7477 NP_109597 R388I not found in SNVbox database
7723 NP_705833 L272I not found in SNVbox database
605 NP_705833 E404K not found in SNVbox database
1622 NP_705833 L435S not found in SNVbox database
3541 NP_705833 N557K not found in SNVbox database
3871 NP_705833 D8H not found in SNVbox database
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr10:52595936 G>A maps to NM_138932.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:7383055 A>C maps to NM_145891.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AJ-01A-21D-A12Q-09 chr16:7383010 G>A maps to NM_145891.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr16:7568360 G>C maps to NM_145891.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr12:9246089 C>T maps to NM_000014.4 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr12:9251297 G>A maps to NM_000014.4 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr12:9254261 G>T maps to NM_000014.4 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr12:9221428 G>A maps to NM_000014.4 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr12:9242988 C>T maps to NM_000014.4 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:8975285 A>C maps to NM_144670.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr12:9006835 T>C maps to NM_144670.3 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr12:8998790 C>T maps to NM_144670.3 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr12:8995941 C>T maps to NM_144670.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr12:8975819 C>A maps to NM_144670.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr12:8998091 A>T maps to NM_144670.3 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr22:43089315 G>C maps to NM_017436.4 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:137843657 G>A maps to NM_016161.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BD-01A-11W-A050-09 chr12:53714437 G>A maps to NM_015665.5 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:125558449 C>T maps to NM_023928.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr12:125550165 C>A maps to NM_023928.3 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:151545639 G>T maps to NM_001086.2 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr3:151535238 C>A maps to NM_001086.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr4:170991749 G>A maps to ENST00000509167 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06P-01A-11W-A019-09 chr4:170988515 G>A maps to ENST00000509167 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:171009668 A>C maps to ENST00000509167 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:69723195 A>C maps to NM_014911.3 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:69747978 T>G maps to NM_014911.3 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:69723168 C>T maps to NM_014911.3 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:69736496 G>T maps to NM_014911.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:69759246 G>A maps to NM_014911.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:69746259 A>G maps to NM_014911.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr17:74464755 G>T maps to NM_001166579.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr17:74466050 G>T maps to NM_001166579.1 *253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:70295060 C>G did not map to a codon.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr16:70295011 G>A maps to ENST00000418685 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr16:70296392 C>T maps to ENST00000418685 L517L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AN-A0FX-01A-11W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr17:41103845 T>G maps to NM_001136042.2 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr17:41113323 C>G maps to NM_001136042.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:105948529 C>T maps to NM_015423.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:121769563 G>A maps to NM_005763.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr16:8857981 G>A maps to NM_001127448.1 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:8862751 A>C maps to NM_001127448.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:8841991 C>T maps to NM_001127448.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr16:8862090 C>T maps to NM_001127448.1 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr9:107584790 C>A maps to NM_005502.3 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr9:107562236 G>A maps to NM_005502.3 I1602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr17:67190106 G>A maps to NM_080282.3 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr17:67181630 G>A maps to NM_080282.3 I828I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr17:67183896 C>T maps to NM_080282.3 W752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr17:67212356 C>A did not map to a codon.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr2:215896642 G>A maps to NM_015657.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr2:215839539 G>A maps to NM_173076.2 F1810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:216002877 A>C maps to NM_173076.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:215851423 G>A maps to NM_173076.2 I1335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr2:215831625 G>A maps to NM_173076.2 L1944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr2:215818579 G>A maps to NM_173076.2 L2215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr7:48335358 T>G maps to NM_152701.3 L3006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:48319378 C>G maps to NM_152701.3 S2863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr7:48311642 T>C maps to NM_152701.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:48319346 C>T maps to NM_152701.3 F2852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:48321035 C>T maps to NM_152701.3 L2941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr7:48511180 T>C maps to NM_152701.3 D4320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr7:48431571 C>T maps to NM_152701.3 G3903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr7:48545980 C>T maps to NM_152701.3 D4447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:48311832 T>A maps to NM_152701.3 L857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr7:48567932 T>A maps to NM_152701.3 T4782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:48266956 C>T maps to NM_152701.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:48626865 A>G maps to NM_152701.3 K4874K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:48313841 C>T maps to NM_152701.3 L1527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:48316002 C>G maps to NM_152701.3 S2247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:48237924 C>T maps to NM_152701.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr7:48308664 C>G maps to NM_152701.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:139912042 G>A maps to ENST00000355090 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R3-01A-31D-A14K-09 chr9:139905719 G>A maps to ENST00000355090 L1977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr9:139911973 C>T maps to ENST00000355090 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr16:2345607 G>C maps to NM_001089.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:2331099 C>T maps to NM_001089.2 L1429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24M-01A-11D-A167-09 chr16:2345721 C>T maps to NM_001089.2 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr16:2339578 G>T maps to NM_001089.2 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr1:94522222 G>A maps to NM_000350.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:94577115 C>T maps to NM_000350.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:94543383 A>C maps to NM_000350.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:94543392 A>C maps to NM_000350.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:94480236 G>A maps to NM_000350.2 V1774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:94488946 T>C maps to NM_000350.2 E1554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr1:94481380 C>G maps to NM_000350.2 V1742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:67310504 G>A maps to ENST00000392677 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr17:67283781 A>G maps to ENST00000392677 H671H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:67079432 A>C maps to NM_080284.2 G1465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:67080463 T>G maps to NM_080284.2 S1431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:67083573 C>A maps to NM_080284.2 E1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:67119455 C>A maps to NM_080284.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:67102266 T>C maps to NM_080284.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr17:67080497 T>C did not map to a codon.
Sequencing variant TCGA-E9-A1RD-01A-11D-A159-09 chr17:67081185 C>T maps to NM_080284.2 A1389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr17:67081245 C>T maps to NM_080284.2 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A4E0-01A-12D-A25Q-09 chr17:67080626 C>T maps to NM_080284.2 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr19:1045034 C>G maps to NM_019112.3 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:66871834 A>C maps to NM_007168.2 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:66872766 A>C did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr17:66891113 C>T maps to NM_007168.2 Q895Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08J-01A-11W-A019-09 chr17:66872767 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:66913592 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:66920855 C>T maps to NM_007168.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:66872813 C>T maps to NM_007168.2 Q1370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr17:66981199 C>T maps to NM_080283.3 K1426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:67047216 G>A maps to NM_080283.3 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr7:87135239 C>T maps to NM_000927.3 T1203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr7:87175253 T>C maps to NM_000927.3 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr7:87225096 G>A maps to NM_000927.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:87179301 C>T maps to NM_000927.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr7:87179585 C>T maps to NM_000927.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:87178678 C>T maps to NM_000927.3 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr7:87175262 G>A maps to NM_000927.3 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr7:87225123 T>C maps to NM_000927.3 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr7:87144684 C>T maps to NM_000927.3 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:87148736 G>A maps to NM_000927.3 F944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:229683294 G>C maps to NM_012089.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:169814581 C>T maps to NM_003742.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:169847320 C>A maps to NM_003742.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:169825986 A>G maps to NM_003742.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr2:169870850 T>A maps to NM_003742.2 K38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr2:169780188 C>T maps to NM_003742.2 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr2:169869944 G>A maps to NM_003742.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:169780193 C>A maps to NM_003742.2 E1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr7:87060833 C>T maps to NM_018849.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:87037514 G>A maps to NM_018849.2 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:87041263 G>A maps to NM_018849.2 R957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr7:87042988 C>T maps to NM_018849.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr7:87069529 G>T maps to NM_018849.2 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr7:20793122 T>C maps to NM_001163941.1 S1190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:20685386 C>T maps to NM_001163941.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr7:20668354 T>C maps to NM_001163941.1 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:220077976 G>A maps to NM_005689.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:220080802 G>C maps to NM_005689.2 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:74289281 A>C did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:74289262 C>A did not map to a codon.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr23:74318815 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr23:74296385 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:74296458 T>C did not map to a codon.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr23:74273322 T>C did not map to a codon.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr23:74296483 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr7:150732798 C>T maps to ENST00000297504 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr12:123419950 G>A maps to NM_203444.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr16:16200630 C>T maps to ENST00000399408 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr16:16150132 G>A maps to ENST00000399408 W553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:16150142 G>A maps to ENST00000399408 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr16:16150073 G>A maps to ENST00000399408 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:16101737 C>G maps to ENST00000399408 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr16:16208803 C>A maps to ENST00000399408 I1097I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr6:43403562 C>G maps to NM_033450.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ST-01A-12D-A099-09 chr16:48204013 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:48221245 G>C maps to NM_032583.3 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:48248818 G>A maps to NM_032583.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr16:48172232 T>C maps to NM_033226.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr16:48139205 G>A maps to NM_033226.2 V839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:48139205 G>A maps to NM_033226.2 V839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr16:48173211 C>T maps to NM_033226.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr10:101591522 C>T maps to NM_000392.3 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr10:101601846 C>G maps to NM_000392.3 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr13:95830022 G>A maps to NM_005845.3 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr13:95861806 C>A maps to NM_005845.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr3:183685545 C>T maps to NM_005688.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:183667818 C>T maps to NM_005688.2 W1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:16284022 G>A maps to NM_001171.5 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:16315480 C>A maps to NM_001079528.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr16:16276376 G>A maps to NM_001171.5 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr16:16284083 G>A maps to NM_001171.5 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr11:17449889 T>G maps to ENST00000302539 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr11:17434215 G>A maps to ENST00000302539 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:17416822 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:17483288 G>A maps to ENST00000302539 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr11:17496467 C>A maps to ENST00000302539 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr12:22025599 G>A maps to NM_005691.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr12:21962816 C>T maps to NM_005691.2 K1428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr23:153008482 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:153001903 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1L6-01A-11D-A13L-09 chr23:153005553 A>G did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:152991468 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr23:152994736 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr12:39947820 G>A maps to NM_005164.3 Q706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr1:94955531 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:74764730 C>G maps to NM_005050.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr14:74758988 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:30558153 T>G maps to NM_001025091.1 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:30546269 G>C maps to NM_001025091.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:30553698 G>A maps to NM_001025091.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr7:150921060 C>T maps to NM_005692.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:150923403 G>A maps to NM_005692.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr3:183911227 C>T maps to NM_018358.2 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:43691252 C>T maps to NM_004915.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr21:43711693 G>A maps to NM_004915.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr21:43714662 C>T maps to NM_004915.3 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr21:43645821 G>A maps to NM_004915.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr21:43716450 C>G maps to NM_004915.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr4:89060990 G>A maps to NM_004827.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr11:119028975 C>T maps to NM_001142505.1 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:119029032 C>T maps to NM_001142505.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:119029575 C>G maps to NM_001142505.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr11:119027389 T>A did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr2:44065695 G>C maps to NM_022436.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:44073412 G>A maps to NM_022437.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr2:44071746 G>A maps to NM_022437.2 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr2:44102319 C>T maps to NM_022437.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr3:111710567 G>T maps to NM_018394.2 *307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr3:111700646 G>A maps to NM_018394.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr7:73151592 A>T maps to NM_148912.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:25295603 C>T maps to NM_015600.3 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:25290080 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:19231712 C>A maps to NM_138340.4 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr14:23078767 G>A maps to NM_022060.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr3:43740767 G>A maps to NM_016006.4 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:17411903 G>T maps to NM_024527.4 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr3:100595365 G>T maps to ENST00000471714 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:100617685 C>T maps to ENST00000471714 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr9:133750253 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr1:179079444 T>A maps to NM_007314.3 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:179095775 C>T maps to NM_007314.3 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr10:116233706 C>T maps to ENST00000277895 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr4:8034383 C>T maps to NM_001130087.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:148630047 C>T maps to NM_014945.2 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr9:136131415 G>A maps to NM_020469.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr9:136131307 G>A maps to NM_020469.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr7:150553776 G>A maps to ENST00000416793 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:150558195 C>A maps to ENST00000416793 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr7:150557702 C>T maps to ENST00000416793 N676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr17:962029 G>C maps to NM_021962.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr17:960313 C>T maps to NM_021962.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr17:913993 G>C maps to NM_021962.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr17:1012302 C>T maps to NM_001092.3 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr17:953382 C>T maps to NM_021962.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr8:107781890 C>T maps to NM_139166.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr8:107773357 G>C maps to NM_139166.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:26598832 C>G maps to NM_013375.2 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr3:127395141 C>T maps to NM_172027.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:34186250 G>C maps to NM_145804.2 S657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr11:34192618 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:35604996 A>C maps to NM_198834.1 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr17:35453999 A>G maps to NM_198834.1 P2274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:35454053 C>A maps to NM_198834.1 L2256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:35518823 G>A maps to NM_198834.1 S1740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr17:35641833 G>A maps to NM_198834.1 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:35615232 G>A maps to NM_198834.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:35605518 T>A maps to NM_198834.1 K721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:109690860 T>G maps to NM_001093.3 G1981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:109577275 C>A maps to NM_001093.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:109700239 C>T maps to NM_001093.3 I2251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:109671747 C>T maps to NM_001093.3 L1415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:109700260 C>T maps to NM_001093.3 L2258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr12:109654461 G>T maps to NM_001093.3 V1130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr12:109694026 G>T maps to NM_001093.3 V2083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:112140023 T>G maps to NM_001136538.1 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:112184920 G>A maps to NM_001136538.1 Q806Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:132358389 C>T maps to NM_032169.4 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:7124145 C>T maps to ENST00000356839 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:89388736 T>G maps to NM_013227.3 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr15:89416110 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:89401539 C>A maps to NM_013227.3 S1908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr15:89388986 G>T maps to NM_013227.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr15:89401122 A>T maps to NM_013227.3 A1769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr17:7251306 G>A maps to NM_014716.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr3:195102672 G>A maps to NM_012287.5 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:108009650 G>A maps to NM_000019.3 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr6:160189619 T>A maps to NM_005891.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr6:160189601 C>T maps to NM_005891.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr17:43220875 T>C maps to NM_001135706.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr10:27529275 C>T maps to ENST00000375888 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr10:27486359 C>G maps to ENST00000375888 *535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:180399375 C>A maps to NM_032360.3 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr17:31439027 G>A maps to NM_183377.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr17:31415883 C>T maps to NM_183377.1 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:50472220 A>C maps to NM_020039.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HU-01A-11W-A050-09 chr2:220402755 T>C maps to NM_018674.4 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:44102733 C>T maps to NM_032592.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr11:44069729 G>A maps to NM_001031854.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:44075056 G>A did not map to a codon.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr17:61562386 C>A maps to NM_152830.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr17:61570871 C>T maps to NM_000789.3 F996F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr17:61557229 C>T maps to NM_000789.3 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr17:61557695 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:15591570 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15596417 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15607527 A>C did not map to a codon.
Sequencing variant TCGA-E2-A15L-01A-11D-A12B-09 chr23:15610357 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:76701615 C>T maps to NM_018367.5 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:23532179 T>G maps to NM_014977.3 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr14:23530618 C>T maps to NM_014977.3 E1162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:23532277 A>G maps to NM_014977.3 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:40042516 A>C maps to ENST00000401700 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr17:40042363 C>T did not map to a codon.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr7:96810328 T>C maps to NM_020186.2 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr9:32431798 T>C maps to NM_002197.2 Y603Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr9:32427426 C>T maps to NM_002197.2 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr22:41923398 C>T maps to ENST00000396512 I712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr1:55067004 C>A maps to NM_015547.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr14:74042018 A>G maps to NM_006821.4 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr14:74058809 C>T maps to NM_152331.3 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:23748990 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr23:23723972 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:73945641 C>T maps to NM_004035.6 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:47269661 G>C maps to NM_001610.2 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:141011695 C>T maps to NM_001037172.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr19:51297065 G>C maps to NM_033068.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr12:6753325 G>T maps to NM_032489.2 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr12:6756500 G>T maps to NM_032489.2 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr23:70832364 G>C did not map to a codon.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr23:70828944 A>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70800699 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70823862 G>A did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:70832260 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr23:70832731 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:125547820 C>A maps to NM_001612.5 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr15:78485846 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:78471058 C>T maps to NM_015162.4 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr15:78475049 G>A maps to NM_015162.4 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr19:6183235 C>T maps to NM_030924.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr17:48538640 C>T maps to ENST00000427954 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:185724637 G>A maps to NM_001995.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr4:185678827 C>T maps to NM_001995.2 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr23:108911439 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:108926402 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:108926711 T>C did not map to a codon.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr23:108921589 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:108926089 A>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:108924258 G>A did not map to a codon.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr23:108926448 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:114154736 A>C maps to NM_016234.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr10:114168280 T>C did not map to a codon.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr10:114172995 C>T maps to NM_016234.3 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:131323824 G>A maps to NM_001009185.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr5:131323821 G>T maps to NM_001009185.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr16:20636768 G>C maps to NM_052956.2 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr16:20487094 G>A maps to NM_001010845.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr16:20554292 C>T maps to NM_182617.3 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr16:20576154 G>A maps to NM_182617.3 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:20554524 C>T maps to NM_182617.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:20788846 C>T maps to NM_005622.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:7480956 G>A maps to NM_001080454.1 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr12:7473394 T>G maps to NM_001080454.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr16:20442396 T>C did not map to a codon.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr16:20442355 T>A maps to NM_017888.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr16:20442561 C>T maps to NM_017888.2 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr16:20442561 C>T maps to NM_017888.2 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr16:20422835 C>A maps to NM_017888.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr16:20448430 C>T maps to NM_017888.2 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr16:20429439 C>T maps to NM_017888.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr20:24988538 G>A maps to NM_032501.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr20:33502155 C>T maps to NM_001076552.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr12:81610678 G>C did not map to a codon.
Sequencing variant TCGA-A8-A07Z-01A-11W-A019-09 chr12:81503341 T>C maps to NM_024560.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:81647430 C>T maps to NM_024560.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr1:229567560 G>A maps to NM_001100.3 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:229568110 C>T maps to NM_001100.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr1:229568793 G>A maps to NM_001100.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:5568350 C>A did not map to a codon.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr7:5569206 G>T maps to NM_001101.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:56777573 G>A maps to NM_001017992.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:74136180 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr3:179291211 C>G maps to NM_004301.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr7:100245119 T>A maps to NM_016188.4 K236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:111625372 G>T maps to NM_006687.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr9:111625618 C>T maps to NM_006687.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr9:111617310 C>T maps to NM_006686.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr19:8808019 G>A maps to NM_178525.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr19:8807971 G>A maps to NM_178525.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr14:69343864 G>C maps to NM_001130004.1 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:69378870 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr14:69387786 G>A maps to NM_001130004.1 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:236908061 C>T maps to NM_001103.2 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:236912557 G>A maps to NM_001103.2 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:236912432 A>T maps to NM_001103.2 K509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr1:236918428 G>T maps to NM_001103.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr1:236914953 T>A did not map to a codon.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr1:236924430 C>G maps to NM_001103.2 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:236914891 C>T maps to NM_001103.2 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15E-01A-11D-A12B-09 chr1:236883432 C>A maps to NM_001103.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr11:66318786 T>C maps to NM_001104.1 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr11:66322630 C>T maps to NM_001104.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:66318768 C>T maps to NM_001104.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr11:66322679 G>T did not map to a codon.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr19:39220041 C>T maps to NM_004924.3 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:39217679 C>T maps to NM_004924.3 D758D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr2:65480994 C>T maps to NM_001005386.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr2:65480892 A>G maps to NM_001005386.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:114699933 G>T maps to NM_005721.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr20:37400365 C>T maps to NM_024855.3 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr20:37380923 C>A maps to NM_024855.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr12:100604126 C>G maps to NM_022496.3 Y190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr3:53908255 A>C maps to NM_022899.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:53902778 G>A maps to NM_022899.4 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:127185210 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:127185608 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr23:127185891 T>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:127185425 C>G did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:127185865 A>G did not map to a codon.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr23:127185326 C>G did not map to a codon.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr2:158655951 G>T maps to NM_001111067.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr12:52370171 C>T maps to NM_020328.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:52370121 G>T maps to NM_020328.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr12:52379130 C>T maps to NM_020328.3 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr12:52387770 A>T maps to NM_020328.3 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr12:52374848 G>A maps to NM_020328.3 W226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:158406836 A>C maps to NM_145259.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:158412649 G>A maps to NM_145259.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr2:158412842 T>G maps to NM_145259.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr2:148657334 T>G maps to NM_001616.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FX-01A-11D-A13L-09 chr3:38519698 C>T maps to NM_001106.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JE-01A-11D-A13L-09 chr3:38520669 A>T maps to NM_001106.3 K240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr20:43255194 C>T maps to NM_000022.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr4:123304954 T>G maps to NM_139243.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:84228108 T>C maps to NM_139174.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:43639254 T>C maps to ENST00000422466 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:58913776 A>C maps to NM_001110.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr10:127760204 C>T maps to NM_003474.4 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr1:155029768 C>A maps to NM_207197.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr2:9634771 G>A maps to NM_003183.4 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr2:9633945 A>G maps to NM_003183.4 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:39467046 C>A maps to NM_014237.2 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr8:39495189 C>T maps to NM_014237.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr5:156907993 G>C maps to ENST00000394020 S909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:156991408 C>A maps to ENST00000430702 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:156921771 C>T maps to ENST00000430702 E544E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D8-A27G-01A-11D-A16D-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:156997986 T>C maps to ENST00000432888 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr8:39695671 G>A maps to NM_001464.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P5-01A-11D-A142-09 chr8:39695677 G>A maps to NM_001464.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr8:39627084 A>G maps to NM_001464.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:70925043 G>C maps to NM_003813.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:70924506 A>C maps to NM_003813.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr14:70924843 C>T maps to NM_003813.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr14:70924449 C>T maps to NM_003813.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:87743931 C>G maps to NM_021723.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:87825799 C>T maps to NM_021723.3 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr2:207435498 G>T maps to NM_003812.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L8-01A-11D-A13L-09 chr2:207406801 A>G maps to NM_003812.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R3-01A-31D-A14K-09 chr2:207406858 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:24199143 T>G maps to NM_014265.4 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:175896720 C>A maps to NM_014269.4 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr4:175897707 G>A maps to NM_014269.4 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr20:3649961 G>C maps to NM_025220.2 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr20:3655439 G>C maps to NM_025220.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr20:3655265 G>C maps to NM_025220.2 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:24323267 C>A maps to ENST00000380789 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr8:24300019 G>C maps to ENST00000380789 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr8:38961170 T>A maps to NM_003816.2 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr8:24249787 G>A maps to NM_014479.3 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr8:24259484 T>G maps to NM_014479.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr8:24257810 G>A maps to NM_014479.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:24259556 G>A maps to NM_014479.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:28212299 C>T maps to NM_006988.3 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15A-01A-11D-A12B-09 chr21:28214902 G>A maps to NM_006988.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:33576497 T>G maps to NM_030955.2 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:33577082 T>G maps to NM_030955.2 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr9:136319569 C>T maps to NM_139025.3 A1026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr10:72468453 C>T maps to NM_139155.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr10:72520350 G>A maps to NM_139155.2 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr11:130318912 C>T maps to NM_139055.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr11:130340997 T>G did not map to a codon.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr11:130343334 C>T maps to NM_139055.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:5306828 A>C maps to NM_139056.2 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr5:5186342 C>T maps to NM_139056.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr5:5262782 G>A maps to NM_139056.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr5:5242242 T>A maps to NM_139056.2 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr5:5237178 T>C maps to NM_139056.2 D707D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr5:5318311 G>A maps to NM_139056.2 P1159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr15:100537591 G>A maps to NM_139057.2 Q932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr15:100801808 C>A maps to NM_139057.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SU-01A-11D-A099-09 chr16:77326975 G>A maps to NM_199355.2 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:77355033 A>C maps to NM_199355.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr16:77353946 G>A maps to NM_199355.2 I777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr16:77327077 C>T maps to NM_199355.2 E1028E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr16:77398162 G>A maps to NM_199355.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:129001210 G>A maps to NM_133638.3 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr5:128977607 C>T maps to NM_133638.3 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr5:129030516 C>T maps to NM_133638.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr5:129040063 C>T maps to NM_133638.3 R1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr5:178585811 G>A maps to NM_014244.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:43846145 C>T maps to ENST00000389420 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:43825143 T>C maps to ENST00000389420 P1084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr12:43833861 G>A maps to ENST00000389420 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr4:73179509 C>T maps to NM_014243.1 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr4:73161389 G>A maps to NM_014243.1 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr4:73149356 G>A maps to NM_014243.1 S1038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr4:73185062 C>A maps to NM_014243.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:161168096 C>T maps to NM_005099.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:161168057 A>C maps to NM_005099.4 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:161166021 C>T maps to NM_005099.4 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:161161332 G>T maps to NM_005099.4 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr21:28302260 T>C maps to NM_007038.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:28296883 G>A maps to NM_007038.3 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr21:28315780 G>T maps to NM_007038.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr5:64521996 G>A maps to NM_197941.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr15:79064139 G>T maps to ENST00000258883 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr15:79090437 G>A maps to ENST00000258883 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr15:79056046 C>T maps to ENST00000258883 W1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr15:79068548 G>T maps to ENST00000258883 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr11:130286094 G>A maps to NM_007037.4 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr3:64587685 C>T maps to NM_182920.1 R1317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr3:64666905 G>C maps to NM_182920.1 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:64640041 C>A maps to NM_182920.1 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr9:18474247 G>C maps to NM_001040272.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr9:18662041 G>A maps to NM_001040272.4 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr9:18908544 G>A maps to NM_001040272.4 *1763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr9:18775841 G>A maps to NM_001040272.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr9:18892386 G>T maps to NM_001040272.4 R1548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr9:18639297 C>G maps to NM_001040272.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr9:136405813 A>G maps to ENST00000393061 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr15:84611515 C>A maps to NM_207517.2 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr15:84657562 G>A maps to NM_207517.2 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:84373149 G>T maps to NM_207517.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:84539558 G>T maps to NM_207517.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr15:84639384 C>A maps to NM_207517.2 C880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr15:84611368 G>T maps to NM_207517.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr15:84651455 T>C maps to NM_207517.2 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr15:84488588 C>T maps to NM_207517.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr15:84539659 G>A maps to NM_207517.2 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:150528804 C>T maps to ENST00000369039 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:150530561 C>T maps to ENST00000369039 N796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BO-01A-23D-A12B-09 chr19:1507613 G>A maps to NM_213604.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr7:966262 C>T maps to NM_006869.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:29283266 C>T maps to ENST00000394782 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:154561930 G>A maps to ENST00000292205 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr21:46596032 G>A maps to NM_015833.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr10:1246062 G>A maps to NM_018702.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:1279753 G>A maps to NM_018702.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr10:1279720 T>C maps to NM_018702.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr6:143759816 G>A maps to NM_182503.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:140374484 A>G maps to NM_052853.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr7:140373339 C>T maps to NM_052853.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MS-A51U-01A-31D-A25Q-09 chr7:140373766 C>T maps to NM_052853.3 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr7:45717646 C>T maps to NM_021116.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:45701779 C>T maps to NM_021116.2 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr1:167791334 G>A maps to NM_018417.4 Q1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:167873125 C>T maps to NM_018417.4 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr1:167823633 C>G maps to NM_018417.4 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr1:167865857 A>G maps to NM_018417.4 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:167873161 C>T maps to NM_018417.4 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N3-01A-12D-A159-09 chr1:167793765 G>T maps to NM_018417.4 R1334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:7817094 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr5:7520912 C>T maps to NM_020546.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr5:7707848 G>A maps to NM_020546.2 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:7414699 T>C maps to NM_020546.2 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr5:7709445 A>G maps to NM_020546.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr5:7802446 C>G maps to NM_020546.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr5:7820753 C>G maps to NM_020546.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr5:7709481 C>T maps to NM_020546.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:25141244 G>A maps to NM_004036.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr2:25065184 G>A maps to NM_004036.3 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr2:25141735 G>T maps to NM_004036.3 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:24795527 G>A maps to NM_139247.3 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr14:24799202 G>A maps to NM_139247.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr14:24788636 G>T maps to NM_139247.3 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr3:123051482 C>T maps to NM_183357.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr3:123022987 G>T maps to NM_183357.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr12:49167397 C>T maps to NM_015270.3 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:50344680 G>A maps to NM_001114.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr16:50348997 T>C maps to NM_001114.3 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr8:131792943 G>T maps to NM_001115.2 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr8:131826439 G>T maps to NM_001115.2 R930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr8:132051961 G>C maps to NM_001115.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr8:132051877 C>T maps to NM_001115.2 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr16:4164944 G>A maps to NM_001116.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:4016693 C>T maps to NM_001116.3 Q1048Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr16:4042210 G>A maps to NM_001116.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr16:4164420 G>A maps to NM_001116.3 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr7:31104524 C>T maps to ENST00000409489 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:2930126 C>T maps to NM_014189.2 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr4:2930219 G>A maps to NM_014189.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:2900188 G>A maps to NM_014189.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr2:70906009 C>T maps to NM_001185054.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr2:70905997 G>A maps to NM_001185054.1 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:70919585 C>T maps to NM_001185054.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr2:70931512 G>A maps to NM_001185054.1 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr10:111860428 C>T maps to NM_016824.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:100200632 T>C maps to NM_000667.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr4:100232777 G>T maps to NM_000668.4 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:99997595 G>A maps to NM_000671.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr4:100003225 C>G maps to NM_000671.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:3502844 C>T maps to NM_018269.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A425-01A-11D-A243-09 chr3:186572123 C>T maps to NM_004797.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr3:186572474 C>T maps to NM_004797.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:1887037 C>T maps to NM_024551.2 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr10:75960543 G>T maps to NM_006721.2 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr11:10327890 C>G maps to NM_001124.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr20:49508349 G>A maps to NM_181442.1 D967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:77896194 G>T maps to NM_014913.3 E967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:77893625 C>T maps to NM_014913.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr18:77894252 C>A maps to NM_014913.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr18:77895839 C>T maps to NM_014913.3 H848H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B5-01A-21D-A12Q-09 chr18:77895773 C>T maps to NM_014913.3 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr18:77895021 C>T maps to NM_014913.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:203134925 G>A maps to NM_001048230.1 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr22:24829518 G>A maps to NM_000675.4 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr1:112042832 C>T maps to NM_000677.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr15:73044811 C>T maps to NM_031284.4 W454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:73044752 G>A maps to NM_031284.4 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr3:119306586 C>A maps to NM_001125.2 C312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr13:114107722 C>T maps to NM_138430.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:36557533 G>A maps to NM_017825.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr8:26722330 G>T maps to ENST00000356368 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr8:26627932 G>A maps to ENST00000356368 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr8:26722153 G>A maps to ENST00000356368 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr20:4229169 C>T maps to NM_000678.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:4229076 G>A maps to NM_000678.3 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr10:112838986 C>T maps to NM_000681.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:148206708 G>A maps to NM_000024.5 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:37823789 C>T maps to NM_000025.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr22:40755271 G>A maps to ENST00000428371 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr1:244615098 G>T maps to NM_001126.3 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr14:105207542 G>A maps to NM_199165.1 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:44146361 A>C maps to NM_001129.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:44151650 T>G did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr7:44153559 C>G maps to NM_001129.3 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:19653049 C>T maps to NM_001114176.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr4:7802237 C>T maps to NM_001134647.1 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:148689610 G>A maps to NM_152406.2 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:116070168 C>A maps to NM_001001936.1 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:116060264 G>C maps to NM_001001936.1 S576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:116100469 C>A maps to NM_001001936.1 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:87968166 A>C maps to NM_001166693.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:87968532 A>C maps to NM_001166693.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr4:87967341 G>A maps to NM_001166693.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr4:87968538 C>T maps to NM_001166693.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr23:147744199 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:147891429 G>A did not map to a codon.
Sequencing variant TCGA-A2-A259-01A-11D-A16D-09 chr23:148039965 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr23:148055075 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:147743619 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:147744060 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:148039952 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:148039961 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:148037454 G>T did not map to a codon.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr23:147800747 A>G did not map to a codon.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr23:147744009 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:147733532 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:148059970 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:148037135 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr23:148037945 C>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:148062290 G>C did not map to a codon.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr23:148037436 T>C did not map to a codon.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr23:148037857 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr23:147743941 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr23:148037759 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:148037680 G>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:148037887 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr23:147743845 C>A did not map to a codon.
Sequencing variant TCGA-C8-A133-01A-32D-A12B-09 chr23:148037577 G>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:148055003 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr23:147733595 G>T did not map to a codon.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr23:147743963 C>T did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr2:100182031 G>A maps to NM_001025108.1 I1037I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr2:100194862 C>T maps to NM_001025108.1 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr2:100210556 C>T maps to NM_001025108.1 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr5:132270411 G>A maps to NM_014423.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:132270039 T>G maps to NM_014423.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr5:132228738 C>T maps to NM_014423.3 K793K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr5:132270372 C>T maps to NM_014423.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr18:12367316 A>C maps to NM_006796.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:236839415 C>A maps to NM_001037131.1 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:236659076 G>T maps to NM_001037131.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:58126637 G>C maps to NM_001122772.1 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YI-01A-21D-A23C-09 chr10:46342648 T>C maps to ENST00000355953 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr10:46342648 T>C maps to ENST00000355953 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr10:75456919 A>C maps to NM_001144000.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr10:51769057 G>A maps to NM_001077665.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr10:51465570 G>A maps to ENST00000416142 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr10:51225622 A>G maps to ENST00000425119 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr15:86810229 A>G maps to NM_152336.2 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr15:86838638 C>T maps to NM_152336.2 R746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr15:87531305 C>T maps to NM_152336.2 L1058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr15:86702162 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr15:87097659 G>A maps to NM_152336.2 E916E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:47698890 A>G maps to ENST00000357610 H693H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:49711500 G>A maps to NM_032785.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr7:100159885 C>T maps to NM_006076.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:100327047 T>G maps to NM_000645.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:100350167 C>T maps to ENST00000311030 R865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr1:100350008 T>C did not map to a codon.
Multiple mappings detected for codon TCGA-B6-A402-01A-11D-A23C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr6:32138200 C>T did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:161574408 G>A maps to NM_020133.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr4:84516077 C>T maps to NM_032717.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:16834590 G>A maps to ENST00000223274 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:88207585 A>C maps to ENST00000395847 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr9:88233909 G>A maps to ENST00000395847 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:88200481 G>A maps to ENST00000395847 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:115304210 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:115303624 C>A did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:115304468 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:11806253 C>T maps to NM_001040196.1 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr2:241810812 G>A maps to NM_000030.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr5:35013130 C>T maps to NM_031900.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr1:247040512 C>A maps to ENST00000428671 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr1:247014468 C>G maps to ENST00000428671 V1651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:247024357 C>T maps to ENST00000428671 P1363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:247004161 G>A maps to ENST00000428671 N2287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr1:247076642 C>T maps to ENST00000428671 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr1:247079595 C>A maps to ENST00000428671 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:247031054 C>T maps to ENST00000428671 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:247030634 T>C maps to ENST00000428671 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:247053341 T>C maps to ENST00000428671 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr1:247027258 T>C maps to ENST00000428671 E1207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr20:32878391 G>A maps to NM_000687.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr20:32873244 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:110563429 C>T maps to NM_006621.4 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr7:129064780 C>T maps to NM_015328.3 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr1:27876097 C>A maps to NM_001029882.2 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr1:27878125 G>A maps to NM_001029882.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:135776912 G>A maps to NM_017651.4 R435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr6:135787469 A>T maps to NM_017651.4 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr6:135787285 G>A maps to NM_017651.4 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr11:62285190 G>A maps to NM_001620.1 I5566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr11:62300538 C>A maps to NM_001620.1 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62285136 A>C maps to NM_001620.1 G5584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62285313 A>C maps to NM_001620.1 G5525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62290188 A>C maps to NM_001620.1 G3900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62292534 A>C maps to NM_001620.1 G3118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62292567 A>C maps to NM_001620.1 G3107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62292918 A>C maps to NM_001620.1 G2990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62294070 A>C maps to NM_001620.1 G2606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62295255 A>C maps to NM_001620.1 G2211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62297838 A>C maps to NM_001620.1 G1350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62298222 A>C maps to NM_001620.1 G1222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:62290071 C>T maps to NM_001620.1 K3939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:62296326 C>T maps to NM_001620.1 K1854K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:62285901 G>C maps to NM_001620.1 L5329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr11:62295894 C>T maps to NM_001620.1 L1998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr11:62297976 T>C maps to NM_001620.1 G1304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:62300601 C>T maps to NM_001620.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr11:62299854 T>C maps to NM_001620.1 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr14:105417179 G>C maps to NM_138420.2 L1536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr14:105415952 G>A maps to NM_138420.2 P1945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr14:105410060 C>T maps to NM_138420.2 K3909K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr14:105420634 G>A maps to NM_138420.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr14:105413153 G>A maps to NM_138420.2 D2878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:105410729 G>A maps to NM_138420.2 L3686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:105416669 G>A maps to NM_138420.2 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:105409444 G>A maps to NM_138420.2 L4115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr14:105416975 G>A maps to NM_138420.2 D1604D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr14:105409679 G>A maps to NM_138420.2 L4036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr14:105414689 G>T maps to NM_138420.2 L2366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr14:105409721 G>A maps to NM_138420.2 S4022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:105410651 G>T maps to NM_138420.2 P3712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr14:105418952 C>G maps to NM_138420.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr14:105406829 G>C maps to NM_138420.2 L4986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr14:105412343 G>A maps to NM_138420.2 F3148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr5:413493 A>G maps to NM_020731.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:186338514 A>G maps to ENST00000273784 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr1:222885593 G>A maps to NM_022831.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr1:222876530 G>A maps to NM_022831.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr1:222849465 G>A maps to NM_022831.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr23:129263971 G>C did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:129290550 G>C did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr23:129263588 A>T did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:129299562 A>C did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr6:143486275 A>T maps to NM_016108.2 K119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:106967918 G>T maps to NM_001624.2 G538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr6:106967047 T>A maps to NM_001624.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr6:106968545 A>T maps to NM_001624.2 K747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:159033296 A>G maps to NM_004833.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:67250640 C>T maps to NM_003977.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:65656504 C>T maps to NM_013410.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:77987613 G>T maps to NM_174858.1 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:55184057 T>G maps to ENST00000427138 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr17:55197672 C>T maps to ENST00000427138 Y942Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr17:55183676 G>A maps to ENST00000427138 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr13:42876456 C>G maps to NM_016248.2 S1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:42874232 C>T maps to NM_016248.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr13:42882611 C>T maps to NM_016248.2 Q1714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:151671391 T>G maps to NM_005100.3 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr6:151672993 G>A maps to NM_005100.3 Q1156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:151670276 G>T maps to NM_005100.3 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:86124247 A>C maps to NM_006738.4 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr15:86124220 G>A maps to NM_006738.4 K974K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:86286811 C>A maps to NM_006738.4 A2720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HU-01A-11W-A050-09 chr15:86123002 G>A maps to NM_006738.4 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr15:86077098 C>T maps to NM_006738.4 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr15:86207933 C>A maps to NM_006738.4 S1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr15:86266396 G>A maps to NM_006738.4 K2201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr23:119037309 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr23:119037536 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:119037308 A>G did not map to a codon.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr9:112898772 C>T maps to NM_007203.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:112898609 A>C maps to NM_007203.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr12:4747363 T>G did not map to a codon.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr12:4737716 G>A maps to NM_006422.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:49957297 A>T did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:49957661 C>T did not map to a codon.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr23:49958364 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:49958209 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr23:49957445 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr23:49957344 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr23:49957910 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:49957749 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1JH-01A-11D-A188-09 chr23:49958928 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:49957211 C>A did not map to a codon.
Sequencing variant TCGA-E2-A1L8-01A-11D-A13L-09 chr23:49958244 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr23:49957993 T>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:64935420 T>G maps to NM_004857.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:64936323 T>A maps to NM_004857.3 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr14:33290717 G>A maps to NM_004274.4 E1233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr19:15511969 G>C maps to NM_014371.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr7:91652212 C>G maps to NM_005751.4 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:91729155 T>G maps to NM_005751.4 Y3623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:91659281 A>T maps to NM_005751.4 K1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:91726194 C>T maps to NM_005751.4 R3308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr7:91630766 C>G maps to NM_005751.4 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr7:91643581 A>G maps to NM_005751.4 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr7:91667986 A>G maps to NM_005751.4 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr6:109820404 G>A maps to NM_001145128.2 Q1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:109816582 C>T maps to NM_001145128.2 P1792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:109837845 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr1:39463916 C>T maps to NM_024595.2 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr9:117120302 G>A maps to NM_030767.4 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:109359766 G>C maps to NM_152763.3 S761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:109380247 G>C maps to NM_152763.3 S487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:109394985 C>A maps to NM_152763.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:109359683 C>A maps to NM_152763.3 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr7:134136357 C>A maps to NM_001628.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:5043770 G>A maps to NM_001354.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr10:5043761 G>A maps to NM_001354.4 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr10:4884036 G>A maps to NM_001040177.1 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:4879733 G>A maps to NM_001040177.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:4889401 C>T maps to NM_001040177.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:19595189 C>T maps to NM_201252.3 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr14:105238713 C>A maps to NM_001014432.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr19:50373174 C>T maps to ENST00000391835 *277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr19:40761099 G>A maps to NM_001626.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr19:40741972 C>T maps to NM_001626.3 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr1:243727149 A>G maps to NM_005465.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr1:243828161 G>A maps to NM_005465.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:53526407 T>C maps to ENST00000425875 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr9:116155797 T>C maps to ENST00000277315 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:52248108 C>T maps to ENST00000441729 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr3:52239959 G>C maps to ENST00000441729 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr23:55039949 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:55052359 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:55046762 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:55052254 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr23:55046895 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr23:55042137 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr23:55052440 C>G did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:55046842 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:74285357 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:105243279 G>T maps to NM_001627.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr3:105253612 C>T maps to NM_001627.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr19:49964939 G>C maps to NM_153329.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:97366658 C>A maps to NM_002860.3 G750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr9:75545878 C>T maps to NM_000689.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr9:75516162 G>C maps to NM_000689.3 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr9:75540495 C>T maps to NM_000689.3 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr9:75540486 A>C maps to NM_000689.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr9:75533708 C>T maps to NM_000689.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr15:58284995 G>T maps to NM_003888.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:101434159 G>A maps to NM_000693.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:101433159 C>T maps to NM_000693.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:101438316 C>T maps to NM_000693.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:125879693 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:125874321 C>A maps to ENST00000273450 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:125876305 C>T maps to ENST00000273450 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:125874328 C>T maps to ENST00000273450 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr12:105456677 G>A maps to NM_001034173.3 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr12:105443687 G>A maps to NM_001034173.3 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr12:105418255 A>C maps to NM_001034173.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:19555063 C>T maps to NM_001031806.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:19576545 G>A maps to NM_001031806.1 *509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:67787215 G>A maps to NM_001161473.1 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr11:67786654 G>A maps to NM_001161473.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr11:67433784 A>C did not map to a codon.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr6:24528349 G>C maps to NM_170740.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr6:135271074 C>T maps to NM_022568.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr1:165667702 G>A maps to NM_000696.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr9:104187271 G>A maps to NM_000035.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:26902012 A>C maps to NM_005165.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WT-01A-11D-A10G-09 chr12:34177060 T>G maps to NM_032834.3 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:34175614 C>T maps to NM_032834.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr12:34179102 A>G maps to NM_032834.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr12:38712082 A>C maps to NM_001013620.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GY-01A-11W-A071-09 chr13:52586562 C>T maps to NM_001004127.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr22:50301579 G>A maps to NM_024105.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr23:110970224 G>A did not map to a codon.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:110970672 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:110970142 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:111003083 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr23:110951472 T>C did not map to a codon.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr23:111003140 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:110964850 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:63876979 A>T maps to ENST00000263440 K222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr11:77812018 C>T maps to NM_024079.4 K524K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E2-A1LH-01A-11D-A14G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:29430128 G>A maps to NM_004304.3 Y1282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr2:29416320 G>A maps to NM_004304.3 N1544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr2:29432664 G>A maps to NM_004304.3 R1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr2:29917809 C>T maps to NM_004304.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:107403093 C>T maps to ENST00000417449 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:107396318 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0CZ-01A-11W-A050-09 chr2:3721690 T>C maps to ENST00000403787 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T7-01A-21D-A099-09 chr2:3729304 T>C did not map to a codon.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr2:73799945 G>T maps to NM_015120.4 E3647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:73799857 T>G maps to NM_015120.4 G3617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:73747066 G>A maps to NM_015120.4 Q3234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:73677667 G>A maps to NM_015120.4 E1337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr2:73646387 G>A maps to NM_015120.4 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr2:73718056 C>T maps to NM_015120.4 Q2990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:6904979 A>C maps to NM_000697.2 P337P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AC-A23H-01A-11D-A159-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:6905054 G>A maps to NM_000697.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:6913413 C>G maps to NM_000697.2 S594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr17:7951169 T>C maps to NM_001141.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J7-01A-11W-A050-09 chr10:45878088 G>A maps to NM_000698.2 W103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr17:8000124 C>G did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr17:8012649 G>A maps to ENST00000380149 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr4:113352475 C>G maps to NM_025144.3 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:113353096 A>C maps to NM_025144.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr18:56246891 A>C maps to NM_052947.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:56203455 G>A maps to NM_052947.3 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr18:56202121 G>C maps to NM_052947.3 S1766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:85384060 A>C maps to NM_020778.4 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr15:85382268 T>C maps to NM_020778.4 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr2:233244600 G>T maps to NM_001632.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr2:233271845 G>A maps to NM_031313.2 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:202611348 A>C maps to NM_020919.3 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:202569271 C>T maps to NM_020919.3 E1581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr2:202590161 T>C maps to NM_020919.3 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr2:202619362 C>T maps to NM_020919.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr2:202483805 G>A maps to NM_001168221.1 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:202358221 C>A maps to NM_001168221.1 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:202358407 C>A maps to NM_001168221.1 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr2:202356524 T>C maps to NM_001168221.1 Q1513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr2:202410311 C>T maps to NM_001168221.1 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:203817331 A>C maps to NM_024744.14 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr2:203826060 T>A maps to NM_024744.14 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:44289130 C>T maps to NM_021926.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr11:44289063 G>A maps to NM_021926.3 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr11:44297152 C>T maps to NM_021926.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr8:11188821 G>A maps to NM_054028.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:33998839 A>C maps to NM_001167595.1 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:71465263 C>A maps to NM_016519.4 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr4:71471930 A>G maps to NM_016519.4 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:116823785 C>T maps to NM_001633.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:46455179 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr11:46564006 C>T maps to ENST00000458649 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr11:46563999 C>A maps to ENST00000458649 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:46563793 G>T maps to ENST00000458649 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr11:46567260 C>T maps to ENST00000458649 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:46564006 C>G maps to ENST00000458649 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X6-01A-11D-A14K-09 chr11:46419044 G>A maps to ENST00000458649 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr11:46568821 C>T maps to ENST00000458649 V73V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A2-A1FW-01A-11D-A13L-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AC-A23H-01A-11D-A159-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B6-A0I8-01A-11W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr23:11316683 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0C3-01A-21D-A12Q-09 chr23:11316985 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:53825112 A>C maps to NM_020547.2 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:53818997 C>G maps to NM_020547.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:110050163 G>C maps to NM_020703.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:47471773 C>A maps to NM_001143668.1 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr12:47471789 C>T maps to NM_001143668.1 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:49756805 G>C maps to NM_198722.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr3:49755911 G>A maps to NM_198722.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr12:31862279 G>A maps to NM_001113402.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:31850718 T>C maps to NM_001113402.1 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr12:31862322 A>T maps to NM_001113402.1 Y25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:112035177 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:112065610 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:112033895 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:112035177 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:112058601 A>C did not map to a codon.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr23:112065719 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:112058766 C>T did not map to a codon.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr23:112058872 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:112048214 A>G did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:112058818 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:94533453 A>C maps to NM_130847.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr11:94532835 G>A maps to NM_130847.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr11:94501721 G>A maps to NM_130847.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:115220584 G>C maps to NM_000036.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr1:115226820 T>C maps to NM_000036.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:115221037 C>T maps to NM_000036.2 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr1:115220951 A>G did not map to a codon.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr1:115236069 T>A did not map to a codon.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr1:115223010 G>A maps to NM_000036.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr1:115223010 G>A maps to NM_000036.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr1:110171113 C>A maps to ENST00000393689 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr11:10483071 G>T maps to NM_000480.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr11:10483075 C>T maps to NM_000480.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr11:10500162 G>A maps to NM_000480.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:38429446 A>C maps to NM_001635.3 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr7:38431519 G>A maps to NM_001635.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr7:38424483 G>A maps to NM_001635.3 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr7:38502652 G>T maps to NM_001635.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr1:104161639 T>C maps to NM_000699.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:104163235 G>T maps to ENST00000305865 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:104166589 C>T maps to ENST00000305865 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr1:104166495 T>C maps to ENST00000305865 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr1:104116890 C>T maps to NM_020978.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr1:104114361 T>C maps to ENST00000305865 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:104114772 C>T maps to ENST00000305865 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:104116526 C>T maps to NM_020978.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:104117916 A>G maps to NM_020978.3 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr7:2748832 C>A maps to NM_133463.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:2748351 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:66246372 C>T maps to NM_016627.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QJ-01A-12D-A19Y-09 chr2:112552426 C>T maps to NM_022662.2 P1447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:112592359 A>G maps to NM_022662.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:73983704 T>G maps to NM_173473.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:140082003 C>T maps to NM_013366.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr4:25408875 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:25391814 A>G maps to ENST00000510092 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr4:25395931 G>T maps to ENST00000510092 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:121746348 C>T maps to NM_016237.4 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr12:121746365 C>A maps to NM_016237.4 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr12:110819686 C>T maps to NM_016238.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:110813983 C>T maps to NM_016238.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:77274281 G>A maps to NM_015305.3 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr1:213174227 C>A maps to NM_144567.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:213178656 G>A maps to NM_144567.3 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr8:108509558 C>A maps to NM_001146.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr8:108359217 G>C maps to NM_001146.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr20:896546 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr20:865877 C>T maps to NM_015985.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr1:178834293 T>G maps to NM_004673.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr9:129870473 C>A maps to NM_012098.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr9:129851265 G>C maps to NM_012098.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:8430845 C>G maps to NM_139314.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:101762072 T>G maps to NM_178127.4 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr11:101777840 G>A maps to NM_178127.4 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr1:11254591 C>T maps to NM_021146.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr8:41615630 T>A maps to ENST00000415018 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr8:41525808 C>T maps to ENST00000415018 K1790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:41574524 C>T maps to ENST00000415018 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr8:41553929 G>A maps to ENST00000415018 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr8:41573205 A>G maps to ENST00000415018 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:114195738 G>A maps to NM_001148.4 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:114275341 T>C maps to NM_001148.4 P1856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:114275419 A>C maps to NM_001148.4 S1882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:114095591 C>T maps to NM_001148.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr4:114274876 G>A maps to NM_001148.4 K1701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr4:114199617 C>T maps to NM_001148.4 N595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr4:114158315 C>T maps to NM_001148.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr4:114177048 C>G maps to NM_001148.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:114117623 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:114253194 C>T maps to NM_001148.4 Q1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr4:114158315 C>T maps to NM_001148.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr4:114277294 C>T maps to NM_001148.4 S2507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:61847991 A>C maps to NM_020987.2 G1151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:61830573 G>T maps to NM_020987.2 S3355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:61965606 T>C maps to NM_020987.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr10:61842432 T>C maps to NM_020987.2 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr2:190569784 C>G maps to NM_144708.3 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr2:190593521 C>T maps to NM_144708.3 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:190606107 C>T maps to NM_144708.3 I1247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr17:54431264 C>T maps to NM_153228.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:4075887 C>A maps to NM_016376.3 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr17:4080475 A>T maps to NM_016376.3 L908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:139889223 G>T maps to ENST00000253810 T1256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:139885378 T>G maps to ENST00000253810 G1111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr5:139884446 C>T maps to ENST00000253810 Q1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:139864796 C>G maps to ENST00000253810 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr5:139908990 C>T maps to ENST00000253810 Q2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr19:17394277 G>T maps to NM_152363.4 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:133306758 C>T maps to NM_015114.1 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr2:241463461 C>A maps to ENST00000401804 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:241496665 G>A maps to ENST00000401804 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr16:89351968 G>A maps to NM_013275.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:89351986 G>A maps to NM_013275.4 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:89349093 C>A maps to NM_013275.4 E1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr16:89347632 C>A maps to NM_013275.4 E1773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:89347282 T>C maps to NM_013275.4 K1889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:9254426 G>T maps to NM_015208.3 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr18:9182462 G>A maps to NM_015208.3 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr18:9257246 G>T maps to NM_015208.3 E1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr1:70781222 G>A maps to NM_030816.4 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr11:67057823 C>T maps to NM_207354.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:5922262 G>C maps to NM_001009941.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:73984503 A>C maps to NM_032217.3 G1363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IL-01A-11D-A14G-09 chr4:73942662 A>C maps to NM_032217.3 P2582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T7-01A-21D-A099-09 chr10:99337562 C>T maps to NM_020349.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:99343449 C>T maps to NM_020349.2 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr9:69423557 C>T maps to NM_001098805.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr9:69423557 C>T maps to NM_001098805.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BJ-01A-11W-A071-09 chr9:69421945 T>C maps to NM_001098805.1 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr9:69421945 T>C maps to NM_001098805.1 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr19:4212476 G>A maps to ENST00000262970 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr10:27326983 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:27329050 C>A maps to NM_014915.2 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr10:27326931 A>G maps to NM_014915.2 Y809Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr10:27382292 A>G maps to NM_014915.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr19:33095252 G>A maps to NM_032139.2 F857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr19:33098717 G>A maps to NM_032139.2 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr19:33090933 T>C maps to NM_032139.2 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:33131254 G>C maps to NM_032139.2 S314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:33131261 G>A maps to NM_032139.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr19:33134216 G>A maps to NM_032139.2 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:33117719 G>C maps to NM_032139.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr19:33134042 C>A maps to NM_032139.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:37431190 G>T maps to ENST00000374660 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr10:37430799 T>A maps to ENST00000374660 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr10:37508552 G>T maps to ENST00000374660 E1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr10:37486215 C>G maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr10:37422842 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr18:14763683 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr18:14782551 T>C maps to NM_001145029.1 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KD-01A-12D-A20S-09 chr18:14852310 G>A maps to NM_001145029.1 E1337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr18:14850234 G>T maps to NM_001145029.1 E1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:14852065 G>T maps to NM_001145029.1 E1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr18:14850374 G>A maps to NM_001145029.1 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr18:14843060 C>G maps to NM_001145029.1 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:93988975 G>C did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:52283228 G>A maps to NM_182608.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr1:145473723 C>T maps to NM_001039888.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:145473930 C>T maps to NM_001039888.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15F-01A-11D-A10Y-09 chr1:145473654 C>T maps to NM_001039888.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:145562453 C>T maps to NM_144698.3 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KI-01A-11D-A14K-09 chr1:145556633 A>G maps to NM_144698.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:97864372 G>A maps to NM_001164315.1 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr2:97783881 C>T maps to NM_001164315.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr2:97868068 C>T maps to NM_001164315.1 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:98197015 G>A maps to NM_025190.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:48774362 G>A maps to NM_052855.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:48777150 G>A maps to NM_052855.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:82938825 T>G maps to ENST00000260047 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:94230118 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:10030563 T>G maps to NM_198798.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr4:125593161 T>A maps to NM_020337.2 K424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:125599894 T>G maps to NM_020337.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:125599963 A>C maps to NM_020337.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:56647895 G>A maps to NM_173595.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr2:71211877 G>A maps to NM_001115116.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:71211940 G>A maps to NM_001115116.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:38229171 G>A maps to NM_138797.2 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr22:38227991 G>A maps to NM_138797.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr5:55407410 G>A maps to NM_024669.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:90331669 G>C maps to ENST00000339746 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr6:35050933 T>C maps to NM_015245.2 Y946Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:34985808 A>C maps to NM_015245.2 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:99194846 G>C maps to NM_152788.3 A1041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:99837458 G>A maps to NM_152788.3 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:101536358 G>A maps to ENST00000375018 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:101518762 C>T maps to ENST00000375018 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:101546392 G>A maps to ENST00000375018 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:101536317 C>T maps to ENST00000375018 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:220098853 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:220098588 C>T maps to NM_001042410.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr7:36450288 C>G maps to NM_018685.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:36446158 C>G maps to NM_018685.2 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr7:36446158 C>G maps to NM_018685.2 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:69978135 C>G maps to NM_018043.5 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:70034016 C>T maps to NM_018043.5 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr11:69957858 A>G maps to NM_018043.5 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:70007265 G>T did not map to a codon.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr11:70007818 C>T maps to NM_018043.5 Y624Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:43591292 C>T maps to NM_018075.3 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:43618202 G>A maps to NM_018075.3 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:5916517 G>A maps to ENST00000356134 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:5685154 G>A maps to ENST00000356134 D823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr12:5848497 G>T maps to ENST00000356134 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr11:26660719 C>G maps to NM_031418.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr11:26484601 G>A maps to NM_031418.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr11:26569061 C>T maps to NM_031418.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:101504218 T>C maps to ENST00000392977 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr12:101504242 C>G maps to ENST00000392977 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr12:101490419 C>T maps to ENST00000392977 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:22283789 C>T maps to NM_213599.2 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W4-01A-11D-A10G-09 chr2:242155636 C>T maps to NM_001001891.3 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:418574 G>A maps to NM_001012302.2 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr11:419604 C>G maps to NM_001012302.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:69076864 C>A maps to NM_006305.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:48866671 A>G maps to NM_012404.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr1:150202959 G>C maps to NM_030920.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:90348549 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:90349346 C>A maps to NM_001150.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:90349715 G>A maps to NM_001150.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr2:69472436 G>A maps to NM_032208.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr10:46122004 C>T maps to NM_001128324.1 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr10:46121713 A>C maps to NM_001128324.1 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:124748000 T>G maps to NM_001003954.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr8:124693589 G>A maps to NM_001003954.1 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr4:122590855 G>C maps to NM_001154.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr4:122607521 G>A maps to NM_001154.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:75147488 C>T maps to NM_004034.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:150967078 G>A maps to NM_003568.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr7:36661341 G>A maps to NM_001177506.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr7:36698845 A>G maps to NM_001177506.1 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr7:36552856 C>T maps to NM_001177506.1 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:40996918 C>T maps to NM_009590.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr17:40997998 A>T maps to NM_009590.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr17:41008380 C>T maps to NM_003734.2 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr17:41004613 G>A maps to NM_003734.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:201459996 C>T maps to NM_001159.3 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:201521603 C>T maps to NM_001159.3 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:201527625 C>T maps to NM_001159.3 F1159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr2:201523929 C>T maps to NM_001159.3 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:29736710 T>G maps to NM_001127.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr22:29747815 T>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr22:29727889 G>A maps to NM_001127.3 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:29750739 T>C maps to NM_001127.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr22:29737710 G>A maps to NM_001127.3 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr22:29727486 G>A maps to NM_001127.3 F825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr22:29727808 C>T maps to NM_001127.3 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr16:71799442 G>A maps to ENST00000423132 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:24035548 G>A maps to NM_003917.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr14:24030619 C>T maps to NM_003917.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr19:16339651 C>T maps to NM_001130524.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:10692014 G>C maps to ENST00000453102 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr19:10692037 C>A maps to ENST00000453102 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr7:100802407 G>T maps to NM_001283.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr19:50295237 C>T maps to NM_014203.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr19:50302176 C>T maps to NM_014203.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr17:33984662 C>T maps to NM_001030006.1 N614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:33953639 C>T maps to NM_001030006.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:183898909 G>T maps to ENST00000411763 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr5:77590301 G>A maps to NM_003664.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr5:77590364 T>A maps to NM_003664.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:83331506 G>A maps to NM_004644.3 G905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr19:2127190 G>C maps to ENST00000355272 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr19:2102198 C>T maps to ENST00000355272 E1207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr10:75889679 G>C maps to NM_207012.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr8:42012399 T>C maps to NM_006803.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:51260497 T>G maps to NM_007347.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:51204291 C>T maps to NM_007347.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr15:51291328 C>T maps to NM_007347.3 Q989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr7:99702513 G>T maps to ENST00000429084 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr7:99704463 C>T maps to ENST00000429084 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr7:99701111 C>T maps to ENST00000429084 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:31542161 G>T maps to NM_007077.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:99065488 G>A maps to NM_181861.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:99080546 G>T maps to NM_181861.1 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:72064696 G>A maps to NM_001163.3 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:72131694 G>A maps to NM_001163.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:72131546 G>A maps to NM_001163.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:72082802 G>C maps to NM_001163.3 S473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr15:29397632 G>T maps to NM_005503.3 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr15:29346221 C>T maps to NM_005503.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:3751443 C>T maps to NM_004886.3 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:6432247 G>T maps to ENST00000389906 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr11:6432495 G>A maps to ENST00000389906 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr10:26851336 G>A maps to NM_019043.3 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:40946935 A>C maps to NM_004307.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr4:41015822 G>T maps to NM_004307.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:112102989 G>T maps to NM_001127510.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:112177958 C>A maps to NM_001127510.2 S2223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XR-01A-11D-A10G-09 chr5:112179285 C>G maps to NM_001127510.2 P2665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WT-01A-11D-A10G-09 chr5:112177344 A>G maps to NM_001127510.2 P2018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr5:112173675 C>T maps to NM_001127510.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr5:112177101 C>T maps to NM_001127510.2 S1937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr19:1468431 C>A maps to NM_005883.2 S1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr14:20924088 G>A maps to NM_080649.1 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:55028813 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:55033188 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr23:55033172 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr23:55028013 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:55029488 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr1:150240460 G>T maps to NM_001077628.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:63571491 C>T maps to NM_031301.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:43342391 G>T maps to NM_001142930.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:43342373 C>T maps to NM_001142930.1 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:43357465 G>T maps to NM_001142930.1 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr2:68765323 G>A maps to NM_173545.2 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr2:68740325 A>T maps to NM_173545.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr11:57004166 G>C maps to NM_005161.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:57004109 G>C maps to NM_005161.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr19:36369537 G>T maps to NM_001024807.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr11:129993588 C>T maps to NM_001642.2 C335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:129993537 C>T maps to NM_001642.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr11:116706640 C>T maps to NM_000039.1 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr1:156562239 G>C maps to ENST00000446584 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:156563831 C>T maps to ENST00000446584 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HB-01A-11W-A071-09 chr11:116692401 G>A maps to NM_000482.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:116661511 G>A maps to NM_052968.4 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr2:21260973 G>A maps to NM_000384.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr2:21247969 A>G maps to NM_000384.2 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr2:21232269 G>T maps to NM_000384.2 T2490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A091-01A-11W-A019-09 chr2:21236080 G>A maps to NM_000384.2 Y1389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:21236185 A>C maps to NM_000384.2 G1354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:21237330 G>T maps to NM_000384.2 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr2:21241872 G>A maps to NM_000384.2 Q1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr2:21226146 A>G maps to NM_000384.2 D4049D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr2:21231855 T>C maps to NM_000384.2 S2628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JU-01A-11D-A13L-09 chr2:21233394 C>T maps to NM_000384.2 L2115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr16:28507282 G>A maps to NM_018690.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr16:28507294 G>A maps to NM_018690.2 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr16:28506484 G>A maps to NM_018690.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr16:28507081 G>C maps to NM_018690.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr12:7802274 T>C maps to NM_001644.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr6:41029072 G>T maps to NM_006789.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr22:39357390 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr22:39380198 C>G maps to ENST00000402182 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:39428251 C>T maps to NM_152426.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr22:39418877 C>T maps to NM_152426.3 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr22:39440104 C>T maps to NM_001006666.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr1:183616995 G>T maps to NM_203454.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:56755653 G>T maps to NM_001638.2 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr17:64219814 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr22:36661743 C>T maps to NM_145343.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:36623806 C>G maps to ENST00000451256 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:36624166 G>A maps to ENST00000451256 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr22:36587939 G>C maps to ENST00000332987 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr22:36587924 C>T maps to ENST00000332987 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr22:36055201 G>A maps to NM_030641.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr22:36054790 C>T maps to NM_030641.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:84309401 A>G did not map to a codon.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr23:84329040 T>A did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr17:58531761 T>C maps to NM_006380.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:105605038 A>G maps to NM_018171.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr9:33443388 C>G maps to NM_004925.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr12:50368231 T>A maps to NM_001652.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr5:115329523 T>A maps to NM_173800.4 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr15:35198908 A>G maps to NM_014691.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:35210545 G>A maps to NM_014691.2 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:66931269 C>A did not map to a codon.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr23:66931345 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:66937360 C>T did not map to a codon.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr23:66766553 C>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:66931472 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr23:66765080 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:66863183 C>T did not map to a codon.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr23:66943561 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47428971 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr23:47430770 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:47426042 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr23:47430835 G>A did not map to a codon.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr23:47429358 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:36214109 C>A did not map to a codon.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr4:36130230 C>A maps to NM_015230.2 V1188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:36069773 G>A maps to NM_015230.2 R1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr5:141052601 G>A maps to NM_022481.5 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:141049550 G>C maps to NM_022481.5 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y2-01A-11D-A159-09 chr5:141049556 G>A maps to NM_022481.5 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118454720 A>C maps to ENST00000359415 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr11:118468586 A>G maps to ENST00000359415 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:75316114 C>T maps to NM_001657.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:228284916 C>G maps to NM_001024228.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:61909528 G>T maps to NM_175609.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr20:61907910 C>T maps to NM_175609.1 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:47193261 G>C maps to NM_032389.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr11:47193041 T>G maps to NM_032389.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr8:68208733 G>A maps to NM_006421.3 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:68179664 C>A maps to NM_006421.3 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr8:68189546 A>G maps to NM_006421.3 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:68137172 A>G maps to NM_006421.3 C1391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0D9-01A-31W-A071-09 chr20:47569306 G>A maps to NM_006420.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:47587773 C>G maps to NM_006420.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:47633847 G>T maps to NM_006420.2 E1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:153802233 A>G maps to NM_001025595.1 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:6501238 A>C maps to NM_012402.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr11:6499365 T>C maps to NM_012402.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:62337708 C>T maps to NM_003224.3 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr20:62337725 G>A maps to NM_003224.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr14:68087660 G>A maps to NM_001172.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:68087649 G>T maps to NM_001172.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr13:107220000 C>T maps to NM_018011.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr13:107220012 G>A maps to NM_018011.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr11:46717590 G>A maps to NM_004308.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr11:46702880 G>A maps to NM_004308.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr4:148985599 G>A maps to NM_024605.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr4:148787877 C>T maps to NM_024605.3 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:32920993 G>T maps to NM_014783.3 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:32928049 C>T maps to NM_014783.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr15:32908480 G>A maps to NM_014783.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr15:32929654 C>A maps to NM_014783.3 S894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr2:144381781 C>T maps to NM_018460.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr2:144525680 C>T maps to NM_018460.3 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:24942174 A>G maps to NM_001006634.1 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:24942414 A>G maps to NM_001006634.1 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:24953403 G>C maps to NM_001006634.1 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr16:24971255 C>G maps to NM_001006634.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:129950557 A>G maps to NM_033515.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:24909206 A>C maps to NM_020824.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr10:24873955 G>A maps to NM_020824.3 S1754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr10:24874321 A>C maps to NM_020824.3 P1632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:49663122 G>C maps to ENST00000417912 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr10:49659121 C>T maps to ENST00000417912 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr4:86916663 A>T maps to NM_001025616.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr4:86863217 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:86852112 C>T maps to NM_031305.2 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr5:142513638 G>A maps to NM_015071.4 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr5:142283103 G>T did not map to a codon.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr18:6890050 C>A maps to ENST00000400091 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:94650458 G>C maps to NM_004815.3 S693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr1:94668511 C>A maps to NM_004815.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:161017608 G>A maps to NM_001025598.1 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:161026204 G>C maps to NM_001025598.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:161018227 G>A maps to NM_001025598.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr3:119101243 C>T maps to NM_020754.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:119132794 A>C maps to NM_020754.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:119133955 T>G maps to NM_020754.2 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:119134690 G>A maps to NM_020754.2 V1305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:128842746 T>G maps to NM_001142685.1 P1204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:128844694 T>G maps to NM_001142685.1 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:128843043 C>T maps to NM_001142685.1 E1105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr23:130219618 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr23:130219990 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:130219632 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:130220303 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:130217157 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr23:130220599 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:130222738 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:130222618 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr23:130218364 A>G did not map to a codon.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr8:145757695 G>A maps to NM_025251.1 H991H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr8:145830969 C>T maps to NM_025251.1 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr8:145770834 C>T maps to NM_025251.1 K773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153175226 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:153176592 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153184654 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr23:153174973 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr14:32623833 C>T maps to NM_001030055.1 Q1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr14:32615467 G>T did not map to a codon.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr14:32561631 T>A maps to NM_001030055.1 L586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:32562265 A>C maps to NM_001030055.1 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:32561796 C>A maps to NM_001030055.1 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr23:11196300 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr23:11162154 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:11160420 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:11682549 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr23:11206972 A>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:11272782 C>T did not map to a codon.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr23:11162145 C>T did not map to a codon.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:11162203 C>A did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr23:11206926 G>C did not map to a codon.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr22:45204249 C>T maps to ENST00000361473 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:57869714 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:57872535 C>T maps to ENST00000393797 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr19:42410773 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:42409362 G>A maps to NM_199002.1 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:42396864 G>T maps to NM_199002.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:1842704 C>T maps to ENST00000398564 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Q-01A-21W-A050-09 chr1:17964410 C>A maps to NM_018125.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:18021722 T>G maps to NM_018125.3 G1085G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr1:17991020 G>A maps to NM_018125.3 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:156908246 A>C maps to NM_198236.1 P1385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:156917168 C>T maps to NM_198236.1 K805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:156946798 C>G maps to NM_198236.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:156910104 T>C maps to NM_198236.1 T1209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr1:156915882 G>A maps to NM_198236.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:156917129 G>C maps to NM_198236.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:156917198 G>A maps to NM_198236.1 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr11:120352171 G>T maps to NM_015313.2 G1481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:120348898 G>A maps to NM_015313.2 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr11:120347957 A>T maps to NM_015313.2 A1132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:8222850 A>C maps to NM_173728.3 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr17:8219171 T>C maps to NM_173728.3 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr17:8221892 C>T maps to NM_173728.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:73021836 T>G maps to NM_014786.3 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr11:73022274 C>T maps to NM_014786.3 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr11:73064009 C>T maps to NM_014786.3 Q1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr19:7504981 C>T maps to NM_001130955.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:7529467 C>G maps to NM_001130955.1 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr19:7509312 G>A maps to NM_001130955.1 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:16525744 G>A maps to NM_153213.3 C717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:16534658 G>A maps to NM_153213.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr1:16525099 C>A maps to NM_153213.3 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:155920203 G>T maps to NM_001162383.1 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:155927619 G>A maps to NM_001162383.1 N533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18S-01A-11D-A12B-09 chr1:155932873 C>T maps to NM_001162383.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr1:155922539 G>A maps to NM_001162383.1 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:56789059 G>A maps to NM_001128615.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr4:106510537 C>T maps to ENST00000420470 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:131801928 G>T maps to NM_015320.2 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:144060667 C>T maps to NM_005435.3 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr7:144062631 C>G maps to NM_005435.3 S957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135761739 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135767927 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr23:135764931 A>T did not map to a codon.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr23:135827434 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr23:135772825 T>C did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:135750294 C>T did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:135767915 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr13:111930017 C>T maps to NM_001113511.1 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr13:111955405 G>A maps to ENST00000218789 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr13:111806289 C>T maps to NM_001113511.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:62944578 C>T did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:62885816 G>T did not map to a codon.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr23:62917052 G>A did not map to a codon.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr23:62894023 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr23:62917108 C>T did not map to a codon.
Sequencing variant TCGA-BH-A201-01A-11D-A14K-09 chr23:62875544 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:62944455 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr1:27057726 C>T maps to NM_006015.4 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr1:27092808 C>T maps to NM_006015.4 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SB-01A-21D-A25Q-09 chr1:27057873 C>T maps to NM_006015.4 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:27101595 A>C maps to NM_006015.4 A1626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:27106007 C>T maps to NM_006015.4 P1873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:27087557 C>G maps to NM_006015.4 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr1:27106497 C>T maps to NM_006015.4 Q2037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr1:27087879 C>T maps to NM_006015.4 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr1:27057933 C>T maps to NM_006015.4 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr1:27057873 C>T maps to NM_006015.4 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr1:27087441 G>A maps to NM_006015.4 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr1:27057873 C>T maps to NM_006015.4 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr6:157522353 G>A maps to ENST00000367148 T1582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:157505481 A>T maps to ENST00000367148 K1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr12:46245927 C>G maps to NM_152641.2 S1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr12:46211463 C>T maps to NM_152641.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EX-01A-11D-A13L-09 chr12:46242690 G>A maps to NM_152641.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:46240702 G>A maps to NM_152641.2 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:58814544 C>T maps to NM_002892.3 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:235345180 G>C maps to NM_016374.5 S1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr1:235345090 G>C maps to NM_016374.5 S1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:63852665 A>C maps to NM_032199.2 T1148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr10:63662060 G>C maps to NM_032199.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:63851360 A>C maps to NM_032199.2 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr15:72855838 T>C maps to NM_005744.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:49012301 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:101789417 T>G maps to NM_001177.3 *182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr5:175798849 G>A maps to NM_173664.4 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:100240740 G>C did not map to a codon.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr23:100229142 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:93768358 T>C maps to NM_182896.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr5:53182435 C>T maps to NM_019087.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr17:79650735 C>G maps to NM_001040025.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr2:153591547 C>T maps to NM_152522.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:66534537 C>A maps to NM_018120.4 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr7:102732967 G>A maps to NM_031905.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr7:102738802 C>T maps to NM_031905.3 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:109258195 G>A maps to NM_032131.4 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:109283313 C>T maps to NM_032131.4 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:109282823 G>A maps to NM_032131.4 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr10:23326257 G>A maps to NM_173081.3 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:28229608 C>T maps to NM_018076.2 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:28260102 C>T maps to NM_018076.2 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:28250536 G>C maps to NM_018076.2 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:28196615 G>A maps to NM_018076.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:31473253 C>T maps to ENST00000408912 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:19166168 C>T maps to ENST00000392336 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr17:73106585 C>T maps to NM_024585.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:137942263 C>T maps to ENST00000469044 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr2:232123799 G>A maps to ENST00000359743 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:232121297 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr2:232156118 C>T maps to ENST00000359743 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr23:100807920 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr23:100809227 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:100808036 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr23:100808301 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:100808690 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:100808832 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr23:100911423 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:100910987 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0GZ-01A-11W-A071-09 chr23:100912410 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:100911131 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:100911529 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:100880199 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:100880572 G>T did not map to a codon.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr23:100880820 A>G did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:100880811 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08J-01A-11W-A019-09 chr23:101858457 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr23:101858439 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:101858322 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:101857233 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:101857286 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:101858438 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr23:101858402 G>T did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:101858367 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:101857505 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27T-01A-11D-A16D-09 chr23:101858271 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:100871323 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:100871480 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr1:150807077 C>A maps to NM_001668.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:80762576 C>T maps to NM_014862.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:13408206 T>C maps to ENST00000403290 N595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr11:13381919 C>T maps to ENST00000403290 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr7:98951678 G>C maps to NM_006409.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr7:98942097 C>T maps to NM_006409.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:98941934 G>A maps to NM_006409.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr7:98946501 G>T maps to NM_006409.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr7:98991735 T>C maps to NM_005720.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr7:98988554 G>A maps to NM_005720.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:219114118 C>T maps to NM_005731.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:219110142 G>T maps to NM_005731.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr3:9845591 G>A maps to ENST00000453882 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:183599739 G>A maps to ENST00000294742 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:169485915 G>A maps to NM_032487.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:169487267 G>T maps to NM_032487.4 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr3:169487257 G>T maps to NM_032487.4 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr3:35770831 G>A maps to ENST00000458225 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr3:35785362 C>A maps to ENST00000458225 Y647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:35723354 G>T maps to ENST00000458225 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr3:35725219 A>G maps to ENST00000458225 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr3:35724360 C>T maps to ENST00000458225 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P5-01A-11D-A142-09 chr3:35833913 C>A maps to ENST00000458225 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:69496526 G>A did not map to a codon.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr23:69501556 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:69495967 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr19:18120411 G>C maps to NM_015683.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr19:18119535 G>A maps to NM_015683.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:4902705 G>A maps to NM_001080523.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18S-01A-11D-A12B-09 chr19:4891117 A>C maps to NM_001080523.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:2825380 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:2873544 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:2853179 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr23:2853147 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:2861116 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:2852961 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:3002326 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr23:3019141 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr23:3030431 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:66416438 T>G maps to NM_014960.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:66416408 T>C maps to NM_014960.3 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr23:2933207 C>T did not map to a codon.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr23:2936643 G>T did not map to a codon.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr4:114823651 G>A maps to NM_024590.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:94918722 G>T maps to NM_198150.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:77003401 C>T maps to NM_001130016.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:3661292 C>T maps to NM_001079536.1 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:231132972 A>G maps to NM_022786.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:19960534 C>T maps to NM_001670.2 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr22:19959494 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:25028417 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:104638148 T>G maps to NM_020682.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:104636764 G>T maps to NM_020682.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr10:104638239 C>T maps to NM_020682.3 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr10:52003087 C>T maps to NM_019893.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr10:52502734 C>T maps to NM_001079516.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr8:131140242 C>G maps to NM_018482.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr8:131172125 G>A maps to NM_018482.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr8:131179787 C>T maps to NM_018482.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:9496398 G>T maps to NM_003887.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr2:9531254 C>T maps to NM_003887.2 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:9525430 C>T maps to NM_003887.2 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:23768755 G>C maps to NM_017707.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr1:23759633 C>A maps to NM_017707.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr2:239353147 C>T maps to NM_001040445.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr23:15306046 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:63445341 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:63445285 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:63445040 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr7:123256325 A>G maps to NM_080928.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr17:42255077 A>T maps to NM_080863.4 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:76397784 G>A maps to NM_080868.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr1:76387977 C>T maps to NM_080868.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr14:94420822 C>T maps to ENST00000434324 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr14:94417513 G>A maps to ENST00000434324 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr4:177146415 T>A maps to NM_080874.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr9:132404203 C>A maps to NM_017873.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:15267032 C>T did not map to a codon.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr23:15272919 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:15270444 G>T did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr23:15262743 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr22:30221108 G>A maps to NM_032204.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr22:30197089 T>C maps to NM_032204.3 K526K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr22:30189365 G>A maps to NM_032204.3 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A133-01A-32D-A12B-09 chr22:30189407 G>A maps to NM_032204.3 Y620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr22:30221652 G>A maps to NM_032204.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:100964163 A>C maps to NM_006828.2 G1989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr11:8959450 G>A maps to NM_020646.1 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:14231276 G>A maps to NM_018154.2 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:155448822 G>A maps to ENST00000368346 R1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr1:155313174 G>A maps to ENST00000368346 L2746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr1:155311855 G>A maps to ENST00000368346 I2782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr1:155311816 G>C maps to ENST00000368346 Y2795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr8:37967941 C>T maps to NM_004674.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:32848254 A>C maps to NM_001672.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr7:65546941 C>T maps to NM_000048.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr23:1755427 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr23:1743207 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:1536954 A>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:1551178 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr23:1522339 T>G did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:1558026 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:1554632 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr23:1522275 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:97488552 G>C maps to NM_183356.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr17:3392581 C>T maps to NM_000049.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:3379678 G>T maps to NM_000049.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr17:3386851 T>A maps to NM_000049.2 Y164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr19:51017027 C>T did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:104570687 C>T maps to NM_001080464.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:62566124 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:62430670 C>A maps to NM_004318.3 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr8:62460692 C>T maps to NM_004318.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr16:29913170 C>T maps to NM_181718.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr22:26829766 C>T maps to NM_020437.4 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr1:197111818 G>T maps to NM_018136.4 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:197102623 G>T maps to NM_018136.4 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr1:197059074 C>T maps to NM_018136.4 L3323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:197073412 G>C maps to NM_018136.4 L1656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:197061147 G>A maps to NM_018136.4 F3111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:197113230 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:197069572 G>A maps to NM_018136.4 T2936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr1:197112484 G>T maps to NM_018136.4 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:95227237 G>A maps to NM_017680.4 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:79952732 C>T maps to ENST00000306729 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:79966992 G>A maps to ENST00000306729 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:96798456 G>T maps to NM_001002036.3 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr1:176915213 G>T maps to ENST00000281881 C707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:176852044 G>A maps to ENST00000281881 L1112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr1:176918358 C>A maps to ENST00000281881 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:177001649 C>T maps to ENST00000281881 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr1:177133536 G>A maps to ENST00000281881 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr1:176913117 C>A maps to ENST00000281881 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr1:176863700 C>T maps to ENST00000281881 Q987Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:119188273 T>G maps to ENST00000313400 T1292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:119626002 C>T maps to ENST00000313400 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr20:31021534 C>T maps to ENST00000375687 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr20:31022689 A>G maps to ENST00000375687 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr20:31023223 G>T maps to ENST00000375687 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:31024378 T>C maps to ENST00000375687 G1288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:31024522 G>A maps to ENST00000375687 G1336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr20:31023331 A>G maps to ENST00000375687 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr20:31021320 A>G maps to ENST00000375687 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr20:31023751 C>G maps to ENST00000375687 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr2:25967089 C>A maps to NM_018263.4 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:25966073 C>T maps to NM_018263.4 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:25976475 G>A maps to NM_018263.4 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:25982355 G>A maps to NM_018263.4 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr2:25994377 T>C maps to NM_018263.4 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr2:25973202 G>A maps to NM_018263.4 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:25965239 C>T maps to NM_018263.4 Q1322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BM-01A-11D-A21Q-09 chr18:31320368 C>T maps to NM_030632.1 Q1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr18:31325064 G>C maps to NM_030632.1 T1751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr18:31326468 C>T maps to NM_030632.1 A2219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr18:31322952 G>A maps to NM_030632.1 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1QZ-01A-21D-A167-09 chr18:31325520 G>A maps to NM_030632.1 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr18:31325406 C>T maps to NM_030632.1 I1865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:117003765 G>A maps to NM_130768.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr8:124340529 C>T maps to NM_014109.3 R1256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr8:124360462 T>C maps to NM_014109.3 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:124373836 C>A maps to NM_014109.3 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr8:124351572 A>C maps to NM_014109.3 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr8:124381413 T>C maps to NM_014109.3 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr8:124358469 C>T maps to NM_014109.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:24086360 C>A maps to NM_017552.1 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr2:24046431 A>T maps to NM_017552.1 C609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr2:24011445 T>C maps to NM_017552.1 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr1:1430986 C>T maps to NM_031921.4 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr1:1426041 G>A maps to NM_031921.4 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr17:29196616 C>G maps to NM_024857.3 S1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:29196662 A>G maps to NM_024857.3 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:29192720 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr17:29220889 T>C maps to NM_024857.3 G1673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr19:3908272 C>T maps to NM_033064.4 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr10:123549741 T>C maps to NM_001001976.1 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr1:212791560 G>A maps to NM_001674.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:212788563 C>T maps to NM_001674.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JH-01A-11D-A188-09 chr22:39917836 T>C maps to NM_182810.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:161771861 C>T maps to NM_007348.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A086-01A-11W-A019-09 chr6:32088602 T>C maps to NM_004381.4 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr6:32094894 T>C maps to NM_004381.4 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:14613534 A>C maps to NM_018179.3 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:14610210 C>T maps to NM_018179.3 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr16:10524749 C>T maps to NM_024997.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr11:72533923 G>T maps to NM_033388.1 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr11:64668489 C>T maps to ENST00000421419 R1400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr11:64666106 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:64681347 C>A maps to ENST00000421419 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr11:64665324 C>T maps to ENST00000421419 Q1662Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr11:64679446 G>A maps to ENST00000421419 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr11:64668019 C>T maps to ENST00000421419 T1472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:64677213 A>G maps to ENST00000421419 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NE-01A-21D-A14K-09 chr11:64674263 C>T maps to ENST00000421419 E952E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NE-01A-21D-A14K-09 chr11:64674995 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:96800037 T>G maps to NM_018036.5 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:96809560 G>A maps to NM_018036.5 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr14:96809458 T>G maps to NM_018036.5 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr14:96777941 C>A maps to NM_018036.5 V1309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr23:107381040 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:107381126 C>G did not map to a codon.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr23:107374542 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr23:107396924 G>T did not map to a codon.
Sequencing variant TCGA-A7-A13H-01A-11D-A228-09 chr2:242590739 T>C maps to ENST00000337606 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr6:106649943 G>A maps to NM_004849.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr2:220089423 A>C maps to NM_024085.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:220088389 G>A maps to NM_024085.3 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr2:220090179 C>T maps to NM_024085.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:294743 G>T maps to ENST00000409479 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr11:289953 C>T maps to ENST00000409479 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:51087315 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:51058287 T>C maps to ENST00000358385 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr2:38527428 T>C maps to NM_001135673.1 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:63410930 G>A maps to NM_015459.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:108200997 G>A maps to NM_000051.3 L2455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:108100033 C>T maps to NM_000051.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr11:108235934 C>T maps to NM_000051.3 R2993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr11:108196268 C>T maps to NM_000051.3 Q2269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr11:108186736 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:108235934 C>T maps to NM_000051.3 R2993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr11:108121487 G>T maps to NM_000051.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr11:108114710 G>C maps to NM_000051.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr12:7047645 G>A maps to NM_001940.3 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:7050912 C>T maps to NM_001940.3 H1181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:69991101 G>C maps to NM_145178.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:85991298 G>A maps to NM_032827.6 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr15:25928588 G>A maps to NM_024490.3 F1112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr15:25932864 G>A maps to NM_024490.3 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr5:160113186 G>T maps to NM_025153.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:160047420 G>A maps to NM_025153.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:160059228 C>T maps to NM_025153.2 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14U-01A-11D-A228-09 chr5:160097652 C>T maps to NM_025153.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr5:160033804 G>A maps to NM_025153.2 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr13:113439564 G>A maps to NM_032189.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr13:113464931 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:113505388 G>A maps to NM_032189.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr13:113439502 G>T maps to NM_032189.3 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KI-01A-11D-A14K-09 chr13:113512468 C>G maps to NM_032189.3 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr13:113532583 G>A maps to NM_015205.2 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr13:113488901 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr13:113481186 C>A maps to NM_032189.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:182590209 A>T maps to NM_014616.1 K645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:182559899 G>T maps to NM_014616.1 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:182584202 G>T maps to NM_014616.1 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:138869361 C>G did not map to a codon.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr23:138864798 A>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:138844148 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr23:138901508 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr23:138845569 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr23:138886718 G>A did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:138878431 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:138880453 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr23:138825728 C>T did not map to a codon.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr23:138897072 A>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:25264522 G>A maps to NM_001185085.1 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr13:25281420 C>T maps to NM_001185085.1 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr13:25272824 C>T maps to NM_001185085.1 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr13:25264552 C>T maps to NM_001185085.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr19:19756231 C>G maps to NM_020410.2 *1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A143-01A-11D-A10Y-09 chr19:19766176 G>T maps to NM_020410.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A145-01A-11D-A10Y-09 chr19:19762518 G>A maps to NM_020410.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:17314650 G>A maps to NM_022089.2 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr1:17316488 G>A maps to NM_022089.2 Q808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:194154625 C>G did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:193151689 G>C maps to NM_032279.2 S929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr3:193132429 G>A maps to NM_032279.2 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr3:193182726 A>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:193081940 G>A maps to NM_198505.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:192992929 G>A maps to NM_198505.2 F1186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr3:193016986 T>C maps to NM_198505.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr3:193032845 G>A maps to NM_198505.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr1:116931551 C>G maps to NM_000701.7 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:160093109 C>T maps to NM_000702.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr1:160106728 C>T maps to NM_000702.3 H916H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr19:42472977 G>A maps to ENST00000441343 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:42474444 G>A maps to ENST00000441343 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr1:160123014 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr1:160124839 T>C maps to NM_144699.3 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:160143453 G>C maps to NM_144699.3 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr1:160145984 C>A maps to NM_144699.3 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:169096636 C>T maps to NM_001677.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IA-01A-11W-A050-09 chr1:169076072 C>G maps to NM_001677.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:7556728 C>T maps to NM_001678.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr3:141622515 C>G maps to NM_001679.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr23:119513400 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr23:119509271 C>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:119512628 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:119500622 G>A did not map to a codon.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr16:28895953 G>T maps to NM_173201.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr16:28889995 G>T maps to NM_173201.3 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr16:28909328 C>A maps to NM_173201.3 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr12:110778618 C>T maps to NM_170665.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr12:110780235 C>T maps to NM_170665.3 N767N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr17:3846792 C>T maps to NM_174953.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr12:90003785 C>T maps to ENST00000428670 Q790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:90005089 A>C maps to ENST00000428670 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:90028993 A>C maps to ENST00000428670 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:89985068 G>A maps to ENST00000428670 R1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr12:90024402 G>A maps to ENST00000428670 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr12:90005122 C>T maps to ENST00000428670 Q698Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:89996932 G>A maps to ENST00000428670 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:10430012 G>T maps to NM_001001331.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XG-01A-11D-A14G-09 chr3:10370590 G>A maps to NM_001001331.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr23:152807216 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr23:152827662 G>A did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr23:152835129 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:152821596 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:152825293 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:152826284 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr23:152822474 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr23:152807209 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr23:152807836 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:152827698 A>T did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr23:152821797 G>C did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:152845590 G>C did not map to a codon.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr23:152825328 G>A did not map to a codon.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr23:152818567 G>A did not map to a codon.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr1:203696642 G>T maps to NM_001001396.1 E1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:203652419 G>A maps to NM_001001396.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:203702397 C>T maps to NM_001001396.1 V1119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr3:130714934 C>T maps to NM_001001486.1 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr16:84488551 C>A maps to ENST00000416219 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:84474521 C>A maps to ENST00000416219 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr13:114303694 C>T maps to NM_000705.3 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr18:43667039 T>G maps to NM_001001937.1 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr1:112002197 A>G maps to NM_001688.4 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:54063125 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr19:41939223 A>G maps to ENST00000417807 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr23:153657487 C>A did not map to a codon.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:153662002 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:153660670 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:153664077 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:40456896 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:40660600 C>T maps to NM_001130021.1 D708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr17:40653306 G>A maps to NM_001130020.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr12:124218489 G>A maps to NM_012463.3 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr12:124229202 G>A maps to NM_012463.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr12:124241428 C>T maps to NM_012463.3 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:138429869 C>T maps to NM_130840.2 W492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:138430010 G>A maps to NM_130840.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr7:138437429 G>C maps to NM_130840.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:138437531 A>G maps to NM_130840.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr7:138418882 G>A maps to NM_130840.2 H563H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:2569733 C>G maps to NM_001694.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr8:87153719 G>T maps to NM_152565.1 E175*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AR-A0TX-01A-11D-A099-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:71192112 C>T maps to NM_001692.3 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr2:71191566 G>C did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr2:71189936 G>T maps to NM_001692.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr8:20074769 T>C maps to NM_001693.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr8:20067921 C>G maps to NM_001693.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr8:20061993 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr8:104053147 G>A maps to NM_001695.4 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr8:104063353 T>C maps to NM_001695.4 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr6:31513276 G>A maps to NM_130463.2 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:198492670 G>C maps to ENST00000489986 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:54742050 C>A maps to NM_015941.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:54656216 G>A maps to NM_015941.2 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr23:77245316 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:77298176 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr23:77271370 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:77254128 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:77245056 G>T did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:77289123 G>C did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:77294385 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr23:77244985 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr23:77268399 A>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:77245409 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:77294442 G>C did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr23:77289219 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr13:52544778 C>T maps to NM_000053.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr13:52518394 G>T maps to NM_000053.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr13:52548305 C>T maps to NM_000053.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr13:52511650 C>T maps to NM_000053.2 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr13:52531743 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:42526831 C>T maps to NM_006095.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:42590346 C>G did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr13:26155955 G>C did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr13:26535726 G>C maps to NM_016529.4 L1066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr13:26129205 G>A maps to NM_016529.4 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr18:55361812 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:55319781 T>G maps to NM_005603.4 A1065A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BH-A0B6-01A-11D-A19Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr18:55355711 A>G maps to NM_005603.4 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr1:154300292 T>G maps to NM_020452.3 A6A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A7-A0DA-01A-31D-A10Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:1799949 G>T maps to NM_138813.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr19:1796812 C>A maps to NM_138813.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:50336859 C>T maps to NM_024837.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:50339640 C>T maps to NM_024837.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:50221404 G>C maps to NM_006045.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XS-01A-22D-A10G-09 chr20:50287754 C>T maps to NM_006045.1 W360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr20:50234063 G>A maps to NM_006045.1 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr1:47119503 G>A maps to NM_022745.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr3:142234358 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:142242884 G>A maps to NM_001184.3 R1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr3:142231144 T>C maps to NM_001184.3 K1603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:142231156 C>G maps to NM_001184.3 L1599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:117226685 G>A maps to NM_207303.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr23:76849192 C>G did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr23:76938061 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:76931790 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:76938481 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:76938533 G>C did not map to a codon.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr23:76812971 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:76855268 A>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:76891540 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:76937355 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:76937586 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:76938942 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:76939513 C>A did not map to a codon.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr23:76939542 A>T did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:76912111 A>T did not map to a codon.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr23:76937078 T>C did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:76938591 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr23:76813031 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr23:76890105 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr23:76940060 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:76937960 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr23:76940007 T>C did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:76938780 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:76972616 G>C did not map to a codon.
Sequencing variant TCGA-A2-A1FX-01A-11D-A13L-09 chr6:16306706 C>T maps to NM_000332.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr12:111926530 T>C maps to NM_002973.3 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:111891574 T>G maps to NM_002973.3 P1273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:111893856 T>G maps to NM_002973.3 P1240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:111923575 G>A maps to NM_002973.3 Q960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr12:111908399 G>A maps to NM_002973.3 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24T-01A-11D-A167-09 chr12:111951203 C>T maps to NM_002973.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:111923575 G>A maps to NM_002973.3 Q960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:111954042 C>T maps to NM_002973.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:111923660 A>C maps to NM_002973.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:28848081 A>C maps to NM_145714.1 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr16:28844516 G>A maps to NM_148414.1 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr16:28842079 C>T maps to NM_148414.1 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr16:28843676 C>T maps to NM_148414.1 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr16:28845926 G>C maps to NM_148414.1 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y2-01A-11D-A159-09 chr16:28847725 G>T maps to NM_148414.1 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr23:13337011 T>A did not map to a codon.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr23:13337898 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:13337694 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr3:63965738 A>C maps to NM_001177387.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:63973892 T>C maps to NM_001177387.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:105260693 G>A maps to NM_020725.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr7:105254754 T>A maps to NM_020725.1 K676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:110032906 G>T maps to NM_153340.4 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:110031014 C>T maps to NM_153340.4 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr2:74754621 A>G maps to ENST00000258081 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr1:1309282 C>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:8110612 C>T maps to NM_004217.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr19:57743592 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:69064929 C>T maps to NM_015570.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr7:70255690 G>A maps to NM_015570.2 E1163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr7:69364340 G>T maps to NM_015570.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr7:70252255 C>T maps to NM_015570.2 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr7:69364483 G>A maps to NM_015570.2 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:58207949 G>A maps to NM_006576.3 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:32535326 G>A maps to NM_015060.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:99437778 G>T maps to NM_021732.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:206231045 C>T maps to NM_000707.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr23:153172075 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr23:153171698 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr23:153171404 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr23:69458162 A>T did not map to a codon.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr23:69459688 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:69459752 C>T did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:69459633 C>G did not map to a codon.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr23:69456922 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr23:69262053 C>T did not map to a codon.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr23:69263412 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:69263345 C>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:69261800 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:69269745 G>A did not map to a codon.
Sequencing variant TCGA-A8-A091-01A-11W-A019-09 chr16:396380 C>T maps to NM_003502.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:343606 G>A maps to NM_003502.3 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr17:63533716 G>A maps to NM_004655.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:63533812 G>C maps to NM_004655.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SU-01A-11D-A099-09 chr17:79173240 G>A maps to ENST00000269392 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr17:79180951 G>A maps to ENST00000269392 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr3:28365571 G>A maps to NM_022461.3 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:103842084 C>A maps to NM_148174.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr3:160804029 G>T maps to NM_033168.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:33246236 T>G maps to NM_003782.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr13:31903711 C>T maps to NM_194318.3 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr13:31891804 C>T maps to NM_194318.3 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr13:31797102 T>C maps to NM_194318.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr13:31803343 C>A maps to NM_194318.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr11:66114071 G>A maps to NM_006876.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr2:62450519 C>T maps to NM_006577.5 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JC-01A-11W-A071-09 chr19:17922585 G>A maps to NM_014256.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr11:76751716 C>T maps to ENST00000354301 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr16:67183398 G>A maps to NM_033309.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr17:80915077 G>A maps to NM_001009905.1 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:47236527 C>T maps to NM_153446.2 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:47246923 C>G maps to NM_153446.2 S512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr17:47236487 C>A maps to NM_153446.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr17:47246210 C>T maps to NM_153446.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:666817 G>T maps to NM_173593.3 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr12:657407 C>T maps to NM_173593.3 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr9:33135285 T>C maps to NM_001497.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr3:118945871 G>C maps to NM_212543.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr18:29211064 G>A maps to NM_004775.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr5:177031458 C>G maps to NM_007255.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:104130413 C>G maps to NM_001701.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:104125294 G>T maps to NM_001701.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:104133259 G>A maps to NM_001701.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:104133442 G>A maps to NM_001701.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr9:104125000 G>A maps to NM_001701.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:104130593 G>A maps to NM_001701.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr11:117164598 G>A maps to NM_012104.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr21:42598251 C>T maps to NM_012105.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr21:42617983 A>G maps to NM_012105.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr21:30699315 C>T maps to NM_206866.1 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:90660492 C>T maps to NM_001170794.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr6:90660210 G>A maps to NM_001170794.1 C538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LH-01A-31D-A18P-09 chr6:57048817 C>T maps to NM_004282.3 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr10:121431831 C>T maps to NM_004281.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:38067575 C>T maps to NM_004874.2 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr8:38067545 C>T maps to NM_004874.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr17:79414863 G>A maps to ENST00000436173 R1322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:40750962 C>G maps to NM_014952.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:32205599 C>G maps to NM_001703.2 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:32196703 C>T maps to NM_001703.2 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr1:32210309 C>T maps to NM_001703.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:32203098 C>T maps to NM_001703.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr6:70070786 C>T maps to NM_001704.2 R1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr6:70071316 G>A maps to NM_001704.2 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr6:69703811 A>G maps to NM_001704.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr7:97984399 G>C maps to NM_018842.4 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr7:97933660 G>A maps to NM_018842.4 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:97939889 G>A maps to NM_018842.4 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr7:97937086 G>C maps to NM_018842.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:97939889 G>A maps to NM_018842.4 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:1390983 T>G did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr16:1392616 C>G maps to NM_003933.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr16:1395870 C>T maps to NM_003933.4 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:102839148 G>T did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr16:88098919 C>T maps to NM_001173543.1 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr2:215657117 C>T maps to NM_000465.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:215610500 G>A maps to NM_000465.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr9:135458231 C>T maps to NM_020064.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr9:135458333 G>C maps to NM_020064.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr11:129306881 G>T maps to NM_003658.4 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr5:17275510 C>T maps to NM_006317.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:17275435 G>A maps to NM_006317.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:31498877 A>G maps to ENST00000417556 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:31602023 A>C maps to NM_080686.2 P1577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr6:31605344 G>T maps to NM_080686.2 G2152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr1:171535914 C>G maps to ENST00000392078 S2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr1:171527108 C>G maps to ENST00000392078 S1953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:171549010 G>T maps to ENST00000392078 L2439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:171557637 A>C maps to ENST00000392078 A2731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr1:171506484 C>T maps to ENST00000392078 R793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:171544265 A>G maps to ENST00000392078 S2318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr1:171494043 A>G maps to ENST00000392078 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:31608185 T>C maps to ENST00000404765 E1038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr11:64756806 G>A maps to NM_138456.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr19:49459540 G>A maps to NM_138761.3 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr14:35240798 C>T maps to NM_013448.2 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:35343774 C>T maps to NM_013448.2 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr14:35331500 G>A maps to NM_013448.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr14:35245192 A>T maps to NM_013448.2 L922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr14:35264069 C>T maps to NM_013448.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:72913004 C>T maps to NM_032408.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:72891323 C>A maps to NM_032408.3 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:72892479 C>T maps to NM_032408.3 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:57009155 G>T maps to NM_013449.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr12:56995557 C>T maps to NM_013449.3 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr12:56995587 C>T maps to NM_013449.3 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:160205737 A>C maps to NM_013450.2 G1639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:160206227 T>G maps to NM_013450.2 S1618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:160206293 T>G maps to NM_013450.2 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:160206299 T>G maps to NM_013450.2 S1594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:160206383 T>G maps to NM_013450.2 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr2:160181322 G>A maps to NM_013450.2 Q2118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr2:160295652 G>C maps to NM_013450.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:160189131 T>C maps to NM_013450.2 K1954K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr19:47725122 T>C maps to NM_001127240.1 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr11:27148981 G>A maps to NM_003986.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:27078796 G>A maps to NM_003986.2 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:76740141 G>C maps to NM_024685.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr4:123664880 G>T maps to NM_152618.2 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr4:123664819 G>C maps to NM_152618.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:123664135 C>T maps to NM_152618.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:56531756 A>C maps to NM_031885.3 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr16:56553672 G>A maps to NM_031885.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr15:73024023 C>T maps to NM_033028.3 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr2:170344337 G>A maps to ENST00000419050 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr4:122765150 A>G maps to NM_176824.1 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:122749601 G>A maps to NM_176824.1 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr7:33573687 A>G maps to NM_198428.2 Q807Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:33573621 G>A maps to NM_198428.2 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr7:33545130 C>T maps to NM_198428.2 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:33388753 T>C maps to NM_198428.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:156618498 A>G maps to NM_021948.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:152967531 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:152969537 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr23:152986356 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr23:152986327 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr16:75267802 C>A maps to NM_001170714.1 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr20:52574000 T>C maps to NM_003657.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:52570098 C>A maps to NM_003657.2 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:52674690 G>A maps to NM_003657.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr20:52570136 G>T maps to NM_003657.2 S505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:115113328 C>T maps to NM_005872.2 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:59161888 C>T maps to ENST00000407086 R827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:58987999 G>A maps to ENST00000407086 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr19:49310292 C>G maps to NM_001190.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:49309944 C>T maps to NM_001190.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr19:49299686 G>A maps to NM_001190.3 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:50232711 G>C maps to NM_181708.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:165547489 G>T maps to NM_000055.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18I-01A-11D-A12B-09 chr3:165504043 C>A maps to NM_000055.2 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr19:41903743 G>A maps to NM_000709.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:41920063 T>C did not map to a codon.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr16:31123510 C>A maps to NM_005881.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:60689266 T>G maps to NM_022893.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr2:60688384 G>T maps to NM_022893.3 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr14:99697760 G>A maps to NM_138576.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A145-01A-11D-A10Y-09 chr20:30309574 T>A maps to NM_138578.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:111881519 A>C maps to NM_138621.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:111921717 G>A maps to NM_138621.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr19:50169137 G>T maps to NM_138639.1 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr14:23778023 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-E2-A15G-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:6928490 A>C maps to NM_181844.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr17:6927076 C>T maps to NM_181844.3 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:147091301 A>C maps to NM_004326.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:147092750 A>C maps to NM_004326.2 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:118770851 A>G maps to NM_182557.2 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr11:118772066 C>T maps to NM_182557.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:136599745 A>C maps to NM_014739.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:136589441 G>T maps to NM_014739.2 S752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr16:81303768 T>A maps to NM_017429.2 Y283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr16:81279116 C>T maps to NM_017429.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr11:112086970 C>G maps to NM_031938.4 S515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr11:112064317 C>T maps to NM_031938.4 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr23:39932240 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:39923695 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:39911451 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:39934251 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:39923728 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr23:39933527 G>T did not map to a codon.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr23:39922162 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0I5-01A-11W-A100-09 chr23:39923605 C>T did not map to a codon.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr23:39937174 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:39913234 T>C did not map to a codon.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr23:39923039 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr23:39937121 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr23:39922953 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr23:39933224 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr23:39931967 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr23:39922992 G>T did not map to a codon.
Sequencing variant TCGA-A7-A13F-01A-11D-A12Q-09 chr23:129150176 C>T did not map to a codon.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr23:129148839 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:129147770 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:129147497 T>C did not map to a codon.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr23:129149945 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:129158974 T>C did not map to a codon.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr23:129189982 G>A did not map to a codon.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr23:129155088 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:129171438 G>T did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:129148106 G>A did not map to a codon.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr23:129149800 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:129146579 C>G did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:129171505 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr23:129147781 C>T did not map to a codon.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr23:129147754 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr23:129149214 C>G did not map to a codon.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr23:129189955 G>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr22:23655134 G>T maps to NM_004327.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PV-01A-11D-A28B-09 chr22:23523317 C>T maps to NM_004327.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:96707348 G>A maps to NM_000623.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:96707645 C>T maps to NM_000623.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:70837389 A>C maps to NM_018429.2 S2044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:70759923 G>A maps to NM_018429.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:70818169 C>T maps to NM_018429.2 F1682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr5:70858269 C>T maps to NM_018429.2 R2556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr5:70793120 T>C maps to NM_018429.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:18198701 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:18194143 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr23:18195776 G>A did not map to a codon.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr23:18234760 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:18192345 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:18221771 A>G did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:18221805 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1RD-01A-11D-A159-09 chr4:42145870 C>A maps to NM_207406.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr6:56857342 C>A maps to NM_152731.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr6:56879946 C>T maps to NM_152731.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr6:56857349 C>T maps to NM_152731.2 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr11:61729921 C>A maps to NM_001139443.1 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr11:61725643 C>T maps to NM_001139443.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:12866251 A>G maps to NM_017682.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr12:70072562 C>A maps to NM_032735.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:70049403 G>A maps to NM_032735.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:45250337 G>A maps to NM_153274.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:205595 A>C maps to NM_016526.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr11:205995 G>A maps to NM_001098787.1 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:102564876 T>G did not map to a codon.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr23:102471237 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:14761576 C>T maps to NM_016561.2 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:17495392 G>A maps to NM_001195.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:17475656 G>A maps to NM_001195.3 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr20:17475258 G>C maps to NM_001195.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:152773775 T>G did not map to a codon.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr23:152771477 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:152773842 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr23:152770765 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:102004633 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:102005077 T>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:102004802 G>A did not map to a codon.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr23:102004786 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:65494150 G>A maps to NM_152414.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:5021411 G>A maps to NM_003670.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:78376541 C>T maps to NM_017614.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:60560009 G>A maps to NM_001080512.1 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr12:32520613 G>A maps to NM_001714.2 Q925Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:32369266 G>A maps to NM_001714.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr12:32491860 C>T maps to NM_001714.2 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr2:127806176 G>A maps to NM_139343.1 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:51685632 T>G maps to NM_016293.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr12:51685680 C>T maps to NM_016293.2 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr2:32836513 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:32631602 T>C maps to NM_016252.3 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr2:32640644 A>G maps to NM_016252.3 Q762Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr2:32824939 C>T maps to NM_016252.3 F4655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr2:32718728 T>A maps to NM_016252.3 T2821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:53793411 C>T maps to NM_033341.3 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr13:103468895 C>T maps to NM_017693.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr13:103459615 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1J3-01A-11D-A13L-09 chr13:103490992 A>G maps to NM_017693.3 K374K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr15:91304367 G>T maps to NM_000057.2 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr15:91312738 G>A maps to NM_000057.2 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr15:91304485 G>T did not map to a codon.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr17:28598288 C>T maps to NM_000386.2 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr17:28598354 C>A maps to NM_000386.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr17:28613876 A>C maps to NM_000386.2 Y169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr17:28612498 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr10:97951824 G>A maps to NM_013314.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr10:97983710 G>A maps to NM_013314.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:56112985 G>A maps to NM_001487.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:56112991 C>T maps to NM_001487.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr1:169347608 G>T maps to NM_003666.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr10:22618335 T>G maps to NM_005180.6 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:22033755 G>A maps to NM_006129.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:22037983 A>C maps to NM_006129.4 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr8:22052370 G>A maps to NM_006129.4 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SX-01A-12D-A099-09 chr23:50659300 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:50659373 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:50659263 C>T did not map to a codon.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr23:50659108 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr23:50654111 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr20:6759580 C>T maps to NM_001200.2 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A143-01A-11D-A10Y-09 chr4:79832816 C>A maps to NM_198892.1 S1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr4:81967615 G>A maps to NM_001201.2 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr14:54416965 G>T maps to NM_130850.2 C337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:55620351 T>C maps to NM_021073.2 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:55739515 C>A maps to NM_021073.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr7:34125683 G>A maps to NM_133468.3 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr4:96052583 C>T maps to ENST00000440890 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr2:203329575 C>T maps to NM_001204.6 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr2:203242212 C>T maps to NM_001204.6 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr2:203383636 G>A maps to NM_001204.6 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr2:203421090 T>C maps to NM_001204.6 N901N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr2:203242212 C>T maps to NM_001204.6 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr2:203417446 G>A maps to NM_001204.6 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr2:203420013 T>C maps to NM_001204.6 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr10:43312806 C>T maps to NM_014753.3 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr10:43292557 A>G maps to NM_014753.3 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr23:15554528 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr23:15552434 A>G did not map to a codon.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr23:15540600 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:15536089 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15536098 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15540567 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15540575 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15540588 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:15544189 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr23:15568079 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr15:83926274 C>T maps to NM_001717.3 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr15:83933255 G>A maps to NM_001717.3 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr9:16738359 C>A maps to NM_017637.5 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr9:16436121 G>A maps to NM_017637.5 D690D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr9:16552752 C>T maps to NM_017637.5 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:16435794 G>A maps to NM_017637.5 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr10:133784251 G>C maps to NM_004052.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr3:113005657 C>T maps to ENST00000273395 S1099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:112969481 G>T maps to ENST00000273395 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr3:113003408 C>T maps to ENST00000273395 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr4:13605526 C>T maps to NM_148894.2 E999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr4:13603396 G>T maps to NM_148894.2 G1709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:13603246 A>C maps to NM_148894.2 G1759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:13603252 A>C maps to NM_148894.2 G1757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:13603747 A>C maps to NM_148894.2 G1592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:13605282 C>A maps to NM_148894.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:13617086 A>G maps to NM_148894.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr4:13605937 G>A maps to NM_148894.2 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr4:13604572 G>T maps to NM_148894.2 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:242501812 C>T maps to NM_032515.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr7:134346543 G>A maps to NM_001724.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr6:3140668 T>A maps to NM_004332.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr20:36962893 C>T maps to NM_001725.2 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr22:32810301 C>T maps to NM_174932.2 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr20:31631124 G>A maps to NM_174897.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr17:65850251 T>C maps to ENST00000321892 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A082-01A-11W-A019-09 chr17:65925452 C>T maps to ENST00000321892 G2126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:65871670 G>C did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:65908823 C>A maps to ENST00000321892 G1734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr17:65909294 C>A maps to ENST00000321892 I1891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr7:140500216 C>A maps to NM_004333.4 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr17:41245984 T>C maps to ENST00000471181 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr17:41245389 C>A maps to ENST00000471181 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr17:41228539 A>G maps to ENST00000471181 S1505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr17:41223255 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr17:41256164 G>A maps to ENST00000471181 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr17:41244295 A>T maps to ENST00000471181 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr17:41244478 C>T maps to ENST00000471181 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr13:32953475 T>G maps to NM_000059.3 L2926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr13:32932066 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:32972492 A>C maps to NM_000059.3 P3281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr13:32969048 C>T maps to NM_000059.3 N3160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:154344338 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:154327649 G>A did not map to a codon.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr23:154317543 G>A did not map to a codon.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr22:50191766 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:32944105 A>C maps to ENST00000395289 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:32946108 T>G maps to ENST00000395289 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:136901436 C>T maps to NM_007371.3 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:15355562 C>T maps to NM_058243.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr16:50353828 G>T maps to NM_001173984.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr5:137480864 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr5:870648 C>T maps to NM_001009877.2 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:891868 G>A maps to NM_023924.4 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:876275 G>A maps to NM_001009877.2 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:865649 C>T maps to NM_001009877.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr5:870669 G>A maps to NM_001009877.2 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:92442613 G>A maps to ENST00000347608 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:28268662 C>G maps to NM_004899.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr2:28521316 C>G maps to NM_004899.3 Y349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr2:28464260 G>A did not map to a codon.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr14:105695167 C>A maps to NM_001519.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr17:59821952 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:59926561 G>T maps to NM_032043.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B5-01A-21D-A12Q-09 chr17:59821811 G>A maps to NM_032043.2 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr5:34915890 G>A maps to NM_018321.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr11:66105189 C>T maps to NM_001024957.1 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:9787514 C>T maps to NM_001003694.1 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr6:36198259 G>A maps to NM_015695.2 K1164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:36181705 A>C maps to NM_015695.2 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr6:36181963 C>G maps to NM_015695.2 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr23:135574242 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:135570622 G>T did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr23:135570327 G>T did not map to a codon.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr23:135574434 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr23:135570651 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr11:1471017 C>T maps to NM_003957.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr11:1466827 C>T maps to NM_003957.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr11:1477888 C>T maps to NM_003957.2 H637H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr21:40571201 C>A maps to NM_018963.3 E1714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr21:40569276 G>A maps to NM_018963.3 D1906D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr21:40571241 T>C maps to NM_018963.3 L1700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr21:40670463 G>A maps to NM_018963.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr23:79999554 A>G did not map to a codon.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr23:79989643 C>G did not map to a codon.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr23:79932419 T>A did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:79990630 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:79948514 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:79999578 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:79985495 C>G did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:80064046 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:79932157 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:79971732 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:79990691 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:79959037 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr23:79980463 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:79978165 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:79939567 T>C did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:79932202 C>T did not map to a codon.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr23:79990687 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr23:79979247 T>C did not map to a codon.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr23:79951433 C>T did not map to a codon.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr23:79947370 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:32842046 A>C maps to NM_001143888.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr1:32849610 C>G maps to NM_001143888.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:32842064 G>A maps to NM_001143888.1 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:580450 C>T maps to NM_001728.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr3:49701898 C>T maps to NM_003458.3 P3884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr3:49695518 A>T maps to NM_003458.3 K2844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:49692118 C>T maps to NM_003458.3 A1710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:49693238 G>T maps to NM_003458.3 E2084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr3:49698236 A>T maps to NM_003458.3 K2987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:15733438 C>T maps to ENST00000382346 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr11:122850009 G>A maps to NM_001098169.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:122848485 A>G maps to NM_001098169.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:93787058 T>C did not map to a codon.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr15:83710633 T>G maps to NM_025238.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr12:108012009 C>A maps to NM_001018072.1 A769A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A8-A08R-01A-11W-A050-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BH-A0BW-01A-11D-A10Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr17:72357931 A>C maps to ENST00000440684 P906P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BH-A0DD-01A-31D-A12Q-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BH-A0DD-01A-31D-A12Q-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A8-A091-01A-11W-A019-09 chr20:11903290 T>C maps to NM_014962.2 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr20:11904103 A>G maps to NM_014962.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FH-01A-12D-A13L-09 chr20:11904304 C>T maps to NM_014962.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr20:11903404 G>A maps to NM_014962.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14O-01A-31D-A10Y-09 chr14:105716213 C>T maps to NM_033271.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:93709171 G>C maps to NM_001002860.2 S949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:38562051 A>G maps to NM_052893.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr11:111367980 T>C maps to NM_017589.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:100615647 C>G did not map to a codon.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr23:100613404 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr23:100614282 C>T did not map to a codon.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr23:100617171 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:100609674 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr23:100629585 T>C did not map to a codon.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr23:100615094 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:100617648 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr3:112185098 A>C maps to NM_181780.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:26509395 A>C maps to NM_001732.2 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66H-01A-11D-A29N-09 chr6:26505348 C>A maps to NM_001732.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:26385555 C>A maps to NM_001197237.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XW-01A-11D-A23C-09 chr6:26406395 C>T maps to NM_007048.5 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:26406423 T>C maps to NM_007048.5 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr6:26412969 A>G maps to NM_194441.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr6:26406423 T>C maps to NM_007048.5 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr6:26406395 C>T maps to NM_007048.5 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr6:26368859 C>T maps to NM_001197246.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:26368937 C>T maps to NM_001197246.1 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:26369079 T>C maps to NM_001197246.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr6:26368440 C>T maps to NM_001197246.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr6:26451999 A>G maps to NM_006994.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr6:32372956 C>T maps to ENST00000468270 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr5:180429675 G>A maps to NM_197975.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr5:180429702 G>A maps to NM_197975.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr5:180377135 G>A maps to NM_001040462.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr10:103295202 G>C maps to NM_033637.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr2:111419364 C>T maps to NM_004336.3 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:111416308 T>C maps to NM_004336.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:111416319 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:40462773 T>G maps to ENST00000412359 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr15:40498521 G>A maps to ENST00000412359 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:40494851 C>G maps to ENST00000412359 S578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:116633413 C>T maps to NM_032725.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr6:105581323 C>A maps to NM_007073.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr6:41899223 C>A maps to NM_004053.3 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:41895230 G>T maps to NM_004053.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr17:56395673 G>A maps to NM_004758.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:56400672 G>A maps to NM_004758.2 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr2:201682950 C>T maps to ENST00000452790 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr10:88728306 A>T maps to NM_006829.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr10:121618636 T>C maps to NM_024834.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:121618681 C>T maps to NM_024834.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr10:98742127 A>C maps to NM_015652.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr10:124457368 T>C maps to NM_001010912.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr10:124457722 T>A maps to NM_001010912.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr10:124457605 G>A maps to NM_001010912.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr10:135170745 C>T maps to NM_001098483.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr10:21805344 G>A maps to NM_207371.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr10:21805479 T>C maps to NM_207371.3 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr10:21805479 T>C maps to NM_207371.3 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr10:5788357 C>T maps to NM_017782.4 Q992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:5789808 C>G maps to NM_017782.4 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:5784152 C>A maps to NM_017782.4 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:5790499 G>T maps to NM_017782.4 E1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr10:5798684 C>G maps to NM_017782.4 S2239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:5798655 A>G maps to NM_017782.4 L2229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XG-01A-31D-A243-09 chr10:5789184 G>T maps to NM_017782.4 V1267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr10:102748458 C>T maps to NM_021830.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EI-01A-11D-A27P-09 chr10:102750655 C>T maps to NM_021830.4 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:72538310 A>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:99968077 A>G maps to ENST00000314594 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:99968875 G>A maps to ENST00000314594 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr10:104614093 G>A maps to NM_001136200.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:11908537 G>A maps to NM_153256.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr10:50916661 G>T maps to NM_182554.2 *158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:75671526 G>C maps to NM_001001791.2 L124L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C8-A275-01A-21D-A16D-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr10:32983900 T>C maps to ENST00000375025 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr10:33165291 C>T maps to NM_024688.2 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:33134843 T>G maps to ENST00000375025 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:33018263 T>C maps to ENST00000375025 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr10:32977991 G>T maps to ENST00000375025 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:50532195 G>T maps to NM_001135196.1 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JJ-01A-11W-A071-09 chr10:50532173 A>G maps to NM_001135196.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr10:50294066 G>C maps to NM_001031746.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr10:103699621 G>A maps to NM_024541.2 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:105903344 C>A maps to ENST00000389588 E1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr10:105932287 C>T maps to ENST00000389588 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr10:118424327 C>T maps to ENST00000388884 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:134743247 G>A maps to ENST00000368586 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr10:134754564 C>A did not map to a codon.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr10:85944485 C>A maps to NM_207373.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr11:8947243 C>A maps to NM_020643.2 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr11:64875773 C>T maps to NM_013265.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:64877358 G>A maps to NM_013265.2 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:64875383 C>T maps to NM_013265.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr11:68029196 C>G maps to NM_022338.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr11:76175092 C>G maps to ENST00000393457 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:57509322 C>T maps to NM_170746.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr11:57509075 C>T maps to NM_170746.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:33566595 G>C maps to ENST00000389726 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr11:33667476 G>A maps to ENST00000389726 S1594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr11:128772496 G>T maps to NM_145013.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:128774419 C>T maps to NM_145013.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:62437401 G>C maps to ENST00000431002 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr11:111156466 G>A maps to NM_198498.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr11:111156556 G>A maps to NM_198498.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr11:111953458 C>G maps to NM_018195.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:16776452 A>G maps to NM_014267.5 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:16776440 T>G maps to NM_014267.5 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A082-01A-11W-A019-09 chr11:122828072 G>A maps to NM_024806.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:108276181 A>G maps to NM_152587.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:66605862 C>G maps to ENST00000360962 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr11:82643267 G>A maps to NM_145018.3 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr11:63585289 G>A maps to NM_138471.1 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr11:111385610 C>G maps to NM_207430.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr11:61547363 G>A maps to NM_001127392.1 Q766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr11:61537880 G>A maps to NM_001127392.1 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:61538992 G>A maps to NM_001127392.1 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:45928733 G>A maps to NM_001080446.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:27081204 G>A maps to NM_018164.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr12:27068940 C>G maps to NM_018164.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr12:107360900 C>T maps to NM_152261.2 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A4E0-01A-12D-A25Q-09 chr12:110924357 A>G maps to NM_013300.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:82850526 T>A maps to NM_032230.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:32134354 C>T maps to NM_018169.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:32136268 G>T maps to NM_018169.3 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr12:32137220 C>G maps to NM_018169.3 S1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr12:13526233 C>T maps to ENST00000318426 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:4626231 G>C maps to NM_020374.2 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr12:40034768 G>C maps to NM_001031748.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:40085853 C>T maps to NM_001031748.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:49073591 G>A maps to NM_017822.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:52467634 C>G maps to NM_021934.4 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr12:52467487 G>A maps to NM_021934.4 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr12:88383051 G>C maps to NM_152589.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr12:88380149 C>T maps to NM_152589.1 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr12:88420368 G>T maps to NM_152589.1 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:88388500 C>T maps to NM_152589.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr12:88380087 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:112666531 T>G maps to NM_001109662.2 P2029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:112666531 T>G maps to NM_001109662.2 P2029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:112621039 G>A maps to NM_001109662.2 R3432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:112685975 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:112707610 G>A maps to NM_001109662.2 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:112708207 C>T maps to NM_001109662.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A4E0-01A-12D-A25Q-09 chr12:112664522 T>C maps to NM_001109662.2 L2126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr12:112703011 T>C maps to NM_001109662.2 K680K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr12:64712480 G>C maps to NM_001170633.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:50513912 C>T maps to NM_032901.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:97093793 G>T maps to ENST00000342887 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:80771626 G>A did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:80615886 C>T maps to NM_173591.3 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr12:80765806 G>A maps to NM_173591.3 G2239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr12:80650137 C>T maps to NM_173591.3 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr12:80647294 C>T maps to NM_173591.3 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr12:80770936 C>T maps to NM_173591.3 I2263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr12:123738229 C>T maps to NM_001143905.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:64609477 G>A maps to ENST00000311915 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr12:48578199 C>T maps to NM_001013635.3 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr12:93100670 G>A maps to NM_001037671.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr13:46946337 T>G maps to NM_025113.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:46942903 T>G maps to NM_025113.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr13:46946583 C>T maps to NM_025113.2 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr13:39587681 C>T maps to NM_025138.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:39587342 T>G maps to NM_025138.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr13:39587531 G>A maps to NM_025138.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:31526899 G>T maps to NM_152325.1 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:73321177 G>T maps to ENST00000377815 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:57052486 T>C maps to NM_017799.3 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:90764655 C>T maps to NM_017970.2 W538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AO-01A-11D-A12Q-09 chr14:90754813 G>A maps to NM_017970.2 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr14:50101795 G>T maps to NM_018139.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr14:57960232 G>A maps to NM_018168.2 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr14:45716463 G>C maps to NM_018353.4 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr14:93652790 C>T maps to NM_001098621.1 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr14:74825095 C>A maps to NM_018228.2 S537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr14:76621083 C>G maps to NM_017926.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr14:60591900 T>G maps to ENST00000404681 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:60581790 C>T maps to ENST00000404681 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr14:93673346 C>G maps to NM_032490.4 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:90263657 G>A maps to NM_145231.2 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr14:90397925 C>A maps to NM_145231.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr14:80971344 C>A maps to NM_152446.3 E1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr14:104040484 C>T maps to ENST00000445352 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:78174464 C>A maps to NM_031210.4 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:78174486 G>C maps to NM_031210.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr14:91681802 C>G maps to NM_001102368.1 S540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr14:91671098 T>C maps to NM_001102368.1 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:99182638 T>G maps to NM_182560.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr14:24774207 G>A maps to NM_174913.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr14:24771258 C>G maps to NM_174913.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:58599979 A>T maps to ENST00000438670 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr14:58471474 G>A maps to ENST00000438670 D786D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr14:60938268 C>T did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr14:60938272 G>A maps to NM_174978.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:60938453 T>C maps to NM_174978.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr14:60938272 G>A maps to NM_174978.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:77492920 G>A maps to NM_024496.2 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:74206009 T>G maps to NM_001043318.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:74194159 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr14:95921719 G>T maps to NM_152592.3 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr14:95934202 C>T maps to NM_152592.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23E-01A-11D-A159-09 chr14:100793565 G>A maps to NM_207117.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr14:100793544 C>T maps to NM_207117.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr14:103566607 G>T maps to NM_001077594.1 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr14:103566714 G>A maps to NM_001077594.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:105958998 G>A maps to ENST00000392523 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr14:105965156 G>T maps to ENST00000392523 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:23467938 A>C maps to NM_021944.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:23456600 C>T maps to NM_021944.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr15:34382542 C>T maps to NM_020154.2 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:93015503 T>G maps to NM_153040.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr15:49659664 G>A maps to NM_152647.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr15:90447195 G>A maps to ENST00000398333 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:90454023 T>C maps to ENST00000398333 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr15:75498683 G>T maps to NM_015492.4 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr15:75498914 C>T maps to NM_015492.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:75498613 C>T maps to NM_015492.4 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:75500455 T>A maps to NM_015492.4 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:90167668 A>C maps to NM_152259.3 P1376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:90168721 C>G maps to NM_152259.3 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr15:65871805 A>G maps to ENST00000420799 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr15:38990577 C>G maps to NM_207444.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:39544368 T>G maps to NM_207445.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:39544725 G>A maps to NM_207445.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr15:34647277 G>A maps to ENST00000438749 Q463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr15:44093967 C>A maps to NM_016400.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr16:15675101 G>A maps to NM_033201.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr16:67697207 C>A maps to NM_032140.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr16:4562820 G>A maps to ENST00000359075 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr16:29756059 G>A maps to NM_175900.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr16:58043923 C>T maps to NM_024598.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr16:2510694 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:2512164 C>G maps to NM_025108.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr16:2510937 G>A maps to NM_025108.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr16:19580755 C>G maps to NM_020314.5 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:19702747 G>A maps to NM_020314.5 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:15973704 G>A maps to NM_144600.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr16:15973704 G>C maps to NM_144600.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:89783150 C>T maps to NM_004913.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:67168335 A>C maps to NM_025187.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:67174454 G>A maps to NM_025187.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr16:4790473 C>T maps to NM_139170.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:9210738 A>C maps to NM_014117.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr16:1889429 A>G maps to NM_001163560.2 C348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr16:2260648 C>T maps to NM_182563.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:58148821 G>A maps to NM_013242.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06T-01A-11W-A019-09 chr16:5110366 C>T maps to ENST00000350219 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:5105256 G>A maps to ENST00000350219 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:3543955 A>C maps to NM_001080524.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr16:1470147 G>C maps to NM_001010878.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:30035048 A>C maps to NM_001109660.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:32906011 G>C maps to NM_207454.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr17:42739710 G>A maps to NM_001145080.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr17:42745435 C>G maps to NM_001145080.2 Y719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr17:72952019 C>T maps to NM_030630.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr17:72948428 C>T maps to NM_030630.2 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr17:29226267 T>C maps to NM_024683.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:29226321 G>A maps to NM_024683.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:43333074 G>A maps to NM_152343.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr17:56620128 C>T maps to NM_001038704.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr17:56620395 G>A maps to NM_001038704.1 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ES-01A-11D-A135-09 chr17:6920582 G>A maps to NM_001142798.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T1-01A-21D-A099-09 chr17:42226187 C>T maps to NM_024032.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr17:42230003 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr17:42225491 C>T maps to NM_024032.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr17:42232257 G>A maps to NM_024032.3 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:45481283 T>G maps to NM_152347.4 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:45421526 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:45438864 G>A maps to NM_152347.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr17:80401963 G>A maps to NM_001193657.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:58506841 G>A maps to NM_181707.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:8132721 A>C maps to NM_025099.5 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr17:8151339 C>A maps to NM_025099.5 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:57288710 G>A maps to NM_018149.6 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:57289067 T>C maps to NM_018149.6 H552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr17:57288017 C>A maps to NM_018149.6 Y202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr17:7329369 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr17:72588619 G>A maps to NM_152460.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr17:35736109 C>T maps to NM_173625.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr17:71232433 A>G maps to NM_017941.4 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr17:59489465 G>T maps to NM_203425.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr17:79632281 G>A maps to NM_001039842.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:74729373 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr17:74729123 C>G maps to ENST00000317409 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:13645424 A>C maps to NM_181481.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr18:33554979 T>C maps to NM_031446.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr18:43820136 G>A maps to NM_145055.3 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr18:30926331 G>T maps to NM_001105528.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr18:20936609 G>A maps to NM_032933.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:21096372 C>T maps to NM_013326.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr18:21109596 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:30193647 G>A maps to NM_001031726.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:58485512 A>G maps to NM_152474.4 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AP-01A-11D-A12Q-09 chr19:30505831 A>G maps to NM_003796.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EI-01A-11D-A27P-09 chr19:758148 G>A maps to NM_173481.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr19:900925 G>T maps to NM_138774.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:3551103 G>A maps to NM_021731.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr19:3620797 G>T maps to NM_021231.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr19:3619188 G>A maps to NM_021231.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr19:2280861 C>T maps to NM_198532.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr19:33464468 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr19:50661561 C>T maps to NM_152358.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr19:16620383 G>A maps to NM_032207.2 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:16617586 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:7570272 C>T maps to NM_198534.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:36497501 A>C maps to ENST00000455847 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr19:40834428 C>T maps to ENST00000357884 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:40832363 G>A maps to ENST00000357884 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:55677312 T>C maps to ENST00000301249 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr19:13888906 G>A maps to NM_014047.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr19:12779223 G>A maps to NM_016145.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:14006306 G>A maps to ENST00000454313 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr19:10200683 C>T maps to NM_018381.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr7:7283156 T>G maps to NM_020156.3 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:119760466 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:119760859 T>G did not map to a codon.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr23:119760250 C>A did not map to a codon.
Sequencing variant TCGA-HN-A2OB-01A-21D-A27P-09 chr23:119760369 A>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:22987413 T>G maps to NM_000491.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr5:159776690 G>A maps to NM_031908.4 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr5:159776462 G>A maps to NM_031908.4 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:34043071 C>T maps to NM_181435.4 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:34043143 C>T maps to NM_181435.4 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:47611498 G>A maps to NM_031909.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr11:47611486 G>A maps to NM_031909.2 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:37578278 G>A maps to NM_182486.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:1144796 C>G maps to NM_207419.3 V42V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A1-A0SK-01A-12D-A099-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr13:24895392 A>G maps to NM_178540.3 K163K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AN-A046-01A-21W-A050-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AN-A04D-01A-21W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr13:24471038 T>G maps to NM_001007537.1 G29G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AN-A04D-01A-21W-A050-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AN-A0FY-01A-11W-A050-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D8-A1JP-01A-11D-A13L-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr13:24465973 G>A maps to NM_001135816.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:7177804 G>A maps to NM_001734.3 Q639Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr12:7177193 C>T maps to NM_001734.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:111494409 G>A maps to NM_018372.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:155290919 A>T maps to NM_001039517.1 C120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr1:210016795 G>A maps to NM_014388.6 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:210001506 C>T maps to NM_014388.6 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr1:162343894 G>A maps to NM_182581.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr1:169818726 G>C maps to NM_018186.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:169388366 C>A maps to ENST00000367806 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:169390681 C>A maps to ENST00000367806 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr1:207195326 C>T maps to NM_023938.5 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr1:231474279 C>T maps to NM_032018.4 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr1:179399654 A>G maps to NM_144696.4 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr1:179335673 G>T maps to NM_144696.4 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr1:11017750 C>T maps to NM_001170754.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:11017131 T>C maps to NM_001170754.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr1:11014109 G>A maps to NM_001170754.1 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr1:170955836 G>T maps to NM_001163629.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:170931074 G>C maps to NM_001163629.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:170916666 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr1:182908336 C>G maps to ENST00000287709 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:182920473 A>T maps to ENST00000287709 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:67559238 G>A maps to NM_001013674.1 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr1:67581049 C>A maps to NM_001013674.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr1:92709921 G>C maps to NM_001012425.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:169762214 C>A maps to NM_033418.1 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:1018320 G>A maps to ENST00000448924 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:116666916 C>T maps to NM_152367.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr1:116663693 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:57258332 A>G maps to NM_001004303.4 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:57254751 G>A maps to NM_001004303.4 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:57189332 G>A maps to NM_001004303.4 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:75038228 A>G maps to NM_001002912.4 D1055D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:75055315 A>C maps to NM_001002912.4 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:75055629 G>A maps to NM_001002912.4 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:75055548 C>A maps to NM_001002912.4 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr1:75078443 G>A maps to NM_001002912.4 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr1:75037346 C>A maps to NM_001002912.4 T1349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:55119567 A>C maps to ENST00000454855 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr1:55175823 G>A maps to ENST00000454855 Q1341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:55145598 G>A maps to ENST00000454855 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:55166887 G>T maps to ENST00000454855 E1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:55277763 G>T maps to NM_001110533.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:156314449 T>C maps to NM_144627.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FF-01A-11W-A050-09 chr1:11766687 C>T maps to NM_198545.3 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:161335345 G>T maps to NM_001013625.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:36181334 G>T maps to NM_152374.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:36181600 G>A maps to NM_152374.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr1:162351891 G>A maps to NM_001135240.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr1:185135758 C>A maps to NM_001105518.1 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:185245788 G>A maps to NM_001105518.1 Q854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr1:185173859 G>A maps to NM_001105518.1 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:28209487 A>C maps to NM_001105556.1 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:28208593 G>T maps to NM_001105556.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:28209286 A>C maps to NM_001105556.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:154187025 G>A maps to NM_001098616.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr1:43240517 T>G maps to NM_024097.2 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:150259146 A>C maps to NM_144697.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr1:197875017 G>A maps to NM_001024594.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr1:226180126 A>G maps to NM_152608.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:151021204 C>T maps to NM_017860.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr1:233092095 A>G maps to NM_032324.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr1:222892338 G>A maps to NM_144695.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr1:222897496 A>G maps to NM_144695.2 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:109197411 G>A maps to ENST00000370031 I108I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BH-A18T-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr1:25572974 C>T maps to NM_020317.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:16330803 C>A maps to NM_178840.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr1:223568467 G>T maps to NM_152610.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:228362452 C>T maps to NM_001010867.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr1:209956184 C>G maps to NM_152485.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:153610785 G>A maps to NM_015607.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr1:54561995 G>A maps to ENST00000371331 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr1:54534541 C>A maps to ENST00000371331 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24T-01A-11D-A167-09 chr1:54562089 C>T maps to ENST00000371331 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr1:43868972 G>A maps to ENST00000310739 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:156264263 C>T maps to NM_144580.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:172558232 A>C maps to ENST00000367723 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:172554176 G>T maps to ENST00000367723 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr1:156897416 C>A maps to NM_144702.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr1:156901796 C>A maps to NM_144702.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:226736784 C>G maps to ENST00000366788 L60L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BH-A18Q-01A-12D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr6:31896623 G>A maps to ENST00000477310 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:9510334 G>A maps to NM_012261.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr20:54941258 C>T maps to NM_080821.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:61574908 G>A maps to NM_017896.2 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr20:61572952 C>T maps to NM_017896.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr20:42831599 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr20:35445812 C>A maps to NM_080627.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IJ-01A-11D-A142-09 chr20:35443693 C>A maps to NM_080627.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr20:18377115 C>T maps to NM_001099407.1 K537K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr20:35731194 G>T maps to ENST00000343811 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr20:34618473 T>G maps to ENST00000373973 Y545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:30598283 G>A maps to ENST00000300415 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr20:30605927 G>T maps to ENST00000300415 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr20:58519657 C>T maps to NM_022106.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr20:31659971 C>T maps to NM_182658.1 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr20:31652641 C>T maps to NM_182658.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:31671647 T>G maps to NM_182519.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr20:31692614 G>T did not map to a codon.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr20:31678568 G>A maps to NM_182519.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr20:3275241 C>G maps to NM_001009984.1 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:3274856 C>A maps to NM_001009984.1 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr20:62187735 T>C maps to NM_024059.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr20:61430925 C>T maps to NM_018270.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr20:35236206 C>T maps to NM_018840.4 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr20:20232262 T>C maps to ENST00000389655 Y731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr20:20269356 C>T maps to ENST00000389655 F970F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr20:20278907 C>A maps to ENST00000389655 I1103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr20:20269468 C>T maps to ENST00000389655 Q1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr20:3736173 G>A maps to NM_001039140.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr20:3802781 C>T maps to NM_018347.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr20:1161623 G>A maps to NM_018354.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr20:1161833 G>T maps to NM_018354.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:746382 G>A maps to NM_033409.3 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr20:31765967 C>T maps to NM_080574.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JE-01A-11D-A13L-09 chr20:31756983 C>T maps to NM_080574.2 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr20:31760834 G>A maps to NM_080574.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:31811623 T>G maps to NM_178466.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:31815360 G>T maps to NM_178466.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IU-01A-11D-A14G-09 chr20:17950657 C>T maps to NM_052865.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr20:10603921 C>T maps to NM_001009608.1 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:10603714 C>T maps to NM_001009608.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr20:259037 C>T maps to NM_153269.1 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr21:45919819 C>A did not map to a codon.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr21:45947264 G>C maps to ENST00000443468 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:33641383 G>A maps to NM_018944.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr21:47706934 C>T maps to NM_058181.1 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr21:33974173 C>T maps to NM_021254.2 *291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr21:30464780 A>G maps to NM_020152.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr21:46380033 T>C maps to NM_058190.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr22:38340199 C>T maps to NM_032561.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:32330256 T>C maps to NM_015372.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:32108526 G>A maps to NM_173566.2 F1766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:32109740 C>A maps to NM_173566.2 E1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr22:32109099 T>G maps to NM_173566.2 R1575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr22:29455032 A>G maps to NM_015370.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr22:45599779 G>A maps to NM_001009880.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr21:43342089 G>A maps to NM_015500.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:118984905 A>C maps to NM_014807.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118981766 T>G maps to NM_014807.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118981974 A>C maps to NM_014807.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118981989 A>C maps to NM_014807.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr11:73789583 C>T maps to ENST00000334126 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZX-01A-12D-A29N-09 chr11:73849825 C>T maps to ENST00000334126 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:73748604 A>C maps to ENST00000334126 G1933G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr11:73849779 T>A maps to ENST00000334126 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G0-01A-11D-A13L-09 chr2:27802527 C>A maps to NM_032266.3 S1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr2:27802012 G>C maps to NM_032266.3 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:27802762 A>C maps to NM_032266.3 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:27801841 C>T maps to NM_032266.3 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:27804052 G>A maps to NM_032266.3 E1538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:27802519 G>A maps to NM_032266.3 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr2:26998353 C>T maps to NM_017877.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:26998494 C>T maps to NM_017877.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr2:26998431 G>A maps to NM_017877.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr2:26671655 C>T maps to NM_145038.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FK-01A-11D-A27P-09 chr2:70377625 T>C maps to NM_017880.1 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr2:24261103 G>A maps to NM_025203.2 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr2:200826645 C>T maps to NM_024520.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr2:99449357 T>C maps to NM_207362.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr2:99443461 C>T maps to NM_207362.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr2:99448831 C>T maps to NM_207362.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr2:200797831 G>C maps to NM_001039693.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:219227512 C>G maps to NM_198559.1 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:219227618 G>A maps to NM_198559.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr2:219232515 C>T maps to NM_198559.1 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr2:219232222 G>C maps to NM_198559.1 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:55433496 G>T maps to NM_152385.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18S-01A-11D-A12B-09 chr2:74803670 T>A maps to NM_138804.3 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr2:211018778 C>T maps to NM_152519.2 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:211019075 G>A maps to NM_152519.2 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr2:85836559 G>A maps to NM_001013649.3 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr2:29295687 A>G maps to NM_001029883.1 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr2:29295822 G>A maps to NM_001029883.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:29296152 C>T maps to NM_001029883.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr2:29293782 C>T maps to NM_001029883.1 V1115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:29296749 C>T maps to NM_001029883.1 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr2:29296695 T>C maps to NM_001029883.1 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr2:29293998 G>T maps to NM_001029883.1 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SG-01A-11D-A142-09 chr2:54587644 T>C maps to NM_001100396.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:74040625 A>G maps to NM_001080474.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr2:228476364 A>G maps to NM_020161.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:24413376 C>A maps to NM_001040710.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr2:24406368 C>T maps to NM_001040710.1 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:242811979 C>T maps to NM_173821.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr2:63631315 G>T maps to NM_015910.4 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr2:63714607 G>A maps to NM_015910.4 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:63605644 C>T did not map to a codon.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr2:85097824 G>A maps to ENST00000409520 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:85051093 C>T maps to ENST00000409520 W439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:85066303 A>G maps to ENST00000409520 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr19:6718309 G>A maps to NM_000064.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr12:8212310 C>A maps to NM_004054.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr3:119434579 G>A maps to NM_033364.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:14703098 G>T maps to NM_016474.4 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:14706595 C>T maps to NM_016474.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr3:14708386 G>A maps to NM_016474.4 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr3:14725872 C>T maps to NM_032137.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:14746068 A>C maps to NM_032137.4 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:14724384 C>T maps to NM_032137.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:14746119 C>T maps to NM_032137.4 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr3:14725872 C>T maps to NM_032137.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr3:14769949 G>T maps to NM_032137.4 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr3:99886580 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr3:128292137 G>A maps to NM_007354.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:118866292 A>C maps to NM_152539.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr3:118865110 C>T maps to NM_152539.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr3:118865254 C>T maps to NM_152539.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr3:11831993 C>T maps to ENST00000455809 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr3:196434579 C>A maps to NM_032898.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:37459026 C>A maps to NM_178342.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:88205419 G>T maps to NM_173824.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr3:43122776 C>T maps to NM_032806.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:196234826 C>A maps to NM_001077657.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr3:196234916 G>A maps to NM_001077657.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:50324237 C>T maps to NM_153215.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:50324282 C>G maps to NM_153215.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X6-01A-11D-A14K-09 chr3:157289742 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr3:143708574 C>G maps to NM_173552.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:192635512 G>A maps to NM_178496.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr3:49311551 C>T maps to NM_198562.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:56667530 A>C maps to ENST00000447900 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr3:56716827 G>A maps to ENST00000447900 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr3:56681155 G>A maps to ENST00000447900 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:69056902 C>T maps to ENST00000383701 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:31995116 C>T maps to ENST00000425700 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:207314501 C>A maps to NM_000715.3 S442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:207286435 C>T maps to NM_000715.3 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr4:57842680 C>G maps to NM_032313.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:100434273 C>T maps to NM_032149.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr4:113468472 C>A maps to NM_018392.4 E1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:113502846 C>T maps to NM_018392.4 R1470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:113541343 C>T maps to NM_018392.4 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr4:113508771 C>T maps to NM_018392.4 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:113539166 T>C maps to NM_018392.4 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr4:113461085 C>T maps to NM_018392.4 L2035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr4:8469961 C>T maps to NM_152544.2 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:128951735 C>T maps to ENST00000454347 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr4:128938553 G>C maps to ENST00000454347 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:121957700 C>T maps to NM_024574.3 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr4:121961157 C>T maps to NM_024574.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr4:71200896 C>T maps to NM_033122.3 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr4:165878323 C>T maps to NM_153027.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr4:71024260 C>T maps to NM_214711.3 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:184603898 T>A maps to NM_021942.4 Y376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr4:184626158 C>T maps to NM_021942.4 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr4:164436572 G>A maps to ENST00000509657 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr4:3255095 G>A maps to NM_001042690.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr4:140187980 C>T maps to ENST00000260011 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr4:5982065 C>A did not map to a codon.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr4:5977631 G>A maps to ENST00000324058 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr4:5966749 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr4:146601432 C>A maps to NM_001080531.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr4:146601495 A>G maps to NM_001080531.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr4:5528054 A>G maps to NM_005750.2 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr9:123777516 G>A maps to NM_001735.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr9:123778622 C>T maps to NM_001735.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:123794433 G>A maps to NM_001735.2 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr9:123731361 G>A maps to NM_001735.2 Y1399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr5:133304254 C>T maps to NM_020199.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr5:134782576 T>C maps to NM_130848.2 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr5:134782594 G>T maps to NM_130848.2 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr5:31545751 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:139574106 A>C maps to NM_032412.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:36200343 C>A maps to NM_001085411.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr5:43505872 G>A maps to NM_198566.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:56207268 T>C maps to NM_153706.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr5:93732077 C>T maps to ENST00000513200 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr5:93856325 G>C maps to ENST00000513200 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr5:93856499 G>A maps to ENST00000513200 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:93739281 G>T maps to ENST00000513200 S960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr5:93805803 C>G maps to ENST00000513200 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:43039620 C>T maps to NM_001014279.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr5:172537651 C>T maps to NM_153607.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr5:172550081 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:37176051 A>G maps to NM_023073.3 T1979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:37181008 A>G maps to NM_023073.3 G1840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr5:37108549 G>A maps to NM_023073.3 L3088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:179271181 T>C maps to NM_016175.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr5:7835544 G>T maps to NM_001089584.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IU-01A-11D-A14G-09 chr5:131796261 C>T maps to NM_001013717.1 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:41161914 A>C maps to NM_001115131.1 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr5:41153969 G>A maps to NM_001115131.1 Y744Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:32260987 C>A maps to ENST00000447241 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:32261366 C>T maps to ENST00000447241 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr6:165715772 C>T maps to NM_144980.3 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr6:30617374 G>A maps to NM_001161376.1 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr6:30615301 G>A maps to NM_001161376.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr6:47846155 C>T maps to NM_001013732.3 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr6:47847115 T>C maps to NM_001013732.3 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:47846039 C>G maps to NM_001013732.3 *847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr6:48035985 G>A maps to NM_001013732.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr6:54025333 C>T maps to ENST00000502396 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:54066988 C>T maps to ENST00000502396 F892F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr6:53883885 G>T maps to ENST00000514921 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr6:43476522 G>A maps to NM_001012974.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr6:43475011 T>A maps to NM_001012974.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:97720876 G>A maps to NM_198468.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:121482198 G>A maps to ENST00000275159 D899D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr6:121577340 C>G maps to ENST00000275159 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr6:121615778 G>A maps to ENST00000275159 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:4099315 G>A maps to NM_001085401.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr6:118803029 C>A maps to NM_001042475.2 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr6:118953700 A>G maps to NM_001042475.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr6:118886717 G>T maps to NM_001042475.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FG-01A-11D-A13L-09 chr6:74072568 G>T maps to NM_001017361.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:36294353 T>G maps to NM_001010903.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr6:36291138 G>T maps to NM_001010903.4 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr6:31741188 A>G maps to NM_025258.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr6:157713933 C>G maps to NM_018452.4 *142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:157714018 G>A maps to NM_018452.4 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:31627048 G>A maps to NM_021184.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:127901509 G>A maps to NM_001010905.1 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:24706364 C>G maps to NM_030939.4 *230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr6:170176589 T>A maps to NM_018341.1 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr6:35704941 C>T maps to NM_145028.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:36867364 C>T maps to NM_152734.3 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr6:151907143 C>T maps to ENST00000367290 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr6:151939083 G>C maps to ENST00000367290 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr6:151857536 G>T maps to ENST00000367290 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr6:151869572 A>G maps to ENST00000367290 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:40958262 T>G maps to NM_000587.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr5:40959617 A>G maps to NM_000587.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr7:40220544 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:31735221 A>C maps to NM_006658.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr7:86825960 C>T maps to NM_024315.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:6639566 C>T maps to NM_024067.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr7:6634118 C>A maps to NM_024067.2 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:6859572 C>A did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:6859401 G>A maps to NM_198097.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:6859416 G>T maps to NM_198097.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr7:23349134 G>C maps to NM_138446.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr7:23338985 C>T maps to NM_138446.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr7:148311309 C>A maps to NM_145304.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr7:30197079 C>T maps to NM_152793.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:99755253 A>C did not map to a codon.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr7:23729010 C>G maps to NM_199136.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:134851533 G>A maps to NM_024033.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr7:112124978 C>G maps to NM_182597.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:48086096 G>T maps to ENST00000430738 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr7:48092458 T>A maps to ENST00000430738 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr7:48080991 C>T maps to ENST00000430738 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr7:120629842 C>A maps to NM_024913.4 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:120935616 C>T maps to NM_024913.4 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr7:120767164 C>T maps to NM_024913.4 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:120768503 C>T maps to NM_024913.4 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr7:112462137 C>T maps to NM_152556.2 W293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr7:112462310 C>A maps to NM_152556.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:100054572 C>T maps to ENST00000426357 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr7:100061588 G>A maps to ENST00000426357 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr7:89933314 G>T maps to NM_001039706.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr7:108524577 C>G maps to NM_001024607.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:6370358 C>A maps to NM_001037163.1 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:57378101 G>A maps to NM_000562.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr9:139840386 G>T maps to NM_000606.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr9:139841101 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr8:144126092 G>T maps to NM_173687.2 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27A-01A-11D-A167-09 chr8:69381035 C>G maps to NM_052958.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr8:40011155 C>T maps to NM_020130.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:67590110 A>C maps to NM_019607.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr8:67793180 A>G maps to NM_173518.4 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:10557965 G>A maps to NM_001040032.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:27922137 C>T maps to ENST00000341513 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr8:27887896 G>A maps to ENST00000341513 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr8:73982159 C>T maps to NM_153225.3 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr8:38385861 T>G maps to NM_207412.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr9:35664116 G>A maps to NM_032818.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr9:98669391 C>G maps to NM_001010895.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:98703780 A>G maps to NM_001010895.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:132084458 C>T maps to NM_001012715.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr9:131587071 G>A maps to NM_016390.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr9:131050993 G>C maps to NM_001040011.1 *236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:131038594 G>C maps to NM_001040011.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr9:131048298 G>A maps to NM_001040011.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:131038976 C>T maps to NM_001040011.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr9:7799563 C>A maps to NM_033428.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr9:96097915 G>A maps to NM_001098808.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr9:96097672 G>A maps to NM_001098808.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:35043447 A>C maps to NM_203299.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:35044317 A>C maps to NM_203299.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:72520982 G>A maps to NM_001010940.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:139888232 T>G maps to NM_183241.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr9:88842312 T>A did not map to a codon.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr9:139379381 G>A maps to NM_152571.2 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr9:139379394 C>T maps to NM_152571.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr9:135374975 G>A maps to NM_207417.1 G207G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GI-A2C9-01A-11D-A21Q-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:34381417 G>A maps to NM_032596.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:97844864 T>G maps to NM_001193329.1 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:97844998 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr9:97563248 C>T maps to NM_001193329.1 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:103213185 C>T maps to NM_001198805.1 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr9:140510462 C>T maps to NM_032937.4 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr9:111903755 A>G maps to NM_014334.2 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr9:77613612 G>A maps to NM_152420.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr9:77631272 T>C maps to NM_152420.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr9:116191455 T>C maps to ENST00000451722 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:116191542 G>A maps to ENST00000451722 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr9:111849488 G>A maps to NM_032012.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr9:111849506 G>A maps to NM_032012.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:132377801 G>A maps to NM_199350.3 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr9:132382052 G>T maps to NM_199350.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:86571085 G>A maps to NM_032307.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr9:71155565 C>T maps to NM_153237.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3HN-01A-11D-A20S-09 chr9:27548293 A>G maps to NM_018325.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:27566854 A>G maps to NM_018325.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr9:132595745 C>T maps to NM_016520.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:90500949 A>C maps to NM_178828.4 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:90502986 G>A maps to NM_178828.4 Q1195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr9:90497817 C>T maps to NM_178828.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:26892704 C>T maps to NM_024828.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:114454524 T>G maps to NM_173521.3 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:114470193 C>A maps to NM_173521.3 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:114520455 C>A maps to NM_173521.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RP-01A-21D-A099-09 chr9:114518626 T>C maps to NM_173521.3 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:114454074 G>A maps to NM_173521.3 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:139720234 G>A maps to NM_001173988.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr9:135759366 C>T maps to ENST00000372136 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr9:15874579 C>T maps to NM_173550.2 F1173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr9:136266927 G>A maps to NM_153710.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr8:86241929 G>A maps to NM_001738.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr19:49142644 G>A maps to NM_001217.3 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr19:49143043 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr19:49142210 G>A maps to NM_001217.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:49143053 G>C maps to NM_001217.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:49142594 G>C maps to NM_001217.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr15:63638801 G>A maps to NM_001218.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr1:150233918 G>A maps to NM_012113.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:150234560 A>G maps to NM_012113.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr17:58235471 T>C maps to NM_000717.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:15790678 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:15793408 C>A did not map to a codon.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr16:66884453 G>A maps to NM_005182.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:35679329 T>C maps to NM_001216.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:231624757 C>T maps to NM_001130850.1 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr13:49925032 C>T maps to NM_001079670.1 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr1:227174269 C>A maps to NM_020247.4 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:227149178 C>T maps to NM_020247.4 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr22:24573574 C>T maps to NM_012295.3 A2103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:24563176 C>T maps to NM_012295.3 L1860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr22:24515497 G>T maps to NM_012295.3 E1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr22:24480533 G>A maps to NM_012295.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr22:24573643 C>G maps to NM_012295.3 S2126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:60969218 G>A maps to NM_031215.2 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr11:67287357 G>A maps to NM_016366.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr19:48537514 G>A maps to NM_019855.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:48543979 G>A maps to NM_019855.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr18:21736509 G>T maps to NM_012189.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr18:21739932 G>T maps to NM_138644.1 G347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:65145335 A>G maps to ENST00000371073 G1101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:65099909 C>T maps to ENST00000371073 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:65139110 G>A maps to ENST00000371073 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr19:13339551 G>A maps to NM_001127221.1 L1863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr19:13370400 C>T maps to NM_023035.2 V1459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JS-01A-11D-A13L-09 chr19:13370457 C>T maps to NM_023035.2 K1440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:13370460 C>T maps to NM_023035.2 W1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:140954104 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr9:140953541 A>T maps to ENST00000277549 A1496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr9:140943755 G>A maps to ENST00000277549 A1234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr9:140777193 A>T did not map to a codon.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr9:140901244 A>T maps to ENST00000277549 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A153-01A-12D-A12B-09 chr9:140952285 G>A maps to ENST00000277549 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr9:140943767 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0T1-01A-21D-A099-09 chr12:2714891 C>T maps to NM_199460.2 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr12:2794919 C>T maps to NM_199460.2 D1947D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:2595324 C>T maps to NM_199460.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr12:2602509 C>T maps to NM_199460.2 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr12:2711018 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0IA-01A-11W-A050-09 chr12:2676747 G>A maps to NM_199460.2 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DT-01A-21D-A12B-09 chr12:2800325 G>A maps to NM_199460.2 E2209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr12:2558200 C>A maps to NM_199460.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr3:53842706 C>T maps to NM_001128840.1 C1927C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr3:53839093 C>T maps to NM_001128840.1 F1890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DO-01B-11D-A12B-09 chr3:53779688 C>T maps to NM_001128840.1 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr1:181680206 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:181690904 T>G maps to ENST00000357570 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr1:181767516 G>A maps to ENST00000357570 P2163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:181725097 C>T maps to ENST00000357570 N1332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr1:181688961 C>T maps to ENST00000357570 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:181767969 G>A maps to ENST00000357570 *2314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:181705571 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr1:181685254 C>A maps to ENST00000357570 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:49088210 T>G did not map to a codon.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr23:49065104 C>T did not map to a codon.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr23:49065755 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:49072932 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:49081267 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:49077520 C>T did not map to a codon.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr23:49082870 A>T did not map to a codon.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr23:49071971 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr23:49071851 G>A did not map to a codon.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr23:49066792 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:49075817 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:49088140 T>C did not map to a codon.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr23:49062123 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr23:49083479 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr23:49065765 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr23:49076143 A>G did not map to a codon.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr23:49065115 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr23:49063554 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr23:49083474 G>A did not map to a codon.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr23:49071880 A>T did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:49071936 C>T did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:49074447 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr17:48695485 G>C maps to NM_018896.3 L1768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr17:48683515 G>A maps to NM_198397.1 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:48683489 G>T maps to NM_198397.1 E1510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr17:48646554 T>C maps to NM_018896.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr17:48695610 C>T maps to NM_018896.3 G1778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr17:48650138 C>G maps to NM_018896.3 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr17:48681623 C>T maps to NM_018896.3 F1426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr17:48668852 C>A maps to NM_018896.3 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr17:48646590 C>G maps to NM_018896.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr17:48703502 C>G maps to NM_018896.3 T2175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr16:1254328 G>A maps to NM_021098.2 W774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr16:1265024 C>G maps to NM_021098.2 V1661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:1261573 C>T maps to NM_021098.2 R1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr22:40075815 C>A maps to NM_021096.3 I1828I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr22:40057233 G>A maps to NM_021096.3 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr22:40043827 T>C maps to NM_021096.3 H488H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr22:40055476 C>T maps to NM_021096.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:201046053 G>A maps to NM_000069.2 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr1:201038704 G>T maps to NM_000069.2 I795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:201030418 C>T maps to NM_000069.2 K1077K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:201012644 C>T maps to NM_000069.2 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:201028334 G>A maps to NM_000069.2 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DN-01A-11D-A17W-09 chr1:201030400 C>T maps to NM_000069.2 K1083K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr7:81636993 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:50415160 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr3:50415438 C>G maps to ENST00000435965 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr3:50413607 G>A maps to ENST00000435965 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr3:50404846 G>A maps to ENST00000435965 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr3:54676225 C>T maps to NM_018398.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:55108163 T>G maps to NM_018398.2 G1069G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr12:1949959 C>T maps to NM_172364.4 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:37331622 C>T maps to NM_000723.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr10:18827197 C>A maps to NM_201596.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr10:18690013 G>A maps to NM_201570.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr12:49220165 G>A maps to NM_000725.2 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:152727056 C>G maps to NM_000726.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:24372910 A>C maps to NM_006539.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:65021036 C>T maps to NM_014405.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr17:65026606 C>T maps to NM_014405.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr17:64876779 G>A maps to NM_014404.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr19:54481412 C>T maps to NM_031895.5 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr1:174977785 G>A maps to NM_014412.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:27464810 G>C maps to NM_004341.3 V1972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:27449091 C>T maps to NM_004341.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:27460409 G>A maps to NM_004341.3 Q1520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr11:115111078 G>A maps to NM_014333.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SB-01A-11D-A142-09 chr3:85932471 C>T maps to NM_153184.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr3:86010720 G>A maps to NM_153184.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:159166749 G>A maps to NM_021189.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr1:159170669 C>T maps to NM_021189.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:44127493 T>C maps to NM_145296.1 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr3:62578365 C>T maps to ENST00000383709 K461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr3:62499311 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr3:62423868 C>G maps to ENST00000383709 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr3:62503857 G>A maps to ENST00000383709 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:122526106 G>T maps to NM_001167940.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:121985735 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:122111513 C>A maps to NM_001167940.1 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:7373467 C>T maps to NM_001170692.1 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr11:14992710 G>A maps to NM_001741.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr12:54109012 C>A maps to NM_020898.2 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr12:54110178 T>C maps to NM_020898.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:46928951 G>T maps to ENST00000448105 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr2:188216645 C>A did not map to a codon.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr7:134618764 G>A maps to NM_033138.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr7:134613540 G>A maps to NM_033138.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr10:105207211 G>C maps to NM_015916.4 Y223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr14:90870838 C>T maps to NM_006888.4 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr14:90870227 C>T maps to NM_006888.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:5567122 C>T maps to NM_005185.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr10:5567449 C>T maps to NM_005185.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr1:1848266 C>T maps to NM_138705.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr7:71868339 C>T maps to NM_031468.3 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B7-01A-12D-A10Y-09 chr7:71743767 G>A maps to NM_031468.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr7:71275371 C>A maps to NM_031468.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:16601238 G>C maps to NM_145046.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr19:16593494 C>T maps to NM_145046.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:9803417 G>A maps to NM_003656.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr10:12595304 G>A maps to NM_153498.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:149633073 A>C maps to NM_015981.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:149636384 A>C maps to NM_015981.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr5:149618305 G>T maps to NM_015981.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:44286721 G>C maps to NM_001220.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr4:114438799 A>T maps to ENST00000515496 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr10:75612978 T>C maps to ENST00000423381 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr5:110814118 C>T maps to NM_001744.4 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:3776720 G>A maps to ENST00000381771 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:121686435 G>C maps to NM_006549.3 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr9:138714835 C>A maps to ENST00000409386 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:138714304 G>A maps to ENST00000409386 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:138774802 G>A maps to ENST00000409386 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr9:138714310 A>T maps to ENST00000409386 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr9:138714463 C>A maps to ENST00000409386 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:7700470 C>T maps to NM_015215.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:7724937 C>T maps to NM_015215.2 I777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:7309643 G>A maps to NM_015215.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr17:4872987 C>T maps to NM_015099.3 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr17:4872101 C>T maps to NM_015099.3 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:67696163 G>A maps to NM_018448.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:67698920 G>A maps to NM_018448.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr12:67696172 G>A maps to NM_018448.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr3:12849814 C>G maps to NM_001162499.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:64973986 G>A maps to NM_005186.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:241536360 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:241531439 G>A maps to NM_023083.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr19:39221789 G>A maps to NM_144691.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:30974020 G>C maps to ENST00000295055 S395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:223940584 G>A maps to NM_001748.4 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr15:42703521 C>T maps to NM_000070.2 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr15:42681293 T>C maps to NM_000070.2 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42693953 G>A maps to NM_000070.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr15:42646652 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr15:42652164 C>T maps to NM_000070.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:110489935 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr23:110496377 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:110491213 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:110494948 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr23:110494201 C>G did not map to a codon.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr1:230895282 C>T maps to NM_006615.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:30872033 T>G maps to NM_001002259.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:30873794 G>A maps to NM_001002259.1 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr12:30872132 C>A maps to NM_001002259.1 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr12:30904068 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:5914690 G>A maps to ENST00000394521 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:5914425 C>T maps to ENST00000394521 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr5:35921197 G>A maps to NM_144647.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:116544383 G>T maps to NM_006136.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:116557788 C>T maps to NM_006136.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:19683161 G>A maps to ENST00000375145 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr22:37912134 G>A maps to NM_014550.3 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr22:37906380 T>A maps to NM_014550.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr7:2983932 G>A maps to NM_032415.4 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:2951847 G>A maps to NM_032415.4 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr7:2979468 G>T maps to NM_032415.4 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:2954873 C>A maps to NM_032415.4 E946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:2987383 C>T maps to NM_032415.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:2979487 C>T maps to NM_032415.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr7:2962873 G>T maps to NM_032415.4 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr17:78171931 C>T maps to NM_024110.2 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr17:78178978 C>T maps to NM_024110.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr5:40843353 T>C maps to NM_032587.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr5:40854019 A>T maps to NM_032587.3 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:40843428 T>G maps to NM_032587.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr5:40841760 A>C maps to NM_032587.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:40854269 C>T maps to NM_032587.3 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:48734037 G>C maps to NM_001184900.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr9:139259655 G>A maps to NM_052813.4 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr9:139264847 C>A maps to NM_052813.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr9:139265794 G>A maps to NM_052813.4 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:11031536 A>C maps to NM_199141.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:11015738 C>T maps to NM_199141.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr19:11031599 C>T maps to NM_199141.1 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr11:3059365 G>A maps to NM_001014437.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr11:3061079 C>A maps to NM_001014437.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:3061127 C>T maps to NM_001014437.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:3062148 G>A maps to NM_001014437.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:25314104 G>C maps to NM_018272.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr15:40913335 C>T maps to NM_170589.3 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr15:40917570 G>A maps to NM_170589.3 L1729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:40949291 C>T maps to NM_170589.3 Y2205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SD-01A-11D-A10Y-09 chr23:41379770 T>C did not map to a codon.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr23:41413140 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr23:41419041 G>A did not map to a codon.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr23:41416284 C>T did not map to a codon.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr23:41530685 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:41393987 T>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:41495898 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr23:41646460 G>C did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:41390310 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:41413094 C>T did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr16:2229627 G>A maps to NM_020764.3 S1247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr17:73497205 G>A maps to NM_020753.3 T1188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:73503686 A>G maps to NM_020753.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:73500658 G>A maps to NM_020753.3 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:104903811 C>A maps to NM_033292.2 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:104905103 C>T maps to NM_033292.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:185550445 C>A maps to NM_032991.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:104819395 A>G maps to NM_001225.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr4:110610589 G>A maps to NM_001226.3 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:202149750 C>T maps to NM_001080125.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RP-01A-21D-A099-09 chr2:202141633 G>T maps to NM_001080125.1 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:202131301 G>A maps to NM_001080125.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P3-01A-11D-A142-09 chr2:202131410 C>T maps to NM_001080125.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:202131497 C>T maps to NM_001080125.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr6:90566807 C>T maps to NM_012115.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr6:90583528 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:90578726 A>G maps to NM_012115.3 A1906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr6:90564539 C>T maps to NM_012115.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AL-01A-21D-A12Q-09 chr6:90572906 T>C maps to NM_012115.3 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:15831196 C>T maps to NM_001229.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr1:160165314 C>T maps to NM_001231.4 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr1:160167382 G>A maps to NM_001231.4 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr3:121980841 C>T maps to NM_001178065.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr5:96101007 A>G maps to ENST00000508830 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr5:96100941 C>T maps to ENST00000508830 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:10720543 G>A maps to NM_001079843.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:65784557 G>A maps to NM_053054.3 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:65793667 C>T maps to NM_053054.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:43931840 C>T maps to NM_172095.1 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr15:43940232 C>T maps to NM_172095.1 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:134344658 C>T maps to NM_178019.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:26517875 C>T maps to NM_198137.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:92159550 C>T maps to NM_024764.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr14:92102917 T>C maps to NM_024764.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr14:92189492 G>C maps to NM_024764.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr14:92047328 C>T maps to NM_024764.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:116166682 C>T maps to NM_001753.4 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr3:8787228 G>A maps to NM_001234.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr16:67100702 T>C did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr16:67070594 G>A maps to NM_022845.2 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:67063683 C>T maps to NM_022845.2 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr16:67070633 C>A maps to NM_022845.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr11:119103159 G>T maps to NM_005188.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr11:119142561 G>A maps to NM_005188.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr11:119148505 G>A maps to NM_005188.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr11:119170208 C>A maps to NM_005188.2 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:105422909 T>G maps to NM_170662.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:105421039 G>T maps to NM_170662.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr3:105421210 A>T maps to NM_170662.3 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:45297489 A>C maps to NM_012116.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:107399334 A>C maps to NM_024814.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:107399370 A>C maps to NM_024814.2 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:107399568 A>C maps to NM_024814.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24T-01A-11D-A167-09 chr14:24898143 G>T maps to NM_001039771.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr20:54579032 C>T maps to NM_080617.4 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:44485529 C>T maps to ENST00000398168 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:70871837 T>C maps to NM_201453.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P0-01A-11D-A142-09 chr17:46148871 T>A maps to ENST00000442683 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:77758810 C>T maps to NM_005189.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr17:77758180 C>T maps to NM_005189.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:77758103 C>T maps to NM_005189.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr7:26248126 A>G maps to NM_016587.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:77809492 C>A maps to NM_003655.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:77808810 C>T maps to NM_003655.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:39066995 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:14029384 A>C maps to NM_017721.4 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:14037404 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:97778986 G>T maps to NM_001159747.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:97786971 C>T maps to NM_001159747.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:70520781 G>T maps to NM_018237.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr10:70482303 C>T maps to NM_018237.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr10:70507133 C>T maps to NM_018237.2 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr18:57115242 A>T maps to NM_133459.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:42906701 C>A maps to NM_001296.4 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr18:66721310 G>A maps to NM_024781.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr19:56160841 C>T maps to NM_013301.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr9:35660614 G>A maps to NM_174923.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:219870846 T>G maps to NM_194302.2 P1606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr2:219895963 C>T maps to NM_194302.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr2:219895497 G>A maps to NM_194302.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr18:47787563 C>A maps to NM_145020.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr4:186383862 C>G did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr4:185593490 G>T maps to NM_152683.2 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr4:185612859 C>T maps to NM_152683.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr5:114611094 G>A maps to NM_001040440.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr5:114611287 A>G maps to NM_001040440.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr16:58287991 G>T maps to NM_014157.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr19:48821778 G>A maps to NM_144577.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr19:48800319 G>A maps to NM_144577.3 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr22:29177136 G>A maps to NM_173510.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr23:48924823 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr23:48921457 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:48922180 C>T did not map to a codon.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr23:48922005 C>G did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr19:33424375 C>T maps to NM_032816.3 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:33424387 G>C maps to NM_032816.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:33417110 G>C maps to NM_032816.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:33378729 A>G maps to NM_032816.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr5:68581192 G>A maps to NM_176816.3 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr5:68616154 T>C maps to NM_176816.3 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr5:68595847 T>G maps to NM_176816.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr7:23682550 G>A maps to NM_138771.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:31692416 G>T maps to NM_194300.2 E1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:42777324 C>T maps to NM_144719.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr3:42777252 C>T maps to NM_144719.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr3:42754738 C>T maps to NM_144719.3 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr19:13870016 C>T maps to NM_030818.2 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:92978028 C>T maps to NM_017667.2 F738F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:92883183 T>C maps to NM_017667.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:92979255 G>T maps to NM_017667.2 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr16:57760056 G>A maps to NM_032269.5 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:57752314 T>C maps to NM_032269.5 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr7:128441409 G>T maps to NM_022742.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr7:128434805 G>A maps to NM_022742.3 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr7:128455957 C>T maps to NM_022742.3 N1112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr2:109432416 T>C maps to NM_144978.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:123674920 C>G maps to NM_022757.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr2:179718297 A>G maps to NM_173648.3 Y1038Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr2:179730514 G>A maps to NM_173648.3 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:74708187 G>C maps to ENST00000393965 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:16675968 C>T maps to NM_014695.1 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:16638063 G>T maps to NM_014695.1 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:16638915 G>T maps to NM_014695.1 E1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr17:16665799 C>T maps to NM_014695.1 Y1280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr17:18528550 G>A did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr17:18498094 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr17:18498076 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr17:18528418 C>G did not map to a codon.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr7:76797008 A>G maps to NM_020879.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:76903797 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr10:106166472 G>T maps to NM_001008723.1 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18S-01A-11D-A12B-09 chr10:106153121 T>C maps to NM_001008723.1 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:159028731 G>A maps to NM_138803.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:124857165 T>G maps to NM_025004.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:124857538 C>T maps to NM_025004.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr2:197521748 C>T maps to NM_001080539.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr19:49913125 G>T maps to NM_144688.4 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr22:30768208 C>G maps to NM_001017437.2 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr22:30766397 C>A maps to NM_001017437.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr4:77317568 A>T maps to NM_001042784.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:133379010 T>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:93722091 G>A maps to NM_206886.2 E1299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:93648931 C>A maps to NM_206886.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:26582245 C>T maps to NM_022778.2 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:26584670 C>T maps to NM_022778.2 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:49098534 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:49099382 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:49106128 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:27605730 G>A maps to NM_018246.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PV-01A-11D-A28B-09 chr1:3679227 C>G maps to NM_152492.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:32667637 C>T maps to ENST00000421922 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:12940513 C>A maps to NM_031455.3 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr10:13043198 G>A maps to NM_031455.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr1:43108212 G>T maps to NM_001080850.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr15:74622636 C>T maps to ENST00000321288 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:27371946 C>A maps to NM_030771.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr11:27379073 G>C maps to NM_030771.1 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr3:126153122 C>T maps to ENST00000505024 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:180379750 A>G maps to NM_181426.1 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr3:180359799 G>A maps to NM_181426.1 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:180334333 G>T maps to NM_181426.1 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:180334471 G>A maps to NM_181426.1 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:78032434 C>T maps to NM_017950.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:78059890 G>A maps to NM_017950.2 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr17:8638832 C>A maps to NM_144681.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr17:62530745 C>G maps to NM_138363.1 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr17:62533818 C>T maps to NM_138363.1 F796F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr17:63898299 T>C maps to NM_145036.3 Q711Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr17:61838663 G>A maps to NM_020198.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr3:128758633 C>G maps to NM_024768.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr3:128755857 G>C maps to NM_024768.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:191098054 G>T maps to NM_178335.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:191093367 C>T maps to NM_178335.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr3:191093232 C>T maps to NM_178335.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:113172492 C>T maps to NM_144718.3 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:113187237 C>T maps to NM_144718.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:113187048 A>G maps to NM_144718.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr3:113166913 G>T maps to NM_144718.3 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:113225374 A>C maps to NM_144718.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr12:102437881 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:28512343 T>G maps to NM_032141.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr12:119966482 G>A maps to NM_178499.3 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:119966455 T>A maps to NM_178499.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr12:119937942 G>A maps to NM_178499.3 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr12:119968835 C>T maps to NM_178499.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr19:46506714 C>T maps to NM_001080402.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:123285985 C>T maps to NM_201435.3 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:111342485 C>T maps to NM_152591.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr12:49298847 C>T maps to NM_033124.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:93148213 A>C maps to NM_181645.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr11:93097376 C>T maps to NM_181645.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr5:150564002 C>G did not map to a codon.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr5:150566945 C>A did not map to a codon.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr10:32856782 A>G maps to NM_001026383.1 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr10:32745229 C>T maps to NM_001026383.1 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr11:32636345 C>T maps to NM_001008391.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr2:132288158 C>T maps to NM_138770.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr2:130897468 C>T maps to NM_207310.1 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:521047 C>T maps to NM_032358.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:773018 C>G did not map to a codon.
