4991 NP_001070868 P46L not found in SNVbox database
5280 NP_001070868 T314P not found in SNVbox database
6270 NP_109597 G36V not found in SNVbox database
9217 NP_705833 N699D not found in SNVbox database
2092 NP_001070868 I751M not found in SNVbox database
2860 NP_705833 T904R not found in SNVbox database
3085 NP_001070868 P350H not found in SNVbox database
3721 NP_001070868 F576C not found in SNVbox database
4543 NP_705833 A305S not found in SNVbox database
4620 NP_705833 S741C not found in SNVbox database
4910 NP_001070868 W687C not found in SNVbox database
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr19:58863914 A>T maps to NM_130786.3 L116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr10:52601745 T>A maps to NM_138932.2 K81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr10:52575930 C>A maps to NM_138932.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr10:52569666 A>T maps to NM_138932.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr16:7568249 C>T maps to NM_145891.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr16:7726798 C>G maps to NM_145891.2 Y339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr16:7383010 G>A maps to NM_145891.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr12:9230404 G>A maps to NM_000014.4 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr12:9242557 C>T maps to NM_000014.4 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr12:8998035 A>T did not map to a codon.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:9000254 C>A maps to NM_144670.3 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr12:9008180 G>A maps to NM_144670.3 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:9000290 C>T maps to NM_144670.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr3:137849688 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr3:137843363 T>C maps to NM_016161.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr3:137850002 A>G maps to NM_016161.2 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr12:53708551 A>T maps to NM_015665.5 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr12:53702265 C>A maps to NM_015665.5 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:151475279 T>C maps to NM_207365.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:12711236 G>T maps to NM_001013630.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr2:69732800 T>C maps to NM_014911.3 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:69757188 G>A maps to NM_014911.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:70301661 G>A maps to ENST00000418685 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr6:44274035 C>A maps to NM_020745.2 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr6:44270801 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr7:121766488 T>A maps to NM_005763.3 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr17:79094951 A>T maps to NM_001080395.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr17:79102326 G>A maps to NM_001080395.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:107578435 C>T maps to NM_005502.3 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr9:107581906 G>A maps to NM_005502.3 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:67189984 T>C maps to NM_080282.3 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:215845227 G>A maps to NM_173076.2 H1573H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:215818762 G>A maps to NM_173076.2 Y2154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:215840567 A>G maps to NM_173076.2 Y1774Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr2:215880303 G>T maps to NM_173076.2 C622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr2:215820032 C>A maps to NM_173076.2 G2096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr7:48313954 C>T maps to NM_152701.3 N1564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr7:48634310 G>A maps to NM_152701.3 E4882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr7:48284202 G>A maps to NM_152701.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr7:48452146 G>A maps to NM_152701.3 T4142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr7:48556329 T>A maps to NM_152701.3 T4550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:48506567 C>T maps to NM_152701.3 N4277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr7:48411808 C>A maps to NM_152701.3 A3616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:48314278 G>A maps to NM_152701.3 K1672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr9:139906469 C>T maps to ENST00000355090 L1817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr9:139908395 G>C maps to ENST00000355090 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139908707 G>A maps to ENST00000355090 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139915956 G>A maps to ENST00000355090 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr9:139907276 C>G maps to ENST00000355090 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:94548961 G>A maps to NM_000350.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr1:94568672 G>T maps to NM_000350.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:94528185 A>T maps to NM_000350.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:94476402 G>T maps to NM_000350.2 Y1889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:94568686 G>A maps to NM_000350.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:94522329 A>G maps to NM_000350.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr1:94486857 A>G maps to NM_000350.2 Y1652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:94546178 G>A maps to NM_000350.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr17:67280185 G>C maps to ENST00000392677 S767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr17:67092894 A>C maps to NM_080284.2 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:1059068 G>T maps to NM_019112.3 G1816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr19:1047001 A>G maps to NM_019112.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:1047001 A>G maps to NM_019112.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr17:66933089 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr17:66924116 A>G maps to NM_007168.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr17:66883566 G>C maps to NM_007168.2 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:66981099 G>A maps to NM_080283.3 I1435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr17:67023933 G>A maps to NM_080283.3 H546H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:87196209 C>A maps to NM_000927.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr2:169842724 A>C maps to NM_003742.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:87051486 A>G maps to NM_018849.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr7:20685685 T>A maps to NM_001163941.1 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:20778603 A>G did not map to a codon.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr7:20682903 A>C maps to NM_001163941.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr7:20739467 A>G maps to NM_001163941.1 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:20778686 G>A maps to NM_001163941.1 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr2:220075788 G>C maps to NM_005689.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr2:220075155 C>T maps to NM_005689.2 Q766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:220074989 G>A maps to NM_005689.2 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr23:74290343 A>C did not map to a codon.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr23:74273331 C>T did not map to a codon.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr7:150731894 C>T maps to ENST00000297504 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr16:16108475 C>T maps to ENST00000399408 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:43402468 G>A maps to NM_033450.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr16:48244894 G>A maps to NM_032583.3 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:48210874 G>A maps to NM_032583.3 R1166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr10:101552067 A>G maps to NM_000392.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr10:101569943 C>T maps to NM_000392.3 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:101559079 G>A maps to NM_000392.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr17:48734447 C>T maps to NM_003786.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr13:95862960 C>A maps to NM_005845.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr16:16256865 G>A maps to NM_001171.5 R1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr12:21960402 G>A maps to NM_005691.2 V1442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr12:22068793 G>T maps to NM_005691.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr12:22065832 G>T maps to NM_005691.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr12:21991034 T>A maps to NM_005691.2 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:21962861 G>A maps to NM_005691.2 C1413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr23:153008674 G>A did not map to a codon.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr23:153006075 C>T did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr23:153008475 T>C did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr23:153008482 G>A did not map to a codon.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr23:153008787 G>A did not map to a codon.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr1:94953299 T>C maps to ENST00000454898 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr1:94884102 C>T maps to ENST00000454898 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:146041305 G>A did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr4:89016749 A>G maps to NM_004827.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:89039326 A>G maps to NM_004827.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:119025496 G>A maps to NM_001142505.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr11:119024754 G>A maps to NM_001142505.1 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:27346839 C>G maps to NM_032604.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:51368557 C>T maps to ENST00000337334 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr17:27889658 C>A maps to NM_198147.2 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:43744052 T>C maps to NM_016006.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:58242369 A>T maps to NM_020676.5 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr19:17405545 G>T maps to NM_024527.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr2:204259530 G>T maps to ENST00000295851 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:47299546 T>C maps to NM_016428.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr9:133748370 C>T maps to NM_007313.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr9:133760874 C>T maps to NM_007313.2 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr9:133738355 G>A maps to NM_007313.2 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr9:133759488 C>A maps to NM_007313.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:133759485 G>A maps to NM_007313.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr10:116307473 C>T maps to ENST00000277895 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr7:150553626 G>C maps to ENST00000416793 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr7:150555108 C>T maps to ENST00000416793 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr8:107773579 G>A maps to NM_139166.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr8:107773582 G>A maps to NM_139166.4 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr8:107773723 C>T maps to NM_139166.4 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr8:107773282 C>G maps to NM_139166.4 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:26597327 A>T maps to NM_013375.2 K40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr3:127396050 C>A maps to NM_172027.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr3:127396056 C>T maps to NM_172027.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr17:35640307 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr17:35581912 C>T maps to NM_198834.1 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:35615280 A>T maps to NM_198834.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:109661639 A>G maps to NM_001093.3 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr12:109577275 C>A maps to NM_001093.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:109692083 C>T maps to NM_001093.3 L2037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr12:109577281 G>A maps to NM_001093.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:112183961 T>C maps to NM_001136538.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:112186992 C>T maps to NM_001136538.1 V918V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr12:112167662 G>T maps to NM_001136538.1 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr11:134131682 C>T maps to NM_014384.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr2:211057526 C>G did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:124800166 G>A maps to NM_001609.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:7125373 C>T maps to ENST00000356839 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7127678 T>C maps to ENST00000356839 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr15:89398461 C>T maps to NM_013227.3 F882F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr15:89382023 C>G maps to NM_013227.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr15:89399907 T>C maps to NM_013227.3 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr15:89402127 C>A maps to NM_013227.3 S2104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr15:89395178 T>A maps to NM_013227.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr15:89391156 C>T maps to NM_013227.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr15:89398668 T>A maps to NM_013227.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:7250506 G>A maps to NM_014716.3 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:195006525 T>C maps to NM_012287.5 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:1229952 C>T maps to NM_030649.2 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr17:43215197 G>A did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr10:27529389 G>A maps to ENST00000375888 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr10:15120705 T>A maps to NM_001039844.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr12:50453581 C>T maps to NM_020039.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr12:50472360 G>A did not map to a codon.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr7:150746016 G>A maps to NM_020321.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:150747622 G>A maps to NM_020321.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr2:220402024 C>A maps to NM_018674.4 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr11:44104722 G>A maps to NM_032592.3 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:44079984 C>T maps to NM_001031854.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:61561774 G>C maps to NM_000789.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:61566073 C>T maps to NM_000789.3 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr17:61557827 G>A maps to NM_000789.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:15591565 C>A did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:15618973 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr23:15585871 T>A did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:19435059 C>T maps to NM_001010887.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr14:23549553 G>T maps to NM_014977.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:23549775 T>C maps to NM_014977.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:40025022 T>C maps to ENST00000401700 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr17:40054058 C>A maps to ENST00000401700 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:40028341 A>T maps to ENST00000401700 I956I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr17:40061041 G>T maps to ENST00000401700 G389G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KO-8408-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr17:40049425 T>C maps to ENST00000401700 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr9:32434666 C>T maps to NM_002197.2 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr22:41911895 T>C maps to ENST00000396512 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr22:41914521 G>A maps to ENST00000396512 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr6:24701749 A>T maps to NM_018473.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr14:74036024 C>G maps to NM_006821.4 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr14:74086149 T>C maps to NM_001037162.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr1:6399499 G>T maps to NM_007274.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr20:44483906 G>T maps to NM_005469.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:23723160 G>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:23723675 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr23:23754069 G>A did not map to a codon.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr3:58512374 T>C maps to NM_003500.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:58517531 C>A maps to NM_003500.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr4:8416610 G>A maps to NM_003501.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr1:147124276 A>G maps to NM_016361.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr3:141011819 G>T maps to NM_001037172.1 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr3:141011926 T>C maps to NM_001037172.1 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr23:70824234 G>A did not map to a codon.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr23:70823809 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr23:70824425 T>C did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr15:78486922 G>A maps to NM_015162.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr15:78526759 G>A maps to NM_015162.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr19:6182802 C>T maps to NM_030924.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr17:48538730 G>C maps to ENST00000427954 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:48541576 A>G did not map to a codon.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr17:48548423 A>G maps to ENST00000427954 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:89169103 G>A maps to NM_174917.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:185724471 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr4:185694255 T>C maps to NM_001995.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr23:108912270 A>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:108912279 A>G did not map to a codon.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr23:108926065 G>C did not map to a codon.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr16:20651788 C>T maps to NM_052956.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:20559487 G>A maps to NM_182617.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr16:20570685 A>G maps to NM_182617.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:20787238 C>T maps to NM_005622.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr12:7459280 C>A maps to NM_001080454.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr12:7469735 C>T maps to NM_001080454.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr16:20430732 G>A maps to NM_017888.2 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr12:81503484 T>C did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr12:81647353 C>T maps to NM_024560.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:81503480 C>T maps to NM_024560.2 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:81503374 C>T maps to NM_024560.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr5:56777709 G>A maps to NM_001017992.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:35083347 G>T maps to NM_005159.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:35085734 G>A maps to NM_005159.4 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:79478135 T>C did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:74128512 T>C maps to NM_001615.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr3:179298769 G>T maps to NM_004301.3 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr14:69349270 C>G maps to NM_001130004.1 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr1:236891014 C>T maps to NM_001103.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr1:236924370 C>A maps to NM_001103.2 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr19:39216362 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr14:58701184 C>T maps to NM_018477.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:152522194 C>T maps to NM_020445.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr7:152522194 C>T maps to NM_020445.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:37383624 T>C maps to NM_024855.3 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr3:53908275 G>A maps to NM_022899.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr3:53913971 T>C maps to NM_022899.4 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr23:127185629 T>A did not map to a codon.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr23:127185830 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr23:127185838 C>A did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr1:2938840 C>A maps to NM_080431.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:158630597 A>G did not map to a codon.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr2:158595005 T>C maps to NM_001111067.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr2:158443711 C>A maps to NM_145259.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr3:38519722 G>A maps to NM_001106.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr12:52312802 T>C maps to NM_001077401.1 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52023048 G>C maps to ENST00000463937 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52022537 A>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr11:67412338 A>G maps to NM_080658.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr4:123332502 C>T maps to NM_139243.3 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr16:84228708 G>A maps to NM_139174.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr8:39537678 C>G maps to NM_014237.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr8:39550200 T>A did not map to a codon.
Alternatively spliced codon TCGA-KM-8639-01A-11D-2397-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr5:156997986 T>C maps to ENST00000432888 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr8:39666985 C>T did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr14:70924612 C>T maps to NM_003813.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr7:87795202 C>A maps to NM_021723.3 C711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr7:87607667 A>G maps to NM_021723.3 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr2:207457433 C>T maps to NM_003812.2 Y684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:207413074 G>T maps to NM_003812.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:24209519 T>C maps to NM_014265.4 H733H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr8:24170912 T>C maps to NM_014265.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr4:175898845 C>T maps to NM_014269.4 R724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr4:175899078 C>T maps to NM_014269.4 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr4:175896894 G>A maps to NM_014269.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr4:175899000 T>C maps to NM_014269.4 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:39044453 A>G maps to NM_145004.5 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr8:38965347 A>G maps to NM_145004.5 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr20:3655258 G>A maps to NM_025220.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:38871522 C>T maps to NM_003816.2 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:33658353 A>G maps to NM_030955.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr5:33576383 G>A maps to NM_030955.2 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr5:33881334 G>C maps to NM_030955.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr9:136305498 G>T maps to NM_139025.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr9:136290646 A>G did not map to a codon.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr10:72496470 C>T maps to NM_139155.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr15:100594116 T>C maps to NM_139057.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:100871169 G>A maps to NM_139057.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr16:77387746 C>T maps to NM_199355.2 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr16:77353973 G>A maps to NM_199355.2 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr16:77325308 C>A maps to NM_199355.2 G1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:128797257 G>C maps to NM_133638.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr5:129015554 C>T maps to NM_133638.3 R863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:128983498 T>C maps to NM_133638.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr5:128990038 A>G maps to NM_133638.3 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr5:178559877 G>A maps to NM_014244.4 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr5:178555035 G>A maps to NM_014244.4 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:178553060 G>T maps to NM_014244.4 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr12:43769951 C>T did not map to a codon.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr12:43896208 C>T did not map to a codon.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr12:43777459 C>A maps to ENST00000389420 V1566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:43825140 C>T maps to ENST00000389420 W1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr12:43862443 T>G maps to ENST00000389420 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr12:43825221 G>A maps to ENST00000389420 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:73205261 A>G maps to NM_014243.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr1:161166009 A>T maps to NM_005099.4 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr21:28338044 A>T maps to NM_007038.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr5:64483841 C>G did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr15:79058943 A>T maps to ENST00000258883 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr15:79090347 G>A maps to ENST00000258883 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:79090323 A>C maps to ENST00000258883 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr15:79092749 G>C maps to ENST00000258883 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr9:18906803 G>A maps to NM_001040272.4 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr9:18706838 C>T maps to NM_001040272.4 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr9:136419612 C>T maps to ENST00000393061 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:84581895 C>T maps to NM_207517.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr15:84592740 T>C maps to NM_207517.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr1:150531785 C>A maps to ENST00000369039 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:150532262 G>A maps to ENST00000369039 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:1506085 G>A maps to NM_213604.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:154569309 G>A maps to ENST00000292205 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr1:154574686 A>T maps to ENST00000292205 L187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr21:46642102 C>A maps to NM_015833.3 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr7:140373651 G>A maps to NM_052853.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr7:45725769 G>A maps to NM_021116.2 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr7:45747950 T>C maps to NM_021116.2 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr5:7706857 A>T maps to NM_020546.2 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr5:7816983 C>T maps to NM_020546.2 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr14:24801008 G>C maps to NM_139247.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:24793366 C>A maps to NM_139247.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr14:24788627 G>T maps to NM_139247.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:50338446 C>T maps to NM_001114.3 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr16:50348997 T>A maps to NM_001114.3 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:132052525 G>A maps to NM_001115.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:4029167 G>A maps to NM_001116.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr16:4043481 A>T maps to NM_001116.3 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr16:4029167 G>A maps to NM_001116.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr16:4164713 G>A maps to NM_001116.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr18:907674 G>A maps to NM_001117.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr2:70919543 G>T maps to NM_001185054.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:70910815 G>A maps to NM_001185054.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr10:111877146 C>T maps to NM_016824.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:111878342 A>G did not map to a codon.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr4:100203571 C>T maps to NM_000667.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:100239947 G>C maps to NM_000668.4 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr4:100231923 T>C maps to NM_000668.4 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr4:100234995 G>A maps to NM_000668.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:100057628 G>T maps to ENST00000505590 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr17:15848765 C>T maps to NM_000676.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr1:112042592 G>A maps to NM_000677.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:112042772 G>A maps to NM_000677.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:112031473 G>C maps to NM_020683.6 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr15:73045221 C>A maps to NM_031284.4 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr8:26722372 A>C maps to ENST00000356368 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr20:4229280 A>G maps to NM_000678.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:96781258 C>T maps to NM_000682.5 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr2:96780985 C>T maps to NM_000682.5 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr11:67050627 T>C maps to NM_001619.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr22:40742591 C>G maps to NM_000026.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr7:44153703 C>T maps to NM_001129.3 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr12:19665399 G>C did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr4:7811365 T>C maps to NM_001134647.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr4:7783207 C>A maps to NM_001134647.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:7770722 G>T maps to NM_001134647.1 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr5:148687091 C>T maps to NM_152406.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr10:116100455 G>A maps to NM_001001936.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:88053422 C>T maps to NM_001166693.1 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr4:88029421 A>T maps to NM_001166693.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr23:148035249 C>A did not map to a codon.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr23:148037493 C>A did not map to a codon.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr23:148037883 C>T did not map to a codon.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr23:147924507 C>T did not map to a codon.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr2:100199271 G>A maps to NM_001025108.1 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:100623249 G>A maps to NM_001025108.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr2:100623381 G>A maps to NM_001025108.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr5:132228041 C>T maps to NM_014423.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr5:132270291 T>G maps to NM_014423.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr18:12367033 A>T maps to NM_006796.2 L161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr4:178357479 T>A maps to NM_000027.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr2:236706508 G>A maps to NM_001037131.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:75457453 T>C maps to NM_001144000.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr10:51769498 C>T maps to NM_001077665.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr10:51464816 T>A maps to ENST00000416142 K570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr15:86806022 A>G maps to NM_152336.2 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr15:86940774 C>T maps to NM_152336.2 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr15:87217501 A>G did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:87066158 C>A maps to NM_152336.2 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr15:86808033 C>A maps to NM_152336.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr11:47713656 T>C maps to ENST00000357610 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr1:49119016 G>A maps to NM_032785.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:48999846 A>G maps to NM_032785.3 *504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr2:27291527 A>G maps to NM_021831.5 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:228399579 C>G maps to NM_001135187.1 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr7:100160276 C>T maps to NM_006076.4 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr7:100160552 C>T maps to NM_006076.4 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr5:76348571 T>C maps to NM_018046.4 Y469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr5:76326663 C>T maps to NM_018046.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr7:141336814 A>T maps to NM_018238.3 K242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:100327976 C>G maps to ENST00000311030 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr1:100349948 G>T maps to ENST00000311030 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr1:100336393 G>A maps to ENST00000311030 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr1:100353593 A>G maps to ENST00000311030 E915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr9:139581686 G>A maps to NM_006412.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:41467378 C>T maps to NM_178819.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr4:84502829 A>G maps to NM_032717.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:984365 C>T maps to NM_198576.2 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:957702 C>A maps to NM_198576.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:978745 C>T maps to NM_198576.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:88207489 C>T maps to ENST00000395847 T851T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:115303623 T>G did not map to a codon.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr4:109681435 G>T maps to NM_031279.3 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr4:109667937 T>C maps to NM_031279.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:177642284 C>T maps to NM_153373.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr5:177649896 T>C maps to NM_153373.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr1:247061602 G>T maps to ENST00000428671 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:247081659 T>G maps to ENST00000428671 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr20:32880314 T>C did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr20:32873356 G>T maps to NM_000687.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:110561172 G>A did not map to a codon.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr1:27874969 C>T maps to NM_001029882.2 W1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:27875713 G>A maps to NM_001029882.2 Y971Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:27874261 G>A maps to NM_001029882.2 H1455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr6:135644422 C>A maps to NM_017651.4 E1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr11:62297274 G>A maps to NM_001620.1 D1538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr11:62290073 T>A maps to NM_001620.1 K3939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:62301414 C>T maps to NM_001620.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr11:62294616 C>T maps to NM_001620.1 G2424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:62286930 G>A maps to NM_001620.1 S4986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr14:105413708 G>T maps to NM_138420.2 T2693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:105410342 C>A maps to NM_138420.2 V3815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr14:105412622 A>G maps to NM_138420.2 A3055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr14:105416510 G>C maps to NM_138420.2 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr14:105408994 C>A maps to NM_138420.2 E4265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:105413290 C>A maps to NM_138420.2 E2833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr14:105413492 C>T maps to NM_138420.2 A2765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr14:105418154 G>C maps to NM_138420.2 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr14:105418039 G>A maps to NM_138420.2 Q1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr14:105416366 A>C maps to NM_138420.2 G1807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:105409721 G>A maps to NM_138420.2 S4022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr14:105418154 G>C maps to NM_138420.2 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr14:105413648 A>G maps to NM_138420.2 D2713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr14:105413681 A>G maps to NM_138420.2 S2702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr14:105415199 G>C maps to NM_138420.2 L2196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr14:105415736 C>T maps to NM_138420.2 K2017K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr14:105412334 C>T maps to NM_138420.2 P3151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr14:105416222 G>A maps to NM_138420.2 A1855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr14:105410416 G>A maps to NM_138420.2 L3791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr14:105410434 G>A maps to NM_138420.2 L3785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr14:105411956 G>A maps to NM_138420.2 D3277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr14:105418148 A>T maps to NM_138420.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr14:105410381 T>C maps to NM_138420.2 K3802K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr14:105412346 C>T maps to NM_138420.2 K3147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr14:105406109 A>C maps to NM_138420.2 G5226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr7:17369577 T>A maps to NM_001621.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:353962 C>T maps to NM_020731.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr5:413517 A>G maps to NM_020731.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr5:413517 A>G maps to NM_020731.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr14:77929007 T>C maps to NM_012111.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:186335069 G>T maps to ENST00000273784 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr23:129265666 G>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:129270134 G>C did not map to a codon.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr23:129265758 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr23:129290573 T>G did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr23:129289190 G>A did not map to a codon.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr23:129281736 G>A did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr6:107009362 T>C maps to NM_001624.2 C1634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr6:106968601 G>A maps to NM_001624.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:106960431 C>G maps to NM_001624.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr1:26663758 G>A maps to NM_001039775.3 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr1:26664086 C>A maps to NM_001039775.3 E1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr17:6331787 C>T maps to NM_014336.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr1:33478982 G>A maps to NM_001625.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr17:55183913 G>T maps to ENST00000427138 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr17:55184150 T>C maps to ENST00000427138 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr17:55197615 G>A maps to ENST00000427138 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:19845194 C>G maps to NM_007202.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr17:19823385 T>C maps to NM_007202.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr13:42875948 C>T maps to NM_016248.2 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr6:151670458 C>A maps to NM_005100.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr6:151672018 A>G maps to NM_005100.3 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr6:151673068 C>T maps to NM_005100.3 D1181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:151671481 A>G maps to NM_005100.3 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr15:86198697 C>T maps to NM_006738.4 T1475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:86269659 C>G maps to NM_006738.4 L2259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr9:112918732 G>T maps to NM_007203.4 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr12:4747325 C>A maps to NM_006422.2 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr23:49963343 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr23:49957226 T>A did not map to a codon.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr14:33068659 T>A maps to NM_004274.4 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr14:33015691 A>T maps to NM_004274.4 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr14:33292169 G>C maps to NM_004274.4 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr14:33293955 C>T maps to NM_004274.4 R2313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr19:15465830 T>C maps to NM_005858.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr7:91668039 C>G maps to NM_005751.4 S1549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr7:91722411 A>G maps to NM_005751.4 E3120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:91631867 A>G maps to NM_005751.4 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr7:91631220 A>T maps to NM_005751.4 K664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr9:117130824 T>A maps to NM_030767.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:46032693 T>C did not map to a codon.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr7:134136493 C>A maps to NM_001628.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr7:134133230 T>C maps to NM_001628.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr7:134261182 G>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:134260619 C>T maps to ENST00000418096 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr10:5009192 T>C maps to NM_001353.5 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr10:5254674 C>T maps to NM_001818.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr1:19611596 A>G maps to NM_012067.2 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:19611545 A>G maps to NM_012067.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr19:50374935 G>A maps to ENST00000391835 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:243800912 C>T maps to NM_005465.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr9:116154421 G>T maps to ENST00000277315 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr9:116151741 G>A maps to ENST00000277315 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr9:116153878 C>T maps to ENST00000277315 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr3:52246386 G>A maps to ENST00000441729 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:52233379 C>A maps to ENST00000441729 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr23:55051155 T>C did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr23:55039930 C>A did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr23:55051163 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr23:55046922 C>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:55051150 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr10:97366698 T>G maps to NM_002860.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr10:97371064 G>A maps to NM_002860.3 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr9:75545842 T>C maps to NM_000689.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr9:75555087 G>A maps to NM_000689.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr15:101427814 C>A maps to NM_000693.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:105433492 C>T maps to NM_001034173.3 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:105464484 G>A maps to NM_001034173.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr17:19641665 C>T maps to NM_000691.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr11:67787233 A>T maps to NM_001161473.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr6:24528316 T>C maps to NM_170740.1 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr14:74531620 C>A maps to NM_005589.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr5:125891621 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr1:165652236 G>T maps to NM_000696.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr9:104192183 G>A maps to NM_000035.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr9:104187207 G>A maps to NM_000035.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:5129068 C>T maps to NM_019109.4 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr12:34179314 C>A maps to NM_032834.3 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr12:34179834 A>G maps to NM_032834.3 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr22:50303614 C>T maps to NM_024105.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr23:111002971 G>A did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr23:110996019 A>G did not map to a codon.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr23:110987972 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr23:110987995 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:110964870 T>A did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:110987896 G>T did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr9:101980773 G>A maps to NM_033087.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr3:183961712 G>T maps to NM_005787.5 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr13:37539813 C>T maps to NM_013338.4 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr11:77817938 T>C maps to NM_024079.4 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr12:109530324 T>A maps to NM_001145375.1 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr11:43905564 T>C maps to NM_139178.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr17:18111565 C>T maps to ENST00000261650 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:73680748 A>G maps to NM_015120.4 E2364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr2:73677724 T>A maps to NM_015120.4 A1356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:73680676 T>C maps to NM_015120.4 N2340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr2:73827934 T>C maps to NM_015120.4 R3932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr2:73836706 C>T maps to NM_015120.4 Q4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:73675808 A>T maps to NM_015120.4 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:4542863 G>A maps to NM_001140.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr17:8000097 C>T maps to ENST00000380149 E817E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr2:233322957 T>C maps to NM_001631.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr18:56202372 T>C maps to NM_052947.3 K1682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr18:56205105 A>T maps to NM_052947.3 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:56191245 C>T maps to NM_052947.3 P1850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:85407684 G>A maps to NM_020778.4 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr15:85360310 G>T maps to NM_020778.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:21889673 C>A maps to NM_000478.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:21887144 C>T maps to NM_000478.4 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:233246012 C>A maps to NM_001632.3 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr2:233246012 C>T maps to NM_001632.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr2:233274093 C>T maps to NM_031313.2 Y412Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr2:202593233 C>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:202591541 T>C maps to NM_020919.3 R1009R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:202626256 G>A maps to NM_020919.3 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:202589117 G>A maps to NM_020919.3 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr2:202598154 G>A maps to NM_020919.3 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr3:46725270 C>T did not map to a codon.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr2:202438994 G>T maps to NM_001168221.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:203848265 A>G maps to NM_024744.14 Q699Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:110604110 G>T maps to NM_006492.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr8:11189124 C>A maps to NM_054028.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr8:11189463 C>T maps to NM_054028.1 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr8:11189484 G>T maps to NM_054028.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr17:7385620 C>T maps to NM_001102614.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr17:7386124 C>T maps to NM_001102614.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:33998824 A>G maps to NM_001167595.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr9:116840414 C>T maps to NM_001633.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:46419221 G>A maps to ENST00000458649 G1225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr6:111214752 T>C maps to NM_001634.4 A313A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A4-8312-01A-11D-2396-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr23:11316959 T>C did not map to a codon.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr16:56396895 A>G maps to NM_001144.4 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr19:2251511 T>A maps to NM_000479.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:2249495 C>T maps to NM_000479.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:49755707 G>A maps to NM_198722.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr14:103389066 C>T maps to NM_030943.3 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr14:103394800 A>T maps to NM_030943.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr23:112048308 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:112022637 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:112022643 A>G did not map to a codon.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr11:94554896 C>G maps to NM_130847.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:134080583 C>A maps to ENST00000514516 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:115221049 A>G maps to NM_000036.2 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:115221021 T>A maps to NM_000036.2 K375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr1:115218254 G>C maps to NM_000036.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr1:115220102 G>C maps to NM_000036.2 Y452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:110168779 A>T did not map to a codon.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr1:104160100 C>A maps to NM_000699.2 C13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:112615902 T>C maps to NM_022662.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:112608403 A>G maps to NM_022662.2 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr4:25398291 G>C maps to ENST00000510092 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr4:25415321 G>A maps to ENST00000510092 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr12:121758186 C>A did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr12:110813920 T>C maps to NM_016238.2 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:110815265 A>T maps to NM_016238.2 L464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr12:110825590 A>G maps to NM_016238.2 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr1:213178425 A>G maps to NM_144567.3 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr8:108276470 T>C maps to NM_001146.3 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr8:108334356 C>G did not map to a codon.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr20:896632 G>A maps to NM_015985.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr9:129870362 T>G maps to NM_012098.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:129870869 C>T maps to NM_012098.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:41547821 G>A maps to ENST00000415018 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr4:114277952 C>T maps to NM_001148.4 Q2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:114290828 A>T maps to NM_001148.4 I3826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr4:114275927 C>T maps to NM_001148.4 R2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:114276400 G>A maps to NM_001148.4 G2209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr4:114290873 G>A maps to NM_001148.4 P3841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr4:114278578 T>C maps to NM_001148.4 S2935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr10:61835268 C>T maps to NM_020987.2 Q1790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr10:61833420 A>G maps to NM_020987.2 Y2406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr10:61829376 T>C maps to NM_020987.2 G3754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr10:61835850 A>T maps to NM_020987.2 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830132 G>A maps to NM_020987.2 F3502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830688 G>C maps to NM_020987.2 S3317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr10:61815748 T>C maps to NM_020987.2 E4244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65223119 T>G did not map to a codon.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr17:54452061 A>G maps to NM_153228.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:14713039 G>A maps to NM_054027.4 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr5:14711322 T>A maps to NM_054027.4 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:139876771 T>C maps to ENST00000253810 H971H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:139864823 T>C maps to ENST00000253810 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr5:139905890 C>T maps to ENST00000253810 C1601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:139876315 A>G maps to ENST00000253810 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr7:92027911 C>A maps to NM_019004.1 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:91957149 T>C maps to NM_019004.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr7:92019369 T>C maps to NM_019004.1 Y664Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:113270031 C>T maps to NM_178510.1 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr19:17396341 C>T maps to NM_152363.4 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr2:241439471 C>T maps to ENST00000401804 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:241465101 C>T maps to ENST00000401804 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr10:92679009 G>A maps to NM_014391.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr16:89345491 G>A maps to NM_013275.4 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:89345818 G>A maps to NM_013275.4 D2377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr18:9211597 T>C maps to NM_015208.3 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:9257290 T>C maps to NM_015208.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr18:9254692 G>A maps to NM_015208.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr1:70781172 G>C maps to NM_030816.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:73956462 T>A maps to NM_032217.3 S2294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr10:99342110 C>T maps to NM_020349.2 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr10:90591733 C>T maps to NM_144590.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr2:97505514 T>C maps to NM_144994.7 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:33113432 G>T maps to NM_032139.2 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15765924 G>A maps to NM_015199.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr3:15755031 A>G did not map to a codon.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr3:15726731 C>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr18:21214113 C>T did not map to a codon.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr10:37418818 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:94005882 T>C maps to NM_032290.3 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr1:145566759 T>C maps to NM_144698.3 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:145561664 C>T maps to NM_144698.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr2:97849371 T>C maps to NM_001164315.1 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr2:98201806 C>T maps to NM_025190.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr2:198001336 C>A maps to NM_001195144.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:197889958 T>C maps to NM_001195144.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr11:94231478 C>T maps to NM_017704.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:125592786 A>G maps to NM_020337.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr5:55412458 G>T maps to NM_024669.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr4:77817361 T>C maps to NM_001029870.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:110373073 C>T maps to NM_023016.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr23:118893384 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:90333670 T>C maps to ENST00000339746 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr7:117876196 C>T maps to ENST00000357099 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr14:102973995 G>C maps to NM_152326.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr6:35051231 C>A maps to NM_015245.2 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:100048988 C>G did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:99640157 G>A maps to NM_152788.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr12:100377919 G>A maps to NM_152788.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr16:4776982 G>C maps to NM_133450.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr16:21261381 C>G maps to NM_145865.2 Y165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:36445952 T>C maps to NM_018685.2 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3443-01A-01D-0966-08 chr3:43642046 A>G maps to NM_018075.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr11:26569052 C>T maps to NM_031418.2 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr11:26465369 C>T maps to NM_031418.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr11:22291962 G>A maps to NM_213599.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr2:242154263 G>A maps to NM_001001891.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr15:69072439 C>A maps to NM_006305.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr12:48866683 C>T maps to NM_012404.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr1:150199044 T>C maps to NM_030920.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:150199056 C>T maps to NM_030920.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:150199044 T>C maps to NM_030920.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr15:90342492 G>C maps to NM_001150.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr15:90342656 C>A maps to NM_001150.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr15:90349607 T>C maps to NM_001150.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:69409662 T>G maps to NM_032208.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:80992808 C>A did not map to a codon.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr4:169085401 T>C maps to NM_007193.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr4:169108554 C>A maps to NM_007193.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr4:169108557 C>A maps to NM_007193.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr15:60641323 T>G maps to NM_001002858.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr4:79531259 A>T maps to NM_005139.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:79516548 A>G maps to NM_005139.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr2:70037723 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr2:70008702 C>A maps to NM_001153.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr4:122604560 G>T maps to NM_001154.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr5:150518239 G>T maps to NM_001155.4 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr5:150514008 G>A maps to NM_001155.4 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr17:40997545 T>C maps to NM_009590.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:201478583 C>T maps to NM_001159.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr16:71789971 C>T maps to ENST00000423132 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:24032847 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr14:24032630 A>T maps to NM_003917.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr14:24030556 T>C maps to NM_003917.2 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:50305817 C>T maps to NM_014203.2 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:50305239 G>A maps to NM_014203.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:984671 C>T maps to ENST00000332231 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr17:33951513 G>A maps to NM_001030006.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:183898701 T>G maps to ENST00000411763 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr5:77316581 G>A maps to NM_003664.3 Q976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr15:83349315 C>T maps to NM_004644.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr10:75884278 G>A maps to NM_207012.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:75898089 T>C maps to NM_207012.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr15:51217399 A>T maps to NM_007347.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:51294807 T>G maps to NM_007347.3 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr7:99700546 T>C maps to ENST00000429084 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:99100324 T>C maps to NM_181861.1 H886H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:99093183 A>C did not map to a codon.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr9:72131196 G>A maps to NM_001163.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr15:29385398 G>T maps to NM_005503.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr15:29346527 G>A maps to NM_005503.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:29368273 C>A maps to NM_005503.3 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:3754019 G>C maps to NM_004886.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:6431908 G>A maps to ENST00000389906 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:40818109 T>A maps to NM_004307.1 *760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr4:41015684 G>A maps to NM_004307.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr5:139941189 T>C maps to ENST00000354402 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:1468066 C>T maps to NM_005883.2 P1589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr19:1460856 G>T did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr19:1469818 G>C maps to NM_005883.2 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:10471913 G>A maps to ENST00000423585 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr1:159557957 G>A maps to NM_001639.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr14:20925020 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr15:63569839 C>T maps to NM_031301.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:43350299 A>T maps to NM_001142930.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr1:10502398 A>G maps to NM_199294.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr2:68772384 C>T maps to NM_173545.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr19:36362559 T>A maps to NM_001024807.1 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr19:36362617 G>A maps to NM_001024807.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr19:36370070 C>A maps to NM_001024807.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr2:21251316 G>A maps to NM_000384.2 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr2:21224844 C>A maps to NM_000384.2 A4483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:21233355 T>C maps to NM_000384.2 S2128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr2:21224730 A>G maps to NM_000384.2 I4521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr2:21225675 C>T maps to NM_000384.2 G4206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:21260847 G>A maps to NM_000384.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:28508785 A>G maps to NM_018690.2 E799E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr12:7807217 G>A maps to NM_001644.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr12:7802196 C>T maps to NM_001644.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:41021139 G>A maps to NM_006789.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr22:39380187 G>A maps to ENST00000402182 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr22:39425421 A>G maps to NM_152426.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr22:39441013 T>A maps to NM_145298.5 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:39482534 C>G maps to NM_021822.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr11:116703545 T>C maps to ENST00000360377 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr22:36661664 C>T maps to NM_145343.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr22:36122930 G>A maps to NM_030642.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr22:36055618 C>G maps to NM_030641.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr6:31625013 C>G maps to NM_019101.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr23:23874428 T>A did not map to a codon.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr23:23874421 T>C did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr23:84310893 A>G did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr21:27348293 A>C maps to NM_000484.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr21:27328003 G>C maps to NM_000484.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr3:57280132 C>A maps to NM_012096.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr3:57291080 T>A did not map to a codon.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr3:57283561 T>A maps to NM_012096.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr9:32988091 T>A maps to NM_001195248.1 K71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:30951658 G>A maps to ENST00000509504 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:154294467 C>T maps to NM_080429.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:154294470 C>T maps to NM_080429.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr11:77314712 T>C maps to NM_173039.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr2:241631446 G>C maps to ENST00000429564 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:241631410 C>A maps to ENST00000429564 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr2:241631667 T>C maps to ENST00000429564 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr18:24436384 T>A maps to NM_001650.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr9:33395107 G>A maps to NM_001170.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr9:33387072 G>A maps to NM_001170.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr9:33386468 C>T maps to NM_001170.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr9:33386143 G>A maps to NM_001170.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr15:58458900 T>C maps to NM_020980.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr5:115350146 G>A maps to NM_173800.4 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr15:35189881 T>G maps to NM_014691.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr15:35196563 C>T maps to NM_014691.2 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:66765166 A>T did not map to a codon.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr23:66765718 C>T did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr23:47426119 T>G did not map to a codon.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr23:47428170 A>T did not map to a codon.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr11:72418404 G>T maps to NM_001040118.2 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:72404806 G>A maps to NM_001040118.2 H1246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr4:36081902 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:36152574 G>T maps to NM_015230.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr5:141046055 G>T maps to NM_022481.5 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr5:141033933 T>C maps to NM_022481.5 P1406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr5:141046055 G>T maps to NM_022481.5 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr8:143694489 G>A maps to NM_015193.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr1:228285382 G>A maps to NM_001024228.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr12:49334776 T>C maps to NM_001659.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:47195001 A>C maps to NM_032389.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr22:43213793 A>G maps to NM_014570.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:43236981 G>A maps to NM_014570.4 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr8:68111270 A>G maps to NM_006421.3 I1816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr8:68112660 T>C maps to NM_006421.3 L1785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr20:47628618 C>A maps to NM_006420.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr20:47604915 C>T maps to NM_006420.2 H784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr20:47612353 G>A maps to NM_006420.2 Q1052Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr20:47605056 T>A maps to NM_006420.2 Y797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr20:47587773 C>G maps to NM_006420.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:47641989 C>T maps to NM_006420.2 Y1632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr11:6499970 A>T maps to NM_012402.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr14:68086726 C>G maps to NM_001172.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:46702649 G>A maps to NM_004308.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:32916474 C>T maps to NM_014783.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr15:32929466 T>C maps to NM_014783.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr15:30919055 G>T maps to NM_001039841.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr2:143913196 C>T maps to NM_018460.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr2:143959764 A>G maps to NM_018460.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr16:24942354 G>C maps to NM_001006634.1 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr10:24873802 T>C maps to NM_020824.3 G1805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr10:24886904 G>A maps to NM_020824.3 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr10:49667743 C>T maps to ENST00000417912 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr2:69034591 G>A maps to NM_001007231.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr2:69045085 C>A maps to NM_001007231.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:94639722 C>T maps to NM_004815.3 W1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr3:119133103 T>C maps to NM_020754.2 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr11:128840159 G>A maps to NM_001142685.1 Q1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:128839968 C>T maps to NM_001142685.1 K1699K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:128933814 A>G maps to NM_001142685.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:36275073 G>A maps to ENST00000007510 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:36279063 C>T maps to ENST00000007510 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:130215817 G>A did not map to a codon.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr23:130218267 C>T did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr23:130219619 C>A did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr23:130219621 G>T did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr8:145759518 G>A maps to NM_025251.1 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr14:32563339 T>G maps to NM_001030055.1 Y1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr14:32619204 A>G maps to NM_001030055.1 P1347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr23:11204519 A>T did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr1:17939551 G>T did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:17907126 G>T maps to NM_018125.3 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr1:17990993 C>A maps to NM_018125.3 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr11:120300473 C>T maps to NM_015313.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:73066675 C>G maps to NM_014786.3 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:73073119 G>T maps to NM_014786.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:73073257 G>T maps to NM_014786.3 V1556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:7521289 G>A did not map to a codon.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:155932491 C>G maps to NM_001162383.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr3:56787576 G>C maps to NM_001128615.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr7:144070337 A>G maps to NM_005435.3 E1367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr7:144070325 A>G maps to NM_005435.3 R1363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:135754262 G>C did not map to a codon.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr23:135829735 C>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:135825891 A>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr13:111885552 G>A maps to NM_001113511.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:27107194 C>A maps to NM_006015.4 S2269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr1:27100917 T>C maps to NM_006015.4 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:27106454 A>C maps to NM_006015.4 P2022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:27094307 G>T maps to NM_006015.4 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr1:27106544 C>A maps to NM_006015.4 C2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:157520040 G>C maps to ENST00000367148 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:157527599 G>A maps to ENST00000367148 K1815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:46285792 G>A did not map to a codon.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr12:46230713 T>C maps to NM_152641.2 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr12:46245700 C>A maps to NM_152641.2 V1265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:971935 C>G maps to NM_005224.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr14:58827677 G>T maps to NM_002892.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr14:58831551 A>C maps to NM_002892.3 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr14:58790269 G>T maps to NM_002892.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr14:58830900 T>A maps to NM_002892.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr1:235386543 T>C maps to NM_016374.5 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr1:235345428 C>T maps to NM_016374.5 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:97216936 G>A maps to NM_212481.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr10:63852306 C>A maps to NM_032199.2 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:63699985 A>G maps to NM_032199.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:63700093 G>A maps to NM_032199.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr15:72848194 T>C maps to NM_005744.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr13:50204840 C>T maps to NM_138450.5 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr10:18957459 T>C maps to NM_178815.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:18806887 C>T maps to NM_015161.1 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr10:28274096 A>G maps to NM_018076.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:28270469 T>C maps to NM_018076.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:31475858 C>T maps to ENST00000408912 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:137982981 C>T maps to ENST00000469044 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:100912451 G>A did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr23:100880894 T>A did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:101857943 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:101857825 A>T did not map to a codon.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr23:101858508 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:100871359 G>T did not map to a codon.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr1:150804292 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:150804345 A>G maps to NM_001668.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr11:13387082 C>A maps to ENST00000403290 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr7:98988629 A>G maps to NM_005720.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:98990334 C>T maps to NM_005720.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr15:52844223 C>T maps to NM_006628.4 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr3:35763133 C>T maps to ENST00000458225 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr23:69498390 T>C did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:74985122 G>A maps to NM_004041.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr5:90671370 T>C maps to NM_020801.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr22:51065092 C>G maps to ENST00000395624 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:51064678 G>A maps to ENST00000395624 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:78076226 C>T maps to NM_000046.3 W532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr23:2836006 G>C did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr23:2826884 T>C did not map to a codon.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr23:2833630 A>G did not map to a codon.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr23:2832695 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr23:2835963 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr23:2832695 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:2835992 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:2835994 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:2836006 G>C did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:2836046 C>T did not map to a codon.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr23:2827910 C>G did not map to a codon.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr23:2867364 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr23:2861168 C>T did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr23:3028195 C>T did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr23:3007542 T>C did not map to a codon.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr23:2990178 A>T did not map to a codon.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr23:2951180 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr23:2928174 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:2933299 C>A did not map to a codon.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr11:3681531 C>T maps to NM_004314.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:14993940 C>T maps to NM_021071.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr22:19967488 A>G maps to NM_001670.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr23:25022840 C>A did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr2:239353297 G>A maps to NM_001040445.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:150878301 C>G maps to ENST00000422024 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr23:15320874 A>G did not map to a codon.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr23:63445176 A>G did not map to a codon.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr7:123257652 G>T maps to NM_080928.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr17:42249678 G>A maps to NM_080863.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr7:95157533 C>T maps to NM_016116.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:177136795 T>C maps to NM_080874.3 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr9:132400145 T>A maps to NM_017873.2 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr12:48543457 T>C maps to NM_024095.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr22:30197984 G>A maps to NM_032204.3 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr6:101296248 T>A maps to NM_006828.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr12:103352210 G>C maps to NM_004316.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:8959459 G>T maps to NM_020646.1 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr1:155308159 G>C maps to ENST00000368346 R2846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr1:155385551 G>A maps to ENST00000368346 D1997D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:155451418 T>C maps to ENST00000368346 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:155313420 G>A maps to ENST00000368346 R2703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr8:37967895 G>T did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr8:37978551 G>A maps to NM_004674.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr23:1748788 C>T did not map to a codon.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr23:1546875 A>G did not map to a codon.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr23:1537001 C>G did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:1540610 G>C did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr23:1537880 C>T did not map to a codon.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr23:1537001 C>G did not map to a codon.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr7:97487670 C>A maps to NM_183356.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr14:104565245 C>T maps to NM_001080464.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:62460749 C>T maps to NM_004318.3 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:197069638 G>A maps to NM_018136.4 I2914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:197111689 G>T maps to NM_018136.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr1:197055988 A>G maps to NM_018136.4 S3425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:197087082 A>G maps to NM_018136.4 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr17:79941540 C>T maps to ENST00000306729 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr9:133333870 C>A maps to NM_000050.4 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr9:133342186 G>C did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr2:96789863 C>A maps to NM_001002036.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:96789882 G>C maps to NM_001002036.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr9:119802149 A>G maps to ENST00000313400 C457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:119202961 G>T maps to ENST00000313400 V1236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr20:31024480 G>T maps to ENST00000375687 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr20:31023503 G>T maps to ENST00000375687 E997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr20:31024235 G>T maps to ENST00000375687 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr2:25967151 G>C maps to NM_018263.4 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:25972918 C>T maps to NM_018263.4 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr2:25966454 C>T maps to NM_018263.4 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:31263417 A>G maps to NM_030632.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr18:31318453 G>C maps to NM_030632.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr18:31325883 T>C maps to NM_030632.1 P2024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr2:24108652 G>A maps to NM_017552.1 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr1:1458173 C>G maps to NM_018188.3 A315A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KL-8338-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr1:1403813 C>T maps to NM_001039211.2 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr1:1391259 C>T maps to NM_001039211.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:1389870 C>T maps to NM_001039211.2 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:29220518 A>T maps to NM_024857.3 K1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr17:29162088 T>A maps to NM_024857.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr19:3907732 C>T maps to NM_033064.4 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr10:123503287 C>T maps to NM_001001976.1 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr10:123683800 G>A maps to NM_001001976.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr2:175986169 A>C did not map to a codon.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr1:161762091 C>T maps to NM_007348.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr1:161790870 T>C maps to NM_007348.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr12:53937185 C>G maps to NM_001130059.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr12:53931333 A>T maps to NM_001130059.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:14628903 T>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr12:14613822 C>T maps to NM_018179.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr16:10525096 C>G maps to NM_024997.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:234178665 G>T maps to ENST00000392018 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr2:234173558 T>C maps to ENST00000392018 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr11:64673942 G>A maps to ENST00000421419 Q1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr11:64681628 C>T maps to ENST00000421419 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr11:64664286 G>A maps to ENST00000421419 D1737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:107381401 T>G did not map to a codon.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:242606246 G>T maps to ENST00000337606 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr2:242610737 T>C maps to ENST00000337606 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr3:11348440 C>A maps to NM_006395.2 C80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr3:11354776 G>T did not map to a codon.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr3:11389434 G>T maps to NM_006395.