Sequencing variant TCGA-E2-A15L-01A-11D-A12B-09 chr19:46915827 C>T maps to NM_032040.3 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr3:112357486 C>T maps to ENST00000447230 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr11:96117311 G>A maps to NM_024725.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:85627277 T>C did not map to a codon.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr11:65658673 C>T maps to NM_006848.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr11:60609810 C>T maps to NM_024098.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:66359835 G>A maps to NM_018219.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:55546074 G>A maps to ENST00000436346 N1076N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:55599631 C>A maps to ENST00000436346 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr14:91779975 C>T maps to NM_001080414.2 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:91770046 C>T maps to NM_001080414.2 E1211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr14:91810001 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr14:91780359 C>T maps to NM_001080414.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr6:13791082 C>T maps to NM_001031713.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr6:13801534 G>A maps to NM_001031713.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:124421637 C>G maps to NM_025140.1 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:118753907 C>A maps to NM_019044.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr5:169023705 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:36170026 A>C maps to NM_005893.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:32684554 G>A maps to NM_005408.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:32685047 C>T maps to NM_005408.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:34340800 G>T maps to NM_005064.3 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:75401298 G>T maps to NM_006072.4 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr17:34641453 C>T maps to NM_207007.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:68463733 G>A did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:50053903 A>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:50052694 T>C did not map to a codon.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr23:50053141 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:50052753 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:50053024 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr23:50094617 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:50052922 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:50053927 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr23:50090647 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr23:50031865 A>C did not map to a codon.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr23:50037883 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr23:50051514 G>A did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:50053999 C>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:50053242 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:4388033 C>T maps to NM_001759.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:41903791 G>A maps to NM_001760.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr19:30313494 C>T maps to NM_001238.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:95893940 T>C maps to NM_057749.1 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:95906148 C>T maps to NM_057749.1 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr4:78082827 C>G maps to NM_004354.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr5:86695301 T>A maps to NM_001239.3 K261*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A2-A0T5-01A-21D-A099-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:159686770 G>A maps to NM_024565.5 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HB-01A-11W-A071-09 chr5:159686722 C>T maps to NM_024565.5 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:99973476 A>C maps to ENST00000437596 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:99959022 G>A maps to ENST00000437596 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr14:99969203 A>G maps to ENST00000437596 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr1:1328841 T>C did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr12:49086992 G>C maps to NM_001240.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:55670507 G>C maps to ENST00000442196 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr15:55651930 G>A maps to ENST00000442196 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr3:46245441 G>T maps to NM_001295.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr3:46399978 C>T maps to NM_001123396.1 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr3:46399914 C>T maps to NM_001123041.2 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22D-01A-11D-A159-09 chr3:46400008 C>T maps to NM_001123396.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:46307027 C>T maps to NM_178328.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ES-01A-11D-A10Y-09 chr3:32995696 G>A maps to NM_005508.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr6:167550464 G>A maps to NM_004367.5 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr17:38711514 G>A maps to NM_001838.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr3:45942990 C>T maps to NM_031200.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:46449776 C>G maps to NM_001130910.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:46450226 C>G maps to NM_001130910.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr11:66366698 C>G maps to NM_005125.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:69991455 C>T maps to NM_006431.2 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:156305629 G>A maps to NM_005998.4 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:156303430 G>A maps to NM_005998.4 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr2:62104096 C>T maps to NM_006430.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:62100345 C>A maps to NM_006430.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:62107466 G>A maps to NM_006430.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr17:33269813 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:33258058 C>T maps to NM_006584.3 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr17:33259454 C>T maps to NM_006584.3 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr2:73471839 C>T maps to NM_006429.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr21:30428849 A>C maps to NM_006585.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:30432942 A>C maps to NM_006585.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:30434564 C>G did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr22:17071959 C>T maps to NM_014406.4 W494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr1:117576698 C>T maps to NM_004258.3 D1014D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:74512953 G>T maps to NM_133493.3 E964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:838146 C>A maps to NM_139030.3 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:7647965 A>C maps to NM_004244.4 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:7640573 T>C maps to NM_004244.4 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr12:7550863 G>A maps to ENST00000416109 C585C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:7559416 A>C maps to ENST00000416109 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:7586249 A>C maps to ENST00000416109 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr12:7556210 G>T maps to ENST00000416109 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr12:7531856 G>A maps to ENST00000416109 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:43859873 A>C maps to NM_020406.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr16:28948419 G>A maps to NM_001178098.1 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr1:158225972 C>T maps to NM_001763.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr1:158150917 C>T maps to NM_001766.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:158326631 G>A maps to NM_030893.3 W371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr1:158326559 C>T maps to NM_030893.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr1:158324192 C>T maps to NM_030893.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr1:158326376 C>T maps to NM_030893.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:117311359 T>C maps to NM_001767.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr1:117311090 G>T maps to NM_001767.3 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:112066508 C>A maps to NM_001004196.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr3:112546235 A>G maps to NM_001008784.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr3:112545930 A>G maps to NM_001008784.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr3:112538664 G>A maps to NM_001008784.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr2:71062660 G>A maps to NM_015717.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr19:35828817 G>A maps to NM_001771.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr19:35827244 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr19:35827137 C>G maps to NM_001771.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:35826996 C>T maps to NM_001771.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr18:67613971 G>C maps to NM_006566.2 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr1:160832437 G>T maps to NM_001166663.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FB-01A-11D-A17D-09 chr1:167404659 C>T maps to NM_198053.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:66082605 T>G maps to NM_020404.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr11:66082628 G>A maps to NM_020404.2 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:6560130 C>T maps to NM_001242.4 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:47580253 A>G maps to NM_012120.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:47563747 A>C maps to NM_012120.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:47471169 C>T maps to NM_012120.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr16:30364695 C>T maps to NM_006110.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr17:72613389 G>A maps to ENST00000426295 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr17:72518948 G>T maps to NM_174892.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr17:72700704 G>C maps to ENST00000412086 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:72699222 C>A maps to ENST00000412086 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:41926055 C>T maps to NM_145273.3 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr17:41939192 C>T maps to NM_145273.3 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:51742870 T>A maps to NM_001772.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr19:51729329 C>T maps to NM_001772.3 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr19:51738412 G>T maps to NM_001772.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:208061238 A>C maps to NM_001025109.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:208062089 G>C maps to NM_001025109.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:208061171 G>A maps to NM_001025109.1 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr7:80303417 T>G maps to NM_001127444.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:6928463 G>A did not map to a codon.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr12:6926434 G>A maps to NM_000616.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:6925450 G>A maps to NM_000616.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr12:6925369 C>T maps to NM_000616.4 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr20:44750512 C>T maps to NM_001250.4 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BS-01A-11D-A12Q-09 chr23:135732437 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:35198252 G>T maps to NM_000610.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr11:35226170 G>C maps to NM_000610.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr1:207940996 G>C did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:207930398 C>T maps to NM_172359.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:107776387 C>T maps to NM_001777.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr3:107766131 C>T maps to NM_198793.2 *306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr11:60886751 T>C maps to NM_014207.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:60886844 C>T maps to NM_014207.3 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:207498022 G>T maps to NM_001114752.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:117057434 T>C maps to NM_001779.2 *251W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IE-01A-11D-A188-09 chr11:33731839 G>A maps to NM_203331.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr1:157803093 C>T maps to NM_005894.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr1:157805922 C>A maps to NM_005894.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr11:60776306 G>C maps to NM_006725.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr12:56119344 C>T maps to NM_001780.4 *239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr12:9907738 C>T maps to NM_001781.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr12:9907273 G>A maps to NM_001781.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr9:35618080 C>T maps to NM_001782.2 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr9:35618270 C>T maps to NM_001782.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:35610684 G>C maps to NM_001782.2 S339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:35616075 C>T maps to NM_001782.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:62006621 C>A maps to NM_001039933.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr3:119263559 G>A maps to NM_005191.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr6:14131890 C>T maps to NM_004233.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:160535224 G>A maps to NM_001184879.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr1:160523826 G>T maps to NM_001184879.1 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr3:121825276 G>C maps to NM_175862.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:121825333 A>C maps to NM_175862.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr2:87085531 A>G maps to NM_172213.3 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr12:6344724 C>G maps to NM_001769.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr12:6344724 C>G maps to NM_001769.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr12:6344724 C>G maps to NM_001769.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr12:6344724 C>G maps to NM_001769.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EA-01A-11D-A10Y-09 chr20:23066475 G>A maps to NM_012072.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr20:23065763 G>A maps to NM_012072.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:23066229 G>T maps to NM_012072.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:111342637 G>C maps to NM_198196.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:14508748 T>G did not map to a codon.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr19:14507217 T>C maps to NM_078481.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:2638450 A>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:2641386 A>G did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:2641358 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1JH-01A-11D-A188-09 chr23:2641395 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:149984483 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr23:149999737 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:43022932 C>T maps to NM_138477.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:43028134 G>A maps to NM_138477.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr15:43025327 C>T maps to NM_138477.2 W475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:12280462 C>T maps to NM_006023.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:12238267 C>T maps to NM_006023.2 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr1:100921010 A>G maps to NM_033312.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:100928261 G>A maps to NM_033312.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr1:100960454 C>T maps to NM_033312.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr5:54436169 G>C maps to NM_001170402.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr5:54429339 G>C maps to NM_001170402.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr20:3782016 C>T maps to NM_021873.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr5:137621469 G>A maps to NM_001790.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr17:45214684 T>C maps to NM_001114091.1 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:45201280 C>A maps to NM_001114091.1 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr17:45214546 G>A maps to NM_001114091.1 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr19:532053 G>A maps to NM_004359.1 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr6:110550071 C>T maps to NM_015891.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr1:227216474 C>A maps to ENST00000366766 E1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:227219068 G>C maps to ENST00000366766 V1235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr1:227300566 C>T maps to ENST00000366766 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr1:227259958 G>C maps to ENST00000366766 S926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr14:103465920 G>A maps to NM_006035.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr14:103406000 G>A maps to NM_006035.3 H1591H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr14:103416190 G>T maps to NM_006035.3 V1120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr14:103466002 G>A maps to NM_006035.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr14:103452868 G>C maps to NM_006035.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr11:64600122 C>G maps to NM_017525.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr11:64606638 C>A maps to NM_017525.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr11:64597719 G>A maps to NM_017525.2 R1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr22:37964205 C>T maps to NM_152243.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22D-01A-11D-A159-09 chr22:37964418 T>C maps to NM_152243.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr6:44360502 G>A maps to NM_001253.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:44390474 C>T maps to NM_001253.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr6:44413390 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:38457242 G>A maps to NM_001254.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr17:38450219 G>A maps to NM_001254.3 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr17:38450650 C>T maps to NM_001254.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:105478142 G>A maps to NM_145701.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr2:174224155 T>C maps to NM_031942.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr2:174224197 G>A maps to NM_031942.4 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:174228556 C>G maps to NM_031942.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:174223537 C>T maps to NM_031942.4 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr3:45152067 C>A maps to NM_022842.3 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:45134772 G>A maps to NM_022842.3 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr16:68844243 G>T maps to NM_004360.3 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr16:68845756 C>T maps to NM_004360.3 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr16:68835595 C>T maps to NM_004360.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EX-01A-21W-A050-09 chr16:68849627 C>T maps to NM_004360.3 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr16:68835595 C>T maps to NM_004360.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr16:68867257 T>A maps to NM_004360.3 Y835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr16:68845756 C>T maps to NM_004360.3 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr16:68862094 T>A maps to NM_004360.3 L728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr16:68856128 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:68849662 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr16:68849603 C>T maps to NM_004360.3 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr16:68846064 C>T maps to NM_004360.3 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr16:68772217 C>T maps to NM_004360.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr16:68856112 C>T maps to NM_004360.3 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr16:68842646 C>T maps to NM_004360.3 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr16:68835595 C>T maps to NM_004360.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr16:68862075 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr16:68844174 C>T maps to NM_004360.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr16:68835628 C>T maps to NM_004360.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RQ-01A-11D-A10Y-09 chr16:68772217 C>T maps to NM_004360.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr16:68842646 C>T maps to NM_004360.3 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr16:68849576 G>T maps to NM_004360.3 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr16:68772217 C>T maps to NM_004360.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr16:68844098 G>A did not map to a codon.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr16:68835595 C>T maps to NM_004360.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr16:68772217 C>T maps to NM_004360.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr16:68856128 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27T-01A-11D-A16D-09 chr16:68846165 G>A maps to NM_004360.3 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr16:68772217 C>T maps to NM_004360.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr16:68845761 G>A maps to NM_004360.3 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L8-01A-11D-A13L-09 chr16:68844244 G>A did not map to a codon.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr16:68847224 C>T maps to NM_004360.3 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr16:68857366 A>T maps to NM_004360.3 K668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PV-01A-11D-A28B-09 chr16:68862075 G>A did not map to a codon.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr16:68772217 C>T maps to NM_004360.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr16:68847303 G>A maps to NM_004360.3 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MS-A51U-01A-31D-A25Q-09 chr16:68849435 A>T maps to NM_004360.3 K447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RV-01A-12D-A28B-09 chr16:68849630 G>T maps to NM_004360.3 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr16:68856093 G>A maps to NM_004360.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr16:68845756 C>T maps to NM_004360.3 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06N-01A-11W-A019-09 chr5:24491919 G>T maps to NM_006727.3 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr5:24511480 G>A maps to NM_006727.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr16:65016036 G>A maps to NM_001797.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B1-01A-21D-A12Q-09 chr16:65016150 G>A maps to NM_001797.2 N351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:21817098 G>A maps to NM_004061.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:21752075 G>A maps to NM_004061.3 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr16:83378510 G>C maps to ENST00000268613 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:89246630 G>A maps to NM_004933.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr16:89254602 C>T maps to NM_004933.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr16:66945977 C>A maps to NM_004062.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr16:66946465 C>A maps to NM_004062.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr8:95172378 C>G maps to NM_001144663.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr8:95183114 C>A maps to NM_001144663.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:64172429 A>C maps to NM_021153.2 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr18:64211461 C>T did not map to a codon.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr18:64239348 G>A maps to NM_021153.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr18:25572678 A>G maps to NM_001792.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:59166486 C>T maps to NM_031891.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr20:44839112 G>T maps to NM_021248.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr20:44869707 C>T maps to NM_021248.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr20:44815341 G>A maps to NM_021248.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr10:73563077 C>G maps to ENST00000398860 L2596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr10:73553338 C>T maps to ENST00000398860 D2223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:73485219 C>T maps to ENST00000398860 H1179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr10:73491897 G>A maps to ENST00000398860 P1295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:23523779 G>C maps to NM_022478.3 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:58574647 C>G maps to NM_177980.2 S676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:58547016 C>T maps to NM_177980.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr20:58559802 T>G maps to NM_177980.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr20:58564053 G>T maps to NM_177980.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:58559718 A>G maps to NM_177980.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr20:58560081 C>T maps to NM_177980.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr20:58559736 A>G maps to NM_177980.2 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PG-01A-11D-A142-09 chr20:58559786 T>A maps to NM_177980.2 L212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr16:68714902 C>T maps to NM_001793.4 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:68716272 C>T maps to NM_001793.4 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:60498600 G>A maps to NM_001794.2 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr5:31294262 C>T maps to NM_004932.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr5:31294331 C>A maps to NM_004932.2 Y164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr18:63430236 G>A maps to NM_004361.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr18:63491904 G>A maps to NM_004361.2 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr18:63529955 C>A maps to NM_004361.2 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr16:61689530 A>G maps to NM_001796.2 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FL-01A-11D-A13L-09 chr16:62055217 A>G maps to NM_001796.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr16:62055070 C>T maps to NM_001796.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr5:26881403 C>T maps to NM_016279.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr5:26890043 G>A maps to NM_016279.3 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:85968078 A>C maps to NM_033100.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:85961561 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr10:85970821 C>G maps to NM_033100.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr10:85968096 G>A maps to NM_033100.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:176002428 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:176004675 C>T maps to NM_001171976.1 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:176004542 G>A maps to NM_001171976.1 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr5:176002161 C>G maps to NM_001171976.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr7:105662854 C>T maps to NM_152750.4 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr11:624854 C>T maps to NM_021924.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr16:29872461 A>G maps to NM_006319.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr10:62553684 G>A maps to NM_001786.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:89757938 G>A maps to NM_052988.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr1:1635322 C>A maps to NM_024011.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:1635703 G>T maps to NM_024011.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:1647825 C>T maps to NM_024011.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr1:1573245 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:1572318 G>C maps to ENST00000401097 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr17:37627546 G>T maps to NM_016507.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:37627608 G>A maps to NM_016507.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr17:37619061 T>A maps to NM_016507.2 Y246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr7:90377066 T>C maps to NM_012395.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr7:90377006 C>T maps to NM_012395.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:90547037 C>T maps to NM_012395.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr7:90585060 G>C maps to NM_012395.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr23:47086097 A>C did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:47086815 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr23:47088129 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:96691098 C>T maps to NM_002595.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr1:205494301 G>C maps to NM_212503.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr1:205494289 G>T maps to NM_212503.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr1:205500481 G>A maps to NM_212503.2 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:205496932 C>T maps to NM_212503.2 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:205499424 G>A maps to NM_212503.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:205499814 T>C maps to NM_212503.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr6:110942345 G>C maps to NM_015076.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:110943341 G>A maps to NM_015076.3 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:111136228 C>T maps to NM_015076.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:73998135 C>G maps to NM_001258.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr17:73998014 G>A maps to NM_001258.2 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr20:31948285 G>A maps to ENST00000357886 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr20:31946929 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:31960459 C>A maps to ENST00000357886 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr20:31967343 G>A maps to ENST00000357886 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr9:123239713 T>A maps to NM_018249.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:123232426 G>A maps to NM_018249.4 Q644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr9:123292326 C>A maps to NM_018249.4 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr9:123201945 T>C maps to NM_018249.4 E1151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:123298717 C>T maps to NM_018249.4 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:123334251 G>A maps to NM_018249.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:123301348 G>C maps to NM_018249.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:92244465 C>T maps to NM_001145306.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:130550295 G>A maps to ENST00000373265 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr6:21198271 G>T maps to NM_017774.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr4:76529119 G>A maps to ENST00000307465 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr2:39456598 G>A maps to ENST00000395035 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:18622625 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:18671595 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:18602448 A>G did not map to a codon.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr23:18631362 C>A did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:18664153 G>C did not map to a codon.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr23:18668702 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr23:18638041 G>T did not map to a codon.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr23:18622481 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr6:36652170 C>G maps to ENST00000448526 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr12:12870852 C>A maps to NM_004064.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr12:12871243 C>T maps to NM_004064.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr12:12870852 C>A maps to NM_004064.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:12871085 G>T maps to NM_004064.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:12870830 C>T maps to NM_004064.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:12871193 C>T maps to NM_004064.3 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr19:10677826 G>A maps to NM_079421.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr23:139866172 T>G did not map to a codon.
Sequencing variant TCGA-E9-A3X8-01A-31D-A22X-09 chr23:139865866 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:22358681 G>A maps to NM_001802.1 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr17:72998157 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr17:15508673 T>A maps to ENST00000455584 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HB-01A-11W-A071-09 chr4:85540675 C>T maps to NM_001263.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr20:5165584 C>A maps to NM_003818.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr20:5155846 G>T maps to NM_003818.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:31084116 T>G maps to NM_001264.4 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:31085091 A>C maps to NM_001264.4 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr3:133306839 C>T maps to NM_017548.4 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr13:28537413 C>T maps to NM_001265.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr23:72674299 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:4943914 A>C maps to ENST00000328908 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr6:4943947 C>T maps to ENST00000328908 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr6:4937915 C>T maps to ENST00000328908 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:80646630 G>A maps to NM_152342.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P3-01A-11D-A142-09 chr16:80646645 C>A maps to NM_152342.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:43023313 C>T maps to NM_001712.4 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:43023124 G>A maps to NM_001712.4 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr19:45209091 C>T maps to ENST00000396750 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr19:51981842 G>T maps to NM_001080405.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr19:51984818 C>G maps to NM_001080405.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:45010248 C>T maps to NM_001102597.1 E585E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr19:45017247 G>A maps to NM_001102597.1 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr19:42085716 C>T maps to NM_001098506.1 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:42083791 C>G maps to NM_001098506.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:42222137 A>C maps to NM_004363.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr22:18022210 C>T maps to ENST00000400579 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:18028672 A>C maps to ENST00000400579 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr22:17976443 A>G maps to ENST00000400579 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr22:17978530 C>T maps to ENST00000400579 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr22:18022654 G>A maps to ENST00000400579 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr22:17619468 G>A maps to NM_033070.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:135939813 T>G maps to NM_001807.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr9:135944523 C>T maps to NM_001807.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr9:135944523 C>T maps to NM_001807.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr9:135944194 C>T maps to NM_001807.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A278-01A-11D-A167-09 chr9:135944194 C>T maps to NM_001807.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr1:15793990 C>T maps to ENST00000375924 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:15807648 G>A maps to ENST00000442979 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:22310303 C>T maps to NM_007352.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr11:47494729 G>A maps to NM_001172639.1 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr11:47494724 G>A maps to NM_001172639.1 D442D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D8-A146-01A-31D-A10Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr11:47498506 C>A maps to NM_001172639.1 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:47498972 C>T maps to NM_001172639.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr10:11299827 G>A maps to NM_006561.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr18:35145385 G>A maps to NM_020180.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr15:72579623 A>G maps to NM_052840.4 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:46930595 G>A maps to NM_014246.1 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr22:46930418 G>C maps to NM_014246.1 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr22:46929989 A>G maps to NM_014246.1 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr22:46785189 G>A maps to NM_014246.1 H2184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr22:46795612 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr22:46763748 G>T maps to NM_014246.1 S2652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:109795430 T>A maps to NM_001408.2 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:109795767 C>T maps to NM_001408.2 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:109803736 C>G maps to NM_001408.2 V1344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:109804502 G>A maps to NM_001408.2 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr1:109812435 G>T maps to NM_001408.2 R2367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr1:109804508 C>G maps to NM_001408.2 Y1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:109795619 C>T maps to NM_001408.2 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:109795442 G>C maps to NM_001408.2 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:109806317 C>G maps to NM_001408.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:109813146 G>T maps to NM_001408.2 E2470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:48685786 C>T maps to NM_001407.2 V2295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr3:48696404 G>A maps to NM_001407.2 V1221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:48696382 G>A maps to NM_001407.2 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr3:48694416 T>C maps to NM_001407.2 V1371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14T-01A-11D-A10Y-09 chr3:48699137 C>T maps to NM_001407.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr3:48694737 G>A maps to NM_001407.2 V1264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr3:48677876 G>C maps to NM_001407.2 Y3047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr16:2580810 A>C maps to NM_001048212.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr16:2580795 C>T maps to NM_001048212.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:788468 C>T maps to NM_016564.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:90037805 G>A maps to NM_145039.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:68385220 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr4:68355812 G>A maps to NM_001812.2 Q848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr4:104064460 C>A maps to NM_001813.2 E1750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr4:104061022 C>A maps to NM_001813.2 E2043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr4:104066765 A>G maps to NM_001813.2 L1496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr1:214816024 C>A maps to NM_016343.3 V1448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:214816318 G>A maps to NM_016343.3 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr1:214794221 T>C maps to NM_016343.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:100356175 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:100382502 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:100403009 T>C did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:100387248 C>T did not map to a codon.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr23:100382635 G>A did not map to a codon.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:100387394 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr13:25479532 T>C maps to NM_018451.3 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:25480609 A>C maps to NM_018451.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr13:25479706 C>T maps to NM_018451.3 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr5:64850677 A>G maps to NM_022145.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr1:173780349 G>A maps to NM_001127181.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr2:25039531 C>A maps to NM_024322.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr2:25040615 C>T maps to NM_024322.2 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RX-01A-11D-A25Q-09 chr9:95094595 G>A maps to NM_001012267.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr6:49438721 G>C maps to NM_018132.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:67865145 G>A maps to NM_025082.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27W-01A-11D-A16D-09 chr6:126669610 G>A did not map to a codon.
Sequencing variant TCGA-A7-A4SB-01A-21D-A25Q-09 chr9:123929865 C>T maps to NM_007018.4 Q1919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:123888036 T>G maps to NM_007018.4 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr9:123880757 G>A maps to NM_007018.4 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr9:123880637 G>A maps to NM_007018.4 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:123930432 A>G maps to NM_007018.4 K1968K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr9:123904481 C>G maps to NM_007018.4 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:122724185 G>C maps to NM_153223.3 S457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr5:122685674 G>A maps to NM_153223.3 R897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr5:122714067 C>A maps to NM_153223.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr4:56883873 C>T maps to NM_025009.3 R955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:49076221 C>T maps to NM_001194998.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FE-01A-11D-A19Y-09 chr15:49085544 G>A maps to NM_001194998.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr15:49048258 G>A maps to NM_001194998.1 I1062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr15:49036476 T>C maps to NM_001194998.1 E1265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr11:117280409 G>A maps to NM_014956.4 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:117280451 G>A maps to NM_014956.4 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr1:243289813 G>A maps to NM_014812.2 F1564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr18:13099580 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:13103574 A>C maps to NM_032142.3 P2313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:13015424 G>A maps to NM_032142.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr18:13055943 G>T maps to NM_032142.3 E1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr20:34054870 C>T maps to NM_007186.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:34057804 G>A maps to NM_007186.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:34092673 G>A maps to NM_007186.3 L2159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:34091185 G>A maps to NM_007186.3 Q1663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NG-01A-21D-A14K-09 chr20:34057760 G>T maps to NM_007186.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr20:34084420 G>C maps to NM_007186.3 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr20:34054795 C>T maps to NM_007186.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:88478576 G>C maps to NM_025114.3 S1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr12:88514772 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr12:88474171 C>T maps to NM_025114.3 Q1671Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr1:180047634 C>G maps to NM_014810.4 Y1935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr1:180065243 C>G maps to NM_014810.4 V2997V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:179961336 G>T maps to NM_014810.4 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:180053274 C>T maps to NM_014810.4 L2083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr1:180053300 C>T maps to NM_014810.4 I2091I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:180003095 A>G maps to NM_014810.4 S1275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:179989445 T>G maps to NM_014810.4 L846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:179959670 A>G maps to NM_014810.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:180062699 C>A maps to NM_014810.4 S2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr10:95279500 A>G maps to NM_018131.4 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr11:95561158 G>A maps to NM_014679.3 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr3:134266254 G>A maps to NM_025180.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:65300102 C>T maps to NM_015147.2 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr2:65298634 G>C maps to NM_015147.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:138224287 G>T maps to NM_024491.2 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr9:80877836 G>A maps to NM_001098802.1 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:80858511 T>C maps to NM_001098802.1 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:131198081 C>A maps to NM_016174.4 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr9:131196436 G>A maps to NM_016174.4 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:47085890 G>A maps to NM_022766.5 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:182403817 C>A did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr16:66972117 G>A maps to NM_003869.5 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr16:67006795 C>T maps to NM_024922.5 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr16:55907860 C>T maps to NM_001143685.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:55899994 G>A maps to NM_001143685.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:67038093 C>G maps to ENST00000326686 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:151997149 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:57003591 G>C maps to NM_000078.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:31914321 G>A maps to ENST00000437789 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr1:196683021 A>T maps to NM_000186.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr1:196684805 G>T maps to NM_000186.3 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr1:196695951 C>T maps to NM_000186.3 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:196659316 A>G maps to NM_000186.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:196977765 C>T maps to ENST00000367414 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:196963291 G>A maps to ENST00000367414 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:196971780 A>G maps to ENST00000367414 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr1:196967315 G>A maps to ENST00000367414 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:196971636 G>A maps to ENST00000367414 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr1:196973944 A>G maps to ENST00000367414 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:110681501 A>C maps to ENST00000394635 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:35182734 G>A maps to NM_138638.4 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr2:201997757 G>T maps to NM_001127183.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:47485562 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr23:47485755 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr23:47485821 C>T did not map to a codon.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr23:47489180 G>C did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:47485762 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:117282580 C>T maps to NM_000492.3 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr7:117188874 A>T maps to NM_000492.3 K464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr6:87796030 C>T maps to NM_000735.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr19:49526241 G>C maps to ENST00000448402 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr19:49557571 T>C maps to ENST00000377280 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:151509345 C>T maps to NM_020770.2 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:151491177 T>C maps to NM_020770.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr1:151492731 C>T maps to NM_020770.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr15:57754041 T>C maps to NM_032866.3 Y785Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr15:57746009 G>A maps to NM_032866.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:57836732 G>A maps to NM_032866.3 G1146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:57730763 G>A maps to NM_032866.3 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr15:57816867 C>G maps to NM_032866.3 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:27325081 G>C maps to ENST00000404694 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:41247842 G>A maps to NM_024111.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr17:48545781 G>A maps to NM_001267.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr19:4428842 C>T maps to NM_005483.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:4409317 G>A maps to NM_005483.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr21:37771830 A>G maps to NM_005441.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr10:50863478 T>G maps to NM_020549.4 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:98238623 G>C maps to NM_001270.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr5:98236685 T>G maps to NM_001270.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:146759363 C>T maps to NM_004284.3 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr1:146756022 G>A did not map to a codon.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr15:93527729 G>A maps to NM_001271.3 K1079K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr15:93510695 A>G maps to NM_001271.3 E714E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr15:93499826 C>T maps to NM_001271.3 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr15:93545465 G>A maps to NM_001271.3 E1399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:93552538 C>T maps to NM_001271.3 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr17:7798779 C>T maps to NM_001005271.2 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:7808966 G>A maps to NM_001005271.2 R1448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:7809181 C>A maps to NM_001005271.2 G1470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr12:6688059 C>A maps to ENST00000309577 E1673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:6690830 T>G maps to ENST00000309577 A1583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr12:6702334 G>A maps to ENST00000309577 D858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr12:6707088 C>T maps to ENST00000309577 W621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:6692025 A>C maps to ENST00000309577 G1436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:6700886 A>C maps to ENST00000309577 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:6707237 G>A maps to ENST00000309577 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr12:6696711 T>C maps to ENST00000309577 K1239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr12:6697538 G>A maps to ENST00000309577 G1130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr12:6715438 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr12:6680151 C>T maps to ENST00000309577 V1896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B6-01A-31D-A12Q-09 chr12:6690306 A>G maps to ENST00000309577 D1632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:6692482 C>T maps to ENST00000309577 W1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr1:6202325 G>A maps to NM_015557.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:6204081 A>C did not map to a codon.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr1:6191718 G>T maps to NM_015557.2 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr1:6166464 G>C maps to NM_015557.2 P1949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XR-01A-11D-A10G-09 chr1:6206324 G>A maps to NM_015557.2 Y583Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:6215762 C>T maps to NM_015557.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr20:40033793 G>A maps to NM_032221.3 P2529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:40126083 G>A maps to NM_032221.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr20:40049604 T>G maps to NM_032221.3 V1890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr20:40081462 C>T maps to NM_032221.3 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24O-01A-11D-A167-09 chr20:40065974 C>G did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr20:40043951 C>T maps to NM_032221.3 Q2271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr20:40126067 G>A maps to NM_032221.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr20:40043945 G>C maps to NM_032221.3 V2273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:40117093 G>A maps to NM_032221.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr20:40076583 G>T maps to NM_032221.3 Y1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr20:40045304 G>A maps to NM_032221.3 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr8:61693869 C>A maps to NM_017780.2 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr8:61773584 G>C maps to NM_017780.2 G2577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr8:61765544 G>C maps to NM_017780.2 L2087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr8:61777879 T>A maps to NM_017780.2 A2794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:61654171 C>T maps to NM_017780.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr14:21871619 G>A maps to NM_001170629.1 I1170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:21868195 C>T maps to NM_001170629.1 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:21861363 G>A maps to NM_001170629.1 L2123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr14:21863270 C>A maps to NM_001170629.1 V1730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr14:21869199 G>A maps to NM_001170629.1 R1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr14:21859708 C>A maps to NM_001170629.1 L2326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr16:53308139 G>A maps to ENST00000219084 V1631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:53283932 A>G maps to ENST00000219084 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr16:53337713 G>A maps to ENST00000219084 R1932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr19:16652819 G>A maps to NM_006387.5 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr12:133438212 C>G maps to NM_001161344.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr14:93397598 G>A maps to NM_001275.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr14:93392990 C>A maps to NM_001275.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:93390550 G>A maps to NM_001275.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H6-01A-21W-A071-09 chr20:5903618 C>T maps to NM_001819.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:5903755 G>A maps to NM_001819.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:203149663 G>A maps to NM_001276.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:203152861 C>T maps to NM_001276.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:203154337 G>A maps to NM_001276.2 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr1:203151920 G>A maps to NM_001276.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B1-01A-21D-A12Q-09 chr1:203154334 G>C maps to NM_001276.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr23:72804294 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:72783180 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:900963 G>C maps to NM_001142676.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:203186160 G>A maps to NM_003465.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:67833264 G>C maps to NM_001277.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr22:51018483 A>G maps to NM_005198.4 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr22:51019009 C>A maps to NM_005198.4 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr3:370002 C>T maps to NM_006614.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr3:430975 C>T maps to NM_006614.2 Y763Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr3:436515 A>T maps to NM_006614.2 K1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr3:447267 C>T maps to NM_006614.2 Y1183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr23:85302526 T>C did not map to a codon.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr23:85128089 A>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:85213943 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:85149240 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr23:85282500 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:85236771 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:85211230 G>T did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr1:241797529 T>C maps to NM_001821.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr1:241798026 C>A maps to NM_001821.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:59063682 G>A maps to NM_014453.2 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:32436336 A>T maps to NM_176812.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:175779832 G>A maps to NM_001822.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr2:175673726 G>A maps to NM_001822.4 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr21:19635192 C>T maps to NM_024944.2 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:41555043 A>C maps to NM_007236.4 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:41571017 C>T maps to NM_007236.4 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr2:220404536 G>A maps to NM_024536.5 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:220405715 G>A maps to NM_024536.5 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr7:150932658 C>T maps to NM_019015.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr12:102117532 C>T maps to NM_020244.2 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr23:110035324 G>C did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr23:109963074 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr23:110035315 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:136699830 T>G maps to NM_001006628.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:136699710 C>T maps to NM_001006628.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr1:240071941 G>T maps to NM_000740.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr1:240071785 C>A maps to NM_000740.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr1:240072277 C>A maps to NM_000740.2 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:46407129 A>G maps to NM_000741.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0RX-01A-21D-A099-09 chr11:46406904 C>T maps to NM_000741.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:46408062 G>T maps to NM_000741.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr2:175618462 G>A maps to NM_001039523.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr2:175613361 G>A maps to NM_001039523.2 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr2:175618973 G>A maps to NM_001039523.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr11:3687754 G>C maps to NM_020402.2 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr15:32460484 C>T maps to NM_001190455.1 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr15:32460484 C>T maps to NM_001190455.1 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GY-01A-11W-A071-09 chr15:32460484 C>T maps to NM_001190455.1 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:32450725 C>T maps to NM_001190455.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr4:40351123 C>T maps to NM_017581.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr17:7359154 C>A maps to NM_000747.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr1:154543985 C>T maps to NM_000748.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:154548272 C>T maps to NM_000748.2 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr15:78921527 G>A maps to NM_000750.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr12:105151385 C>T maps to NM_018413.5 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr12:105150938 C>T maps to NM_018413.5 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr7:2473032 C>T maps to NM_018641.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:2472870 G>A maps to NM_018641.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:125805521 A>C maps to NM_015892.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:125804102 C>T maps to NM_015892.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr10:125804129 G>A maps to NM_015892.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A227-01A-11D-A159-09 chr3:142840437 G>A maps to NM_004267.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr10:73767169 C>A maps to NM_004273.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:75563694 C>T maps to NM_024533.3 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr16:75564024 G>A maps to NM_024533.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr23:46433864 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr19:34180250 C>T maps to NM_022467.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:101775742 G>A maps to NM_014918.4 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:129521228 C>T maps to NM_175856.4 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:129243965 T>C maps to NM_175856.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr5:129520401 C>T maps to NM_175856.4 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr5:129520289 G>A maps to NM_175856.4 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr16:842804 C>G maps to ENST00000317063 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:845740 C>A maps to ENST00000317063 I953I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr16:839676 C>T maps to ENST00000317063 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr16:847929 C>T maps to ENST00000317063 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:101953143 A>C maps to NM_001278.3 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr14:65392795 C>T maps to ENST00000448390 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:96936857 G>A maps to NM_004804.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:57473133 A>C maps to NM_020313.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:57473234 C>A maps to NM_020313.2 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:78401628 G>A maps to NM_006383.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:26805697 G>A maps to NM_001029881.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr19:42794461 C>A maps to NM_015125.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr19:42791540 C>G maps to NM_015125.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr19:42793199 C>T maps to NM_015125.3 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr18:12254818 C>T maps to ENST00000342845 R2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr16:10997663 G>T maps to NM_000246.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr16:10996534 T>C maps to NM_000246.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:65490841 A>C maps to NM_003613.3 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X7-01A-11D-A14K-09 chr15:65495781 C>A maps to NM_003613.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr15:65496642 C>T maps to NM_003613.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr19:19654869 C>T maps to NM_153221.2 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:1271006 C>G maps to ENST00000413636 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr3:50645370 T>C maps to NM_013324.5 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:120139492 G>A maps to ENST00000392521 F1826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr12:120295449 G>A maps to ENST00000392521 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:120166327 G>A maps to ENST00000392521 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr23:71521747 A>G did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:71521828 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07Z-01A-11W-A019-09 chr9:130931779 G>A maps to NM_012127.2 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr13:53035901 C>G maps to NM_001098525.1 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr11:46839991 A>G maps to ENST00000415402 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:46799087 C>T maps to ENST00000415402 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr14:103988689 C>T maps to NM_001823.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:43891359 G>A maps to ENST00000413657 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:80562046 A>C maps to NM_001825.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:80555034 C>A maps to NM_001825.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:122217668 A>C maps to NM_015282.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:122204964 C>T maps to NM_015282.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:122273281 A>G maps to NM_015282.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:33705002 C>A maps to ENST00000359576 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr3:33552253 C>T maps to ENST00000359576 V1380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:86951097 C>T maps to NM_001285.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:86964396 A>C maps to NM_001285.3 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:86951096 C>T maps to NM_001285.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr1:86952405 C>T maps to NM_001285.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NG-01A-21D-A14K-09 chr1:86942162 C>T maps to NM_001285.3 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:86921062 A>C maps to NM_006536.5 V895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BJ-01A-11W-A071-09 chr1:86904569 C>A maps to NM_006536.5 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr1:86919247 T>G maps to NM_006536.5 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr7:143028367 C>T maps to NM_000083.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:143043344 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:184069894 C>T maps to NM_004366.4 W774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr3:184072689 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr4:170610224 C>T maps to NM_173872.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr4:170557239 G>T did not map to a codon.
Sequencing variant TCGA-A8-A08O-01A-21W-A071-09 chr23:10176392 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23E-01A-11D-A159-09 chr23:10180563 G>T did not map to a codon.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr23:10176284 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:10180692 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:10176332 G>C did not map to a codon.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr23:10181871 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:10174757 C>G did not map to a codon.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr23:10176292 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:49853533 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr23:49845353 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:11898656 C>G maps to ENST00000376496 V823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:11900278 G>C maps to NM_001286.2 *870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:1511648 G>A maps to ENST00000382745 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr16:1500620 G>A maps to ENST00000382745 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr16:1497551 G>T maps to ENST00000382745 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr1:16350314 C>T maps to NM_004070.3 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:16356295 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:16349185 C>A maps to NM_004070.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:16356469 C>T maps to NM_004070.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RY-01A-21D-A28B-09 chr1:16360143 T>C maps to NM_004070.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A086-01A-11W-A019-09 chr1:16373086 G>A maps to NM_000085.3 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:16377453 G>T maps to NM_000085.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr13:96086158 G>A maps to NM_182848.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:170150447 C>G maps to NM_005602.5 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr21:37833354 T>G maps to NM_001146077.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr21:37833618 G>A maps to NM_001146077.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr3:190105966 C>G maps to NM_006580.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:31538401 T>C maps to NM_012131.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr21:31538836 T>A maps to NM_012131.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:137729228 G>A maps to NM_016369.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:43204089 A>C did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr1:43203907 G>C maps to NM_148960.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:106171607 C>G did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:106171826 C>G did not map to a codon.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr23:106171890 C>T did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr8:8560423 G>T maps to NM_194284.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr7:73245797 C>A maps to NM_001305.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr22:19511924 G>A maps to NM_003277.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:3065665 G>A maps to NM_021195.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr21:31587664 A>G maps to NM_199328.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:31587871 G>A maps to NM_199328.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:31588138 G>A maps to NM_199328.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr21:31587859 G>A maps to NM_199328.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr21:31587808 G>A maps to NM_199328.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr16:3063851 C>G maps to NM_020982.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:51871789 G>A maps to NM_152353.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NE-01A-21D-A14K-09 chr17:6980306 C>A did not map to a codon.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr12:10134653 T>C maps to ENST00000355690 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr12:10137480 C>T maps to ENST00000355690 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr16:11154763 C>T maps to ENST00000409790 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr16:11071087 G>T maps to ENST00000409790 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr19:14705308 C>T maps to NM_207390.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr16:69985382 G>A maps to NM_182619.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:9840571 C>T maps to NM_001004419.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:9845422 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr12:9833615 T>G maps to NM_001004419.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr12:7894053 T>A maps to NM_130441.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr12:8689858 G>T maps to NM_014358.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:71039686 A>C maps to NM_173535.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr19:7832456 C>G maps to NM_014257.4 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr12:8618226 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:8618152 T>G maps to NM_001007033.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr12:10213789 G>A maps to NM_207345.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:141315153 G>A maps to NM_004362.2 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:154528131 C>G did not map to a codon.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr23:154528457 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:154563717 C>T did not map to a codon.
Sequencing variant TCGA-E9-A227-01A-11D-A159-09 chr9:139889216 C>T maps to NM_004669.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:45917118 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:36081682 G>A maps to ENST00000360731 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:157218851 T>G maps to NM_001195555.1 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr12:122812588 G>A maps to ENST00000302528 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:122837294 G>C maps to ENST00000302528 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:122862452 G>C maps to ENST00000302528 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr12:122845562 G>A maps to ENST00000302528 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:122773064 G>C maps to ENST00000302528 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr12:122825431 G>C maps to ENST00000302528 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Q-01A-11D-A12B-09 chr12:122825971 G>A maps to ENST00000302528 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:73790668 C>T maps to NM_003388.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr7:73753225 C>T maps to NM_003388.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr19:36517497 C>T maps to NM_015526.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:36515354 G>C maps to NM_015526.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr2:29366666 C>A maps to ENST00000379543 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr2:29386782 A>T maps to ENST00000379543 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr2:201718658 G>T maps to NM_001162407.1 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:155237913 A>C maps to ENST00000368361 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:178044392 C>A maps to NM_020666.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr14:95677071 G>A maps to NM_024734.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr14:95669353 G>A maps to NM_024734.3 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:57428679 C>G maps to NM_006831.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:57428874 C>T maps to NM_006831.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr19:45494524 C>G maps to NM_001294.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr15:65459106 G>C maps to NM_006660.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr4:17528650 G>A maps to NM_001079827.2 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr10:129676622 G>A maps to NM_152311.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:36212415 C>T maps to NM_022111.3 E935E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr1:36204751 G>A maps to NM_022111.3 R1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Q-01A-21W-A050-09 chr3:140251266 C>T maps to NM_022131.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr3:140277568 C>G maps to NM_022131.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:140122609 C>T maps to NM_022131.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:7293956 A>C maps to NM_014718.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:7301654 G>A maps to NM_014718.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr12:7310619 C>T maps to NM_014718.3 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr12:7310622 T>C maps to NM_014718.3 D939D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr12:7293851 G>A maps to NM_014718.3 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:7301601 G>T maps to NM_014718.3 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N8-01A-11D-A142-09 chr9:36211698 C>T maps to NM_007096.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr17:57746198 A>G maps to NM_004859.3 K730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:57760138 T>C maps to NM_004859.3 T1250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr8:27457502 G>A maps to NM_001831.2 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:100543600 C>T maps to NM_206808.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr14:24975398 C>A maps to NM_001836.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr12:22214245 G>T maps to NM_018686.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:22213809 G>T maps to NM_018686.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr2:6990087 G>A maps to NM_207315.2 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XR-01A-11D-A10G-09 chr16:66613572 G>A maps to NM_144673.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:66620991 A>G maps to NM_144673.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:23847568 C>T maps to ENST00000339180 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr3:32490992 C>T maps to NM_138410.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr3:32491025 C>T maps to NM_138410.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr5:79033447 T>C maps to NM_153610.3 L2954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:79033021 C>T maps to NM_153610.3 L2812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:79026762 T>G maps to NM_153610.3 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:79027197 A>C maps to NM_153610.3 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:79031052 A>C maps to NM_153610.3 P2155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:79028540 C>G maps to NM_153610.3 S1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:79034304 G>A maps to NM_153610.3 E3239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:79034764 G>T maps to NM_153610.3 E3393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:79034947 G>T maps to NM_153610.3 G3454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:79028838 C>T maps to NM_153610.3 D1417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:88364007 C>T maps to NM_173538.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr8:88365982 G>A maps to NM_173538.2 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:72244216 G>T maps to NM_032649.5 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr4:47938685 G>A maps to NM_001142564.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr23:150912603 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:150908061 G>T did not map to a codon.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr23:150911870 C>G did not map to a codon.
Sequencing variant TCGA-BH-A1EW-01A-11D-A135-09 chr23:150911668 G>A did not map to a codon.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr23:150912894 G>A did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:150911599 A>T did not map to a codon.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr2:99013186 G>A maps to NM_001298.2 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:99008335 C>T maps to NM_001298.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:99006234 C>T maps to NM_001298.2 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr2:99013588 C>T maps to NM_001298.2 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:6262771 G>C maps to NM_001037329.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A096-01A-11W-A019-09 chr16:57951249 G>A maps to NM_001297.4 Y696Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:57921860 A>C maps to NM_001297.4 G1120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:57974197 C>T maps to NM_001297.4 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr16:57965654 G>T maps to NM_001297.4 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr16:57921788 C>T maps to NM_001297.4 A1144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr16:57921824 G>T maps to NM_001297.4 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:87588297 C>A maps to NM_019098.4 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IA-01A-11W-A050-09 chr8:87623884 C>T maps to NM_019098.4 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr14:54896976 A>C did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:66050244 G>A maps to NM_182553.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:224553691 C>T maps to NM_014184.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr1:26509859 G>A maps to ENST00000374253 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:26513678 C>T maps to ENST00000374253 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:26514739 C>G maps to ENST00000374253 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:21450880 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:21627212 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:21667120 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:21670582 G>C did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:21444709 G>T did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:21444777 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr23:21627268 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr23:21458840 C>G did not map to a codon.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr23:21581524 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr23:21450848 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr23:21666974 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr23:21450901 C>A did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:21670488 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr6:154754626 C>T maps to NM_173515.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr6:154762479 G>A maps to NM_173515.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr6:154771285 G>A maps to NM_173515.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:11658676 C>T maps to NM_001299.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:101090508 G>A maps to NM_020348.2 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr10:104679433 C>T maps to NM_017649.3 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr10:104836879 G>A maps to NM_017649.3 Q857Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr2:97498310 C>T maps to NM_017623.4 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:97427968 C>T maps to NM_020184.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr16:58564182 C>T maps to NM_016284.3 V2082V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr16:58589800 G>A maps to NM_016284.3 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:58579342 T>G maps to NM_016284.3 P1353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:58577649 G>T maps to NM_016284.3 S1432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:58573835 G>A maps to NM_016284.3 Q1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr16:58585041 T>C maps to NM_016284.3 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:54647842 G>A maps to NM_014516.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:135100011 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:179996272 T>C maps to NM_015455.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:40120675 C>T maps to NM_033133.4 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A278-01A-11D-A167-09 chr17:40125629 A>C maps to NM_033133.4 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:155301641 C>A maps to NM_001103176.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr12:56708703 C>A maps to NM_014255.5 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:42905862 C>A maps to NM_006586.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr9:34552693 G>C maps to NM_147164.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:34552232 T>G maps to NM_147164.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:34557647 G>C maps to NM_147164.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr9:17486985 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr12:41352941 C>T maps to NM_001843.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:41419004 C>T maps to NM_001843.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:41337524 A>G maps to NM_001843.2 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr12:41337929 C>A maps to NM_001843.2 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr1:205038688 G>A maps to NM_005076.3 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:205030994 C>T maps to NM_005076.3 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:205033453 C>T maps to NM_005076.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:74347204 G>A maps to NM_020872.1 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:74535627 C>A maps to NM_020872.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr3:74418525 T>C did not map to a codon.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr3:3085387 A>G maps to NM_175607.1 K937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BJ-01A-11W-A071-09 chr3:3084015 T>C maps to NM_175607.1 S807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr3:2787337 G>C maps to NM_175607.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:3067927 C>T maps to NM_175607.1 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr3:3080620 C>A maps to NM_175607.1 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr11:100211930 T>A maps to NM_014361.2 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr11:100095464 G>A maps to NM_014361.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr3:1320095 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr3:1424981 C>T maps to NM_014461.2 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr3:1415620 C>G maps to NM_014461.2 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr3:1444012 G>A maps to NM_014461.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr17:40837253 C>T maps to NM_003632.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr17:40847560 G>A maps to NM_003632.2 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr17:40849570 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:147926765 T>G maps to NM_014141.5 G1092G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr7:147600693 C>T maps to NM_014141.5 N712N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr7:146471393 C>T maps to NM_014141.5 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:147336228 C>T maps to NM_014141.5 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr7:146829360 G>T maps to NM_014141.5 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NG-01A-21D-A14K-09 chr7:146536956 G>T maps to NM_014141.5 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr9:39100103 C>T maps to NM_033655.3 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr9:39177395 C>T maps to NM_033655.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22D-01A-11D-A159-09 chr9:39103828 G>A maps to NM_033655.3 D816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr9:39287975 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:76495851 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr16:76555163 A>G maps to NM_033401.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:125504941 C>T maps to NM_130773.2 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:125555850 C>T maps to NM_130773.2 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr2:125204420 G>A maps to NM_130773.2 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr2:125405530 G>A maps to NM_130773.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr2:125671837 C>T maps to NM_130773.2 S1298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:7851862 C>G maps to NM_001037144.4 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:7842980 C>T maps to NM_001037144.4 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr17:7847522 C>T maps to NM_001037144.4 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr17:40714738 G>A maps to NM_001042532.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:40714750 C>T maps to NM_001042532.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr17:40715173 C>T maps to NM_001042532.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr17:40715278 C>T maps to NM_001042532.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr7:51096584 C>T maps to ENST00000395542 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr2:165542500 T>C maps to ENST00000392717 S1190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr2:165551132 A>T maps to ENST00000392717 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:71202304 G>C maps to NM_018714.2 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr17:71203395 G>A did not map to a codon.
Sequencing variant TCGA-GM-A3XG-01A-31D-A243-09 chr17:71197881 C>A maps to NM_018714.2 S639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:230819334 G>A maps to NM_007357.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr13:46065674 T>C did not map to a codon.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr13:46065552 A>G maps to NM_031431.2 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr13:46070344 G>A maps to NM_031431.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:107167691 G>A maps to NM_006348.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr16:23457181 G>T maps to NM_153603.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr16:69370509 G>A maps to NM_032382.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr16:69370509 G>A maps to NM_032382.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:69369071 G>C maps to NM_032382.4 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:55027621 G>A maps to NM_004645.2 C327C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BH-A18G-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:103468815 T>C maps to NM_080629.2 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr1:103474021 A>C maps to NM_080629.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr1:103461543 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr6:75857511 C>G maps to ENST00000322507 V1432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:75811747 A>C maps to ENST00000322507 G2812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:75861681 G>T maps to ENST00000322507 R1301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr6:75833787 T>C maps to ENST00000322507 T2249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr6:75893165 G>A maps to ENST00000322507 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr6:75866153 G>A maps to ENST00000322507 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr6:75893096 G>A maps to ENST00000322507 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr6:75814969 G>A maps to ENST00000322507 C2739C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:71658487 A>C maps to ENST00000356340 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:71682480 T>G maps to ENST00000356340 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr10:71562272 C>A maps to ENST00000356340 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:71677049 A>G maps to ENST00000356340 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr8:121237325 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:121290693 C>T maps to NM_021110.1 R1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr8:121170399 A>G maps to NM_021110.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr8:121222031 C>T maps to NM_021110.1 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:101832092 G>A maps to NM_001855.3 Q1364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:32122648 A>C maps to NM_001856.3 G1347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr1:32127284 G>A maps to NM_001856.3 G1234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr1:32131198 G>T maps to NM_001856.3 G1159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr10:105801281 G>A maps to NM_000494.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr10:105793002 G>A maps to NM_000494.3 F1429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr10:105811266 G>A maps to NM_000494.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr21:46888326 C>A maps to ENST00000359759 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Z-01A-11D-A167-09 chr21:46875482 G>A maps to ENST00000359759 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr21:46911227 C>T maps to ENST00000359759 D1134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr21:46896296 A>G maps to ENST00000359759 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr21:46907402 C>T maps to ENST00000359759 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr21:46925825 G>C maps to ENST00000359759 V1469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr21:46925148 A>C maps to ENST00000359759 P1405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:70778331 A>G maps to NM_001858.4 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr6:70610188 C>G maps to NM_001858.4 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr6:70840094 G>T maps to NM_001858.4 G455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:70916617 G>A maps to NM_001858.4 Q1079Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr6:70637852 C>T maps to NM_001858.4 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr17:48271769 G>A maps to NM_000088.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr17:48266585 C>T maps to NM_000088.3 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr7:94034182 T>A maps to NM_000089.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:94047824 C>G maps to NM_000089.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr7:94056943 C>A maps to NM_000089.3 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:94053755 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr7:94057752 C>T maps to NM_000089.3 H1225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr7:94041433 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr20:61939942 C>G maps to ENST00000326996 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr20:61942975 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr20:61936826 C>T maps to ENST00000326996 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:61929274 G>A maps to ENST00000326996 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr6:55940288 G>T maps to NM_030820.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr6:55925687 C>T did not map to a codon.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr8:139647306 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr8:139701177 A>G maps to NM_152888.1 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:139749808 A>C maps to NM_152888.1 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:139629191 C>A maps to NM_152888.1 G1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr8:139675983 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr8:139638435 G>A maps to NM_152888.1 I1238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr8:139767454 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:139614390 C>G maps to NM_152888.1 G1384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:177669365 A>C maps to ENST00000390654 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:177686745 A>C maps to ENST00000390654 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr1:86249997 G>A maps to NM_152890.5 R1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr4:109817821 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:109782109 T>C maps to ENST00000333642 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:109784540 A>C maps to ENST00000333642 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:117045990 T>G maps to NM_032888.2 G1294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr9:116930356 C>T maps to NM_032888.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:117044774 C>T maps to NM_032888.2 G1270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:7472283 A>C maps to NM_001037763.2 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:7410429 G>A maps to NM_001037763.2 Q998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr7:7561588 C>A maps to NM_001037763.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:48370912 G>T maps to NM_001844.4 S1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr2:189875537 G>C maps to NM_000090.3 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr2:189872622 C>T maps to NM_000090.3 Q1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr13:110845183 T>C maps to NM_001845.4 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr13:110833734 A>C maps to NM_001845.4 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr13:110839538 C>T maps to NM_001845.4 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr13:110847368 C>A did not map to a codon.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr13:111143634 G>C maps to NM_001846.2 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:111141853 C>T maps to NM_001846.2 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr2:228163515 A>G maps to NM_000091.4 P1290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr2:228111411 G>T maps to NM_000091.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DN-01A-11D-A17W-09 chr2:228141147 G>T maps to NM_000091.4 G659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr2:227872736 C>T maps to ENST00000396625 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr2:227872898 G>A maps to ENST00000396625 P1548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:227942675 G>A maps to ENST00000396625 R641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:227946855 A>C maps to ENST00000396625 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr2:227872835 G>A maps to ENST00000396625 C1569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:227974002 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:107834340 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:107823934 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:107829954 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:107920852 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:107929280 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr23:107829951 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr23:107924994 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr23:107924150 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:107935989 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr23:107814669 G>T did not map to a codon.
Sequencing variant TCGA-E9-A1QZ-01A-21D-A167-09 chr23:107823801 A>G did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:107863631 A>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:107840777 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:107422037 A>C did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:107420160 C>G did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:107421947 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:107435806 T>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:107434674 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:107414091 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:107457344 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:107433720 C>A did not map to a codon.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr23:107435783 C>A did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:107436903 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr23:107412745 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr23:107402722 C>A did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:107418927 C>A did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr23:107403828 C>T did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:107436868 G>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:107400446 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr9:137707821 A>G maps to NM_000093.3 E1370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr9:137591854 G>A maps to NM_000093.3 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr9:137650105 C>T maps to NM_000093.3 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:137702138 G>C maps to NM_000093.3 G1171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr2:189904112 A>T maps to NM_000393.3 A1270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:189927993 A>C maps to NM_000393.3 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr2:189943787 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr19:10084292 G>A maps to NM_015719.3 R1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:10108822 A>C maps to NM_015719.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:10071215 C>T maps to NM_015719.3 T1703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr19:10108092 G>C maps to NM_015719.3 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr19:10088136 G>A maps to NM_015719.3 G1046G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr19:10087233 C>T maps to NM_015719.3 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr21:47407423 C>T maps to NM_001848.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr21:47423449 C>T maps to NM_001848.2 D870D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr21:47532001 G>A maps to NM_001849.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:47545702 G>A maps to NM_001849.3 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr21:47549149 C>G maps to NM_058174.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr21:47539718 C>T maps to NM_001849.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr21:47552402 G>A maps to NM_001849.3 E999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr2:238290028 C>A maps to NM_004369.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IY-01A-21D-A21Q-09 chr2:238303515 T>A maps to NM_004369.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:238268799 A>C maps to NM_004369.3 G2071G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr2:238283133 G>A maps to NM_004369.3 V1200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr2:238283232 G>A maps to NM_004369.3 I1167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:238290023 G>A maps to NM_004369.3 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:238234209 G>A maps to NM_004369.3 C3162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr2:238303251 C>T maps to NM_004369.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:238285969 G>A maps to NM_004369.3 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr2:238253584 G>A maps to NM_004369.3 Y2391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr2:238280435 G>T maps to NM_004369.3 I1408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RX-01A-11D-A25Q-09 chr3:130159256 A>G maps to ENST00000312481 T2025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:130110298 G>A maps to ENST00000312481 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr3:130188287 C>A maps to ENST00000312481 I2480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:130095626 C>T maps to ENST00000312481 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:130116893 C>T maps to ENST00000312481 D1310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:130174353 G>T maps to ENST00000312481 E2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:130188204 G>T maps to ENST00000312481 E2453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr3:130098666 G>A maps to ENST00000312481 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr3:130187807 C>T maps to ENST00000312481 Y2320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RP-01A-21D-A099-09 chr3:130159661 G>A maps to ENST00000312481 S2160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr3:130119917 T>C maps to ENST00000312481 H1345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr3:130116893 C>T maps to ENST00000312481 D1310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr3:130110115 T>G maps to ENST00000312481 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P0-01A-11D-A142-09 chr3:130095410 G>A maps to ENST00000312481 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr3:130290046 C>G maps to NM_001102608.1 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr3:48612825 G>A maps to NM_000094.3 P2042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:48606849 A>C maps to NM_000094.3 G2548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:48627146 T>G maps to NM_000094.3 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:48631838 A>C maps to NM_000094.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:48623526 G>A maps to NM_000094.3 Q1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr3:48625778 C>A maps to NM_000094.3 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JI-01A-21W-A100-09 chr3:48609589 G>A maps to NM_000094.3 D2331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr3:48630810 C>T maps to NM_000094.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr3:48617225 T>G maps to NM_000094.3 R1716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr3:99513746 G>A maps to ENST00000429802 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:71003883 G>A maps to NM_001851.4 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:70984476 T>C did not map to a codon.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr6:70942385 G>A maps to NM_001851.4 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:70935662 G>A maps to NM_001851.4 N851N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr6:70935662 G>A maps to NM_001851.4 N851N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr1:40778133 T>A maps to NM_001852.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:61472047 A>G maps to NM_001853.3 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr20:61458147 G>A maps to NM_001853.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr20:61458598 C>T maps to NM_001853.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:120116066 G>A maps to NM_006438.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:335126 T>G maps to NM_130386.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr18:357408 C>A maps to NM_130386.2 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr18:331726 G>A maps to NM_130386.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr3:15515752 C>G maps to NM_005677.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:149468586 C>A maps to NM_016094.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr10:22606825 G>A maps to NM_012071.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr8:146076482 G>A maps to NM_001081003.1 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr20:31315778 G>A maps to NM_053041.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23E-01A-11D-A159-09 chr11:36297761 G>A maps to NM_014186.3 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr11:36300037 G>A maps to NM_014186.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr19:18897404 G>A maps to NM_000095.2 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr19:18902063 G>C maps to NM_000095.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3X8-01A-31D-A22X-09 chr22:19956087 G>T maps to NM_001135162.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr1:160261647 C>T maps to NM_001098398.1 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:160280017 T>C maps to NM_001098398.1 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr1:160280026 G>A maps to NM_001098398.1 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:160276145 C>T maps to NM_001098398.1 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:160275508 G>A maps to NM_001098398.1 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:160279993 G>A maps to NM_001098398.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:139092189 G>C maps to NM_004766.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr3:139092648 T>C maps to NM_004766.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr19:19016389 G>A maps to NM_007263.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr3:128973841 G>A maps to NM_016128.3 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr3:128996135 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:130148492 G>A maps to NM_012133.4 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr7:130146585 C>G maps to NM_012133.4 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JU-01A-11D-A13L-09 chr4:83971137 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr7:99687263 G>T maps to NM_006833.4 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:57490418 C>T maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr4:47676479 G>C maps to NM_006587.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr4:47676507 G>C maps to NM_006587.2 S420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:109055907 G>A maps to ENST00000420959 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr17:27948433 G>A maps to ENST00000345068 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:4412093 G>C maps to NM_024535.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr16:4458193 C>A maps to NM_024535.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr16:4408083 G>A maps to NM_024535.3 D826D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr17:14110528 G>T maps to NM_001303.3 *444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:119396137 G>C maps to ENST00000484810 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr3:119396061 C>T maps to ENST00000484810 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr20:30227900 G>A did not map to a codon.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr2:98262608 C>A maps to NM_001862.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:120876254 G>A maps to NM_004373.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:46736980 C>A maps to NM_130902.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr4:46737163 G>A maps to NM_130902.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:63742176 C>T maps to NM_004074.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:148896324 G>A maps to NM_000096.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr3:148896319 A>G maps to NM_000096.3 F920F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:148896219 C>A maps to NM_000096.3 E954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:148928070 C>A maps to NM_000096.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W3-01A-11D-A10G-09 chr3:148930394 G>A maps to NM_000096.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr16:19547332 C>T maps to NM_014711.4 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr16:19548274 A>G maps to NM_014711.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr16:19556522 C>G maps to NM_014711.4 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr7:130027698 C>T maps to NM_001868.2 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:130021574 C>A maps to NM_001868.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:129916569 C>T maps to NM_001869.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr3:148603938 C>A maps to NM_001870.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A082-01A-11W-A019-09 chr7:129939178 C>T maps to NM_016352.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr7:130007390 C>T maps to NM_080385.4 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr7:130003342 T>G maps to NM_080385.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr8:68346440 T>C maps to NM_020361.4 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:17025305 A>C maps to ENST00000443236 G1320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr19:17040006 A>G maps to ENST00000443236 Y1020Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr19:17014625 G>T maps to ENST00000443236 I1488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr19:17108121 G>T maps to ENST00000443236 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J7-01A-11W-A050-09 chr19:17032749 G>A maps to ENST00000443236 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr19:17017900 C>T maps to ENST00000443236 A1353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:17014403 C>G maps to ENST00000443236 V1536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr19:17015306 G>A maps to ENST00000443236 F1418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:17003993 G>C maps to ENST00000443236 V1918V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:148558713 C>T maps to NM_001871.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr13:46629930 G>T maps to NM_001872.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:28778810 C>G maps to NM_001304.4 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:28750579 G>T maps to NM_001304.4 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:28769411 G>T maps to NM_001304.4 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:28754559 A>G maps to NM_001304.4 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr15:83240147 G>A maps to ENST00000261723 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr4:15054050 C>G maps to NM_001177382.1 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr4:15054068 C>G maps to NM_001177382.1 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr4:15009074 G>A maps to NM_001177382.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:93841169 A>C maps to NM_014912.4 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr10:93870934 C>A maps to NM_014912.4 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr5:173317752 A>G maps to NM_030627.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:173378903 T>C maps to NM_030627.2 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:173380154 C>T maps to NM_030627.2 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr5:175307020 G>A maps to NM_001008220.1 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:75122505 T>G maps to NM_001030005.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:194063181 G>A maps to NM_001080513.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr3:194063050 G>A maps to NM_001080513.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr3:194062060 C>T maps to NM_001080513.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:87570601 T>C maps to NM_003909.3 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:131261487 G>A maps to ENST00000502818 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr3:131388573 G>T maps to ENST00000502818 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr3:131268918 G>A maps to ENST00000502818 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BO-01A-23D-A12B-09 chr6:36713226 G>A maps to NM_020939.1 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:24545067 C>A maps to NM_006032.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr12:39079359 G>T maps to NM_153634.2 Y401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:39117597 G>T maps to NM_153634.2 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr12:39161455 G>A maps to NM_153634.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:211466996 T>G maps to NM_001122633.1 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:211452780 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:211469849 C>T maps to NM_001122633.1 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr8:145623022 A>C maps to NM_013291.2 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:145634419 G>A maps to NM_013291.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr8:145619107 G>A maps to NM_013291.2 I1335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:145625826 C>T maps to NM_013291.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr8:145621562 C>T maps to NM_013291.2 Q993Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr14:92628063 A>G maps to NM_017437.1 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:92625616 A>C maps to NM_017437.1 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:92627466 T>C maps to NM_017437.1 H711H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:1249258 C>T maps to NM_017871.4 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:61183743 G>C maps to NM_024811.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:68542876 G>C maps to NM_001876.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr11:68574940 G>A maps to NM_001876.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr11:68566685 G>T maps to NM_001876.3 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr22:51015381 G>A maps to NM_152245.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr22:51007767 C>T maps to NM_152245.2 *773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr22:51015420 G>A maps to NM_152245.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr22:51012016 C>T maps to NM_152245.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:50195589 G>A maps to NM_152359.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:50210804 C>G maps to NM_152359.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Y-01A-21W-A050-09 chr23:88008776 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:88008975 C>T did not map to a codon.
Sequencing variant TCGA-AC-A5EI-01A-11D-A27P-09 chr23:88008506 T>A did not map to a codon.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr23:88008721 C>T did not map to a codon.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr20:2778612 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr20:2774880 C>T maps to NM_019609.4 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr20:2779432 G>A maps to NM_019609.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr10:125521406 G>T maps to NM_198148.2 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr1:207669638 G>A maps to NM_000651.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:207684912 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:207741167 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr1:207697076 G>A maps to NM_000651.4 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr1:207791575 G>A maps to NM_000651.4 L2350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:207890888 G>T maps to NM_175710.1 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr1:207870998 G>A maps to NM_175710.1 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr1:207644372 C>G maps to NM_001006658.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr1:207651344 G>A maps to NM_001006658.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr1:207648367 T>A maps to NM_001006658.2 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XX-01A-21D-A23C-09 chr15:78632840 G>C did not map to a codon.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr12:94244019 C>G maps to NM_003805.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:1675983 T>G maps to NM_020825.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:1723943 C>T maps to NM_020825.3 F1236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr16:1724027 C>G maps to NM_020825.3 V1264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:1724027 C>T maps to NM_020825.3 V1264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr16:1712793 G>A maps to NM_020825.3 R876R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr16:1719081 C>T maps to NM_020825.3 Q1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr9:131860610 G>A maps to NM_000755.3 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr9:131860625 G>A maps to NM_000755.3 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr9:131864750 C>T maps to NM_000755.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr7:65579836 G>T maps to NM_001142414.1 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr2:208434995 C>T maps to NM_134442.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr9:35733102 C>G maps to NM_006368.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr19:4171689 C>T maps to NM_032607.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:28610008 T>G maps to NM_182898.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:28547354 G>T maps to NM_182898.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr7:28547243 G>A maps to NM_182898.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr7:28848829 G>A maps to NM_182898.2 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr16:3779641 C>G maps to NM_004380.2 V1802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr16:3900660 G>T maps to NM_004380.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:3900735 C>T maps to NM_004380.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr11:85375463 C>G maps to NM_001039618.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:35467875 T>C maps to ENST00000429130 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr5:76264652 C>T maps to NM_001882.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:76251688 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:30702424 G>A maps to ENST00000348438 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XS-01A-22D-A10G-09 chr7:30704715 G>A maps to ENST00000348438 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr2:36583698 G>C maps to NM_016441.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr2:36764582 C>T maps to NM_016441.2 H839H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr4:1388649 C>T maps to NM_175918.3 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr4:1389288 C>T maps to NM_175918.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:49819839 C>T maps to NM_001131.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr8:75925199 A>G maps to NM_031461.5 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr8:75898248 C>T maps to NM_031461.5 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr23:1314926 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr17:29130961 G>C maps to NM_015986.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr17:29123273 G>A maps to NM_015986.3 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr20:6011955 G>A maps to NM_019095.4 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FW-01A-11D-A17D-09 chr20:6017786 C>T maps to NM_019095.4 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:5827260 T>G maps to NM_001014809.1 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr4:5844876 C>T maps to NM_001014809.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:5862759 C>T maps to NM_001014809.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:20020422 G>A maps to NM_016652.4 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr20:20033187 C>T maps to NM_016652.4 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:152384673 G>A maps to NM_016190.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:152382486 A>G maps to NM_016190.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr1:17274956 T>C maps to NM_014675.3 A882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr1:17249171 C>T maps to NM_014675.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr1:17263260 G>A maps to NM_014675.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr1:17266457 G>T maps to NM_014675.3 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr1:17264147 G>C maps to NM_014675.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr1:17264938 T>C maps to NM_014675.3 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr1:17250934 C>T maps to NM_014675.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:87005250 A>C maps to NM_001143935.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr7:87005202 G>A maps to NM_001143935.1 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr7:87011254 G>A maps to NM_001143935.1 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr1:159683854 C>A maps to NM_000567.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XW-01A-11D-A23C-09 chr10:99640045 A>G maps to NM_018058.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:18886533 G>A maps to NM_001098482.1 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr1:153923849 C>T maps to NM_181715.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr11:45882530 G>A maps to NM_021117.3 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr11:45880385 A>T maps to NM_021117.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:111781131 C>A maps to NM_001885.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:97660029 T>G maps to ENST00000182096 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:97614823 A>G maps to ENST00000182096 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr2:208993006 G>A maps to NM_020989.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr2:208993165 C>A maps to NM_020989.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr2:208994510 C>T maps to NM_020989.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I5-01A-11W-A100-09 chr2:208988841 G>A maps to NM_006891.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:208986458 G>A maps to NM_006891.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:21288835 G>A maps to NM_001888.3 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr16:21288826 G>A maps to NM_001888.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:75184933 G>A maps to NM_001889.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr21:34969636 G>A maps to ENST00000416217 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:56679747 G>A maps to NM_004077.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06P-01A-11W-A019-09 chr12:53552402 G>A maps to NM_015989.4 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:151908825 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:151908882 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr23:151908832 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:115267857 C>T maps to NM_001130523.1 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:115284279 C>T maps to NM_001130523.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:110465848 G>A maps to NM_000757.4 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:149433882 A>C did not map to a codon.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr5:149449827 G>A maps to NM_005211.3 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr5:149450042 G>A maps to NM_005211.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:1428414 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:1407733 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:1428337 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr23:1407466 T>A did not map to a codon.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr22:37325586 C>T maps to ENST00000262825 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr22:37325761 C>T maps to ENST00000262825 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:19263578 A>C maps to NM_018371.4 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr8:19277863 C>T maps to NM_018371.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:43678728 T>G maps to NM_018590.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:43651250 C>T maps to NM_018590.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr8:2967830 G>A maps to NM_033225.5 Q2153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr8:3076792 G>A maps to NM_033225.5 F1552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr8:3216672 C>T did not map to a codon.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr8:2824185 G>T maps to NM_033225.5 I3002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0D9-01A-31W-A071-09 chr8:3165942 A>T maps to NM_033225.5 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr8:3889445 G>A maps to NM_033225.5 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:2807842 G>A maps to NM_033225.5 A3408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:3165332 A>C maps to NM_033225.5 G1278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:3265490 C>T maps to NM_033225.5 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr8:2910129 G>T maps to NM_033225.5 S2505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr8:3855432 T>C maps to NM_033225.5 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr8:3000128 T>G maps to NM_033225.5 G2033G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I5-01A-11W-A100-09 chr8:2823393 A>G maps to NM_033225.5 Y3061Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr8:3057329 C>T maps to NM_033225.5 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr8:3265701 G>T maps to NM_033225.5 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr8:3057295 G>A maps to NM_033225.5 L1712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr8:2975987 G>A maps to NM_033225.5 G2121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SG-01A-11D-A142-09 chr1:34090711 G>A maps to ENST00000373381 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:33999408 T>G maps to ENST00000373381 P3286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr1:34046409 G>A maps to ENST00000373381 L2404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr1:34312488 G>C maps to ENST00000373381 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr1:34276436 G>T maps to ENST00000373381 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:34204849 G>A maps to ENST00000373381 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr1:34076839 G>A maps to ENST00000373381 I2008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:34291355 C>T maps to ENST00000373381 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A249-01A-11D-A167-09 chr1:34052730 G>T maps to ENST00000373381 L2258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr8:113237152 T>G maps to NM_198123.1 A3657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr8:113358356 G>A maps to NM_198123.1 C2137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:113276018 G>A maps to NM_198123.1 P3237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:114186098 A>C maps to NM_198123.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr8:113662561 C>T maps to NM_198123.1 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:113323299 G>A maps to NM_198123.1 R2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr8:113988069 A>G maps to NM_198123.1 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr8:113841930 T>G maps to NM_198123.1 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr8:113516055 T>A maps to NM_198123.1 G1682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr4:70823233 G>A maps to NM_001891.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:148930499 C>A maps to NM_001025105.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr5:148885085 G>C maps to NM_001025105.1 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:37678472 C>T maps to NM_145203.5 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr15:64495364 G>A maps to NM_022048.3 H341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr19:1978886 G>A maps to NM_001319.6 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr15:75982427 C>T maps to NM_001897.4 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr15:75983020 G>A maps to NM_001897.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr15:75968730 C>T maps to NM_001897.4 V2043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr15:75977997 C>A maps to NM_001897.4 V1278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:68049833 G>C maps to ENST00000389042 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:68007968 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:68070683 T>C maps to ENST00000389042 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr8:67986495 T>C maps to ENST00000389042 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:67988730 G>A maps to ENST00000389042 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:68087601 C>T maps to ENST00000389042 Q1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27I-01A-11D-A16D-09 chr8:68062078 A>G maps to ENST00000389042 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr8:67988760 C>T maps to ENST00000389042 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:39185505 G>A maps to NM_033027.3 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr2:166532859 C>T maps to ENST00000409420 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr2:166514343 C>T maps to ENST00000409420 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr2:166535902 G>C maps to ENST00000409420 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:201458005 C>A maps to NM_001193572.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr12:77253421 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:77254188 G>A maps to NM_001321.1 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:18143129 C>T maps to NM_020536.4 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:23433218 A>C did not map to a codon.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr20:23807083 G>A maps to NM_001322.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr20:23546646 G>A maps to NM_080610.2 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr3:122060395 C>T maps to NM_005213.3 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr20:54978524 C>G maps to NM_001033522.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr20:54974291 C>T maps to NM_001033522.1 D305D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr23:100083081 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr23:100078981 G>A did not map to a codon.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr23:100087874 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:53458880 C>G maps to NM_015235.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:53457841 G>A maps to NM_015235.2 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SD-01A-11D-A10Y-09 chr20:23420937 C>T maps to NM_138283.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr20:23424674 G>A maps to NM_138283.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:134947484 A>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:120008887 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr23:120009252 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:120008752 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:120009244 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0EW-01A-21D-A10Y-09 chr23:153881612 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:153881772 T>C did not map to a codon.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr23:153881597 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr7:143965404 T>A maps to NM_198495.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:39818101 T>C maps to ENST00000396158 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:39818140 A>C maps to ENST00000396158 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:39818164 A>C maps to ENST00000396158 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:39819416 A>C maps to ENST00000396158 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr14:39818098 T>A maps to ENST00000396158 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr14:39796099 C>T maps to ENST00000396158 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:132031203 C>T maps to NM_001145659.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:1232006 G>A maps to NM_001328.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:126714660 T>G maps to NM_022802.2 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr10:126681265 G>A maps to NM_022802.2 Y925Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr10:126683157 G>A maps to NM_022802.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr16:67645307 G>A maps to NM_006565.3 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RI-01A-11W-A071-09 chr16:67645517 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr16:67644836 A>G maps to NM_006565.3 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr16:67655430 G>T maps to NM_006565.3 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr16:67645097 T>A maps to NM_006565.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr16:67662442 A>T maps to NM_006565.3 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A156-01A-11D-A12B-09 chr16:67644795 G>T maps to NM_006565.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr16:67670627 G>T maps to NM_006565.3 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:56099180 C>T maps to ENST00000423479 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:58217396 C>T maps to NM_005730.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:132270448 G>T maps to NM_001901.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr1:70890018 G>T maps to NM_001902.5 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:70895526 C>G maps to NM_001902.5 Y213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr1:70897809 C>T maps to NM_001902.5 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FX-01A-11D-A13L-09 chr5:138264933 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:138119051 C>T maps to ENST00000355078 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr5:138117645 C>T maps to ENST00000355078 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr5:138145809 C>T maps to ENST00000355078 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr10:69299407 T>A maps to NM_013266.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr10:68280417 G>A maps to NM_013266.2 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr3:41266592 G>A maps to NM_001904.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr3:41268805 T>A maps to NM_001904.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr3:41268808 C>T maps to NM_001904.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:9910781 C>T maps to ENST00000361853 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr20:36431298 G>T maps to NM_030877.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr11:57569468 C>G maps to NM_001085458.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr23:16685674 C>T did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:16720989 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr23:16711262 C>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:10800561 C>T maps to NM_014633.3 G1144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr11:10794774 G>A maps to NM_014633.3 E894E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BH-A0H9-01A-11W-A071-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:44520932 C>T maps to NM_000308.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:11708389 G>T maps to NM_147783.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:206317584 G>A maps to ENST00000361052 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr1:206331148 G>A maps to ENST00000361052 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr14:25044493 C>T maps to NM_001911.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:150779185 G>T maps to NM_000396.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:99795260 G>A maps to NM_001333.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr11:65650289 A>G maps to NM_001335.3 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:65650876 G>T maps to NM_001335.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr7:117398013 C>T maps to NM_033427.2 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr7:117432080 G>C maps to NM_033427.2 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr7:117431491 C>T maps to NM_033427.2 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr7:117450854 G>A maps to NM_033427.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:112999853 A>C maps to NM_018704.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr16:88781475 G>A maps to ENST00000378384 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:17142043 A>G maps to NM_001081.3 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:16957858 C>A maps to NM_001081.3 E2391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:16960707 G>A maps to NM_001081.3 Q2305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr10:16975113 A>G maps to NM_001081.3 C2032C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr10:16916413 C>G maps to NM_001081.3 L3065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr10:16960642 T>C maps to NM_001081.3 G2326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:16957943 G>A maps to NM_001081.3 F2362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:16957100 C>T maps to NM_001081.3 V2427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:17146499 T>A maps to NM_001081.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr10:16945995 G>A maps to NM_001081.3 H2677H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr10:16990570 G>A maps to NM_001081.3 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr10:104184497 C>A maps to NM_024040.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:148463717 T>C maps to NM_003592.2 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr10:35333604 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr2:225346621 G>C maps to NM_003590.3 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:225378294 G>A maps to NM_003590.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:225376275 T>C maps to NM_003590.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr2:225362532 G>A maps to NM_003590.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XR-01A-11D-A14K-09 chr13:113897391 G>A maps to NM_001008895.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr13:113899464 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:119678469 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr23:119694134 G>C did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:119660674 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:119691861 C>T did not map to a codon.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr23:119678366 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr23:119679330 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr23:119691820 C>A did not map to a codon.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr23:119673223 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:107965236 A>G maps to NM_003478.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr11:107925434 A>G maps to NM_003478.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr11:107965572 C>T maps to NM_003478.3 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr11:107965647 A>G maps to NM_003478.3 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr6:43010838 G>T maps to NM_001168370.1 R1229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:43013137 A>C maps to NM_001168370.1 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:43013068 C>T maps to NM_001168370.1 R1062R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:43010723 T>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:43005598 G>A maps to NM_001168370.1 Q1726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr6:43017143 C>T did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr6:43019029 C>G maps to NM_001168370.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr6:43172795 T>C maps to ENST00000354495 A1525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr6:33384456 T>C maps to NM_001014433.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr7:101713689 C>T maps to ENST00000360264 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr7:101844814 G>A maps to ENST00000360264 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr7:101840508 A>T maps to ENST00000360264 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N3-01A-12D-A159-09 chr7:101740744 G>T maps to ENST00000360264 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:111785939 A>C maps to NM_015267.3 P1424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:111652115 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:94705286 A>C maps to NM_016403.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:94705307 A>C maps to NM_016403.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:180835740 G>A maps to NM_020943.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr17:36958377 C>G maps to NM_017748.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr17:36971289 G>A maps to NM_017748.3 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr5:64081366 C>T maps to NM_005869.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:49032932 T>G maps to NM_025087.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:49009314 C>T maps to NM_025087.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr4:48996813 A>G maps to NM_025087.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr4:48990512 C>G maps to NM_025087.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr21:18933137 C>G maps to NM_001338.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr21:18931411 G>A maps to NM_001338.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:18924179 G>A maps to NM_001338.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr21:18933746 A>G maps to NM_001338.3 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr2:219029616 G>C maps to NM_000634.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr2:219000456 C>T maps to NM_001168298.1 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KD-01A-12D-A20S-09 chr23:70837001 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:70837026 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:70836739 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr23:70836242 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24P-01A-11D-A167-09 chr23:70836774 C>T did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:70837214 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr23:70836845 A>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:136873299 C>T maps to NM_001008540.1 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:118764306 C>T maps to NM_001716.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:237489125 C>T maps to NM_020311.2 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr2:237489605 C>T maps to NM_020311.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr18:47810866 C>T maps to NM_001101654.1 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:105393505 G>A maps to NM_025212.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr4:105412002 G>A maps to NM_025212.1 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr5:139060485 G>A maps to NM_016463.7 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:30578392 A>C did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:30578015 C>T did not map to a codon.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr23:35984769 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr23:35985881 A>G did not map to a codon.
Sequencing variant TCGA-A2-A3KC-01A-11D-A20S-09 chr23:35989850 G>T did not map to a codon.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr23:35969263 C>T did not map to a codon.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr23:35993901 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr23:35993846 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:35969362 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:35989990 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:35989718 T>C did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:35966470 C>G did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr23:35984725 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:35993897 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:35984796 T>C did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:35989889 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:19973550 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:19984267 C>A did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr23:19971132 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr23:19971987 G>T did not map to a codon.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr23:19984271 T>A did not map to a codon.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr23:75392997 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:75394727 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:75395421 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr23:75397564 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:45051236 T>G did not map to a codon.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr23:45013240 A>G did not map to a codon.
Sequencing variant TCGA-E2-A1L9-01A-11D-A13L-09 chr23:45011032 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:45013387 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr23:40489944 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr23:40506282 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr23:148627222 T>A did not map to a codon.
Sequencing variant TCGA-AR-A24Z-01A-11D-A167-09 chr23:148628333 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HU-01A-11W-A050-09 chr23:148627390 T>G did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr23:148628333 C>G did not map to a codon.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr23:149100973 T>A did not map to a codon.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr23:149101991 T>C did not map to a codon.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr23:106486491 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:106459905 T>G did not map to a codon.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr23:106456140 G>A did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr23:134294369 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:134292175 G>C did not map to a codon.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr23:118694272 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118675340 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:105905388 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:105879797 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:105868385 G>C did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:105855829 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr23:105855471 G>A did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:105868339 C>G did not map to a codon.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr23:105905446 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr23:105879794 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr23:105921403 C>T did not map to a codon.
Sequencing variant TCGA-A1-A0SD-01A-11D-A10Y-09 chr23:23956734 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:23934360 C>A did not map to a codon.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr23:23934437 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:23953446 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:23953534 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:23957413 C>G did not map to a codon.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr23:23956747 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:36117973 A>G did not map to a codon.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr23:115593149 T>G did not map to a codon.
Sequencing variant TCGA-A2-A0T7-01A-21D-A099-09 chr23:70324241 A>G did not map to a codon.
Sequencing variant TCGA-A8-A09V-01A-11D-A045-09 chr23:70323922 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:70325952 C>T did not map to a codon.
Sequencing variant TCGA-AR-A24R-01A-11D-A167-09 chr23:70325860 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:70324636 G>A did not map to a codon.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr23:139038827 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr23:139038666 T>C did not map to a codon.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr18:71959065 C>T maps to NM_148923.2 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr17:4060160 G>T maps to NM_144611.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr17:4053206 C>T maps to NM_144611.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:7690526 A>C maps to NM_016229.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:54649920 C>T maps to NM_001031672.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:61124158 G>A maps to NM_001161454.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:61120476 A>G maps to NM_001161454.1 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr11:61120578 G>C maps to NM_001161454.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr23:37665783 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:37664366 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:37670092 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:145151519 C>T maps to NM_001916.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:145151385 C>T maps to NM_001916.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:22956469 C>T maps to NM_014608.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr15:22933647 G>A maps to NM_014608.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr15:22926025 C>T maps to NM_014608.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P3-01A-11D-A142-09 chr15:22928473 T>A maps to NM_014608.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:156786029 C>T maps to ENST00000442283 Y922Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:156747678 C>T maps to ENST00000442283 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0RX-01A-21D-A099-09 chr17:74527736 G>A maps to NM_134268.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:145677910 G>A maps to NM_138496.1 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr8:145677766 G>C maps to NM_138496.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr23:83129610 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:83128336 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr23:83128428 G>T did not map to a codon.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr23:83129528 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:105767464 T>G maps to NM_001340.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:105767536 T>G maps to NM_001340.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr9:105767683 G>C maps to NM_001340.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:50828136 G>A maps to ENST00000311559 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:50783749 A>G maps to ENST00000311559 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr15:74631004 G>A maps to NM_000781.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr8:143957770 G>A maps to ENST00000377675 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P6-01A-11D-A142-09 chr8:143998608 G>A maps to NM_000498.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr8:143994089 C>G maps to NM_000498.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:104592374 G>A maps to NM_000102.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AO-01A-11D-A12Q-09 chr15:75015348 T>C maps to NM_000499.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:75042204 A>C maps to NM_000761.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:75042573 G>C maps to NM_000761.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr2:204154589 T>C maps to ENST00000429815 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:32008362 T>G did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:32008450 C>T maps to NM_000500.5 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:52775542 A>G maps to NM_000782.4 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr20:52782316 C>A maps to NM_000782.4 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr20:52789445 A>T did not map to a codon.
Sequencing variant TCGA-BH-A1FD-01A-11W-A14Q-09 chr20:52773722 G>A maps to NM_000782.4 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr20:52786154 C>A maps to NM_000782.4 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr10:94834967 C>T maps to NM_000783.3 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr2:72371200 C>A maps to NM_019885.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr2:219674427 C>T maps to NM_000784.3 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13H-01A-11D-A228-09 chr19:41596101 G>T did not map to a codon.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr19:41596334 C>T maps to NM_000766.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:41595961 C>T maps to NM_000766.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr19:41596462 G>A maps to NM_000766.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr19:41596357 C>A maps to NM_000766.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:41354537 G>A maps to NM_000762.5 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr19:41384688 G>A maps to NM_000764.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:41388070 C>T maps to NM_000764.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:41518201 G>C did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr10:96443635 G>A maps to NM_000772.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:96447537 C>T maps to NM_000772.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr10:96447985 C>T maps to NM_000772.2 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr10:96535204 G>A maps to NM_000769.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr10:96580362 C>A maps to NM_000769.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:96796917 T>G maps to NM_000770.3 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:42524866 G>A maps to NM_000106.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr10:135340910 C>T maps to NM_000773.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:41631414 C>A maps to NM_000774.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr19:41627363 C>T maps to NM_000774.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr19:41703774 C>T maps to ENST00000301173 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr19:41704618 C>T maps to ENST00000301173 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24K-01A-11D-A167-09 chr19:41704415 A>T maps to ENST00000301173 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr19:41709353 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:46563858 T>C did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr7:99366073 C>T maps to NM_017460.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr7:99358486 G>T maps to NM_017460.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:99247812 T>C maps to NM_000777.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr7:99306818 G>C maps to ENST00000292414 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:47398485 T>G maps to ENST00000371904 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr1:47407051 G>T maps to ENST00000371904 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:47406940 G>T maps to ENST00000371904 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14T-01A-11D-A10Y-09 chr1:47610235 C>T maps to NM_001010969.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:47283831 G>A maps to NM_001099772.1 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:47280918 C>T maps to NM_001099772.1 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:16025599 C>G maps to NM_021187.3 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:16038069 G>T maps to NM_021187.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr19:16038291 A>T maps to NM_021187.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:15789132 C>A maps to NM_023944.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:16000452 G>C maps to NM_001082.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr19:16003163 C>A maps to NM_001082.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr19:15662125 C>T maps to NM_173483.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr19:15757898 C>T maps to NM_000896.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:15730299 G>C did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr4:187130352 C>T maps to ENST00000511608 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:187131687 G>T maps to NM_207352.3 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:47512150 T>G maps to NM_178033.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr1:47489662 G>A maps to NM_178033.1 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:47581262 C>T maps to NM_178134.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr8:59405043 G>C maps to NM_000780.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr8:59404034 C>T maps to NM_000780.3 *505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CU-01A-12W-A050-09 chr8:65527679 G>A maps to NM_004820.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr8:65528611 T>C maps to NM_004820.3 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr8:65528638 G>C maps to NM_004820.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr8:65509377 T>A maps to NM_004820.3 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr8:65527648 G>A maps to NM_004820.3 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:10199054 C>T maps to NM_001037160.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr23:77528442 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:77528531 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:77528735 T>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:77529167 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr23:77528895 G>T did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr23:77528832 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr13:49281045 C>T maps to NM_020377.2 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr17:76705781 C>A maps to NM_004762.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr19:48981326 G>A maps to NM_017457.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr7:6210235 C>T maps to ENST00000396741 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr7:6210580 G>A maps to ENST00000396741 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:37690714 G>A maps to NM_013385.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr22:37690714 G>A maps to NM_013385.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr2:158272419 C>T maps to NM_004288.4 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr2:158300388 C>T maps to NM_004288.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:158300406 A>G maps to NM_004288.4 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:24709375 A>C maps to NM_015330.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:24709375 A>C maps to NM_015330.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr22:24765208 C>G maps to NM_015330.2 S1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr17:20156816 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr17:20130835 C>T maps to NM_001033553.1 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:27852723 A>C maps to ENST00000435845 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr21:27840936 G>A maps to ENST00000435845 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr21:27945193 G>C maps to ENST00000435845 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr4:4411346 C>A maps to NM_001040101.1 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:4389430 T>C maps to NM_001040101.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr14:59830427 C>T maps to NM_014992.1 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:39855369 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:39869079 C>T maps to ENST00000398904 F938F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:39855320 G>A maps to ENST00000398904 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr6:39847225 G>A maps to ENST00000398904 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:57480803 G>C maps to ENST00000371231 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr5:39383283 G>A maps to NM_001343.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr5:39383202 G>A maps to NM_001343.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr9:124519318 G>A maps to ENST00000408936 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:124530893 C>G maps to ENST00000408936 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr23:86071091 T>C did not map to a codon.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr23:85769371 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:85404051 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:85404025 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:85950092 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr23:85404050 C>G did not map to a codon.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr23:85403984 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:86082771 G>C did not map to a codon.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr14:59113587 C>T maps to NM_016651.5 Y749Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:49569308 A>C maps to NM_004393.4 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:61511556 C>T maps to NM_006133.2 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr11:61508015 C>G maps to NM_006133.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr11:61106622 C>T maps to NM_015533.3 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:61111710 C>T maps to NM_015533.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr3:49055970 C>T maps to NM_001009996.1 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:13084300 A>C maps to NM_152654.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr12:109288101 C>T maps to NM_001917.4 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr12:109278916 C>G maps to NM_001917.4 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:155701154 C>T maps to NM_004632.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr9:90321696 G>A maps to NM_004938.2 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr9:90252866 T>A maps to NM_004938.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr9:90256920 C>G maps to NM_004938.2 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr9:90220078 G>T maps to NM_004938.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:64332424 C>T maps to NM_014326.3 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr19:3964284 C>T maps to NM_001348.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:159672275 G>T maps to NM_001017920.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:100756829 C>G maps to NM_014395.2 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr2:136680408 T>C maps to NM_001349.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:173808665 C>T maps to NM_018122.4 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr6:33288192 A>G maps to NM_001350.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:33289224 G>C maps to NM_001350.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14O-01A-31D-A10Y-09 chr19:1418353 G>T maps to NM_018959.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr19:1432661 C>T maps to NM_018959.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:51634211 A>C maps to NM_014764.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:51634818 A>C maps to NM_014764.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr9:121929781 C>G maps to NM_014618.2 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr9:121929943 G>A maps to NM_014618.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr9:121929580 A>C maps to NM_014618.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr9:121971043 G>A maps to NM_014618.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr9:121930378 C>T maps to NM_014618.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr9:121929961 G>C maps to NM_014618.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:87525811 A>G maps to NM_006716.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:136507372 C>T maps to NM_000787.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr20:44037636 C>G maps to NM_001048226.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr3:137892402 G>C maps to NM_016216.3 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr3:137890541 C>A maps to NM_016216.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr3:137886066 A>C maps to NM_016216.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:20177891 C>T maps to ENST00000227256 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15P-01A-11D-A10Y-09 chr11:20177993 G>A maps to ENST00000227256 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr9:37861270 C>G maps to NM_024345.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr14:24586890 C>T maps to NM_025230.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr14:24587303 C>T maps to NM_025230.4 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr9:34125206 G>A maps to NM_015397.3 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr23:125685531 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr23:125685741 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:125685655 C>G did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:125685469 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr23:125685703 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:125685956 G>A did not map to a codon.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr23:125686113 A>C did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:125686219 G>A did not map to a codon.
Sequencing variant TCGA-A8-A083-01A-21W-A019-09 chr23:125298648 T>A did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr23:125298655 C>G did not map to a codon.
Sequencing variant TCGA-AO-A12H-01A-11D-A10Y-09 chr23:125299409 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr23:125298869 A>T did not map to a codon.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr23:125298897 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:73408475 A>T maps to NM_015604.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:41983922 C>T maps to NM_001029955.3 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr4:41984627 G>A maps to NM_001029955.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr4:41984213 G>A maps to NM_001029955.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr8:88885922 C>A maps to NM_152418.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:88885902 G>A maps to NM_152418.3 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr14:69521488 G>A maps to NM_003861.2 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr1:168044670 T>A maps to ENST00000367840 *952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:168044616 G>T maps to ENST00000367840 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:168034922 G>A maps to ENST00000367840 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:168034844 C>T maps to ENST00000367840 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SD-01A-11D-A10Y-09 chr1:160210107 C>T maps to NM_015726.3 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr1:160209534 C>G maps to NM_015726.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr23:27998515 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:27998943 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr23:27997689 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:27999138 C>A did not map to a codon.
Sequencing variant TCGA-AR-A1AJ-01A-21D-A12Q-09 chr23:27999023 A>T did not map to a codon.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr23:27999268 G>T did not map to a codon.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr23:27999080 C>A did not map to a codon.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr23:27765791 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:27766111 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr23:27765437 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr23:27765578 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr23:27765024 G>A did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:27765803 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr23:27765410 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr3:98538118 C>A maps to ENST00000326857 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr3:98518305 G>A maps to ENST00000326857 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr18:50976882 A>T maps to NM_005215.3 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:50832016 C>T maps to NM_005215.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr18:50450135 G>T maps to NM_005215.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr18:50432562 C>A maps to NM_005215.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr18:50278517 C>T maps to NM_005215.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:31287063 A>G maps to NM_181807.2 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr6:24174966 G>T maps to NM_016356.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr1:32678162 C>T maps to NM_001099434.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr11:6652951 G>C maps to NM_003737.2 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr4:155242002 C>T maps to NM_017639.3 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr4:155157391 C>T maps to NM_017639.3 L2349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:155219189 T>C maps to NM_017639.3 E1637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr4:155411019 G>T maps to NM_001142552.1 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NE-01A-21D-A14K-09 chr4:155241642 G>C maps to NM_017639.3 S1181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr4:155254227 G>A maps to NM_017639.3 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:2290146 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:71888181 C>G maps to ENST00000504952 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr13:36686077 G>A maps to NM_004734.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr13:36700118 G>A maps to NM_004734.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr13:36367616 C>T did not map to a codon.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr13:36686247 G>T maps to NM_004734.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:151169477 C>T maps to NM_001040261.4 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr4:151153907 C>T maps to NM_001040261.4 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr4:151153940 C>T maps to NM_001040261.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr3:36759618 G>A maps to NM_033403.1 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr10:115607026 T>C maps to NM_014881.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:114454080 G>A maps to NM_022836.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RU-01A-11D-A28B-09 chr10:14968883 A>G maps to NM_001033855.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr3:53381532 C>G maps to ENST00000480258 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:53346357 C>T maps to ENST00000480258 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr5:112321589 C>T maps to NM_152624.4 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr1:155020577 A>T maps to NM_152494.3 K601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:155018650 C>T maps to NM_152494.3 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr1:155018633 G>T maps to NM_152494.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:154991031 T>G maps to NM_144622.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:154991074 G>C maps to NM_144622.2 S756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:183815717 C>T maps to NM_001012732.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:74594519 G>A maps to NM_004082.4 Q738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr12:57925869 G>A maps to ENST00000434715 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr5:150112929 C>T maps to NM_001135643.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr3:182683348 C>A maps to NM_020640.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:114112364 A>C maps to NM_001014283.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr13:114138362 A>G maps to NM_001014283.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:20871507 G>T maps to NM_173475.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:20873716 A>C maps to NM_173475.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:20873484 G>A maps to NM_173475.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RU-01A-11D-A28B-09 chr16:20873623 G>A maps to NM_173475.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:110644538 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:110574208 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:85816196 C>T maps to NM_012137.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr11:61094350 C>T maps to NM_001923.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr11:47237947 G>A maps to NM_000107.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:47254426 C>T maps to NM_000107.2 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr7:50611609 G>A maps to NM_000790.3 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr11:103907555 G>A maps to NM_001001711.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:74034580 C>T maps to NM_019058.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr4:101108851 T>C maps to NM_145244.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:101108932 G>A maps to NM_145244.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FB-01A-11D-A17D-09 chr6:30859823 G>T maps to NM_013994.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:30861151 C>A maps to NM_013994.2 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr6:30864587 C>T maps to NM_013994.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr1:162729696 C>T maps to NM_006182.2 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr1:162746030 G>A maps to NM_006182.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr1:162746134 G>A maps to NM_006182.2 W753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:162729639 C>T maps to NM_006182.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:15758355 C>T maps to NM_004939.1 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr11:108577471 A>G maps to NM_004398.2 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:31244702 C>T maps to NM_030653.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:31247695 G>A maps to NM_030653.3 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:31247701 G>A maps to NM_030653.3 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr12:31244702 C>T maps to NM_030653.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:118579546 T>G maps to NM_006773.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:118586965 C>A maps to NM_006773.3 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:118577294 A>G maps to NM_006773.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:70400063 C>G maps to NM_018332.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:49230684 C>T maps to NM_004818.2 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr14:94524188 G>T maps to NM_020414.3 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr14:94526826 G>A maps to NM_020414.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr11:125787145 G>A maps to NM_013264.3 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr23:134680716 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:134683698 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:134685925 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:134713932 A>C did not map to a codon.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr23:134713801 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:134683684 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:134713876 A>C did not map to a codon.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr23:134706901 C>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:134686018 C>T did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:134715539 C>A did not map to a codon.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr23:134711193 G>A did not map to a codon.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr20:47839852 G>T maps to NM_017895.7 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:47841657 A>G maps to NM_017895.7 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr9:135513748 C>T maps to NM_138620.1 *586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr19:14523993 G>T maps to ENST00000451994 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:41202028 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:41204736 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:41206170 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:41203504 C>A did not map to a codon.
Sequencing variant TCGA-AO-A03L-01A-41W-A071-09 chr23:41201887 C>T did not map to a codon.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr23:41204454 G>A did not map to a codon.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr23:41202081 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:41200787 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:41196695 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:41203587 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr23:41205486 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:55081638 C>T maps to NM_024415.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:61895376 G>A maps to NM_203499.1 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:61864560 C>G maps to NM_203499.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07Z-01A-11W-A019-09 chr12:12974214 A>G maps to NM_016355.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr12:12974613 A>C maps to NM_016355.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr19:19035753 C>T maps to NM_019070.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr19:19035753 C>T maps to NM_019070.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr17:62499307 T>G maps to NM_004396.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:62498635 C>A maps to NM_004396.3 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:132625196 G>C maps to NM_175066.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr12:132626393 C>G did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:35981175 C>T maps to NM_007010.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr23:23018657 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:23019753 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:23019817 T>A did not map to a codon.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:23018404 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0IH-01A-11D-A10Y-09 chr12:113599786 C>T maps to NM_001111322.1 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:32492506 A>C maps to NM_014314.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr9:32481364 G>C maps to NM_014314.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr9:32481394 G>A maps to NM_014314.3 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr9:32491383 A>G maps to NM_014314.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr1:200613626 A>G maps to NM_001031725.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28O-01A-11D-A228-09 chr1:200635367 G>A maps to NM_001031725.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr1:200635771 G>A maps to NM_001031725.4 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:169190080 C>A maps to NM_017631.5 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:169204665 C>T maps to NM_017631.5 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:169305834 G>A maps to NM_001012967.1 L1348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr11:654015 G>A maps to NM_021008.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr9:118164402 G>C maps to NM_017418.2 *71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:161092973 C>T maps to ENST00000368005 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr19:42703631 C>T maps to NM_133328.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:35287431 G>A maps to NM_022047.3 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr6:35277529 C>T maps to NM_022047.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:71548592 A>C maps to NM_001002035.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr6:50016313 T>C maps to NM_001037498.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:30037880 C>T maps to NM_153324.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Z-01A-11D-A167-09 chr4:9446285 A>C maps to NM_001040448.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr20:239785 G>T maps to NM_207469.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr14:100615658 G>C maps to NM_206918.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr9:126371760 C>G did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr9:126146023 G>A maps to NM_020946.1 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr9:126520094 T>A maps to NM_020946.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr9:126392665 C>T maps to NM_020946.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:197522229 G>A maps to NM_001195215.1 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:197621421 G>A maps to NM_001195215.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr1:197515102 G>A maps to NM_001195215.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr19:6480062 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:140301261 T>G maps to NM_015689.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:140268611 C>T maps to NM_015689.3 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr1:115168326 A>G maps to ENST00000393274 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr1:111742286 T>C maps to NM_024901.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:142161046 C>T maps to NM_014957.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr8:142161848 C>T maps to NM_014957.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:66044752 C>T maps to ENST00000443035 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:65994123 G>C maps to ENST00000443035 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr15:66022016 C>T did not map to a codon.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr15:65960401 G>C maps to ENST00000443035 S1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr1:153916697 T>C maps to NM_014856.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr1:153912953 C>T maps to NM_014856.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr1:153916787 G>A maps to NM_014856.2 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:19299255 A>C maps to NM_017925.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:19346105 G>A maps to NM_017925.4 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr11:9225257 G>A maps to NM_015213.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr11:9167306 G>A maps to NM_015213.2 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr11:9200590 A>G maps to NM_015213.2 N495N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:9165778 G>A maps to NM_015213.2 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:9165017 G>A maps to NM_015213.2 Q1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:31605370 C>A maps to NM_144973.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:31632841 G>A maps to NM_144973.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:31545555 C>A maps to NM_144973.3 E1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr12:31632973 A>G maps to NM_144973.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr12:31579328 T>C maps to NM_144973.3 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr12:100660824 C>T maps to ENST00000422147 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:100657284 C>A maps to ENST00000422147 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:100660752 C>G maps to ENST00000422147 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:32188762 C>T maps to NM_001136029.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr22:32239672 C>G maps to NM_001136029.1 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr22:32275715 G>C maps to NM_001136029.1 R1328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr22:32180824 G>T maps to NM_001136029.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:121019104 G>A maps to NM_022783.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr11:33054212 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr11:33047293 C>T maps to NM_001077242.1 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:16189253 G>A maps to NM_015954.2 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr12:16115829 G>T maps to NM_015954.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr8:124042881 T>C maps to NM_024295.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr2:220283540 C>T maps to NM_001927.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr15:89074360 G>T maps to NM_017996.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr15:89074905 G>A maps to NM_017996.3 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:11035628 C>T maps to NM_014015.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr16:11035706 G>A maps to NM_014015.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr1:10527262 G>C maps to NM_004401.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:24745878 A>C maps to NM_001127453.1 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr7:24738783 A>T maps to NM_001127453.1 L451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:24756891 C>G maps to NM_001127453.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:117228549 G>C maps to NM_015404.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:179320771 C>G maps to NM_001042702.3 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr2:179319226 C>G maps to NM_001042702.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr8:145541990 G>A maps to NM_012079.4 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr8:145542157 C>T maps to NM_012079.4 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr11:75508200 A>T did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:69397491 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:69424871 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:69424166 C>G did not map to a codon.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr23:69424915 A>G did not map to a codon.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr23:69424318 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:69421893 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:19130242 T>G maps to NM_022719.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IK-01A-11D-A17G-09 chr22:19127487 G>C maps to NM_022719.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr22:19121846 C>T maps to NM_022719.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr22:19121834 C>A maps to NM_022719.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:56335968 T>C maps to NM_201554.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24R-01A-11D-A167-09 chr7:14737755 T>C maps to NM_004080.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr7:14216524 C>T did not map to a codon.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr7:14797339 T>C maps to NM_004080.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:14758164 A>G did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr2:234357966 G>A maps to NM_152879.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:234359583 T>A maps to NM_152879.2 C685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr2:234359580 G>A maps to NM_152879.2 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:234350625 C>A maps to NM_152879.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr17:54940025 C>A maps to NM_003647.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr17:54912560 C>A maps to NM_003647.2 C135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KD-01A-12D-A20S-09 chr3:185879389 A>G did not map to a codon.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr3:185882703 G>T maps to NM_001346.2 C733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr3:186015249 A>G maps to NM_001346.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr3:185985539 C>T maps to NM_001346.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr13:42752317 C>T maps to NM_178009.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr7:137148263 C>T maps to NM_004717.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr7:137263038 G>A maps to NM_004717.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr7:137293717 G>C maps to NM_004717.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr23:50111994 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:50122991 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:50135374 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:50146135 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr23:50129372 A>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:50119145 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:50136226 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr23:50213255 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr23:50146531 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:50135429 T>C did not map to a codon.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr23:50135383 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr4:955822 C>G maps to NM_001347.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:46397490 C>T maps to NM_001105540.1 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr11:46398098 G>A maps to NM_001105540.1 R917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr2:74154070 C>T maps to NM_080916.1 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr1:55319844 G>C maps to NM_014762.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr11:71155929 G>C maps to NM_001360.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr11:71146438 C>A maps to NM_001360.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:26784299 G>C maps to NM_024887.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:26764699 G>A maps to NM_024887.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:26795576 C>G maps to NM_024887.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr1:26784374 G>A maps to NM_024887.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:26764735 G>A maps to NM_024887.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr19:49439287 G>C did not map to a codon.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr19:49438312 C>T maps to NM_014475.3 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr10:99359501 G>A maps to NM_138413.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:93780120 C>A maps to NM_001195643.1 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr19:12792433 G>A maps to NM_001930.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P0-01A-11D-A142-09 chr19:12788174 G>A maps to NM_001930.2 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr14:24760121 C>G maps to NM_001136050.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr17:34956182 G>A maps to NM_024308.3 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr13:52345422 G>A maps to NM_001031719.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr17:27225509 C>T maps to NM_144683.3 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr14:24112420 G>T maps to NM_182908.4 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr14:24114450 A>G maps to NM_182908.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:24423023 C>G maps to NM_021004.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr14:24424345 G>A maps to NM_021004.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr14:24470240 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr14:60616217 G>A maps to NM_016029.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr14:60616169 G>A maps to NM_016029.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:2184965 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:2343247 A>G did not map to a codon.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr10:12111088 C>G maps to NM_018706.5 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr10:12126635 A>G maps to NM_018706.5 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr10:12126593 C>G maps to NM_018706.5 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:24578091 G>C maps to NM_001358.2 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr4:24529617 G>A maps to NM_001358.2 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr4:24557983 G>A maps to NM_001358.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr6:30623035 A>G maps to NM_003587.4 D913D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:54570700 T>C maps to NM_019030.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:47859510 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:47859551 A>C maps to NM_138615.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr3:47890692 C>T maps to NM_138615.2 Q981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr3:47889001 G>T maps to NM_138615.2 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr3:47882664 C>G maps to NM_138615.2 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr10:127527668 A>G maps to NM_018180.2 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr17:5356906 T>C maps to ENST00000457531 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:5354240 C>T maps to ENST00000457531 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:47856604 C>T maps to NM_014681.5 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr19:47884111 C>T maps to NM_014681.5 Q1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr20:37662881 G>A maps to NM_021931.3 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:72132859 C>T maps to NM_014003.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:39033742 G>A maps to NM_198963.1 N1258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr2:39050358 G>T maps to NM_198963.1 R1023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:39083578 G>A maps to NM_198963.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:40262749 G>A maps to NM_024119.2 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:41585182 C>T maps to NM_004941.1 Q706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:41598849 A>C maps to NM_004941.1 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr1:182853846 C>T maps to NM_001357.4 I1120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:140960327 T>G maps to ENST00000398557 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr5:140958162 G>A maps to ENST00000398557 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr23:96200576 A>G did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:96369846 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:95990780 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:96603144 G>C did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:96213048 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr23:95993636 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:96854257 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr23:96185792 T>A did not map to a codon.
Sequencing variant TCGA-EW-A1P6-01A-11D-A142-09 chr23:96684717 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr13:60407363 C>T maps to NM_001042517.1 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr14:95572023 C>T maps to NM_177438.2 Q1028Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:95597887 A>G maps to NM_177438.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0D9-01A-31W-A071-09 chr20:61542481 C>T maps to NM_033081.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr20:61513155 T>C maps to NM_033081.2 P1384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:61524223 C>T maps to NM_033081.2 Q1064Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:61537437 G>T maps to NM_033081.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:61542561 G>A maps to NM_033081.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr20:61512735 T>G maps to NM_033081.2 P1524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr20:61523337 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr20:61542835 C>T maps to NM_033081.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr5:61699153 C>G maps to NM_014473.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr1:54370426 C>T maps to NM_000792.5 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr1:54371906 G>A maps to NM_000792.5 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr14:80677772 G>A maps to NM_001007023.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:80677713 G>A maps to NM_001007023.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr21:47983836 C>T maps to ENST00000318711 L1387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr21:47974149 G>A maps to ENST00000318711 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr21:47966832 C>T maps to ENST00000318711 N801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr21:47910570 C>G maps to ENST00000318711 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:51097987 G>T maps to NM_173602.2 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr12:51076994 G>A maps to NM_173602.2 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr10:323354 G>A maps to NM_014974.2 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:402401 G>A maps to NM_014974.2 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:394616 G>A maps to NM_014974.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LJ-01A-12D-A19Y-09 chr10:373068 C>T maps to NM_014974.2 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr10:395376 C>T maps to NM_014974.2 S1001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr10:486823 G>T maps to NM_014974.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:2717405 G>A maps to NM_145173.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr9:93375797 G>A maps to NM_017594.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr1:68512641 G>A maps to NM_004675.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10A-01A-21D-A10Y-09 chr13:73349501 C>T maps to NM_014953.3 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr15:66618591 G>A maps to NM_001143688.1 W697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:66615122 C>T maps to NM_001143688.1 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr1:231885723 G>T maps to NM_001164537.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:231830349 G>A maps to NM_001164537.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:231829665 C>T maps to NM_001164537.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:223178468 G>T maps to NM_032890.2 E1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:223177300 G>A maps to NM_032890.2 E854E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:223177729 C>T maps to NM_032890.2 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:223177876 C>T maps to NM_032890.2 V1046V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr1:223178035 C>G maps to NM_032890.2 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:223177180 C>T maps to NM_032890.2 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr1:223176629 C>T maps to NM_032890.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr15:40659880 C>G maps to NM_033510.1 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DD-01A-31D-A12Q-09 chr15:40660862 C>T maps to NM_033510.1 C850C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr23:154002896 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:153995617 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:153993195 T>G did not map to a codon.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr23:154005111 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr11:65545692 T>G maps to NM_138368.3 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr10:54074292 G>A maps to NM_012242.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr11:12020296 G>C maps to ENST00000450094 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr8:42232279 C>T maps to NM_014420.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr19:49878065 G>A maps to NM_014419.3 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08X-01A-21W-A019-09 chr8:12957976 G>A maps to NM_182643.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr8:12957133 G>A maps to NM_182643.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:38138086 C>T maps to NM_007335.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr3:196846392 G>A maps to NM_004087.2 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:196863523 A>C maps to NM_004087.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:197023228 G>A maps to NM_004087.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr11:83984228 G>A maps to NM_001142700.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr11:83195171 G>A maps to NM_001142699.1 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A425-01A-11D-A243-09 chr23:69712378 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr23:69671831 C>T did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:69717041 C>A did not map to a codon.
Sequencing variant TCGA-EW-A1IX-01A-12D-A142-09 chr23:69722030 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:7096883 G>A maps to NM_001365.3 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:79581385 G>C maps to NM_004747.3 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:79554686 C>T maps to NM_004747.3 P1822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr10:79567579 G>A maps to NM_004747.3 G1590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr18:3879837 C>T maps to NM_004746.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr18:3879222 C>T maps to NM_004746.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr8:1497330 A>T maps to ENST00000357934 K180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:1497431 C>T maps to ENST00000357934 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr8:1645362 G>A maps to ENST00000357934 W891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr1:35350652 G>T maps to NM_001080418.1 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:55655898 C>A did not map to a codon.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr14:55647929 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:101198415 C>T maps to NM_003836.5 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:39989619 C>T maps to NM_016941.3 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:39994718 C>T maps to NM_016941.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr17:48070937 C>T maps to NM_005220.2 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:96650194 A>G maps to NM_005221.5 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr7:96653898 G>A maps to NM_005221.5 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr7:96651582 A>G maps to NM_005221.5 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr7:96639202 G>A maps to NM_005222.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KC-01A-11D-A20S-09 chr10:124339283 C>T maps to ENST00000368915 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr10:124351806 C>A maps to ENST00000368915 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr1:46977812 C>T maps to NM_147192.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr1:46976926 G>T maps to NM_147192.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P5-01A-11D-A142-09 chr1:46977790 G>A maps to NM_147192.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr23:31792150 C>T did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:32717248 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr23:32482758 C>T did not map to a codon.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr23:31950255 T>A did not map to a codon.
Sequencing variant TCGA-A7-A5ZX-01A-12D-A29N-09 chr23:32361403 C>G did not map to a codon.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr23:32867883 G>T did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr23:32482763 T>C did not map to a codon.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr23:32382794 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr23:31462682 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr23:32481658 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:32305720 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr23:32407758 T>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:31697676 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:32382736 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:32472825 C>G did not map to a codon.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr23:31279128 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:31224748 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:31525419 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:31747749 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:32305670 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:32328391 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:32459311 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:31525512 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:31697690 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:32456488 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr23:32364091 G>A did not map to a codon.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr23:32459414 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr23:32662396 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr23:32503136 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr23:31950336 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr23:32717337 T>C did not map to a codon.
Sequencing variant TCGA-BH-A1FL-01A-11D-A13L-09 chr23:31200939 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr23:32380913 C>G did not map to a codon.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr23:31187563 T>A did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:32429983 T>C did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:31496246 G>C did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:32380913 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:31241176 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:32662402 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:31341727 G>C did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:32305753 G>T did not map to a codon.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr23:32328198 C>T did not map to a codon.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr23:31152231 G>T did not map to a codon.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr23:32591672 T>G did not map to a codon.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr23:31165492 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1N8-01A-11D-A142-09 chr23:31200884 A>T did not map to a codon.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr23:31792300 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr23:32613969 T>G did not map to a codon.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr23:32366617 G>T did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:32716092 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr23:32364149 G>T did not map to a codon.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr23:32591706 C>T did not map to a codon.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr23:31198555 G>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:32360360 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:78340259 T>C maps to NM_013391.2 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr5:78328516 G>A maps to NM_013391.2 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr5:78350098 G>A maps to NM_013391.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:35991277 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:88583797 G>T maps to NM_004407.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr9:847103 C>T maps to NM_021951.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:1056879 A>C maps to NM_181872.4 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr9:990338 G>A maps to NM_021240.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr9:22451645 T>A maps to NM_022160.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:53930485 G>A maps to NM_033067.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr1:53927224 G>A maps to NM_033067.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:118485160 A>C maps to NM_005509.4 P1213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:118487624 T>G maps to NM_005509.4 G1532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr5:118513860 G>T maps to NM_005509.4 E2353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr5:118482537 C>G maps to NM_005509.4 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:118464936 G>A maps to NM_005509.4 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:118479552 C>G maps to NM_005509.4 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr5:118500330 G>A maps to NM_005509.4 W1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr15:51857357 G>C maps to NM_001174116.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr15:51766784 C>G maps to NM_001174116.1 V2323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:51773347 G>A maps to NM_001174116.1 A1985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:51828901 G>C maps to NM_001174116.1 S592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr15:51773278 T>C maps to NM_001174116.1 K2008K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr10:70190363 G>A maps to NM_001080449.1 H765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr10:70231705 G>A maps to NM_001080449.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr10:70182494 G>A maps to NM_001080449.1 D873D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr10:70179589 G>C maps to NM_001080449.1 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:52383094 C>G maps to ENST00000273600 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:52406971 G>A maps to ENST00000273600 L2296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr3:52404635 G>A maps to ENST00000273600 K2134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:52387624 T>C maps to ENST00000273600 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr3:52365311 G>T maps to ENST00000273600 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr3:52396483 C>T maps to ENST00000273600 Y1687Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:52430734 G>A maps to ENST00000273600 E3908E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:52400783 G>A maps to ENST00000273600 L1882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr3:52360795 C>T maps to ENST00000273600 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr3:52423502 C>T maps to ENST00000273600 D3238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:124337865 T>G maps to NM_207437.3 G2017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:124415058 C>T maps to NM_207437.3 F4123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:124265776 C>A maps to NM_207437.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:124319951 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:124352082 G>T maps to NM_207437.3 G2295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:124362405 C>T maps to NM_207437.3 R2657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:124416306 C>T maps to NM_207437.3 S4229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr12:124362320 G>A maps to NM_207437.3 L2628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr12:124387591 C>T maps to NM_207437.3 V3131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:124335529 G>A maps to NM_207437.3 V1948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr12:124349243 C>A maps to NM_207437.3 I2219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:124398953 C>T maps to NM_207437.3 L3359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr12:124414287 C>G maps to NM_207437.3 L4080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr7:21744131 T>C maps to NM_003777.3 G2125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr7:21730484 C>T maps to NM_003777.3 L2016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:21640532 G>A maps to NM_003777.3 E1080E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:21657331 C>A maps to NM_003777.3 I1402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:21641029 G>T maps to NM_003777.3 E1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:21678628 C>T maps to NM_003777.3 F1635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:21813516 C>A maps to NM_003777.3 S3086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:21882183 G>T maps to NM_003777.3 E3579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr7:21784507 G>T maps to NM_003777.3 L2786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12H-01A-11D-A10Y-09 chr7:21639511 C>T maps to NM_003777.3 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:21840867 C>T maps to NM_003777.3 N3387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:21818682 G>A maps to NM_003777.3 V3155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr7:21640548 G>A did not map to a codon.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr3:57419476 A>G maps to NM_178504.4 N1555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:57443480 C>G maps to NM_178504.4 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:57391426 C>A maps to NM_178504.4 E2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr3:57443860 G>A maps to NM_178504.4 N983N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr17:76455993 C>T maps to ENST00000389840 G3161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr17:76492021 G>A maps to ENST00000389840 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12O-01A-11D-A10Y-09 chr17:76487631 G>A maps to ENST00000389840 R2174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr17:76567115 C>G did not map to a codon.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr17:76471536 G>A maps to ENST00000389840 D2764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr17:76567382 G>A maps to ENST00000389840 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:7671380 T>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:7696444 A>C maps to NM_020877.2 P2497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr17:7690335 C>T maps to NM_020877.2 I2196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:7720734 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:7727152 T>G maps to NM_020877.2 G3777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:7660480 G>T maps to NM_020877.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:7720726 C>T maps to NM_020877.2 I3338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:7671379 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:7681675 C>T maps to NM_020877.2 T1810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:7691441 C>T maps to NM_020877.2 L2260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr16:21117907 T>C maps to NM_017539.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr16:21011633 C>T maps to NM_017539.1 Q2111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr16:21078623 C>T maps to NM_017539.1 K1166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:20996485 G>A maps to NM_017539.1 I2526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr16:21078620 C>T maps to NM_017539.1 K1167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:21086872 G>A maps to NM_017539.1 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr16:20976175 G>A maps to NM_017539.1 G3010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr16:21115811 T>C maps to NM_017539.1 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P7-01A-21D-A142-09 chr16:21170741 G>C maps to NM_017539.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr5:13708336 G>A maps to NM_001369.2 L4411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr5:13841154 G>A maps to NM_001369.2 Q1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr5:13901543 G>A maps to NM_001369.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr5:13719036 G>A maps to NM_001369.2 N4151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:13701434 C>T maps to NM_001369.2 T4483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:13842010 G>A maps to NM_001369.2 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:13944505 G>T maps to NM_001369.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr5:13866370 G>A maps to NM_001369.2 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AJ-01A-21D-A12Q-09 chr5:13735414 C>T maps to NM_001369.2 P3862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24T-01A-11D-A167-09 chr5:13770960 G>A maps to NM_001369.2 R3168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr5:13871097 G>A maps to NM_001369.2 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:13714558 A>G maps to NM_001369.2 A4360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:13735430 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:13708287 G>A maps to NM_001369.2 L4428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr5:13735384 G>A maps to NM_001369.2 I3872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr5:13759059 G>A maps to NM_001369.2 L3438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr2:84881839 T>C maps to NM_001370.1 F1897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:84777117 A>C maps to NM_001370.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:84864426 G>T maps to NM_001370.1 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:84846925 T>G maps to NM_001370.1 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr2:84949762 C>A maps to NM_001370.1 A3269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr2:84846871 C>T maps to NM_001370.1 A1212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr2:196737066 G>T maps to NM_018897.2 L2180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:196720639 A>C maps to NM_018897.2 G2830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:196673491 G>A maps to NM_018897.2 R3333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:196834763 C>A maps to NM_018897.2 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr2:196749475 G>A maps to NM_018897.2 R1866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:196642547 G>A maps to NM_018897.2 I3680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:196834701 C>T maps to NM_018897.2 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr2:196762432 T>C maps to NM_018897.2 V1535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:196636481 G>A maps to NM_018897.2 Q3779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr2:196723281 G>A maps to NM_018897.2 I2661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr2:196729474 C>A maps to NM_018897.2 E2302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr6:38813486 G>A maps to ENST00000327475 S1649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr6:38840838 C>T maps to ENST00000327475 I2453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:38840463 A>C maps to ENST00000327475 A2369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:38913261 G>C maps to ENST00000327475 L3997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:38980273 C>G maps to ENST00000327475 L4513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:38825466 C>T maps to ENST00000327475 F1957F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:38867566 C>T maps to ENST00000327475 R3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:38905787 C>T maps to ENST00000327475 R3856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr6:38854683 G>T maps to ENST00000327475 G2781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H6-01A-21W-A071-09 chr6:38851105 G>A maps to ENST00000327475 L2658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr6:38816465 T>A maps to ENST00000327475 Y1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr6:38759339 T>C maps to ENST00000327475 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:11584122 G>A maps to NM_001372.3 V1220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:11790215 C>A maps to NM_001372.3 A3682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr17:11520809 G>A maps to NM_001372.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:11511579 T>G maps to NM_001372.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:11778414 C>G maps to NM_001372.3 L3464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr17:11783515 C>T maps to NM_001372.3 R3534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr17:11522984 G>T maps to NM_001372.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr17:11572850 C>T maps to NM_001372.3 Y1031Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr17:11597315 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr17:11726131 G>A maps to NM_001372.3 Q3009Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:11584200 G>A maps to NM_001372.3 P1246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr17:11772530 C>T maps to NM_001372.3 A3338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr9:34500813 C>A maps to NM_012144.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr9:34493196 G>A maps to NM_012144.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr9:34514446 C>G maps to NM_012144.2 S542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr9:34500838 T>G did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr9:34514509 G>A maps to NM_012144.2 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24R-01A-11D-A167-09 chr17:72310297 G>A maps to NM_023036.4 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr17:72308230 G>A maps to NM_023036.4 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:4498774 T>G maps to NM_005147.4 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr16:4484515 C>T maps to NM_005147.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr15:78566656 C>T maps to NM_018602.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr15:78565506 C>T maps to NM_018602.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:78568071 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:74104793 A>C maps to NM_017626.4 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:100824994 G>A maps to NM_001031723.2 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr2:220144581 C>T maps to NM_006736.5 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:78478873 T>G maps to NM_007034.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr1:78481909 G>A maps to NM_007034.3 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:34990774 C>T maps to NM_001135005.1 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr9:34990766 T>G maps to NM_001135005.1 L47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:41257856 C>A maps to NM_145174.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr3:128181428 C>T maps to NM_153330.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:22193535 A>G maps to NM_022365.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr2:183597232 G>A maps to NM_018981.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:183624000 G>A maps to NM_018981.1 Q704Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:6697504 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:6697332 C>T maps to NM_018198.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:6697263 G>T maps to NM_018198.3 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:6738480 C>T maps to NM_018198.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:132193830 G>T maps to NM_015268.3 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:132196902 C>T maps to NM_015268.3 A876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr3:132245097 G>A maps to NM_015268.3 Q2118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr3:132247139 C>G maps to NM_015268.3 L2163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr3:132153450 A>G maps to NM_015268.3 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr3:132224253 A>T maps to NM_015268.3 K1665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:56221319 G>A maps to NM_032364.5 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:56221446 G>A maps to NM_032364.5 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr12:56221461 C>T maps to NM_032364.5 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr1:15890820 C>G maps to NM_015291.2 S522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr1:15892575 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr15:41060224 G>A maps to NM_018163.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr3:180702453 A>G maps to NM_145261.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:31392333 C>A maps to NM_181706.4 Y13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:25174348 G>A maps to NM_016544.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr2:25174423 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr2:25180734 C>A maps to NM_016544.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr13:96329520 C>T maps to NM_006260.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:27500864 G>A maps to NM_173650.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr1:65855272 C>A maps to ENST00000371069 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:38023343 C>T maps to NM_003462.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr23:153631300 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr16:2287302 G>A did not map to a codon.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr16:2288403 C>G maps to NM_001374.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:58183603 C>T maps to NM_004944.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:12989583 T>G maps to NM_001375.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:230271999 G>T maps to NM_139072.3 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XR-01A-11D-A14K-09 chr2:230312185 G>T maps to NM_139072.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:6588480 G>T maps to NM_144666.2 L3914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:6585251 C>T maps to NM_144666.2 C3394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:6587872 G>T maps to NM_144666.2 E3755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr11:6519528 C>G maps to NM_144666.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr11:6592505 C>T maps to NM_144666.2 H4588H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:6579371 G>A maps to NM_144666.2 V2949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr11:6541508 G>A maps to NM_144666.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:6578696 T>C maps to NM_144666.2 N2724N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr11:6587992 G>T maps to NM_144666.2 E3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:32895574 C>T maps to ENST00000381000 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:10922974 C>T maps to NM_001005361.2 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:10870470 C>T maps to NM_001005361.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr19:10935730 A>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:10887806 C>T maps to NM_001005361.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:172356383 C>T maps to ENST00000359070 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr1:172356292 C>T maps to ENST00000359070 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr10:101637037 G>T maps to ENST00000342239 S1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr10:101715244 G>C maps to ENST00000342239 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr10:101646290 G>C maps to ENST00000342239 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr19:10291056 G>A maps to NM_001130823.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr19:10250459 G>T maps to NM_001130823.1 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:10257156 C>A maps to NM_001130823.1 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr19:10260161 G>A maps to NM_001130823.1 I851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:25469588 A>G maps to NM_175629.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:25523046 C>T maps to NM_175629.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:25467059 G>A maps to NM_175629.1 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr20:31376691 G>A maps to NM_006892.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AT-01A-11D-A12Q-09 chr10:98092127 C>T maps to NM_004088.3 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr10:98087354 G>C maps to NM_004088.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:44424003 G>A maps to NM_052951.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:94335492 G>T maps to NM_014597.4 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr16:30020843 G>A maps to NM_003586.2 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr16:30018122 C>T maps to NM_003586.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr16:30018134 G>T maps to NM_003586.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:128859961 C>T maps to ENST00000398025 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr10:128908589 C>T maps to ENST00000398025 I844I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:129242508 A>G maps to ENST00000398025 T1838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U0-01A-11D-A10G-09 chr2:225702538 G>C maps to NM_014689.2 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24O-01A-11D-A167-09 chr2:225661752 G>C maps to NM_014689.2 A1585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:225659733 C>T maps to NM_014689.2 K1672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr2:225652078 C>T maps to NM_014689.2 E1818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr2:225738766 G>T maps to NM_014689.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:117752670 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:117732034 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:117752645 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:117782983 C>T did not map to a codon.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr23:117742259 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr23:117814518 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr23:117788765 G>T did not map to a codon.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr23:117752579 G>C did not map to a codon.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr23:117758500 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr23:117679332 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr23:117782983 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr23:117749568 G>C did not map to a codon.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr23:117722097 A>T did not map to a codon.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr23:117699983 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr23:117815152 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr23:117739286 C>T did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr23:117679990 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr23:117785949 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:117819731 G>A did not map to a codon.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr23:117743297 G>C did not map to a codon.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr23:117722170 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:117809964 A>C did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:117770338 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr23:117777489 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr5:169135222 C>T maps to NM_004946.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr5:169145738 G>A maps to NM_004946.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr5:169494674 C>T maps to NM_004946.2 F1543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr3:51417595 G>T maps to NM_004947.4 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr3:51378785 G>T maps to NM_004947.4 R1295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr3:51101916 G>T maps to NM_004947.4 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:111580175 C>T maps to ENST00000428084 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr7:111575670 C>T maps to ENST00000428084 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:111423965 G>A maps to ENST00000428084 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:111451975 G>C maps to ENST00000428084 S987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr8:25193754 G>A maps to NM_024940.6 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:25174583 G>A maps to NM_024940.6 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr8:25237859 G>T maps to NM_024940.6 E1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:25156536 C>T maps to NM_024940.6 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr19:11313274 G>A maps to ENST00000319867 I1784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:11323970 G>A maps to ENST00000319867 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:11361687 C>G maps to ENST00000319867 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:63003603 T>G maps to ENST00000371140 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:63027332 A>C maps to ENST00000371140 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:62962168 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:63113856 C>A maps to ENST00000371140 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:62960020 T>C maps to ENST00000371140 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr1:63005435 G>T maps to ENST00000371140 S1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr1:62970399 G>C maps to ENST00000371140 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:62959996 C>T maps to ENST00000371140 L1722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr9:377062 C>T maps to NM_203447.3 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:377197 C>T maps to NM_203447.3 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr9:390475 C>T maps to NM_203447.3 F960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:99462536 C>G maps to ENST00000428223 L1713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr13:99534234 C>T maps to ENST00000428223 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr2:74783919 C>T maps to NM_001381.3 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:74781923 C>T maps to NM_001381.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr20:53205224 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:53205256 C>G maps to NM_018431.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:53226983 C>A maps to NM_018431.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:3478249 C>G maps to ENST00000389653 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr6:31938576 G>A maps to NM_005510.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:31938176 G>A maps to NM_005510.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:34954522 C>A maps to NM_017613.2 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr6:83877654 C>G maps to NM_015018.2 T2389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr6:83872605 C>T maps to NM_015018.2 R2354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr6:83845440 C>T maps to NM_015018.2 R992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr6:83847714 C>T maps to NM_015018.2 L1318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr6:83869519 C>A maps to NM_015018.2 S2268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr6:83841992 T>G maps to NM_015018.2 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr21:37612130 G>A maps to NM_005128.2 W982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr21:37617883 C>T maps to NM_005128.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr21:37665769 A>T maps to NM_005128.2 G2266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr19:2211748 G>T did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:2223287 C>T maps to ENST00000221482 N1133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:2216366 C>T maps to ENST00000221482 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr19:2191090 C>A maps to ENST00000221482 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr19:2220126 G>T maps to ENST00000221482 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr6:30919363 T>C maps to NM_080870.3 P1041P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr16:68011675 C>T maps to NM_022357.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr16:68010013 G>C maps to NM_022357.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr16:68014004 G>A maps to NM_022357.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr11:65116379 G>A maps to NM_006268.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr11:65113787 C>T maps to NM_006268.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr11:65107854 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:44436767 T>C maps to NM_001384.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:44437173 G>A maps to NM_001384.4 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr1:44435937 G>T maps to NM_001384.4 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr1:44437410 A>G maps to NM_001384.4 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr2:116101488 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr2:116497432 G>A maps to NM_020868.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr2:116101438 C>T maps to NM_020868.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:116101462 C>T maps to NM_020868.3 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:116599869 T>A maps to NM_020868.3 C780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:116503732 C>T maps to NM_020868.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:116447288 A>G maps to NM_020868.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr7:154564563 G>T maps to NM_130797.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr7:154561217 C>T maps to NM_130797.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr15:65799694 T>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:65804678 C>T maps to NM_197960.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:65777496 A>G maps to NM_197960.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:4689734 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr3:109031470 G>A maps to NM_138815.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr3:109027095 C>G maps to NM_138815.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr12:7867842 T>C maps to NM_199286.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:109052729 G>A maps to NM_018189.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr3:109056309 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:64015111 G>C maps to NM_173812.4 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr12:64055198 C>T maps to NM_173812.4 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr19:32923704 C>T maps to NM_001172774.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr8:95782691 G>A maps to NM_181787.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:95789984 C>T maps to NM_181787.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr8:95796031 T>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:98015202 A>C maps to NM_000110.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:97770897 G>C maps to NM_000110.3 S739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:97544612 G>A maps to NM_000110.3 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:98058911 C>T maps to NM_000110.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:105441825 T>G maps to NM_001385.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:146780344 C>T maps to NM_001197294.1 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr5:146777318 G>T maps to NM_001197294.1 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr10:134006320 G>A maps to NM_006426.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr2:27165482 G>A maps to NM_020134.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr2:27167564 G>A maps to NM_020134.3 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr2:27169787 C>T maps to NM_020134.3 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:74749892 C>A maps to NM_133637.2 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:102302141 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr12:102315028 T>C maps to NM_018370.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:65688407 A>C maps to ENST00000376991 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr11:113286298 G>A maps to ENST00000355319 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr11:113281553 G>A maps to ENST00000355319 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:640488 C>G maps to NM_000797.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A091-01A-11W-A019-09 chr4:9784609 C>A maps to NM_000798.4 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:18002986 G>A maps to NM_001388.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:50599323 G>A maps to NM_001080520.1 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr23:100497358 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:100486735 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr23:100493981 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:28672104 C>A maps to ENST00000438199 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr18:28574328 G>A maps to NM_001941.3 R835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:41561082 A>C maps to NM_001389.3 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr21:41710061 G>C maps to NM_001389.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr21:41496178 G>A maps to NM_001389.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr21:42064817 G>C maps to NM_001389.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr21:41710184 G>A maps to NM_001389.3 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr21:41719609 C>T maps to NM_001389.3 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr21:41459119 A>C maps to NM_001389.3 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr21:41465723 G>A maps to NM_001389.3 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr11:117342752 T>C did not map to a codon.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr11:117375738 C>T maps to NM_020693.2 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr11:117306504 T>C maps to NM_020693.2 P1637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr11:117351188 C>T maps to NM_020693.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:117299064 G>A maps to NM_020693.2 S2107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr11:117651334 G>A maps to NM_020693.2 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:116752195 G>A maps to NM_013352.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr6:116756905 T>C maps to NM_013352.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr6:116757739 C>A maps to NM_013352.2 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MS-A51U-01A-31D-A25Q-09 chr6:116756764 G>A maps to NM_013352.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr18:65179784 G>A maps to NM_032160.2 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:65178586 C>A maps to NM_032160.2 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr18:65181125 T>C maps to NM_032160.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr18:65178249 C>T maps to NM_032160.2 W1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:28906913 C>T maps to NM_001942.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr18:29098200 G>T did not map to a codon.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr18:29054364 C>T maps to NM_001944.2 Q795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr18:29041207 G>T maps to NM_001944.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:28968332 C>T maps to NM_001134453.1 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr20:35395196 G>A maps to NM_001145315.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr20:35381195 G>A maps to NM_001145315.1 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr6:7567657 G>A maps to NM_004415.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr6:7583867 C>T maps to NM_004415.2 L2125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr6:7567628 C>T maps to NM_004415.2 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr6:7578089 C>T maps to NM_004415.2 Q986*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A1-A0SP-01A-11D-A099-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-A2-A0YD-01A-11D-A10G-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-A7-A56D-01A-11D-A27P-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AC-A2BK-01A-11D-A21Q-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:88535002 G>T maps to NM_014208.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:88533961 T>C maps to NM_014208.3 G208G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AR-A0U0-01A-11D-A10G-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D8-A143-01A-11D-A10Y-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D8-A1X9-01A-12D-A159-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D8-A27M-01A-11D-A16D-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-E2-A156-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-E2-A15I-01A-21D-A135-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-E9-A22E-01A-11D-A159-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr6:56480617 C>T maps to ENST00000281662 K3113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr6:56323955 G>A maps to ENST00000361203 I7493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr6:56394932 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:56328482 T>G maps to ENST00000361203 R7375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:56458619 A>C maps to ENST00000361203 G3978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:56485102 C>T maps to ENST00000281662 E1807E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:56494133 T>C maps to ENST00000361203 E1252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:56504571 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr6:56399924 G>A maps to ENST00000361203 Q5435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr6:56484031 T>A maps to ENST00000281662 I2164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:56354314 T>C maps to ENST00000361203 K6739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr6:56485201 A>C maps to ENST00000281662 A1774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr6:56324026 C>A maps to ENST00000361203 G7470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:205156710 G>A maps to NM_015375.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:205132056 G>A maps to NM_015375.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr5:118264306 G>A maps to NM_173666.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr12:113534595 C>A maps to NM_004416.2 S572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:113530987 G>A maps to NM_004416.2 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:113515418 C>T maps to NM_004416.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:122288190 C>T maps to NM_138287.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:122287952 C>T maps to NM_138287.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:122284778 A>G maps to NM_138287.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:122288504 T>G maps to NM_138287.3 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr11:58949803 G>T maps to NM_015177.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr11:58949647 G>A maps to NM_015177.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:242619703 G>A maps to NM_012145.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:45444529 C>T maps to NM_175940.1 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:45457063 C>A maps to NM_175940.1 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:45396386 G>A maps to NM_014080.4 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr15:45396251 C>T did not map to a codon.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr15:45388166 G>A maps to NM_014080.4 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr15:45392972 C>G maps to NM_014080.4 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr15:45389583 G>A maps to NM_014080.4 I1233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr15:45398768 G>C maps to NM_014080.4 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:45409844 C>T maps to NM_144565.2 S440S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BH-A0HF-01A-11W-A071-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E9-A1NE-01A-21D-A14K-09 chr15:45406841 G>A maps to NM_207581.3 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:76803732 G>A maps to NM_001003892.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr10:76818228 G>T maps to NM_001003892.1 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:80019597 C>A did not map to a codon.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr7:107215656 G>T maps to NM_181581.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12F-01A-11D-A10Y-09 chr5:172195857 G>A maps to NM_004417.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr1:221913040 T>G maps to NM_007207.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:74000984 C>T maps to NM_003584.2 E172E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AC-A3W5-01A-11D-A228-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr10:76857642 C>T maps to ENST00000356369 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr10:76868888 C>T maps to NM_001007272.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr12:12630477 G>C maps to NM_030640.2 Y429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr12:12630055 G>C maps to NM_030640.2 S570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr12:12630251 G>A maps to NM_030640.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr12:12672817 G>A maps to NM_030640.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr12:12630317 G>A maps to NM_030640.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr22:31059954 G>A maps to NM_152511.3 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr2:96810079 G>A maps to NM_004418.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:44703609 G>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:44703468 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:33451072 G>A maps to NM_024025.1 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr8:33451225 G>T maps to NM_024025.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr1:167097766 C>T maps to NM_001080426.1 D1133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr1:167095567 C>T maps to NM_001080426.1 N400N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr12:89743171 G>A maps to NM_001946.2 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr12:89744752 A>G maps to NM_001946.2 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:1580208 G>A maps to NM_004420.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr23:152915601 T>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:152915643 G>T did not map to a codon.
Sequencing variant TCGA-A2-A04Y-01A-21W-A050-09 chr1:1275141 C>A maps to ENST00000378888 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr17:7129291 G>A maps to NM_004422.2 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:183888224 C>T maps to NM_004423.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr18:46808426 C>T maps to NM_017653.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr14:102467877 G>T maps to NM_001376.4 E1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:102496050 T>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr14:102505054 C>A maps to NM_001376.4 L3692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr14:102516406 G>A did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr14:102474585 G>A maps to NM_001376.4 L1963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:102442137 T>C did not map to a codon.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr14:102508352 A>T maps to NM_001376.4 K4036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:95657608 A>C maps to NM_004411.4 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:95657617 A>C maps to NM_004411.4 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr7:95665025 T>C maps to NM_004411.4 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:32612232 G>A maps to NM_016141.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr11:103106511 G>T maps to NM_001080463.1 E3227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:103229062 C>G maps to NM_001080463.1 L4051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:103019264 C>G maps to NM_001080463.1 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:103004287 C>G maps to NM_001080463.1 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr2:44032337 C>T maps to NM_001193464.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:120935919 G>A maps to NM_003746.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr16:80577174 A>C maps to NM_130897.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr23:37700303 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0BA-01A-11W-A071-09 chr21:38884542 A>G maps to NM_001396.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr12:68051049 G>A maps to NM_006482.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:206821148 A>G maps to NM_003582.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:206821775 A>C maps to NM_003582.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:206820843 C>T maps to NM_003582.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr1:206821262 G>T maps to NM_003582.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr1:206810307 A>G maps to NM_001004023.1 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr12:4705772 G>A maps to NM_003845.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr12:4702195 G>T maps to NM_003845.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr2:71871093 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06N-01A-11W-A019-09 chr2:71828630 G>A maps to NM_001130987.1 P1300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:71909713 C>T maps to NM_001130987.1 F2076F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:71788903 G>T maps to NM_001130987.1 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:71894638 C>T maps to NM_001130987.1 I1817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:71753453 C>T maps to NM_001130987.1 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr2:71913615 C>T maps to NM_001130987.1 F2118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:71883419 G>A maps to NM_001130987.1 K1585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr2:207530592 C>A did not map to a codon.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr15:55742418 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr15:55727257 T>C did not map to a codon.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr13:96234511 A>G maps to NM_198968.2 D860D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr13:96293773 C>A maps to NM_198968.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr3:137807222 G>A maps to NM_173543.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr3:137800588 G>C maps to NM_173543.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:108344739 C>T maps to NM_014648.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr3:108407717 C>T maps to NM_014648.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr20:32267775 C>A maps to NM_005225.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AU-01A-11D-A12Q-09 chr1:23847526 C>T maps to NM_004091.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr1:23857033 C>A maps to NM_004091.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr16:67226204 C>T maps to NM_001950.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:67228645 G>T maps to NM_001950.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:11593805 C>T maps to NM_198256.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L9-01A-11D-A13L-09 chr12:77439989 C>T maps to NM_203394.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:19252337 C>T maps to NM_024680.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:19252193 A>C maps to NM_024680.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:2282220 A>G maps to NM_004424.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:2285080 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0ST-01A-12D-A099-09 chr3:15469354 G>A maps to NM_033083.6 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr14:35002707 C>T maps to NM_018453.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:35005481 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:110563121 G>A maps to ENST00000276658 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr5:158135081 G>C maps to NM_024007.3 S550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DD-01A-31D-A12Q-09 chr5:158523387 G>A maps to NM_024007.3 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:48382366 G>T did not map to a codon.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr23:48385404 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:74897828 C>G did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr10:74923575 C>T maps to NM_001135752.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:21563236 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:21586796 G>A maps to NM_001397.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:183967550 C>G maps to NM_014693.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:184001628 G>A maps to NM_014693.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr3:184003268 C>A maps to NM_014693.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr3:183976325 C>G maps to NM_032331.3 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr2:233345460 T>A maps to NM_004826.2 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr6:127611346 G>T maps to NM_001139510.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:53364851 T>C maps to ENST00000371522 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr10:11789357 T>C maps to NM_024693.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr10:11789449 G>C maps to NM_024693.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr10:135179585 C>T maps to NM_004092.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:150484177 C>T maps to ENST00000369049 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:11624889 A>C maps to NM_016581.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:172537996 G>A maps to ENST00000392692 T905T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr23:69247729 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:69176942 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:69177015 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr23:68836475 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:65824308 T>C did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:65819497 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr23:65819448 C>T did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr23:65819548 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:65824936 G>C did not map to a codon.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr23:65824950 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr2:109546676 G>A maps to ENST00000376651 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr2:109547440 C>T maps to ENST00000376651 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr15:74925171 C>G maps to NM_025083.3 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr15:74925123 G>T maps to NM_025083.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr16:67914875 C>T maps to NM_014329.3 C838C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr16:67913011 C>A maps to NM_014329.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:67913802 C>T maps to NM_014329.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr14:21216104 C>T maps to NM_006683.4 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:5248876 C>T maps to NM_014674.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:83402619 A>C maps to NM_005711.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr6:12294559 G>T maps to NM_001955.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr20:57876516 G>A maps to NM_207034.1 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr20:57899429 C>T maps to NM_207034.1 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:148453721 G>T maps to NM_001957.3 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr13:78492255 G>A maps to ENST00000377211 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr13:78474077 A>G maps to ENST00000377211 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07Z-01A-11W-A019-09 chr12:93195435 C>T maps to NM_003566.3 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:93213143 A>C maps to NM_003566.3 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:93220058 C>T maps to NM_003566.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XR-01A-11D-A10G-09 chr12:93192856 A>T maps to NM_003566.3 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr12:93170705 G>A maps to NM_003566.3 Q1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr12:93244970 A>G maps to NM_003566.3 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr8:144669009 A>T maps to NM_032378.4 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr8:144662367 A>G maps to NM_032378.4 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:3977867 G>C maps to NM_001961.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr19:3980543 C>T maps to NM_001961.3 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr16:22268145 C>T maps to NM_013302.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr16:22291591 G>T maps to NM_013302.3 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:22295257 C>A maps to NM_013302.3 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr3:127983620 C>A maps to NM_021937.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:60451217 G>A maps to NM_001144933.1 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr17:60451214 G>T maps to NM_001144933.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr12:3757679 C>G maps to NM_032680.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr17:28419934 T>G maps to NM_198529.3 L1434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr17:28380486 G>T maps to NM_198529.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NG-01A-21D-A14K-09 chr17:28417633 G>A maps to NM_198529.3 V1293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr22:44079632 G>A maps to NM_022785.3 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr22:44004465 G>A maps to NM_022785.3 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr22:44178058 C>T did not map to a codon.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr22:44127684 C>T maps to NM_022785.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:64011605 C>G maps to NM_032437.2 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:64011714 G>C maps to NM_032437.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:56145145 A>C maps to NM_001039349.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr2:56097973 G>A maps to NM_001039349.1 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr2:56145043 T>G maps to NM_001039349.1 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr2:56149539 C>T maps to NM_001039349.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr13:22070299 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0BO-01A-23D-A12B-09 chr8:16944528 A>G maps to NM_181723.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:44120502 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:44109463 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:44101448 C>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:44094562 C>G did not map to a codon.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr23:44101420 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:155041461 G>A maps to NM_005227.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:106722975 G>A maps to NM_001962.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr23:68060251 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr23:68060259 G>A did not map to a codon.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr8:132966109 A>G maps to NM_015137.3 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr14:23829242 G>A maps to NM_005864.2 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:23830035 G>A maps to NM_005864.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr14:23826503 C>T maps to NM_005864.2 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr17:42929857 G>A maps to NM_004247.3 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:110866275 C>G maps to NM_001963.4 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr4:110882134 A>G maps to NM_001963.4 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:13618112 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr23:13618175 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr23:13645205 T>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:13636125 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:13626501 A>G did not map to a codon.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr6:32135278 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr5:38407075 C>A maps to ENST00000354891 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:38418271 C>A maps to ENST00000354891 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr7:55249077 C>G maps to NM_005228.3 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:55220347 C>T maps to NM_005228.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr7:55223634 C>A maps to NM_005228.3 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr7:55268033 C>A maps to NM_005228.3 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr5:137801479 G>A maps to NM_001964.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:137802701 A>C maps to NM_001964.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr5:137802623 G>C maps to NM_001964.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr5:137803325 C>T maps to NM_001964.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr8:22548603 C>T maps to NM_004430.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr2:73519007 C>T maps to NM_001965.3 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:63217920 A>C maps to NM_015252.3 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr11:65351788 C>G maps to NM_001099409.1 V1057V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr11:65351857 C>G maps to NM_001099409.1 Y1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr11:65351788 C>T maps to NM_001099409.1 V1057V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:64621906 G>A maps to NM_006795.2 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:64621972 G>T maps to NM_006795.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr11:64622047 C>T maps to NM_006795.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr11:64622245 G>A maps to NM_006795.2 N388N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:64627437 G>A maps to NM_006795.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr19:48229478 C>T maps to NM_014601.3 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y2-01A-11D-A159-09 chr19:48239729 G>C maps to NM_014601.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr2:31483604 G>A maps to NM_014600.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42193118 G>C maps to NM_139265.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42202043 G>A maps to NM_139265.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr15:42192878 G>A maps to NM_139265.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr15:42192995 G>A maps to NM_139265.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EX-01A-21W-A050-09 chr9:140710463 G>A maps to NM_024757.4 A1108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr9:140710463 G>A maps to NM_024757.4 A1108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:140648627 G>A maps to NM_024757.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr9:140672360 C>T maps to NM_024757.4 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr9:140729275 C>T maps to NM_024757.4 C1256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr9:140672411 G>A maps to NM_024757.4 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr11:125445239 C>T maps to ENST00000278903 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:20148682 T>G did not map to a codon.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr23:20148713 C>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:20150341 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr7:6077155 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0EA-01A-11D-A10Y-09 chr7:6085746 T>A maps to NM_014413.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr2:88885397 C>A maps to NM_004836.5 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:88857340 G>A maps to NM_004836.5 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:40318191 G>A maps to NM_001013703.2 E1468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr15:40246167 A>T maps to NM_001013703.2 K193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:75473392 A>C maps to NM_014239.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr14:75470299 A>T maps to NM_014239.3 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:45444132 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr1:45323457 G>A maps to NM_020365.3 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr2:27591876 G>A maps to NM_172195.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:183859752 T>G maps to NM_003907.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:183859752 T>G maps to NM_003907.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:183859756 C>T maps to NM_003907.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr3:183856021 C>T maps to NM_003907.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:36372655 C>G maps to NM_012199.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GY-01A-11W-A071-09 chr1:36358235 G>A maps to NM_012199.2 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:36474554 C>T maps to NM_024852.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr1:36509127 C>T maps to NM_024852.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:36307243 C>T maps to NM_017629.2 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr23:24082439 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:24089732 A>T did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:24082436 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:120797949 A>C maps to NM_003750.2 G1176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr7:2409145 C>T maps to ENST00000314800 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:36919317 G>A maps to NM_003753.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr22:36907703 G>A maps to NM_003753.3 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr8:109260901 G>A maps to NM_001568.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr8:109228676 A>G maps to NM_001568.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr11:8013645 G>T maps to ENST00000449102 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr11:8016559 C>T maps to ENST00000449102 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr19:10226168 G>A maps to NM_003755.3 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:38259031 C>T maps to ENST00000262832 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr22:38273868 G>A maps to ENST00000262832 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:7480799 C>T maps to NM_001416.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr3:186503951 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr22:31867873 G>C maps to NM_019843.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr22:31858941 G>A maps to NM_019843.3 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DN-01A-11D-A17W-09 chr22:31851271 G>A maps to NM_019843.3 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:10828815 A>C maps to ENST00000429377 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14T-01A-11D-A10Y-09 chr1:21167443 G>A maps to NM_001198801.1 T1302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:73588724 C>T maps to NM_022170.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L8-01A-11D-A13L-09 chr7:73609622 A>G maps to NM_022170.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr14:103803550 C>G maps to NM_183004.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:100009492 C>T maps to NM_015904.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:100015795 C>G maps to NM_015904.3 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:99998686 C>T maps to NM_015904.3 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr2:99988164 T>A maps to NM_015904.3 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:33868519 T>C maps to NM_002212.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr18:48510607 G>A maps to NM_018696.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr17:12897060 G>A maps to NM_018127.6 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr17:12913974 T>C maps to NM_018127.6 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr17:12897054 G>A maps to NM_018127.6 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr19:8032480 T>G maps to ENST00000351593 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:50666726 C>T maps to NM_021952.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:50572058 A>G maps to NM_001144775.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr13:41517239 G>T maps to NM_172373.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr13:41515218 G>C maps to NM_172373.3 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr13:41515070 G>C maps to NM_172373.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:139980484 C>G maps to ENST00000379550 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr4:139980595 C>A maps to ENST00000379550 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr4:139981716 G>T maps to ENST00000379550 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr1:201984384 C>G maps to NM_004433.4 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:129203482 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:129200907 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:129201240 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:129200982 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr23:129201170 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W5-01A-11D-A10G-09 chr23:129206309 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr23:129203348 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr23:129201240 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr22:37771055 G>A maps to NM_052906.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr22:37770125 G>A maps to NM_052906.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:47497482 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47500669 G>A did not map to a codon.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr23:47498440 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr23:47500695 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:47498366 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr23:47500825 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:47496234 T>C did not map to a codon.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr23:47498687 G>C did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr12:96641457 C>T maps to NM_005230.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:37298951 G>A maps to NM_014800.9 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr7:36934508 G>A maps to NM_014800.9 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:37262230 C>A maps to NM_014800.9 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:45014803 G>A maps to ENST00000439931 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:45002082 G>A maps to ENST00000439931 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:45003904 G>A maps to ENST00000439931 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr20:44999095 G>A maps to ENST00000439931 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr20:45021782 C>A did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr16:67235310 G>A maps to NM_024712.3 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr7:73474243 T>A maps to ENST00000358929 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:103986364 C>T maps to NM_152310.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:80636018 C>T maps to NM_022726.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr6:53133925 C>T maps to ENST00000370918 *327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr6:53140986 G>C maps to ENST00000370918 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr5:60060093 G>A maps to NM_024930.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr18:33722825 C>T maps to ENST00000442325 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:33726232 T>G maps to ENST00000442325 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr8:27989917 C>T maps to NM_018091.5 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:79470884 C>T maps to NM_022159.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr1:79383582 A>G maps to NM_022159.3 Y538Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr1:79357326 C>T maps to NM_022159.3 W631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr1:79403527 T>A maps to NM_022159.3 K242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr4:101396226 G>C maps to NM_016242.3 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:101200767 C>T maps to ENST00000397927 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr7:101091051 G>T maps to ENST00000397927 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U0-01A-11D-A10G-09 chr18:2891303 G>A maps to NM_032048.2 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr20:39993700 C>T maps to NM_052846.1 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:39991350 C>T maps to NM_052846.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr14:100406370 C>T maps to NM_001008707.1 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:46124833 G>A maps to NM_001193268.1 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr19:46130076 C>T maps to NM_001193268.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr11:62371660 C>T maps to ENST00000278845 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62376501 T>C maps to ENST00000278845 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FL-01A-11D-A13L-09 chr11:62378385 G>A maps to ENST00000278845 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:42544565 G>C did not map to a codon.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr2:42472823 A>T maps to NM_019063.3 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:42530294 C>T maps to NM_019063.3 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:89210435 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr14:89212616 G>T maps to ENST00000380664 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr14:89153605 G>T maps to ENST00000380664 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:10626884 G>A maps to NM_001424.4 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:6937655 G>A maps to ENST00000381407 K886K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr19:6919733 C>T maps to ENST00000381407 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr19:14876519 C>T maps to NM_013447.2 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr19:14884858 G>A maps to NM_013447.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr19:14863284 C>T maps to NM_013447.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr19:14749062 G>C maps to NM_032571.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:155255354 C>T maps to NM_001427.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25C-01A-11D-A167-09 chr1:225707101 C>T maps to ENST00000284563 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:225742782 G>A maps to ENST00000284563 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:225707047 C>T maps to ENST00000284563 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:225700685 A>G maps to ENST00000284563 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:71500212 A>C maps to NM_031889.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:71501556 A>C maps to NM_031889.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:71501592 A>C maps to NM_031889.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:71500260 C>A maps to NM_031889.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr4:71508642 T>C maps to NM_031889.2 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr5:73931215 G>A maps to NM_003633.2 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr9:130605383 C>A maps to NM_001114753.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AL-01A-21D-A12Q-09 chr9:130580641 T>C maps to NM_001114753.1 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr9:130580443 G>A maps to NM_001114753.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:130579443 G>A maps to NM_001114753.1 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:77079916 A>G maps to NM_001042573.1 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr17:77081764 G>A maps to NM_001042573.1 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr18:677833 C>T maps to ENST00000319815 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr13:43810835 G>A maps to NM_001127615.1 D550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr13:43810873 C>A maps to NM_001127615.1 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr23:129769018 A>C did not map to a codon.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr23:129804094 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr23:129822966 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:132203609 A>C maps to NM_006208.2 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr6:132201018 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:120602771 G>A maps to NM_006209.3 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr8:120598502 G>C maps to NM_006209.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr6:132041439 T>C maps to NM_005021.3 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:132054738 G>A maps to NM_005021.3 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:46107847 A>C maps to NM_014936.4 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr6:46135384 C>A maps to NM_021572.4 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr4:185038158 G>A maps to NM_153343.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:40139767 C>T maps to NM_152512.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr22:40161425 C>A maps to NM_152512.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr22:40283458 A>G maps to NM_152512.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr10:97602251 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:74438594 A>C maps to NM_001249.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WT-01A-11D-A10G-09 chr14:74436745 A>G maps to NM_001249.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr20:25196321 G>A maps to NM_001247.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr22:41572385 C>T maps to NM_001429.3 L1639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:41564859 A>C maps to NM_001429.3 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:41573462 A>C maps to NM_001429.3 P1916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr22:41545098 C>T maps to NM_001429.3 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr22:41489025 G>A maps to NM_001429.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr22:41521912 C>T maps to NM_001429.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:132514308 A>C maps to ENST00000333577 P1851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YI-01A-21D-A23C-09 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:132554137 C>A maps to ENST00000333577 S3027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:132508391 G>A maps to ENST00000333577 E1623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr12:132562208 G>A maps to ENST00000333577 P3157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr12:132504702 C>T maps to ENST00000333577 Q1499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr2:46574116 C>A maps to NM_001430.4 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr2:46607727 G>A maps to NM_001430.4 W639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr1:29314145 T>A maps to NM_001166005.1 L66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr20:34807720 C>T maps to NM_012156.2 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr20:34775660 C>G maps to NM_012156.2 Y283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:131201316 A>G maps to NM_001431.3 N621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr6:131247795 G>C maps to NM_001431.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr18:5434035 G>T maps to NM_012307.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:111966007 A>C maps to NM_019114.3 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:120848066 C>T maps to NM_020909.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr2:120836079 G>T maps to NM_020909.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr2:120903829 T>C maps to NM_020909.3 H586H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr10:32576024 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:32581464 T>C maps to NM_025209.2 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr2:149539234 G>A maps to NM_015630.3 E581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:149520237 G>T did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr4:75174840 G>A maps to ENST00000413830 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:143090941 C>A maps to NM_005232.4 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr1:38185167 T>G maps to NM_001099439.1 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:16456788 G>A maps to NM_004431.3 I867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr1:16458582 G>A maps to NM_004431.3 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr3:89391073 C>T maps to NM_005233.5 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr3:89176422 G>T maps to NM_005233.5 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:222308222 A>G maps to NM_004438.3 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:222428887 G>C maps to NM_004438.3 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:222307702 G>C maps to NM_004438.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:66356344 A>C maps to NM_004439.5 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr4:66286191 G>T maps to NM_004439.5 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr4:66280011 G>T maps to NM_004439.5 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:96945243 A>C maps to NM_001080448.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:96706412 C>T maps to NM_001080448.2 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:97251320 G>T maps to NM_001080448.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr6:94120422 C>A maps to NM_004440.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:93964515 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:93967994 G>A maps to NM_004440.3 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:93979355 G>C maps to NM_004440.3 S491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:22903005 G>A maps to NM_020526.3 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:22927461 C>A maps to NM_020526.3 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr3:134884888 C>A maps to NM_004441.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr3:134670325 G>C maps to NM_004441.4 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:134885849 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:134825413 G>A maps to NM_004441.4 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr3:134851667 C>T maps to NM_004441.4 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr3:134911475 C>T maps to NM_004441.4 Y647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr3:134670250 C>G maps to NM_004441.4 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr1:23191664 G>T maps to ENST00000400191 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr1:23191469 C>T maps to ENST00000400191 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:23111288 C>T maps to ENST00000400191 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr1:23111018 C>T maps to ENST00000400191 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A249-01A-11D-A167-09 chr1:23111510 C>T maps to ENST00000400191 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr3:184299397 T>C maps to NM_004443.3 P995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:184295791 C>T maps to NM_004443.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr7:100410500 C>T maps to NM_004444.4 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:100420100 C>T maps to NM_004444.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:142566373 A>G maps to NM_004445.3 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr7:142568300 G>A maps to NM_004445.3 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr7:142568629 G>A maps to NM_004445.3 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:27399055 G>A maps to ENST00000458037 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:27358451 G>C maps to ENST00000458037 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr8:27369411 G>C maps to ENST00000458037 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:92515872 G>A did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:92495764 C>A maps to NM_173567.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr19:56200356 C>T maps to NM_001130071.1 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr19:56190109 C>A maps to NM_001130071.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr19:56206662 C>T maps to NM_001130071.1 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr17:19215400 C>T maps to NM_014964.4 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:48619017 A>C maps to NM_017957.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr17:48616613 C>T maps to NM_017957.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr8:144940614 G>A maps to NM_031308.1 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr8:144947298 C>T maps to NM_031308.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr8:144941721 C>G maps to NM_031308.1 A1900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A202-01A-11D-A14K-09 chr8:144945135 G>A maps to NM_031308.1 D762D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr8:144941900 G>A maps to NM_031308.1 Q1841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr8:144940299 G>A maps to NM_031308.1 R2374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:220198563 C>T maps to NM_004446.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:51869126 A>T maps to NM_001981.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr1:51910582 G>C maps to NM_001981.2 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr19:16528436 G>A maps to ENST00000455140 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr19:16514561 C>T maps to ENST00000455140 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr19:16528785 C>T maps to ENST00000455140 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr19:16548607 C>T maps to ENST00000455140 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:15784424 A>C maps to NM_004447.5 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr12:15777329 G>A maps to NM_004447.5 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr19:55598980 G>A maps to NM_133180.2 *724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr19:55598980 G>C maps to NM_133180.2 *724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr1:110300156 C>T maps to NM_139053.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr13:43500513 A>G maps to NM_001002264.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:56276524 C>T maps to NM_000502.4 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:91371910 G>T maps to NM_004950.4 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:27186249 T>G maps to NM_005702.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr17:27185467 G>A maps to NM_005702.2 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:27187543 C>T maps to NM_005702.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:96124325 A>C maps to NM_016442.3 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:96215569 C>T maps to NM_001130140.1 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr17:37879580 G>T maps to NM_004448.2 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr17:37868681 C>T maps to NM_004448.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr5:65370886 C>G maps to ENST00000506030 L1271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:65349720 C>T maps to ENST00000506030 Q859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:65321314 G>A maps to ENST00000506030 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr5:65310495 G>C did not map to a codon.
Sequencing variant TCGA-AO-A12A-01A-21D-A10Y-09 chr12:56479000 C>T maps to NM_001005915.1 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr12:56488313 G>C maps to NM_001982.2 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:56490387 C>A maps to NM_001982.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:212248369 T>G maps to NM_005235.2 P1299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:212615429 C>A did not map to a codon.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr2:212289006 C>T maps to NM_005235.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:212285276 C>T maps to NM_005235.2 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:212578305 T>C maps to NM_005235.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr12:1137552 T>C maps to NM_178040.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:56026098 G>A maps to ENST00000460849 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr3:56026143 G>A maps to ENST00000460849 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr3:56468947 G>A maps to ENST00000460849 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr19:45924517 G>C maps to NM_202001.2 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:45918178 G>T maps to NM_202001.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr19:45856498 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:128047294 G>T maps to NM_000122.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:128050293 G>A maps to NM_000122.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr16:14041639 C>T maps to NM_005236.2 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:14026114 G>T maps to NM_005236.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr13:103510686 C>T maps to NM_000123.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr10:50690882 C>A maps to NM_000124.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr10:50732755 G>A maps to ENST00000515869 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:50732503 T>C maps to ENST00000515869 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr10:50678495 C>T maps to NM_000124.2 E1170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:71425688 C>G did not map to a codon.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:71426033 A>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:71425224 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:71426164 A>C did not map to a codon.
Sequencing variant TCGA-AC-A3HN-01A-11D-A20S-09 chr23:71428268 T>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:71428541 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:71425474 T>C did not map to a codon.
Sequencing variant TCGA-AR-A24Z-01A-11D-A167-09 chr23:71426993 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:71426742 C>G did not map to a codon.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr23:71425080 G>T did not map to a codon.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr23:71427062 T>C did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:71428225 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr19:42753285 G>A maps to NM_006494.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr21:39817364 G>A maps to NM_001136154.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr21:39817427 G>C maps to NM_001136154.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr5:172324038 C>T maps to NM_001031711.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:34143976 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr20:34130640 A>G maps to ENST00000447986 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr20:34144962 A>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:8877910 C>G maps to NM_153332.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr8:8869081 G>C maps to NM_153332.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:44820584 C>T maps to NM_024066.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr8:614676 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:37611456 C>T maps to NM_007175.6 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:43296733 G>C maps to NM_018538.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr1:43296766 C>A maps to NM_018538.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:158177977 A>C maps to NM_001009959.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:158181184 C>A maps to NM_001009959.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:5805086 T>G maps to NM_024896.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SG-01A-11D-A142-09 chr17:62130250 G>A maps to NM_001433.3 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr17:62137921 C>T maps to NM_001433.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr16:23722311 G>A maps to NM_033266.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr16:23722312 G>C maps to NM_033266.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:15091358 C>T maps to NM_152321.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:15087834 C>T maps to NM_152321.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WY-01A-11D-A10G-09 chr12:15068439 G>A maps to NM_152321.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AO-01A-11D-A12Q-09 chr12:112460209 C>G maps to NM_006817.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr6:11104835 A>G maps to NM_207582.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr11:124628268 G>A maps to NM_138961.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr18:19110360 G>T maps to NM_052911.2 Y822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr8:27634127 G>C maps to NM_001017420.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:13763476 C>A maps to NM_016649.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr20:13756550 C>A maps to NM_016649.3 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr12:53670884 C>A maps to NM_012291.4 I653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E9-01B-11D-A10Y-09 chr12:53663661 C>A maps to NM_012291.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr12:53680433 C>G maps to NM_012291.4 S1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A143-01A-11D-A10Y-09 chr1:6511894 C>T maps to NM_031475.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:152382233 C>G maps to NM_001122741.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:152265368 G>A maps to NM_001122741.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr14:64746759 T>G maps to NM_001437.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr8:95690587 G>T maps to NM_017697.3 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr8:95658490 C>T maps to NM_017697.3 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:76957919 C>A maps to NM_004452.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:216680403 C>T maps to NM_001438.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:103495262 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:103497467 A>C did not map to a codon.
Sequencing variant TCGA-AO-A03L-01A-41W-A071-09 chr23:103499461 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:103499123 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:56531111 A>C maps to NM_001184796.1 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr12:56531335 T>C maps to NM_001184796.1 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:56531158 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:56524861 G>A maps to NM_001184796.1 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr12:56522357 C>T maps to NM_001184796.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:158557430 G>A maps to NM_020728.2 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr7:158529791 T>G maps to NM_020728.2 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr7:158552763 C>T maps to NM_020728.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr7:158555811 G>T maps to NM_020728.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:138178096 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr3:138186957 G>A maps to NM_031913.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr2:67631499 T>C maps to NM_019002.3 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr5:137844061 G>A maps to NM_004730.2 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr15:76578062 T>A maps to NM_000126.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr19:51857487 G>A maps to NM_001014763.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:159603494 G>A maps to NM_004453.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:128359260 A>C maps to NM_001143820.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:128359311 A>C maps to NM_001143820.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr11:128354829 G>C maps to NM_001143820.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr11:128350167 G>A maps to NM_001143820.1 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:40194728 C>T maps to NM_005239.4 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr21:40191519 T>A maps to NM_005239.4 L302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr7:13949272 G>T maps to NM_004956.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr3:185823092 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr12:12022706 C>T maps to NM_001987.4 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:12022745 C>T maps to NM_001987.4 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:12038879 T>A maps to NM_001987.4 Y391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr6:36343649 G>C maps to NM_016135.2 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:5747025 G>T maps to NM_153717.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr4:5812120 G>T maps to NM_153717.2 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr4:5721018 G>A maps to NM_153717.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr4:5564814 G>C maps to NM_147127.4 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr4:5667276 G>A maps to NM_147127.4 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr4:5624639 G>A maps to NM_147127.4 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:29645754 C>A maps to NM_001003927.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr1:93163491 A>G maps to NM_005665.4 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:93029228 C>T maps to NM_005665.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:93101761 C>T maps to NM_005665.4 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr19:7918194 G>A maps to NM_001159944.1 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr19:7917979 G>A maps to NM_001159944.1 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr17:74005589 C>T maps to NM_001988.2 E1232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:74019441 G>A maps to NM_001988.2 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:74004965 C>T maps to NM_001988.2 R1440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr2:176948444 C>T maps to NM_001080458.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr22:29693827 C>T maps to NM_013986.3 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr22:29670254 A>G maps to NM_013986.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr14:69695781 C>A maps to NM_001193363.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:140243648 C>G maps to NM_017820.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr6:619509 T>C maps to NM_018303.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:491138 C>T maps to NM_018303.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:637807 G>C maps to NM_018303.4 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:454016 G>A maps to ENST00000315013 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr5:446328 G>A maps to ENST00000315013 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr5:457048 C>G maps to ENST00000315013 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr5:447697 C>T maps to ENST00000315013 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:45731005 G>A maps to NM_138568.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3X8-01A-31D-A22X-09 chr19:45735068 G>A maps to NM_138568.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:132937877 T>G maps to NM_021807.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:133002138 C>G maps to NM_021807.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr14:57696454 A>G maps to ENST00000340918 H433H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:94653265 G>T maps to NM_019053.4 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14T-01A-11D-A10Y-09 chr10:94653132 G>A maps to NM_019053.4 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr2:72802667 G>A maps to NM_015189.1 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr17:74079729 C>T maps to NM_001145297.2 *736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr3:38537965 G>A maps to NM_005107.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr1:11147519 G>A maps to NM_001001998.1 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:122734397 T>G maps to NM_001034194.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:122734397 T>G maps to NM_001034194.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:122732757 C>T maps to NM_001034194.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr11:108381163 C>T maps to NM_015065.2 Q1690Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:108385507 G>A maps to NM_015065.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:108381247 G>A maps to NM_015065.2 N1662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr11:108380563 C>A maps to NM_015065.2 G1890G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:108385390 C>T maps to NM_015065.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr8:118842507 A>C maps to NM_000127.2 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:118811983 C>T maps to NM_000127.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr8:118830769 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:44135749 T>G maps to NM_000401.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:101343415 G>A maps to NM_001439.2 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr8:28595119 C>G maps to NM_001440.2 Y787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:72127862 C>T maps to NM_000503.4 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:72229892 A>C maps to NM_000503.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr8:72211887 A>G maps to NM_000503.4 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:45633691 T>C maps to ENST00000360649 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr20:45801426 G>A maps to ENST00000360649 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr20:45702957 T>C maps to ENST00000360649 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:28354402 A>C maps to NM_001990.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:133802607 C>T maps to ENST00000452339 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:133844247 G>A maps to ENST00000452339 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr6:65767561 G>T maps to ENST00000370616 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:40864450 T>G maps to ENST00000264646 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:40880880 G>A maps to ENST00000264646 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr7:148508732 G>C maps to NM_004456.3 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:148525901 G>A maps to NM_004456.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr6:159188098 G>A maps to NM_001111077.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr13:113803434 G>A maps to NM_000504.3 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr5:176832168 G>A maps to NM_000505.3 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr6:6182293 C>A maps to NM_000129.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:6266928 G>A maps to NM_000129.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:6251073 G>A maps to NM_000129.3 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr6:6152106 G>A maps to NM_000129.3 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:197024938 T>A maps to NM_001994.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:46747679 C>T maps to NM_000506.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr11:46750992 A>T maps to NM_000506.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:76028610 C>T maps to NM_001992.3 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:76028892 G>A maps to NM_001992.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:76129178 G>A maps to NM_005242.4 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr5:76128710 C>T maps to NM_005242.4 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr1:95001578 G>T maps to NM_001993.4 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr1:169487736 C>A maps to ENST00000367796 S2091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:169511441 A>G maps to ENST00000367796 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:169509733 G>A maps to ENST00000367796 Q1537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:169510292 T>C maps to ENST00000367796 Q1350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr1:169509635 A>G maps to ENST00000367796 P1569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr13:113771833 C>T maps to NM_000131.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr13:113771884 C>T maps to NM_000131.3 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XS-01A-11D-A22X-09 chr23:154156941 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:154157863 G>C did not map to a codon.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr23:154090057 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:154132578 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:154133100 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:154156921 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:154159894 A>G did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:154194286 G>C did not map to a codon.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr23:154194830 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:154091403 G>A did not map to a codon.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr23:154088863 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr23:154194349 T>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:154065913 C>G did not map to a codon.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr23:154157955 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr23:154124398 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr23:154133267 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:154132572 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr23:154182269 C>T did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr23:154158486 A>C did not map to a codon.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr23:154159943 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1RD-01A-11D-A159-09 chr23:154133121 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr23:154133159 C>A did not map to a codon.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr23:154133243 A>G did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:154159466 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:138630620 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr1:46874198 G>C maps to NM_001441.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:46879246 A>G maps to NM_001441.2 *580W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:57458463 T>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:57337163 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:57337118 C>T did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:57358157 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr23:57358082 A>G did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr2:88425756 G>A maps to NM_001443.1 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:82441795 C>T maps to NM_001105281.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr8:82437316 G>A maps to NM_001105281.1 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr5:159640762 T>G maps to NM_001040442.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr5:159661861 G>A maps to NM_001040442.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:61580762 C>T maps to NM_013402.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr11:61608166 T>A maps to NM_004265.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr11:61615737 C>G maps to NM_004265.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LQ-01A-22D-A18P-09 chr17:72889675 G>C maps to ENST00000310226 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr1:50907188 G>A maps to NM_007051.2 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr5:175875472 T>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:80467428 G>A maps to NM_000137.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr15:80454633 C>G maps to NM_000137.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr16:1877748 C>T maps to NM_001018104.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr2:96071354 C>T maps to NM_016044.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr2:97757394 G>A maps to NM_199336.1 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:50295018 T>G maps to NM_012306.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr12:50291850 G>A maps to NM_012306.2 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr17:293239 G>A maps to NM_182705.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:55187405 A>C did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr5:14601227 G>A maps to NM_019018.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr5:14693018 C>G maps to NM_138348.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr5:14687727 A>G maps to NM_138348.4 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr10:14816536 C>T maps to NM_031453.2 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr10:14563236 G>A maps to NM_031453.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr9:74489591 C>A maps to NM_016014.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr15:81046554 C>A maps to NM_021214.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr8:59059799 C>T maps to NM_147189.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr8:59059478 C>T maps to NM_147189.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr2:45605 G>A maps to NM_001077710.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr11:58920328 G>A maps to NM_198847.2 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:58919902 G>A maps to NM_198847.2 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr11:58893516 C>G maps to NM_198947.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:2816742 T>G maps to NM_022760.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:2816865 T>G maps to NM_022760.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:2816742 T>G maps to NM_022760.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:38879878 T>G maps to NM_138389.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr7:143573578 C>A maps to NM_014719.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr7:143556201 C>T maps to NM_014719.1 E740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr7:143417624 G>C maps to ENST00000441159 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr3:57632136 G>A maps to NM_152678.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr2:203630189 C>A maps to NM_173511.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:203630267 C>T maps to NM_173511.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr11:126120561 C>G maps to NM_024556.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr9:96326562 C>G maps to ENST00000333936 S1061*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GM-A3NW-01A-21D-A228-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:54160447 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr23:54161502 T>A did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr23:54143206 C>G did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:54112177 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:54114264 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:54117848 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:54159178 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr23:54099575 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:54112278 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr23:54142995 A>G did not map to a codon.
Sequencing variant TCGA-A8-A083-01A-21W-A019-09 chr23:133923289 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:133915916 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:133906272 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr23:133923129 A>G did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr23:133906239 C>T did not map to a codon.
Sequencing variant TCGA-AR-A1AU-01A-11D-A12Q-09 chr23:133955535 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:63409935 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:63410059 A>G did not map to a codon.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr23:63411446 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:63413063 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:63410162 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0BA-01A-11W-A071-09 chr23:63412048 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:63411277 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18M-01A-11D-A12B-09 chr23:63411026 G>C did not map to a codon.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr23:63410048 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:63412319 C>G did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:63410387 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr23:63410673 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:63412445 G>C did not map to a codon.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr23:63411642 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:63410169 C>T did not map to a codon.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr23:63412662 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:131522017 G>A maps to NM_001105195.1 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:131519825 G>T maps to NM_001105195.1 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XO-01A-11D-A10G-09 chr13:51855019 G>C maps to NM_145019.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr13:51854668 G>A maps to NM_145019.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr7:22985375 C>T maps to NM_032581.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:201846307 C>T maps to NM_173822.3 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:201887607 C>G maps to NM_173822.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr23:134166664 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:134186114 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr23:134186076 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr23:134185955 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:134186090 G>C did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:134185807 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr23:134156264 G>A did not map to a codon.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr23:134156442 A>C did not map to a codon.
Sequencing variant TCGA-AR-A24T-01A-11D-A167-09 chr1:184764695 C>T maps to NM_052966.2 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:17662652 T>G maps to ENST00000332386 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:17641687 C>A maps to ENST00000335393 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:184056251 C>T maps to NM_144635.4 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:16385198 G>T maps to NM_182623.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr1:16386007 T>C maps to NM_182623.2 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:92964428 G>A did not map to a codon.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr2:220045922 G>A maps to NM_024293.4 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:220047074 A>C maps to NM_024293.4 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:71234911 G>T maps to NM_001162529.1 E709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr6:71243516 C>T maps to NM_001162529.1 Q1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr6:71186933 C>A maps to NM_001162529.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr8:139209857 G>A maps to NM_015912.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:139164905 G>T maps to NM_015912.3 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:139164464 G>A maps to NM_015912.3 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr8:139164076 T>A maps to NM_015912.3 K881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr2:70524438 G>A maps to ENST00000430566 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:70524438 G>C maps to ENST00000430566 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr2:70527970 C>T did not map to a codon.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr4:89649698 A>G maps to NM_014883.2 D1019D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:89653250 G>A maps to NM_014883.2 F915F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr4:89744131 C>A maps to NM_001015045.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:137289149 G>A maps to NM_016603.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr10:61029862 G>T maps to ENST00000442566 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:61122178 G>A maps to ENST00000442566 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:187084673 A>C maps to ENST00000356371 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr4:187077210 C>T maps to ENST00000356371 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr2:283134 G>A maps to NM_001002919.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:55085648 G>T maps to NM_176782.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr5:79797659 T>C maps to NM_205548.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr5:175511988 C>A maps to NM_001079529.2 C8*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E2-A2P6-01A-11D-A19Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr9:18950826 G>C maps to NM_153707.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr9:19032888 G>A maps to NM_153707.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:82575372 C>T maps to NM_001008226.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr13:108518416 C>T maps to NM_001080396.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr13:108518299 G>C maps to NM_001080396.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr23:68725886 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:68725796 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr14:24608638 G>A maps to NM_016049.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:6238628 G>A maps to NM_032127.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr11:6232927 G>A maps to NM_032127.3 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr10:116602859 C>T maps to NM_020940.3 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr8:21951948 A>G did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr2:62067331 G>C maps to ENST00000404929 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr14:74412990 C>T maps to NM_152445.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr8:79629670 C>A maps to NM_016010.2 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr14:75537977 G>C maps to NM_024643.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr14:75537317 C>T maps to NM_024643.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr11:73141810 G>C maps to ENST00000064778 Y25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr5:74096703 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr5:74078856 C>A maps to NM_015566.1 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr5:74096760 A>G maps to NM_015566.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AB-01A-11W-A050-09 chr15:99023895 C>A maps to NM_182562.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr10:15255675 G>A maps to NM_001010924.1 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr10:15255344 C>A maps to NM_001010924.1 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr10:15255093 C>A maps to NM_001010924.1 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr10:15256056 T>C maps to NM_001010924.1 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr2:187611927 G>A maps to NM_177454.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr2:187626829 C>G maps to NM_177454.3 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr2:187626599 G>T maps to NM_177454.3 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr5:99871632 C>G maps to NM_198507.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr10:126523294 C>T maps to NM_032182.3 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr10:102705187 G>T maps to NM_001136123.1 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:102684176 A>G maps to NM_001136123.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr2:97613615 T>C maps to ENST00000417561 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr2:97617139 T>C maps to ENST00000417561 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:29246026 G>A maps to NM_199280.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CV-01A-31D-A10Y-09 chr14:45431732 C>T maps to ENST00000361462 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:45475464 G>T maps to ENST00000361462 E967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr14:45473546 T>A maps to ENST00000361462 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr6:119297155 G>T maps to NM_024581.4 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:119282951 T>G maps to NM_024581.4 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr6:119345693 G>A maps to NM_024581.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:119297137 C>A maps to NM_024581.4 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr6:119327761 G>C maps to NM_024581.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:49998301 G>C maps to NM_032130.2 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr10:15858875 C>T maps to NM_024948.2 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:30831163 G>A maps to NM_032222.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:30876277 T>C maps to NM_032222.2 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr7:30818061 A>C maps to NM_032222.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr7:30876301 A>G maps to NM_032222.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr9:71998864 A>T maps to NM_001127608.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:91844537 A>G maps to NM_001145065.1 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr4:91230077 C>T maps to NM_001145065.1 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:86131657 G>T maps to ENST00000372088 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr16:57188234 G>A maps to NM_024946.2 I244I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A2-A0T4-01A-31D-A099-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:2648435 C>A maps to ENST00000324666 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:176951588 A>C maps to ENST00000442143 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:150384647 C>A maps to NM_152394.3 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr3:150421568 T>C maps to NM_152394.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr10:128974472 G>A maps to NM_001039762.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr10:128974482 C>T maps to NM_001039762.2 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:103411547 C>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:103420341 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr23:103430807 C>T did not map to a codon.
Sequencing variant TCGA-A2-A3XX-01A-21D-A23C-09 chr3:68788350 C>A did not map to a codon.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr17:66533882 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:66538247 G>T maps to NM_017565.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr1:179013002 C>T maps to NM_014864.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:195706 C>T maps to NM_020223.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:51890689 A>G maps to NM_001005751.1 K1246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr10:47946861 G>A maps to NM_018232.1 K1166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr10:88988362 G>T maps to NM_001099338.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr10:88988293 G>A maps to NM_001099338.1 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr9:97082783 C>G maps to NM_017561.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:97080988 G>A maps to NM_017561.1 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:97088184 C>T maps to NM_017561.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr9:99698809 C>A maps to NM_001170741.1 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr10:124671227 C>G maps to NM_001029888.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr10:124672466 C>A maps to NM_001029888.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:124608795 T>G maps to NM_152644.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:116833356 C>T maps to NM_153711.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr6:116784534 G>A maps to NM_001010919.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr18:10761022 C>T maps to NM_022068.2 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr18:10705743 G>A maps to NM_022068.2 S1750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr18:10773431 G>A maps to NM_022068.2 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr18:10761001 G>A maps to NM_022068.2 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr18:10759832 C>G maps to NM_022068.2 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:10807217 G>A maps to NM_022068.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:153736152 A>T did not map to a codon.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr7:121011388 G>A maps to NM_014888.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr10:120871383 G>C maps to NM_207009.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr6:82461504 C>A maps to ENST00000369756 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:118166485 C>T maps to NM_017709.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:79698161 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LM-01A-11D-A17W-09 chr23:79698446 G>T did not map to a codon.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr23:34150227 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr23:34148881 C>T did not map to a codon.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr23:34149178 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0AB-01A-11W-A050-09 chr23:34149383 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:34149095 A>G did not map to a codon.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr23:34148764 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:34149896 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:34148694 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:34150199 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:34148935 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr23:34148874 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:34149896 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr23:34961960 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:34961467 G>A did not map to a codon.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr23:34962203 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:34961254 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr23:34961801 C>T did not map to a codon.
Sequencing variant TCGA-AO-A12F-01A-11D-A10Y-09 chr23:34960975 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:34961040 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr23:34962577 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JU-01A-11D-A13L-09 chr23:34962643 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:34962380 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr23:34961413 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:34962125 G>A did not map to a codon.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr23:34961261 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr23:34961514 G>A did not map to a codon.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr23:37027581 C>T did not map to a codon.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr23:37029579 G>T did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:37026643 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:37028374 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:37027246 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:37028866 G>C did not map to a codon.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr23:37026497 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:37027606 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr23:37027221 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr23:37029348 C>A did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:37028629 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr23:37027407 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:37026521 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr23:37026806 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr23:37028634 C>T did not map to a codon.
Sequencing variant TCGA-E2-A15L-01A-11D-A12B-09 chr23:37026637 C>T did not map to a codon.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr23:37026994 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:37028316 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:37028694 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr13:37584781 C>T maps to NM_001014286.2 Q703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:37583934 G>A maps to NM_001014286.2 F738F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:16742327 G>A maps to NM_030797.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:16745328 C>A maps to NM_030797.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr2:16742264 C>A maps to NM_030797.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr2:16740778 G>C maps to NM_030797.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr8:130867880 G>A maps to NM_016623.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr23:153674858 C>T did not map to a codon.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr23:153678579 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr10:126370496 G>T maps to NM_014661.3 C195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:137680988 A>C maps to NM_001135647.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr5:137681243 C>T maps to NM_001135647.1 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr6:136560809 G>C maps to NM_138419.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr1:26153134 G>A maps to NM_001099626.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:114569281 C>T maps to NM_182495.5 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:101535800 C>G maps to NM_145037.2 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr11:114453662 C>A maps to NM_001077639.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr17:641190 T>A maps to NM_024792.1 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr23:152860003 C>A did not map to a codon.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr23:152858122 A>G did not map to a codon.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr23:152860088 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr23:152853865 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr18:29848310 C>T maps to ENST00000269209 Q718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr18:29890259 G>A maps to ENST00000269209 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:177245551 C>A maps to NM_021165.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:177250075 C>A maps to NM_021165.2 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr1:177199233 C>T maps to NM_021165.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr1:190250699 A>G maps to NM_199051.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr1:190068152 C>T maps to NM_199051.1 Q432Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr1:190067726 A>G maps to NM_199051.1 N574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr12:31435669 C>A maps to NM_001135812.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:59064338 C>T maps to NM_001040450.1 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr17:6348480 C>G maps to NM_001195228.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:67573655 T>G did not map to a codon.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr16:67580079 C>T maps to NM_001193523.1 Q1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:24818811 G>C maps to NM_014722.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RX-01A-11D-A25Q-09 chr20:49209054 C>G maps to NM_080829.2 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:49221280 T>G maps to NM_080829.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr20:49219049 C>T maps to NM_080829.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:139617772 C>T maps to NM_152421.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:119410810 T>G did not map to a codon.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr23:119418989 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:119410839 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:119425190 A>G did not map to a codon.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr23:119421018 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:212798746 A>C maps to NM_153606.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr1:212798329 C>T maps to NM_153606.3 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:212798753 G>T maps to NM_153606.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr1:212799871 C>T maps to NM_153606.3 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:156589955 A>G maps to NM_130899.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IU-01A-11D-A14G-09 chr5:156589496 C>T maps to NM_130899.2 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr5:156592822 G>A maps to NM_130899.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr7:128317708 C>T maps to NM_001012454.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr1:120839838 T>C maps to NM_001100910.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr1:78309070 T>C maps to NM_198549.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:131804680 G>A maps to NM_032809.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr9:39887041 C>A maps to ENST00000377642 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:43627222 T>G maps to NM_001145196.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr9:43624849 C>T maps to NM_001145196.1 R1279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr9:134151293 G>A maps to NM_033387.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr1:166135413 G>A maps to NM_001017961.3 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:59813529 C>T maps to NM_152450.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:38156641 G>A maps to NM_001170792.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr15:41028780 G>A maps to NM_018145.1 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr8:87498795 C>A maps to NM_016033.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr8:87489535 G>A maps to NM_016033.2 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr8:124195569 T>G maps to NM_032899.4 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S0-01A-21D-A25Q-09 chr6:54805817 T>C maps to NM_001010872.1 Y683Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:54805004 A>C maps to NM_001010872.1 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr20:33876298 G>A maps to NM_178468.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr20:33875225 G>A maps to NM_178468.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:33875617 G>A maps to NM_178468.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr20:37580526 C>T maps to NM_030919.2 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr19:49107071 G>A maps to NM_017708.3 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr8:12044261 G>A maps to NM_001083537.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr8:12283472 C>T maps to NM_001137610.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr8:12286608 T>C maps to NM_001137610.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DG-01A-21D-A12Q-09 chr8:12283472 C>T maps to NM_001137610.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr8:12283472 C>T maps to NM_001137610.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr12:8376711 C>A maps to NM_018088.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr8:124818462 G>T maps to NM_144963.2 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:33810292 A>C maps to ENST00000395190 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:38776775 T>G maps to NM_173611.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:38762572 C>T maps to NM_173611.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr19:38895680 C>G maps to NM_174905.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:8763153 C>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:8763372 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr23:8998339 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr23:9000381 C>A did not map to a codon.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr23:8997416 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:8995992 T>C did not map to a codon.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr23:9000175 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:13061328 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:13061256 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr16:89809342 G>A maps to NM_000135.2 F1210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:14862650 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr23:14871185 T>A did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr23:14861740 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:97873873 G>A maps to NM_000136.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr9:97873828 T>C maps to NM_000136.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr9:97873906 A>G maps to NM_000136.2 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:10130559 T>C maps to NM_033084.3 I1203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr3:10089639 C>T maps to NM_033084.3 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr3:10089627 C>T maps to NM_033084.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr3:10107573 G>T maps to NM_033084.3 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:35426159 A>C maps to NM_021922.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:35078686 G>T maps to NM_004629.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr9:35076496 T>C maps to NM_004629.1 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr15:89843029 G>C did not map to a codon.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr15:89849397 C>T maps to NM_001113378.1 Y1170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:89828361 C>T maps to NM_001113378.1 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr15:89838175 T>G maps to NM_001113378.1 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr15:89838217 G>C maps to NM_001113378.1 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:58457009 C>G did not map to a codon.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr14:45644731 A>G maps to NM_020937.2 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:45665673 C>T maps to NM_020937.2 F1880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr10:127697977 C>T maps to ENST00000368692 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:163044749 A>C maps to NM_004460.2 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:163039978 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:163044821 C>T maps to NM_004460.2 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr2:163072472 G>A maps to NM_004460.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr11:13721952 C>T maps to NM_032228.5 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:13716449 G>A maps to NM_032228.5 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr13:99083457 C>T maps to NM_005766.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr13:98865602 C>G maps to NM_005766.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr13:99093080 C>T maps to NM_005766.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SX-01A-12D-A099-09 chr2:242312706 T>A did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr2:242380740 T>A maps to NM_014808.2 L394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr6:5545515 C>T maps to NM_006567.3 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr17:80039174 G>A maps to NM_004104.4 L2154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr17:80040423 G>A maps to NM_004104.4 G1966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EW-01A-11D-A135-09 chr17:80042924 G>A maps to NM_004104.4 G1465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr17:80047260 C>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:80051191 C>T maps to NM_004104.4 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:80053313 C>T maps to NM_004104.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr7:150774050 C>G maps to NM_006712.3 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr7:150774080 G>A maps to NM_006712.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr2:207656459 G>A maps to NM_014929.3 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr5:7867556 C>A maps to NM_024091.3 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr4:187535468 G>A maps to ENST00000260147 D3038D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:187629076 A>C maps to ENST00000260147 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:187629724 G>C maps to ENST00000260147 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr4:187524065 G>A maps to ENST00000260147 Q3828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr4:187539185 G>A maps to ENST00000260147 Q2855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:150943057 T>G maps to NM_001447.2 P1134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr5:150946623 G>A maps to NM_001447.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr5:150948303 C>T maps to NM_001447.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:150924612 A>C maps to NM_001447.2 G2025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:150906914 G>C maps to NM_001447.2 L3396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:150931081 C>T maps to NM_001447.2 S1414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr5:150947877 C>T maps to NM_001447.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr5:150924227 G>A maps to NM_001447.2 Q2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr5:150924171 C>T maps to NM_001447.2 Q2172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr5:150946113 A>G maps to NM_001447.2 Y793Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:92523113 T>C maps to ENST00000298047 F1447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr11:92620184 G>T maps to ENST00000298047 P4319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:92600121 C>T maps to ENST00000298047 F3958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr11:92087135 G>T maps to ENST00000298047 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr11:92086867 A>G maps to ENST00000298047 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr11:92531858 C>T maps to ENST00000298047 L1894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr11:92568090 G>A maps to ENST00000298047 L3309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:126241180 T>C maps to NM_024582.4 D1205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:126370102 T>G maps to NM_024582.4 G2644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:126369916 C>G maps to NM_024582.4 V2582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:126411443 T>C maps to NM_024582.4 C4489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr4:126411925 C>A maps to NM_024582.4 S4650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr4:126337774 C>G maps to NM_024582.4 S2339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:126328237 T>C maps to NM_024582.4 H1837H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr4:126237641 C>T maps to NM_024582.4 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RD-01A-11D-A159-09 chr4:126336087 G>A maps to NM_024582.4 G1990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr23:150884627 G>T did not map to a codon.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr23:150890385 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0RT-01A-21D-A099-09 chr23:150890414 G>C did not map to a codon.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr23:150889972 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr17:73924154 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:40331153 A>C maps to NM_001436.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr3:13661228 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr3:13661248 G>A maps to NM_001165035.1 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:13649652 C>A maps to NM_001165035.1 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:13667999 G>A maps to NM_001165035.1 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr3:13669371 G>A maps to NM_001165035.1 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:112917317 G>A maps to NM_153214.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr15:48787332 G>T maps to NM_000138.4 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr15:48719824 C>T maps to NM_000138.4 Q2381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr15:48818432 G>A maps to NM_000138.4 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:48707866 A>C maps to NM_000138.4 Y2639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr15:48802319 G>T maps to NM_000138.4 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr15:48780598 G>A maps to NM_000138.4 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18S-01A-11D-A12B-09 chr15:48788402 C>A maps to NM_000138.4 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FD-01A-11W-A14Q-09 chr15:48707818 C>T maps to NM_000138.4 A2655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr5:127645091 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:127863563 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:127610375 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XG-01A-11D-A14G-09 chr5:127597565 C>T maps to NM_001999.3 G2742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr5:127681109 G>A maps to NM_001999.3 C1052C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr19:8140057 A>G maps to NM_032447.3 D2533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:8156388 T>G maps to NM_032447.3 P1997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr19:8176939 G>A maps to NM_032447.3 H1294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr19:8155007 G>A maps to NM_032447.3 C2053C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr19:8131063 G>A maps to NM_032447.3 I2723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr16:30678912 G>T maps to ENST00000356166 G682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr7:102453789 C>G maps to NM_145032.3 *736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:1702884 G>T maps to NM_152441.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr12:1702884 G>A maps to NM_152441.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15A-01A-11D-A12B-09 chr5:107216862 G>A maps to NM_001163315.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr7:5540157 G>T maps to ENST00000312577 S581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:5540849 G>A maps to ENST00000312577 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:30958078 G>A maps to NM_001099784.2 Q572Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr3:33416910 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr3:33416838 C>T maps to NM_012157.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr3:33420175 G>C did not map to a codon.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr15:63889650 C>T maps to NM_203373.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FV-01A-11D-A17D-09 chr13:77595878 G>A maps to NM_012158.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr4:15613941 G>C maps to NM_012161.3 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr4:15638231 G>A maps to NM_012161.3 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:145580145 G>A maps to NM_012162.1 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr5:15500793 G>C maps to NM_012304.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:15936679 C>T maps to NM_012304.3 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr16:67196942 G>A maps to NM_018378.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr9:37537586 G>A maps to NM_012166.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:48046192 C>A maps to NM_001190274.1 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr18:71797869 G>C maps to NM_001142958.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr18:71740755 G>C maps to NM_001142958.1 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr18:71740746 G>A maps to NM_001142958.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr10:5945068 C>T maps to NM_032807.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr10:5951232 C>A maps to NM_032807.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr10:5945052 G>A maps to NM_032807.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HB-01A-11W-A071-09 chr10:5963219 G>T did not map to a codon.
Sequencing variant TCGA-E9-A5FK-01A-11D-A27P-09 chr1:11708828 G>A maps to NM_012168.4 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr12:117603391 C>T maps to NM_033624.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr15:76225244 G>C maps to NM_147188.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr8:385682 C>A maps to NM_183421.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:39516185 G>A maps to NM_178820.3 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:224318193 G>A maps to NM_015176.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:146126452 A>C maps to NM_032145.4 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr8:124518724 G>T maps to NM_058229.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr8:124526555 T>C maps to NM_058229.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr14:39870682 G>A maps to NM_203301.3 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr14:39900892 A>C maps to NM_203301.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:55818481 C>T maps to NM_152231.1 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:147803582 C>T maps to NM_205836.1 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr5:41934238 G>T maps to NM_012176.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr2:73490822 C>T maps to ENST00000295133 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:16577862 G>A maps to NM_018994.1 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A3DX-01A-21D-A20S-09 chr1:16641841 C>T maps to NM_018994.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:101146032 G>C maps to NM_001029860.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:101154163 C>T maps to NM_001029860.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr1:11718331 G>T maps to ENST00000376768 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr3:196296085 G>A maps to NM_001105573.1 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:46215013 G>C maps to NM_001080469.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr1:11732059 G>A maps to NM_018438.5 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr22:32881083 G>A maps to NM_012179.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr4:175184102 G>T maps to NM_012180.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:18661705 C>T maps to ENST00000395665 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr17:18668053 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr5:171295749 G>A maps to NM_012300.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr3:48419898 G>C maps to NM_207102.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:123527010 C>G maps to NM_012164.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:123526845 C>T maps to NM_012164.3 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr10:103427731 C>T maps to ENST00000331272 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr4:153251994 C>T maps to NM_033632.2 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27A-01A-11D-A167-09 chr12:117448249 C>T maps to NM_153348.2 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr1:207134287 A>G maps to NM_001170631.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr19:55399641 C>G maps to NM_002000.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr19:55399554 T>C maps to NM_002000.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr1:159275776 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:40392454 A>C maps to NM_003890.2 G2683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr19:40421280 G>A maps to NM_003890.2 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06N-01A-11W-A019-09 chr19:40367786 G>A maps to NM_003890.2 C4391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr19:40392481 A>G maps to NM_003890.2 S2674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr19:40367762 A>G maps to NM_003890.2 A4399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:40368714 G>A maps to NM_003890.2 G4211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:40362868 C>T maps to NM_003890.2 L5067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr19:40377033 G>A maps to NM_003890.2 N3796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr19:40383694 T>C maps to NM_003890.2 G3305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:40367447 G>A maps to NM_003890.2 C4504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:40433014 G>A maps to NM_003890.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr19:40370212 G>A maps to NM_003890.2 D4151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:40368618 G>A maps to NM_003890.2 G4243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:40392718 G>A maps to NM_003890.2 N2595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:40406018 G>A maps to NM_003890.2 C1609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr19:40377033 G>A maps to NM_003890.2 N3796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LL-01A-11D-A17W-09 chr19:40377033 G>A maps to NM_003890.2 N3796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr19:40368618 G>A maps to NM_003890.2 G4243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr19:40392718 G>A maps to NM_003890.2 N2595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr19:40407986 G>A maps to NM_003890.2 A1578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr19:40370470 G>A maps to NM_003890.2 G4065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr19:40383694 T>C maps to NM_003890.2 G3305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr19:40377033 G>A maps to NM_003890.2 N3796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr19:40377033 G>A maps to NM_003890.2 N3796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr19:40408746 C>T maps to NM_003890.2 L1364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr19:40366142 G>A maps to NM_003890.2 D4697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr19:40376679 G>T maps to NM_003890.2 C3914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:40433878 C>T maps to NM_003890.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:149761829 C>T maps to NM_000566.3 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr1:120927201 G>A maps to NM_001017986.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr1:161475283 G>A maps to NM_001136219.1 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr1:161641359 C>T maps to NM_004001.4 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:161518250 G>C maps to NM_000569.6 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:161600156 C>T did not map to a codon.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr1:161600163 G>T maps to ENST00000367964 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr19:50017359 C>T maps to NM_004107.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr19:17889451 C>T maps to NM_015122.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr19:17883271 C>T maps to NM_015122.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:72302348 C>T maps to NM_138782.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr5:141025748 G>A maps to ENST00000354789 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr11:72552499 G>A maps to ENST00000409314 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr9:137808242 C>A maps to NM_002003.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr9:137804957 C>T maps to NM_002003.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:137777127 G>C maps to NM_004108.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr9:137772750 G>A maps to NM_004108.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:27700000 C>A maps to NM_003665.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:157740394 G>A maps to NM_030764.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:157737210 C>G maps to NM_030764.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:157740421 G>A maps to NM_030764.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:157738282 A>G maps to NM_030764.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:157666097 C>T maps to NM_052939.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr1:157667170 G>T maps to NM_052939.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:157660234 C>G maps to NM_052939.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr1:157669485 T>C maps to NM_052939.3 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr1:157557673 G>A maps to NM_031282.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:157556083 G>A maps to NM_031282.2 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr1:157514744 A>C maps to NM_031281.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr1:157514864 C>A maps to NM_031281.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:159778910 C>T maps to NM_001004310.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:155290321 C>G maps to NM_001135821.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr1:155290279 C>T maps to NM_001135821.1 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr1:155290276 G>A maps to NM_001135821.1 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:110333083 G>A maps to NM_004109.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:111747363 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr19:4793215 C>T maps to NM_018708.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr15:68582868 T>A maps to NM_015322.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr5:108290581 T>C maps to NM_005246.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:124968315 T>C did not map to a codon.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr8:125047695 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr8:125076804 A>G maps to NM_001039112.2 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:125072856 C>T maps to NM_001039112.2 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr8:125047695 G>T did not map to a codon.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr7:19184756 C>A maps to NM_152898.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr7:19184706 C>T maps to NM_152898.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:91437039 C>T maps to NM_002005.3 Y734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr3:186370418 G>A maps to NM_014375.2 *383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr11:125325837 G>A maps to NM_005103.4 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:62355758 C>T maps to NM_018008.3 *460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:62357787 C>G maps to NM_018008.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr3:62356988 C>A maps to NM_018008.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:35850151 A>C maps to NM_005304.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr19:35849944 C>T maps to NM_005304.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr4:155487117 T>C maps to NM_005141.4 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:54472831 G>A did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:54496511 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr9:95773517 A>G maps to NM_033086.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:32735052 T>G maps to NM_139241.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr12:32791665 G>A maps to NM_139241.2 Q660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:32761021 T>C maps to NM_139241.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:32793346 G>A maps to NM_139241.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr12:32778623 C>T maps to NM_139241.2 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr3:14963442 C>T maps to NM_152536.3 D1196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr3:14861792 C>T maps to NM_152536.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:14861603 C>T maps to NM_152536.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:14965557 C>T maps to NM_152536.3 F1327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:14862971 C>T maps to NM_152536.3 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:14862848 A>G maps to NM_152536.3 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr3:14964006 C>T maps to NM_152536.3 C1253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:95566495 C>T maps to NM_018351.3 Q822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:7344850 G>A maps to NM_004112.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YC-01A-11D-A117-09 chr23:137793116 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:137717748 G>A did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:137715073 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:137715088 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr23:76709702 C>A did not map to a codon.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr23:76711931 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr8:21903692 G>C maps to NM_003867.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr5:170883697 C>T maps to NM_003862.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:170883685 G>A maps to NM_003862.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24O-01A-11D-A167-09 chr5:170883787 C>A maps to NM_003862.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:16850658 T>C maps to NM_019851.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:4481813 A>C maps to NM_020638.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr12:4479738 G>T maps to NM_020638.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr12:4479577 G>A maps to NM_020638.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr12:4479709 C>T maps to NM_020638.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr11:69625282 G>A maps to NM_005247.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr11:69588112 G>T maps to NM_002007.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr4:81188145 C>T maps to NM_004464.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr4:81196117 C>T maps to NM_004464.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr12:4554430 G>C maps to NM_020996.1 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr12:4554415 G>A maps to NM_020996.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr15:49716608 C>T maps to NM_002009.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:103534552 C>T maps to NM_033163.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr10:103534570 G>C maps to NM_033163.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr8:38273483 G>A maps to NM_001174067.1 N617N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr8:38314913 T>C maps to NM_001174067.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:38277217 G>A maps to NM_001174067.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr8:38271456 G>A maps to NM_001174067.1 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr8:38282146 G>A maps to NM_001174067.1 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr8:38275445 G>A maps to NM_001174067.1 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:38272341 G>A maps to NM_001174067.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:167417804 A>G maps to NM_007045.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:167447389 G>A maps to NM_007045.2 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:27116367 G>T maps to NM_015633.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr12:27107175 C>T maps to NM_015633.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:123241688 G>T maps to NM_001144913.1 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr10:123239385 G>A maps to ENST00000351936 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr4:1808374 C>T maps to NM_000142.4 H711H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr5:176522627 C>T maps to NM_213647.1 D575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr5:176523631 G>A maps to NM_213647.1 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr5:176519684 C>G maps to NM_213647.1 Y319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:155533683 T>C maps to ENST00000407946 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr4:155531294 C>T maps to ENST00000407946 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:155533354 T>C did not map to a codon.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr4:155533320 T>A maps to ENST00000407946 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr4:155533232 C>A maps to ENST00000407946 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr1:60103947 G>A maps to NM_001113411.1 K374K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr1:60073503 C>T maps to NM_001113411.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:76825880 G>A maps to NM_006682.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:241680544 A>C maps to NM_000143.3 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr4:153897754 T>G maps to NM_033393.2 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr23:135290661 G>A did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr23:135288737 G>A did not map to a codon.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr23:135291481 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135290059 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:135288564 G>A did not map to a codon.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr23:135279278 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:38463127 T>C maps to NM_004468.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:97058461 T>G maps to NM_020482.4 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:67265425 C>T maps to NM_013241.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr16:67265710 G>A maps to NM_013241.2 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr18:34238118 C>T maps to NM_025135.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr18:34320687 G>T maps to NM_025135.2 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr11:27016366 G>T maps to NM_203371.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr11:65651445 C>G maps to NM_198897.1 *365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr12:108913080 G>A maps to NM_007076.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:108913233 G>A maps to NM_007076.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:110064464 A>C maps to NM_014845.5 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:15381242 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:15376293 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:15381256 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:164466815 G>C maps to NM_018086.2 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr6:76022556 G>A maps to NM_015687.2 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:76072488 C>A maps to NM_015687.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:76023498 C>T maps to NM_015687.2 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27A-01A-11D-A167-09 chr3:99568866 G>A maps to NM_001042459.1 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr4:54319223 C>A maps to NM_030917.3 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:42935515 G>A maps to NM_001080472.1 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr20:42935836 G>A maps to NM_001080472.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:39973387 C>T maps to NM_021939.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:39977249 C>T maps to NM_021939.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:115959277 T>A maps to ENST00000446284 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:115928408 C>T maps to ENST00000446284 T1228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr9:115931532 G>C maps to ENST00000446284 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr9:115931999 G>A maps to ENST00000446284 Q1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr2:24285914 C>A maps to NM_054033.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:2910380 G>A maps to NM_002014.3 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr12:2909685 G>A maps to NM_002014.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr6:35610570 C>A maps to NM_001145775.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:35588007 C>T maps to NM_001145775.1 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr19:18648425 G>A maps to NM_012181.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:18652708 G>A maps to NM_012181.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:18652633 C>G maps to NM_012181.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr7:33044890 G>A maps to NM_007270.3 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:33035889 G>C maps to NM_007270.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:108397330 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:154956391 C>A maps to NM_025207.4 C74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:154961213 G>T maps to NM_025207.4 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr1:154961308 C>G maps to NM_025207.4 Y367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:154960717 C>T maps to NM_025207.4 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr17:17122396 G>C maps to NM_144997.5 S333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr1:152283147 G>T maps to NM_002016.1 S1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr1:152282657 G>A maps to NM_002016.1 A1568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06N-01A-11W-A019-09 chr1:152283964 G>T maps to NM_002016.1 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:152282640 G>C maps to NM_002016.1 S1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:152282817 G>C maps to NM_002016.1 S1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:152279357 T>C maps to NM_002016.1 S2668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:152286350 C>T maps to NM_002016.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:152287133 C>G maps to NM_002016.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr1:152280686 C>A maps to NM_002016.1 V2225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr1:152283131 C>A maps to NM_002016.1 V1410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EU-01A-11D-A135-09 chr1:152276138 C>T maps to NM_002016.1 Q3741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr1:152280539 C>T maps to NM_002016.1 Q2274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr1:152285535 G>T maps to NM_002016.1 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr1:152277092 C>T maps to NM_002016.1 R3423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A4E0-01A-12D-A25Q-09 chr1:152283587 C>T maps to NM_002016.1 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr1:152329633 T>A maps to NM_001014342.2 K210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr1:152329343 T>C maps to NM_001014342.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:152327897 A>T maps to NM_001014342.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:152327924 C>T maps to NM_001014342.2 Q779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:152328380 C>T maps to NM_001014342.2 Q627Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr1:152324738 G>A maps to NM_001014342.2 D1841D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr1:152329960 T>A maps to NM_001014342.2 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr11:128628221 G>A did not map to a codon.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr11:128680834 C>A maps to NM_002017.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr11:128680831 C>T maps to NM_002017.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr17:18157405 C>T maps to NM_002018.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:18149710 G>A maps to NM_002018.2 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr17:18149364 C>T maps to NM_002018.2 E1093E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr14:21552964 C>T maps to NM_018071.3 I1281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr14:21543296 G>T maps to NM_018071.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:21546584 G>A maps to NM_018071.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:142505476 C>A maps to NM_207414.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr8:142489404 G>A maps to NM_207414.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr8:142517234 A>G maps to NM_207414.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:84605966 A>C maps to NM_001001670.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:84608546 A>C maps to NM_001001670.2 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:84606896 C>T maps to NM_001001670.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:84607175 C>T maps to NM_001001670.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:84607751 G>A maps to NM_001001670.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153595193 A>C did not map to a codon.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr23:153581201 T>G did not map to a codon.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr23:153586900 C>T did not map to a codon.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr23:153594794 A>T did not map to a codon.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr23:153593203 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:153592704 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153582800 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153585973 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153586610 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153596429 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:153585878 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:153593612 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr23:153593246 G>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:153583245 T>C did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:153585989 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:153595101 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:153580967 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:153590633 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:153592630 A>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:153594506 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr23:153599397 G>A did not map to a codon.
Sequencing variant TCGA-GM-A5PV-01A-11D-A28B-09 chr23:153582334 T>A did not map to a codon.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr23:153587943 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:58090878 T>G maps to NM_001164317.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:58135955 T>G did not map to a codon.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr3:58124078 G>C maps to NM_001164317.1 G1675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr3:58140518 T>C maps to NM_001164317.1 A2243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr7:128485244 C>T maps to NM_001458.4 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr7:128485099 C>A maps to NM_001458.4 S1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr7:128496687 C>G maps to NM_001458.4 V2456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr7:128495364 C>T maps to NM_001458.4 L2416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr7:128491584 C>A maps to NM_001458.4 T1915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr17:27211281 C>A maps to ENST00000394906 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr17:27207859 G>C maps to ENST00000394906 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr11:63884803 C>A maps to NM_013280.4 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:86089114 A>C maps to NM_013231.4 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12A-01A-21D-A10Y-09 chr14:86089045 G>A maps to NM_013231.4 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr14:86088322 C>T maps to NM_013231.4 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr14:86088199 C>G maps to NM_013231.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:86089276 T>C maps to NM_013231.4 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr20:14307922 G>C maps to NM_198391.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr13:28942780 T>G maps to NM_001160030.1 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr13:29005429 G>A maps to NM_002019.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr13:28588648 C>T maps to NM_004119.2 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr13:28602381 G>A maps to NM_004119.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr13:28644704 G>A maps to NM_004119.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr5:180056358 C>T maps to NM_182925.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr5:180045773 T>C maps to NM_182925.4 Q999Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:180049833 C>T maps to NM_182925.4 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr5:180046346 C>T maps to NM_182925.4 E889E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:213046101 G>A maps to NM_014053.2 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:213061313 C>A maps to NM_014053.2 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:76088462 A>C maps to NM_017791.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:2988356 C>T maps to ENST00000399667 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr16:2988209 G>C maps to ENST00000399667 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06N-01A-11W-A019-09 chr15:33256331 A>G maps to NM_001103184.2 Y815Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr1:240601453 C>T maps to ENST00000406993 F1811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:240286596 C>T maps to ENST00000406993 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:240519170 G>A maps to ENST00000406993 Q1750Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr1:240256069 C>T maps to ENST00000406993 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr1:240371327 G>A maps to ENST00000406993 A1215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr1:240370994 G>A maps to ENST00000406993 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr1:240370373 G>A maps to ENST00000406993 V897V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr1:240370289 C>G maps to ENST00000406993 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66H-01A-11D-A29N-09 chr1:240370193 G>A maps to ENST00000406993 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr17:43314957 G>A maps to NM_005892.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:43318500 A>G maps to NM_005892.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr2:153504367 C>T maps to NM_052905.3 R1076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr2:153488523 C>G maps to NM_052905.3 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:153473672 C>G maps to NM_052905.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr1:171251161 C>T maps to NM_002021.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:171236743 G>A maps to NM_002021.1 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:171251125 G>A maps to NM_002021.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr1:171251332 C>A maps to NM_002021.1 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr1:171250103 C>T maps to NM_002021.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr1:171174756 G>C maps to NM_001460.2 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:171173074 A>G maps to NM_001460.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr1:171162533 G>T maps to NM_001460.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:171083155 G>A maps to NM_006894.5 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr1:171086557 C>T maps to NM_006894.5 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr1:171083266 G>C maps to NM_006894.5 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr1:171303693 G>A maps to NM_002022.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr1:146656160 T>C maps to NM_001144829.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:203316864 C>T maps to NM_002023.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:147007127 A>C did not map to a codon.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr23:147026496 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:147026441 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr23:147026506 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:147014260 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:147010188 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr23:147027088 C>G did not map to a codon.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr23:147024826 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:147084782 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:147088317 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr2:216271006 C>A maps to NM_212482.1 V980V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:216271892 T>G maps to NM_212482.1 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:216274747 G>A maps to NM_212482.1 Y677Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:216298143 G>A maps to NM_212482.1 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr2:216262531 C>A maps to NM_212482.1 E1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr17:80699259 C>T maps to NM_022158.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr9:132689620 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:132740794 G>T maps to NM_015033.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr6:159635992 C>T maps to NM_032532.2 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr6:159621605 C>T maps to NM_032532.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr6:159670104 C>A maps to NM_032532.2 T1575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:159650874 C>G maps to NM_032532.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr6:159660684 C>A maps to NM_032532.2 V1439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr6:159670140 G>T maps to NM_032532.2 V1587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr13:49580376 T>C maps to NM_001079673.1 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:49749514 A>G maps to NM_001079673.1 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr13:49781422 G>A maps to NM_001079673.1 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr3:172070864 C>A maps to NM_022763.3 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:27716325 A>C maps to NM_022823.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr1:33333875 G>A maps to ENST00000291421 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SU-01A-11D-A099-09 chr1:109268546 C>T maps to NM_001144937.1 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr1:109256137 T>G maps to NM_001144937.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr17:33456559 C>T maps to NM_017559.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr4:159791485 G>A maps to ENST00000379346 Q961Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:65494209 T>G maps to ENST00000448390 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr11:49175783 T>C maps to NM_004476.1 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr11:49190795 G>A maps to NM_004476.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14U-01A-11D-A228-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr11:71906690 C>T maps to NM_016729.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:71850523 C>G maps to ENST00000442948 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:94038941 T>A did not map to a codon.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr14:75746764 T>G maps to NM_005252.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr14:75748072 C>T maps to NM_005252.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:45974092 C>T maps to NM_006732.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr2:28635011 G>A maps to NM_005253.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr20:22562871 C>T maps to NM_021784.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr19:46376174 C>T maps to NM_004497.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr6:1610937 C>A maps to NM_001453.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr1:63789205 G>A maps to NM_012183.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:114257231 C>T maps to NM_012184.4 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr9:70177572 G>A maps to NM_001126334.1 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:47882466 C>T maps to NM_012186.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:47882373 C>T maps to NM_012186.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:1390569 C>T maps to NM_001452.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:1390508 C>T maps to NM_001452.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:29237810 C>T maps to NM_005249.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X6-01A-11D-A14K-09 chr14:29237627 C>T maps to NM_005249.3 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KD-01A-12D-A20S-09 chr5:169535083 C>T maps to NM_012188.4 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr5:169535449 G>A maps to NM_012188.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr12:8197501 C>T maps to NM_018416.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr12:8200739 C>T maps to NM_018416.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:42654599 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:42657007 T>G maps to NM_001198850.1 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr16:86612424 C>T maps to NM_005250.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr12:2977869 C>T maps to NM_202002.1 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr17:26861800 G>A maps to NM_003593.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:26861407 C>T maps to NM_003593.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:48573478 G>A maps to NM_002158.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr6:108985250 G>A maps to NM_001455.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:70321367 A>C did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr23:70321378 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70316734 G>T did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:70316803 T>A did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr23:70321045 T>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:70316623 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr23:70321265 C>G did not map to a codon.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr3:71096184 A>T maps to NM_032682.4 L191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:71247210 G>C maps to NM_001012505.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr3:71161785 T>C maps to NM_032682.4 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr3:71026977 C>A did not map to a codon.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr3:71101698 G>A maps to NM_032682.4 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr23:49113996 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:49107845 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr23:55650718 G>T did not map to a codon.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr23:55650934 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr11:126147520 G>T maps to NM_017547.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:126145283 C>T maps to NM_017547.3 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:130566832 T>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:74665363 T>C maps to NM_001112808.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:74665372 C>T maps to NM_001112808.2 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:79173628 A>C maps to NM_025074.6 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:79343116 A>C maps to NM_025074.6 A1547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:79367921 C>T maps to NM_025074.6 L1966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr4:79391187 C>A maps to NM_025074.6 G2438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr4:79328835 G>A maps to NM_025074.6 V1383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr4:79236806 G>T maps to NM_025074.6 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:79462127 G>A maps to NM_025074.6 E3963E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr4:79188076 G>A maps to NM_025074.6 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:79410059 C>G maps to NM_025074.6 L2928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PG-01A-11D-A142-09 chr4:79462037 G>A maps to NM_025074.6 Q3933Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr9:14868948 C>T maps to ENST00000380880 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:14737549 A>C maps to ENST00000380880 G2131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr9:14819422 C>G maps to ENST00000380880 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr9:14769771 G>A maps to ENST00000380880 T1721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:14746970 G>A maps to ENST00000380880 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr9:14792818 G>T maps to ENST00000380880 A1304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr9:14776227 C>T maps to NM_001177704.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr13:39264279 C>A maps to NM_207361.4 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr13:39263886 C>T maps to NM_207361.4 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr13:39446911 C>A maps to NM_207361.4 R2673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A247-01A-11D-A167-09 chr13:39261492 C>G maps to NM_207361.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr10:135439802 C>T maps to ENST00000443774 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr10:135439802 C>T maps to ENST00000443774 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr6:116289837 G>A maps to NM_002031.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:116381276 A>C maps to NM_002031.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:116264330 G>A maps to NM_002031.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:168468076 G>A maps to NM_024919.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:85863081 C>T maps to NM_174938.4 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:85958183 C>T maps to NM_174938.4 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:85924482 C>T maps to NM_174938.4 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr10:13782555 G>A maps to NM_018027.3 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr10:13743359 G>A maps to NM_018027.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr10:13852854 C>G maps to NM_018027.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr10:13699218 C>T maps to NM_018027.3 A790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr10:13705477 G>A maps to NM_018027.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr14:52187001 C>T maps to ENST00000344768 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr14:52186812 G>C maps to ENST00000344768 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:52169258 C>T maps to ENST00000344768 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:131212278 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:131212884 A>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:131214254 T>C did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:131212588 G>T did not map to a codon.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr23:131233521 A>T did not map to a codon.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr23:131220042 A>T did not map to a codon.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr9:37708486 C>T maps to NM_014907.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr9:37737220 C>T maps to NM_014907.2 H510H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr9:37692652 G>A maps to NM_014907.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:49389049 A>C maps to NM_001018071.3 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr10:49452892 C>G did not map to a codon.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr10:49379162 G>C maps to NM_001018071.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr10:49431218 G>T maps to NM_001018071.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A247-01A-11D-A167-09 chr10:49448465 G>A maps to NM_001018071.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr23:12735861 G>A did not map to a codon.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr23:12722602 A>T did not map to a codon.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr23:12627985 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr23:12735774 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:12720092 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:12627995 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:12734316 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:12735140 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:12736041 G>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:12627930 G>C did not map to a codon.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr23:12632958 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:12734820 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:12627959 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:12736311 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:12736123 A>G did not map to a codon.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr23:12734332 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr23:12722502 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr23:12736088 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr23:12734857 C>T did not map to a codon.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr23:12704306 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr23:12736551 C>A did not map to a codon.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr23:12736882 G>T did not map to a codon.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr23:12516807 G>A did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr13:32863811 C>T maps to NM_023037.2 L2838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr13:32783134 C>G maps to NM_023037.2 V1388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:32723919 C>T maps to NM_023037.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr13:32721439 C>T maps to NM_023037.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr13:32835904 C>T maps to NM_023037.2 S2523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr13:32698786 T>C maps to NM_023037.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr4:48542835 T>C maps to NM_015030.1 R1943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:48566993 A>G maps to NM_015030.1 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr4:48512869 G>C maps to NM_015030.1 V2759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr14:44973847 T>C maps to NM_032135.3 E781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr14:44975062 A>G maps to NM_032135.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr14:44973862 A>C maps to NM_032135.3 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr7:5644990 C>T maps to ENST00000340250 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr17:79495874 G>A maps to NM_001077182.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr15:83437669 C>G maps to NM_001007122.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr2:49295406 G>A maps to NM_000145.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:49210298 C>G maps to NM_000145.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr2:49191056 A>C maps to NM_000145.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:40057929 C>A maps to NM_152597.4 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr2:186625769 A>G maps to NM_173651.2 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr2:186670215 C>T maps to NM_173651.2 Q5484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr2:186653386 G>A maps to NM_173651.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr2:186656656 C>T maps to NM_173651.2 N1687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:186659335 G>A maps to NM_173651.2 L2580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr5:52778851 C>T maps to NM_013409.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:120130713 A>G maps to NM_007085.4 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:132939614 C>T maps to NM_015082.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr5:132535017 C>T maps to NM_015082.1 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:162307213 T>C maps to NM_020116.3 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr21:47565363 C>T maps to ENST00000397748 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23E-01A-11D-A159-09 chr23:31089760 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:49469964 C>T maps to NM_000146.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RI-01A-11W-A071-09 chr5:121187813 C>T maps to NM_177478.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:2274963 G>T maps to NM_013393.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:61897287 A>C maps to NM_017647.3 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:61897485 C>T maps to NM_017647.3 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:61901719 C>G maps to NM_017647.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr6:37427447 G>A maps to NM_015050.2 L361L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AN-A0XW-01A-11D-A10G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr1:78414917 A>G maps to ENST00000436586 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:133498198 T>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:133501830 T>G maps to NM_003934.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr9:133498184 C>T maps to NM_003934.1 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:70506490 C>T maps to NM_145059.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr16:70513501 C>T maps to NM_145059.2 I1058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr16:70508499 G>A maps to NM_145059.2 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr23:44386523 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:44386526 G>A did not map to a codon.
Sequencing variant TCGA-AR-A5QP-01A-11D-A28B-09 chr23:154261713 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr15:91422702 G>A maps to NM_002569.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr15:91423398 G>A maps to NM_002569.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr19:49254064 T>C maps to NM_000148.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr10:75532726 C>G maps to NM_173540.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:49206872 G>A maps to NM_001097638.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr11:94278567 C>A maps to NM_002033.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr11:94278444 C>T maps to NM_002033.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr19:5866758 G>A maps to NM_002034.2 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr19:5867085 C>T maps to NM_002034.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr19:5832190 G>A maps to NM_001040701.1 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:66188493 T>G maps to NM_178155.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr6:96651552 C>T maps to NM_006581.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr19:50315564 C>T maps to NM_025129.4 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:50311870 C>T maps to NM_025129.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr3:180685863 C>T maps to NM_005087.3 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr3:180687949 C>G maps to NM_005087.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr3:180685878 T>G maps to NM_005087.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr17:7496416 C>T maps to NM_004860.3 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PV-01A-11D-A28B-09 chr17:7507082 C>T maps to NM_004860.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:35632069 C>T maps to NM_005031.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr19:35614359 G>C maps to NM_021910.2 *114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EX-01A-21W-A050-09 chr19:35649291 G>A maps to NM_001164605.1 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr5:39203056 C>T maps to ENST00000263405 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr3:46008080 C>T maps to NM_024513.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr3:46007804 C>G maps to NM_024513.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:46008713 G>A maps to NM_024513.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr6:112015899 T>C maps to NM_153047.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr3:197505307 G>A maps to NM_032288.6 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:197497047 C>T maps to NM_032288.6 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:90895682 C>T maps to NM_003505.1 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3HN-01A-11D-A20S-09 chr12:130648818 C>T maps to NM_007197.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:130648737 C>T maps to NM_007197.3 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr17:42636264 C>T maps to NM_001466.3 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:28385477 C>T maps to NM_017412.3 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr11:86663461 G>A maps to NM_012193.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr2:208633331 G>A maps to NM_003468.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:202900865 G>A maps to NM_003507.1 W499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:202899453 G>A maps to NM_003507.1 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr7:72849170 G>A maps to NM_003508.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:31074843 C>T maps to NM_017769.3 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr14:31071092 C>T maps to NM_017769.3 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153763481 T>G did not map to a codon.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr23:153761879 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:153760986 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr23:153760235 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:78083793 C>T maps to NM_001079804.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr17:78087102 C>G maps to NM_001079804.1 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:144361461 T>C maps to NM_207123.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:144390326 G>A maps to NM_207123.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:153940740 C>T did not map to a codon.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr23:153928294 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr23:153925487 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153927706 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:153940943 G>C did not map to a codon.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr23:153924212 G>A did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:153924264 C>G did not map to a codon.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr23:153940822 G>A did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr23:153908515 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:153924288 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:17449244 A>C maps to NM_001037814.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:17451046 G>A maps to NM_001037814.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr22:17468926 C>T maps to NM_001037814.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr17:7144762 G>A maps to NM_007278.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr6:29588976 G>A maps to NM_001470.2 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr6:29589963 C>A maps to NM_001470.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr6:29589895 G>A maps to NM_001470.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr6:29599374 A>T maps to NM_001470.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr9:101148011 G>T maps to NM_005458.7 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr9:101470749 G>A maps to NM_005458.7 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr9:101052988 G>A maps to NM_005458.7 H901H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:101133760 C>T maps to NM_005458.7 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:161292754 C>A maps to NM_001127648.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr5:161302574 G>A maps to NM_001127648.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27I-01A-11D-A16D-09 chr5:161324181 C>T maps to NM_001127648.1 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr23:151376600 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr23:151453147 T>A did not map to a codon.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr23:151358337 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:151366131 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:151336963 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr23:151514122 G>T did not map to a codon.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr4:46973127 T>C maps to NM_000809.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr4:46981080 G>T maps to NM_000809.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr15:27188365 C>T maps to NM_000810.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:27185189 G>A maps to NM_000810.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:161119076 C>T maps to NM_000811.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr5:161116328 C>T maps to NM_000811.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:47163372 C>A maps to NM_000812.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:47427692 C>T maps to NM_000812.3 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr23:151128422 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151124003 T>G did not map to a codon.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr23:151129810 A>T did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr4:46060586 T>C maps to NM_173536.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:161524771 C>T maps to NM_198903.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr15:27725919 G>A maps to NM_033223.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr23:151815557 C>T did not map to a codon.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:151815454 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr23:151815562 A>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151808885 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr23:151821276 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:151821344 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr23:151821056 G>A did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr23:151808899 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:97744432 G>A maps to NM_001105580.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr3:97731405 A>G maps to NM_001105580.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:92220725 G>A maps to NM_006705.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr19:13065284 G>A maps to NM_052850.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr3:30892433 C>A did not map to a codon.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr23:49173739 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:49179680 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr23:49192768 G>A did not map to a codon.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr23:49192695 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12O-01A-11D-A10Y-09 chr23:49236864 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:49230848 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr4:882687 C>A maps to NM_005255.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:860254 G>C maps to NM_005255.2 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr4:870397 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr11:68458383 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr11:65810934 C>T maps to NM_033036.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr11:65810976 C>T maps to NM_033036.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:88407817 A>C maps to NM_000153.2 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr15:49611903 C>T maps to NM_002044.2 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:88902641 C>T maps to NM_000512.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:88893183 C>G maps to NM_000512.4 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:151818671 G>A maps to NM_022087.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr7:151807731 T>A did not map to a codon.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr9:101594188 A>T maps to NM_024642.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr9:101589094 C>T maps to NM_024642.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:101597548 T>G maps to NM_024642.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr9:101594116 C>T maps to NM_024642.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr2:155115570 A>T maps to NM_052917.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:155099311 C>T maps to NM_052917.2 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr2:31165079 A>C maps to NM_024572.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:31165079 A>C maps to NM_024572.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:31152340 C>T maps to NM_024572.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr1:230384984 G>A maps to NM_004481.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr1:230381834 C>A maps to NM_004481.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr2:166618454 T>C maps to NM_004482.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr2:166611524 G>A maps to NM_004482.3 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr2:158115247 G>A maps to NM_014568.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:158140916 C>T maps to NM_014568.1 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr12:51758020 G>A maps to NM_007210.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XO-01A-11D-A10G-09 chr12:51771042 G>A maps to NM_007210.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:174225220 G>A maps to NM_017423.2 W447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr4:174216641 C>T maps to NM_017423.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr4:174223290 T>C maps to NM_017423.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:4874618 C>T maps to NM_017417.1 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:4855363 C>T maps to NM_017417.1 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:4848373 C>A maps to NM_017417.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr12:4855387 C>T maps to NM_017417.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:132837565 G>A maps to NM_001122636.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr12:132685674 G>A maps to NM_001122636.1 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr12:132905683 C>A maps to NM_001122636.1 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr3:16216720 G>A maps to NM_054110.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:16269005 G>T maps to NM_054110.4 *640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr11:11454294 C>G maps to NM_198516.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr11:11394112 C>T maps to NM_198516.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:11362440 G>A maps to NM_198516.2 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:151711820 C>T maps to NM_145292.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr7:151699797 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr7:151716745 C>T maps to NM_145292.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr4:173961205 T>A maps to NM_001034845.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr4:173150859 G>A maps to NM_001034845.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:56688524 G>A maps to NM_033106.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr18:74962761 C>G maps to NM_001480.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:34647846 C>T maps to NM_000155.2 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr11:62396765 T>C maps to NM_198335.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr11:62396293 G>A maps to NM_198335.2 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr11:62394093 T>G maps to NM_198335.2 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr15:42621622 C>G maps to NM_198141.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:42632944 C>T maps to NM_198141.2 Y715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr19:36035878 C>T maps to NM_014364.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr9:128099859 C>G maps to NM_015635.2 S983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr9:130153010 C>A maps to NM_032293.4 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr9:130155391 T>A maps to NM_032293.4 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr9:130095400 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:30661110 G>T maps to NM_002047.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:30671998 C>A maps to NM_002047.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr7:30649280 A>G maps to NM_002047.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A425-01A-11D-A243-09 chr21:34889371 G>T maps to NM_001136006.1 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr21:34897278 C>T maps to NM_001136006.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr21:34876574 C>T maps to NM_001136006.1 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:89560989 G>C maps to NM_002048.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr17:34072742 G>A maps to NM_139285.2 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:101018310 G>A maps to NM_174942.1 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr12:100994201 C>T maps to NM_174942.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr13:114529990 G>A maps to ENST00000357389 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr13:114529999 C>T maps to ENST00000357389 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr13:114541066 G>C maps to ENST00000357389 L188L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AN-A046-01A-21W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:48652430 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr23:48650323 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr23:48652248 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr10:8100439 C>G maps to NM_001002295.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr10:8115700 G>C did not map to a codon.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr10:8111496 G>A maps to NM_001002295.1 W329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr10:8100448 G>A maps to NM_001002295.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr10:8111549 A>T maps to NM_001002295.1 K347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr20:61048599 A>G maps to NM_080473.4 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr18:19761418 A>G maps to NM_005257.3 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr19:19603407 C>T maps to ENST00000404158 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr19:19612062 G>A maps to ENST00000404158 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:153784599 T>C maps to NM_020699.2 E476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:120897760 G>C maps to NM_176818.2 *137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:35737780 A>C maps to NM_020944.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr4:22749084 T>C maps to NM_020973.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr7:56051542 C>G maps to NM_001483.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr3:81754673 G>A maps to ENST00000264326 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr3:81635275 T>G maps to ENST00000264326 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr3:81692074 G>A maps to ENST00000264326 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr3:81627202 G>A maps to ENST00000264326 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr10:104135341 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:104117887 A>C maps to NM_004193.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:89519114 C>A maps to NM_002053.2 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:89524632 G>A maps to NM_002053.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:89479027 G>A maps to NM_018284.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr1:89656942 C>T did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr1:89660994 C>G maps to NM_052941.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr1:89662871 G>A maps to NM_052941.4 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:89730584 C>T maps to NM_052942.3 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr1:89849787 G>A maps to NM_198460.2 Q535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:89848299 C>G maps to NM_198460.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr22:38208967 T>C maps to NM_001171690.1 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:127224900 A>C maps to NM_024523.5 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:109087261 G>T maps to NM_181453.3 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:109109116 C>T maps to NM_181453.3 R1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr2:109086704 C>A maps to NM_181453.3 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr2:109102989 A>G maps to NM_181453.3 S1272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr21:34127559 C>T maps to NM_016631.3 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr21:34133371 G>A maps to NM_016631.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr14:55310746 G>A maps to NM_001024024.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:44190552 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:53365146 A>C maps to NM_001498.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:94362250 G>A maps to NM_002061.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:52993141 G>A maps to NM_003643.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:10882011 C>A maps to NM_004752.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr6:10876742 G>A maps to NM_004752.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:120575567 C>T maps to NM_006836.1 G2148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:120593460 G>A maps to NM_006836.1 N1125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr12:120582589 C>T maps to NM_006836.1 L1735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:120575104 G>A maps to NM_006836.1 Q2228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr12:120613010 C>T maps to NM_006836.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr12:120602271 C>A maps to NM_006836.1 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:10529557 T>G maps to NM_145649.4 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:10529248 G>A maps to NM_145649.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr15:59910997 C>T maps to NM_004751.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr15:57931736 C>T maps to NM_001018090.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:57967240 G>T maps to NM_001018090.3 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr15:57929915 A>G maps to NM_001018090.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr9:74810495 G>C maps to ENST00000238018 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24R-01A-11D-A167-09 chr8:75263606 C>T maps to NM_018972.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr8:75275184 T>G maps to NM_018972.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr20:42907675 C>G maps to NM_024034.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:48428694 C>A maps to NM_004962.2 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr12:7842581 A>G maps to NM_020634.1 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr12:7843250 C>T maps to NM_020634.1 Q106Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AC-A2FB-01A-11D-A17D-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BH-A0HF-01A-11W-A071-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr8:97157009 G>A maps to NM_001001557.2 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:20871055 C>T maps to NM_182828.2 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08O-01A-21W-A071-09 chr23:153670140 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr23:153668415 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:153667352 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr23:153668756 G>A did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:153668820 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:5815854 C>A maps to NM_001494.3 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:5808031 T>C maps to NM_001494.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:5827882 C>T maps to NM_001494.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr17:57352537 G>A maps to NM_001165993.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10A-01A-21D-A10Y-09 chr17:57326132 C>T maps to NM_182569.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:69652253 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr23:69650938 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:69652506 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:69650966 A>G did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:69650935 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr11:76990359 T>A maps to ENST00000376217 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr5:154282236 C>A did not map to a codon.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr5:154316740 T>G maps to NM_015465.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:39006138 G>T maps to NM_024775.9 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:39008832 G>A maps to NM_024775.9 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:14027286 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:17962026 A>C maps to NM_001130009.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:933449 G>T maps to NM_015949.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:42985464 G>A maps to NM_002055.3 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:92948571 C>T maps to NM_005263.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr5:179757777 C>G maps to NM_005110.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:179755314 G>A maps to NM_005110.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr5:179731846 G>T maps to NM_005110.2 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:118029027 G>C maps to NM_005264.4 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr5:137589524 G>A maps to NM_001496.3 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr6:55216081 G>A maps to NM_207410.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr22:38016264 G>A maps to ENST00000381756 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:23478979 A>C maps to NM_015044.4 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr17:73239561 C>T maps to NM_138619.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr7:30538451 G>C maps to NM_024051.3 Y130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:85781380 A>C maps to NM_000821.4 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr2:85777242 C>G maps to NM_000821.4 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr19:38876803 G>A maps to NM_152657.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr17:34942556 G>T maps to NM_024835.3 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:34941764 C>T maps to NM_024835.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr17:34937778 C>T maps to NM_024835.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr1:235505825 A>G maps to NM_001037277.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr22:24621544 G>A maps to NM_001099781.1 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:24622607 C>T maps to NM_001099781.1 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr22:24621311 T>C maps to NM_001099781.1 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:33451190 G>A maps to NM_178026.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr20:23966754 C>A maps to NM_178311.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr20:23966411 G>T maps to NM_178311.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr22:22988910 G>A maps to ENST00000215938 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr22:22988910 G>A maps to ENST00000215938 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr17:61994782 G>A maps to NM_000515.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:61957632 G>T maps to NM_022558.2 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr17:61957655 G>A maps to NM_022558.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr17:61958445 G>C maps to NM_002059.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr10:85901315 T>G maps to ENST00000436406 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr7:31014651 C>G maps to NM_000823.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr2:233655445 C>T maps to ENST00000373566 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:233659530 A>C maps to ENST00000373566 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A252-01A-11D-A167-09 chr2:233655499 C>T maps to ENST00000373566 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:233697793 G>A maps to ENST00000373566 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr7:150417440 C>T maps to NM_130759.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr7:150390168 C>A maps to NM_015660.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:150390099 C>T maps to NM_015660.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr7:150389496 C>T maps to NM_015660.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr7:150325502 G>A maps to ENST00000438845 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:150217319 C>T maps to NM_153236.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr7:150164190 G>T maps to NM_175571.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:150171336 C>A maps to NM_175571.2 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:85715276 C>T maps to NM_016095.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr8:41397267 G>A maps to NM_032336.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr8:41397270 G>T maps to NM_032336.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr8:41397267 G>A maps to NM_032336.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr1:78546504 C>T maps to NM_017655.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr19:3586585 C>T maps to NM_133261.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr19:46181246 G>T maps to NM_000164.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr19:46181213 G>C maps to NM_000164.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr17:27903566 G>A maps to NM_001085454.1 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:110385282 C>T maps to NM_057169.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr6:90604249 G>T maps to NM_032602.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr6:90605437 G>T maps to NM_032602.1 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr6:90604283 C>T maps to NM_032602.1 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:20716914 G>A maps to NM_021954.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr13:20717289 G>A maps to NM_021954.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:35260296 C>T maps to NM_002060.2 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:147380471 G>A maps to NM_005267.4 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:147381069 G>T maps to NM_005267.4 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr1:39341551 G>T maps to NM_030772.4 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:70443810 C>G did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:70444261 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:35227253 G>C maps to NM_153212.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:35227505 C>T maps to NM_153212.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr13:20797607 C>A maps to NM_001110221.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:87994372 T>G maps to NM_198568.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr15:35044894 C>T maps to NM_020660.1 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IE-01A-11W-A050-09 chr17:38519721 C>A maps to ENST00000337376 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr10:35896911 C>T maps to NM_153368.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:30714175 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:30671718 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:30686135 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:30686234 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:30737549 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:30738756 G>A did not map to a codon.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr23:30671664 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr4:80329027 G>T maps to NM_033214.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr4:80327944 G>A maps to NM_033214.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr4:80329159 G>A maps to NM_033214.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:141917687 G>A maps to NM_001039547.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:86421330 A>C maps to NM_025211.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:100653842 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:100652807 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr23:100658890 C>G did not map to a codon.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr23:100662775 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:100652886 A>G did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:100655658 G>C did not map to a codon.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr2:220102661 C>T maps to NM_024506.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:134217272 C>T maps to NM_138342.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr11:134238553 G>T maps to NM_138342.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr11:134179637 G>A maps to NM_001080407.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr11:134179637 G>A maps to NM_001080407.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:8095166 C>T maps to NM_138426.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:69548654 C>T maps to NM_015554.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:69561129 C>T maps to NM_015554.1 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:6553490 C>T maps to NM_000170.2 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:6644692 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:51687140 T>G maps to NM_181789.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr9:131277846 C>T maps to NM_001003722.1 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:131296227 G>A maps to NM_001003722.1 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr12:57859575 C>T maps to NM_005269.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:57864697 A>C maps to NM_005269.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:121747899 G>C maps to NM_005270.4 R1470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr2:121708926 C>T maps to NM_005270.4 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:121712908 C>G maps to NM_005270.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:42064931 C>T maps to NM_000168.5 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr7:42085090 G>A maps to NM_000168.5 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr7:42005085 G>A maps to NM_000168.5 N1195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr7:42079678 G>T maps to NM_000168.5 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr1:54059933 C>T maps to NM_147193.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:4385104 C>G maps to NM_032575.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr9:4117902 G>A maps to NM_001042413.1 H525H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr9:3856174 A>C maps to NM_001042413.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:673717 A>C maps to ENST00000397393 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr6:39033992 C>G maps to NM_002062.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr6:39046889 G>A maps to NM_002062.3 V319V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A8-A07R-01A-21W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr17:9739688 C>A maps to NM_004246.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:9757870 C>T maps to NM_004246.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr17:9764489 C>T maps to NM_004246.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr5:151231106 C>G maps to NM_001146040.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr23:14627176 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:175649777 G>A maps to NM_006529.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr23:102962272 C>T did not map to a codon.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr23:102968563 C>T did not map to a codon.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr4:158065055 C>T maps to NM_001166060.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr1:193065755 C>G maps to NM_016066.3 *166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr1:193074651 C>T maps to NM_016066.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr10:131967699 C>T maps to NM_006541.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:191760404 C>T maps to NM_014905.3 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr2:191827681 C>T maps to NM_014905.3 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr12:129467538 C>T maps to ENST00000442111 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr12:129383810 G>A maps to ENST00000442111 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr19:17688076 C>T maps to NM_024656.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:183938427 G>C maps to NM_015101.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:183920241 G>A maps to NM_015101.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr3:52729290 A>C maps to NM_018446.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr12:110290497 C>T maps to NM_016433.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr10:88820731 A>G maps to NM_005271.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr23:120182735 A>G did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:120182612 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr23:120181769 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr23:120181965 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr1:182354559 C>T maps to NM_002065.5 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr1:182355486 G>A maps to NM_002065.5 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:58722667 T>G maps to NM_080661.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr16:4867658 G>A maps to NM_032569.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:70068152 A>C maps to NM_178439.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IU-01A-11D-A14G-09 chr6:1930369 T>C maps to NM_001500.2 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr14:54947648 G>A maps to NM_004124.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:39826171 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr19:19746226 C>T maps to NM_016573.2 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:19748734 C>T maps to NM_016573.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:19751357 G>A maps to NM_016573.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr19:19740897 C>T maps to NM_016573.2 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:49759421 G>A maps to NM_013334.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:16290771 C>T maps to NM_006877.3 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr6:16279066 T>C maps to NM_006877.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:155652735 G>T maps to NM_003875.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:3119347 G>T maps to NM_002067.2 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:3113467 C>A maps to NM_002067.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:2770815 C>T maps to NM_007353.2 *382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:2771102 G>A maps to NM_007353.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:2771045 C>T maps to NM_007353.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:63010886 C>A maps to NM_006572.4 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr9:80049396 G>C maps to NM_004297.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr9:80043863 G>A maps to NM_004297.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W4-01A-11D-A10G-09 chr19:3151785 C>G maps to NM_002068.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr20:57428535 G>A maps to NM_080425.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:110148666 G>A maps to NM_005272.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:110155434 C>A maps to NM_005272.3 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr7:80108224 C>T maps to NM_001102386.1 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:19794229 C>A maps to NM_053004.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr22:19794229 C>G maps to NM_053004.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr5:180665140 G>C maps to NM_006098.4 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr5:180666576 C>T maps to NM_006098.4 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CU-01A-12W-A050-09 chr12:6952160 C>T maps to NM_002075.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:6955959 C>T maps to NM_002075.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr9:36246268 C>T maps to NM_001128227.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:848772 G>A maps to NM_016541.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr6:30513923 C>T maps to NM_005275.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr1:38061423 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:52728120 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr3:52724623 G>A maps to NM_014366.4 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:54578328 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0XR-01A-11D-A10G-09 chr23:54574725 G>T did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:54574725 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr23:54586951 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr23:54578043 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr23:54569443 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr23:54577448 G>T did not map to a codon.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr23:54585016 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr6:42931380 T>C maps to NM_018960.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr1:231406537 C>T maps to NM_014236.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr1:231396287 C>T maps to NM_014236.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27T-01A-11D-A16D-09 chr14:53247395 C>A did not map to a codon.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr12:102158935 G>A maps to NM_024312.4 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr12:102224413 G>A maps to NM_024312.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr16:1412631 G>A maps to NM_032520.4 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:1412860 G>A maps to NM_032520.4 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L8-01A-11D-A13L-09 chr12:65133263 G>A maps to ENST00000418919 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr12:65122795 G>A maps to ENST00000418919 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr9:127674284 C>T maps to NM_002077.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:127689005 C>T maps to NM_002077.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr9:127660908 T>C maps to NM_002077.3 Q442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:131020256 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr9:131024000 C>T maps to NM_004486.4 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr12:133384793 G>A maps to NM_005895.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:133349837 G>T maps to NM_005895.3 A1450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:133393372 C>T maps to NM_005895.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr12:133351860 C>A maps to NM_005895.3 E1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:37367847 C>T maps to NM_001172713.1 Q1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:37368484 C>G maps to NM_001172713.1 S1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:37388710 C>A maps to NM_001172713.1 S2182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:93263949 T>G maps to NM_005113.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:75562411 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:75580503 T>G did not map to a codon.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr10:99619285 C>T maps to NM_001010917.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr15:34676191 C>T maps to NM_181077.3 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr15:34820135 G>A maps to NM_001023567.4 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr3:121415259 G>T maps to ENST00000393667 V1370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:121413969 A>C maps to ENST00000393667 G1800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:121417376 C>A maps to ENST00000393667 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:121415751 G>A maps to ENST00000393667 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24M-01A-11D-A167-09 chr3:121416507 C>T maps to ENST00000393667 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr3:121409629 G>A maps to ENST00000393667 R2861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:121414698 A>G maps to ENST00000393667 I1557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr3:121416390 A>G maps to ENST00000393667 N993N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:167742832 A>C maps to NM_014498.3 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr9:88650388 C>T maps to ENST00000376023 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:150621201 T>C maps to ENST00000369003 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr1:155823535 T>C maps to ENST00000368331 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:155783568 G>A maps to ENST00000368331 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr1:155753881 T>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:155753796 A>G maps to ENST00000368331 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:155823270 G>A maps to ENST00000368331 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:155747442 C>T maps to ENST00000368331 Q687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:155735932 G>A maps to ENST00000368331 R1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:155744916 C>T maps to ENST00000368331 Q742Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:155733330 G>A maps to ENST00000368331 L1500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:117894638 T>G maps to NM_020399.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr1:170521401 A>T maps to NM_152281.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:170501402 G>C maps to NM_152281.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:171818230 A>C maps to NM_015530.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr17:28817221 C>T maps to NM_004871.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AT-01A-11D-A12Q-09 chr8:37792594 G>A maps to NM_152413.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr16:20329727 C>G maps to NM_001007240.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr16:20335273 G>C maps to NM_001007240.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr16:20331054 G>C maps to NM_001007240.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:20335309 C>A maps to NM_001007240.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr3:194118426 C>T maps to NM_004488.2 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr3:194117823 G>A maps to NM_004488.2 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr19:55543872 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:55543612 G>C maps to NM_001083899.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr19:55525716 G>T maps to NM_001083899.1 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr19:55526127 G>A maps to NM_001083899.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr1:167024280 G>T maps to NM_005814.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr1:167024316 G>A maps to NM_005814.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr1:167038306 G>A maps to NM_005814.1 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:145138726 T>C maps to NM_003801.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr10:113920521 T>G maps to NM_020918.4 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr10:113923489 C>T maps to NM_020918.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:96691751 G>A maps to NM_207328.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr2:96689095 G>A maps to NM_207328.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr2:96689145 A>G maps to NM_207328.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr19:33602732 G>A maps to NM_018025.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr19:33585131 A>G maps to NM_018025.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr19:33602731 C>A maps to NM_018025.2 S563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:217793290 C>A maps to NM_018040.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:217793584 C>A maps to NM_018040.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr1:217688213 T>G maps to NM_018040.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:217784357 A>G maps to NM_018040.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr1:156565375 G>A maps to NM_015590.3 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr17:42477335 C>T maps to NM_001002909.2 E703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:42478763 A>C maps to NM_001002909.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr17:42476444 G>A maps to NM_001002909.2 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:42478351 G>A maps to NM_001002909.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:56542136 G>A maps to NM_001127236.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr7:99769763 C>T maps to NM_152742.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr7:99769784 C>T maps to NM_152742.1 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:99771587 C>G maps to NM_152742.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr23:132887944 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:132887639 G>T did not map to a codon.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr23:132887697 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1P5-01A-11D-A142-09 chr23:132887945 G>A did not map to a codon.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr23:132458220 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr13:92408590 A>C maps to NM_004466.4 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr13:92345579 G>A maps to NM_004466.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr13:92345972 G>A maps to NM_004466.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr20:5556510 A>C maps to NM_019593.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr3:32180206 C>T maps to NM_015141.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr2:157439306 G>A maps to NM_000408.4 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:1132344 C>T maps to NM_001505.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr11:64702633 T>A maps to NM_130769.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:67243227 G>T maps to NM_020806.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:34872411 C>T maps to NM_000175.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48972149 C>A did not map to a codon.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr23:48980040 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0HU-01A-11W-A050-09 chr23:48972278 T>C did not map to a codon.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr23:48978772 G>T did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:13795517 C>T did not map to a codon.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr23:13834992 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:13835018 T>C did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:27216557 G>A maps to NM_018066.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr7:23300073 G>T did not map to a codon.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr7:23306202 T>C maps to ENST00000435486 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr7:23309657 T>C maps to ENST00000435486 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06P-01A-11W-A019-09 chr23:136112379 G>C did not map to a codon.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr23:136113229 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:136112552 G>A did not map to a codon.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr23:136113329 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:136113256 T>C did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr23:136112851 C>T did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:136112923 C>T did not map to a codon.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr19:6731902 C>T maps to NM_001080452.1 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr19:6731092 G>A maps to NM_001080452.1 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr12:123187140 G>A maps to NM_177551.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:123186990 G>C maps to NM_177551.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:123187335 C>T maps to NM_177551.3 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:46977496 G>A maps to ENST00000283297 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr6:46975028 T>C maps to ENST00000283297 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr6:46982476 G>A maps to ENST00000283297 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr23:135405033 A>T did not map to a codon.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr23:135455155 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135427229 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135427268 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135428004 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135428007 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135428063 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135428446 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135429059 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135429243 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135429255 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135429615 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135430583 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135430845 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135430955 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135431310 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135431381 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135431602 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135431876 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135432069 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135432260 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:135429315 G>A did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr23:135475729 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135426898 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135431991 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135482171 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135496376 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr23:135429690 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:135431749 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr23:135428726 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:135429148 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:135427023 A>G did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr23:135405373 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:135480085 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:135405372 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:135441600 A>G did not map to a codon.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr23:135427510 C>T did not map to a codon.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr2:26534174 G>A maps to NM_001145168.1 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:26541773 C>T maps to NM_001145168.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr2:26533778 C>T maps to NM_001145168.1 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr2:26534504 G>A maps to NM_001145168.1 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:26538504 C>T maps to NM_001145168.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr16:57601827 G>A maps to ENST00000349457 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:46867793 A>C maps to NM_015234.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:46836644 G>A maps to NM_015234.4 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:46826783 C>T maps to NM_015234.4 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr6:46826225 G>A maps to NM_015234.4 C1138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:46834802 G>A maps to NM_015234.4 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:46839703 G>T maps to NM_015234.4 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:46826993 G>C maps to NM_015234.4 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr6:46847553 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:129519123 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:129518471 C>A did not map to a codon.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr23:129518881 G>C did not map to a codon.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr13:27333625 C>T maps to NM_005288.3 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr10:95326767 C>T maps to NM_181745.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr4:22390353 C>T maps to NM_145290.2 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:22389591 T>G maps to NM_145290.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr4:22415368 G>C maps to NM_145290.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr4:22390712 G>C maps to NM_145290.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:142715041 G>C maps to NM_198569.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:142691310 C>T maps to NM_198569.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:142630779 A>G maps to NM_198569.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr3:100354666 T>G maps to NM_032787.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:100378561 T>G maps to NM_032787.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr3:100373699 A>C maps to NM_032787.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr12:131623711 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr12:131476807 C>T maps to NM_198827.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A143-01A-11D-A10Y-09 chr12:131488810 C>T maps to NM_198827.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr14:53098945 T>C maps to NM_001099652.1 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:20043380 G>T maps to NM_001002911.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:20043734 G>T maps to NM_001002911.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:20043419 A>G maps to NM_001002911.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:37780042 G>A maps to NM_181791.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:37780195 G>A maps to NM_181791.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:37780201 G>A maps to NM_181791.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:37780045 A>C maps to NM_181791.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr7:37780219 C>A maps to NM_181791.1 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr17:72365632 G>A maps to NM_181790.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:72366768 C>T maps to ENST00000440684 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr17:72366696 C>T maps to ENST00000440684 H1095H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EM-01A-11W-A050-09 chr23:9716673 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DG-01A-21D-A12Q-09 chr23:9707632 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:9714089 T>A did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:9693795 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:1097298 C>T maps to NM_138445.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr3:154138884 T>C maps to NM_001038705.1 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr3:154146675 A>G maps to NM_001038705.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr3:98251077 G>A maps to NM_005290.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:94957229 C>T maps to NM_199243.1 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:145894850 G>A maps to NM_194251.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:6313984 G>A maps to NM_207370.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr2:175311475 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:119886427 G>A maps to NM_153002.2 H632H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:25465206 C>A maps to NM_020752.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr10:25887794 C>G maps to NM_020752.2 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr3:169802101 G>C maps to NM_014373.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr2:128409205 C>T maps to NM_005291.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:53105959 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0RT-01A-21D-A099-09 chr23:53106369 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:53106177 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:53106577 C>T did not map to a codon.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr23:78426995 T>A did not map to a codon.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr23:78427389 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr23:78427211 A>G did not map to a codon.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr23:78426997 G>T did not map to a codon.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr23:78426711 C>A did not map to a codon.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr17:36486442 C>T maps to ENST00000398597 K1004K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr17:36485057 C>T maps to ENST00000398597 W1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr13:95273461 C>T maps to NM_180989.4 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr13:95271494 C>T maps to NM_180989.4 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr12:57389643 G>A maps to NM_007264.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:99947550 T>C maps to NM_004951.4 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:107115431 G>A maps to NM_005295.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:200842890 G>A maps to NM_005298.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr10:125447553 C>T maps to NM_153442.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:125426498 C>T maps to NM_153442.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:27721268 C>T maps to NM_005281.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:51274288 C>G maps to NM_001506.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr19:51273961 G>T maps to NM_001506.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr23:41555292 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:41555229 T>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:41555259 T>A did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr23:41555197 C>G did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr23:41555704 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:202092630 C>G maps to NM_004767.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:133174866 C>T maps to NM_001508.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr2:133175157 G>T maps to NM_001508.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BA-01A-11W-A071-09 chr2:133175211 C>T maps to NM_001508.2 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:133402800 C>T maps to NM_001508.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:133402995 C>G maps to NM_001508.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr19:46094650 G>C maps to NM_005282.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:46094965 G>A maps to NM_005282.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr2:105859374 C>T maps to NM_007227.3 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr23:150348635 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:150349820 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr23:150349051 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr23:150349191 C>T did not map to a codon.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr23:150348959 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr1:174417938 C>A maps to NM_005684.4 C230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr1:174417410 C>A maps to NM_005684.4 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:231775233 C>T maps to NM_005683.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr2:231774801 G>A maps to NM_005683.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:57695731 C>T maps to NM_005682.5 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:57689381 G>A maps to NM_005682.5 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr1:110086348 C>G maps to NM_031936.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15E-01A-11D-A12B-09 chr1:110086561 C>T maps to NM_031936.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:51989736 C>T maps to NM_080865.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:19021144 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:19022966 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:19026099 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:19042053 G>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:19039285 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:19017177 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:19021228 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr23:19027880 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:19017263 C>G did not map to a codon.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr23:19021074 C>G did not map to a codon.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr23:19031862 G>A did not map to a codon.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr23:19017273 C>A did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:19028891 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr14:91701373 G>A maps to ENST00000238699 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr2:54081233 G>C maps to NM_006794.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr2:54081560 A>G maps to NM_006794.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:47844307 T>C maps to NM_018485.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:123214246 G>T maps to NM_032554.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr12:123214163 G>A maps to NM_032554.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:94129616 G>C maps to NM_016540.3 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr12:54757016 G>A maps to NM_020370.2 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr1:101004698 C>T maps to NM_022049.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:145791154 C>G maps to NM_001097612.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:57713198 C>T maps to NM_170776.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr16:57713120 C>T maps to NM_170776.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr16:57710129 G>A maps to NM_170776.4 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr16:57719563 C>T maps to NM_170776.4 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr5:90086904 T>C maps to NM_032119.3 S4753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr5:90052315 G>T maps to NM_032119.3 E3876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:89943342 T>G maps to NM_032119.3 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:89969929 G>A maps to NM_032119.3 V1663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:90004653 G>T maps to NM_032119.3 E2918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:90084102 C>T maps to NM_032119.3 S4623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr5:89981682 C>T maps to NM_032119.3 Q2121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A227-01A-11D-A159-09 chr5:89948175 C>T maps to NM_032119.3 R1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr5:90049485 C>A maps to NM_032119.3 L3739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:101911192 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:101909940 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:101908853 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:101911384 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr23:101912417 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:101910196 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:101912815 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:101912280 G>A did not map to a codon.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr23:101912270 T>G did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:101910383 G>C did not map to a codon.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr23:101910989 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:101911238 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:101969920 A>T did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:101971742 A>T did not map to a codon.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr23:101971945 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:101971234 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:101972187 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr23:101972005 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:101970775 G>C did not map to a codon.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr23:101971060 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:101972128 C>G did not map to a codon.
Sequencing variant TCGA-OL-A5RU-01A-11D-A28B-09 chr23:101971060 G>A did not map to a codon.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr17:72436046 C>T maps to NM_022036.2 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr12:13102973 C>T maps to NM_018654.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:13103173 G>A maps to NM_018654.1 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr6:117128089 G>T maps to NM_148963.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27I-01A-11D-A16D-09 chr6:117130686 C>G maps to NM_148963.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr10:46999521 G>A maps to NM_014696.3 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr10:46999029 C>T maps to NM_014696.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr4:90170955 C>A maps to NM_198281.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr4:90169140 G>T maps to NM_198281.2 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr17:80010319 T>C maps to NM_212492.1 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:7216539 G>A maps to NM_004489.4 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AU-01A-11D-A12Q-09 chr17:7217446 G>A maps to NM_004489.4 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr17:7218276 C>G did not map to a codon.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr17:7216884 A>G did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:139244163 C>T maps to NM_001145638.1 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AL-01A-21D-A12Q-09 chr9:139229080 C>T maps to NM_001145638.1 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr9:139231982 T>C maps to NM_001145638.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr1:109440721 G>T maps to NM_013296.4 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr8:145730242 G>T maps to NM_005309.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:46956199 G>T maps to NM_133443.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr16:46962905 G>C maps to NM_133443.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr19:1106406 C>T maps to NM_002085.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr19:35504260 G>C maps to NM_020895.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr11:123479406 G>A maps to ENST00000456860 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr11:123481043 C>G maps to ENST00000456860 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr11:123489813 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr11:123476186 G>A did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr3:113623049 C>T maps to NM_017577.4 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr22:47070635 C>T maps to NM_015124.2 Y489Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr22:40364071 G>C maps to NM_004810.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:52407498 G>C maps to NM_181711.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:50686923 C>T maps to NM_005311.4 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IH-01A-11D-A10Y-09 chr7:50663153 T>A maps to NM_005311.4 K540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr2:11725302 C>A maps to NM_014668.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:11718468 C>G maps to NM_014668.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr2:11720881 C>T maps to NM_014668.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:11752668 G>T maps to NM_014668.3 E1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12O-01A-11D-A10Y-09 chr2:11772120 C>T maps to NM_014668.3 D1566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:11696748 T>C maps to NM_014668.3 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:11767229 G>A maps to NM_014668.3 Q1483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:240656739 C>G maps to NM_022469.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:240656325 C>T maps to NM_022469.3 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr1:240656379 G>C maps to NM_022469.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A096-01A-11W-A019-09 chr8:102571040 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr8:102570698 C>T maps to NM_024915.3 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:102661726 G>A maps to NM_024915.3 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr8:102555523 C>T maps to NM_024915.3 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:24657984 T>C maps to NM_021180.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr5:153143996 C>T maps to NM_001114183.1 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr5:153175110 C>T maps to NM_001114183.1 Y782Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:153085553 G>T maps to NM_001114183.1 E584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12A-01A-21D-A10Y-09 chr5:153056564 G>A maps to NM_001114183.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr5:153030052 C>A maps to NM_001114183.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:153078608 C>T maps to NM_001114183.1 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr5:153149726 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr4:158262490 C>T maps to NM_000826.3 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:158224869 C>G maps to NM_000826.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:122528947 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:122532571 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr23:122551280 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr23:122536949 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr23:122536847 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr23:122616871 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:122460031 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr23:122387163 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:122528931 G>A did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:122561909 G>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:122598858 G>A did not map to a codon.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr23:122598836 C>A did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr23:122538637 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr23:122599567 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr23:122387186 T>C did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:122319693 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:122598761 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr23:122528858 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:105623815 A>C maps to NM_000829.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:87966205 T>G maps to NM_017551.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:87362125 C>T maps to NM_017551.2 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:87484361 C>T maps to NM_017551.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:87362185 C>T maps to NM_017551.2 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:31015151 G>A maps to ENST00000327783 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr21:30909632 G>C maps to ENST00000327783 S923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr6:102337556 C>T maps to NM_021956.4 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr6:102337556 C>T maps to NM_021956.4 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr6:102069878 C>T maps to NM_021956.4 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr6:101847170 G>A maps to NM_021956.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L8-01A-11D-A13L-09 chr6:102376326 A>C maps to NM_021956.4 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr1:37307536 C>A maps to NM_000831.3 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:37291370 G>T maps to NM_000831.3 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:37267520 G>A maps to NM_000831.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EU-01A-11D-A135-09 chr11:120833361 C>T maps to NM_014619.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr11:120852905 G>A maps to NM_014619.2 W829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr16:9857874 C>A maps to NM_000833.3 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr16:9862752 C>T maps to NM_000833.3 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr16:9923468 C>T maps to NM_000833.3 W606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr12:14018977 C>T maps to NM_000834.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr12:13716855 C>A maps to NM_000834.3 E1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr12:13716940 G>A maps to NM_000834.3 A1077A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr12:13716418 C>G maps to NM_000834.3 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:13906513 C>T maps to NM_000834.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:13717033 G>A maps to NM_000834.3 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr12:13724844 G>A maps to NM_000834.3 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SJ-01A-11D-A099-09 chr17:72846849 G>A maps to NM_000835.3 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr17:72850910 G>A maps to NM_000835.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr17:72846368 G>A maps to NM_000835.3 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr17:72840606 G>A maps to NM_000835.3 I797I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr19:48945082 C>T maps to NM_000836.2 D770D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr19:48922956 G>A maps to NM_000836.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:48945551 C>G maps to NM_000836.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:48945554 C>T maps to NM_000836.2 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr9:104499856 C>T maps to NM_133445.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr9:104341569 A>G maps to NM_133445.2 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr9:104499592 G>A maps to NM_133445.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr9:104433298 G>A maps to NM_133445.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr9:104375771 G>A maps to NM_133445.2 T884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:1005497 C>T maps to NM_138690.1 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:145065973 T>G did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr8:145066882 G>A maps to NM_001009184.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:58001340 G>A maps to NM_015532.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:66839142 T>G maps to ENST00000359742 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:66765533 C>T maps to ENST00000359742 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr12:66788017 G>C maps to ENST00000359742 S700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:14552700 C>T maps to ENST00000507975 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:14537939 G>T maps to ENST00000507975 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr23:48838242 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48834732 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48838216 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0XO-01A-11D-A10G-09 chr23:48837668 C>T did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:48831587 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr23:48853757 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr23:48839810 C>T did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:48841751 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:48839760 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr13:114322007 C>T maps to NM_002929.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:3021498 C>T maps to NM_182982.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr4:3040212 C>T maps to NM_182982.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr4:2986303 C>A maps to NM_182982.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr10:121201554 G>T maps to NM_005308.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:176863206 G>A maps to NM_002082.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:141497503 C>T maps to NM_139209.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr3:141499535 C>T maps to NM_139209.2 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr19:47492816 G>T maps to NM_004491.4 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr19:47422144 C>T maps to NM_004491.4 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr19:47492897 G>A maps to NM_004491.4 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GY-01A-11W-A071-09 chr19:47424157 C>G maps to NM_004491.4 Y742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr19:47422651 C>T maps to NM_004491.4 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:47424130 C>T maps to NM_004491.4 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr19:47424344 C>T maps to NM_004491.4 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr19:47440519 G>A did not map to a codon.
Sequencing variant TCGA-AC-A2FF-01A-11D-A17D-09 chr6:146720187 C>A maps to NM_000838.3 C671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr3:51743247 C>T maps to NM_000839.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr7:86415884 G>A maps to NM_000840.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr7:86468644 C>T maps to NM_000840.2 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:86468740 A>C maps to NM_000840.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr7:86468222 C>T maps to NM_000840.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:86415800 G>A maps to NM_000840.2 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr7:86493601 T>C maps to NM_000840.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr5:178408822 G>T maps to NM_000843.3 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr5:178410024 G>A maps to NM_000843.3 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr5:178408702 C>T maps to NM_000843.3 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr7:126173065 G>A maps to NM_001127323.1 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:126173509 T>G maps to NM_001127323.1 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:126409994 G>A maps to NM_001127323.1 Y427Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr7:126173297 C>T maps to NM_001127323.1 W713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr7:126079179 G>C maps to NM_000845.2 S907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L9-01A-11D-A13L-09 chr7:126173164 G>T maps to NM_001127323.1 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr17:42427674 C>A maps to NM_002087.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr17:42427850 T>G maps to NM_002087.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:16142182 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:16170720 A>C did not map to a codon.
Sequencing variant TCGA-AR-A2LL-01A-11D-A17W-09 chr23:16170431 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr23:16142100 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr4:71697362 C>A maps to NM_002092.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr13:113980338 C>T maps to NM_024719.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr19:48953638 C>T maps to NM_031485.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr4:42895456 C>T maps to NM_001080476.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr5:145252321 G>A maps to NM_001080516.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:130762326 A>C maps to NM_031415.2 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:130765005 G>C maps to NM_031415.2 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr8:130774953 G>C maps to NM_031415.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BA-01A-11W-A071-09 chr8:130777948 G>A maps to NM_031415.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:42744159 C>A maps to NM_019884.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:119721033 A>C maps to NM_002093.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr3:119585460 T>G maps to NM_002093.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr3:119812254 G>C maps to NM_002093.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:124065344 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:124079488 C>T maps to NM_000177.4 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr16:12009403 C>T maps to NM_002094.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr23:51487621 T>A did not map to a codon.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr23:51488497 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0JI-01A-21W-A100-09 chr23:51488352 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr23:51488513 A>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:51488001 T>C did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:51487019 C>T did not map to a codon.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr23:51487775 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr8:30553914 C>G maps to NM_000637.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:30553958 C>A maps to NM_000637.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IJ-01A-11D-A142-09 chr8:30557644 G>A maps to NM_000637.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:52767199 G>A maps to NM_000847.4 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr6:52770566 G>T maps to NM_000847.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr6:52849323 G>A maps to NM_001512.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr6:52701122 G>A maps to NM_153699.1 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:142962180 C>A maps to NM_001143679.1 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:110280958 C>T maps to NM_000849.4 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr10:106014942 C>T maps to NM_004832.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr11:67353657 C>G maps to NM_000852.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr4:54966573 G>A maps to NM_133267.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr2:144764837 A>G maps to NM_001164629.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr8:30472232 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:30436511 G>A maps to NM_002095.4 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr19:6380408 G>C maps to NM_002096.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:6381745 G>A maps to NM_002096.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr19:6380393 C>G maps to NM_002096.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr13:45694816 G>A maps to NM_004128.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:18373960 G>T maps to NM_005316.3 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr12:124144424 C>T maps to NM_001516.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr7:73961493 G>A maps to NM_016328.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:73927242 G>A maps to NM_016328.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:73938399 G>A did not map to a codon.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr7:74237281 G>A maps to NM_173537.2 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr7:74212295 G>A maps to NM_173537.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr7:74538955 A>G maps to NM_001003795.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:74536716 G>A maps to NM_001003795.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr7:74536690 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:27474859 A>C did not map to a codon.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr16:27506804 G>A maps to NM_001520.3 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:27494390 G>A maps to NM_001520.3 R1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:27480780 C>T maps to NM_001520.3 V1635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:27512665 C>A did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr16:27499929 G>C maps to NM_001520.3 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:27551025 G>A maps to NM_001521.2 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:27552348 G>A maps to NM_001521.2 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24P-01A-11D-A167-09 chr2:197662519 C>T did not map to a codon.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr2:197654047 G>C maps to NM_012086.2 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr9:135917589 G>A maps to NM_001122823.1 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr22:39111930 G>C maps to NM_004286.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:1042141 G>T maps to NM_012341.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:1044977 G>A maps to NM_012341.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr20:60771000 G>A maps to NM_015666.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:42355073 C>T maps to NM_176791.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:108626925 C>T maps to NM_005459.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28O-01A-11D-A228-09 chr1:42620391 G>C maps to NM_007102.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:42619186 G>A maps to NM_007102.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr1:42619171 C>G maps to NM_007102.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr11:106810892 C>A maps to ENST00000282249 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DN-01A-11D-A17W-09 chr4:156629402 A>G maps to NM_001130684.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr4:156724916 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr4:156721139 C>T maps to ENST00000502959 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr12:14774138 G>A maps to NM_004963.3 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr12:14822719 A>C maps to NM_004963.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr12:14798207 G>A maps to NM_004963.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr17:7912873 C>T maps to NM_000180.3 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr17:7911259 G>T maps to NM_000180.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:108684642 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr23:108718510 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:108696851 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:108625349 G>C did not map to a codon.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr23:108718456 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:108638634 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr23:108635296 A>T did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr23:108696998 A>C did not map to a codon.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr23:108718515 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:108652303 C>T did not map to a codon.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr23:108635323 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:228335368 G>A maps to ENST00000366720 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr2:189452660 A>G maps to NM_016315.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:73016710 A>T maps to NM_001080393.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr3:73024282 C>A maps to NM_001080393.1 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr3:73004302 C>T maps to NM_001080393.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr3:148714087 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:2779636 A>C did not map to a codon.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr23:2773100 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:2779625 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:2779691 C>T did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr23:2761049 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr23:2761382 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr23:2761347 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr23:2774659 C>G did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:49494594 C>T maps to NM_002103.4 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:49494639 C>T maps to NM_002103.4 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr12:21733377 A>G maps to NM_021957.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:21712042 T>C maps to NM_021957.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr12:21693463 A>C maps to NM_021957.3 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr5:54403621 G>A maps to NM_006144.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:54327359 C>T maps to NM_002104.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:154113467 G>A did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr12:14927766 G>A maps to NM_177925.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr11:118965981 G>A maps to NM_002105.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr5:134705191 G>A maps to NM_138610.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr23:103267769 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:31944955 G>A maps to NM_001013699.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr1:9305182 G>T maps to NM_004285.3 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:42997319 G>A maps to NM_012205.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:43015731 G>C maps to NM_012205.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr2:42997322 G>A maps to NM_012205.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:99227699 T>G maps to NM_014282.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:99227624 T>G maps to NM_014282.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr9:99252295 G>A maps to NM_014282.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr6:105239458 G>A maps to NM_020771.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18I-01A-11D-A12B-09 chr6:105198287 G>A maps to NM_020771.3 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr6:105244541 G>C maps to NM_020771.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr6:105224703 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:15609478 T>C maps to NM_012260.2 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr3:15642906 G>A maps to NM_012260.2 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr3:15613243 C>T maps to NM_012260.2 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr2:26417471 C>T maps to NM_000182.4 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WV-01A-11D-A10G-09 chr2:26432728 T>C maps to NM_000182.4 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr16:1869957 G>A maps to NM_005326.4 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:153855389 G>C maps to NM_004821.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:174450056 G>A maps to NM_021973.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:7864302 C>T maps to NM_017545.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:39887780 C>A maps to ENST00000310778 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr17:39889033 T>C maps to ENST00000310778 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:89424726 G>A maps to NM_178232.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr15:89424726 G>A maps to NM_178232.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:19369470 G>T maps to NM_023002.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr11:46625235 G>T maps to NM_173811.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:140056373 A>C maps to NM_002109.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:140056699 A>C maps to NM_002109.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:122626672 C>T maps to NM_005328.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:172822935 G>A maps to NM_003642.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr4:2233654 C>G maps to NM_024511.5 *604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr19:36110618 C>T maps to NM_015302.1 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr23:152728091 C>T did not map to a codon.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr23:152722093 G>A did not map to a codon.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr23:152721080 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:17179894 A>C maps to NM_033417.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr5:156456794 G>A maps to NM_001173393.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr5:156482503 A>C maps to NM_001173393.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:154248119 G>A maps to NM_006118.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:139722245 C>T maps to NM_001945.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr5:139722293 A>G maps to NM_001945.2 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr11:5275626 A>C maps to ENST00000399563 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:135371785 C>A did not map to a codon.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr6:135299855 G>A maps to NM_006620.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr23:11136710 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr23:11136673 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153222818 T>G did not map to a codon.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr23:153224816 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr23:153218021 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr23:153220766 G>T did not map to a codon.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr23:153219073 G>A did not map to a codon.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr23:153225482 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153218310 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153222965 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr23:153215006 T>C did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:153223546 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr23:153219200 C>T did not map to a codon.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr23:153222201 C>A did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr23:153220422 T>G did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr23:153220494 T>G did not map to a codon.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr23:153224851 G>A did not map to a codon.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr23:153220824 C>T did not map to a codon.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr23:153220380 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:3073235 G>C maps to NM_017885.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:104480762 C>G maps to NM_013320.2 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr12:104458501 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr12:104487162 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:30659554 C>T maps to NM_002110.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr3:121361819 G>A maps to NM_005335.4 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr3:121376168 C>A maps to NM_005335.4 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:45353207 C>G maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr5:45267190 C>A maps to NM_021072.2 G595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr5:45262055 G>A maps to NM_021072.2 D880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr5:45645499 C>T maps to NM_021072.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:603699 C>T maps to NM_001194.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:613252 C>T maps to NM_001194.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:73615748 T>C maps to NM_005477.2 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr1:32089152 G>A maps to NM_001525.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:32085274 C>T maps to NM_001525.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:32092458 C>T maps to NM_001525.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr6:55147108 C>T maps to NM_001526.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr6:55142341 G>A maps to NM_001526.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:36394702 C>T maps to NM_014266.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RP-01A-21D-A099-09 chr1:32768219 A>G did not map to a codon.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr1:32793145 G>A maps to NM_004964.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr1:32798617 G>A maps to NM_004964.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr1:32796495 G>T maps to NM_004964.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr22:50688544 C>T maps to NM_032019.5 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr3:13546038 C>A maps to NM_024827.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:240056336 C>T maps to NM_006037.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:239975186 G>A maps to NM_006037.3 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr2:240066377 G>A maps to NM_006037.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:42170739 C>T maps to NM_001015053.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr17:42161000 C>T maps to NM_001015053.1 W793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr23:48682345 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:48672896 A>C did not map to a codon.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr23:48672894 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:48672896 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:48678615 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:48681409 G>A did not map to a codon.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr23:48665032 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48681417 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr23:48674947 G>T did not map to a codon.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr23:48682593 A>G did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:48681326 G>C did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:48672885 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr23:48661391 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:48681989 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr23:48675746 T>A did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:48681534 A>T did not map to a codon.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr23:48681344 T>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:48190854 G>C maps to NM_015401.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:48185713 G>A maps to NM_015401.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr23:71571587 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:71715092 G>C did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:71681926 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:71684451 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:18705918 G>C maps to NM_178425.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr7:18833075 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:156721132 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:156713978 C>T maps to NM_001126050.1 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:6968401 T>G did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr23:7023815 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr23:6975751 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:7023748 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:242178169 G>A maps to NM_005336.3 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:242181872 A>C did not map to a codon.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr2:242170254 G>A maps to NM_005336.3 D1131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr2:242179046 C>T maps to NM_005336.3 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr2:242179381 G>A maps to NM_005336.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr23:83723942 C>T did not map to a codon.
Sequencing variant TCGA-A2-A1G0-01A-11D-A13L-09 chr23:83730289 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:83723724 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:83581231 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:83591866 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr23:83581198 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:83616511 C>T did not map to a codon.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr23:83724461 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:83724167 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:83724309 T>G did not map to a codon.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr23:83724315 G>C did not map to a codon.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr1:236749562 A>C maps to NM_018072.5 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr1:236738058 C>A maps to NM_018072.5 E1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr1:236739581 C>A maps to NM_018072.5 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr7:825271 C>T maps to NM_017802.3 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr7:810168 C>T maps to NM_017802.3 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr16:50102689 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:50138962 G>A maps to NM_182922.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr16:50112755 G>T maps to NM_182922.2 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:50102696 C>T maps to NM_182922.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:50120138 C>T maps to NM_182922.2 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:31852861 G>A maps to ENST00000389961 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:31856418 G>A maps to ENST00000389961 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr14:31763187 C>T maps to ENST00000389961 K1908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr14:31762748 G>T maps to ENST00000389961 S1962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr14:31763214 G>A maps to ENST00000389961 I1899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr14:31844037 T>C maps to ENST00000389961 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:37247805 G>A maps to NM_019024.1 Q1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:37284540 G>A maps to NM_019024.1 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr2:37306264 T>C maps to NM_019024.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:58156107 G>A maps to NM_022070.4 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr8:145255362 C>T maps to NM_032450.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:145245804 C>G maps to NM_032450.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr8:145246703 C>T maps to NM_032450.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr5:41058281 G>A maps to ENST00000296803 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr5:41009483 C>T maps to ENST00000296803 A1107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:41004558 G>A maps to ENST00000296803 V1362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:41048428 C>A maps to ENST00000296803 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr5:41005743 G>A maps to ENST00000296803 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:41009476 C>A maps to ENST00000296803 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:41018804 T>C maps to ENST00000296803 Q888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr5:41058278 C>T maps to ENST00000296803 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr5:41033172 G>A maps to ENST00000296803 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:138734174 G>A maps to NM_014320.2 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr6:139487769 C>T maps to NM_016217.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr14:31605748 G>C maps to NM_015382.2 Y1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:31585632 G>A maps to NM_015382.2 V1809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:31642856 T>G maps to NM_015382.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr10:93256089 C>T maps to ENST00000446394 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr10:93220310 G>A maps to ENST00000446394 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Q-01A-21W-A050-09 chr7:43590144 C>T maps to NM_015052.3 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr7:43484585 G>A maps to NM_015052.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr7:43482154 C>T maps to NM_015052.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr7:43484511 G>T maps to NM_015052.3 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:43540892 A>C maps to NM_015052.3 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:43484777 T>C maps to NM_015052.3 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr7:43548588 G>A maps to NM_015052.3 S1296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:43580830 G>C maps to NM_015052.3 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr7:43591894 C>A maps to NM_015052.3 I1490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr2:197189775 G>A maps to NM_020760.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr2:197136014 T>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:197085560 A>C maps to NM_020760.1 G1417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:197194347 A>C maps to NM_020760.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr3:124732409 A>G maps to NM_020733.1 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:124689578 C>A maps to NM_020733.1 G1355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:124732037 T>G maps to NM_020733.1 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:124692595 C>T maps to NM_020733.1 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr3:124731511 G>A maps to NM_020733.1 Q971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:66717933 G>A maps to NM_033647.2 K823K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr12:66698652 G>A maps to NM_033647.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:66703994 G>A maps to NM_033647.2 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:65147274 G>C maps to NM_014877.3 S748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:65074571 G>A maps to NM_014877.3 I1875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:65105788 G>T maps to NM_014877.3 S1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:65110474 G>A maps to NM_014877.3 R1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:65134097 G>A maps to NM_014877.3 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:65162699 G>A maps to NM_014877.3 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr17:65074481 C>T maps to NM_014877.3 K1905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr17:65074604 G>A maps to NM_014877.3 G1864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:124805829 G>A maps to NM_152722.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr11:124794752 G>A maps to NM_152722.4 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr7:92826859 G>C maps to ENST00000453812 S382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr7:92848660 T>A maps to ENST00000453812 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr23:65392231 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:65486388 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:65382718 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:65390555 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:65408349 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr23:65475996 C>G did not map to a codon.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr23:65427136 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr23:65418839 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr23:65408291 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:65409532 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:65415032 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr23:65417627 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1NG-01A-21D-A14K-09 chr23:65420444 C>T did not map to a codon.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr23:65409614 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:93826751 G>T maps to NM_001098672.1 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:63937809 C>G maps to ENST00000261887 V3650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:63972326 T>C maps to ENST00000261887 A2166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr15:63964893 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr15:63935168 G>C maps to ENST00000261887 S3807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr15:63970198 G>C maps to ENST00000261887 P2305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr15:64067207 T>C maps to ENST00000261887 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr15:63964738 C>T maps to ENST00000261887 V2667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr15:28408362 C>T maps to NM_004667.4 L3541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr15:28474382 G>A maps to NM_004667.4 R1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:28451474 G>A maps to NM_004667.4 Q2375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AB-01A-11W-A050-09 chr15:28421866 A>G maps to NM_004667.4 S3160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr15:28446655 T>A maps to NM_004667.4 R2554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IH-01A-11D-A10Y-09 chr15:28357016 G>A maps to NM_004667.4 I4799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:28436125 C>T maps to NM_004667.4 L2878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr15:28419643 C>A maps to NM_004667.4 S3318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:28525308 G>A maps to NM_004667.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr15:28386673 G>T maps to NM_004667.4 V3973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:89627933 C>A maps to NM_014606.1 I992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr10:69832856 G>T maps to NM_022079.2 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:69785427 A>C maps to NM_022079.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:69832820 A>C maps to NM_022079.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr10:69684842 C>A maps to NM_022079.2 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr10:69692461 C>T maps to NM_022079.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr4:89388331 C>A maps to NM_016323.2 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr4:89388331 C>A maps to NM_016323.2 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr4:89334349 G>A maps to NM_017912.3 W497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:934930 C>G maps to NM_001142467.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr17:80393720 C>T maps to NM_173620.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr17:43227033 G>A maps to NM_006460.2 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:80677500 C>T maps to NM_001040708.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:80677449 A>T maps to NM_001040708.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr8:80679522 C>T maps to NM_001040708.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr8:80677524 G>A maps to NM_001040708.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr1:40092513 G>A maps to NM_014571.3 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:40098332 C>T maps to NM_014571.3 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr1:145415807 G>A maps to NM_213653.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:81339533 C>T maps to NM_000601.4 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr4:3445880 C>T maps to ENST00000511533 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr4:3445880 C>T maps to ENST00000511533 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:43033330 C>T maps to ENST00000458501 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr1:210637882 C>T maps to NM_001170580.1 Y297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr3:42740388 G>T maps to NM_020707.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:100118805 C>T maps to NM_001127258.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:100118586 C>T maps to NM_001127258.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr14:100118810 C>G maps to NM_001127258.1 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:100138716 C>A maps to NM_001127258.1 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:222721349 G>A maps to NM_024746.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:70820798 G>A maps to ENST00000432224 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr14:62187183 T>C maps to ENST00000394997 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr14:62193472 C>G maps to ENST00000394997 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr10:102296310 G>A maps to ENST00000442724 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr19:46815778 G>A maps to NM_152795.2 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:175816402 C>T maps to NM_138820.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:119003410 G>A maps to NM_198971.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:75183427 T>G maps to NM_005338.4 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr7:75192286 C>T maps to NM_005338.4 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:75192344 G>C maps to NM_005338.4 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr7:75221830 C>T maps to NM_005338.4 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr12:123333100 C>G maps to NM_003959.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EW-01A-21D-A10Y-09 chr7:139257729 G>C maps to NM_022740.4 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr7:139305146 C>T maps to NM_022740.4 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr7:139416106 C>A maps to NM_022740.4 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:139281599 G>A maps to NM_022740.4 G860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:139257858 T>C maps to NM_022740.4 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:33370298 G>A maps to NM_005734.3 V867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:33373168 G>A maps to NM_005734.3 E941E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:33360385 G>A maps to NM_005734.3 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:40895446 G>C maps to NM_144685.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FR-01A-11D-A13L-09 chr19:40889791 G>A maps to NM_144685.3 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr22:19348810 T>C maps to NM_003325.3 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:19338951 G>A maps to NM_003325.3 R956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr22:19349294 C>T maps to NM_003325.3 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr22:19349344 G>A maps to NM_003325.3 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr22:19346929 C>T maps to NM_003325.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:26056107 C>T maps to NM_005319.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:26056116 C>A maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr6:26056284 G>T maps to NM_005319.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:26234496 C>T maps to NM_005320.2 *222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr6:26199317 G>A maps to NM_021065.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr6:26217366 G>A maps to NM_021052.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr6:26217378 G>T maps to NM_021052.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:27101161 A>G maps to NM_021064.4 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr6:27115266 G>A maps to NM_080596.1 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr6:27115248 C>G maps to NM_080596.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr6:27776368 A>T maps to NM_003509.2 K128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr6:27782386 G>A maps to NM_021066.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr6:27782244 C>A maps to NM_021066.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr6:27805931 C>T maps to NM_003510.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr6:27860569 T>A maps to NM_003514.2 K120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr6:27860645 G>A maps to NM_003514.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr6:26043594 C>A maps to NM_021062.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr6:26043569 C>A maps to NM_021062.2 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr6:26123994 C>G maps to NM_003526.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr6:26123903 C>A maps to NM_003526.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:26158659 C>A maps to NM_138720.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:26184322 C>G maps to NM_003523.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:26200094 G>A maps to NM_003522.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:26216589 C>T maps to NM_003518.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr6:26252225 T>G maps to NM_003524.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr6:26251946 G>A maps to NM_003524.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr6:26273271 G>A maps to NM_003525.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr6:27100193 C>A maps to NM_021058.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr6:27114439 C>T maps to NM_080593.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr6:27806522 G>A maps to NM_003520.3 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr6:27861509 C>T maps to NM_003527.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr6:26032005 C>A maps to NM_003537.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr6:26032135 C>T maps to NM_003537.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:26032114 C>A maps to NM_003537.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr6:26271387 G>A maps to NM_003534.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:27778003 G>A maps to NM_003536.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:26027257 C>A maps to NM_003544.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:26189127 C>T maps to NM_003539.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:26188993 C>A maps to NM_003539.3 *104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:26205069 G>T maps to NM_003545.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:26204904 G>A maps to NM_003545.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr6:26205021 C>T maps to NM_003545.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr6:26247073 G>C maps to NM_003547.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr6:27107359 C>G maps to NM_003495.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:27798994 C>T maps to NM_003541.2 *104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr1:149858865 C>G maps to NM_003517.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr1:149858595 C>A maps to NM_003517.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr1:149858775 C>G maps to NM_003517.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr1:149858553 G>A maps to NM_003517.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr1:149857968 G>A maps to NM_003528.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr1:149784972 C>T maps to NM_001123375.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:14923904 G>T maps to NM_175054.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:12161806 C>A maps to NM_002114.2 S2208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr6:12164531 G>A maps to NM_002114.2 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:12125791 T>C maps to NM_002114.2 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:12161697 C>T maps to NM_002114.2 R2172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr6:12121103 C>G maps to NM_002114.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr6:143093048 G>A maps to NM_006734.3 R943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr6:143091477 G>A maps to NM_006734.3 Y1466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr6:143074258 C>T maps to NM_006734.3 K2442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr6:143092671 C>G maps to NM_006734.3 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:42049025 G>A maps to NM_024503.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr1:41978909 G>C maps to NM_024503.3 P1994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EX-01A-21W-A050-09 chr10:71154850 C>T maps to ENST00000439900 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr10:71144574 C>T maps to ENST00000439900 C616C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:71158401 G>C maps to ENST00000439900 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr10:71060617 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:75107614 C>A maps to NM_000189.4 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr2:75107454 C>T maps to NM_000189.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr10:71007229 G>T maps to NM_025130.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr19:37853954 C>T maps to NM_181786.2 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:37838096 C>T maps to NM_181786.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr19:37853115 C>A maps to NM_181786.2 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr19:37853009 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr6:29910603 C>A maps to ENST00000376806 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr6:29910603 C>A maps to ENST00000376806 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr6:29910335 C>T maps to ENST00000376806 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:29911953 G>T maps to ENST00000376806 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr6:31324103 G>A maps to ENST00000428231 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr6:31239009 G>A maps to ENST00000383329 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr6:31238991 G>C maps to ENST00000383329 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr6:31239445 G>A maps to ENST00000383329 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr6:32917496 T>C maps to NM_006120.3 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:32609761 C>T maps to NM_002122.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:32709261 G>A maps to NM_020056.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CZ-01A-11W-A050-09 chr6:32632632 C>T maps to ENST00000374943 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BS-01A-11D-A12Q-09 chr6:32634372 C>T maps to ENST00000374943 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr6:32634372 C>T maps to ENST00000374943 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr6:32552155 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr6:32551997 G>A maps to NM_002124.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr6:32557477 C>A maps to NM_002124.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:32549463 T>C maps to NM_002124.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr6:32549547 G>A maps to NM_002124.2 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr6:32549562 G>A maps to NM_002124.2 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr6:32497904 G>T maps to NM_002125.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr6:29693317 G>T maps to NM_001098479.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr17:53342934 G>A maps to NM_002126.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr3:148750057 G>A maps to NM_003071.3 D993D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:221054581 C>G maps to NM_021958.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr1:221054584 A>C maps to NM_021958.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25C-01A-11D-A167-09 chr1:185962312 G>C did not map to a codon.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr1:186106711 G>T maps to NM_031935.2 L4555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr1:185880812 G>A maps to NM_031935.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr1:186010159 C>T maps to NM_031935.2 R2066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:186014910 A>C maps to NM_031935.2 P2132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:185969324 C>T maps to NM_031935.2 V1341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:186031691 A>G maps to NM_031935.2 V2491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:186034376 A>G maps to NM_031935.2 P2507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:186120828 C>T maps to NM_031935.2 L4950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr1:185892720 C>A maps to NM_031935.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr1:186026399 T>C maps to NM_031935.2 P2393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr1:186023071 G>A maps to NM_031935.2 S2272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr1:186086185 T>A maps to NM_031935.2 Y3874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr15:77763313 G>A maps to NM_018200.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr15:77759648 G>A maps to NM_018200.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:77769895 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:3575617 G>A maps to NM_006339.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr19:3574547 C>T maps to NM_006339.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:34208574 G>A maps to NM_145899.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr23:150155774 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:150154161 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:150156381 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr23:150156318 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr6:55441923 G>C maps to NM_019036.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:74650359 C>T maps to NM_000859.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr5:74640148 A>G maps to NM_000859.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:43294890 G>C maps to NM_002130.6 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr5:43294938 G>T maps to NM_002130.6 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr5:43298902 C>T maps to NM_002130.6 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr5:43294890 G>C maps to NM_002130.6 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr1:120301759 G>T maps to NM_005518.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr23:80371789 G>T did not map to a codon.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr23:80370667 T>G did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr23:80371737 C>A did not map to a codon.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr22:35661430 C>A maps to NM_001003681.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:1083180 G>A maps to NM_012292.2 G928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr19:1073547 C>T maps to NM_012292.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr5:162905689 G>T maps to NM_001142556.1 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr5:162910043 G>A maps to NM_001142556.1 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr5:162891727 G>A did not map to a codon.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr22:35789488 G>A maps to NM_002133.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr22:35779122 C>T maps to NM_002133.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr16:4559693 C>G maps to NM_001127205.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr17:73132262 C>T maps to NM_016185.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr17:36099430 G>A maps to NM_000458.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IE-01A-11D-A188-09 chr20:43052730 C>T maps to ENST00000338692 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr20:43036107 G>A maps to ENST00000338692 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr8:76465338 T>C maps to NM_004133.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr5:137089509 C>T maps to NM_006805.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr7:26233302 C>A maps to NM_031243.2 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr2:178080347 C>T maps to NM_194247.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr5:177634109 T>C maps to NM_031266.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:21702334 G>A maps to NM_031314.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr10:43882981 T>A maps to NM_001098204.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:179043939 G>A maps to NM_005520.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:179044635 G>T maps to NM_005520.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:100668169 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:100668169 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:100667406 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr23:100668304 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr23:100667033 T>A did not map to a codon.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr23:100668218 C>A did not map to a codon.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr23:100667604 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:70101399 A>G maps to NM_012207.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:39334665 C>T maps to ENST00000221419 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr19:39329198 G>T maps to ENST00000221419 Y465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr1:23660096 G>A maps to ENST00000414299 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr1:23648157 T>C did not map to a codon.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr1:245027314 G>A maps to NM_031844.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:245021465 A>G maps to NM_031844.2 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:41774179 C>T maps to NM_007040.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr11:62487501 C>T maps to NM_001079559.1 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24P-01A-11D-A167-09 chr4:83350515 G>A maps to NM_031372.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr2:38795341 C>G maps to NM_138394.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:38829675 C>T maps to NM_138394.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr15:83523512 G>T maps to NM_199330.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:23745734 G>A maps to NM_020834.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:60331544 A>G maps to NM_015888.4 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr1:60333999 G>T maps to NM_015888.4 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr8:42873639 A>G maps to NM_032410.3 *719W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:150672638 T>A maps to NM_032132.4 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:150676670 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:30514991 C>T maps to NM_152510.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr7:27134949 G>A maps to NM_005522.4 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr7:27213490 C>A maps to NM_018951.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:27211757 G>A maps to NM_018951.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:27222522 G>C maps to NM_005523.5 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr7:27238808 C>G maps to NM_000522.4 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr7:27148061 G>A maps to NM_153631.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:27203248 G>A maps to NM_152739.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr17:46608134 G>A maps to NM_002144.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr17:46607828 G>A maps to NM_002144.3 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr17:46805421 C>T maps to NM_006361.5 W178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr17:46628037 C>T maps to NM_002146.4 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr17:46670816 G>A maps to NM_002147.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr12:54379357 C>G maps to NM_017409.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:54369061 G>A maps to NM_014212.3 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr12:54448688 G>C maps to NM_153633.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr12:54448949 G>A maps to NM_153633.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:54403415 C>A maps to NM_022658.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:54394136 C>T maps to NM_006897.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:176981647 C>T maps to NM_002148.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr2:176958330 G>A maps to NM_000523.3 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:177033860 C>T maps to NM_006898.4 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr2:176996276 C>T maps to NM_019558.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr16:72094179 C>T maps to NM_005143.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:21076288 C>T maps to NM_016287.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr1:21076219 A>G maps to NM_016287.3 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr2:10560113 C>T maps to NM_002149.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:40149704 G>A maps to NM_016257.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:122294312 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr19:35540194 T>G maps to NM_182983.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:100179912 G>A maps to NM_000195.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr3:148871408 G>A maps to NM_032383.3 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KD-01A-12D-A20S-09 chr22:26868809 G>A maps to NM_022081.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr22:26860226 T>G maps to NM_022081.4 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:26854462 C>T maps to NM_022081.4 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr22:26859978 C>T maps to NM_022081.4 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:18306956 G>A maps to NM_181507.1 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr4:84231231 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr10:100904058 A>G maps to NM_021828.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr10:100374726 C>G maps to NM_021828.4 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr11:6452494 G>C maps to NM_000613.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:6453143 G>T maps to NM_000613.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:6452442 A>G maps to NM_000613.2 *463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr3:192988398 C>A maps to NM_020386.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr19:49657821 C>A maps to NM_002152.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:49654781 G>T maps to NM_002152.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr19:49655282 G>C maps to NM_002152.2 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:186395437 T>C maps to NM_000412.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr3:11301538 C>G maps to NM_001098211.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr3:11301810 C>A maps to NM_001098211.1 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:175111226 G>T maps to NM_001131055.1 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:152191269 A>T maps to NM_001009931.1 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:152192115 G>A maps to NM_001009931.1 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:152187861 A>G maps to NM_001009931.1 Y2081Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr1:152185556 G>A maps to NM_001009931.1 Q2850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr1:152186442 A>G maps to NM_001009931.1 H2554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H5-01A-21D-A10Y-09 chr1:152191464 G>A maps to NM_001009931.1 R880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr1:152186442 A>G maps to NM_001009931.1 H2554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr1:152186613 C>G maps to NM_001009931.1 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr1:152192918 G>A maps to NM_001009931.1 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr1:152186613 C>G maps to NM_001009931.1 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr1:152191389 G>A maps to NM_001009931.1 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:87538856 T>C did not map to a codon.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr16:22926831 G>A maps to NM_006043.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr16:22926627 C>T maps to NM_006043.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr16:22926862 C>T maps to NM_006043.1 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr17:13399615 A>T maps to NM_006042.1 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BA-01A-11W-A071-09 chr16:26147358 T>C maps to NM_006040.2 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:26147544 G>A maps to NM_006040.2 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr16:26147247 C>T maps to NM_006040.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:114379008 G>A maps to NM_153612.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr2:129075960 T>C maps to NM_004807.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr2:129075960 T>C maps to NM_004807.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr23:131762533 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr23:131762941 T>C did not map to a codon.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr23:131762770 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr23:131762516 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:132091142 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr23:131762776 A>C did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:131762562 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr13:97485349 G>A maps to NM_153456.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr23:53460759 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:53459269 G>A did not map to a codon.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr4:88258483 G>A maps to NM_016245.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr9:99064320 C>T maps to NM_000197.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SG-01A-11D-A142-09 chr5:118835163 C>T maps to NM_000414.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr12:57181032 T>A maps to NM_003725.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:57178646 C>T maps to NM_003725.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:162773288 G>A maps to NM_016371.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:162769552 C>G maps to NM_016371.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr1:162767618 T>C maps to NM_016371.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr6:33172844 G>A maps to NM_014234.3 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr16:30997511 G>A maps to NM_025193.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:115200847 G>T maps to NM_032303.4 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr9:115200811 A>T maps to NM_032303.4 K234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:56540555 G>A maps to NM_001080439.1 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:56540484 G>T maps to NM_001080439.1 C400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:44218083 T>G maps to NM_007355.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr6:44220996 G>A maps to NM_007355.2 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr6:44221292 C>T maps to NM_007355.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr6:44218044 G>A maps to NM_007355.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr6:44219553 G>A maps to NM_007355.2 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr12:104337514 G>C did not map to a codon.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr12:104332120 G>T maps to NM_003299.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr10:118439272 C>T did not map to a codon.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr10:118439099 C>T maps to NM_025015.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr10:118458151 C>T maps to NM_025015.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:3731520 C>T maps to NM_052970.4 Q458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr21:15750637 C>T maps to NM_006948.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:14912622 G>T maps to NM_016299.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr6:31783754 T>C maps to NM_005345.5 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:31779257 A>C maps to NM_005527.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:132424818 C>T maps to NM_002154.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:132424802 A>G maps to NM_002154.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:128726846 G>A maps to ENST00000438626 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr4:128751920 G>A maps to ENST00000438626 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HU-01A-11W-A050-09 chr9:128001806 G>A maps to NM_005347.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr11:122929478 G>A maps to NM_006597.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr5:137909536 G>C maps to NM_004134.6 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:137893675 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:16342075 C>T maps to ENST00000375714 *259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr17:40275311 G>T maps to NM_033194.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:122478176 C>A maps to NM_024610.4 G155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr19:55790901 C>G maps to NM_012267.4 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr2:64683523 T>A maps to NM_014181.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr2:198363533 C>T maps to NM_199440.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:198358178 C>T maps to NM_199440.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:22154745 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:22216563 G>A maps to NM_005529.5 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr1:22179534 G>T maps to NM_005529.5 I2156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DD-01A-31D-A12Q-09 chr1:22167761 G>A maps to NM_005529.5 S3115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr1:22174304 G>A maps to NM_005529.5 I2634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:22160415 A>G maps to NM_005529.5 L3575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:22174271 C>T maps to NM_005529.5 Q2645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:20398234 C>G maps to NM_001098520.1 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr23:135584978 G>A did not map to a codon.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr23:135592322 G>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:135593710 G>A did not map to a codon.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr23:135581800 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135593994 C>T did not map to a codon.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr23:135586548 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr23:135593305 G>A did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:135594141 C>T did not map to a codon.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr23:135593485 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr23:135582351 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:135592334 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:135593358 T>C did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:135593185 G>A did not map to a codon.