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr7:150714121 C>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:150720229 G>A maps to NM_173681.5 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr2:216184410 G>T maps to NM_004044.6 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr2:216211657 T>C maps to NM_004044.6 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr11:108155201 T>C did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr11:108153495 T>A maps to NM_000051.3 S1212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr11:108202713 A>T maps to NM_000051.3 R2580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr11:108106449 A>T maps to NM_000051.3 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr11:108199912 A>T maps to NM_000051.3 R2419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr16:81069750 C>G maps to NM_015251.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:7046364 C>G maps to NM_001940.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr12:7045494 A>C maps to NM_001940.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:7045911 G>A maps to NM_001940.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr12:7045905 G>A maps to NM_001940.3 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:85981695 G>T maps to NM_032827.6 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr15:25959388 C>G did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr15:25972304 A>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr15:25966974 A>G maps to NM_024490.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:25981204 G>A maps to NM_024490.3 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr15:25959133 C>T maps to NM_024490.3 W677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr5:160061394 G>A maps to NM_025153.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr4:47538704 C>G maps to NM_020453.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:47538505 C>A maps to NM_020453.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr4:47560000 G>A maps to NM_020453.3 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:113474212 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr13:113508718 G>A maps to NM_032189.3 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr23:138857090 C>G did not map to a codon.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr23:138827925 C>T did not map to a codon.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr23:138908946 T>C did not map to a codon.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr23:138840002 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr23:138880881 A>C did not map to a codon.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr23:138823232 G>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:138884414 C>T did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr13:25276071 G>T did not map to a codon.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr13:25266643 C>T maps to NM_001185085.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr19:19767886 C>A maps to NM_020410.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr1:17313020 G>A maps to NM_022089.2 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr3:193120482 A>G maps to NM_032279.2 S1183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr3:193174888 C>T maps to NM_032279.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr3:193039502 C>A maps to NM_198505.2 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr1:116937891 A>T maps to NM_000701.7 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr1:116936277 T>C maps to NM_000701.7 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:116943757 G>T maps to NM_000701.7 E909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:160105303 C>A maps to NM_000702.3 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr19:42490381 C>A did not map to a codon.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr1:169076144 C>T maps to NM_001677.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr3:141626057 T>C maps to NM_001679.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr23:119509281 C>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:119509327 T>G did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr23:119504656 G>A did not map to a codon.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr23:119500535 C>T did not map to a codon.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr16:28898564 C>A maps to NM_173201.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr12:110720426 G>C did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr17:3851043 G>T maps to NM_174953.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:10387741 G>A maps to NM_001001331.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr23:152811578 A>G did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:152826335 C>T did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr23:152823736 C>T did not map to a codon.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr23:152823627 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:130673863 C>T maps to NM_001001486.1 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr16:84495697 G>C maps to ENST00000416219 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr19:36054146 C>T maps to NM_000704.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr12:57037242 A>G maps to NM_001686.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr12:57036239 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr12:57036240 C>A did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:153657421 C>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:153662707 A>G did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr23:153662579 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr17:40639357 C>T maps to NM_001130020.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr7:138417831 G>A maps to NM_130840.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr16:67487538 G>A maps to NM_004691.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr5:172410943 C>T maps to NM_003945.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr2:71190717 C>A maps to NM_001692.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr2:10923346 T>C maps to NM_001039362.1 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr23:77244941 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr23:77254040 A>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr23:77268390 T>A did not map to a codon.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr23:77275863 T>C did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr13:52548107 A>T maps to NM_000053.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr13:52548875 G>A maps to NM_000053.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr4:42509033 G>A maps to NM_006095.2 I695I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr4:42581896 G>T maps to NM_006095.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr13:26125479 C>A maps to NM_016529.4 S299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr13:26148984 G>T maps to NM_016529.4 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr18:55319398 G>A maps to NM_005603.4 G1089G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr18:55399033 A>G maps to NM_005603.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:154314971 C>T maps to NM_020452.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr1:154315637 C>T maps to NM_020452.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:1807165 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr19:1787179 C>A maps to NM_138813.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr19:1789555 C>T maps to NM_138813.2 Q883Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr15:50336886 T>A maps to NM_024837.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr15:50154546 C>T maps to NM_024837.2 Q1064Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr15:50168714 C>T maps to NM_024837.2 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr20:50221536 C>G maps to NM_006045.1 A942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr20:50329571 C>T maps to NM_006045.1 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr20:50292727 A>T maps to NM_006045.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr18:76870366 G>A maps to NM_198531.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr18:77090009 A>G did not map to a codon.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr3:142275325 G>A maps to NM_001184.3 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr3:142274791 A>T maps to NM_001184.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr3:142281208 A>T maps to NM_001184.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:142238532 G>A maps to NM_001184.3 L1454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:142272664 A>G did not map to a codon.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr3:48506400 G>T maps to NM_130384.1 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr3:48498817 T>C did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr3:48488464 C>T maps to NM_130384.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr10:117075205 C>T maps to NM_207303.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:117093810 T>C maps to NM_207303.2 H1019H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr10:117024694 A>G maps to NM_207303.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr10:117075178 G>A maps to NM_207303.2 E990E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr23:76777787 G>T did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr23:76813065 C>T did not map to a codon.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr23:76939123 C>G did not map to a codon.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr23:76890184 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr23:76855279 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr23:76952168 T>A did not map to a codon.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr23:76875908 C>A did not map to a codon.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr23:76938883 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:76888846 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:76777833 C>A did not map to a codon.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr6:16328214 C>T maps to NM_000332.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr6:16328274 C>T maps to NM_000332.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr6:16326645 G>A maps to NM_000332.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:111926344 A>G maps to NM_002973.3 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr16:28847660 A>T maps to NM_148414.1 R1052*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-5875-01A-11D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:13337344 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr7:105254437 C>T maps to NM_020725.1 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:42275085 C>A maps to NM_020218.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:74756586 G>C maps to ENST00000258081 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr7:70229863 C>G maps to NM_015570.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr7:70228159 G>A maps to NM_015570.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr7:70255255 C>T maps to NM_015570.2 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr7:70255843 A>G maps to NM_015570.2 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr7:70231280 C>T maps to NM_015570.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr7:70231265 G>A maps to NM_015570.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:58204235 C>T maps to NM_006576.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr12:58207207 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr12:63543858 G>T maps to NM_000706.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr23:153171714 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr23:153170603 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr16:396563 G>A maps to NM_003502.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr16:354432 G>A maps to NM_003502.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr17:63532472 G>T maps to NM_004655.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr7:99573622 G>T maps to NM_001185.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr17:79166552 C>T maps to ENST00000269392 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr3:28368356 T>C maps to NM_022461.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:103848545 C>T maps to NM_148174.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr19:831826 C>T maps to NM_001700.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr13:31821209 A>G maps to NM_194318.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr11:76750645 C>T maps to ENST00000354301 L17L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G7-6792-01A-21D-1961-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-IZ-8195-01A-31D-2396-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr19:41932062 A>G maps to NM_198540.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr19:41932578 G>A maps to NM_198540.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:67183947 C>T maps to NM_033309.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:67184130 G>C maps to NM_033309.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr12:58020622 G>A maps to NM_001478.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr17:47246987 C>A maps to NM_153446.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr12:658989 C>T maps to NM_173593.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr12:657231 G>A maps to NM_173593.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr12:667219 C>A maps to NM_173593.3 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr11:375477 C>T maps to NM_178537.4 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr3:118945880 C>T maps to NM_212543.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr20:48273174 G>A maps to NM_004776.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr18:29207085 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr18:29218624 C>T maps to NM_004775.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr18:29218693 G>A maps to NM_004775.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr9:104125252 T>C maps to NM_001701.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:90660213 G>A maps to NM_001170794.1 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:90661557 C>T maps to NM_001170794.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:104027516 A>T maps to NM_001015049.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr21:11097540 C>A did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr21:11058196 G>A maps to NM_182482.2 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr21:11058229 C>A maps to NM_182482.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr17:79425868 G>T maps to ENST00000436173 E1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:79424536 C>T maps to ENST00000436173 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr17:79426335 G>A maps to ENST00000436173 E1926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:32207415 C>A maps to NM_001703.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:32203281 G>A maps to NM_001703.2 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:69943307 A>T maps to NM_001704.2 I869I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr6:70071055 C>A maps to NM_001704.2 V1297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr6:69685177 A>G maps to NM_001704.2 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr17:79027520 G>A maps to NM_017451.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:97933660 G>A maps to NM_018842.4 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:38483171 G>T maps to NM_025045.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr22:38483171 G>T maps to NM_025045.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr16:1398015 C>G maps to NM_003933.4 Y1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr16:1389513 G>A maps to NM_003933.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr6:33545339 G>A maps to ENST00000360661 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:88105727 G>A maps to NM_001173543.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr16:88052145 C>T maps to NM_001173543.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr16:88105724 G>A maps to NM_001173543.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr3:52438514 C>A maps to NM_004656.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr3:52441469 C>A maps to NM_004656.2 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr3:52439305 A>C maps to NM_004656.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr3:52439912 G>A maps to NM_004656.2 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr3:52440294 G>A maps to NM_004656.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr3:52437781 G>C maps to NM_004656.2 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr3:52437162 G>C maps to NM_004656.2 Y627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr3:52443728 C>T did not map to a codon.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr3:52439875 G>T maps to NM_004656.2 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr3:52442566 G>A maps to NM_004656.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr3:52443567 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr3:52443573 G>A maps to NM_004656.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr3:52441303 G>A maps to NM_004656.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr3:52437167 T>A maps to NM_004656.2 K626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr3:52443567 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr3:52439310 C>A did not map to a codon.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr6:31598497 C>A maps to NM_080686.2 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr6:31593610 C>T maps to NM_080686.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr9:134308049 C>G maps to NM_013318.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr9:134357756 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:134334700 G>A maps to NM_013318.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:171526992 A>C maps to ENST00000392078 P1914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr1:171501661 A>C maps to ENST00000392078 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr1:171556218 T>A maps to ENST00000392078 P2609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr1:171560736 A>G maps to ENST00000392078 R2816R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A4-A5DU-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:49464329 T>C maps to NM_004324.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr14:35264069 C>A maps to NM_013448.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr14:35295322 A>G maps to NM_013448.2 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:35242929 A>G maps to NM_013448.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr14:35269497 T>A maps to NM_013448.2 K354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr7:72892731 C>G maps to NM_032408.3 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr7:72907198 T>C maps to NM_032408.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr7:72863960 A>G maps to NM_032408.3 C1213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr7:72861633 C>T maps to NM_032408.3 E1268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr2:160194249 C>A maps to NM_013450.2 E1830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr11:66287215 C>G maps to NM_024649.4 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:76740156 A>G maps to NM_024685.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr12:76741470 A>G maps to NM_024685.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:123663958 T>C maps to NM_152618.2 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr4:123664663 T>C maps to NM_152618.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr16:56535331 C>T maps to NM_031885.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr16:56535340 G>A maps to NM_031885.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:56531662 G>A maps to NM_031885.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:56518731 G>A maps to NM_031885.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr3:107463493 C>T maps to NM_001142568.1 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr19:45322914 T>A maps to NM_005581.3 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:45322836 A>C did not map to a codon.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:156626161 G>T maps to NM_021948.3 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr16:75269476 A>C maps to NM_001170714.1 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:94054730 C>T maps to NM_003567.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:94048424 G>T maps to NM_003567.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr1:94057947 G>A maps to NM_003567.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:94054977 T>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:52601912 G>A maps to NM_003657.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr17:58952031 C>A maps to ENST00000407086 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr17:58786583 A>T maps to ENST00000407086 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr17:59118254 T>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:59445724 C>T maps to ENST00000407086 C851C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr10:127520152 T>G maps to NM_016567.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr2:60780393 G>A maps to NM_022893.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr14:99641321 C>T maps to NM_138576.2 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr18:60985488 G>A maps to NM_000633.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr20:30253880 A>G maps to NM_138578.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr19:50169226 G>A maps to NM_138639.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr19:50169187 G>T maps to NM_138639.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr14:23776984 C>A maps to NM_004050.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:187446246 G>A maps to NM_001706.4 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr12:122481897 C>T maps to NM_020993.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr12:122492741 G>C maps to NM_020993.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:30899186 C>T maps to NM_004765.2 *218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr1:147092834 C>T maps to NM_004326.2 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:147086308 A>C maps to NM_004326.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:118771982 C>T maps to NM_182557.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:118773515 C>A maps to NM_182557.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr11:118779363 C>T maps to NM_182557.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr6:136596667 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr11:112064373 T>C maps to NM_031938.4 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:39932879 G>T did not map to a codon.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr23:39932147 A>G did not map to a codon.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr23:39911577 A>C did not map to a codon.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr23:39931682 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr23:39921478 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr23:39922968 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr23:39923131 G>T did not map to a codon.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr23:39913557 A>G did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr23:129148821 G>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:129173134 A>G did not map to a codon.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr23:129147822 A>C did not map to a codon.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr23:129147105 G>T did not map to a codon.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr23:129150164 G>A did not map to a codon.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr23:129149053 A>G did not map to a codon.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr23:129146950 G>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:129190043 T>C did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:23656858 T>A maps to NM_004327.3 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr4:104000885 G>T maps to NM_020139.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr5:70855947 G>A maps to NM_018429.2 V2460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr5:70800507 C>T maps to NM_018429.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr5:70798506 G>A maps to NM_018429.2 K710K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:101012902 G>A maps to NM_020836.3 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr23:18219955 C>G did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr23:18195782 A>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:49208390 C>A maps to NM_024603.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr11:61725622 G>A maps to NM_001139443.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:61730353 C>T maps to NM_001139443.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr19:12867046 C>T maps to NM_017682.2 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:12865477 C>T maps to NM_017682.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr12:70087466 G>A maps to NM_032735.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:14755822 G>T maps to NM_016561.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr16:14738463 C>T maps to NM_016561.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:133119013 G>A maps to NM_003571.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr23:152773749 C>T did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr23:102004857 G>C did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr23:102004559 G>A did not map to a codon.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr23:102005103 G>T did not map to a codon.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr23:102004676 G>T did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr10:60558279 A>G maps to NM_001080512.1 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr12:32369297 G>T maps to NM_001714.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr12:32481359 G>C maps to NM_001714.2 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:32491839 C>A maps to NM_001714.2 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:51690949 T>A did not map to a codon.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr12:51696508 G>A maps to NM_016293.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:22488016 G>A maps to NM_018688.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr11:102239262 T>C maps to NM_001166.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr11:102248742 G>A maps to NM_001166.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:32664735 T>C maps to NM_016252.3 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr2:32640715 C>A maps to NM_016252.3 S786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:32673958 C>A maps to NM_016252.3 V1527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:32626578 C>T maps to NM_016252.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr2:32694460 A>G did not map to a codon.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr2:32617104 A>G did not map to a codon.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr8:11412943 C>G maps to ENST00000427279 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr8:11412979 C>A maps to ENST00000427279 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr8:11415474 C>T maps to ENST00000427279 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr17:28598330 T>C maps to NM_000386.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr8:22037968 G>A maps to NM_006129.4 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:50658964 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:50658767 A>T did not map to a codon.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr4:79808403 T>C maps to NM_198892.1 D676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr4:79786782 T>C maps to NM_198892.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr4:81967318 C>T maps to NM_001201.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr1:39987054 C>T maps to NM_181809.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr10:88681452 G>A did not map to a codon.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr10:43288426 T>C maps to NM_014753.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr10:43312104 A>G maps to NM_014753.3 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr23:15549468 A>G did not map to a codon.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr23:15540570 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:83933198 C>T maps to NM_001717.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr9:16419220 A>G maps to NM_017637.5 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:26240663 C>G maps to NM_004331.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:112993347 C>G maps to ENST00000273395 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr3:112969549 G>T maps to ENST00000273395 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr3:112969402 C>T maps to ENST00000273395 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr4:13615199 T>C maps to NM_148894.2 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:13592028 G>A maps to NM_148894.2 S2730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr6:3137662 C>T maps to NM_004332.2 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr20:36940336 C>T maps to NM_001725.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr22:32831774 A>T maps to NM_174932.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr17:65909127 A>T maps to ENST00000321892 K1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr17:65942186 C>T maps to ENST00000321892 Q2581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr17:65889529 C>T maps to ENST00000321892 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr12:112098448 G>C maps to NM_006768.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:112096634 G>A maps to NM_006768.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:41203098 G>A maps to ENST00000471181 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr17:41244424 T>C maps to ENST00000471181 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr13:32906982 G>A maps to NM_000059.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr13:32911476 A>T maps to NM_000059.3 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr23:154299903 A>C did not map to a codon.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr23:154344344 G>A did not map to a codon.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr23:154344461 A>T did not map to a codon.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr22:50216912 A>G maps to ENST00000342989 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr6:32944713 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32945958 C>G maps to ENST00000395289 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32947798 C>G maps to ENST00000395289 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:32945265 T>C maps to ENST00000395289 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:15350518 C>T maps to NM_058243.2 E1132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr19:15350593 G>A maps to NM_058243.2 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:15353720 G>T maps to NM_058243.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr5:137480909 A>G maps to NM_139199.1 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr5:137506597 C>T maps to NM_139199.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr5:137488284 T>C maps to NM_139199.1 E914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr5:137502345 A>T maps to NM_139199.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:884145 C>T maps to NM_001009877.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:864639 G>T maps to NM_001009877.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr5:864654 C>T maps to NM_001009877.2 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:891952 G>A maps to NM_023924.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3427-01A-01D-0966-08 chr1:92430267 G>T maps to ENST00000347608 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:92470104 G>A maps to ENST00000347608 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr1:92470111 G>T maps to ENST00000347608 E856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:92445157 G>A maps to ENST00000347608 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:28532987 C>T maps to NM_199192.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:125509639 C>A maps to NM_080626.5 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:167893735 C>T maps to NM_001143674.1 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr6:166778931 T>C maps to ENST00000360961 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr6:166780319 T>C maps to ENST00000360961 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr3:9785379 C>G maps to NM_001003694.1 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr6:36175214 A>T maps to NM_015695.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr6:36185715 A>G maps to NM_015695.2 K1004K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr23:135570316 C>A did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr23:135570528 A>G did not map to a codon.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr19:55816166 G>T maps to NM_032430.1 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:55805596 G>T maps to NM_032430.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:1466622 C>T maps to NM_003957.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:1466526 G>C maps to NM_003957.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr21:40572253 A>G maps to NM_018963.3 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr21:40665926 G>T maps to NM_018963.3 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr21:40568694 T>C maps to NM_018963.3 R2100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr23:79939595 T>C did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:79932815 G>T did not map to a codon.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr23:79941023 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr23:79991540 C>G did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr23:79948520 C>T did not map to a codon.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr23:79989614 A>G did not map to a codon.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr23:79932728 T>C did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:80001212 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:62458108 C>T maps to NM_001130702.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:49689058 C>A maps to NM_003458.3 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr10:93768665 T>G maps to NM_003972.2 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:107713244 G>A maps to NM_001018072.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr16:3640656 G>T maps to NM_032444.2 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr16:3641169 C>T maps to NM_032444.2 W823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:124057336 C>T maps to ENST00000368994 Y216Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B0-5085-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr19:1993132 C>T maps to NM_017797.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:1986876 C>G maps to NM_017797.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:1986501 G>A maps to NM_017797.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr19:1986957 G>A maps to NM_017797.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr1:52552414 G>A maps to NM_152265.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr1:203274778 C>T maps to NM_006763.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr1:203276484 T>A maps to NM_006763.2 C132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:203276559 C>T maps to NM_006763.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr21:18977200 C>A maps to NM_001130914.1 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr5:180377359 T>A maps to NM_001040462.2 L440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr5:180376248 C>T maps to NM_001040462.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr5:180338540 C>T maps to NM_001040462.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr5:180475149 C>T maps to NM_152547.4 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr2:111399712 G>A maps to NM_004336.3 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:45472881 G>A maps to NM_007021.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr10:115894781 T>A maps to NM_018017.2 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr10:115891082 A>G maps to NM_018017.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr10:115917413 G>A maps to NM_018017.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr10:115885643 C>A did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr10:121598083 A>G maps to NM_024834.2 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:98741938 T>G maps to NM_015652.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr10:124457697 C>A maps to NM_001010912.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr10:96967147 G>A maps to NM_207321.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:127418871 A>T maps to ENST00000356792 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr10:127422204 A>T maps to ENST00000356792 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr10:127426982 A>T maps to ENST00000356792 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr10:5789389 G>T maps to NM_017782.4 E1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr10:5789076 A>C maps to NM_017782.4 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr10:5781660 C>T maps to NM_017782.4 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr10:11894169 C>T maps to NM_153256.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr10:73521775 C>A maps to NM_022153.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr10:99349704 A>T maps to NM_001009997.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr10:50532032 G>A maps to NM_001135196.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:50534402 C>T maps to NM_001135196.1 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr10:103789496 C>T maps to NM_024541.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr10:105893488 T>C maps to ENST00000389588 K1496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr10:105924007 T>C maps to ENST00000389588 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:105928499 A>T did not map to a codon.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr10:118424300 G>A maps to ENST00000388884 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr10:134261286 C>T maps to NM_173541.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr10:134261474 A>G maps to NM_173541.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr11:111754534 T>C maps to NM_022761.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:8940959 T>G maps to NM_020642.3 L189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr11:64875905 C>A maps to NM_013265.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:68029862 C>T maps to NM_022338.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr11:76171049 A>G maps to ENST00000393457 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr11:33565133 C>T maps to ENST00000389726 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr11:6231319 C>T maps to NM_173525.2 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr11:30352521 C>T maps to NM_152316.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr11:30352899 G>A maps to NM_152316.1 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr11:16774368 T>A maps to NM_014267.5 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:77580811 G>A maps to NM_024684.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr11:64717340 C>T did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr11:61549235 C>T maps to NM_001127392.1 R986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr11:61545942 C>T maps to NM_001127392.1 N665N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr11:61537796 A>C maps to NM_001127392.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr12:53700058 G>A maps to NM_021640.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr12:53693592 C>T maps to NM_021640.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr12:27059271 T>A maps to NM_018164.2 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr12:27075597 A>G maps to NM_018164.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr12:110207029 G>A maps to NM_032829.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr12:32134404 T>C maps to NM_018169.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:32136954 T>A maps to NM_018169.3 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr12:21680691 G>C maps to NM_030572.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:21679900 G>T did not map to a codon.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr12:40076778 A>T maps to NM_001031748.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr12:49073491 C>A maps to NM_017822.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr12:121444124 A>G maps to NM_022895.1 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr12:112650434 G>C maps to NM_001109662.2 G2323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr12:112673070 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr12:112688105 G>C maps to NM_001109662.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr12:112668607 G>A maps to NM_001109662.2 P1901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr12:6804738 C>T maps to NM_153685.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr12:6806816 C>T maps to NM_153685.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:48888592 T>C maps to NM_152319.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr12:80750653 A>G maps to NM_173591.3 Q1984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr12:80650145 A>C maps to NM_173591.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:80655787 C>T maps to NM_173591.3 H634H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr12:64615825 G>C maps to ENST00000311915 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr13:50495710 A>G maps to NM_020456.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr13:42031875 G>A maps to NM_014059.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr13:46918948 G>A maps to NM_025113.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr13:46946277 G>A maps to NM_025113.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr13:39596541 A>T maps to NM_025138.3 Y217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr13:103418815 C>A maps to NM_138779.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr13:43362793 A>C maps to NM_182508.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr13:44456456 G>T maps to NM_153218.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr13:37269301 G>A maps to NM_203451.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr14:76118233 T>C did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr14:57960295 T>A maps to NM_018168.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:45711248 A>C maps to NM_018353.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr14:93652728 C>T maps to NM_001098621.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr14:74825561 C>G maps to NM_018228.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr14:50579392 T>C maps to NM_024558.2 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr14:93670050 C>T maps to NM_032490.4 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr14:77880340 C>T maps to NM_001113475.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr14:59950689 A>C maps to NM_144581.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr14:104029448 G>A maps to ENST00000445352 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr14:91681815 C>T maps to NM_001102368.1 H544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr14:77327094 G>A maps to NM_194287.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr14:73959008 G>A maps to NM_024644.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr14:77844366 A>G maps to NM_001010860.1 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr14:77844712 A>C maps to NM_001010860.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr14:77844690 A>G maps to NM_001010860.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr14:77844921 C>T maps to NM_001010860.1 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:77844645 G>A maps to NM_001010860.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr14:77846825 T>C did not map to a codon.
Alternatively spliced codon TCGA-B1-5398-01A-02D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr14:24773483 G>A did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr14:60921716 A>T did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr14:77493793 T>C maps to NM_024496.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr14:77492044 C>G maps to NM_024496.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr14:77493793 T>C maps to NM_024496.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr14:77493793 T>C maps to NM_024496.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr14:77493793 T>C maps to NM_024496.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr14:74205844 G>A maps to NM_001043318.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr14:95910938 A>G maps to NM_152592.3 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr14:65053587 G>A maps to NM_172365.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr14:103570686 G>A maps to NM_001077594.1 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr14:103568980 A>C maps to NM_001077594.1 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:103568932 G>A maps to NM_001077594.1 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr14:103576542 C>T maps to NM_001077594.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr14:23467860 A>C maps to NM_021944.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr15:24923230 T>A maps to NM_018958.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:24921073 A>G maps to NM_018958.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:24923446 T>A maps to NM_018958.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr15:24923341 C>T maps to NM_018958.2 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr15:93016233 T>C maps to NM_153040.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:75499126 C>A maps to NM_015492.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:75499666 C>T maps to NM_015492.4 C426C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B4-5835-01A-11D-1669-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr15:90126124 T>A maps to NM_152259.3 L288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:90138744 T>C maps to NM_152259.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr15:90128973 C>T maps to NM_152259.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:90118912 C>A maps to NM_152259.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr15:90119272 C>T maps to NM_152259.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:90167320 G>A maps to NM_152259.3 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr15:65871973 G>T maps to ENST00000420799 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr15:40628800 C>T maps to NM_207380.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:38988924 G>C maps to NM_207444.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr15:34647721 G>T maps to ENST00000438749 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr15:90785078 G>T maps to NM_001013657.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:90784688 G>A maps to NM_001013657.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr15:74032953 C>T maps to NM_001039614.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr15:73852254 T>A maps to NM_001042367.1 *267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:73843451 A>G maps to NM_001042367.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr15:73735651 G>T maps to NM_001042367.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:81094971 G>A maps to NM_152337.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:2511751 C>T maps to NM_025108.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr16:19613022 G>T maps to NM_020314.5 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr16:15977976 A>G maps to NM_144600.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:67168084 T>C maps to NM_025187.3 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:67166429 T>G did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr16:49407978 G>A maps to NM_144602.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:67702136 C>G maps to NM_001012984.2 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr17:80369359 G>T maps to NM_175902.4 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr17:21147502 G>A maps to NM_152914.2 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr17:42228327 G>C did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:80405454 C>T did not map to a codon.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr17:34182252 T>C maps to NM_152781.2 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr17:34185481 G>T maps to NM_152781.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr17:79518168 A>G maps to NM_025161.5 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr17:7330113 G>A maps to NM_175734.4 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr17:30660438 T>C maps to NM_022344.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr17:30666860 C>A maps to NM_022344.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:71231746 T>G maps to NM_017941.4 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:74729097 C>A maps to ENST00000317409 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr18:77797400 G>A maps to NM_024805.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr18:30795587 T>A maps to NM_001105528.1 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr18:71816321 C>G maps to NM_014177.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr19:30193855 G>T maps to NM_001031726.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:757668 C>T maps to NM_173481.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr19:757467 C>A maps to NM_173481.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr19:1236021 C>T maps to ENST00000382477 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:3546267 G>A maps to NM_021731.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:2275749 G>A maps to NM_198532.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr19:50666388 G>A maps to NM_152358.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr19:40827908 G>T maps to ENST00000357884 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:36253152 G>A did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:13996868 C>G did not map to a codon.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr19:14000171 C>T maps to ENST00000454313 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:1010405 G>A maps to NM_001033026.1 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr19:44237822 G>A maps to NM_019108.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr7:7278069 A>G maps to NM_020156.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr1:22973840 C>A maps to NM_172369.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:159781880 G>A maps to NM_031908.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:47611594 G>C maps to NM_031909.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:119210049 G>C maps to NM_015645.3 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:119210070 G>C maps to NM_015645.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:24895239 G>A maps to NM_178540.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr13:24465622 G>A maps to NM_001007537.1 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr12:7252315 T>C maps to NM_016546.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr12:7177660 T>G maps to NM_001734.3 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr12:7177888 G>T maps to NM_001734.3 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr1:111494479 A>T maps to NM_018372.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr1:200860814 A>G maps to NM_018265.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:210006561 G>T maps to NM_014388.6 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:162344113 T>C maps to NM_182581.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:169806132 C>T maps to NM_018186.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr1:169822054 G>A maps to NM_018186.2 W830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr1:169391257 A>G maps to ENST00000367806 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr1:207200937 G>C maps to NM_023938.5 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:231489082 A>G maps to NM_032018.4 K482K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:231474335 C>T maps to NM_032018.4 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:24105127 A>G maps to NM_020362.4 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr1:24106409 C>G maps to NM_020362.4 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr1:170965677 G>T maps to NM_001163629.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:182922004 C>G maps to ENST00000287709 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr1:182869150 G>A maps to ENST00000287709 N712N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:182921875 C>T maps to ENST00000287709 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr1:67561004 C>T maps to NM_001013674.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr1:12820748 G>A maps to NM_152290.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr1:116670805 G>A maps to NM_152367.2 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:112019441 A>C maps to NM_174896.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:75101999 G>T maps to NM_001002912.4 T189T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-7501-01A-11D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:3807423 G>A maps to NM_207356.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr1:55119456 T>A maps to ENST00000454855 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:55166857 C>T maps to ENST00000454855 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr1:156309582 G>C did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:11771906 G>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:11775242 C>T maps to NM_198545.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:109649720 G>A maps to NM_001122961.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr1:230991423 C>T maps to NM_032800.2 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:184476744 G>T maps to NM_030806.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:23696042 A>C maps to ENST00000507744 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr1:185143986 C>T maps to NM_001105518.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr1:186355193 T>C maps to NM_017847.5 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr1:234509988 G>T maps to ENST00000424237 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:150258999 T>A maps to NM_144697.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:85718362 A>G maps to NM_198077.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:226180617 T>C maps to NM_152608.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:151021075 A>G maps to NM_017860.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr1:109191480 G>T maps to ENST00000370031 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr1:25569163 A>C maps to NM_020317.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr1:16332450 G>C maps to NM_178840.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr1:223568376 C>T maps to NM_152610.2 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:223567035 C>T maps to NM_152610.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:156706430 T>C maps to NM_015997.3 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr1:156706496 G>A maps to NM_015997.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr1:156264684 T>G maps to NM_144580.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr1:156264684 T>G maps to NM_144580.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr1:32682462 A>T maps to NM_019118.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr1:156897771 A>G maps to NM_144702.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr1:34677971 A>G maps to NM_001134734.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr20:9495508 C>T maps to NM_012261.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr20:55101051 C>T maps to NM_001012971.3 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:55111248 C>T maps to NM_001013646.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr20:42825742 G>C maps to NM_016470.6 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr20:31892697 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:35467799 G>A maps to NM_080627.2 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:18414379 C>T maps to NM_001099407.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr20:35772167 G>A maps to ENST00000343811 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr20:2795844 C>T maps to NM_080739.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr20:60987770 C>T maps to NM_080833.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr20:34611537 C>A maps to ENST00000373973 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr20:61167748 G>A maps to NM_178463.3 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr20:31657701 T>A maps to NM_182658.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr20:31671266 T>C maps to NM_182519.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr20:61427955 G>A maps to NM_018270.4 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr20:20123552 G>A maps to ENST00000389655 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr20:34832709 G>T maps to NM_015511.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr20:34828158 G>C maps to NM_015511.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr20:1161647 G>A maps to NM_018354.1 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr20:1161560 C>T maps to NM_018354.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr20:31815350 G>A maps to NM_178466.3 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:17950810 C>A maps to NM_052865.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr20:10604012 G>T maps to NM_001009608.1 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr21:45919680 C>T maps to ENST00000443468 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr21:45949792 G>A maps to ENST00000443468 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr21:33651271 C>T maps to NM_018944.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr21:47588273 C>T maps to NM_001142854.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr21:47722404 G>A maps to NM_058180.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr21:46363675 G>A maps to NM_058190.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:24106286 G>A maps to NM_182520.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr22:32797732 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:19839715 G>A maps to NM_024627.5 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr22:32113206 C>G maps to NM_173566.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr22:29456414 T>C maps to NM_015370.1 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr22:45601730 C>A maps to NM_001009880.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:73814556 T>A maps to ENST00000334126 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr11:73753115 G>T maps to ENST00000334126 S1881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:27802447 G>A maps to NM_032266.3 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr2:220038161 T>A maps to NM_015680.4 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr2:20990105 A>T maps to ENST00000381090 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr2:24261023 G>C maps to NM_025203.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr2:24261377 G>C maps to NM_025203.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr2:99449444 C>T maps to NM_207362.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:219222407 C>T maps to NM_198559.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:219222363 C>T maps to NM_198559.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:210889860 C>T maps to NM_152519.2 W844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr2:210889825 G>A did not map to a codon.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr2:210896229 A>T maps to NM_152519.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr2:29295854 G>A maps to NM_001029883.1 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr2:54587527 G>T maps to NM_001100396.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr2:170505753 C>A maps to NM_001085447.1 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr2:228497786 G>A maps to NM_020161.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr2:63401908 A>G maps to NM_015910.4 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr2:85066360 G>T maps to ENST00000409520 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr19:6714021 C>A maps to NM_000064.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr19:6712357 G>A maps to NM_000064.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr3:119242474 G>T maps to NM_016589.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:62317064 T>A maps to NM_020685.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3923-01A-01D-1458-08 chr3:14731558 C>T maps to NM_032137.4 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr3:118865299 C>A maps to NM_152539.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:196434642 C>A maps to NM_032898.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr3:129023467 C>T maps to NM_001006109.1 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:128998743 C>T maps to NM_001006109.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr3:88199300 C>T maps to NM_173824.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:50324294 T>A did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:161064027 G>T maps to NM_001040100.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr3:143691274 C>A maps to NM_173552.3 S34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr3:48956090 T>A maps to NM_001123040.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr3:138669386 C>T maps to NM_001040061.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr4:57842812 C>T maps to NM_032313.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr4:100443801 G>A maps to NM_032149.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr4:113510904 A>G maps to NM_018392.4 D1034D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:170671700 G>A maps to NM_017867.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr4:170663224 C>T maps to NM_017867.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:170658831 G>T maps to NM_017867.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:170678992 T>C maps to NM_017867.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:128905553 C>T maps to ENST00000454347 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr4:113066759 G>A maps to NM_152400.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr4:99064289 C>A maps to NM_174952.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr4:184600618 T>C maps to NM_021942.4 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr4:3257592 C>T maps to NM_001042690.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr9:123719561 C>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:123783918 C>G maps to NM_001735.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr5:134782501 C>T maps to NM_130848.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr5:175740818 T>G maps to ENST00000443967 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr5:102611691 C>T maps to NM_033211.2 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:43490824 C>A maps to NM_198566.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr5:156770120 C>A maps to NM_001001343.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr5:37168940 T>C maps to NM_023073.3 K2395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:37121779 A>G maps to NM_023073.3 L2988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr5:37221453 T>A maps to NM_023073.3 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr5:64933558 C>T maps to NM_001093755.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:64956552 T>G maps to NM_001093755.1 Y242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:442634 C>T maps to NM_138464.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr6:32260988 T>C maps to ENST00000447241 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr6:43193767 C>A maps to NM_199184.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr6:13470344 T>C maps to NM_033069.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:53989446 T>C maps to ENST00000502396 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr6:3723938 G>A maps to NM_183373.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr6:3751741 G>T maps to NM_183373.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:31079877 G>T maps to NM_014070.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:74135069 A>G maps to NM_138441.2 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr6:74161502 A>G maps to NM_138441.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:42994981 C>T maps to NM_033112.2 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr6:97629853 A>T maps to NM_198468.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr6:121433800 G>T maps to ENST00000275159 C1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:121576520 T>A maps to ENST00000275159 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:2623683 C>A maps to NM_152554.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr6:36298371 C>T maps to NM_001010903.4 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr6:36294404 G>C maps to NM_001010903.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr6:157744465 A>G maps to NM_018452.4 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr6:31627291 A>G maps to NM_021184.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:31627424 A>G maps to NM_021184.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr6:127901449 G>A maps to NM_001010905.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr6:127902328 T>G maps to NM_001010905.1 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr6:170162544 T>A maps to NM_018341.1 L293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr6:170179295 T>A maps to NM_018341.1 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr6:151894313 G>A maps to ENST00000367290 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr6:151857577 T>C maps to ENST00000367290 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr7:42949680 C>T maps to NM_001099858.1 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr7:2577861 A>G maps to NM_152743.3 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr7:2577852 C>G maps to NM_152743.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr7:2578284 G>A maps to NM_152743.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr7:150028095 G>A maps to NM_138434.2 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:66410207 T>C maps to NM_017994.4 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr7:99753404 G>A maps to NM_018275.3 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr7:23728935 C>T maps to NM_199136.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:23724138 A>T maps to NM_199136.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr7:100033304 G>C maps to NM_145030.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr7:100085829 G>A maps to ENST00000423930 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr7:100087002 C>T maps to ENST00000423930 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr7:100087170 C>A maps to ENST00000423930 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:48081006 C>A maps to ENST00000430738 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr7:120765872 G>T did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:120907349 A>G maps to NM_024913.4 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr7:120629776 C>G maps to NM_024913.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr7:100061218 G>A maps to ENST00000426357 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr7:89937152 C>T maps to NM_001039706.2 N845N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr7:47698324 G>A maps to NM_001123065.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr7:108524165 A>G maps to NM_001024607.1 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr1:57351709 A>T maps to NM_000562.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr8:144124474 C>G maps to NM_173687.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr8:69351860 G>A maps to NM_052958.2 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr8:69621308 C>G maps to NM_052958.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr8:444510 T>C maps to NM_175075.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr8:67590119 C>A maps to NM_019607.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr8:67405942 T>A maps to NM_152765.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr8:144654815 T>C maps to NM_001100878.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr8:12879057 T>C maps to NM_020844.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr8:117954927 G>A maps to NM_001025357.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr9:131587283 A>T maps to NM_016390.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr9:138387376 G>A maps to NM_001048265.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr9:130475073 C>A maps to NM_001012502.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr9:35044752 G>A maps to NM_203299.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr9:139959179 A>G maps to NM_178448.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr9:88844485 C>T maps to NM_001010907.1 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr9:139379130 G>A maps to NM_152571.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr9:139739642 T>C maps to NM_001080482.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr9:99413723 T>C maps to NM_153698.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr9:34397496 C>T maps to NM_032596.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr9:97823037 C>T maps to NM_001193329.1 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr9:111853339 G>A maps to NM_032012.3 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr9:86570340 C>T maps to NM_032307.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:86571235 G>A maps to NM_032307.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:214550 G>T maps to NM_152569.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr9:215108 G>T maps to NM_152569.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:136333114 G>A maps to NM_017586.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:27556770 C>T maps to NM_018325.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr9:132593304 G>T maps to NM_016520.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr9:90501483 C>T maps to NM_178828.4 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr9:90502737 G>T maps to NM_178828.4 L1112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr9:90500481 C>T maps to NM_178828.4 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:26842571 G>A maps to NM_024828.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr9:114518733 C>A maps to NM_173521.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr9:139722994 G>A maps to NM_001173988.1 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139730291 C>T maps to NM_001173988.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr9:117400850 T>C maps to ENST00000374049 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr9:15745612 C>T maps to NM_173550.2 D885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr8:86163152 A>T maps to NM_198584.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:58234006 C>T maps to NM_000717.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr23:15768233 C>G did not map to a codon.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr23:15790715 C>T did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr1:9019021 T>C maps to ENST00000413627 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr16:66887325 G>A maps to NM_005182.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr8:61192347 C>T maps to NM_004056.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr2:231682473 C>T maps to NM_001130850.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr1:227174151 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr1:227171878 G>A maps to NM_020247.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:24447424 T>A maps to NM_012295.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr22:24434872 C>A maps to NM_012295.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr22:24451597 C>T maps to NM_012295.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr22:24456571 C>T maps to NM_012295.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr22:24472139 C>T maps to NM_012295.3 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr18:20814664 G>A maps to NM_001100619.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr20:60971620 G>A maps to NM_031215.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr20:60967981 C>G maps to NM_031215.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr20:60982023 C>T maps to NM_031215.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr18:21735911 T>A maps to NM_138644.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:65143847 T>C maps to ENST00000371073 C1033C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr1:65117973 T>C maps to ENST00000371073 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr19:13325350 G>A maps to NM_023035.2 Q1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr19:13366049 G>T maps to NM_023035.2 I1542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr19:13325356 G>A maps to NM_023035.2 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:13346024 G>A maps to NM_023035.2 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr19:13319692 A>G maps to NM_023035.2 H2223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr19:13340906 G>A maps to NM_023035.2 D1843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr9:140809199 C>A maps to ENST00000277549 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:140943669 T>C maps to ENST00000277549 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:140865970 C>T maps to ENST00000277549 C491C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr12:2800281 G>T maps to NM_199460.2 E2195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:2719718 G>T maps to NM_199460.2 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr12:2566763 A>T maps to NM_199460.2 K217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr12:2800178 G>A maps to NM_199460.2 A2160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr12:2711090 G>T maps to NM_199460.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:2716230 C>T maps to NM_199460.2 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:2763056 C>T maps to NM_199460.2 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr12:2783695 C>T maps to NM_001129829.1 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr3:53777117 G>T maps to NM_001128840.1 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:53757944 C>T maps to NM_001128840.1 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr1:181453104 T>C maps to ENST00000357570 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr1:181705480 G>A maps to ENST00000357570 V1111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:181701627 G>A maps to ENST00000357570 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr23:49072840 C>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:49071829 T>C did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr23:49071690 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr23:49066822 G>A did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr23:49084508 G>A did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr17:48652947 C>T maps to NM_018896.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr17:48647165 T>A did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr16:1251874 C>T maps to NM_021098.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr16:1257813 C>T maps to NM_021098.2 V1036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr16:1252258 A>G maps to NM_021098.2 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr16:1265530 C>T maps to NM_021098.2 L1728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr16:1268484 C>T maps to NM_021098.2 G1907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr16:1250558 T>C maps to NM_021098.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr22:39966975 C>T maps to NM_021096.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr22:40062012 T>A did not map to a codon.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr1:201047116 C>A maps to NM_000069.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr1:201041937 C>T maps to NM_000069.2 E724E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr1:201058499 C>A maps to NM_000069.