Sequencing variant TCGA-E9-A2JT-01A-22D-A18P-09 chr23:135593756 G>C did not map to a codon.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr4:70898888 G>A maps to NM_000200.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:63257402 G>A maps to NM_000524.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr6:78172232 G>A maps to NM_000863.1 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr6:78172400 C>T maps to NM_000863.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr6:78172316 G>C maps to NM_000863.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:23519995 G>A maps to NM_000864.4 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:47409027 C>A maps to NM_000621.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr13:47409442 G>A maps to NM_000621.3 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr13:47409634 C>A maps to NM_000621.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr2:231988412 G>C maps to NM_000867.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XX-01A-21D-A23C-09 chr23:114141665 G>T did not map to a codon.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr23:114082685 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:114082716 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:114082646 A>C did not map to a codon.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr23:114141230 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:114141976 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1P0-01A-11D-A142-09 chr23:114141529 C>T did not map to a codon.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr23:114082706 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:113860483 G>C maps to NM_213621.3 *517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr11:113815319 C>T maps to NM_006028.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr11:113815301 C>T maps to NM_006028.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:183777384 C>G maps to NM_130770.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:183772650 C>T maps to NM_130770.2 F70F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A8-A0A6-01A-12W-A071-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:183756197 T>G maps to NM_001145143.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr3:183755825 G>A maps to NM_001145143.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr3:183753876 C>T maps to NM_001145143.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr3:183823578 C>A maps to NM_182589.2 L264L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AN-A0XT-01A-11D-A10G-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-E2-A14N-01A-31D-A135-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr7:154863223 C>T maps to NM_024012.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:92509170 C>T maps to NM_019859.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:92617140 G>A maps to NM_019859.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:124268260 G>A maps to NM_002775.4 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:74758058 C>T maps to NM_013247.4 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr4:8294068 C>T maps to NM_053044.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr4:8305970 T>A maps to NM_053044.3 Y387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr8:38832595 C>G maps to NM_153692.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr4:3162103 G>T maps to NM_002111.6 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr4:3134376 C>T maps to NM_002111.6 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:3235056 C>T maps to NM_002111.6 L2811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BO-01A-23D-A12B-09 chr4:3148606 C>G maps to NM_002111.6 S1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr4:3179078 G>A maps to NM_002111.6 L1476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr21:33331188 C>T maps to NM_014586.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:33371430 A>C maps to NM_014586.1 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:48016404 C>T maps to NM_004507.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr23:53570823 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:53587266 T>G did not map to a codon.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr23:53652125 A>G did not map to a codon.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr23:53575990 C>T did not map to a codon.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr23:53561636 G>A did not map to a codon.
Sequencing variant TCGA-A7-A3J1-01A-11D-A20S-09 chr23:53602624 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr23:53573666 C>G did not map to a codon.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr23:53573460 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr23:53644082 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:53560334 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:53562390 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr23:53565353 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:53596650 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:53610640 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:53642740 G>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:53561009 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53560293 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53566023 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53574687 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53577888 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:53675210 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr23:53661225 A>T did not map to a codon.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr23:53563525 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr23:53589796 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr23:53617396 A>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:53616682 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:53644040 C>A did not map to a codon.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr23:53588773 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:53570802 G>A did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:53631743 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:53575139 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:53655569 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:53589823 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr23:53581745 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr23:53561597 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr23:53562451 A>C did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:53589092 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:53563166 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:53589160 G>C did not map to a codon.
Sequencing variant TCGA-LL-A5YN-01A-11D-A28B-09 chr23:53631551 G>C did not map to a codon.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr23:53610742 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:50357749 C>G maps to NM_033158.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:50330901 G>A maps to NM_003549.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr16:70989286 C>A maps to NM_032821.2 E2102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr16:71163692 A>G maps to NM_032821.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr16:70993580 G>A maps to NM_032821.2 I2036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr16:70928401 C>T maps to NM_032821.2 A3065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr16:70942228 G>A maps to NM_032821.2 I2773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:70989398 C>G maps to NM_032821.2 L2064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr16:71008517 G>A maps to NM_032821.2 R1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr16:71163692 A>G maps to NM_032821.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr16:70993565 A>G maps to NM_032821.2 H2041H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr16:70841560 C>T maps to NM_032821.2 L5095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr16:70900082 G>T maps to NM_032821.2 T3819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr16:70852400 G>A maps to NM_032821.2 I4833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr16:71098724 G>C maps to NM_032821.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr16:71163611 C>T maps to NM_032821.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:70884494 G>A maps to NM_032821.2 C4168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr16:70871622 G>C maps to NM_032821.2 V4403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr11:118926848 C>T maps to NM_001130991.1 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:21531359 G>C maps to NM_000415.2 *90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr9:94985651 G>A maps to ENST00000375660 Q1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr9:95027829 T>A maps to ENST00000375660 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:95025285 G>A maps to ENST00000375660 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T7-01A-21D-A099-09 chr1:220269534 C>T maps to NM_018060.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr1:220275716 C>A maps to NM_018060.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:220284182 T>C maps to NM_018060.3 H461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:220316388 A>G maps to NM_018060.3 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:220273921 G>T maps to NM_018060.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:220300109 T>C maps to NM_018060.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:88723674 C>T maps to NM_004967.3 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:88723880 C>T maps to NM_004967.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr6:82924533 A>G maps to NM_015525.2 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr7:8167560 A>G maps to ENST00000422063 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr7:8153624 A>G maps to ENST00000422063 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:203676512 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr2:203653622 G>A maps to NM_138468.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr17:62083990 C>A maps to NM_001099789.1 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:52870087 C>T maps to NM_016513.4 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:52883202 G>C maps to NM_016513.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr6:52876588 C>T maps to NM_016513.4 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:204820494 C>G maps to NM_012092.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr21:45648917 C>G maps to NM_015259.4 *303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr21:45651312 C>A maps to ENST00000400379 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:94291538 C>T maps to NM_004969.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A248-01A-11D-A167-09 chr10:94234711 G>A maps to NM_004969.3 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr2:209113242 C>T maps to NM_005896.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:78454028 C>T maps to NM_005530.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr23:153055670 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:153055738 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:148584846 T>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:148564414 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr23:148571917 G>T did not map to a codon.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr23:148568513 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:148579794 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr23:148568555 T>G did not map to a codon.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr23:148584950 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:148568836 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:181058943 C>A maps to NM_016545.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:158986468 A>C maps to ENST00000295809 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr1:159021842 A>G maps to ENST00000295809 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr1:159021524 G>A maps to ENST00000295809 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:158985710 T>C maps to ENST00000295809 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:158990207 A>G maps to ENST00000295809 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr17:41164294 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr17:41165359 C>G maps to NM_005533.4 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A248-01A-11D-A167-09 chr17:41165617 C>T maps to NM_005533.4 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:79120817 C>A maps to NM_006417.4 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:79125146 C>T maps to NM_006417.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:91162829 T>G maps to NM_001548.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0D9-01A-31W-A071-09 chr10:91143441 T>C maps to NM_001010987.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr10:91143778 G>T maps to NM_001010987.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr10:91066306 G>A maps to NM_001547.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr10:91099110 C>A maps to NM_001549.4 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr10:91178166 T>G maps to NM_012420.2 L404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:91178389 C>G maps to NM_012420.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DD-01A-31D-A12Q-09 chr11:319873 G>A maps to NM_021034.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr9:21367847 C>T maps to NM_006900.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:21217190 C>T maps to NM_002173.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr9:21227803 C>A maps to NM_021268.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr9:21384860 C>T maps to NM_000605.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr9:21304985 G>C maps to NM_002169.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr9:21201825 G>T maps to NM_021057.2 Y113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr21:34721849 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr21:34717588 C>T maps to NM_000629.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr21:34625118 A>C maps to NM_207585.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr21:34635688 C>T maps to NM_207585.1 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr21:34617289 A>G maps to NM_207585.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr9:21077513 G>A maps to NM_002176.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr9:21481117 G>A maps to NM_176891.4 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr9:21481248 G>A maps to NM_176891.4 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr12:68552012 A>G maps to NM_000619.2 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:137524671 C>A maps to NM_000416.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr9:27524612 G>A maps to NM_020124.2 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:112096971 G>A maps to NM_001007245.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr3:50326326 G>A maps to ENST00000336089 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr3:129180116 C>T maps to NM_052985.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr3:129234419 C>T maps to NM_052985.2 F1132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr3:129207206 G>A maps to NM_052985.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr3:129183528 C>A maps to NM_052985.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr3:129200410 C>G maps to NM_052985.2 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:1607967 G>A maps to NM_014714.3 D789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr16:1570260 G>A maps to NM_014714.3 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:1621411 G>T maps to NM_014714.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A249-01A-11D-A167-09 chr16:1575898 C>A maps to NM_014714.3 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr16:1570680 C>T maps to NM_014714.3 Q1194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:27707129 A>C maps to NM_015662.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:27706175 C>A maps to NM_015662.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:27668691 G>A maps to NM_015662.1 L1612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:27672429 C>A did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr2:27707102 G>A maps to NM_015662.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:27688294 T>C maps to NM_015662.1 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr20:42275616 T>C maps to NM_016004.2 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr20:42271261 C>T maps to NM_016004.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:42264643 T>G maps to NM_016004.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr20:42271137 A>G maps to NM_016004.2 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr3:160095281 T>A maps to ENST00000326448 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr3:159976354 T>A maps to ENST00000483754 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr13:21172875 G>A maps to NM_175605.3 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:69385789 A>C did not map to a codon.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr23:69353825 C>T did not map to a codon.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr15:65623552 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:65621901 C>T maps to NM_004884.3 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr15:65627715 G>A maps to NM_004884.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr15:65694818 G>A maps to NM_020962.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr15:65676705 C>A maps to NM_020962.1 E1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr15:99465385 G>A maps to NM_000875.3 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr15:99500586 C>T maps to NM_000875.3 F1340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:47118820 G>A maps to NM_006546.3 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:185376146 C>T maps to NM_006548.4 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:185363396 C>T maps to NM_006548.4 K574K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:185410496 C>A maps to NM_006548.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:185542724 C>T maps to NM_006548.4 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr3:185369914 G>T maps to NM_006548.4 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:23391171 C>T maps to NM_006547.2 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr7:23352362 A>G maps to NM_006547.2 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr6:160489289 T>C maps to NM_000876.2 A1375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr6:160461697 C>T maps to NM_000876.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr6:160496979 C>T maps to NM_000876.2 F1756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr6:160500676 A>G maps to NM_000876.2 G1848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:160510201 G>A maps to NM_000876.2 K2128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr6:160477533 C>T maps to NM_000876.2 Q925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:160482884 C>T maps to NM_000876.2 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr16:1840819 C>T maps to NM_001146006.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr16:1841613 G>A maps to NM_001146006.1 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr7:45928352 C>T maps to NM_000596.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr7:45956970 C>T maps to NM_001013398.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:217542936 G>A maps to NM_000599.3 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr19:46627330 G>A maps to NM_207393.1 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr1:201178469 G>A maps to NM_001164586.1 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr11:68678968 G>A maps to NM_002180.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr11:68678992 C>T maps to NM_002180.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr19:51831945 C>G maps to NM_001101372.1 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr23:130409528 T>C did not map to a codon.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr23:130409476 G>T did not map to a codon.
Sequencing variant TCGA-A8-A096-01A-11W-A019-09 chr23:130410200 A>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:130409513 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:130411004 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:130407800 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:130410078 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:130416512 T>C did not map to a codon.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr23:130409565 G>T did not map to a codon.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr23:130411976 G>T did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:130412088 G>T did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr23:130419140 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr23:130416482 T>C did not map to a codon.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr23:130408819 C>T did not map to a codon.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr23:130409099 G>T did not map to a codon.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr23:130410057 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr23:130409211 G>T did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:151163472 C>T maps to NM_178822.4 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr3:151155622 T>C maps to NM_178822.4 T2242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:151166298 A>C maps to NM_178822.4 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:151163431 G>C maps to NM_178822.4 S1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr3:151166526 A>T maps to NM_178822.4 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr3:151165428 G>T maps to NM_178822.4 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr3:151162893 T>A maps to NM_178822.4 P1625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr3:151164276 A>C maps to NM_178822.4 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr1:18691739 A>G maps to NM_032880.4 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr11:18739610 G>A maps to NM_173588.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:18735827 G>A maps to NM_173588.3 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr11:18727601 C>T maps to NM_173588.3 V1224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr1:117131544 G>A maps to NM_001542.2 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr1:117146249 A>G maps to NM_001542.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:117122182 G>A maps to NM_001542.2 F1075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ES-01A-11D-A135-09 chr1:117127360 G>T maps to NM_001542.2 C938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:117142950 G>T maps to NM_001542.2 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr1:117142613 G>A maps to NM_001542.2 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr21:41137564 C>G maps to NM_001080444.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr1:160063722 G>C maps to NM_052868.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr1:160062102 T>C maps to NM_052868.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr1:160063722 G>C maps to NM_052868.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:159901699 C>A maps to NM_001135050.1 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:159904598 G>A maps to NM_001135050.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr1:159900121 G>A maps to NM_001135050.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr1:159901652 G>A maps to NM_001135050.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr11:133801653 G>A maps to NM_014987.1 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:133790400 C>T maps to NM_014987.1 K1073K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L6-01A-11D-A13L-09 chr11:133790478 G>A maps to NM_014987.1 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr2:219925126 C>A maps to NM_002181.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr2:219920402 C>G maps to NM_002181.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:140037203 G>T maps to NM_006083.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:111668704 A>G maps to NM_003640.3 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr9:111674595 C>G maps to NM_003640.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27I-01A-11D-A16D-09 chr9:111663919 G>A maps to NM_003640.3 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr8:42174287 G>T maps to NM_001556.2 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr1:206658370 C>T maps to NM_014002.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr1:206658613 G>A maps to NM_014002.3 K529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr1:206648209 C>T maps to NM_014002.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:206658610 G>A maps to NM_014002.3 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr1:206649566 C>T maps to NM_014002.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:50468069 C>T maps to NM_006060.3 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr17:37922576 C>T maps to NM_012481.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr12:56428779 C>T maps to NM_022465.3 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr10:124753898 G>A maps to NM_022466.5 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:117869437 G>A maps to NM_001558.3 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr11:117859103 G>A maps to NM_001558.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr9:34655291 C>T maps to NM_001142784.1 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr9:34655615 C>T maps to NM_001142784.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:159713201 C>T maps to NM_000882.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:158743779 G>A maps to NM_002187.2 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:117895248 C>G did not map to a codon.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr23:114242506 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr23:114250276 C>G did not map to a codon.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr23:114242610 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr23:114242576 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr23:114242524 T>C did not map to a codon.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr23:114244200 A>C did not map to a codon.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr23:114239779 G>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:81572014 C>T maps to NM_172217.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr15:81598848 C>T maps to NM_172217.3 H1256H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:81592432 C>A maps to NM_172217.3 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr6:52053963 C>A maps to NM_002190.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:52052588 A>C maps to NM_002190.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr5:148754153 G>A maps to NM_014443.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr5:148756492 G>A maps to NM_014443.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr22:17577965 G>A maps to NM_014339.5 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:53891710 G>A maps to NM_018725.3 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr3:9974334 C>T maps to NM_153461.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr3:9959097 C>T maps to NM_153461.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:57144295 C>A maps to NM_017563.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr3:57139977 G>A maps to NM_017563.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr3:57132383 G>A maps to NM_017563.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr11:71712519 G>A maps to NM_001145057.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr11:71712370 G>C did not map to a codon.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr2:102988434 T>C maps to NM_003855.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr1:206972244 C>A maps to NM_153758.2 C2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:113817023 G>C maps to NM_173170.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:113785617 G>T maps to NM_173178.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:113736244 T>G maps to NM_019618.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:102793212 C>T maps to NM_000877.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr2:102644697 G>A maps to NM_004633.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:102641100 G>A maps to NM_004633.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr3:190362052 C>A maps to NM_002182.3 Y356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr3:190321987 A>T maps to NM_002182.3 K46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:29973933 G>T did not map to a codon.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr23:29935649 G>T did not map to a codon.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr23:29301287 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07Z-01A-11W-A019-09 chr23:29935617 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:29301119 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:29972751 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:29973316 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:29301119 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:29686610 G>A did not map to a codon.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr23:29417322 C>G did not map to a codon.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr23:29935695 T>G did not map to a codon.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr23:29301320 G>A did not map to a codon.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr23:29414525 C>G did not map to a codon.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr23:104512184 G>C did not map to a codon.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr23:104961444 G>A did not map to a codon.
Sequencing variant TCGA-AR-A2LL-01A-11D-A17W-09 chr23:105011475 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:104440362 G>C did not map to a codon.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr2:102964504 C>A maps to NM_016232.4 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:102959638 T>G did not map to a codon.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr6:137330611 C>A maps to NM_014432.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr6:137323192 G>A maps to NM_014432.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:123536875 T>G maps to NM_021803.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr6:137482868 G>A maps to NM_052962.2 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr6:137476182 C>A maps to NM_052962.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:67666481 C>G maps to NM_144701.2 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:23842572 C>T maps to NM_022789.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:28511193 C>T maps to NM_145659.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr19:14150607 C>T maps to NM_004843.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr19:39734334 G>A maps to ENST00000392072 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr1:24496054 C>T maps to NM_170743.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:39787500 T>C maps to NM_172140.1 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr22:37540123 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr23:70330749 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:70328514 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:55209368 G>A maps to NM_139017.4 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr16:3119019 A>G maps to ENST00000416912 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:1497590 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:1501284 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:1471271 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:1475213 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr23:1475124 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr19:50397596 C>T maps to NM_172374.1 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr16:27374148 A>T maps to NM_000418.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr16:27375081 G>A maps to NM_000418.2 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:22771135 C>T maps to NM_000600.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:154401670 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:154407478 G>A maps to NM_000565.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:55237577 C>A maps to NM_002184.3 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr5:55237583 C>A maps to NM_002184.3 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:155233502 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:155237195 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:121720278 G>A maps to ENST00000344209 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr1:153635020 C>A maps to NM_004515.2 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr19:10781783 C>T maps to NM_017620.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:10793295 G>A maps to NM_017620.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:10781687 G>C maps to NM_017620.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr19:10795140 G>C maps to NM_001137673.1 *707Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:6631243 A>C maps to NM_001014795.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr11:6631266 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:86371533 G>A maps to NM_006839.2 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr17:43922886 C>T maps to NM_175882.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr17:43923000 T>C maps to NM_175882.2 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24T-01A-11D-A167-09 chr17:43923373 C>A maps to NM_175882.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr17:43924167 C>G maps to NM_175882.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:12009920 T>C maps to NM_014214.1 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr18:12030412 C>T maps to NM_014214.1 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:22030765 A>G maps to NM_018439.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:128033078 G>A maps to NM_000883.3 Y594Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr3:49066744 C>T maps to NM_000884.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr3:49065175 G>C maps to NM_000884.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr3:100976550 G>A maps to NM_016247.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:100964820 A>C maps to NM_016247.2 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:100964784 C>T maps to NM_016247.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:62253531 C>A maps to NM_176877.2 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr1:62374108 A>G maps to NM_176877.2 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:4892805 C>T maps to NM_001167987.1 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr17:4892727 G>T maps to NM_001167987.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:61897584 C>T maps to NM_001040694.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr14:105180654 C>T maps to ENST00000252520 A1052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr13:111372215 G>A maps to NM_005537.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr13:111371873 C>T maps to NM_005537.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr13:111368179 C>G maps to NM_005537.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr7:41729910 G>C maps to NM_002192.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr7:41739756 G>C maps to NM_002192.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr7:41729514 C>T maps to NM_002192.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr7:41729850 G>A maps to NM_002192.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr12:57843319 C>T maps to NM_005538.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:30795235 C>G maps to NM_006774.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr15:41364196 G>A maps to NM_017553.1 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H6-01A-21W-A071-09 chr2:74684834 G>C maps to ENST00000452361 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:206921317 G>A maps to NM_017759.4 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:206920990 G>A maps to NM_017759.4 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr16:30012781 G>A maps to NM_173618.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:191233907 C>T maps to NM_002194.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr2:191236037 A>G maps to NM_002194.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr2:99189390 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr2:99175924 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr2:99204010 G>A maps to NM_001134224.1 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A3DX-01A-21D-A20S-09 chr4:143181717 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:134523912 C>A maps to NM_005539.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr1:38354000 T>C maps to ENST00000373026 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:38409555 G>T maps to ENST00000373026 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:38343875 G>T maps to ENST00000373026 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr2:233925286 C>T maps to ENST00000359570 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:233986822 G>T maps to ENST00000359570 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr10:121583334 C>T maps to NM_014937.2 Q724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:121582586 T>C maps to NM_014937.2 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr22:31524533 C>G maps to ENST00000331075 S696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:31529470 T>C did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr11:71939468 C>T maps to NM_001567.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:71946991 A>C maps to NM_001567.3 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr11:71939421 C>T maps to NM_001567.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:71940779 C>G maps to NM_001567.3 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr11:15170707 G>A maps to NM_001031853.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:15212254 G>A maps to NM_001031853.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:118865891 G>A maps to NM_016133.2 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:118854308 A>C maps to NM_016133.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr2:118864686 C>G maps to NM_016133.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:118864431 C>T maps to NM_016133.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:67263790 T>A maps to NM_005478.3 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A247-01A-11D-A167-09 chr14:36005144 C>A maps to NM_032594.3 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr19:7117095 G>A maps to NM_000208.2 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:7122973 C>T maps to NM_000208.2 K1095K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:7172400 C>A maps to NM_000208.2 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr1:156823930 G>A maps to NM_014215.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:156819149 G>A maps to NM_014215.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr7:1512807 G>A maps to ENST00000389470 F2204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:1533498 C>T maps to ENST00000389470 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:1539235 G>A maps to ENST00000389470 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr7:1527562 C>T maps to ENST00000389470 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr7:1529305 C>T maps to ENST00000389470 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:19694645 G>A maps to NM_018142.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J7-01A-11W-A050-09 chr8:19679948 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr8:19694624 C>T maps to NM_018142.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:106621096 T>C maps to NM_020395.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JS-01A-11D-A13L-09 chr4:106604453 T>A maps to NM_020395.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr17:59967188 G>A maps to NM_020748.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:59967156 C>T maps to NM_020748.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr17:59949624 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:59984940 G>A maps to NM_020748.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr1:153735213 G>A maps to ENST00000428986 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:153733388 C>A maps to ENST00000428986 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:153742292 C>T maps to ENST00000428986 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:153730073 C>T maps to ENST00000428986 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:153730148 C>T maps to ENST00000428986 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:77632421 G>A maps to NM_033547.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr11:77618840 A>G maps to NM_033547.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr11:77639510 T>A maps to NM_033547.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62414521 T>G maps to NM_030628.1 S1010S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:51948401 T>G maps to NM_012141.2 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr13:52026592 G>T maps to NM_012141.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr1:212141941 C>T maps to NM_015434.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr8:95869178 C>T maps to NM_017864.2 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr8:28627465 G>A maps to NM_018250.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:103059202 C>T maps to NM_014425.2 Q931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:103062874 C>G maps to NM_014425.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:33694577 C>T maps to NM_054111.4 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:59956181 A>C maps to NM_152230.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr10:59956130 C>T maps to NM_152230.4 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A126-01A-11D-A10M-09 chr5:61781289 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:44423180 C>T maps to NM_014652.3 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr1:44413298 G>T maps to NM_014652.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr1:44422561 T>C maps to NM_014652.3 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr14:24652346 C>G maps to ENST00000458132 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:24655585 T>G maps to ENST00000458132 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:9466642 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:30787095 G>A maps to NM_006390.3 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr12:30834603 C>A maps to NM_006390.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr12:30823922 G>T maps to NM_006390.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:201841955 C>T maps to NM_018085.4 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr1:201798351 G>A maps to NM_018085.4 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr9:95381787 A>G maps to NM_022755.5 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr9:95378176 G>A maps to NM_022755.5 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:237374266 C>T maps to ENST00000457693 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr2:237240001 C>T maps to ENST00000457693 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr2:237405936 G>A maps to ENST00000457693 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:32673499 G>A maps to NM_001160042.1 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr12:113633597 G>A maps to ENST00000416617 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:2618126 G>C maps to NM_152558.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:51929352 C>A did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr3:51897215 T>C maps to NM_203424.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:51863729 T>G did not map to a codon.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr3:51864468 G>A maps to NM_001085479.1 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr3:197670852 G>A maps to NM_001134435.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr3:197659061 G>A maps to NM_001134435.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr3:197619513 T>C maps to NM_001134435.1 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:91009561 G>A maps to NM_003870.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:91016136 G>C maps to NM_003870.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr5:75967585 C>A maps to NM_006633.2 S949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr5:75993879 G>C maps to NM_006633.2 L1425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:75973154 G>T maps to NM_006633.2 E1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr5:75993916 C>T maps to NM_006633.2 Q1438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr5:75906998 G>A maps to NM_006633.2 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr5:75969809 G>A maps to NM_006633.2 K1081K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr5:75871576 T>C maps to NM_006633.2 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:156520118 G>A maps to NM_178229.4 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18I-01A-11D-A12B-09 chr1:156499902 C>T maps to NM_178229.4 L1466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:156531791 G>C maps to NM_178229.4 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:156531731 G>T maps to NM_178229.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr1:156533414 G>A maps to NM_178229.4 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr3:12977012 C>A maps to ENST00000429247 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr3:12977057 G>A maps to ENST00000429247 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr23:53265516 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:53276154 C>T did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:53276286 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:53280312 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:53264092 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:53283758 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:53267460 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53277314 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr23:53268409 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr23:53283877 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:53276253 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:53267380 C>T did not map to a codon.
Sequencing variant TCGA-OL-A5RU-01A-11D-A28B-09 chr23:53265539 C>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:123109375 G>A maps to NM_178827.4 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr7:123097472 C>A maps to NM_178827.4 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153284455 T>G did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:153281521 C>G did not map to a codon.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr23:153282464 A>T did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:153278075 T>C did not map to a codon.
Sequencing variant TCGA-E2-A14O-01A-31D-A10Y-09 chr23:153284684 C>A did not map to a codon.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr23:153278097 C>T did not map to a codon.
Sequencing variant TCGA-OL-A66H-01A-11D-A29N-09 chr6:79577331 G>A maps to NM_001010844.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr3:10276204 C>T maps to NM_001570.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:10258683 C>T maps to NM_001570.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr12:66597503 A>C maps to NM_007199.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:66620553 G>A maps to NM_007199.2 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr12:66638268 A>C maps to NM_007199.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr15:78775775 G>A maps to NM_004136.2 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:401422 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr16:85954812 C>G maps to NM_002163.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr16:85952386 C>T maps to NM_002163.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr14:24633977 C>T maps to NM_006084.4 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:44097101 G>T maps to NM_001007561.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr2:227662968 C>T maps to NM_005544.2 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr23:107978507 G>C did not map to a codon.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr23:107978146 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr23:107979178 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:107977786 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:107977912 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:107978065 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:107978377 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:107976537 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:107979342 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr23:107976113 C>G did not map to a codon.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr23:107978001 C>T did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:107978763 C>T did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr5:1878505 G>A maps to NM_016358.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:50687232 C>T maps to NM_002202.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:74467696 C>T maps to NM_201526.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:74468368 C>G maps to NM_201526.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr15:74426741 C>T maps to NM_001130137.1 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:74425643 C>T maps to NM_001130137.1 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr14:77942060 G>A maps to NM_199296.2 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr5:128448598 C>T maps to NM_016048.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr22:35480374 G>C did not map to a codon.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr22:35478526 G>A maps to NM_001008494.1 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr12:2932052 G>T maps to NM_018463.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:2929321 G>A maps to NM_018463.3 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr12:2929345 G>A maps to NM_018463.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:314097 C>T maps to NM_032039.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:314834 C>T maps to NM_032039.2 H491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:52211421 C>T maps to NM_181501.1 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr5:52193331 G>A maps to NM_181501.1 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr5:52243218 A>T maps to NM_181501.1 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr1:145538041 C>A maps to NM_003637.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:145537185 C>G maps to NM_003637.3 S786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr1:145535833 C>G maps to NM_003637.3 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr1:145539029 C>T maps to NM_003637.3 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr1:145530312 C>T maps to NM_003637.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr15:68599781 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr15:68624256 G>A maps to ENST00000423218 H570H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:68642964 G>A maps to ENST00000423218 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:68642961 G>A maps to ENST00000423218 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr15:68631958 G>T maps to ENST00000423218 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr15:68612681 T>A maps to ENST00000423218 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr5:52361804 C>T maps to NM_002203.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr5:52363034 C>T maps to NM_002203.3 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:42458328 G>T maps to NM_000419.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:48148879 T>C maps to NM_002204.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:48156612 C>G maps to NM_002204.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr17:48156480 G>T maps to NM_002204.2 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:182363437 G>C maps to NM_000885.4 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr2:182399015 C>T maps to NM_000885.4 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr2:182339923 G>A maps to NM_000885.4 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:182374491 A>C maps to NM_000885.4 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:54795427 T>C maps to NM_002205.2 Q776Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:56091781 A>C maps to ENST00000347027 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:56096913 C>T maps to ENST00000347027 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr10:15628599 C>T maps to NM_003638.1 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:15617486 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:15686061 C>A maps to NM_003638.1 G456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:15714659 C>T maps to NM_003638.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:15617551 C>T maps to NM_003638.1 W805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr10:15573047 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:15628629 C>T maps to NM_003638.1 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr10:15697405 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:37818951 G>T maps to NM_002207.2 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr16:31422066 C>A maps to ENST00000444228 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr16:31424208 G>A maps to ENST00000444228 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr16:31425770 G>C did not map to a codon.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr17:3620002 C>T maps to NM_002208.4 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:30485580 G>A maps to NM_002209.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:30485580 G>A maps to NM_002209.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr16:30515579 A>C maps to NM_002209.2 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:31342566 C>T maps to NM_001145808.1 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr16:31341485 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr16:31340572 C>G maps to NM_001145808.1 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr16:31336601 G>T maps to NM_001145808.1 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr2:187521034 G>T maps to NM_002210.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:187511545 A>C maps to NM_002210.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr2:187540545 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr2:187516747 G>T maps to NM_002210.3 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr2:187455103 C>G maps to NM_002210.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr16:31384614 A>G maps to NM_000887.3 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr16:31371717 C>T maps to NM_000887.3 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr16:31374514 C>G maps to NM_000887.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr16:31373986 C>T maps to NM_000887.3 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr16:31373962 G>T maps to NM_000887.3 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:31374655 C>T maps to NM_000887.3 H557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:31383823 G>A maps to NM_000887.3 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:31388160 C>T maps to NM_000887.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr10:33217184 T>C maps to ENST00000374956 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:33199372 G>A maps to ENST00000374956 Q648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr10:33218840 T>C maps to ENST00000374956 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:70524436 C>A did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:3938652 G>A maps to NM_170678.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:46306785 G>A maps to NM_000211.3 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:46330267 C>T maps to NM_000211.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr21:46319037 C>A maps to NM_000211.3 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr21:46306282 C>A maps to NM_000211.3 *770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr21:46308698 C>T maps to NM_000211.3 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr21:46311908 G>T maps to NM_000211.3 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr21:46306291 A>T maps to NM_000211.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:45362031 A>C maps to NM_000212.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr1:63920060 G>A maps to ENST00000371092 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr17:73723281 C>A maps to NM_001005619.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr3:124567322 C>G maps to NM_002213.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr3:124487899 G>A maps to NM_002213.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr3:124578167 G>T maps to NM_002213.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FV-01A-11D-A17D-09 chr3:124567274 G>A maps to NM_002213.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr2:160993969 C>A maps to NM_000888.3 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:161055737 A>G maps to NM_000888.3 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr12:53587621 G>T maps to NM_000889.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr7:20418797 C>T maps to NM_002214.2 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr13:102250554 G>A maps to NM_004791.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr13:102220050 C>G maps to NM_004791.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:102227835 T>G maps to NM_004791.1 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr3:52814346 G>T maps to NM_002215.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr3:52818384 G>C maps to NM_002215.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr3:52822302 C>T maps to NM_002215.2 C687C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr10:7773952 G>A maps to NM_002216.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:7769756 G>C maps to NM_002216.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:7763622 C>T maps to NM_002216.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr10:7769037 T>G maps to NM_002216.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:7786201 C>T maps to NM_002216.2 F789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:52839833 G>A maps to NM_002217.3 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr3:52858545 G>A maps to ENST00000485816 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:52860574 G>T maps to ENST00000485816 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:52861122 G>A maps to ENST00000485816 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr3:52850985 G>A maps to ENST00000485816 H800H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr3:52863160 C>T maps to ENST00000485816 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr10:7618854 G>T maps to ENST00000256861 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr10:7621821 G>A maps to ENST00000256861 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr10:7658058 A>T maps to ENST00000256861 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr23:54781527 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr23:54777708 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:54780364 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54784175 T>A did not map to a codon.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr23:54785404 C>G did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:54785120 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr23:54817310 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:54817416 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:54784293 G>A did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr23:54780123 G>T did not map to a codon.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr23:54784949 G>C did not map to a codon.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr5:156635916 G>A maps to NM_005546.3 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:156641278 C>T maps to NM_005546.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:160846492 A>G maps to NM_017625.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr1:160850396 A>G maps to NM_017625.2 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr1:160851090 G>A maps to NM_017625.2 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:160921009 A>C maps to NM_080878.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr1:160924177 T>G maps to NM_080878.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr1:160920835 G>C maps to NM_080878.2 Y146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr1:160922452 A>G maps to NM_080878.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr1:160921036 C>T maps to NM_080878.2 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:160924222 G>C maps to NM_080878.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:78622669 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr23:78616642 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:78619022 T>A did not map to a codon.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr14:93412700 G>C maps to NM_014216.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr14:93424626 G>A maps to NM_014216.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr1:226825420 G>A maps to NM_002221.3 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr19:41231345 T>G did not map to a codon.
Sequencing variant TCGA-E2-A14T-01A-11D-A10Y-09 chr19:41235233 G>T maps to NM_025194.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XS-01A-11D-A22X-09 chr3:4821277 C>T maps to ENST00000356617 H2110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr3:4699914 C>T maps to ENST00000356617 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:4726850 C>T maps to ENST00000356617 H1217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C3-01A-21D-A12Q-09 chr3:4856840 T>C maps to ENST00000356617 A2600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr3:4699855 G>T maps to ENST00000356617 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr12:26551827 C>T maps to NM_002223.2 K2559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:26553192 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:26551857 G>A maps to NM_002223.2 S2549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr12:26647217 C>T maps to NM_002223.2 Q1746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr12:26580851 T>G maps to NM_002223.2 A2313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:26750046 G>A maps to NM_002223.2 D1341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr12:26748415 G>A maps to NM_002223.2 F1454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:26592093 G>C maps to NM_002223.2 L2203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr6:33663497 C>T maps to ENST00000374316 Q2653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0RX-01A-21D-A099-09 chr6:33655052 G>A maps to ENST00000374316 S2042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:33656490 C>T maps to ENST00000374316 F2209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr6:33647762 C>T maps to ENST00000374316 H1359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:96992959 C>A maps to ENST00000420728 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr16:19126676 C>T maps to NM_001034841.3 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:35138277 A>C maps to NM_003024.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:35190572 T>G maps to NM_003024.2 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr21:35172110 G>A did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr21:35258720 C>G maps to NM_003024.2 V1658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr15:40710372 C>T maps to NM_002225.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr1:152883340 G>T maps to NM_005547.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24P-01A-11D-A167-09 chr1:185276770 A>T maps to NM_006469.4 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:185276196 C>T maps to NM_006469.4 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr2:128262379 C>A maps to NM_017969.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr2:128253597 G>A maps to NM_017969.2 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr2:128260969 C>A maps to NM_017969.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:128244194 G>A maps to NM_017969.2 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:128261085 G>T maps to NM_017969.2 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr2:128250922 T>G maps to NM_017969.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:150719276 G>A maps to NM_203395.2 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr6:150715288 C>T maps to NM_203395.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr20:10627608 G>A maps to NM_000214.2 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr20:10639265 G>A maps to NM_000214.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr20:10644609 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:105614669 G>A maps to NM_002226.3 C709C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:105615579 G>A maps to NM_002226.3 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:9934814 C>G maps to NM_032492.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr3:9934707 C>T maps to NM_032492.3 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:65310573 T>G did not map to a codon.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr1:65307284 C>G did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr9:5044447 T>G maps to NM_004972.3 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr9:5022118 C>A maps to NM_004972.3 Y44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:17951134 G>A maps to NM_000215.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:17945531 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:17950340 C>T maps to NM_000215.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr19:17945964 C>T maps to NM_000215.3 E658E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:6087284 C>T maps to NM_001099433.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:6083469 G>A maps to NM_001099433.1 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:147019298 G>A maps to NM_014790.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr5:147019218 G>A maps to NM_014790.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr10:133967267 C>T maps to NM_001105521.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr21:27012165 G>C maps to NM_021219.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:134014271 C>T maps to NM_032801.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:15507633 C>T maps to NM_004973.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:27934995 T>G maps to NM_175061.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr10:64957270 T>G maps to NM_032776.1 A1848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:64968091 C>A maps to NM_032776.1 E1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:64974824 G>A maps to NM_032776.1 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr10:64974080 G>A maps to NM_032776.1 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr10:64975355 G>T maps to NM_032776.1 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr1:227921281 G>A maps to NM_023007.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:27221800 C>A maps to NM_001145348.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:78533273 G>A maps to NM_152405.4 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:78586969 C>T maps to NM_152405.4 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:78533502 G>T maps to NM_152405.4 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr22:39085344 T>G maps to NM_014876.5 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:75156988 G>A maps to NM_020647.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr8:143745923 G>A maps to NM_003724.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:96125258 C>G maps to NM_003772.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr19:2254464 G>A maps to NM_144616.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:23442684 G>T maps to NM_032876.4 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr19:12902830 C>T maps to NM_002229.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:12903463 C>T maps to NM_002229.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr17:39919552 C>T maps to NM_021991.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:39919444 C>G maps to NM_021991.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:8553306 C>A did not map to a codon.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr23:8553428 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:8565078 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr23:8591690 T>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:8555970 G>A did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr3:124174097 G>A maps to NM_001024660.3 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:124175524 C>T maps to NM_001024660.3 D1266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:124160829 C>G maps to NM_001024660.3 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:124281709 G>A maps to NM_001024660.3 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr3:124380760 C>T maps to NM_001024660.3 L2110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:124132496 G>T maps to NM_001024660.3 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr3:124181438 C>A maps to NM_001024660.3 I1328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr3:124415016 G>C maps to NM_001024660.3 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr9:712823 C>G maps to NM_015158.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr9:742356 C>T maps to NM_015158.2 V1283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr19:11287321 C>A maps to NM_015493.6 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr19:11289298 G>T maps to NM_015493.6 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:11287448 G>C maps to NM_015493.6 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr19:8399295 G>C maps to NM_198471.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:8387755 G>A maps to NM_198471.2 C811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr1:62739851 G>A maps to NM_181712.4 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr1:62740106 C>T maps to NM_181712.4 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:75665398 T>G maps to NM_001130089.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SB-01A-11D-A142-09 chr17:40272380 G>A maps to NM_021078.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr17:40266619 G>A maps to NM_021078.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XS-01A-11D-A22X-09 chr3:20167542 C>T maps to NM_003884.4 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:20189799 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:20168995 C>T maps to NM_003884.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr3:20161093 C>A maps to NM_003884.4 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr3:20167518 G>T maps to NM_003884.4 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:65481119 G>A maps to NM_182710.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr13:30782678 A>C maps to NM_032116.3 *491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr16:57775729 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:15439018 C>T maps to NM_201628.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr1:14925607 G>T maps to NM_201628.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr10:102824286 G>T maps to NM_030929.4 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:170367115 T>G maps to NM_006063.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:170377482 G>T maps to ENST00000419050 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr2:170366848 C>T maps to NM_006063.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:127642769 C>G maps to NM_207335.2 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr3:127642152 G>A maps to NM_207335.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr15:65370331 C>T maps to NM_001101362.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:47599452 G>A maps to NM_018095.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr11:47599059 C>A maps to NM_018095.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr3:42730495 C>T maps to NM_152393.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:41705645 T>G maps to NM_152903.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:41705200 G>A maps to NM_152903.4 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:41767844 G>A maps to NM_032138.4 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:67054596 T>G maps to NM_032505.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr3:67054332 G>A maps to NM_032505.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr2:85276733 C>T maps to NM_020122.4 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:5021755 A>C maps to NM_000217.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:5021915 G>T maps to NM_000217.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr12:5021914 C>T maps to NM_000217.2 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:111146714 G>A maps to NM_004974.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:111215865 C>T maps to NM_002232.3 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:30032938 A>C maps to NM_002233.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:30033211 G>T maps to NM_002233.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr11:30033316 G>T maps to NM_002233.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr12:5153646 C>T maps to NM_002234.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:5153828 C>T maps to NM_002234.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr12:5155076 C>T maps to NM_002234.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr12:4919671 C>T maps to NM_002235.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr12:4920088 C>T maps to NM_002235.3 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:4920418 G>A maps to NM_002235.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:6155659 A>C maps to NM_003636.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr1:6100693 G>C maps to NM_003636.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr1:6142260 G>T maps to NM_003636.3 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:47990587 G>T maps to NM_004975.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:47991436 G>A maps to NM_004975.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr8:73480016 G>A maps to NM_004770.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:73849473 C>T maps to NM_004770.2 H628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr8:73480343 C>A maps to NM_004770.2 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr8:73480415 C>T maps to NM_004770.2 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr8:73848354 A>G maps to NM_004770.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:17794170 G>A maps to NM_004976.4 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:17793648 C>T maps to NM_001112741.1 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr11:17794065 C>T maps to NM_001112741.1 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:75444658 G>A maps to NM_139137.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr12:75444551 G>A maps to NM_139137.2 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr19:50827192 G>A maps to NM_004977.2 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr23:48826430 A>C did not map to a codon.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr23:48825776 C>G did not map to a codon.
Sequencing variant TCGA-B6-A0RP-01A-21D-A099-09 chr23:48823410 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:48825563 G>A did not map to a codon.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr23:48825563 G>A did not map to a codon.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr23:48826173 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr23:48825987 A>T did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr7:120387848 A>G maps to NM_012281.2 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr7:119915570 C>T maps to NM_012281.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:119914820 G>A maps to NM_012281.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:112323332 G>C maps to ENST00000315987 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr1:112525096 G>A maps to ENST00000315987 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr1:112524763 G>A maps to ENST00000315987 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:112319679 G>A maps to ENST00000315987 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RQ-01A-11D-A10Y-09 chr2:11053550 G>A maps to NM_002236.4 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:11053361 C>T maps to NM_002236.4 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr2:11052863 C>T maps to NM_002236.4 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:49626118 T>G maps to NM_002237.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr20:49626536 G>A maps to NM_002237.3 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr16:84270971 G>A maps to NM_172347.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr16:84256442 C>A maps to NM_172347.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr1:210857057 C>A maps to NM_172362.2 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr1:210856853 C>T maps to NM_172362.2 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr7:150654492 G>A maps to NM_000238.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:49937856 T>C did not map to a codon.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr12:49951309 T>G maps to NM_012284.1 T942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:40321596 C>T maps to NM_012285.2 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:40323835 C>A maps to NM_012285.2 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr14:63473098 G>A maps to NM_139318.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr14:63473180 A>G maps to NM_139318.3 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr14:63174897 C>A maps to NM_139318.3 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr14:63174801 G>A maps to NM_139318.3 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:61611485 C>T maps to NM_030779.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr17:61619776 C>A maps to NM_030779.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr17:61611455 T>C maps to NM_030779.2 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr2:163374254 G>T maps to NM_033272.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr2:163694985 G>A maps to NM_033272.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:163256807 T>G maps to NM_033272.2 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:163228504 G>C maps to NM_033272.2 S1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:163241398 G>A maps to NM_033272.2 Q921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:163291795 G>A maps to NM_033272.2 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:163291987 G>A maps to NM_033272.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr3:19575050 G>A maps to NM_144633.2 W928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:160011386 T>G maps to NM_002241.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr1:160011188 A>G maps to NM_002241.4 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr11:17408654 C>T maps to NM_000525.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A249-01A-11D-A167-09 chr11:17408780 G>T maps to NM_000525.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr11:17408789 G>T maps to NM_000525.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:21319232 G>A maps to NM_021012.4 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr17:21319178 C>T maps to NM_021012.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr17:21319340 C>T maps to NM_021012.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:233632924 G>T maps to NM_002242.4 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:233633332 G>C maps to NM_002242.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:48967727 C>G maps to NM_170720.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RD-01A-11D-A159-09 chr19:48967592 C>T maps to NM_170720.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:39672031 C>G maps to NM_170736.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WV-01A-11D-A10G-09 chr17:68128758 G>A maps to NM_018658.1 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr17:68128509 C>T maps to NM_018658.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr17:68171872 C>T maps to NM_000891.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr2:155555499 C>T maps to NM_002239.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr2:155711276 G>T maps to NM_002239.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr22:38823441 G>A maps to NM_152868.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:128781575 C>T maps to NM_000890.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:39087042 G>A maps to NM_002240.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr21:39087021 T>C maps to NM_002240.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:21919226 T>G maps to NM_004982.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:21918862 C>A maps to NM_004982.2 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr14:88729860 G>C maps to NM_138318.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:88693720 G>T maps to NM_138318.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr14:90650489 A>T maps to NM_022054.2 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:43378956 G>A maps to ENST00000372861 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:39283145 T>G maps to NM_001135105.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:39290283 A>C maps to NM_032115.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:39286909 C>A did not map to a codon.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr6:39284657 T>G maps to NM_032115.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr1:215408280 C>G maps to NM_001017425.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:64064699 G>A maps to ENST00000422670 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:39159241 G>A maps to NM_003740.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr6:39162068 G>A maps to NM_003740.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr19:38817293 C>G maps to NM_004823.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A126-01A-11D-A10M-09 chr8:140631061 G>A maps to NM_016601.2 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr10:78674712 G>A maps to NM_001161352.1 I999I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:78708959 A>G maps to NM_001161352.1 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr10:78943190 T>A maps to NM_001161352.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr5:169805860 C>T maps to NM_004137.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr3:178560677 C>T maps to NM_005832.3 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:178968843 G>A maps to NM_014407.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr3:178968568 G>A maps to NM_171828.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr3:178984450 C>T maps to NM_171828.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr5:113740532 G>A maps to NM_021614.2 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr1:154842329 T>C maps to NM_002249.4 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr1:154680664 C>T maps to NM_002249.4 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr1:154842242 A>C maps to NM_002249.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:154698439 C>T maps to NM_002249.4 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr1:154842242 A>C maps to NM_002249.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr19:44278609 C>T maps to NM_002250.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr20:62073860 G>T maps to NM_172107.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:62062703 G>T maps to NM_172107.2 Y379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr8:133150244 G>C maps to NM_004519.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr8:133142087 C>T maps to NM_004519.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr8:133192478 G>A maps to NM_004519.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr8:133182582 G>A maps to NM_004519.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr1:41300695 C>T maps to NM_004700.3 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr1:41296812 T>G maps to NM_004700.3 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Q-01A-21W-A050-09 chr6:73843188 G>A maps to NM_001160133.1 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:73815080 A>C maps to NM_001160133.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:73904265 C>A maps to NM_001160133.1 S662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:73751696 C>T maps to NM_001160133.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:73751705 C>T maps to NM_001160133.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr8:99440887 C>T maps to NM_020697.2 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14U-01A-11D-A228-09 chr8:99440758 G>A maps to NM_020697.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr2:18112661 C>T maps to NM_002252.3 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr9:138676623 C>T maps to ENST00000298480 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:138645812 C>T maps to ENST00000298480 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr9:138669335 C>T maps to ENST00000298480 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:196197465 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:196197454 G>A maps to NM_198503.2 R1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:196295845 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr1:196227572 C>A maps to NM_198503.2 E988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:196274446 C>A maps to NM_198503.2 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:196397236 G>A maps to NM_198503.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:196295946 C>A maps to NM_198503.2 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr8:110980574 C>T maps to NM_014379.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr9:2729630 G>A maps to NM_133497.2 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr9:2729624 C>T maps to NM_133497.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:2729534 C>T maps to NM_133497.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:24081181 G>A maps to NM_001142730.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr16:29937237 G>A maps to NM_178863.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr5:143853656 T>C maps to NM_020768.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr22:37455387 C>T maps to ENST00000403888 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr22:37457642 C>T maps to ENST00000403888 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:201369514 C>A maps to NM_152387.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:67327654 G>T maps to NM_001100915.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr6:36447444 C>G maps to NM_173562.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr11:77885302 C>A maps to NM_001029859.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr1:215793687 T>C maps to NM_016121.3 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:215775436 G>A maps to NM_016121.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:215792601 C>T maps to NM_016121.3 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr1:215768801 C>T maps to NM_016121.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr13:45768345 G>A maps to NM_198404.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr16:2745958 C>T maps to NM_018992.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr7:66103259 G>T maps to ENST00000451741 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr7:6509385 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:23405609 A>C maps to NM_001009999.2 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr6:18197352 C>T maps to ENST00000388870 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr11:66995612 C>T maps to NM_012308.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr11:67010478 G>T did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr11:66985341 C>T maps to NM_012308.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr12:121986849 C>T maps to ENST00000377071 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr12:121878876 C>A maps to ENST00000377071 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr12:121878933 G>T maps to ENST00000377071 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr2:86709792 T>C maps to NM_001146688.1 F966F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:86712077 T>C maps to NM_001146688.1 N1036N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr2:86693920 T>C maps to NM_001146688.1 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:44137197 C>G maps to NM_014663.2 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:44134890 G>A maps to NM_014663.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:5041184 G>T maps to NM_015015.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr19:5150385 G>A maps to NM_015015.2 G1013G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:5077435 C>T maps to NM_015015.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr19:5144266 C>G maps to NM_015015.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CU-01A-12W-A050-09 chr9:6793071 G>A maps to NM_015061.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr9:6887969 A>T maps to NM_015061.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:6849508 T>G maps to NM_015061.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:7103846 C>T maps to NM_015061.3 R863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12H-01A-11D-A10Y-09 chr11:94730905 A>T maps to NM_018039.2 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr11:94758973 C>T maps to NM_001161630.1 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr11:94760220 G>A maps to NM_001161630.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr11:94759548 C>A maps to NM_001161630.1 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:404771 T>G maps to NM_001042603.1 P1474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr12:406342 A>G maps to NM_001042603.1 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr12:465640 C>T maps to NM_001042603.1 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:202698836 C>A maps to ENST00000367264 E1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:53225907 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:53225893 C>T did not map to a codon.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr23:53225217 G>A did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr23:53240702 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr23:53223538 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:53230804 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr23:53247016 A>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:53223475 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:53223477 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:53224231 C>G did not map to a codon.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr23:53247463 G>A did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:44921974 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr23:44896935 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:44949988 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:44820631 C>G did not map to a codon.
Sequencing variant TCGA-AO-A12A-01A-21D-A10Y-09 chr23:44942775 T>C did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr23:44969494 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:44945127 A>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:44942008 A>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:44949996 T>C did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr23:44913105 G>C did not map to a codon.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr17:7752914 G>A maps to NM_001080424.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr4:55980406 C>G maps to NM_002253.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:10600509 C>A maps to NM_203500.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:142658953 A>C maps to NM_000420.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr7:142640099 G>A maps to NM_000420.2 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr7:142649694 C>T maps to NM_000420.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr12:91449977 A>G maps to NM_007035.3 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr12:91449419 G>A maps to NM_007035.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr12:91449596 C>T maps to NM_007035.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr12:91445254 C>T maps to NM_007035.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr6:73951883 A>G maps to ENST00000370385 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr1:32502509 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr1:32495998 G>A maps to NM_006559.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr6:62688081 A>G maps to NM_152688.2 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:136470168 C>T maps to NM_006558.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:2837291 A>C maps to NM_014878.4 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:2837401 C>G did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:19563659 G>A maps to NM_015047.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:19557342 G>T maps to NM_015047.1 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr1:19545922 C>T maps to NM_015047.1 Q952Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr17:26965605 G>C maps to NM_014680.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:26960089 A>G maps to NM_014680.2 H1225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:26943633 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:26965611 G>A maps to NM_014680.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:26964012 G>A maps to NM_014680.2 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr17:26962558 G>C maps to NM_014680.2 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr17:26966442 C>G maps to NM_014680.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr5:141309822 C>T maps to NM_014773.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr8:48614555 G>T maps to NM_001080394.1 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr8:48309072 G>A maps to NM_001080394.1 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr8:48647972 C>T maps to NM_001080394.1 I903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr8:48586494 C>G maps to NM_001080394.1 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr16:71956528 C>T maps to NM_014761.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BM-01A-11D-A21Q-09 chr17:73491095 G>T maps to ENST00000375248 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr17:73489890 C>T maps to ENST00000375248 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XX-01A-21D-A23C-09 chr8:126073416 G>A maps to ENST00000377985 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr8:126073341 C>T maps to ENST00000377985 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr8:126059485 G>A maps to ENST00000377985 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:197427634 C>A maps to NM_014687.1 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:6862901 G>T maps to NM_014743.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:6863222 G>T maps to NM_014743.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr4:6865759 A>G maps to NM_014743.2 E1217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr4:6863767 A>T maps to NM_014743.2 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:42832737 C>T maps to NM_015349.1 Q932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:75142431 C>T maps to NM_001039479.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr6:24559334 G>C maps to NM_014809.3 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:24596613 G>A maps to NM_014809.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr1:35908579 T>C maps to NM_024874.4 K902K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr9:114156469 G>A maps to NM_001080398.1 V1142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr9:114156469 G>C maps to NM_001080398.1 V1142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:114159316 T>G maps to NM_001080398.1 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr9:114176802 C>A maps to NM_001080398.1 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:114172338 G>A maps to NM_001080398.1 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr20:36641849 C>T maps to NM_014657.1 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IX-01A-12D-A142-09 chr20:36641776 G>A maps to NM_014657.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr6:127765376 A>G maps to NM_014702.4 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:4826022 C>T maps to ENST00000450194 L1136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:4820889 C>A maps to ENST00000450194 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr16:15718666 C>T maps to NM_014647.3 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BA-01A-11W-A071-09 chr16:15692756 T>C maps to NM_014647.3 Q1646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr16:15728700 G>A maps to NM_014647.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JE-01A-11D-A13L-09 chr16:15702216 T>A maps to NM_014647.3 T1371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr16:15698048 C>T maps to NM_014647.3 L1463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr1:43908289 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:43908005 G>A maps to NM_015284.2 Q1748Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:43908578 G>C maps to NM_015284.2 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:43896997 C>G maps to NM_015284.2 S761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:43892770 G>A maps to NM_015284.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr1:43892389 C>T maps to NM_015284.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr1:47148999 G>A maps to NM_014774.2 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr1:3662659 G>C did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr12:22627751 G>C maps to ENST00000446597 S659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:22670986 T>G maps to ENST00000446597 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:27761259 C>G maps to NM_015202.2 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr16:27709760 C>T maps to NM_015202.2 N351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:3739735 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr13:42267041 T>A maps to NM_015058.1 K1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:58965601 A>C maps to ENST00000354386 P1417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr14:58925190 A>G maps to ENST00000354386 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr9:138379214 G>A maps to NM_014811.3 V953V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr9:138377840 G>T maps to NM_014811.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr11:46686402 C>A maps to NM_001142673.1 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:46667425 T>C maps to NM_001142673.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr17:6503708 G>C maps to NM_014804.2 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:6483150 A>C maps to NM_014804.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:39877865 T>G maps to NM_015038.1 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:39877268 A>T maps to NM_015038.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr6:96971167 G>A did not map to a codon.
Sequencing variant TCGA-AR-A2LL-01A-11D-A17W-09 chr18:8784387 G>A maps to ENST00000456698 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr18:8796351 C>A maps to ENST00000456698 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr18:8784555 G>C maps to ENST00000456698 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:55836402 A>C maps to NM_014924.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr14:55852814 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr1:155886453 C>T maps to NM_014949.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:75561274 T>C maps to NM_015037.2 *1843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr10:75561183 G>A maps to NM_015037.2 Q1812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr10:75559812 G>A maps to NM_015037.2 V1570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:154542960 C>G maps to NM_001131007.1 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr4:154479492 C>G maps to NM_001131007.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:154506764 T>C did not map to a codon.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr4:154471281 T>C maps to NM_001131007.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:5464642 A>C maps to NM_015325.1 P1732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:5463629 C>T maps to NM_015325.1 Q1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:5466494 C>T maps to NM_015325.1 Q1981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:5473834 G>A maps to NM_015325.1 W2129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr5:5462875 G>A maps to NM_015325.1 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr5:5464609 G>A maps to NM_015325.1 P1721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr5:5457496 G>T maps to NM_015325.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:84862694 T>C maps to NM_014895.2 K1066K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:84913770 C>T maps to NM_014895.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr18:29480940 T>C maps to NM_014939.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr18:29497564 C>A maps to NM_014939.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr18:29496331 G>A maps to NM_014939.3 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr18:29470717 G>A maps to NM_014939.3 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr18:29487547 G>A maps to NM_014939.3 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr15:79748797 G>A maps to NM_015206.2 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:105546179 T>C maps to NM_015275.1 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr9:34971432 C>G maps to NM_015297.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:123156059 A>C maps to NM_015312.3 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr4:123111227 G>T maps to NM_015312.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr4:123151229 C>A maps to NM_015312.3 R1063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr4:123159398 C>T maps to NM_015312.3 Q1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr4:123239409 G>A maps to NM_015312.3 R3593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr4:123168475 C>T maps to NM_015312.3 R1826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr4:123254964 G>T did not map to a codon.
Sequencing variant TCGA-A2-A25C-01A-11D-A167-09 chr7:141365077 G>A maps to NM_001080392.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr15:81225626 C>T maps to NM_018689.1 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr15:81212547 C>A maps to NM_018689.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr15:81216987 C>G maps to NM_018689.1 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr15:81176527 T>C maps to NM_018689.1 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr23:118230487 G>C did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:118222227 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:118222230 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:118222236 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:118221101 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:118222088 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:118243103 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3HN-01A-11D-A20S-09 chr23:118215341 C>A did not map to a codon.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr23:118221385 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118220835 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118222905 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118239002 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:118220633 C>A did not map to a codon.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr23:118221785 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr23:118222465 C>A did not map to a codon.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr23:118221585 G>T did not map to a codon.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr23:118221919 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr23:118223588 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr23:118284463 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr23:118223624 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr23:118221703 C>T did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:118227689 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:118221556 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr23:118215409 C>T did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:118239019 C>A did not map to a codon.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr23:118284279 G>A did not map to a codon.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr23:118221419 A>T did not map to a codon.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr23:118242397 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr4:57180615 G>A maps to NM_020722.1 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr4:57181863 C>A maps to NM_020722.1 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr4:57182103 C>A maps to NM_020722.1 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:24790377 A>C maps to NM_019590.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:24834958 A>C maps to NM_019590.3 P1846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:24721999 C>T maps to NM_019590.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr10:24810807 T>C maps to NM_019590.3 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:24832224 G>A maps to NM_019590.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr10:24508618 A>G maps to NM_019590.3 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:24722056 G>T maps to NM_019590.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SU-01A-11D-A099-09 chr6:138599687 C>T maps to NM_020340.4 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:138610955 G>A maps to NM_020340.4 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:138619873 C>T maps to NM_020340.4 F1260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr6:138655268 C>A maps to NM_020340.4 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:128690193 C>T maps to NM_020741.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr3:128706483 G>A maps to NM_020741.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:44249015 G>C maps to NM_015443.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:44249260 G>C maps to NM_015443.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr17:44116047 C>T maps to NM_015443.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr10:72289739 T>G maps to NM_014431.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15F-01A-11D-A10Y-09 chr10:70748749 T>C maps to NM_015634.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr2:97302707 G>A maps to ENST00000421845 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr2:97276809 G>C maps to ENST00000421845 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr2:97267391 G>A maps to ENST00000421845 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:97274299 C>T maps to ENST00000421845 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XG-01A-11D-A14G-09 chr2:97302833 T>C maps to ENST00000421845 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:86521168 A>G maps to NM_001142749.2 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr18:34646884 A>C maps to NM_020776.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr18:34415223 C>G maps to NM_020776.1 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr18:34752975 T>C maps to NM_020776.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:52901590 G>C maps to NM_019600.2 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:52901012 C>A maps to NM_019600.2 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr11:101828904 A>C maps to NM_020802.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:101832650 C>T maps to NM_020802.2 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr1:232943639 T>C maps to NM_019090.2 N957N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr1:232940797 G>A maps to NM_019090.2 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:94156522 T>G maps to ENST00000393153 G2443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:94128948 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr14:93962757 G>T maps to ENST00000393153 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr14:94088693 G>A maps to ENST00000393153 Q1727Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr14:94088207 C>T maps to ENST00000393153 N1565N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr14:94088951 C>A maps to ENST00000393153 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr14:94097184 C>T maps to ENST00000393153 R1905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:95504987 G>C maps to NM_015496.3 S1567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:95518780 G>A maps to NM_015496.3 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:95523889 C>T maps to NM_015496.3 T971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:186096981 G>A maps to NM_020827.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:5765497 C>T maps to ENST00000414202 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr9:5762596 G>A maps to ENST00000414202 Q683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:30317150 A>C maps to NM_020848.2 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:30315896 A>C maps to NM_020848.2 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:30318311 T>G maps to NM_020848.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:30317578 G>A maps to NM_020848.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr12:13208572 G>A maps to NM_020853.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr12:13208584 G>T maps to NM_020853.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr18:59854855 C>A maps to NM_020854.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:59878436 C>G maps to NM_020854.3 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr18:59895750 A>T maps to NM_020854.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr18:59895759 G>A maps to NM_020854.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:226516193 T>G maps to NM_020864.1 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr1:33233705 C>A maps to NM_020888.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr3:108298526 C>A maps to NM_020890.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr3:108276093 C>T maps to NM_020890.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr3:108287043 T>A maps to NM_020890.2 K411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr9:100085181 G>T maps to ENST00000375206 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:100105798 G>T maps to ENST00000375206 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:100105818 G>A maps to ENST00000375206 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:100119935 G>T maps to ENST00000375206 G1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr9:100137843 C>G maps to ENST00000375206 A1594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr4:1343482 G>A maps to NM_020894.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr4:1343344 C>T maps to NM_020894.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr4:1348586 C>G maps to NM_020894.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr9:35105680 G>C maps to NM_025182.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:7681484 C>G maps to NM_001080429.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:138601599 C>T maps to NM_001164665.1 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:138603448 G>C maps to NM_001164665.1 S308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr6:56918698 G>T maps to NM_020931.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr1:180886054 G>T maps to NM_020950.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:180910279 G>C maps to NM_020950.1 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:180905639 C>T maps to NM_020950.1 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:43532579 G>A maps to NM_020964.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:43432479 G>A maps to NM_020964.2 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr18:43483980 G>C maps to NM_020964.2 P1477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr18:43503332 T>C maps to NM_020964.2 Q913Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:18376507 C>T maps to NM_001145304.1 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr4:175224933 C>T maps to NM_001145314.1 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr4:175224963 G>C maps to NM_001145314.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:176812260 G>C maps to NM_030650.1 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:77579856 A>C maps to NM_033426.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr14:77576158 G>A maps to NM_033426.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr20:36869428 C>A maps to NM_001029864.1 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:36845690 G>A maps to NM_001029864.1 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:36851969 G>A maps to NM_001029864.1 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I5-01A-11W-A100-09 chr20:36856566 G>A maps to NM_001029864.1 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12O-01A-11D-A10Y-09 chr20:36874486 C>T maps to NM_001029864.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr20:36869995 G>T maps to NM_001029864.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr20:36868032 G>A maps to NM_001029864.1 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:20789450 C>T maps to NM_017794.3 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:20789381 T>C maps to NM_017794.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr9:20990141 G>A maps to NM_017794.3 L1675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr9:20944724 G>T maps to NM_017794.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr1:233512265 C>T maps to NM_032435.2 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr1:233515007 G>A maps to NM_032435.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr1:233490630 C>A maps to NM_032435.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr1:233482293 A>G maps to NM_032435.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:233515232 C>G maps to NM_032435.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:105881239 A>C maps to NM_032424.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:105881233 G>C maps to NM_032424.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:61315523 G>T maps to NM_001129993.1 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr2:61324842 C>G maps to NM_001129993.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr6:111583512 G>A maps to NM_153369.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr8:22464824 C>G maps to NM_021174.5 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:113378737 T>G maps to NM_001009899.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:113377642 T>C maps to NM_001009899.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr3:113380215 G>A maps to NM_001009899.2 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:113379493 C>T maps to NM_001009899.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr23:73963036 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:73962126 T>C did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:73962609 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:73960910 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr23:73961665 G>A did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:73964214 C>T did not map to a codon.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr23:73961111 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:73963608 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr23:73960663 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27W-01A-11D-A16D-09 chr23:73960045 C>T did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:73961156 G>T did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr23:73962902 C>G did not map to a codon.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr23:73963323 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr23:73961190 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr23:73962008 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr23:73964064 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DM-01A-11D-A17W-09 chr23:73962854 C>T did not map to a codon.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr23:73961058 T>A did not map to a codon.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr9:6007234 G>A maps to NM_001017969.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:5920430 T>G maps to NM_001017969.2 A1855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:5920349 T>G maps to NM_001017969.2 T1882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr9:5921684 A>G maps to NM_001017969.2 T1437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr2:8943113 C>T maps to NM_020738.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:8926447 A>C maps to NM_020738.2 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:8940592 A>C maps to NM_020738.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:8871260 C>T maps to NM_020738.2 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:8931195 G>A maps to NM_020738.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr2:8888078 G>A maps to NM_020738.2 Q1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr6:17781437 G>C maps to NM_022113.4 Y1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:17837132 C>T maps to NM_022113.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:17856347 C>A maps to NM_022113.4 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr6:17799619 G>C maps to NM_022113.4 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:17797020 G>A maps to NM_022113.4 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:29025022 G>C maps to NM_015254.3 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr8:28967485 G>C maps to NM_015254.3 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr8:29003918 G>A maps to NM_015254.3 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr8:29043903 A>T maps to NM_015254.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:200571174 A>C maps to NM_014875.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:200523594 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:44854635 G>T maps to NM_020242.2 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:44847349 G>T maps to NM_020242.2 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr3:44826335 G>T did not map to a codon.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr20:16474995 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:16407782 A>C maps to NM_024704.4 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr20:16496279 C>T maps to NM_024704.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr1:20998491 G>A maps to NM_020816.2 D887D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:21016679 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:20998629 G>A maps to NM_020816.2 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:21014089 G>A maps to NM_020816.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:28084021 C>T maps to NM_031217.3 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr17:43009057 G>A maps to ENST00000438933 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:72349060 G>A maps to NM_153209.3 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr17:72350925 C>T maps to NM_153209.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr17:72346875 C>G maps to NM_153209.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr17:72341084 C>T maps to NM_153209.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr2:241713622 G>A maps to ENST00000373308 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:241676564 C>A maps to ENST00000373308 E1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr2:241710386 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr1:10355753 A>T maps to ENST00000377086 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:10363813 C>G maps to NM_183416.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr1:10332315 T>C maps to ENST00000377086 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:4903597 G>A maps to NM_006612.5 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:137518126 C>G maps to NM_005733.2 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:91486271 G>T maps to ENST00000416354 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr10:91497969 G>A maps to ENST00000416354 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr10:91503680 C>G maps to ENST00000416354 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:91483861 T>C did not map to a codon.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr10:91498015 C>T maps to ENST00000416354 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr10:91518584 G>A maps to ENST00000416354 Q1572Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:39726825 T>G maps to ENST00000395670 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:39725548 G>A maps to ENST00000395670 C1032C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr12:39764026 T>C maps to ENST00000395670 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:39763644 A>G maps to ENST00000395670 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr1:200973932 G>A maps to NM_017596.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr1:200959736 G>C maps to NM_017596.2 V934V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr1:200960091 G>A maps to NM_017596.2 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JB-01A-11D-A13L-09 chr1:200959274 C>T maps to NM_017596.2 E1007E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:34259646 T>G maps to NM_194313.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:34306377 G>A maps to NM_194313.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr9:34255842 G>T maps to NM_194313.2 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr6:168440804 G>A maps to NM_030615.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr6:168439274 C>G maps to NM_030615.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr14:104638169 C>T maps to NM_015656.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr1:245583002 C>T maps to NM_018012.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr1:245850727 C>T maps to NM_018012.3 D1481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr1:245850802 C>T maps to NM_018012.3 F1506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr1:245582981 G>T maps to NM_018012.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr1:245851144 C>T maps to NM_018012.3 G1620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr1:245530509 G>A maps to NM_018012.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr1:245704135 G>T maps to NM_018012.3 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:86502078 C>A maps to NM_017576.1 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr9:86485436 G>C maps to NM_017576.1 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:86518065 G>C maps to NM_017576.1 S456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr9:86485474 T>A maps to NM_017576.1 K906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:61669520 G>T maps to NM_001098511.1 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr17:51902100 C>T maps to NM_032559.4 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr17:51900534 G>A maps to NM_032559.4 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr17:51901203 C>T maps to NM_032559.4 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr17:51900666 G>A maps to NM_032559.4 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr20:30898743 C>T maps to NM_004798.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr20:30898413 C>T maps to NM_004798.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr20:30898617 C>T maps to NM_004798.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:26203691 G>T maps to NM_002254.6 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:69615654 G>A did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr23:69639952 G>C did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr23:69594087 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:69573522 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:69516984 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr23:69615616 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr23:69550015 G>C did not map to a codon.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr23:69521792 C>G did not map to a codon.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr23:69639609 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr23:69623827 A>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:69563754 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:69625734 G>A did not map to a codon.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr23:69510349 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1JS-01A-11D-A13L-09 chr23:69521826 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:69572500 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr23:69606485 G>T did not map to a codon.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr23:69510362 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr23:69623810 G>A did not map to a codon.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr23:69596000 G>A did not map to a codon.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr23:69615825 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:154396043 C>G maps to NM_001099293.1 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr12:57969054 G>A maps to NM_004984.2 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr12:57975303 C>T maps to NM_004984.2 Y954Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr10:32322813 C>A maps to NM_004521.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:32306076 G>A maps to NM_004521.2 Q919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:149806435 C>A maps to NM_004522.1 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr2:149806934 C>T maps to NM_004522.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr6:39325123 G>A maps to NM_145027.4 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:39507920 A>C maps to NM_145027.4 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:39563937 G>T maps to NM_145027.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:169961352 G>A maps to NM_014970.2 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr1:170008429 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:33374264 T>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr6:33372651 A>G maps to NM_002263.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr6:33374169 C>T maps to NM_002263.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:33377465 G>T maps to NM_002263.3 *674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr6:33371564 T>C maps to NM_002263.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:145697643 T>G did not map to a codon.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr16:57828978 G>A maps to NM_005550.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr10:7816804 A>C maps to NM_012311.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr19:55263946 G>T maps to NM_015868.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr19:55325454 G>A maps to ENST00000396289 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr19:55325382 T>A maps to ENST00000396289 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr19:55325454 G>A maps to ENST00000396289 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AL-01A-21D-A12Q-09 chr19:55325454 G>A maps to ENST00000396289 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr19:55325454 G>A maps to ENST00000396289 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr19:55351147 G>A maps to NM_012314.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr19:55341435 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr1:158047871 C>T maps to ENST00000368173 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:158063195 C>T maps to ENST00000368173 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C3-01A-21D-A12Q-09 chr1:158059317 G>T maps to ENST00000368173 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr19:36357207 C>T maps to NM_199180.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:36353863 C>T maps to NM_199180.2 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr19:36351483 C>T maps to NM_199180.2 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr19:36357342 A>G maps to NM_199180.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr11:126294696 C>T maps to NM_032531.3 E705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr11:126391324 C>T maps to NM_032531.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr11:126396532 C>T maps to NM_032531.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr19:918592 C>T maps to NM_032551.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:55565920 G>T maps to NM_000222.2 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:33638179 G>T maps to NM_004795.3 E966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:39436041 G>A maps to NM_175737.3 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr11:66033218 C>T maps to NM_022822.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr19:45848975 C>T maps to NM_177417.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:103664028 G>T maps to NM_005655.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr2:10192627 T>G maps to NM_003597.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr3:126071323 G>A maps to NM_014079.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr3:126062721 C>A maps to NM_014079.3 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr1:44595380 C>G maps to NM_173484.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PG-01A-11D-A142-09 chr2:207988823 A>T maps to NM_003709.2 L136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr23:56291988 G>T did not map to a codon.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr23:56292170 G>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:50249115 G>T maps to NM_014315.2 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:42985433 G>C did not map to a codon.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr22:50987926 G>A maps to NM_138433.3 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:161069458 G>A maps to NM_152366.4 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:161069896 G>A maps to NM_152366.4 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr13:70281928 C>T did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr13:70535548 A>G maps to NM_020866.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:202894212 G>C maps to NM_021633.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:117033136 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:117044001 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr23:117033309 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr23:117033282 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:117054216 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr23:117053568 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:117053568 T>C did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr18:30321921 G>A maps to NM_020805.1 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr18:30321984 T>C maps to NM_020805.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr18:30267119 T>C maps to NM_020805.1 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr23:24006790 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:24024794 C>A did not map to a codon.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr23:24024510 G>A did not map to a codon.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr1:900504 G>C maps to NM_198317.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr1:899383 G>A maps to NM_198317.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:897820 C>T maps to NM_198317.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr3:47385247 G>A maps to NM_025010.4 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr1:173725094 A>G maps to NM_014458.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:20819206 G>A maps to NM_032775.3 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr22:20800741 C>T maps to NM_032775.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:170592606 C>T maps to NM_144711.5 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr15:86311421 G>C maps to NM_022480.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr15:86311928 C>T maps to NM_022480.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:86312360 G>C maps to NM_022480.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:18779976 G>A maps to NM_018316.1 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:137071326 A>C maps to NM_017415.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:239057646 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr2:239049613 C>T maps to NM_198582.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:53519884 A>G maps to NM_001003760.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr23:21675571 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr23:21674414 C>T did not map to a codon.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr16:84690715 G>A maps to NM_024731.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr16:84690685 C>T maps to NM_024731.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr8:124663966 G>T maps to NM_001081675.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:86877240 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr23:86772967 T>A did not map to a codon.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr23:86880628 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:86869456 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0EI-01A-11D-A10Y-09 chr23:86887331 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:86888817 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:86773200 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:39083599 G>T maps to NM_015990.4 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27T-01A-11D-A16D-09 chr4:39114837 A>G maps to NM_015990.4 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LJ-01A-12D-A19Y-09 chr3:183225933 C>T maps to NM_130446.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E9-01B-11D-A10Y-09 chr3:183209732 G>A maps to NM_130446.2 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr3:183209882 C>A maps to NM_130446.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr7:23212572 T>G maps to NM_001031710.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:23213709 T>G maps to NM_001031710.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:23180526 C>A maps to NM_001031710.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:88085133 A>C maps to NM_020803.3 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr4:88106440 G>A maps to NM_020803.3 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:21334137 G>A maps to NM_018847.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr9:21334378 A>G maps to NM_018847.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr9:21333115 T>A maps to NM_018847.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:51323211 C>T maps to NM_002257.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr19:51323271 G>A maps to NM_002257.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr19:51526350 G>T maps to NM_144947.1 C231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr19:51535183 G>A maps to NM_019598.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr19:51537844 A>G maps to NM_019598.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N8-01A-11D-A142-09 chr19:51563337 A>G maps to NM_015596.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:51330209 C>A maps to NM_017509.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:51380014 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1Y2-01A-11D-A159-09 chr19:51361805 C>T maps to NM_001648.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25F-01A-11D-A167-09 chr19:51452256 G>A maps to NM_012427.4 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr19:51470540 G>A maps to NM_001012964.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:187159466 G>T maps to ENST00000511608 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:187172698 G>T maps to ENST00000511608 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:48713897 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:48692640 C>T maps to NM_001135629.2 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr2:48722822 C>T maps to NM_001135629.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr2:48668099 C>A maps to NM_001135629.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:9747965 C>T maps to NM_002258.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr12:9985924 C>T maps to NM_016523.1 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:135025316 C>T maps to ENST00000368572 F1399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr10:135020747 C>T maps to ENST00000368572 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr12:123058839 T>C maps to NM_014708.4 N765N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:123061575 G>A maps to NM_014708.4 Q907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:123089154 G>T maps to NM_014708.4 E1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr12:123068875 G>C maps to NM_014708.4 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr3:122146502 A>G maps to NM_002264.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IX-01A-12D-A142-09 chr13:50296657 G>A maps to NM_002267.3 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EU-01A-11D-A135-09 chr3:160283040 T>C maps to NM_002268.3 Q10Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:117037437 C>G maps to NM_002269.2 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:117013466 T>C maps to NM_002269.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:32620198 G>A maps to NM_012316.4 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr1:152733638 C>G maps to NM_001025231.1 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:152733329 T>C maps to NM_001025231.1 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:152733173 G>A maps to NM_001025231.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr19:47979890 C>A maps to NM_007059.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr17:8272526 G>A maps to NM_213597.2 D468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr19:10664627 C>T maps to NM_023008.3 *710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:10668269 G>T maps to NM_023008.3 Y531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr19:10670169 C>T maps to NM_023008.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:75900636 C>T maps to NM_007043.6 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr12:53069279 G>A maps to NM_006121.3 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:53073853 A>G maps to NM_006121.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr12:53071192 G>A maps to NM_006121.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:38978705 A>C maps to NM_000421.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr17:38978657 C>T maps to NM_000421.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr17:39022940 A>G maps to NM_000223.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:39661748 A>C maps to NM_153490.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:39659615 G>A maps to NM_153490.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:39672353 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:39674866 T>C maps to NM_002275.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XO-01A-11D-A10G-09 chr12:53344650 C>T maps to NM_000224.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr12:53344578 C>A maps to NM_000224.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr17:39684180 C>A maps to NM_002276.4 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr12:53040549 G>T maps to NM_000423.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr12:53042055 G>A maps to NM_000423.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr17:39092672 A>T maps to NM_015515.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr17:38857430 G>A maps to NM_019016.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:38859681 A>C maps to NM_019016.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr17:38907419 C>T maps to NM_181534.3 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:38926131 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:38935966 G>A maps to NM_181537.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr17:38935975 G>A maps to NM_181537.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr17:38933367 G>T maps to NM_181537.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:38955995 T>C maps to NM_181535.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:53189430 T>C maps to ENST00000309505 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:53189592 T>C maps to ENST00000309505 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr17:39551242 G>T maps to ENST00000393998 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr17:39623316 G>A maps to NM_002278.3 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:39525756 C>T maps to ENST00000394004 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr17:39534311 C>G maps to NM_021013.3 *437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr17:39633897 G>T maps to NM_002280.4 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr17:39637325 G>T maps to NM_002280.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:39637139 G>A maps to NM_002280.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr17:39637187 C>A maps to NM_002280.4 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:39643671 C>T maps to NM_003771.4 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr17:39645737 C>A maps to NM_003771.4 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr17:39645669 A>G maps to NM_003771.4 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr17:39596720 G>C maps to NM_006771.3 Y151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:39137135 C>T maps to NM_182497.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr12:52910584 G>A maps to NM_000424.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:52912905 G>T maps to NM_000424.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr12:52913582 G>T maps to NM_000424.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:52862992 G>A maps to NM_173086.4 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr12:52867104 G>A maps to NM_173086.4 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr12:52943868 C>T maps to NM_033448.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:52938504 G>A maps to NM_033448.2 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr12:52981584 G>A maps to NM_080747.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:53003054 C>A maps to NM_175068.2 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:52827015 C>T maps to ENST00000252245 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:52824396 G>A maps to ENST00000252245 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr12:53164970 A>G maps to NM_015848.4 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr12:53167401 G>A maps to NM_015848.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:53165955 G>A maps to NM_015848.4 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr12:53086262 G>A maps to NM_175078.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr12:53086215 G>A maps to NM_175078.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:53233249 G>A maps to NM_173352.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr12:53225305 G>C maps to NM_175834.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr12:52681779 C>T maps to NM_002281.3 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr12:52681496 C>T maps to NM_002281.3 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr12:52681911 C>G maps to NM_002281.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:52789543 G>A maps to NM_033033.3 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:52714753 G>A maps to NM_002282.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr12:52714810 G>A maps to NM_002282.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr12:52760886 G>A maps to NM_002283.3 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:52754750 G>T maps to NM_002283.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr12:52700001 C>G maps to NM_002284.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr12:52698792 G>C maps to NM_002284.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr12:52699842 G>C did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr17:39728034 G>T maps to NM_000226.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:39724858 G>A maps to NM_000226.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr17:39724451 C>T maps to NM_000226.3 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr17:39724601 C>T maps to NM_000226.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr17:39724822 C>T maps to NM_000226.3 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr21:46067172 C>T maps to NM_198692.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12A-01A-21D-A10Y-09 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr21:45994018 C>T maps to NM_198687.1 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr21:46000149 G>T maps to NM_198694.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr21:46011699 G>A maps to NM_198688.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr21:46011675 C>T maps to NM_198688.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr21:46020874 C>G maps to ENST00000380102 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr21:46020574 C>T maps to ENST00000380102 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr21:46032256 C>T maps to NM_198695.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr21:32253423 G>C maps to NM_175858.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr21:31798068 C>T maps to NM_181622.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr21:31802937 G>A maps to NM_181600.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr21:31812764 C>T maps to NM_181623.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:32410705 A>C maps to NM_001099219.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr21:32007596 C>T maps to NM_181616.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr21:31692281 G>C maps to NM_203405.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr17:39324181 C>T maps to NM_033187.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr17:39324271 C>T maps to NM_033187.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LH-01A-31D-A18P-09 chr17:39316499 G>A maps to NM_032524.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr17:39240790 C>T maps to ENST00000377731 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr17:39240790 C>T maps to ENST00000377731 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:39262176 C>T maps to ENST00000377731 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr17:39262242 C>A maps to ENST00000377731 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr17:39261861 T>C maps to NM_001146041.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:1606197 T>C maps to NM_001005922.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr11:71276830 C>G maps to ENST00000422553 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr11:71276950 T>C maps to ENST00000422553 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr11:1718780 A>G maps to NM_001012416.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:71259912 A>G maps to ENST00000422553 G119G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BH-A18G-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr21:31986142 A>G maps to NM_181602.1 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr21:31964847 A>G maps to NM_181605.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr21:31964877 C>T maps to NM_181605.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr1:155145339 G>C maps to NM_173852.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr1:155145234 A>G maps to NM_173852.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:117962946 C>G maps to ENST00000339824 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:118198909 G>A maps to ENST00000339824 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr12:117962667 G>A maps to ENST00000339824 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr12:118293371 G>A maps to ENST00000339824 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr12:118199252 G>A maps to ENST00000339824 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr12:117962829 G>A maps to ENST00000339824 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:119205718 G>A maps to NM_152305.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:119209418 C>T maps to NM_152305.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr14:56114769 G>A maps to NM_001079521.1 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr14:56101367 C>T maps to NM_001079521.1 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr14:56107111 C>T maps to NM_001079521.1 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr3:134323233 C>T maps to NM_178554.4 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:143799653 A>C maps to NM_003937.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SD-01A-11D-A10Y-09 chr23:153132280 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153135596 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153135896 T>G did not map to a codon.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:153129443 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr23:153128303 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr23:153136573 A>G did not map to a codon.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr23:153133853 T>G did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr23:153130154 G>T did not map to a codon.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr23:153130894 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr23:153134144 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:153128185 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr23:153133790 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr23:153129921 A>G did not map to a codon.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr23:153134350 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr1:62676023 C>T maps to NM_019079.4 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:62676789 G>T maps to NM_019079.4 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr1:62673211 C>T maps to NM_019079.4 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr14:50732074 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:50769674 G>A maps to NM_024884.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:50750612 C>A maps to NM_024884.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr20:42143190 C>T maps to NM_015478.6 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr20:42157309 G>A maps to NM_032107.4 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr20:42169424 T>C maps to NM_032107.4 C766C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-C8-A12U-01A-11D-A10Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:42164829 G>A maps to NM_032107.4 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JE-01A-11D-A13L-09 chr20:42143724 G>A maps to NM_032107.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JE-01A-11D-A13L-09 chr20:42161474 G>A maps to NM_032107.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr22:41613206 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:41621038 G>A maps to NM_031488.4 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr22:41626158 G>A maps to NM_031488.4 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr22:41613160 G>A maps to NM_031488.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:130370958 A>C maps to NM_032438.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr6:130392141 C>T maps to NM_032438.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:130425708 C>T maps to NM_032438.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:6263966 T>G maps to NM_173464.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr18:6093493 C>T maps to NM_173464.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I5-01A-11W-A100-09 chr18:6171938 A>G maps to NM_173464.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:63433550 T>G maps to NM_032857.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:71553219 G>A maps to NM_016027.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr12:6882448 C>T maps to NM_002286.5 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr12:6882467 C>T maps to NM_002286.5 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr19:55019379 C>T maps to NM_002288.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr18:7046345 G>A maps to NM_005559.2 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr18:6959368 C>T maps to NM_005559.2 A2583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr18:7050725 A>C maps to NM_005559.2 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr18:7032991 G>C maps to NM_005559.2 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr18:6993718 C>A maps to NM_005559.2 V1643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr18:7036045 G>A maps to NM_005559.2 Y593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr6:129722391 C>T maps to NM_000426.3 S1823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr6:129712679 C>T maps to NM_000426.3 R1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:129581939 A>C maps to NM_000426.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:129465143 G>A maps to NM_000426.3 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr6:129468132 T>A maps to NM_000426.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr6:129835645 C>T maps to NM_000426.3 L3039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr18:21533029 A>C maps to ENST00000416669 P3273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:21483959 G>T maps to ENST00000416669 E2130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr18:21427491 G>A maps to ENST00000416669 T1334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr18:21481287 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr18:21419893 G>T did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr18:21417016 C>T maps to ENST00000416669 D1021D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:112441615 G>C maps to NM_001105206.1 S1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:112440397 C>T maps to NM_001105206.1 L1594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:112441586 G>A maps to NM_001105206.1 L1522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr20:60937536 G>A maps to NM_005560.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr20:60889468 G>A maps to NM_005560.3 L2799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr20:60904937 G>A maps to NM_005560.3 Y1338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr20:60889976 G>A maps to NM_005560.3 Q2692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:107618512 G>A maps to NM_002291.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:107594131 C>T maps to NM_002291.2 Q974Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr7:107576030 G>A maps to NM_002291.2 T1339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr7:107594138 G>T maps to NM_002291.2 S972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr7:107569872 C>A maps to NM_002291.2 E1577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr7:107618512 G>A maps to NM_002291.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr3:49159430 A>C maps to NM_002292.3 G1623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:49160242 C>T maps to NM_002292.3 Q1489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:49160161 G>A maps to NM_002292.3 I1516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr3:49166018 C>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr3:49169563 G>A maps to NM_002292.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr3:49163266 G>A maps to NM_002292.3 Q801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:209796404 A>C maps to NM_000228.2 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:107749690 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:107696106 A>T maps to NM_007356.2 L1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr7:107763588 A>T maps to NM_007356.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:183091056 C>T maps to NM_002293.3 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:183097763 G>A maps to NM_002293.3 E1053E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr9:133907490 C>T maps to ENST00000355048 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:133963172 C>T maps to ENST00000355048 I1494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DD-01A-31D-A12Q-09 chr9:133945107 C>T maps to ENST00000355048 N980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr23:119562413 G>C did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:119589361 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:119589283 A>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:119590608 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:119573088 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:119581880 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr23:119565294 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:119575636 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:119589288 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:182871808 T>G maps to NM_014398.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:37515014 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:37515046 A>G did not map to a codon.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr23:37431624 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:17609059 G>T maps to NM_015907.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr4:17585130 G>A maps to NM_015907.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr4:17586654 C>G maps to NM_015907.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr8:98817647 C>G maps to ENST00000378722 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr22:33670433 G>A maps to NM_133642.3 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:154173459 G>A maps to ENST00000377643 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr5:154172348 G>A maps to ENST00000377643 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:154170242 T>C maps to ENST00000377643 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:129019457 C>G maps to NM_018078.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr4:129043386 G>C maps to NM_178043.1 *523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr10:860732 G>A maps to NM_015155.1 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr10:882384 G>T maps to NM_015155.1 C236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr10:875658 G>A maps to NM_015155.1 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W5-01A-11D-A10G-09 chr15:71125332 G>A maps to NM_018357.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:113568855 C>T maps to ENST00000509061 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr5:145539014 C>T maps to NM_020117.9 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:45561758 C>T maps to NM_015340.3 Q755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:64743517 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr23:64737979 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr23:64734715 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:64749664 C>T did not map to a codon.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr23:64754389 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1FL-01A-11D-A13L-09 chr19:18994906 G>A maps to NM_021267.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr1:150941433 G>A maps to NM_181746.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:150939651 A>G maps to NM_181746.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr1:150939290 G>A maps to NM_181746.2 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr15:101009638 C>T maps to ENST00000394113 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr15:101019662 T>C maps to ENST00000394113 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr12:50524369 C>G maps to NM_147190.2 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:150005195 C>T maps to NM_004690.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr13:21563387 G>T maps to NM_014572.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:21557890 C>A maps to NM_014572.2 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JU-01A-11D-A13L-09 chr1:203743055 A>T maps to NM_017773.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr11:111414804 G>C maps to ENST00000375615 L89L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EW-A1P5-01A-11D-A142-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EW-A1P5-01A-11D-A142-09 chr2:30457270 C>T maps to NM_030915.3 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr1:225600339 A>G maps to NM_194442.1 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr2:74725095 G>A maps to NM_001009812.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr2:74725248 C>T maps to NM_001009812.1 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:68119167 C>T maps to ENST00000380035 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr15:68118405 G>A maps to ENST00000380035 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr15:68124618 G>A maps to ENST00000380035 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr6:80198926 G>A maps to NM_181714.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr21:40795104 G>A maps to NM_152505.3 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr21:40795030 C>A maps to NM_152505.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr21:40778155 T>C maps to NM_152505.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:67977875 A>G maps to NM_000229.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:152800091 C>T maps to NM_178348.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr1:152800019 C>T maps to NM_178348.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RU-01A-11D-A28B-09 chr1:152800193 C>T maps to NM_178348.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:152784993 C>T maps to NM_178349.1 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:152648634 T>A maps to NM_178429.2 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr1:152595498 T>G maps to NM_178431.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr1:152552175 G>A maps to NM_032563.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:152552373 T>G maps to NM_032563.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr1:32741214 C>T maps to ENST00000373562 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr1:32742226 G>A maps to ENST00000373562 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:30863241 A>C maps to NM_182551.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr9:130913970 C>G maps to ENST00000373013 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr9:139651509 G>C maps to ENST00000371689 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:46722522 A>C maps to NM_002298.4 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr5:169720328 A>G maps to NM_005565.3 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:169677829 G>C maps to NM_005565.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:136547150 G>A maps to NM_002299.2 L1851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr2:136594163 G>A maps to NM_002299.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr2:136566445 G>T maps to NM_002299.2 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr2:136548357 C>T maps to NM_002299.2 W1735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr2:136566346 A>G maps to NM_002299.2 T1190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:66856309 C>T maps to NM_207338.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr10:103867909 G>A maps to NM_001113407.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HB-01A-11W-A071-09 chr4:16504397 C>T maps to NM_001290.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:88476469 G>T maps to NM_001171610.1 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:18425289 G>A maps to NM_001165414.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr19:11241988 G>A maps to NM_000527.4 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr19:11221352 C>T maps to NM_000527.4 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr1:54479915 G>A maps to NM_001010978.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr11:36119973 A>G maps to NM_174902.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:140271167 C>G did not map to a codon.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr23:140270876 C>T did not map to a codon.
Sequencing variant TCGA-E9-A249-01A-11D-A167-09 chr23:140271017 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:140270785 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr22:44893162 G>A maps to NM_032287.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr22:44892893 G>A maps to NM_032287.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:132209724 C>T maps to NM_052971.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:156710887 G>T maps to NM_001004316.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr1:153177230 C>T maps to NM_001010857.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr19:54660721 G>A maps to NM_024316.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:54967263 C>T maps to ENST00000431846 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:66085698 C>T maps to NM_002303.5 F828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr1:66064358 C>G maps to NM_002303.5 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:189700849 G>A maps to NM_018192.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr12:6947181 C>T maps to NM_014262.3 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:1818527 G>A maps to NM_012318.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:1838206 C>A maps to NM_012318.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:1838290 C>G maps to NM_012318.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr4:1836570 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr4:1834626 A>G maps to NM_012318.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr8:38258463 C>T maps to ENST00000379957 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr11:63279228 G>T maps to NM_001142535.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr19:40199875 C>T maps to NM_203471.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr19:40196606 G>T maps to NM_203471.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27I-01A-11D-A16D-09 chr22:37966364 C>A maps to NM_006498.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:76972104 G>A maps to NM_005567.3 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr17:76968194 C>T maps to NM_005567.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr19:39292706 G>A maps to NM_006149.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:25974090 G>A maps to NM_009587.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:95549885 C>T maps to NM_005097.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr4:25005662 G>A maps to NM_018176.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:22006074 A>C maps to NM_139278.2 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SX-01A-12D-A099-09 chr11:27393923 A>C maps to NM_018490.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:27390283 G>A maps to NM_018490.2 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:27405887 C>T maps to NM_018490.2 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr12:71978444 G>C maps to NM_003667.2 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:71978450 A>C maps to NM_003667.2 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:71977910 C>T maps to NM_003667.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr12:71974204 T>C did not map to a codon.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr12:71833916 G>A maps to NM_003667.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr12:71898465 G>T did not map to a codon.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr1:202287563 C>T maps to NM_001017403.1 Y711Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr1:202287824 G>T maps to NM_001017403.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:202287365 T>C maps to NM_001017403.1 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr6:63990177 G>A maps to NM_016571.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:63990606 A>G maps to NM_016571.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:63990011 G>A maps to NM_016571.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr6:63989961 A>T maps to NM_016571.2 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:206770511 G>A maps to NM_006893.2 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:206776374 G>C maps to NM_006893.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:48915275 G>A maps to NM_000233.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr2:48936097 C>A maps to NM_000233.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr13:40175302 A>G maps to NM_005780.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:111874826 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr3:9547778 G>T maps to NM_198560.2 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:35773536 T>C maps to NM_182548.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr1:180243386 C>T maps to NM_033343.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:113907047 G>A maps to NM_022363.2 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr9:124971973 C>T maps to NM_014368.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:75622660 A>C maps to NM_001001933.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr1:197889139 C>T maps to NM_020204.2 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:197898304 C>A maps to NM_020204.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:197898202 A>G maps to NM_020204.2 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr1:197890706 C>T maps to NM_020204.2 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr22:30639825 G>A maps to NM_002309.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr5:38493887 C>G did not map to a codon.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr5:38496649 T>C maps to NM_002310.5 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr5:38490330 G>A maps to NM_002310.5 Q710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr5:38504177 G>C maps to NM_002310.5 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr5:38504177 G>C maps to NM_002310.5 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:48631250 G>A maps to NM_000234.1 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:48643315 G>A maps to NM_000234.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr19:48640790 G>A maps to NM_000234.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr19:48640922 C>A maps to NM_000234.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:33321329 G>A maps to NM_013975.3 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:33325242 T>C maps to NM_013975.3 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:33310109 G>A maps to NM_013975.3 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr13:108862658 T>A maps to NM_001098268.1 K320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:55107146 A>C maps to NM_006863.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:55107400 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr19:55106796 C>A maps to NM_006863.1 C197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr19:55098710 C>A maps to NM_001130917.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr19:55087517 C>T maps to NM_001130917.1 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr19:54848303 G>A maps to NM_012276.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr19:54818709 T>C maps to NM_021250.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr19:54744773 G>T maps to ENST00000245620 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr19:54742957 G>A maps to NM_024318.2 H439H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr19:54745620 G>A maps to ENST00000270464 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr19:54780305 C>T maps to ENST00000391747 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:54721252 G>A maps to NM_001081450.1 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28O-01A-11D-A228-09 chr19:54725994 G>A maps to NM_001081450.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:54723031 G>C maps to NM_001081450.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:55176602 C>G maps to ENST00000391733 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:54756346 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr19:54756785 G>T maps to NM_001081442.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr19:54758226 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr19:51890454 T>A maps to NM_030657.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr12:50571617 G>T maps to NM_001113546.1 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr12:50571542 C>A maps to NM_001113546.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:41664931 G>A maps to NM_014988.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:41608008 T>C maps to NM_014988.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S0-01A-21D-A25Q-09 chr7:73535624 C>T maps to NM_002314.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr2:109293129 A>G maps to NM_001193484.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr2:109292432 G>T maps to NM_001193484.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr2:109293129 A>G maps to NM_001193484.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr6:105526462 A>T maps to NM_001004317.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:226426716 C>T maps to ENST00000366807 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr1:226426760 G>T maps to ENST00000366807 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr9:27950414 C>T maps to NM_152570.1 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr9:27950342 G>A maps to NM_152570.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr9:27949217 G>A maps to NM_152570.1 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr1:151774340 G>T maps to NM_001004432.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:151774543 C>A maps to NM_001004432.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr15:101120810 G>A maps to NM_001040616.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr15:101115306 A>T maps to NM_001040616.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:90982281 A>G maps to NM_000235.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr19:42911524 C>G maps to NM_005357.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:42931007 T>G maps to NM_005357.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr19:42911524 C>T maps to NM_005357.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr18:47110099 G>A maps to NM_006033.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr3:185245368 G>C maps to NM_139248.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:90366447 C>T maps to NM_001010939.2 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr10:90512356 C>G maps to NM_001080518.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:90521991 C>T maps to NM_001102469.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr10:90530615 C>A maps to NM_001102469.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:99779271 C>A maps to NM_015929.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24K-01A-11D-A167-09 chr2:99778926 C>T maps to NM_015929.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr5:96460223 A>G maps to NM_153234.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr5:96430595 G>T maps to NM_153234.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AU-01A-11D-A12Q-09 chr17:18145295 C>T maps to NM_004140.3 R955R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RX-01A-11D-A25Q-09 chr17:73560439 C>T maps to NM_001031803.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr17:73564695 C>T maps to NM_001031803.1 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr17:73560622 G>A maps to NM_001015002.1 *357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr17:73566548 G>A maps to NM_001031803.1 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr12:66522787 G>A maps to NM_032338.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr18:57006120 A>G maps to NM_005570.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr15:75111589 C>G maps to NM_021819.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:75116717 A>C maps to NM_021819.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr2:97405747 C>G maps to NM_001142292.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr7:156619308 G>A maps to ENST00000354505 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr7:156521382 T>C maps to ENST00000354505 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr12:49491487 G>A maps to NM_018113.2 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3X8-01A-31D-A22X-09 chr6:70500243 G>A maps to NM_018368.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:36117854 A>G maps to NM_001007527.1 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66H-01A-11D-A29N-09 chr5:36114620 A>T maps to NM_001007527.1 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr5:36104191 G>A maps to NM_001007527.1 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr3:197751547 C>T maps to NM_001136049.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:2434312 G>C maps to NM_032737.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr19:2431810 G>A maps to NM_032737.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr11:33886167 G>A maps to NM_005574.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr13:76430697 C>T maps to ENST00000357063 I1539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr13:76381849 T>A maps to ENST00000357063 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W3-01A-11D-A10G-09 chr13:76370782 A>G maps to ENST00000357063 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr1:201869750 T>C maps to NM_012134.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr3:69168310 G>A maps to NM_198271.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr3:69167915 C>G maps to NM_198271.3 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr3:69171351 C>T maps to NM_198271.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:97822149 T>G maps to NM_014916.3 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:97821192 G>C maps to NM_014916.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:97822929 C>T maps to NM_014916.3 T1051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr7:97822388 C>G maps to NM_014916.3 S871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr7:97823712 C>T maps to NM_014916.3 D1312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:97816227 C>T maps to NM_014916.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr19:49001388 C>G maps to NM_001080434.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr19:49014821 G>A maps to NM_001080434.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr9:129455804 C>A maps to NM_001174147.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:54342966 T>G maps to NM_001126328.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr4:54364836 G>T maps to NM_001126328.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:54364969 A>T maps to NM_001126328.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr4:54374204 G>A maps to NM_001126328.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr16:22545338 T>C maps to NM_001135865.1 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr19:40172130 C>A did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr19:19258545 G>A maps to ENST00000410050 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr19:19257860 G>A maps to ENST00000410050 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:5693718 A>C maps to NM_004793.2 G794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:5692071 G>A maps to NM_004793.2 Q951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr19:5708351 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:100911960 G>A maps to NM_198461.3 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:118123502 G>C did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:118123496 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr23:118140132 A>G did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr1:153233505 C>T maps to NM_000427.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr5:121411135 G>A maps to NM_002317.5 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:23159593 G>A maps to NM_002318.2 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr8:23177556 C>T maps to NM_002318.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JS-01A-11D-A13L-09 chr8:23174486 G>A maps to NM_002318.2 Y537Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr8:23198632 G>A maps to NM_002318.2 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr2:74763221 G>A maps to NM_032603.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr10:100017454 A>G maps to NM_032211.6 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr10:100021812 G>A maps to NM_032211.6 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:161006193 A>C maps to NM_005577.2 G1391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr6:161056224 G>A maps to NM_005577.2 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr6:160968969 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr6:161015050 G>A maps to NM_005577.2 Q1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr6:161016384 C>T did not map to a codon.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr6:161012000 C>T maps to NM_005577.2 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr6:161071368 C>T did not map to a codon.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr6:161071403 G>A maps to NM_005577.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr9:113637889 G>A maps to NM_057159.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr19:19735339 G>A maps to NM_004720.5 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr23:78011419 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:78010753 A>C did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:78010426 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr12:6730246 C>T maps to ENST00000435659 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:1479768 C>T maps to NM_024830.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr15:34654802 A>T maps to NM_153613.2 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr15:34655636 C>T maps to NM_153613.2 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr1:82445610 T>A maps to ENST00000370717 L1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr4:62778465 C>T maps to ENST00000506720 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr4:62800718 C>T maps to ENST00000506720 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr4:62897273 C>T maps to ENST00000506720 F1179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:2960672 C>A maps to NM_014646.2 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr18:2937723 C>G maps to NM_014646.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr18:2960805 C>T maps to NM_014646.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr20:39977739 T>A maps to NM_022896.1 L189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr8:19818492 C>G maps to NM_000237.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr8:19797004 G>A maps to NM_000237.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr17:56329629 A>T maps to NM_006151.2 K290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:56321412 C>T maps to NM_006151.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr17:56332272 C>T maps to NM_006151.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr17:56344803 G>A maps to NM_006151.2 K596K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:188202461 A>C maps to NM_005578.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr3:188584022 C>G maps to NM_005578.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr19:11470278 C>T maps to NM_022737.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr19:11468357 A>G maps to NM_001170635.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr19:11473232 C>G maps to NM_001170635.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr19:815749 G>A maps to NM_024888.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:99767347 C>A maps to NM_014839.4 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr1:99772370 A>T maps to NM_014839.4 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:58317478 T>G maps to NM_004811.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15P-01A-11D-A10Y-09 chr11:58345492 G>A maps to NM_001143995.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr4:155665726 C>T maps to NM_004744.3 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:151749399 T>G maps to NM_006726.3 P1701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:151749399 T>G maps to NM_006726.3 P1701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr4:151850193 C>T maps to NM_006726.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr4:151199018 C>A maps to NM_006726.3 L2829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RI-01A-11W-A071-09 chr4:151392803 C>T maps to NM_006726.3 E2224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HB-01A-11W-A071-09 chr4:151412072 T>A maps to NM_006726.3 R2160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:151511903 G>A maps to NM_006726.3 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A248-01A-11D-A167-09 chr4:151935686 T>C maps to NM_006726.3 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr4:151749585 C>T maps to NM_006726.3 E1639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr13:47303079 A>C maps to NM_001164211.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:47315871 A>C maps to NM_001164211.1 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:47315874 A>C maps to NM_001164211.1 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr13:47243212 C>G maps to NM_001164211.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:114391182 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:114400905 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:114347860 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:114400487 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:114400481 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:114422890 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr23:114357647 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr23:114414223 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:114419068 G>T did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr3:197574832 G>T maps to ENST00000425562 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr7:100179963 G>A maps to NM_002319.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr7:100180050 G>C maps to NM_002319.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:40400498 G>A maps to NM_020737.1 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:66625781 C>T maps to NM_024036.4 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr14:42361010 C>A maps to NM_152447.3 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:42356628 A>C maps to NM_152447.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr14:42360995 G>A maps to NM_152447.3 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:4538287 C>T maps to NM_052972.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr7:133863334 G>A maps to NM_144648.1 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:133842801 G>T maps to NM_144648.1 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24K-01A-11D-A167-09 chr7:133842881 A>G maps to NM_144648.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr7:133886231 G>A did not map to a codon.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr3:66463428 A>G maps to NM_015541.2 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr3:66431241 C>T maps to NM_015541.2 V938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:113650362 G>C maps to NM_014813.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:59283812 T>G maps to NM_153377.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:59271205 C>A maps to NM_153377.3 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr10:85993928 G>A maps to NM_015613.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr10:85991724 A>G maps to NM_015613.2 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr10:85984683 C>A maps to NM_001017924.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr4:110789052 C>A maps to NM_198506.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr4:110772989 C>T maps to NM_198506.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:110772998 G>C maps to NM_198506.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr12:57591444 C>T maps to NM_002332.2 Q3094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:57556254 G>C maps to NM_002332.2 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr12:57595391 C>T maps to NM_002332.2 P3486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr12:57552401 G>T maps to NM_002332.2 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr12:57567572 C>A maps to NM_002332.2 I1119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:57559870 G>A maps to NM_002332.2 Q892Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:57592377 G>T maps to NM_002332.2 E3201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:57604144 C>T maps to NM_002332.2 L4212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr6:150174186 G>A maps to NM_032832.5 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr8:105503584 C>T maps to NM_013437.4 Q632Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr2:141283539 G>A maps to NM_018557.2 F2633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr2:141660639 G>A maps to NM_018557.2 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:141294171 T>G maps to NM_018557.2 S2540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr2:141762943 G>A maps to NM_018557.2 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr2:141528483 T>C maps to NM_018557.2 G1864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr2:141806576 C>T maps to NM_018557.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr2:141819657 G>A maps to NM_018557.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr2:141806594 C>T maps to NM_018557.2 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr2:141607770 G>A maps to NM_018557.2 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr2:141356268 C>T maps to NM_018557.2 E2375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr2:170177380 C>T maps to NM_004525.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IY-01A-21D-A21Q-09 chr2:170100024 T>C maps to NM_004525.2 T1146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:169989104 T>G maps to NM_004525.2 S4569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:170025079 G>A maps to NM_004525.2 G3868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:170092351 A>G maps to NM_004525.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr2:170177302 C>A maps to NM_004525.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:170147507 C>T did not map to a codon.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr2:170115632 G>T maps to NM_004525.2 Y805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr4:186291898 G>A maps to ENST00000362004 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr4:186296781 C>T maps to ENST00000362004 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr11:46880599 T>C maps to ENST00000256991 R1929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr11:46894757 G>A maps to ENST00000256991 H1537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WT-01A-11D-A10G-09 chr11:46916347 G>A maps to ENST00000256991 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:46920201 C>A maps to ENST00000256991 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:68171129 G>C maps to NM_002335.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr11:68205944 G>A maps to NM_002335.2 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr11:68115417 G>A maps to NM_002335.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:25750758 C>T maps to NM_001135772.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr12:12334289 G>A maps to NM_002336.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:12312057 C>T maps to NM_002336.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr12:12397347 C>T maps to NM_002336.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr1:53715174 G>A maps to NM_004631.3 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:44170829 C>A maps to NM_133259.3 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr2:44173271 G>C maps to NM_133259.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr6:53784343 G>A maps to NM_018214.4 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:53787446 G>A maps to NM_018214.4 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:53764613 G>T maps to NM_018214.4 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr6:53784397 C>T maps to NM_018214.4 D403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr12:70004048 G>T maps to NM_201550.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr12:70004327 C>T maps to NM_201550.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:195152 C>A maps to NM_001080478.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:195143 C>T maps to NM_001080478.1 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr5:195275 C>T maps to NM_001080478.1 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:194080848 T>G maps to NM_001135057.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:194080857 G>T maps to NM_001135057.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr3:194080617 G>A maps to NM_001135057.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr3:194080749 C>T maps to NM_001135057.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr6:25600889 G>A maps to NM_017640.5 R1156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr6:25471407 C>T maps to NM_017640.5 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr6:25500450 C>T maps to NM_017640.5 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:25610305 G>A maps to NM_017640.5 P1292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:25516006 C>T maps to NM_017640.5 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:25471440 C>T maps to NM_017640.5 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr14:24528875 T>G maps to NM_138360.3 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr14:24525585 C>T maps to NM_138360.3 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr7:102574413 G>A maps to NM_001031692.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr10:50121645 C>T maps to NM_001006939.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:26996330 C>T maps to NM_022901.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:46592973 C>T maps to NM_024512.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr12:7019119 C>T maps to NM_201650.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EI-01A-11D-A27P-09 chr19:18507239 T>C maps to NM_145256.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:99892628 G>A maps to NM_144598.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr15:99926305 G>C maps to NM_144598.2 *368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:169574571 C>T maps to NM_024727.2 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:76372513 G>C maps to NM_001128922.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:76371262 G>C maps to NM_001128922.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr11:76372513 G>C maps to NM_001128922.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:76372552 C>A did not map to a codon.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr11:76371883 C>G maps to NM_001128922.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr3:196386693 G>T maps to NM_198565.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr3:196387260 C>A maps to NM_198565.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr3:169524689 G>T maps to NM_001172779.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:67412589 G>A maps to NM_018296.5 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr17:44374709 A>G maps to NM_014834.4 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr17:44408125 G>A maps to NM_014834.4 R1161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr17:44374709 A>G maps to NM_014834.4 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:44627782 C>T maps to NM_001006607.2 L1569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr17:62865211 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:30348554 G>A maps to ENST00000327564 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:30348458 G>A maps to ENST00000327564 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr3:26751432 G>A maps to NM_052953.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr7:127670237 G>T maps to NM_022143.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:127670273 G>A maps to NM_022143.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr1:46745909 G>A maps to ENST00000254454 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr1:46763261 C>G maps to ENST00000254454 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr12:122685098 G>A maps to NM_001098519.1 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr17:45909568 G>A maps to NM_033413.3 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:45914449 C>T maps to NM_033413.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr17:17907780 G>A maps to NM_031294.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:17900947 G>A maps to NM_031294.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr15:71211474 T>C maps to NM_017691.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:71256255 T>C maps to NM_017691.3 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr19:51022087 G>A maps to NM_001080457.1 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr19:51022416 G>T maps to NM_001080457.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr19:51021652 C>A maps to NM_001080457.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3X8-01A-31D-A22X-09 chr19:51021607 C>T maps to NM_001080457.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:40136876 C>T maps to NM_020929.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr16:84203705 G>A maps to NM_178452.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H3-01A-11D-A12Q-09 chr16:84203705 G>A maps to NM_178452.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr11:56949487 C>T maps to NM_001005210.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr3:120067640 C>G maps to NM_001099678.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr4:52861774 A>T maps to NM_001024611.1 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr4:52861807 C>A maps to NM_001024611.1 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr1:70505049 C>T maps to NM_020794.2 Y1143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr1:70446129 A>G maps to NM_020794.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:131669650 C>A maps to NM_001127244.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:131670663 C>T maps to NM_001127244.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:131670393 C>G maps to NM_001127244.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:90049783 G>A maps to NM_015350.2 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:90049387 G>A maps to NM_015350.2 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr1:90400207 T>C maps to NM_001134479.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:90399944 G>T maps to NM_001134479.1 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:90400313 C>T maps to NM_001134479.1 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr19:7964303 C>T maps to NM_025061.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:7964036 G>A maps to NM_025061.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr19:7964375 C>T maps to NM_025061.3 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:86027663 G>T maps to NM_033402.4 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:238671279 C>A maps to NM_001137552.1 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr2:238672521 C>T maps to NM_001137552.1 D722D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr2:238672125 T>C maps to NM_001137552.1 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr3:37114316 G>A maps to NM_006309.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr3:37152547 G>C maps to NM_006309.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:85450904 A>C maps to NM_001079910.1 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:74492645 C>A maps to NM_001105659.1 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr3:169546578 G>A maps to NM_001080460.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr3:169540419 G>A maps to NM_001080460.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:169539936 C>G maps to NM_001080460.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:169540269 C>T maps to NM_001080460.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T7-01A-21D-A099-09 chr15:101565084 G>A maps to NM_024652.3 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr15:101549211 C>T maps to NM_024652.3 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr15:101567953 G>T maps to NM_024652.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:101555578 A>G maps to NM_024652.3 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:101593285 A>G maps to NM_024652.3 V1283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr15:101595247 C>T maps to NM_024652.3 F1384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr12:40745468 C>T maps to NM_198578.3 G2170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:40681224 C>G maps to NM_198578.3 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr12:40643747 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr12:40745429 T>G maps to NM_198578.3 A2157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr12:40687421 T>A maps to NM_198578.3 L922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:40704387 C>G maps to NM_198578.3 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr3:3886975 G>A maps to NM_020873.5 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr1:204587203 G>C maps to NM_201630.1 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0D9-01A-31W-A071-09 chr7:110762900 A>T maps to NM_018334.4 K25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JT-01A-22D-A18P-09 chr7:110763865 C>T maps to NM_018334.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FN-01A-11W-A050-09 chr20:6025282 G>A maps to NM_152611.3 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:80529759 C>T maps to NM_178839.4 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr2:80530773 G>A maps to NM_178839.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr2:80530005 C>G maps to NM_178839.4 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr2:80530638 G>T maps to NM_178839.4 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr2:80530608 C>T maps to NM_178839.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr5:138210117 G>C maps to NM_015564.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr10:68687690 C>A maps to NM_178011.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:77746142 C>T maps to NM_001134745.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:77746928 C>A maps to NM_001134745.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr9:130223501 G>A maps to NM_001005374.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:130223477 G>C maps to NM_001005374.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr3:54959015 G>A maps to NM_020678.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr3:54958789 G>A maps to NM_020678.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr12:1943502 C>A maps to NM_001163926.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr11:71819712 G>A maps to NM_001145309.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr3:115529226 G>A maps to NM_002338.3 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr3:194371714 A>G maps to NM_018385.2 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr3:194387182 C>T maps to NM_018385.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:194379778 C>G maps to NM_018385.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr8:38033805 G>A maps to NM_014462.1 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr19:34699900 G>A maps to NM_001114093.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr20:60705736 G>T maps to NM_144703.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:60699715 G>A maps to NM_144703.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:14223155 C>T maps to NM_014463.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr4:147104111 G>A maps to NM_007080.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr11:1904705 G>A maps to ENST00000381758 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr21:47611797 C>T maps to NM_002340.5 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr2:33585832 G>T maps to ENST00000354476 P1391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr2:33482525 G>A maps to ENST00000354476 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr2:33590448 G>C maps to ENST00000354476 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:33359905 C>T maps to ENST00000354476 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:33413718 C>G maps to ENST00000354476 S501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13F-01A-11D-A12Q-09 chr14:74975370 G>A maps to NM_000428.2 H1196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr14:74995672 G>A maps to NM_000428.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:65310654 A>C maps to NM_001130144.2 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr19:41123061 C>T maps to ENST00000308370 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr19:41133241 G>T maps to ENST00000308370 E1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10A-01A-21D-A10Y-09 chr19:41125310 G>T maps to ENST00000308370 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr3:46497445 G>A maps to NM_002343.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IE-01A-11W-A050-09 chr3:46492155 C>T maps to NM_002343.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr3:46501160 A>G maps to NM_002343.3 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr15:41797649 C>T maps to NM_002344.5 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr15:41797487 G>A maps to NM_002344.5 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr6:144178936 G>A maps to NM_032860.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr6:144184639 G>A maps to NM_032860.3 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr7:139097294 A>G did not map to a codon.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr1:23418606 T>C maps to NM_001142546.1 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:23419977 A>C maps to NM_001142546.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:23419094 G>A maps to NM_001142546.1 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr1:23418096 A>G maps to NM_001142546.1 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr11:24759770 G>T maps to NM_001009909.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:114537905 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:114524332 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:114524373 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:114536622 A>G did not map to a codon.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr23:114524333 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:143867011 C>T maps to NM_003695.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:143866693 G>T maps to NM_003695.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:31678346 A>C maps to NM_001003693.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr8:144239708 G>A maps to NM_001130478.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr2:160750485 T>A maps to NM_001198759.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:160706651 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:160692126 C>A maps to NM_001198759.1 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr2:160690696 T>C maps to NM_001198759.1 P1233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:160667155 G>C maps to NM_001198759.1 S1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr2:160714972 T>A maps to NM_001198759.1 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:160793999 G>A maps to ENST00000263285 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr1:160769717 C>G maps to ENST00000263285 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr8:74939030 G>A maps to NM_015364.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr8:74922236 G>A maps to NM_015364.4 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:4269646 A>C maps to NM_017816.2 L370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr8:143856614 G>A maps to NM_177457.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr8:143856610 G>A maps to NM_177457.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr8:143833839 C>T maps to NM_205545.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:43965791 G>C maps to NM_014400.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr2:150325178 C>T maps to NM_194317.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr2:150017280 G>A maps to NM_177964.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr16:20931493 G>A maps to NM_020424.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:52016996 C>A maps to NM_153374.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr5:89814774 G>C maps to NM_198273.1 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:100269516 G>C maps to NM_152449.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:100269824 C>A maps to NM_152449.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr1:235922443 G>A maps to NM_000081.2 Q2237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr1:235922288 T>A maps to NM_000081.2 R2288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:235945332 A>G maps to NM_000081.2 S1639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:235972814 C>A maps to NM_000081.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:235872543 C>T maps to NM_000081.2 A3330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:235967815 A>G maps to NM_000081.2 A1181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr1:235860497 G>T maps to NM_000081.2 V3483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:235909788 G>A maps to NM_000081.2 L2607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr1:235940492 G>C maps to NM_000081.2 S1777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr1:235872549 A>C maps to NM_000081.2 P3328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr10:29580825 T>C maps to NM_032517.4 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:30915043 G>A maps to NM_183058.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr17:34264774 G>A maps to NM_020426.1 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:45869968 G>A maps to NM_020347.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr22:21343955 C>T maps to NM_006767.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr22:21351224 C>A maps to NM_006767.3 C792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr22:21348558 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:20112662 G>A maps to NM_021020.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:20110691 C>T maps to NM_021020.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr13:36050008 C>T maps to NM_005584.4 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr13:36049882 C>T maps to NM_005584.4 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:36049384 A>C maps to NM_005584.4 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr4:151504780 G>C maps to NM_006439.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:20198912 T>G maps to NM_182762.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:20199080 G>A maps to NM_182762.3 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr7:20198201 C>T maps to NM_182762.3 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr7:20193844 G>A maps to NM_182762.3 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr1:39889704 C>G maps to ENST00000361689 L3323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr1:39950402 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr1:39823075 G>A maps to ENST00000361689 Q1756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:39799603 T>G maps to ENST00000289893 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:39853532 G>T maps to ENST00000361689 E2945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr1:39798342 C>G maps to ENST00000289893 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr1:39851165 C>T maps to ENST00000361689 Q2575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr1:39851425 G>A maps to ENST00000361689 L2661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr1:39918357 G>A maps to ENST00000361689 A4813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:39824489 C>G maps to ENST00000361689 S1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr1:39797713 G>T maps to ENST00000289893 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr1:39775286 G>A maps to ENST00000361689 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:39797743 G>A maps to ENST00000289893 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr1:39854170 T>C maps to ENST00000361689 R3157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr20:15866445 A>G maps to ENST00000310348 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:16030488 G>T maps to ENST00000310348 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr4:120986905 C>T maps to NM_002358.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:501804 C>T maps to NM_130760.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr11:47296329 C>A maps to NM_003682.3 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:47317506 T>G maps to NM_003682.3 G1220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:47300611 G>T maps to NM_003682.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:47297572 C>A maps to NM_003682.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr11:47304167 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:47330182 G>A maps to NM_003682.3 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr4:1330720 C>T maps to ENST00000505177 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:166985512 G>A maps to NM_032858.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr1:166963266 G>T maps to NM_032858.1 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr1:166959029 C>T maps to NM_032858.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr16:79632802 C>A maps to NM_005360.4 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:145161368 T>G did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr8:145160612 T>C maps to NM_032272.4 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr17:79880759 C>T maps to NM_002359.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr19:35786322 C>T maps to NM_002361.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:152482174 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151303737 T>G did not map to a codon.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr23:151303065 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr23:151303749 C>A did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:148798080 C>G did not map to a codon.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr23:148798315 C>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:148798334 A>T did not map to a codon.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr23:148797954 G>A did not map to a codon.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr23:151900719 A>C did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:151900208 T>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151899894 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151899937 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151900303 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:151900218 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr23:151900502 C>G did not map to a codon.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr23:151900086 G>C did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:151899871 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr23:151899974 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:151900150 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:151900473 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr23:151900529 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1P5-01A-11D-A142-09 chr23:151900137 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151935260 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr23:151935226 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr23:151936111 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:151092212 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:151092145 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1FL-01A-11D-A13L-09 chr23:151092940 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr23:151092750 C>T did not map to a codon.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr23:151869613 G>C did not map to a codon.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr23:151869894 C>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:149013454 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:149014001 G>C did not map to a codon.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr23:30268638 G>A did not map to a codon.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr23:30269533 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:30269358 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:30269643 A>C did not map to a codon.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr23:30268684 C>G did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr23:30269314 C>A did not map to a codon.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr23:30268879 T>C did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:30269444 G>A did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr23:27839449 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:27839429 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:27840227 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:27840082 G>T did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr23:27840070 T>C did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr23:27839535 C>T did not map to a codon.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr23:27840128 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr23:35820493 C>A did not map to a codon.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr23:35821239 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:35821045 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr23:35820756 G>A did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:35820373 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr23:35820502 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:26157614 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr23:26157852 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr23:26157579 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr23:30237090 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:30254732 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr23:30254046 T>C did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr23:30254771 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:30254804 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:30254051 G>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:30260295 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:30261062 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr23:30260726 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:30260719 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0W5-01A-11D-A10G-09 chr23:30261120 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr23:30260917 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:30260711 G>T did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr23:30260875 C>G did not map to a codon.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr23:26213142 G>C did not map to a codon.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr23:26212914 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:26212639 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:26212722 G>T did not map to a codon.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr23:26212564 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:26212602 G>C did not map to a codon.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr23:26212546 T>G did not map to a codon.
Sequencing variant TCGA-A8-A09T-01A-11W-A019-09 chr23:140994264 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:140995924 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:140994640 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:140994849 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:140993953 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr23:140995479 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:140995392 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr23:140994860 C>G did not map to a codon.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr23:140993499 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr23:140995859 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:141291000 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:141290719 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:141291014 C>T did not map to a codon.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr23:141290905 G>C did not map to a codon.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr23:141291555 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0GY-01A-11W-A071-09 chr23:141291739 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr23:141291032 C>G did not map to a codon.
Sequencing variant TCGA-EW-A2FV-01A-11D-A17D-09 chr23:141290730 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr23:140985037 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr23:140969317 C>G did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:140969421 A>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:140984786 C>A did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:140969431 A>G did not map to a codon.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr23:140985321 T>A did not map to a codon.
Sequencing variant TCGA-B6-A0IH-01A-11D-A10Y-09 chr23:140983080 G>A did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:140983303 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:140953295 C>T did not map to a codon.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr23:51644928 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr23:51638305 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:51644658 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:51640911 G>T did not map to a codon.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr23:51639992 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:51641409 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr23:51640686 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr23:51638614 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:54841886 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr23:54841169 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:54837514 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr23:54836183 G>T did not map to a codon.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr23:75648641 A>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:75649825 C>T did not map to a codon.
Sequencing variant TCGA-AO-A126-01A-11D-A10M-09 chr23:75649279 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:75649539 C>A did not map to a codon.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr23:75651057 T>C did not map to a codon.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr23:75649512 C>G did not map to a codon.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr23:75651134 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:75650038 A>G did not map to a codon.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr23:75648838 G>A did not map to a codon.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr23:75004119 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:75004013 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:75003458 G>C did not map to a codon.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr23:75004101 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:75004400 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0EI-01A-11D-A10Y-09 chr23:75004147 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:75003628 C>G did not map to a codon.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr23:75004572 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DG-01A-21D-A12Q-09 chr23:55478907 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0EM-01A-11W-A050-09 chr15:23890164 G>A maps to NM_019066.4 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:23890428 G>A maps to NM_019066.4 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr15:23890636 G>T maps to NM_019066.4 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:65376919 T>G maps to NM_001033057.1 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr3:65361489 G>C maps to NM_001033057.1 S1042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr7:77789381 G>A maps to NM_012301.3 I935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:79082423 C>T maps to NM_012301.3 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:114196629 A>C maps to NM_001142782.1 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:114224864 G>A maps to ENST00000369617 V1145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:114185086 C>T maps to NM_001142782.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr1:114092194 A>T maps to NM_001142782.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr1:114184724 C>G maps to NM_001142782.1 S518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:114165575 G>A maps to NM_001142782.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr23:49021386 C>T did not map to a codon.
Sequencing variant TCGA-AR-A1AX-01A-11D-A12Q-09 chr23:49021217 A>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:49021635 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:49022628 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:10766110 G>A maps to NM_018048.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:10758912 G>A maps to NM_018048.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:77084725 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:33346628 C>T maps to NM_032509.3 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AT-01A-11D-A12Q-09 chr9:72727929 T>C maps to NM_153267.4 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr9:72723277 G>A maps to NM_153267.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr9:72723398 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:72659139 G>A maps to NM_153267.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr5:179193105 G>A maps to NM_014757.4 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:179193519 G>A maps to NM_014757.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr11:95826165 G>A maps to NM_032427.1 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:95825556 G>A maps to NM_032427.1 H546H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A4E0-01A-12D-A25Q-09 chr11:95712201 A>G maps to NM_032427.1 D1127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr4:140811602 G>A maps to ENST00000509479 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:140810735 T>G maps to ENST00000509479 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr4:140811095 C>T maps to ENST00000509479 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr4:140811110 C>T maps to ENST00000509479 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr4:140640647 T>C maps to ENST00000509479 Q1082Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:149631068 A>T did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:149639504 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr23:149680749 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:149639039 C>A did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:149639245 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:149638570 T>G did not map to a codon.
Sequencing variant TCGA-BH-A1FG-01A-11D-A13L-09 chr23:149613878 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:149639114 C>T did not map to a codon.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr23:149638545 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr6:119569482 A>G maps to NM_005907.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr6:119628073 T>C maps to NM_005907.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr1:118039455 C>T maps to NM_006699.3 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:117910924 C>G maps to NM_006699.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:118035767 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr1:117910859 C>T maps to NM_006699.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr1:118003224 C>G maps to NM_006699.3 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr1:117944861 G>A maps to NM_006699.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08X-01A-21W-A019-09 chr5:109091134 T>C maps to NM_002372.2 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:109091065 T>G maps to NM_002372.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr5:109183373 C>T maps to NM_002372.2 I953I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:109155378 C>T maps to NM_002372.2 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr5:109183449 C>T maps to NM_002372.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:109120579 T>C maps to NM_002372.2 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:91456165 G>A maps to NM_006122.2 E843E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:91450542 G>A maps to NM_006122.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr19:12760742 C>A maps to NM_000528.3 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:12763059 G>A maps to NM_000528.3 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr19:12768877 G>C maps to NM_000528.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr19:12769246 G>A maps to NM_000528.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:12768310 G>A maps to NM_000528.3 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:6610947 G>A maps to NM_015274.1 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr4:6621676 C>T maps to NM_015274.1 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr4:6578363 C>T maps to NM_015274.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr4:6598858 G>A maps to NM_015274.1 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr15:75649183 G>A maps to NM_006715.2 N869N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:75651117 G>A maps to NM_006715.2 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr15:75653436 C>T maps to NM_006715.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr4:103556106 C>T maps to NM_005908.3 E751E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr4:103592458 G>C maps to NM_005908.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:103578870 G>A maps to NM_005908.3 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:38265583 C>T maps to NM_001113482.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr23:43590601 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:43652715 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:43640730 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:43702918 A>G did not map to a codon.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr23:43698177 G>T did not map to a codon.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr23:43626802 G>T did not map to a codon.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr23:43656375 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr15:43814495 G>A maps to ENST00000382031 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr15:43817717 G>A maps to ENST00000382031 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:43816967 C>A maps to ENST00000382031 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:43818324 G>T maps to ENST00000382031 E1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:43820639 C>T maps to ENST00000382031 S2561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr15:43820167 C>A maps to ENST00000382031 S2404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:43816226 C>A maps to ENST00000382031 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr15:43814970 G>T maps to ENST00000382031 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr15:43814750 G>A maps to ENST00000382031 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr5:71495433 C>T maps to NM_005909.3 L2084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:71495040 T>G maps to NM_005909.3 G1953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:71490033 C>A maps to NM_005909.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr5:71492253 C>T maps to NM_005909.3 D1024D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr5:71479589 C>T maps to NM_005909.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr5:71499537 G>A maps to NM_005909.3 V2387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:172945067 C>T maps to NM_199227.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr2:172945133 A>T maps to NM_199227.1 *336C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr19:17836888 C>T maps to NM_018174.4 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr2:210574676 C>G maps to NM_002374.3 S1591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr2:210558834 T>C maps to NM_002374.3 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:210565007 T>G maps to NM_002374.3 G1510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr2:210518056 G>T maps to NM_002374.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:210559606 C>T maps to NM_002374.3 R905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr2:210574869 G>A maps to NM_002374.3 A1655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr2:210560611 G>T maps to NM_002374.3 E1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr2:210559281 C>T maps to NM_002374.3 Y796Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:210557364 G>C maps to NM_002374.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:66729196 C>T maps to NM_002755.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07Z-01A-11W-A019-09 chr17:11998992 T>A maps to ENST00000415385 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr17:12043201 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:11958294 C>T maps to ENST00000415385 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr17:12028689 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:12032509 C>T maps to ENST00000415385 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr17:12044462 G>C did not map to a codon.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr17:12011211 A>T maps to ENST00000415385 K218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr17:12032458 G>T maps to ENST00000415385 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YI-01A-31D-A10M-09 chr15:67873161 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:68061992 C>T maps to NM_145160.1 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr5:56161283 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr5:56170972 G>T maps to NM_005921.1 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr5:56178256 C>G maps to NM_005921.1 S1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr5:56178410 C>T maps to NM_005921.1 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr5:56178168 C>T maps to NM_005921.1 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr5:56160760 G>A maps to NM_005921.1 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr5:56161794 C>A maps to NM_005921.1 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr5:56174908 A>T maps to NM_005921.1 K690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr5:56183346 G>A maps to NM_005921.1 E1419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr5:56176547 C>T maps to NM_005921.1 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr5:56168739 C>T maps to NM_005921.1 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W5-01A-11D-A10G-09 chr5:56177499 A>T maps to NM_005921.1 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18M-01A-11D-A12B-09 chr5:56178570 G>T maps to NM_005921.1 E1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr5:56178168 C>T maps to NM_005921.1 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr5:56178084 C>T maps to NM_005921.1 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr5:56178576 G>T maps to NM_005921.1 E1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr5:56181806 C>G maps to NM_005921.1 S1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr5:56168739 C>T maps to NM_005921.1 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:40698483 G>A maps to NM_002446.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr11:65380869 C>A maps to NM_002419.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr11:65365762 C>G maps to NM_002419.3 *848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr11:65374960 C>T maps to NM_002419.3 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G0-01A-11D-A13L-09 chr12:53876973 C>T did not map to a codon.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr3:185165735 G>A maps to ENST00000392515 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:185169087 C>T maps to NM_004721.3 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:185165696 G>C maps to NM_004721.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr3:185191456 G>T maps to NM_004721.3 E780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr23:19387186 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:19410219 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:19392776 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:19433295 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:19478235 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr23:19478184 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr23:19390836 G>A did not map to a codon.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr23:19391797 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr2:128084358 T>A maps to NM_006609.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr6:161470387 G>T maps to NM_005922.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:161529875 T>A maps to NM_005922.2 G1407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:161523000 C>A maps to NM_005922.2 S1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:161508887 C>T maps to NM_005922.2 R909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr6:161507646 C>G maps to NM_005922.2 S835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:161533712 T>C maps to NM_005922.2 P1511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr6:161507646 C>A maps to NM_005922.2 S835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr6:161502010 C>T maps to NM_005922.2 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr6:161510421 G>A maps to NM_005922.2 Q964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr6:137019706 G>A maps to NM_005923.3 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr6:136878949 C>G maps to NM_005923.3 G1357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:136934280 G>A maps to NM_005923.3 Q798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr1:27682954 G>C maps to NM_004672.3 Y1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr6:91257870 T>G maps to NM_145331.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr6:91261892 G>A maps to NM_145331.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr3:48040185 C>T maps to ENST00000426837 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr3:47951253 C>A maps to ENST00000426837 E1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr3:47957723 G>A maps to ENST00000426837 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr19:39092117 G>A maps to NM_001042600.1 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr19:39098532 C>T maps to NM_001042600.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr19:39096099 C>T maps to NM_001042600.1 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr19:39098646 G>C maps to NM_001042600.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr19:39104521 G>C maps to NM_001042600.1 Y177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:64567839 G>C maps to NM_004579.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:39499673 G>A maps to NM_003618.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr2:39519954 T>C maps to NM_003618.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr2:39552676 G>A maps to NM_003618.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr2:102482934 G>T maps to NM_145686.2 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:102480404 A>C maps to NM_145686.2 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr2:102476238 G>A maps to NM_145686.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:102441848 C>T maps to NM_145686.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:102456319 G>A maps to NM_145686.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:102456439 G>A maps to NM_145686.2 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr14:50952847 G>A maps to NM_198794.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr11:75298781 G>C maps to NM_033063.1 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr11:75298415 G>A maps to NM_033063.1 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:136710530 A>G maps to NM_001198609.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:136710560 C>T maps to NM_001198609.1 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:36642136 C>T maps to NM_018067.3 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr23:20070997 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:20060745 A>C did not map to a codon.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr23:20043895 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr23:20030639 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr23:20069028 G>C did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:20030533 C>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:135309523 T>A did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr6:36103592 G>A maps to NM_002754.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr6:36040653 C>T maps to NM_139012.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr8:144803947 G>A maps to NM_139021.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:55529445 G>A maps to NM_144578.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A145-01A-11D-A10Y-09 chr18:48256049 C>T maps to NM_002747.3 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr18:48255620 G>A maps to NM_002747.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr15:52356302 T>C maps to NM_002748.3 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0D9-01A-31W-A071-09 chr10:49609775 C>T maps to NM_139049.1 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:1798617 C>T maps to NM_015133.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr5:179676087 G>A maps to NM_002752.4 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr5:179663438 G>C maps to NM_002752.4 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:128322033 G>A maps to NM_001006617.1 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr1:206904485 G>A maps to NM_032960.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr3:50683585 A>C maps to NM_004635.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:50679146 T>G maps to NM_004635.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr12:112323731 C>G maps to NM_139078.1 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42115322 C>G maps to NM_001128608.1 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr15:42113196 G>C maps to NM_001128608.1 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr15:42110266 C>T maps to NM_001128608.1 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A153-01A-12D-A12B-09 chr15:42115927 C>T maps to NM_001128608.1 I1300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:31421536 C>T maps to NM_012325.2 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:31434458 G>A maps to NM_012325.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:44067365 A>C maps to NM_001123066.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14U-01A-11D-A228-09 chr17:44061291 C>A maps to NM_001123066.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr17:44087761 C>T maps to NM_001123066.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr17:60814610 C>A maps to NM_152598.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr17:60821779 C>T maps to NM_152598.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr17:60821842 C>G maps to NM_152598.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr5:10390503 A>C maps to NM_005885.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr5:10410283 G>A maps to NM_005885.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:160605207 T>G maps to NM_022826.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:160604369 C>G maps to NM_022826.2 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr10:45956753 C>T maps to NM_145021.4 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr2:119735464 A>G maps to NM_006770.3 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr2:119727688 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr2:119750775 G>A maps to NM_006770.3 W443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr1:220824017 G>A maps to NM_018650.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr11:63669753 C>T maps to NM_001039469.2 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:57884026 G>A maps to NM_004990.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr12:57910282 G>A maps to NM_004990.2 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr2:198570603 C>T maps to NM_138395.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:71663365 C>T maps to NM_001017967.2 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr6:160328343 C>G maps to NM_002377.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:160328583 C>T maps to NM_002377.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr6:29454671 C>T maps to NM_052967.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:29455046 G>A maps to NM_052967.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:29454983 A>G maps to NM_052967.1 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr6:29454743 G>A maps to NM_052967.1 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr6:29455331 G>A maps to NM_052967.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:186954134 C>A maps to NM_139125.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr3:186953801 A>T maps to NM_139125.3 Y619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr3:186953789 G>A maps to NM_139125.3 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr3:186968078 C>T maps to NM_139125.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr3:186970995 C>T maps to NM_139125.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr1:11106965 G>A maps to NM_006610.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AB-01A-11W-A050-09 chr19:12984564 G>A maps to NM_014975.2 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:12975947 G>T maps to NM_014975.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ES-01A-11D-A135-09 chr19:12976828 C>T maps to NM_014975.2 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:18254638 C>T maps to NM_015016.1 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:18245682 G>A maps to NM_015016.1 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:66459593 C>T maps to NM_001164664.1 R1529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr5:66432389 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr2:85769378 A>G maps to NM_005911.4 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr1:31188154 G>A maps to NM_002379.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr8:98900331 G>T maps to ENST00000254898 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr8:99006789 G>C maps to ENST00000254898 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr20:43926556 C>T did not map to a codon.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr20:3846667 G>C maps to NM_020746.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:3844921 A>C maps to NM_020746.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J3-01A-11D-A13L-09 chr20:3835300 G>A maps to NM_020746.3 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr16:29819562 C>G maps to NM_001042539.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr16:29821525 C>T maps to NM_002383.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:29819913 G>A maps to NM_001042539.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr22:36007098 C>T maps to NM_203377.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:47800615 G>A maps to ENST00000424334 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr18:47800630 G>A maps to ENST00000424334 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr19:1585125 C>T maps to NM_003926.5 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:1582690 C>T maps to NM_003926.5 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:129155811 G>A maps to NM_003925.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr2:149247299 T>C maps to ENST00000404807 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr2:149227716 C>T maps to ENST00000404807 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr2:149247497 G>T maps to ENST00000404807 E1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr12:57922184 C>T maps to NM_052897.3 R888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr12:57922154 C>T maps to NM_052897.3 R878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr12:57919305 C>T maps to NM_052897.3 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RD-01A-11D-A159-09 chr12:57921443 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr14:36781171 G>A maps to NM_016586.2 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:131573582 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:131573611 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:131516234 G>T did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:131540294 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr6:20152997 C>T maps to NM_001080480.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:20126777 A>C maps to NM_001080480.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr6:20144467 G>A maps to NM_001080480.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:54692349 C>A maps to NM_024298.3 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr19:54691159 G>A maps to NM_024298.3 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:54677851 G>A maps to NM_024298.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr16:84101989 T>A maps to NM_003791.2 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:21857899 C>T did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr23:21871595 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:21871565 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:21871529 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:21863499 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr23:21886677 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:21900732 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:21900633 C>G did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:21887781 G>A did not map to a codon.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr20:54824147 C>T maps to ENST00000371389 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr18:58039363 C>T maps to NM_005912.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr18:58038838 G>T maps to NM_005912.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr18:13826447 G>A maps to NM_005913.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr11:119182248 G>T maps to NM_006500.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZX-01A-12D-A29N-09 chr11:119181177 T>A did not map to a codon.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr11:119182272 G>C maps to NM_006500.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr11:119183642 C>T maps to NM_006500.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr23:103349779 C>T did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:103349789 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:112364656 G>A maps to NM_001085377.1 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr5:70930838 G>A maps to NM_022132.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:138727744 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:138687894 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:138699718 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr23:138689911 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:138698559 C>T did not map to a codon.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:138680640 A>T did not map to a codon.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr13:113750782 C>T maps to NM_001112732.1 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:113728861 C>T maps to NM_001112732.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr13:113699675 G>T did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr13:113719305 C>T maps to NM_001112732.1 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:182994745 C>G did not map to a codon.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr2:47135038 C>T maps to NM_001171506.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:100382335 C>T maps to NM_032503.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:100369052 C>G maps to NM_032503.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr6:100369061 G>A maps to NM_032503.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr1:150551358 A>T maps to NM_021960.4 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr10:13251285 T>A maps to NM_182751.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr10:13228240 G>A maps to NM_182751.2 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:127336830 G>A maps to NM_004526.2 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr3:127325046 G>T maps to NM_004526.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr3:127327259 G>A maps to NM_004526.2 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr6:52129520 G>T maps to ENST00000419835 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr6:52146917 C>T maps to ENST00000419835 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr21:47692479 G>A maps to NM_003906.3 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr21:47663505 G>A maps to NM_003906.3 S1723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:47664967 C>T maps to NM_003906.3 L1597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr21:47687011 C>T maps to NM_003906.3 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr21:47663637 T>C did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr21:47697513 C>T maps to NM_003906.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:48875551 C>T maps to NM_182746.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr8:48883291 G>A maps to NM_182746.1 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr8:48887463 G>A maps to NM_182746.1 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr8:48882406 G>A maps to NM_182746.1 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr8:48888381 G>T maps to NM_182746.1 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr2:136598405 C>G maps to NM_005915.4 *822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:99690707 G>C maps to NM_005916.3 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:99694959 G>A maps to NM_005916.3 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr7:99695337 G>T maps to NM_005916.3 S339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr6:119245056 G>A maps to ENST00000316316 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr19:7593048 G>A maps to NM_020533.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr19:7592839 C>T maps to NM_020533.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:85405235 C>T maps to NM_153259.2 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:85487857 A>G maps to NM_018298.9 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr1:85486833 G>C maps to NM_018298.9 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr8:6302475 A>G maps to NM_024596.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:6302398 C>T maps to NM_024596.3 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr5:94353074 T>G maps to NM_024717.4 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr15:94910917 T>A maps to NM_018349.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr15:94927323 C>A maps to NM_018349.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr15:95013627 C>T maps to NM_018349.3 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SJ-01A-11D-A099-09 chr23:119738712 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:119739327 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr6:30673104 C>G maps to NM_014641.2 V1285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr6:30673674 G>T maps to NM_014641.2 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:30673815 T>G maps to NM_014641.2 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:30675208 T>G maps to NM_014641.2 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:30680998 A>C maps to NM_014641.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:30672141 G>C maps to NM_014641.2 V1606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr6:30671701 G>C maps to NM_014641.2 S1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:37605978 A>C maps to ENST00000505425 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CH-01A-21W-A019-09 chr6:37622128 C>T maps to ENST00000297153 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr6:37620060 G>A maps to ENST00000297153 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:47613279 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr14:47530632 T>A maps to NM_001113498.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:63822564 T>C maps to NM_005917.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:63824531 G>A did not map to a codon.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr12:68696588 G>A maps to NM_017440.4 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:68707260 G>A maps to NM_017440.4 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:68720624 G>A maps to NM_017440.4 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr12:68720670 G>A maps to NM_017440.4 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:68707512 G>C maps to NM_017440.4 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr1:204513769 T>G maps to NM_002393.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr6:90450018 C>T maps to NM_014611.1 L1509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr6:90397096 G>A maps to NM_014611.1 Q3806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr6:90400448 C>T maps to NM_014611.1 L3564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:90409322 C>T maps to NM_014611.1 Q2998Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:90383866 G>A maps to NM_014611.1 V4401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:90374211 C>A maps to NM_014611.1 E4744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr6:90406152 C>T maps to NM_014611.1 E3103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr6:90380733 G>T maps to NM_014611.1 L4620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18S-01A-11D-A12B-09 chr6:90410500 A>T maps to NM_014611.1 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:90366469 C>G maps to NM_014611.1 S5078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:48465961 C>T maps to NM_002396.4 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:48446852 C>T maps to NM_002396.4 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr18:48458668 G>A maps to NM_002396.4 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:86158118 G>A maps to NM_001014811.1 Y456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr3:168849289 C>T maps to NM_004991.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr3:168833700 C>T maps to NM_004991.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr3:168802735 C>T maps to NM_004991.3 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:168807966 G>A maps to NM_004991.3 D1074D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr3:168813029 G>A maps to NM_004991.3 C951C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr23:153296804 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:153296880 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03L-01A-41W-A071-09 chr23:153296384 C>G did not map to a codon.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr23:153297781 G>A did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr17:37564555 G>A maps to NM_004774.3 V1306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SG-01A-11D-A142-09 chr23:70361799 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:70340836 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:70352255 T>G did not map to a codon.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr23:70345961 C>G did not map to a codon.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr23:70357091 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr23:70339988 G>T did not map to a codon.
Sequencing variant TCGA-A8-A083-01A-21W-A019-09 chr23:70340967 A>T did not map to a codon.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr23:70340010 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:70345252 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:70351943 A>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:70356303 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:70352038 G>C did not map to a codon.
Sequencing variant TCGA-AR-A24T-01A-11D-A167-09 chr23:70352767 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr23:70361813 A>G did not map to a codon.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr23:70344906 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr23:70357673 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:70352289 C>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:70340924 G>A did not map to a codon.