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr1:201013476 C>G maps to NM_000069.2 A1592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr1:201017770 T>A maps to NM_000069.2 T1460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:201034980 G>T maps to NM_000069.2 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:201060822 G>A maps to NM_000069.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:50513566 G>T maps to ENST00000435965 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr12:2022186 A>G did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr17:37333728 C>T maps to NM_000723.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr17:37341383 C>T maps to NM_000723.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:37341118 T>A did not map to a codon.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr12:49221582 G>A maps to NM_000725.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr2:152709961 T>C maps to NM_000726.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr22:36960523 G>A maps to NM_006078.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr17:65021006 C>T maps to NM_014405.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr17:64875147 G>A maps to NM_014404.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr1:174973752 C>T maps to NM_014412.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:174975971 A>G maps to NM_014412.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:27440796 C>A maps to NM_004341.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr2:27456648 C>T maps to NM_004341.3 V1124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr3:85961676 G>A maps to NM_153184.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:85851254 A>C maps to NM_153184.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr1:159161759 G>A maps to NM_021189.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:159170639 C>T maps to NM_021189.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:159169658 G>A maps to NM_021189.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr1:159170697 G>T maps to NM_021189.3 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr3:62499342 A>G maps to NM_183394.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr3:62498424 C>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:122081598 A>G maps to NM_001167940.1 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr7:122269334 A>G maps to NM_001167940.1 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:7334268 T>C maps to NM_001170692.1 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:7373332 C>T maps to NM_001170692.1 E573E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:71419535 C>T maps to NM_001740.4 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr11:14991620 C>T maps to NM_001741.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr10:105215350 C>A maps to NM_001001412.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:90870814 C>T maps to NM_006888.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr10:12595349 G>T maps to NM_153498.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:209781276 T>C maps to NM_020439.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:114434487 G>A maps to ENST00000515496 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:48266892 T>C maps to NM_004345.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr9:138703211 G>A maps to ENST00000409386 N1595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr9:138713194 C>T maps to ENST00000409386 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:4877037 T>C maps to NM_015099.3 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr17:4872276 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:67699343 G>A maps to NM_018448.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:12858740 G>A maps to NM_001162499.1 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr17:76991240 C>A maps to NM_138793.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr6:17556591 A>G maps to NM_006366.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:17507927 T>C maps to NM_006366.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3427-01A-01D-0966-08 chr2:241534489 C>A maps to NM_023083.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr6:44148400 T>G did not map to a codon.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr19:39233679 C>T maps to NM_144691.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:39226898 G>A maps to NM_144691.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr19:39225511 T>A did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:39226165 G>T maps to NM_144691.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:39226802 G>A maps to NM_144691.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr1:223954129 A>C maps to NM_001748.4 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:223936793 G>C maps to NM_001748.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr15:42695071 C>T maps to NM_000070.2 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr11:76804732 C>T maps to ENST00000360841 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr23:110491969 G>A did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr23:110494189 T>G did not map to a codon.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr23:110494225 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr19:36632119 C>T maps to NM_001749.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr11:34074125 C>T maps to NM_005898.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr12:30888128 C>T maps to NM_001002259.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr19:5914494 G>T maps to ENST00000394521 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr1:113192052 A>T maps to NM_006135.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr7:116533093 A>T maps to NM_006136.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:18891594 C>T maps to NM_033328.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr22:37898634 C>G maps to NM_014550.3 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr22:37912255 T>C maps to NM_014550.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr22:37888768 C>T maps to NM_014550.3 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr7:2951853 G>A maps to NM_032415.4 N1032N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:2959067 G>A maps to NM_032415.4 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr7:2956955 G>A maps to NM_032415.4 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr11:104971441 G>A maps to NM_001007232.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr5:40843665 T>G maps to NM_032587.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr5:40852477 G>A maps to NM_032587.3 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr19:48715113 C>A maps to NM_001184900.1 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr9:139266449 G>C maps to NM_052813.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr9:139262145 C>T maps to NM_052813.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr19:11019855 G>A maps to NM_199141.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr11:3022345 A>C maps to NM_001014437.2 *832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr12:25347861 G>C maps to NM_001082972.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr12:25264774 A>T maps to NM_018272.3 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:38319004 G>A maps to NM_007359.4 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:40913800 A>T maps to NM_170589.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr15:40949237 A>T did not map to a codon.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr23:41428919 C>T did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr23:41448781 G>C did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:2233882 G>A maps to NM_020764.3 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr11:104901191 A>C maps to NM_033292.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:15164632 C>T maps to NM_012114.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:185552221 G>T maps to NM_032991.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr6:90573112 T>A maps to NM_012115.3 L562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr1:160167357 G>C did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr1:160167356 A>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr20:55027380 G>A maps to NM_020356.3 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:10713662 G>A maps to NM_001079843.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:10714627 G>A maps to NM_001079843.1 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:10713845 G>A maps to NM_001079843.1 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr11:34478279 T>C maps to NM_001752.3 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:65788965 C>T did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43940127 G>A maps to NM_172095.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:26520357 T>C maps to NM_198137.1 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:26524567 G>A maps to NM_198137.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:38850107 A>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:38853149 T>C maps to NM_021185.4 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr19:38857908 C>T maps to NM_021185.4 C909C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr7:116166676 C>T maps to NM_001753.4 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr3:8787537 G>A maps to NM_001234.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr16:88945788 G>A maps to NM_005187.5 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr16:88958663 C>T maps to NM_005187.5 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:107398635 C>T maps to NM_024814.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr7:107395873 G>A maps to NM_024814.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr21:37518698 C>A maps to NM_001236.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr4:169931207 G>T maps to NM_032783.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr9:69206733 C>T maps to NM_001085457.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:46152377 G>A maps to ENST00000442683 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr7:26251699 A>T did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr22:39262465 C>T maps to NM_014292.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:39066950 G>A maps to NM_015373.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr4:15511766 G>A maps to NM_001080522.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr10:70547738 T>G maps to NM_018237.2 L979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr18:57106798 C>G maps to NM_133459.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr16:57562849 C>A maps to NM_033212.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:55749244 T>C maps to ENST00000339012 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr9:35660624 C>T maps to NM_174923.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:219868975 T>C maps to NM_194302.2 P1751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:219886631 G>C maps to NM_194302.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr2:219892422 A>G maps to NM_194302.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr18:47792750 G>A maps to NM_145020.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr4:186382295 A>G maps to NM_152775.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr19:48809520 G>A maps to NM_144577.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr19:48807246 C>T maps to NM_144577.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:21989094 C>G maps to NM_152612.2 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr22:21989452 C>T maps to NM_152612.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr23:48919828 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr23:48919829 T>G did not map to a codon.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr23:48923284 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:33444681 T>A maps to NM_032816.3 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr19:18054505 C>T maps to NM_001136203.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr5:68581284 G>C maps to NM_176816.3 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr7:31683359 C>A maps to NM_194300.2 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr3:42777230 G>A maps to NM_144719.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:92905517 T>C maps to NM_017667.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr7:128434748 G>A maps to NM_022742.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr2:179701994 A>T maps to NM_173648.3 A1317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr17:20768729 A>G maps to NM_001004306.1 *222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr17:20769995 C>A maps to NM_001004306.1 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr17:20768802 C>T maps to NM_001004306.1 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr17:20769963 C>A maps to NM_001004306.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr7:76916143 C>T maps to NM_020879.2 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr2:159033037 G>A maps to NM_138803.3 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr2:159312933 A>T maps to NM_138803.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr4:24810061 G>A maps to NM_001130726.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:24838060 G>T maps to NM_001130726.2 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr19:11537535 G>A maps to NM_145045.4 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr22:30766352 C>A maps to NM_001017437.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr22:30766637 C>G maps to NM_001017437.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr23:133379665 G>T did not map to a codon.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr23:133379665 G>A did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:133379027 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr23:133378952 C>A did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:46086773 G>T maps to NM_001114938.2 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr1:26584684 G>A maps to NM_022778.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr23:49105113 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:49106625 C>T did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:3679838 A>G maps to NM_152492.2 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr1:43055003 T>C maps to NM_001080850.2 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:96273431 G>A maps to NM_182496.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:78058618 C>T maps to NM_017950.2 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr17:8647474 C>T maps to NM_144681.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr17:62506378 C>A maps to NM_138363.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr3:48475151 A>G maps to NM_024661.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr3:113166964 C>T maps to NM_144718.3 E782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr17:28512532 G>T maps to NM_032141.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:80115740 C>T maps to ENST00000445854 E708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr3:122102041 A>G maps to NM_001017928.2 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:82747060 C>A maps to NM_014167.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:119968787 C>T maps to NM_178499.3 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:123307923 C>A maps to NM_201435.3 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:120428097 C>T maps to NM_207311.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr12:120510406 G>A maps to NM_207311.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr16:3081003 G>A maps to NM_001103175.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:56649977 A>C maps to NM_001141947.1 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr3:56649271 C>T maps to NM_001141947.1 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr10:32854548 G>T did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:32676506 T>C maps to NM_001008391.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr2:132288264 G>T maps to NM_138770.1 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr2:132288326 C>T maps to NM_138770.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr2:130897217 T>C maps to NM_207310.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr2:37315581 C>T maps to ENST00000379187 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr2:37319306 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr2:37321280 A>G maps to ENST00000379187 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr1:100613724 C>T maps to NM_019083.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr16:775559 C>T maps to NM_001031737.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr3:112357945 G>T maps to ENST00000447230 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr3:112357864 G>A maps to ENST00000447230 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr11:96104274 T>A maps to NM_024725.3 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:118869165 C>T maps to NM_198489.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr2:56419910 C>T maps to NM_001080433.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr11:65658487 C>T maps to NM_006848.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:60609626 G>T maps to NM_024098.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr11:66359724 G>A maps to NM_018219.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:55566740 T>G maps to ENST00000436346 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr11:64111335 C>A maps to NM_032251.5 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr14:91779453 C>A maps to NM_001080414.2 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr14:91755524 G>A maps to NM_001080414.2 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:91776234 C>G maps to NM_001080414.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr12:28458579 A>T did not map to a codon.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:118732796 G>T maps to NM_019044.4 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr2:118766137 A>G maps to NM_019044.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:41826333 C>T maps to NM_052848.1 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:36170074 C>T maps to NM_005893.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3923-01A-01D-1458-08 chr11:6292568 C>T maps to NM_176875.2 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:34340314 G>A maps to NM_005064.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:34661942 A>G maps to NM_006664.2 *113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:45112358 C>T maps to NM_001029835.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr13:37014311 C>T maps to NM_003914.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr4:122743633 A>G maps to NM_001237.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:59407027 C>T maps to NM_004701.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr15:59409485 T>C maps to NM_004701.2 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr15:59408906 A>T maps to NM_004701.2 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr23:50052671 G>A did not map to a codon.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr23:50090766 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr23:50053810 G>T did not map to a codon.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr23:50054337 C>A did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr6:100009546 T>A maps to NM_005190.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:4398011 T>C maps to NM_001759.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr6:41904302 A>G maps to NM_001760.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr15:43482263 A>C maps to NM_012142.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:43478361 T>A maps to NM_012142.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr16:2506612 G>A maps to NM_001761.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr16:2506954 G>A maps to NM_001761.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr16:2481269 C>T maps to NM_001761.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:78082687 C>T maps to NM_004354.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:86695280 C>A maps to NM_001239.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr4:77969662 G>T maps to NM_006835.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:132084159 C>A maps to NM_001039780.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:1334455 G>A maps to NM_030937.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:135711410 A>G maps to NM_058241.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr3:46415325 C>T maps to NM_001100168.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr12:69985845 G>T maps to NM_006431.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:156294857 A>G maps to NM_005998.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:10263418 G>A maps to NM_012073.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr2:73467610 T>C maps to NM_006429.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:117568203 C>T maps to NM_004258.3 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:74517870 C>T maps to NM_133493.3 D1085D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr12:7636080 C>G maps to NM_004244.4 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:7654023 A>C maps to NM_004244.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr12:7527158 C>T maps to ENST00000416109 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr12:7510008 G>A maps to ENST00000416109 A1461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:7528455 T>A maps to ENST00000416109 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr12:7527335 G>T maps to ENST00000416109 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:109690200 C>T maps to NM_006016.4 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr5:66479406 G>A maps to NM_005582.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr5:66478707 T>G maps to NM_005582.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr16:28944419 C>T maps to NM_001178098.1 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr1:158226666 C>T maps to NM_001763.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr1:158260922 G>A did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:158262060 C>T maps to NM_001765.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:112059810 G>C maps to NM_001004196.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr2:71060813 G>C maps to NM_015717.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:7810713 G>A maps to NM_021155.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr19:7809903 G>T maps to NM_021155.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr19:35827038 G>T maps to NM_001771.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:35828751 C>T maps to NM_001771.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr9:5457409 G>A maps to NM_014143.3 V128V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5120-01A-01D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:72522163 G>T maps to NM_174892.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr17:72700847 T>A maps to ENST00000412086 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51738930 G>A maps to NM_001772.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr7:80302112 A>T maps to NM_001127444.1 K385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:6924066 T>A maps to NM_000616.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr23:135730559 C>T did not map to a codon.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr11:35208448 T>A did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:26646660 G>T did not map to a codon.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr12:56121063 G>A maps to NM_001780.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:42384962 T>C maps to NM_001783.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr17:62009606 C>T maps to NM_001039933.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr6:14118277 C>A maps to NM_004233.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr1:160523748 C>T maps to NM_001184879.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr12:6334632 A>G maps to NM_001769.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr20:23066498 G>A maps to NM_012072.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr23:2658824 C>T did not map to a codon.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr13:49852532 C>T maps to NM_030911.3 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr15:43021464 G>A maps to NM_138477.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr1:100964715 A>T maps to NM_033312.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr1:100964517 A>G maps to NM_033312.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:43828620 G>A did not map to a codon.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr5:137524672 C>T maps to NM_004661.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr5:137621757 G>A maps to NM_001790.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:45247408 C>T did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr17:45234324 G>A maps to NM_001114091.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr17:45234649 A>G maps to NM_001114091.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:4706078 A>G maps to NM_017913.2 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413229 C>G maps to NM_001039802.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413328 C>G maps to NM_001039802.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr1:227213827 C>T maps to ENST00000366766 V1486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr1:227227834 C>A maps to ENST00000366766 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr1:227192737 A>G maps to ENST00000366766 P1644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:227288694 T>C maps to ENST00000366766 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr14:103430981 C>T maps to NM_006035.3 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr14:103418833 C>A did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr11:64601932 T>C maps to NM_017525.2 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr11:64597204 G>T maps to NM_017525.2 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr11:64600191 C>A maps to NM_017525.2 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr11:64601932 T>C maps to NM_017525.2 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr2:37873388 T>A maps to NM_006449.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:44414437 C>A maps to NM_001253.2 S800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:44390389 T>C maps to NM_001253.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr8:25341647 C>T maps to ENST00000434814 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:25341584 G>A maps to ENST00000434814 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr2:174231882 G>A maps to NM_031942.4 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr3:45127492 C>T maps to NM_022842.3 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr3:45136962 A>G maps to NM_022842.3 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:68853182 A>C maps to NM_004360.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr16:68862135 C>T maps to NM_004360.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr16:65038637 C>T maps to NM_001797.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr16:65006840 G>T maps to NM_001797.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:21783500 C>T maps to NM_004061.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr16:83816958 C>A maps to ENST00000268613 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr16:89246669 T>C maps to NM_004933.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:66949282 T>A did not map to a codon.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr5:19747189 A>C maps to NM_004934.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr5:19838882 A>T maps to NM_004934.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr18:64172225 A>G maps to NM_021153.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr18:64172300 G>A maps to NM_021153.2 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr18:25591823 G>A maps to NM_001792.3 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr18:25532270 A>T maps to NM_001792.3 L856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr18:59195204 G>A maps to NM_031891.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr10:73442208 C>T maps to ENST00000398860 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr10:73499529 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:73406334 C>T maps to ENST00000398860 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr14:23524348 T>A maps to NM_022478.3 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr20:60511820 C>T maps to NM_001794.2 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:31323225 T>G maps to NM_004932.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr18:63547746 G>T maps to NM_004361.2 G659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr18:63477169 C>T maps to NM_004361.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr16:61851426 C>A maps to NM_001796.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr16:61761057 G>A maps to NM_001796.2 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr16:61935248 C>T maps to NM_001796.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr16:61935266 T>G maps to NM_001796.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr16:61851420 C>A maps to NM_001796.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:61851549 C>T maps to NM_001796.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr5:26890657 C>T maps to NM_016279.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr16:89753116 G>C did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:89760631 C>T maps to NM_052988.4 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:1638913 G>T maps to NM_024011.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr1:1647843 G>A maps to NM_024011.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr1:1571828 A>G maps to ENST00000401097 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:37619371 T>C did not map to a codon.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr17:37681092 C>T maps to NM_016507.2 Q1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr17:37657500 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr7:40134551 A>G maps to NM_003718.4 R1504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr7:40134338 T>C maps to NM_003718.4 P1433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr7:90355878 A>T did not map to a codon.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr2:202687538 C>T maps to ENST00000450471 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr2:202700486 G>T did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr12:56363323 G>A maps to NM_001798.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr9:90585695 G>T maps to NM_001039803.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr17:73998204 C>A maps to NM_001258.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:30815100 C>T maps to NM_003885.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr2:219825192 C>T maps to NM_003936.3 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr20:31946926 G>T maps to ENST00000357886 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr20:31946923 G>A maps to ENST00000357886 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr17:46058012 C>T maps to NM_176096.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr7:92252375 A>G maps to NM_001145306.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr13:26923219 G>A maps to NM_001260.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr9:130548495 C>G maps to ENST00000373265 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr6:20781421 G>C maps to NM_017774.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr4:76521461 G>T maps to ENST00000307465 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:76532404 T>C maps to ENST00000307465 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr4:76529104 T>A maps to ENST00000307465 K231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:133655129 T>C maps to NM_001113575.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:18646491 G>C did not map to a codon.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr23:18622765 G>T did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr23:18622978 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:18622811 G>A did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:36652170 C>A maps to ENST00000448526 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr12:12871757 G>C did not map to a codon.