Sequencing variant TCGA-C8-A27A-01A-11D-A167-09 chr23:70344920 G>T did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:70349588 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr23:70357653 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:70342619 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:70346869 G>T did not map to a codon.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr23:70345259 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr23:70356251 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr23:70355013 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr3:151107819 C>G maps to NM_053002.4 S1800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:151073778 C>A maps to NM_053002.4 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:151134120 C>T maps to NM_053002.4 Q2072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:150877656 T>C maps to NM_053002.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr3:151127065 G>A maps to NM_053002.4 A1917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr3:150840682 T>A maps to NM_053002.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr3:151075104 C>A maps to NM_053002.4 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr3:151095875 C>T maps to NM_053002.4 L1430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:60088224 T>G maps to NM_005121.2 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:60023860 G>A maps to NM_005121.2 Q2165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:60028298 G>A maps to NM_005121.2 Q2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:60142515 A>G maps to NM_005121.2 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:60062381 G>A maps to NM_005121.2 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr17:60088031 T>A maps to NM_005121.2 K616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:116406834 C>T maps to NM_015335.4 G2045G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:40542222 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:40562737 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:40570493 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:40586057 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:40571484 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0FF-01A-11W-A050-09 chr23:40511086 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:40560456 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:40569290 C>T did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:40573795 C>T did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr23:40514244 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:40573050 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr22:20918842 G>A maps to NM_001003891.1 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr22:20907441 A>G maps to NM_001003891.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:93527178 A>C maps to NM_004268.4 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:57472687 C>G maps to ENST00000431606 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:136213392 A>C did not map to a codon.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr6:131948805 C>A maps to ENST00000403834 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr6:131912471 G>A maps to ENST00000403834 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25C-01A-11D-A167-09 chr6:131921248 G>A maps to ENST00000403834 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr6:131908937 G>A maps to ENST00000403834 R1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:131948547 A>C maps to ENST00000403834 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:131919504 G>A maps to ENST00000403834 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr6:131912639 G>A maps to ENST00000403834 R1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr6:131946080 G>A maps to ENST00000403834 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr17:38189362 C>T maps to NM_014815.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr17:38176103 C>T maps to NM_014815.3 E929E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr17:38187822 G>A maps to NM_014815.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr19:50335257 C>T maps to NM_030973.3 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:50335407 G>A maps to NM_030973.3 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr17:6554833 G>C maps to NM_016060.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr13:48651421 C>T maps to NM_014166.2 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr5:156566069 C>A maps to NM_004270.4 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr1:43852270 G>C maps to NM_052877.3 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:100250837 G>C did not map to a codon.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr5:88047757 G>A maps to NM_002397.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr5:88018446 G>A maps to NM_002397.4 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr5:88056819 C>T maps to NM_001193347.1 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:156437436 T>C maps to NM_005920.2 *522W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YI-01A-31D-A10M-09 chr16:3306364 G>T maps to NM_000243.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G0-01A-11D-A13L-09 chr16:3293863 A>G maps to NM_000243.2 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:3294547 G>A maps to NM_000243.2 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:3299508 G>T maps to NM_000243.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr16:3293383 C>T maps to NM_000243.2 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:3293878 A>T maps to NM_000243.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:126705650 C>A maps to NM_032446.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27I-01A-11D-A16D-09 chr5:126792856 T>C maps to NM_032446.2 N1090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr15:66206078 G>A maps to NM_032445.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr15:66257397 G>A maps to NM_032445.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr19:42855838 C>T maps to ENST00000251268 F1009F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr19:42875613 C>T maps to ENST00000251268 R2417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:42848851 C>G maps to ENST00000251268 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr19:42841096 G>T maps to ENST00000251268 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr19:42862377 G>A maps to ENST00000251268 L1698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:42128504 C>A maps to NM_152513.3 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr22:42177710 C>T maps to NM_152513.3 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr2:66664936 G>A maps to ENST00000407092 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:37376048 G>C maps to NM_170675.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:36643023 G>T maps to NM_014791.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:32117106 C>T maps to NM_015955.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr11:64577194 G>C maps to NM_130804.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr6:46803034 G>A maps to NM_005588.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:46793147 C>A maps to NM_005588.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:46793030 C>A maps to NM_005588.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr6:46802998 C>T maps to NM_005588.2 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr6:46766376 C>G maps to NM_005588.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr18:29797729 G>A maps to NM_005925.2 Q631Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr18:29797014 C>T maps to NM_005925.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr18:29775425 A>G maps to NM_005925.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr7:100028414 T>A maps to NM_019606.5 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:88767249 T>G maps to ENST00000395102 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:88766592 G>A maps to ENST00000395102 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr4:88766793 C>T maps to ENST00000395102 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr2:112779074 C>T maps to NM_006343.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JJ-01A-11W-A071-09 chr2:112786350 C>T maps to NM_006343.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:116380976 A>C maps to NM_001127500.1 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:116395449 G>A maps to NM_001127500.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:99962253 G>T maps to NM_015143.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:99964477 G>T maps to NM_015143.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EI-01A-11D-A27P-09 chr4:99955393 G>T maps to NM_015143.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:99969960 C>T maps to NM_015143.2 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:95888733 G>T maps to NM_006838.3 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr12:95905672 A>T maps to NM_006838.3 K323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:81042909 C>G maps to NM_001004431.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr17:81043179 G>C maps to NM_001004431.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:2405550 G>C maps to NM_024086.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:2341477 C>T maps to NM_024086.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:2323419 G>A maps to NM_024086.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr14:21464954 G>A maps to NM_001029991.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr12:58162853 G>A maps to ENST00000408972 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:132395101 C>T maps to NM_014064.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr9:132397667 C>T maps to NM_014064.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr11:62434165 T>G maps to NM_001043229.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr11:62433974 G>T maps to NM_001043229.1 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:171765634 C>T maps to NM_015935.4 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr1:171763539 G>A maps to NM_015935.4 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:171753158 G>T maps to NM_015935.4 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:128141828 G>A maps to NM_018396.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr7:128141819 A>G maps to NM_018396.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr18:2567035 A>G maps to NM_022840.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr2:170676118 T>C maps to NM_014168.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:156047129 G>A maps to NM_001093725.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12O-01A-11D-A10Y-09 chr15:82336478 G>A maps to NM_032246.3 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr18:48702726 G>A maps to NM_016626.4 H658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr1:17301447 C>T maps to NM_017459.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:17301447 C>T maps to NM_017459.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:153432987 T>G maps to NM_005927.4 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr4:170913068 G>A maps to NM_021647.6 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr2:228211953 G>A maps to NM_020194.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SB-01A-21D-A25Q-09 chr15:89444792 G>A maps to NM_005928.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr15:89450545 C>G maps to NM_005928.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr3:196748287 C>A maps to NM_005929.5 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:196735738 G>C maps to NM_005929.5 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12V-01A-11D-A10Y-09 chr3:179107926 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:12066641 A>C maps to NM_014874.3 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:12064573 T>C maps to NM_014874.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr17:74772589 C>T maps to NM_024311.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr17:74763466 G>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr17:74737111 C>T maps to NM_024311.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:145735752 T>G maps to NM_138431.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:205548899 C>A maps to NM_181644.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:191301649 G>T maps to NM_017694.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:191301690 C>T maps to NM_017694.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr2:191362339 A>C maps to NM_017694.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:191354509 C>T maps to NM_017694.3 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr4:678307 G>A maps to ENST00000404286 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr2:103335115 C>A maps to NM_032718.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr15:42041006 A>T maps to ENST00000219905 P1844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42041378 C>G maps to ENST00000219905 S1907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42041581 C>A maps to ENST00000219905 S1975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:42021427 C>T maps to ENST00000219905 R1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:42046669 G>A maps to ENST00000219905 E2397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr15:42057207 C>G maps to ENST00000219905 L2672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:41961441 C>G maps to ENST00000219905 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr15:41989019 G>A maps to ENST00000219905 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr15:42041685 C>T maps to ENST00000219905 Q2010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr7:141763363 G>A maps to ENST00000475668 L1441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr7:141765158 G>A maps to ENST00000475668 Q1503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:141794560 C>T maps to ENST00000475668 I2453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:141705407 C>T maps to ENST00000475668 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr7:141752212 C>T maps to ENST00000475668 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:141755405 C>T maps to ENST00000475668 R1121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:141736723 C>G maps to ENST00000475668 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr2:99279577 A>C maps to NM_012214.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr2:99272903 G>A maps to NM_012214.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:99242245 G>A maps to NM_012214.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr2:99274685 C>T maps to NM_012214.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr5:179226610 C>T maps to NM_054013.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr5:179225427 G>A maps to NM_054013.3 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr2:135206252 C>T maps to NM_002410.3 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr2:135107490 C>T maps to NM_002410.3 Q410*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E2-A15A-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr17:74902193 G>A maps to NM_198955.1 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr7:88424031 T>A maps to NM_152706.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr10:131565071 C>A maps to NM_002412.3 C176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr10:131506230 G>A maps to NM_002412.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RQ-01A-11D-A10Y-09 chr10:131565092 C>T maps to NM_002412.3 S183S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EW-A1PD-01A-11D-A142-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr16:4715103 G>T maps to NM_015246.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:41282968 C>T maps to NM_006533.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:222837365 T>C maps to NM_198551.2 P1763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:222832962 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:222828094 C>T maps to NM_198551.2 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr1:222801434 G>A maps to NM_198551.2 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr1:222803198 C>T maps to NM_198551.2 D879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr1:222828135 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:222825649 T>A maps to NM_198551.2 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr1:222827735 G>A maps to NM_198551.2 Q1461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:19371400 T>G maps to NM_020774.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr18:19426997 C>T maps to NM_020774.2 R769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr6:109767567 A>G maps to NM_022765.3 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr11:12265627 C>G maps to NM_014632.2 S918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:12183806 C>G maps to NM_014632.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:12263915 G>A maps to NM_014632.2 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr11:12225819 C>G maps to NM_014632.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr22:18371884 G>A maps to NM_015241.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr22:18293575 T>G maps to NM_015241.2 R1817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:12316063 A>C maps to NM_032867.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr11:12371383 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:38327900 A>C maps to NM_033386.2 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr22:38333085 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:38328624 G>A maps to NM_033386.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr23:10535322 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:10442786 G>A did not map to a codon.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr23:10535363 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:10535384 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr23:10534971 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:10450568 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr23:10442721 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr23:10491175 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:10442696 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DN-01A-11D-A17W-09 chr23:10535214 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:107169921 C>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:107167683 T>G did not map to a codon.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr23:107170051 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:73262963 G>A maps to NM_020679.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr1:12081869 G>T maps to NM_021933.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr1:12081866 G>A maps to NM_021933.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr17:4799334 C>T maps to NM_153827.4 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:4800500 G>A maps to NM_153827.4 V1306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr7:7636042 A>T maps to NM_019005.3 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr13:24460600 A>G maps to NM_005932.3 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr10:129921414 G>A maps to NM_002417.4 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr10:129899950 G>A maps to NM_002417.4 R3092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:129901623 G>T maps to NM_002417.4 S2827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr10:129901070 C>T maps to NM_002417.4 R3011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:10385933 C>T maps to NM_170784.1 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:10393433 G>A maps to NM_170784.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr22:40825738 G>A maps to NM_020831.3 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr22:40807870 C>A maps to NM_020831.3 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:14334206 T>G maps to NM_014048.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr16:14339390 C>T maps to NM_014048.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:131071995 G>T maps to NM_013255.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:47048951 C>T maps to NM_003684.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr1:47037768 G>A maps to NM_003684.4 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr19:2042425 C>G maps to NM_199054.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr19:2041143 G>T maps to NM_199054.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr3:12623429 C>G maps to NM_014160.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JC-01A-11W-A071-09 chr15:23811711 C>T maps to NM_005664.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr17:56285903 T>G maps to NM_017777.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr9:5897574 C>T maps to NM_005511.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr9:5892542 G>A maps to NM_005511.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr22:50506876 G>T maps to NM_015166.3 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr22:50512643 C>T did not map to a codon.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr22:50500032 G>A maps to NM_015166.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:6858086 A>G maps to NM_005439.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:37092141 T>A maps to NM_000249.3 *757K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:37067126 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr3:37042541 G>T maps to NM_000249.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:75515641 G>A maps to NM_001040108.1 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr14:75515437 T>G maps to NM_001040108.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr11:118350901 C>T maps to NM_001197104.1 Q1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118343655 A>C maps to NM_001197104.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118372516 A>C maps to NM_001197104.1 T2150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118376137 A>C maps to NM_001197104.1 P3177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:118343827 C>T maps to NM_001197104.1 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr11:118392844 C>G maps to NM_001197104.1 P3959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:118344571 C>T maps to NM_001197104.1 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AT-01A-11D-A12Q-09 chr11:118354911 G>A maps to NM_001197104.1 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr11:118371700 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr11:118375783 G>A maps to NM_001197104.1 P3059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:118376470 C>T maps to NM_001197104.1 I3288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr11:118359385 G>T maps to NM_001197104.1 E1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr12:49443898 C>A maps to NM_003482.3 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:49445935 T>G maps to NM_003482.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr12:49444768 G>C maps to NM_003482.3 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:49445581 T>G maps to NM_003482.3 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:49445158 G>A maps to NM_003482.3 H769H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr12:49445332 C>T maps to NM_003482.3 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr12:49424515 G>T maps to NM_003482.3 I4569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr12:49428418 G>A maps to NM_003482.3 L3462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A259-01A-11D-A16D-09 chr7:152027749 G>A maps to ENST00000355193 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr7:151879135 G>A maps to ENST00000355193 Q1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06P-01A-11W-A019-09 chr7:151904385 T>C maps to ENST00000355193 P1280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr7:151891575 C>A maps to ENST00000355193 E1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:151879633 G>A maps to ENST00000355193 Q1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:151860830 T>G maps to ENST00000355193 P3277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:151879295 T>G maps to ENST00000355193 S1883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:151879376 A>G maps to ENST00000355193 P1856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:151879442 T>G maps to ENST00000355193 P1834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:151877801 C>T maps to ENST00000355193 L2381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:151917667 G>A maps to ENST00000355193 Q1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr7:151845840 T>A maps to ENST00000355193 K4448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr7:152132814 G>C maps to ENST00000355193 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:151845579 G>A maps to ENST00000355193 R4535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr7:151945473 G>C maps to ENST00000355193 S682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr7:151919732 C>A maps to ENST00000355193 E1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr7:151880093 C>A maps to ENST00000355193 E1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr7:151860727 G>A maps to ENST00000355193 Q3312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr7:151945450 C>A maps to ENST00000355193 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr7:151878505 G>A maps to ENST00000355193 Q2147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr7:151945600 C>A maps to ENST00000355193 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:151880188 G>C maps to ENST00000355193 S1712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr7:151868350 G>A maps to ENST00000355193 Q3151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr7:151960148 A>T maps to ENST00000355193 C417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr7:152012424 T>G did not map to a codon.
Sequencing variant TCGA-E2-A1L9-01A-11D-A13L-09 chr7:152012229 G>A maps to ENST00000355193 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr7:151921672 C>T maps to ENST00000355193 W1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr7:151891153 G>A maps to ENST00000355193 Q1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr7:151880168 G>A maps to ENST00000355193 Q1719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr7:151896462 G>A maps to ENST00000355193 Q1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66H-01A-11D-A29N-09 chr7:151949698 A>T maps to ENST00000355193 C467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:36211032 C>T maps to NM_014727.1 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:36216489 C>T maps to NM_014727.1 F1251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:36220953 G>A maps to NM_014727.1 R1668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WY-01A-11D-A10G-09 chr19:36220092 G>T maps to NM_014727.1 E1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr7:104748201 C>T maps to NM_182931.2 R1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr7:104753374 C>T maps to NM_182931.2 S1724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:104748224 G>A maps to NM_182931.2 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:104681466 C>G maps to NM_182931.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:104715185 C>G maps to NM_182931.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr10:21827789 T>A maps to NM_004641.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr10:21884362 T>A maps to NM_004641.3 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AU-01A-11D-A12Q-09 chr6:168289973 T>G maps to ENST00000400822 L325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr6:168312076 C>T maps to ENST00000400822 Q648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr6:168312081 C>G maps to ENST00000400822 Y649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr13:49796404 G>A maps to NM_001507.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:238434428 G>T maps to NM_024101.5 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr2:238449563 A>G maps to NM_024101.5 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr2:238461046 C>T maps to NM_024101.5 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:238436065 C>T maps to NM_024101.5 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:83948796 G>A maps to NM_012213.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:109996960 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:45974865 A>C maps to NM_015506.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr1:45974589 T>A maps to NM_015506.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr1:45974547 G>A maps to NM_015506.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr2:150443602 A>G maps to NM_015702.2 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr17:53491547 A>T maps to NM_012329.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr17:53471850 A>T maps to NM_012329.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:53481165 T>C maps to NM_012329.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:154886404 T>G maps to NM_007289.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr3:154889934 C>T maps to NM_007289.2 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr23:135053262 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr22:24122653 C>T maps to NM_005940.3 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr22:24121531 G>C maps to NM_005940.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr11:102822756 C>A maps to NM_002427.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr14:23314528 A>G maps to NM_004995.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr8:89339423 G>A maps to NM_005941.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr8:89130938 C>T maps to NM_005941.4 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:56236192 C>T maps to NM_002429.4 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr16:55536777 C>G maps to NM_004530.4 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:55523665 C>T maps to NM_004530.4 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr10:127461251 T>C maps to NM_147191.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:33842405 C>A maps to NM_006690.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr16:3107151 C>A maps to NM_022468.4 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr20:44639872 C>T maps to NM_004994.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr20:44637579 G>A maps to NM_004994.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr20:44639884 C>T maps to NM_004994.2 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr4:90856573 G>A maps to NM_007351.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr4:90857361 T>A maps to NM_007351.2 L844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W3-01A-11D-A10G-09 chr10:88703811 G>A maps to NM_024756.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr10:99222426 G>T maps to ENST00000422291 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:99219136 G>C maps to ENST00000422291 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:99237134 G>T maps to ENST00000422291 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr22:28194899 T>C maps to NM_002430.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr1:158817522 C>T maps to NM_002432.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr1:158813902 G>A maps to NM_002432.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:56748601 T>G maps to NM_018365.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr14:93650052 C>A maps to NM_022151.4 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr11:1492540 C>A maps to NM_001172223.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr4:71844866 C>T maps to ENST00000396051 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:74386336 G>A maps to NM_018221.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr18:33785061 G>A maps to NM_017947.2 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr18:33785148 C>T maps to NM_017947.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:52402959 C>T maps to NM_004531.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:29633971 G>A maps to NM_002433.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr16:77228811 G>T maps to NM_014940.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:77232018 C>T maps to NM_014940.2 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr12:62959109 C>T maps to ENST00000393630 Q1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr3:108682296 A>G maps to NM_014429.3 R921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr3:108705759 G>A maps to NM_014429.3 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr3:108723918 G>A maps to NM_014429.3 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr21:37713804 G>A maps to ENST00000290384 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:106186348 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:106185939 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:106224594 C>A did not map to a codon.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr23:106229352 G>T did not map to a codon.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr23:106205309 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr23:106228453 C>T did not map to a codon.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr23:106221351 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:79183336 G>A maps to NM_206839.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:102931314 T>G did not map to a codon.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr23:102931121 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:102931366 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr23:102931275 T>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:2319696 G>A maps to NM_024848.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr1:2319729 C>T maps to NM_024848.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr10:99379351 C>T maps to NM_001098831.1 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr9:124936829 C>T maps to NM_198469.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr8:57026279 G>A maps to NM_005372.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr1:220964934 C>A maps to NM_022746.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr1:220971247 C>T maps to NM_022746.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr1:220986672 A>T maps to NM_022746.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr1:220953545 C>T maps to NM_017898.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr1:220936308 T>C maps to NM_017898.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr23:14934368 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr23:14910869 T>A did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr23:14915212 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:113236788 C>G maps to NM_020963.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr1:113242559 C>T maps to NM_020963.3 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:113232168 C>T maps to NM_020963.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr22:50582665 C>T maps to NM_018995.2 F833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr22:50591631 C>A maps to NM_018995.2 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr22:50584152 C>T maps to NM_018995.2 D847D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SU-01A-11D-A099-09 chr6:132643997 G>A maps to NM_015529.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:13150578 G>T maps to ENST00000319217 I1187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr9:13192135 T>C maps to ENST00000319217 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:13176325 C>A maps to ENST00000319217 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr9:13222405 G>A maps to ENST00000319217 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RX-01A-11D-A25Q-09 chr11:58979530 G>A maps to NM_001039396.1 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr11:58979627 G>A maps to NM_001039396.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr11:58978652 G>A maps to NM_001039396.1 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:58979699 A>G maps to NM_001039396.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:133184 C>T maps to NM_002434.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:135461 C>T maps to NM_002434.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr2:71375163 A>T maps to NM_005791.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr13:20220771 G>T maps to ENST00000414242 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:123703047 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr15:75188520 C>T maps to NM_002435.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:43818358 A>C maps to NM_005373.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:56355506 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr17:56356744 G>A maps to ENST00000340482 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:56353031 G>A maps to ENST00000340482 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr17:56356464 G>C maps to ENST00000340482 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr23:154033609 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:154009962 T>C did not map to a codon.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr23:154020089 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:154007614 T>C did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:154012324 C>G did not map to a codon.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr17:41960569 C>A did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr2:202557735 C>T maps to NM_033066.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:67759249 A>G maps to NM_022474.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr7:24718894 T>C maps to ENST00000409253 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr10:28412994 C>A maps to NM_173496.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr18:11884557 G>A maps to ENST00000344987 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr18:11886743 G>A maps to ENST00000344987 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr18:11886608 C>T maps to ENST00000344987 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:15494711 C>T maps to NM_001128423.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24K-01A-11D-A167-09 chr19:18304728 G>A maps to NM_032683.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr1:167741688 C>T maps to NM_003953.5 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:167741608 C>A maps to NM_003953.5 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:118133339 G>T maps to NM_144765.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:118110949 A>G maps to NM_198275.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr1:181021546 C>T maps to NM_001531.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:181024395 C>T maps to NM_001531.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr21:33679041 G>A maps to ENST00000445271 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr6:84799079 C>A maps to NM_138409.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr6:84798938 C>T maps to NM_138409.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:138119419 C>A maps to NM_001085049.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr17:60765921 C>A maps to NM_006039.3 S1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr17:60743533 C>T maps to NM_006039.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr17:60767629 C>T maps to NM_006039.3 L1286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:60751428 C>T maps to NM_006039.3 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr11:94194140 T>C maps to NM_005591.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:6711284 G>A maps to NM_203462.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr4:6711320 A>G maps to NM_203462.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:68773714 C>T maps to NM_145015.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr11:18955815 C>T maps to NM_147199.3 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr11:18955911 C>T maps to NM_147199.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr11:19077007 T>C maps to NM_054030.2 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:66203552 C>T maps to NM_016050.3 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr11:66204714 C>T maps to NM_016050.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:55049887 T>C maps to NM_014175.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:59574083 A>C maps to NM_017840.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:59574020 G>A maps to NM_017840.3 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:1337463 C>G maps to NM_017971.3 *150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr1:156708152 G>A maps to NM_145729.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XR-01A-11D-A14K-09 chr17:48447870 G>A maps to NM_016504.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr3:131188557 C>T maps to ENST00000425847 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr2:86434314 C>T maps to NM_016622.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:54670806 C>T maps to NM_016491.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23E-01A-11D-A159-09 chr17:73897304 C>T maps to NM_032478.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:73895239 C>T maps to NM_032478.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr19:10363299 C>T maps to NM_146387.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr17:36478435 T>A maps to NM_032351.3 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr17:36474594 T>C maps to NM_032351.3 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr17:36478037 G>A maps to NM_032351.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SG-01A-11D-A142-09 chr15:89008086 G>A maps to NM_022163.3 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:6601582 G>A maps to NM_016497.3 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr12:6602121 G>T maps to NM_016497.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr14:23302666 A>G maps to NM_178336.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:74699266 C>T maps to NM_053050.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:228295775 G>T maps to NM_181462.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:89015950 C>T maps to NM_022839.3 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr15:89020218 G>A did not map to a codon.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr15:89020269 G>A maps to NM_022839.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr10:75011557 G>A maps to NM_016065.3 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr6:30587732 C>T maps to NM_014046.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr6:30587567 T>A maps to NM_014046.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JS-01A-11D-A13L-09 chr4:84377235 C>T maps to NM_016067.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:138395684 C>G maps to NM_016034.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr9:138395756 G>T maps to NM_016034.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr9:138395774 C>T maps to NM_016034.3 P229P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BH-A18V-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr3:15094075 G>A maps to NM_022497.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:71519557 G>A maps to ENST00000513900 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:71616003 T>C maps to ENST00000513900 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:71524186 C>T maps to ENST00000513900 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr5:71521973 C>T maps to ENST00000513900 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr8:80831316 C>G maps to NM_014018.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr5:44813384 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr12:27890495 C>T maps to NM_021821.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr2:95767454 C>T maps to NM_031902.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr2:95775736 T>C maps to NM_031902.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr17:73261940 G>A maps to NM_015971.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr2:105665627 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1N8-01A-11D-A142-09 chr6:24409714 G>T maps to NM_020662.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:60184015 G>A maps to NM_032597.3 W525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr11:60540905 G>A maps to NM_001098835.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr11:59861501 C>T maps to NM_000139.4 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:59863090 G>T maps to NM_000139.4 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:60105377 A>C maps to NM_139249.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:60476148 C>T maps to NM_031457.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:17998318 C>T maps to NM_001105569.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr2:47702264 C>T maps to NM_000251.1 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr5:80071553 A>T maps to NM_002439.3 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr5:79950578 C>T maps to NM_002439.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr1:76365304 T>C maps to NM_002440.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:76269498 C>T maps to NM_002440.2 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:76349501 G>A maps to NM_002440.2 Q701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr6:31713096 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:48026681 T>G maps to NM_000179.2 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:48026708 T>G maps to NM_000179.2 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:48026508 G>T maps to NM_000179.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:48027885 C>T maps to NM_000179.2 R922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr17:38290098 C>T maps to ENST00000398532 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P0-01A-11D-A142-09 chr17:38282587 G>A maps to ENST00000398532 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:135871020 G>A maps to NM_018133.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr3:135870741 T>A maps to NM_018133.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr23:11783688 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:11778558 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr23:11783718 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:11786798 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:11790740 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:11779009 C>G did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr23:11779629 T>C did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:234774857 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr16:816660 C>T maps to NM_013404.4 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:830631 G>A maps to NM_001025190.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr16:820068 G>T maps to NM_001025190.1 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr9:35754069 C>A maps to NM_001044264.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr23:64957137 G>A did not map to a codon.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr23:64959698 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:64958993 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr23:64958833 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr23:64955187 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr8:10285662 T>C maps to NM_012331.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr8:10285773 C>T maps to NM_012331.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr10:23393166 G>A maps to ENST00000277598 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr3:49723822 A>G maps to NM_020998.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:49933681 T>G maps to NM_002447.2 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr23:131202596 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:190927170 G>C maps to NM_005259.2 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr4:4864567 G>T maps to NM_002448.3 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr5:174156268 C>T maps to NM_002449.4 Q163*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C8-A26Y-01A-11D-A16D-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr16:56667261 C>T maps to NM_176870.2 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:62365555 G>A maps to NM_004739.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr11:62365547 C>T maps to NM_004739.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr2:42871361 C>T maps to ENST00000405094 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:154294233 C>T did not map to a codon.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr23:154290172 G>T did not map to a codon.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr23:154292280 C>T did not map to a codon.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr8:97258549 T>C maps to NM_015942.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AL-01A-21D-A12Q-09 chr12:107372348 T>C maps to NM_025198.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:107371775 G>A maps to NM_025198.3 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr1:93594861 G>A maps to NM_007358.3 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr1:93602436 C>G maps to NM_007358.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:64867570 C>T maps to NM_005956.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr14:64879188 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:64924930 G>A did not map to a codon.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr14:64898263 C>A maps to NM_005956.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr14:64894166 C>T maps to NM_005956.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr6:151277146 C>T maps to NM_015440.3 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:74425783 C>T maps to NM_006636.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:74432939 G>C maps to NM_006636.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr15:80181579 G>A maps to NM_006441.3 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr2:55470654 C>T maps to NM_002453.2 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr23:149828219 G>C did not map to a codon.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr23:149787532 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr23:149809751 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:149828936 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:149764985 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:149765018 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:149814259 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:149828867 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr23:149814335 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IH-01A-11D-A10Y-09 chr23:149814174 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr23:149783131 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr23:149826403 G>C did not map to a codon.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr23:149828873 T>C did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr23:149905752 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr15:31233954 G>C maps to NM_017762.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr15:31239428 G>C maps to NM_017762.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr1:149903190 G>T maps to NM_001145862.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr5:32263226 G>A maps to NM_001040446.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A153-01A-12D-A12B-09 chr5:32233992 G>C maps to NM_001040446.1 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:32230234 G>A maps to NM_001040446.1 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:9714434 G>A maps to NM_001077525.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:95578203 G>T maps to NM_016156.5 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:56572388 C>T maps to NM_004687.4 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr17:56582888 G>T maps to NM_004687.4 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr23:63548743 C>A did not map to a codon.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr23:63490846 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:63548722 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:63579390 A>G did not map to a codon.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr23:63488917 T>C did not map to a codon.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr23:63488611 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:11162408 A>C maps to NM_015458.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr11:92714859 C>A maps to NM_005959.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr6:74176210 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr6:74171765 G>T maps to NM_001123226.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr1:11300582 G>C maps to NM_004958.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr1:11217312 C>T maps to NM_004958.3 E1455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:11317199 A>C maps to NM_004958.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06T-01A-11W-A019-09 chr1:11187854 C>T maps to NM_004958.3 E2014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:11307745 C>T maps to NM_004958.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:11177098 G>A maps to NM_004958.3 V2326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:11288916 G>A maps to NM_004958.3 F946F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr1:11317204 C>A maps to NM_004958.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr10:30602779 G>A maps to ENST00000358107 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr1:236988692 C>T maps to NM_000254.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:237054514 T>G maps to NM_000254.2 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:236959007 C>A maps to NM_000254.2 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr1:237015843 A>C maps to NM_000254.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:41814501 A>C maps to NM_004294.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr5:7878077 G>A maps to NM_024010.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr5:7886773 C>T maps to NM_024010.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:7883322 C>G maps to NM_024010.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr8:125711806 G>A maps to NM_014751.4 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr8:125577934 G>A maps to NM_014751.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr16:70713719 C>T maps to NM_138383.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:100527948 A>G maps to ENST00000511045 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr4:100521862 C>G maps to ENST00000511045 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr4:100530059 G>T maps to ENST00000511045 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:100521725 C>T maps to ENST00000511045 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N3-01A-12D-A159-09 chr4:100510903 T>C maps to ENST00000511045 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr8:17612529 G>A maps to NM_001001924.2 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr13:29933489 G>A maps to NM_001033602.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr13:30066849 A>G maps to NM_001033602.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:29600550 A>C maps to NM_001033602.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:29599593 G>A maps to NM_001033602.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:29599938 C>A maps to NM_001033602.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr13:29933531 C>T maps to NM_001033602.2 G1023G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr13:29600958 C>G maps to NM_001033602.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr13:29599119 G>A maps to NM_001033602.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr13:29600607 C>T maps to NM_001033602.2 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr2:177188192 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr1:155162589 G>A maps to ENST00000425082 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr11:26582734 C>T maps to NM_001135091.1 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr11:26586727 C>T maps to NM_001135091.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr19:9066847 C>T maps to NM_024690.2 E6866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:9046758 T>G maps to NM_024690.2 P11624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr19:9091121 C>G maps to NM_024690.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr19:9089882 C>T maps to NM_024690.2 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr19:9064045 G>A maps to NM_024690.2 T7800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr19:9058645 T>C maps to NM_024690.2 T9600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr19:9090875 C>A maps to NM_024690.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr19:9064815 A>G maps to NM_024690.2 L7544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:9045771 T>G maps to NM_024690.2 P11953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:9048195 T>G maps to NM_024690.2 S11145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:9067939 T>G maps to NM_024690.2 P6502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:9087902 T>G maps to NM_024690.2 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:9062049 G>A maps to NM_024690.2 Q8466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:9066055 G>A maps to NM_024690.2 L7130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:9062815 T>C maps to NM_024690.2 T8210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:9077622 C>A maps to NM_024690.2 E3275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:9087800 G>T maps to NM_024690.2 V1338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:9090526 C>A maps to NM_024690.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr19:9061492 C>A maps to NM_024690.2 G8651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:9071380 T>C maps to NM_024690.2 P5355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr19:9061378 T>C maps to NM_024690.2 T8689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr19:9066266 G>C maps to NM_024690.2 S7060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr19:9074464 G>A maps to NM_024690.2 V4327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AT-01A-11D-A12Q-09 chr19:9085517 A>G maps to NM_024690.2 S2099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr19:9007505 G>A maps to NM_024690.2 S13154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr19:9004896 C>T maps to NM_024690.2 E13307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr19:9065989 A>G maps to NM_024690.2 P7152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr19:9019326 G>C maps to NM_024690.2 S12520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr19:9091400 T>C maps to NM_024690.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:9007830 C>T maps to NM_024690.2 R13131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr19:9062671 G>T maps to NM_024690.2 S8258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr19:9063010 C>T maps to NM_024690.2 V8145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr19:9049090 G>C maps to NM_024690.2 S10847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr19:9000462 C>T maps to NM_024690.2 T13507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:9046938 C>T maps to NM_024690.2 L11564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:8976843 C>T maps to NM_024690.2 L14074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr19:9089492 G>T maps to NM_024690.2 T774T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:9046788 C>G maps to NM_024690.2 T11614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:9068488 G>A maps to NM_024690.2 V6319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr19:8982253 C>T maps to NM_024690.2 L14007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr19:9069331 G>A maps to NM_024690.2 H6038H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr19:9076600 T>G maps to NM_024690.2 T3615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A3DX-01A-21D-A20S-09 chr19:8994488 G>A maps to NM_024690.2 N13801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J3-01A-11D-A13L-09 chr19:9038119 T>A maps to NM_024690.2 T12052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr19:9072871 T>G maps to NM_024690.2 T4858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:9033259 G>A maps to NM_024690.2 L12122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr7:100676652 T>A maps to NM_001040105.1 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr7:100684340 C>G maps to NM_001040105.1 S3215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr7:100684335 A>G maps to NM_001040105.1 P3213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr7:100678734 C>G maps to NM_001040105.1 T1346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:100678794 A>C maps to NM_001040105.1 T1366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:100679715 A>C maps to NM_001040105.1 T1673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:100683213 A>C maps to NM_001040105.1 T2839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr7:100678769 C>G maps to NM_001040105.1 S1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:100683066 C>T maps to NM_001040105.1 S2790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr7:100679921 C>G maps to NM_001040105.1 S1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:100681241 C>G maps to NM_001040105.1 S2182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:100675011 C>T maps to NM_001040105.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr7:100683507 C>T maps to NM_001040105.1 T2937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr7:100684488 C>A maps to NM_001040105.1 P3264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr7:100680492 T>A maps to NM_001040105.1 P1932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr7:100676391 T>C maps to NM_001040105.1 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:100684536 C>T maps to NM_001040105.1 S3280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr11:1092239 G>A maps to ENST00000441003 Q1353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:1093499 C>T maps to ENST00000441003 T1773T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:1101058 C>T maps to ENST00000441003 I2486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr11:1093103 C>A maps to ENST00000441003 T1641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr3:195452667 C>G maps to ENST00000447234 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09V-01A-11D-A045-09 chr3:195452667 C>G maps to ENST00000447234 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr3:195452688 C>T maps to ENST00000447234 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr3:195452667 C>G maps to ENST00000447234 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr3:195452004 C>T maps to ENST00000447234 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr6:30955397 C>A maps to NM_001010909.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr6:30955118 A>T maps to NM_001010909.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr3:195490501 G>A maps to NM_018406.5 F4685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr11:1254321 G>A maps to ENST00000447027 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KC-01A-11D-A20S-09 chr11:1280245 G>A maps to ENST00000447027 T5559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr11:1266560 G>A maps to ENST00000447027 R2820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr11:1272401 C>A maps to ENST00000447027 V4767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:1268930 A>C maps to ENST00000447027 A3610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:1271765 C>G maps to ENST00000447027 P4555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr11:1272880 C>G maps to ENST00000447027 S4927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr11:1268930 A>C maps to ENST00000447027 A3610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr11:1264013 G>C maps to ENST00000447027 L1971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr11:1251805 G>A maps to ENST00000447027 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr11:1266536 G>T maps to ENST00000447027 L2812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KI-01A-11D-A14K-09 chr11:1268063 C>T maps to ENST00000447027 A3321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr11:1268930 A>C maps to ENST00000447027 A3610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr11:1268930 A>C maps to ENST00000447027 A3610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr11:1269971 C>T maps to ENST00000447027 I3957I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr11:1269275 C>G maps to ENST00000447027 L3725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:1268666 C>T maps to ENST00000447027 T3522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr11:1268477 G>A maps to ENST00000447027 G3459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr11:1261519 C>A maps to ENST00000447027 I1298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr11:1265474 G>A maps to ENST00000447027 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr11:1267310 A>C maps to ENST00000447027 T3070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RV-01A-12D-A28B-09 chr11:1268036 G>A maps to ENST00000447027 P3312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:1016001 G>A maps to NM_005961.2 Q2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:1026074 G>A maps to NM_005961.2 Y871Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:1025238 C>T maps to NM_005961.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr4:71347000 A>C maps to NM_152291.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:71346685 A>C maps to NM_152291.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr4:71347315 C>A maps to NM_152291.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr14:57749706 C>T maps to ENST00000431972 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr23:105450895 G>C did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr23:105450902 A>G did not map to a codon.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr23:105450667 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr23:105450344 C>T did not map to a codon.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr23:105450850 T>G did not map to a codon.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr23:105449659 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:113562967 A>C maps to ENST00000189978 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:113547900 C>T maps to ENST00000189978 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr9:113457775 C>G maps to ENST00000189978 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:113449438 C>G maps to ENST00000189978 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A145-01A-11D-A10Y-09 chr12:110034357 C>G maps to NM_001114185.1 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:29845166 C>T maps to NM_017458.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr16:29848116 G>A maps to NM_017458.3 W249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr16:29853119 C>T maps to NM_017458.3 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr16:29851674 C>A maps to NM_017458.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr21:42824597 G>A maps to NM_001144925.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr21:42812921 G>T maps to NM_001144925.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr21:42770840 A>G maps to NM_002463.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr2:70164404 C>A maps to NM_002357.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr23:3261748 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr23:3242308 C>T did not map to a codon.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr23:3242906 C>A did not map to a codon.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr23:3241922 A>G did not map to a codon.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr23:3242929 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:3228968 T>C did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:3242092 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:3238468 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:3229460 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:3238648 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:3240106 C>T did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:3241060 C>T did not map to a codon.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr23:3261810 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:3228183 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:3229371 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:3241251 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:3241425 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:3248192 T>C did not map to a codon.
Sequencing variant TCGA-B6-A0RT-01A-21D-A099-09 chr23:3228363 C>T did not map to a codon.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr23:3248431 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr23:3238685 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr23:3239605 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr23:3238810 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:3228562 T>C did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr23:3239761 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr23:3238283 A>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:3248092 C>A did not map to a codon.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr23:3241891 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:3236005 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr23:3228240 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr23:3238220 C>A did not map to a codon.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr23:3235329 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:3242462 C>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:3248696 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr23:3235330 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr23:3241187 A>C did not map to a codon.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr23:3239600 T>C did not map to a codon.
Sequencing variant TCGA-E9-A249-01A-11D-A167-09 chr23:3229026 T>C did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:3229057 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:54377505 G>A maps to NM_001020818.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr6:135511398 G>A maps to NM_001130173.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:4451589 G>A maps to NM_001105538.1 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr17:4452658 C>T maps to NM_001105538.1 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr8:67488507 C>A maps to NM_001080416.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr20:42343799 C>T maps to NM_002466.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr12:102040636 G>A maps to NM_002465.2 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:102057261 G>A maps to NM_002465.2 T760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:102067395 C>A maps to NM_002465.2 I935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr12:102045069 C>T maps to NM_002465.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X7-01A-11D-A14K-09 chr12:102053565 C>T maps to NM_002465.2 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:50954181 C>T maps to NM_004533.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr19:50939057 G>A maps to NM_004533.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr19:50964797 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr19:50957612 G>A maps to NM_004533.3 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr19:50945507 C>T maps to NM_004533.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr11:47363597 C>T maps to ENST00000399249 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:47365083 G>C maps to ENST00000399249 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:47374180 C>T maps to ENST00000399249 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr11:47367797 C>T maps to ENST00000399249 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:109840083 A>C maps to NM_001010985.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr13:77651359 G>A maps to NM_015057.4 Q3883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr13:77862347 G>C maps to NM_015057.4 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:77670473 G>A maps to NM_015057.4 R3309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:77724894 G>A maps to NM_015057.4 R2369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:77742766 G>T maps to NM_015057.4 V1970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr13:77673129 G>C maps to NM_015057.4 S2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JU-01A-11D-A13L-09 chr13:77748600 G>A maps to NM_015057.4 R1832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr13:77655722 G>A maps to NM_015057.4 R3753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:48603378 G>A maps to NM_032133.4 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:48597008 G>A maps to NM_032133.4 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr6:153043115 C>T maps to NM_025107.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr3:38180430 A>T maps to NM_001172567.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr3:38182755 C>G maps to NM_001172567.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EM-01A-11W-A050-09 chr15:48441259 C>T maps to NM_016132.3 W536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr15:48443699 G>A maps to NM_016132.3 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:241070505 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr17:10408306 A>G maps to NM_005963.3 Y837Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr17:10419369 G>C maps to NM_005963.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:10409216 G>A maps to NM_005963.3 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr17:10399731 G>T maps to NM_005963.3 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:10397960 A>G maps to NM_005963.3 S1832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr17:10399278 G>T maps to NM_005963.3 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr17:10411878 G>A maps to NM_005963.3 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr17:10406520 T>A maps to NM_005963.3 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr17:10416982 G>A maps to NM_005963.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr17:8396258 G>A maps to ENST00000360416 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr17:8383633 C>T maps to ENST00000360416 V1797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:8480562 A>G maps to ENST00000360416 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:8424484 G>A maps to ENST00000360416 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:15835427 C>T maps to NM_001040114.1 K924K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:15833937 G>T maps to NM_001040114.1 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr16:15831388 C>T maps to NM_001040114.1 Q1077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr16:15831385 G>T maps to NM_001040114.1 I1078I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr16:15931821 G>T maps to NM_001040114.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:15818512 G>C maps to NM_001040114.1 L1376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr16:15878553 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr16:15797865 T>C maps to NM_001040114.1 G1974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:10224964 C>A maps to NM_003802.2 E999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr17:10233720 C>T maps to NM_003802.2 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr17:10243509 A>T maps to NM_003802.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:10227359 C>T maps to NM_003802.2 E971E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr17:10210332 G>A maps to NM_003802.2 Q1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr17:10265676 G>A maps to NM_003802.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr17:10213132 G>A maps to NM_003802.2 H1557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:50758519 A>C maps to NM_001145809.1 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr19:50713889 C>T maps to NM_001145809.1 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr19:50750309 C>T maps to NM_001145809.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr3:108220615 G>C maps to NM_014981.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr3:108158715 G>T maps to NM_014981.1 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr3:108129756 G>A maps to NM_014981.1 Q1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr3:108159993 C>T maps to NM_014981.1 E943E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr17:10450931 G>A maps to NM_017534.5 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr17:10424653 C>T maps to NM_017534.5 V1923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr17:10443329 C>T maps to NM_017534.5 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr17:10435108 C>T maps to NM_017534.5 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr17:10447096 G>A maps to NM_017534.5 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr17:10432036 A>G maps to NM_017534.5 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:10535127 A>C did not map to a codon.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr17:10543516 C>T maps to NM_002470.2 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr17:10547933 A>G maps to NM_002470.2 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:10542776 A>G maps to NM_002470.2 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr17:10558306 G>A maps to NM_002470.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:10549036 C>T maps to NM_002470.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:10368807 T>G maps to NM_017533.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr17:10366410 G>C maps to NM_017533.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LH-01A-31D-A18P-09 chr17:10366487 G>A maps to NM_017533.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr17:10358114 G>A maps to NM_017533.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15E-01A-11D-A12B-09 chr17:10346781 G>T maps to NM_017533.2 A1910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr17:10355545 G>A maps to NM_017533.2 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr14:23858705 G>A maps to NM_002471.3 Q1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr14:23862940 C>T maps to NM_002471.3 K954K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr14:23867982 G>C maps to NM_002471.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr14:23884325 G>A maps to NM_000257.2 Q1813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr14:23884897 C>T maps to NM_000257.2 R1699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr14:23885224 C>T maps to NM_000257.2 Q1647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr14:23894536 G>A maps to NM_000257.2 R793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr20:33577723 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr20:33581195 C>T maps to NM_020884.3 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W3-01A-11D-A10G-09 chr20:33568851 C>T maps to NM_020884.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr20:33586314 G>A maps to NM_020884.3 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr20:33584936 C>G maps to NM_020884.3 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr17:10318469 A>G maps to NM_002472.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr17:10301948 G>A maps to NM_002472.2 N1330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:36692886 A>C did not map to a codon.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr22:36705365 G>A maps to NM_002473.4 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr22:36689867 G>A maps to NM_002473.4 D1293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr22:36681951 C>G maps to NM_002473.4 R1703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr22:36697606 G>C maps to NM_002473.4 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr22:36684951 C>A maps to NM_002473.4 E1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr22:36690230 C>T maps to NM_002473.4 K1248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr22:36680271 G>A maps to NM_002473.4 Q1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr22:36737525 G>A maps to NM_002473.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:211163222 G>A maps to NM_079420.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr2:211163234 G>T maps to NM_079420.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:101266274 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:56553407 T>G maps to NM_079423.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:56548625 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0DD-01A-31D-A12Q-09 chr20:35177630 C>T maps to NM_006097.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr3:123419230 G>A maps to NM_053025.3 N1028N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr3:123456282 C>T maps to NM_053025.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:123385990 C>T maps to NM_053025.3 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr3:123512532 G>A maps to NM_053025.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:123376170 G>A maps to NM_053025.3 Q1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr3:123376020 C>A maps to NM_053025.3 E1414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr3:123452939 C>T maps to NM_053025.3 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:30414463 C>T maps to NM_033118.3 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr16:46764602 A>G maps to NM_182493.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:169501310 C>A maps to NM_018657.4 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr5:16666899 C>T maps to NM_012334.2 V2026V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr5:16680190 G>C maps to NM_012334.2 Y1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr5:16761622 C>T maps to NM_012334.2 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:16670937 G>C maps to NM_012334.2 L1860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr5:16711285 C>T maps to NM_012334.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr17:18044984 C>T maps to ENST00000205890 A1850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr17:18082135 C>A maps to ENST00000205890 A3515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr17:18075555 C>T maps to ENST00000205890 I3434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr13:109672249 C>T maps to NM_015011.1 Y907Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr13:109779749 G>A maps to NM_015011.1 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr13:109707854 C>T maps to NM_015011.1 Q1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr13:109777493 T>C maps to NM_015011.1 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:27421768 G>A maps to NM_078471.3 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr17:27434124 A>C maps to NM_078471.3 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:27414016 G>A maps to NM_078471.3 T1883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr17:27424324 C>T maps to NM_078471.3 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr17:27493079 C>T maps to NM_078471.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr22:26224778 C>A maps to ENST00000407587 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr22:26422500 A>G maps to ENST00000407587 S2189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr22:26224904 C>T maps to ENST00000407587 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr22:26422842 C>G maps to ENST00000407587 L2303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr22:26423469 A>T maps to ENST00000407587 S2512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr17:34863743 T>C maps to NM_001163735.1 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:57422604 A>C maps to NM_005379.2 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr12:57422604 A>C maps to NM_005379.2 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:57431418 A>C maps to NM_005379.2 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:57434982 C>T maps to NM_005379.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:1383838 G>A maps to NM_001080779.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:31039077 T>G maps to NM_015194.1 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:31087537 G>T maps to NM_015194.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr17:30981575 C>T maps to NM_015194.1 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:59445901 G>A maps to NM_004998.2 Y989Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:8615497 C>T maps to NM_012335.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr19:8601261 G>A maps to NM_012335.3 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr19:8592340 C>T maps to NM_012335.3 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr19:8587612 C>A maps to NM_012335.3 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:109831242 A>C maps to NM_001101421.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:109845624 C>G maps to NM_001101421.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr10:26462783 G>A maps to NM_017433.4 E1197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:26312956 A>C maps to NM_017433.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr10:26359065 G>A maps to NM_017433.4 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr10:26436363 C>T maps to NM_017433.4 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr10:26243888 C>T maps to NM_017433.4 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr10:26243834 C>T maps to NM_017433.4 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JE-01A-11D-A13L-09 chr10:26446237 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:26465628 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr10:26463155 A>G maps to NM_017433.4 E1321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:171242758 C>T maps to NM_138995.3 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:171243682 C>G maps to NM_138995.3 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15P-01A-11D-A10Y-09 chr2:171240239 G>A maps to NM_138995.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr2:171240299 C>T maps to NM_138995.3 C422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr15:52643661 G>T maps to ENST00000358212 S1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:52635371 C>A maps to ENST00000358212 E1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:52646160 G>A maps to ENST00000358212 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr15:52620093 C>T maps to ENST00000358212 R1555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:52662436 G>A maps to ENST00000358212 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr15:52667643 G>A maps to ENST00000358212 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:52646093 C>A maps to ENST00000358212 E1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr18:47511088 G>A maps to NM_001080467.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:47438437 G>A maps to NM_001080467.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr18:47463623 A>G maps to NM_001080467.2 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr15:52553128 C>A maps to NM_018728.3 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:52517714 G>A maps to NM_018728.3 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:52556401 C>T maps to NM_018728.3 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr15:52517714 G>A maps to NM_018728.3 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:52574996 G>C maps to NM_018728.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr11:76872062 C>T maps to NM_000260.3 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:76892549 C>G maps to NM_000260.3 S940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:76918338 C>T maps to NM_000260.3 F1916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr11:76903323 G>T did not map to a codon.
Sequencing variant TCGA-E2-A10A-01A-21D-A10Y-09 chr11:76872023 C>T maps to NM_000260.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr2:128370128 G>T maps to ENST00000389524 E1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:128339973 C>A maps to ENST00000389524 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:128378019 A>C maps to ENST00000389524 P1142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:128317308 C>T maps to ENST00000389524 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:128347710 C>T maps to ENST00000389524 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A126-01A-11D-A10M-09 chr2:128364878 C>A maps to ENST00000389524 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr15:72252307 G>A maps to ENST00000424560 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr15:72144512 G>C maps to ENST00000424560 L2216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:72197348 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr19:17311481 T>G maps to NM_004145.3 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr19:17314023 C>T maps to NM_004145.3 C1649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:12666388 G>A did not map to a codon.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr17:12655754 C>T maps to NM_001146312.1 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr10:95085597 C>T maps to NM_013451.3 Q1752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr10:95072845 G>C maps to NM_013451.3 L1940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:95111508 G>A maps to NM_013451.3 F1192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr10:95191209 C>T maps to NM_013451.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr10:95093658 C>G maps to NM_013451.3 R1525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr18:3090725 C>T maps to NM_003803.3 E1313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:2071150 T>A maps to NM_003970.2 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr8:2054292 C>G maps to NM_003970.2 Y968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr8:2064058 C>G maps to NM_003970.2 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:2024236 C>T maps to NM_003970.2 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr8:2024278 C>T maps to NM_003970.2 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr8:1998980 C>G maps to NM_003970.2 S34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YC-01A-11D-A117-09 chr1:24409110 G>A maps to ENST00000330966 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr1:24402670 G>A maps to ENST00000330966 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr5:137211661 C>A maps to NM_006790.2 C167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:75391840 G>A maps to NM_021245.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr4:120072075 C>A maps to NM_016599.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr10:69881872 C>T maps to NM_032578.2 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:69934371 A>C maps to NM_032578.2 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:69881326 C>T maps to NM_032578.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr10:69961610 G>T maps to NM_032578.2 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:40275441 C>A maps to NM_015460.2 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:59142676 C>T maps to NM_001085487.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr8:41790604 G>A maps to NM_006766.3 F1711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr8:41790652 A>G maps to NM_006766.3 P1695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:76788733 T>G maps to NM_012330.2 G1384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:76737185 T>G maps to NM_012330.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:76781832 A>G maps to NM_012330.2 E1072E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr10:76789123 G>A maps to NM_012330.2 K1514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr10:76788709 A>G maps to NM_012330.2 G1376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:62839630 C>G maps to NM_004535.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr2:1812866 G>A maps to ENST00000399161 I1051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P5-01A-11D-A142-09 chr2:1926289 C>T maps to ENST00000399161 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr16:48596337 G>T maps to NM_153029.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr13:33018232 C>T maps to NM_033111.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:33110065 C>A maps to ENST00000505213 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:30255356 A>C maps to NM_013240.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:30250539 A>C maps to NM_013240.3 L171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153197766 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr23:153197828 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:153197995 G>A did not map to a codon.
Sequencing variant TCGA-A2-A3XS-01A-11D-A22X-09 chr4:80246827 C>T maps to NM_032693.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A082-01A-11W-A019-09 chr4:80246827 C>T maps to NM_032693.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A143-01A-11D-A10Y-09 chr4:140280937 G>A maps to NM_057175.3 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:41891016 C>T maps to NM_024561.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:41899886 T>C maps to NM_024561.4 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:20013187 A>G maps to NM_016100.3 V114V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BH-A0HA-01A-11D-A12Q-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr20:20003099 T>C maps to NM_016100.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr12:112513492 G>C maps to NM_024953.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr12:112492279 G>T maps to NM_024953.3 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:112492343 C>G maps to NM_024953.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr12:112509714 G>A maps to NM_024953.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:88632434 C>T maps to NM_024635.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:76852391 C>T maps to NM_014435.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr11:64825816 C>T maps to ENST00000340252 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr3:174814751 G>A maps to NM_207015.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:57485519 T>G maps to NM_005967.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr12:57110261 T>C maps to NM_001113203.1 V1684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr17:59668408 G>A maps to NM_199290.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr17:59668403 G>A maps to NM_199290.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr19:13248139 C>T maps to NM_052876.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr19:13247175 C>G maps to NM_052876.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:71185448 G>A maps to NM_018161.4 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr11:71185526 C>T maps to NM_018161.4 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr11:71212358 C>T maps to NM_018161.4 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr11:71189511 G>A maps to NM_018161.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:71305508 C>T maps to NM_017567.4 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr9:130825868 G>T maps to NM_197956.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr13:101712241 C>T maps to NM_052867.2 P1611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr13:102047686 G>T maps to NM_052867.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:101742292 G>A maps to NM_052867.2 F1098F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:102029094 A>G maps to NM_052867.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr13:101755599 G>A maps to NM_052867.2 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr13:101828726 T>G did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr13:102029100 C>T maps to NM_052867.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr13:101777014 G>A maps to NM_052867.2 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr7:105893542 G>A maps to NM_005746.2 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:25597052 A>C maps to NM_152667.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:76444397 G>A maps to NM_139207.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:72434296 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:72434142 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr23:72433776 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:72433718 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr23:72433233 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr23:92927933 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:92927868 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:92927656 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:92927780 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:2979661 C>A maps to ENST00000399624 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NE-01A-21D-A14K-09 chr11:2975877 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr18:10546340 C>T maps to NM_003826.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:50865321 C>A maps to NM_004851.1 G85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr15:60741134 A>G maps to NM_024611.4 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr15:60760322 G>A maps to NM_024611.4 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr18:55287866 A>G maps to NM_004539.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr18:55274370 C>G maps to NM_004539.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr18:55269588 G>A maps to NM_004539.3 Q505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr11:78189714 C>G maps to NM_024678.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr1:46066129 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr1:46072991 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr1:46079799 G>A maps to NM_002482.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:34160971 C>T maps to NM_024662.2 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr11:34160962 C>T maps to NM_024662.2 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr3:50334918 G>A maps to NM_012191.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:201789053 A>C maps to ENST00000367296 T1876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:201777847 G>A maps to ENST00000367296 L1352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:201758892 C>T maps to ENST00000367296 A1064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:201752733 C>G maps to ENST00000367296 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr1:201772759 C>G maps to ENST00000367296 S1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr1:201751994 C>T maps to ENST00000367296 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:19890544 T>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:19954974 C>T maps to ENST00000396087 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr11:19961291 G>T maps to ENST00000396087 G730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:20057564 T>C maps to ENST00000396087 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:78400971 G>T maps to NM_014903.4 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:78542660 G>T maps to NM_014903.4 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XO-01A-11D-A10G-09 chr12:78444718 C>T maps to NM_014903.4 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr12:78594277 C>A maps to NM_014903.4 P2225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:78598795 C>T maps to NM_014903.4 Q2284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z5-01A-41D-A243-09 chr12:78582466 T>C maps to NM_014903.4 L1967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr2:15374757 C>T maps to NM_015909.2 Q2019Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:15417007 G>A maps to NM_015909.2 R1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:15698716 C>T maps to NM_015909.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr2:15432701 T>A maps to NM_015909.2 A1662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr13:36239285 C>T maps to ENST00000400445 V2788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FG-01A-11D-A13L-09 chr13:35785238 G>C maps to ENST00000400445 V1857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr13:35756526 C>T maps to ENST00000400445 L1565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr13:35517229 C>T maps to ENST00000400445 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:204002927 G>T maps to NM_001114132.1 E1508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:204031987 C>T maps to NM_001114132.1 R1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:204016193 G>A maps to NM_001114132.1 Q1794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr2:204037477 T>G maps to NM_001114132.1 T2046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr2:204058610 G>T maps to NM_001114132.1 E2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr3:47045884 T>G did not map to a codon.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr3:47045356 C>T maps to NM_015175.1 A1924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr3:47045823 C>T maps to NM_015175.1 Q2047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr1:16905868 G>A maps to NM_017940.3 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:16901177 C>T maps to NM_017940.3 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr1:16905868 G>A maps to NM_017940.3 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14O-01A-31D-A10Y-09 chr1:16909219 T>C maps to NM_017940.3 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:145293419 C>T maps to NM_001039703.4 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:145368596 C>T maps to NM_001039703.4 F3525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr1:145318951 A>G maps to NM_001039703.4 Q925Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:145299868 C>T maps to NM_001039703.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:145368576 G>T maps to NM_001039703.4 E3519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr1:148009509 G>A maps to ENST00000310701 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:21800025 C>T maps to NM_032264.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr1:144827097 C>T maps to NM_001037675.2 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr17:41362091 G>A maps to NM_005899.3 *967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr17:41349047 G>T maps to NM_005899.3 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr11:113076801 C>T maps to ENST00000316851 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr11:113140961 C>A maps to ENST00000316851 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr21:22664442 A>T maps to NM_004540.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SU-01A-11D-A099-09 chr19:19338573 G>A maps to NM_004386.2 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:19360665 A>G maps to NM_004386.2 K1304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr19:19327773 G>T maps to NM_004386.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr12:6630247 C>G maps to NM_014865.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr11:134073801 C>G did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr11:134047317 C>T maps to NM_015261.2 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:17841403 G>T maps to NM_022346.3 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:17843963 G>A maps to NM_022346.3 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr4:17816952 C>T maps to NM_022346.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:158486139 G>C maps to NM_017760.5 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr22:50960791 G>T maps to NM_001185011.1 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:100424411 C>T maps to NM_002486.4 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr19:39690989 G>T maps to NM_001001414.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr1:36030850 C>T maps to NM_001014839.1 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:172351309 G>A maps to NM_001146276.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:74202953 C>T maps to NM_000265.4 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:183559437 G>C maps to NM_001127651.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr1:183543636 C>G maps to NM_001127651.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:183532636 G>A maps to NM_001127651.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr1:183556057 G>A maps to NM_001127651.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:136664689 T>G maps to NM_006153.4 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr2:106509511 C>T maps to NM_001004720.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:106497970 C>T maps to NM_001004720.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:183850955 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:183853876 G>A maps to NM_205842.1 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:54910760 A>G maps to NM_005337.4 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:133540645 T>C maps to NM_207363.2 V1246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:133543152 G>A maps to NM_207363.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr2:133541245 G>A maps to NM_207363.2 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:133539535 G>T maps to NM_207363.2 T1616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr2:133541461 C>T maps to NM_207363.2 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr2:133539970 T>C maps to NM_207363.2 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:133540872 C>A maps to NM_207363.2 E1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr2:133636434 G>T maps to NM_207363.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr12:50188849 C>A maps to NM_001037806.3 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:232321357 T>G maps to NM_005381.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:24952560 A>C maps to NM_003743.4 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:24952581 A>C maps to NM_003743.4 S1033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr8:71060628 G>A maps to NM_006540.2 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:71069090 T>G maps to NM_006540.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr8:71087080 A>C maps to NM_006540.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:71039234 C>T maps to NM_006540.2 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:71060583 G>T maps to NM_006540.2 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr8:71068736 C>T maps to NM_006540.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr8:71069224 G>A maps to NM_006540.2 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:46268321 T>G maps to NM_181659.2 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:46255810 C>T maps to NM_181659.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:46266470 C>G maps to NM_181659.2 S819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:44691319 G>A maps to NM_020967.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr20:44692113 G>A maps to NM_020967.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:33345515 C>T maps to NM_014071.2 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr20:33330150 G>A maps to NM_014071.2 H1303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr20:33364230 G>A maps to NM_014071.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr6:126206414 C>T maps to NM_181782.4 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr17:16024443 C>A maps to ENST00000395857 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr17:15989750 G>A maps to ENST00000395857 Q1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr17:15975530 G>A maps to ENST00000395857 R1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr17:15965431 G>A maps to ENST00000395857 Q1807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23E-01A-11D-A159-09 chr17:16012111 C>A maps to ENST00000395857 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:16042500 C>A did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr17:16047010 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr17:15943799 G>A maps to ENST00000395857 Q2245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr17:15983301 T>A maps to ENST00000395857 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WY-01A-11D-A10G-09 chr17:16049834 G>A maps to ENST00000395857 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H3-01A-11D-A12Q-09 chr17:16012216 T>A maps to ENST00000395857 K689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:16075193 G>A maps to ENST00000395857 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr17:15989635 G>T maps to ENST00000395857 S1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:15995174 A>G maps to NM_001190438.1 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr17:16062145 C>T maps to ENST00000395857 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr17:15965425 G>A maps to ENST00000395857 R1809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:124882662 A>C did not map to a codon.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr12:124816870 C>A maps to NM_006312.4 E2307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:124887086 C>T maps to NM_006312.4 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:124816952 C>T maps to NM_006312.4 L2279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr19:55417944 G>A maps to NM_004829.5 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr19:55420646 A>G maps to NM_004829.5 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr6:41318436 C>G maps to NM_004828.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr6:41304104 C>A maps to NM_004828.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr1:160327967 C>T maps to NM_015331.2 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:160323996 A>C maps to NM_015331.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:160323979 C>T maps to NM_015331.2 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A278-01A-11D-A167-09 chr13:80113887 C>A maps to NM_019080.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:23932067 C>T maps to NM_002487.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr15:23931599 C>T maps to NM_002487.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr15:29561243 G>A maps to NM_138704.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr15:29561354 G>A maps to NM_138704.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr9:140109081 G>T maps to NM_001144026.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr8:134251150 G>C maps to NM_006096.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:134256606 C>T maps to NM_006096.3 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:21490554 G>C maps to NM_201537.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr14:21486164 G>A maps to NM_201537.1 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:35284790 G>A maps to ENST00000373803 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:58537742 G>A maps to NM_001130487.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr5:149907410 C>T maps to NM_001543.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:149907580 G>A maps to NM_001543.4 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr5:149921220 G>A maps to NM_001543.4 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr5:149915314 C>T maps to NM_001543.4 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr10:75567933 T>G maps to NM_003635.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr4:119176788 G>T maps to NM_004784.2 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:115767002 T>C maps to NM_022569.1 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr4:115997883 T>G maps to NM_022569.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr4:115791932 A>G maps to NM_022569.1 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr23:119007278 G>A did not map to a codon.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr23:119005895 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr23:119005891 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1FD-01A-11W-A14Q-09 chr23:119005894 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr19:8381507 G>A maps to NM_005001.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:4764072 C>T maps to NM_005002.4 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr15:41687185 G>C maps to NM_016013.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr3:179341749 A>G maps to NM_002492.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr19:1390883 C>T maps to NM_024407.4 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr21:44329105 C>G maps to NM_021075.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr21:44324235 G>T maps to NM_021075.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Y-01A-21W-A050-09 chr2:152420118 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:152402428 C>T maps to NM_001164507.1 V6850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:152500595 A>C maps to NM_001164507.1 G2564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:152402957 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr2:152506757 T>A maps to NM_001164507.1 K2455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr2:152495885 C>A maps to NM_001164507.1 E2968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:152483719 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:152547255 C>T maps to NM_001164507.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:152472568 G>A maps to NM_001164507.1 L3746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr2:152466573 C>A maps to NM_001164507.1 E4027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:152466466 C>T maps to NM_001164507.1 V4062V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:152483695 C>T maps to NM_001164507.1 Q3389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr2:152350315 C>T maps to NM_001164507.1 V8215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:152450703 T>C maps to NM_001164507.1 K4778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr2:152543947 G>A maps to NM_001164507.1 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr2:152541306 A>G maps to NM_001164507.1 Y940Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr2:152580857 C>T maps to NM_001164507.1 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr2:152506884 A>G maps to NM_001164507.1 Y2412Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr10:21177024 C>A did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr10:21097580 C>A maps to ENST00000430741 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr10:21097451 C>T maps to ENST00000430741 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr8:91929751 C>T maps to NM_022351.4 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12G-01A-11D-A10M-09 chr8:91937789 G>A maps to NM_022351.4 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:84012113 G>T maps to NM_019065.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:16778397 G>A maps to NM_018090.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:97339469 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr15:56209008 C>T maps to ENST00000508342 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr18:55990550 G>A maps to NM_001144967.1 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L6-01A-11D-A13L-09 chr18:56018245 C>T maps to NM_001144967.1 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr6:11191330 C>T maps to NM_006403.3 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:11190430 G>A maps to NM_006403.3 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr6:11188467 G>A maps to NM_006403.3 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:11190370 C>T maps to NM_006403.3 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:11185571 G>A maps to NM_006403.3 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr8:24813738 G>C maps to ENST00000221169 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr8:24772013 C>T maps to NM_005382.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:24775740 T>G maps to NM_005382.2 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:24774572 G>T did not map to a codon.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr8:24771590 G>A maps to NM_005382.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr8:24771947 G>A maps to NM_005382.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:72748150 A>C maps to NM_173808.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr15:75647143 C>T maps to NM_024608.2 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr4:178274471 C>T maps to NM_018248.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IA-01A-11W-A050-09 chr4:178274552 C>T maps to NM_018248.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:170477098 G>A maps to ENST00000507142 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr4:170321764 G>A maps to ENST00000507142 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:170476893 C>T maps to ENST00000507142 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:27332818 C>T maps to ENST00000396636 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:27394315 C>A maps to ENST00000396636 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr3:131068490 G>A maps to NM_024800.4 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:130962290 C>T maps to NM_024800.4 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:211847750 G>A maps to NM_002497.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr13:52707286 G>A maps to NM_002498.2 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr3:52786049 T>C maps to NM_003157.4 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:52780207 G>A maps to NM_003157.4 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr13:52663414 G>A maps to NM_199289.1 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr9:127083781 C>T maps to NM_001166171.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:198222168 G>C did not map to a codon.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr14:75584014 T>C maps to NM_033116.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr14:75585574 G>T maps to NM_033116.4 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:75576447 G>A maps to NM_033116.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr14:75580952 G>A maps to NM_033116.4 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr14:75577040 T>C maps to NM_033116.4 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr14:75572696 G>A maps to NM_033116.4 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:20968883 T>G maps to NM_006157.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr11:21250896 C>T maps to NM_006157.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:21135144 G>A maps to NM_006157.3 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr11:20940826 C>T maps to NM_006157.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr11:20805316 T>G maps to NM_006157.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:45173748 G>C maps to NM_001145107.1 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:45173690 C>T maps to NM_001145107.1 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:45000973 G>A maps to NM_001145107.1 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr12:45269655 G>A maps to NM_001145107.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:73581571 A>C maps to NM_002499.3 P1245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:73590863 G>A maps to NM_002499.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Y-01A-21W-A050-09 chr1:156639944 T>G maps to NM_006617.1 P1345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:156642722 A>C maps to NM_006617.1 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:156640298 C>A maps to NM_006617.1 P1227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:156639697 C>A maps to NM_006617.1 E1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:156645030 G>A maps to NM_006617.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr1:156640028 T>C maps to NM_006617.1 G1317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr18:70417576 G>T maps to NM_153181.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:47163218 G>A maps to NM_018092.3 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:47162344 C>G maps to NM_018092.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr6:31827912 G>A maps to NM_000434.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:233899280 C>T maps to NM_005383.2 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:105331385 C>T maps to NM_004210.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:44519338 C>A maps to NM_080749.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr2:182543041 G>A maps to NM_002500.2 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:182543320 C>T maps to NM_002500.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr12:55420712 C>T maps to NM_021191.2 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:78395129 G>T maps to NM_144573.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Q-01A-21W-A050-09 chr17:29548938 G>A maps to NM_001042492.2 W571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr17:29528087 A>T maps to NM_001042492.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr17:29556188 C>T maps to NM_001042492.2 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:29654785 G>A maps to NM_001042492.2 R1846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr17:29527589 C>T maps to NM_001042492.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr17:29562790 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:29653201 G>T maps to NM_001042492.2 E1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr17:29585446 C>G maps to NM_001042492.2 S1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr17:29585515 C>G maps to NM_001042492.2 S1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr17:29527589 C>T maps to NM_001042492.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:29563040 T>C did not map to a codon.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr17:29541467 G>C did not map to a codon.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr17:29684040 C>G maps to NM_001042492.2 S2601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr22:30057311 C>A maps to NM_181832.2 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr22:30074207 G>A maps to NM_181832.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:204953167 G>A maps to ENST00000367172 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr1:204942491 C>T maps to ENST00000367172 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:204966376 C>A maps to ENST00000367172 T1061T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr16:69725788 A>T maps to NM_138713.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:69681171 A>C maps to NM_138713.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:69727438 A>C maps to NM_138713.2 P1237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr16:69703976 G>A maps to NM_138713.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:69693764 T>C maps to NM_138713.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr18:77193710 G>A maps to NM_172387.1 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr20:50140350 G>A maps to NM_012340.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr20:50090598 C>G maps to NM_012340.3 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr20:50048859 G>A maps to NM_012340.3 C822C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr16:68156616 C>T maps to NM_173165.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:68156493 A>C maps to NM_173165.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SJ-01A-11D-A099-09 chr14:24845881 G>A maps to NM_001136022.1 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:24845725 C>A maps to NM_001136022.1 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr14:24845638 C>A maps to NM_001136022.1 C795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr14:24836346 A>C maps to NM_001136022.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr17:46136576 C>T maps to ENST00000362042 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr17:46136892 C>T maps to ENST00000362042 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr17:46136903 C>T maps to ENST00000362042 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:46136804 G>A maps to ENST00000362042 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:46136063 C>T maps to ENST00000362042 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr17:46128580 C>G maps to ENST00000362042 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:178096427 T>G maps to NM_006164.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:178095530 T>C maps to NM_006164.3 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr7:26224736 T>C maps to NM_004289.6 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr7:26224283 T>C maps to NM_004289.6 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr7:26224322 T>C maps to NM_004289.6 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr1:61869881 G>A maps to NM_001145512.1 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr1:61848996 G>A maps to NM_001145512.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr9:14307138 C>G maps to ENST00000397581 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr19:3381781 C>T maps to ENST00000269778 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:94172890 A>C maps to NM_005384.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr19:13186432 C>G maps to ENST00000397661 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:103522111 C>G maps to NM_003998.3 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:103527726 G>A maps to NM_003998.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:104160249 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:104156689 C>T maps to NM_001077494.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:35871601 C>A maps to NM_020529.2 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr19:39390821 C>G maps to NM_002503.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr19:39396098 C>T maps to NM_002503.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:31525609 C>T maps to NM_005007.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:145657805 G>A maps to NM_013432.4 N1199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr11:129751712 T>A maps to NM_006165.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr11:129762648 T>C maps to NM_006165.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr20:34262521 G>A maps to NM_021100.4 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:34262464 C>T maps to NM_021100.4 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr2:69642365 A>G maps to NM_001002755.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:69623384 G>C maps to NM_001002755.1 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:33351757 A>C maps to NM_002504.4 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:104517030 C>A maps to NM_006166.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr12:104519902 G>A maps to NM_006166.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:41236498 G>A maps to ENST00000308733 *459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:41228645 G>A maps to ENST00000308733 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr14:77735656 C>G maps to NM_021257.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:23946771 C>T maps to NM_015514.1 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr2:233839576 A>G maps to NM_019850.2 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr2:233785248 G>A maps to NM_019850.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:233785115 G>A maps to NM_019850.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:115829302 A>G maps to NM_002506.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr17:47589365 C>T maps to NM_002507.3 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:102632689 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr23:102632640 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:102632567 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr3:25761535 T>G maps to NM_018297.3 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr3:25770770 C>T maps to NM_018297.3 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:103949981 C>T maps to NM_178833.4 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr2:220022357 A>G maps to NM_024782.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr13:39616425 G>A maps to NM_001012754.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr22:42071107 C>A maps to ENST00000402458 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:17746432 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr23:17745317 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:17745770 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:17743895 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:17744667 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:17750085 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:17739706 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:17746841 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr23:17744060 C>T did not map to a codon.
Sequencing variant TCGA-AR-A24O-01A-11D-A167-09 chr23:17705912 C>T did not map to a codon.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr23:17705939 T>C did not map to a codon.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr23:17705955 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr23:17750231 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr23:17743643 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:17750096 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr23:17744274 G>C did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr23:17705939 T>C did not map to a codon.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr23:17746846 C>T did not map to a codon.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr23:17750268 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr23:71359431 A>C did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:71358847 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:71358700 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr23:71360542 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr23:71359815 C>T did not map to a codon.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr23:71359876 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:71360030 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:71359751 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr23:71360163 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr23:71359228 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr23:71363116 T>A did not map to a codon.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr1:236192955 C>T maps to NM_002508.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr1:236189205 C>T maps to NM_002508.2 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:236157146 G>A maps to NM_002508.2 H851H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:236212243 C>A maps to NM_002508.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:236211998 C>T maps to NM_002508.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:52474620 C>A maps to NM_007361.3 E1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:52481847 G>A maps to NM_007361.3 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr14:52481991 C>T maps to NM_007361.3 E1010E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr14:52509644 G>A maps to NM_007361.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr14:52493940 G>A maps to NM_007361.3 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr2:201764123 C>T maps to NM_001136039.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr14:51206033 G>T maps to NM_020921.3 R1874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr14:51223741 G>A maps to NM_020921.3 Q1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:51204880 C>A maps to NM_020921.3 E1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr14:51237254 G>A maps to NM_020921.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr14:51228555 T>C maps to NM_020921.3 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr14:51238048 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:95888857 G>A maps to NM_004148.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:675157 G>A maps to NM_016533.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr12:675137 G>A maps to NM_016533.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr20:25498422 G>T maps to NM_025176.4 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr20:25443171 C>T maps to NM_025176.4 Q1143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:23049287 G>A maps to NM_144599.4 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr4:48037624 G>A maps to NM_207330.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:156895772 A>C maps to NM_001099287.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:36984829 T>G maps to NM_133433.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:36984841 T>G maps to NM_133433.3 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:36985402 T>G maps to NM_133433.3 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:37020978 G>A maps to NM_133433.3 Q1776Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:36986158 G>A maps to NM_133433.3 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr5:37007573 C>T maps to NM_133433.3 Q1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:36995902 G>T maps to NM_133433.3 E1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr5:37020922 C>T maps to NM_133433.3 R1758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:36985781 C>T maps to NM_133433.3 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr22:29951935 C>T maps to NM_003634.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:29956726 G>C maps to NM_003634.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr3:52521223 C>G maps to NM_007184.3 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:31656837 G>A maps to NM_024522.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YC-01A-11D-A117-09 chr23:119077496 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr23:119077366 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:119059226 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:119059263 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr6:28227178 C>A maps to NM_001007531.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:28228225 G>A maps to NM_001007531.1 Q359Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr5:1033614 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr19:45662101 G>A maps to NM_198478.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr23:118723825 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr23:118724266 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr23:118724233 T>C did not map to a codon.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr20:21492968 C>T maps to NM_002509.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:21492890 G>C maps to NM_002509.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr10:101294772 G>A maps to NM_145285.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr10:101292920 T>A maps to NM_145285.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:172659766 G>A maps to NM_004387.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr4:13543810 G>A maps to NM_001189.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr10:134598421 A>G maps to NM_177400.2 *278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr17:33463229 C>T maps to NM_018096.3 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr3:173322405 C>A maps to NM_014932.2 C6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RY-01A-31D-A25Q-09 chr23:70375089 G>A did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:70367893 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:70367815 C>T did not map to a codon.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr23:70389454 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr23:70386912 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr23:70384047 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:70389299 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:70375089 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr23:70375069 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:70389242 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1P6-01A-11D-A142-09 chr23:70389879 A>C did not map to a codon.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr23:5821685 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:5811276 T>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:5821583 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr23:5811008 G>A did not map to a codon.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr23:5947365 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr23:5811359 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr23:5811183 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:5821329 G>A did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:5811038 G>T did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:5821685 C>T did not map to a codon.
Sequencing variant TCGA-AR-A24Z-01A-11D-A167-09 chr17:26370123 C>T maps to NM_016231.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:26495571 G>A maps to NM_016231.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15L-01A-11D-A12B-09 chr5:65088424 C>T maps to NM_020726.4 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr16:3611701 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:3602206 C>T maps to ENST00000448023 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:3602202 C>A maps to ENST00000448023 E828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18I-01A-11D-A12B-09 chr16:3611737 C>T maps to ENST00000448023 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr2:32475387 G>A maps to NM_021209.4 H515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:32466147 G>C maps to NM_021209.4 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:32475708 G>A maps to NM_021209.4 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr2:32476277 G>A maps to NM_021209.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr2:32475165 C>T maps to NM_021209.4 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SJ-01A-11D-A099-09 chr16:57059664 C>T maps to NM_032206.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr16:57075468 C>T maps to NM_032206.3 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr16:57068127 C>T maps to NM_032206.3 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:57095610 C>G maps to NM_032206.3 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr17:5418123 C>A maps to NM_033004.3 E1458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr17:5461873 G>A maps to NM_033004.3 H714H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr11:7982711 A>T maps to NM_176821.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr11:7984894 C>A maps to NM_176821.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr11:7982327 T>A maps to NM_176821.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr19:56320355 C>T maps to NM_145007.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr19:54313211 C>T maps to ENST00000391773 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr19:54310780 G>C maps to ENST00000391773 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr19:54312950 C>T maps to ENST00000391773 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr19:56423842 G>C maps to NM_176810.2 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr19:56424552 G>A maps to NM_176810.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:56407312 A>C maps to NM_176810.2 *1044E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:56424033 A>G maps to NM_176810.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:56424579 G>A maps to NM_176810.2 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RT-01A-21D-A099-09 chr19:56423853 G>C maps to NM_176810.2 Y443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:56443488 G>A maps to NM_176810.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:7064921 G>A maps to NM_176822.3 K555K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:55497647 C>A maps to NM_017852.3 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr19:55489136 C>T maps to NM_017852.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr19:55501560 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr19:55494671 C>T maps to NM_017852.3 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr19:55493528 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr1:247588839 C>T maps to NM_004895.4 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:247597528 C>T maps to NM_004895.4 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr19:56363562 C>G maps to NM_134444.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr19:56379194 T>A maps to NM_134444.4 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr19:56372910 T>G maps to NM_134444.4 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr19:56569641 G>A maps to NM_153447.4 E1112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FM-01A-11D-A13L-09 chr19:56515225 C>G maps to NM_153447.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr19:56515219 G>A maps to NM_153447.4 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:284397 C>T maps to NM_138329.1 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr19:55451232 G>A maps to ENST00000446217 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:55450563 C>T maps to ENST00000446217 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:55451493 C>T maps to ENST00000446217 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr19:55447630 C>G maps to ENST00000446217 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr19:55451244 C>T maps to ENST00000446217 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RV-01A-12D-A28B-09 chr19:55451643 G>A maps to ENST00000446217 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr19:56466065 C>T maps to NM_176811.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr19:56490780 C>A maps to NM_176811.2 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr19:56243390 A>G maps to NM_176820.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr19:56243876 A>T maps to NM_176820.2 C440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr19:56243837 G>A maps to NM_176820.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:56223332 C>T maps to NM_176820.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:119050496 C>T maps to NM_024618.2 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:119044704 C>T maps to NM_024618.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr11:119050479 C>T maps to NM_024618.2 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:160942831 G>C maps to ENST00000472947 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr16:449628 C>T maps to ENST00000382940 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr2:152139453 A>G maps to NM_004688.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr16:4511846 G>C maps to NM_020677.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr2:101087010 C>T maps to NM_001011717.1 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr17:43183001 C>T maps to NM_021079.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr17:43138786 C>A maps to NM_021079.3 C30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr10:15151733 G>T maps to ENST00000378143 Y512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:15161457 G>A maps to ENST00000378143 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:56466708 G>A maps to NM_006681.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr2:232393176 G>A maps to NM_006056.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:151771982 C>T maps to NM_020167.4 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr5:151771791 G>T maps to NM_020167.4 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr5:151784139 G>A maps to NM_020167.4 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr11:114168853 C>A maps to NM_006169.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr11:114183078 G>C maps to NM_006169.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:43644381 T>G maps to NM_182977.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr16:69788554 G>C maps to NM_014062.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:144097352 A>G maps to ENST00000467773 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:96093960 C>T maps to NM_022451.9 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr10:96106313 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr10:96101464 G>A maps to NM_022451.9 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr16:50744979 C>T maps to NM_022162.1 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr16:50745993 A>C maps to NM_022162.1 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:10808823 C>A maps to NM_024894.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr17:65722666 G>A maps to NM_015462.3 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:38083949 C>T maps to NM_024313.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr18:31803106 G>C maps to NM_003787.4 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KC-01A-11D-A20S-09 chr9:33468139 G>A maps to NM_022917.4 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr9:33464967 G>A maps to NM_022917.4 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr9:33470120 C>T maps to NM_022917.4 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:33469228 G>A maps to NM_022917.4 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr9:33467128 G>A maps to NM_022917.4 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr9:33467239 G>A maps to NM_022917.4 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:13620559 T>G maps to NM_016167.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Y-01A-21W-A050-09 chr9:95077553 A>C maps to NM_017948.5 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:95062251 C>T maps to NM_017948.5 Q1074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:95077076 G>A maps to NM_017948.5 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr9:95077793 T>C maps to NM_017948.5 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr1:6593397 C>G maps to NM_024654.4 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr1:6610528 G>A maps to NM_024654.4 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:14935256 G>A maps to ENST00000456867 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr16:14966095 C>A maps to ENST00000456867 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:70516864 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:70517737 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:2951856 A>C maps to NM_003703.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr4:2945908 C>T maps to NM_003703.1 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LJ-01A-12D-A19Y-09 chr12:6677048 C>T maps to ENST00000382421 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr12:6666266 G>C maps to ENST00000382421 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr20:2636060 A>G maps to NM_006392.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr2:203162127 C>T maps to NM_015934.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:117698389 C>T maps to ENST00000338101 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:117768589 G>A maps to ENST00000338101 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr12:117691525 G>T maps to ENST00000338101 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr12:117680510 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:162302839 G>A maps to NM_014697.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:162335291 C>T maps to NM_014697.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:26101429 G>A maps to NM_000625.4 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:26116656 G>A maps to NM_000625.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:26105952 G>A maps to NM_000625.4 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr17:26087754 G>A maps to NM_000625.4 H968H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:150704042 G>A maps to NM_000603.4 K629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr7:150698506 C>T maps to NM_000603.4 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr19:50059663 G>A maps to NM_015953.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:139401291 G>A maps to NM_017617.3 F1259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:139393654 C>T maps to NM_017617.3 T1997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D3-01A-11D-A10Y-09 chr1:120458201 G>A maps to NM_024408.2 G2381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr1:120491103 G>A maps to NM_024408.2 Y895Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:120484366 C>T maps to NM_024408.2 Q921Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr1:120458146 G>A maps to NM_024408.2 R2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr19:15272362 G>A maps to NM_000435.2 Q2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr19:15276819 G>A maps to NM_000435.2 D1815D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr19:15281152 C>T maps to NM_000435.2 A1701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:15291537 G>T maps to NM_000435.2 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr19:15296368 G>C maps to NM_000435.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr6:32187942 C>A maps to NM_004557.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr6:32188296 G>C maps to NM_004557.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr6:32190849 C>G maps to NM_004557.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr14:26939693 C>T maps to NM_006491.2 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr23:100117161 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:100103624 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr23:100103699 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:100105158 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:100105270 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:155764535 C>T maps to NM_015718.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr6:155750118 C>T maps to NM_015718.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr6:155750166 G>T maps to NM_015718.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr6:155750088 T>A maps to NM_015718.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr11:89135608 G>C maps to NM_016931.3 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr11:89073284 T>C maps to NM_016931.3 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr11:89075270 A>G maps to NM_016931.3 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr11:89106651 A>G maps to NM_016931.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:89075297 G>A maps to NM_016931.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr16:2029830 C>T maps to NM_172168.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:2030975 G>A maps to NM_172168.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr16:2029884 G>A maps to NM_172168.1 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XG-01A-11D-A14G-09 chr14:34269261 G>A maps to NM_001164749.1 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr11:66192384 C>A maps to NM_178864.3 S675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:66188754 C>T maps to NM_178864.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:66192502 C>T maps to NM_178864.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:108062882 A>C maps to NM_002519.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr11:108032048 G>C maps to NM_002519.2 S1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr18:21114478 C>T maps to NM_000271.4 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr18:21119842 G>A maps to NM_000271.4 C909C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr18:21134738 G>A maps to NM_000271.4 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr18:21119418 G>A maps to NM_000271.4 F937F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr7:44579386 G>C maps to NM_013389.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr7:44578656 G>A maps to NM_013389.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr17:45608783 C>T maps to NM_006310.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:110919221 T>C maps to NM_000272.3 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:110902118 A>G maps to NM_000272.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:132427045 G>A maps to ENST00000393156 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr1:5926437 A>T maps to NM_015102.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:6029190 G>A maps to NM_015102.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:6046244 G>C maps to NM_015102.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr1:5940237 G>A maps to NM_015102.2 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr1:5927908 C>G maps to NM_015102.2 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr19:36336321 G>A maps to NM_004646.3 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr19:36332656 G>T maps to NM_004646.3 A925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr19:36321760 G>A maps to NM_004646.3 Y1193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr1:179520517 G>A maps to NM_014625.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:182787763 C>T maps to NM_030769.1 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr17:79526302 G>A maps to NM_017921.2 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:79556050 C>T maps to NM_017921.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr17:79526292 T>G maps to NM_017921.2 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr10:103542240 T>C maps to NM_006993.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:106819081 G>A maps to ENST00000503451 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr4:106890053 C>G maps to ENST00000503451 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr1:153661753 C>T maps to NM_000906.3 F885F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:35809216 A>G maps to NM_003995.3 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr9:35801759 G>A maps to NM_003995.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr16:136808 C>G maps to ENST00000399953 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr7:98257808 T>C maps to NM_002523.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr22:39222745 G>T maps to NM_014293.2 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr22:39219198 C>T maps to NM_014293.2 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr22:39218757 C>G maps to NM_014293.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:25266321 T>G maps to NM_022150.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr4:164247684 G>A maps to NM_000909.4 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:38253471 T>G maps to NM_021724.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr17:38253555 C>A maps to NM_021724.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr3:24003870 C>T maps to NM_005126.4 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr3:24018853 C>T maps to NM_005126.4 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:24004050 G>A maps to NM_005126.4 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:47289527 C>T maps to NM_005693.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:100928776 G>C maps to ENST00000392986 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:100904595 C>T maps to ENST00000392986 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr3:119531720 C>T maps to NM_022002.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:119535969 C>T maps to NM_022002.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FF-01A-11W-A050-09 chr1:161200618 G>A maps to NM_001077482.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr3:15055259 C>T maps to NM_003298.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr3:15065705 G>A maps to NM_003298.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr6:108497705 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr15:72106380 C>T maps to NM_014249.2 H341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr19:17355840 C>G maps to NM_005234.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:142689724 G>A maps to NM_001024094.1 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr4:149075852 G>A maps to ENST00000511528 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:52448894 T>G maps to ENST00000360284 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr12:52448564 C>G maps to ENST00000360284 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr12:52448795 G>A maps to ENST00000360284 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr12:52451282 C>T maps to ENST00000360284 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr9:102609748 C>T maps to NM_173200.1 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr9:102595690 C>T maps to NM_173200.1 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:102590585 G>T maps to NM_173200.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr9:102590380 G>A maps to NM_173200.1 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:200080382 C>T maps to NM_205860.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:200090048 C>T maps to NM_205860.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr9:127285048 C>A maps to NM_033334.2 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:115356934 G>T maps to ENST00000369358 Y1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr10:115348778 G>T maps to ENST00000369358 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WY-01A-11D-A10G-09 chr10:115370291 G>A maps to ENST00000369358 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:27657998 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:27664624 C>T maps to ENST00000379863 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:107790513 G>A maps to ENST00000379032 D1256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:107807428 G>A maps to ENST00000379032 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:107849982 C>T maps to ENST00000379032 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:107820850 C>T maps to ENST00000379032 Q889Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr7:107820769 C>T maps to ENST00000379032 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr7:107834871 C>T maps to ENST00000379032 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FW-01A-11D-A17D-09 chr7:107823284 C>T maps to ENST00000379032 W795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr7:107831698 G>A maps to ENST00000379032 Y644Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr1:52257715 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr7:129350353 A>G maps to ENST00000393231 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr8:32621346 G>T maps to NM_013956.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr8:32621718 G>A maps to NM_013956.3 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:139267079 C>T maps to NM_013982.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr21:16338288 G>C maps to NM_003489.3 S742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:9009802 G>T maps to NM_020645.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FX-01A-11D-A13L-09 chr23:105132398 G>A did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr23:105168990 C>A did not map to a codon.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr23:105153825 G>A did not map to a codon.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr23:105179170 G>T did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:105139452 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:105167110 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:105167222 A>C did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:105193652 C>T did not map to a codon.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr23:105153758 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:105144611 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:105156651 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:105132357 C>A did not map to a codon.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr23:105152944 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr23:105152798 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:67920003 C>T maps to NM_198443.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr10:33545246 C>A maps to NM_003873.5 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:33475377 G>A maps to NM_003873.5 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:33502421 A>C maps to NM_003873.5 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:206659745 C>T maps to NM_201266.1 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:51254724 G>A maps to ENST00000404971 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr2:50758374 C>T maps to ENST00000404971 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:50733714 A>G maps to ENST00000404971 N845N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr11:64416347 A>G maps to NM_015080.3 N1047N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:80164018 T>G maps to NM_004796.4 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:80328292 G>T maps to NM_004796.4 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr14:79423677 T>G maps to NM_004796.4 L417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr14:80328255 G>A maps to NM_004796.4 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr5:176562355 A>G maps to NM_022455.4 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:176721022 C>T maps to NM_022455.4 I2218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr5:176562115 C>T maps to NM_022455.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr5:176721811 G>A maps to NM_022455.4 E2481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr5:176721685 G>A maps to NM_022455.4 L2439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr5:176638367 G>T maps to NM_022455.4 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr23:152036193 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:152014896 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr23:152018962 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:44832678 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:59498559 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr16:27238138 G>A maps to NM_145080.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr16:27238061 G>A maps to NM_145080.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr5:6600146 C>G maps to NM_017755.5 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr3:93803062 C>T maps to NM_022072.3 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr3:93783282 G>C maps to NM_022072.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:72717682 A>C maps to NM_148956.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:72718966 G>A maps to NM_148956.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WT-01A-11D-A10G-09 chr7:72718329 A>G maps to NM_148956.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:72717628 G>A maps to NM_148956.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:72718260 G>A maps to NM_148956.2 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:18903416 C>A maps to NM_182543.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr2:18745289 C>G maps to ENST00000455492 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr2:18766031 G>A maps to ENST00000455492 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr7:33066430 G>A maps to NM_001002010.1 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:116436852 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:52561685 G>A maps to NM_001134231.1 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr3:52563264 G>T maps to NM_001134231.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr12:104174076 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:104179220 A>C maps to NM_001031701.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr6:86201887 T>C maps to NM_002526.2 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr6:86197086 G>A maps to NM_002526.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr6:86195079 G>A maps to NM_002526.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr17:17248214 C>T maps to ENST00000379552 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:5603724 G>A maps to NM_001102654.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24M-01A-11D-A167-09 chr16:2093637 C>T maps to NM_002528.5 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr12:96063917 T>C maps to NM_021229.3 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr1:107963748 T>C maps to NM_001113228.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr1:107691448 G>A maps to NM_001113226.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:107691310 G>A maps to NM_001113226.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr9:135073543 C>T maps to NM_032536.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr9:135073813 C>T maps to NM_032536.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr9:87635260 C>T maps to NM_006180.3 Y771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr9:87563382 A>T maps to NM_006180.3 K591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:87325698 C>T maps to NM_006180.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:87636237 G>C maps to NM_006180.3 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BM-01A-11D-A21Q-09 chr9:87342735 G>T maps to NM_006180.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:87342752 C>T maps to NM_006180.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:87570323 C>T maps to NM_006180.3 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr15:88671940 C>A did not map to a codon.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr15:88678458 G>A maps to NM_001012338.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr15:88576184 G>A maps to NM_001012338.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr20:61340825 G>A maps to NM_002531.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr20:61340966 C>T maps to NM_002531.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr2:11800209 G>A maps to NM_012344.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:11800245 G>T maps to NM_012344.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr12:106461704 C>A maps to NM_014840.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr1:205272578 C>T maps to ENST00000441520 *673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr7:151052932 G>A maps to ENST00000355851 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:32030677 T>G maps to NM_025152.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr19:49424448 G>A maps to NM_006184.5 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:17331215 C>A maps to ENST00000458064 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr1:27268242 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:110293354 G>A maps to NM_032869.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr8:110308644 C>A maps to NM_032869.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:110305594 G>T maps to NM_032869.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:162884607 G>T maps to NM_145266.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:2284289 C>T maps to NM_198954.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:51076060 G>A did not map to a codon.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr23:51238951 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:51238930 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr5:102888117 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr10:74890576 C>T maps to NM_015901.4 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr16:4744070 G>C maps to NM_032349.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:145588434 C>T maps to NM_001012758.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr11:63995110 C>T maps to NM_032344.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:34256663 G>A maps to NM_006703.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:12214821 G>A maps to ENST00000378937 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr4:123814027 A>G maps to NM_007083.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr4:88356369 C>T maps to NM_024047.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:163309204 C>T maps to NM_145697.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr1:163298073 C>T maps to NM_145697.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr13:45554946 C>T maps to NM_012345.2 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:27614140 G>A maps to NM_020772.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:71716289 G>A maps to ENST00000393695 L1946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:71727201 C>T maps to ENST00000393695 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:71725098 G>C maps to ENST00000393695 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr11:71726684 G>A maps to ENST00000393695 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr11:71726409 G>T maps to ENST00000393695 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:73749115 C>T maps to NM_001005743.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr19:41173888 C>T maps to NM_004756.3 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr19:41173888 C>T maps to NM_004756.3 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:69094516 G>A maps to NM_020401.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr1:229619832 C>T maps to NM_018230.2 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:229635511 G>A maps to NM_018230.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BM-01A-11D-A21Q-09 chr6:17637762 A>T maps to ENST00000430136 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr6:17629105 T>C maps to ENST00000430136 Q1139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:37370989 G>A maps to NM_153485.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr5:37330152 G>T maps to NM_153485.1 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr5:37371052 C>T maps to NM_153485.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:47800713 G>A maps to NM_015231.1 D1418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr11:47869780 G>C maps to NM_015231.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr9:131768006 C>T maps to NM_015354.1 F1607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr9:131760903 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:131764195 C>T maps to NM_015354.1 Q1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:131752484 C>T maps to NM_015354.1 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr9:131711512 G>C maps to NM_015354.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:131768562 C>T maps to NM_015354.1 I1663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:135323339 C>T maps to NM_015135.2 L1767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:135261102 G>A maps to NM_015135.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:135261084 T>C maps to NM_015135.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:135261124 C>T maps to NM_015135.2 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr3:13364911 C>T maps to NM_024923.2 Q1555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:13407448 G>A maps to NM_024923.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:13429820 G>A maps to NM_024923.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr3:13418985 G>A maps to NM_024923.2 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:13399720 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:154125326 T>C maps to NM_207308.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr1:154062064 G>A maps to NM_207308.2 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr9:134108839 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:134021644 A>C maps to ENST00000451030 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:134014703 C>T maps to ENST00000451030 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr9:134103691 T>C maps to ENST00000451030 T2017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:134049691 G>A maps to ENST00000451030 V1049V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IJ-01A-11D-A142-09 chr9:134027157 T>G maps to ENST00000451030 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr9:134010373 C>T maps to ENST00000451030 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:150067513 C>A maps to NM_198887.1 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66H-01A-11D-A29N-09 chr22:45574233 C>A maps to NM_007172.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:50411866 G>A maps to NM_012346.4 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr17:73204680 G>A maps to NM_024844.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr16:56782314 C>T maps to NM_014669.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:3721867 T>C maps to NM_016320.4 E1238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr11:3697417 G>A maps to NM_016320.4 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr16:67902250 G>A maps to NM_005796.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:224492452 A>G maps to NM_002533.2 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr19:16926009 G>A maps to ENST00000438489 W1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr19:16860607 G>T maps to ENST00000438489 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XR-01A-11D-A10G-09 chr19:16860187 G>A maps to ENST00000438489 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr19:16870119 G>A maps to ENST00000438489 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr19:16872910 C>T maps to ENST00000438489 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr19:16860391 C>A maps to ENST00000438489 C313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:62567904 G>C maps to NM_006362.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr11:62561770 T>C maps to NM_006362.4 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:101571968 T>G did not map to a codon.
Sequencing variant TCGA-E9-A3X8-01A-31D-A22X-09 chr23:101576789 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr23:102339331 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:102334987 G>T did not map to a codon.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr23:102332670 C>T did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:102338140 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:102338583 G>C did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:102338575 C>G did not map to a codon.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:101096036 C>T did not map to a codon.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:101096476 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:101095498 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:101096071 C>G did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:101092627 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr23:101097745 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr23:101096720 G>A did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:101096302 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr17:729228 C>T maps to NM_022463.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr17:722711 G>T maps to NM_022463.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:17571357 C>G maps to NM_138454.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr9:91159323 C>G maps to NM_001161625.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr7:8791149 C>T maps to NM_152745.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr12:57619523 C>T maps to NM_007224.3 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr20:23334770 G>A maps to NM_013248.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr23:108785737 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:108780218 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:24885064 C>A maps to NM_025081.2 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:24878310 G>C maps to NM_025081.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr14:24880590 C>G maps to NM_025081.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr14:24878031 C>A maps to NM_025081.2 C344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:120096396 C>T maps to NM_178507.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:113446924 T>G maps to NM_016817.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:113433194 C>T maps to NM_016817.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr12:113440771 G>C maps to NM_016817.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:113405874 G>A maps to NM_006187.2 E1000E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:113405313 C>T maps to NM_006187.2 F927F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:121458767 C>A maps to NM_003733.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:121458801 G>A maps to NM_003733.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:121471333 G>A maps to NM_003733.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:151735644 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:56619452 T>G maps to NM_024068.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:138438622 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:228527795 C>T maps to NM_001098623.1 F5803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:228528890 C>T maps to NM_001098623.1 I5931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:228432210 T>C maps to NM_001098623.1 D1140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr1:228467645 C>G maps to NM_001098623.1 P2507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:228400245 C>T maps to NM_001098623.1 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr1:228432171 C>T maps to NM_001098623.1 C1127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr1:228538600 C>T maps to NM_001098623.1 Q6126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr1:228464917 A>C maps to NM_001098623.1 R2220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr1:228451892 G>C maps to NM_001098623.1 L1554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:228509153 C>G maps to NM_001098623.1 S4871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr1:228402100 C>G maps to NM_001098623.1 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr1:228511201 C>T maps to NM_001098623.1 Q5183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr1:228552691 G>A maps to NM_001098623.1 P6284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr1:228521395 C>A maps to NM_001098623.1 V5323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr1:228482538 G>A maps to NM_001098623.1 T3818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr1:228495194 A>T maps to NM_001098623.1 T4143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr1:228496061 C>T maps to NM_001098623.1 S4239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:228509241 C>T maps to NM_001098623.1 F4900F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DM-01A-11D-A17W-09 chr1:228494728 C>A maps to NM_001098623.1 L4018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr1:228462357 C>T maps to NM_001098623.1 S1923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:220418355 G>A maps to NM_015311.2 G1643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr2:220435006 G>A maps to NM_015311.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr2:220432022 G>A maps to NM_015311.2 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr2:220428131 G>A maps to NM_015311.2 G875G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr2:220431780 G>A maps to NM_015311.2 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr8:133058113 G>A maps to ENST00000262283 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:28171385 G>A maps to NM_000275.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr4:48835498 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:128674764 C>T did not map to a codon.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr23:128722976 G>C did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:128701281 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:128709950 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:128695188 C>G did not map to a codon.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr23:128692911 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:128723900 C>T did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:128723902 G>A did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:128709148 A>T did not map to a codon.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr23:128692643 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:71063771 A>C maps to NM_017855.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr4:71068003 T>G maps to NM_017855.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr2:10584252 C>T maps to NM_002539.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:131236002 G>T maps to NM_153435.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr9:131256859 G>A maps to NM_153435.1 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr9:131256859 G>A maps to NM_153435.1 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:86848879 C>T did not map to a codon.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr19:463918 C>T maps to NM_182577.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr23:123615785 C>A did not map to a codon.
Sequencing variant TCGA-A7-A3IY-01A-21D-A21Q-09 chr23:123519750 G>T did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:123695608 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr23:123680766 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr23:123785794 C>G did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:123654413 T>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:123515041 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:123695591 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:123779164 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:123787527 T>G did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr23:123518122 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:123805645 A>T did not map to a codon.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr23:123630945 A>G did not map to a codon.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr23:123518515 C>T did not map to a codon.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr23:123539063 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr23:123779071 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr23:123630872 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:123657270 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:123518322 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr23:123615596 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr23:123539083 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:123556287 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr23:123554339 G>A did not map to a codon.
Sequencing variant TCGA-BH-A201-01A-11D-A14K-09 chr23:123514547 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:123514645 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:123517988 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr23:123556235 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr23:123539029 C>T did not map to a codon.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr23:123663728 C>A did not map to a codon.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:123518526 C>T did not map to a codon.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:123839048 T>G did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr5:167675131 G>A maps to NM_001122679.1 E2387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr5:167631624 C>T maps to NM_001122679.1 R1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr5:167545417 C>T maps to NM_001122679.1 C645C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr5:167674942 C>A maps to NM_001122679.1 T2324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr4:183594305 C>A maps to NM_001080477.1 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr4:183720879 C>A maps to NM_001080477.1 V2492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr4:183714371 C>T maps to NM_001080477.1 R2183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr4:183635306 G>A maps to NM_001080477.1 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr4:183603097 G>T maps to NM_001080477.1 G656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr4:183676016 A>G maps to NM_001080477.1 S1499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:78380177 A>C maps to NM_001098816.2 G2404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr11:78412584 C>T maps to NM_001098816.2 W1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:78383320 C>T maps to NM_001098816.2 E1850E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr11:78437178 C>A maps to NM_001098816.2 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:78423689 G>A maps to NM_001098816.2 S1297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr11:78387424 G>T maps to NM_001098816.2 V1756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr11:78440580 C>T maps to NM_001098816.2 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SJ-01A-11D-A099-09 chr23:13776560 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:13778449 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr23:13778584 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:13785325 G>C did not map to a codon.
Sequencing variant TCGA-AR-A24K-01A-11D-A167-09 chr23:13774755 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:13778538 C>G did not map to a codon.
Sequencing variant TCGA-BH-A202-01A-11D-A14K-09 chr23:13781896 G>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:13764544 G>C did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:13764996 A>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:44736516 G>C maps to ENST00000444676 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr7:44713498 G>A maps to ENST00000444676 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr10:50966464 G>A maps to NM_018245.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr10:50966590 C>T maps to NM_018245.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:61441000 C>T maps to NM_007346.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MS-A51U-01A-31D-A25Q-09 chr20:61444664 G>A maps to NM_007346.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:72011677 G>T maps to NM_024576.3 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr3:9792080 G>C maps to NM_016821.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70757737 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70775169 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:70793551 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr23:70767781 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:70787537 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr23:70776922 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr10:74692228 C>T maps to NM_152635.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:138011558 C>G maps to NM_014279.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:102270204 A>C maps to ENST00000338858 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr13:53624149 G>T maps to NM_006418.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr11:7530893 T>C maps to NM_198474.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:161953686 G>A maps to ENST00000451379 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr1:161953617 G>A maps to ENST00000451379 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:161970067 G>A maps to ENST00000451379 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr1:114523991 C>T maps to NM_020190.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr1:114523967 C>T maps to NM_020190.2 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr1:114523757 G>A maps to NM_020190.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:137814986 G>A maps to NM_175747.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:137814824 G>A maps to NM_175747.2 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr6:74079479 C>A maps to NM_001080507.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:193343891 T>G maps to NM_130837.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr3:193355803 C>T maps to NM_130837.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:46087995 C>G maps to NM_001017989.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr19:46087902 A>G maps to NM_001017989.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12F-01A-11D-A10Y-09 chr11:132290113 G>T maps to NM_002545.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R3-01A-31D-A14K-09 chr11:132527108 C>A maps to NM_002545.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr23:67339170 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr23:67414315 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr23:67431961 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr23:67417077 A>G did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:67273541 G>T did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr8:145112527 G>A maps to ENST00000360660 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr8:145108231 G>A maps to ENST00000360660 H917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:153421832 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0BJ-01A-11W-A071-09 chr23:153421963 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr23:153416305 C>T did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:153418541 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153496170 A>C did not map to a codon.
Sequencing variant TCGA-A8-A086-01A-11W-A019-09 chr23:153461446 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:153461462 G>A did not map to a codon.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr7:128412692 C>T maps to NM_001708.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr7:128415771 G>A maps to NM_001708.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12V-01A-11D-A10Y-09 chr10:88416982 C>T maps to NM_001030015.2 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr6:47754320 C>T maps to ENST00000489301 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr20:62729632 C>T maps to NM_000913.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr6:154412312 G>T maps to NM_001145279.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr6:154412456 T>C maps to NM_001145279.1 Y431Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr10:13169758 C>T maps to NM_021980.4 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr10:13174128 A>G maps to NM_021980.4 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr11:7960263 G>A maps to NM_001003745.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:7949368 G>A maps to NM_001004461.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:48596595 G>A maps to NM_001004134.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr12:48596742 G>A maps to NM_001004134.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:55735241 G>T maps to NM_001005491.1 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:55735852 G>A maps to NM_001005491.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:55735720 G>C maps to NM_001005491.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07Z-01A-11W-A019-09 chr6:29408424 C>T maps to NM_013941.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr6:29407975 C>T maps to NM_013941.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:22037945 C>T maps to NM_001005465.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr11:123886800 C>T maps to NM_001004462.1 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr11:123886541 C>T maps to ENST00000375021 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr11:123901063 C>T maps to ENST00000375021 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr19:15918841 C>T maps to NM_013940.2 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A096-01A-11W-A019-09 chr19:15839335 G>A maps to NM_013939.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr19:16060404 T>G maps to NM_001004465.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:16059847 G>T maps to NM_001004465.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:16060033 C>T maps to NM_001004465.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr19:15905355 C>T maps to NM_001004466.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr19:15904917 C>T maps to NM_001004466.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:159409769 G>C maps to NM_012351.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:159410498 G>T maps to NM_012351.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr1:159283942 G>A maps to NM_001004467.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:159505111 G>C maps to NM_001004469.1 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr1:159505695 G>C maps to NM_001004469.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:158435936 C>T maps to NM_001004473.1 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:158435689 C>T maps to NM_001004473.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr1:158390578 C>T maps to NM_001004476.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:158390017 C>T maps to NM_001004476.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:158450420 G>T maps to NM_001004472.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr11:123847944 T>A maps to NM_001004474.1 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr11:123848323 G>A maps to NM_001004474.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr11:123848194 G>T maps to NM_001004474.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr1:158368835 G>A maps to NM_001004475.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr11:59480613 G>A maps to NM_001005324.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr1:158548882 A>C maps to NM_001004477.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr14:20665886 G>A maps to NM_001005503.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr14:20665592 G>A maps to NM_001005503.1 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr14:19377727 C>A maps to NM_001013354.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr14:19378226 C>T maps to NM_001013354.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:19378130 C>T maps to NM_001013354.1 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr1:248004655 G>A maps to NM_001001959.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr6:29342373 T>G maps to NM_030959.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:45799215 G>A maps to NM_001004297.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr9:107298626 G>T maps to NM_001001961.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr9:107298537 G>C maps to NM_001001961.1 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:107289307 G>A maps to NM_001001919.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr9:107379681 A>C maps to NM_001001956.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr9:107380083 G>A maps to NM_001001956.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:107456837 C>T maps to NM_001004484.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr9:107457128 G>T maps to NM_001004484.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:247835509 C>T maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:130678344 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr9:35869717 C>T maps to NM_001004487.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr1:248512378 C>T maps to NM_001001918.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:248512855 A>C maps to NM_001001918.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:248512624 G>A maps to NM_001001918.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr1:248512624 G>T maps to NM_001001918.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr1:248845387 G>C maps to NM_001004734.1 S73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:248845113 C>T maps to NM_001004734.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:248844943 G>C maps to NM_001004734.1 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr17:3119720 C>T maps to NM_014565.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:3300919 G>C maps to NM_003553.2 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr17:3337084 C>A maps to NM_003554.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:3336292 A>C maps to NM_003554.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:15198730 C>G maps to NM_001004713.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:125240100 G>A maps to NM_001004451.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:125273829 C>T maps to NM_054107.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:125437458 C>A maps to NM_001005234.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr9:125487176 G>A maps to NM_001005235.1 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:9204423 C>T maps to ENST00000305465 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr19:9204486 C>A maps to ENST00000305465 C192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr9:125289197 G>A maps to ENST00000359439 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:125288930 G>T maps to ENST00000359439 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:125315549 C>T maps to NM_001004457.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr9:125377240 C>T maps to NM_012364.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr11:57982599 G>A maps to NM_001004458.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr11:57983025 C>T maps to NM_001004458.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr11:57971578 G>A maps to NM_001004459.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr7:144015840 G>A maps to NM_001005287.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr7:144015462 G>A maps to NM_001005287.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:144015331 C>T maps to NM_001005287.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr7:143793108 C>T maps to NM_001004135.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:143792799 G>A maps to NM_001004135.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr7:143826249 A>T maps to NM_001001659.1 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:143807337 C>T maps to NM_001005480.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr7:143747697 T>C maps to NM_012365.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr7:143956460 T>C maps to NM_001005328.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W4-01A-11D-A10G-09 chr7:143956460 T>C maps to NM_001005328.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr7:143956460 T>C maps to NM_001005328.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr11:6789588 G>A maps to NM_001004490.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr11:6790158 G>A maps to NM_001004490.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:248128842 C>T maps to NM_001004491.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr1:248128806 C>T maps to NM_001004491.1 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr6:29055015 C>A maps to NM_001005226.2 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr6:29054989 A>G maps to NM_001005226.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr6:27925572 C>G maps to NM_012367.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:3406242 C>G maps to NM_012368.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr1:247695645 G>A maps to NM_198074.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr11:6913662 G>A maps to NM_003700.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr11:6913560 T>G maps to NM_003700.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:143657555 C>T maps to NM_012369.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:143657695 C>T maps to NM_012369.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr1:247752383 C>T maps to NM_001001915.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr1:247752245 C>A maps to NM_001001915.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr1:247752098 C>T maps to NM_001001915.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr1:247769546 C>T maps to NM_001001914.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:247769657 C>T maps to NM_001001914.1 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:247769441 C>G maps to NM_001001914.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr1:248685864 G>T maps to NM_001013355.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:114089922 G>C maps to ENST00000374428 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr1:248262901 C>A maps to NM_175911.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:248262772 C>T maps to NM_175911.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:248263204 C>T maps to NM_175911.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr1:248202360 G>A maps to NM_001004686.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr1:248202361 C>T maps to NM_001004686.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:248224538 C>T maps to NM_001004687.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:248112737 C>A maps to NM_001001963.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr1:248112344 G>A maps to NM_001001963.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:248113010 C>G maps to NM_001001963.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr1:248402478 C>T maps to NM_017504.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:248402649 C>T maps to NM_017504.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:248402509 C>T maps to NM_017504.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:248309123 C>G maps to NM_001004690.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr1:248487710 G>A maps to NM_001004691.1 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:248569615 A>C maps to NM_030904.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr1:248570402 T>G maps to NM_030904.1 *370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:248569792 C>T maps to NM_030904.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr1:248756769 C>T maps to NM_001004693.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:248757015 G>A maps to NM_001004693.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr1:248789814 G>T maps to NM_001001964.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:248458058 G>A maps to NM_001004692.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:248616622 C>T maps to NM_001004136.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr1:248616355 C>A maps to NM_001004136.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr1:248637178 T>A maps to NM_001005495.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:248637361 C>T maps to NM_001005495.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr1:248637259 C>A maps to NM_001005495.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr1:248737770 G>T maps to NM_001001821.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr1:248737929 G>A maps to NM_001001821.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr1:248737983 C>T maps to NM_001001821.1 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:248737566 G>A maps to NM_001001821.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr1:248524974 T>C maps to NM_001004696.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr1:248551589 G>A maps to NM_001005471.1 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:248551532 G>C maps to NM_001005471.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:248551040 C>T maps to NM_001005471.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr1:248084510 T>C maps to NM_001005522.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:248058938 C>T maps to NM_001001957.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:247655208 T>C maps to NM_001004698.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr5:180166344 C>T maps to NM_001001657.1 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr5:180166707 C>T maps to NM_001001657.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr5:180166206 G>C maps to NM_001001657.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr19:8841767 G>T maps to NM_001004699.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr19:8841851 C>G maps to NM_001004699.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:3181518 G>A maps to NM_002551.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:3181563 G>A maps to NM_002551.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:55135706 G>A maps to NM_001005275.1 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr11:55135637 T>C maps to NM_001005275.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr11:55136012 C>T maps to NM_001005275.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:55111278 T>G maps to NM_001005274.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr11:48511195 C>A maps to NM_001005512.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:51412278 C>T maps to NM_001005272.3 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr11:51412083 G>A maps to NM_001005272.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr11:51411540 C>T maps to NM_001005272.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:48238978 C>G maps to NM_001005470.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:55371783 C>T maps to NM_001004700.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr11:55371450 G>A maps to NM_001004700.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr11:50003440 C>T maps to NM_001005270.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:50003191 G>A maps to NM_001005270.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr11:49974336 T>C maps to NM_001001955.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:55322696 C>T maps to NM_001001920.1 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr11:55321982 G>C maps to NM_001001920.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr11:55322144 C>T maps to NM_001001920.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr11:55321991 A>G maps to NM_001001920.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr11:55340442 C>G maps to NM_001004701.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr11:51515860 G>T maps to NM_001004703.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:55433073 A>G maps to NM_001004704.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:56232786 G>A maps to NM_012374.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:59245561 C>A maps to NM_001004705.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr11:59245265 C>T maps to NM_001004705.1 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr11:59245265 C>T maps to NM_001004705.1 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr11:59271953 G>A maps to NM_001004706.1 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr11:59225032 C>A maps to NM_001004708.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr14:22133491 C>T maps to NM_001001912.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr14:22133390 C>A maps to NM_001001912.1 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr14:22133649 G>T maps to NM_001001912.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr15:102358586 C>G maps to NM_001001674.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr19:110857 A>G maps to NM_001005240.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr8:116433 G>A maps to NM_001005504.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr15:102346323 C>T maps to NM_001005326.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr14:20404130 C>T maps to NM_001004063.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr14:20404298 C>T maps to NM_001004063.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr14:20444045 C>T maps to NM_001005486.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr14:20444651 G>C maps to NM_001005486.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr14:20345238 G>T maps to NM_001005501.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr14:20344473 G>T maps to NM_001005501.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr14:20529102 A>G maps to NM_001004717.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr14:20528299 C>T maps to NM_001004717.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:20528646 A>G maps to NM_001004717.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr14:20248567 T>C maps to NM_001005500.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr14:20248531 A>G maps to NM_001005500.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr14:20248543 G>A maps to NM_001005500.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr14:20248586 T>C maps to NM_001005500.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr15:22369003 C>A maps to NM_001004719.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:22368952 C>T maps to NM_001004719.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr14:20296297 G>T maps to NM_001004723.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EW-01A-21D-A10Y-09 chr15:22382594 A>G maps to NM_001005241.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr15:22383381 C>A maps to NM_001005241.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr14:20612250 C>G maps to NM_001004724.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr14:20216050 C>A maps to NM_172194.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr14:20215638 C>G maps to NM_172194.1 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr11:55419047 G>A maps to NM_001004059.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr11:55419086 C>G maps to NM_001004059.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:48285504 C>G maps to NM_001004726.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr11:48286092 C>T maps to NM_001004726.1 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr11:48285567 G>T maps to NM_001004726.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr11:4976553 A>G maps to NM_001004748.1 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr11:4976682 G>A maps to NM_001004748.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr11:4976925 T>A maps to NM_001004748.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr11:4967816 T>A maps to NM_001005329.1 K172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:5322876 G>A maps to NM_033179.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:5322606 C>T maps to NM_033179.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:5364631 G>A maps to NM_001005567.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr11:5373048 T>A maps to NM_001004750.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr11:4661646 G>A maps to NM_001004751.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr11:4661472 G>T maps to NM_001004751.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr11:4661784 C>T maps to NM_001004751.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:5020400 C>T maps to NM_001004755.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:5444284 A>C maps to NM_001004757.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr11:5443510 C>A maps to NM_001004757.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:5444149 C>G maps to NM_001004757.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr11:4869757 C>T maps to NM_001004758.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:5221546 G>T maps to NM_001004760.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr11:5153188 G>T maps to NM_001005160.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr11:6191247 G>A maps to NM_001004052.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr11:6190728 G>T maps to NM_001004052.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:4388712 T>G maps to NM_001005161.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr11:4389300 G>A maps to NM_001005161.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr11:5906157 G>C maps to NM_001005165.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr11:5905806 C>T maps to NM_001005165.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr11:5905605 G>A maps to NM_001005165.1 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr11:5862419 G>C maps to ENST00000379946 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr11:5878437 C>A maps to NM_001005168.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:5566324 G>T maps to NM_001005289.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:4615426 C>A maps to ENST00000450052 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:4608425 C>T maps to NM_001005170.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:5068501 C>T maps to NM_001001916.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr11:4510283 C>T maps to NM_001005171.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:4471426 A>C maps to NM_001005172.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr11:4470850 A>T maps to NM_001005172.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:4471051 C>G maps to NM_001005172.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr11:4566605 C>A maps to NM_001004137.1 Y62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:4566806 C>T maps to NM_001004137.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:4566887 C>G maps to NM_001004137.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr11:5841831 C>T maps to NM_001005174.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr11:5842493 T>G maps to NM_001005174.1 L310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr11:5799612 G>A maps to NM_001001922.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr11:4825511 C>T maps to ENST00000380382 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr11:6048682 G>A maps to NM_001001917.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr11:6048718 G>C maps to NM_001001917.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr11:6048394 G>A maps to NM_001001917.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:6024171 G>A maps to NM_001005179.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr11:6024336 C>T maps to NM_001005179.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr11:5757882 C>G maps to NM_001005180.2 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:6129490 G>A maps to NM_001005181.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr11:59211430 C>T maps to NM_001004728.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:59211306 T>C maps to NM_001004728.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:59132344 A>C maps to NM_001004729.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr11:56431679 C>T maps to NM_001004730.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:55798439 A>C maps to NM_001001921.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr11:55798415 C>T maps to NM_001001921.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:58125987 C>T maps to NM_001005489.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr11:58126185 G>A maps to NM_001005489.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:58274816 G>A maps to NM_001005218.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr11:58170264 A>G maps to NM_001005469.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:125551609 A>C maps to NM_001001923.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr9:125551553 G>T maps to NM_001001923.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr11:55540971 C>G maps to NM_001001967.1 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr11:55563054 G>A maps to NM_001004735.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:55563651 C>T maps to NM_001004735.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:55607000 C>G maps to NM_001005496.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:55761831 T>C maps to NM_003697.1 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr11:55761641 G>A maps to NM_003697.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr3:97851849 G>A maps to NM_001005338.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HI-01A-11D-A099-09 chr3:97851562 T>C maps to NM_001005338.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr3:97851915 C>T maps to NM_001005338.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr3:97868792 T>C maps to NM_001005514.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:97888445 C>T maps to NM_001005515.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr3:98002000 C>T maps to NM_001005482.1 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:97983946 C>T maps to NM_001005479.1 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:55703531 G>A maps to NM_006637.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr3:98217027 C>T maps to NM_001004737.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr3:98217147 C>T maps to NM_001004737.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr3:98110240 C>A maps to NM_001005516.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr3:98073611 T>C maps to NM_001005517.1 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:55579137 T>C maps to NM_001004738.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:55579223 C>T maps to NM_001004738.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr11:55595569 G>A maps to NM_001004739.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr11:55595296 G>T maps to NM_001004739.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:56380306 C>T maps to NM_001004740.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr11:56344870 G>T maps to NM_001004741.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr11:56310544 G>A maps to NM_001005245.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:56310646 C>T maps to NM_001005245.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr11:56310391 C>A maps to NM_001005245.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr11:56310310 G>T maps to NM_001005245.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr11:56309908 G>C maps to NM_001005245.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr11:56237367 G>T maps to NM_001004742.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr11:56237826 G>A maps to NM_001004742.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr11:56258638 G>A maps to NM_001005282.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:7817781 G>A maps to NM_153444.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr11:56185675 T>C maps to NM_001004744.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:56043560 A>C maps to NM_001004745.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr11:56000598 A>T maps to NM_001004746.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr11:55999764 C>T maps to NM_001004746.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:56000013 G>A maps to NM_001004746.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr11:56019959 T>C maps to NM_001004747.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr11:56020649 A>G maps to NM_001004747.1 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A24A-01A-11D-A167-09 chr6:29323444 G>T maps to NM_030876.5 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:55681413 G>A maps to NM_001001960.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WT-01A-11D-A10G-09 chr11:55681317 C>T maps to NM_001001960.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr11:6816235 G>T maps to NM_003696.2 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr7:143701739 C>G maps to NM_001005281.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:143701937 C>T maps to NM_001005281.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:143701586 C>G maps to NM_001005281.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr7:143701863 C>T maps to NM_001005281.1 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P7-01A-21D-A142-09 chr2:240969516 G>A maps to NM_001005853.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:240969291 G>C maps to NM_001005853.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr2:240984859 T>C maps to NM_173351.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:55714604 C>A maps to NM_001005182.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr12:55846917 A>G maps to NM_054105.1 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr12:55846935 G>C maps to NM_054105.1 *313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr12:55688857 G>C maps to NM_001005493.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr12:55794893 G>A maps to NM_001005518.1 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:55794566 A>G maps to NM_001005518.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr12:55886698 T>C maps to NM_001005519.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:55641292 C>T maps to NM_001005490.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr12:55641890 C>T maps to NM_001005490.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr12:55820675 C>G maps to NM_001005183.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr1:247875784 G>T maps to NM_001005286.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr1:247875682 G>A maps to NM_001005286.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:158670001 G>T maps to NM_001005279.1 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr1:158687141 G>C maps to ENST00000368146 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LH-01A-31D-A18P-09 chr1:158725033 G>A maps to NM_001005184.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:158725147 C>T maps to NM_001005184.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr1:158735695 A>T maps to NM_001005185.1 Y259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr1:158735725 G>A maps to NM_001005185.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr14:21109616 G>A maps to NM_001001968.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr14:21109742 G>C maps to NM_001001968.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:123814089 T>A maps to NM_001005187.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr11:123814410 A>T maps to NM_001005187.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:142749601 A>C maps to NM_001001667.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:123624914 G>A maps to NM_001005188.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr1:158517487 G>C maps to NM_001005189.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr19:14952056 G>T maps to NM_001005190.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr19:14992032 G>A maps to NM_030901.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:14910447 G>T maps to NM_198944.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr19:14910072 C>G maps to NM_198944.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr19:14910315 G>A maps to NM_198944.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:15052451 C>G maps to NM_012377.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr19:15053103 G>A maps to NM_012377.1 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr19:15053235 G>A maps to NM_012377.1 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22D-01A-11D-A159-09 chr19:15052845 C>T maps to NM_012377.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr19:15052875 C>T maps to NM_012377.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr19:9296714 G>A maps to NM_175883.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W4-01A-11D-A10G-09 chr19:9296534 C>T maps to NM_175883.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr19:9324862 G>T maps to NM_001005191.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr19:9325093 G>T maps to NM_001005191.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr19:9362660 C>T maps to NM_001079935.1 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:9361811 C>T maps to NM_001079935.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr19:9225563 C>T maps to ENST00000293614 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr19:9213394 C>T maps to NM_001005193.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:9237503 C>T maps to NM_001001958.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:124440641 G>C maps to NM_001005194.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr11:124412710 T>A maps to NM_001005195.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:124413043 A>G maps to NM_001005195.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr11:124412896 G>T maps to NM_001005195.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr11:124253146 A>G maps to NM_001005468.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr11:124252387 G>A maps to NM_001005468.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:124310651 A>G maps to NM_012378.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr11:124310047 A>G maps to NM_012378.1 *312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:124180215 G>A maps to NM_001002917.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr11:124180242 G>C maps to NM_001002917.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr11:123777207 C>T maps to NM_001005197.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:56058163 G>A maps to NM_001005199.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:56058172 G>A maps to NM_001005199.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:56058342 A>G maps to NM_001005199.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr11:55872937 C>T maps to NM_001005200.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:55890733 G>T maps to NM_001005201.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:55860881 C>T maps to NM_001003750.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr11:56127892 C>A maps to NM_001005205.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08O-01A-21W-A071-09 chr11:56114029 G>A maps to NM_001002907.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr11:56114083 G>A maps to NM_001002907.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:56085817 C>T maps to NM_001005202.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr11:56086126 C>A maps to NM_001005202.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr12:48920157 G>A maps to NM_001005203.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:142724057 C>T maps to NM_001001658.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr7:141618800 A>T maps to NM_001001656.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:56467913 C>G maps to NM_001013358.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr11:56468330 A>C maps to NM_001013358.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr11:57947557 C>A maps to NM_001005212.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr11:57947194 T>G maps to NM_001005212.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:201785790 G>A maps to NM_006190.4 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr2:201790581 C>T maps to NM_006190.4 W375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:103844670 G>A maps to NM_002553.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:103848353 C>A did not map to a codon.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr7:103801543 A>G maps to NM_002553.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr9:117092259 C>T maps to NM_000608.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr12:58114297 C>T maps to NM_006812.3 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:58088531 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr22:31289973 G>A maps to NM_030758.3 K787K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr22:31301871 C>T maps to NM_030758.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr3:31725408 G>A maps to NM_017784.4 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FB-01A-11D-A17D-09 chr3:31871578 G>A maps to NM_017784.4 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr3:31871603 C>T maps to NM_017784.4 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr3:31871636 G>A maps to NM_017784.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr3:31725366 C>T maps to NM_017784.4 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:125313606 G>T maps to NM_022776.4 S13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr18:21761132 G>T maps to NM_080597.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:21914261 C>A maps to NM_080597.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr18:21759702 G>A maps to NM_080597.2 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr20:60868879 C>A maps to NM_144498.1 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:24905790 C>T maps to NM_015550.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr7:24911624 G>A maps to NM_015550.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:3140804 C>T maps to NM_020896.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EI-01A-11D-A27P-09 chr11:3114833 C>G maps to NM_020896.3 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr11:3147732 C>A maps to NM_020896.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:45885728 C>T maps to NM_145798.2 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:45893813 G>A maps to NM_145798.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EW-01A-11D-A135-09 chr12:76765226 C>T did not map to a codon.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr1:52227564 C>T maps to ENST00000428468 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:52231524 C>T maps to ENST00000428468 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr1:36894015 C>A maps to ENST00000445843 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:90937000 C>G maps to NM_001126111.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr5:38881756 C>G maps to NM_003999.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr5:38924581 G>A maps to NM_003999.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:38886284 T>C maps to NM_003999.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:65345331 G>T maps to NM_178859.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:108395498 G>A maps to NM_014028.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr3:195959934 G>A maps to NM_152672.5 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr3:195956805 T>G maps to NM_152672.5 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr23:38212025 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:38262975 C>T did not map to a codon.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr23:38268239 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:38240605 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:38271224 G>A did not map to a codon.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr16:21728238 G>A maps to ENST00000286149 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr16:21742184 C>G maps to ENST00000286149 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr2:26696084 T>G maps to NM_194248.2 T1216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr2:26696147 G>A maps to NM_194248.2 N1195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr2:26739335 G>A maps to NM_194248.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr4:4199563 G>A maps to NM_177998.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr17:72929468 G>A did not map to a codon.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr17:72923825 T>G maps to NM_178160.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr17:72926761 G>C maps to NM_178160.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:16729138 C>A maps to NM_020157.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr2:241079497 C>T maps to NM_148961.3 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:94505334 C>T maps to NM_023112.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:20224046 G>A maps to NM_015207.1 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr4:146076763 G>C maps to ENST00000447906 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr4:146059244 C>T maps to ENST00000447906 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr4:146062554 G>A maps to ENST00000447906 Q687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr23:48780994 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:69283014 C>T did not map to a codon.
Sequencing variant TCGA-A8-A096-01A-11W-A019-09 chr23:69282425 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr23:69283093 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:69282994 C>T did not map to a codon.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr23:69282968 G>A did not map to a codon.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr15:31947335 C>T maps to ENST00000382902 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:149939360 A>C maps to NM_020205.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:149939360 A>C maps to NM_020205.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:149939378 G>C maps to NM_020205.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr14:57269057 G>A maps to NM_021728.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr14:57270977 C>T maps to NM_021728.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr14:57268781 G>A maps to NM_021728.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:29628063 C>T maps to NM_183378.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JI-01A-21W-A100-09 chr12:29604407 C>T maps to NM_183378.2 W875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr12:29649524 A>G maps to NM_183378.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:29644105 G>A maps to NM_183378.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:111957919 C>A maps to ENST00000369728 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:65562748 G>A maps to NM_004561.2 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:65562190 T>C maps to NM_004561.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr14:23239474 C>G maps to NM_005015.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:23237316 C>T maps to NM_005015.3 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:97639803 G>T maps to NM_080818.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr13:97639085 G>A maps to NM_080818.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr13:97639725 G>A maps to NM_080818.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:3803052 A>C maps to NM_002558.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:133198140 C>T maps to NM_170683.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:121666903 T>G did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:121666824 C>G maps to NM_002560.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr22:21380773 A>T maps to NM_005446.3 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr3:152554272 G>C maps to NM_002563.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr3:152554179 C>T maps to NM_002563.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SB-01A-11D-A142-09 chr23:78216688 C>T did not map to a codon.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr23:78216326 G>T did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr23:78216939 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:78216876 A>C did not map to a codon.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr23:78216026 C>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:78216687 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:78216911 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XR-01A-11D-A14K-09 chr23:78216288 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr3:151046414 G>C maps to NM_176894.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr3:151046792 C>T maps to NM_176894.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr11:72946004 C>G maps to NM_176071.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr23:69479265 G>A did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr23:69478550 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:1585256 C>G did not map to a codon.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr23:1585396 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:74803709 G>A maps to NM_000917.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:49042365 T>G maps to NM_177938.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:49042458 A>C maps to NM_177938.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:49028330 C>G maps to NM_177938.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:49041555 C>T maps to NM_177938.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr11:73627699 T>C maps to NM_025155.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr11:73611343 G>A maps to NM_025155.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr20:43559249 G>A maps to NM_001124756.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr13:25670377 C>G maps to NM_030979.2 Y14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr13:25671061 A>G maps to NM_030979.2 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr13:25671128 C>T maps to NM_030979.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr1:40027753 G>C maps to NM_001135653.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr23:90690697 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:90691597 A>G did not map to a codon.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr11:65983633 C>T maps to NM_018026.2 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:105860931 C>T maps to ENST00000458164 Q880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:105834824 G>A maps to ENST00000458164 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08O-01A-21W-A071-09 chr1:17567194 G>T maps to NM_013358.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr1:17395658 G>T maps to NM_007365.2 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09V-01A-11D-A045-09 chr1:17575712 G>A maps to NM_016233.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27T-01A-11D-A16D-09 chr1:17597588 T>C maps to NM_016233.2 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr1:17714945 G>A maps to NM_207421.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FV-01A-11D-A17D-09 chr1:17699574 C>T maps to NM_207421.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr9:138454701 A>G maps to NM_002571.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:39880903 C>A maps to NM_019088.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr17:2573486 C>T maps to NM_000430.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:117034544 T>G maps to NM_002572.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:117034544 T>G maps to NM_002572.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:26310507 G>A maps to NM_000437.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr8:81897316 C>T maps to NM_018440.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr8:81905417 G>T maps to NM_018440.3 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:49459342 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:49454039 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr23:49459369 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr23:49454098 C>G did not map to a codon.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr23:55117825 A>G did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr23:55117844 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:55102532 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr23:55248234 G>C did not map to a codon.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr23:55248224 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:103246666 A>C maps to NM_000277.1 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr4:57314717 G>T maps to NM_001079525.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr5:138699535 C>T maps to NM_001033112.1 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:77054951 G>A maps to NM_001128620.1 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:110459701 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:110406823 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:110439163 A>C did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:110388138 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr23:110385363 T>A did not map to a codon.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr23:110366475 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:39668391 C>G maps to NM_005884.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:40564735 C>T maps to NM_020168.4 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BS-01A-11D-A12Q-09 chr15:40557141 C>T maps to NM_020168.4 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr20:9561436 G>A maps to NM_177990.2 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03L-01A-41W-A071-09 chr20:9520174 T>C maps to NM_177990.2 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr20:9546863 G>C maps to NM_177990.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr20:9523319 G>A maps to NM_177990.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:23614971 C>T maps to NM_024675.3 V1123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr16:23614904 G>A maps to NM_024675.3 Q1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:23634363 C>T maps to NM_024675.3 K974K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:23641647 G>A maps to NM_024675.3 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr4:169589472 G>A maps to NM_001166108.1 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:112694276 A>C maps to NM_007203.4 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:112705572 G>A maps to ENST00000413420 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr1:100154697 G>A maps to NM_017734.4 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr5:102343194 C>T maps to NM_000919.3 F683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:102343294 G>T maps to NM_000919.3 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:35457466 T>G maps to NM_015430.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr12:56721334 C>A maps to NM_001127460.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr12:56718084 C>A maps to NM_001127460.2 G641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr12:56713157 G>A maps to NM_001127460.2 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr12:56713710 C>T maps to NM_001127460.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr13:28794502 G>T maps to NM_175854.7 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr13:28834663 C>T maps to NM_175854.7 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr13:28855480 C>G maps to NM_175854.7 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr5:167984617 A>G maps to NM_024594.2 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:167995967 G>A maps to NM_024594.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr5:167984581 G>A maps to NM_024594.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:2452259 G>A maps to ENST00000425477 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:50616034 G>A maps to NM_052839.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr11:124489689 G>A maps to NM_052959.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr10:135193581 C>T maps to NM_152911.2 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr5:78919236 C>T maps to NM_173797.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr19:39591968 C>T maps to NM_001004318.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr14:73720539 G>A maps to ENST00000427855 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr7:4900571 C>T maps to NM_020144.4 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr7:4901039 G>A maps to NM_020144.4 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr7:4900823 C>T maps to NM_020144.4 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:60987416 G>T maps to NM_022894.3 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr9:119106917 C>T maps to NM_002581.3 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:119033602 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr9:119115960 T>A maps to NM_002581.3 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr9:119106884 C>T maps to NM_002581.3 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr9:119097219 C>T maps to NM_002581.3 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr9:118950075 G>A maps to NM_002581.3 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:118950120 G>A maps to NM_002581.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:176564440 G>C maps to NM_020318.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:176738741 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:176668446 C>A maps to NM_020318.2 I986I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:176564695 G>A maps to NM_020318.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr1:176769268 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:176659423 A>G maps to NM_020318.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr10:89474610 G>A maps to NM_001015880.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr10:89505675 C>A maps to NM_001015880.1 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr4:79845077 C>T maps to NM_001040202.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:156214982 C>A maps to NM_024897.2 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr6:52268805 C>G maps to ENST00000361841 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr10:34400414 C>T maps to NM_019619.3 Q1251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:34558595 T>G maps to NM_019619.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:34649031 G>C maps to NM_019619.3 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:34759097 G>C maps to NM_019619.3 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:34739261 G>A maps to NM_019619.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:206050530 A>C maps to ENST00000406610 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:206480218 A>C maps to ENST00000406610 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:206165384 C>T maps to ENST00000406610 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr16:67695949 C>T maps to NM_016948.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr18:77917707 G>A maps to NM_032510.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr6:162622174 G>C maps to NM_004562.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:162622237 G>T maps to NM_004562.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FV-01A-11D-A17D-09 chr6:161969945 C>A maps to NM_004562.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:75938166 A>C maps to NM_015393.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:75938250 A>C maps to NM_015393.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr1:226562031 C>T maps to NM_001618.3 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:226573297 G>A maps to NM_001618.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:226568859 C>T maps to NM_001618.3 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr12:3939169 T>C maps to NM_020367.4 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:3921318 G>T maps to NM_020367.4 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr7:139756695 G>A maps to NM_022750.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr3:122418981 G>A maps to NM_017554.2 K527K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:122419357 G>T maps to NM_017554.2 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:122296640 C>T maps to NM_001113523.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:20813205 A>G maps to NM_005484.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:20819269 C>A maps to NM_005484.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:20825601 C>T maps to NM_005484.3 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr14:20824783 G>A maps to NM_005484.3 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:51979012 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr13:25068830 G>T maps to NM_006437.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:25000641 G>A maps to NM_006437.3 F1647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:72557475 C>A maps to NM_020214.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr15:72552859 G>A maps to NM_020214.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr5:50091196 C>A maps to ENST00000505697 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr5:50055553 A>T maps to ENST00000505697 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr5:50090980 T>A maps to ENST00000505697 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:122255021 T>G maps to NM_031458.2 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:12534908 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:12534908 T>G did not map to a codon.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr11:12399199 C>T maps to NM_018222.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr22:44514986 C>T maps to NM_001003828.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:44395434 T>G maps to NM_001003828.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:150839660 A>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:150789404 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:150844586 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr23:150780206 T>A did not map to a codon.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr23:150789491 C>A did not map to a codon.
Sequencing variant TCGA-E2-A15P-01A-11D-A10Y-09 chr23:150832808 G>A did not map to a codon.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr23:150832672 G>T did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr2:242076634 G>C maps to ENST00000358649 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:242076463 G>A maps to ENST00000358649 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr2:242080103 C>T maps to ENST00000358649 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:242082327 C>T maps to ENST00000358649 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:59418264 G>A maps to NM_152716.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr22:31731813 C>T maps to NM_014323.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr12:79990323 G>A maps to NM_002583.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr20:21687301 C>A maps to NM_006192.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:223086013 A>G maps to NM_181459.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:127255098 A>C maps to NM_006193.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr7:127253882 C>A maps to NM_006193.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:37006506 T>G maps to NM_016734.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:36882082 C>T maps to NM_016734.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr11:31816280 G>A maps to NM_001604.4 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:18960956 C>T maps to NM_002584.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:18961013 C>T maps to NM_002584.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr2:113993060 G>A maps to NM_003466.3 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr7:154760836 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr7:154753358 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:27667907 C>A maps to NM_018492.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr6:138539211 G>A maps to NM_021635.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:52621380 G>A maps to ENST00000296302 V1037V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr3:52643678 A>G maps to ENST00000296302 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:19675751 T>G maps to NM_025245.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:154918316 C>T maps to NM_020524.2 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr11:66617202 G>T maps to NM_022172.2 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:72645665 C>T maps to NM_000281.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:53854844 C>G maps to NM_005016.5 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr12:53849273 G>A maps to NM_005016.5 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr21:47349883 C>T maps to NM_020528.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr13:101020766 C>G maps to NM_000282.3 S562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr13:101167709 C>T maps to NM_000282.3 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr3:135974723 C>T maps to NM_001178014.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZX-01A-12D-A29N-09 chr3:136048837 T>G maps to NM_001178014.1 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:136019952 T>G maps to NM_001178014.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr3:136012614 C>T maps to NM_001178014.1 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr5:141244044 G>T maps to NM_032420.2 Y617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:141243816 T>G maps to NM_032420.2 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr5:141243273 C>G maps to NM_032420.2 V874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr4:134071573 G>A maps to NM_032961.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XO-01A-11D-A10G-09 chr4:134071405 C>T maps to NM_032961.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr4:134073568 C>T maps to NM_032961.1 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr4:134073304 C>T maps to NM_032961.1 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr4:134072135 C>T maps to NM_032961.1 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr4:134084409 C>T maps to NM_032961.1 R1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr4:134073919 C>T maps to NM_032961.1 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr4:134072728 T>C maps to NM_032961.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr23:91456403 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr23:91090833 G>C did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:91873467 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:91090835 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:91873599 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:91091031 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:91133181 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr23:91873604 C>A did not map to a codon.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr23:91131968 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr23:91873567 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:91873396 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:91134232 G>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:91642763 G>C did not map to a codon.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr23:91873741 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:91134144 A>T did not map to a codon.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr23:91133193 C>A did not map to a codon.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr23:91133193 C>T did not map to a codon.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr10:55582295 A>G maps to NM_001142763.1 I1737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr10:55581734 A>T maps to NM_001142763.1 T1924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr10:55782834 G>T maps to NM_001142763.1 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W4-01A-11D-A10G-09 chr10:55626526 C>A maps to NM_001142763.1 E1203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr13:58208938 T>A maps to NM_001040429.2 G753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr13:58206871 C>T maps to NM_001040429.2 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:138451805 T>G maps to NM_019035.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:138442191 G>C maps to NM_019035.3 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr4:138452905 G>A maps to NM_019035.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr23:99551447 G>T did not map to a codon.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr23:99657714 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:99657818 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:99662736 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:99662856 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr23:99551518 G>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:99551783 G>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:99597038 G>T did not map to a codon.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr23:99662739 G>A did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:99663205 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr23:99663129 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:99662071 G>C did not map to a codon.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr23:99663200 G>T did not map to a codon.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr23:99605658 G>C did not map to a codon.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr23:99661924 G>A did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:99551395 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1X6-01A-11D-A14K-09 chr23:99662739 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr23:99662057 C>G did not map to a codon.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr23:99662745 G>A did not map to a codon.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr23:99551590 C>G did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr23:99663460 G>A did not map to a codon.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr23:99663146 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:61986584 T>G maps to NM_022843.3 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:30725305 A>C maps to NM_001173523.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:30724369 C>T maps to NM_001173523.1 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10B-01A-11D-A10M-09 chr4:30921825 C>T maps to NM_001173523.1 Q1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:67802047 A>C maps to NM_203487.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr13:67801017 G>A maps to NM_203487.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:140165976 G>A maps to NM_018900.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr5:140168169 C>G maps to NM_018900.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr5:140358574 G>C maps to NM_018909.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr5:140166324 G>A maps to NM_018900.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr5:140167620 G>A maps to NM_018900.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JE-01A-11D-A13L-09 chr5:140167728 G>A maps to NM_018900.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr5:140167485 G>A maps to NM_018900.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AB-01A-11W-A050-09 chr5:140236811 G>A maps to NM_018901.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr5:140235800 G>A maps to NM_018901.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:140250091 A>C maps to NM_018902.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:140249092 C>T maps to NM_018902.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:140248984 C>T maps to NM_018902.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CV-01A-31D-A10Y-09 chr5:140256805 G>A maps to NM_018903.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr5:140256727 C>T maps to NM_018903.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:140256670 C>T maps to NM_018903.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140256955 G>C maps to NM_018903.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr5:140256082 C>T maps to NM_018903.2 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:140255158 C>T maps to NM_018903.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr5:140263907 C>T maps to NM_018904.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr5:140263089 C>T maps to NM_018904.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr5:140176057 G>A maps to NM_018905.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr5:140175976 G>A maps to NM_018905.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr5:140176411 G>A maps to NM_018905.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr5:140174749 G>A maps to NM_018905.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr5:140187101 A>G maps to NM_018907.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr5:140188292 C>T maps to NM_018907.2 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr5:140187111 C>T maps to NM_018907.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr5:140188733 C>T maps to NM_018907.2 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr5:140187581 C>T maps to NM_018907.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr5:140188133 G>A maps to NM_018907.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr5:140201500 C>T maps to NM_018908.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr5:140203198 G>A maps to NM_018908.2 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr5:140203027 C>T maps to NM_018908.2 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr5:140209680 C>T maps to NM_018909.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140214099 C>T maps to NM_018910.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:140215410 C>T maps to NM_018910.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr5:140215803 A>G maps to NM_018910.2 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr5:140222343 C>T maps to NM_018911.2 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:140222342 G>A maps to NM_018911.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr5:140222366 C>T maps to NM_018911.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr5:140221571 C>G maps to NM_018911.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:140230161 G>T maps to NM_031857.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr5:140229588 G>A maps to NM_031857.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr5:140230083 G>A maps to NM_031857.1 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr5:140306795 C>T maps to NM_018898.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr5:140346875 C>T maps to NM_018899.5 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr5:140347415 C>T maps to NM_018899.5 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:140432341 A>C maps to NM_013340.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr5:140433271 C>T maps to NM_013340.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:140432383 C>T maps to NM_013340.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr5:140431702 C>T maps to NM_013340.2 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr5:140574446 G>A maps to NM_018930.3 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr5:140573345 C>T maps to NM_018930.3 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr5:140573648 G>T maps to NM_018930.3 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr5:140581056 G>A maps to NM_018931.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr5:140579847 A>G maps to NM_018931.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P0-01A-11D-A142-09 chr5:140580708 C>T maps to NM_018931.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XX-01A-21D-A23C-09 chr5:140590533 G>A maps to NM_018932.3 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr5:140590266 G>A maps to NM_018932.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:140588742 A>G maps to NM_018932.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr5:140590644 C>A maps to NM_018932.3 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr5:140589270 C>T maps to NM_018932.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140593757 G>A maps to NM_018933.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:140595017 C>T maps to NM_018933.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr5:140604696 G>A maps to NM_018934.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr5:140603610 C>T maps to NM_018934.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr5:140604652 G>T maps to NM_018934.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:140605261 G>T maps to NM_018934.2 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Q-01A-11D-A12B-09 chr5:140605356 G>C maps to NM_018934.2 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:140626450 G>A maps to NM_018935.2 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr5:140562835 C>T maps to NM_020957.1 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr5:140562338 C>T maps to NM_020957.1 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr5:140563930 T>C maps to NM_020957.1 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:140564254 G>C maps to NM_020957.1 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr5:140475556 T>C maps to NM_018936.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IA-01A-11W-A050-09 chr5:140481609 C>T maps to NM_018937.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr5:140480787 T>C maps to NM_018937.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr5:140503863 G>T maps to NM_018938.2 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr5:140502503 C>T maps to NM_018938.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140502767 G>A maps to NM_018938.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr5:140516084 G>T maps to NM_015669.2 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr5:140516842 G>A maps to NM_015669.2 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr5:140531178 C>A maps to NM_018939.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr5:140531490 C>T maps to NM_018939.2 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr5:140553378 C>G maps to NM_018940.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr5:140553978 C>T maps to NM_018940.2 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr5:140554696 G>T maps to NM_018940.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr5:140552632 C>T maps to NM_018940.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr5:140560002 C>T maps to NM_019120.2 F796F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:140559582 C>T maps to NM_019120.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:140558613 C>T maps to NM_019120.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:140559921 A>G maps to NM_019120.2 K769K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140711610 C>T maps to NM_018912.2 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140712449 G>A maps to NM_018912.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140890724 G>A maps to NM_018915.2 K928K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:140711000 T>C maps to NM_018912.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr5:140712320 T>A maps to NM_018912.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr5:140711822 G>A maps to NM_018912.2 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr5:140795060 C>A maps to NM_018913.2 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3HN-01A-11D-A20S-09 chr5:140793053 G>A maps to NM_018913.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:140793452 C>T maps to NM_018913.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:140802356 C>T maps to NM_018914.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr5:140802473 G>A maps to NM_018914.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr5:140812077 C>A maps to NM_003735.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:140812002 G>A maps to NM_003735.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr5:140810541 G>A maps to NM_003735.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr5:140719242 G>C maps to NM_018915.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KI-01A-11D-A14K-09 chr5:140720952 G>A maps to NM_018915.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GY-01A-11W-A071-09 chr5:140720424 G>A maps to NM_018915.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr5:140720607 T>C maps to NM_018915.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:140725165 C>T maps to NM_018916.3 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr5:140724178 G>A maps to NM_018916.3 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:140725480 C>T maps to NM_018916.3 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr5:140725927 G>A maps to NM_018916.3 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr5:140724037 G>A maps to NM_018916.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:140725633 C>T maps to NM_018916.3 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr5:140725489 A>C maps to NM_018916.3 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr5:140736101 C>A maps to NM_018917.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140735108 G>T maps to NM_018917.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr5:140735309 C>T maps to NM_018917.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr5:140737103 C>T maps to NM_018917.2 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:140736992 C>T maps to NM_018917.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr5:140744718 C>T maps to NM_018918.2 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:140745243 A>C maps to NM_018918.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:140744613 G>A maps to NM_018918.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:140744574 G>A maps to NM_018918.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr5:140755395 A>C maps to NM_018919.2 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:140754846 C>T maps to NM_018919.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:140755875 C>T maps to NM_018919.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr5:140754952 G>T maps to NM_018919.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr5:140755126 G>T maps to NM_018919.2 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:140753949 G>A maps to NM_018919.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr5:140764697 C>T maps to NM_018920.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr5:140763959 G>T maps to NM_018920.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr5:140764796 C>T maps to NM_018920.2 D777D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr5:140764679 G>A maps to NM_018920.2 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr5:140764592 C>T maps to NM_018920.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr5:140774002 C>A maps to NM_032088.1 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:140774122 C>T maps to NM_032088.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:140772610 G>A maps to NM_032088.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr5:140784571 G>T maps to NM_018921.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JU-01A-11D-A13L-09 chr5:140784340 C>T maps to NM_018921.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IY-01A-21D-A21Q-09 chr5:140731008 G>A maps to NM_018922.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr5:140731701 G>A maps to NM_018922.2 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr5:140730084 G>A maps to NM_018922.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr5:140731548 G>A maps to NM_018922.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr5:140731308 G>A maps to NM_018922.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr5:140731959 G>A maps to NM_018922.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Q-01A-11D-A12B-09 chr5:140731437 G>A maps to NM_018922.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr5:140740550 T>C maps to NM_018923.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr5:140739808 C>G maps to NM_018923.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:140741847 C>T maps to NM_018923.2 R716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr5:140751316 C>T maps to NM_018924.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr5:140752363 C>A maps to NM_018924.2 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr5:140768707 C>T maps to NM_003736.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140768027 G>T maps to NM_003736.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140768278 G>A maps to NM_003736.2 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140769358 C>G maps to NM_003736.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr5:140768681 G>T maps to NM_003736.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr5:140769217 A>T maps to NM_003736.2 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr5:140769019 G>T maps to NM_003736.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr5:140769343 C>T maps to NM_003736.2 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:140788896 C>T maps to NM_018926.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:140788731 G>A maps to NM_018926.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr5:140789280 C>G maps to NM_018926.2 Y504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr5:140797617 C>T maps to NM_018927.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:140856513 T>G maps to NM_002588.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr5:140857179 A>G maps to NM_002588.2 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr5:140866200 T>C maps to NM_018928.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:140866368 A>C maps to NM_018928.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr5:140869113 C>T maps to NM_018929.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:140869184 C>T maps to NM_018929.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:140870732 G>A maps to NM_018929.2 Q642Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr2:120362808 C>G maps to NM_001029996.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr11:82877732 A>G maps to NM_015885.3 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:82880098 C>T maps to NM_015885.3 R908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr11:82892089 C>T maps to NM_015885.3 Q1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr11:82877652 C>T maps to NM_015885.3 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr11:82877693 A>G maps to NM_015885.3 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26E-01A-11D-A167-09 chr2:74734187 G>A maps to NM_032673.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:74733152 G>A maps to NM_032673.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:93011091 T>G maps to NM_032373.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:113852541 C>A maps to ENST00000246505 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr13:113838711 T>C maps to ENST00000246505 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:44575024 T>G did not map to a codon.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr20:44574945 C>T maps to NM_022104.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:44574936 C>T maps to NM_022104.3 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr14:24572734 C>T maps to NM_004563.2 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:24569342 C>T maps to NM_004563.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:24573118 C>T maps to NM_004563.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr14:24567420 C>A maps to NM_004563.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr7:82579109 A>T maps to NM_033026.5 I3598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:82582444 T>G maps to NM_033026.5 S2608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:82764192 T>G maps to NM_033026.5 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr7:82578884 C>T maps to NM_033026.5 K3673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr7:82784866 G>A maps to NM_033026.5 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr7:82764213 G>A maps to NM_033026.5 T884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr7:82545703 C>T maps to NM_033026.5 Q3866Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr7:82584706 A>G maps to NM_033026.5 S1854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr7:82784779 G>A maps to NM_033026.5 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr7:82579906 C>A maps to NM_033026.5 E3333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:82579160 C>T maps to NM_033026.5 L3581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr7:82467654 G>A maps to NM_033026.5 Q4701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr7:82784525 T>C maps to NM_033026.5 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr8:17872348 T>G maps to NM_006197.3 Y1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:17819684 T>C did not map to a codon.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr20:62891425 C>T maps to NM_018257.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:62904722 C>T maps to NM_018257.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr21:47845791 G>A maps to NM_006031.5 L2409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:47746322 T>G maps to NM_006031.5 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:47754669 G>C maps to NM_006031.5 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr21:47819610 T>C maps to NM_006031.5 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr21:47766850 C>T maps to NM_006031.5 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr14:71540425 C>T maps to NM_014982.2 L1673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:233136089 G>A maps to NM_014801.3 I1763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:233136209 C>T maps to NM_014801.3 K1723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:233136145 C>A maps to NM_014801.3 E1745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr1:233136232 C>A maps to NM_014801.3 E1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:233161097 C>A maps to NM_014801.3 E1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr1:233394470 C>T maps to NM_014801.3 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr11:65387068 G>A maps to NM_032223.2 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:65384756 C>G maps to NM_032223.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:65403970 G>A maps to NM_032223.2 R1901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:100205425 G>A maps to NM_002593.3 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr7:100203381 C>G maps to NM_002593.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr3:142539867 G>A maps to NM_013363.3 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr19:7696694 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr5:95746672 C>A maps to NM_000439.4 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:95768599 G>A maps to NM_000439.4 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr5:95744024 C>T maps to NM_000439.4 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr20:17207982 G>A maps to NM_002594.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:1488078 G>A maps to NM_017573.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:1486857 G>T maps to NM_017573.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15L-01A-11D-A12B-09 chr19:1482436 C>T maps to NM_017573.3 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B5-01A-21D-A12Q-09 chr19:1482991 G>A maps to NM_017573.3 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:78601082 G>A maps to NM_001190482.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr9:78722165 G>C did not map to a codon.
Sequencing variant TCGA-AC-A2BM-01A-11D-A21Q-09 chr15:101929763 G>A maps to NM_002570.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr15:101910614 G>T maps to NM_002570.3 S548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr11:117098038 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:117077850 G>A maps to NM_004716.2 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:55512284 T>C maps to NM_174936.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:70504173 A>T maps to NM_016297.3 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr2:70503935 C>T maps to NM_016297.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr3:195968821 G>T maps to NM_005017.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr23:24625918 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr23:24608282 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:24608143 T>C did not map to a codon.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr23:24608285 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:24580565 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr23:24580503 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr2:242793269 G>A maps to NM_005018.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:105181187 T>C maps to NM_014976.1 D787D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FD-01A-11W-A14Q-09 chr10:105200304 C>T maps to NM_014976.1 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr10:105179383 C>T maps to NM_014976.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr10:105200071 G>T maps to NM_014976.1 E1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:33863450 T>C maps to NM_001162429.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr3:33905539 A>G maps to NM_001162429.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr9:125582780 C>T maps to NM_005388.4 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr2:101186078 G>A maps to NM_024065.4 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:774047 G>C maps to NM_182612.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr6:165848787 G>T maps to NM_001130690.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:166075456 C>T maps to NM_001130690.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr6:165863748 C>T maps to NM_001130690.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr6:165832133 G>T maps to NM_001130690.1 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:178936813 A>G maps to NM_016953.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr3:57543002 T>C maps to NM_177966.5 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:57543083 G>A maps to NM_177966.5 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr7:31887634 C>T maps to NM_001191057.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr7:31917593 C>A maps to NM_001191057.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr7:31862801 C>T maps to NM_001191057.1 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr11:72295772 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W3-01A-11D-A10G-09 chr11:72290427 C>G did not map to a codon.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr12:20766423 C>T maps to NM_000921.3 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr12:20766492 C>T maps to NM_000921.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:20807048 G>T maps to NM_000921.3 E1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr12:20807083 G>A maps to NM_000921.3 E1043E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr12:20799760 C>T maps to NM_000921.3 Y814Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr12:20787974 G>A maps to NM_000921.3 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:20709645 T>A did not map to a codon.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr12:20522502 G>A maps to NM_000921.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr12:20806921 C>T maps to NM_000921.3 F989F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr11:14865385 A>G maps to NM_000922.3 R778R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:14880746 G>A maps to NM_000922.3 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr11:14808116 T>C maps to NM_000922.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr19:10572599 G>A maps to NM_001111307.1 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr19:10568681 C>T maps to NM_001111307.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:66834513 C>T maps to NM_001037341.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:18321999 C>T maps to NM_000923.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A133-01A-32D-A12B-09 chr19:18333012 C>G maps to NM_000923.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:58270586 A>G maps to NM_001104631.1 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:144873980 G>T maps to NM_014644.4 S1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:144877066 C>G maps to NM_014644.4 L1540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr1:144918871 G>A maps to NM_014644.4 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr1:144904728 C>T maps to NM_014644.4 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr1:145075853 G>C maps to NM_022359.5 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr1:145075682 C>T maps to NM_022359.5 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr4:120432237 A>G maps to NM_001083.3 H684H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:120484076 C>A maps to NM_001083.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:120422365 G>A maps to NM_001083.3 Q817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr4:120473720 C>T maps to NM_001083.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr5:149310671 G>A maps to NM_000440.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr5:149310661 G>A maps to NM_000440.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:149275995 C>A maps to NM_000440.2 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:149276339 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr10:95372793 G>C maps to NM_006204.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr10:95386561 G>A maps to NM_006204.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr8:66753614 C>T maps to ENST00000401827 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:85669544 C>T maps to NM_002605.2 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:76649194 C>G maps to NM_003719.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr5:76700557 C>T maps to NM_003719.3 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr21:44153464 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr22:39636859 G>T maps to NM_033016.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr4:157689124 G>A maps to NM_016205.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:55129882 C>T maps to NM_006206.4 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr4:55133782 C>G maps to NM_006206.4 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:149501506 G>A maps to NM_002609.3 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr5:149513323 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr23:19371263 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:19373833 G>A did not map to a codon.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr23:19362211 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:19373843 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:34988273 A>C maps to NM_003477.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:34988327 A>C maps to NM_003477.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:35016491 G>T maps to NM_003477.2 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:335567 C>T maps to NM_006849.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:44053673 C>G maps to NM_005313.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:148712056 C>A maps to NM_004911.4 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:122842911 G>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:122842971 C>T maps to NM_006810.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr3:122811241 G>A maps to NM_006810.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr1:26448561 C>T maps to NM_152835.3 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr16:20387446 G>A maps to NM_174924.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:20396156 C>T maps to NM_174924.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr16:20387484 G>A maps to NM_174924.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr23:24552116 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:97028543 A>G maps to NM_020992.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr4:95539202 A>T maps to NM_006457.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:95506854 C>T maps to NM_006457.3 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:176923432 G>A maps to NM_005451.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr8:94934413 C>T maps to NM_001161778.1 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:2636864 G>A maps to NM_002613.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:2645821 C>T maps to NM_002613.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr16:70154553 G>A maps to NM_017990.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr16:70177495 T>C maps to NM_017990.3 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr20:30534326 C>A maps to NM_030815.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:39871073 A>C maps to NM_001100399.1 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr4:39846301 C>T maps to NM_001100399.1 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr13:33315237 T>G maps to ENST00000400481 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr13:33275521 C>T maps to ENST00000400481 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:107780456 T>G maps to NM_020381.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:107531711 T>C maps to NM_020381.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr16:15103549 C>T maps to NM_015027.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr16:15127252 G>A maps to NM_015027.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr20:1961217 G>C maps to NM_024411.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:69509158 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr5:32088971 T>C maps to NM_178140.2 N1806N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:31983722 T>G maps to NM_178140.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:31995785 C>A maps to NM_178140.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:32098720 C>T maps to NM_178140.2 I2733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr5:32089646 T>G maps to NM_178140.2 A2031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr23:153068870 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:153070649 A>C did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:153070216 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153070070 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153073862 G>A did not map to a codon.