Sequencing variant TCGA-B0-4707-01A-01W-1359-10 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr9:21971183 T>G maps to NM_001195132.1 R58R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-4163-01A-02W-1382-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr4:184367367 G>C maps to NM_017632.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:22006243 G>A maps to NM_004936.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:139866439 A>G did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:139866439 A>G did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr23:139865946 G>A did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:139866076 C>T did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:139865790 C>G did not map to a codon.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr17:15498177 C>T maps to ENST00000455584 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr20:5157343 C>A maps to NM_003818.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr3:133302926 T>C maps to NM_017548.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr23:72673462 G>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr16:80654829 G>T maps to NM_152342.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr19:43031328 G>A maps to NM_001712.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr19:42132311 G>A maps to NM_001817.2 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr19:42219788 C>A maps to NM_004363.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:42213710 C>A maps to NM_004363.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:42225040 C>G maps to NM_004363.2 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr19:42260805 C>T maps to NM_002483.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr19:33792386 G>A maps to NM_004364.3 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr19:33792411 G>T maps to NM_004364.3 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793107 G>T maps to NM_004364.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793119 G>T maps to NM_004364.3 Y67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr22:17690278 G>A maps to NM_017424.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr22:18028579 T>A maps to ENST00000400579 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr22:18021868 C>T maps to ENST00000400579 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr22:18021910 C>T maps to ENST00000400579 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr22:18029227 T>C maps to ENST00000400579 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:15793928 C>T maps to ENST00000375924 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:22310246 C>T maps to NM_007352.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:151688471 G>A maps to NM_007185.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr1:151678745 C>T maps to NM_007185.4 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr18:34855138 G>A maps to NM_020180.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr18:34833812 C>T maps to NM_020180.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr18:34846535 G>T maps to NM_020180.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr19:3293437 C>A maps to NM_021938.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr19:3281240 G>A maps to NM_021938.3 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:46765597 A>G maps to NM_014246.1 A2621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr22:46807518 G>T maps to NM_014246.1 G1583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:46930991 G>A maps to NM_014246.1 Y692Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr22:46806459 T>G did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:46931729 G>A maps to NM_014246.1 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr1:109801210 G>C maps to NM_001408.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:109801120 C>T maps to NM_001408.2 T1126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:109810543 C>A maps to NM_001408.2 R2060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:48692762 T>A maps to NM_001407.2 T1602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:48699893 G>A maps to NM_001407.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr3:48694146 G>A maps to NM_001407.2 C1461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr3:48694701 G>A maps to NM_001407.2 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:48697289 G>T maps to NM_001407.2 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr20:3765588 A>G maps to NM_001810.5 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:68380077 A>G maps to NM_001812.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr4:104097154 C>A maps to NM_001813.2 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr4:104117118 A>C maps to NM_001813.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:214830402 T>C maps to NM_016343.3 H2871H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:214815374 G>T maps to NM_016343.3 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:214813547 A>T maps to NM_016343.3 K623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr23:100381783 G>A did not map to a codon.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr5:64847409 C>T maps to NM_022145.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:173780411 G>C maps to NM_001127181.2 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:42342455 C>G maps to NM_024053.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:42341238 G>A maps to NM_024053.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr6:126669609 A>G did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr9:123870183 A>T maps to NM_007018.4 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr5:122685708 A>T maps to NM_153223.3 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr4:56884017 G>T maps to NM_025009.3 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr4:56825851 C>T maps to NM_025009.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr15:49052451 A>T maps to NM_001194998.1 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:49030736 G>A maps to NM_001194998.1 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr11:117244471 G>A maps to NM_014956.4 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr11:117265694 C>T maps to NM_014956.4 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr11:117214945 G>T maps to NM_014956.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr18:13056676 C>A maps to NM_032142.3 S1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr18:13049582 A>G maps to NM_032142.3 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr20:34053566 G>C did not map to a codon.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr12:88471485 G>T maps to NM_025114.3 T1858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:88514779 A>C maps to NM_025114.3 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:180044160 C>T maps to NM_014810.4 L1858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr11:95564237 A>T maps to NM_014679.3 K441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:95561020 A>G maps to NM_014679.3 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr2:65299147 T>G maps to NM_015147.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr5:612535 C>T maps to NM_018140.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr18:12701061 T>C maps to NM_024899.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr3:101476745 T>C maps to ENST00000327230 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr22:47116100 G>A maps to NM_022766.5 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:55886919 C>T maps to NM_001143685.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr16:67029714 T>C maps to ENST00000326686 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:196654323 A>G maps to NM_000186.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:196918738 G>A maps to ENST00000367421 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:196762627 C>T maps to NM_021023.5 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr1:196744040 C>T maps to NM_021023.5 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr23:47489069 G>A did not map to a codon.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr23:47485782 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr23:47487500 C>T did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr7:117199624 C>A maps to NM_000492.3 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr7:117251653 T>G maps to NM_000492.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:88105045 G>A maps to NM_001195308.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr1:151496774 C>T maps to NM_020770.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:151509761 C>T maps to NM_020770.2 Y1184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr1:151497209 G>T maps to NM_020770.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr15:57836714 C>G maps to NM_032866.3 Y1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:57816813 C>T maps to NM_032866.3 T968T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:57808994 G>T maps to NM_032866.3 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr14:54996812 A>G maps to NM_006568.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr14:55004492 C>T maps to NM_006568.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr10:90966989 C>T maps to NM_003956.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr19:4433325 C>T maps to NM_005483.2 H821H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:4428836 G>A maps to NM_005483.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:4409548 G>A maps to NM_005483.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr19:4433328 G>A maps to NM_005483.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr10:50833614 C>T maps to NM_020549.4 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr7:132470403 T>A maps to ENST00000448878 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:146747122 C>A maps to NM_004284.3 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr15:93545456 G>A maps to NM_001271.3 E1396E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CJ-4871-01A-01D-1373-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:7805977 C>A maps to NM_001005271.2 Y1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr17:7806303 C>T maps to NM_001005271.2 G1199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:6707539 G>A maps to ENST00000309577 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr1:6214897 A>C maps to NM_015557.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr1:6204187 G>A maps to NM_015557.2 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:6212525 G>A maps to NM_015557.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:40143494 C>A maps to NM_032221.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr20:40116334 C>T maps to NM_032221.3 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr20:40033766 G>A maps to NM_032221.3 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr8:61769233 T>C maps to NM_017780.2 F2465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr8:61757863 C>T maps to NM_017780.2 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr8:61654761 T>C maps to NM_017780.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr16:53340242 T>C maps to ENST00000219084 N2238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr16:53320219 T>G maps to ENST00000219084 V1718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr16:53358032 G>A maps to ENST00000219084 K2640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr16:53358032 G>A maps to ENST00000219084 K2640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr3:53853055 C>A maps to NM_018397.4 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr22:29091807 G>A maps to NM_001005735.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr20:5903083 C>T maps to NM_001819.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:5903026 A>G maps to NM_001819.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr20:5903113 G>A maps to NM_001819.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr20:5903929 T>C maps to NM_001819.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr1:111860637 C>T maps to NM_201653.2 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:111862961 C>T maps to NM_201653.2 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:203188446 C>T maps to NM_003465.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:203188923 G>T maps to NM_003465.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr1:203186949 C>T maps to NM_003465.2 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr22:51018474 A>C maps to NM_005198.4 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr23:85213895 A>C did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr16:89713673 C>A maps to NM_001083314.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:89717998 G>C maps to NM_001083314.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr8:23116261 G>A maps to NM_152272.3 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr21:19629057 G>A maps to NM_024944.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr11:89956062 G>A maps to NM_012124.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr15:41535938 T>C did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:220404815 A>T maps to NM_024536.5 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr7:150932431 C>T maps to NM_019015.1 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr3:184102983 G>T maps to NM_003741.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:184098192 A>C maps to NM_003741.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr15:30664488 A>G maps to NM_139320.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr7:136699839 C>T maps to NM_001006628.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3443-01A-01D-0966-08 chr11:46407117 C>T maps to NM_000741.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:46407570 C>A maps to NM_000741.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr15:34355730 G>A maps to NM_012125.3 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:175612867 A>T maps to NM_001039523.2 L478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr2:175614793 A>G maps to NM_001039523.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr2:175614799 G>A maps to NM_001039523.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr20:61981904 G>A maps to NM_000744.5 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr20:61987734 T>C maps to NM_000744.5 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:61981544 C>T maps to NM_000744.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr4:40356026 C>T maps to NM_017581.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:154544110 C>A maps to NM_000748.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5568-01A-01D-1534-10 chr15:78922277 C>T maps to NM_000750.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr15:78921470 G>A maps to NM_000750.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:101009957 C>A maps to NM_004854.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr10:73767937 C>T maps to NM_004273.4 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:73768162 C>T maps to NM_004273.4 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr16:71570903 C>A maps to NM_001166395.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr23:46433703 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr23:46434587 A>C did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:34180262 G>A maps to NM_022467.3 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr18:24496339 G>T maps to NM_031422.4 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr15:101717679 G>T maps to NM_014918.4 T774T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:129241298 C>T maps to NM_175856.4 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr5:129520379 G>T maps to NM_175856.4 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr16:845818 A>G maps to ENST00000317063 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr10:101969425 G>A maps to NM_001278.3 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr14:24774972 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:24775202 G>C maps to NM_014430.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr3:9908859 C>T maps to ENST00000430427 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr16:11001310 C>T maps to NM_000246.3 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr16:10997753 T>A did not map to a codon.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr15:65499357 G>T maps to NM_003613.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:65490141 G>A maps to NM_003613.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:65494240 C>A maps to NM_003613.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:175215407 T>C maps to NM_004882.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr16:69199287 C>T maps to NM_032830.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:120150414 G>C maps to ENST00000392521 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr12:120128174 G>A maps to ENST00000392521 P1989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr6:139694868 A>G maps to NM_006079.3 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr13:53035797 A>T maps to NM_001098525.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:113509842 C>A did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:46799003 G>C maps to ENST00000415402 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:103988668 G>A maps to NM_001823.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr2:122206530 T>C maps to NM_015282.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr3:33648251 T>C did not map to a codon.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr3:33586216 G>A maps to ENST00000359576 H1099H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr19:40225078 G>A maps to NM_001828.4 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr1:86947887 A>G maps to NM_001285.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr1:86957041 G>A maps to NM_001285.3 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:86890014 C>T maps to NM_006536.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr1:86913357 T>C maps to NM_006536.5 N627N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:67135056 G>T maps to NM_013246.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr7:143020427 C>A maps to NM_000083.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr7:143049048 G>A maps to NM_000083.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr3:184071154 C>A maps to NM_004366.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:184079225 C>G maps to NM_004366.4 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr23:10176318 C>T did not map to a codon.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr23:10180544 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:10162969 C>G did not map to a codon.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr23:49853519 G>A did not map to a codon.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr23:49840553 A>G did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr23:49851499 C>T did not map to a codon.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr23:49834548 A>G did not map to a codon.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:11894063 T>C maps to ENST00000376496 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:11894361 G>T maps to ENST00000376496 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr21:37833693 G>A maps to NM_001146077.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr23:106171624 C>A did not map to a codon.
Sequencing variant TCGA-B2-4099-01A-02D-1458-08 chr7:73183929 C>G maps to NM_001306.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:73184304 C>T maps to NM_001306.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr7:73245665 C>T maps to NM_001305.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr16:3065983 C>T maps to NM_021195.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr16:3063764 C>A maps to NM_020982.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr19:51228702 C>T maps to NM_002975.2 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr12:10131626 C>T maps to ENST00000355690 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:38724315 C>T maps to NM_175060.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr16:11217729 C>G maps to ENST00000409790 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr16:69988259 G>A maps to NM_182619.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr16:70211265 G>A maps to NM_173619.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:71036917 G>A maps to NM_173535.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr19:7796206 T>C did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:8618082 G>A maps to NM_001007033.1 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr12:10205355 C>T maps to NM_207345.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr12:9885605 G>A maps to NM_172004.2 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr23:154563724 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr21:36042940 C>T maps to ENST00000360731 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr12:122826193 T>G maps to ENST00000302528 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:73752799 A>T maps to NM_003388.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr2:29383259 C>T maps to ENST00000379543 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:201719789 T>G maps to NM_001162407.1 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr2:201721414 T>C maps to NM_001162407.1 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr2:201721534 C>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:178044363 T>C maps to NM_020666.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:178050362 C>A maps to NM_020666.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:92816353 T>G maps to NM_001025232.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr14:95657992 G>A maps to NM_024734.3 Q973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr8:1728426 C>G maps to NM_018941.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:56301653 A>T maps to NM_004898.2 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr4:56319288 C>A maps to NM_004898.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:72005413 C>T maps to NM_030813.3 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr11:72012969 G>A maps to NM_030813.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr5:1344896 C>A maps to NM_030782.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr15:65471323 C>T maps to NM_006660.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr3:150659492 G>T maps to NM_001195794.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr1:36205124 A>T maps to NM_022111.3 L1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr1:9801266 C>T maps to NM_001009566.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:9809528 G>A maps to NM_001009566.1 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:7295477 G>T maps to NM_014718.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr12:7302197 T>C maps to NM_014718.3 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr9:36209296 C>T maps to NM_007096.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:57746159 C>T maps to NM_004859.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:3554720 T>C maps to NM_015041.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr16:3586165 C>T maps to NM_015041.1 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr8:62212688 C>T maps to NM_173519.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr8:62412011 A>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:66612902 G>A maps to NM_052999.3 *287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:66670439 T>A maps to NM_178818.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr3:32433538 G>C maps to NM_138410.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr5:79032747 T>C maps to NM_153610.3 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr5:79025640 A>G maps to NM_153610.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr18:72234668 G>T did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr18:72247363 A>G did not map to a codon.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr18:72234589 T>C maps to NM_032649.5 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr18:72180799 T>A maps to NM_018235.2 L250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr19:42893090 G>A maps to NM_032488.3 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:150912422 G>A did not map to a codon.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:150912763 G>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr23:150912595 C>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:150906985 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr23:150911738 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr23:150912324 G>A did not map to a codon.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr16:57984388 T>C maps to NM_001297.4 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr1:26514972 G>A maps to ENST00000374253 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr1:26509851 C>T maps to ENST00000374253 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:21519645 A>C did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr23:21667029 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr23:21450760 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr6:154743777 C>T maps to NM_173515.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr10:101151191 A>G did not map to a codon.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr2:97483237 A>C maps to NM_017623.4 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:97428004 C>A maps to NM_020184.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr16:58577564 A>G maps to NM_016284.3 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr16:58622798 C>T maps to NM_016284.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr16:58585657 A>T maps to NM_016284.3 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr3:32750280 T>A maps to NM_015442.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:70704757 C>T maps to NM_014515.5 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr19:54648052 G>A maps to NM_014516.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr7:135095314 A>T maps to NM_001190850.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr7:135079030 T>C maps to NM_001190850.1 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr4:78650047 C>T maps to ENST00000512485 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr4:78641755 G>A maps to ENST00000512485 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr8:17088228 T>C maps to NM_013354.5 *286W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr6:88853865 C>T maps to NM_016083.4 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:88853688 G>A maps to NM_016083.4 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:40730406 G>A maps to NM_024877.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr9:17394560 T>C maps to NM_017738.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr9:17416023 T>A maps to NM_017738.2 L984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:17332673 G>A maps to NM_017738.2 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:41316145 C>T maps to NM_001843.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr1:205041695 A>C maps to NM_005076.3 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:205028741 C>A maps to NM_005076.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr11:100226890 C>G maps to NM_014361.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:40849968 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr17:40844514 A>T did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr7:147336209 G>A maps to NM_014141.5 W637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr7:146829476 T>C maps to NM_014141.5 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr7:146829389 C>T maps to NM_014141.5 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:39140599 G>A maps to NM_033655.3 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:39177437 G>A maps to NM_033655.3 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr16:76509833 A>T did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr2:125555790 C>G maps to NM_130773.2 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:40717243 G>T did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:40715164 G>A maps to NM_001042532.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr9:140158761 G>A maps to NM_015456.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr14:31355024 C>T maps to NM_004086.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:71196857 G>A maps to NM_018714.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr17:71197741 T>C maps to NM_018714.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr13:46054426 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr16:70546245 T>A maps to NM_015386.2 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr13:40268841 A>G maps to ENST00000255468 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr1:103468817 G>A maps to NM_080629.2 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr1:103444414 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr1:103428307 G>A maps to NM_080629.2 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:103405990 C>A did not map to a codon.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr1:103453263 T>C maps to NM_080629.2 E821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr6:33133476 G>A maps to NM_080680.2 A1533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr6:75864168 G>C maps to ENST00000322507 T1176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr6:75843573 C>A maps to ENST00000322507 L1888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:75861880 T>C maps to ENST00000322507 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr8:121259909 C>T maps to NM_021110.1 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:121170483 A>G maps to NM_021110.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr8:121237424 A>T maps to NM_021110.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr9:101777793 A>C maps to NM_001855.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr9:101748183 C>A maps to NM_001855.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr9:101829276 T>G maps to NM_001855.3 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr1:32138104 T>A did not map to a codon.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:32146504 C>T did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:105793763 A>G maps to NM_000494.3 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr10:105830253 G>T maps to NM_000494.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr21:46930114 G>A maps to ENST00000359759 Q1626Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr21:46924433 A>C maps to ENST00000359759 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr21:46925136 T>C maps to ENST00000359759 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr21:46912468 G>A maps to ENST00000359759 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr6:70878566 C>T maps to NM_001858.4 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:70646795 A>G maps to NM_001858.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr6:70733566 G>T maps to NM_001858.4 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr6:70639450 C>A maps to NM_001858.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr6:70873232 A>T did not map to a codon.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:48266573 A>G maps to NM_000088.3 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr17:48267075 A>T maps to NM_000088.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr7:94029505 A>T did not map to a codon.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr20:61945125 G>T maps to ENST00000326996 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr6:56035908 G>A maps to NM_030820.3 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr6:55933842 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:56044472 A>G maps to NM_030820.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:139729065 A>G did not map to a codon.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr8:139845295 C>T maps to NM_152888.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr8:139707080 C>A maps to NM_152888.1 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr8:139767733 T>C maps to NM_152888.1 K656K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr8:139674281 G>A maps to NM_152888.1 A1077A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr8:139606434 G>A maps to NM_152888.1 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:86362086 T>G maps to NM_152890.5 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr1:86453337 C>A did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr1:86289365 A>G did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:109790279 T>C maps to ENST00000333642 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr4:109810855 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:109783656 C>T maps to ENST00000333642 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr9:117026663 G>T maps to NM_032888.2 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr9:117052532 C>G maps to NM_032888.2 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:7472277 G>A maps to NM_001037763.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr2:189860858 C>T maps to NM_000090.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:189867766 C>T maps to NM_000090.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr13:110833683 C>T maps to NM_001845.4 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr13:110827562 A>C did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr13:111102706 C>A maps to NM_001846.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr13:111125465 T>A maps to NM_001846.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr13:111144510 T>C maps to NM_001846.2 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:228112293 A>G maps to NM_000091.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:227945176 T>C maps to ENST00000396625 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:227872133 C>T maps to ENST00000396625 Q1660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:107930822 C>G did not map to a codon.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr23:107930859 G>A did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:107929323 G>T did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr23:107935976 G>T did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:107938640 G>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:107938133 G>A did not map to a codon.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr23:107868986 T>G did not map to a codon.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr23:107909821 C>T did not map to a codon.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr23:107849992 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr23:107924994 C>T did not map to a codon.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr23:107457372 G>A did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:107447617 C>G did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr23:107433649 T>G did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr23:107400257 C>T did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr23:107431169 G>A did not map to a codon.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr23:107420104 C>T did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr23:107681170 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr23:107434728 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr23:107430495 T>A did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:137734001 G>C did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:189912940 T>C maps to NM_000393.3 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr19:10071470 G>T maps to NM_015719.3 Y1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr19:10116390 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr19:10090546 G>A maps to NM_015719.3 R894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr19:10091505 A>C maps to NM_015719.3 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr21:47409685 G>T maps to NM_001848.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr21:47422536 C>A maps to NM_001848.2 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr21:47420242 A>C did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr21:47421873 G>A did not map to a codon.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr21:47533974 C>A maps to NM_001849.3 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr21:47542787 G>A did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:238280360 C>T maps to NM_057165.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:238234212 A>T maps to NM_004369.3 V3161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr2:238280963 C>T maps to NM_004369.3 R1232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:238275564 C>T maps to NM_004369.3 S1755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr2:238249677 A>C maps to NM_004369.3 A2627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr2:238249155 G>C maps to NM_004369.3 S2801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr3:130095638 A>G maps to ENST00000312481 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:130113787 A>G maps to ENST00000312481 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr3:130287095 C>T maps to NM_001102608.1 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr3:130284102 A>G maps to NM_001102608.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr3:130289956 C>T maps to NM_001102608.1 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr3:48623283 C>T maps to NM_000094.3 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr3:48609478 C>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:48602897 G>A maps to NM_000094.3 A2824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr3:99514148 T>G maps to ENST00000429802 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr3:99514922 G>A maps to ENST00000429802 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:36564105 A>G maps to NM_005202.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr6:70942324 T>A maps to NM_001851.4 K822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:71003974 G>A maps to NM_001851.4 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr20:61468579 C>T maps to NM_001853.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:120101990 G>A did not map to a codon.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr8:120118231 T>C maps to NM_006438.3 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:120114629 A>G maps to NM_006438.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr2:3691554 C>T maps to ENST00000418971 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr18:480712 G>T maps to NM_130386.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr18:346952 C>A maps to NM_130386.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr10:22605387 G>A maps to NM_012071.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr13:76101978 G>A maps to NM_203497.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr20:31291228 C>A maps to NM_053041.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr11:36302300 T>G maps to NM_014186.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr19:18901410 G>A maps to NM_000095.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr22:19956114 A>G maps to NM_001135162.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:160305058 A>G maps to NM_001098398.