Sequencing variant TCGA-BH-A201-01A-11D-A14K-09 chr23:153073933 G>C did not map to a codon.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr10:102783751 G>A maps to NM_001195263.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:21995785 T>G maps to ENST00000424898 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr3:73657823 G>T maps to NM_015009.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr12:41967118 C>T maps to NM_001164595.1 H846H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr12:41967238 G>A maps to NM_001164595.1 K886K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:41961628 G>A maps to NM_001164595.1 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr1:160183047 G>A maps to ENST00000368075 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr12:118574085 G>C maps to NM_002567.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:22570924 G>A maps to NM_144962.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:22675166 G>A maps to NM_144962.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr6:4116162 G>C maps to NM_206836.2 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:4116137 C>T maps to NM_206836.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr7:94293358 G>A maps to NM_001172437.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:57327379 G>A maps to NM_006210.2 F810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr19:57326916 G>A maps to NM_006210.2 R965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr11:66236346 G>T maps to NM_145065.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr17:4594695 T>A maps to ENST00000301396 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr8:57358416 C>T maps to NM_001135690.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr8:57354325 G>A maps to NM_001135690.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr19:33892708 G>A maps to NM_000285.3 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr19:33991852 G>A maps to NM_000285.3 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:8051086 G>A maps to NM_002616.2 N431N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr17:8051336 G>A maps to NM_002616.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:8049970 C>T maps to NM_002616.2 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr2:239164478 G>A maps to NM_022817.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:239161561 C>T maps to NM_022817.2 A1034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:239164300 G>A maps to NM_022817.2 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:239165683 A>G maps to NM_022817.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25F-01A-11D-A167-09 chr1:7890054 T>A maps to ENST00000377532 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr1:7886603 G>A maps to ENST00000377532 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:7886708 A>C maps to ENST00000377532 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr1:7890054 T>A maps to ENST00000377532 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr1:7890054 T>A maps to ENST00000377532 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L6-01A-11D-A13L-09 chr1:7890054 T>A maps to ENST00000377532 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr1:7890054 T>A maps to ENST00000377532 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:152637188 G>A maps to NM_004564.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr7:92120665 C>A maps to NM_000466.2 E1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr7:92122350 G>T maps to NM_000466.2 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:145522531 C>T maps to NM_003846.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:145522858 C>T maps to NM_003846.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr1:10596277 G>T maps to NM_004565.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr1:10678419 C>T maps to NM_004565.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:45937776 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr8:77896090 A>G maps to NM_001172087.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr12:7343050 G>A maps to NM_001131023.1 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:7343047 C>A maps to NM_001131023.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr6:42934185 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr6:42934115 G>A maps to NM_000287.3 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:74719800 C>T maps to NM_002620.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr17:8172308 G>A maps to NM_012393.2 Q1248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:139625620 G>A maps to NM_002622.4 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr5:139680101 C>T maps to NM_002622.4 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr20:52835690 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr6:33258200 G>A maps to NM_001185181.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:54978379 G>A did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:207243669 C>T maps to NM_006212.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr21:45742919 C>T maps to NM_002626.4 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:48525121 T>G maps to NM_001166686.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:48528605 C>T maps to NM_001166686.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr12:48528757 C>T maps to NM_001166686.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr12:48539432 C>A maps to NM_001166686.1 S833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr12:48539017 T>C maps to NM_001166686.1 D777D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr12:48538877 G>A maps to NM_001166686.1 W757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr10:3159020 C>T maps to NM_002627.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:4849195 C>T maps to NM_005022.2 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr10:99190256 C>G maps to NM_002629.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr23:77224587 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:77224912 C>T did not map to a codon.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr23:77224967 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr2:197709277 G>A maps to NM_024989.3 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:3845300 C>A maps to NM_014489.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr11:3845297 C>T maps to NM_014489.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:28254874 C>A maps to NM_032507.3 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr6:28269871 G>A maps to NM_032507.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J7-01A-11W-A050-09 chr1:249210905 G>A maps to NM_170725.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr1:249210806 C>G maps to NM_170725.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:50723440 G>A maps to ENST00000515869 R1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:230492711 G>C maps to ENST00000321327 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18M-01A-11D-A12B-09 chr1:230492717 G>A maps to ENST00000321327 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr1:230459308 G>A maps to ENST00000321327 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr8:97847336 G>T maps to ENST00000325141 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:10473183 C>G maps to NM_002631.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:77369390 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr23:77373595 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:77380824 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:77378811 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr23:77378338 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:77359847 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:77373624 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27T-01A-11D-A16D-09 chr23:77378414 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr6:49753828 C>A maps to NM_138733.4 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr6:49754483 C>T maps to NM_138733.4 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr6:49753844 G>T maps to NM_138733.4 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr19:17628660 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr19:17627088 G>A maps to NM_012088.2 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:15590170 A>C maps to NM_052890.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:153283096 G>C maps to NM_052891.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr1:153312920 G>A maps to NM_020393.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr1:153317676 G>C maps to NM_020393.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr1:64100531 G>T maps to NM_002633.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:37848903 G>T maps to NM_018290.3 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:37846058 C>A maps to NM_018290.3 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr11:74062495 C>G maps to NM_173582.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IL-01A-11D-A14G-09 chr19:18474257 C>T maps to NM_017712.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118377132 C>A did not map to a codon.
Sequencing variant TCGA-BH-A1EW-01A-11D-A135-09 chr23:118377190 G>A did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:118370395 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:76388700 C>T maps to NM_024419.3 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:13228272 C>T maps to NM_030948.1 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WV-01A-11D-A10G-09 chr6:13206101 A>T maps to NM_030948.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr6:13273142 G>A maps to NM_030948.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr6:143929460 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:144081676 T>G maps to NM_001100164.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:58348346 C>G maps to NM_080672.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr20:58342409 G>A maps to NM_080672.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:28792953 A>C maps to NM_023923.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:28764912 C>G maps to NM_023923.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:125944094 G>A maps to NM_032177.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr12:7076336 C>T maps to NM_001144831.1 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr12:7075639 G>A maps to NM_001144831.1 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr12:9085306 T>C maps to ENST00000433083 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr1:33837946 C>T maps to ENST00000419414 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr3:169846804 G>A maps to NM_024947.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr3:169846621 G>T maps to NM_024947.3 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:169847253 G>A maps to NM_024947.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:169815092 G>C maps to NM_024947.3 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:22237178 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr23:22231058 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:22094543 G>A did not map to a codon.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr23:22132592 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr23:22245689 T>A did not map to a codon.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr23:22208619 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr23:22056653 G>C did not map to a codon.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr13:50098310 C>G maps to NM_001040443.1 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:27239656 C>T maps to NM_001033561.1 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BA-01A-11W-A071-09 chr17:27238153 G>A maps to NM_001033561.1 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:11022503 T>C maps to ENST00000303905 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:11075295 T>C maps to ENST00000303905 C495C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr7:11022483 C>T maps to ENST00000303905 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:133909366 C>T maps to ENST00000448712 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:46898406 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:46917721 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:46887305 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:46915518 G>T did not map to a codon.
Sequencing variant TCGA-D8-A143-01A-11D-A10Y-09 chr23:46887477 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:46884153 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XR-01A-11D-A14K-09 chr23:46913560 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:129776882 T>G maps to NM_199320.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:123624963 T>G maps to NM_015651.1 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:123620359 G>C maps to NM_015651.1 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:96425263 C>T maps to NM_005392.3 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:96439924 G>A maps to NM_005392.3 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr20:34528958 G>A maps to NM_016436.4 K962K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr8:133849985 C>T maps to ENST00000395386 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:45967432 T>G maps to ENST00000257821 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr22:45312306 G>A maps to NM_138415.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr6:64404654 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:64422919 A>C maps to NM_015153.2 P1812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:64423051 A>C maps to NM_015153.2 P1856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:64394965 C>G maps to NM_015153.2 S448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:64395605 G>T maps to NM_015153.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr23:133527636 G>A did not map to a codon.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr23:133559243 A>T did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr23:133547522 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:52456898 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:54043157 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr23:54069224 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53966664 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53966870 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54012303 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54044119 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr23:54014273 C>G did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr23:54020122 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr23:54069104 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:54037618 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr23:54026387 C>T did not map to a codon.
Sequencing variant TCGA-D8-A145-01A-11D-A10Y-09 chr23:54028587 C>T did not map to a codon.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr23:54020224 T>C did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:53966852 T>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:79675690 A>G maps to NM_017934.5 P1096P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:79655834 G>A maps to NM_017934.5 R1505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:79725352 G>C maps to NM_017934.5 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:71855031 T>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:71823054 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:71800898 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:71830978 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr23:71813105 T>A did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr23:71823049 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:71800922 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr23:71830972 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr23:71855079 G>A did not map to a codon.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr23:18911701 G>T did not map to a codon.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr23:18942251 G>T did not map to a codon.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr23:18954267 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:18969325 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:18942525 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:18944650 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:18970659 C>A did not map to a codon.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr23:18969225 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr23:18961826 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr23:18943842 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:18936865 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:18918817 C>G did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:18954232 G>A did not map to a codon.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr23:18949832 C>A did not map to a codon.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr23:18944632 G>A did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:18961898 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:47682454 G>A maps to NM_000293.2 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr11:118516530 C>A maps to NM_015157.2 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr11:118520792 G>A maps to NM_015157.2 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr3:111604183 A>G maps to NM_001134438.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:111681099 C>T maps to NM_001134438.1 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24M-01A-11D-A167-09 chr19:44008075 A>G maps to NM_198850.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr19:43999762 G>A maps to NM_198850.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr18:60572514 A>G maps to NM_194449.2 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:60646417 G>A maps to NM_194449.2 V1636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:60587215 G>A maps to NM_194449.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:71712725 T>C maps to NM_015020.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr4:41748264 C>T maps to NM_003924.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr9:139745247 C>T maps to NM_014172.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr11:607852 G>C maps to ENST00000264555 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:601668 C>T maps to ENST00000264555 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr11:605237 G>A maps to ENST00000264555 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:114269049 G>A maps to NM_006608.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr7:77578992 A>C did not map to a codon.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr10:13325815 G>A maps to NM_006214.3 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr10:13325694 G>T maps to NM_006214.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr8:22084433 C>T maps to NM_014759.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr6:36930981 C>A maps to NM_153370.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:36930960 A>C maps to NM_153370.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr6:36922583 A>G maps to NM_153370.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr20:43804745 T>C maps to NM_002638.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr10:99410714 C>T maps to ENST00000416867 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:99426327 G>A maps to ENST00000416867 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr4:25278650 C>T maps to NM_018323.3 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr22:21096565 G>A maps to NM_058004.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:151274389 G>C maps to NM_002651.2 S572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr1:151266605 G>A maps to NM_002651.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:151280085 G>T maps to NM_002651.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr1:151274424 G>T maps to NM_002651.2 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:44398375 C>T maps to NM_173206.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:4028788 C>T maps to NM_015897.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:4033536 G>A maps to NM_015897.2 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr11:85722143 C>A maps to ENST00000393343 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr2:230020680 C>T did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr15:65114489 C>G maps to ENST00000333425 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr15:65114689 G>A maps to ENST00000333425 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr23:15349900 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:15349470 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:15349847 T>G did not map to a codon.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr23:15339869 C>T did not map to a codon.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr23:15342879 T>A did not map to a codon.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr23:15343248 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr15:55633009 G>C maps to ENST00000164305 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:515576 C>T maps to NM_001127178.1 H487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:16221194 C>T maps to NM_004278.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr18:59828373 C>A maps to NM_176787.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr9:35090232 G>A maps to NM_032634.2 Q967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr9:35095508 G>A maps to NM_032634.2 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr21:38437923 T>C maps to NM_153681.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr16:633503 C>G maps to NM_148920.1 S718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:633150 T>G maps to NM_148920.1 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr16:628899 C>T maps to NM_148920.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr20:44045205 G>A maps to NM_015937.4 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr20:44044825 C>T maps to NM_015937.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr20:33231979 G>A maps to NM_080476.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr3:196674231 A>C maps to NM_025163.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:49952840 A>G maps to NM_017916.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:49954099 C>T maps to NM_017916.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr10:98469720 G>A maps to NM_152309.2 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr11:17124375 A>G maps to NM_002645.2 A1228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:204411713 G>C maps to NM_002646.3 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr1:204394860 G>A maps to NM_002646.3 L1532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:204412634 C>A maps to NM_002646.3 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr12:18435177 G>T maps to NM_004570.4 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr12:18435044 T>C maps to NM_004570.4 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr18:39593428 A>G maps to ENST00000398870 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr3:178941945 A>G maps to NM_006218.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:178928089 G>A maps to NM_006218.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:178917559 C>T maps to NM_006218.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr3:178937444 T>G maps to NM_006218.2 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr3:178916822 C>T maps to NM_006218.2 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr3:178941972 C>T maps to NM_006218.2 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:138382745 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:138474621 G>C maps to NM_006219.1 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr1:9777150 C>G maps to ENST00000361110 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:9781570 C>T maps to ENST00000361110 C651C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr7:106523499 C>T maps to NM_002649.2 D884D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:106526631 C>T maps to NM_002649.2 F975F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:106509619 G>A maps to NM_002649.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr5:67589268 A>G maps to ENST00000396611 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:67591075 C>T maps to ENST00000396611 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:67589187 C>T maps to ENST00000396611 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:46509512 G>T maps to NM_001114172.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EX-01A-21W-A050-09 chr2:209212649 C>T maps to NM_015040.3 S1759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr2:209218800 C>T maps to NM_015040.3 F2008F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28O-01A-11D-A228-09 chr2:209215531 C>A maps to NM_015040.3 L1824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:209201653 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr7:99987589 C>G maps to NM_013439.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:99957092 C>T maps to ENST00000413850 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:48771428 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:48771451 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:48771838 A>C did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr23:48775084 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr23:48772371 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr7:76984910 G>A maps to NM_017439.3 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr7:77006203 T>C maps to NM_017439.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr7:142829238 C>T maps to NM_002652.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:22830772 G>A maps to NM_005028.4 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr17:36955584 C>T maps to NM_003559.4 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:151215028 A>G maps to NM_001135638.1 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:151214634 C>G maps to NM_001135638.1 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr1:151209080 C>T maps to NM_001135638.1 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr9:71532630 T>C maps to NM_003558.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:3638911 C>T maps to NM_012398.2 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:15474116 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15425669 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15477803 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:32015675 G>A maps to ENST00000422296 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr22:32019789 C>T maps to NM_014338.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:1444909 G>A maps to ENST00000313486 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr17:1456443 C>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:28292611 A>G maps to NM_012399.3 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr22:28293117 C>T maps to NM_012399.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr17:65548391 A>T maps to NM_012417.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr11:67270036 C>T maps to NM_004910.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr11:67261511 C>A maps to NM_004910.2 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27T-01A-11D-A16D-09 chr11:67260512 G>A maps to NM_004910.2 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr11:67263647 C>T did not map to a codon.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr12:123497205 G>A maps to NM_020845.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RQ-01A-11D-A10Y-09 chr17:6380353 G>A maps to NM_031220.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:3190234 G>A maps to ENST00000380989 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr4:111539733 G>C maps to NM_153426.1 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr12:130831526 G>A maps to NM_004764.4 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr12:130833871 C>T maps to NM_004764.4 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:130827555 C>T maps to NM_004764.4 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr12:130833915 G>A maps to NM_004764.4 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr12:130839527 C>T maps to NM_004764.4 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:22141725 G>A maps to NM_001135721.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr22:25115534 C>T maps to NM_001008496.2 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J3-01A-11D-A13L-09 chr22:25158415 C>T maps to NM_001008496.2 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr22:25147425 C>T maps to NM_001008496.2 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr22:25131763 G>A maps to NM_001008496.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr23:68383056 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:68381748 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:68382055 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:68382675 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:68381468 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:68381727 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:68382801 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:68382827 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:68382500 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:68382696 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:68382749 C>G did not map to a codon.
Sequencing variant TCGA-E2-A14O-01A-31D-A10Y-09 chr23:68382546 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1R3-01A-31D-A14K-09 chr23:68382136 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr16:2159445 G>A maps to NM_001009944.2 Q1908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr16:2161708 C>A maps to NM_001009944.2 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J1-01A-11D-A20S-09 chr16:2147329 G>A maps to NM_001009944.2 F3465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:2152429 G>A maps to NM_001009944.2 F3051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr16:2158581 G>A maps to NM_001009944.2 Q2196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr16:2140300 G>C maps to NM_001009944.2 L4143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr16:2149968 A>C maps to NM_001009944.2 R3272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr7:47917119 G>A maps to NM_138295.3 T1210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:47855018 G>A maps to NM_138295.3 I2334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr7:47897211 A>G maps to NM_138295.3 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr7:47969107 C>T maps to NM_138295.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L6-01A-11D-A13L-09 chr7:47969010 G>A maps to NM_138295.3 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr16:81193422 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0I5-01A-11W-A100-09 chr16:81193366 G>T maps to NM_052892.3 V1252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr4:88940607 A>C did not map to a codon.
Sequencing variant TCGA-AR-A0U0-01A-11D-A10G-09 chr10:102049823 G>C maps to NM_016112.2 S733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:102056046 G>C maps to NM_016112.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:137243570 T>C maps to ENST00000230643 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P3-01A-11D-A142-09 chr5:137226170 G>A maps to ENST00000230643 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:46654365 G>A maps to NM_006071.1 F1618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr22:46654719 A>C maps to NM_006071.1 P1500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr22:46654200 T>G maps to NM_006071.1 I1673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr22:46654178 G>A maps to NM_006071.1 R1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr22:46653440 G>A maps to NM_006071.1 L1927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr22:46657362 G>T maps to NM_006071.1 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr22:46656330 A>T maps to NM_006071.1 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr6:51776624 A>T maps to NM_138694.3 V2154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:51512838 T>C maps to NM_138694.3 S3796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:51927318 G>A maps to NM_138694.3 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr6:51890476 A>G maps to NM_138694.3 N1377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr6:51944777 G>A maps to NM_138694.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DG-01A-21D-A12Q-09 chr6:51512916 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:51768415 G>A maps to NM_138694.3 C2325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:51913410 C>T maps to NM_138694.3 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:51921763 G>C maps to NM_138694.3 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:110509425 A>G maps to ENST00000426474 G3508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr8:110503325 G>A maps to ENST00000426474 G3370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr8:110464391 C>A maps to ENST00000426474 A2130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24O-01A-11D-A167-09 chr8:110454341 T>C maps to ENST00000426474 Y1437Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr8:110418567 C>T maps to ENST00000426474 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr8:110523135 G>C maps to ENST00000426474 L3843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr8:110400724 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr8:110447417 G>C did not map to a codon.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr8:110394763 C>A maps to ENST00000426474 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr8:110491845 G>C maps to ENST00000426474 G3052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr6:123038977 T>C maps to ENST00000368446 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:43243274 C>T maps to NM_181805.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr1:155265233 C>T maps to ENST00000423816 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr15:72492896 G>T maps to ENST00000419739 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr19:14569082 C>A maps to NM_213560.1 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr19:14551134 G>A maps to NM_213560.1 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:89237459 G>T maps to NM_006256.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RI-01A-11W-A071-09 chr1:89299056 C>T maps to NM_006256.2 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr9:131476615 C>T maps to NM_013355.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:131469041 G>A maps to NM_013355.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr9:131476874 G>T maps to NM_013355.3 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:131482031 G>A maps to NM_013355.3 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr11:125237867 C>T maps to NM_022062.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr11:125255461 G>A maps to NM_022062.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:201282463 C>G maps to NM_000299.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr1:201282595 G>A maps to NM_000299.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr12:32977059 C>G maps to NM_004572.3 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:32955376 C>T maps to NM_004572.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:32955342 C>A maps to NM_004572.3 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:159481553 G>A maps to NM_003628.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:159526289 C>T maps to NM_003628.3 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:159537086 G>A maps to NM_003628.3 Q1159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:119325651 C>T maps to NM_015900.2 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr3:119336878 G>C maps to NM_015900.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr3:119327721 A>T maps to NM_015900.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr10:74714296 G>A maps to NM_032562.2 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr10:74702433 G>A maps to NM_032562.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr16:68283256 C>A maps to NM_012320.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IF-01A-11D-A142-09 chr12:120763746 C>A maps to NM_000928.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:20499353 C>T maps to NM_001105572.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:20442968 A>C maps to ENST00000442610 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:20471183 T>C did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr22:31536079 A>G maps to NM_015715.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:186901923 T>G maps to NM_024420.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr1:186880522 T>A did not map to a codon.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr19:48578069 G>A maps to NM_003706.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23G-01A-11D-A20S-09 chr19:48558216 G>A maps to NM_003706.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42373775 G>T maps to NM_178034.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr15:42284982 G>A maps to NM_001080490.1 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr15:42292463 C>T maps to NM_001080490.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:42434400 A>C maps to ENST00000397272 G779G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr22:38509508 C>T maps to NM_003560.2 K729K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr6:46678353 C>T maps to NM_001168357.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr2:160798453 G>A maps to NM_007366.4 V1409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr2:160901624 G>T maps to NM_007366.4 C51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:160901312 A>G maps to NM_007366.4 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr2:160832692 A>G maps to NM_007366.4 H827H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LH-01A-31D-A18P-09 chr23:133700447 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr11:59810969 G>A maps to NM_173801.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr4:84026090 G>A maps to NM_001130715.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:145477821 C>T maps to NM_001029869.1 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:42038189 C>G maps to NM_000930.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr10:75675048 G>A maps to NM_002658.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:28836896 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr2:28775832 C>T maps to NM_153021.4 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:14688647 G>A maps to NM_024829.5 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:113824888 G>A maps to NM_173542.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:113818607 C>T maps to NM_173542.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr12:113826337 G>A maps to NM_173542.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:8769280 G>T maps to NM_015192.2 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr20:8769094 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr20:8713939 C>A maps to NM_015192.2 Y648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr20:8721039 G>T maps to NM_015192.2 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:40596199 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:64026029 G>A maps to NM_000932.2 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:64029068 C>T maps to NM_000932.2 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:9374233 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:9376257 C>T maps to NM_001172646.1 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FH-01A-12D-A13L-09 chr20:9353020 G>A maps to NM_001172646.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:38049300 G>C maps to NM_001130964.1 S766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr3:38051648 G>A maps to NM_001130964.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:219500655 T>G did not map to a codon.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr2:219492899 C>T maps to ENST00000432688 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A091-01A-11W-A019-09 chr10:95791948 G>A maps to ENST00000371380 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr10:96018634 C>T maps to ENST00000371380 S1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:95791726 T>C maps to ENST00000371380 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr20:39791130 C>T maps to NM_002660.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:39800882 C>G maps to NM_002660.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr20:39802847 C>T maps to NM_002660.2 R1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr20:39796489 A>G did not map to a codon.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr20:39792359 C>A maps to NM_002660.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FW-01A-11D-A17D-09 chr20:39795423 G>A maps to NM_002660.2 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr16:81939109 C>T maps to NM_002661.2 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr16:81990424 T>C maps to NM_002661.2 V1232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr16:81902857 C>A maps to NM_002661.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr16:81914539 C>A maps to NM_002661.2 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FX-01A-11D-A13L-09 chr3:155232585 C>A maps to ENST00000340059 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr3:155200811 C>A maps to ENST00000340059 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr3:155311893 G>A maps to ENST00000340059 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr3:155303907 C>A maps to ENST00000340059 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr3:155203417 G>T maps to ENST00000340059 R909R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KC-01B-11D-A159-09 chr3:155201157 G>T maps to ENST00000447496 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:2422689 C>T maps to NM_014638.2 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr1:2430265 C>T maps to NM_014638.2 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15E-01A-11D-A12B-09 chr1:2430565 C>T maps to NM_014638.2 H826H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:2435865 C>G maps to NM_014638.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr2:198948972 G>A maps to NM_006226.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr3:17053573 G>A maps to NM_001144382.1 W908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr3:17052802 G>A maps to NM_001144382.1 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:17051209 C>T maps to NM_001144382.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr3:17052712 C>A maps to NM_001144382.1 C621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:207348 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:209788 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr23:208196 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr3:111439671 G>A maps to ENST00000312791 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:111426887 G>A maps to ENST00000312791 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:18852884 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr12:18837201 T>A maps to ENST00000266505 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr12:18852862 G>A maps to ENST00000266505 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr3:171431830 A>G maps to NM_002662.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:171405269 C>A maps to NM_002662.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:4711583 C>T maps to NM_002663.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr17:4711090 C>T maps to NM_002663.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr19:40880503 T>G maps to NM_012268.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X6-01A-11D-A14K-09 chr19:40883953 G>A maps to NM_012268.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr14:105397277 C>G maps to NM_138790.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:242451669 T>G maps to NM_152666.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr1:242253179 G>A maps to NM_152666.2 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr1:242287769 C>T maps to NM_152666.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr15:45884474 G>C did not map to a codon.
Alternatively spliced codon TCGA-D8-A27R-01A-11D-A16D-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr8:145007426 G>A maps to NM_201380.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr8:145049452 G>A maps to NM_000445.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr8:145024475 C>T maps to NM_201380.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr8:145001189 G>A maps to NM_201380.2 A1437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:145006648 C>A maps to NM_201380.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr8:144997235 G>A maps to NM_201380.2 A2424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15A-01A-11D-A12B-09 chr8:145004698 C>T maps to NM_201380.2 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr8:144995813 C>T maps to NM_201380.2 T2862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr2:68621249 C>T maps to NM_002664.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr2:68607461 G>C maps to NM_002664.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr8:38827054 C>T maps to NM_021623.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:38808378 T>G maps to NM_021623.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr8:38775522 C>T maps to NM_021623.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179360368 A>C maps to NM_019091.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EX-01A-21W-A050-09 chr19:49363611 G>A maps to NM_020904.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:49364729 G>A maps to NM_020904.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr19:49355487 G>C maps to NM_020904.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr19:49364910 G>A maps to NM_020904.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr12:19511184 A>G maps to ENST00000429027 E1049E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:204218353 C>T maps to ENST00000367191 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:204228863 C>A maps to ENST00000367191 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:204228734 C>A maps to ENST00000367191 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:16810672 G>A maps to ENST00000448080 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:16816094 T>G maps to ENST00000448080 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:30087518 C>T maps to ENST00000440706 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr7:30088946 C>G maps to ENST00000440706 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr8:96166775 T>C maps to NM_024613.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:151161917 T>C maps to NM_001029884.1 N1348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr6:151055038 G>A maps to NM_001029884.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr6:151055038 G>A maps to NM_001029884.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr6:151055077 C>A maps to NM_001029884.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr19:39915204 A>T maps to NM_022835.2 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:39913628 C>A maps to NM_022835.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:39912765 C>T maps to NM_022835.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:39914676 T>G maps to NM_022835.2 A968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:39915424 G>T maps to NM_022835.2 G1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:65208034 C>T maps to ENST00000394691 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr5:151656 C>T maps to NM_052909.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:173085 G>C maps to NM_052909.3 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:6556590 G>A maps to NM_198681.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr12:6426506 C>T maps to NM_001144856.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08O-01A-21W-A071-09 chr14:68042722 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:68044076 C>G maps to NM_020715.2 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr14:68029172 C>T maps to NM_020715.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr2:43992707 A>T maps to NM_172069.3 R1485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr2:43919672 A>G maps to NM_172069.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr2:43924308 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:43871928 A>G maps to NM_172069.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr2:43937468 G>A maps to NM_172069.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr17:40826428 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr17:40826402 G>A maps to NM_024927.4 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr17:43545834 G>A maps to NM_014798.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr2:208841567 C>T maps to NM_001080475.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:208866249 C>A maps to NM_001080475.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr2:208841407 G>A maps to NM_001080475.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr2:208811100 G>C maps to NM_001080475.2 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:901935 C>T maps to ENST00000379409 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:150123145 C>T maps to ENST00000443480 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:161135824 G>C did not map to a codon.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr6:161173945 T>G maps to NM_000301.3 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:161152103 C>T maps to NM_000301.3 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr6:161128785 G>A maps to NM_000301.3 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:90213325 C>T maps to NM_002666.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr15:90210241 C>G maps to NM_002666.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:19120943 C>A maps to NM_001122.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr19:4513409 G>A maps to NM_001080400.1 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr19:4512291 C>T maps to NM_001080400.1 V546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr19:4529858 G>A maps to NM_001013706.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr19:4534065 A>G maps to NM_001013706.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr19:4525793 G>A maps to NM_001013706.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr16:23701344 G>A maps to NM_005030.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr16:23690576 C>G maps to NM_005030.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr20:21143056 C>T maps to NM_018474.4 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:57752384 G>A maps to NM_006622.2 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr5:57750793 G>A maps to NM_006622.2 Q604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr1:45271020 C>T maps to NM_004073.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr1:45271307 C>G maps to NM_004073.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:45268476 G>A maps to NM_004073.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:45266519 C>T maps to NM_004073.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr4:128804490 G>A maps to NM_014264.4 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr3:145794676 T>A maps to NM_182943.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr3:145841965 G>A maps to NM_182943.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:145788885 A>G maps to NM_182943.2 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr3:145809640 C>T maps to NM_182943.2 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr7:100853848 G>A maps to NM_001084.4 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr7:100854921 C>T maps to NM_001084.4 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr7:100860011 G>A maps to NM_001084.4 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr23:103044307 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:49030741 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:49028370 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:49029796 T>C did not map to a codon.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr3:142403209 C>T maps to NM_001172312.1 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:114879342 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:114868365 G>C did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:114869258 G>A did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr23:114844607 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:114871267 A>G did not map to a codon.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr23:114883856 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:114868383 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr20:44533471 C>T maps to NM_006227.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr20:44533592 C>T maps to NM_006227.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:17487788 C>A maps to NM_031310.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:17476093 C>G did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr17:37234232 G>A maps to NM_020405.4 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr10:20534364 C>T maps to NM_032812.7 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:20290836 C>T maps to NM_032812.7 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A041-01A-11W-A050-09 chr10:20290911 C>A maps to NM_032812.7 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr10:20357103 G>T maps to NM_032812.7 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr3:126736735 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:126722198 T>G maps to NM_032242.3 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:126739144 C>G maps to NM_032242.3 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:126724937 G>A maps to NM_032242.3 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr3:126736503 C>T maps to NM_032242.3 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:208213055 C>T maps to NM_025179.3 E1470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr1:208216495 G>T maps to NM_025179.3 R1309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:153698348 G>C did not map to a codon.
Sequencing variant TCGA-A2-A259-01A-11D-A16D-09 chr23:153696521 G>T did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:153693507 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:153689878 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr23:153689606 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153688843 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153691976 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153699599 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:153689481 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:153691780 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr23:153699918 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr23:153694158 G>A did not map to a codon.
Sequencing variant TCGA-GM-A4E0-01A-12D-A25Q-09 chr23:153694399 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr7:131982948 G>T maps to NM_020911.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:132169687 G>A maps to NM_181775.3 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:132174104 G>C maps to NM_020911.1 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:131887454 G>A maps to NM_020911.1 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr7:131883299 G>C maps to NM_020911.1 V894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:132174146 G>A maps to NM_020911.1 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:132193071 C>G maps to NM_020911.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A091-01A-11W-A019-09 chr3:48454156 G>A maps to NM_001130082.1 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:48459321 G>A maps to NM_001130082.1 S1124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:50718988 G>T maps to NM_012401.2 I1368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr22:50728317 G>A maps to NM_012401.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr22:50720381 G>A maps to NM_012401.2 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr22:50727189 G>A maps to NM_012401.2 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr22:50717395 C>T maps to NM_012401.2 P1478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr22:50718175 G>C maps to NM_012401.2 L1424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:153036042 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:153039723 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr23:153032800 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr23:153041489 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr23:153032506 C>G did not map to a codon.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr23:153032740 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr23:153040400 A>G did not map to a codon.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr23:153043429 C>T did not map to a codon.
Sequencing variant TCGA-E9-A24A-01A-11D-A167-09 chr23:153043071 C>A did not map to a codon.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr23:153031696 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr12:94563008 C>T maps to NM_005761.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:94692559 G>A maps to NM_005761.1 W1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:94634313 C>G maps to NM_005761.1 S725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr12:94673273 C>T maps to NM_005761.1 I1208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:205814470 G>A maps to NM_152491.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr1:205813219 G>A maps to NM_152491.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr16:72166722 C>T maps to NM_031293.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:74328400 A>G maps to NM_033247.2 *436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr15:74324914 C>T maps to NM_033238.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr17:15134332 C>T maps to NM_000304.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr2:190682786 A>T maps to NM_000534.4 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr7:6031634 T>C maps to NM_000535.5 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:6017293 C>T maps to NM_000535.5 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:6022615 C>T maps to NM_000535.5 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:6026982 C>T maps to NM_000535.5 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr1:154904863 G>A maps to NM_006556.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:152937643 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr23:152937597 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr23:152937333 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:219209286 G>A maps to NM_015488.4 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr19:50370347 C>T maps to NM_007254.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr6:160222207 C>A maps to NM_173516.1 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:160240033 C>T maps to NM_173516.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:160240300 G>T maps to NM_173516.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr6:160232781 C>T maps to NM_173516.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B1-01A-21D-A12Q-09 chr10:118318676 C>T maps to NM_000936.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:118357353 G>T maps to NM_006229.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr10:118351337 C>T maps to NM_006229.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr10:118202577 G>A maps to NM_001011709.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr10:118196374 C>T maps to NM_001011709.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr8:26365955 A>G maps to NM_007257.5 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:152225893 A>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:152226003 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:152226241 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:152225790 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:152225667 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:152159223 C>G did not map to a codon.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr23:152159874 C>T did not map to a codon.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr23:152159357 A>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:152159202 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr19:46973871 G>A maps to NM_018215.3 Q141*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E2-A1B4-01A-11D-A12Q-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr19:46998317 C>T maps to ENST00000377652 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SU-01A-11D-A099-09 chr17:37825993 C>G maps to NM_002686.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr17:37826536 C>A maps to NM_002686.3 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr6:36262088 C>T maps to ENST00000457797 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:36259106 C>T maps to ENST00000457797 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:7890131 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:7625553 G>A maps to NM_001166111.1 G1250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr19:7605076 C>T maps to NM_001166111.1 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr19:7601417 C>T maps to NM_001166111.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RX-01A-11D-A25Q-09 chr9:140372520 G>A maps to NM_001098537.1 N949N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr9:140437117 C>A maps to NM_001098537.1 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr9:140356759 C>T maps to NM_001098537.1 Q1172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr9:140417222 T>A maps to NM_001098537.1 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr17:46023745 A>T maps to NM_018129.3 K202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr12:89818991 G>T maps to NM_172240.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:89819117 A>C maps to NM_172240.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:89864263 G>A maps to NM_172240.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr1:53537272 C>T maps to NM_153703.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr1:53544663 C>T maps to NM_153703.4 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr19:14044770 C>G maps to NM_024825.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:131189072 G>T maps to NM_001018111.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:127379390 G>T maps to NM_015720.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:84634290 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:84601035 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:84585966 C>A did not map to a codon.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr23:84563183 C>A did not map to a codon.
Sequencing variant TCGA-E9-A247-01A-11D-A167-09 chr23:84634255 G>T did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:84614598 G>T did not map to a codon.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr20:30803130 C>T maps to NM_015352.1 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr21:46705635 G>A maps to NM_133635.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AY-01A-21W-A019-09 chr1:166819225 G>A maps to NM_017542.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr23:24859808 A>T did not map to a codon.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr23:24721367 G>C did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr23:24830921 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:24745161 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:25014004 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:24906168 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:24839690 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:24844656 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:24746047 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:24759534 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:24761361 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:25013997 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:24717573 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:24830821 T>C did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:24735566 G>C did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:24760173 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:24753570 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr23:24722585 G>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr11:65064613 G>A maps to NM_002689.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A202-01A-11D-A14K-09 chr11:65064613 G>A maps to NM_002689.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:65062087 T>C maps to NM_002689.2 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:50906814 C>T maps to ENST00000391817 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:44156073 G>A maps to NM_006230.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr17:26677508 G>A maps to NM_015584.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr17:26680330 A>C maps to NM_015584.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr22:42992320 G>T maps to ENST00000415122 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr22:42981865 C>T maps to ENST00000415122 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:133218850 A>C maps to ENST00000455752 G1698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3HN-01A-11D-A20S-09 chr12:133252322 G>A maps to ENST00000455752 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr12:133220437 G>A maps to ENST00000455752 G1428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr12:133220065 G>C maps to ENST00000455752 G1460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr12:133202329 G>A maps to ENST00000455752 L2189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr12:133240730 C>T maps to ENST00000455752 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr14:50118019 A>T maps to NM_002692.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:116171213 C>T maps to NM_017443.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr15:89870411 C>T maps to NM_002693.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:62492749 C>A maps to NM_007215.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr6:43578460 G>T did not map to a codon.
Sequencing variant TCGA-AO-A12A-01A-21D-A10Y-09 chr6:43571739 G>A maps to NM_006502.2 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:103344475 C>T maps to NM_013274.3 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr7:44118409 C>A maps to NM_013284.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr3:121151151 T>G maps to ENST00000393672 *2728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:121207339 C>A maps to ENST00000393672 E1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:121217466 G>A maps to ENST00000393672 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr3:121207553 A>G maps to ENST00000393672 D1544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr3:121228969 G>A maps to ENST00000393672 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr2:86327171 G>A maps to NM_015425.3 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr2:86308728 G>A maps to NM_015425.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr2:86260894 C>G maps to NM_015425.3 L1350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr2:113321940 A>G maps to ENST00000458012 P1P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A086-01A-11W-A019-09 chr2:113333167 C>T maps to NM_019014.4 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:113317068 G>A maps to NM_019014.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr2:113325614 G>A maps to NM_019014.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr2:113317038 G>A maps to NM_019014.4 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr6:43488438 C>G maps to NM_203290.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr6:43487160 C>T maps to NM_203290.1 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:7416964 A>C maps to NM_000937.4 S1794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:7416985 A>C maps to NM_000937.4 S1801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:7417048 A>C maps to NM_000937.4 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:7417090 A>C maps to NM_000937.4 S1836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:7407064 C>T maps to NM_000937.4 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:7404380 C>T maps to NM_000937.4 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr17:7404269 G>A maps to NM_000937.4 E631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr4:57888326 C>T maps to NM_000938.1 F810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:57891077 T>G maps to NM_000938.1 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr4:57889848 C>T maps to NM_000938.1 Q930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr16:57504902 G>T maps to NM_032940.2 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr16:57503882 C>T maps to NM_032940.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr11:62533186 G>A maps to NM_002696.2 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr7:102116677 A>G maps to ENST00000393794 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr10:79745019 C>T maps to NM_007055.3 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr10:79784450 C>T maps to NM_007055.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr8:22107967 C>T maps to NM_001722.2 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr16:22337484 C>T maps to NM_018119.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr16:22337443 C>T maps to NM_018119.2 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr1:145457307 C>A maps to NM_032305.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr16:103517 G>A maps to NM_016310.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:103473 A>C did not map to a codon.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr7:72413873 T>C maps to ENST00000434423 N1114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:72416245 C>T maps to ENST00000434423 F1217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:72412439 G>A maps to ENST00000434423 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:72416771 A>G maps to ENST00000434423 *1250W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr7:53103483 C>G maps to NM_182595.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AD-01A-11W-A071-09 chr2:25384120 C>A maps to NM_001035256.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:46655662 T>G did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:46662732 C>T maps to ENST00000371986 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr9:134382846 G>T maps to NM_007171.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr14:77751975 C>G did not map to a codon.
Sequencing variant TCGA-E2-A14Q-01A-11D-A12B-09 chr14:77757675 C>T maps to NM_013382.5 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:76247565 T>C maps to NM_012230.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr7:94944671 G>T maps to NM_000446.5 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr8:99146754 G>A maps to NM_015029.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr8:99162828 G>A maps to NM_015029.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27A-01A-11D-A167-09 chr8:99168385 C>G maps to NM_015029.2 Y722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr8:99158820 T>A maps to NM_015029.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr8:99146854 C>T maps to NM_015029.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:30101470 A>G maps to NM_006627.2 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:121017675 C>A maps to NM_015918.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr12:121018956 C>A maps to NM_015918.3 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr3:119379072 C>T maps to NM_022135.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:119378820 A>C maps to NM_022135.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:119367223 G>A maps to NM_022135.2 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:48374290 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48369814 G>A did not map to a codon.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr23:48372916 C>T did not map to a codon.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr23:48368216 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr23:48378799 A>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr13:38145545 C>T maps to NM_006475.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:43152472 A>G maps to NM_001005365.2 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr18:14542699 C>T maps to ENST00000444806 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YI-01A-31D-A10M-09 chr2:132022030 C>T maps to NM_001083538.1 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr2:132022030 C>T maps to NM_001083538.1 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr2:132022030 C>T maps to NM_001083538.1 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr2:132022030 C>T maps to NM_001083538.1 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P1-01A-31D-A14G-09 chr2:132022030 C>T maps to NM_001083538.1 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr2:130832872 G>A maps to NM_001099771.2 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:130858274 C>A maps to NM_001099771.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr2:130832041 G>A maps to NM_001099771.2 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr2:130832164 C>T maps to NM_001099771.2 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr2:130832164 C>T maps to NM_001099771.2 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr2:130832872 G>A maps to NM_001099771.2 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr2:130832872 G>A maps to NM_001099771.2 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr2:130832872 G>A maps to NM_001099771.2 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr2:130832872 G>A maps to NM_001099771.2 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:16267011 A>C maps to NM_001136213.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr22:16275278 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr22:16287405 G>A maps to NM_001136213.1 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr14:19990640 C>T maps to ENST00000439503 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr14:20020112 C>T maps to ENST00000439503 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr14:20020112 C>T maps to ENST00000439503 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr14:20020112 C>T maps to ENST00000439503 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr1:167382292 C>A maps to NM_002697.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:42626660 A>C did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:42599708 C>T maps to ENST00000342301 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18I-01A-11D-A12B-09 chr19:42599575 G>A maps to ENST00000342301 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr11:120180258 C>T maps to NM_014352.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N4-01A-11D-A14K-09 chr6:99283255 G>C maps to NM_005604.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr23:82763377 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:82764285 G>T did not map to a codon.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr23:82763875 G>T did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr23:82763505 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:82763663 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:82764177 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr23:82764245 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr13:79175723 G>A maps to NM_006237.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr4:147561515 C>T maps to NM_004575.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr5:145719175 G>A maps to NM_002700.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:128429114 C>G maps to NM_001159542.1 S335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr7:39503849 G>C maps to NM_007252.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:39472785 C>T maps to NM_007252.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr7:39503975 T>C maps to NM_007252.3 H589H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr7:39125578 G>A maps to NM_007252.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr7:39379418 C>T maps to NM_007252.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:10218531 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:54721767 G>A maps to NM_176895.1 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr10:122278378 C>A maps to NM_001030059.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:4662872 G>C maps to NM_203453.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr6:35393843 G>A maps to NM_006238.4 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:23797538 G>C maps to NM_013261.3 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A247-01A-11D-A167-09 chr4:23815385 G>A maps to NM_013261.3 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr5:149212266 C>T maps to NM_133263.3 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:149206234 G>C did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr5:149216612 A>C maps to NM_133263.3 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr4:57268336 T>C maps to NM_002703.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr15:75341500 C>T maps to NM_021823.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr20:62152892 C>T maps to ENST00000370177 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SX-01A-12D-A099-09 chr23:18800499 G>T did not map to a codon.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr23:18768067 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:18822165 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr23:18822012 A>C did not map to a codon.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr23:18748317 C>T did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr23:18822126 C>A did not map to a codon.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr23:18824525 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr23:18824536 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr23:18822015 G>C did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr23:18767946 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:18807362 A>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:18797189 G>C did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:18842150 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr4:76782041 G>A maps to NM_006239.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr4:76804228 C>G did not map to a codon.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr4:76797715 G>A maps to NM_006239.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:70194313 G>T maps to NM_003626.2 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr11:70171059 G>T maps to NM_003626.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr11:70171068 G>C maps to NM_003626.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr12:81839410 G>C maps to NM_003625.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:81839382 G>C maps to NM_003625.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr12:81732973 G>A maps to NM_003625.2 R845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:81762605 C>T maps to NM_003625.2 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr12:81657055 A>G maps to NM_003625.2 F1223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:49652004 C>T maps to NM_003660.2 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:49652820 C>T maps to NM_003660.2 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:49643253 G>A maps to NM_003660.2 K759K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr19:49644725 C>A maps to NM_003660.2 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr1:203024613 G>A maps to ENST00000367238 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr12:27799033 G>T maps to NM_003622.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:27844710 G>A maps to NM_003622.3 G905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SJ-01A-11D-A099-09 chr11:7650733 G>T maps to NM_003621.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr11:7672915 C>G maps to NM_003621.2 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:7674391 C>T maps to NM_003621.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:7647042 G>T maps to NM_003621.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:143767698 A>G maps to NM_001123068.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:159631980 G>C maps to NM_005038.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr4:159636498 G>A maps to NM_005038.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:81113561 G>A maps to NM_005729.3 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:170492642 C>T maps to NM_004792.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr2:170487450 C>T maps to NM_004792.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GZ-01A-11W-A071-09 chr2:170493411 A>G maps to NM_004792.2 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:36823698 G>A maps to NM_016059.4 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr6:149867099 G>A maps to NM_139126.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr14:50065855 C>T maps to NM_152329.3 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr15:43831722 A>G maps to NM_001130858.2 R1148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr5:102502944 G>A maps to ENST00000451606 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A082-01A-11W-A019-09 chr16:4937210 G>A maps to NM_002705.4 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr16:4934650 C>T maps to NM_002705.4 Q1335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr16:4944580 C>T maps to NM_002705.4 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr16:4947725 G>A maps to NM_002705.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr16:4987025 C>T maps to NM_002705.4 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr2:44429051 C>T maps to NM_002706.4 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr2:44428732 C>G maps to NM_002706.4 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr17:58734120 G>C maps to NM_003620.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr17:58740528 C>A maps to NM_003620.3 C478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr17:58740763 C>A maps to NM_003620.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr17:56833489 G>A maps to NM_014906.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:57057970 C>G maps to NM_014906.3 S616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr17:57043168 C>G maps to NM_014906.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr12:63042361 G>A maps to NM_020700.1 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr1:113253092 A>G maps to NM_005167.5 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr3:160783284 C>T maps to NM_139245.2 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:52283690 C>G maps to NM_144641.2 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr1:161140233 A>T maps to NM_001122764.1 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:161137814 C>A maps to NM_001122764.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:67168586 G>A maps to NM_001008709.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XG-01A-11D-A14G-09 chr11:67166578 T>A maps to NM_001008709.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BS-01A-11D-A12Q-09 chr12:111160056 A>G maps to NM_002710.2 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:30574586 G>A maps to NM_002714.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr6:30569977 A>G maps to NM_002714.2 H816H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:80187671 C>A maps to NM_001143885.1 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:80266598 A>C maps to NM_001143885.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr12:80199487 C>T maps to NM_001143885.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr1:202318210 C>T maps to ENST00000367270 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:202418188 C>A maps to ENST00000367270 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:202398058 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:55623916 G>C maps to NM_017607.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:204379264 C>T maps to NM_032833.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr20:37529304 C>T maps to NM_015568.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:54975817 T>G maps to NM_006741.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:113519369 C>A maps to NM_002711.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr7:113519205 A>G maps to NM_002711.3 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr7:113520081 C>A maps to NM_002711.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr7:113558744 C>A maps to NM_002711.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:113519949 G>A maps to NM_002711.3 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:113522198 G>A maps to NM_002711.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr8:8998782 G>A maps to NM_024607.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:93390235 C>T maps to NM_005398.4 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:49138467 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:49143235 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:49143509 C>T did not map to a codon.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr23:49142943 T>G did not map to a codon.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr1:28176725 C>T maps to NM_014110.4 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CM-01A-31W-A050-09 chr7:94855424 A>G maps to NM_001166160.1 K703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr7:94919429 C>T maps to NM_001166160.1 R1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:94750033 T>G maps to NM_001166160.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:94917886 C>T maps to NM_001166160.1 Q1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:94917888 G>A maps to NM_001166160.1 Q1257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:94879486 C>G maps to NM_001166160.1 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr19:52729059 T>G maps to NM_014225.5 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:52693366 C>T maps to NM_014225.5 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr11:111613317 T>C maps to NM_181699.2 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:146017812 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr5:145969746 G>A maps to ENST00000394414 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:135721941 T>G maps to NM_002718.4 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr3:135721398 G>A maps to NM_002718.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr3:135745747 T>G maps to NM_002718.4 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:135721143 T>C maps to NM_002718.4 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr3:135721059 C>A maps to NM_002718.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr3:135720976 C>T maps to NM_002718.4 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:299557 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:299629 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:308341 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:35579137 C>G did not map to a codon.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr1:212515538 G>T maps to NM_006243.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr11:64700358 G>A maps to NM_006244.3 W413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr11:64693373 G>A maps to NM_006244.3 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr14:102384166 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:102359335 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr6:42976143 C>T maps to NM_006245.2 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:42977067 G>A maps to NM_006245.2 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:101947177 G>A maps to NM_000944.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:102019577 C>G maps to NM_000944.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr8:22355572 G>C maps to ENST00000397775 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:104357017 G>A maps to NM_147180.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr9:104356696 G>A maps to NM_147180.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr18:9588771 T>C maps to NM_001042388.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr18:9550109 C>T maps to NM_001042388.1 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:73114210 C>T maps to NM_174907.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:94718120 C>T maps to NM_058237.1 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr14:94744954 G>C did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr19:46890422 G>A maps to NM_006247.2 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:46886681 C>T maps to NM_006247.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr19:46891946 C>T maps to NM_006247.2 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:244852549 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:103900658 A>C maps to NM_015062.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:103906589 G>T maps to NM_015062.3 E1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:40544321 A>G maps to ENST00000372783 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:32122469 C>T maps to NM_138717.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr12:110983716 G>C maps to NM_139283.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:42018892 C>A maps to NM_002722.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48760317 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr23:48760063 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:48759631 G>A did not map to a codon.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr23:48760063 C>T did not map to a codon.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr23:48759290 G>C did not map to a codon.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr1:19653906 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:11304360 C>T maps to NM_152391.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr23:48931490 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr19:8564532 G>A maps to NM_032152.4 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr22:22892666 G>C maps to NM_206954.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr22:22890902 C>T maps to NM_206954.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13G-01A-11D-A13L-09 chr1:12853414 A>G maps to NM_023013.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:12856051 C>T maps to NM_023013.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr1:12954598 C>G maps to NM_001039361.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:12952851 T>C maps to NM_001039361.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr1:12954759 T>G maps to NM_001039361.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:12888388 A>C maps to NM_001146344.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:13448454 G>T maps to NM_001024661.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:13448421 G>C maps to NM_001024661.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:13474916 C>T maps to NM_001099850.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr1:13474982 G>A maps to NM_001099850.1 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:12918986 G>A maps to NM_023014.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr1:12919595 C>T maps to NM_023014.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr1:12919910 G>A maps to NM_023014.1 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr1:13036692 A>G maps to NM_001100631.1 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:12939781 A>G maps to ENST00000376192 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:12939850 G>A maps to ENST00000376192 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr1:12939781 A>G maps to ENST00000376192 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J1-01A-11D-A20S-09 chr1:12939781 A>G maps to ENST00000376192 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:12939610 C>T maps to ENST00000376192 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:12980231 G>A maps to NM_001012277.1 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ST-01A-12D-A099-09 chr1:12980231 G>A maps to NM_001012277.1 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T1-01A-21D-A099-09 chr1:12980231 G>A maps to NM_001012277.1 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr1:12980231 G>A maps to NM_001012277.1 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr1:12980073 T>A maps to NM_001012277.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:12979941 C>T maps to NM_001012277.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr1:12980231 G>A maps to NM_001012277.1 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr1:12980231 G>A maps to NM_001012277.1 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr10:135165567 G>T maps to ENST00000423766 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr10:135165630 C>T maps to ENST00000423766 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:11507488 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:11507488 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:11546153 T>G maps to NM_006248.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:11546339 T>G maps to NM_006248.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:11546525 T>G maps to NM_006248.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:11420308 T>G maps to NM_006249.4 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr12:11420172 G>A maps to NM_006249.4 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:11461448 T>G maps to NM_002723.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:11461637 T>G maps to NM_002723.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:11461736 T>G maps to NM_002723.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:156756494 C>T maps to NM_005973.4 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr17:74538647 C>T maps to NM_001077620.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr6:106553636 C>A maps to NM_001198.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr6:106553786 C>T maps to NM_001198.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:45246194 C>T maps to NM_020229.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr11:45245849 G>A maps to NM_020229.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr11:45203409 C>T maps to NM_020229.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:100060927 C>T maps to ENST00000359773 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr8:70981495 C>T maps to NM_024504.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:70981429 C>T maps to NM_024504.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr8:70981479 G>A maps to NM_024504.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr21:43279762 G>A maps to NM_022115.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr21:43222949 G>A maps to NM_022115.3 S1321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SB-01A-21D-A25Q-09 chr1:3328443 C>T maps to NM_022114.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr1:3329040 C>T maps to NM_022114.3 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:14107346 A>C maps to NM_012231.4 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr1:14106176 G>A maps to NM_012231.4 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:14108960 C>G maps to NM_012231.4 V1557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:14108568 C>T maps to NM_012231.4 Q1427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr12:108134959 G>A maps to NM_012406.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr12:108150666 G>C maps to NM_012406.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr4:121739571 C>A maps to NM_018699.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr4:121616406 C>T maps to NM_018699.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:23527068 C>T maps to NM_020227.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:23527740 C>T maps to NM_020227.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:120936581 C>T maps to NM_006793.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr23:23697374 A>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:23704420 G>C did not map to a codon.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr2:27355592 C>T maps to NM_013388.4 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr5:145214805 G>A maps to NM_182960.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr1:203452614 G>A maps to NM_201348.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:105726243 G>A maps to NM_002726.4 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09T-01A-11W-A019-09 chr2:44556196 G>A maps to NM_001171603.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr2:44559717 T>A maps to NM_001171603.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:47269205 G>A maps to NM_020820.3 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr20:47254269 G>A maps to NM_020820.3 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr20:47309236 C>A maps to NM_020820.3 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr8:69104583 C>A maps to NM_024870.2 L1476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:68972970 G>T maps to NM_024870.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:69017564 G>T maps to NM_025170.4 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LM-01A-11D-A17W-09 chr8:69046351 C>T maps to NM_024870.2 V1275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr8:69069647 C>T maps to NM_024870.2 V1441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr8:69002850 G>A maps to NM_024870.2 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr10:72360526 G>A maps to NM_005041.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:72358690 G>A maps to NM_005041.4 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr11:57147149 G>A maps to NM_006093.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:186275712 G>T maps to NM_005807.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A143-01A-11D-A10Y-09 chr1:186277244 C>A maps to NM_005807.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr1:186280193 C>T maps to NM_005807.3 F1176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr12:11036777 G>A maps to NM_006250.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr20:62195419 G>A maps to NM_001037335.2 H1585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:62197420 G>C maps to NM_001037335.2 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr20:62191560 G>A maps to NM_001037335.2 I2540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr20:62197237 C>T maps to NM_001037335.2 E979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IE-01A-11W-A050-09 chr12:42853697 A>T maps to NM_153026.2 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:42854278 C>A maps to NM_153026.2 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:64132655 C>A maps to NM_198859.3 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15L-01A-11D-A12B-09 chr3:64133123 C>A maps to NM_198859.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr3:64133157 G>A maps to NM_198859.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:49032243 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr23:49032266 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr23:49032340 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:49034492 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr23:49034431 G>A did not map to a codon.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr23:49034758 G>T did not map to a codon.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr6:41752674 G>A maps to NM_013397.5 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:57140789 C>A maps to NM_000946.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr5:40775556 A>G maps to NM_206907.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr5:40798177 G>A maps to NM_206907.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr5:40771908 A>G maps to NM_206907.3 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr12:120118060 G>A maps to NM_006253.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr1:146639407 G>T maps to NM_005399.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:146638125 G>A maps to NM_005399.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr19:14213651 G>A maps to NM_002730.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:84679969 G>A maps to NM_182948.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr9:71628861 C>A maps to NM_002732.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr7:151265912 T>C maps to NM_016203.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:151265921 G>A maps to NM_016203.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24U-01A-11D-A167-09 chr17:66526497 C>T maps to NM_212472.1 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr17:66521902 T>C maps to NM_212472.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr17:66511560 C>T maps to NM_212472.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr17:66511663 C>T maps to NM_212472.1 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr7:720285 G>C maps to NM_002735.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr3:48802460 C>T maps to NM_004157.2 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:106786854 A>C maps to NM_002736.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr17:64731689 C>T maps to NM_002737.2 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr17:64800106 G>A maps to NM_002737.2 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr16:24135277 G>C maps to NM_002738.6 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr16:24196451 T>C maps to NM_002738.6 Y518Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr16:24043542 C>T maps to NM_002738.6 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr16:24104238 C>G maps to NM_002738.6 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr16:24135280 G>A maps to NM_002738.6 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:53223998 A>C maps to NM_212539.1 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr3:53223072 G>C did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr11:6340458 G>A maps to NM_145040.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:46386872 A>C maps to NM_005400.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr2:46313345 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:46234613 T>C maps to NM_005400.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:46372291 C>T maps to NM_005400.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr2:46234724 G>A maps to NM_005400.2 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr19:54403867 C>T maps to NM_002739.3 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr19:54385849 G>A maps to NM_002739.3 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:54403524 A>G maps to NM_002739.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:54407908 C>T maps to NM_002739.3 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr19:54403951 C>T maps to NM_002739.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:6506291 G>A maps to NM_006257.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr14:30107712 C>A maps to NM_002742.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:37496796 C>A maps to NM_005813.3 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr2:37501723 A>G maps to NM_005813.3 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr2:37507070 T>C maps to NM_005813.3 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:37499525 A>G maps to NM_005813.3 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr2:37501750 G>T maps to NM_005813.3 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr8:48839892 C>T maps to NM_006904.6 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:48792180 G>A maps to NM_006904.6 L1701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:48752647 G>A maps to NM_006904.6 F2460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr8:48839764 G>T maps to NM_006904.6 S803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr8:48694775 C>T maps to NM_006904.6 L3811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr8:48811082 G>A maps to NM_006904.6 I1137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr10:54048488 A>G maps to NM_001098512.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr4:82092952 G>A maps to NM_006259.1 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr4:82125819 C>A maps to NM_006259.1 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr4:82126024 C>T maps to NM_006259.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr4:82027040 G>C maps to NM_006259.1 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr11:76062797 G>A maps to NM_004705.2 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:3592656 T>G did not map to a codon.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr23:3592643 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:3539328 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:3544505 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr23:3592795 A>C did not map to a codon.
Sequencing variant TCGA-BH-A201-01A-11D-A14K-09 chr23:3544505 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr4:148564056 G>A maps to NM_138364.2 Q694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr4:148559723 G>A maps to NM_138364.2 Q833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr4:148575484 T>C maps to NM_138364.2 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr21:48080770 C>G maps to NM_206962.1 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr21:48064219 C>A maps to NM_206962.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr21:48084229 C>T maps to NM_206962.1 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr11:20414538 C>T maps to NM_005788.3 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr11:20417382 C>T maps to NM_005788.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:23395966 C>T maps to NM_006109.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr16:68379633 G>T maps to NM_019023.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr20:4705265 G>A maps to NM_012409.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:4680570 C>T maps to NM_001080123.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:18908914 C>T maps to NM_016335.4 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr19:36303323 G>A maps to NM_021232.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:36303417 G>C maps to NM_021232.1 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr19:36297348 A>G maps to NM_021232.1 Y404Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:110998921 C>T maps to NM_032414.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr3:71821980 T>C did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr2:68872961 C>A maps to NM_138964.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr2:68882404 C>T maps to NM_138964.2 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:68873195 C>T maps to NM_138964.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr20:5294673 G>A maps to NM_144773.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:16000006 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:15995621 G>A maps to NM_006017.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:95952918 G>A maps to NM_144707.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr2:95944748 G>A maps to NM_144707.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr2:95945628 A>G maps to NM_144707.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr2:95946988 G>A did not map to a codon.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr8:37635576 C>T maps to NM_007198.3 C261C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr8:37633452 G>A maps to NM_007198.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr14:75321978 G>A maps to ENST00000445876 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr13:113826029 C>T maps to ENST00000342783 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:13658487 G>T maps to NM_003675.3 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FF-01A-11W-A050-09 chr10:13642248 G>A maps to NM_003675.3 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:150316908 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:150318497 C>T maps to NM_004698.2 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr1:150307462 G>A maps to NM_004698.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:109235462 G>T maps to NM_018061.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr9:116038853 C>T maps to NM_004697.3 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr9:116053922 C>T maps to NM_004697.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr2:153525673 G>A maps to ENST00000410080 R645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:153532998 A>G maps to ENST00000410080 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr2:153520243 A>G maps to ENST00000410080 D735D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:50025191 T>C maps to NM_001031698.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:50025227 A>C maps to NM_001031698.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:50025641 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:50037941 G>C maps to NM_001031698.1 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:4032152 G>A maps to NM_003913.4 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:4032362 T>G maps to NM_003913.4 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr20:62658960 G>A maps to NM_012469.3 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr20:62641604 G>C maps to NM_012469.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr17:1582136 C>T maps to NM_006445.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:1580871 G>T maps to NM_006445.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:1579899 G>A maps to NM_006445.3 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr17:1554096 C>T maps to NM_006445.3 *2336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr23:106893240 A>G did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:12817442 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:12809624 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr23:12837705 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:74328410 C>T maps to NM_002766.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr17:18785978 C>T maps to NM_002767.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr16:30664307 C>T maps to NM_024031.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr5:120022379 G>A maps to NM_016644.1 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:42814038 A>C maps to NM_199285.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:138739116 G>A maps to NM_001013650.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IA-01A-11W-A050-09 chr3:138762901 G>A maps to NM_001134657.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:10999886 A>C maps to NM_007244.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr22:45182382 G>A maps to ENST00000352766 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:36458965 C>A maps to NM_001160167.1 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr11:36453428 C>T maps to NM_001160167.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:176882157 C>T maps to NM_001174101.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:126860370 A>C maps to ENST00000330542 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:37312565 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:37312733 G>C did not map to a codon.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr23:150869480 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr6:32117478 C>T maps to NM_030651.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03L-01A-41W-A071-09 chr1:170695521 G>A maps to NM_022716.2 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr7:142459747 C>T maps to ENST00000486171 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr16:2871055 C>A maps to NM_006799.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr16:2903952 A>G maps to NM_022119.3 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr16:2763622 G>A maps to NM_031948.3 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:2762621 C>T maps to NM_031948.3 *291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:33797967 C>A maps to NM_007343.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr6:84233450 G>A maps to NM_153362.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:84234347 C>T maps to NM_153362.2 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:84233643 C>T maps to NM_153362.2 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr3:46754417 C>T maps to NM_013270.4 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:31096161 A>G maps to NM_001039503.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr8:10383205 A>G maps to NM_198464.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr8:10390542 C>T maps to NM_198464.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr16:31143758 G>A maps to NM_002773.3 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr16:31144596 G>T maps to NM_002773.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:55930810 T>C maps to NM_173814.4 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:150999787 A>C maps to NM_021222.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr1:151006388 T>C maps to NM_021222.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:79321863 C>A maps to NM_015225.2 E1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr9:79324906 C>T maps to NM_015225.2 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr9:79323853 G>A maps to NM_015225.2 L1112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr9:79239390 C>A maps to NM_015225.2 L3055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:79461545 A>T maps to NM_015225.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr9:79320727 G>A maps to NM_015225.2 V2154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N8-01A-11D-A142-09 chr9:79324111 A>T maps to NM_015225.2 G1026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr9:79322730 G>A maps to NM_015225.2 R1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr19:40902116 G>C maps to NM_181882.2 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr19:40901698 G>A maps to NM_181882.2 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr19:40902908 G>C maps to NM_181882.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr19:40903118 G>C maps to NM_181882.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr19:40902281 G>T maps to NM_181882.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14T-01A-11D-A10Y-09 chr10:73594254 G>A maps to ENST00000373120 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr10:73579278 C>T maps to ENST00000373120 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr10:104172163 G>A maps to NM_002779.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:139193007 C>T maps to NM_032289.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr5:139193031 C>T maps to NM_032289.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr5:139189066 C>T maps to NM_032289.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:139221910 C>G maps to NM_032289.2 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr5:139193040 C>T maps to NM_032289.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr8:18457915 G>T maps to ENST00000440756 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:18730166 A>C maps to ENST00000440756 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr2:113940770 C>T maps to NM_012455.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:36237745 T>C maps to NM_172341.1 *102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr19:43376162 G>A maps to NM_006905.2 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr19:43373184 C>T maps to NM_006905.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:43519386 G>C maps to ENST00000306308 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:43570752 C>A did not map to a codon.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr19:43233452 G>A maps to NM_021016.3 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:43699291 A>C maps to NM_002780.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:43699147 G>A maps to NM_002780.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr19:43690497 G>A maps to ENST00000270059 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr19:43420538 G>C maps to NM_002782.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:43433597 G>C maps to NM_002783.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr19:43430737 G>T maps to NM_002783.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:43259202 G>A maps to NM_182707.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:43762546 G>A maps to NM_002784.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:43763216 G>A maps to NM_002784.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:15472748 C>G did not map to a codon.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr9:15486060 C>G maps to NM_001128217.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr9:15489982 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr16:67942875 C>G maps to NM_006742.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr8:87076598 G>C maps to ENST00000276616 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr14:58727738 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr14:58727695 C>T maps to NM_002788.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:109957928 C>T maps to NM_002790.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr1:109957928 C>T maps to NM_002790.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr20:60714887 C>T maps to NM_002792.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr20:60714887 C>T maps to NM_002792.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr18:23731888 G>T maps to NM_144662.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr18:23713973 C>T maps to NM_144662.2 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:67969494 G>A maps to NM_002801.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr14:23512054 C>T maps to NM_001099780.1 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr14:23511784 G>T maps to NM_001099780.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:90731484 C>A maps to NM_002802.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr7:103004750 T>C maps to NM_002803.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr17:40726210 C>T maps to NM_016556.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr19:40485742 G>T maps to NM_006503.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:61908769 A>C maps to NM_002805.5 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr14:53177880 C>T maps to NM_002806.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr14:53184855 T>G maps to NM_002806.3 L210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:231943446 T>C maps to NM_002807.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr17:65337028 G>C maps to NM_002816.3 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BV-01A-11W-A019-09 chr11:244465 G>A maps to NM_002817.3 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr11:250837 G>A maps to NM_002817.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04A-01A-21W-A050-09 chr2:162175350 T>G maps to NM_005805.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr17:38140649 C>G maps to NM_002809.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr17:38140604 C>T maps to NM_002809.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:38153807 G>T maps to NM_002809.2 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:151239034 C>G maps to ENST00000368881 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:63999217 C>A maps to ENST00000492933 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr14:24605500 C>G maps to NM_176783.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr17:40993570 C>T maps to NM_176863.1 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:54176299 G>A maps to NM_014614.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:54150228 G>C maps to NM_014614.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:54155411 C>A maps to NM_014614.2 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr20:1099508 G>A maps to NM_006814.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:1108103 G>A maps to NM_006814.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr18:12718541 A>G maps to NM_020232.4 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr13:20283699 C>A maps to NM_001042414.1 G400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr7:56088779 G>A maps to NM_004577.3 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:77310854 T>G maps to NM_003978.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr18:43571949 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:28477475 C>T maps to NM_001164721.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:72333320 C>T maps to NM_001099666.1 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:810753 C>A maps to NM_002819.4 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:808429 G>A maps to NM_002819.4 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:804186 G>T maps to NM_002819.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:97272422 T>G maps to ENST00000370197 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:97243417 G>A maps to ENST00000370197 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LI-01A-12D-A159-09 chr7:99021451 T>C maps to NM_001198879.1 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:86355070 G>A maps to NM_017952.5 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr9:98220333 G>A maps to NM_000264.3 C1043C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:98231098 C>T maps to NM_000264.3 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:98209243 G>A maps to NM_000264.3 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:45289024 C>T maps to NM_003738.4 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr23:23411287 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr23:23397728 A>T did not map to a codon.
Sequencing variant TCGA-A8-A06P-01A-11W-A019-09 chr23:23412004 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BJ-01A-11W-A071-09 chr23:23398005 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr23:23411646 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr23:23353125 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DO-01B-11D-A12B-09 chr23:23411482 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:23410823 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr23:23397793 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr1:11591049 C>T maps to NM_020780.1 S1063S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr1:11594442 G>A maps to NM_020780.1 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:27702555 G>A maps to NM_001034842.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr10:27702624 C>T maps to NM_001034842.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr8:97274285 G>C maps to NM_014754.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr10:89653839 C>G maps to NM_000314.4 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:89685280 C>A maps to NM_000314.4 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JA-01A-11W-A071-09 chr10:89692779 T>A maps to NM_000314.4 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr10:89712017 T>C did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr10:89720708 C>G maps to NM_000314.4 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr10:89720708 C>G maps to NM_000314.4 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr10:89692934 T>G maps to NM_000314.4 L140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr14:52741543 G>C maps to NM_000953.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr14:52735143 C>T maps to NM_000953.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr14:52793937 G>A did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr14:52793970 A>C maps to NM_000956.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr14:52782108 G>A maps to NM_000956.3 T281T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E2-A15S-01A-11D-A10Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:71512882 C>T maps to ENST00000354608 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr5:40681724 G>A maps to NM_000958.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr5:40692392 C>T maps to NM_000958.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr9:130883441 C>T maps to NM_025072.5 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr1:117504033 C>T maps to NM_020440.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr20:48164523 G>A maps to NM_000961.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:114345823 A>C maps to NM_001146108.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr14:74340784 A>G maps to NM_152444.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:186646839 G>A maps to NM_000963.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:186648331 C>T maps to NM_000963.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:186644408 C>T maps to NM_000963.2 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:186643895 T>C did not map to a codon.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr1:186648295 G>A maps to NM_000963.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:209308165 C>T maps to NM_005048.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr8:27288484 C>T maps to NM_004103.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr20:62163968 G>A maps to NM_005975.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr20:62163954 G>A maps to NM_005975.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr6:43099858 G>A maps to NM_002821.3 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:43109508 C>T maps to NM_002821.3 N574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14T-01A-11D-A10Y-09 chr12:6879110 G>T maps to NM_002824.4 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr19:50360969 C>G maps to NM_017432.3 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:96857614 C>T maps to ENST00000434261 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr9:96860127 G>A maps to ENST00000434261 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:112915488 T>C maps to ENST00000392596 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:77256042 T>G maps to NM_002835.3 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr4:87720272 G>T maps to NM_080685.2 E2146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:87653743 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:87671905 C>G maps to NM_080685.2 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:87724872 C>T maps to NM_080685.2 L2178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr4:87691102 G>A maps to NM_080685.2 V1562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12B-01A-11D-A10M-09 chr1:214543009 G>A maps to NM_005401.4 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr1:214557334 G>A maps to NM_005401.4 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr2:131127381 C>A maps to NM_014369.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr10:46584513 T>C maps to NM_001042357.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr14:88974300 T>C maps to NM_007039.3 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr14:88962791 C>T maps to NM_007039.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:114401700 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr1:114376999 T>A maps to NM_015967.5 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T7-01A-21D-A099-09 chr3:47451453 C>T maps to NM_015466.2 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr3:47450965 C>T maps to NM_015466.2 N619N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:47453830 G>T maps to NM_015466.2 E1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:7064126 C>T maps to ENST00000416215 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:202127407 C>G maps to ENST00000309017 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr1:202127398 G>A maps to ENST00000309017 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:75816618 G>A maps to NM_002833.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:75801284 G>C maps to NM_002833.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr15:75815502 T>C maps to NM_002833.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:2998480 G>A maps to NM_002836.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr20:2967451 C>T maps to NM_002836.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr12:70974954 G>C maps to NM_001109754.1 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Z-01A-11D-A167-09 chr12:70946686 C>A maps to NM_001109754.1 E1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WV-01A-11D-A10G-09 chr12:70925883 T>C maps to NM_001109754.1 K2145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr12:70925901 G>A maps to NM_001109754.1 L2139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:71029496 G>A maps to NM_001109754.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr12:70933794 G>A maps to NM_001109754.1 R1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr12:70928672 C>A maps to NM_001109754.1 L2048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr12:70964941 T>G maps to NM_001109754.1 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr12:70974894 G>A maps to NM_001109754.1 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:70953345 G>A maps to NM_001109754.1 I1497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr12:70938400 C>G maps to NM_001109754.1 L1810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr1:198676019 T>G maps to ENST00000271610 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr1:198704338 A>G maps to ENST00000271610 K787K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:198721854 G>T maps to ENST00000271610 E1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:198691596 C>G maps to ENST00000271610 S571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N5-01A-11D-A14G-09 chr1:198697544 C>T maps to ENST00000271610 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr9:8471021 C>T maps to NM_002839.3 E1159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr9:8504362 C>A maps to NM_002839.3 G574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:8507408 T>C maps to NM_002839.3 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:8526636 T>C maps to NM_002839.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:8525026 G>A maps to NM_002839.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15A-01A-11D-A12B-09 chr9:8500900 C>A maps to NM_002839.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr9:8518118 G>A maps to NM_002839.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr10:129871638 G>A maps to NM_006504.4 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr10:129866448 C>T maps to NM_006504.4 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr1:44084967 G>A maps to NM_002840.3 V1552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:62216897 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:62254774 G>A maps to NM_002841.3 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:62240891 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr19:55693163 G>A maps to NM_002842.3 Y1102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr19:55715305 G>A maps to NM_002842.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:48164576 T>C maps to NM_002843.3 Y850Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr6:128410948 G>A maps to ENST00000368210 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:128718726 T>G maps to ENST00000368210 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:128291386 G>A maps to ENST00000368210 Y1454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:128505865 C>T maps to ENST00000368210 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr6:128404924 C>A maps to ENST00000368210 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XS-01A-22D-A10G-09 chr18:8088801 C>T maps to NM_001105244.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr18:8076451 G>T did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr18:8296427 G>A maps to NM_001105244.1 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr18:7888191 C>T maps to NM_001105244.1 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr18:8244067 G>A maps to NM_001105244.1 K771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:220166325 A>C maps to NM_002846.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:220161521 C>T maps to NM_002846.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr2:220155280 C>A maps to NM_002846.3 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr7:158282451 G>A maps to NM_002847.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr7:157926523 G>A maps to NM_002847.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:15652374 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:15656882 G>T maps to NM_030667.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr12:15661532 G>T maps to NM_030667.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:5221137 G>A maps to NM_002850.3 Q1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XX-01A-21D-A23C-09 chr20:41306713 G>A maps to ENST00000373198 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:40714430 G>A maps to ENST00000373198 F1325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:40770575 G>A maps to ENST00000373198 R939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:41385108 G>A maps to ENST00000373198 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:41420062 C>T maps to ENST00000373198 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:40790036 C>T maps to ENST00000373198 T901T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr20:41100906 G>A maps to ENST00000373198 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:29637971 G>A maps to NM_005704.4 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr1:29652165 C>A maps to NM_005704.4 S1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:29644306 C>T maps to NM_005704.4 I1197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:121608161 C>T maps to NM_002851.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr7:121624109 G>A maps to NM_002851.2 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr7:121695125 C>T maps to NM_002851.2 I2171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr17:40556902 G>C maps to NM_012232.5 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr17:40557213 T>A maps to NM_012232.5 K222*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AC-A23H-01A-11D-A159-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:159854866 A>C maps to NM_004219.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr4:37962150 C>T maps to NM_006607.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:37962570 A>C maps to NM_006607.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr8:144900365 G>A maps to NM_078480.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:31406058 C>G maps to ENST00000373741 *1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr1:31439033 C>T maps to ENST00000373741 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr1:31478855 G>A maps to ENST00000373741 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr2:20455817 G>A maps to ENST00000361078 F868F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:30889437 C>T maps to NM_013357.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:30889905 C>T maps to NM_013357.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:61192231 C>T maps to NM_144709.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr2:61238926 A>G maps to NM_144709.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr2:61233763 A>C maps to NM_144709.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:44124247 G>T maps to NM_031292.3 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:44139859 C>A maps to NM_031292.3 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:37213028 C>G maps to NM_002854.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:45161047 A>C maps to NM_006505.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:110837623 T>G maps to NM_015480.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr3:110831213 G>C maps to NM_015480.1 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr1:161042510 G>A maps to NM_030916.2 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr12:108086666 G>A maps to NM_007062.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr2:1653367 G>A maps to NM_012293.1 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:1653127 G>A maps to NM_012293.1 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr2:1670055 G>A maps to NM_012293.1 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr2:1680708 G>A maps to NM_012293.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr2:1687850 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:52284469 C>A maps to NM_144651.4 P1288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr8:52384838 C>T maps to NM_144651.4 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:52412307 C>A maps to NM_144651.4 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr8:52370198 G>A maps to NM_144651.4 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EX-01A-11D-A13L-09 chr8:52321347 G>A maps to NM_144651.4 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr8:52336141 T>G maps to NM_144651.4 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr8:52321105 G>T maps to NM_144651.4 G1026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:52252212 G>A maps to NM_144651.4 Q1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:58351612 C>T maps to NM_017771.3 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:120651737 G>A maps to NM_001080855.1 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr16:31213060 G>A maps to NM_013258.4 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:191179037 G>A maps to NM_001083308.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr20:25273189 C>G maps to NM_002862.3 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr20:25229005 C>T maps to NM_002862.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:158906838 C>T maps to NM_152501.3 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:100152323 C>A did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:42030475 C>T did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr12:9321483 T>A maps to NM_002864.2 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr12:9312949 C>T maps to NM_002864.2 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr12:9346693 C>T maps to NM_002864.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:49136806 T>G maps to NM_005051.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:49137391 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:49136833 G>T maps to NM_005051.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:17493919 G>C maps to NM_000320.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:37594514 A>C maps to NM_012413.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:46198867 A>C maps to NM_017659.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr19:46196813 G>A maps to NM_017659.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:46196026 C>G maps to NM_017659.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr16:29706324 C>G maps to NM_014298.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr3:49067886 A>G maps to NM_198880.1 *777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr3:49084616 A>G maps to NM_198880.1 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:74274260 C>T maps to NM_032134.1 L1476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:74290027 G>A maps to NM_032134.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:74271963 G>C maps to NM_032134.1 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:74300971 C>T maps to NM_032134.1 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr17:74303557 G>T maps to NM_032134.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr11:32954675 T>C maps to NM_001076786.1 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:32954423 T>C maps to NM_001076786.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:32953655 A>C maps to NM_001076786.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr11:32955887 G>A maps to NM_001076786.1 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr11:32956871 T>A maps to NM_001076786.1 S1227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr1:180144453 A>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:180153134 A>C maps to NM_002826.4 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3QP-01A-11D-A22X-09 chr1:180165577 T>C maps to NM_002826.4 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr1:180147982 G>A maps to NM_002826.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr1:180151337 C>T maps to NM_002826.4 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:180165580 C>T maps to NM_002826.4 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr9:139110970 C>T maps to NM_181701.3 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr9:139100960 C>A maps to NM_181701.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr3:113785092 C>G maps to ENST00000485050 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr12:57660597 G>A maps to ENST00000438036 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr20:42972037 C>T maps to NM_178491.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr20:42965926 C>T maps to NM_178491.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr2:26350786 G>A maps to NM_016131.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr15:66180166 C>T maps to ENST00000435304 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:66170176 G>A maps to ENST00000435304 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:8464849 C>T maps to NM_004218.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:37735005 G>A maps to NM_001002814.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr8:37720511 C>T maps to NM_001002814.2 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr8:37730534 G>A maps to NM_001002814.2 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr16:569770 G>A maps to NM_014700.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr17:29858681 C>T maps to NM_032932.3 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr17:29758838 A>G maps to NM_032932.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr2:73316120 G>A maps to NM_015470.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr1:153955064 C>T maps to NM_002870.2 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:123954461 A>G maps to NM_016322.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr9:123943766 A>G maps to NM_016322.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr2:238484087 C>T maps to NM_022449.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:72164418 C>T maps to NM_014999.2 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:56928355 C>T maps to NM_020673.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr6:57061378 G>A maps to NM_016277.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr1:156039537 G>T maps to NM_020387.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:2201890 C>T maps to NM_014353.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09T-01A-11W-A019-09 chr11:82698728 G>A maps to NM_014488.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr11:82693236 G>A maps to NM_014488.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FD-01A-11W-A14Q-09 chr11:82708279 G>T maps to NM_014488.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr23:129318288 C>A did not map to a codon.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr23:129306146 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr23:129318408 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr17:72725504 G>A maps to NM_175738.4 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr17:72736905 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:87883070 A>C maps to NM_022337.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:154490156 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:154490163 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr23:154490355 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr23:154493387 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr23:154493494 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:18313508 G>T maps to NM_002866.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:18309659 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:11436205 G>A maps to NM_004283.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:135870804 G>A maps to NM_001172435.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr2:135848701 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:220340906 C>A maps to ENST00000358951 E973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr1:220325076 G>C maps to ENST00000358951 V1299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:220355609 G>A maps to ENST00000358951 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr23:102755365 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:102755665 G>T did not map to a codon.
Sequencing variant TCGA-BH-A1FG-01A-11D-A13L-09 chr23:102755500 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:102192644 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:102192924 A>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:69502671 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr1:229434757 G>A maps to NM_004578.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr19:41286350 T>A maps to ENST00000419646 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr19:41285990 C>T maps to ENST00000419646 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BS-01A-11D-A12Q-09 chr17:40280335 G>A maps to NM_201434.1 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr1:205739861 T>G maps to NM_003929.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr1:205739908 C>T maps to NM_003929.2 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:13727288 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:103080349 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:103080649 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr23:103080632 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr23:103080688 T>G did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr23:103080360 G>T did not map to a codon.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr23:103080671 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr17:5235302 C>T maps to NM_004703.4 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr17:5253831 C>T maps to NM_004703.4 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EA-01A-11D-A10Y-09 chr16:28935781 C>T maps to NM_024816.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr9:127994884 A>G maps to NM_005833.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:125752411 A>C maps to NM_012197.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr9:125863867 G>A maps to NM_012197.3 R971R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr9:125746847 G>T maps to NM_012197.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr1:174927025 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:24736011 T>G maps to NM_182836.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr14:24740087 C>T maps to NM_182836.1 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr14:24738316 G>C maps to NM_182836.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr22:37628022 G>A maps to NM_002872.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr22:37627983 G>A maps to NM_002872.3 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr12:50410432 G>T maps to NM_013277.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:50387973 G>A maps to NM_013277.3 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:8955389 G>A maps to NM_020165.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:117859870 C>T maps to NM_006265.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:13059100 A>C maps to NM_005053.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr19:13059324 C>G maps to NM_005053.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:13059578 G>C maps to NM_005053.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:131940516 G>A maps to NM_005732.3 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr15:41022085 A>G maps to NM_002875.4 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr2:17698739 T>A maps to NM_001099218.2 K315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr8:95399224 G>A maps to NM_012415.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr8:95384608 G>T maps to NM_012415.2 S841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr8:95399324 T>C maps to NM_012415.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:95419751 G>A maps to NM_012415.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:46743952 G>T maps to NM_003579.3 *748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:46739836 G>A maps to NM_003579.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:51664814 T>G maps to NM_015106.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr3:51673685 G>A maps to NM_015106.2 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:110941659 G>A maps to NM_152442.3 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr6:150240755 C>T maps to NM_001001788.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr6:150239332 C>G maps to NM_001001788.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr11:36597220 G>A maps to NM_000448.2 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr11:36596584 C>T maps to NM_000448.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr14:102698064 A>G maps to NM_014226.1 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr17:17697696 C>T maps to ENST00000395776 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr17:17696486 C>G maps to ENST00000395776 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:17819744 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr23:17818738 T>G did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:17819187 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr23:17818731 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:17819377 C>T did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:17818566 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr23:17819681 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:121050754 G>A maps to NM_002881.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:9525755 T>G maps to NM_006788.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr18:9533748 C>T maps to NM_006788.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A201-01A-11D-A14K-09 chr18:9524596 C>T maps to NM_006788.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr14:36096647 T>G maps to NM_194301.2 R1663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr14:36192402 A>T maps to NM_194301.2 L645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr14:36207802 G>A maps to NM_194301.2 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr20:20585840 C>T maps to NM_020343.3 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr20:20493752 C>T maps to NM_020343.3 V1420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FN-01A-11W-A050-09 chr20:20517352 G>A maps to NM_020343.3 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr20:20553659 G>A maps to NM_020343.3 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:20610049 G>C maps to NM_020343.3 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr20:20585863 G>A maps to NM_020343.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:20582458 G>A maps to NM_020343.3 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr20:37182574 T>G maps to NM_020336.2 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:37126020 C>T maps to NM_020336.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr20:37177428 A>T maps to NM_020336.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:129974505 G>A maps to NM_014636.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:129957409 G>A maps to NM_014636.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr1:178780487 A>G maps to NM_152663.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr20:32664861 C>T maps to NM_016732.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:131359145 G>A maps to ENST00000392369 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:20113871 C>T maps to NM_002882.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:170720957 C>G maps to NM_022897.3 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:170722916 G>A maps to NM_022897.3 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:109368405 C>T maps to NM_006267.4 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:109384011 C>G maps to NM_006267.4 L2339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr2:109380098 C>G maps to NM_006267.4 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr19:5917814 G>A maps to NM_007322.2 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr19:5917931 C>T maps to NM_007322.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr19:5918622 G>A maps to NM_007322.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr19:5925679 G>A maps to NM_007322.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr5:36262046 G>C maps to NM_001161429.1 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:6015409 C>T maps to NM_012416.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr9:6012610 T>C maps to NM_012416.2 E999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:112237961 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:21926031 G>A maps to NM_001145658.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr1:21928253 G>A maps to NM_001145658.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr1:21924471 C>T maps to NM_001145658.1 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:2883660 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:99273630 T>C maps to NM_001100426.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr13:98086994 C>T maps to NM_021033.6 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr3:152880776 C>T maps to NM_002886.2 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P0-01A-11D-A142-09 chr23:131348320 T>C did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr9:134503378 G>A maps to NM_198679.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:160235762 T>G maps to NM_014247.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:160243586 C>T maps to NM_014247.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr4:160252681 G>T maps to NM_014247.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:160252650 T>A maps to NM_014247.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr12:48141336 G>A maps to NM_001098531.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A096-01A-11W-A019-09 chr2:173891807 G>C did not map to a codon.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr2:173825507 C>T maps to NM_007023.3 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:22170701 C>A maps to ENST00000344041 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:22259537 C>A maps to ENST00000344041 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:22233009 C>T maps to ENST00000344041 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:130846054 G>A maps to ENST00000514667 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr5:130769160 G>A maps to ENST00000514667 H1362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:130764663 G>A maps to ENST00000514667 Q1621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr5:130840455 G>A maps to ENST00000514667 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr17:38345156 G>A maps to ENST00000456989 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:204313534 G>A maps to ENST00000374493 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:204326612 G>A maps to ENST00000374493 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr17:38508725 C>T maps to NM_001145301.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:38506061 G>A maps to NM_001145301.2 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:25542810 G>T maps to NM_000965.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr3:25470350 C>T maps to NM_000965.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr3:25622089 C>T maps to NM_000965.3 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:25622071 G>A maps to NM_000965.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr3:25622056 A>T maps to NM_000965.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr3:25542764 C>A maps to NM_000965.3 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr12:53609501 G>C maps to NM_000966.4 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:63312300 G>A maps to NM_004585.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr11:63312153 G>A maps to NM_004585.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr5:86676365 C>T maps to NM_002890.1 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr3:141292063 G>T did not map to a codon.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr3:141277775 G>T maps to ENST00000452898 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr13:114786881 C>T maps to ENST00000389544 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr13:114766362 C>T maps to ENST00000389544 K603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:178427486 T>G maps to ENST00000263528 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr19:15563551 C>T maps to NM_022904.1 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:15563563 G>T maps to NM_022904.1 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JH-01A-11D-A188-09 chr22:35943098 C>T maps to NM_014310.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr15:79298691 G>A maps to NM_002891.4 Y650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:79312446 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:79282605 G>A maps to NM_002891.4 F1063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:79317727 T>C maps to NM_002891.4 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:79339278 G>T maps to NM_002891.4 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr15:79296366 G>A maps to NM_002891.4 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr15:79317804 G>A maps to NM_002891.4 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr15:79310204 G>A maps to NM_002891.4 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A125-01A-11D-A10M-09 chr5:80390149 G>A maps to NM_006909.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr5:80382662 C>T maps to NM_006909.1 H427H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:38811529 C>T maps to NM_005739.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr15:38805031 C>T maps to NM_005739.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:64496380 G>A maps to ENST00000320253 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr11:64506870 G>T maps to ENST00000320253 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:33774811 G>A maps to NM_170672.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr2:33749575 C>G maps to NM_170672.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr19:38910823 G>A maps to ENST00000405332 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr19:38916710 C>T maps to ENST00000405332 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr19:49228117 C>A maps to NM_017805.2 G743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr19:49227976 G>A maps to NM_017805.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr19:49230687 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr13:27847232 C>T maps to NM_206827.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr4:53731599 C>T maps to NM_023940.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:65351706 C>T maps to NM_016563.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:4768400 C>G did not map to a codon.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr20:4776603 G>A maps to NM_014737.2 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr20:4773209 C>T maps to NM_014737.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:45478051 C>T maps to NM_032023.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:45478084 G>A maps to NM_032023.3 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr11:563349 G>A maps to ENST00000431809 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:65243505 C>T maps to ENST00000294428 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr18:56939730 C>T maps to NM_013435.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr13:49039500 C>G maps to NM_000321.2 S829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr13:48934161 T>G maps to NM_000321.2 L206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr13:49050905 G>T maps to NM_000321.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr13:49030342 T>G maps to NM_000321.2 Y606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:49039420 G>C maps to NM_000321.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:48939107 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr13:48955537 C>T maps to NM_000321.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr13:48934188 C>G maps to NM_000321.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr13:48916746 C>T maps to NM_000321.2 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A202-01A-11D-A14K-09 chr13:48934188 C>A maps to NM_000321.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr13:49050874 T>A maps to NM_000321.2 C853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr13:49037901 G>C maps to NM_000321.2 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr13:48954372 T>C maps to NM_000321.2 Y498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr13:48953759 C>T maps to NM_000321.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr8:53596280 T>G did not map to a codon.
Sequencing variant TCGA-AR-A2LO-01A-31D-A18P-09 chr8:53588957 G>T maps to NM_014781.4 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr8:53548622 A>G maps to NM_014781.4 N1448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr8:53569189 T>A maps to NM_014781.4 K1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MS-A51U-01A-31D-A25Q-09 chr8:53568767 A>G maps to NM_014781.4 A1207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:5104214 C>T maps to NM_021163.3 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Z-01A-11D-A167-09 chr1:33117548 C>T maps to NM_005610.2 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr1:33138483 C>T maps to NM_005610.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr1:33117548 C>A maps to NM_005610.2 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr1:33123069 G>T maps to NM_005610.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr1:205069183 C>T maps to NM_005057.3 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr16:24567189 C>T maps to NM_006910.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:24578775 A>C maps to NM_006910.4 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr16:24578809 C>T maps to NM_006910.4 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:24574617 T>A did not map to a codon.
Sequencing variant TCGA-E9-A1R3-01A-31D-A14K-09 chr16:24560352 A>G maps to NM_032626.5 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:16863949 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:16863180 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:16887271 G>T did not map to a codon.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr23:16871847 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:20562313 G>T maps to ENST00000360790 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr18:20572914 T>A maps to ENST00000360790 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr20:18474698 G>A maps to NM_006606.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr20:35651109 T>C maps to NM_002895.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr20:35696492 A>G maps to NM_002895.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XG-01A-11D-A14G-09 chr20:35689642 C>T maps to NM_002895.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr20:35693876 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:47035948 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47028798 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:47041644 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr23:47044962 C>T did not map to a codon.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr23:47028832 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr23:47045971 G>A did not map to a codon.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr23:47028776 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:34242644 T>G maps to NM_001198838.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr20:34242680 T>G maps to NM_001198838.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:34242527 T>G maps to NM_001198838.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:34241692 G>A maps to NM_001198838.1 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr20:34241979 G>C maps to NM_001198838.1 S422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr8:94746789 C>A maps to NM_203390.2 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:94746031 A>C maps to NM_203390.2 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:94746436 T>G maps to NM_203390.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:94746460 T>G maps to NM_203390.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr8:94748064 G>A maps to NM_203390.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr8:94747081 G>A maps to NM_203390.2 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr11:66392811 C>T maps to NM_006328.3 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08H-01A-21W-A019-09 chr3:51430438 C>T maps to NM_013286.4 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:155145465 A>C maps to NM_014892.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:155148330 A>C maps to NM_014892.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:155153553 A>C maps to NM_014892.3 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:155153571 A>C maps to NM_014892.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:155153607 A>C maps to NM_014892.3 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:155154382 C>T maps to NM_014892.3 Q1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:155148304 G>T did not map to a codon.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr5:150076367 C>T maps to NM_018047.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr14:23374449 G>A maps to NM_001077351.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr14:23371048 G>A maps to NM_001077351.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:73574557 G>T maps to NM_021239.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr14:73570126 A>G maps to NM_021239.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:79929468 G>A maps to ENST00000438737 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr13:79911272 C>T maps to ENST00000438737 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr13:79896573 G>A maps to ENST00000438737 F949F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:145641281 G>A maps to NM_018989.1 Q701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:145641353 C>T maps to NM_018989.1 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr23:48434029 T>A did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr1:235301418 G>A maps to NM_015014.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:235316074 C>A maps to NM_015014.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr20:34312572 G>A maps to NM_184234.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:66407220 T>A maps to NM_002896.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:106332066 C>A did not map to a codon.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr23:106310810 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:106312493 T>G did not map to a codon.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr23:106331857 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:36125259 C>T maps to NM_024321.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:36128362 C>T maps to NM_024321.3 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:178988301 A>T maps to ENST00000456670 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:40440151 G>A maps to NM_001098634.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:40440208 C>T maps to NM_001098634.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr4:40440361 G>C maps to NM_001098634.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr3:50154521 C>T maps to NM_005778.2 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr3:50005865 T>C maps to NM_005777.2 H336H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AN-A0AK-01A-21W-A019-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:161141318 T>G maps to NM_016836.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr3:29781332 C>T maps to NM_001003793.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:135960219 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:135957680 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:135956542 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr23:135961211 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:129536313 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:129543275 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:89449113 A>C maps to NM_019610.5 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:89448794 G>A maps to NM_019610.5 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr11:7110464 C>G maps to NM_014469.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:139257745 G>A maps to NM_002899.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:48388822 C>T maps to NM_002900.2 Q685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr10:48383986 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr12:7280865 G>A maps to NM_031491.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr1:173916615 C>G maps to NM_172071.2 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr9:125618152 G>C maps to NM_001100588.1 S820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr9:125616340 G>A maps to NM_001100588.1 Q1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr9:125642123 C>T maps to NM_001100588.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:125659701 G>A maps to NM_001100588.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr9:125652666 C>T maps to NM_001100588.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr21:35890531 T>G maps to NM_004414.5 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:24859649 T>C maps to NM_013441.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr1:24859682 C>T maps to NM_013441.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr1:24857755 C>T maps to NM_013441.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr13:49075942 A>T maps to NM_001268.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:28858718 G>T maps to NM_001048194.2 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:17743034 G>A maps to NM_018715.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:17739609 C>T maps to NM_018715.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr11:66613001 T>G maps to NM_005133.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr9:4841273 G>T maps to NM_005772.3 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr19:50045942 G>T maps to NM_020650.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:103173722 C>T maps to NM_015156.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr17:9808317 G>T maps to NM_002903.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr1:211652656 C>T maps to NM_183059.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:68159248 G>A maps to NM_016026.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr14:68156952 G>A maps to NM_016026.3 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:68151904 C>T maps to NM_016026.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr12:56118202 C>T maps to NM_002905.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr12:56118163 G>A maps to NM_002905.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:56118262 G>A maps to NM_002905.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:110128532 A>C maps to ENST00000405097 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:24648881 T>G maps to NM_005132.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr14:24644762 C>T maps to NM_005132.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr9:36052307 T>C maps to NM_021111.2 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:21623139 G>A maps to NM_032941.2 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr12:21639493 C>T maps to NM_032941.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr8:145738068 C>G maps to ENST00000428558 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:145737118 C>A maps to ENST00000428558 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr8:145739482 C>T maps to ENST00000428558 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr8:145739719 C>T maps to ENST00000428558 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KC-01A-11D-A20S-09 chr17:73657111 G>A maps to NM_004259.5 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:73624333 G>A maps to NM_004259.5 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr17:73661204 G>A maps to NM_004259.5 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:137780193 C>T maps to ENST00000378339 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr10:65380601 G>T maps to NM_001001330.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr2:79350283 A>G maps to NM_002909.4 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15D-01A-11D-A10Y-09 chr2:79350037 T>C maps to NM_002909.4 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr2:79312687 G>T maps to NM_006507.3 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:79314714 G>A maps to NM_006507.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr2:79253872 G>T maps to NM_001008387.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr2:61145425 G>A maps to NM_002908.2 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:61128172 G>T maps to NM_002908.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr2:61149039 A>G maps to NM_002908.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:45515437 C>T maps to ENST00000221452 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GY-01A-11W-A071-09 chr4:37640082 C>A maps to NM_001085399.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr4:37651122 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:103473982 C>T did not map to a codon.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr7:103130321 C>T maps to ENST00000428762 Q3210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr7:103191641 G>T maps to ENST00000428762 C2058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:103205744 G>A maps to ENST00000428762 V1730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:103205790 G>C maps to ENST00000428762 S1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:73102242 A>C maps to NM_152222.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:30070280 C>A maps to NM_014012.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr20:30070111 C>G maps to NM_014012.4 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:204125432 G>T maps to NM_000537.3 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153208405 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:153209419 T>C did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr12:27850131 G>T maps to NM_001029874.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:150068458 G>A maps to NM_001099695.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:150069010 C>T maps to NM_001099695.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:17153382 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:17065587 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr23:17024440 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:17047735 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:8421517 A>C maps to NM_012102.3 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr1:8426005 C>T maps to NM_012102.3 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr4:57777581 G>T maps to NM_005612.4 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr10:43597898 C>T maps to NM_020975.4 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KI-01A-11D-A14K-09 chr10:43609955 G>A maps to NM_020975.4 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr10:43607664 T>C maps to NM_020975.4 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr2:85570863 G>A maps to NM_017750.3 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr2:85571789 G>A maps to NM_017750.3 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr2:100046337 G>C maps to NM_016316.2 S504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CU-01A-12W-A050-09 chr2:100019353 G>A maps to NM_016316.2 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr2:100065946 C>T maps to NM_016316.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:100019233 C>G maps to NM_016316.2 V1138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:111665170 G>A maps to NM_002912.3 R2499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24R-01A-11D-A167-09 chr19:1825882 G>A maps to NM_020695.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr4:39308301 G>A maps to ENST00000381897 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr4:39308262 C>G maps to ENST00000381897 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr4:39310355 G>C maps to ENST00000381897 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr3:186508117 G>C maps to NM_181573.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:186507945 G>A maps to NM_181573.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:186507766 C>T maps to NM_181573.2 Q361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:94991895 T>A maps to NM_001131065.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr22:32589027 G>T maps to NM_001098527.2 C139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr22:32587022 C>G maps to NM_001098527.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:53138047 C>T maps to NM_052859.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:16419312 A>C maps to NM_015150.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:198480649 G>A maps to NM_144629.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:198540113 C>T maps to NM_144629.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:198498525 C>A maps to NM_144629.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr1:176012390 T>G maps to NM_022457.5 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr1:176012376 A>T maps to NM_022457.5 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:74662503 A>C maps to NM_018124.3 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr19:14073673 C>A maps to NM_002918.4 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr19:6007780 G>A maps to NM_000635.3 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr9:3225065 T>C maps to NM_134428.1 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:107080790 A>C maps to ENST00000357881 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:107103123 C>T maps to ENST00000357881 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr12:106995095 G>A maps to ENST00000357881 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:117245848 C>T maps to NM_173560.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:56386019 G>A maps to NM_022841.5 I1302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr15:56386800 G>C maps to NM_022841.5 S1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr19:19304794 C>T maps to NM_003721.2 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:19308330 T>C maps to NM_003721.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr19:19309500 G>A maps to NM_003721.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr19:19312526 G>A maps to NM_003721.2 *261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:100479276 G>A maps to NM_001134666.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:109694796 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:109694111 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:109694925 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:109695034 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:109695159 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:109694738 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:109694562 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr23:109697416 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr23:109694014 A>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:109696096 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr23:109694148 C>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:109696854 T>G did not map to a codon.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr23:109694661 A>G did not map to a codon.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr23:109696710 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IB-01A-11W-A050-09 chr23:109694758 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:109695583 T>C did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:109696069 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:109694515 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr23:109694770 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:109695734 G>C did not map to a codon.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr23:71351177 G>C did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:71350650 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr1:183816894 C>T maps to NM_015149.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:183711313 G>T maps to NM_015149.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr19:11526648 G>A maps to NM_001161616.1 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr19:11507983 C>T maps to NM_001161616.1 K656K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr19:11512790 G>C maps to NM_001161616.1 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr19:11527721 G>A maps to NM_001161616.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:24039359 T>G maps to ENST00000382833 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr22:24040041 G>A maps to ENST00000382833 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:93588830 A>C maps to NM_020211.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:93616197 G>C maps to NM_020211.2 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HI-01A-11D-A099-09 chr5:98115335 C>T maps to NM_001012761.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr23:46952338 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:73205404 C>T maps to NM_001080479.2 Q1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr9:35751660 G>A maps to ENST00000456972 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr2:88083848 T>C maps to NM_001078170.2 E898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr2:107041152 G>A maps to ENST00000304514 N1090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:107040732 A>C maps to ENST00000304514 G1230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:107041449 G>T maps to ENST00000304514 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr2:107049423 C>A maps to ENST00000304514 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr2:107084738 A>G maps to ENST00000304514 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:107040335 C>A maps to ENST00000304514 E1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AX-01A-11D-A12Q-09 chr2:107041127 G>A maps to ENST00000304514 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R3-01A-31D-A14K-09 chr2:107029549 C>T maps to ENST00000304514 A1752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr2:108479274 A>G maps to NM_182588.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr2:108499276 G>A maps to NM_182588.2 T1738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr2:108487658 C>T maps to NM_182588.2 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr2:108479239 C>T maps to NM_182588.2 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:113157341 G>C maps to NM_005054.2 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr10:86017647 G>T did not map to a codon.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr10:86014114 C>T maps to ENST00000358110 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr1:192545957 C>G maps to NM_002922.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:121259768 G>T maps to NM_001005339.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr16:324237 T>G maps to NM_183337.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr4:3441257 C>G maps to NM_198229.2 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2OB-01A-21D-A27P-09 chr4:3319690 G>A maps to NM_198229.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:176798516 T>C maps to ENST00000398128 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr5:176793927 C>T maps to ENST00000398128 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr1:192150503 C>T maps to NM_130782.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr8:54852242 C>T maps to NM_170587.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:101083656 A>G maps to NM_015668.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr8:101075865 G>C maps to NM_015668.3 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr8:101020623 C>T maps to NM_015668.3 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr8:100994226 G>A maps to NM_015668.3 Q1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr9:116247926 C>T maps to NM_144488.4 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr9:116241772 C>T maps to NM_144488.4 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr1:163044343 T>A maps to NM_001102445.2 C301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:163044338 C>T maps to NM_001102445.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:163131766 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr1:240976994 G>A maps to ENST00000407727 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr1:240966281 G>C maps to ENST00000407727 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr1:241094015 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr1:240990396 C>A did not map to a codon.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr1:240975338 C>A maps to ENST00000407727 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:240969543 G>A maps to ENST00000407727 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:63904997 C>T maps to NM_001029875.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr5:63894217 T>A maps to NM_001029875.1 L213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06N-01A-11W-A019-09 chr1:182616031 G>C maps to NM_033345.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:63204105 C>T maps to NM_003835.3 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FE-01A-11D-A13L-09 chr6:49582474 G>A maps to NM_000324.2 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U0-01A-11D-A10G-09 chr2:227731980 G>T maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:74472979 C>T maps to NM_024599.5 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:74471186 G>C maps to NM_024599.5 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr17:74469973 C>A maps to NM_024599.5 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr17:30648094 C>T maps to NM_138328.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:156351625 A>G maps to NM_020407.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr15:90016020 G>T maps to NM_016321.1 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr15:90026414 G>A maps to NM_016321.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WT-01A-11D-A10G-09 chr12:49459215 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:20647564 C>A maps to NM_004040.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr2:20647543 C>T maps to NM_004040.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:62648542 G>A maps to NM_014836.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr8:22862904 C>T maps to NM_001160036.1 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr5:95084069 C>G maps to NM_014899.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:66838014 T>C maps to NM_014578.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr4:40245080 C>T maps to NM_004310.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr14:63757636 G>A maps to NM_020663.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SX-01A-12D-A099-09 chr2:46803350 A>G maps to NM_012249.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:30498101 T>C maps to NM_001033568.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr17:30551655 C>G maps to NM_001033568.1 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr16:723515 C>T maps to NM_138769.1 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:119249599 T>C did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:119249528 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr23:119293025 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr23:119292961 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:119297566 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:119211022 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr23:119293080 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr23:119293090 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:119211053 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:144461120 C>A maps to ENST00000422773 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr8:144463487 A>T maps to ENST00000422773 K512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr19:33493751 G>A maps to NM_033103.4 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr19:33470934 G>A maps to NM_033103.4 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:53454978 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:53454978 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:53453287 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr23:53453288 G>A did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr11:209306 G>T maps to NM_021932.4 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr11:209709 G>T maps to NM_021932.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr11:210569 G>C did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:209436 G>T maps to NM_021932.4 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:209669 G>A maps to NM_021932.4 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:12846951 G>A maps to NM_014859.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr17:12799746 G>A maps to NM_014859.4 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:12847443 C>T maps to NM_014859.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr5:38958579 G>A maps to ENST00000296782 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr5:38952358 T>C maps to ENST00000296782 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr5:38944600 G>C maps to ENST00000296782 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr5:38949950 C>T maps to ENST00000296782 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:152322144 T>G maps to NM_018151.4 G2037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr2:152324647 T>G maps to NM_018151.4 T2245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:152289600 T>C maps to NM_018151.4 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:124008108 C>T maps to NM_178314.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr12:124008164 G>A maps to NM_178314.3 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:123957183 C>T maps to NM_178314.3 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr12:130892282 G>A maps to NM_015347.4 N971N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr12:130921494 C>A maps to NM_015347.4 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr12:130926627 G>A maps to NM_015347.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr12:130927140 G>A maps to NM_015347.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr12:130898668 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr12:130926615 G>T maps to NM_015347.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr12:130941039 C>G did not map to a codon.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr12:130935808 C>T maps to NM_015347.4 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr22:20457059 C>G maps to NM_015672.1 V1414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:104709397 T>G maps to NM_001100117.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:105025834 A>C maps to NM_001100117.2 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:105263948 A>C maps to NM_001100117.2 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:104948869 G>T maps to NM_001100117.2 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:41095015 C>G maps to NM_014747.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr20:19970722 G>A maps to ENST00000255006 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr20:19915792 G>A maps to ENST00000255006 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr14:93118023 C>G maps to NM_024832.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr14:93118713 C>A maps to NM_024832.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr7:105205802 C>T maps to NM_021930.4 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr6:7405581 C>G maps to NM_031480.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr6:7393370 C>T maps to NM_031480.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr6:3081256 C>T maps to NM_003804.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr6:3111035 G>A did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr8:90777696 C>T maps to NM_003821.5 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr14:24808753 G>A maps to NM_006871.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:106144759 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:106145376 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:106144712 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:155874116 G>C maps to ENST00000368322 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr1:155874569 A>T maps to ENST00000368322 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr18:40503614 G>A maps to NM_002930.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:40702531 C>T maps to NM_012421.3 R720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:40704441 C>T maps to NM_012421.3 V1356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:40702531 C>T maps to NM_012421.3 R720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr1:40654737 A>G maps to NM_012421.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr1:40697287 G>A maps to NM_012421.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:40701829 G>T maps to NM_012421.3 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:73812247 G>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:73812680 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:73814165 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr23:73812044 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:5300361 C>T maps to NM_134441.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr16:67683045 G>A maps to NM_001013838.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:67685160 T>G maps to NM_001013838.1 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:67684004 C>T maps to NM_001013838.1 H712H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A153-01A-12D-A12B-09 chr16:67685826 C>T maps to NM_001013838.1 D864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr16:67682004 C>T maps to NM_001013838.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr9:86617622 C>T maps to NM_024945.2 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr6:151748624 T>A maps to NM_017909.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr6:151738412 C>A did not map to a codon.
Sequencing variant TCGA-C8-A133-01A-32D-A12B-09 chr6:151743698 C>A maps to NM_017909.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr14:21359856 A>G maps to NM_002935.2 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:21167835 T>G maps to NM_194431.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr14:21511330 G>A maps to NM_032572.3 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr14:21024982 G>T maps to NM_001110361.1 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr14:21026772 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0ST-01A-12D-A099-09 chr19:12917876 G>A maps to NM_006397.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr1:182551305 G>A maps to NM_021133.3 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:31495401 C>T maps to NM_013235.4 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:31526196 G>A maps to NM_013235.4 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr12:49251829 G>A maps to NM_014470.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:49259481 C>T maps to NM_014470.3 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr2:151326602 C>T maps to NM_005168.3 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:120995233 C>T maps to ENST00000458409 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr2:86831286 G>A maps to NM_005667.3 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr2:86832075 C>T maps to NM_005667.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr15:59373483 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:119005242 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:119005375 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr23:119004954 T>C did not map to a codon.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr23:119005192 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:119005191 C>T did not map to a codon.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr23:119005096 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr23:119005193 C>T did not map to a codon.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr23:119004943 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:49739543 G>A maps to NM_022064.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr3:49750024 C>A maps to NM_022064.2 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A099-01A-11W-A019-09 chr23:105937247 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:106034296 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:105970596 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr23:105937521 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:105970245 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr3:149678698 C>T maps to NM_007282.4 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr5:179440192 C>A maps to NM_018434.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr7:122338267 T>G maps to NM_139175.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:122338357 G>A maps to NM_139175.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:29326193 G>A maps to NM_032322.3 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:141354477 A>C maps to NM_183399.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr5:141359788 G>A maps to NM_183399.1 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:141359788 G>A maps to NM_183399.1 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr2:7164586 G>A maps to NM_014746.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:158601063 G>A maps to NM_144726.2 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr7:122342505 G>T maps to NM_198085.1 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr7:122342072 G>A maps to NM_198085.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:30365114 C>T maps to NM_015565.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr21:30342947 G>A maps to NM_015565.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr21:30332983 G>C maps to NM_015565.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:196199118 C>T maps to NM_152617.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:196199265 C>T maps to NM_152617.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr13:25424487 T>G maps to ENST00000381927 G1086G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr8:42711535 C>T maps to NM_030954.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr6:13977595 C>G maps to NM_001165033.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr8:101271467 G>A maps to NM_183419.1 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:101273924 A>C maps to NM_183419.1 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr8:101271359 G>C maps to NM_183419.1 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr1:185060755 C>T maps to NM_007212.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr9:104302597 A>C maps to NM_019592.5 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DG-01A-21D-A12Q-09 chr1:6272427 C>T maps to NM_207396.2 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr1:6271953 G>A maps to NM_207396.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr4:1107206 T>G maps to NM_001131034.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr17:78320720 G>A maps to NM_020914.4 P2911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr17:78313851 G>C maps to NM_020914.4 L1944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:78346802 G>A maps to NM_020914.4 L4309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:78321588 G>T maps to NM_020914.4 E3201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:78351595 G>A maps to NM_020914.4 E4564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:78320639 G>A maps to NM_020914.4 Q2884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:78320423 T>C maps to NM_020914.4 I2812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr17:78358924 A>G maps to NM_020914.4 Q4852Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr17:78306164 C>T maps to NM_020914.4 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A145-01A-11D-A10Y-09 chr17:78264524 C>T maps to NM_020914.4 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:78280204 C>T maps to NM_020914.4 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:78307960 C>A maps to NM_020914.4 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr17:78263573 T>G maps to NM_020914.4 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:117150622 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr6:125397898 C>T maps to NM_152553.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:79191223 G>C maps to NM_024546.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr1:44877904 C>T maps to ENST00000453887 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr11:119206392 C>T maps to NM_032015.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:119206923 G>A maps to NM_032015.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:24617259 C>T maps to NM_017999.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr14:24617077 C>T maps to NM_017999.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr7:156450901 G>A maps to NM_001184997.1 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:121854107 A>C maps to NM_194271.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr12:121853972 G>A maps to NM_194271.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr9:36344830 A>G maps to NM_022781.4 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:56601467 C>T maps to NM_194359.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr12:56607764 C>A maps to NM_194359.1 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr12:56600314 G>A maps to NM_194359.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr13:26788188 C>T maps to NM_005977.3 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr13:26788507 G>C maps to NM_005977.3 S504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:141464079 C>G maps to NM_014245.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:141464117 G>A maps to NM_014245.3 *114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:37336597 T>G maps to NM_003958.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr6:37349062 T>C maps to NM_003958.3 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr11:499130 G>C maps to NM_203389.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr11:502135 G>A maps to NM_203389.1 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr10:90122431 G>A maps to NM_001031709.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr10:90341438 G>A maps to NM_001031709.2 G84G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AO-A0J9-01A-11W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr17:685929 G>A maps to ENST00000397393 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:201969070 C>T maps to NM_020216.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr16:2313110 C>T maps to NM_080594.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr3:78666818 C>G maps to NM_002941.3 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr3:78737827 T>A maps to NM_002941.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:78700969 C>T maps to NM_002941.3 W908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr3:77612342 C>T maps to ENST00000332191 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr3:77571961 A>G maps to ENST00000332191 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr3:77147252 G>T maps to ENST00000332191 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr11:124742416 C>T maps to NM_022370.3 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:124742308 G>A maps to NM_022370.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:124739878 C>G maps to NM_022370.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:124756684 T>G maps to NM_019055.5 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:124764190 G>T maps to NM_019055.5 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr11:124763621 C>T maps to NM_019055.5 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr18:18586383 G>A maps to NM_005406.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr18:18572890 A>G maps to NM_005406.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PV-01A-11D-A28B-09 chr18:18546961 A>G maps to NM_005406.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:11332422 C>T maps to NM_004850.3 Q1338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:11338704 G>C maps to NM_004850.3 S1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr2:11355159 A>T maps to NM_004850.3 L581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr9:115038243 C>T maps to NM_001163790.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr11:62381061 G>T maps to NM_000327.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr3:123688910 G>A maps to NM_017578.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr3:123694369 G>A maps to NM_017578.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr3:125690995 C>T maps to NM_001012337.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr3:125694465 C>T maps to NM_001012337.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:64516388 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:64624666 C>G maps to NM_005012.2 S393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:64643811 C>T maps to NM_005012.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr9:94486603 G>A maps to NM_004560.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr9:94495596 C>T maps to NM_004560.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr9:77300401 C>T maps to ENST00000396204 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:151787668 C>T maps to ENST00000392697 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:117706914 A>G maps to NM_002944.2 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:117710572 G>A maps to NM_002944.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr6:117642470 G>A maps to NM_002944.2 R1910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr6:117658500 C>T maps to NM_002944.2 W1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr6:117658377 C>T maps to NM_002944.2 T1735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr6:117632211 G>C maps to NM_002944.2 V2068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr8:55534762 C>T maps to NM_006269.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:55540660 G>T maps to NM_006269.1 E1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:55542259 G>T maps to NM_006269.1 E1940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:55539011 C>A maps to NM_006269.1 S857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr8:55533669 C>T maps to NM_006269.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:55533669 C>T maps to NM_006269.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr8:55539492 G>A maps to NM_006269.1 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr8:55540309 C>T maps to NM_006269.1 Q1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SQ-01A-21D-A142-09 chr8:10466299 G>A maps to NM_178857.5 Q1770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr8:10480627 G>T maps to NM_178857.5 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:10465892 A>C maps to NM_178857.5 G1905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:10466144 T>C maps to NM_178857.5 G1821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:10470384 C>T maps to NM_178857.5 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HU-01A-11W-A050-09 chr8:10466219 G>T maps to NM_178857.5 G1796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr23:46713074 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:46713149 C>T did not map to a codon.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr23:46696578 C>G did not map to a codon.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr23:46736939 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:96139470 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr23:96139694 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:96140073 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:96139823 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:41819478 C>T maps to NM_015540.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr15:41821753 G>A maps to NM_015540.2 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr15:41820177 G>A maps to NM_015540.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:92789577 T>G maps to NM_024813.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr1:92789085 A>G maps to NM_024813.2 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr1:92789907 C>T maps to NM_024813.2 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:48062805 G>A maps to NM_024604.2 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FO-01A-11D-A17W-09 chr2:210881289 G>A maps to NM_199229.1 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:68895511 C>A maps to NM_000329.2 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:84945164 C>T maps to NM_025065.6 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr23:38160591 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr23:38146054 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:38145106 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:38145214 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:38176594 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:38158322 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:38146232 C>G did not map to a codon.
Sequencing variant TCGA-AR-A24X-01A-11D-A167-09 chr23:38146401 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:38144854 C>A did not map to a codon.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr23:38145734 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr23:38160624 C>A did not map to a codon.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr23:38182683 G>A did not map to a codon.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr23:38145825 T>C did not map to a codon.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr23:38146287 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:38146012 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:21770704 T>C maps to NM_020366.3 N183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IK-01A-11D-A17G-09 chr16:53706823 T>C maps to NM_015272.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr12:113307579 G>A maps to NM_001143854.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr2:89034082 C>T maps to NM_144563.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr23:153628243 C>G did not map to a codon.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr23:153628160 A>C did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:153628918 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0W5-01A-11D-A10G-09 chr6:35436735 G>A maps to NM_007104.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:35438058 C>G maps to NM_007104.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:47017914 C>T maps to NM_001035006.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr18:47017222 A>C maps to NM_001035006.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr17:37358624 G>A maps to NM_000981.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MS-A51U-01A-31D-A25Q-09 chr17:27047043 G>A maps to NM_000984.5 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr22:39711521 C>G maps to NM_000967.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:100646779 T>G did not map to a codon.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr23:100646802 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:2002909 G>A maps to NM_005061.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr15:66795049 G>A maps to NM_000968.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:93301751 C>G maps to NM_000969.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LI-01A-12D-A159-09 chr12:112846112 G>C maps to NM_001024662.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr8:74204932 G>T maps to ENST00000396470 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr8:74204478 G>A maps to ENST00000396470 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:146015838 A>C maps to NM_000973.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T1-01A-21D-A099-09 chr12:120636934 A>G maps to NM_053275.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr12:120634623 T>C maps to NM_053275.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr20:35858459 C>T maps to NM_002951.3 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AU-01A-11D-A12Q-09 chr10:92656099 C>T maps to ENST00000458617 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr10:92660381 A>T maps to ENST00000458617 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LM-01A-11D-A17W-09 chr18:33647352 A>G maps to NM_018170.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:36676791 G>C maps to NM_021215.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr20:36676791 G>A maps to NM_021215.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr20:36718277 G>C did not map to a codon.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr1:150444408 A>G maps to NM_015203.3 K995K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:150443697 C>T maps to NM_015203.3 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr1:150444378 G>A maps to NM_015203.3 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:150443733 A>C maps to NM_015203.3 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr1:150444066 A>G maps to NM_015203.3 Q881Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:150443265 C>T maps to NM_015203.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:149826501 A>C maps to NM_005617.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr5:149825181 G>A maps to NM_005617.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr19:39924347 G>T maps to NM_001020.4 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr8:56985780 C>G maps to NM_001146227.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr20:60963387 C>T maps to NM_001024.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr23:71493101 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr23:71494956 G>C did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr23:71493126 G>T did not map to a codon.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr9:19379493 T>C maps to NM_001010.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:26882030 G>A maps to NM_001006665.1 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr6:166923826 G>T maps to ENST00000510118 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr6:166952215 C>T maps to ENST00000510118 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:20183076 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:20174288 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:20183108 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:20213248 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr23:20185729 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr23:20195138 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr23:20212320 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:20213260 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr23:83411144 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:83402051 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr23:83361976 T>C did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr23:83319325 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:83372092 G>A did not map to a codon.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr23:83352799 A>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:83389806 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr17:58011558 A>G maps to NM_003161.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr11:67196635 G>A maps to NM_003952.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr11:67200918 G>T did not map to a codon.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr1:213303215 C>T maps to NM_012424.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J1-01A-11D-A20S-09 chr14:75375555 T>G maps to NM_031464.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:54705144 G>T maps to NM_001013.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:152128200 G>A maps to NM_001122965.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:152129394 G>T maps to NM_001122965.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr1:152130350 C>G maps to NM_001122965.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr1:152128041 A>G maps to NM_001122965.1 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr17:78923267 G>A maps to NM_020761.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:78820338 C>T maps to NM_020761.2 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr17:78897382 G>A maps to NM_020761.2 P906P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr17:78704421 G>T maps to NM_020761.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JS-01A-11D-A13L-09 chr11:126075477 G>A maps to NM_032795.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr2:219457091 G>A maps to NM_005444.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:39311644 G>C maps to NM_022157.2 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LH-01A-31D-A18P-09 chr6:90097117 G>A maps to NM_021244.4 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:50139932 G>A maps to NM_006270.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:17640693 G>C maps to ENST00000377813 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr20:17596585 C>G maps to ENST00000377813 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr20:17602409 G>A maps to ENST00000377813 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr6:7226852 G>A maps to NM_001003699.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:7211828 T>G maps to NM_001003699.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:7229819 A>C maps to NM_001003699.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr6:7230725 G>C maps to NM_001003699.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A133-01A-32D-A12B-09 chr6:7189438 A>G maps to NM_001003699.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr4:110756590 C>T maps to NM_006583.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr2:10269009 A>G maps to NM_001165931.1 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:15157140 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:15162054 T>C maps to NM_018427.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:15180233 G>A maps to NM_018427.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr21:45223489 T>G maps to NM_003683.5 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr21:45222218 G>A maps to NM_003683.5 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr10:99130257 G>A maps to NM_015179.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:99118364 A>C maps to NM_015179.3 G1240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:99141180 C>T maps to NM_015179.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FE-01A-11D-A19Y-09 chr10:99118292 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr10:99132554 C>T maps to NM_015179.3 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:218480876 C>G maps to NM_016052.3 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:6621411 G>A maps to NM_015324.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:51969379 G>A maps to NM_004704.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr23:18662717 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0DV-01A-21D-A12Q-09 chr17:48557114 G>A maps to NM_018346.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr17:48560767 G>T maps to NM_018346.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:7018228 C>T maps to NM_080657.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr1:114308630 G>A maps to NM_018364.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr1:114340404 T>C maps to NM_018364.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:15988078 T>C maps to NM_006511.1 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:15987463 T>C maps to NM_006511.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr1:15987817 C>T maps to NM_006511.1 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr11:77404596 C>G maps to NM_016578.3 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr7:6820476 C>T maps to NM_173565.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:116949423 T>G maps to NM_001010892.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr6:116938342 C>G maps to NM_001010892.2 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr19:46307977 G>A maps to NM_030785.3 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:46318101 G>A maps to NM_030785.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:46307900 G>C maps to NM_030785.3 S421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr1:38078564 G>T maps to NM_001038633.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:57246891 C>T maps to NM_133368.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:123001880 C>T maps to NM_023012.5 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr19:12945619 T>C maps to NM_031429.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr19:12936702 G>A maps to NM_031429.1 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr19:12939556 G>A maps to NM_031429.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:100740416 C>T maps to NM_001130841.1 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr22:23401816 C>A maps to NM_014433.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr20:62322278 G>C maps to ENST00000482936 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr20:62311270 G>A maps to ENST00000482936 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr20:62293269 C>T maps to ENST00000482936 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr20:62319308 G>T maps to ENST00000482936 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr2:74653444 T>G maps to NM_001015055.1 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr2:74659724 T>C maps to NM_001015055.1 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr14:101350747 G>A maps to NM_001134888.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr14:101350432 G>A maps to NM_001134888.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr14:101350111 T>A maps to NM_001134888.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27A-01A-11D-A167-09 chr14:101349799 G>A maps to NM_001134888.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr19:45991898 A>T maps to NM_005619.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BF-01A-21D-A12Q-09 chr19:45997922 C>T maps to NM_005619.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:63486545 C>A maps to ENST00000377819 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr2:55214628 G>A maps to NM_020532.4 F1073F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BS-01A-11D-A12Q-09 chr6:107070839 A>G maps to NM_032730.4 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y2-01A-11D-A159-09 chr6:107070755 C>A maps to NM_032730.4 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr17:1840863 G>C maps to NM_178568.2 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr17:1839852 C>T maps to NM_178568.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr11:57235331 C>T maps to NM_178570.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:187416723 G>A maps to NM_001004312.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr3:187088788 G>A maps to NM_022147.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr18:67759381 A>G maps to NM_173630.3 A1369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IE-01A-11W-A050-09 chr18:67863737 G>A maps to NM_173630.3 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EA-01A-11D-A10Y-09 chr18:67727269 C>A maps to NM_173630.3 E1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:179016621 C>T maps to NM_025158.3 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:70143577 G>A maps to NM_017987.4 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr10:70153887 T>A maps to NM_017987.4 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr10:70156613 C>T maps to NM_017987.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:41143192 G>A maps to NM_173079.2 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:87407140 C>T maps to NM_138290.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FB-01A-11D-A17D-09 chr21:36259141 T>A maps to NM_001754.4 K117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr21:36164863 G>A maps to NM_001754.4 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IH-01A-11D-A10Y-09 chr21:36206715 G>A maps to NM_001754.4 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr21:36206752 C>T maps to NM_001754.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr21:36252852 C>G did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr8:93088268 G>A maps to NM_175634.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr8:92998436 G>A maps to NM_175634.2 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:92988196 C>T maps to NM_175634.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr8:92982888 G>A maps to NM_175634.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H6-01A-21W-A071-09 chr8:92972571 C>T maps to NM_175634.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:93088281 C>T did not map to a codon.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr6:45512999 C>T maps to ENST00000359524 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr6:45399749 G>T maps to ENST00000359524 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:45480141 C>A maps to ENST00000359524 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:25228981 G>A maps to NM_001031680.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr1:155298045 C>G maps to NM_001105203.1 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:155294932 C>T maps to NM_001105203.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:127816332 G>A maps to NM_003707.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:127819556 C>A maps to NM_003707.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr3:127800191 G>A maps to NM_003707.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YN-01A-11D-A28B-09 chr21:30391544 C>G maps to NM_016940.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr1:95710161 A>T maps to NM_015485.4 K161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:184577114 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:159573000 G>T maps to ENST00000440678 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr5:33937027 G>A maps to NM_016568.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr9:137309061 C>T maps to NM_002957.4 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:165386386 G>A maps to NM_006917.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr1:165370565 G>A maps to NM_006917.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr1:165398093 T>G maps to NM_006917.4 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:165386310 G>A maps to NM_006917.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr1:165380212 G>A maps to NM_006917.4 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr19:39018369 G>A maps to NM_000540.2 E3590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr19:39025993 C>T maps to NM_000540.2 G3826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr19:38976763 G>A maps to NM_000540.2 G1823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09V-01A-11D-A045-09 chr19:38976253 G>A maps to NM_000540.2 S1653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr19:38966089 G>A maps to NM_000540.2 T1431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:38979987 G>T maps to NM_000540.2 E1907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:39075590 G>C maps to NM_000540.2 L4885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:38958301 G>A maps to NM_000540.2 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:39025385 C>A maps to NM_000540.2 L3762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:38954466 G>A maps to NM_000540.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr19:38954139 C>T maps to NM_000540.2 R885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr19:38993591 C>T maps to NM_000540.2 F2636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:39055672 C>T maps to NM_000540.2 F4233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr19:38948693 C>T maps to NM_000540.2 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr19:38959724 C>A maps to NM_000540.2 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:39003070 C>T maps to NM_000540.2 L3140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr19:38942505 C>T maps to NM_000540.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr19:39018354 C>T maps to NM_000540.2 D3585D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr1:237586391 G>T maps to NM_001035.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CH-01A-21W-A019-09 chr1:237947545 C>T maps to NM_001035.2 N4178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:237753281 C>G maps to NM_001035.2 S1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr1:237890430 A>G maps to NM_001035.2 L3590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr1:237947086 T>C maps to NM_001035.2 D4025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:237948217 C>T maps to NM_001035.2 L4402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:237947260 C>T maps to NM_001035.2 F4083F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:237947455 C>A maps to NM_001035.2 V4148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:237972335 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr1:237870516 C>A maps to NM_001035.2 I3283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr1:237801706 G>A maps to NM_001035.2 V2281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:237604720 C>T maps to NM_001035.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HI-01A-11D-A099-09 chr1:237954733 T>C maps to NM_001035.2 Y4494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr1:237813232 C>T maps to NM_001035.2 A2523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr1:237532862 C>T maps to NM_001035.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr1:237608816 T>C maps to NM_001035.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:237895410 G>T maps to NM_001035.2 L3667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr1:237608771 C>G maps to NM_001035.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:237893592 T>C maps to NM_001035.2 Y3624Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr1:237777584 C>T maps to NM_001035.2 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr1:237948028 G>A maps to NM_001035.2 Q4339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr1:237924276 G>T maps to NM_001035.2 E3809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr1:237995856 T>G maps to NM_001035.2 S4938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr1:237550636 C>G maps to NM_001035.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr15:34094086 G>A maps to NM_001036.3 E3312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr15:33927950 G>A maps to NM_001036.3 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr15:33961575 C>T maps to NM_001036.3 Q1881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr15:34115274 T>G did not map to a codon.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr15:33927941 C>T maps to NM_001036.3 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr15:33928728 C>T maps to NM_001036.3 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr15:34130642 C>T maps to NM_001036.3 T4154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr15:33988663 G>T maps to NM_001036.3 E2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr15:34129916 C>T maps to NM_001036.3 F3912F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr15:34113752 C>T maps to NM_001036.3 L3649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr15:33952546 G>A maps to NM_001036.3 V1515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18R-01A-11D-A12B-09 chr15:34113499 C>T maps to NM_001036.3 L3615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr15:34140622 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr15:33954818 G>A maps to NM_001036.3 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr15:33954809 G>A maps to NM_001036.3 T1693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr15:34123204 C>T maps to NM_001036.3 D3792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr15:34064134 C>A maps to NM_001036.3 S2944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr15:33765739 G>T did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr15:33923485 G>T maps to NM_001036.3 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr15:33954809 G>A maps to NM_001036.3 T1693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr15:33944993 C>T maps to NM_001036.3 N1406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr15:34049767 C>A maps to NM_001036.3 A2892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr15:34156377 G>A maps to NM_001036.3 E4835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr15:33954809 G>A maps to NM_001036.3 T1693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr15:34080596 G>T maps to NM_001036.3 A3256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:151958688 T>C maps to NM_002966.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:153598798 G>C maps to NM_001024210.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:153410673 G>C maps to NM_001045479.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:101704656 G>A maps to NM_001400.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:101705562 G>A maps to NM_001400.4 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AQ-01A-11D-A12Q-09 chr19:10334726 G>A maps to NM_004230.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:91616711 C>T maps to NM_005226.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:91617140 C>T maps to NM_005226.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr9:91616634 C>T maps to NM_005226.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr19:3179899 G>A maps to NM_003775.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:18290865 T>C maps to NM_199161.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr11:18269510 G>T maps to NM_030754.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:18253072 A>G maps to NM_006512.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr11:18124893 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:64811983 A>C maps to ENST00000301885 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:23907075 C>A maps to NM_014363.4 E3647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:23907633 C>A maps to NM_014363.4 E3461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:23913540 C>A maps to NM_014363.4 E1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H6-01A-21W-A071-09 chr13:23930147 T>G did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr13:23905512 G>A maps to NM_014363.4 L4168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr13:23928977 G>C maps to NM_014363.4 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr13:23912086 G>C maps to NM_014363.4 T1976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr13:23910499 G>A maps to NM_014363.4 A2505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr19:47653512 C>T maps to NM_005500.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr19:5641893 G>A maps to ENST00000433404 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:234237144 C>T maps to NM_000541.4 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:234255500 G>A maps to NM_000541.4 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:134994975 A>T did not map to a codon.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr23:134995007 A>G did not map to a codon.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr23:134991156 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr23:134991071 A>G did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:134987482 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:134978439 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:134993747 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:134994096 C>T did not map to a codon.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr23:134994547 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr23:134986703 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr23:134990729 T>G did not map to a codon.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr23:134988614 T>C did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:134993409 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JF-01A-11D-A13L-09 chr23:134992587 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:134991925 A>G did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr23:134995025 C>G did not map to a codon.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr23:134988301 G>T did not map to a codon.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr23:134993473 G>C did not map to a codon.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr16:51171178 T>A maps to ENST00000251020 S1273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12H-01A-11D-A10Y-09 chr16:51175175 G>A maps to ENST00000251020 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:51185092 C>T maps to ENST00000251020 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr16:51175499 G>T maps to ENST00000251020 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr14:21991857 G>A maps to NM_005407.1 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr14:21991731 G>A maps to NM_005407.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr20:50405594 C>T maps to NM_020436.3 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr20:50400809 G>A maps to NM_020436.3 V1052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr20:50407392 C>T maps to NM_020436.3 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X7-01A-11D-A14K-09 chr20:50408673 G>A maps to NM_020436.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr19:14199330 C>T maps to ENST00000269724 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr6:130475972 A>C maps to ENST00000457563 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr14:55251056 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr19:39847653 C>T maps to NM_018028.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr3:169644814 C>G maps to NM_182610.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr3:169644853 T>C maps to NM_182610.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:92731164 G>A maps to NM_017654.3 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:92733847 G>A maps to NM_017654.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr7:92733022 G>T maps to NM_017654.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:92763634 G>C maps to NM_152703.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:92761791 C>A maps to NM_152703.2 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:128774073 T>G maps to NM_001145928.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr2:128750776 A>T maps to NM_001145928.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:128767865 C>A maps to NM_001145928.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:128767877 A>G maps to NM_001145928.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:55751014 C>A maps to ENST00000443936 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr19:55743171 G>A maps to ENST00000443936 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr11:68305347 G>A maps to NM_001164160.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:68315554 G>A maps to NM_001164160.1 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:136555503 G>T maps to NM_007101.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr9:136550314 C>T maps to NM_007101.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr9:136594963 G>T maps to NM_007101.3 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr9:136531949 G>T maps to NM_007101.3 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr9:136535740 G>A maps to NM_007101.3 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr17:26723194 G>T maps to ENST00000379061 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:26711584 C>T maps to ENST00000379061 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:109779109 G>A maps to ENST00000369923 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr1:109756667 C>G maps to ENST00000369923 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:39412196 C>T maps to NM_017827.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:39416864 C>A maps to NM_017827.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr11:65744011 C>T maps to NM_005146.4 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:65745367 G>T maps to NM_005146.4 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr11:65744185 G>A maps to NM_005146.4 E602E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr6:148867224 C>T maps to NM_015278.3 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:128926672 T>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:100550982 C>T maps to NM_194292.1 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr23:23801964 T>C did not map to a codon.
Sequencing variant TCGA-AR-A1AP-01A-11D-A12Q-09 chr23:23803898 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:7530313 C>T maps to ENST00000380466 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:18427908 T>G maps to ENST00000332610 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:18436022 T>C maps to ENST00000332610 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:200193422 G>A maps to NM_001172509.1 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr23:84349171 A>T did not map to a codon.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr23:84349939 C>T did not map to a codon.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr23:84362456 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr23:84363425 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:66460353 C>G maps to NM_016038.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr22:50893514 G>A maps to ENST00000337034 L1547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:50885851 C>A maps to ENST00000337034 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr22:50898964 G>A maps to ENST00000337034 L1058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr22:50899060 G>C maps to ENST00000337034 Y1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr22:50903480 G>T maps to ENST00000337034 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr11:9875161 G>A maps to NM_030962.3 R821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:10052690 A>C maps to NM_030962.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:10024131 C>A maps to NM_030962.3 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr11:9853807 G>A maps to NM_030962.3 V1205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr12:123795659 C>G maps to NM_001167856.1 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:123813289 G>A maps to NM_001167856.1 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr12:123789179 C>A maps to NM_001167856.1 G1239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr12:123794130 C>A did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr19:1127656 G>A maps to NM_014963.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:39966000 G>A maps to NM_006455.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:50156059 C>G maps to NM_021228.2 S805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:50148657 C>T maps to NM_021228.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr19:50161136 C>T maps to NM_021228.2 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:127781101 G>C maps to NM_173690.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr15:75143799 A>C maps to NM_005697.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:155231933 C>T maps to NM_005698.2 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:75304188 T>G did not map to a codon.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr15:75305051 C>T maps to ENST00000361900 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr3:47463967 G>A maps to NM_012235.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:47462166 C>G maps to NM_012235.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr3:47484390 G>A maps to NM_012235.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:77096878 T>C maps to ENST00000324767 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LN-01A-21D-A18P-09 chr15:76763567 C>T maps to ENST00000324767 L1021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr8:27528480 C>T maps to NM_016240.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:27767261 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr8:27845102 G>A maps to NM_173833.5 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:125292370 T>G maps to NM_005505.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr12:125292446 G>T maps to NM_005505.4 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr4:77100834 C>T maps to NM_005506.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:83626522 A>C maps to NM_001037582.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr4:83552509 C>G maps to NM_001037582.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:78184242 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:31107336 C>T maps to ENST00000311943 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:54231505 A>C maps to NM_152540.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr4:54231619 A>T maps to NM_152540.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr4:54011746 G>A maps to NM_152540.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:224462746 T>G maps to NM_003469.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr2:224462620 C>T maps to NM_003469.4 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:51975584 C>T maps to NM_013243.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr15:32988744 C>T maps to NM_001144757.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr11:62009820 C>T maps to NM_006551.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IO-01A-11D-A142-09 chr11:62065068 G>A maps to NM_206998.1 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:61976232 G>A maps to NM_002407.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr19:35085142 G>A maps to NM_001025591.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr19:35085447 G>T maps to NM_001025591.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:12668844 G>A maps to NM_001112706.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr7:12620846 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr4:129964597 C>T maps to NM_144643.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:239005490 C>T maps to NM_016510.4 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr1:41617300 G>A maps to NM_001031694.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr1:41512121 G>C maps to NM_001031694.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:41579177 G>A maps to NM_001031694.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:17768234 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr23:17768274 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:17768338 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr23:17768112 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:18276273 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:18323136 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:18323136 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:18264848 G>A did not map to a codon.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr23:18278328 T>C did not map to a codon.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr23:18342119 T>C did not map to a codon.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr3:38753807 G>A maps to NM_006514.2 I1311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:38783991 T>G maps to NM_006514.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:38797325 C>A maps to NM_006514.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr3:38802769 G>A maps to NM_006514.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:38938591 G>C maps to ENST00000302328 S716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr3:38938446 G>A maps to ENST00000302328 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr3:38889048 G>C maps to ENST00000302328 L1504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr2:166848243 G>C maps to NM_001165963.1 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:166848777 C>T maps to NM_001165963.1 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:166904220 G>T maps to NM_001165963.1 Y362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr19:35530583 G>A maps to NM_001037.4 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:166210775 C>T maps to NM_001040142.1 N998N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr2:166245631 C>A maps to NM_001040142.1 I1772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr2:166246183 G>A maps to NM_001040142.1 E1956E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W3-01A-11D-A10G-09 chr2:166245337 C>T maps to NM_001040142.1 Y1674Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:166020197 G>A maps to NM_006922.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr2:166020191 G>T maps to NM_006922.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr2:165947250 C>T maps to NM_006922.3 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:165946940 G>A maps to NM_006922.3 Q1908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr17:62045590 C>T maps to NM_000334.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr17:62049997 G>A maps to NM_000334.4 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr17:62025336 G>A maps to NM_000334.4 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr17:62026000 G>A maps to NM_000334.4 V1038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:62038791 C>A did not map to a codon.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr17:62034710 G>A maps to NM_000334.4 C729C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr17:62019252 G>A maps to NM_000334.4 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr17:62019024 G>A maps to NM_000334.4 D1539D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr17:62018349 G>A maps to NM_000334.4 D1764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:62019084 G>A maps to NM_000334.4 F1519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:62020327 C>T maps to NM_000334.4 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr17:62026012 C>T maps to NM_000334.4 E1034E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:38651375 G>A maps to NM_001099404.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:38601832 G>A maps to NM_001099404.1 I1350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:38647443 C>A maps to NM_001099404.1 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:38655496 C>T maps to NM_001099404.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr3:38593035 C>T maps to NM_001099404.1 S1609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:38616940 G>T maps to NM_001099404.1 G1171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr3:38647464 C>A maps to NM_001099404.1 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr3:38627265 C>T maps to NM_001099404.1 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:167327217 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:167289025 C>T maps to NM_002976.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:167313381 C>A maps to NM_002976.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr2:167301343 G>A maps to NM_002976.2 N518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr12:52082601 G>A maps to NM_014191.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:52156411 G>C maps to NM_014191.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr12:52200942 T>C maps to NM_014191.2 R1891R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr2:167159747 C>T maps to ENST00000303354 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YI-01A-31D-A10M-09 chr2:167099092 C>T maps to ENST00000303354 R1183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:167141109 T>G maps to ENST00000303354 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr2:167060935 C>T maps to ENST00000303354 K1480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr2:167055874 G>A maps to ENST00000303354 V1759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:167129103 G>A maps to ENST00000303354 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr16:23360075 G>A maps to ENST00000307331 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr4:141294857 G>A maps to NM_001153484.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:55065575 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:144892909 G>A maps to NM_182706.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:144895653 G>C maps to NM_182706.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr7:29963713 C>T maps to NM_001145514.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:29983716 A>C maps to NM_001145514.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:45917621 G>A maps to NM_138355.3 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:45917716 G>A maps to NM_138355.3 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:175263037 C>T maps to NM_024583.4 F9F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AN-A0AK-01A-21W-A019-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:43619222 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr22:43634955 C>T maps to NM_173050.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr22:43634853 C>T maps to NM_173050.2 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr11:9080883 T>C maps to ENST00000457346 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:9081967 C>T maps to ENST00000457346 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:35200678 G>A maps to ENST00000394681 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr6:35213838 C>T maps to ENST00000394681 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr11:65294576 G>T maps to NM_020680.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr11:65305348 C>T maps to NM_020680.3 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr11:65293725 C>T maps to NM_020680.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:65293614 C>G maps to NM_020680.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Y-01A-21W-A019-09 chr12:100676853 C>T maps to NM_017988.4 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:169831923 C>A maps to NM_181093.2 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr1:169857903 A>C maps to NM_181093.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr1:169825045 C>T maps to NM_181093.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr4:76891501 C>G maps to NM_018115.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr4:76878696 A>T maps to NM_018115.2 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:76878804 G>A maps to NM_018115.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr2:20403761 C>A maps to NM_001006946.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:20402586 C>T maps to NM_001006946.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:31350003 G>A maps to NM_014654.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:43964514 G>A maps to NM_002999.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr8:59492211 G>A maps to NM_005625.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:1293000 G>A maps to NM_080489.4 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:50253455 G>A maps to NM_004713.3 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr9:139301959 G>T maps to NM_001039707.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr5:236616 G>A maps to NM_004168.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr11:111958686 G>A maps to NM_003002.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:4051819 A>C maps to NM_152744.3 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:4259822 C>A maps to NM_152744.3 T1874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:4056934 C>T maps to NM_152744.3 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr7:4285427 A>C maps to NM_152744.3 S2124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr7:4249711 C>T maps to NM_152744.3 N1819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr7:4213861 G>A maps to NM_152744.3 R1603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr17:71410869 G>A maps to NM_001144952.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:71415321 G>C maps to NM_001144952.1 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr17:71375644 G>T maps to NM_001144952.1 Y1602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr17:71431697 G>A maps to NM_001144952.1 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr2:192700906 C>T maps to NM_004657.5 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr8:57214112 C>A maps to NM_138969.2 G286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr8:57228666 T>G maps to NM_138969.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:57317826 G>A maps to NM_148897.2 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:113867089 C>T maps to NM_138432.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr17:26691975 G>A maps to NM_001080837.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr3:10354320 C>T maps to ENST00000343726 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr22:30818389 G>A maps to NM_012429.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06T-01A-11W-A019-09 chr22:30891390 G>A maps to NM_174977.3 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:30890861 G>A maps to NM_174977.3 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr22:30891944 G>A maps to NM_174977.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr16:5038172 C>T maps to NM_014692.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr16:5038148 G>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:139357506 A>G maps to NM_014866.1 N1575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:177901869 T>G maps to NM_033127.2 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr1:177905471 G>A maps to NM_033127.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:177930797 G>A maps to NM_033127.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:42610511 C>G maps to NM_032970.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr20:18523791 G>A maps to NM_001172745.1 W547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:134039560 G>A maps to NM_021982.1 E793E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr5:134059306 C>T maps to NM_021982.1 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr5:134011802 C>T maps to NM_021982.1 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr5:134032904 C>T maps to NM_021982.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr5:133997100 C>A maps to NM_021982.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr4:110448568 C>T maps to NM_006323.2 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr4:110460810 C>T maps to NM_006323.2 Q1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:110384066 G>A maps to NM_006323.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:110415769 G>T did not map to a codon.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr4:110384523 C>T maps to NM_006323.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A145-01A-11D-A10Y-09 chr4:110454804 T>G maps to NM_006323.2 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr10:75525330 C>T maps to NM_198597.1 C450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr10:75528882 C>T maps to NM_198597.1 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr10:75530079 C>T maps to NM_198597.1 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr10:75520489 G>C maps to NM_198597.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:102267699 C>A maps to NM_015490.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J5-01A-11W-A050-09 chr10:102247411 C>T maps to NM_015490.3 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr10:102266116 C>T maps to NM_015490.3 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:169700700 T>G did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr6:108246120 A>C maps to NM_007214.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:91953428 G>A maps to NM_024077.3 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr15:49309149 G>A maps to NM_001193489.1 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:49320845 G>C maps to NM_001193489.1 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr17:80282640 C>A maps to NM_003004.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr14:81953844 C>T maps to NM_005065.4 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr14:81969227 C>A did not map to a codon.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr14:81955631 A>G maps to NM_005065.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr20:13912404 C>A maps to NM_025229.1 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr20:13830251 T>A did not map to a codon.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr20:13846123 C>A maps to NM_025229.1 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:25806330 C>T maps to NM_015187.3 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr4:25750061 C>T maps to NM_015187.3 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:25849036 G>A maps to NM_015187.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr1:169698644 C>T maps to NM_000450.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr1:169696915 G>A maps to NM_000450.2 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U0-01A-11D-A10G-09 chr1:169679647 C>T maps to NM_000655.4 W18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr22:50649204 C>T maps to NM_031454.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr1:169578895 G>A maps to NM_003005.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr3:150321283 T>A maps to NM_016275.3 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr7:83675754 T>G maps to NM_006080.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:83764202 G>T maps to NM_006080.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr3:50310759 G>A maps to NM_004636.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr7:80418801 C>A maps to NM_006379.2 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:80427530 G>A maps to NM_006379.2 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:80394493 G>A maps to NM_006379.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr7:84670041 G>A maps to NM_152754.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:84697513 T>C maps to NM_152754.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr7:84649619 T>A maps to NM_152754.2 K478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr7:84644490 G>C maps to NM_152754.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr7:83119462 G>A maps to NM_012431.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:83035375 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:82997141 A>G maps to NM_012431.2 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:50220386 G>A maps to NM_004186.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr3:50211373 C>T maps to NM_004186.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr3:50225260 C>T maps to NM_004186.3 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr3:50224044 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1L9-01A-11D-A13L-09 chr3:52469819 G>A maps to NM_020163.1 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:156146368 C>T maps to NM_022367.3 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:90760782 C>G maps to NM_198925.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr9:92017793 G>A maps to NM_006378.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:91993810 G>A maps to NM_006378.3 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr2:74902497 C>G maps to NM_004263.3 L453L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AC-A23H-01A-11D-A159-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:102743095 C>T maps to NM_017893.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:102740652 C>T maps to NM_017893.2 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr5:9066542 G>T maps to NM_003966.2 C763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr5:9154768 G>A maps to NM_003966.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr5:9108317 G>A maps to NM_003966.2 C669C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IY-01A-21D-A21Q-09 chr3:122631792 G>A maps to NM_001031702.2 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr3:122641111 G>A maps to NM_001031702.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr3:122630347 G>A maps to NM_001031702.2 T1027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:115813552 T>G maps to ENST00000257414 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr5:115782653 A>G maps to ENST00000257414 Y933Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr19:4555003 G>A maps to NM_032108.3 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:48052586 C>T maps to NM_153618.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr15:48059232 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27W-01A-11D-A16D-09 chr15:48052558 G>A maps to NM_153618.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr20:43837006 C>T maps to NM_003007.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:43850671 C>T maps to NM_003008.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:43850896 T>C maps to NM_003008.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr12:48439118 G>A maps to ENST00000004980 R641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr12:48468347 T>A maps to ENST00000004980 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:185304284 G>A maps to ENST00000427465 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:185337232 C>G maps to ENST00000427465 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr17:7468904 G>C did not map to a codon.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr6:76412368 G>A maps to NM_015571.2 W766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr6:76380372 C>A maps to NM_015571.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:101083787 C>A maps to NM_020654.3 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:101062690 A>G maps to NM_020654.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:101083809 T>C maps to NM_020654.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr10:13378338 C>T maps to NM_012247.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr5:42801109 G>C maps to NM_001093726.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr16:30393471 G>C maps to NM_052838.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr16:30392784 C>A maps to NM_052838.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:110303649 C>T maps to ENST00000356688 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr16:4834056 G>A maps to NM_144605.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr16:4829724 G>A maps to NM_144605.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:242265526 C>T maps to ENST00000391972 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:42392934 A>C maps to NM_145733.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr22:42388723 C>G maps to NM_145733.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr17:56598441 C>G maps to NM_004574.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr22:19707719 G>C maps to NM_002688.5 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr22:19708173 G>A maps to NM_002688.5 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:118771005 C>G did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr7:35942762 C>T maps to NM_001788.4 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr5:132101176 C>G maps to NM_001098811.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EW-01A-11D-A135-09 chr17:75471845 C>T maps to NM_001113495.1 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:158532534 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:17981061 C>T maps to NM_012139.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr1:31905814 C>T maps to NM_178865.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:31896631 C>T maps to NM_178865.4 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:43138621 G>A maps to NM_006811.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:44087638 G>A maps to ENST00000319327 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr5:79439629 G>A maps to NM_001174072.1 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr5:79439629 G>A maps to NM_001174072.1 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr14:94849022 G>C maps to NM_001127707.1 Y184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:94848935 G>A maps to NM_001127707.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr14:94849256 G>A maps to NM_001127707.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr14:94756846 C>T maps to NM_001100607.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:94756903 G>C maps to NM_001100607.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr14:94912878 C>A maps to NM_001080451.1 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr14:94909048 G>C maps to NM_001080451.1 S388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:94956040 G>A maps to NM_173850.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr14:94953678 C>G maps to NM_173850.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr14:94964317 G>A maps to NM_173850.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr14:94953738 G>T maps to NM_173850.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J1-01A-11D-A20S-09 chr14:95029839 G>T maps to NM_006215.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr14:94770756 A>C maps to NM_001756.3 *406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:105278252 T>G did not map to a codon.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr23:105278232 A>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:105279124 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:105280611 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr23:105278293 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:94929465 G>C maps to NM_175739.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EI-01A-11D-A10Y-09 chr14:94933669 T>A maps to NM_175739.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr18:61602230 C>T maps to NM_005024.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:61379842 C>T maps to NM_080475.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr18:61383309 G>A maps to NM_080475.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:61234180 C>G maps to ENST00000382768 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:61306948 C>G maps to NM_002974.2 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr6:2955874 A>C maps to ENST00000316782 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr18:61463606 T>C maps to NM_001040147.1 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:2890789 G>A maps to NM_004155.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr6:2892087 G>A maps to NM_004155.4 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr22:21134010 C>G maps to NM_000185.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08X-01A-21W-A019-09 chr7:100776988 G>A maps to NM_000602.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr7:100773700 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:100773723 C>T maps to NM_000602.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr7:100777175 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr7:100771745 G>T maps to NM_000602.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr7:100773846 G>T maps to NM_000602.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:224866464 G>A maps to NM_001136530.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BM-01A-11D-A21Q-09 chr17:1679824 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:57369595 C>T maps to ENST00000403558 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:75280188 T>G maps to NM_001235.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr3:167525055 T>C maps to NM_005025.4 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:167170821 C>A did not map to a codon.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr3:167184945 A>G maps to NM_006217.3 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IX-01A-12D-A142-09 chr3:167183402 C>G maps to NM_006217.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:64863615 G>A maps to NM_014755.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SB-01A-21D-A25Q-09 chr19:40947663 C>T maps to NM_203344.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12F-01A-11D-A10Y-09 chr1:28598250 C>T maps to NM_031459.3 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:42533105 C>T maps to NM_015559.2 G1267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:42643263 C>T maps to NM_015559.2 F1464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr18:42643575 C>G maps to NM_015559.2 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr16:30970120 C>T maps to NM_014712.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:30976316 C>T maps to NM_014712.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr16:30977151 T>A maps to NM_014712.1 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr16:30975563 C>T maps to NM_014712.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr3:47084163 G>A maps to NM_014159.6 L2375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:47165586 G>C maps to NM_014159.6 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:47164272 G>C maps to NM_014159.6 S618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:47163681 G>T maps to NM_014159.6 S815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:47163992 G>A maps to NM_014159.6 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr3:47163293 A>C maps to NM_014159.6 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr3:47103759 C>T maps to NM_014159.6 E2062E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:99865090 G>C maps to NM_032233.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:99925515 C>A maps to NM_032233.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr4:140432837 G>A maps to NM_030648.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:150923290 C>T maps to NM_001145415.1 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr9:135211681 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:135139997 G>A maps to ENST00000372169 F2583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:135204367 C>A maps to ENST00000372169 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:135202957 G>A maps to ENST00000372169 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr9:135206815 G>A maps to ENST00000372169 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr17:27308920 C>T maps to NM_178860.4 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JB-01A-11D-A13L-09 chr17:27286097 C>A maps to NM_178860.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr17:27296862 G>A maps to NM_178860.4 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr16:29907122 C>A maps to NM_201575.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr16:29896967 G>C maps to NM_201575.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr16:29899945 C>G maps to NM_201575.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:64534714 G>A maps to NM_201995.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr11:64533496 G>A maps to NM_201995.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr11:64535091 C>T maps to NM_201995.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr22:30733775 C>T maps to NM_005877.4 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A440-01A-11D-A243-09 chr19:2245451 C>A maps to NM_007165.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:38423887 G>A maps to NM_006802.2 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr2:198274676 C>A maps to NM_012433.2 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:198273150 C>G maps to NM_012433.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:198285248 C>T maps to NM_012433.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:24297060 G>A maps to NM_016047.3 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr2:24291325 C>T maps to NM_016047.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr2:24291244 C>G maps to NM_016047.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:65835429 C>T maps to NM_006842.2 Q782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EI-01A-11D-A10Y-09 chr11:65819872 C>T maps to NM_006842.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:70590859 T>G maps to NM_012426.4 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr16:70595639 G>T maps to NM_012426.4 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:70566407 A>G maps to NM_012426.4 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:70566470 G>T maps to NM_012426.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr16:70595600 G>A maps to NM_012426.4 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:149898613 G>A maps to NM_005850.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr19:19414552 G>C maps to NM_172231.2 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr22:31942921 G>A maps to NM_001007467.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr22:32009791 C>T maps to NM_001007467.1 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr3:52947575 G>T maps to NM_016329.3 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:52941318 A>C maps to NM_016329.3 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr10:7318922 T>C maps to NM_001018039.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:7325872 T>G maps to NM_001018039.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:27189720 G>T maps to NM_006142.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:27189736 C>T maps to NM_006142.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr1:35658566 G>T maps to NM_005066.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:35650152 A>C maps to NM_005066.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:41122838 G>A maps to NM_003012.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr8:41166388 C>T maps to NM_003012.4 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr17:56084324 G>A maps to NM_006924.4 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr1:70694185 G>A maps to NM_004768.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr1:70716187 T>C did not map to a codon.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr1:70716045 A>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr5:65466526 T>G maps to NM_001077199.1 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr5:65474671 C>T maps to NM_001077199.1 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr5:65466527 A>T maps to NM_001077199.1 K413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr6:89808453 G>T maps to ENST00000452027 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr19:19115424 G>A maps to NM_001017392.3 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr19:19136589 C>G maps to NM_001017392.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:33066595 C>A maps to NM_020706.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr21:33073364 T>C maps to NM_020706.2 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr21:33076191 A>G maps to NM_020706.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr21:33044074 G>A maps to NM_020706.2 N1027N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12F-01A-11D-A10Y-09 chr19:45571724 G>C maps to NM_007056.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:1718125 G>C did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr23:1712626 C>G did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr23:1712953 C>T did not map to a codon.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr23:1719551 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:1714351 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr6:99853926 C>A maps to NM_032870.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr11:94801109 C>G maps to NM_032102.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:46321649 C>A maps to NM_004719.2 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:29485896 G>A maps to NM_005626.4 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:70235392 T>G did not map to a codon.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr12:132241103 A>C maps to NM_004592.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr1:168204350 C>T maps to NM_199344.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr14:36946265 G>A maps to NM_001101341.1 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr10:81372137 C>T maps to NM_001093770.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:85892749 C>T maps to NM_198843.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:85892441 C>G maps to NM_198843.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09V-01A-11D-A045-09 chr10:104489150 G>A maps to NM_178858.4 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr10:104486422 C>T maps to NM_178858.4 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr10:102794459 A>G maps to NM_030971.3 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr10:120917219 A>C maps to NM_213649.1 L166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr2:73215385 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr17:48247562 G>C maps to NM_000023.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:48246599 G>A maps to NM_000023.2 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr17:48247652 G>A maps to NM_000023.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:94257669 G>A maps to NM_001099401.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:94259145 A>G maps to NM_001099401.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr8:14412341 G>A maps to NM_139167.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr8:13965682 G>T maps to NM_139167.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr8:13965706 C>T maps to NM_139167.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:153840605 C>A maps to NM_015595.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:67101646 A>C maps to NM_032291.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:67126206 G>A maps to ENST00000237247 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:134492861 T>G maps to NM_001143676.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:134491429 C>T maps to NM_001143676.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr6:134492798 G>C maps to NM_001143676.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr6:134493421 G>T maps to NM_001143676.1 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr8:42977593 G>A maps to NM_032237.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr20:42204865 G>A maps to NM_016276.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:42208628 T>C maps to NM_016276.3 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:8233986 C>T maps to NM_001080826.1 E644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr15:77425880 A>G maps to NM_024776.2 C1181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr15:77406584 G>A maps to NM_024776.2 S1718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr8:67748218 T>C maps to NM_013257.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr17:26938660 C>T maps to NM_001174103.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr10:52103556 C>A maps to ENST00000361543 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:108824543 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:108829841 C>T maps to NM_152621.5 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:20225111 T>C maps to NM_001012410.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr10:72604348 G>A maps to NM_003901.3 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:72604357 G>C maps to NM_003901.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:223389674 T>C maps to NM_152386.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:78188915 G>A maps to NM_000199.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:25313623 G>C did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:2280274 C>T maps to NM_014853.2 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:40801714 C>T maps to NM_015705.4 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:40802611 C>A maps to NM_015705.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr22:40800416 C>T maps to NM_015705.4 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr5:64981224 G>C maps to NM_019072.2 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr16:28884849 G>A maps to NM_001145795.1 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr16:28883118 C>G maps to NM_001145795.1 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:101943911 C>T maps to ENST00000306803 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:123480596 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr1:156784031 G>A maps to NM_001161441.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr1:156784869 G>A maps to NM_001161441.1 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr19:6755276 C>T maps to NM_005490.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr19:6754087 C>T maps to NM_005490.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:130501095 C>A maps to NM_170600.2 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr8:19221742 A>C maps to NM_022071.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DT-01A-21D-A12B-09 chr1:21048380 G>A maps to ENST00000444387 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr21:40871771 T>G maps to NM_007341.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:40834350 C>T maps to NM_007341.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr23:80552724 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:80457736 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr23:80532646 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr22:38039003 G>A maps to NM_018957.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr22:38046693 T>G maps to NM_018957.3 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr2:235951350 G>A maps to NM_014521.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:235951290 C>T maps to NM_014521.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:235950795 C>G maps to NM_014521.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:152080502 A>G maps to NM_001009555.3 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr9:17761475 T>A maps to NM_003026.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr15:84241414 C>T maps to ENST00000434347 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:87208821 G>C maps to ENST00000482504 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:87181435 G>A maps to ENST00000482504 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr9:131772129 G>T maps to ENST00000372554 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr9:131771579 G>C maps to ENST00000372554 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:19606865 A>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:19564083 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:19702028 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:19713835 A>C did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:19764459 T>G did not map to a codon.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr23:19854374 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr23:19568117 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:19701972 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JS-01A-11D-A13L-09 chr23:19764521 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1XR-01A-11D-A14K-09 chr23:19560228 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr10:105363028 G>T maps to ENST00000369774 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr10:105362403 C>T maps to ENST00000369774 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:105372947 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr5:171766110 G>A maps to NM_001017995.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr5:171766137 G>A maps to NM_001017995.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr5:171766089 G>C maps to NM_001017995.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr4:170017807 C>T maps to NM_020870.3 Q843Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:170037743 C>T maps to NM_020870.3 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr4:170057684 G>A maps to NM_020870.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A086-01A-11W-A019-09 chr4:8242513 G>A maps to NM_018986.3 T1281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:8216248 C>T maps to NM_018986.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:8211493 C>T maps to NM_018986.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr4:8228800 C>G maps to NM_018986.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr5:148421115 C>T maps to NM_024577.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:148417942 G>A maps to NM_024577.3 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:51190855 G>C maps to ENST00000391814 S791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:51191281 G>A maps to ENST00000391814 R736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:51219645 G>C maps to ENST00000391814 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr19:51165692 G>A maps to ENST00000391814 P2013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr19:51217198 G>T maps to ENST00000391814 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr19:51219969 G>A maps to ENST00000391814 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr19:51201172 G>C maps to ENST00000391814 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:70331453 T>G maps to ENST00000338508 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr11:70805675 G>C maps to ENST00000338508 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr11:70803542 G>T maps to ENST00000338508 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A126-01A-11D-A10M-09 chr11:70331576 G>A maps to ENST00000338508 D1601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:70742675 C>T did not map to a codon.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr11:70336385 G>C maps to ENST00000338508 S843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr11:70331426 G>C maps to ENST00000338508 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr8:145154195 A>C maps to NM_030974.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H5-01A-21D-A10Y-09 chr8:145154288 G>A maps to NM_030974.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:154942697 G>C maps to NM_001130040.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr19:434768 G>A maps to NM_012435.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A041-01A-11W-A050-09 chr9:91727507 T>G maps to NM_016848.5 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:154471711 G>A maps to NM_001010846.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IP-01A-11D-A045-09 chr15:45470456 A>G maps to ENST00000437903 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:26620749 T>G maps to NM_001007538.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr4:42403143 G>A maps to NM_001080505.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:201859620 C>T maps to NM_198149.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr1:201859607 C>G maps to NM_198149.2 S91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:48510835 T>G maps to NM_016479.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:41084068 C>T maps to NM_138392.3 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr17:18232667 C>G maps to NM_004169.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:18238960 G>A maps to NM_004169.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:57626533 C>T maps to NM_005412.5 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr23:591784 G>A did not map to a codon.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr3:157823480 C>T maps to NM_003030.4 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr17:3524660 G>A maps to NM_013276.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr6:146240554 G>A maps to ENST00000367503 R1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:146275930 C>T maps to ENST00000367503 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:146256485 C>T maps to ENST00000367503 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:146256179 C>T maps to ENST00000367503 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr3:72866533 C>A maps to NM_018130.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr23:9914856 C>T did not map to a codon.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr23:9864380 G>C did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr23:9864048 G>A did not map to a codon.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr23:9863793 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:9864399 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:9900719 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:9900767 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:9914782 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:9863479 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:9900233 C>T did not map to a codon.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr23:9864211 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:9863011 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:9900560 G>T did not map to a codon.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr23:9900267 C>T did not map to a codon.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr23:9914799 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr23:9841725 A>G did not map to a codon.
Sequencing variant TCGA-E2-A15E-01A-11D-A12B-09 chr23:9905361 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr4:77660024 A>C maps to NM_020859.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr4:77675772 G>T maps to NM_020859.3 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr23:50381256 C>A did not map to a codon.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr23:50376534 G>A did not map to a codon.
Sequencing variant TCGA-A2-A25F-01A-11D-A167-09 chr23:50350781 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:50351125 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:50376560 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:50341288 C>T did not map to a codon.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr23:50377357 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BT-01A-11D-A12Q-09 chr23:50350795 G>A did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:50350777 T>G did not map to a codon.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr23:50350781 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr23:50350571 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:50377930 G>C did not map to a codon.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr23:50350475 G>C did not map to a codon.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr23:50377365 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr23:50377006 T>G did not map to a codon.
Sequencing variant TCGA-EW-A2FW-01A-11D-A17D-09 chr23:50378350 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr3:164785126 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr3:164716393 G>A maps to NM_001041.3 R1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr3:164735431 A>G maps to NM_001041.3 Y1221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr3:164716430 C>T maps to NM_001041.3 G1479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr16:48396329 G>A maps to NM_001006610.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr13:46358081 G>C maps to NM_198849.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:113323817 C>T maps to ENST00000393830 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:113325916 C>T maps to ENST00000393830 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:117052582 G>A maps to NM_001040455.1 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:117062705 C>G maps to NM_001040455.1 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr11:117063013 C>T maps to NM_001040455.1 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr11:117054808 G>C maps to NM_001040455.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:117052205 G>A maps to NM_001040455.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr11:117063052 C>T maps to NM_001040455.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr20:3687267 G>A maps to NM_023068.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr20:3683871 G>A maps to NM_023068.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:3682157 G>T maps to NM_023068.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr20:3684514 G>A maps to NM_023068.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr20:3680053 C>T maps to NM_023068.3 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr20:3677445 G>A maps to NM_023068.3 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr20:3673309 G>A maps to NM_023068.3 H1296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DD-01A-12D-A27P-09 chr20:3673773 C>T maps to NM_023068.3 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr19:51920148 C>T maps to NM_033130.4 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr19:51918503 C>A maps to NM_033130.4 G421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr19:50462686 T>C maps to NM_052884.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:50463851 C>T maps to NM_052884.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr19:52004713 G>T maps to NM_053003.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr18:43422080 C>T maps to NM_213602.2 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr19:52132740 G>A maps to ENST00000222107 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr19:52130889 C>T maps to ENST00000222107 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:52132710 G>A maps to ENST00000222107 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr19:52130754 G>A maps to ENST00000222107 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr19:52034506 G>T maps to NM_001245.5 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DO-01B-11D-A12B-09 chr19:52033694 G>A maps to NM_001245.5 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:52032987 G>T maps to NM_001245.5 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:51646009 A>G maps to NM_014385.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr19:51647819 C>A maps to NM_014385.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:51960769 C>A maps to NM_014442.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:51628530 G>A maps to NM_014441.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr19:51631730 A>T maps to NM_014441.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:44840965 G>A maps to NM_173354.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr21:44838353 G>A maps to NM_173354.3 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr11:116730051 C>T maps to ENST00000445177 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:116747070 A>G maps to ENST00000445177 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr11:116732605 G>A maps to ENST00000445177 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr11:116798096 C>A did not map to a codon.
Sequencing variant TCGA-BH-A201-01A-11D-A14K-09 chr11:116766966 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:116827663 C>T maps to ENST00000445177 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:116827732 C>T maps to ENST00000445177 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr12:56351003 A>G maps to NM_006928.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr12:56355433 T>C maps to NM_006928.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr12:56349110 G>A maps to NM_006928.3 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr12:56349317 T>A maps to NM_006928.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr6:100897265 G>A maps to ENST00000262901 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr6:100897297 G>A maps to ENST00000262901 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr6:100841735 T>C maps to ENST00000262901 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr21:38117438 T>G maps to NM_009586.2 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:38095421 C>T maps to NM_005069.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OX-01A-11D-A142-09 chr21:38095374 C>T maps to NM_005069.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:75705121 T>G maps to NM_001145357.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:75705148 A>G maps to NM_001145357.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:75702227 C>T maps to NM_001145357.1 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:65417951 T>G did not map to a codon.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr14:72138129 A>G maps to NM_015556.1 G850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RX-01A-11D-A25Q-09 chr14:72138261 C>T maps to NM_015556.1 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr14:72171447 T>C maps to NM_015556.1 Y1219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:72152207 A>C maps to NM_015556.1 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:72055317 C>T maps to NM_015556.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:72055815 G>A maps to NM_015556.1 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr14:72085582 A>C maps to NM_015556.1 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr14:72139138 C>T maps to NM_015556.1 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr14:72139288 C>A maps to NM_015556.1 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr1:232607133 G>C maps to NM_020808.3 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr1:232561449 C>G maps to NM_020808.3 R1505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr1:232581366 G>A maps to NM_020808.3 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr1:232650899 A>C maps to NM_020808.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:232601163 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr19:38631958 A>G maps to NM_015073.1 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:38673347 A>C maps to NM_015073.1 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr19:38689101 G>A maps to NM_015073.1 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr19:38694841 G>T maps to NM_015073.1 L1732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:1903211 C>T maps to ENST00000400068 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:1585667 C>T maps to NM_001135844.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr20:1538281 G>T maps to ENST00000381621 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr20:1617131 C>T maps to NM_018556.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr19:39371528 C>T maps to NM_012237.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr6:13599263 G>C maps to NM_012241.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr19:4174717 G>A maps to NM_016539.2 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr17:79872223 C>G maps to NM_016538.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IL-01A-11D-A14G-09 chr9:35649943 G>A maps to NM_014450.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr14:61113135 G>A maps to NM_005982.3 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr14:61115627 C>A maps to NM_005982.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr2:45169909 G>T maps to NM_005413.3 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr14:61190201 G>T maps to NM_017420.4 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:47908573 C>T maps to NM_145060.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr13:21742332 C>A maps to NM_145061.5 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:2236017 C>T maps to NM_003036.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:2234755 C>G maps to NM_003036.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr3:170078979 G>T maps to NM_005414.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RY-01A-31D-A25Q-09 chr6:31928495 G>T maps to NM_006929.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr6:31931757 C>T maps to NM_006929.4 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:31930341 C>T maps to NM_006929.4 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr5:54624573 T>C maps to NM_015360.4 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr20:35262007 C>G maps to NM_032214.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr4:48343848 G>A maps to NM_020846.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:48384855 A>C maps to NM_020846.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr4:48424069 C>T maps to NM_020846.1 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:160604687 C>T did not map to a codon.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr1:160582298 C>T maps to NM_003037.2 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr1:160718251 C>A maps to NM_021181.3 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr1:160722906 C>G maps to NM_021181.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:159921618 G>A maps to NM_033438.3 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr13:103701762 C>T maps to NM_000452.2 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr23:153716702 G>T did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr23:153716007 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:153717202 A>G did not map to a codon.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr23:153716036 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:48490952 C>G maps to NM_152679.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr8:82606130 C>T maps to NM_001010893.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:82606775 T>C maps to NM_001010893.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:87745029 C>T maps to NM_197965.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:147431097 G>C maps to ENST00000507030 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr15:48580713 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:48521449 C>A maps to NM_000338.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:127522268 A>C maps to NM_001046.2 P1195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:56936404 G>A maps to NM_000339.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr16:67981663 G>T maps to NM_005072.4 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr20:44681680 C>T maps to NM_001134771.1 F844F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr20:44664068 G>T maps to NM_001134771.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr5:1073783 G>A maps to NM_006598.2 Y735Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr3:124829134 C>G maps to NM_001195483.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr3:124826850 C>T maps to NM_001195483.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr7:100457799 G>C maps to NM_020246.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr7:100456720 C>T maps to NM_020246.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr7:100453403 C>A maps to NM_020246.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr7:100456723 C>T maps to NM_020246.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr7:122769491 G>A maps to NM_022444.3 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:26821424 G>A maps to NM_001145975.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr17:26817850 C>T maps to NM_001145975.1 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr17:26818765 C>A maps to NM_001145975.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:45212256 G>A maps to NM_022829.5 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr20:45192148 C>T maps to NM_022829.5 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr20:45242259 G>A maps to NM_022829.5 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:135375975 T>C maps to NM_012450.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr7:135377129 G>T maps to NM_012450.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:43314268 C>A maps to NM_001146037.1 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr13:99338506 C>T maps to NM_005073.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:129299501 G>A maps to ENST00000376744 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:6945054 G>A maps to NM_153357.1 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:91195820 G>A maps to NM_213606.3 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr10:91198596 C>T maps to NM_213606.3 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr10:91198587 G>C maps to NM_213606.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr10:91198854 G>A maps to NM_213606.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:230911082 G>A maps to NM_152527.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr2:230910839 G>A maps to NM_152527.4 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:73749119 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:73749121 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:73744261 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr23:73744297 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr23:73751292 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:80195569 G>A maps to NM_001042423.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08J-01A-11W-A019-09 chr17:73100131 A>C maps to ENST00000450736 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr17:66267700 G>C maps to NM_004694.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:66274362 G>A maps to NM_004694.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:66267691 G>T maps to NM_004694.4 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr22:38474562 G>A maps to NM_013356.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:61414048 A>C maps to NM_194298.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr10:61412688 G>A maps to NM_194298.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr6:25921429 G>T maps to NM_005835.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr6:25921484 G>A maps to NM_005835.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:25921448 C>T maps to NM_005835.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:25924048 C>G maps to NM_005835.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr6:25776821 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr6:25769213 T>C maps to NM_005495.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:25776932 C>T maps to NM_005495.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr6:74331661 C>T maps to NM_012434.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:22396410 G>A maps to NM_020346.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr12:100813923 C>G maps to NM_139319.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr12:100796148 G>A maps to NM_139319.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr12:100795585 C>A maps to NM_139319.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr8:20008220 G>T maps to NM_001135691.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:20028925 T>C maps to NM_001135691.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr8:20036763 G>C maps to NM_001135691.2 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:119027221 G>A maps to NM_003054.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr10:119017347 G>A maps to NM_003054.4 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:169446715 G>A maps to NM_006996.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr1:169446893 T>G maps to NM_006996.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr2:228563716 G>C maps to NM_025243.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:228563695 A>G maps to NM_025243.3 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr9:4583112 G>A maps to NM_004170.5 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr5:36608579 C>T maps to NM_004172.4 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XP-01A-11D-A117-09 chr2:65243808 T>C did not map to a codon.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr2:65217238 G>T maps to NM_003038.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr19:15061144 G>A maps to NM_005071.1 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:15075173 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:15083566 G>A maps to NM_005071.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr1:53569222 G>T maps to NM_006671.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr2:113405015 C>T maps to NM_005415.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:113417045 T>G maps to NM_005415.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:113404597 C>T maps to NM_005415.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:42294940 G>A maps to NM_006749.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:42295030 G>A maps to NM_006749.3 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr8:42297141 G>A maps to NM_006749.3 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:63064903 C>T maps to NM_001039752.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr11:64323713 G>T maps to NM_018484.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr11:64338507 G>A maps to NM_018484.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A091-01A-11W-A019-09 chr11:64368332 G>C maps to NM_144585.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27I-01A-11D-A16D-09 chr11:64361227 G>T maps to NM_144585.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:38317564 C>T maps to NM_004256.3 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:38354925 C>T maps to NM_004803.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:116574175 A>T maps to NM_018420.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr1:116609326 C>T maps to NM_018420.2 Q518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr1:116609286 G>T maps to NM_018420.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr14:23816807 C>T maps to NM_020372.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:23816857 G>A maps to NM_020372.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr11:2943414 C>A maps to NM_002555.5 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr11:62996779 G>A maps to NM_199352.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:62996882 G>C maps to NM_199352.3 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr6:160858229 G>A maps to ENST00000392145 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr6:160864752 G>T maps to ENST00000392145 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr6:160858112 G>A maps to ENST00000392145 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr6:160858217 C>T maps to ENST00000392145 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr5:131676321 C>A maps to NM_003059.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:131721158 G>A maps to ENST00000435065 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr6:43269377 C>T maps to ENST00000372585 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr11:62761058 C>A maps to ENST00000430500 G456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr11:63137554 C>T maps to NM_080866.2 H9H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr20:4843514 G>A maps to NM_203327.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr15:65946273 C>T maps to NM_004727.2 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr20:19662507 C>T maps to NM_020689.3 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr15:48413270 G>A maps to NM_205850.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr12:113754438 G>A maps to NM_024959.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr22:19164681 G>C maps to NM_005984.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr22:19163983 C>T maps to NM_005984.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:79681981 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:4841315 A>C did not map to a codon.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr17:4842371 C>G maps to NM_003562.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:172683315 G>A maps to NM_003705.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr7:95906629 G>A maps to NM_001160210.1 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:95820547 A>C maps to NM_001160210.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr23:129474325 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:129480617 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr23:129483302 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr23:129474312 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr10:70243320 A>C maps to NM_152707.2 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:48936158 G>T maps to NM_000387.4 C23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:48896536 G>A maps to NM_000387.4 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AU-01A-11D-A12Q-09 chr11:793560 G>A maps to NM_001191061.1 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:792900 C>T maps to NM_001191061.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr9:130863452 G>T maps to ENST00000373069 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:46630142 T>G maps to NM_004277.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:101370743 A>C maps to NM_031212.3 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:98995191 G>A maps to NM_213611.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EO-01A-11W-A050-09 chr13:45971425 T>A maps to NM_001010875.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr13:45983069 G>A maps to NM_001010875.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr4:128665851 T>C maps to NM_031291.2 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:9613783 C>T maps to NM_032315.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:16063211 C>T maps to NM_207348.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:16065219 C>T maps to NM_207348.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:140692581 T>G maps to NM_001104647.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr3:140695208 C>T maps to NM_001104647.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr19:6430136 C>A maps to NM_173637.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr19:19218750 G>T maps to NM_178526.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr23:118540556 A>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118585979 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:118586863 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr23:118586829 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr1:156169757 C>A maps to NM_014655.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:118603761 A>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:1510814 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:1508404 G>A did not map to a codon.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr12:58018732 G>T maps to NM_133489.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr17:78195380 C>T maps to NM_173626.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:149360494 G>T maps to NM_000112.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:107420159 G>A maps to NM_000111.2 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr7:107408025 C>A maps to NM_000111.2 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:107329553 C>G maps to NM_000441.1 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:107335076 A>G maps to NM_000441.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr7:103051935 G>T maps to ENST00000354356 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:103051988 G>A maps to ENST00000354356 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:35918969 C>T maps to NM_052961.3 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:205895722 C>T maps to NM_134325.2 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:205896724 G>A maps to NM_134325.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:205884081 G>A maps to NM_134325.2 Q868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr19:17597395 G>A maps to NM_198580.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr9:131105548 C>A maps to NM_005094.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr9:131115027 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:59010587 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr19:59009983 G>T maps to NM_012254.2 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr5:128326090 G>A maps to NM_001017372.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr15:45557309 C>T maps to NM_004212.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr15:45564977 C>T maps to NM_004212.3 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr9:86902988 G>T maps to NM_022127.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:44200650 C>G maps to ENST00000313248 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:66136071 G>C maps to NM_001532.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:73115967 C>T maps to NM_018344.5 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr10:73111333 C>A maps to NM_018344.5 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr7:5336822 C>G maps to NM_153247.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr7:5338961 C>T maps to NM_153247.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr1:43393368 G>A maps to NM_006516.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:43393371 G>A maps to NM_006516.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr1:43396748 G>A maps to NM_006516.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:43392840 G>A maps to NM_006516.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr22:24210688 G>T maps to NM_030807.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr6:134350197 G>A maps to NM_145176.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr6:134349969 G>T maps to NM_145176.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr12:40422142 G>A maps to NM_052885.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr12:40223927 A>G maps to NM_052885.3 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr12:40158268 T>C maps to NM_052885.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CL-01A-11D-A10Y-09 chr3:170736325 A>G maps to NM_000340.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr3:170715730 A>C maps to NM_000340.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr12:8074172 A>G maps to NM_006931.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R5-01A-11D-A14K-09 chr12:8086480 T>G maps to NM_006931.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr17:7187849 T>C maps to NM_001042.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr17:7187612 C>T maps to NM_001042.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N3-01A-12D-A159-09 chr20:62373243 G>A maps to NM_020062.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:9097665 T>G maps to NM_003039.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:9082984 G>A maps to NM_207420.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr4:9836552 G>A maps to NM_020041.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr1:211749098 A>G maps to NM_021194.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:220091780 C>T maps to NM_018713.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr15:45814233 G>A maps to NM_013309.4 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr5:68419203 G>C maps to NM_022902.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr5:68419173 G>A maps to NM_022902.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr8:118165273 G>C maps to NM_173851.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:42020144 G>T maps to NM_006345.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:42020149 C>G maps to NM_006345.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:115925088 C>A maps to ENST00000394724 Y164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr20:37356318 G>A maps to NM_080552.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr20:37353516 C>G maps to NM_080552.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:155571375 G>A maps to NM_004733.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr5:176815138 T>A maps to NM_003052.4 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr5:176813237 C>G maps to NM_003052.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr4:25671394 C>T maps to NM_006424.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr9:140126582 C>T maps to NM_080877.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr6:88216122 G>T maps to NM_006416.4 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr6:88221165 C>G maps to NM_006416.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:48760727 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr23:48761928 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr23:48762370 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr5:139947419 C>G maps to NM_080670.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr6:44222442 T>C maps to NM_178148.2 *433W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr6:8417216 C>T maps to NM_001142540.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:45832723 C>T maps to NM_018389.4 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18S-01A-11D-A12B-09 chr1:67519642 C>A maps to NM_015139.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr1:67486084 A>C maps to NM_015139.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr19:16678953 G>T maps to NM_024881.4 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr19:16683055 C>T maps to NM_024881.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr12:69158495 C>T maps to NM_018656.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J1-01A-11D-A20S-09 chr6:118475628 C>T maps to NM_001029858.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:234367367 C>T maps to NM_173508.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IG-01A-11W-A050-09 chr1:234452418 C>T maps to NM_173508.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr1:234367370 C>T maps to NM_173508.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr1:234041448 G>A maps to NM_173508.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:150856194 A>C maps to NM_078483.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:150867631 A>C maps to NM_078483.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:150843173 C>T maps to NM_078483.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:150856221 C>T maps to NM_078483.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr5:150846796 G>T maps to NM_078483.2 G153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr5:150696503 G>A maps to NM_181776.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr5:150682786 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr11:124954752 G>C maps to NM_198277.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr11:124946651 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:118898960 G>A maps to NM_001164278.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr12:46600986 C>A maps to NM_030674.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr12:46754959 C>T maps to NM_018976.4 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:46758432 C>G maps to NM_018976.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:46758940 G>A maps to NM_018976.4 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr3:50252844 C>T maps to NM_006841.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:47173643 C>A maps to NM_018018.4 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:47173741 C>A maps to NM_018018.4 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr12:47163174 G>A maps to NM_018018.4 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr12:47173626 G>T maps to NM_018018.4 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:47178889 C>A maps to NM_018018.4 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr23:48326102 G>C did not map to a codon.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr23:48326121 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:48317387 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:84066952 G>A maps to NM_001080442.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:54960638 G>A maps to NM_173514.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr5:54923792 C>G maps to NM_173514.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr5:54931404 A>G maps to NM_173514.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr5:54965417 T>C maps to NM_173514.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr5:54931482 C>T maps to NM_173514.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr5:54929601 G>A maps to NM_173514.2 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:196578277 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:196544849 A>G maps to NM_001127257.1 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr10:18250620 C>T maps to NM_001145195.1 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:18254616 C>G maps to NM_001145195.1 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:47434988 C>G maps to NM_001128225.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HN-01A-11D-A099-09 chr11:47436877 C>T maps to NM_001128225.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:22275338 G>T maps to NM_001135153.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr8:145638247 G>A maps to NM_130849.2 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr12:56630188 A>C maps to NM_001135195.1 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr18:33691197 G>A maps to NM_012319.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr6:33169324 C>G maps to NM_006979.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KD-01A-12D-A20S-09 chr14:69920015 C>T maps to NM_018375.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr11:62652117 C>T maps to NM_001012661.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GZ-01A-11W-A071-09 chr2:190430089 A>G maps to NM_014585.5 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr2:190437614 A>C maps to NM_014585.5 L115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr1:205779275 G>A maps to NM_173854.4 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr11:57263601 G>A maps to NM_003627.5 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:57263538 G>A maps to NM_003627.5 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:57263538 G>A maps to NM_003627.5 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:57252589 G>A maps to NM_003627.5 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FE-01A-11D-A19Y-09 chr11:57177568 G>A maps to ENST00000428603 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A3Z6-01A-11D-A23C-09 chr11:57182166 G>A maps to ENST00000428603 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr19:10742749 C>T maps to NM_020428.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr19:10747166 C>T maps to NM_020428.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr1:95330334 G>C maps to NM_001114106.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NG-01A-21D-A14K-09 chr1:95311007 C>T maps to NM_001114106.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr1:75685019 C>T maps to NM_152697.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr1:75693465 C>T maps to NM_152697.4 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr1:75693409 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr1:75684230 T>C maps to NM_152697.4 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BQ-01A-21D-A10Y-09 chr1:8390662 G>A maps to ENST00000377479 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr1:8385358 A>G maps to ENST00000377479 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr5:33984319 C>A maps to NM_016180.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:142238314 C>T maps to NM_001080431.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JI-01A-21W-A100-09 chr8:142228730 G>A maps to NM_001080431.1 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:26726704 G>A maps to ENST00000440501 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:26732243 G>A maps to ENST00000440501 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr17:26729307 G>A maps to ENST00000440501 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:29292006 A>C maps to NM_001135919.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr13:29284960 G>A maps to NM_001135919.1 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:19480670 G>A maps to ENST00000395585 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr17:19452968 G>A maps to ENST00000395585 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:48172901 C>T maps to NM_017842.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr17:42328556 C>T maps to NM_000342.3 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr17:42330735 C>T maps to NM_000342.3 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr2:162711542 T>G maps to NM_001178015.1 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:162738875 C>T maps to NM_001178015.1 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XX-01A-21D-A23C-09 chr20:3209990 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:3215415 G>C maps to NM_001174090.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XS-01A-22D-A10G-09 chr20:3214873 G>A maps to NM_001174090.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:3214189 G>A maps to NM_001174090.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr20:3211606 G>C maps to NM_001174090.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr2:27910884 C>A maps to NM_018158.2 S734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:150768693 T>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:150772560 G>A maps to NM_003040.3 Q1089Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr7:150773263 G>A maps to NM_003040.3 E1212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:220501565 C>T maps to NM_201574.2 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:220505648 C>T maps to NM_201574.2 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:220501550 C>T maps to NM_201574.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr4:72316952 G>C maps to NM_001098484.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr4:72205156 C>T maps to NM_001098484.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr4:72400044 G>A maps to NM_001098484.2 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:74482966 G>A maps to NM_021196.3 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr2:74477541 G>A maps to NM_021196.3 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:27450960 G>A maps to ENST00000454389 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr3:27418336 C>T did not map to a codon.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr12:51888748 C>G maps to NM_001039960.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:51890847 C>G maps to NM_001039960.1 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:139752359 G>T maps to ENST00000507527 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:32480936 T>G maps to NM_000343.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:32439354 C>A maps to NM_000343.3 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr22:32506049 C>T maps to NM_000343.3 H615H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:18922810 C>T maps to NM_152351.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr17:18922823 C>T maps to NM_152351.3 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:18922756 C>T maps to NM_152351.3 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr16:24920356 G>A maps to NM_052944.2 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr11:26725446 G>A maps to NM_178498.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr16:31496153 C>G maps to ENST00000431354 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:31499001 C>T maps to ENST00000431354 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr22:32631033 C>T maps to NM_014227.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr22:32614515 G>A maps to NM_014227.2 H655H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr22:32626964 C>G maps to NM_014227.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:17983484 G>A maps to NM_000453.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:17992985 C>T maps to NM_000453.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr19:17988648 C>T maps to NM_000453.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:27423438 G>A maps to NM_021095.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:27430196 G>A maps to NM_021095.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XV-01A-11D-A10G-09 chr2:108604634 G>C maps to NM_021815.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:108626920 A>G maps to NM_021815.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:101587554 A>C maps to NM_145913.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr12:101555847 G>A maps to NM_145913.3 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr12:101581286 G>C maps to NM_145913.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:48705106 G>C maps to NM_001135181.1 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:48699339 C>T maps to NM_001135181.1 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr1:48698154 C>T maps to NM_001135181.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr1:48699330 G>A maps to NM_001135181.1 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr3:11064045 C>T maps to NM_003042.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr3:11059538 G>A maps to NM_003042.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr3:10960031 T>C maps to NM_014229.1 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:313808 G>A maps to NM_003044.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr12:313733 G>A maps to NM_003044.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr12:352956 G>A maps to NM_016615.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:331754 G>A maps to NM_016615.3 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:351810 G>A maps to NM_016615.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:351813 C>A maps to NM_016615.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr23:115574820 T>C did not map to a codon.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr23:115584213 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:115585532 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:115582835 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:49796529 G>A maps to NM_014037.2 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr19:49793935 G>A maps to NM_014037.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr19:49812931 G>A maps to NM_014037.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:110734721 C>T maps to NM_001010898.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:110737301 C>T maps to NM_001010898.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr5:1219061 C>T maps to NM_001003841.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J3-01A-11D-A13L-09 chr5:1216681 C>T maps to NM_001003841.2 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:55729243 C>T maps to NM_001043.3 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr16:55719075 C>T maps to NM_001043.3 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:45801402 C>G maps to NM_020208.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:45800526 G>A maps to NM_020208.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:45804463 G>A maps to NM_020208.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr5:1441546 G>T maps to NM_001044.4 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:1416256 C>A maps to NM_001044.4 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr17:28545923 G>A maps to ENST00000394821 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:20652251 C>T maps to NM_004211.3 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr11:20652302 C>T maps to NM_004211.3 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:20636288 T>C maps to NM_004211.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr11:20676317 C>G maps to NM_004211.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr3:14487330 C>T maps to NM_001134367.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:152960585 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:152955959 A>T did not map to a codon.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr23:152956983 G>A did not map to a codon.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr1:44476554 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:30096463 A>C maps to NM_003045.4 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr13:30091322 G>A maps to NM_003045.4 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr13:30091319 G>A maps to NM_003045.4 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:87229944 C>T maps to NM_138817.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr3:170201116 G>A maps to NM_020949.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr3:170201191 C>T maps to NM_020949.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr23:70149700 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr23:70145946 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70146751 T>A did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:70149841 C>T did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr23:70148348 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr23:70149573 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:21385747 G>A maps to NM_004173.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr16:87902746 G>A maps to NM_003486.5 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr14:23245481 G>A maps to NM_001126106.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr14:23609768 G>A maps to NM_012244.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr14:23609735 G>T maps to NM_012244.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr14:23607215 G>C maps to NM_012244.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:33334769 G>A maps to NM_014270.4 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr19:33355670 G>A maps to NM_014270.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:47940725 C>T maps to NM_015063.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr14:70633482 G>A maps to NM_183002.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:70633414 A>C maps to NM_183002.1 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr14:70527616 G>A maps to NM_183002.1 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:70634611 G>A maps to NM_183002.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I2-01A-11W-A050-09 chr14:70515730 C>A maps to NM_183002.1 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr1:27436073 G>C maps to NM_003047.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12O-01A-11D-A10Y-09 chr1:27429180 G>A maps to NM_003047.3 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:27436082 G>A maps to NM_003047.3 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:111958818 C>T maps to NM_183061.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CQ-01A-21W-A050-09 chr1:173542379 G>A maps to NM_178527.3 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:173472457 G>C maps to NM_178527.3 V1106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:173552699 T>C maps to NM_178527.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr1:173493932 G>A maps to NM_178527.3 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr2:103310910 C>G maps to NM_003048.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:103236534 C>T maps to NM_003048.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr2:103274407 C>G maps to NM_003048.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr2:103095466 C>T maps to NM_001011552.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KP-01A-11D-A13L-09 chr16:67289833 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:67289056 C>T maps to NM_004594.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr16:67283104 G>T did not map to a codon.
Sequencing variant TCGA-A8-A083-01A-21W-A019-09 chr23:135126694 A>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135098869 A>C did not map to a codon.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr23:135126843 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr23:135112302 T>C did not map to a codon.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr23:135126699 T>A did not map to a codon.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr23:135077033 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:46466592 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr23:46618329 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr23:46491043 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr23:46539150 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr23:46508205 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:46521523 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr20:48431649 C>T maps to ENST00000417961 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr3:143412149 C>T did not map to a codon.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr12:21453306 C>T maps to NM_134431.3 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:21457361 A>G maps to NM_134431.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr12:21445245 G>A maps to NM_134431.3 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:21358918 A>C maps to NM_006446.4 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:21353575 C>T maps to NM_006446.4 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr12:21028167 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr12:20885885 G>C maps to NM_017435.4 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr12:20893299 G>A maps to NM_017435.4 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr3:133661571 G>T maps to NM_005630.2 S501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:133666197 G>A maps to NM_005630.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr3:133664055 G>A maps to NM_005630.2 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr11:74880254 G>T maps to NM_007256.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:92647640 C>G maps to NM_013272.3 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr15:92638111 A>T maps to NM_013272.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr20:61299500 C>T maps to NM_016354.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr20:61300420 C>G maps to NM_016354.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr5:101631644 G>A maps to NM_180991.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr5:101572690 G>A maps to NM_180991.4 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr8:70588855 A>G maps to NM_030958.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr5:101834401 C>T maps to NM_173488.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr5:101813401 T>A maps to NM_173488.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr17:33679924 G>C maps to NM_152270.3 S719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:33680923 C>T maps to NM_152270.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr17:33749141 G>A maps to NM_018042.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:33749891 G>C maps to NM_018042.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr17:33802085 G>T maps to ENST00000361112 Y570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:33805115 C>T maps to ENST00000361112 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr17:33768151 G>C maps to NM_144682.5 S719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr17:33768826 G>A maps to NM_144682.5 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12H-01A-11D-A10Y-09 chr17:33592828 G>A maps to NM_144975.3 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:98763828 C>T maps to NM_003061.2 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:98923168 A>C maps to NM_003061.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:98794277 G>A maps to NM_003061.2 I796I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:20598061 A>C maps to ENST00000273739 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:20620616 G>A maps to ENST00000273739 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr4:20541117 C>T maps to ENST00000273739 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr5:168181005 C>G maps to NM_003062.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:168135105 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr5:168310286 G>A maps to NM_003062.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QP-01A-11D-A28B-09 chr13:84455449 G>A maps to NM_052910.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr13:84453896 G>A maps to NM_052910.1 Y582Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr13:84454772 G>A maps to NM_052910.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr23:144905076 G>C did not map to a codon.
Sequencing variant TCGA-A8-A06T-01A-11W-A019-09 chr23:144903964 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:144904957 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:144906172 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:144905544 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:144906448 C>A did not map to a codon.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr23:144905275 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr23:144904062 C>T did not map to a codon.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr23:144906242 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr23:144905066 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr23:144905706 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:164906571 G>A maps to NM_014926.2 R683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr3:164908084 C>T maps to NM_014926.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr3:164905804 C>G maps to NM_014926.2 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr3:164906170 C>T maps to NM_014926.2 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr23:142716452 G>C did not map to a codon.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr23:142718043 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:142716964 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:142718209 C>A did not map to a codon.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr23:142717847 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr23:142718313 C>A did not map to a codon.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr23:142717798 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr23:142718154 T>C did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:142716422 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:88329424 G>A maps to NM_015567.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr13:88328770 C>T maps to NM_015567.1 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr13:88328416 G>A maps to NM_015567.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr13:86368269 C>A maps to NM_032229.2 G792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:105762852 T>G maps to NM_014720.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:105762037 G>T maps to NM_014720.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr3:57846446 C>T maps to ENST00000428312 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr5:159842202 C>T maps to NM_006425.4 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr4:146475146 C>T maps to NM_001003688.1 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr4:146467879 A>G maps to NM_001003688.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr18:45368210 G>C maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:45368210 G>C maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr18:48584559 C>T maps to NM_005359.5 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr18:48604753 G>T maps to NM_005359.5 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:71567694 G>A maps to NM_001044305.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:40881846 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:128631941 G>C did not map to a codon.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr23:128657221 C>T did not map to a codon.
Sequencing variant TCGA-A2-A1FX-01A-11D-A13L-09 chr23:128631870 A>T did not map to a codon.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr23:128641921 G>T did not map to a codon.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:128602782 C>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:128605203 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:128632006 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:128638728 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr23:128650474 C>G did not map to a codon.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr23:128649966 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:2039662 C>T maps to NM_003070.3 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr9:2097428 G>A maps to NM_003070.3 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr19:11170527 G>T maps to NM_001128849.1 E1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr19:11152149 G>A maps to NM_001128849.1 P1478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr19:11113751 C>T maps to NM_001128849.1 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr19:11129677 C>G maps to NM_001128849.1 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:11123623 G>T did not map to a codon.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr4:144468590 C>T maps to NM_003601.2 Q903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:144464811 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:144465013 G>A maps to NM_003601.2 E687E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:144446670 G>A maps to NM_003601.2 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:95206185 G>A maps to NM_001128429.1 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr4:95173941 T>G maps to NM_001128429.1 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:217293397 C>A maps to NM_014140.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0AB-01A-11W-A050-09 chr3:47676718 G>C maps to NM_003074.3 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr3:47719704 A>G maps to NM_003074.3 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:50484355 C>A maps to NM_003076.4 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr17:61910317 G>A maps to NM_001098426.1 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:53430527 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A9-01A-11W-A019-09 chr23:53439189 C>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:53409196 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr23:53423504 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:53409441 G>A did not map to a codon.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr23:53432454 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:53423294 A>T did not map to a codon.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr23:53430746 C>G did not map to a codon.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr23:53439173 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr23:53436123 C>A did not map to a codon.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr22:45795230 G>T maps to NM_148674.3 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr22:45802481 G>A maps to NM_148674.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr22:45804621 G>A maps to NM_148674.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr9:106862468 G>A maps to NM_001042550.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FX-01A-11W-A050-09 chr9:106880573 A>G maps to NM_001042550.1 K638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr9:106877034 G>C maps to NM_001042550.1 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:160132287 C>T maps to NM_005496.3 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr3:160131389 A>G maps to NM_005496.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:160146628 A>G maps to NM_005496.3 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:72965053 C>T maps to NM_015110.3 R972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr9:72913048 G>C maps to NM_015110.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr2:17897523 C>A maps to ENST00000381272 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:17884468 A>G maps to ENST00000381272 N725N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:17906558 C>A maps to ENST00000381272 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:2784501 C>T maps to NM_015295.2 R1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr18:2743898 C>T maps to NM_015295.2 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:2666918 C>T maps to NM_015295.2 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr17:18167939 C>T maps to NM_148886.1 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr22:39907906 G>A maps to NM_019008.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr17:18219649 T>C maps to NM_144775.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:18220113 G>A maps to NM_144775.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr14:91942311 T>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:55844402 G>A maps to NM_001122964.1 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:55842595 C>T maps to NM_001122964.1 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:18826946 A>C maps to ENST00000389467 G3444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:18844386 A>C maps to ENST00000389467 G2889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:18887490 G>T maps to ENST00000389467 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr16:18826808 G>C maps to ENST00000389467 L3490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr16:18872049 C>T maps to ENST00000389467 Q1248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr16:18828729 G>A maps to ENST00000389467 A3320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr16:18863733 G>A maps to ENST00000389467 L1607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr16:18872049 C>T maps to ENST00000389467 Q1248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr16:18839446 G>T maps to ENST00000389467 S3217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:18827804 G>C maps to ENST00000389467 S3375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr16:18865075 G>A maps to ENST00000389467 Q1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A4E0-01A-12D-A25Q-09 chr16:18893627 C>A maps to ENST00000389467 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr16:18879676 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:156235761 T>G maps to NM_015327.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:156230286 G>A maps to NM_015327.2 R746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr1:156235969 G>C maps to NM_015327.2 S486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:1989102 A>C maps to NM_017575.4 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr17:2147959 G>A maps to NM_017575.4 T905T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr17:2203077 C>T maps to NM_017575.4 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr17:2203542 G>A maps to NM_017575.4 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr1:183511501 G>A maps to NM_173156.2 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr7:128850817 G>A maps to NM_005631.4 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:128852288 C>T maps to NM_005631.4 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:128850844 G>A maps to NM_005631.4 K564K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr20:4163034 C>A maps to ENST00000443211 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:4162971 T>G maps to ENST00000443211 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr11:6412016 T>G maps to NM_000543.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:68404920 G>A maps to NM_018667.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr2:130910972 C>T maps to NM_017951.4 Q687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:130934149 G>A maps to NM_017951.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:123124875 G>A maps to NM_006714.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:28279861 C>T maps to NM_014474.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:71232644 A>C maps to NM_012390.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:71232704 A>C maps to NM_012390.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:71232425 A>T maps to NM_012390.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:22010729 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr22:31486976 C>A maps to ENST00000454496 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr22:31485770 A>G maps to ENST00000454496 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr11:57313408 G>T maps to ENST00000457912 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:57310507 G>A maps to ENST00000457912 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr11:57314113 C>T maps to ENST00000457912 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:98630673 C>T maps to NM_020429.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:88367478 C>T maps to NM_198274.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr2:88390553 C>T maps to NM_198274.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr2:88405935 G>A maps to NM_198274.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SX-01A-12D-A099-09 chr1:214491453 A>G maps to NM_020197.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr1:214504345 C>T maps to NM_020197.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:246078939 G>A maps to NM_001167740.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr1:246490555 G>A maps to NM_001167740.1 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr17:1703985 G>T maps to NM_052928.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr17:1703214 C>T maps to NM_052928.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:73451123 G>A maps to NM_006062.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:73452826 C>T maps to NM_006062.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr20:48604478 C>G maps to NM_005985.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr16:88747604 G>A maps to NM_178310.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr16:88747982 G>C maps to NM_178310.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr22:21237757 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr1:227935802 G>A maps to NM_053052.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:227947064 G>A maps to NM_053052.3 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr6:84303248 G>A maps to NM_014841.2 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr6:84372141 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:139277850 C>T maps to NM_003086.2 W590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr5:121786698 G>A maps to ENST00000379533 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:121776430 C>T maps to ENST00000379533 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr5:121785557 C>G maps to ENST00000379533 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr5:121780265 T>A maps to ENST00000379533 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr5:121786791 C>A maps to ENST00000379533 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr7:127731926 C>T maps to NM_014390.2 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PE-01A-11D-A142-09 chr2:241989249 C>T maps to NM_001080437.1 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:38018287 C>T maps to NM_024700.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:1285647 C>G maps to ENST00000381876 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:43344693 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:96963380 A>C maps to NM_014014.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:96961279 G>A maps to NM_014014.3 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XO-01A-11D-A10G-09 chr2:96964155 A>G maps to NM_014014.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr2:96943288 A>G maps to NM_014014.3 R1973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr2:96944591 G>A maps to NM_014014.3 L1760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:96944571 C>T maps to NM_014014.3 Q1766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr16:105792 G>A maps to NM_024571.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:123950358 C>G maps to NM_180699.2 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:123950611 C>G maps to NM_180699.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr1:31769547 G>A maps to ENST00000446633 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr19:49610880 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:16721631 C>T maps to NM_198220.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:46191652 G>T maps to NM_004597.5 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:46190963 C>T maps to NM_004597.5 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr15:25222050 G>T maps to NM_022805.2 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:69304155 A>C maps to NM_006750.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Y-01A-21D-A12B-09 chr16:69294159 A>G maps to NM_006750.3 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CP-01A-11W-A050-09 chr8:51449299 C>T maps to NM_018967.2 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr8:51569548 G>A maps to NM_018967.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:51705322 C>T maps to NM_018967.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr8:51503449 C>A maps to NM_018967.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24M-01A-11D-A167-09 chr2:1094037 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr2:1312321 C>T maps to NM_018968.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A273-01A-11D-A16D-09 chr15:75901959 G>T maps to ENST00000371091 Y189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr14:78205184 G>A maps to NM_012245.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:78184741 A>C maps to NM_012245.2 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:78184849 A>C maps to NM_012245.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr15:64415705 T>C maps to NM_003099.3 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:27599022 G>A maps to NM_014748.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:27599540 C>T maps to NM_014748.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:53814486 C>T maps to NM_052870.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:53839148 C>T maps to NM_001102575.1 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:130780194 G>A maps to NM_014758.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10A-01A-21D-A10Y-09 chr16:50709815 C>T maps to NM_182854.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr20:44463688 A>C maps to NM_033421.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr5:122337114 A>G maps to ENST00000395451 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SB-01A-21D-A25Q-09 chr4:186284579 G>A maps to NM_031953.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:186260570 G>A maps to NM_031953.2 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr1:151665017 G>A maps to ENST00000458013 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:151665460 C>T maps to ENST00000458013 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:151630880 A>T maps to ENST00000458013 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:12450108 G>A maps to NM_001080530.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:108544179 G>A maps to NM_003795.4 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr9:115567231 T>C maps to NM_001012994.1 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr8:101642560 C>T maps to NM_152628.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:101642581 G>A maps to NM_152628.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:65620231 C>T maps to NM_152760.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr15:75949546 C>T maps to NM_153271.1 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr3:125216187 C>T maps to NM_003794.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr20:17934761 C>A did not map to a codon.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr14:35045012 G>C maps to NM_152233.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr1:99167431 G>A maps to NM_015976.4 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr1:99150447 C>G maps to NM_015976.4 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:179310327 C>A maps to NM_003101.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr1:179308635 C>T maps to NM_003101.4 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:53499383 C>T maps to NM_003578.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:107811909 G>A maps to NM_018013.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr6:107908292 G>T maps to NM_018013.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr14:55510647 G>T maps to NM_199421.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CU-01A-12W-A050-09 chr17:36522191 C>T maps to NM_014598.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AT-01A-11D-A12Q-09 chr17:36508489 A>G maps to NM_014598.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr6:160109176 G>A maps to NM_000636.2 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr13:36748876 A>G maps to ENST00000511166 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr13:36776200 A>G maps to ENST00000511166 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:599150 C>T maps to NM_005632.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A086-01A-11W-A019-09 chr21:34924650 G>A maps to NM_138927.1 E1038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr21:34922544 G>T maps to NM_138927.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr21:34922289 T>C maps to NM_138927.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr21:34926936 C>T maps to NM_138927.1 H1800H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr10:97096416 G>C maps to NM_001034954.1 S1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr10:97106170 C>T maps to NM_001034954.1 Q807Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr10:97096373 C>G maps to NM_001034954.1 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr10:97170459 G>A maps to NM_001034954.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr4:186545550 C>T maps to ENST00000355634 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr4:186544314 C>T maps to ENST00000355634 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr4:186544245 C>G maps to ENST00000355634 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr8:22424225 G>A maps to NM_005775.4 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr10:108427517 C>T maps to NM_001013031.1 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:108923815 C>A maps to NM_001013031.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:108366942 G>T maps to NM_001013031.1 S1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:108536423 A>G maps to NM_001013031.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr10:108339233 T>G did not map to a codon.
Sequencing variant TCGA-E2-A15A-01A-11D-A12B-09 chr10:108380240 C>T maps to NM_001013031.1 W914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr10:108536408 C>T maps to NM_001013031.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr4:7725557 G>A maps to NM_020777.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr4:7728553 G>A maps to NM_020777.2 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr4:7714486 C>T maps to NM_020777.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr10:106974226 C>T maps to NM_014978.1 C801C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr10:106737217 G>A maps to NM_014978.1 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr15:45353335 C>T maps to NM_003104.5 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr11:121425981 C>T maps to NM_003105.5 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr11:121458741 G>A maps to NM_003105.5 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:121477605 T>G maps to NM_003105.5 G1667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:121425981 C>T maps to NM_003105.5 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:121414376 G>A maps to NM_003105.5 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FN-01A-11W-A050-09 chr11:121466410 G>T maps to NM_003105.5 T1483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr11:121477956 A>T maps to NM_003105.5 T1708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr1:109878930 T>C maps to NM_002959.4 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr2:39281773 G>C maps to NM_005633.3 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:39237795 G>A maps to NM_005633.3 D813D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:39250248 A>G maps to NM_005633.3 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr2:39239445 G>A maps to NM_005633.3 I737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:50597446 C>A maps to NM_006939.2 G1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr14:50671069 C>A maps to NM_006939.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:38370134 C>T maps to NM_006941.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr22:38369663 G>A maps to NM_006941.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr20:307341 G>T maps to NM_006943.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:137483946 G>A maps to NM_004189.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr3:137484309 C>T maps to NM_004189.2 G228G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A1-A0SB-01A-11D-A142-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:181430270 C>G maps to NM_003106.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:139586631 C>T did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:139586808 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1IL-01A-11D-A14G-09 chr23:139586875 G>T did not map to a codon.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr5:157073788 G>A maps to NM_178424.1 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr6:21594935 G>T maps to NM_003107.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:23728678 G>A maps to NM_006940.4 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr12:23887620 G>A maps to NM_006940.4 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr8:10587808 G>A maps to NM_031439.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr17:70120526 G>C maps to NM_000346.3 *510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr17:70117907 C>T maps to NM_000346.3 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr12:53776063 T>C maps to NM_138473.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:231307768 C>G maps to NM_001080391.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr2:231308966 G>A maps to NM_001080391.1 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr2:231102990 G>T maps to NM_007237.4 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr2:231266470 G>T maps to NM_138402.4 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:45993625 A>C maps to NM_003110.5 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:45994051 T>G maps to NM_003110.5 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:174777919 G>C maps to NM_003111.4 S636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr7:21550871 C>T maps to NM_003112.3 N780N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:21469371 C>T maps to NM_003112.3 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr17:45924910 G>A maps to NM_199262.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr17:45925603 C>G maps to NM_199262.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr17:45925438 C>T maps to NM_199262.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr17:45925417 G>A maps to NM_199262.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr12:53722733 T>C maps to NM_001173467.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:88763692 G>T maps to NM_030960.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:101196182 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:101237469 G>A maps to NM_003114.3 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:214794710 T>G maps to NM_024532.3 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:214149242 G>C maps to NM_024532.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr2:214215281 G>A maps to NM_024532.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr2:214160806 A>T maps to NM_024532.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr1:118535190 C>T maps to NM_206996.2 P1753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:118574469 C>A maps to NM_206996.2 E1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:118634278 G>A maps to NM_206996.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:34206843 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr17:26912941 G>A maps to NM_006461.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:22634685 C>T maps to ENST00000376603 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr10:22680767 G>T maps to ENST00000376603 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr9:35811634 G>A maps to NM_001039592.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr17:49083546 C>G maps to ENST00000376407 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr17:49075938 C>T maps to ENST00000376407 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr7:123594425 C>T maps to NM_001174046.1 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr7:123599692 C>G maps to NM_001174046.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr7:123599782 T>A maps to NM_001174046.1 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr7:123594491 A>T maps to NM_001174046.1 K290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr23:140786505 G>A did not map to a codon.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr23:140785799 G>A did not map to a codon.
Sequencing variant TCGA-A1-A0SN-01A-11D-A142-09 chr23:142795592 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr23:142795496 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:142803694 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:142795503 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr23:142596805 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:52826371 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:52825542 C>G did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr5:151047099 G>C maps to NM_003118.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:88415324 A>C maps to NM_004684.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:88411521 G>T maps to NM_004684.4 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr4:88415071 G>A maps to NM_004684.4 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:84986375 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr1:85018791 C>T maps to ENST00000263717 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr13:24860362 T>C maps to ENST00000424834 D808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr13:24860453 C>T maps to ENST00000424834 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr13:24797936 G>A maps to ENST00000424834 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr13:24860470 G>A maps to ENST00000424834 K844K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr3:172835389 T>A maps to NM_031955.5 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:172694805 A>C maps to NM_031955.5 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:172737319 T>C maps to NM_031955.5 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08O-01A-21W-A071-09 chr1:217975164 A>G maps to NM_138796.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:217947773 T>G maps to NM_138796.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr4:52943136 G>A maps to NM_145263.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr11:133712411 G>A maps to NM_174927.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr20:48524760 G>A maps to NM_006038.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr1:16730301 G>C maps to NM_198546.1 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr1:16735619 T>C maps to NM_198546.1 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:45695560 C>A maps to NM_024063.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:48821395 A>G maps to NM_019073.2 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:88862530 G>T maps to NM_018418.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr15:97328266 C>T maps to NM_173499.3 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr8:145101811 C>T maps to NM_198572.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:49919800 A>G maps to NM_023071.3 Q467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:201334653 T>A maps to ENST00000409151 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:64938905 T>G maps to NM_001008778.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:64940420 T>G maps to NM_001008778.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr7:44040869 C>T maps to NM_175064.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:99912207 A>C maps to NM_001004351.4 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr7:99905563 C>G maps to NM_001004351.4 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:8659710 C>G maps to NM_001128076.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr5:35814582 C>T maps to NM_024867.3 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr5:35740103 G>A maps to NM_024867.3 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:35704660 G>T maps to NM_024867.3 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr5:35654759 C>T maps to NM_024867.3 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:220326763 A>C maps to NM_005876.4 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FF-01A-11W-A050-09 chr2:220333725 C>T maps to NM_005876.4 A1149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr2:220354391 A>C maps to NM_005876.4 P2884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr1:16260813 G>C maps to NM_015001.2 L2693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr1:16262319 G>A maps to NM_015001.2 V3195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:16257057 A>C maps to NM_015001.2 T1441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:16257636 A>C maps to NM_015001.2 P1634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr1:16261458 C>T maps to NM_015001.2 S2908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr1:16258803 G>C maps to NM_015001.2 V2023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:16257358 C>T maps to NM_015001.2 R1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr1:16255131 G>C maps to NM_015001.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr1:16260481 G>T maps to NM_015001.2 E2583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr1:16257011 T>A maps to NM_015001.2 L1426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr1:16254873 G>C maps to NM_015001.2 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr1:16261572 G>A maps to NM_015001.2 Q2946Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr1:16260888 G>A maps to NM_015001.2 V2718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr1:16254678 G>A maps to NM_015001.2 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr1:16257913 C>T maps to NM_015001.2 Q1727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr1:16262614 C>T maps to NM_015001.2 Q3294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:16265816 G>T maps to NM_015001.2 P3630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr1:16254904 C>T maps to NM_015001.2 R724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr1:16262704 C>T maps to NM_015001.2 Q3324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr15:44905734 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:44898235 T>C maps to NM_025137.3 T1169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:44881459 G>C maps to NM_025137.3 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr15:44900704 G>A maps to NM_025137.3 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr13:36905607 G>T maps to NM_001142294.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RI-01A-11W-A071-09 chr13:36886474 T>G maps to NM_001142294.1 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr13:36886555 C>T maps to NM_001142294.1 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13F-01A-11D-A12Q-09 chr19:49129266 C>T maps to NM_020126.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:228883175 A>C maps to NM_001142644.1 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:228881963 G>A maps to NM_001142644.1 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr2:228884270 A>T maps to NM_001142644.1 Y433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr2:228884720 T>C maps to NM_001142644.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr2:228882872 G>T maps to NM_001142644.1 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:228882605 G>A maps to NM_001142644.1 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr19:50931496 C>A maps to NM_003121.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr12:101871391 G>C maps to ENST00000299272 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr9:91090080 G>A maps to NM_006717.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr23:57162735 G>A did not map to a codon.
Sequencing variant TCGA-AC-A2FE-01A-11D-A19Y-09 chr23:57162384 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:57146945 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr23:57146371 G>C did not map to a codon.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr5:147204247 G>A maps to NM_003122.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr5:147481390 T>C maps to NM_001127698.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:147503413 C>T maps to NM_001127698.1 R853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:147475425 G>A maps to NM_001127698.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr15:41148156 C>T maps to NM_181642.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr18:12479721 G>A maps to NM_001128626.1 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr16:89924756 C>T maps to NM_032451.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr16:29675523 G>T maps to NM_003123.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr17:4389849 C>T maps to NM_182538.4 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr20:55909041 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr5:136320886 G>A maps to NM_004598.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2OB-01A-21D-A27P-09 chr11:14281247 G>A did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr11:14280994 C>T maps to NM_006108.2 C553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:1161403 C>G maps to NM_012445.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr17:47696470 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:139308478 G>T maps to NM_001001664.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr4:88902646 C>T maps to NM_001040058.1 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr2:234959681 G>T maps to NM_006944.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:2344415 T>C maps to NM_152988.2 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:121204080 C>T maps to NM_139015.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:121220514 G>A maps to NM_139015.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr2:73118644 C>T maps to NM_003124.4 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr2:73115497 G>A maps to NM_003124.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:38614450 G>T maps to NM_152594.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr2:65571978 G>T maps to NM_181784.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:152957747 T>C maps to NM_005987.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:152957714 T>A maps to NM_005987.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr1:152957723 G>A maps to NM_005987.3 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr1:153043173 G>A maps to NM_001017418.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:153043215 C>A maps to NM_001017418.1 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr1:153043219 G>T maps to NM_001017418.1 C32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr1:153085067 G>A maps to NM_001014450.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr1:153122538 A>G maps to NM_001014291.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr1:152975897 T>G maps to NM_005416.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr4:124323701 C>G maps to NM_199327.1 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:124323316 G>T maps to NM_199327.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:155003850 A>C did not map to a codon.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr23:155004150 T>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:155004220 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:155003546 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:155004067 G>A did not map to a codon.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr23:155004062 C>T did not map to a codon.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr23:155003722 C>T did not map to a codon.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr5:141694298 T>A maps to NM_030964.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr5:141694223 G>A maps to NM_030964.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:53460124 C>T maps to NM_032840.2 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr11:55653690 G>A maps to NM_032681.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr11:55657465 C>T maps to NM_032681.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr1:158608013 C>T maps to NM_003126.2 L1666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr1:158615007 C>T maps to NM_003126.2 K1388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:158653163 C>T maps to NM_003126.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:158595953 G>C maps to NM_003126.2 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:158654936 G>A maps to NM_003126.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr1:158608031 C>G did not map to a codon.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr1:158647584 T>C maps to NM_003126.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr1:158585118 G>A maps to NM_003126.2 D2225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr1:158648297 A>T maps to NM_003126.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr1:158644208 G>A maps to NM_003126.2 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr1:158590172 C>T maps to NM_003126.2 E2068E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A229-01A-31D-A17G-09 chr1:158583565 C>A maps to NM_003126.2 E2312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr1:158650471 G>A maps to NM_003126.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr14:65253820 G>A maps to ENST00000389723 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr14:65239967 C>T maps to ENST00000389723 P1720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr14:65263385 C>T maps to ENST00000389723 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr14:65220358 G>A maps to ENST00000389723 P2170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr14:65267587 T>G did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:54856886 C>T maps to NM_003128.2 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr2:54874275 G>A maps to NM_003128.2 Q1625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr2:54870173 G>T maps to NM_003128.2 E1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:54858525 C>T maps to NM_003128.2 Y1114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr11:66468702 G>C maps to NM_006946.2 S956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:66458880 G>A maps to NM_006946.2 A1813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1BC-01A-11D-A14G-09 chr11:66475052 G>C maps to NM_006946.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr19:41021283 C>T maps to NM_020971.2 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr19:40996085 G>A maps to NM_020971.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr19:40978680 G>A maps to NM_020971.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr19:41008788 G>A maps to NM_020971.2 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:42180139 G>C maps to ENST00000320955 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:42182385 G>A maps to ENST00000320955 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr15:42162651 G>A maps to ENST00000320955 Q1852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr15:42173269 A>G maps to ENST00000320955 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:94843196 G>A maps to NM_006415.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr9:94821571 A>G maps to NM_006415.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr20:13029711 C>G maps to NM_018327.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr20:13090783 G>T maps to NM_018327.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr11:18636608 G>A maps to NM_194285.2 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr11:18636797 G>A maps to NM_194285.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr11:18636179 G>T maps to NM_194285.2 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:18633885 C>A maps to NM_194285.2 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr8:126021463 G>C maps to NM_003129.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr5:179260247 C>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:179263499 C>T maps to NM_003900.4 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr2:45789853 C>T maps to NM_018079.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr2:45774704 G>A maps to NM_018079.4 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr2:45812871 G>A maps to NM_018079.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:36024661 C>T maps to ENST00000373558 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:30734380 A>C maps to NM_006662.2 A1330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr16:30736381 A>C maps to NM_006662.2 P1879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr16:30724857 G>A maps to NM_006662.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:30721027 A>C maps to NM_006662.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:30736381 A>C maps to NM_006662.2 P1879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr16:30718894 G>A maps to NM_006662.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr16:30749898 A>T maps to NM_006662.2 G2846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:30744670 C>T maps to NM_006662.2 T2066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr16:30731616 A>C maps to NM_006662.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr16:30745236 G>T maps to NM_006662.2 E2173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:76028109 G>A maps to NM_080744.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:76023177 G>C maps to NM_080744.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:6651953 G>T did not map to a codon.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr5:6663006 G>A maps to NM_001047.2 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:56225576 C>T maps to NM_024592.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A133-01A-32D-A12B-09 chr17:17716751 G>T maps to NM_001005291.2 A1078A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr22:42281015 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr22:42290842 C>T maps to NM_004599.2 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr22:42276901 G>C maps to NM_004599.2 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr6:43141676 G>C maps to NM_003131.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:64502760 G>C maps to NM_020762.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr12:64485058 T>A maps to NM_020762.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:64383791 G>C maps to NM_020762.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr1:206611341 C>T maps to ENST00000414359 N477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr1:206611341 C>T maps to ENST00000414359 N477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr1:206634387 G>T maps to ENST00000414359 E870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr1:206611446 C>A maps to ENST00000414359 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:9055515 G>A maps to NM_014850.2 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr3:9068658 C>T maps to NM_014850.2 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:87839421 A>C maps to NM_003130.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr16:4247811 G>A maps to ENST00000330063 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:11116763 G>T maps to NM_003132.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:112200209 T>C maps to NM_003135.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr17:74042251 G>C maps to NM_014230.2 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:74035867 T>G maps to NM_014230.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr17:74041392 A>T maps to NM_014230.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr4:57355615 C>T maps to NM_006947.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:104807827 C>G maps to ENST00000336613 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr7:104844104 C>A maps to ENST00000336613 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:104787033 G>T maps to ENST00000336613 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:104809656 A>G maps to ENST00000336613 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:153047643 C>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:153047248 G>A did not map to a codon.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr11:126134964 A>G maps to NM_003139.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr11:126136688 G>A maps to NM_003139.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:133526668 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:38024060 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr23:38016147 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr23:99921785 G>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:99919931 G>C did not map to a codon.
Sequencing variant TCGA-GM-A2DC-01A-11D-A18P-09 chr23:99920274 C>T did not map to a codon.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr22:26884127 A>C maps to NM_001013694.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr1:24975441 G>A maps to NM_005839.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:24981552 A>C maps to NM_005839.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:24981344 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:2812583 A>C maps to NM_016333.3 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:2812961 A>C maps to NM_016333.3 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:2813072 A>C maps to NM_016333.3 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:2813075 A>C maps to NM_016333.3 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:2813156 A>C maps to NM_016333.3 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:2816960 A>C maps to NM_016333.3 T2144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr16:2816576 C>T maps to NM_016333.3 R2016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr16:2817326 G>A maps to NM_016333.3 A2266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr16:2815373 G>A maps to NM_016333.3 Q1615Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr16:2814999 C>T maps to NM_016333.3 Q1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr12:119583289 C>T maps to NM_194286.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr12:119419692 G>A maps to NM_194286.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr7:100482031 C>T maps to NM_015908.5 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:100484669 C>G maps to NM_015908.5 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr18:23612479 A>G maps to ENST00000415083 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:60749633 C>T maps to NM_198935.1 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr20:60733750 G>A maps to NM_198935.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:170666791 G>T did not map to a codon.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr2:170663548 G>A maps to NM_003142.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr5:81046828 G>C maps to ENST00000380182 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr1:54722838 G>A maps to NM_145716.2 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:18541703 A>C maps to NM_032627.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:182780670 A>C maps to NM_001130445.1 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr2:182794292 C>A maps to NM_006751.5 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr12:109186214 C>T maps to NM_018984.3 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr12:109201437 C>T maps to NM_018984.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr12:109181919 C>A maps to NM_018984.3 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:109186592 G>A maps to NM_018984.3 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:109182840 C>A maps to NM_018984.3 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr12:109185904 G>A maps to NM_001161330.1 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr17:28022485 G>A maps to NM_033389.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr11:67077325 C>T maps to NM_017857.3 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr11:67079318 G>A maps to NM_017857.3 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr12:26383693 C>T maps to NM_005086.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:149476191 C>A maps to NM_198455.2 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:149484607 C>G maps to NM_198455.2 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:149500158 C>T maps to NM_198455.2 P2596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr7:149500336 T>G maps to NM_198455.2 Y2622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr7:149489164 C>T maps to NM_198455.2 Q1805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr7:149475873 G>A maps to NM_198455.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UP-01A-11D-A28B-09 chr7:149482038 G>A maps to NM_198455.2 A943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:7295634 C>T maps to ENST00000474597 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr3:156260994 T>C maps to ENST00000467789 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr23:153063794 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr11:57101999 G>A maps to NM_003146.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr11:57099624 C>A did not map to a codon.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr14:38679346 C>T maps to NM_001049.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr17:71165748 T>A maps to NM_001050.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr22:37603629 C>A maps to NM_001051.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr20:23016932 C>T maps to NM_001052.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr20:23016491 C>T maps to NM_001052.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr20:23016497 C>T maps to NM_001052.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr20:23016518 C>T maps to NM_001052.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12V-01A-11D-A10Y-09 chr20:23017091 G>T maps to NM_001052.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr20:23016242 C>T maps to NM_001052.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr20:23016839 C>T maps to NM_001052.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr16:1129032 G>C maps to NM_001053.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr16:1129134 C>T maps to NM_001053.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:48125764 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:85122062 C>A maps to NM_001166417.1 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:85122087 G>A maps to NM_001166417.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr1:85130214 G>A maps to NM_001166417.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr1:85136469 T>C maps to NM_001166417.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr23:48214152 G>C did not map to a codon.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr23:48214615 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48244832 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:48244060 C>G did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:48270248 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:48054500 A>C did not map to a codon.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr23:48049612 G>T did not map to a codon.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr23:52677373 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr8:53038648 A>T maps to NM_014682.2 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr8:53074079 G>A maps to NM_014682.2 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr15:80191305 C>A maps to NM_001100880.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XS-01A-11D-A14K-09 chr8:134477070 G>A maps to NM_173344.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr16:70428925 A>G maps to NM_006927.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:98512544 G>A maps to ENST00000493584 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr11:8728715 G>A maps to NM_005418.3 F829F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr11:8737242 C>T maps to NM_005418.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:186790684 G>T maps to NM_003032.2 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HB-01A-11W-A071-09 chr2:107459974 G>A maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:107423286 G>A maps to NM_001142351.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XG-01A-11D-A14G-09 chr2:107423301 G>A maps to NM_001142351.1 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:74623527 T>G maps to NM_018414.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:74625460 G>T maps to NM_018414.3 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:74622471 G>A maps to NM_018414.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr17:74639651 G>C maps to NM_018414.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:74623563 G>A maps to NM_018414.3 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr17:74623303 C>T maps to NM_018414.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:130658580 T>G maps to NM_013443.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr9:130656838 G>C maps to NM_013443.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SF-01A-11D-A142-09 chr7:116593629 C>T maps to ENST00000323984 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr7:116863012 A>G maps to NM_021908.2 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr1:113161561 G>T maps to NM_017744.4 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:113134186 G>A maps to NM_017744.4 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr15:92981771 G>C maps to NM_006011.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr18:55027375 T>C maps to NM_015879.2 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:100231433 G>A maps to NM_005668.4 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr5:100238608 C>T maps to NM_005668.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr5:100238562 C>A maps to NM_005668.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr18:44336459 C>T maps to NM_013305.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr3:52550706 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr3:52548171 C>T maps to NM_015136.2 Y1163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:52544366 T>C maps to NM_015136.2 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22A-01A-11D-A159-09 chr3:52544483 C>A maps to NM_015136.2 C916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr3:52548715 G>T did not map to a codon.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr12:104106174 A>G maps to NM_017564.9 S1455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:104121094 A>C maps to NM_017564.9 A1634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr12:104140457 G>T maps to NM_017564.9 E2074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr12:104129267 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:104146996 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr3:36484977 G>A maps to NM_003149.1 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr17:37371457 G>T maps to NM_198993.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr17:37369271 A>C maps to NM_198993.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr12:57637999 G>A maps to NM_145064.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:136082219 G>C maps to NM_005862.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr3:136096564 C>T maps to NM_005862.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr3:136062774 T>C maps to NM_005862.2 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10F-01A-11D-A10M-09 chr3:136088051 G>A maps to NM_005862.2 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr23:123199792 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0SX-01A-12D-A099-09 chr23:123195703 G>T did not map to a codon.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr23:123200023 G>A did not map to a codon.
Sequencing variant TCGA-A7-A0CH-01A-21W-A019-09 chr23:123220475 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:123179049 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:123164892 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:123179105 A>G did not map to a codon.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr23:123195112 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr23:123196790 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:123196824 T>C did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:123182866 C>G did not map to a codon.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr23:123211833 A>G did not map to a codon.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr23:123181290 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr7:99798462 T>C maps to NM_012447.2 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr7:99799581 C>A maps to NM_012447.2 S771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr7:72470052 G>T maps to ENST00000308103 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:72470028 T>A maps to ENST00000308103 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:66774031 C>G maps to NM_022906.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr10:17702461 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:17756739 T>C maps to NM_003473.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr10:17686364 C>T maps to NM_003473.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr2:152982823 C>T maps to NM_005843.4 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr2:152977210 C>T maps to NM_005843.4 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr2:74074848 G>A maps to NM_213622.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr10:90672856 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:4325219 G>C maps to ENST00000314714 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr19:4324464 G>C maps to ENST00000314714 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr11:72492196 G>T maps to NM_006645.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr13:33859765 G>A maps to NM_178006.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr13:33739511 A>G maps to NM_178007.2 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr17:37809975 C>T maps to NM_006804.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:67939203 A>C did not map to a codon.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr23:67938427 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr23:67937328 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr23:67938432 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0C1-01B-11D-A12B-09 chr23:67940159 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr23:67937722 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr23:67941498 A>C did not map to a codon.
Sequencing variant TCGA-E9-A22D-01A-11D-A159-09 chr23:67935134 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:191862978 G>C maps to NM_007315.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:56744934 A>G maps to NM_005419.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:56743378 G>A maps to NM_005419.3 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr17:40468876 G>A maps to NM_139276.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr2:192012875 C>T maps to NM_003151.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr2:191896228 T>A maps to NM_003151.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr2:191922751 G>A maps to NM_003151.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr17:40451779 C>T maps to NM_003152.3 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr17:40453428 G>T maps to NM_003152.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr17:40370188 G>C maps to NM_012448.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr17:40376886 C>T did not map to a codon.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr12:57500357 G>A maps to NM_003153.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:57492847 A>C maps to NM_003153.4 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:57493637 G>A maps to NM_003153.4 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:57496108 G>A maps to NM_003153.4 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:57498952 G>A maps to NM_003153.4 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr12:57499082 C>T maps to NM_003153.4 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:47739673 G>A maps to NM_017453.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:74529673 T>C maps to NM_001164380.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr7:89789119 C>T maps to ENST00000433102 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr7:89790306 G>A maps to ENST00000433102 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr7:87913446 A>T maps to NM_024636.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr7:87910331 C>G maps to NM_024636.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:47746629 C>T maps to NM_001048166.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr1:47728697 C>T maps to NM_001048166.1 Q902Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr11:4112908 C>T maps to NM_003156.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr4:27009201 C>T maps to ENST00000382009 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr4:27009195 G>T maps to ENST00000382009 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:171520586 A>C maps to NM_005990.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr5:171533634 C>T maps to NM_005990.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr19:1218491 C>T maps to NM_000455.4 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SD-01A-11D-A10Y-09 chr2:220479254 G>A maps to NM_052902.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr2:220476371 C>T maps to NM_052902.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr2:197010663 G>A maps to NM_004226.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr2:197010663 G>A maps to NM_004226.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr8:99591914 A>G maps to ENST00000354930 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr7:23751905 G>T did not map to a codon.
Sequencing variant TCGA-BH-A1FD-01A-11W-A14Q-09 chr5:146750275 G>C maps to NM_001112724.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:5468440 G>A maps to NM_018401.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr10:134022578 G>A maps to NM_173575.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RV-01A-11D-A099-09 chr11:8435218 C>T maps to NM_030906.2 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:8483384 G>A maps to NM_030906.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr20:2097462 T>C maps to NM_080836.3 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:219557366 C>T maps to NM_015690.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:27470916 A>G maps to NM_015000.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:168986077 T>G maps to NM_013233.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:168994616 G>A maps to NM_013233.2 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:169020358 G>C maps to NM_013233.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:43607179 C>A maps to NM_006282.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr20:62275114 C>T maps to NM_015894.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr8:27099196 G>A maps to NM_030795.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:74276415 C>T maps to NM_004809.3 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:74277123 C>T maps to NM_004809.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr9:35101258 C>T maps to NM_013442.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:48808575 C>T maps to NM_172311.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr2:48809569 C>T maps to NM_172311.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr2:48808392 C>T maps to NM_172311.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:81862358 T>G maps to NM_033104.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr10:70644055 G>T maps to NM_001130161.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J7-01A-11W-A050-09 chr10:70644127 C>T maps to NM_001130161.2 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:184930788 C>T maps to NM_020225.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr15:74487714 G>A maps to ENST00000449139 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QH-01A-11D-A18P-09 chr12:16050833 C>A maps to ENST00000025399 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:16036559 A>G maps to ENST00000025399 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:125898321 G>A maps to NM_018387.4 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr9:125923336 C>T maps to NM_018387.4 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66K-01A-11D-A29N-09 chr9:125909223 T>A maps to NM_018387.4 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:43892867 G>C maps to NM_153700.2 L1619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FY-01A-11W-A050-09 chr2:37085128 C>T maps to NM_003162.2 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:37129875 A>G maps to NM_003162.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:31364698 G>C maps to NM_001083893.1 S771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr14:31381307 T>C maps to NM_001083893.1 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr14:31381223 A>C maps to NM_001083893.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr19:47240083 G>A maps to NM_001039877.1 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr19:47242076 C>T maps to NM_001039877.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:7252143 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:7223128 A>T did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:31661215 A>G maps to NM_178862.1 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr16:731864 C>T maps to NM_005861.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:731456 G>A maps to NM_005861.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr19:13260550 C>A maps to NM_003765.1 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr19:13260581 G>T maps to NM_003765.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr6:144508474 G>A maps to NM_003764.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr9:102730739 C>T maps to NM_017919.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr9:102713415 G>A maps to NM_017919.2 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr3:93733951 G>A maps to NM_001001850.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr12:131297511 G>C maps to NM_194356.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr11:59554571 C>G maps to NM_004177.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr11:62574964 G>T maps to NM_003164.3 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr11:62598706 C>G maps to NM_003164.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr11:62595055 G>A maps to NM_003164.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr1:180957442 G>A maps to NM_005819.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:180974599 C>G did not map to a codon.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr6:132792637 C>T maps to NM_003569.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:130440789 G>A maps to NM_003165.3 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:109294877 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:109336202 G>C did not map to a codon.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr6:147636832 A>C maps to NM_001127715.1 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr6:147525811 C>T maps to NM_001127715.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr6:147684753 G>C maps to NM_001127715.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:147684706 C>T maps to NM_001127715.1 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr3:120977985 T>C maps to NM_014980.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:120952484 C>T maps to NM_014980.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:121097678 C>T maps to NM_014980.2 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr14:25288272 G>A maps to NM_014178.6 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:75643110 G>A maps to NM_016086.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr5:32601184 C>T maps to NM_006713.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr13:48563102 G>A maps to NM_003850.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr12:118852238 C>G did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr12:118821843 C>T maps to NM_022491.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr12:118839609 G>C maps to NM_022491.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr8:70550876 C>T maps to NM_001128206.1 Q809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr20:46365492 C>T maps to NM_001161841.1 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr16:28617551 C>G maps to NM_177529.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CH-01A-21W-A019-09 chr16:29472810 A>G maps to ENST00000395400 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr16:30212153 A>G maps to ENST00000354723 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23E-01A-11D-A159-09 chr16:29472810 A>G maps to ENST00000395400 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr16:29472810 A>G maps to ENST00000395400 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LM-01A-11D-A17W-09 chr16:29472810 A>G maps to ENST00000395400 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:108910796 A>C maps to ENST00000437390 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr2:108998293 T>C maps to NM_006588.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr4:70707774 T>C maps to NM_005420.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr19:49094927 C>T maps to NM_177973.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:44221915 C>A maps to NM_014351.3 G274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr2:37402346 A>G maps to NM_001032377.1 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:203079095 G>T maps to ENST00000409368 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr2:203084811 A>C maps to ENST00000409368 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr17:73177268 A>T maps to NM_006937.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LL-01A-11D-A142-09 chr20:31572970 C>T maps to NM_080675.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr14:21840140 G>A maps to NM_007192.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:39963949 C>G maps to NM_003169.3 S789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:39960833 C>T maps to NM_003169.3 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:39959501 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr19:39955655 C>G maps to NM_003169.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1N3-01A-12D-A159-09 chr19:39964081 C>T maps to NM_003169.3 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:27023949 T>G maps to NM_003170.3 G1353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:27015212 C>T maps to NM_003170.3 I1037I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:27018008 G>A maps to NM_003170.3 A1187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr17:27009874 G>T did not map to a codon.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr2:27876561 C>T maps to NM_014860.1 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:70946250 T>G maps to NM_003171.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:136220649 G>A maps to NM_003172.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr9:136227990 C>T maps to NM_017503.3 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:136231780 C>A maps to NM_033161.2 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:114864565 C>A did not map to a codon.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr1:223441873 C>A maps to NM_017982.3 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr3:33249408 C>T maps to NM_015551.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr3:33194512 C>A maps to NM_015551.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:48565945 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:48558623 G>A did not map to a codon.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr23:48557405 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr11:67947666 G>A maps to NM_017635.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr17:30325874 G>A maps to NM_015355.2 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr15:91769861 G>T maps to NM_014848.4 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:75587083 G>A maps to NM_014979.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr9:113192279 A>C maps to ENST00000374463 V1848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr9:113168447 C>T maps to ENST00000374463 V3147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr9:113312282 C>T maps to ENST00000374463 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:113169374 T>G maps to ENST00000374463 S2838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:113194754 T>G maps to ENST00000374463 S1743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr9:113169976 C>A maps to ENST00000374463 E2638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:113169050 G>A maps to ENST00000374463 L2946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:113141790 G>C maps to ENST00000374463 S3418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:113168822 C>G maps to ENST00000374463 G3022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr10:29813435 G>A maps to NM_021738.2 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr10:29811406 T>C maps to NM_021738.2 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:29801714 C>T maps to NM_021738.2 A1155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr12:109311863 C>T maps to NM_018711.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:109316517 C>T maps to NM_018711.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr23:16737864 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr23:16775410 G>C did not map to a codon.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr23:16774819 C>A did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr8:110590146 C>G maps to NM_001099744.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:115428912 G>A maps to NM_003176.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:115398094 C>T maps to NM_003176.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr20:58453082 C>A maps to NM_014258.2 G987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr20:58467481 C>A did not map to a codon.
Sequencing variant TCGA-AR-A2LJ-01A-12D-A19Y-09 chr20:58491608 C>A maps to NM_014258.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr20:58460988 G>A maps to NM_014258.2 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr20:58470577 G>A maps to NM_014258.2 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr6:10926594 C>T maps to NM_001040274.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:10913128 G>A maps to NM_001040274.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:10927483 G>T maps to NM_001040274.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr6:10935309 C>A maps to NM_001040274.2 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr6:10911065 A>G maps to NM_001040274.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr19:15224593 C>T maps to NM_033025.4 D676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:85647954 C>G maps to NM_032184.1 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr19:46333416 G>A maps to NM_004819.2 D548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr19:46341873 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:46341762 C>A maps to NM_004819.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr19:46319769 G>A maps to NM_004819.2 A1108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr19:46334727 A>C maps to NM_004819.2 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:47432350 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:47464779 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47436003 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:47432290 T>A did not map to a codon.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr23:47436040 T>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:12232085 G>A maps to NM_133625.3 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr3:12203642 C>T maps to NM_133625.3 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr22:33260984 G>A maps to NM_003490.3 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr22:33402386 A>G maps to NM_003490.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr1:33160552 G>A maps to NM_030786.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06P-01A-11W-A019-09 chr6:86350198 G>A maps to NM_006372.4 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:86350231 C>A maps to NM_006372.4 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr6:86351073 C>T maps to NM_006372.4 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1L9-01A-11D-A13L-09 chr6:86332253 T>C maps to NM_006372.4 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr6:152623078 C>T maps to NM_182961.2 E5822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:152671845 A>C maps to NM_182961.2 G3880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr6:152576052 G>A maps to NM_182961.2 Q6478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr6:152453308 G>C maps to NM_182961.2 S8681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr6:152454416 A>G maps to NM_182961.2 S8665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:152540176 G>T maps to NM_182961.2 A7335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:152762357 T>C maps to NM_182961.2 V1352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:152565760 C>A maps to NM_182961.2 E6535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:152763329 G>A maps to NM_182961.2 I1296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr6:152529114 C>A maps to NM_182961.2 E7606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr6:152763221 T>C maps to NM_182961.2 E1332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr6:152652193 G>A maps to NM_182961.2 V4542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr6:152650987 C>T maps to NM_182961.2 L4944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr6:152558035 C>T maps to NM_182961.2 L6705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr6:152706961 C>T maps to NM_182961.2 R2833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr6:152847286 G>A maps to NM_182961.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:152770739 C>T maps to NM_182961.2 E1144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr6:152599232 G>T maps to NM_182961.2 L6188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IG-01A-11D-A142-09 chr6:152861112 G>A maps to NM_182961.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IL-01A-11D-A14G-09 chr6:152751744 G>A maps to NM_182961.2 R1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr6:152570398 T>C did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr14:64488684 C>T maps to NM_182914.2 V1821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr14:64494450 C>T maps to NM_182914.2 F2218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:64491914 G>T maps to NM_182914.2 E2010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:64516496 G>T maps to NM_182914.2 E2516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:64591862 G>T maps to NM_182914.2 E4497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr14:64608065 C>G maps to NM_182914.2 S4995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr14:64636984 G>A maps to NM_182914.2 R5680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:64604686 C>G maps to NM_182914.2 L4943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr14:64457238 C>T maps to NM_182914.2 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr14:64547349 G>A maps to NM_182914.2 L3780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr14:64691727 G>A maps to NM_182914.2 V6827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr14:64692243 G>C maps to NM_182914.2 *6908Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr19:48879376 A>T maps to NM_012451.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr21:34099182 C>T maps to NM_003895.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr21:34003517 T>C maps to NM_003895.3 L1542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr21:34012089 C>G did not map to a codon.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr21:34072326 G>C maps to NM_003895.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr6:158505093 G>C maps to NM_003898.3 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:158507989 A>C maps to NM_003898.3 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr6:158516837 C>G maps to NM_003898.3 A1311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:158505057 C>T maps to NM_003898.3 D1020D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr6:158480366 G>T maps to NM_003898.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:99671030 T>G maps to ENST00000336292 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RG-01A-11W-A071-09 chr15:99671358 G>T maps to ENST00000336292 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr15:99673181 G>A maps to ENST00000336292 R1538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr5:150028532 C>T maps to NM_001166209.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr5:150028361 G>A maps to NM_001166209.1 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr4:119810232 G>T maps to NM_133477.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr4:119944646 C>T maps to NM_133477.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr4:119952719 G>A maps to NM_133477.2 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SG-01A-11D-A142-09 chr10:75406544 C>T maps to NM_001114133.1 R955R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr3:63466632 G>A did not map to a codon.
Sequencing variant TCGA-BH-A202-01A-11D-A14K-09 chr3:63594946 C>T maps to NM_001130003.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:63466555 C>T maps to NM_001130003.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:35913622 A>C maps to NM_007247.4 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:35914003 T>C maps to NM_007247.4 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:35902635 T>C maps to NM_007247.4 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:35902443 G>A maps to NM_007247.4 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:49055487 A>G did not map to a codon.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr23:49050647 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:105733466 C>T maps to NM_006754.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:79689853 G>C maps to NM_005639.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:33559899 G>A maps to NM_198992.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:155850388 G>A maps to NM_152280.4 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr1:155851076 C>A maps to NM_152280.4 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:45265779 C>G maps to NM_020826.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:210187038 C>T maps to NM_001146261.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:46969349 G>T maps to NM_031912.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:62542003 C>A maps to NM_031914.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr14:62547603 C>G maps to NM_031914.2 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr14:62463083 C>G maps to NM_031914.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr16:19278386 G>T maps to NM_016524.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr16:19194880 C>T maps to NM_016524.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:202573741 G>A maps to NM_177402.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr19:51129220 G>A maps to NM_001160329.1 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:51128490 G>A maps to NM_001160329.1 H545H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr19:51135657 C>A maps to NM_001160329.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr19:51132703 C>T maps to NM_001160329.1 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:40850380 A>C maps to NM_020783.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:40850401 A>C maps to NM_020783.3 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:114640499 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:114682358 C>T maps to ENST00000369545 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12V-01A-11D-A10Y-09 chr1:114640408 G>A maps to ENST00000369545 Y485Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:114646334 C>A maps to ENST00000369545 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr1:114640499 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:61295495 G>A maps to NM_004200.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:1858525 G>A maps to NM_138567.3 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr11:7335087 C>A maps to NM_175733.3 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JU-01A-11D-A13L-09 chr11:7324288 G>A maps to NM_175733.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr1:27680339 G>A maps to NM_001193308.1 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:85435305 G>A maps to ENST00000359152 Q1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr6:159084347 G>A maps to ENST00000297239 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:159086486 G>A maps to ENST00000297239 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:159184341 C>T maps to ENST00000297239 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:99934401 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:99942063 G>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:99956242 T>C did not map to a codon.
Sequencing variant TCGA-AR-A1AW-01A-21D-A12Q-09 chr23:99936232 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr23:99956629 C>T did not map to a codon.
Sequencing variant TCGA-E9-A247-01A-11D-A167-09 chr23:99942107 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:37932903 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:37981417 G>T did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:37969612 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1BD-01A-11D-A12Q-09 chr23:37893156 A>T did not map to a codon.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr6:166571841 G>C maps to NM_003181.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr6:166575968 G>A maps to NM_003181.2 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr6:132967073 A>G maps to NM_138327.1 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:132938299 C>A maps to NM_001033080.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:132939134 G>T maps to NM_001033080.1 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:132938708 G>T maps to NM_001033080.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr6:132938837 C>A maps to NM_001033080.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:132874340 T>G maps to NM_053278.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:132859625 T>C maps to NM_175057.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr6:132859521 C>T maps to NM_175057.3 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:30872358 C>G did not map to a codon.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr23:30873404 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:30873373 G>A did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:30873284 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1X6-01A-11D-A14K-09 chr23:30872397 C>T did not map to a codon.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr23:30873309 G>A did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr23:30873430 C>T did not map to a codon.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr23:30877659 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:97364150 C>A maps to NM_003182.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr7:97361935 C>G maps to NM_003182.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:38646275 A>C maps to ENST00000379931 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:38684894 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr8:38677316 C>A maps to ENST00000379931 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr8:38693780 C>T maps to ENST00000379931 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr10:124008182 C>G maps to NM_206862.2 V2806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr10:123985897 G>A maps to NM_206862.2 P2542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:123954632 A>C maps to NM_206862.2 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:123988979 A>C maps to NM_206862.2 P2672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:123846637 G>A maps to NM_206862.2 L1541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:123847393 C>T maps to NM_206862.2 C1793C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr10:123845983 G>A maps to NM_206862.2 V1323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr4:1742587 G>T maps to NM_006342.1 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr2:75280767 A>G maps to NM_001058.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:75425985 G>A maps to NM_001058.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:75278397 G>T maps to NM_001058.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr2:75280857 C>A maps to NM_001058.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:104579456 G>A maps to NM_001059.2 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr1:166839060 C>T maps to NM_053053.3 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr17:35822221 C>T maps to NM_001166105.1 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GZ-01A-11W-A071-09 chr17:35837017 G>A maps to NM_001166105.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr4:7055892 C>T maps to NM_152293.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:70683845 G>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:70586248 G>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:70643862 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70602466 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr23:70627429 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr23:70607213 T>G did not map to a codon.
Sequencing variant TCGA-AO-A0JJ-01A-11W-A071-09 chr23:70678131 T>A did not map to a codon.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr23:70604807 A>G did not map to a codon.
Sequencing variant TCGA-AO-A12F-01A-11D-A10Y-09 chr23:70608655 A>G did not map to a codon.
Sequencing variant TCGA-AR-A1AL-01A-21D-A12Q-09 chr23:70602700 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:70683833 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:70607297 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0W4-01A-11D-A10G-09 chr23:70598835 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XC-01A-11D-A14G-09 chr23:70627445 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr23:70617193 C>T did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:109607255 G>A maps to NM_005645.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:34171775 T>G maps to NM_139215.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr17:34147184 G>A maps to NM_139215.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr9:32634817 G>A maps to NM_153809.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr9:32633549 T>C maps to NM_153809.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:32635409 G>T maps to NM_153809.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr9:32634452 G>A maps to NM_153809.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:32631257 G>A maps to NM_153809.2 I1440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr9:32632814 G>T maps to NM_153809.2 G921G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr9:32631491 G>C maps to NM_153809.2 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:120810086 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr8:120774728 G>A maps to NM_003184.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr10:8005971 G>T maps to NM_031923.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:7866500 A>C maps to NM_031923.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:7860722 C>A maps to NM_031923.2 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr10:8055755 G>A maps to NM_031923.2 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr10:8006834 C>G maps to NM_031923.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr20:60578310 G>C maps to NM_003185.3 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:23866324 G>A maps to ENST00000418698 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:23901146 C>T maps to ENST00000418698 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:229738111 C>A maps to NM_014409.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:229738610 G>A maps to NM_014409.3 V101V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A7-A0DA-01A-31D-A10Y-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-A8-A0A6-01A-12W-A071-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr7:99711748 G>A maps to ENST00000472509 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:62545601 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:100538457 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:100547876 C>T did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:100531447 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:100538493 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr23:100530995 T>A did not map to a codon.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr23:100537336 T>A did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:42044896 G>A maps to NM_138572.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:68662386 C>A maps to NM_016283.4 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RQ-01A-11D-A10Y-09 chr11:117075032 C>A maps to NM_003186.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr3:111730661 A>C maps to NM_001008272.1 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:160076338 A>C maps to NM_033394.2 T1213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:159954287 A>C maps to NM_033394.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:160086358 T>C maps to NM_033394.2 T1474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:160035381 C>T maps to NM_033394.2 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:160005674 G>A maps to NM_033394.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr2:160031600 A>G maps to NM_033394.2 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:160035599 C>T maps to NM_033394.2 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr2:160006962 C>G maps to NM_033394.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:61497800 A>C maps to ENST00000389520 S1496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr17:61315385 A>G maps to ENST00000389520 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:61498463 T>G maps to ENST00000389520 G1717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:61473153 C>G maps to ENST00000389520 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:61490919 G>A maps to ENST00000389520 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:61176554 C>T maps to ENST00000389520 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:61498331 A>G maps to ENST00000389520 S1673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr17:27818871 G>T maps to NM_020791.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr17:27778589 C>T maps to NM_020791.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:29989482 T>G did not map to a codon.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr16:29994056 C>T maps to NM_016151.2 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr12:118610294 C>T maps to NM_016281.3 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr6:32813448 G>A maps to NM_000593.5 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:32813493 G>C maps to NM_000593.5 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:32797290 C>T maps to ENST00000452392 Q606Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:6562311 T>C maps to NM_018009.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr4:16193019 G>A maps to NM_153365.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:16188197 C>T maps to NM_153365.2 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RT-01A-21D-A099-09 chr1:234565070 C>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:53895904 G>T maps to NM_134323.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr12:53895207 C>T maps to NM_134323.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr12:53895942 C>T maps to NM_134323.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr5:33456147 T>C maps to ENST00000455217 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:33462212 T>G maps to ENST00000455217 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:33467053 C>T maps to ENST00000455217 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr1:150471488 C>T maps to NM_025150.3 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:150463905 G>A maps to NM_025150.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A426-01A-22D-A243-09 chr15:102241330 G>A maps to NM_152334.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:102261471 C>T maps to NM_152334.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr1:6639316 C>G maps to NM_138697.3 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42U-01A-12D-A243-09 chr1:6637089 G>A maps to NM_138697.3 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr1:19180889 G>C maps to NM_152232.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:19166641 G>A maps to NM_152232.2 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr1:1268386 C>G maps to NM_152228.1 Y454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:1267308 C>T maps to NM_152228.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:1267242 G>A maps to NM_152228.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr1:1269621 G>C maps to NM_152228.1 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr12:10978406 A>C maps to NM_023921.1 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:122635652 G>A maps to NM_016945.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr7:141464470 C>T maps to NM_016943.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:141464824 T>C maps to NM_016943.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr7:141463991 C>T maps to NM_016943.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A202-01A-11D-A14K-09 chr7:141673069 G>T maps to NM_176817.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:143175672 C>T maps to NM_176883.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr12:11338817 G>A maps to NM_181429.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr12:11244633 G>A maps to ENST00000422992 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr12:11244645 T>C maps to ENST00000422992 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr12:11244633 G>A maps to ENST00000422992 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr12:11244645 T>C maps to ENST00000422992 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:141490679 C>A maps to NM_018980.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:11139339 C>T maps to NM_176890.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr12:11138560 C>T maps to NM_176890.2 *300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr7:143141396 G>A maps to NM_177437.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr12:10959165 A>G maps to NM_023918.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr12:10958814 G>T maps to NM_023918.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:13398116 G>C maps to NM_017714.2 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A278-01A-11D-A167-09 chr20:13415694 A>G maps to NM_017714.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr16:71602631 G>A maps to NM_000353.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DK-01A-21W-A071-09 chr8:125528003 G>T maps to NM_032026.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr3:10301825 T>C maps to NM_014760.3 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr3:10291218 C>A maps to NM_014760.3 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr1:212985603 G>A maps to NM_001146171.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr7:27839636 G>A maps to ENST00000409980 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:3567566 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr23:153642518 G>A did not map to a codon.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr4:38020061 C>T maps to NM_015173.2 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr4:38029466 T>C maps to NM_015173.2 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr16:30380862 T>G maps to NM_015527.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr16:30380862 T>G maps to NM_015527.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr11:67171807 C>T maps to NM_198517.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr4:7026814 C>T maps to NM_001113361.1 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:72316974 A>C maps to NM_022771.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr17:77921631 T>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:100962586 G>A maps to NM_018421.3 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr9:101006298 G>C maps to NM_018421.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr15:74178432 C>T maps to NM_153356.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr15:74177161 C>A maps to NM_153356.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr15:74177363 G>T maps to NM_153356.1 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr6:37252158 G>T maps to NM_017772.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:100020999 T>G maps to ENST00000394144 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:100002472 G>A maps to ENST00000394144 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:100009478 T>C maps to ENST00000394144 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:100037970 G>A maps to ENST00000394144 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr3:99979900 G>C maps to ENST00000394144 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:2546964 C>T maps to ENST00000434757 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr16:2548279 C>A maps to ENST00000434757 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr16:2549399 C>T maps to ENST00000434757 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr23:48418940 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:48399754 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:48418992 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:48419089 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:48418496 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:48418593 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:48419225 G>A did not map to a codon.
Sequencing variant TCGA-E9-A1N8-01A-11D-A142-09 chr23:48418749 T>C did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:48398282 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr23:48399819 G>C did not map to a codon.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr15:78305169 T>A maps to NM_144572.1 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr17:34493596 C>T maps to NM_001001417.5 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr17:34497336 G>A maps to NM_001001417.5 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr13:75936433 C>A maps to ENST00000431480 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr13:75876478 G>A maps to ENST00000431480 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr13:75930354 G>A maps to ENST00000431480 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:17202619 G>A maps to NM_001134381.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr3:17415992 C>T maps to NM_001134381.1 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr2:101648788 C>T maps to NM_001102426.1 W611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr2:101646083 C>T maps to NM_001102426.1 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:101670692 C>A maps to NM_001102426.1 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr2:101667086 C>T maps to NM_001102426.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr23:106066620 C>T did not map to a codon.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr23:106096863 T>C did not map to a codon.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr23:106117063 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr23:106097453 T>G did not map to a codon.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr23:106116841 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:106082595 C>T did not map to a codon.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr23:106065363 C>A did not map to a codon.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr23:106093308 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:106065206 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr23:106066567 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:141578946 A>C maps to NM_015130.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr4:141598221 G>T maps to NM_015130.2 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr4:141578723 A>G maps to NM_015130.2 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr5:179302038 G>A maps to NM_198868.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr5:179294844 C>G maps to NM_198868.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr19:36611613 C>T maps to NM_001281.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr3:186272044 T>G maps to NM_001134415.1 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr3:186272077 G>A maps to NM_001134415.1 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:80755679 T>C did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr17:80882912 C>T maps to NM_005993.4 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:120916473 C>T maps to NM_152715.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr12:64878169 C>G maps to NM_013254.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr12:64875759 A>G maps to NM_013254.3 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr17:45785814 G>T maps to NM_014726.2 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:45787925 T>C maps to NM_014726.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr23:9659622 T>C did not map to a codon.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr23:9683008 G>T did not map to a codon.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr23:9661203 T>C did not map to a codon.
Sequencing variant TCGA-A8-A06O-01A-11W-A019-09 chr23:9661243 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:9659626 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr23:9661416 G>T did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:9621719 C>T did not map to a codon.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr3:176771559 C>G did not map to a codon.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr3:176744189 T>A maps to NM_024665.4 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr3:176771658 G>A maps to NM_024665.4 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JB-01A-11D-A13L-09 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr6:170871090 G>A maps to NM_003194.4 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:162276717 G>A maps to NM_006593.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr11:124494847 G>T maps to NM_032811.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr11:124495578 G>A maps to NM_032811.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr22:19751740 C>T maps to NM_080647.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr11:67399311 G>A maps to NM_005995.4 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr11:67399342 G>A maps to NM_005995.4 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A082-01A-11W-A019-09 chr6:85446534 C>T maps to NM_001080508.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr6:85457661 G>T maps to NM_001080508.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:168262408 G>T maps to NM_005149.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A132-01A-31D-A10Y-09 chr1:168262380 G>C did not map to a codon.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr7:35280489 C>A did not map to a codon.
Sequencing variant TCGA-A7-A13H-01A-11D-A228-09 chr17:45822176 G>A maps to NM_013351.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:45820053 C>T maps to NM_013351.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13H-01A-11D-A228-09 chr23:79279631 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:79286516 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:79279655 C>T did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr23:79278588 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:79277897 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr23:79282217 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr23:79278718 G>T did not map to a codon.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr23:79279599 T>A did not map to a codon.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr12:115118831 C>T maps to NM_016569.3 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:115117318 C>T maps to NM_016569.3 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A28Q-01A-11D-A16D-09 chr12:115120615 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr17:59560292 C>T maps to ENST00000393853 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:59557552 G>A maps to ENST00000393853 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr12:114804030 T>A maps to NM_000192.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr14:92264127 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AM-01A-11W-A050-09 chr14:92249446 A>T maps to NM_001128596.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr17:37821695 G>A maps to NM_003673.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr23:101382273 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:101381907 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:101382107 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:101381907 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:102864205 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:102864442 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr23:102864235 G>A did not map to a codon.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr23:102528975 T>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:101396081 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:101396100 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:101396222 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr23:101396133 T>G did not map to a codon.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr23:102586399 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:13680712 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:13681277 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:13680986 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr23:13680945 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:24086038 C>T maps to NM_003198.2 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr1:24075527 G>A maps to NM_003198.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr18:44561515 C>G maps to NM_016427.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr18:44560633 G>A maps to NM_016427.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5S0-01A-11D-A28B-09 chr18:44561452 G>A maps to NM_016427.2 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr18:44542946 G>A maps to NM_001100817.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr5:145859430 G>A maps to NM_006706.3 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr5:145888736 C>T maps to NM_006706.3 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:145843285 A>C maps to NM_006706.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:145882936 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr5:145838841 C>A maps to NM_006706.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:133107550 A>C maps to NM_174937.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:57523417 A>C maps to NM_207036.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr15:57524925 C>G maps to NM_207036.1 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:42605809 A>C maps to NM_005650.1 G1834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:42607081 A>C maps to NM_005650.1 G1410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:42609385 A>C maps to NM_005650.1 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:42609448 A>C maps to NM_005650.1 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr22:42608680 G>A maps to NM_005650.1 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:1615707 C>G maps to NM_003200.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr18:52921802 A>G maps to ENST00000398339 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr18:52928696 C>T maps to ENST00000398339 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr18:52896159 G>A maps to ENST00000398339 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr18:52899810 C>T maps to ENST00000398339 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr18:52896201 G>A maps to ENST00000398339 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:133451687 G>A maps to ENST00000395029 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr5:133473796 C>T maps to ENST00000395029 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr2:85361197 C>G maps to NM_031283.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XL-01A-11D-A10M-09 chr10:114849223 T>C maps to NM_001146283.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DO-01B-11D-A12B-09 chr1:152079923 G>A maps to NM_007113.2 V1923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:152083124 G>C maps to NM_007113.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:152060520 C>T maps to NM_001008536.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr12:110346446 G>A maps to NM_032300.4 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr12:110341867 G>C maps to NM_032300.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr5:149777995 G>A maps to ENST00000451292 Q1511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr5:149755375 C>G maps to ENST00000451292 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr6:167591955 C>T maps to NM_001145121.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr6:167591955 C>T maps to NM_001145121.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr12:106729427 C>T maps to NM_152772.1 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr12:106734741 T>A maps to NM_152772.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr3:49450056 G>A maps to NM_022171.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr6:44250152 C>A maps to NM_182539.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr1:67242935 T>G maps to NM_152665.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A1H3-01A-31D-A13L-09 chr12:111085645 A>C maps to NM_001082538.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr12:111085555 C>A maps to NM_001082538.2 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:111064184 T>C maps to NM_001082538.2 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr12:124189163 C>T maps to NM_024809.3 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:124156154 G>T maps to NM_024809.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:124189163 C>T maps to NM_024809.3 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr10:97442428 G>A maps to ENST00000371217 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:24666934 C>T maps to NM_016614.2 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr10:115973856 T>C maps to NM_198795.1 H732H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr10:115986918 G>C maps to NM_198795.1 V1088V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:154516498 C>G maps to NM_001098475.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr1:154516882 C>A maps to NM_001098475.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr1:154516981 C>T maps to NM_001098475.1 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr13:61057958 G>A maps to NM_001146070.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr13:61141756 A>C maps to NM_001146070.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr1:179659889 T>C maps to ENST00000444136 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr1:179604941 C>A maps to ENST00000444136 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr1:179609513 G>A maps to ENST00000444136 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr9:100245336 T>C maps to NM_014290.2 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr1:151748588 C>T maps to NM_001083965.1 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr1:151751326 G>A maps to NM_001083965.1 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr11:12785960 C>G maps to NM_021961.5 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:49846610 A>C maps to NM_003598.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr6:35446092 G>A maps to ENST00000357281 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr6:35446242 G>A maps to ENST00000357281 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr4:48230589 C>T maps to NM_003215.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:48152922 G>A maps to NM_003215.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr4:48148340 C>A did not map to a codon.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr4:65180390 T>A maps to NM_001010874.4 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr4:65175564 T>C maps to NM_001010874.4 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr11:120989315 G>A maps to NM_005422.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr11:121000429 G>T maps to NM_005422.2 V817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr11:121023638 C>T maps to NM_005422.2 C1385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr11:121039472 C>A maps to NM_005422.2 Y1946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr11:121000387 G>A maps to NM_005422.2 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:114045947 G>A maps to NM_058222.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr9:27169622 C>T maps to NM_000459.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:27157841 T>G maps to NM_000459.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:27228263 G>A maps to NM_000459.3 Q1087Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr9:27169493 G>A maps to NM_000459.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr9:27157943 C>A maps to NM_000459.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr9:27183604 C>G maps to NM_000459.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:27197532 T>C maps to NM_000459.3 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04Q-01A-21W-A050-09 chr17:6733604 T>G maps to NM_053285.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:36551435 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr17:15234728 G>A maps to NM_031898.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr16:10721460 C>T maps to NM_144674.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr16:10769863 G>T maps to NM_144674.1 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr16:10788508 C>T maps to NM_144674.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr16:10783849 C>T maps to NM_144674.1 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:1547068 C>T maps to NM_016111.3 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:1557646 C>T maps to NM_016111.3 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:1544311 C>A maps to NM_016111.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr12:53457539 C>T maps to NM_170754.2 F1368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:20851644 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr14:20846383 T>G maps to NM_007110.4 A1840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr14:20873629 C>A maps to NM_007110.4 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr14:20856086 G>C maps to NM_007110.4 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr16:58018667 C>T maps to NM_199046.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:58018604 G>T maps to NM_199046.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:1293842 G>T maps to NM_198253.2 Y386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr5:1260684 G>C maps to NM_198253.2 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr7:115892484 T>C maps to NM_015641.2 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr7:115890507 G>A maps to NM_015641.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr12:117494612 G>A maps to ENST00000392545 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:45810736 T>G maps to NM_007170.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:45923280 G>A maps to NM_007170.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr1:45821106 C>T maps to NM_007170.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:45821061 A>T maps to NM_007170.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr10:70406739 A>G maps to NM_030625.2 E1418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:70333954 G>A maps to NM_030625.2 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:70406322 T>C maps to NM_030625.2 D1279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr10:70451291 C>G maps to NM_030625.2 L2044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr10:70451415 C>T maps to NM_030625.2 Q2086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr10:70406121 A>G maps to NM_030625.2 K1212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr10:70450997 C>T maps to NM_030625.2 L1946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr10:70405671 T>C maps to NM_030625.2 D1062D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr4:106155362 T>C maps to ENST00000513237 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr4:106196473 C>T maps to ENST00000513237 Q1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr4:106190765 G>C did not map to a codon.
Sequencing variant TCGA-A8-A08X-01A-21W-A019-09 chr2:74275538 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:74275428 C>G maps to ENST00000409262 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:74328502 C>T maps to ENST00000409262 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DN-01A-11D-A17W-09 chr2:74273625 G>T maps to ENST00000409262 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr9:103065952 G>A maps to NM_017746.3 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:103091438 C>A maps to NM_017746.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr9:103092447 G>A maps to NM_017746.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:69772022 C>A did not map to a codon.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr23:69749697 C>T did not map to a codon.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr23:69773226 A>G did not map to a codon.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr23:69890250 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:69898655 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr23:70073143 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr23:104464662 T>G did not map to a codon.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr23:104464130 G>A did not map to a codon.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr23:104464755 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:107224368 T>G did not map to a codon.
Sequencing variant TCGA-A8-A08X-01A-21W-A019-09 chr23:107224729 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:107224702 A>C did not map to a codon.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr17:56688646 C>T maps to ENST00000240361 Q359Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A4Z1-01A-21D-A25Q-09 chr17:56665336 C>T maps to ENST00000240361 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:30703536 T>C maps to NM_031271.3 K999K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr8:30700080 G>A maps to NM_031271.3 C2151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H3-01A-11D-A12Q-09 chr8:30705429 C>T maps to NM_031271.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A138-01A-11D-A10Y-09 chr8:30700782 T>C maps to NM_031271.3 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr8:30705356 C>A maps to NM_031271.3 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr8:30701523 T>C maps to NM_031271.3 V1670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:62289936 C>T maps to NM_018469.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr3:51708439 A>C maps to NM_015926.4 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:133472538 C>G maps to NM_001063.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr6:10415191 G>A maps to ENST00000379613 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:10410367 C>T maps to ENST00000379613 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:50807996 C>T maps to ENST00000263046 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr6:50683205 C>A maps to NM_172238.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:36055627 C>T maps to NM_178548.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr16:4322743 C>A maps to NM_003223.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr12:51501077 G>A maps to NM_005653.4 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:51493561 C>T maps to NM_005653.4 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:51512434 G>C maps to NM_005653.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:122004537 G>A maps to NM_014553.2 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:141693018 C>T maps to NM_001178139.1 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr3:141671858 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:132352053 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:132351893 C>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:132351620 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr23:48887845 G>A did not map to a codon.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr23:48896922 T>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:48887885 T>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:48895888 T>C did not map to a codon.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr23:48887873 T>A did not map to a codon.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr23:48895567 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr6:41652768 C>T maps to ENST00000343317 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr6:41658741 C>T maps to ENST00000343317 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:115580654 C>A maps to NM_012252.2 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JT-01A-31D-A13L-09 chr21:43767727 G>A maps to NM_005423.4 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:100467134 G>A maps to NM_001007565.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr3:100432552 T>C maps to NM_001007565.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr3:100432574 C>T maps to NM_001007565.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:26895342 G>A maps to NM_012143.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr2:188331769 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr2:188332558 G>A maps to NM_006287.4 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27A-01A-11D-A167-09 chr7:93519524 C>A maps to NM_006528.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr7:93516140 C>T maps to NM_006528.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:54611422 A>C maps to NM_013342.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr7:100224403 G>C maps to NM_003227.3 Y706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr7:100238597 C>A did not map to a codon.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr3:195802198 G>A maps to NM_001128148.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:133918957 C>T maps to NM_003235.4 N1220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:134030206 G>A maps to NM_003235.4 L2249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03U-01B-21D-A10M-09 chr8:133899092 A>G maps to NM_003235.4 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr8:133984054 C>T maps to NM_003235.4 R1998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr8:133910444 G>T maps to NM_003235.4 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr8:133948003 C>T maps to NM_003235.4 R1646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr8:134030035 C>A maps to NM_003235.4 L2192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr14:76446978 C>T maps to NM_003239.2 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr14:76446996 C>A maps to NM_003239.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A041-01A-11W-A050-09 chr5:135385249 C>T maps to NM_000358.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr5:135389689 C>T maps to NM_000358.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr3:30732949 G>A maps to NM_001024847.2 W546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr3:30713658 C>T maps to NM_001024847.2 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr1:92185006 C>T maps to NM_003243.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr20:35219311 G>T did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:89177795 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr14:24724645 G>A maps to NM_000359.2 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr14:24718578 G>A maps to NM_000359.2 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr14:24723362 G>A maps to NM_000359.2 N740N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr20:36779423 G>A maps to NM_004613.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr20:36776434 G>A maps to NM_004613.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:36770539 C>T maps to NM_004613.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:36789840 G>A maps to NM_004613.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr20:36766743 C>T maps to NM_004613.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54X-01A-11D-A25Q-09 chr20:36766788 T>C did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr20:2297757 C>T maps to NM_003245.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:44952808 C>T maps to NM_003241.3 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:43531129 T>C maps to NM_201631.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07L-01A-11W-A019-09 chr15:43525858 C>T maps to NM_201631.3 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr20:2413156 G>A maps to NM_198994.2 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr20:2378599 C>T maps to NM_198994.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr15:43579532 G>A maps to NM_052955.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr15:43569148 G>C maps to NM_052955.2 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:85554056 G>A maps to ENST00000409015 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:56723587 A>C maps to NM_024831.6 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:56695305 G>T did not map to a codon.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr8:56711670 G>T maps to NM_024831.6 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr20:57564938 G>A maps to NM_198976.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:43514200 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:43787408 A>C maps to ENST00000330266 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr8:42693458 T>C maps to NM_018105.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr8:42693371 G>A maps to NM_018105.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:72070746 A>G maps to NM_031435.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:242572452 C>T maps to NM_015963.5 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr19:36526356 C>T maps to NM_152658.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:83828936 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr4:83839428 C>T maps to NM_024672.4 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr15:39874436 C>T maps to NM_003246.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:39885725 C>T maps to NM_003246.2 Q1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr15:39880381 G>A maps to NM_003246.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr15:39884926 T>C maps to NM_003246.2 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr15:39885372 C>T maps to NM_003246.2 R980R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr15:39886349 C>G maps to NM_003246.2 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IY-01A-21D-A21Q-09 chr6:169641883 G>A maps to NM_003247.2 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:169648727 G>A maps to NM_003247.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:169648907 G>A maps to NM_003247.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr6:169626379 T>C maps to NM_003247.2 E811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr1:155167680 G>C maps to NM_007112.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr1:155176015 G>C maps to NM_007112.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr5:79375017 G>A maps to NM_003248.4 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:79368164 T>G maps to NM_003248.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:79335984 C>A maps to NM_003248.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr5:79374936 C>T maps to NM_003248.4 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:375703 T>C maps to NM_016585.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:375709 C>T maps to NM_016585.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr1:151826026 G>A maps to NM_182578.3 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:128134915 T>G maps to NM_001164685.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:128222053 G>A maps to NM_001164685.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr5:157166414 A>T maps to NM_017872.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:25314044 C>G maps to NM_024838.4 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr10:25313397 C>T maps to NM_024838.4 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr2:88482534 C>T maps to NM_018271.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr18:226823 G>C maps to NM_005131.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr23:122820418 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:122758013 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:122771966 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:122765547 A>G did not map to a codon.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr23:122754798 T>A did not map to a codon.
Sequencing variant TCGA-E9-A1R0-01A-22D-A16D-09 chr23:122840714 T>A did not map to a codon.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr23:122830636 G>T did not map to a codon.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr23:122766799 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr5:175388334 T>C maps to NM_032361.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:29908075 T>G maps to NM_003678.4 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:29940565 G>A maps to NM_003678.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr16:3075809 G>A maps to NM_024339.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:3077654 C>T maps to NM_024339.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24R-01A-11D-A167-09 chr19:2807033 C>T maps to NM_003249.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:38243000 C>T maps to NM_003250.5 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr11:77774953 C>G maps to NM_003251.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03V-01A-11D-A10Y-09 chr13:52971732 G>A maps to NM_018676.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr15:71704116 C>T maps to NM_024817.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YI-01A-31D-A10M-09 chr7:11509515 C>T maps to ENST00000423059 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:11450848 C>T maps to ENST00000423059 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:11501711 G>A maps to ENST00000423059 N809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:11446993 C>T maps to ENST00000423059 V1285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr7:11676318 G>A maps to ENST00000423059 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:11464339 C>T maps to ENST00000423059 V1122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr7:11486989 T>G maps to ENST00000423059 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr2:138373749 C>T maps to ENST00000272643 C1146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:137988704 C>T maps to ENST00000272643 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr2:138033555 G>A maps to ENST00000272643 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr2:138208560 C>T maps to ENST00000272643 R1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr3:9406883 A>G maps to NM_015453.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:9412820 T>C maps to NM_015453.2 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:134121158 A>C maps to NM_199298.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:70444096 A>C maps to NM_022173.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:32624208 C>T maps to NM_003253.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr21:32492858 G>A maps to NM_003253.2 Q1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr21:32639060 G>A maps to NM_003253.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RY-01A-21D-A28B-09 chr21:32624172 G>A maps to NM_003253.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:155561806 C>T maps to ENST00000456144 I1104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:155451382 C>A maps to ENST00000456144 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr6:155561719 C>T maps to ENST00000456144 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:4816954 G>A maps to NM_182919.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr1:43783619 G>A maps to NM_005424.2 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:43774786 C>T maps to NM_005424.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr1:43773136 G>A maps to NM_005424.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:113199407 G>A maps to NM_052864.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr11:65124037 C>T maps to NM_145719.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09K-01A-11W-A019-09 chr4:153690941 C>G maps to NM_145720.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr4:153691715 T>C maps to NM_145720.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr5:149375539 C>T maps to NM_030953.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:3350380 A>C maps to NM_033208.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr16:3349849 A>T maps to NM_033208.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr12:56817647 G>A maps to NM_003920.3 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr16:4390378 C>A maps to NM_016069.8 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr17:904306 G>C maps to NM_013337.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:902166 C>T maps to NM_013337.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15P-01A-11D-A10Y-09 chr10:51592554 T>C maps to NM_006327.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr19:8006001 G>A maps to NM_006351.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:7993024 G>A maps to NM_006351.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr19:7998979 G>A maps to NM_006351.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr19:7999108 G>A maps to NM_006351.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:39978707 C>G maps to NM_001001563.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:39971351 C>A maps to NM_001001563.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FU-01A-11D-A14G-09 chr19:39973555 G>A maps to NM_001001563.1 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr19:39976915 G>A maps to NM_001001563.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr23:100601590 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr23:100603572 G>T did not map to a codon.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr23:47442868 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr22:33245469 G>A maps to NM_000362.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr22:33245466 G>A maps to NM_000362.4 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:54173488 C>T maps to NM_014464.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr6:54254621 G>T maps to NM_014464.3 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr6:54173423 C>T maps to NM_014464.3 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:156396103 G>A maps to NM_015508.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P6-01A-11D-A142-09 chr3:156396271 T>A maps to NM_015508.4 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:66641442 G>A maps to NM_017858.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr1:168160638 A>G maps to NM_152902.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr1:168168158 T>C maps to NM_152902.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr11:126162825 C>T maps to NM_148910.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:43472734 T>G maps to NM_001146016.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr6:43471368 C>T maps to NM_001146016.1 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr15:30025015 A>C maps to NM_003257.3 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr15:30024833 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr15:30003158 C>T maps to NM_003257.3 E1416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr15:30024678 C>A maps to NM_003257.3 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:3747916 C>T maps to NM_014428.1 Y849Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153540978 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153555941 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:153553733 C>A did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:27052390 G>A maps to NM_138463.3 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:3011062 G>A maps to NM_003260.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KI-01A-11D-A14K-09 chr15:70347453 G>A maps to NM_005078.2 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr15:70347637 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr9:82227581 C>T maps to ENST00000376537 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:82320814 T>G maps to ENST00000376537 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:2980132 G>A maps to NM_001143986.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr19:2987727 G>T maps to NM_001143986.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr4:166913987 C>T maps to ENST00000507499 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27R-01A-11D-A16D-09 chr4:166999052 A>T did not map to a codon.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr4:167012407 T>C maps to ENST00000507499 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A079-01A-21W-A019-09 chr9:35717227 C>A maps to NM_006289.3 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr9:35714847 G>C maps to NM_006289.3 S927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr9:35713253 G>C maps to NM_006289.3 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr9:35704101 C>T maps to NM_006289.3 G2039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr9:35724266 C>T maps to NM_006289.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr9:35708475 T>G maps to NM_006289.3 A1444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr15:63032863 C>G maps to NM_015059.2 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A4-01A-11W-A019-09 chr15:63029120 C>T maps to NM_015059.2 Q1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15G-01A-11D-A12B-09 chr15:63102179 C>T maps to NM_015059.2 F2240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RY-01A-31D-A25Q-09 chr4:38798934 C>T maps to NM_003263.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TM-01A-11D-A228-09 chr4:38798934 C>T maps to NM_003263.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:38799038 C>A maps to NM_003263.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr4:38798934 C>T maps to NM_003263.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr4:38798997 T>C maps to NM_003263.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr4:38775801 T>C maps to NM_030956.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YN-01A-11D-A28B-09 chr4:38777096 G>A maps to NM_030956.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr4:154624746 C>T maps to NM_003264.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr4:154626260 C>T maps to NM_003264.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr4:186998035 C>G maps to NM_003265.2 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:120476788 C>T maps to NM_138554.3 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr9:120475508 C>A maps to NM_138554.3 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr9:120474782 C>G maps to NM_138554.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:223283802 G>A maps to NM_003268.5 I857I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:223286289 G>A maps to NM_003268.5 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr1:223286091 C>A maps to NM_003268.5 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr1:223284237 G>C maps to NM_003268.5 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ES-01A-11D-A10Y-09 chr23:12904270 A>G did not map to a codon.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr23:12904334 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:12904083 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:12904836 C>T did not map to a codon.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr23:12905868 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr23:12903834 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr23:12905641 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr23:12906028 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1L7-01A-11D-A142-09 chr23:12903897 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:12939335 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:12939869 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:12937807 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:12939569 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr23:12938974 G>A did not map to a codon.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr23:12938875 G>A did not map to a codon.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr23:12937271 A>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:12937582 T>G did not map to a codon.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr23:12937621 C>T did not map to a codon.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr23:12940142 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr23:12939276 C>A did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr3:52255598 G>C maps to ENST00000494383 R1064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr3:52255703 G>A maps to ENST00000494383 F1029F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr3:149095217 G>A maps to ENST00000383054 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:196050699 G>A maps to NM_138461.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:83781629 A>C maps to NM_023003.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr19:19377376 C>A maps to NM_001001524.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr19:19379480 G>T maps to NM_001001524.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr11:64883378 C>T maps to NM_003273.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr12:27127094 C>A maps to NM_016551.2 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:27132786 C>T maps to NM_016551.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr12:27126945 G>A maps to NM_016551.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr8:105361289 C>A maps to NM_030788.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:24663985 A>C maps to NM_006405.5 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr14:24659851 G>A maps to NM_006405.5 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr10:98303889 G>A maps to NM_020123.3 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr20:30729673 G>T maps to NM_014742.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:30749158 C>T maps to NM_014742.3 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:30733155 G>T maps to NM_014742.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RU-01A-11D-A28B-09 chr20:30733012 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:219141750 A>T maps to NM_022152.4 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr12:50136032 C>G maps to NM_001098576.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:75435970 A>C maps to NM_138691.2 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr20:2591084 G>A maps to NM_080751.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:2575595 G>C maps to NM_080751.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:2542638 G>A maps to NM_080751.2 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:2517916 C>T maps to NM_080751.2 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr15:81630255 G>A maps to ENST00000454937 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr15:81625443 C>G maps to ENST00000454937 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:81644151 G>A maps to ENST00000454937 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr16:19481011 G>A maps to NM_001105248.1 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:76122674 G>A maps to NM_007267.6 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr17:76109252 C>T maps to NM_007267.6 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:76116777 G>A maps to NM_007267.6 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:19058513 A>C maps to NM_024847.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:19056733 G>A maps to NM_024847.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:19056742 C>T maps to NM_024847.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr17:76134256 C>T maps to NM_152468.4 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr13:114156089 G>A maps to NM_017905.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:20097809 C>A maps to NM_181719.4 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr1:20066415 G>A maps to NM_181719.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr1:20082236 T>C maps to NM_181719.4 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr1:20009550 G>A maps to NM_181719.4 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DH-01A-11D-A099-09 chr5:140023513 G>A maps to ENST00000252100 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr5:140022221 C>T maps to ENST00000252100 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr19:10943682 C>T maps to NM_006858.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr7:44621753 G>A maps to NM_182547.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr16:69381692 C>A maps to NM_144676.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:77818023 T>G maps to NM_213601.1 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:177022333 C>T maps to NM_017510.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:103310113 C>T maps to NM_001198812.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr9:103334853 C>G maps to NM_001198812.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62X-01A-11D-A29N-09 chr17:53798215 G>A maps to NM_001099640.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26F-01A-21D-A167-09 chr17:72832375 C>T maps to NM_017728.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr17:72786400 C>T maps to NM_017728.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr17:72832297 C>G maps to NM_017728.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr17:41368592 T>C maps to NM_145041.1 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr7:12258147 G>A did not map to a codon.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr12:48360467 G>A maps to NM_001143842.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr17:8077908 G>C maps to NM_032354.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr3:133109179 T>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:10012308 A>G maps to NM_018447.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:50396185 T>C maps to NM_007024.4 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr3:50392896 T>C maps to NM_007024.4 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:44338118 G>A maps to NM_032256.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:44693419 C>T maps to NM_032256.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15E-01A-11D-A12B-09 chr12:44238678 C>T maps to NM_032256.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr12:122213015 G>T maps to NM_001080825.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr12:122186348 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr12:122186339 G>A maps to NM_001080825.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:4247947 C>A maps to ENST00000382753 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr2:98409037 C>A maps to NM_015348.1 E1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr2:98375463 C>T maps to NM_015348.1 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:98388800 G>A maps to NM_015348.1 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CZ-01A-11W-A050-09 chr12:125834675 C>A maps to NM_052907.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EN-01A-13D-A099-09 chr12:125834883 T>A maps to NM_052907.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr12:126139186 C>A maps to NM_052907.2 C1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr12:125834178 C>G maps to NM_052907.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr12:126137036 C>G maps to NM_052907.2 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr12:125834061 C>A maps to NM_052907.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr12:126138565 C>G maps to NM_052907.2 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CV-01A-31D-A10Y-09 chr12:129569106 G>A maps to NM_133448.2 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr12:129563233 T>A maps to NM_133448.2 K654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:130184751 G>A maps to NM_133448.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr12:130015638 G>A maps to NM_133448.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:32963144 G>T maps to NM_207313.1 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr11:61135441 T>C maps to NM_016464.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:134849411 G>C maps to NM_018295.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr9:139686769 C>G maps to NM_032928.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr19:5724830 G>A maps to NM_152784.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr2:85827040 C>G maps to NM_001031738.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr4:122682807 G>A maps to NM_152399.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr4:38990516 A>C maps to NM_024943.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr19:47549914 G>A maps to NM_017854.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr2:135260480 G>A maps to NM_030923.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr4:56283242 G>A maps to NM_018475.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:56291561 C>T maps to NM_018475.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr7:112424724 T>C maps to NM_022484.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:216960799 G>T maps to NM_138390.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:216964904 C>A maps to NM_138390.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr2:62729607 C>T maps to NM_198276.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr16:75485729 C>T maps to NM_145254.1 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:72419565 C>T maps to NM_173490.6 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:72469363 C>T maps to NM_153217.2 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr4:947132 T>C maps to NM_032326.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr4:952145 C>T maps to NM_032326.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:150490275 G>C maps to NM_014020.3 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:62554929 C>T maps to NM_199337.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:104233462 G>A maps to NM_024789.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:159010741 G>C maps to NM_020823.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr6:159029467 G>C maps to NM_020823.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr2:103414460 T>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:148555440 A>C maps to NM_018241.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:148690403 G>T did not map to a codon.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr23:148685666 G>T did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr23:148690502 A>G did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr16:8890207 C>T maps to NM_015421.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:153247680 C>G did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr20:48699336 G>A maps to NM_199203.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:72090222 C>T maps to NM_018279.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:72091270 A>G maps to NM_018279.3 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr12:57464508 G>A maps to NM_001130963.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr7:19761718 C>G maps to NM_152774.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:19812244 G>A maps to NM_152774.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:74365109 G>A maps to NM_013390.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:74340595 C>T maps to NM_013390.2 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr10:95660751 G>A maps to NM_001134658.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr1:9656052 C>G maps to NM_001130924.2 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:1584285 C>T maps to NM_024600.4 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr19:11453679 A>C maps to NM_198536.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:11456196 T>C maps to NM_198536.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr22:25331449 A>C maps to ENST00000423535 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:37186653 A>C maps to NM_145316.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YF-01A-21D-A10G-09 chr11:124967603 G>A maps to NM_001080546.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:29982864 G>A maps to NM_194280.3 *241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr17:10632346 C>A did not map to a codon.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr11:62558103 C>G maps to NM_001080501.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr11:118404579 C>A maps to NM_032780.3 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BS-01A-11D-A12Q-09 chr23:15682470 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:15646167 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:102968725 G>T did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr23:102968632 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:100349754 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:100349771 C>G did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr2:120194850 C>A maps to NM_183240.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr19:16798953 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr19:16799101 C>T maps to NM_024074.1 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:16791267 G>T maps to NM_024074.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr9:108536282 C>T maps to NM_018112.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr3:119150929 G>C maps to NM_018266.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:119151001 G>A maps to NM_018266.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr11:9316934 C>G did not map to a codon.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr3:14170982 G>A maps to NM_024334.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:34657504 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:54293789 G>A maps to NM_018087.4 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FD-01A-11W-A050-09 chr17:57842468 C>T maps to NM_030938.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr17:57915715 A>G maps to NM_030938.3 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr17:57917166 C>G maps to NM_030938.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr21:34832792 G>A maps to NM_006134.5 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr8:92021020 C>T maps to NM_018710.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:25812148 C>T maps to NM_018202.4 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr1:25775351 G>C maps to NM_018202.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr1:25810702 C>G maps to NM_018202.4 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HI-01A-11D-A135-09 chr1:54509099 G>C maps to ENST00000371338 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:43476615 T>C maps to NM_024956.3 Y588Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J2-01A-21D-A13L-09 chr1:226034839 C>T maps to NM_014698.2 Q775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr1:226040470 C>T did not map to a codon.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr6:44119645 C>T maps to NM_018426.1 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr14:77719718 C>T maps to NM_020431.2 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr8:56668875 G>A maps to ENST00000434581 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:109797207 G>A maps to NM_153015.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:156255127 T>G maps to NM_032323.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr11:700170 T>C maps to ENST00000449452 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:205052740 C>T maps to NM_203376.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr2:112847240 G>C maps to NM_032824.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr2:112873717 T>C maps to NM_032824.2 *556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr3:48658404 G>C maps to NM_001008269.1 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr14:74874369 G>A maps to NM_001105579.1 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr19:41889657 A>G maps to NM_001098821.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr19:41889742 C>T maps to NM_001098821.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:7259741 G>A maps to NM_198154.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr17:26653644 G>C maps to NM_014573.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:31263411 G>A maps to NM_015544.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A252-01A-11D-A167-09 chr3:69072339 T>C maps to NM_007114.2 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:28652026 G>T maps to NM_206832.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr19:4294612 C>T maps to NM_144615.2 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr19:4298145 G>A maps to NM_144615.2 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:4292731 G>C maps to NM_144615.2 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:4292688 G>A maps to NM_144615.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr23:154743675 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:52192462 G>T maps to NM_014547.4 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr15:52161503 C>T maps to NM_014547.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:52155167 G>A maps to NM_014547.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr1:151143395 C>T maps to NM_013353.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:151143932 C>T maps to NM_013353.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr1:151147305 C>A maps to NM_013353.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AP-01A-11D-A12Q-09 chr3:33135081 G>C maps to NM_001039770.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AV-01A-31D-A10Y-09 chr3:33135492 G>A maps to NM_001039770.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr4:68797733 G>A maps to NM_182606.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CU-01A-12W-A050-09 chr4:69094492 A>T maps to NM_182502.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:68693102 C>A maps to NM_004262.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:69343140 G>A maps to NM_014058.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:117789199 T>G maps to ENST00000413475 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr11:117780639 C>T maps to ENST00000413475 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr21:19666645 G>C maps to NM_002772.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr21:19666940 G>T maps to NM_002772.2 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:113563802 G>C maps to NM_030770.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DA-01A-11D-A18P-09 chr11:113570326 T>G maps to NM_030770.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr22:37492105 G>A maps to ENST00000381792 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A7-01A-11W-A019-09 chr3:111768780 C>G maps to ENST00000443106 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:111785246 C>T maps to ENST00000443106 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr3:111795821 C>T maps to ENST00000443106 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B4-01A-11D-A12Q-09 chr23:101769049 T>G did not map to a codon.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr12:29709841 G>A maps to NM_001193451.1 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr12:29709800 C>T maps to NM_001193451.1 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr12:83359522 G>A maps to NM_152588.1 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr12:83289847 C>T maps to NM_152588.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:88566489 A>G maps to NM_181783.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr14:51707048 C>G maps to NM_030755.4 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr18:66354925 G>T maps to NM_019022.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:117853231 A>C maps to NM_002160.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:117826953 T>G maps to NM_002160.2 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr9:117798470 C>G maps to NM_002160.2 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr9:117825310 G>A maps to NM_002160.2 G1306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr9:117848956 G>A maps to NM_002160.2 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr9:117849162 G>A maps to NM_002160.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr9:117825202 G>A maps to NM_002160.2 V1342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:103599097 G>A maps to NM_006291.2 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr6:138200081 C>T maps to NM_006290.2 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:138196964 C>G maps to NM_006290.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:138192622 C>T maps to NM_006290.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr6:138201277 G>T maps to NM_006290.2 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr2:152220569 C>T maps to NM_007115.3 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:152230092 C>A maps to NM_007115.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A041-01A-11W-A050-09 chr5:118728610 C>T maps to NM_014350.2 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:4652150 C>T maps to NM_152362.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:51350621 G>C maps to NM_207381.2 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr8:23069722 G>A maps to NM_003844.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C3-01A-21D-A12Q-09 chr8:22973123 T>C maps to ENST00000356864 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FS-01A-11D-A17D-09 chr18:60036220 A>G maps to NM_003839.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:12061487 T>C maps to NM_001192.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr13:24242896 C>T maps to NM_018647.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:6443375 G>C maps to NM_001065.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:12266989 G>A maps to NM_001066.2 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr6:47253821 C>T maps to NM_014452.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr6:47221132 G>A maps to NM_014452.3 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr6:47254253 G>A maps to NM_014452.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XV-01A-11D-A14K-09 chr20:62328256 G>A maps to ENST00000482936 A1348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr1:7995127 G>A maps to NM_001561.5 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr3:172241141 G>A maps to ENST00000382750 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04H-01B-11D-A10M-09 chr3:172224440 A>G maps to ENST00000382750 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:7464140 G>T maps to NM_003808.3 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr9:117553069 G>A maps to NM_005118.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr9:117552736 G>A maps to NM_005118.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr1:173157703 G>C maps to NM_003326.3 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr9:117692388 C>G maps to NM_001244.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:170828505 G>A maps to NM_015028.2 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr3:170819299 C>T maps to NM_015028.2 E843E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr3:170802952 C>T maps to NM_015028.2 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr3:170819278 G>T maps to NM_015028.2 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr3:170843928 C>T maps to NM_015028.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15H-01A-11D-A12B-09 chr3:170784080 G>A maps to NM_015028.2 G1298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr4:2747220 A>T maps to NM_024309.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:2744010 G>A maps to NM_024309.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:122063918 G>A maps to ENST00000509841 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XT-01A-11D-A14K-09 chr4:122078380 C>T maps to ENST00000509841 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr17:7286593 G>A maps to NM_003985.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr17:7288066 G>T maps to NM_003985.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:9562211 C>T maps to NM_003747.2 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:9588467 C>T maps to NM_003747.2 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:9622297 C>T maps to NM_003747.2 R1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr8:9619111 C>A maps to NM_003747.2 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr11:57081322 G>C maps to NM_033396.2 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:57075951 A>C maps to NM_033396.2 G1411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:57076398 A>C maps to NM_033396.2 G1262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr11:57070109 G>A maps to NM_033396.2 D1502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr11:57069367 T>C maps to NM_033396.2 E1628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IL-01A-11D-A14G-09 chr11:57077319 G>A maps to NM_033396.2 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr10:93572899 A>G maps to NM_025235.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:99848938 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:99849290 A>G did not map to a codon.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr23:99848999 G>A did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:99840057 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:99849280 G>T did not map to a codon.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr1:175067624 C>T maps to NM_022093.1 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr1:175086255 G>A maps to NM_022093.1 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:201379467 C>T maps to ENST00000367312 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr11:1862415 C>T maps to ENST00000381906 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:74834916 C>T maps to NM_001112808.2 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:55649352 G>A maps to NM_003283.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr5:72151659 C>T maps to NM_002270.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr5:72161499 C>T maps to NM_002270.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:12814322 G>A maps to NM_001136196.1 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:12817063 G>C maps to NM_001136196.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr19:12816347 C>T maps to NM_001136196.1 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr19:12830079 G>C maps to NM_001136196.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:128630065 C>A maps to ENST00000471166 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr7:128610252 G>A maps to ENST00000471166 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:128610207 G>A maps to ENST00000471166 D898D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr1:175355300 G>T maps to NM_003285.2 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr1:175365872 C>T maps to NM_003285.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J6-01A-11D-A188-09 chr1:175372510 G>A maps to NM_003285.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr7:5399196 C>T maps to NM_001080495.2 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:5391555 C>G maps to NM_001080495.2 L1788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr7:5355695 C>A maps to NM_001080495.2 L2251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr7:5415755 G>T maps to NM_001080495.2 S903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RC-01A-11D-A159-09 chr7:5352634 T>G maps to NM_001080495.2 S2629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr16:24831604 A>C maps to NM_014494.2 P1742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AT-01A-11D-A12Q-09 chr16:24801087 C>T maps to NM_014494.2 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr16:24817932 A>G maps to NM_014494.2 Q1456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr16:24801525 A>C maps to NM_014494.2 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr16:24788393 C>T maps to NM_014494.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr22:40662370 C>T maps to ENST00000454349 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:40681695 T>G maps to ENST00000454349 G1224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:40677265 C>G maps to ENST00000454349 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:40719020 G>T maps to ENST00000454349 G1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr22:40676007 C>A maps to ENST00000454349 S1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr22:40717092 G>T did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr17:76083109 C>A maps to NM_001142640.1 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:76063871 T>G maps to NM_001142640.1 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr17:76060962 G>A maps to NM_001142640.1 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr17:76083022 G>A maps to NM_001142640.1 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:76067209 C>T maps to NM_001142640.1 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IJ-01A-11D-A142-09 chr17:76089143 G>A maps to NM_001142640.1 W1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr2:218745657 G>A maps to NM_022648.4 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:47344431 C>T maps to NM_022748.11 E940E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr7:47408709 G>C maps to NM_022748.11 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr7:47344560 C>T maps to NM_022748.11 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:47408073 G>A maps to NM_022748.11 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr7:47342641 G>A maps to NM_022748.11 F1121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr7:47342614 G>A maps to NM_022748.11 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CO-01A-13D-A228-09 chr17:38638408 C>A maps to NM_032865.5 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr17:38643407 G>T maps to NM_032865.5 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr6:32021405 C>G maps to ENST00000375244 L2850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr6:32011574 C>T maps to ENST00000375244 S3827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr6:32029330 G>A maps to ENST00000375244 Y2445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:32039827 G>A maps to ENST00000375244 F1643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr6:32021330 C>T maps to ENST00000375244 L2875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F6-01A-11D-A13L-09 chr6:32025868 C>T maps to ENST00000375244 R2597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr6:32065666 C>T maps to ENST00000375244 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr6:32065107 C>T maps to ENST00000375244 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:32023868 C>G maps to ENST00000375244 L2742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr17:48940733 G>A maps to NM_005749.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:41833043 C>T maps to NM_016272.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:45807207 G>A maps to NM_025077.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr22:35729467 C>G maps to ENST00000451197 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54O-01A-11D-A25Q-09 chr17:17786096 C>T maps to NM_001082968.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr17:17786171 G>A maps to NM_001082968.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr20:43577408 G>C maps to NM_006809.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr20:43572096 G>A maps to NM_006809.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AS-01A-11D-A12Q-09 chr19:45406419 C>T maps to NM_006114.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:39704875 C>G maps to NM_003286.2 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr20:39751879 C>A maps to NM_003286.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr8:144406750 C>T maps to NM_052963.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:38552590 G>A maps to ENST00000357601 R1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr17:38557206 A>G maps to ENST00000357601 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JB-01A-11D-A13L-09 chr3:25668733 T>G maps to ENST00000264331 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr17:18205697 C>A maps to NM_004618.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LS-01A-12D-A159-09 chr22:22318571 A>T maps to NM_003935.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr22:22311881 G>A maps to NM_003935.3 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07E-01A-11W-A050-09 chr3:133327396 A>G maps to NM_007027.3 I1469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:133356789 G>T maps to NM_007027.3 S817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr3:133339114 C>T maps to NM_007027.3 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr9:32541996 G>T maps to NM_005802.4 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:132584994 C>T maps to ENST00000437532 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:179815880 C>T maps to NM_145034.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:132569510 G>A maps to NM_014506.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr9:132566430 C>T maps to NM_014506.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:179054886 C>T maps to NM_022371.3 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr8:59750754 A>T maps to NM_014729.2 L270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr8:59764364 C>G did not map to a codon.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr8:59852037 G>A maps to NM_014729.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr20:42697310 G>A maps to ENST00000348077 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr20:42683024 G>A maps to ENST00000348077 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SD-01A-11D-A25Q-09 chr16:52473348 G>A maps to ENST00000407228 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:52484428 G>T maps to ENST00000407228 Y146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08T-01A-21W-A019-09 chr14:21961323 G>T maps to NM_014828.2 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A228-01A-31D-A159-09 chr14:21963402 C>T maps to NM_014828.2 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr17:7578187 C>A maps to NM_001126112.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr17:7577155 C>A did not map to a codon.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-A8-A07O-01A-11W-A019-09 chr17:7579310 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:7579428 T>G maps to NM_001126112.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3OD-01A-11D-A21Q-09 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr17:7578464 G>T maps to NM_001126112.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr17:7577109 G>C maps to NM_001126112.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03L-01A-41W-A071-09 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0JB-01A-11W-A071-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AP-01A-11D-A12Q-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A254-01A-21D-A167-09 chr17:7579314 G>T maps to NM_001126112.1 C124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IE-01A-11W-A050-09 chr17:7577017 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr17:7579345 A>T maps to NM_001126112.1 L114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B7-01A-12D-A10Y-09 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr17:7579311 C>G maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0RX-01A-21D-A099-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18H-01A-11D-A12B-09 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr17:7579520 C>A maps to NM_001126112.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-BH-A202-01A-11D-A14K-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A208-01A-11D-A159-09 chr17:7578289 C>G did not map to a codon.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr17:7577076 C>T maps to NM_001126112.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr17:7577099 T>A maps to NM_001126112.1 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XA-01A-11D-A14G-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr17:7578430 G>A maps to NM_001126112.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr17:7578401 G>T maps to NM_001126112.1 C176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr17:7579590 C>G did not map to a codon.
Sequencing variant TCGA-E2-A1B6-01A-31D-A12Q-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr17:7578555 T>G did not map to a codon.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr17:7577508 C>A maps to NM_001126112.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PA-01A-11D-A142-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr17:7579535 C>A maps to NM_001126112.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr15:43701228 C>A maps to NM_001141980.1 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr15:43701231 G>A maps to NM_001141980.1 F1821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:43739573 A>G maps to NM_001141980.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr15:43700246 G>C maps to NM_001141980.1 L1880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr1:223983916 G>C maps to NM_001031685.2 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr17:27899464 C>T maps to NM_138349.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:24302508 A>C maps to NM_147184.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:24302508 A>C maps to NM_147184.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:24302331 C>G maps to NM_147184.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr8:95952410 T>C maps to NM_033285.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:44004146 G>A maps to NM_014477.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr3:189608637 C>T maps to NM_003722.4 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:189612206 A>C maps to NM_003722.4 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr3:189582202 C>T maps to NM_003722.4 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:189604230 G>A maps to NM_003722.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:113731075 A>G maps to NM_001143819.1 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr8:80992643 C>T maps to NM_001025252.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr8:80956422 G>C maps to NM_001025253.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:18048071 C>T maps to ENST00000341556 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr12:72388263 T>C maps to ENST00000389376 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:72338141 C>A maps to ENST00000389376 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Z-01A-11D-A10Y-09 chr12:72338117 G>C maps to ENST00000389376 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr12:72335392 C>T maps to ENST00000389376 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:6979277 G>A maps to NM_001159287.1 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WW-01A-11D-A10G-09 chr12:6976709 C>T maps to NM_001159287.1 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr7:144245656 A>C maps to NM_022445.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr9:35685267 C>T maps to ENST00000329305 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr9:35689718 A>G maps to ENST00000329305 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:154164458 C>T maps to ENST00000271850 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr1:154144513 A>C maps to NM_153649.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr6:18132370 C>T maps to NM_000367.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr2:1440157 T>C did not map to a codon.
Alternatively spliced codon TCGA-A2-A0EM-01A-11W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:6636545 C>T maps to ENST00000453338 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr11:6637687 G>A maps to ENST00000453338 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr13:103301462 T>G maps to ENST00000376052 Y945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr13:103299561 G>A maps to ENST00000376052 K832K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:21500190 G>A maps to NM_173846.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr14:21499251 G>A maps to NM_173846.4 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr1:186303577 A>T maps to NM_003292.2 A1687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:186314829 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:3542022 C>T maps to NM_182752.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:1291837 A>C maps to ENST00000461509 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:1279625 G>A maps to ENST00000445910 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:1278689 T>A maps to ENST00000445910 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr16:1279649 G>C maps to ENST00000445910 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr7:65705582 C>A maps to NM_003596.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B7-01A-12D-A10Y-09 chr7:65705727 C>T maps to NM_003596.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr22:26936813 G>A maps to NM_003595.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr21:10916376 C>T maps to NM_199261.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr13:20049727 G>T maps to NM_199254.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03O-01A-11W-A019-09 chr3:185641772 C>G did not map to a codon.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr14:103336783 G>T did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr14:103363657 C>T maps to NM_145725.2 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:111913187 T>G maps to ENST00000340026 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:209949002 G>C maps to NM_025228.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr1:209951471 A>G maps to NM_025228.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr1:209953884 G>A maps to NM_025228.2 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr17:27076033 G>A maps to NM_004295.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr17:27075096 G>A maps to NM_004295.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr17:27075545 C>T maps to NM_004295.3 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:211526622 C>T maps to ENST00000427925 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr16:2225152 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr3:49878477 C>A maps to NM_005879.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr3:42229602 G>T maps to NM_001042646.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:42233126 G>C maps to NM_001042646.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr3:42166957 G>A maps to NM_001042646.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr3:42234666 A>G maps to NM_001042646.1 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr2:202260101 G>A maps to NM_015049.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:202265749 G>A maps to NM_015049.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr2:202245616 G>C maps to NM_015049.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:71495480 C>T maps to NM_014294.5 W323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:71510246 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:71520435 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr4:118005643 C>A maps to NM_152402.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr6:52370467 G>A maps to NM_012288.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:52369497 G>A maps to NM_012288.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr6:52369548 G>T maps to NM_012288.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr3:36902451 G>A maps to NM_014831.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr3:36872505 C>T maps to NM_014831.2 V2812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr3:36872499 G>A maps to NM_014831.2 D2814D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr16:3714412 G>A maps to NM_016292.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr21:45479067 C>T maps to NM_003274.4 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:13732584 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr23:13734770 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr16:88926158 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:36603570 G>A maps to NM_014408.3 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:36603504 G>C maps to NM_014408.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr11:118890871 C>T maps to NM_016146.4 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr19:45666464 C>T maps to NM_024108.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:140898131 G>A maps to NM_031466.5 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr8:141468378 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:123786108 T>G maps to NM_006073.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr6:123892140 G>T maps to NM_006073.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XT-01A-11D-A10G-09 chr6:41243862 C>T maps to NM_018643.2 *235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:41129193 C>T maps to NM_018965.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:41160569 G>A maps to ENST00000373108 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr6:41196188 C>A maps to NM_198153.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr6:42200627 C>T maps to NM_033502.2 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr6:42224822 A>T maps to NM_033502.2 L785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr6:42236953 G>T maps to NM_033502.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03R-01A-21W-A050-09 chr6:42222646 C>T maps to NM_033502.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr6:42227275 C>T maps to NM_033502.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr6:42204014 C>T maps to NM_033502.2 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr23:152710882 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:129694817 C>G maps to NM_007117.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr12:73014964 T>C maps to NM_013381.2 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12B-01A-11D-A10M-09 chr12:72956809 C>T maps to NM_013381.2 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr12:72680616 G>A maps to NM_013381.2 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:110100130 C>T maps to NM_003301.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr12:120882701 G>T maps to NM_016399.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FZ-01A-11W-A050-09 chr2:12880595 C>T maps to NM_021643.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr13:50587115 G>A maps to NM_001007278.1 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr9:100862245 G>A maps to NM_033219.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr6:30131730 C>T maps to NM_033229.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr17:15535028 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:15535964 A>G maps to ENST00000455584 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr17:18638607 C>T maps to NM_001037330.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:228601545 C>T maps to NM_016102.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:228598715 A>T maps to NM_016102.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24M-01A-11D-A167-09 chr4:154191509 A>G maps to NM_015271.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A440-01A-11D-A243-09 chr4:154191551 C>A maps to NM_015271.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:4411501 A>C maps to NM_003141.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DP-01A-21W-A071-09 chr11:4409559 C>T maps to NM_003141.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr11:5718548 C>T maps to NM_006074.4 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:64892257 G>C maps to NM_001656.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr5:64892899 G>A maps to NM_001656.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr7:138203953 C>T maps to NM_015905.2 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:138210051 G>A maps to NM_015905.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr17:54990827 G>A maps to NM_005082.4 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr6:30153877 G>C maps to NM_003449.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06P-01A-11W-A019-09 chr19:59061548 C>T maps to NM_005762.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr19:59059686 C>G maps to NM_005762.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:59061136 C>T maps to NM_005762.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:6479438 G>T maps to NM_033278.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr9:119460576 C>T maps to NM_012210.3 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:114969880 C>T maps to NM_015906.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:114944048 C>A maps to NM_015906.3 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:114940463 G>A maps to NM_015906.3 Q1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:5653666 C>T maps to NM_001003819.3 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:57094719 G>A maps to NM_015294.3 R775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YX-01A-11D-A22X-09 chr17:57165758 G>C maps to NM_015294.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr6:25983773 G>A maps to NM_006355.2 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:30297548 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:180661693 C>T maps to NM_033549.3 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr5:180661771 T>C maps to NM_033549.3 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr3:140401813 A>G maps to NM_152616.4 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:140401333 C>T maps to NM_152616.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:140401471 G>A maps to NM_152616.4 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr3:140401894 C>G maps to NM_152616.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr2:96265164 C>T maps to NM_138800.1 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:96260028 G>C maps to NM_138800.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XN-01A-12D-A22X-09 chr2:96265164 C>T maps to NM_138800.1 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr1:155150659 C>G maps to NM_025058.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr17:73872165 T>G maps to NM_033452.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr17:73872003 C>T maps to NM_033452.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr11:5686164 G>A maps to NM_033034.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr7:72727111 G>T maps to NM_178125.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:72732850 G>A maps to NM_178125.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:72738404 G>A maps to NM_178125.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr2:27527882 A>C maps to NM_032546.3 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:27527901 G>T maps to NM_032546.3 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D2-01A-21W-A050-09 chr8:67062590 C>G maps to NM_184085.1 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:67066550 A>C maps to NM_184085.1 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr8:67064727 G>T maps to NM_184085.1 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:67039517 G>A maps to NM_184085.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr8:67040681 C>A maps to NM_184085.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:67062074 C>T maps to NM_184085.1 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr8:67049370 C>T maps to NM_184085.1 N183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:100732398 C>T maps to NM_030961.1 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr7:100732536 C>T maps to NM_030961.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr1:248028176 G>A maps to NM_015431.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr1:248039235 G>A maps to NM_015431.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:160156608 A>G maps to ENST00000483754 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr3:160155836 G>A maps to NM_173084.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr11:5624730 C>G maps to NM_001003819.3 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr4:165961478 G>A maps to NM_152620.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr4:165961496 G>A maps to NM_152620.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr4:165890902 T>C maps to NM_001012414.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr1:231334914 G>A maps to NM_001004342.3 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:231344913 C>T maps to NM_001004342.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr1:231335935 C>T maps to NM_001004342.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr11:4626419 C>T maps to NM_018073.5 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:45059888 G>A maps to NM_182985.3 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr15:45047336 G>A maps to NM_182985.3 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:75034313 G>T maps to ENST00000430211 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:75028333 C>T maps to ENST00000430211 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:104404571 G>A maps to NM_030912.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr14:51561357 G>A maps to ENST00000338969 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr14:51560946 G>A maps to ENST00000338969 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr14:51448552 C>G maps to ENST00000338969 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr4:189068189 C>T maps to NM_178556.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr4:189068231 A>C maps to NM_178556.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr4:189068234 T>A maps to NM_178556.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr5:14287159 A>G maps to NM_007118.2 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0ET-01A-31D-A045-09 chr5:14504591 C>T maps to NM_007118.2 R2834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr5:14492842 C>G maps to NM_007118.2 P2600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:14290895 C>T maps to NM_007118.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:14481718 G>T maps to NM_007118.2 G2153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr5:14358321 G>T maps to NM_007118.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr5:14399175 G>A maps to NM_007118.2 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr5:14363872 G>A maps to NM_007118.2 E808E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr5:14480116 G>A maps to NM_007118.2 L2111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr22:38131374 C>T maps to NM_001039141.2 L1678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:38131259 C>T maps to NM_001039141.2 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr22:38150909 C>G maps to NM_001039141.2 T1802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:38111849 G>A maps to NM_001039141.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:6750385 C>A maps to ENST00000313244 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr14:92436127 G>A maps to NM_004239.3 P1943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HI-01A-11D-A099-09 chr14:92460256 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:230652274 G>A maps to ENST00000389044 I1620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:230679861 G>A maps to ENST00000389044 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XU-01A-11D-A10G-09 chr2:230678608 G>A maps to ENST00000389044 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B1-01A-21D-A12Q-09 chr2:230643193 G>A maps to ENST00000389044 R1746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr15:64689806 A>T maps to NM_016213.4 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr15:64701982 G>A maps to NM_016213.4 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr1:40348987 A>T did not map to a codon.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr6:126333929 C>T maps to NM_001031712.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr11:64084383 G>A maps to NM_016404.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr8:125463551 T>C maps to NM_017956.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:125463369 G>T maps to NM_017956.3 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr22:20100265 G>C maps to ENST00000439169 V584V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C8-A1HG-01A-11D-A135-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:100275495 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0J7-01A-11W-A050-09 chr23:100275553 G>A did not map to a codon.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr23:100274320 C>A did not map to a codon.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr23:100292960 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr14:61442325 A>G maps to NM_020810.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A153-01A-12D-A12B-09 chr14:61444281 G>A maps to NM_020810.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr20:5921752 C>T maps to NM_015939.3 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr2:29092828 C>G maps to NM_017910.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr22:46746200 C>T maps to NM_018006.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr22:46746263 G>A maps to NM_018006.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr1:28880169 G>T maps to NM_017846.4 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr1:28904117 A>T maps to NM_017846.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr3:3189338 A>G maps to NM_182916.2 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr23:54949938 T>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54949180 G>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:54954166 T>C did not map to a codon.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr23:54955698 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr23:54955781 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr23:54950988 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:54956206 T>C did not map to a codon.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr23:54955075 G>A did not map to a codon.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr23:54956592 A>T did not map to a codon.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr12:49717674 T>C maps to NM_005480.3 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:49722996 A>C maps to NM_005480.3 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr1:193051359 C>T maps to NM_004600.5 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr8:72948629 G>T maps to NM_007332.2 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:142521153 C>T maps to ENST00000476941 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:142522878 C>A maps to ENST00000476941 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:142521186 G>A did not map to a codon.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr4:122853548 G>A maps to NM_001130698.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr4:122853578 G>A maps to NM_001130698.1 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12B-01A-11D-A10M-09 chr13:38357161 A>G maps to NM_003306.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr13:38213436 C>G did not map to a codon.