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr1:160310031 C>A maps to NM_001098398.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:160275562 C>G maps to NM_001098398.1 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr11:14510131 T>C did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr11:14510040 A>C maps to NM_001144061.1 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr11:14520432 C>T maps to NM_001144061.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr19:19014154 G>A maps to NM_007263.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr7:130295933 A>G maps to NM_012133.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr17:17184461 T>C maps to NM_003653.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr8:67970383 A>G maps to NM_006837.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr7:99686961 T>C maps to NM_006833.4 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr12:6837090 G>C did not map to a codon.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:238004480 A>G maps to NM_006710.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr17:46103805 C>G maps to NM_016429.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:99823845 T>A maps to NM_017421.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:131095204 G>A maps to NM_016035.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr14:74420178 G>T maps to NM_182476.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr4:47667068 G>A maps to NM_006587.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr16:30198794 T>C maps to NM_007074.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:67207641 A>G maps to NM_020441.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr15:69003111 C>T maps to NM_006091.3 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr17:27948313 G>A maps to ENST00000345068 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr16:4408460 C>T maps to NM_024535.3 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:10510333 C>T maps to ENST00000377049 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr17:14005507 T>A maps to NM_001303.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:13980320 A>G maps to NM_001303.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr17:53042200 C>A maps to NM_004375.3 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:119393996 C>A maps to ENST00000484810 *99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:30231237 G>A maps to NM_032609.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr19:36142195 T>C maps to ENST00000392201 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr19:36142195 T>C maps to ENST00000392201 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:75947672 C>T maps to NM_001865.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr14:93813724 G>T maps to NM_182971.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr3:148928071 T>C maps to NM_000096.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr7:130024429 C>T maps to NM_001868.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr3:148583132 T>C maps to NM_001870.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr7:129938645 A>T maps to NM_016352.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:129962494 T>C maps to NM_016352.3 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:17056400 G>T maps to ENST00000443236 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:17003920 A>C maps to ENST00000443236 *1943E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr19:17036077 A>G maps to ENST00000443236 L1216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:17088186 G>A maps to ENST00000443236 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr3:148559630 A>T maps to NM_001871.2 K166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr17:28750569 G>C maps to NM_001304.4 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:166385728 A>G maps to NM_001873.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr15:83215271 C>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:93999657 A>C maps to NM_014912.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:93999849 A>G maps to NM_014912.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:173370038 T>G maps to NM_030627.2 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr5:173372084 A>G maps to NM_030627.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr4:780369 C>T maps to NM_006651.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr20:34215309 G>T maps to NM_003915.5 Y381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:34219485 A>G maps to NM_003915.5 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr6:36730738 A>G maps to NM_020939.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr6:36759869 A>G maps to NM_020939.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr14:24545746 G>A maps to NM_006032.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:89650106 T>A maps to NM_014427.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr2:207820278 T>A maps to NM_173077.2 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:207833967 G>C maps to NM_173077.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr2:207827298 C>T maps to NM_173077.2 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:98309566 A>T maps to NM_000097.5 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr16:12875237 G>A maps to NM_018340.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr2:211521331 C>A maps to NM_001122633.1 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr8:145634428 G>C maps to NM_013291.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr8:145623273 C>A maps to NM_013291.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:1250911 A>C maps to NM_017871.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr11:61188975 A>C maps to NM_024811.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr11:68575042 C>T maps to NM_001876.3 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:50200611 C>A maps to NM_152359.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr23:88009259 G>A did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:2775210 C>T maps to NM_019609.4 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr20:2776795 C>G maps to NM_019609.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr10:125526487 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr4:8613866 G>A maps to NM_001014447.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:8607800 G>C maps to NM_001014447.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr1:207685000 T>A did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:207669653 G>C maps to NM_000651.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:207896963 T>C maps to NM_175710.1 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr1:207644229 G>T maps to NM_001006658.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr16:1718162 C>T maps to NM_020825.3 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr16:1706143 A>G maps to NM_020825.3 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr16:1705978 A>G maps to NM_020825.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr9:131864767 G>A maps to NM_000755.3 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr1:197446955 C>T maps to NM_201253.2 R1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:197390460 G>C maps to NM_201253.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr3:3209359 T>C maps to NM_016302.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr9:35736113 C>T maps to NM_006368.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr7:28610068 C>T maps to NM_182898.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr16:3860636 G>A maps to NM_004380.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr16:3817814 T>C maps to NM_004380.2 K1052K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:3817822 C>A maps to NM_004380.2 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:3779017 C>T maps to NM_004380.2 G2010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:9984519 G>T maps to NM_001077415.2 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr8:67089640 C>T maps to NM_000756.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr7:30706863 C>A maps to ENST00000348438 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr7:30701794 G>T maps to ENST00000348438 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:36583677 C>G maps to NM_016441.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr6:43275359 T>C maps to ENST00000449267 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr6:43275461 T>C maps to ENST00000449267 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr4:1389121 C>T maps to NM_175918.3 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr4:1388535 G>A maps to NM_175918.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr4:1389129 G>A maps to NM_175918.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr4:1388523 A>G maps to NM_175918.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr4:1389147 T>C maps to NM_175918.3 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr6:49696472 G>T maps to NM_001190986.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr8:75924704 G>A maps to NM_031461.5 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:84940196 G>A maps to NM_031476.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr17:1326914 A>G maps to NM_016823.2 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:5827341 A>T maps to NM_001014809.1 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:20033151 G>A maps to NM_016652.4 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:152384628 C>T maps to NM_016190.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:17270750 G>A maps to NM_014675.3 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr10:99664545 C>T maps to NM_018058.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr10:99655167 G>A maps to NM_018058.4 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr10:99640009 G>A maps to NM_018058.4 C605C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr19:18856653 C>T maps to NM_001098482.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr19:18879482 C>T maps to NM_001098482.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr12:107393577 G>A maps to NM_004075.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr21:44589373 C>G maps to NM_000394.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr3:97595924 A>T maps to ENST00000182096 K15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr13:21063529 T>C maps to NM_015974.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr12:56669790 G>A maps to NM_004077.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr23:151909171 C>A did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr1:115280130 A>G maps to NM_001007553.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:47691343 A>G maps to NM_001316.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr5:149449863 G>T maps to NM_005211.3 Y400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:1407701 G>T did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr23:1422841 G>C did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr23:1413321 G>T did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr1:36932908 C>T maps to NM_156039.3 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr8:19263530 A>T maps to NM_018371.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr8:19297428 C>A maps to NM_018371.4 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:19363315 C>T maps to NM_018371.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:43651226 A>G maps to NM_018590.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr10:43659371 C>T maps to NM_018590.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:3855603 G>A maps to NM_033225.5 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr8:3245040 C>T maps to NM_033225.5 W919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr8:3216672 C>A did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr8:3224563 G>A maps to NM_033225.5 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr8:2832126 T>C maps to NM_033225.5 P2862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:33985174 T>A maps to ENST00000373381 T3573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr1:34238248 G>A maps to ENST00000373381 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr1:34180250 G>A maps to ENST00000373381 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:34209064 A>G maps to ENST00000373381 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr8:113358404 C>A maps to NM_198123.1 V2121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:113421241 T>C maps to NM_198123.1 V1805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr8:113650948 C>A maps to NM_198123.1 E1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr8:113347651 G>T maps to NM_198123.1 T2357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:113249530 G>T maps to NM_198123.1 Y3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr8:113301592 C>A did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr8:113516206 C>G did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr8:113237128 A>G maps to NM_198123.1 C3665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:113988243 A>G maps to NM_198123.1 H388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:113657335 A>G did not map to a codon.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr13:37678646 A>G maps to NM_145203.5 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr13:37679099 T>C maps to NM_145203.5 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr13:37678604 A>G maps to NM_145203.5 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:80202674 C>T maps to NM_001893.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr19:1980182 C>A maps to NM_001319.6 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr5:122911472 A>G maps to NM_001044723.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:470422 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:75980708 C>T maps to NM_001897.4 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:75982865 G>C maps to NM_001897.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr8:68107614 A>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:77257106 A>G maps to NM_001321.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr11:19213959 G>A maps to NM_003476.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr20:23618487 G>A maps to NM_000099.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr20:23548868 G>T maps to NM_080610.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr23:100088268 G>A did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr23:120009344 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr23:120008790 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr23:120009117 T>G did not map to a codon.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr15:71403497 T>G maps to NM_001102658.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr18:19995947 G>C maps to NM_172241.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr14:39783948 A>G maps to ENST00000396158 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr14:39763223 G>A maps to ENST00000396158 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr10:126683132 G>A maps to NM_022802.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr16:67644948 C>T maps to NM_006565.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr20:56099122 A>G maps to ENST00000423479 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr20:56089654 G>A maps to ENST00000423479 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr20:56087701 A>G maps to ENST00000423479 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr18:77475250 G>C maps to NM_004715.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr18:77488984 T>A maps to NM_004715.3 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr18:77513732 C>T maps to NM_004715.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr3:38009345 G>A maps to NM_001008392.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr15:44751275 A>T maps to NM_016396.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr15:44776438 T>G maps to NM_016396.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:70895505 T>C maps to NM_001902.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr1:70897871 C>A maps to NM_001902.5 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr5:138261072 A>C maps to ENST00000355078 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:138147873 G>T maps to ENST00000355078 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:138266341 C>T maps to ENST00000355078 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr2:80782890 G>T maps to ENST00000402739 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr10:67726368 C>A did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr10:68940122 G>A maps to NM_013266.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:41274904 C>T maps to NM_001904.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr11:57573352 G>A did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr17:3550807 C>T maps to NM_001031681.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr23:16685794 A>C did not map to a codon.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr1:15771155 C>T maps to NM_007272.2 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr8:11703215 G>T maps to NM_147783.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr11:66335106 C>T maps to NM_003793.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr14:25043507 G>A maps to NM_001911.2 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr1:150778607 A>T maps to NM_000396.3 Y71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr11:65650834 T>A maps to NM_001335.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:117375371 C>T maps to NM_033427.2 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr7:117417735 A>T maps to NM_033427.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr7:117364733 T>A maps to NM_033427.2 I1438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr7:117396641 G>A maps to NM_033427.2 I1105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:117407221 T>C maps to NM_033427.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:112997121 G>T maps to NM_018704.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr10:16957109 A>G maps to NM_001081.3 N2424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr10:17165679 G>A maps to NM_001081.3 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr10:16919091 A>G maps to NM_001081.3 R2970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr10:16873254 G>T maps to NM_001081.3 P3508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr10:17169881 A>G maps to NM_001081.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr10:16882523 A>G maps to NM_001081.3 G3279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr10:17110703 T>G maps to NM_001081.3 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:16916467 G>T maps to NM_001081.3 I3047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr10:16941135 A>G maps to NM_001081.3 P2819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr10:16967261 G>A maps to NM_001081.3 I2208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr10:104184283 T>A maps to NM_024040.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr7:148454215 C>T maps to NM_003592.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:35324144 G>T maps to NM_001198778.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:225449721 G>T maps to NM_003590.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:225422515 G>A maps to NM_003590.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr2:225342979 T>C maps to NM_003590.3 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr23:119694025 G>T did not map to a codon.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr6:43018714 A>G maps to NM_001168370.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43008725 G>A maps to NM_001168370.1 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr6:43020112 A>G maps to NM_001168370.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr6:43153718 G>A maps to ENST00000354495 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr6:43156327 G>T maps to ENST00000354495 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr6:43188336 G>A maps to ENST00000354495 K2141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43181267 T>C maps to ENST00000354495 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:33384695 C>G did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr7:101923412 G>T did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr7:101882762 G>A maps to ENST00000360264 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:111757855 C>T maps to NM_015267.3 N681N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:180810242 A>G maps to NM_020943.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr5:64314066 C>A maps to NM_005869.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr5:64082385 G>A maps to NM_005869.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr4:49034690 C>T maps to NM_025087.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:49032878 T>G maps to NM_025087.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr4:76943923 A>G maps to NM_001565.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr2:218999550 C>T maps to NM_001168298.1 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:136873380 G>T maps to NM_001008540.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr3:45988807 C>T maps to NM_006564.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr18:47812978 A>G maps to NM_001101654.1 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr18:47808971 G>A maps to NM_001101654.1 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr4:105393488 C>T maps to NM_025212.1 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr23:144909346 C>T did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:30578341 G>T did not map to a codon.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr23:30578380 T>C did not map to a codon.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr23:30577709 G>C did not map to a codon.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr23:35969398 G>A did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:35993322 C>A did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr23:35974188 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:35944235 C>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:35974128 T>C did not map to a codon.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr23:35969402 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr23:19971167 T>C did not map to a codon.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr23:19983777 T>A did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:75394773 T>C did not map to a codon.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr23:75397643 A>G did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr23:45016972 G>A did not map to a codon.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr23:45010907 C>T did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:40506302 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr23:40506318 A>T did not map to a codon.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr23:149100903 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr23:149102005 A>G did not map to a codon.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr23:106462182 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:134303601 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr23:134292202 A>G did not map to a codon.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr23:134294441 G>A did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr23:36156551 T>C did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr23:36103602 A>G did not map to a codon.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr23:36117960 C>T did not map to a codon.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr23:139038423 A>G did not map to a codon.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr23:139038511 G>T did not map to a codon.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr23:139040296 G>A did not map to a codon.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr23:139038873 G>A did not map to a codon.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr23:139038179 C>T did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:61511912 G>A maps to NM_001915.3 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr18:71930703 A>G maps to NM_148923.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr22:43024288 T>A did not map to a codon.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:172409899 T>C maps to NM_024843.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr8:145151519 C>T maps to NM_001916.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr15:22955132 T>C maps to NM_014608.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr15:22956551 C>T maps to NM_014608.2 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr15:22928511 T>C did not map to a codon.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr23:83128363 A>G did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr23:83128850 G>A did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr23:83128528 T>C did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr23:83128043 C>T did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:143957216 G>A maps to ENST00000377675 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr8:143960506 G>A maps to ENST00000377675 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:143956728 C>G did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr8:143957128 G>T maps to ENST00000377675 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr8:143957150 A>C maps to ENST00000377675 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:143958437 C>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr8:143958290 C>T maps to ENST00000377675 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr15:75042327 G>A maps to NM_000761.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr15:75047425 C>T maps to NM_000761.3 N516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr2:72371135 G>T maps to NM_019885.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr10:94828243 C>A maps to NM_183374.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr12:58158258 C>T maps to NM_000785.3 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr2:127950813 G>T maps to NM_001001665.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:41594409 C>T maps to NM_000766.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr10:96534858 G>A maps to NM_000769.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr10:96805618 G>A maps to NM_000770.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr10:96748761 C>T maps to NM_000771.3 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr22:42524794 A>G maps to NM_000106.4 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr22:42523538 A>G maps to NM_000106.4 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr10:135346308 T>C maps to NM_000773.3 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr19:41627950 C>T maps to NM_000774.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:41712374 C>T maps to NM_030622.6 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr7:1023012 C>T maps to NM_017781.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:46563726 A>T maps to NM_016593.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:99328743 T>A maps to ENST00000292414 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr7:99313482 C>A maps to ENST00000292414 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:47402389 A>C maps to ENST00000371904 Y152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr1:47401232 C>T maps to ENST00000371904 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr19:16032976 C>A did not map to a codon.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr19:16032977 T>A did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:15651479 C>T maps to NM_173483.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:15752326 C>A maps to NM_000896.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr8:59404309 A>C maps to NM_000780.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr8:65517237 C>A did not map to a codon.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr23:77528389 G>T did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr19:48977566 C>T maps to NM_017457.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr17:20130772 C>T maps to NM_001033553.1 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr2:242684221 T>A maps to NM_152783.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr4:4389418 C>G maps to NM_001040101.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr14:59835513 A>G maps to NM_014992.1 K1058K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39390644 A>G maps to NM_001343.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39394410 T>C maps to NM_001343.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr5:39376875 T>A maps to NM_001343.2 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:39381654 G>A maps to NM_001343.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr5:39382722 A>C maps to NM_001343.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:39383076 A>G maps to NM_001343.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:39377145 G>T maps to NM_001343.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:39383199 A>G maps to NM_001343.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr13:72204835 G>A maps to ENST00000359684 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr13:72440445 G>A maps to ENST00000359684 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:86087131 A>G did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:85906057 G>C did not map to a codon.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr23:86069819 G>T did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr14:59113725 G>A maps to NM_016651.5 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr14:59113095 G>A maps to NM_016651.5 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr14:59112840 C>T maps to NM_016651.5 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr11:61511888 C>T maps to NM_006133.2 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr11:61504730 C>T maps to NM_006133.2 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr11:61505672 G>A maps to NM_006133.2 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr7:6474528 A>T maps to NM_139179.3 L181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr11:61113378 A>G maps to NM_015533.3 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr19:13080509 G>A maps to NM_152654.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:109290783 G>T maps to NM_001917.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr9:90255296 T>C maps to NM_004938.2 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr9:90321651 C>T maps to NM_004938.2 V1222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr15:64218209 C>A maps to NM_014326.3 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr19:3964715 C>T maps to NM_001348.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr4:100787279 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr4:100738084 A>G maps to NM_014395.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr4:100756842 C>T maps to NM_014395.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:136736936 C>A did not map to a codon.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:136678171 T>C did not map to a codon.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr19:1433801 C>T maps to NM_170711.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr19:1432573 T>C maps to NM_018959.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr3:16633628 C>T maps to NM_001190811.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr3:16638274 A>G maps to NM_001190811.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr3:16630167 C>G maps to NM_001190811.1 *316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr9:121930243 C>T maps to NM_014618.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:42828062 C>T maps to NM_145663.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr2:120128349 C>A maps to NM_001178017.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr2:120129818 A>T did not map to a codon.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr5:176893973 C>A maps to ENST00000393565 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr5:176894481 C>G maps to ENST00000393565 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr16:90075258 C>T maps to ENST00000392973 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr11:20177782 G>A maps to ENST00000227256 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr12:45429898 T>G did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:37800964 G>T maps to NM_024345.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr23:125685458 C>T did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr23:125686495 G>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:125685497 A>C did not map to a codon.
Sequencing variant TCGA-B2-3923-01A-01D-1458-08 chr23:125299312 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:125299513 G>A did not map to a codon.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr8:104444936 T>C maps to NM_015420.6 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:104427571 T>A maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr2:172291645 C>G maps to NM_025000.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:172333420 T>A maps to NM_025000.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr14:73412734 G>A maps to NM_015604.3 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr14:73422349 T>G maps to NM_015604.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:88885731 G>A maps to NM_152418.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr1:168034952 A>T maps to ENST00000367840 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr1:167974002 A>G maps to ENST00000367840 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:160209813 A>G maps to NM_015726.3 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr23:27998266 G>A did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr23:27997689 C>T did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:27766432 G>T did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr23:27766774 C>T did not map to a codon.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr23:27765416 G>A did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr3:98600600 A>G maps to ENST00000326857 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr18:50918088 C>G maps to NM_005215.3 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr18:50985742 T>A maps to NM_005215.3 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr6:24357768 A>T maps to NM_016356.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:155219150 A>T maps to NM_017639.3 P1650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr4:155253990 C>T maps to NM_017639.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr4:155219312 C>T maps to NM_017639.3 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155163875 C>T maps to NM_017639.3 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155254035 C>T maps to NM_017639.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155254287 G>A maps to NM_017639.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr13:36521537 C>T maps to NM_004734.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr13:36383186 A>G maps to NM_004734.4 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr4:151169527 C>A maps to NM_001040261.4 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr10:115609996 T>A maps to NM_014881.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr10:115608964 A>G maps to NM_014881.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr12:91550948 C>T maps to NM_133503.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:53376260 G>T maps to ENST00000480258 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:126201298 G>T did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:155015934 G>T maps to NM_152494.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr1:154995892 G>A maps to NM_144622.2 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr1:155004242 C>T maps to NM_144622.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr13:95121258 G>A maps to NM_001129889.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr16:30435759 G>A maps to NM_024096.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr16:30435592 C>T maps to NM_024096.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:182681754 A>G maps to NM_020640.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:20871210 A>G maps to NM_173475.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr16:20871249 G>A maps to NM_173475.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr4:52765462 T>C maps to ENST00000451288 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr23:110654010 C>T did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:17425184 C>A maps to NM_024050.5 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:61081865 G>A maps to NM_001923.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr11:61070126 T>C maps to NM_001923.3 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:15956838 C>T maps to NM_032341.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr12:57910756 A>G maps to NM_001195056.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr4:101109220 C>A maps to NM_145244.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr6:110714418 C>T maps to NM_003649.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr6:30866811 C>T maps to NM_013994.2 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:30864434 C>T maps to NM_013994.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:162729663 G>A maps to NM_006182.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr2:15746320 A>C maps to NM_004939.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr12:31242980 C>A maps to NM_030653.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr12:31256927 C>G maps to NM_152438.1 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr12:31242980 C>A maps to NM_030653.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr2:118577222 A>G did not map to a codon.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr16:70405335 G>A maps to NM_018332.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:112308357 G>A did not map to a codon.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr12:49233686 C>T maps to NM_004818.2 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr14:94519371 C>T maps to NM_020414.3 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr14:94528592 G>A maps to NM_020414.3 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:125791251 C>A maps to NM_013264.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:134706892 G>T did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr23:134715016 C>T did not map to a codon.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr20:47835897 A>G maps to NM_017895.7 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr20:47835942 A>G maps to NM_017895.7 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr9:135538025 T>C maps to NM_022779.7 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:41203495 C>T did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:41202083 G>C did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr23:41205658 C>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:41200809 T>C did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr23:41202003 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr24:15024910 T>A did not map to a codon.