Sequencing variant TCGA-AQ-A04J-01A-02W-A050-09 chr20:33623022 G>A maps to NM_015638.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A133-01A-32D-A12B-09 chr20:33591391 G>A maps to NM_015638.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr23:111155924 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YI-01A-31D-A10M-09 chr23:111155992 G>T did not map to a codon.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr23:111078325 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09B-01A-11W-A019-09 chr23:111095567 G>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:111078255 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:111022281 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:111195345 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:111155909 C>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:111155771 G>A did not map to a codon.
Sequencing variant TCGA-C8-A1HG-01A-11D-A135-09 chr23:111155831 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr23:111078165 A>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:111155633 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr23:111097214 C>A did not map to a codon.
Sequencing variant TCGA-E9-A1NE-01A-21D-A14K-09 chr23:111024399 T>A did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:111095576 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr23:111025165 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr11:101344346 G>T maps to NM_004621.5 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr11:101324384 G>A maps to NM_004621.5 N880N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr11:101325832 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr5:135692613 G>A maps to NM_020389.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:135567146 G>A maps to NM_020389.2 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:135601911 G>T maps to NM_020389.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr5:135551912 G>A maps to NM_020389.2 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr5:135692810 C>A maps to NM_020389.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18L-01A-32D-A12B-09 chr5:135587469 G>A maps to NM_020389.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:31321582 C>A maps to NM_002420.4 E1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr15:31360097 G>T maps to NM_002420.4 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr15:31334371 G>A maps to NM_002420.4 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YL-01A-21D-A10G-09 chr21:45833783 C>T maps to ENST00000397932 F991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr21:45833777 G>T maps to ENST00000397932 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr21:45789135 G>C maps to ENST00000397932 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr21:45825916 G>C maps to ENST00000397932 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr21:45811189 C>T maps to ENST00000397932 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr21:45821617 C>T maps to ENST00000397932 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr21:45784056 C>G maps to ENST00000397932 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D8-01A-11D-A27P-09 chr21:45821602 C>T maps to ENST00000397932 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:73151468 T>G maps to ENST00000419692 T1474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:73213505 G>A maps to ENST00000419692 I913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HL-01A-11D-A135-09 chr9:73151246 G>T maps to ENST00000419692 C1548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr9:73233935 C>T maps to ENST00000419692 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr19:49703866 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:49684693 C>A maps to NM_017636.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr19:49692302 C>A maps to NM_017636.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr11:2439588 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr9:77423060 G>T maps to NM_017662.4 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr9:77435342 C>G maps to NM_017662.4 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr15:50905026 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:234875329 T>G maps to NM_024080.4 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:234858711 C>G maps to NM_024080.4 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr2:234878391 G>A maps to NM_024080.4 W693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:116426337 C>T maps to NM_014112.2 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:116616176 G>C maps to NM_014112.2 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:116631535 C>T maps to NM_014112.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr8:116426595 C>T maps to NM_014112.2 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr8:116426721 C>A maps to NM_014112.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:3489148 C>T maps to ENST00000399756 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr17:16335538 C>G maps to NM_016113.4 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr17:16335508 C>A maps to NM_016113.4 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr17:16327009 C>T maps to NM_016113.4 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:16335334 T>C maps to NM_016113.4 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr17:16326932 C>G maps to NM_016113.4 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr17:3458078 G>A maps to ENST00000381913 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:110230225 G>A maps to NM_021625.4 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SB-01A-21D-A25Q-09 chr7:142626580 G>C maps to NM_019841.4 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr7:142622658 G>A maps to NM_019841.4 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:142625938 G>A maps to NM_019841.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr7:142573588 G>C maps to NM_018646.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr7:142573241 G>C maps to NM_018646.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:98588154 A>C maps to ENST00000359863 P3227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr7:98528368 G>A maps to ENST00000359863 E1169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr7:98507950 C>T maps to ENST00000359863 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:98495371 C>T maps to ENST00000359863 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:98555623 G>A maps to ENST00000359863 S2077S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr7:98488013 C>T maps to ENST00000359863 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr7:98565272 G>A maps to ENST00000359863 Q2481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:98574179 G>A maps to ENST00000359863 A2671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A209-01A-11D-A17G-09 chr9:131073253 C>A maps to NM_015679.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BM-01A-11W-A071-09 chr9:135797349 C>T maps to NM_000368.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:2127643 A>C maps to NM_000548.3 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr16:2134597 C>T maps to NM_000548.3 R1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:2134656 C>T maps to NM_000548.3 D1478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr16:2136342 C>A maps to NM_000548.3 G1604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr16:2108762 C>T maps to NM_000548.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr13:45148148 G>A maps to NM_183422.2 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr13:45148989 G>A maps to NM_183422.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr13:45010710 C>T maps to NM_006022.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr3:150128828 C>G maps to NM_014779.2 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:150127628 G>A maps to NM_014779.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr3:150176289 C>G maps to NM_014779.2 S737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:106957902 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:106957971 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:107018504 G>A did not map to a codon.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr23:107018375 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr23:106959959 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr23:107018551 C>G did not map to a codon.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr23:106957952 A>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:54695750 G>C maps to NM_001077446.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:73519776 C>A maps to NM_207346.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr17:73519827 T>G maps to NM_207346.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr17:73520469 T>C maps to NM_207346.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZW-01A-12D-A29N-09 chr12:58176984 C>T maps to NM_001172696.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr11:18503242 T>C maps to NM_006292.2 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:99722135 G>A maps to NM_025244.2 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr2:99634760 A>T maps to NM_025244.2 Y658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr2:99651727 G>A maps to NM_025244.2 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr2:99695168 T>A maps to NM_025244.2 K279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr11:65715544 C>T maps to NM_152762.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:115576827 C>T maps to NM_000549.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:81610384 C>T maps to NM_000369.2 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr14:81610006 C>T maps to NM_000369.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr18:72998609 C>G maps to NM_005786.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:72999857 G>A maps to NM_005786.4 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr18:72999677 G>A maps to NM_005786.4 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr18:72999752 C>T maps to NM_005786.4 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EN-01A-11D-A17G-09 chr20:51871631 C>T maps to NM_173485.5 H545H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr20:51872432 C>A maps to NM_173485.5 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27W-01A-11D-A16D-09 chr20:51872711 C>T maps to NM_173485.5 Y905Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr20:51870686 G>A maps to NM_173485.5 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CE-01A-11W-A019-09 chr19:31767506 G>A maps to NM_020856.2 H1064H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:31770203 G>A maps to NM_020856.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QN-01A-12D-A28B-09 chr19:31769936 C>T maps to NM_020856.2 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr19:31768346 G>C maps to NM_020856.2 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr19:31767860 G>A maps to NM_020856.2 I946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr19:31767665 G>A maps to NM_020856.2 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr19:31768091 G>A maps to NM_020856.2 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr5:110411666 G>A maps to NM_033035.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr2:122520631 C>G maps to NM_004622.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr16:67854842 G>A maps to ENST00000339830 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr16:67861264 C>G maps to ENST00000339830 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr12:31116819 C>A maps to NM_001080509.2 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr7:120428908 G>A maps to NM_012338.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:120496757 G>A maps to NM_012338.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr7:16816716 C>T maps to NM_014399.3 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:82277671 C>T maps to NM_030927.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr10:82264497 C>G maps to NM_030927.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr10:82249012 C>T maps to NM_030927.2 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr19:11417277 A>T maps to ENST00000337994 *161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:176081936 C>G maps to NM_012171.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr5:176078753 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr12:85413516 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:85411252 C>T maps to NM_001100917.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AL-01A-21D-A12Q-09 chr1:115615556 T>C maps to NM_005725.4 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr11:2337499 G>A maps to NM_139022.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:99890604 T>G did not map to a codon.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr23:99890579 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:38420831 G>A did not map to a codon.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr23:38533517 C>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:71533562 A>C maps to NM_004616.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr12:71519152 C>T maps to NM_004616.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr12:3388204 C>T maps to ENST00000407263 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr23:53114173 C>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:53112399 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:53116971 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:53114013 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:53113973 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr23:53115365 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:98289178 G>A maps to NM_033512.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:98289556 C>T maps to NM_033512.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr8:98288844 G>A maps to NM_033512.2 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:2227534 C>T maps to NM_018128.4 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AN-01A-11D-A12Q-09 chr23:54470524 C>G did not map to a codon.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr23:54467207 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:3200773 C>T maps to ENST00000398659 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr2:3381439 C>T maps to ENST00000398659 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18J-01A-11D-A12B-09 chr5:112770419 C>T maps to NM_032028.3 A39A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AC-A3BB-01A-21D-A19Y-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B6-A0RG-01A-11W-A071-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C8-A1HJ-01A-11D-A13L-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:19625639 G>A maps to NM_032037.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr8:144696574 G>C maps to NM_003313.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr8:144696345 G>A maps to NM_003313.3 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr9:100368472 T>C maps to NM_139246.4 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr6:43225686 G>A maps to NM_032538.1 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04P-01A-31D-A128-09 chr15:43045172 T>C maps to ENST00000263802 K1162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr15:43038226 T>G maps to ENST00000263802 S1572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr15:43044686 A>G maps to ENST00000263802 C1324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr2:3428378 T>C maps to NM_016030.5 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr11:43411359 C>T maps to NM_018259.5 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:43427131 T>G maps to NM_018259.5 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:75114497 A>G maps to NM_145170.3 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr10:75034277 A>C maps to NM_145170.3 Y986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr10:75113463 G>A maps to NM_145170.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr3:39156149 G>A maps to ENST00000301819 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr3:39167780 A>G maps to ENST00000301819 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:39162577 G>T maps to ENST00000301819 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:166806234 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27K-01A-11D-A16D-09 chr1:55251673 C>T maps to NM_001114108.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:99768842 T>C maps to NM_022905.4 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FJ-01A-11D-A13L-09 chr5:34863072 G>A maps to NM_144725.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:156556332 T>G maps to NM_001105669.2 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:156555598 C>T maps to NM_001105669.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr1:156551234 A>T maps to NM_001105669.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FV-01A-11D-A13L-09 chr17:40091965 C>T maps to ENST00000377543 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:40113432 G>T maps to ENST00000377543 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr17:40091944 C>A maps to ENST00000377543 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:32897448 C>T maps to NM_017735.4 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr4:147724764 G>A maps to ENST00000513335 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr4:147741288 G>A maps to ENST00000513335 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr4:147830217 C>T maps to ENST00000513335 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr21:38511011 G>T maps to NM_003316.3 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr21:38516839 C>T maps to NM_003316.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr21:38572588 G>A maps to NM_003316.3 V1969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:178416234 G>T maps to NM_152517.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:20101479 C>A maps to NM_001008237.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr8:109455892 G>T maps to NM_014673.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr5:94852113 C>A did not map to a codon.
Sequencing variant TCGA-AN-A049-01A-21W-A019-09 chr5:94858949 T>G maps to NM_014639.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:51770778 C>A maps to ENST00000447632 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:51756243 G>A maps to ENST00000447632 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr9:15177714 A>G maps to NM_152574.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr9:15175072 A>G maps to NM_152574.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr9:15190603 T>G maps to NM_152574.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr18:21712495 C>T maps to NM_001135993.1 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:21662875 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr14:20768885 C>A maps to NM_138376.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr2:47249092 C>T maps to ENST00000394850 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr2:47233104 G>A maps to ENST00000394850 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr14:71137835 C>G maps to NM_015351.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:40723220 G>C maps to NM_152479.5 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:135276917 C>A maps to NM_007344.2 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr9:135273708 G>A maps to NM_007344.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr1:117634517 G>A maps to NM_003594.3 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr1:117617613 T>A maps to NM_003594.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:117624492 C>T maps to NM_003594.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:117634490 A>G maps to NM_003594.3 S908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr1:117634445 G>A maps to NM_003594.3 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:43435886 A>C maps to NM_012263.4 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr9:124751815 G>C maps to NM_001139442.1 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr9:124584994 C>T maps to NM_001139442.1 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr22:43569737 G>A maps to NM_015140.3 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:167754551 C>T maps to NM_031949.4 N388N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:9854974 C>T maps to NM_001025930.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:9854980 C>T maps to NM_001025930.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr3:9876578 G>A maps to NM_001025930.3 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:76349194 A>C maps to NM_015072.4 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr14:76173407 T>C maps to NM_015072.4 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr14:76349120 C>T maps to NM_015072.4 Q1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr14:76238122 C>T maps to NM_015072.4 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:46863600 C>G maps to NM_001130918.1 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr17:46894359 C>T maps to NM_001130918.1 A25A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A8-A08R-01A-11W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr20:30486274 G>A did not map to a codon.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr2:179640413 G>T maps to NM_133378.4 I2059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SY-01A-31D-A099-09 chr2:179584559 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr2:179437367 A>T maps to NM_133378.4 Y21929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr2:179469434 C>G maps to NM_133378.4 G15559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25C-01A-11D-A167-09 chr2:179446723 G>A maps to NM_133378.4 T19556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr2:179408031 C>T maps to NM_133378.4 W29655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr2:179442792 G>A maps to NM_133378.4 R20249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr2:179604294 C>A maps to NM_133437.3 G4384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr2:179501200 G>A maps to NM_133378.4 S11183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr2:179417110 C>T maps to NM_133378.4 L27604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179431754 A>C maps to NM_133378.4 G23800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179440253 T>G maps to NM_133378.4 P20967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179466034 T>G maps to NM_133378.4 P15995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179474579 A>C maps to NM_133378.4 G14622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179612156 T>G maps to ENST00000375038 P4992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179640833 A>C maps to NM_133378.4 G1919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179641100 A>C maps to NM_133378.4 G1830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:179641112 A>C maps to NM_133378.4 G1826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:179422693 G>A maps to NM_133378.4 F26561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:179431832 C>A maps to NM_133378.4 V23774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:179482159 C>T maps to NM_133378.4 L13316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:179586853 C>T maps to NM_133378.4 K6268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:179588745 C>T maps to NM_133378.4 E5836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:179596444 G>A maps to NM_133378.4 I4475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:179612624 G>C maps to ENST00000375038 L4836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2BK-01A-11D-A21Q-09 chr2:179444795 A>C maps to NM_133378.4 T19838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr2:179569261 G>A maps to NM_133378.4 I8735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179393746 C>T maps to NM_133378.4 K33009K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179394813 G>T maps to NM_133378.4 L32900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179425490 T>A maps to NM_133378.4 G25888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179442350 G>T maps to NM_133378.4 T20366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179443560 C>T maps to NM_133378.4 S20164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179445321 C>A maps to NM_133378.4 E19694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179477577 G>T maps to NM_133378.4 R14056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179485077 C>T maps to NM_133378.4 P12822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179589083 C>T maps to NM_133378.4 R5762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:179596284 G>A maps to NM_133378.4 I4492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr2:179588691 G>C maps to NM_133378.4 V5854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:179468879 G>A maps to NM_133378.4 R15610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:179597326 G>A maps to NM_133378.4 N4243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr2:179455718 G>A maps to NM_133378.4 R17677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FF-01A-11W-A050-09 chr2:179547547 C>T maps to NM_133378.4 E9746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr2:179400247 A>G maps to NM_133378.4 V31130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr2:179444428 G>A maps to NM_133378.4 R19931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr2:179650715 G>A maps to NM_133378.4 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U0-01A-11D-A10G-09 chr2:179593822 G>A maps to NM_133378.4 T5070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr2:179614479 A>T maps to ENST00000375038 L4218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr2:179422747 G>A maps to NM_133378.4 D26543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr2:179585181 G>A maps to NM_133378.4 V6525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X5-01A-21D-A10G-09 chr2:179427224 A>G maps to NM_133378.4 N25310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr2:179612699 C>T maps to ENST00000375038 L4811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DO-01B-11D-A12B-09 chr2:179449666 A>G maps to NM_133378.4 F18999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:179654085 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr2:179569096 C>G maps to NM_133378.4 L8756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:179489399 A>G maps to NM_133378.4 T12301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:179483182 C>A maps to NM_133378.4 E13100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr2:179527762 C>T maps to NM_133378.4 P10501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr2:179436919 G>A maps to NM_133378.4 R22079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr2:179611634 G>A maps to ENST00000375038 S5166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HK-01A-21D-A13L-09 chr2:179479655 G>A maps to NM_133378.4 A13658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26X-01A-31D-A16D-09 chr2:179587199 G>T maps to NM_133378.4 L6194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr2:179423170 C>G maps to NM_133378.4 L26437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:179656924 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:179396527 C>T maps to NM_133378.4 L32370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:179468912 A>G maps to NM_133378.4 P15599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:179473133 A>G maps to NM_133378.4 N14924N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr2:179477303 C>G did not map to a codon.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr2:179476279 A>G maps to NM_133378.4 C14324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15P-01A-11D-A10Y-09 chr2:179442016 C>T maps to NM_133378.4 A20447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr2:179477136 G>C maps to NM_133378.4 V14137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr2:179640218 G>A maps to NM_133378.4 I2124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr2:179471856 G>A maps to NM_133378.4 I15256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr2:179586823 T>C maps to NM_133378.4 V6278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr2:179427678 G>C maps to NM_133378.4 S25159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr2:179594183 C>T maps to NM_133378.4 L4989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr2:179595298 C>T maps to NM_133378.4 G4743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr2:179435072 G>C maps to NM_133378.4 L22694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YM-01A-11D-A28B-09 chr2:179614553 T>A maps to ENST00000375038 T4193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YO-01A-21D-A28B-09 chr2:179410787 G>A maps to NM_133378.4 C29157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr19:54937906 C>T maps to ENST00000391739 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr17:72245190 G>A maps to NM_032646.5 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:72248378 C>T maps to NM_032646.5 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr17:72233551 G>A maps to NM_032646.5 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:8122479 C>G maps to NM_003320.4 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr12:49580116 G>C maps to NM_006009.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:49523123 G>A maps to NM_006082.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:49523126 C>T maps to NM_006082.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr12:49666772 A>G maps to NM_032704.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr13:19751147 C>T maps to NM_006001.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr13:19751441 G>T maps to NM_006001.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr13:19751649 G>T maps to NM_006001.1 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr13:19748194 G>A maps to NM_006001.1 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:132238048 G>A maps to NM_080386.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:132235828 C>T maps to NM_080386.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:130951526 G>A maps to NM_207312.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:130952657 G>A maps to NM_207312.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr2:130949652 C>T maps to NM_207312.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:220115763 G>A maps to NM_006000.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr10:5435788 C>T maps to NM_024803.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr10:5436289 C>T maps to NM_024803.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr6:30691483 G>C maps to NM_178014.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:57599138 A>C maps to NM_030773.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A2FW-01A-11D-A17D-09 chr20:57597973 G>A maps to NM_030773.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40C-01A-11D-A23C-09 chr19:6501313 C>T maps to NM_006087.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr19:6495768 G>A maps to NM_006087.2 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr19:6495819 C>T maps to NM_006087.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:6495393 C>T maps to NM_006087.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr10:93602 C>T maps to NM_177987.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr10:93893 C>A maps to NM_177987.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CJ-01A-21W-A019-09 chr6:112397207 T>C maps to NM_016262.4 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3HN-01A-11D-A20S-09 chr6:112394010 G>A maps to NM_016262.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:40765752 T>G did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr17:40817561 C>T maps to NM_016437.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:135106139 G>A maps to NM_006659.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr10:135106687 C>T maps to NM_006659.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr13:113212674 G>T maps to NM_006322.4 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08O-01A-21W-A071-09 chr15:43696711 T>C maps to ENST00000399460 Y651Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:43668351 C>G maps to ENST00000399460 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:22861854 G>C maps to NM_052903.4 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:22841054 C>T maps to NM_052903.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr15:22863084 C>T maps to NM_052903.4 C702C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr15:22866751 G>A maps to NM_052903.4 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:50671771 G>A maps to NM_020461.3 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr22:50665187 C>T maps to NM_020461.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:28857236 C>T maps to NM_003321.4 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:151534601 T>G maps to NM_020127.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr1:151536441 G>A maps to NM_020127.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr12:3018747 T>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr12:3048600 G>A maps to NM_003324.4 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr6:158924081 T>G maps to NM_020245.3 G1129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr6:158924159 G>C maps to NM_020245.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:158922908 T>G maps to NM_020245.3 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:158924636 C>T maps to NM_020245.3 N1314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr6:158834164 C>T maps to NM_020245.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr6:158915878 G>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr6:158923523 G>T maps to NM_020245.3 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:50363861 C>A maps to NM_007275.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr11:62348588 C>A maps to NM_022830.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr11:62343414 G>A maps to NM_022830.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:19156619 G>A maps to NM_000474.3 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr4:48081955 C>T maps to NM_003328.2 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr4:48096221 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr4:48115240 A>G maps to NM_003328.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:16838291 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0FS-01A-11W-A050-09 chr23:16838306 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0B4-01A-11W-A019-09 chr23:16859738 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:16847876 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr22:36872854 C>G maps to NM_012473.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:134229286 C>T maps to NM_024715.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EA-01A-11D-A10Y-09 chr5:134210138 C>T maps to NM_024715.3 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr14:52978094 C>A maps to NM_020784.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:53009141 C>A maps to NM_020784.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:9887411 T>G maps to NM_001098529.1 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr18:9888089 C>T maps to NM_001098529.1 C538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr7:37916508 G>A maps to NM_016616.4 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:7904871 C>A maps to NM_030810.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr1:145438999 T>C maps to NM_006472.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr1:145438840 C>A maps to NM_006472.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:145438807 G>T maps to NM_006472.3 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:145440058 G>T maps to NM_006472.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07U-01A-11W-A050-09 chr18:54291575 C>T maps to NM_004786.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:77737611 G>A maps to NM_006701.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:104714973 C>T maps to NM_001093771.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr22:19906522 G>T maps to NM_006440.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr3:126291350 C>A maps to NM_001039783.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr19:10467349 G>A maps to NM_003331.4 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr19:10475417 C>T maps to NM_003331.4 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:10468727 G>A maps to NM_003331.4 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr22:50966116 G>A maps to ENST00000395681 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr22:50967952 C>T maps to ENST00000395681 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YM-01A-11D-A10G-09 chr11:88911666 T>C maps to NM_000372.4 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:41863284 C>T maps to NM_006293.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr15:41860466 C>T maps to NM_006293.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr15:41854887 T>G maps to NM_006293.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr9:12708042 A>G maps to NM_000550.2 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:12702373 T>G maps to NM_000550.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IU-01A-11D-A14G-09 chr9:12698599 G>A maps to NM_000550.2 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DH-01A-11D-A17W-09 chr9:12704688 G>A maps to NM_000550.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:66474574 C>T maps to NM_018264.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr7:66490010 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:66532312 C>T maps to NM_018264.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr7:72093975 G>A maps to NM_001145440.1 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:72159805 G>A maps to NM_001145440.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:72081767 G>T maps to NM_001145440.1 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr21:44513292 G>A maps to NM_001025203.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr1:162560142 A>G maps to ENST00000367925 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RX-01A-11D-A28B-09 chr9:139977162 G>A maps to NM_207309.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr23:47061806 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:47065730 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:47070557 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:47060714 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47072429 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47073737 G>A did not map to a codon.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr23:47070445 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr23:47070623 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr23:47061806 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:47058917 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:47070299 C>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:47073982 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:47074207 G>T did not map to a codon.
Sequencing variant TCGA-D8-A27P-01A-11D-A16D-09 chr23:47073946 A>G did not map to a codon.
Sequencing variant TCGA-E2-A154-01A-11D-A10Y-09 chr23:47065654 A>T did not map to a codon.
Sequencing variant TCGA-GM-A2DD-01A-11D-A17W-09 chr23:47061597 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr19:34960011 C>T maps to NM_005499.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:132387768 G>A maps to NM_024818.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3X8-01A-31D-A22X-09 chr3:132389817 G>C maps to NM_024818.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr4:68492132 C>T maps to NM_018227.5 E821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr9:138845594 G>C maps to NM_016172.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:34234325 C>T maps to NM_001171201.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr9:33923996 A>C maps to NM_018449.2 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:33941793 G>A maps to NM_018449.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:33989071 G>C maps to NM_018449.2 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr9:33923948 A>C maps to NM_018449.2 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr9:33944418 G>A maps to NM_018449.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr1:154227319 C>T maps to NM_014847.3 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr1:154229567 C>T maps to NM_014847.3 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:154229864 G>A maps to NM_014847.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:154223667 T>C maps to NM_014847.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr21:43862565 C>G maps to NM_018961.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:125397060 G>A maps to NM_021009.5 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:125397363 A>G maps to NM_021009.5 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:125398029 A>G maps to NM_021009.5 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr12:125396730 A>G maps to NM_021009.5 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:29523866 A>C maps to NM_006398.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr6:29523761 A>G maps to NM_006398.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XU-01A-12D-A22X-09 chr23:118717177 G>T did not map to a codon.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr6:83728708 G>A maps to NM_198920.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:23929153 C>T maps to NM_003341.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr6:90045150 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr22:21922053 G>T maps to NM_003347.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:57327815 G>A maps to NM_004223.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:142967228 C>G did not map to a codon.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr17:74401325 G>A maps to NM_022066.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr17:74392692 C>T maps to NM_022066.3 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr1:154527993 C>G maps to NM_017582.6 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D6-01A-21D-A27P-09 chr1:154524282 G>A maps to NM_017582.6 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:202302592 G>A maps to NM_014176.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr8:48921028 A>C maps to NM_003350.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:25616213 C>T maps to NM_000462.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:109937547 C>T maps to NM_183415.1 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:109958978 C>G maps to NM_183415.1 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr7:157046808 C>G maps to NM_014671.2 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:157046646 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:118242315 C>T maps to NM_004788.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:10132171 T>C maps to NM_001105562.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03X-01A-21W-A019-09 chr1:10186919 T>C maps to NM_001105562.2 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:10190625 C>G maps to NM_001105562.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr1:10166257 C>G maps to NM_001105562.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NY-01A-11D-A21Q-09 chr19:9939518 G>A maps to NM_024292.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr5:158711930 G>T maps to NM_145049.3 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DX-01A-11D-A10Y-09 chr16:4923064 C>T maps to NM_016936.3 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:4924717 C>T maps to NM_016936.3 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr16:4924573 T>G maps to NM_016936.3 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr7:138944053 G>A maps to NM_173569.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:138968830 A>C maps to NM_173569.3 S1060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr7:138946213 G>C maps to NM_173569.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr9:86294884 C>T maps to NM_013438.4 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr9:86294874 G>A maps to NM_013438.4 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:56591369 C>A did not map to a codon.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr23:56590877 T>G did not map to a codon.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr11:5529921 G>A maps to NM_017481.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:43348618 C>A maps to NM_174916.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:42626012 A>C maps to NM_015255.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr6:42652567 A>G maps to NM_015255.2 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:42644558 G>T maps to NM_015255.2 E1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:42657405 C>T maps to NM_015255.2 L1708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XL-01A-11D-A14K-09 chr6:42585063 C>T maps to NM_015255.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:170732337 C>T maps to ENST00000442603 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr2:170732315 C>G maps to ENST00000442603 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:170936529 A>G maps to ENST00000442603 V1831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr1:19484362 G>C maps to ENST00000375267 L1902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr1:19518986 C>A maps to ENST00000375267 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:19472302 T>G maps to ENST00000375267 A2643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:19478890 A>C maps to ENST00000375267 G2304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:19480423 A>C maps to ENST00000375267 G2156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:19484464 A>C maps to ENST00000375267 G1868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:19481937 C>G maps to ENST00000375267 L2099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:19479818 G>A maps to ENST00000375267 R2270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:19491456 G>T maps to ENST00000375267 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:19504041 G>A maps to ENST00000375267 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:19443821 G>A maps to ENST00000375267 S3572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr1:19481473 G>A maps to ENST00000375267 F2132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr1:19494603 A>C maps to ENST00000375267 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15T-01A-11D-A10Y-09 chr1:19491830 T>C maps to ENST00000375267 V1408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr1:19487464 C>T maps to ENST00000375267 K1784K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R7-01A-11D-A14K-09 chr1:19439334 C>T maps to ENST00000375267 L3828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr8:103299694 G>A maps to NM_015902.4 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr8:103309808 C>T maps to NM_015902.4 E1150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr8:103287947 T>A maps to NM_015902.4 A2206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:103284936 G>A maps to NM_015902.4 R2265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr8:103271311 C>A maps to NM_015902.4 E2668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BD-01A-11W-A050-09 chr8:103298798 C>A maps to NM_015902.4 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:103324593 C>T maps to NM_015902.4 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:103324644 C>T maps to NM_015902.4 Q692Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr14:93686632 T>C maps to NM_175748.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr10:99330207 C>T maps to NM_024954.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:42293019 A>C did not map to a codon.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr17:42287811 G>A maps to NM_014233.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:59343143 G>A maps to NM_001077619.1 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:59343209 A>G maps to NM_001077619.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:4445602 C>G maps to NM_025241.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:196089177 C>T maps to NM_015562.1 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:41262731 C>T maps to NM_004181.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:41266169 C>T maps to NM_004181.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr1:165875180 C>T maps to NM_012474.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr1:165875163 A>T maps to NM_012474.4 K202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IQ-01A-11W-A050-09 chr1:165872482 C>T maps to NM_012474.4 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr1:165865489 C>T maps to NM_012474.4 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C3-01A-21D-A12Q-09 chr1:165872479 G>C maps to NM_012474.4 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:165875171 T>C maps to NM_012474.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15S-01A-11D-A10Y-09 chr1:165859580 G>A maps to NM_012474.4 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr4:141484631 C>T maps to NM_021833.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr11:73687704 C>T maps to NM_003355.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr11:73686075 G>T maps to NM_003355.2 C302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HO-01A-11D-A13L-09 chr11:73687704 C>T maps to NM_003355.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1ET-01A-11D-A135-09 chr11:73717217 C>T maps to NM_003356.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:18600313 T>C maps to NM_001040697.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:186339817 C>T maps to NM_018359.3 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:128930288 G>T maps to NM_020120.3 E1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr2:128939818 C>G maps to NM_020120.3 S1400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr13:96506619 C>T maps to NM_020121.3 W1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A158-01A-11D-A12B-09 chr13:96547534 A>G maps to NM_020121.3 D886D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B1-01A-21D-A12Q-09 chr13:96555314 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr13:96529963 C>T maps to NM_020121.3 V1125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr13:96684188 C>T maps to NM_020121.3 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:64085016 G>T maps to NM_006759.3 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr2:234681045 C>T maps to ENST00000373460 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr2:234669445 C>T maps to NM_000463.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr2:234681066 C>A maps to ENST00000373460 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:234676535 G>A maps to ENST00000373460 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr2:234681078 T>C maps to ENST00000373460 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X6-01A-11D-A14K-09 chr2:234680994 T>C maps to ENST00000373460 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr2:234681012 C>T maps to ENST00000373460 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LE-01A-12D-A19Y-09 chr2:234545371 A>G maps to NM_019075.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:234638269 G>A maps to NM_019093.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J4-01A-11W-A050-09 chr2:234638185 C>T maps to NM_019093.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr2:234622269 C>A maps to NM_019078.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:234601796 C>A maps to NM_001072.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr2:234527063 A>C maps to NM_019076.4 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr2:234526442 A>C maps to NM_019076.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:234580886 C>T maps to ENST00000373460 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:70512676 G>T maps to ENST00000514019 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr4:70460340 G>C maps to ENST00000514019 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr4:70462044 G>A maps to NM_006798.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr4:70504738 G>C maps to ENST00000514019 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr4:69798465 A>G maps to NM_024743.3 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EW-01A-11D-A135-09 chr4:69817412 G>A maps to NM_024743.3 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr4:70070293 G>A maps to NM_001073.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr4:69416555 T>C maps to NM_001076.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr4:69533860 C>T maps to NM_001076.2 W257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr4:69416555 T>C maps to NM_001076.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr4:69512932 C>G maps to NM_001076.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr4:69536303 C>A maps to NM_001076.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr4:70351052 A>G maps to NM_021139.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr4:70350945 C>T maps to NM_021139.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr4:70346545 C>A maps to NM_021139.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08B-01A-11W-A019-09 chr4:69973881 C>T maps to NM_001074.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr5:36039648 A>G maps to NM_174914.3 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:115544203 C>G maps to NM_003360.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr4:115544066 C>T maps to NM_003360.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr19:4930846 G>A maps to ENST00000398240 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr6:34803150 C>T maps to NM_017754.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:34840164 G>T maps to NM_017754.3 E1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U3-01A-11D-A10G-09 chr12:100482726 T>C maps to NM_015054.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr12:100452151 G>C maps to NM_015054.1 S968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J1-01A-11D-A188-09 chr12:100452033 T>A maps to NM_015054.1 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:6477775 A>C maps to NM_152896.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:150266700 A>C maps to NM_025217.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3Q9-01A-11D-A21Q-09 chr6:150267526 A>C maps to NM_025217.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr6:150267714 C>G maps to NM_025217.2 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:132392050 T>G maps to NM_003565.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RY-01A-31D-A25Q-09 chr12:132399949 C>T maps to NM_003565.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:19680998 G>A maps to NM_014683.3 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr17:19700726 G>A maps to NM_014683.3 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr17:19685245 C>T maps to NM_014683.3 E865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:41952878 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr3:41705171 T>C maps to NM_017886.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24L-01A-11D-A167-09 chr3:41942264 G>A maps to NM_017886.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DL-01A-11D-A18P-09 chr3:41942240 G>A maps to NM_017886.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:20352645 G>A maps to ENST00000424589 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr16:20362043 G>A maps to ENST00000424589 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr16:20346822 T>C maps to ENST00000424589 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr21:43508465 C>T maps to NM_173568.3 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07J-01A-11W-A019-09 chr21:43505491 C>T maps to NM_173568.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr21:43557582 C>T maps to NM_173568.3 A1398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:43541249 C>T maps to NM_173568.3 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr21:43505407 G>A maps to NM_173568.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:124449395 C>T maps to NM_000373.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr12:121148294 G>A maps to NM_001080533.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr19:17722611 G>A maps to ENST00000428389 F1625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr19:17780392 G>A maps to ENST00000428389 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr19:17750005 C>T maps to ENST00000428389 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr19:17741461 C>G did not map to a codon.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr19:17756582 G>A maps to ENST00000428389 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr9:35399190 G>A maps to ENST00000396787 T1299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr9:35295822 G>A maps to ENST00000396787 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr15:54305909 C>G maps to ENST00000260323 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:54630587 G>A maps to ENST00000260323 A1538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:54919070 C>G maps to ENST00000260323 L2135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JJ-01A-11W-A071-09 chr15:54825145 C>T maps to ENST00000260323 Q1860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr15:54306761 C>T maps to ENST00000260323 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr15:54556501 T>A maps to ENST00000260323 I1195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A134-01A-11D-A10Y-09 chr15:54590072 A>G maps to ENST00000260323 K1351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr15:54919233 C>T maps to ENST00000260323 Q2190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr15:54793089 C>T maps to ENST00000260323 Q1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FX-01A-11D-A13L-09 chr17:73836635 C>T maps to ENST00000412096 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:73832920 G>A maps to ENST00000412096 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:73835918 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0CR-01A-11D-A228-09 chr15:91491410 C>T maps to NM_018671.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr15:91496461 G>T maps to NM_018671.3 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:33486547 C>A maps to NM_173167.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:99226338 C>T maps to ENST00000409347 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr5:176295945 C>T maps to NM_133369.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr10:73048334 G>A maps to NM_170744.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:73051400 C>T maps to NM_170744.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr10:73046504 C>T maps to NM_170744.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:35406936 G>A maps to ENST00000416672 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr8:35606155 C>G maps to ENST00000416672 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr8:35608204 G>T maps to ENST00000416672 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr8:35583856 G>A maps to ENST00000416672 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr8:35542202 C>G maps to ENST00000416672 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HX-01A-21W-A071-09 chr8:35563479 G>T did not map to a codon.
Sequencing variant TCGA-D8-A142-01A-11D-A10Y-09 chr8:35631899 C>A maps to ENST00000416672 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:67766693 G>T maps to NM_030930.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr7:1275499 G>A maps to NM_001080461.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr22:24909454 T>A did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr22:24919737 C>T maps to NM_016327.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:18960955 G>A maps to ENST00000418384 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr10:12071391 G>C maps to NM_015542.2 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr10:12071465 T>C maps to NM_015542.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr10:12039690 G>A maps to NM_015542.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:12042002 C>A maps to NM_015542.2 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr10:12046628 A>G maps to NM_015542.2 Y468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr10:12071426 G>A maps to NM_015542.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr13:115070304 C>T maps to NM_023011.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr23:118986831 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118971733 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:118979167 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr23:118971939 C>T did not map to a codon.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr23:118971886 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr23:118968923 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:118971804 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:36164156 C>G maps to NM_007000.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:36166879 G>T maps to NM_007000.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26W-01A-11D-A16D-09 chr19:36164377 G>C maps to NM_007000.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr22:45689104 C>T maps to NM_006953.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:76144471 C>T maps to NM_030570.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:158991284 C>G maps to NM_001135098.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr23:74519697 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:74494389 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr23:74519658 G>A did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:74517353 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:33894573 A>T maps to NM_018244.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr22:30163498 C>T maps to ENST00000406782 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:30163494 C>T maps to ENST00000406782 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:21974111 C>T maps to NM_003366.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:21969860 A>G maps to NM_003366.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr16:21979965 G>A maps to NM_003366.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr19:29698493 C>T maps to NM_006003.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AJ-01A-11W-A019-09 chr1:229783408 C>G maps to NM_014777.2 V1353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:229770770 C>T maps to NM_014777.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr7:43916992 G>C maps to NM_001077663.1 S690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:43917816 G>T maps to NM_001077663.1 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:43917966 G>A maps to NM_001077663.1 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:43918062 G>C maps to NM_001077663.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:43918379 G>A maps to NM_001077663.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:43918402 G>T maps to NM_001077663.1 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:43918480 G>C maps to NM_001077663.1 S194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OK-A5Q2-01A-11D-A27P-09 chr3:126224609 G>A maps to NM_001165974.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr1:45480406 G>C did not map to a codon.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr10:127495985 A>G maps to NM_000375.2 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:17330037 C>T maps to NM_018467.3 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr11:17545006 C>A maps to NM_153676.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr11:17531091 C>T maps to NM_153676.3 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr17:72916429 G>A maps to NM_173477.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr17:72916078 G>A maps to NM_173477.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SH-01A-11D-A099-09 chr1:216420206 G>A maps to ENST00000366943 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr1:216498907 G>A maps to ENST00000366943 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr1:216371888 C>T maps to ENST00000366943 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr1:216390732 G>A maps to ENST00000366943 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr1:216138716 G>C maps to ENST00000366943 R2354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr1:215916651 C>T maps to ENST00000366943 V3805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:215933099 G>C maps to ENST00000366943 L3711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:216496859 G>C maps to ENST00000366943 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr1:215901419 G>T maps to ENST00000366943 P4006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:216019235 G>T maps to ENST00000366943 I2995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:216062265 G>T maps to ENST00000366943 Y2575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr1:215953311 C>T maps to ENST00000366943 V3604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr4:76695833 C>G maps to NM_003715.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr1:62905636 T>G maps to NM_003368.4 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RE-01A-11D-A159-09 chr1:62910496 C>T maps to NM_003368.4 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:47100713 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr23:47098832 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr23:47092576 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr23:47101697 C>T did not map to a codon.
Sequencing variant TCGA-E2-A10A-01A-21D-A10Y-09 chr23:47101512 A>G did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:47104783 G>A did not map to a codon.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr23:47104841 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:179474866 G>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:179424843 T>C maps to NM_003940.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr3:179472636 C>A maps to NM_003940.2 S639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:178977 G>T maps to NM_005151.3 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr18:210023 T>C maps to NM_005151.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:62795051 T>A maps to ENST00000280377 I920I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr12:62749201 C>G maps to ENST00000280377 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr12:62786083 A>G maps to ENST00000280377 K779K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr8:11995159 G>C maps to NM_201402.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr3:49154008 G>A maps to ENST00000434032 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr3:49148220 G>T maps to ENST00000434032 I1205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr3:49148492 A>G maps to ENST00000434032 C1143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr3:49152538 C>T maps to ENST00000434032 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr9:132637591 G>A maps to NM_001008563.3 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A2JS-01A-11D-A17W-09 chr9:132637216 C>A maps to NM_001008563.3 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:161132850 G>T maps to NM_012475.4 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:161133387 C>T maps to NM_012475.4 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:55589231 C>T maps to NM_015306.2 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A54Y-01A-11D-A25Q-09 chr1:55591334 C>A did not map to a codon.
Sequencing variant TCGA-GM-A3XL-01A-11D-A22X-09 chr1:55589147 C>T maps to NM_015306.2 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr1:55619827 C>T maps to NM_015306.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3RF-01A-11D-A228-09 chr21:17250131 C>A maps to ENST00000285681 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr21:17246809 G>T maps to ENST00000285681 E954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr21:17199313 A>T maps to ENST00000285681 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr21:17242406 G>A maps to ENST00000285681 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:132161351 A>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:132161375 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:132161847 T>G did not map to a codon.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr23:132159685 A>G did not map to a codon.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr23:132160196 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:113700046 C>A maps to NM_020886.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr11:113723333 G>A maps to NM_020886.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr19:57641240 G>T maps to NM_020903.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr15:63866265 C>T maps to NM_006537.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr15:63866544 C>T maps to NM_006537.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:109494573 A>G maps to NM_032663.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:23098495 G>A maps to NM_020718.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:23117793 A>C maps to NM_020718.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14X-01A-11D-A10Y-09 chr16:23116869 T>C maps to NM_020718.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AI-01A-11D-A12Q-09 chr17:58275781 C>T maps to NM_032582.3 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y3-01A-11D-A159-09 chr17:58275760 G>A maps to NM_032582.3 P1098P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:78181536 G>T maps to NM_015017.3 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr2:61492664 C>T maps to NM_014709.3 W1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr2:61622131 T>C maps to NM_014709.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr2:61473499 G>A maps to NM_014709.3 I2169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:61456066 C>T maps to NM_014709.3 V2421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:61475691 C>T maps to NM_014709.3 T2116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X7-01A-11D-A14K-09 chr2:61468771 G>A maps to NM_014709.3 L2234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:61456054 T>C maps to NM_014709.3 L2425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:61430399 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1XY-01A-11D-A14K-09 chr2:61416189 G>C maps to NM_014709.3 L3296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14R-01A-11D-A10Y-09 chr2:61505420 C>A did not map to a codon.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr2:61441299 C>T maps to NM_014709.3 R2859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr17:76795830 A>T maps to NM_025090.3 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr17:76831511 G>A maps to NM_025090.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr17:76798463 G>T maps to NM_025090.3 V988V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:144106825 G>T maps to NM_032557.5 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr4:144119004 G>A maps to NM_032557.5 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr2:85852771 G>C maps to NM_006590.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr2:85857863 T>G maps to NM_006590.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:49362184 A>G maps to NM_003363.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:234431958 A>C maps to NM_018218.2 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10E-01A-21D-A10M-09 chr2:234428318 T>C did not map to a codon.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr7:6175583 T>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:9578276 A>C maps to NM_153210.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr17:9615432 C>T maps to NM_153210.3 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S0-01A-21D-A25Q-09 chr12:95926682 G>T maps to NM_032147.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr6:99887725 G>C maps to NM_001080481.1 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr4:53468078 A>G maps to NM_022832.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XZ-01A-42D-A23C-09 chr4:53468093 G>A maps to NM_022832.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:11951661 C>T maps to ENST00000399455 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr1:22032269 G>A maps to NM_032236.5 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr1:22032269 G>A maps to NM_032236.5 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:22073595 C>A maps to NM_032236.5 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr1:22084185 G>T maps to NM_032236.5 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:41767667 G>A maps to ENST00000373009 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Q-01A-11D-A12B-09 chr6:41773689 G>A maps to ENST00000373009 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S0-01A-21D-A25Q-09 chr12:6964623 T>C maps to NM_001098536.1 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06R-01A-11D-A015-09 chr23:55513980 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr23:55513915 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:55514072 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr23:55514739 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr4:120181040 A>G maps to NM_019050.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:120192983 G>T maps to NM_019050.2 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr4:120193096 C>T maps to NM_019050.2 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:75258662 T>G maps to NM_152586.3 S1593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr10:75258500 A>G maps to NM_152586.3 Y1647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr10:75277120 A>C maps to NM_152586.3 A1021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr10:75258419 G>A maps to NM_152586.3 I1674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:75289457 A>G maps to NM_152586.3 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NC-01A-12W-A16L-09 chr10:75290087 G>T maps to NM_152586.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:5071408 A>C maps to NM_004505.2 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr17:5048768 C>T maps to NM_004505.2 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:5072192 T>C maps to NM_004505.2 H1120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23C-01A-12D-A167-09 chr10:11505402 A>C maps to NM_001080491.2 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr16:8996317 G>A maps to NM_003470.2 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr15:50769137 T>C maps to NM_005154.3 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:50773899 G>T maps to NM_005154.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr15:50741616 T>G maps to NM_005154.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T3-01A-21D-A10Y-09 chr23:41075184 T>C did not map to a codon.
Sequencing variant TCGA-A7-A26J-01A-11D-A167-09 chr23:41082489 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:41075312 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:41075652 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:40990749 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:41048644 G>C did not map to a codon.
Sequencing variant TCGA-AC-A2FM-01A-11D-A19Y-09 chr23:41073962 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:41010190 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0G0-01A-11W-A050-09 chr23:41076558 C>G did not map to a codon.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr23:41007788 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr23:41025363 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr23:41048626 G>A did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:41047364 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1X7-01A-11D-A14K-09 chr23:41025386 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XZ-01A-11D-A14K-09 chr23:41012239 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr23:41043848 C>G did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:41056703 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr23:41075619 A>C did not map to a codon.
Sequencing variant TCGA-A8-A08I-01A-11W-A019-09 chr13:31195309 G>A maps to NM_005800.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:31233465 C>T maps to NM_005800.4 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr13:31233475 C>T maps to NM_005800.4 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr13:31231752 A>G maps to NM_005800.4 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:129058965 A>C did not map to a codon.
Sequencing variant TCGA-A8-A082-01A-11W-A019-09 chr23:129059020 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:129060219 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3BB-01A-21D-A19Y-09 chr23:129055207 A>G did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:129053402 T>C did not map to a codon.
Sequencing variant TCGA-AR-A2LR-01A-12D-A18P-09 chr23:129053382 C>T did not map to a codon.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr23:129058937 G>A did not map to a codon.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr23:129042695 A>G did not map to a codon.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr23:129063525 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr12:101699821 C>T maps to NM_014503.2 N637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr12:101693780 C>G maps to NM_014503.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr12:101693507 G>A maps to NM_014503.2 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr8:117784062 G>A maps to NM_032334.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:145069572 G>T maps to NM_007124.2 E2711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03P-01A-11W-A019-09 chr6:144838084 G>T did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr6:144780059 C>T maps to NM_007124.2 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr6:144768442 C>T maps to NM_007124.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:144783989 C>T maps to NM_007124.2 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr6:145160370 G>A maps to NM_007124.2 L3376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:144860467 C>G maps to NM_007124.2 L2136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:144835050 C>T maps to NM_007124.2 Q1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr6:145118985 G>A maps to NM_007124.2 V3035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr6:144761486 G>C did not map to a codon.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr6:144772625 G>A maps to NM_007124.2 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3E8-01B-11D-A243-09 chr6:145157644 C>T maps to NM_007124.2 Q3345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr6:144743012 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:75591008 T>G maps to NM_003369.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr2:106717537 G>A maps to ENST00000283148 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:106713194 C>T maps to ENST00000283148 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47517209 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0D0-01A-11W-A019-09 chr12:6574107 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0E1-01A-11W-A071-09 chr17:8064833 G>A maps to ENST00000488857 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr23:155130210 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:155119138 C>A did not map to a codon.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr23:155169386 G>T did not map to a codon.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr1:160389363 C>T maps to NM_020335.2 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr1:160389021 C>T maps to NM_020335.2 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr6:31752261 C>T maps to NM_006295.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr6:30892267 G>A maps to NM_001167734.1 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr14:77242495 A>G maps to NM_014909.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:213146161 C>G maps to NM_001136474.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr1:213145985 G>T maps to NM_001136474.1 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr17:41168368 C>T maps to NM_006373.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr16:77859252 T>G maps to NM_020927.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr16:77913105 C>T maps to NM_020927.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:6833623 C>T maps to NM_005428.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr9:136661556 G>C maps to NM_001134398.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XV-01A-21D-A23C-09 chr1:108226108 C>A did not map to a codon.
Sequencing variant TCGA-AC-A5EI-01A-11D-A27P-09 chr1:108299952 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:108293775 G>A maps to NM_006113.4 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RF-01A-11D-A159-09 chr10:118891743 C>G maps to NM_199131.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:101186182 G>A maps to NM_001078.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:101198113 C>T maps to NM_001078.3 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr1:101190441 T>A maps to NM_001078.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr5:82815166 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:82835238 C>A maps to NM_004385.4 I2139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AV-01A-21D-A12Q-09 chr5:82817938 G>T maps to NM_004385.4 E1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr5:82807964 G>A maps to NM_004385.4 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NF-01A-11D-A14G-09 chr5:82834036 G>T maps to NM_004385.4 E1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RD-01A-11D-A159-09 chr5:82850847 C>T maps to NM_004385.4 G3242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:75849803 T>G maps to NM_014000.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr10:75874587 C>G maps to NM_014000.2 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr10:75860848 A>C maps to NM_014000.2 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr10:75854053 C>T maps to NM_014000.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr10:75868883 C>T maps to NM_014000.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr10:75832607 C>A maps to NM_014000.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr9:35057428 C>T maps to NM_007126.3 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr9:35059572 G>A maps to NM_007126.3 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr8:67547062 A>C maps to NM_025054.4 S1114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr8:67547575 T>C maps to NM_025054.4 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I9-01A-11W-A050-09 chr8:67547341 G>A maps to NM_025054.4 N1021N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr8:67563702 C>T maps to NM_025054.4 K929K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr23:7811287 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:7811637 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0E2-01A-11W-A071-09 chr23:7811258 G>C did not map to a codon.
Sequencing variant TCGA-BH-A42V-01A-11D-A243-09 chr23:7811961 C>T did not map to a codon.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr23:7812006 G>C did not map to a codon.
Sequencing variant TCGA-E2-A14W-01A-11D-A12B-09 chr23:6451835 C>G did not map to a codon.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr23:8433539 G>A did not map to a codon.
Sequencing variant TCGA-A2-A1G4-01A-11D-A13L-09 chr23:8433832 C>T did not map to a codon.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr23:8434391 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:8434324 G>T did not map to a codon.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr23:8433832 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr23:8434063 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr5:133311612 C>T maps to NM_003374.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr12:48240181 C>T maps to NM_001017535.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr4:177650828 G>T maps to NM_005429.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:157213078 G>T maps to NM_001167912.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr17:56056609 C>T maps to NM_007146.2 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr12:95688096 G>A maps to NM_017599.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:135630993 A>C did not map to a codon.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr23:135630755 A>T did not map to a codon.
Sequencing variant TCGA-E2-A15J-01A-11D-A12Q-09 chr3:11684951 A>T maps to NM_001128219.1 L14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FB-01A-11D-A17D-09 chr2:219294018 G>T maps to NM_007127.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:219305527 G>A maps to NM_007127.2 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:219313998 C>T maps to NM_007127.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr2:219314014 C>T maps to NM_007127.2 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:219296866 C>T maps to NM_007127.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr3:38039035 T>G maps to NM_015873.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr14:77900250 C>T maps to ENST00000445370 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AZ-01A-21D-A12Q-09 chr3:42567472 G>T maps to NM_004624.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr7:158902572 C>T maps to ENST00000402066 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr7:158829458 G>T maps to ENST00000402066 Y385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr2:36986165 C>A maps to NM_053276.3 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr2:36994369 T>C maps to NM_053276.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:37041380 C>G maps to NM_053276.3 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SV-01A-11D-A099-09 chr16:31104726 G>A maps to ENST00000319788 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr16:31105924 G>C maps to ENST00000319788 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:150573405 A>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:57967284 C>T maps to NM_020633.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:57967634 A>G maps to NM_020633.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:53770364 G>T maps to NM_173857.2 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr19:53770435 G>A maps to NM_173857.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr6:133078956 A>T maps to NM_004665.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr3:51450831 G>A maps to ENST00000273612 Q1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:51457420 T>G maps to ENST00000273612 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr3:51456159 G>C maps to ENST00000273612 S1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RH-01A-21D-A10Y-09 chr22:22599457 C>T maps to NM_007128.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:118940044 C>G maps to NM_021729.4 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:118942375 C>G maps to NM_021729.4 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr11:118952248 C>T maps to NM_021729.4 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13D-01A-13D-A272-09 chr9:79890417 A>G maps to ENST00000376646 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr9:79865047 G>A maps to ENST00000376646 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr9:79792652 G>A maps to ENST00000376646 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr8:100729480 G>A maps to NM_017890.3 L2204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr8:100523445 A>C maps to NM_017890.3 R1472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:100791208 G>T maps to NM_017890.3 G2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr8:100123446 C>T maps to NM_017890.3 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr8:100791055 C>T maps to NM_017890.3 Q2551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr8:100205157 C>G maps to NM_017890.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr8:100732755 C>T maps to NM_017890.3 L2306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr8:100479735 T>C maps to NM_017890.3 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr8:100832305 C>T maps to NM_017890.3 L3009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A42T-01A-11D-A243-09 chr8:100880676 G>A maps to NM_017890.3 V3817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr8:100791108 G>A maps to NM_017890.3 V2568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:62276050 G>A maps to NM_020821.2 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:62299589 G>A maps to NM_020821.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:62274772 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:62315719 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:12338009 A>C maps to NM_015378.2 P1455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:12338009 A>C maps to NM_015378.2 P1455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:12446263 T>G maps to NM_015378.2 G3835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:12414077 C>G maps to NM_015378.2 S3160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr1:12309332 C>A maps to NM_015378.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A251-01A-12D-A167-09 chr1:12446241 A>G did not map to a codon.
Sequencing variant TCGA-B6-A0WV-01A-11D-A10G-09 chr1:12331105 A>G maps to NM_015378.2 Q676Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:12294402 C>G maps to NM_015378.2 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:12408917 G>A maps to NM_015378.2 V3036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr1:12374321 C>A maps to NM_015378.2 I2362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr1:12405429 G>T did not map to a codon.
Sequencing variant TCGA-E9-A245-01A-22D-A16D-09 chr1:12409219 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1PH-01A-11D-A14K-09 chr1:12368635 A>T maps to NM_015378.2 T2196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:2845109 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:2841665 C>G maps to NM_022575.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr20:2841102 C>G maps to NM_022575.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:2842329 C>T maps to NM_022575.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr20:2840964 G>T maps to NM_022575.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:40931071 C>T maps to NM_032353.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:134104819 G>T maps to NM_052875.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YE-01A-11D-A10G-09 chr8:145649455 G>A maps to NM_183057.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr15:91542958 A>C maps to NM_018668.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:91542264 C>G maps to NM_018668.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr15:91551138 C>G maps to NM_018668.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr13:52990192 A>G maps to NM_016075.2 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03T-01A-21W-A050-09 chr8:17137582 G>T maps to NM_152415.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IE-01A-11W-A050-09 chr15:42458982 C>T maps to ENST00000348544 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr15:42459589 A>G did not map to a codon.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr7:38798011 G>T maps to NM_014396.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:150116910 T>C maps to NM_007259.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr1:150054063 A>G maps to NM_007259.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr1:150054882 A>C maps to NM_007259.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:33237281 A>G maps to NM_022553.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr6:33231847 A>G maps to NM_022553.4 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr6:33235985 C>G did not map to a codon.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr17:559190 C>T maps to NM_001128159.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B7-01A-12D-A10Y-09 chr17:505055 C>T maps to NM_001128159.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr1:151149392 G>A maps to ENST00000354473 F285F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AO-A0JD-01A-11W-A071-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr19:50510824 C>A did not map to a codon.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr19:50491660 G>A maps to NM_016440.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FZ-01A-51D-A17G-09 chr23:107310234 G>T did not map to a codon.
Sequencing variant TCGA-A8-A08A-01A-11W-A019-09 chr23:107320386 A>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:107301372 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:107315907 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:107319420 G>T did not map to a codon.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr23:107316028 G>A did not map to a codon.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr23:107301403 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr23:107316025 G>C did not map to a codon.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr23:107320310 C>T did not map to a codon.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr12:118511687 C>T maps to NM_019086.5 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr12:118511557 G>A maps to NM_019086.5 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr12:118517244 C>T maps to NM_019086.5 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:65247916 A>G did not map to a codon.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr23:65253419 A>T did not map to a codon.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr23:65244945 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JC-01A-11D-A13L-09 chr23:65247937 G>A did not map to a codon.
Sequencing variant TCGA-E2-A56Z-01A-12D-A29N-09 chr1:159826347 G>C maps to NM_001013661.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr14:74726396 C>T maps to NM_182894.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:117690303 G>T maps to NM_024626.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr14:68126639 C>G did not map to a codon.
Sequencing variant TCGA-EW-A2FR-01A-11D-A21Q-09 chr10:116032588 C>T maps to NM_198496.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CV-01A-31D-A10Y-09 chr16:22143004 G>A maps to NM_173615.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr16:22159555 C>T maps to NM_173615.3 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr16:22122216 C>T maps to NM_173615.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr16:22142968 G>A maps to NM_173615.3 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:98736088 T>G maps to NM_144992.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:98744743 G>T maps to NM_144992.4 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:98928330 G>T maps to NM_144992.4 E1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr11:123994095 G>A maps to NM_014622.4 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr11:123993832 C>T maps to NM_014622.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr12:6230459 G>A maps to NM_000552.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr12:6125318 G>T maps to NM_000552.3 V1797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B3-01A-11W-A071-09 chr12:6134805 C>A maps to NM_000552.3 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:6143978 G>T maps to NM_000552.3 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr12:6091107 C>T maps to NM_000552.3 P2377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr12:6230459 G>A maps to NM_000552.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:6092322 G>A maps to NM_000552.3 F2358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr12:6134805 C>T maps to NM_000552.3 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr10:28905245 C>T maps to NM_016628.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:119683236 C>A maps to NM_015836.3 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:119575658 C>A maps to NM_015836.3 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:48543986 A>C did not map to a codon.
Sequencing variant TCGA-A7-A2KD-01A-31D-A21Q-09 chr23:48547821 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr23:48542727 C>G did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:48542740 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr23:48547797 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr23:48546699 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr23:48547759 G>C did not map to a codon.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr23:48545240 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr6:110422809 T>C maps to NM_003931.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr7:123335909 T>C maps to NM_003941.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr7:123324634 C>G did not map to a codon.
Sequencing variant TCGA-C8-A1HJ-01A-11D-A13L-09 chr12:14946764 A>C maps to NM_016312.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:73842838 T>G maps to NM_012478.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:73844681 G>A maps to NM_012478.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:73851354 C>A maps to NM_012478.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr22:42422935 A>C maps to NM_152613.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr13:41656884 A>G maps to NM_007187.3 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr23:102612871 T>G did not map to a codon.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr7:74486512 C>T maps to NM_030798.3 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LH-01A-31D-A18P-09 chr7:70885902 G>T maps to NM_022479.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr7:70886057 G>A maps to NM_022479.1 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RA-01A-11D-A14G-09 chr7:71175846 G>T maps to NM_022479.1 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1AZ-01A-11D-A12Q-09 chr7:73100969 C>A maps to ENST00000423497 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HW-01A-11W-A050-09 chr7:73279579 C>T maps to NM_182504.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:73279591 C>A maps to NM_182504.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr2:224746708 C>T maps to NM_020830.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr13:52325490 G>A maps to NM_052950.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YH-01A-11D-A10G-09 chr4:85617212 C>T maps to NM_014991.4 E2937E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr4:85696134 C>G did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr4:85701311 G>C maps to NM_014991.4 V1438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr4:85758096 C>T maps to NM_014991.4 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr4:85648058 C>T maps to NM_014991.4 E2409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr4:85663021 C>T maps to NM_014991.4 V2042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr4:85748076 C>G maps to NM_014991.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr4:85762416 C>A did not map to a codon.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr4:85654704 G>A maps to NM_014991.4 L2351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DK-01A-21D-A17W-09 chr4:85742537 A>G maps to NM_014991.4 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A03Y-01A-21W-A019-09 chr14:55411175 C>A maps to NM_007086.3 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr14:55411097 T>G maps to NM_007086.3 I1047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3HO-01A-11D-A20S-09 chr4:10117754 G>T maps to NM_017491.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:122648627 T>G maps to NM_018117.11 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr2:203747487 A>T maps to NM_018256.3 Y380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr23:48458723 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:48457209 G>A did not map to a codon.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr23:48458036 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr23:48463344 C>T did not map to a codon.
Sequencing variant TCGA-E2-A15M-01A-11D-A12B-09 chr23:48458900 A>G did not map to a codon.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr23:48462670 A>G did not map to a codon.
Sequencing variant TCGA-E9-A1N9-01A-11D-A14G-09 chr23:48460301 C>T did not map to a codon.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr23:48458085 C>T did not map to a codon.
Sequencing variant TCGA-A7-A3J0-01A-11D-A20S-09 chr4:177041168 T>C maps to NM_170710.4 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:177052720 A>G maps to NM_170710.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr4:177049887 G>C did not map to a codon.
Sequencing variant TCGA-E2-A3DX-01A-21D-A20S-09 chr4:39245930 C>A maps to NM_025132.3 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr14:102675569 C>A maps to ENST00000454394 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr14:102675016 G>A maps to ENST00000454394 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:735943 G>A maps to ENST00000248142 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr1:224592212 A>G maps to NM_025160.6 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:118482188 G>A maps to NM_006784.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr9:116094278 C>T maps to NM_001012361.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:128477067 G>C maps to NM_018383.4 S844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:128471175 G>A maps to NM_018383.4 R1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr2:128477150 T>C maps to NM_018383.4 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr9:131397465 G>A maps to NM_052844.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:20141590 G>A maps to NM_001006657.1 Q630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr2:20131079 C>A maps to NM_001006657.1 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr2:20113973 G>A maps to NM_001006657.1 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr5:110446554 G>T maps to NM_139281.2 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A086-01A-11W-A019-09 chr5:110462514 C>A maps to NM_139281.2 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:1142161 A>C maps to ENST00000416775 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr10:1123882 C>T maps to ENST00000416775 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr10:1149702 T>G maps to ENST00000416775 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M8-01A-11D-A20S-09 chr9:127619644 C>G maps to NM_001045476.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr21:44270218 C>T maps to NM_018669.4 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr21:44279795 G>A maps to NM_018669.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr2:29165224 G>A maps to NM_015131.1 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr2:29169539 C>T maps to NM_015131.1 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr23:117527020 G>A did not map to a codon.
Sequencing variant TCGA-A7-A13F-01A-11D-A12Q-09 chr23:117540915 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:117570665 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A1-01A-11W-A019-09 chr23:117521340 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:117527136 A>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:117570719 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:117575414 G>T did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:117527074 G>C did not map to a codon.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr23:117577582 C>G did not map to a codon.
Sequencing variant TCGA-AR-A5QP-01A-11D-A28B-09 chr23:117566791 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:117570781 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:117570785 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:117528091 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1IY-01A-11D-A188-09 chr23:117578414 G>A did not map to a codon.
Sequencing variant TCGA-GM-A2DI-01A-31D-A18P-09 chr23:117529290 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:48935538 C>G did not map to a codon.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr23:48932525 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:48934350 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr17:80583300 G>A maps to NM_019613.3 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:33254618 G>C maps to NM_005452.5 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr6:33247579 G>A maps to NM_005452.5 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:109517229 G>A maps to NM_001142550.1 R857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr3:167293917 G>A maps to NM_178824.3 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr9:137021656 T>A maps to NM_052821.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr9:137013426 T>C maps to NM_052821.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr3:113122818 A>C maps to NM_001164496.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:113027090 G>C maps to NM_001164496.1 S1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:113013533 C>T maps to NM_001164496.1 Q1791Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:113085109 G>A maps to NM_001164496.1 R831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr3:113010506 G>T maps to NM_001164496.1 S1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr3:113082084 C>T maps to NM_001164496.1 R947R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A570-01A-11D-A29N-09 chr3:113119413 G>T maps to NM_001164496.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr3:113122793 G>A maps to NM_001164496.1 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr3:196288325 A>C maps to NM_182627.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FG-01A-11D-A13L-09 chr2:74652075 A>G maps to NM_032118.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr16:74943794 C>A maps to NM_030581.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr16:74946203 G>C maps to NM_030581.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:49049713 G>A maps to NM_018031.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr7:158723188 G>C maps to NM_018051.4 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr7:158672658 G>A maps to NM_018051.4 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:158672482 C>T maps to NM_018051.4 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:158719111 C>T maps to NM_018051.4 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:36577706 G>A maps to NM_001083961.1 K587K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr1:85564232 G>A maps to NM_145172.3 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr1:241912925 G>T maps to NM_144625.4 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr1:241886719 C>G maps to NM_144625.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr1:241936092 G>T did not map to a codon.
Sequencing variant TCGA-A8-A07P-01A-11W-A019-09 chr12:122437779 C>T maps to NM_144668.4 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr12:122441597 C>T maps to NM_144668.4 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:122395060 G>A maps to NM_144668.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr12:122396243 G>A maps to NM_144668.4 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr8:124132399 C>T maps to NM_145647.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08Z-01A-21W-A019-09 chr8:124132396 C>T maps to NM_145647.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr8:124162366 G>A maps to NM_145647.3 Q1022Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr8:124113133 G>T maps to NM_145647.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JM-01A-21W-A071-09 chr2:228769655 C>T maps to NM_178821.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:228767738 C>T maps to NM_178821.1 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:54591304 G>T maps to NM_015285.2 E1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:54694260 C>T maps to NM_015285.2 I1432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr18:54354206 T>C did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr18:54424177 C>G maps to NM_015285.2 S785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr18:54348615 C>T maps to NM_015285.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr18:54606598 C>T maps to NM_015285.2 Q1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr18:54350049 C>T maps to NM_015285.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr5:37701205 A>C maps to NM_018034.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr5:37379654 C>T maps to NM_018034.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr5:37605228 G>A maps to NM_018034.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A259-01A-11D-A16D-09 chr15:54025258 G>A maps to NM_182758.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr15:54025193 C>T maps to NM_182758.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr15:53907999 G>A maps to NM_182758.2 C801C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A441-01A-11D-A243-09 chr15:54008806 G>T maps to NM_182758.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:62603235 A>C maps to NM_018093.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WS-01A-11D-A10Y-09 chr11:62603452 T>A maps to NM_018093.2 K117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:190323495 C>G maps to NM_032168.1 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr15:44150961 C>T maps to NM_024908.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr15:44119241 G>T maps to NM_024908.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr1:67293562 C>A maps to NM_024763.4 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12W-01A-11D-A10Y-09 chr1:67299694 G>A maps to NM_024763.4 R624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:1636971 G>A maps to NM_001163809.1 G1547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr3:52293747 C>T maps to NM_025222.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr3:52293227 G>A maps to NM_025222.3 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr9:140449870 C>T maps to NM_138778.2 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SE-01A-11D-A099-09 chr7:151093203 C>T maps to ENST00000426624 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:701846 A>C maps to NM_145294.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr16:711732 G>A maps to NM_145294.4 Q1270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr16:708526 G>A maps to NM_145294.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr7:134871825 G>A maps to NM_014149.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:68371768 A>C maps to NM_138458.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A075-01A-11D-A099-09 chr15:90258280 C>T maps to NM_020212.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:90248830 C>G maps to NM_020212.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr15:90255297 C>A maps to NM_020212.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr15:90265344 G>A maps to NM_020212.1 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr1:27622854 C>T maps to ENST00000319394 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr1:27624573 C>T maps to ENST00000319394 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:141418903 C>A maps to NM_001105558.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W3-01A-11D-A10G-09 chr7:141427141 A>T maps to NM_001105558.1 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr20:44108627 C>T maps to NM_006103.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr20:44166722 G>A maps to ENST00000396669 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr20:44168035 G>T maps to ENST00000372665 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr20:44190776 A>C maps to NM_130896.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X7-01A-11D-A10M-09 chr16:683759 C>T maps to NM_053284.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr17:48917948 G>T maps to NM_175575.5 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr17:48913405 G>A maps to NM_175575.5 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr17:48917308 G>A maps to NM_175575.5 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:6303117 G>A maps to NM_006005.3 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:1906106 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:38162117 G>A maps to NM_023034.1 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:38162249 A>G maps to NM_023034.1 C822C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr8:38187390 C>T maps to NM_023034.1 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A247-01A-11D-A167-09 chr8:38173481 G>C maps to NM_023034.1 S645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr8:38172996 C>T maps to NM_023034.1 Q684Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:1985183 G>A maps to NM_005663.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr4:1986592 G>C maps to NM_005663.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr2:175432742 A>G maps to NM_003387.4 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RB-01A-11D-A17G-09 chr2:175436605 C>T maps to NM_003387.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr17:38412740 A>T maps to NM_133264.4 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:29915469 C>T maps to NM_001080529.1 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:66446898 G>A maps to NM_017983.5 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:5265558 A>G maps to NM_015610.3 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr7:5256730 G>A maps to NM_015610.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr8:134237777 C>A maps to NM_003882.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr8:134225360 G>C maps to NM_003882.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S2-01A-12D-A25Q-09 chr20:43353469 C>T maps to NM_003881.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:43355908 A>C maps to NM_003881.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:112386069 A>C maps to NM_198239.1 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:112386120 T>G maps to NM_198239.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr19:15536451 G>C maps to ENST00000389282 V1260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09M-01A-11W-A019-09 chr1:68564425 G>A maps to NM_001002292.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr1:68615924 G>A maps to NM_024911.6 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:68603523 G>C maps to NM_024911.6 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr12:1017843 A>C maps to NM_001184985.1 P2605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:989987 T>C maps to NM_001184985.1 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:990014 A>C maps to NM_001184985.1 T1247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr12:994742 A>C maps to NM_001184985.1 T1851T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr12:936423 G>C maps to NM_001184985.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr12:989089 C>T maps to NM_018979.3 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:1006807 C>T maps to NM_001184985.1 R2397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A40B-01A-11D-A23C-09 chr12:1009693 C>T maps to NM_001184985.1 L2427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:992226 T>C did not map to a codon.
Sequencing variant TCGA-BH-A5J0-01A-11D-A27P-09 chr12:970324 C>G maps to NM_001184985.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5DA-01A-11D-A27P-09 chr12:988981 C>T maps to NM_018979.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr9:96030075 C>T maps to ENST00000297954 Q1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr9:96060332 C>T maps to ENST00000297954 V2006V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:54263719 C>T did not map to a codon.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr23:54263736 G>C did not map to a codon.
Sequencing variant TCGA-A8-A096-01A-11W-A019-09 chr23:54275400 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:54278050 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:54359806 A>C did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:54319421 G>C did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr23:54321118 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54264796 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54275240 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54275488 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:54282243 G>A did not map to a codon.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr23:54275568 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:54275291 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0DQ-01A-11D-A099-09 chr23:54335679 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr23:54319369 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr23:54263732 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr23:54265470 C>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:54319738 C>T did not map to a codon.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr23:54337551 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15A-01A-11D-A12B-09 chr23:54224847 G>A did not map to a codon.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr23:54259336 G>C did not map to a codon.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr23:54337559 G>T did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:40936071 C>T maps to NM_032387.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04T-01A-21W-A050-09 chr12:49374312 C>T maps to NM_005430.3 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:120979272 C>T maps to NM_057168.1 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr7:120969830 G>A maps to NM_057168.1 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr7:116918217 G>A maps to NM_003391.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr7:116955247 A>G maps to NM_003391.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A250-01A-31D-A167-09 chr1:113058810 C>A maps to NM_024494.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr1:113057711 C>T maps to NM_024494.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr1:113057693 C>T maps to NM_024494.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr1:113052033 G>C maps to NM_024494.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr1:228246811 C>T maps to ENST00000366753 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr3:55513564 C>T maps to NM_003392.3 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:13921256 G>C maps to NM_004625.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:13860506 G>A maps to NM_004625.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TY-01A-12W-A12T-09 chr3:13896103 G>A maps to NM_004625.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B7-01A-12D-A10Y-09 chr3:13860452 G>T maps to NM_004625.3 Y346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:137423579 C>T maps to NM_058244.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A3ZX-01A-11D-A23C-09 chr5:137426284 A>G maps to NM_058244.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr5:137426380 G>A maps to NM_058244.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr10:102239668 C>T maps to NM_003393.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr17:7606071 C>A maps to NM_018081.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A256-01A-11D-A167-09 chr17:7592244 C>T maps to NM_018081.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:30933779 C>T maps to NM_000553.4 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr8:30999100 C>T maps to NM_000553.4 C1041C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr8:30982426 C>T maps to NM_000553.4 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:30977829 T>C maps to NM_000553.4 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr6:2785329 G>A maps to NM_020135.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1G0-01A-11D-A13L-09 chr12:108618543 C>T maps to ENST00000261400 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07G-01A-11W-A050-09 chr12:108604054 C>T maps to ENST00000261400 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr12:108634214 C>T maps to ENST00000261400 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AJ-01A-21D-A12Q-09 chr11:32450118 C>T maps to NM_024426.4 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr11:32413551 C>T maps to NM_024426.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr6:160169353 G>T maps to NM_004906.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07F-01A-11W-A019-09 chr6:160163164 C>A maps to NM_004906.3 Y44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr19:34991145 C>A maps to ENST00000270288 S646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:184182395 G>A maps to ENST00000448232 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F2-01A-31D-A13L-09 chr4:184129263 C>T maps to ENST00000448232 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:10102554 A>G did not map to a codon.
Sequencing variant TCGA-A2-A25E-01A-11D-A167-09 chr23:10102559 C>G did not map to a codon.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr23:10106888 C>T did not map to a codon.
Sequencing variant TCGA-A8-A09A-01A-11W-A019-09 chr23:10062265 C>T did not map to a codon.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr23:10046871 A>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:10085169 T>G did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:10085365 C>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:10106782 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1X9-01A-12D-A159-09 chr23:10092350 G>A did not map to a codon.
Sequencing variant TCGA-EW-A1IW-01A-11D-A13L-09 chr23:10058870 C>T did not map to a codon.
Sequencing variant TCGA-EW-A1OY-01A-11D-A142-09 chr23:10066592 T>C did not map to a codon.
Sequencing variant TCGA-C8-A12M-01A-11D-A135-09 chr16:78466447 C>T maps to NM_016373.1 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr8:87460601 A>G maps to NM_007013.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr8:87437450 G>A did not map to a codon.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr8:87464812 C>T maps to NM_007013.3 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TS-01A-11D-A10Y-09 chr16:69922068 A>C maps to NM_007014.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr16:69951723 C>T maps to NM_007014.3 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr16:69973788 G>C maps to NM_007014.3 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr3:149243908 C>A maps to NM_001168278.1 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr3:149374904 G>C maps to NM_001168278.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:7692691 C>T maps to NM_020196.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr19:7687716 G>A maps to NM_020196.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr19:7688748 C>G maps to NM_020196.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:52844168 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JD-01A-11D-A13L-09 chr3:46063166 G>A maps to NM_005283.2 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:2729483 A>G did not map to a codon.
Sequencing variant TCGA-A2-A0CZ-01A-11W-A050-09 chr23:123019869 T>A did not map to a codon.
Sequencing variant TCGA-A8-A07I-01A-11W-A019-09 chr23:123019796 C>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:123020210 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr23:123040997 C>G did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr3:39226262 G>A maps to NM_194293.2 L1558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T6-01A-11D-A099-09 chr2:168104723 C>T maps to NM_152381.5 I2274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr2:168074743 C>T maps to NM_152381.5 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:168102872 T>G maps to NM_152381.5 G1657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:168104945 A>C maps to NM_152381.5 P2348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr2:168106292 C>G maps to NM_152381.5 L2797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:168100928 C>T maps to NM_152381.5 I1009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:168103709 C>T maps to NM_152381.5 F1936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:168107318 C>T maps to NM_152381.5 N3139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A54N-01A-11D-A25Q-09 chr2:168115458 C>T maps to ENST00000420519 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr2:167760154 C>T maps to NM_152381.5 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr2:168106215 C>T maps to NM_152381.5 Q2772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr2:168102293 G>A maps to NM_152381.5 L1464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:168103370 G>A maps to NM_152381.5 E1823E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr2:168103376 G>A maps to NM_152381.5 Q1825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr2:168102467 C>G maps to NM_152381.5 V1522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15I-01A-21D-A135-09 chr2:168115716 A>G maps to ENST00000420519 T920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr2:168104571 G>T maps to NM_152381.5 E2224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:37587559 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:37587123 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:37587604 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0EB-01A-11W-A050-09 chr23:37553704 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr8:56435906 G>A maps to NM_052898.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:56435861 C>T maps to NM_052898.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr8:10755616 T>G maps to NM_173683.3 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RN-01A-12D-A099-09 chr8:10755749 G>A maps to NM_173683.3 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr20:30556265 C>T maps to NM_001011718.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr1:28293113 G>C maps to NM_018053.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr23:100183268 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:100183172 T>G did not map to a codon.
Sequencing variant TCGA-LQ-A4E4-01A-11D-A25Q-09 chr23:100169374 C>G did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr3:14190367 C>T maps to NM_004628.4 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:14208753 C>T did not map to a codon.
Sequencing variant TCGA-E2-A1LK-01A-21D-A14G-09 chr3:14190418 C>T maps to NM_004628.4 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:128886314 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:128902309 T>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:128877935 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0H0-01A-11W-A071-09 chr23:128887189 A>G did not map to a codon.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr23:128889306 A>C did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:128880269 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr22:41265019 C>T maps to NM_022098.2 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:61726026 C>T maps to NM_003400.3 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:61719557 G>C maps to NM_003400.3 S542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14N-01A-31D-A135-09 chr2:61710128 A>G maps to NM_003400.3 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr13:21361136 G>C maps to NM_022459.4 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A425-01A-11D-A243-09 chr13:21417129 T>G maps to NM_022459.4 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BG-01A-11D-A10Y-09 chr13:21382692 G>C maps to NM_022459.4 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr13:21395841 C>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:43534914 G>A maps to NM_020750.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr6:43535088 C>T maps to NM_020750.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:43494462 C>T maps to NM_020750.2 K981K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr16:28177892 A>C maps to NM_015171.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X1-01A-11D-A10G-09 chr16:28187311 G>T maps to NM_015171.2 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr16:28109861 G>C maps to NM_015171.2 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr16:28112955 G>A maps to NM_015171.2 V1033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr8:21842350 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:21827074 C>T maps to ENST00000434536 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr12:64825440 C>G maps to NM_007235.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0SW-01A-11D-A099-09 chr12:64808757 G>A maps to NM_007235.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr12:64815163 G>A maps to NM_007235.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:44056988 T>G maps to NM_006297.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:44057131 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:44047651 C>G maps to NM_006297.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr5:82491605 C>T maps to NM_022406.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr22:42049644 G>A maps to NM_001469.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr3:142131499 C>T maps to NM_019001.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:142142426 G>A maps to NM_019001.3 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr3:142090129 C>A maps to NM_019001.3 E1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr3:142031571 G>T maps to NM_019001.3 L1562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr3:142095322 T>C maps to NM_019001.3 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr20:21314347 G>T maps to NM_012255.3 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FK-01A-11D-A27P-09 chr20:21314340 G>A did not map to a codon.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr11:74556117 C>A maps to NM_182969.1 G635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr11:74574067 T>C maps to ENST00000431210 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A408-01A-12D-A243-09 chr16:17292093 G>A maps to NM_022166.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:48434546 G>T maps to NM_022167.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr17:48433606 C>T maps to NM_022167.2 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr11:102076657 G>A maps to NM_001130145.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr11:102076657 G>A maps to NM_001130145.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr12:32908184 G>A maps to NM_001040436.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:43166673 C>T maps to NM_004559.3 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:183442289 G>A maps to NM_018023.4 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr3:183525828 C>T maps to NM_018023.4 T1341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:69759618 C>T maps to NM_006530.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12U-01A-11D-A10Y-09 chr11:66055108 G>T maps to ENST00000376904 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:38798234 A>C did not map to a codon.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr19:38799893 C>A maps to NM_001039672.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y0-01A-11D-A14K-09 chr19:38798136 G>T maps to NM_001039672.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:54348836 T>C maps to NM_018982.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FK-01A-11W-A050-09 chr23:67718952 G>A did not map to a codon.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr23:67742611 C>G did not map to a codon.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr23:67738654 G>T did not map to a codon.
Sequencing variant TCGA-BH-A1FG-01A-11D-A13L-09 chr23:67741222 A>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:75247274 A>C maps to NM_019589.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:75248350 T>C maps to NM_019589.2 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:75248377 A>C maps to NM_019589.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:75265527 T>G maps to NM_019589.2 G1176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:75245272 G>T maps to NM_019589.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0GZ-01A-11W-A071-09 chr14:75247170 C>T maps to NM_019589.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr10:27425309 G>A maps to NM_139312.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A275-01A-21D-A16D-09 chr17:57430826 G>A maps to NM_001005404.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:38272573 G>A maps to NM_024640.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W5-01A-11D-A228-09 chr2:135741342 G>C maps to NM_025052.3 S1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:135745744 C>A maps to NM_025052.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr2:135779314 G>A maps to NM_025052.3 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr20:61835142 G>C maps to NM_017798.3 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr20:61835024 G>A maps to NM_017798.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr20:61834988 G>A maps to NM_017798.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr1:29064168 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0D1-01A-11W-A050-09 chr8:64087953 C>T maps to ENST00000339066 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:64099493 C>T maps to ENST00000339066 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr7:75959385 C>T maps to NM_012479.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr22:32352685 T>C maps to NM_003405.3 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A62Y-01A-11D-A29N-09 chr23:21874662 G>C did not map to a codon.
Sequencing variant TCGA-AQ-A1H2-01A-11D-A13L-09 chr23:21874874 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr23:21875633 C>G did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr18:72914129 T>G maps to NM_175907.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr2:174055652 T>G did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:173955863 G>A maps to NM_016653.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr2:174130808 G>A maps to NM_016653.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SM-01A-11D-A099-09 chr7:100349611 C>T maps to ENST00000349350 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:100352903 G>A maps to ENST00000349350 K1060K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr7:100365542 G>A maps to ENST00000349350 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BL-01A-11D-A10Y-09 chr7:100349831 G>T maps to ENST00000349350 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr7:100334226 G>T maps to ENST00000349350 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr7:100349542 C>T maps to ENST00000349350 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FL-01A-11D-A27P-09 chr7:100365627 C>T maps to ENST00000349350 L1679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A041-01A-11W-A050-09 chr2:98354540 C>T maps to NM_001079.3 Y569Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr2:98351028 G>A maps to NM_001079.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr2:98340801 G>A maps to NM_001079.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr2:98351823 C>T maps to NM_001079.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr3:167034855 C>T maps to ENST00000307529 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr3:167083757 G>A maps to ENST00000307529 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:2408733 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0E6-01A-11W-A050-09 chr23:2406917 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr23:2407716 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1IU-01A-11D-A14G-09 chr23:2407842 C>T did not map to a codon.
Sequencing variant TCGA-E9-A1NI-01A-11W-A16H-09 chr23:2408673 G>T did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:2408348 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:50277792 G>A maps to NM_014838.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:50277906 C>T maps to NM_014838.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr22:50280504 G>A maps to NM_014838.2 W1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr22:50278869 G>A maps to NM_014838.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr3:101370303 G>A maps to NM_014415.3 N956N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr3:101370348 C>T maps to NM_014415.3 V941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:114121048 T>G maps to NM_001018011.1 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1Y1-01A-21D-A14K-09 chr11:113935218 C>T maps to NM_001018011.1 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr1:16272249 A>C maps to ENST00000375733 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:16274921 G>C maps to ENST00000375733 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PD-01A-11D-A142-09 chr3:114069880 C>T maps to NM_001164342.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:33283445 G>C maps to NM_001145338.1 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:33284489 G>A maps to NM_001145338.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr6:33283625 G>A maps to NM_001145338.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr6:109787657 A>C maps to NM_014797.2 L497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:125680888 C>G maps to NM_020924.2 *442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr9:125681054 C>A maps to NM_020924.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr19:36207191 C>T maps to NM_014383.1 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr23:119388920 C>T did not map to a codon.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr23:119388278 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:119388942 C>A did not map to a codon.
Sequencing variant TCGA-BH-A1FE-01A-11D-A13L-09 chr23:119389141 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:119388223 T>C did not map to a codon.
Sequencing variant TCGA-A2-A1G1-01A-21D-A13L-09 chr3:141161655 A>C maps to NM_001080412.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:141162772 C>T maps to NM_001080412.2 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U2-01A-11D-A10G-09 chr3:141163017 T>C maps to NM_001080412.2 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NA-01A-11D-A142-09 chr3:141162009 G>A maps to NM_001080412.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:7366056 G>A maps to NM_020899.3 H748H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr17:7366442 C>A maps to NM_020899.3 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr1:22839543 G>A maps to NM_014870.3 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr1:22835080 C>G maps to NM_014870.3 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RI-01A-11D-A167-09 chr1:22835659 C>A maps to NM_014870.3 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr1:22828832 G>T maps to NM_014870.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr1:22852822 C>T maps to NM_014870.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:197128625 G>A maps to NM_194314.2 Q865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FV-01A-11W-A019-09 chr1:197169213 G>A maps to NM_194314.2 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HO-01A-11W-A050-09 chr9:129595093 T>C maps to NM_014007.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr9:129594904 C>G maps to NM_014007.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:62407184 C>T maps to NM_025224.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr20:62421189 G>A maps to NM_025224.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr4:4301737 C>T maps to NM_145291.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr9:125673288 G>A maps to NM_006626.4 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr9:125673813 C>A maps to NM_006626.4 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:4054873 C>T maps to NM_015898.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:4055152 C>T maps to NM_015898.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr1:154988893 C>A maps to ENST00000417934 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:154987159 G>C maps to ENST00000417934 L42L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AC-A23H-01A-11D-A159-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr1:33099307 G>A maps to NM_178547.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr1:33116130 G>A maps to NM_178547.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr1:33099257 G>A maps to NM_178547.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr6:33423206 G>A maps to NM_152735.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:203818933 G>A maps to NM_014827.4 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr23:64722082 A>C did not map to a codon.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr23:64717088 A>G did not map to a codon.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr23:64708836 G>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:64721840 T>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:64708807 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:64722248 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:64718921 C>T did not map to a codon.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr23:64722720 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr23:64722505 G>T did not map to a codon.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr23:64722830 C>T did not map to a codon.
Sequencing variant TCGA-C8-A12N-01A-11D-A10Y-09 chr23:64721752 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1JM-01A-11D-A13L-09 chr23:64721695 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr11:110034054 G>A maps to NM_033390.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:110030199 C>A maps to NM_033390.1 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A203-01A-12D-A167-09 chr11:110030001 T>A maps to NM_033390.1 L312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:149795445 C>T maps to NM_207360.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:46541950 G>A maps to ENST00000242848 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:46543500 C>A maps to ENST00000242848 E1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:46543914 C>A maps to ENST00000242848 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr14:89073698 A>C maps to NM_024824.4 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A2-01A-11W-A050-09 chr2:187371486 C>T maps to NM_018471.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:11846601 C>T maps to NM_014153.3 E883E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:11850203 G>A maps to NM_014153.3 Y817Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:11868839 C>T maps to NM_014153.3 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr16:11862258 G>C maps to NM_014153.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr22:41726064 G>A maps to ENST00000351589 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr22:41752440 G>A maps to ENST00000351589 E842E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A124-01A-11D-A10M-09 chr7:138732378 C>A maps to ENST00000464606 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IK-01A-12W-A071-09 chr7:138774480 C>T maps to ENST00000464606 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:138764572 T>G maps to ENST00000464606 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr7:129663532 G>A maps to NM_016478.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:64137671 C>T did not map to a codon.
Sequencing variant TCGA-A8-A090-01A-11W-A019-09 chr1:52933939 C>A did not map to a codon.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:52930845 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:52943418 C>A maps to NM_001009881.2 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr1:52911473 G>A maps to NM_001009881.2 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BO-01A-23D-A12B-09 chr23:117960411 T>C did not map to a codon.
Sequencing variant TCGA-BH-A0EE-01A-11W-A050-09 chr23:117959441 G>A did not map to a codon.
Sequencing variant TCGA-E2-A1B1-01A-21D-A12Q-09 chr23:117959236 C>G did not map to a codon.
Sequencing variant TCGA-E2-A1IE-01A-11D-A188-09 chr23:117960035 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:73524264 G>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:73524274 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr23:73524430 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YG-01A-21D-A10G-09 chr16:87452475 A>G maps to NM_015144.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DE-01A-11D-A10Y-09 chr16:87446721 G>A maps to NM_015144.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0CG-01A-11W-A019-09 chr23:111698591 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:111698507 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:111698552 T>G did not map to a codon.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr23:111698858 G>A did not map to a codon.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:31811815 A>T maps to NM_016505.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Q-01A-11W-A019-09 chr23:103359681 G>C did not map to a codon.
Sequencing variant TCGA-BH-A18T-01A-11D-A12B-09 chr18:60209734 A>T maps to NM_017742.4 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr18:60207018 C>T maps to NM_017742.4 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:77913173 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0D4-01A-11W-A019-09 chr23:77912637 T>A did not map to a codon.
Sequencing variant TCGA-A8-A09W-01A-11W-A019-09 chr23:77913267 T>A did not map to a codon.
Sequencing variant TCGA-AR-A1AM-01A-41D-A228-09 chr23:77913760 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0HL-01A-11W-A050-09 chr23:77913882 A>C did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr9:88938450 A>C maps to NM_024617.3 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:88916364 G>A maps to NM_024617.3 Q1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:88933973 C>A did not map to a codon.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr9:88932176 G>C maps to NM_024617.3 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr9:88920154 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:37327809 C>A maps to NM_032226.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:122983410 C>A maps to NM_017612.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:28454652 C>T maps to NM_001040432.1 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F0-01A-11D-A135-09 chr2:207170989 G>T maps to NM_020923.1 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XF-01A-11D-A14G-09 chr2:207175935 G>A maps to NM_020923.1 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14P-01A-31D-A12B-09 chr2:207175719 C>T maps to NM_020923.1 V2156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr2:207169561 G>T maps to NM_020923.1 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06X-01A-21W-A019-09 chr5:843814 C>T maps to NM_024786.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr5:837563 G>C maps to NM_024786.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IK-01A-11D-A17G-09 chr5:843814 C>T maps to NM_024786.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:131484718 G>A maps to ENST00000372667 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr9:131484018 C>T maps to ENST00000372667 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:74636952 T>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:74651337 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:74644503 C>T did not map to a codon.
Sequencing variant TCGA-E2-A107-01A-11D-A10M-09 chr23:74637023 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr10:99211935 A>G maps to NM_198046.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08G-01A-11W-A019-09 chr12:77199201 C>T maps to NM_015336.2 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27N-01A-11D-A16D-09 chr1:27176929 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09D-01A-11W-A019-09 chr3:195937532 G>A maps to NM_001039617.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:17063262 G>A maps to NM_016353.4 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr13:21955624 G>A maps to ENST00000400590 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr13:21987847 C>A maps to ENST00000400590 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:14639977 T>G maps to NM_178566.4 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:57461341 G>A maps to NM_015457.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr11:57457519 C>T maps to NM_015457.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:128963020 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24V-01A-21D-A167-09 chr23:128948762 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr23:128975838 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:128946744 C>T did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr10:31810830 A>C maps to NM_001174096.1 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr10:31810767 G>A maps to NM_001174096.1 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A243-01A-21D-A167-09 chr8:82626197 C>T maps to NM_024699.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AR-01A-31D-A135-09 chr2:220072392 T>C maps to NM_138802.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HE-01A-11D-A188-09 chr2:220073994 C>T maps to NM_138802.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr8:135669981 T>C maps to ENST00000318135 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr8:135614281 C>A maps to NM_020863.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr12:72037951 G>A maps to NM_144982.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr12:72013171 A>G maps to NM_144982.4 L1689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:72030785 T>C maps to NM_144982.4 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr12:72009005 A>C maps to NM_144982.4 P1745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr16:72831444 C>T maps to NM_006885.3 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr16:72830477 G>A maps to NM_006885.3 Q2035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09R-01A-11W-A019-09 chr16:72830232 C>T maps to NM_006885.3 P2116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:72829036 G>C maps to NM_006885.3 S2515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:72830631 G>A maps to NM_006885.3 L1983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:72831141 C>T maps to NM_006885.3 V1813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr16:72992022 G>A maps to NM_006885.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr16:72830256 C>T maps to NM_006885.3 Q2108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HQ-01A-11W-A050-09 chr16:72830108 G>A maps to NM_006885.3 R2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:72991572 G>A maps to NM_006885.3 T824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr16:72827827 G>C maps to NM_006885.3 S2918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XO-01A-11D-A14K-09 chr16:72832412 G>A maps to NM_006885.3 Q1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14Z-01A-11D-A10Y-09 chr16:72984481 G>A maps to NM_006885.3 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr8:77765960 G>T maps to NM_024721.4 R2268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XW-01A-11D-A23C-09 chr8:77618656 C>T maps to NM_024721.4 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr8:77745628 G>A maps to NM_024721.4 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:77768192 C>T maps to NM_024721.4 C3012C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A129-01A-21D-A10M-09 chr8:77761273 G>C maps to NM_024721.4 G1185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr8:77763443 C>A maps to NM_024721.4 L1429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr8:77775819 C>T maps to NM_024721.4 V3290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JL-A3YW-01A-12D-A23C-09 chr8:77767799 C>T maps to NM_024721.4 D2881D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:75204021 G>A maps to NM_153688.2 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25D-01A-12D-A16D-09 chr15:42743986 G>A maps to NM_022473.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr15:42734372 G>A maps to NM_022473.1 Q1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr15:42742651 C>T maps to NM_022473.1 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr15:42749156 G>A maps to NM_022473.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr15:42710149 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:44832305 G>A maps to ENST00000412927 F685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B8-01A-21W-A071-09 chr19:44834084 C>T maps to ENST00000412927 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr19:44832008 T>G maps to ENST00000412927 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XB-01A-11D-A14G-09 chr19:44831586 C>A maps to ENST00000412927 *925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:36831887 A>C maps to NM_020917.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:36851394 A>G maps to NM_020917.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J2-01A-11W-A050-09 chr18:5291510 C>T maps to NM_003409.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr18:5290994 C>T maps to NM_003409.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr19:57066545 G>T maps to NM_020828.1 G798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:57060375 C>T maps to NM_020828.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr19:57066676 A>G maps to NM_020828.1 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr17:4995114 G>T maps to NM_153018.2 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18U-01A-21D-A12B-09 chr17:4996236 C>T maps to NM_153018.2 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr14:69256806 T>A maps to NM_004926.2 K154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr2:43453433 G>A maps to NM_006887.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr4:188924197 T>G maps to NM_174900.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09E-01A-11W-A019-09 chr6:29640363 G>A maps to NM_001109809.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr20:50803572 G>T maps to NM_018197.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr20:50701560 G>A maps to NM_199427.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18F-01A-11D-A12B-09 chr20:50701380 C>T maps to NM_199427.2 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr20:50701659 T>C maps to NM_199427.2 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr19:36883687 A>G maps to NM_133466.2 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RZ-01A-11D-A28B-09 chr19:36884212 G>A maps to NM_133466.2 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:68598487 C>T maps to NM_133458.2 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr16:68597460 C>T maps to NM_133458.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QQ-01A-11D-A28B-09 chr11:58347038 G>A maps to NM_053023.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr11:64854241 C>T maps to NM_006782.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SE-01A-11D-A25Q-09 chr8:106815175 G>T maps to NM_012082.3 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr8:106815705 A>G maps to NM_012082.3 S1132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FL-01A-11W-A050-09 chr8:106815138 G>A maps to NM_012082.3 K943K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KT-01A-11D-A13L-09 chr8:106815009 C>T maps to NM_012082.3 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr8:106815513 G>A maps to NM_012082.3 Q1068Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr8:106814536 G>T maps to NM_012082.3 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr5:32390508 C>A maps to NM_016107.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr5:32364312 C>T maps to NM_016107.3 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr5:32403301 C>T maps to NM_016107.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J3-01A-11D-A13L-09 chr5:32364330 C>T maps to NM_016107.3 Q962Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:3813854 G>C maps to NM_015174.1 T735T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D8-A140-01A-11D-A10Y-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr19:3834980 G>A maps to NM_015174.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr19:3806015 T>C maps to NM_015174.1 G917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4RW-01A-21D-A25Q-09 chr23:24197365 C>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:24225829 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:24228423 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:24197700 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr23:24228433 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:24225860 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr14:73464633 G>A maps to NM_021260.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr5:79741088 T>C maps to NM_014733.3 C863C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WZ-01A-11D-A10G-09 chr5:79733497 C>T maps to NM_014733.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25B-01A-11D-A167-09 chr15:41099909 A>G maps to NM_001077268.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr15:41099930 G>C maps to NM_001077268.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr15:41105029 C>T maps to NM_001077268.1 N320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XY-01A-11D-A23C-09 chr3:15126257 G>A maps to NM_022340.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:15116190 G>A maps to NM_022340.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:15122258 G>A maps to NM_022340.2 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:15115665 C>A maps to NM_022340.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03N-01B-11D-A10M-09 chr3:15115822 G>A maps to NM_022340.2 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26V-01A-11D-A16D-09 chr3:15115865 G>C maps to NM_022340.2 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr14:68264773 C>T maps to NM_015346.3 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr14:68229057 C>T maps to NM_015346.3 G2077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04U-01A-11D-A10Y-09 chr4:2321937 G>A maps to NM_020972.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr4:2306974 A>G maps to NM_020972.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr4:2306047 A>G maps to NM_020972.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr4:2341250 C>G maps to NM_020972.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr16:2880414 G>C did not map to a codon.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr19:10415799 A>T maps to NM_001103167.1 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr20:62366832 G>T maps to NM_032527.4 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:124267925 A>G maps to NM_007222.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr8:124266321 G>C maps to NM_007222.3 S622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:124267581 G>C maps to NM_007222.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A259-01A-11D-A16D-09 chr8:123964745 G>A maps to NM_014943.3 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:123964307 C>T maps to NM_014943.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr8:123965813 G>A maps to NM_014943.3 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr20:39831957 G>A maps to NM_015035.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:39832165 G>C maps to NM_015035.3 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr23:136652161 C>G did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:136649034 C>T did not map to a codon.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr23:136649098 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Z-01A-11D-A16D-09 chr23:136651210 G>A did not map to a codon.
Sequencing variant TCGA-E2-A15R-01A-11D-A10Y-09 chr23:136649807 C>A did not map to a codon.
Sequencing variant TCGA-BH-A18N-01A-11D-A12B-09 chr13:100617885 C>T maps to NM_033132.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr13:100623857 C>G maps to NM_033132.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr19:57286769 T>C maps to NM_001146326.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18Q-01A-12D-A12B-09 chr19:57286203 G>T maps to NM_001146326.1 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:57647188 A>G maps to NM_052882.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:99627538 G>A maps to NM_003439.1 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr7:99631174 G>A maps to NM_003439.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr16:25251805 C>T maps to NM_001012981.4 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr6:28213379 G>A maps to NM_019110.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A130-01A-31D-A10Y-09 chr6:28214861 C>T maps to NM_019110.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XT-01A-11D-A22X-09 chr7:99110155 G>A maps to NM_014569.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:99110129 C>T maps to NM_014569.3 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:99103903 G>A maps to NM_014569.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr23:101152869 G>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:101139681 C>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:101139429 C>T did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:101139435 A>C did not map to a codon.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr23:101139059 C>G did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr1:40735711 T>C maps to NM_005857.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SP-01A-11D-A099-09 chr23:70462187 G>C did not map to a codon.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr23:70467294 C>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:70469954 G>A did not map to a codon.
Sequencing variant TCGA-B6-A0I5-01A-11W-A100-09 chr23:70464310 G>A did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:70462259 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12Z-01A-11D-A10Y-09 chr23:70472830 G>A did not map to a codon.
Sequencing variant TCGA-D8-A141-01A-11D-A10Y-09 chr23:70461088 T>C did not map to a codon.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr23:70464639 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XM-01A-21D-A14K-09 chr23:70462883 G>A did not map to a codon.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr1:35835659 C>T maps to NM_005095.2 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:35871051 C>G maps to NM_005095.2 S1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:35863123 G>A maps to NM_005095.2 E1059E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr1:35870628 G>C maps to NM_005095.2 R1178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr1:35851041 G>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr1:35836130 C>T maps to NM_005095.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr1:35454131 C>A maps to NM_007167.3 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:50379983 G>A maps to NM_015896.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:4647125 A>C maps to NM_001136046.1 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:4647379 C>T maps to NM_001136046.1 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:75185689 T>G maps to NM_001024593.1 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:45867685 C>T maps to ENST00000471951 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:19790985 T>A maps to NM_033204.2 C396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S1-01A-21D-A25Q-09 chr7:64167461 T>C maps to NM_016220.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr7:64166947 C>G maps to NM_016220.3 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:48785656 G>A maps to NM_153608.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A402-01A-11D-A23C-09 chr19:48789741 C>T maps to NM_153608.1 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr7:6731348 G>C maps to ENST00000330442 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr7:6730907 T>C maps to ENST00000330442 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A27B-01A-11D-A167-09 chr19:9677203 A>G maps to NM_001008727.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr1:247320335 A>G maps to NM_003431.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H9-01A-11W-A071-09 chr1:247320266 A>G maps to NM_003431.2 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr5:43175003 G>A maps to ENST00000509156 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E7-01A-11W-A050-09 chr5:43174805 A>G maps to ENST00000509156 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A573-01A-11D-A29N-09 chr19:58946285 G>A maps to NM_003433.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:18297345 C>G maps to ENST00000401790 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:18296601 C>A maps to ENST00000401790 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr20:18297345 C>G maps to ENST00000401790 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:58579108 C>T maps to NM_007134.1 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:58578709 C>T maps to NM_007134.1 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:58579046 C>T maps to NM_007134.1 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:58578409 C>T maps to NM_007134.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr19:12297990 A>T maps to NM_003437.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr4:367623 G>C maps to NM_003441.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T1-01A-21D-A099-09 chr2:219509720 C>T maps to NM_001105537.1 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F8-01A-11D-A13L-09 chr2:219508613 G>A maps to NM_001105537.1 F875F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr2:219507866 G>A maps to NM_001105537.1 I1124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0EI-01A-11D-A10Y-09 chr11:9494302 A>G maps to NM_003442.5 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr11:9501032 A>G maps to NM_003442.5 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A574-01A-11D-A29N-09 chr19:36727857 A>T maps to NM_007145.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr3:124951818 G>C maps to NM_021964.2 S584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr19:58213788 G>A maps to NM_001085384.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr23:47270115 G>C did not map to a codon.
Sequencing variant TCGA-AR-A1AY-01A-21D-A12Q-09 chr23:47272786 G>C did not map to a codon.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr23:47272096 C>G did not map to a codon.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr8:146156834 G>A maps to NM_006958.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr8:146156996 C>G maps to NM_006958.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr19:53572088 C>T maps to NM_001102603.1 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:28056848 C>T maps to NM_003447.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:44612759 G>T maps to NM_018651.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A274-01A-11D-A16D-09 chr3:44612803 T>C maps to NM_018651.2 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C9-01A-11D-A21Q-09 chr9:97062922 C>G maps to NM_194320.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DA-01A-31D-A10Y-09 chr16:3458759 G>A maps to NM_003450.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0W7-01A-11D-A10Y-09 chr16:3452195 C>T maps to NM_003450.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr19:52090258 C>T maps to NM_007147.2 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:9492218 C>A maps to NM_001172651.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A105-01A-11D-A10M-09 chr17:11881384 A>G maps to NM_144680.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr19:44981988 G>A maps to NM_013256.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:44980939 G>A maps to NM_013256.3 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A204-01A-11D-A159-09 chr19:44980903 A>T maps to NM_013256.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:35232202 C>A maps to ENST00000392232 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:35232518 G>C maps to ENST00000392232 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:35232521 A>G maps to ENST00000392232 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:35232356 C>T maps to ENST00000392232 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr19:35232611 C>T maps to ENST00000392232 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:47836624 C>G did not map to a codon.
Sequencing variant TCGA-BH-A0BP-01A-11D-A10Y-09 chr23:47836618 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr23:47837014 G>A did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:47842724 T>C did not map to a codon.
Sequencing variant TCGA-A7-A26I-01A-11D-A167-09 chr23:152128304 G>A did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr23:152132426 C>T did not map to a codon.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr23:152083320 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:104170578 C>T maps to NM_003452.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr16:71510089 C>T maps to NM_006961.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr6:28121503 G>A maps to NM_006298.2 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr6:28195499 C>T maps to ENST00000425468 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr11:3392235 C>T maps to NM_001130520.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15P-01A-11D-A10Y-09 chr2:95847301 G>A maps to ENST00000453539 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:12243836 C>T maps to NM_021143.2 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:12243956 G>A maps to NM_021143.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:3274080 C>T maps to NM_198088.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LG-01A-21D-A14K-09 chr11:123601455 C>T maps to NM_003455.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AU-01A-11D-A12Q-09 chr17:30678928 C>T maps to ENST00000394679 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IO-01A-11D-A142-09 chr17:30690004 T>C did not map to a codon.
Sequencing variant TCGA-A7-A0CD-01A-11W-A019-09 chr19:22157190 G>T maps to NM_007153.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr19:22156953 A>G maps to NM_007153.3 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr19:22155756 G>A maps to NM_007153.3 Y693Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5EH-01A-11D-A28B-09 chr19:22156812 G>T maps to NM_007153.3 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr19:22155447 C>T maps to NM_007153.3 K796K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr19:22171631 A>C maps to NM_007153.3 L28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A131-01A-11D-A10Y-09 chr19:58153269 G>A maps to NM_006385.3 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:58152606 C>T maps to NM_006385.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr7:148950659 C>T maps to NM_012256.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04X-01A-21W-A050-09 chr16:3191254 C>T maps to NM_001134655.1 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr11:7022735 C>A maps to NM_013249.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A156-01A-11D-A12B-09 chr11:6964814 G>T maps to NM_013250.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LH-01A-11D-A14G-09 chr11:6977209 T>C maps to NM_013250.2 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JK-01A-11D-A13L-09 chr20:52193274 G>T maps to NM_006526.2 Y676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A150-01A-11D-A12B-09 chr20:52192497 A>G maps to NM_006526.2 N935N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R3-01A-31D-A14K-09 chr20:52192683 G>A maps to NM_006526.2 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XW-01A-11D-A14K-09 chr14:21560534 G>A maps to NM_001102454.1 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr10:45499193 C>T maps to NM_006963.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr10:45499205 G>A maps to NM_006963.4 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A56D-01A-11D-A27P-09 chr19:44470974 C>T maps to NM_013359.2 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:44536585 G>A maps to NM_001129996.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AL-01A-11W-A019-09 chr19:44611902 C>T maps to NM_013398.2 H530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:44680726 C>T maps to NM_001032372.1 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr19:44740535 G>A maps to NM_182490.1 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:44739131 G>A maps to NM_182490.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B1-01A-12W-A071-09 chr19:44738969 G>A maps to NM_182490.1 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3YJ-01A-11D-A22X-09 chr19:44933890 T>C maps to NM_014518.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KR-01A-12D-A142-09 chr19:44934253 A>G maps to NM_014518.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X4-01A-11D-A10G-09 chr19:44933793 G>A maps to NM_014518.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:44934556 G>A maps to NM_014518.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr16:71482892 G>A maps to NM_145911.1 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:71483102 C>T maps to NM_145911.1 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:44513051 G>A maps to NM_006300.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr17:5009307 T>C maps to NM_014519.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr17:5013060 A>G maps to NM_014519.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:44771095 C>T maps to NM_181756.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr19:44778657 G>A maps to NM_181756.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:44792420 A>G maps to NM_004234.4 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1NH-01A-11D-A14G-09 chr19:44792858 T>C maps to NM_004234.4 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:74622658 A>C maps to NM_007345.3 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr18:74611134 C>T maps to NM_007345.3 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A400-01A-11D-A23C-09 chr18:74583725 T>C maps to NM_007345.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr18:74625816 C>T maps to NM_007345.3 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JI-01A-11D-A13L-09 chr18:74625748 C>T maps to NM_007345.3 Q984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr18:74620456 C>T maps to NM_007345.3 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04R-01A-41D-A117-09 chr1:244218515 C>T maps to NM_205768.2 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BR-01A-21W-A12T-09 chr1:244218260 G>A maps to NM_205768.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr18:32917213 C>T maps to NM_006965.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:38121070 T>C maps to NM_021045.1 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr8:145947415 G>A maps to NM_138367.1 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr8:145947970 G>A maps to NM_138367.1 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr19:20002370 C>T maps to ENST00000427401 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:24309668 T>C maps to NM_203282.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr19:24309128 G>A maps to NM_203282.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr11:116658326 G>T maps to NM_003904.3 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr11:116655591 G>A maps to NM_003904.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr11:116656231 G>A maps to NM_003904.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P4-01A-21D-A142-09 chr19:37006038 T>C maps to NM_001166038.1 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A50Y-01A-11D-A25Q-09 chr19:37005894 T>A maps to NM_001166038.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:3339441 G>A maps to NM_005741.4 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr16:3336102 C>T maps to NM_005741.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr19:9524013 G>A maps to NM_006631.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr19:9524223 G>A maps to NM_006631.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr16:31926604 C>T maps to NM_003414.4 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr16:31927081 T>C maps to NM_003414.4 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A3NW-01A-21D-A228-09 chr7:64363751 G>C maps to NM_021148.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:58724196 C>G maps to NM_133502.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3KD-01A-12D-A20S-09 chr23:152613218 G>A did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:152612810 A>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:152612649 G>A did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr23:152612504 G>C did not map to a codon.
Sequencing variant TCGA-E2-A1II-01A-11D-A142-09 chr23:152612457 G>A did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:89804229 C>T maps to NM_001113525.1 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IM-01A-11W-A050-09 chr7:111982648 C>G maps to NM_021994.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07W-01A-11W-A019-09 chr19:53303906 A>G maps to NM_006969.3 H397H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:53303165 G>A maps to NM_006969.3 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U0-01A-11D-A10G-09 chr19:53304395 C>T maps to NM_006969.3 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr22:22869162 G>T maps to NM_080740.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr22:22869495 G>T maps to NM_080740.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr22:22842273 G>A maps to NM_080764.2 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A5QM-01A-11D-A27P-09 chr23:129370195 G>T did not map to a codon.
Sequencing variant TCGA-BH-A0HY-01A-11W-A071-09 chr23:129349833 T>C did not map to a codon.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr23:129380917 C>T did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:129380845 T>G did not map to a codon.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr15:56959160 T>A maps to NM_017661.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A0Y5-01A-11D-A14K-09 chr1:200377723 G>C maps to NM_012482.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr7:148895474 A>C maps to NM_003575.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:44351411 C>G maps to NM_181845.1 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:44341305 G>A maps to NM_181845.1 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr19:44351926 C>T maps to NM_181845.1 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:44892085 G>A maps to NM_152354.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr17:15620165 T>C maps to NM_020652.2 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr17:15619790 C>G maps to NM_020652.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr17:18584122 A>G maps to NM_001145045.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CS-01A-11D-A10Y-09 chr6:87865326 C>T maps to NM_015021.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr6:87970158 C>A maps to NM_015021.1 S2271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:87969863 C>T maps to NM_015021.1 R2173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:87971191 G>A maps to NM_015021.1 P2615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:87928330 G>A maps to NM_015021.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr6:87968185 G>A maps to NM_015021.1 Q1613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr6:87966305 C>T maps to NM_015021.1 Q987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PB-01A-11D-A142-09 chr6:87964519 G>A maps to NM_015021.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A409-01A-11D-A243-09 chr21:43413757 G>A maps to NM_020727.4 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12L-01A-11D-A10Y-09 chr21:43411587 G>A maps to NM_020727.4 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr7:99669143 G>A maps to NM_032924.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27H-01A-11D-A16D-09 chr19:35174102 T>C maps to ENST00000221282 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:9270893 G>A maps to NM_020933.4 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr6:43323175 G>A maps to NM_014345.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:43307007 A>C maps to NM_014345.2 G1576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr6:43325019 A>C maps to NM_014345.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr6:43305690 C>T maps to NM_014345.2 G2015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr6:43306893 A>C maps to NM_014345.2 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:44140113 G>T maps to NM_006973.2 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DL-01A-11D-A10Y-09 chr19:53384562 A>G maps to NM_207333.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09I-01A-22W-A050-09 chr6:28297244 G>A maps to NM_030899.4 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr19:58982713 C>T maps to NM_014347.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HU-01A-11W-A050-09 chr19:58983205 C>T maps to NM_014347.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A3QA-01A-61D-A228-09 chr1:90486420 T>A maps to NM_182976.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:58639418 C>T maps to NM_024620.3 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:58639868 G>A maps to NM_024620.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:142155134 G>T maps to NM_014487.4 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RG-01A-11D-A14G-09 chr4:142150851 G>T did not map to a codon.
Sequencing variant TCGA-A2-A0ER-01A-21W-A050-09 chr19:54081067 G>A maps to NM_001079907.1 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:54080795 G>T maps to NM_001079907.1 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:54080888 G>T maps to NM_001079907.1 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EY-01A-11D-A13L-09 chr19:54080626 C>G maps to NM_001079907.1 Y271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:14805937 C>A maps to NM_032433.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GI-A2C8-01A-11D-A16D-09 chr19:14829927 C>T maps to NM_032433.2 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr20:45130336 A>G maps to NM_018102.3 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CW-01A-21D-A10Y-09 chr20:44596987 C>T maps to NM_022095.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:44580824 G>A maps to NM_022095.3 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr10:38344791 C>A maps to NM_006954.1 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:145998980 G>A maps to NM_030580.3 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr8:145999826 C>T maps to NM_030580.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:32358035 G>A maps to ENST00000375200 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr19:53645624 G>T maps to NM_001172674.1 Y153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A226-01A-21D-A159-09 chr19:53643754 G>A maps to NM_001172674.1 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:53643692 C>T maps to NM_001172674.1 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A66J-01A-11D-A29N-09 chr3:44701309 G>A maps to NM_003420.3 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr19:52468720 G>A maps to ENST00000391795 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:52472314 G>A maps to NM_021632.3 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:52472378 G>C maps to NM_021632.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr5:178506092 A>G maps to NM_014594.1 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IC-01A-11W-A050-09 chr5:178503489 C>T maps to NM_014594.1 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr10:64415341 T>C maps to NM_199452.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr5:71739897 C>T maps to NM_152625.1 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr9:99157204 A>G maps to NM_153695.3 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0U1-01A-11D-A10Y-09 chr10:38407206 A>G maps to NM_003421.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W6-01A-12D-A228-09 chr19:37117320 C>G maps to NM_032825.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BW-01A-11D-A10Y-09 chr12:6788133 C>T maps to NM_001135734.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr12:6787582 G>A maps to NM_001135734.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr12:6782581 G>A maps to NM_001135734.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr12:54778268 G>A maps to NM_001130967.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HP-01A-12D-A099-09 chr2:180634301 G>A maps to NM_152520.4 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr2:180311285 C>A maps to NM_152520.4 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A085-01A-11W-A019-09 chr3:21462906 C>T maps to NM_024697.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr3:21478512 G>A maps to NM_024697.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R4-01A-21D-A14G-09 chr6:27369105 C>A maps to NM_001076781.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr7:99091433 G>C maps to NM_032164.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr8:28206664 T>G maps to NM_018660.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr8:28218425 C>T maps to NM_018660.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C0-01A-21W-A071-09 chr18:32822448 T>A maps to NM_001135178.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27F-01A-11D-A16D-09 chr18:72775226 C>G maps to NM_017757.2 L1850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr18:72775895 G>A maps to NM_017757.2 Q2073Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr11:46723027 A>C maps to NM_024741.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr11:46722614 G>A maps to NM_024741.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47307005 A>G did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47308779 A>C did not map to a codon.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr23:47308437 T>C did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr23:47306830 A>G did not map to a codon.
Sequencing variant TCGA-AO-A12D-01A-11D-A10Y-09 chr23:47307055 G>A did not map to a codon.
Sequencing variant TCGA-AR-A24H-01A-11D-A167-09 chr23:47308256 G>C did not map to a codon.
Sequencing variant TCGA-B6-A0I1-01A-11D-A21Q-09 chr23:47308149 G>A did not map to a codon.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr23:47307012 T>C did not map to a codon.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr23:47308384 G>C did not map to a codon.
Sequencing variant TCGA-D8-A1JN-01A-11D-A13L-09 chr23:47307018 C>G did not map to a codon.
Sequencing variant TCGA-E2-A153-01A-12D-A12B-09 chr23:47326821 C>A did not map to a codon.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr23:47307459 T>G did not map to a codon.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr14:74376083 T>G maps to NM_021188.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:8577298 G>A maps to NM_001146175.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0C7-01B-11D-A10Y-09 chr19:8577296 C>A maps to NM_001146175.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09C-01A-11W-A019-09 chr19:53612814 T>C maps to NM_001164309.1 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BC-01A-22D-A099-09 chr19:53612660 C>A maps to NM_001164309.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18K-01A-11D-A12B-09 chr19:53611668 T>C maps to NM_001164309.1 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:58084932 C>A maps to NM_017879.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:58423524 C>A maps to NM_152475.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr19:58004584 G>A maps to NM_001098491.1 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:58005130 T>C maps to NM_001098491.1 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr19:37618813 T>G maps to NM_144689.3 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr16:49672765 T>C maps to NM_015069.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr16:49669759 G>A maps to NM_015069.2 N1101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr16:49660156 T>A maps to NM_015069.2 T1167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr7:148800868 C>T maps to NM_001001661.2 E698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JJ-01A-31D-A14K-09 chr7:148800754 C>T maps to NM_001001661.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YJ-01A-11D-A10G-09 chr19:21240798 C>A maps to NM_025189.3 S562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:21239608 A>C maps to NM_025189.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:21216269 G>A maps to NM_025189.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:52538019 G>A maps to NM_014650.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr16:3434861 G>C maps to ENST00000396852 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr10:31139083 G>A maps to NM_182755.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr10:31138844 T>G maps to NM_182755.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr10:31134087 A>G maps to NM_182755.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IE-01A-11W-A050-09 chr19:11979021 A>T maps to NM_152262.2 K380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr19:12383719 T>C maps to NM_001164276.1 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr19:11943460 A>G maps to NM_152357.2 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:11942304 C>A maps to NM_152357.2 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr19:11942980 C>T maps to NM_152357.2 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:12461473 G>A maps to NM_030824.2 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:12460898 G>A maps to NM_030824.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr3:44490163 G>A maps to NM_181489.5 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12K-01A-21D-A10Y-09 chr23:134493836 G>T did not map to a codon.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr19:44417543 G>A maps to NM_003425.3 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H6-01A-21W-A071-09 chr19:44419340 G>A maps to NM_003425.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr6:57033219 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr5:178392437 C>T maps to NM_182594.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr19:57803102 G>A maps to NM_006635.3 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04N-01A-11D-A10Y-09 chr19:37129665 G>A maps to NM_153257.2 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr19:37129790 G>A maps to NM_153257.2 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr19:37129878 G>C maps to NM_153257.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr19:37130137 G>C maps to NM_153257.2 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CK-01A-11D-A228-09 chr9:109691403 C>T maps to NM_021224.4 S1737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:109690549 G>T maps to NM_021224.4 E1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:109687236 G>A maps to NM_021224.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1F5-01A-12D-A13L-09 chr9:109771898 G>A maps to NM_021224.4 R2421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr9:109689135 G>A maps to NM_021224.4 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IU-01A-11D-A14G-09 chr9:109687059 G>A maps to NM_021224.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr9:109689354 C>T maps to NM_021224.4 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr7:149461946 G>A maps to NM_207336.1 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:53352451 G>A maps to NM_001008801.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26G-01A-21D-A167-09 chr19:57089782 C>A maps to NM_001001668.3 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08F-01A-11W-A019-09 chr19:57089278 G>A maps to NM_001001668.3 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0E0-01A-11W-A071-09 chr19:57089740 T>C maps to NM_001001668.3 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25C-01A-11D-A167-09 chr19:50548575 T>C maps to NM_015428.1 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:50548386 C>T maps to NM_015428.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr7:57194379 C>A maps to NM_033273.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr7:57187651 C>T maps to NM_033273.1 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr16:30408954 G>A maps to ENST00000495929 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr16:30409374 G>A maps to ENST00000495929 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr16:30409374 G>A maps to ENST00000495929 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A152-01A-11D-A12B-09 chr19:52825580 C>T maps to NM_144684.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr19:52824908 C>T maps to NM_144684.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:114304255 G>A maps to NM_133464.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:114289935 G>A maps to NM_133464.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X8-01A-11D-A14K-09 chr9:114293153 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27L-01A-11D-A16D-09 chr9:114290001 G>A maps to NM_133464.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14V-01A-11D-A12B-09 chr9:114305317 T>C maps to NM_133464.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr9:95609115 G>C maps to NM_031486.1 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr10:44111817 G>A maps to NM_145312.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr10:44112690 T>C maps to NM_145312.3 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0CU-01A-12W-A050-09 chr19:20307905 G>T maps to NM_052852.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J9-01A-11W-A050-09 chr19:20308256 C>T maps to ENST00000428290 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:20308649 A>T maps to ENST00000428290 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A2LE-01A-11D-A17W-09 chr10:48371218 C>G maps to NM_153034.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:11917290 C>T maps to NM_152356.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:11917794 C>T maps to NM_152356.3 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:22847409 A>G maps to NM_020855.2 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr19:22847267 C>G maps to NM_020855.2 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:22848027 G>A maps to NM_020855.2 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15O-01A-11D-A10Y-09 chr19:22847202 G>A maps to NM_020855.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:21607593 A>G maps to NM_001076678.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr1:247464342 G>T maps to NM_032752.1 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DF-01A-11D-A17W-09 chr1:247464501 C>A maps to NM_032752.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr19:58868857 C>T maps to NM_198458.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:58868302 G>A maps to NM_198458.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr7:99219166 G>T maps to NM_145115.2 G187*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OL-A66H-01A-11D-A29N-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OL-A66H-01A-11D-A29N-09 chr10:77161111 T>G maps to ENST00000438638 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:19917757 G>T maps to NM_001099269.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr19:32845864 T>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:32844180 C>T maps to NM_014910.4 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:32845206 C>T maps to NM_014910.4 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A081-01A-11W-A019-09 chr9:99521788 G>A maps to NM_014930.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0AW-01A-11W-A071-09 chr9:99521782 C>T maps to NM_014930.1 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0WX-01A-11D-A10G-09 chr2:27825428 G>T did not map to a codon.
Sequencing variant TCGA-EW-A2FW-01A-11D-A17D-09 chr2:27822523 C>T maps to NM_032434.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr20:62592726 G>A maps to NM_020713.1 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A13Y-01A-11D-A10Y-09 chr20:62592678 G>A maps to NM_020713.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr20:62594492 G>C maps to NM_020713.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HN-A2NL-01A-11D-A18P-09 chr2:27601549 G>A maps to NM_144631.4 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07C-01A-11D-A045-09 chr2:95815407 A>T maps to NM_032788.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr18:74091504 T>C maps to ENST00000443185 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07R-01A-21W-A050-09 chr10:97919090 G>C maps to NM_014803.3 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr10:97919630 G>A maps to NM_014803.3 Q1184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A3M7-01A-12D-A21Q-09 chr4:10445843 G>T maps to NM_053042.2 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5UO-01A-11D-A28B-09 chr4:10445819 G>A maps to NM_053042.2 N711N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:14105754 C>A maps to NM_145287.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr18:22805295 C>T maps to NM_015461.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:22805862 G>A maps to NM_015461.2 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr18:22805937 G>A maps to NM_015461.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr18:22806690 C>T maps to NM_015461.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A423-01A-11D-A243-09 chr18:22806795 G>A maps to NM_015461.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:42730114 G>T maps to NM_133444.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:37879979 T>C maps to NM_032453.1 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:37880321 G>A maps to NM_032453.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr19:52919653 G>T maps to NM_032423.2 G517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OZ-01A-11D-A142-09 chr19:52909855 C>T maps to NM_032423.2 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09X-01A-11W-A019-09 chr18:56586481 C>T maps to NM_018181.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr18:56601828 G>A maps to NM_018181.4 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr18:56586091 G>T maps to NM_018181.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Q-01A-11W-A050-09 chr19:52942227 G>A maps to NM_001143939.1 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr19:52941952 G>T maps to NM_001143939.1 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SF-01A-11D-A25Q-09 chr19:30935416 C>T maps to NM_014717.1 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J3-01A-11W-A050-09 chr19:31048069 G>A maps to NM_014717.1 *1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0H7-01A-13W-A071-09 chr19:31038892 G>A maps to NM_014717.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr19:31039201 C>T maps to NM_014717.1 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr19:31039732 C>T maps to NM_014717.1 I1069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1OV-01A-11D-A142-09 chr19:30936547 C>T maps to NM_014717.1 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:38103033 G>T maps to NM_152606.3 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:38103536 A>G maps to NM_152606.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr19:57835120 G>A maps to NM_213598.3 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3W7-01A-11D-A228-09 chr19:58773562 C>T maps to NM_014480.2 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:58773306 C>T maps to NM_014480.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr19:58773060 C>T maps to NM_014480.2 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A255-01A-11D-A167-09 chr19:40521492 G>A maps to NM_178544.3 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A295-01A-11D-A16D-09 chr19:40521667 G>T maps to NM_178544.3 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T7-01A-21D-A099-09 chr19:57910902 G>A maps to NM_001172773.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:57910563 C>T maps to NM_001172773.1 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24N-01A-11D-A167-09 chr19:57908525 C>T maps to NM_001172773.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:57910113 C>T maps to NM_001172773.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JL-01A-11W-A071-09 chr19:58058368 G>A maps to NM_001039654.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FG-01A-11D-A17D-09 chr19:58198257 A>G maps to ENST00000356715 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:58319601 T>A maps to NM_024762.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:2852868 C>G maps to NM_152791.4 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:2852746 C>T maps to NM_152791.4 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr19:2873607 C>T maps to NM_024967.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:7075748 C>T maps to NM_024341.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2B8-01A-11D-A17D-09 chr19:8923820 G>A maps to NM_144693.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:9579822 C>T maps to NM_152476.2 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr19:9584908 C>G maps to NM_152476.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr19:9577764 G>A maps to NM_152476.2 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:12430262 A>C maps to NM_145276.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XJ-01A-11D-A14K-09 chr19:12429835 G>A maps to NM_145276.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:12639151 C>A maps to NM_144976.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J9-01A-11D-A13L-09 chr19:12638669 G>A maps to NM_144976.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3Y0-01A-11D-A23C-09 chr19:36673715 G>C maps to ENST00000355114 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A13E-01A-11D-A272-09 chr19:36674066 A>G maps to ENST00000355114 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:37440918 T>C maps to NM_198539.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08R-01A-11W-A050-09 chr19:37975361 A>C maps to NM_144694.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:37975204 C>T maps to NM_144694.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A5ZV-01A-11D-A28B-09 chr8:125989334 T>C maps to NM_152412.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr8:125989478 A>G maps to NM_152412.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr19:38230530 G>C maps to NM_001172690.1 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:44039688 C>T maps to ENST00000458714 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:52376753 G>A maps to NM_032679.2 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1B0-01A-11D-A12Q-09 chr19:52376690 T>C maps to NM_032679.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1RH-01A-21D-A167-09 chr19:52381690 G>T maps to NM_032679.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr19:52376201 A>C maps to NM_032679.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:53014315 G>T maps to NM_001099694.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:53014743 T>G maps to NM_001099694.1 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr19:53007921 C>T maps to NM_001099694.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24S-01A-11D-A167-09 chr19:53005127 G>A maps to NM_001099694.1 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:56089406 G>A maps to NM_152600.2 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr19:56935299 C>T maps to NM_001159861.1 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr19:56925396 C>T maps to NM_001159861.1 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3TN-01A-11D-A228-09 chr19:37642916 G>A maps to ENST00000356958 H628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FW-01A-11W-A050-09 chr19:37644488 A>G maps to ENST00000356958 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A2P5-01A-11D-A19Y-09 chr19:37643189 G>A maps to ENST00000356958 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KS-01A-11D-A13L-09 chr19:58291157 T>C maps to NM_017652.2 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr19:58287979 C>T maps to NM_017652.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YP-01A-21D-A28B-09 chr19:58290714 A>T maps to NM_017652.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr19:58370800 C>T maps to NM_032828.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:58371048 C>T maps to NM_032828.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B0-01A-21D-A10Y-09 chr3:48309445 C>T maps to NM_016089.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EU-01A-22W-A071-09 chr15:85345428 G>A maps to NM_014630.2 E1203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr15:85326112 T>A maps to NM_014630.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr15:85326353 G>T maps to NM_014630.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18V-01A-11D-A12B-09 chr15:85327555 G>T maps to NM_014630.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr17:5086843 C>T maps to NM_032530.1 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:5086243 T>C maps to NM_032530.1 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I6-01A-11D-A128-09 chr4:87134 A>T maps to NM_182524.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AT-01A-11D-A045-09 chr16:3487524 C>T maps to NM_152457.1 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr16:3486605 C>A maps to NM_152457.1 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AH-01A-11D-A12B-09 chr16:2050139 C>A maps to ENST00000431526 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr19:35249961 G>A maps to NM_001007248.2 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:58490988 G>T maps to NM_025027.3 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KN-01A-11D-A13L-09 chr19:38189030 A>G maps to NM_032689.4 H667H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0EV-01A-11W-A050-09 chr15:64792133 C>T maps to NM_015042.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr15:64966801 C>T maps to NM_015042.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A24Q-01A-12D-A167-09 chr19:52869626 C>A maps to NM_001161425.1 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:53208723 A>G maps to NM_001161500.1 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A3XS-01A-11D-A22X-09 chr19:52443550 C>T maps to NM_001031721.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:52448791 G>A maps to NM_001031721.3 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J8-01A-21D-A045-09 chr19:52448194 C>T maps to NM_001031721.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr19:52496795 G>C maps to ENST00000354939 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr19:52633751 A>C did not map to a codon.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:52618994 G>A maps to NM_178523.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T4-01A-31D-A099-09 chr9:116794995 C>T maps to ENST00000374126 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr3:40528996 C>T maps to NM_001145082.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2QI-01A-12D-A19Y-09 chr3:40529165 C>T maps to NM_001145082.2 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr3:40528622 G>T maps to NM_001145082.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IH-01A-11D-A188-09 chr3:40528667 C>T maps to NM_001145082.2 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JE-01A-11W-A071-09 chr3:40557521 C>G maps to NM_175888.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr3:40554006 G>T did not map to a codon.
Sequencing variant TCGA-AR-A24M-01A-11D-A167-09 chr5:16463792 G>A maps to NM_033414.2 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr8:144733535 A>C maps to NM_014789.3 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:144733407 G>T maps to NM_014789.3 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr8:144732549 C>T maps to NM_014789.3 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr19:12256909 C>T maps to ENST00000439556 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:12256294 G>A maps to ENST00000439556 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FJ-01A-11W-A019-09 chr19:20807491 G>C maps to NM_001076675.2 Y397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr19:20808203 G>C maps to NM_001076675.2 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr19:55995406 C>T maps to NM_033113.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr16:30794529 C>T maps to NM_001080417.1 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A5IZ-01A-11D-A27P-09 chr16:30794370 G>A maps to NM_001080417.1 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1IN-01A-11D-A13L-09 chr16:30793336 G>C maps to NM_001080417.1 S771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr23:47920303 A>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:47920249 C>T did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:47918478 C>A did not map to a codon.
Sequencing variant TCGA-E2-A1LB-01A-11D-A142-09 chr23:47926258 C>T did not map to a codon.
Sequencing variant TCGA-E2-A2P6-01A-11D-A19Y-09 chr23:47919406 T>A did not map to a codon.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr23:47918310 C>T did not map to a codon.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr23:47918373 G>T did not map to a codon.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr2:71591251 C>T maps to NM_014497.3 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DS-01A-11W-A071-09 chr1:91405736 C>A maps to NM_201269.1 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:22291959 A>C did not map to a codon.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr23:22291799 T>A did not map to a codon.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr23:22292143 C>T did not map to a codon.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr23:22291679 C>T did not map to a codon.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr16:31092018 T>G maps to NM_014699.3 G1458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr16:31092214 C>T maps to NM_014699.3 Q1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YK-01A-22D-A117-09 chr1:182025756 G>A maps to NM_001009992.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A1FW-01A-11D-A13L-09 chr1:182025786 G>A maps to NM_001009992.1 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr1:182025763 G>T maps to NM_001009992.1 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XU-01A-11D-A28B-09 chr1:182026755 G>A maps to NM_001009992.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A5PX-01A-12D-A28B-09 chr1:182025618 G>A maps to NM_001009992.1 C509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B9-01A-11W-A071-09 chr7:99158244 G>A maps to NM_001083956.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08J-01A-11W-A019-09 chr9:40773309 C>T maps to NM_033160.5 E655E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RO-01A-22D-A099-09 chr9:40775034 C>T maps to NM_033160.5 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HN-01A-11D-A135-09 chr9:40773231 T>G maps to NM_033160.5 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr3:44636459 C>T maps to NM_173658.1 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr3:44636311 G>A maps to NM_173658.1 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A1AK-01A-21D-A12Q-09 chr3:44636309 C>T maps to NM_173658.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr19:53668565 G>A maps to NM_024733.3 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04W-01A-31D-A10Y-09 chr19:56953657 G>A maps to ENST00000342634 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr16:31073558 C>T maps to NM_001172669.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr16:31072661 C>T maps to NM_001172669.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A14S-01A-11D-A12B-09 chr16:31075618 G>A maps to NM_001172669.1 A77A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E2-A15H-01A-11D-A12B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LL-A440-01A-11D-A243-09 chr16:31075645 C>A maps to NM_001172669.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:247265304 C>T maps to NM_024804.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FC-01A-11D-A13L-09 chr1:247264536 C>G maps to NM_024804.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:247265073 C>T maps to NM_024804.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A093-01A-11W-A019-09 chr19:58231989 G>A maps to ENST00000335820 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr19:58232982 G>C maps to ENST00000335820 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SI-01A-11D-A142-09 chr23:46322224 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:46332438 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr23:46359484 G>C did not map to a codon.
Sequencing variant TCGA-A2-A0EQ-01A-11W-A050-09 chr23:46359951 G>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:46359976 T>C did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:46360442 C>A did not map to a codon.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr23:46360532 C>A did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:23836447 A>G maps to NM_138330.2 C429C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15K-01A-11D-A12Q-09 chr19:23837310 T>A maps to NM_138330.2 K142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5RW-01A-11D-A28B-09 chr19:23836665 C>A maps to NM_138330.2 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:22362985 G>T maps to NM_001001411.2 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22B-01A-11D-A159-09 chr19:53740446 T>A maps to NM_182609.2 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr1:227751426 T>C did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:23927313 G>A maps to NM_138286.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HM-01A-12D-A135-09 chr19:23937694 C>T maps to NM_138286.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27V-01A-12D-A17D-09 chr19:23928057 C>T maps to NM_138286.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A092-01A-11W-A019-09 chr19:20117296 C>T maps to NM_033196.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:20117674 C>T maps to NM_033196.2 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JL-01A-11D-A13L-09 chr19:20117637 C>A maps to NM_033196.2 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T5-01A-21D-A099-09 chr1:26691430 T>G maps to ENST00000436292 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A155-01A-11D-A12B-09 chr1:41006376 C>T maps to NM_152373.3 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0J6-01A-11W-A050-09 chr1:151259888 C>G maps to NM_020832.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A5FK-01A-11D-A27P-09 chr1:151259168 C>T maps to NM_020832.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr16:30616235 C>T maps to NM_138447.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A0JF-01A-11W-A071-09 chr1:249151655 C>T maps to NM_001136036.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr1:249152046 G>C maps to NM_001136036.2 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr1:247150837 C>A maps to NM_020394.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr8:146067400 G>A maps to ENST00000446747 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XW-01A-11D-A10G-09 chr19:12059254 C>G maps to NM_144566.1 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr19:12059453 C>T maps to NM_144566.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IX-01A-12D-A142-09 chr19:53079272 G>A maps to NM_001172655.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr8:37553646 C>T maps to NM_025069.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18P-01A-11D-A12B-09 chr8:81599538 G>A maps to NM_001033723.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr12:8327887 A>G maps to NM_001004328.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr12:8328539 T>C did not map to a codon.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:57133464 C>T maps to NM_021216.4 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A2FE-01A-11D-A19Y-09 chr15:90611205 G>A maps to NM_198526.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr15:90610659 G>A maps to NM_198526.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr15:90617349 G>A maps to NM_198526.2 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06Z-01A-11W-A019-09 chr23:84525673 G>T did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr23:84520174 C>G did not map to a codon.
Sequencing variant TCGA-AN-A0AS-01A-11W-A019-09 chr23:84525071 G>A did not map to a codon.
Sequencing variant TCGA-AR-A0TU-01A-31D-A10G-09 chr23:84526404 C>A did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr23:84520126 G>T did not map to a codon.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr23:84510488 G>A did not map to a codon.
Sequencing variant TCGA-OL-A66I-01A-21D-A29N-09 chr23:84520169 A>C did not map to a codon.
Sequencing variant TCGA-B6-A0RE-01A-11W-A071-09 chr19:21299679 G>C maps to NM_182515.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A076-01A-21W-A019-09 chr7:57528713 A>T maps to NM_001159279.1 K183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AR-01A-11W-A019-09 chr7:57529138 C>A maps to NM_001159279.1 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AQ-A04L-01B-21D-A10M-09 chr16:31734053 C>A maps to NM_001130913.1 Y37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr4:437286 A>G maps to NM_133474.2 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr4:435675 A>G maps to NM_133474.2 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:266263 C>A maps to ENST00000419098 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A094-01A-11W-A019-09 chr19:20728198 A>C maps to NM_001159293.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0DB-01A-11D-A272-09 chr19:57956492 G>A maps to NM_001023561.2 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:57955118 T>G maps to NM_001023561.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr19:57953287 C>T maps to NM_001023561.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A1KF-01A-11D-A13L-09 chr19:57955448 T>G maps to NM_001023561.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XU-01A-11D-A14K-09 chr19:57956838 G>T maps to NM_001023561.2 G775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr17:80788619 G>A maps to NM_024702.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr16:3367199 C>A maps to NM_153028.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:134421117 T>G did not map to a codon.
Sequencing variant TCGA-B6-A0IJ-01A-11W-A050-09 chr23:134427719 T>G did not map to a codon.
Sequencing variant TCGA-B6-A0IO-01A-11W-A050-09 chr23:134427817 G>A did not map to a codon.
Sequencing variant TCGA-B6-A2IU-01A-32D-A19T-09 chr23:134427657 C>T did not map to a codon.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr23:134427657 C>A did not map to a codon.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr23:134426225 G>T did not map to a codon.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr23:134427832 C>T did not map to a codon.
Sequencing variant TCGA-E2-A159-01A-11D-A10Y-09 chr23:134427938 A>C did not map to a codon.
Sequencing variant TCGA-AO-A0JD-01A-11W-A071-09 chr6:35258416 G>A did not map to a codon.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:52794078 T>C maps to NM_001010851.2 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DE-01A-11D-A27P-09 chr16:30537312 C>A maps to NM_024671.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:2934274 G>A maps to NM_021217.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:2933699 G>A maps to NM_021217.2 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr15:35273757 T>C maps to NM_014106.3 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr15:35274400 C>T maps to NM_014106.3 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr15:35274693 A>G maps to NM_014106.3 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T2-01A-11W-A097-09 chr19:58017762 G>A maps to NM_198542.1 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:58018248 C>A maps to NM_198542.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A1-A0SK-01A-12D-A099-09 chr7:149128875 C>T maps to ENST00000440594 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr7:149152834 G>C maps to ENST00000440594 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr7:149152288 G>A maps to ENST00000440594 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A109-01A-11D-A10M-09 chr16:89294297 A>G maps to NM_182531.2 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:40578774 C>A maps to NM_001142579.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A147-01A-11D-A10Y-09 chr19:40581286 A>G maps to NM_001142577.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:40581229 G>A maps to NM_001142577.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:40540982 G>A maps to NM_001005851.2 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr19:40540902 G>T maps to NM_001005851.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr19:40542426 G>A maps to NM_001005851.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:38160236 G>C maps to NM_152605.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:38160560 G>A maps to NM_152605.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:38160577 G>A maps to NM_152605.3 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:38160629 C>T maps to NM_152605.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0RU-01A-11D-A099-09 chr19:38160607 G>A maps to NM_152605.3 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06N-01A-11W-A019-09 chr9:99580377 C>A maps to NM_001001662.1 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr9:99580236 T>G maps to NM_001001662.1 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:99580244 G>C maps to NM_001001662.1 S687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr9:99581356 T>C maps to NM_001001662.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr9:99580393 C>T maps to NM_001001662.1 Q637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr16:30594471 G>A maps to NM_152458.6 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HA-01A-11D-A12Q-09 chr16:30594699 C>T maps to NM_152458.6 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr16:30594327 C>T maps to NM_152458.6 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A108-01A-13D-A10M-09 chr16:30596467 G>A maps to NM_152458.6 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A18G-01A-11D-A12B-09 chr7:148767970 G>A maps to NM_152411.3 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12X-01A-11D-A10Y-09 chr7:148769112 G>T maps to NM_152411.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr9:130206314 G>A maps to NM_007135.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr9:130206324 G>T maps to NM_007135.2 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04C-01A-21W-A050-09 chr19:12739845 C>T maps to NM_153358.2 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:35451235 G>A maps to NM_175872.4 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A2L8-01A-11D-A18P-09 chr19:35449353 G>A maps to NM_175872.4 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A3IZ-01A-11D-A20S-09 chr19:12501312 G>C maps to NM_001080821.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1J8-01A-11D-A13L-09 chr19:12502761 G>A maps to NM_001080821.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr7:127017264 G>T maps to NM_176814.3 C92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0IN-01A-11W-A050-09 chr7:127026204 A>G maps to NM_176814.3 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R6-01A-11D-A14G-09 chr7:127014789 T>C maps to NM_176814.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A4S3-01A-21D-A25Q-09 chr2:185800788 G>A maps to NM_194250.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0WA-01A-11D-A10G-09 chr2:185803356 C>T maps to NM_194250.1 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1ND-01A-11D-A142-09 chr2:185803707 G>T maps to NM_194250.1 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A0X0-01A-21D-A10Y-09 chr7:88964842 T>C maps to NM_181646.2 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:57765159 C>T maps to NM_001023563.3 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:57765875 G>C maps to NM_001023563.3 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr19:57765470 G>A maps to NM_001023563.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OL-A5D7-01A-11D-A27P-09 chr19:53058310 G>A maps to NM_001039886.3 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0T0-01A-22D-A099-09 chr23:47774341 G>C did not map to a codon.
Sequencing variant TCGA-D8-A27M-01A-11D-A16D-09 chr23:47774911 C>A did not map to a codon.
Sequencing variant TCGA-OL-A5RV-01A-12D-A28B-09 chr23:47775906 A>T did not map to a codon.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:53989944 G>A maps to NM_001004301.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:58384384 T>C maps to NM_001144989.1 K791K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A128-01A-11D-A10M-09 chr19:58384393 T>A maps to NM_001144989.1 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AR-A0TX-01A-11D-A099-09 chr16:71895827 C>T maps to ENST00000425432 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr4:146823476 C>A maps to ENST00000508784 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr4:146770594 G>A maps to ENST00000508784 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12P-01A-11D-A10Y-09 chr19:37383373 C>G did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:53117178 G>C maps to NM_018300.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A06U-01A-11W-A019-09 chr20:57769142 G>A maps to NM_178457.1 G1023G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08P-01A-11W-A019-09 chr20:57768843 C>T maps to NM_178457.1 Q924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09G-01A-21W-A019-09 chr20:57769622 C>A maps to NM_178457.1 L1183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EO-01A-11D-A135-09 chr20:57782029 C>T maps to NM_178457.1 R1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1FN-01A-11D-A13L-09 chr20:57768188 T>G maps to NM_178457.1 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A1LA-01A-11D-A142-09 chr20:57768110 T>A maps to NM_178457.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr19:57175336 C>T maps to NM_001005850.1 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr19:52658628 C>T maps to NM_001102657.1 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J5-01A-11D-A13L-09 chr19:52660056 C>G maps to NM_001102657.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A04D-01A-21W-A050-09 chr19:52568484 T>A maps to NM_001136499.1 K884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12T-01A-11D-A10Y-09 chr19:52580297 G>A maps to NM_001136499.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr19:9869047 G>A maps to NM_001077624.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0FT-01A-11W-A050-09 chr19:21131733 C>G maps to NM_003429.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr19:21116930 G>A maps to NM_003429.4 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XQ-01A-11D-A14K-09 chr7:149559203 T>C maps to NM_001099220.1 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr19:12154700 T>C maps to NM_001080404.1 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SA-01A-11D-A25Q-09 chr19:52888047 G>A maps to NM_001145434.1 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A12E-01A-11D-A10M-09 chr19:52888047 G>A maps to NM_001145434.1 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:20229155 G>T maps to NM_007138.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:23544384 C>A maps to NM_003430.2 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2DB-01A-31D-A19Y-09 chr19:23544003 T>A maps to NM_003430.2 K593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PE-A5DC-01A-12D-A27P-09 chr19:23578124 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0EY-01A-11W-A050-09 chr7:64853753 C>T maps to NM_152626.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr19:20045093 G>T maps to NM_031218.3 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:20044990 C>A maps to NM_031218.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr19:20044951 C>A maps to NM_031218.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0DI-01A-21D-A12Q-09 chr19:20045076 C>G maps to NM_031218.3 S438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JG-01B-11D-A13L-09 chr19:22941530 G>A maps to ENST00000397104 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22E-01A-11D-A159-09 chr19:22939509 C>T maps to ENST00000397104 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22G-01A-11D-A159-09 chr19:22939858 A>G maps to ENST00000397104 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YD-01A-11D-A10G-09 chr20:47882677 G>A maps to NM_021035.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A25A-01A-12D-A16D-09 chr20:47865237 G>A maps to NM_021035.2 C1441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr20:47887219 G>A maps to NM_021035.2 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:47870298 G>A maps to NM_021035.2 V1003V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr20:47887532 G>A maps to NM_021035.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr20:47865201 G>A maps to NM_021035.2 F1453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HK-01A-11W-A071-09 chr20:47864112 C>T maps to NM_021035.2 L1816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A146-01A-31D-A10Y-09 chr20:47863857 C>T maps to NM_021035.2 W1901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1P8-01A-11D-A142-09 chr20:47886965 G>A maps to NM_021035.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A095-01A-11W-A019-09 chr1:86123611 C>T maps to NM_017953.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B6-A401-01A-11D-A23C-09 chr16:75033985 G>A maps to ENST00000320619 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr22:29445638 C>G maps to NM_032173.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A15C-01A-31D-A12B-09 chr22:29445671 G>A maps to NM_032173.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09N-01A-11W-A019-09 chr19:5455666 G>A maps to NM_181710.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr11:60637859 C>T maps to NM_207341.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A0YT-01A-11D-A10G-09 chr11:60640694 C>T maps to NM_207341.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08S-01A-11W-A050-09 chr11:60642668 G>T maps to NM_207341.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A26Y-01A-11D-A16D-09 chr11:60637152 C>T maps to NM_207341.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E2-A10C-01A-21D-A10M-09 chr16:21213433 C>T maps to NM_003460.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A244-01A-11D-A167-09 chr16:21221499 G>A maps to NM_003460.1 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A4SC-01A-12D-A25Q-09 chr1:238048464 C>T maps to NM_021186.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr1:238051745 T>G maps to NM_021186.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A140-01A-11D-A10Y-09 chr1:238051690 C>A maps to NM_021186.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1X5-01A-11D-A14G-09 chr1:238051726 C>A maps to NM_021186.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1J3-01A-11D-A13L-09 chr17:38031505 G>A did not map to a codon.
Sequencing variant TCGA-C8-A12Q-01A-11D-A10Y-09 chr3:102181128 C>G maps to NM_175056.1 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1XK-01A-21D-A14K-09 chr3:102187980 T>C did not map to a codon.
Sequencing variant TCGA-AN-A0AK-01A-21W-A019-09 chr10:126671766 G>A maps to NM_017580.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A0D9-01A-31W-A071-09 chr2:135966548 C>A did not map to a codon.
Sequencing variant TCGA-B6-A0I8-01A-11W-A050-09 chr2:136023136 A>C maps to NM_032143.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LL-A5YL-01A-12D-A29N-09 chr2:135965354 G>A maps to NM_032143.2 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr23:15833900 A>C did not map to a codon.
Sequencing variant TCGA-A2-A0CT-01A-31W-A071-09 chr16:3140510 G>A maps to NM_032805.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B5-01A-11D-A12Q-09 chr6:28358959 C>T maps to ENST00000396827 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JP-01A-11D-A13L-09 chr6:28359436 G>A maps to ENST00000396827 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A5XS-01A-11D-A29N-09 chr6:28093430 G>C maps to NM_025231.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A1EV-01A-11D-A135-09 chr6:28097613 G>A maps to NM_025231.1 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A135-01A-11D-A10Y-09 chr19:58601319 G>C maps to NM_001145542.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A1KO-01A-31D-A188-09 chr15:85164373 C>T maps to NM_181877.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A137-01A-11D-A10Y-09 chr15:85164364 G>A maps to NM_181877.3 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0HF-01A-11W-A071-09 chr1:33960295 C>T maps to NM_145238.3 H784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A1HF-01A-11D-A135-09 chr1:33959018 C>T maps to NM_145238.3 C559C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AN-A046-01A-21W-A050-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AR-A2LK-01A-11D-A17W-09 chr7:99654806 C>T maps to NM_145914.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A7-A26H-01A-11D-A167-09 chr6:28403767 C>T maps to NM_001012455.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A0XN-01A-21D-A10G-09 chr6:28403824 G>T maps to NM_001012455.1 C73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0B6-01A-11D-A19Y-09 chr6:28402589 C>T maps to NM_001012455.1 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A097-01A-11W-A050-09 chr15:43658335 A>G maps to NM_152455.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GM-A2D9-01A-11D-A18P-09 chr19:58190193 C>G maps to NM_152677.2 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A3EH-01A-22D-A228-09 chr19:56703341 T>C maps to NM_001080456.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr19:56701488 G>A maps to NM_001080456.2 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr19:56704352 T>G maps to NM_001080456.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A22D-01A-11D-A159-09 chr19:56703239 G>A maps to NM_001080456.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr20:44511365 A>C maps to NM_080603.4 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D8-A1JA-01A-11D-A13L-09 chr2:187703765 C>T maps to NM_182521.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A09Z-01A-11W-A019-09 chr19:13941203 C>T maps to NM_023072.2 C770C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A07B-01A-11W-A019-09 chr1:45516764 C>T maps to NM_020883.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:45484875 G>A maps to NM_020883.1 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr1:45501902 C>A maps to NM_020883.1 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C8-A12Y-01A-11D-A12B-09 chr1:45501825 G>A maps to NM_020883.1 Y680Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr11:113609075 A>C maps to NM_004724.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AO-A03M-01B-11D-A10M-09 chr11:113644307 C>T maps to NM_004724.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A2-A04V-01A-21W-A050-09 chr23:57935543 C>A did not map to a codon.
Sequencing variant TCGA-A8-A084-01A-21W-A019-09 chr23:57935842 C>A did not map to a codon.
Sequencing variant TCGA-A2-A0CX-01A-21W-A019-09 chr23:57620854 G>C did not map to a codon.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr23:57620689 C>G did not map to a codon.
Sequencing variant TCGA-AR-A2LO-01A-31D-A18P-09 chr23:57620699 C>T did not map to a codon.
Sequencing variant TCGA-GM-A2DO-01A-11D-A19Y-09 chr23:57619606 C>T did not map to a codon.
Sequencing variant TCGA-BH-A0DZ-01A-11W-A019-09 chr3:126185055 G>C maps to NM_025112.4 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E9-A1R2-01A-11D-A14G-09 chr1:53267567 T>A maps to NM_024646.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1PC-01B-11D-A21Q-09 chr1:53255691 C>T maps to NM_024646.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A08L-01A-11W-A019-09 chr7:143080093 C>G maps to NM_001010972.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A8-A0A6-01A-12W-A071-09 chr17:3966099 T>G maps to NM_015113.3 P1610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AC-A23H-01A-11D-A159-09 chr17:3954096 C>G maps to NM_015113.3 L1947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AN-A046-01A-21W-A050-09 chr17:3962534 G>A maps to NM_015113.3 R1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BH-A0BZ-01A-31D-A12Q-09 chr17:3980053 C>G did not map to a codon.
Sequencing variant TCGA-D8-A27G-01A-11D-A16D-09 chr17:4005620 C>T maps to NM_015113.3 W554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A1IZ-01A-11D-A188-09 chr17:3919736 G>A maps to NM_015113.3 G2675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EW-A3U0-01A-11D-A228-09 chr1:78098297 G>A maps to NM_015534.4 Q248*. Only missense variants will be evaluated by CHASM.