Sequencing variant TCGA-BP-4804-01A-02D-1373-10 chr5:176942815 A>G maps to NM_016222.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr17:61886960 T>C maps to NM_203499.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr5:134126241 G>A maps to ENST00000452510 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr5:134153323 G>T maps to ENST00000452510 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:62496042 A>G maps to NM_004396.3 *615Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:62500169 T>C maps to NM_004396.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:23018220 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr23:23019107 G>A did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr23:23019820 C>T did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:113596867 G>C maps to NM_001111322.1 R821R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr12:113618758 C>T maps to NM_001111322.1 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr12:113610194 G>A maps to NM_001111322.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr9:32488008 C>T maps to NM_014314.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr9:32459419 G>T maps to NM_014314.3 C810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr11:118656897 C>T maps to NM_004397.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr4:169382990 C>T maps to NM_001012967.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:169317121 C>T maps to NM_001012967.1 R1215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:687970 C>A maps to NM_021008.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr8:91013752 G>A maps to NM_001359.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr16:460351 T>G maps to NM_020664.3 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr16:461364 C>T maps to NM_020664.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr1:161093707 C>A maps to ENST00000368005 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr16:90023965 G>A maps to NM_207514.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr16:90025606 A>G maps to NM_017702.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr8:6783458 A>C maps to NM_001926.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr6:49936557 T>C maps to NM_001037729.1 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr6:49931769 G>A maps to NM_001037499.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr6:49928061 G>T maps to NM_001037499.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr20:29891068 G>A maps to NM_001037731.1 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr20:30037859 T>A maps to NM_153324.2 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr20:238440 T>C maps to NM_207469.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:197684158 A>G did not map to a codon.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr7:140301429 A>C maps to NM_015689.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr7:140301429 A>C maps to NM_015689.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:111734926 C>T maps to NM_024901.3 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:142178353 C>A maps to NM_014957.2 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:142186772 C>T maps to NM_014957.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr8:142186847 C>A maps to NM_014957.2 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr8:142175379 G>A maps to NM_014957.2 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr8:142204325 C>G maps to NM_014957.2 G1197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:66010114 C>G did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr15:66031103 A>G maps to ENST00000443035 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr15:65957693 C>T maps to ENST00000443035 W1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:65983019 C>T maps to ENST00000443035 V1304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr15:66044740 G>A maps to ENST00000443035 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr15:65982750 A>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:153904718 G>A maps to NM_014856.2 G1319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr1:153916541 A>T maps to NM_014856.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr1:153907305 T>C maps to NM_014856.2 Q901Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:153907293 C>T maps to NM_014856.2 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:31551283 C>T maps to NM_144973.3 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr5:59895074 C>A maps to NM_018369.2 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:59894910 T>C maps to NM_018369.2 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr12:100660754 G>A maps to ENST00000422147 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:32193640 A>T maps to NM_001136029.1 K275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr22:32301996 T>G maps to NM_001136029.1 S1479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr22:32198824 G>C did not map to a codon.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr8:121021275 T>C maps to NM_022783.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:89056232 C>T maps to NM_017996.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr7:24758692 G>A maps to NM_001127453.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr7:24738851 T>C maps to NM_001127453.1 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr9:117165102 G>T maps to NM_015404.3 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr8:145540324 G>C maps to NM_012079.4 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr8:145540218 A>T maps to NM_012079.4 *489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:75509460 C>T maps to NM_032564.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr22:19055738 C>A did not map to a codon.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr22:19076917 C>A maps to NM_005137.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr22:20307318 A>G maps to NM_033257.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:20077781 G>C did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:14620498 G>A maps to NM_004080.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:234368473 C>T maps to NM_152879.2 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:185960323 T>A maps to NM_001346.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr13:42793829 T>C maps to NM_178009.2 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:50129520 T>A did not map to a codon.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr23:50147056 G>T did not map to a codon.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr23:50213422 T>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:50144041 T>C did not map to a codon.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr4:961062 G>A maps to NM_001347.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:46388174 G>A maps to NM_001105540.1 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:46401422 G>T maps to NM_001105540.1 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr10:99344531 C>T maps to ENST00000416867 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:99358954 C>T maps to NM_138413.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:79945301 G>A maps to NM_000791.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr17:27225662 C>T maps to NM_144683.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:12628410 T>C maps to NM_004753.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr14:24424291 G>T maps to NM_021004.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr14:24459471 C>T maps to NM_198083.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr10:12142205 C>A maps to NM_018706.5 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr10:12139742 G>A maps to NM_018706.5 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:30622527 C>A maps to NM_003587.4 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr6:30640453 G>T maps to NM_003587.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr6:30623373 C>T maps to NM_003587.4 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:54591350 A>G maps to NM_019030.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr5:54579537 T>C maps to NM_019030.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr3:47891145 G>A maps to NM_138615.2 W1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr3:47882519 C>A maps to NM_138615.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr10:127548369 G>C maps to NM_018180.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr19:47856880 C>G maps to NM_014681.5 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr20:37623475 C>A maps to NM_021931.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr20:37597790 G>T maps to NM_021931.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr20:37632408 T>A maps to NM_021931.3 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:37653977 C>T maps to NM_021931.3 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr3:154022914 T>A maps to NM_020865.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr12:125435350 C>T did not map to a codon.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr17:57663567 A>G maps to NM_024612.4 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr17:57656853 C>T maps to NM_024612.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr17:57676167 T>C maps to NM_024612.4 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr17:57656853 C>T maps to NM_024612.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:39088915 T>C maps to NM_198963.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:40263344 G>A maps to NM_024119.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:41582144 G>A maps to NM_004941.1 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr17:41582096 G>T maps to NM_004941.1 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr1:182827872 A>G maps to NM_001357.4 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr5:140896573 G>T maps to ENST00000398557 A1221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr5:140954548 G>T maps to ENST00000398557 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr23:96369938 G>C did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr23:96212937 C>T did not map to a codon.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr14:95582927 A>G maps to NM_177438.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr14:95577718 C>A maps to NM_177438.2 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:95556879 G>T maps to NM_177438.2 A1908A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr14:95557549 C>A maps to NM_177438.2 R1839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr14:95579560 T>C maps to NM_177438.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr14:95557672 T>C maps to NM_177438.2 K1798K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr20:61527635 G>A maps to NM_033081.2 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr20:61537211 G>A maps to NM_022105.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr1:54370441 A>G maps to NM_000792.5 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr14:80669283 A>G maps to NM_001007023.2 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr21:47958480 G>A maps to ENST00000318711 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr21:47987405 G>T maps to ENST00000318711 V1530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr12:51127943 T>C maps to NM_173602.2 T1336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:51072519 A>G maps to NM_173602.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr10:390775 G>T maps to NM_014974.2 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr10:375378 G>T maps to NM_014974.2 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr10:375465 G>C maps to NM_014974.2 A1220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr10:445050 T>A maps to NM_014974.2 K420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr9:93375536 C>T maps to NM_017594.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr15:66618703 T>C did not map to a codon.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr1:223178701 T>C maps to NM_032890.2 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr1:223178161 T>C maps to NM_032890.2 G1141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr15:40661342 C>T maps to NM_033510.1 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr15:40660394 G>A maps to NM_033510.1 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr15:40660191 C>T maps to NM_033510.1 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr11:65547486 G>A maps to NM_138368.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr4:107846994 G>T maps to NM_014421.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr11:111915860 G>A did not map to a codon.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr11:111930749 C>G maps to NM_001931.4 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:107556127 A>T maps to NM_000108.3 K288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:107545819 T>C maps to NM_000108.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr3:38159472 A>G maps to NM_007335.2 S1554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr3:38139263 C>A maps to NM_007335.2 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:196888576 A>T maps to NM_004087.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr11:83770382 T>C maps to NM_001142699.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr18:3502637 A>G maps to NM_004746.2 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr8:1513949 C>T maps to ENST00000357934 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:35331686 C>T maps to NM_001080418.1 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:101198409 C>T maps to NM_003836.5 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:41222314 G>T did not map to a codon.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr15:41228879 G>A maps to NM_019074.3 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr2:172966927 G>T maps to NM_004405.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr17:48050512 G>C maps to NM_138281.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr1:44684378 A>T maps to NM_019100.4 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr10:124358419 C>G maps to ENST00000368915 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr10:124340397 G>T maps to ENST00000368915 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:124351861 C>A maps to ENST00000368915 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr10:124361508 T>C maps to ENST00000368915 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr10:124399734 C>T maps to ENST00000368915 V2374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:46972768 G>A maps to NM_147192.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr1:46976716 C>T maps to NM_147192.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr23:32862974 T>C did not map to a codon.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr23:31187595 A>T did not map to a codon.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr23:31196784 C>A did not map to a codon.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr23:32834667 A>G did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:31854855 T>G did not map to a codon.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr23:31792261 C>G did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:31496340 T>G did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr23:31152281 C>G did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr23:32408278 G>T did not map to a codon.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr23:32382804 G>C did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr23:31645806 G>T did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:32305750 G>T did not map to a codon.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr5:78347128 A>G maps to NM_013391.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:36003990 G>A maps to NM_033317.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr4:88583133 C>T maps to NM_004407.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:88584222 G>A maps to NM_004407.3 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:88584282 A>G maps to NM_004407.3 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr9:990588 C>T maps to NM_021240.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr1:53925248 C>T maps to NM_033067.1 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:46290078 C>T maps to NM_004943.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr5:118569033 G>T did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr5:118560453 T>C maps to NM_005509.4 T2755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr5:118502424 A>G maps to NM_005509.4 E1695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:118479555 T>C maps to NM_005509.4 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr15:51837939 A>C maps to NM_001174116.1 L257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr15:51778457 G>T maps to NM_001174116.1 S1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr15:51778459 A>G maps to NM_001174116.1 T1764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:51857283 C>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:51790749 T>G maps to NM_001174116.1 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr15:51828387 T>G maps to NM_001174116.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr10:70196868 A>C maps to NM_001080449.1 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr10:70196868 A>C maps to NM_001080449.1 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:52432934 A>G maps to ENST00000273600 V4117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr3:52422875 C>T maps to ENST00000273600 L3204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr12:124272411 A>T maps to NM_207437.3 K434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr7:21784606 A>T maps to NM_003777.3 T2819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr7:21639511 C>T maps to NM_003777.3 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr7:21737743 A>G maps to NM_003777.3 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr7:21678589 C>A maps to NM_003777.3 Y1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr3:57431083 G>T maps to NM_178504.4 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:76451800 G>A maps to ENST00000389840 Y3351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr17:76506510 G>T maps to ENST00000389840 V1393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr17:76496392 G>A maps to ENST00000389840 D1864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr17:76449534 G>T maps to ENST00000389840 V3459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr17:7669720 G>A maps to NM_020877.2 E1199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr17:7689596 C>T maps to NM_020877.2 R2095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr16:21136610 G>C maps to NM_017539.1 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr16:20999307 A>G maps to NM_017539.1 I2227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr16:21065765 C>T maps to NM_017539.1 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr16:21049159 C>A maps to NM_017539.1 E1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr5:13883075 G>T maps to NM_001369.2 A1037A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr5:13753410 A>T maps to NM_001369.2 P3601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:13727613 A>G did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr5:13814811 C>A maps to NM_001369.2 E2378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr5:13708237 C>T maps to NM_001369.2 W4444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr2:84912546 T>C maps to NM_001370.1 I2338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:84846835 T>G maps to NM_001370.1 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:84777108 A>T maps to NM_001370.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr2:84928426 G>T maps to NM_001370.1 L2675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:196753117 A>T maps to NM_018897.2 L1757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:196749320 T>C maps to NM_018897.2 Q1917Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr2:196750887 G>A maps to NM_018897.2 R1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr6:38994430 G>A maps to ENST00000327475 T4596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr6:38758104 G>A maps to ENST00000327475 W890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr17:11778480 C>A maps to NM_001372.3 V3486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr17:11845735 T>A maps to NM_001372.3 C4259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr17:11593687 C>T maps to NM_001372.3 R1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr17:11833187 T>C maps to NM_001372.3 I3961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr17:11865497 A>G maps to NM_001372.3 E4386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:72306226 G>T maps to NM_023036.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr15:78565449 A>G maps to NM_018602.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:186299284 C>T maps to NM_016306.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:78481810 G>A maps to NM_007034.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr7:157177600 T>C maps to NM_058246.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr3:128181551 G>A maps to NM_153330.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:108212286 G>A maps to NM_012328.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:183594618 G>T maps to NM_018981.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr2:183640092 T>C maps to NM_018981.1 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:183623958 T>C maps to NM_018981.1 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr2:183584761 T>A maps to NM_018981.1 L78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr2:183622507 G>A maps to NM_018981.1 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr2:183616890 A>G maps to NM_018981.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr1:6741000 G>A maps to NM_018198.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr3:132245125 G>A did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:132193850 A>G maps to NM_015268.3 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:132196968 T>C maps to NM_015268.3 I898I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr3:132193880 A>G maps to NM_015268.3 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr12:56221610 G>A maps to NM_032364.5 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr12:56221620 A>G maps to NM_032364.5 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr12:56221610 G>A maps to NM_032364.5 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr12:56216894 T>C maps to NM_032364.5 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr13:43652745 A>G did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr13:43652821 A>T maps to NM_013238.2 V103V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B1-A657-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr7:102960088 T>A maps to NM_014377.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr12:49743365 T>C maps to NM_024902.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr9:114429211 T>C maps to NM_004125.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr9:114429093 G>A did not map to a codon.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr7:73097663 G>A maps to NM_032317.2 S30S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EV-5903-01A-11D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:27503081 A>T maps to ENST00000406962 K103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr1:65831860 T>C maps to ENST00000371069 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:38022627 C>T maps to NM_003462.3 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr1:84876611 A>T maps to NM_021233.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr2:230411680 G>T maps to NM_139072.3 C325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr2:230253113 T>G did not map to a codon.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr11:6592960 C>T maps to NM_144666.2 A4669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr11:6585251 C>T maps to NM_144666.2 C3394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr11:6592053 C>T maps to NM_144666.2 R4438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:6592936 G>T maps to NM_144666.2 A4661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:130982345 G>A maps to ENST00000372923 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:32886680 T>C maps to ENST00000381000 Y506Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:172037990 G>A maps to ENST00000359070 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:101716911 G>A maps to ENST00000342239 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr2:25498412 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:25469541 C>T maps to NM_175629.1 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr20:31375211 G>A maps to NM_006892.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr20:31386265 G>T maps to NM_006892.3 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr2:220239738 G>A maps to NM_012100.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr10:98064449 G>T maps to NM_004088.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:94335472 G>A maps to NM_014597.4 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr10:129209145 G>A maps to ENST00000398025 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr10:128830576 T>A maps to ENST00000398025 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr10:129202629 C>T maps to ENST00000398025 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:129216675 G>A maps to ENST00000398025 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr2:225637921 C>T maps to NM_014689.2 V2052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:225661098 T>C maps to NM_014689.2 G1624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr2:225637921 C>G maps to NM_014689.2 V2052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr2:225761076 A>G maps to NM_014689.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr23:117707901 G>T did not map to a codon.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr23:117752677 G>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:117761499 T>C did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr23:117700142 A>T did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr23:117819735 G>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:117731502 A>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:117786021 T>C did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr5:169494674 C>T maps to NM_004946.2 F1543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr5:169504742 T>C maps to NM_004946.2 R1632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr3:51198059 C>T maps to NM_004947.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:51246203 G>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:51315163 G>A maps to NM_004947.4 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr7:111387451 C>T maps to ENST00000428084 K1488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr7:111379462 G>T maps to ENST00000428084 S1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:111368530 C>T maps to ENST00000428084 P1909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr8:25158134 G>T maps to NM_024940.6 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr8:25167944 C>G maps to NM_024940.6 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr8:25203088 C>T maps to NM_024940.6 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr19:11314959 G>A maps to ENST00000319867 P1712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:11326076 T>C maps to ENST00000319867 S1364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr19:11312612 G>A maps to ENST00000319867 H1882H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr1:62979389 A>G maps to ENST00000371140 Y1372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr1:63119665 T>C maps to ENST00000371140 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr1:62961313 A>T maps to ENST00000371140 S1654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr9:406988 T>A maps to NM_203447.3 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr9:304679 G>A maps to NM_203447.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:441957 C>T maps to NM_203447.3 V1813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr13:99481632 G>A maps to ENST00000428223 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:99540612 C>T did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr13:99476684 T>C maps to ENST00000428223 E1699E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr16:57509511 G>A maps to NM_018110.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr16:57508841 C>T maps to NM_018110.3 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr4:3494663 A>C maps to ENST00000389653 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr6:31939425 T>C maps to NM_005510.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr21:34955917 A>C maps to NM_017613.2 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr6:83823097 A>G maps to NM_015018.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:83862076 A>G maps to NM_015018.2 L2040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr6:83862019 T>A maps to NM_015018.2 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr21:37591689 T>C maps to NM_005128.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr21:37603370 C>T maps to NM_005128.2 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:2216710 G>A maps to ENST00000221482 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr19:2214516 G>A maps to ENST00000221482 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:2229789 A>C maps to NM_032482.2 *1538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:2211149 G>A maps to ENST00000221482 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:2210829 C>T maps to ENST00000221482 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr19:2207666 C>T maps to ENST00000221482 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr11:118969111 C>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:118971119 T>G did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr6:30917884 C>G maps to NM_080870.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr16:68009727 G>T maps to NM_022357.3 Y494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:65113419 A>C maps to NM_006268.3 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:65113197 G>A maps to NM_006268.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr1:155112593 C>A maps to NM_018973.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:116510851 C>G maps to NM_020868.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:116572491 T>C maps to NM_020868.3 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr2:116594278 C>A maps to NM_020868.3 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr2:116510750 G>T maps to NM_020868.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr11:66255470 T>A maps to NM_005700.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:66260241 G>A maps to NM_005700.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr2:162865774 G>A maps to NM_001935.3 N621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr19:4719860 A>T did not map to a codon.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr19:4704157 G>A maps to ENST00000357909 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr3:109023470 T>C maps to NM_138815.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:7867785 T>A maps to NM_199286.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:168698361 C>T maps to NM_001937.4 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr7:35029519 C>T maps to NM_015283.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr1:97564119 C>T maps to NM_000110.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:98058808 T>A maps to NM_000110.3 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr8:105479133 C>T maps to NM_001385.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr8:105478932 G>A maps to NM_001385.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:26513188 C>T maps to NM_001197293.1 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr10:134012455 C>A maps to NM_006426.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr1:111667501 G>T maps to NM_178454.4 C67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:174870045 G>A maps to NM_000794.3 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:113295343 A>G maps to ENST00000355319 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr11:113295087 C>T did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:113288846 C>T maps to ENST00000355319 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:113858391 T>A maps to NM_000796.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr3:113890722 G>T maps to NM_000796.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:9784912 C>T maps to NM_000798.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr4:9783961 G>T maps to NM_000798.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr4:9784111 T>C maps to NM_000798.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr23:100497380 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr23:100509875 G>A did not map to a codon.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr18:28720255 G>A maps to NM_024421.2 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr18:28651757 A>G maps to ENST00000438199 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr18:28598102 A>G maps to NM_001941.3 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr18:28611061 C>A maps to NM_001941.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr18:28598132 C>T maps to NM_001941.3 W389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr21:41416059 T>C maps to NM_001389.3 A1776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr21:41385098 G>A maps to NM_001389.3 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr21:41414411 G>A maps to NM_001389.3 L1858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr21:41514494 G>A maps to NM_001389.3 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr21:41384993 G>A maps to NM_001389.3 N2002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr11:117332277 C>G maps to NM_020693.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr11:117647628 G>T maps to NM_020693.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr11:117309652 C>A maps to NM_020693.2 S1457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr11:117307844 G>A maps to NM_020693.2 Y1631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr6:116757865 C>T maps to NM_013352.2 N745N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr18:65181608 A>T maps to NM_032160.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr18:65180322 G>C maps to NM_032160.2 S518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr18:65181491 A>G maps to NM_032160.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr18:28935224 C>T maps to NM_001942.2 H1022H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr18:29116285 T>C maps to NM_001943.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr18:29054159 A>G maps to NM_001944.2 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr18:29046490 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr18:28972162 C>T maps to NM_001134453.1 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr20:35381211 A>T maps to NM_001145315.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:7583191 C>A maps to NM_004415.2 I1899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr6:7562979 T>A maps to NM_004415.2 Y231*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AT-A5NU-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B2-5635-01A-01D-1534-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-GL-A59R-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HE-A5NF-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-IZ-A6M8-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-KN-8421-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr4:88536447 C>T maps to NM_014208.3 D878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr4:88536450 C>T maps to NM_014208.3 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr4:88536456 T>C maps to NM_014208.3 D881D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr4:88536459 C>T maps to NM_014208.3 S882S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KN-8436-01A-11D-2310-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-KN-8436-01A-11D-2310-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-KO-8408-01A-11D-2310-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-KO-8411-01A-11D-2310-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-P4-A5EB-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-PJ-A5Z9-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-Q2-A5QZ-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr6:56463336 T>C maps to ENST00000361203 A3744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr6:56399925 T>C maps to ENST00000361203 E5434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr6:56484744 C>A maps to ENST00000281662 E1927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr6:56394512 G>T maps to ENST00000361203 G5565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr6:56357197 G>A maps to ENST00000361203 Q6651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:56501421 C>T maps to ENST00000361203 W787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr6:56417322 C>A maps to ENST00000361203 E5212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:205132070 G>A maps to NM_015375.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr2:25754364 T>C maps to NM_021907.3 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr2:25754450 T>A maps to NM_021907.3 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:25799754 G>A maps to NM_021907.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr6:15627642 C>A maps to NM_032122.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr5:118280325 A>G maps to NM_173666.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr7:76112347 C>G maps to NM_020892.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:7147937 G>T maps to NM_015343.4 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:7147901 A>G maps to NM_015343.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr15:45453966 G>A maps to NM_175940.1 Q1296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:45445602 G>C maps to NM_175940.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:45427437 A>G maps to NM_175940.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr15:45389451 C>T maps to NM_014080.4 A1277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr15:45398797 G>A maps to NM_014080.4 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr15:45387205 G>A maps to NM_014080.4 H1441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr15:45408397 C>T maps to NM_207581.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr16:68109278 C>A maps to NM_017803.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr16:68071946 T>A maps to NM_017803.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr17:35872565 T>C maps to NM_007026.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr12:12629997 A>T maps to NM_030640.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr2:183960370 G>A maps to NM_080876.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr23:44703516 C>T did not map to a codon.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr23:44703527 C>T did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:167096128 A>G maps to NM_001080426.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:167095900 A>C maps to NM_001080426.1 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:167096183 G>T maps to NM_001080426.1 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:167097706 A>T maps to NM_001080426.1 A1113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:167088686 G>A maps to NM_001080426.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr23:152915554 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:152915502 G>A did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr10:82112338 G>A maps to NM_138812.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr18:46798649 C>G maps to NM_017653.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr14:102505822 C>T maps to NM_001376.4 N3845N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr11:102991434 G>C maps to NM_001080463.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:103093808 T>G maps to NM_001080463.1 L3116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr11:103091359 C>A maps to NM_001080463.1 V2985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:56164456 T>A maps to NM_080677.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:206822276 C>T maps to NM_003582.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:71838424 C>A maps to NM_001130987.1 I1336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr2:71896301 C>A maps to NM_001130987.1 L1869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:207564615 T>C did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr13:96238361 T>C maps to NM_198968.2 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr6:20481596 C>A maps to NM_001949.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr8:86118417 C>A maps to ENST00000256117 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr12:77426861 A>G maps to NM_203394.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr12:77417896 G>T maps to NM_203394.2 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr12:77444476 C>T maps to NM_203394.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr12:77424036 G>T maps to NM_203394.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr3:121591510 C>A maps to NM_018456.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr3:121554182 C>T maps to NM_018456.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:23540827 C>T maps to NM_001083614.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr16:23546344 C>A maps to NM_001083614.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr8:110567064 G>A maps to ENST00000276658 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr5:158250250 A>G maps to NM_024007.3 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr5:158158100 A>G maps to NM_024007.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr5:158526462 G>T maps to NM_024007.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr8:25744373 T>C maps to NM_022659.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:25715867 G>A maps to NM_022659.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr8:25744301 G>T maps to NM_022659.2 C326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr10:131671767 C>A maps to ENST00000355311 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr10:131761927 G>A maps to ENST00000355311 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr19:4237066 A>G maps to NM_005755.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr1:21584022 C>A maps to NM_001397.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:21546591 G>C maps to NM_001397.2 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr3:184001748 T>A maps to NM_014693.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:233347835 A>G maps to NM_004826.2 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:233350796 G>A maps to NM_004826.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr6:127611394 T>C maps to NM_001139510.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:53362194 T>C maps to ENST00000371522 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr19:11618639 G>A maps to NM_016581.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr6:139164270 G>A maps to NM_001195037.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr23:69243091 G>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:65819456 T>G did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:109527286 C>T maps to ENST00000376651 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr2:109513431 G>T maps to ENST00000376651 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:67909956 T>A maps to NM_014329.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:67910483 G>A maps to NM_014329.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:67913802 C>T maps to NM_014329.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr14:21238698 C>T maps to NM_022360.4 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr20:33703673 A>C maps to NM_018217.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr5:83402564 C>A maps to NM_005711.3 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr6:12292679 C>T maps to NM_001955.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr20:57876744 C>T maps to NM_207034.1 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr4:148463688 C>T maps to NM_001957.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr6:74228229 G>T maps to NM_001402.5 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr20:62128978 C>T maps to NM_001958.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr8:144668952 T>A maps to NM_032378.4 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr8:144671243 C>A maps to NM_032378.4 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:22274499 C>T maps to NM_013302.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:22291587 C>T maps to NM_013302.3 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr3:127872505 C>T maps to NM_021937.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr8:49643117 A>T maps to NM_024593.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr8:49647694 G>A maps to NM_024593.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:60484527 T>C maps to NM_001144933.1 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr17:28407884 G>C maps to NM_198529.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:28405488 G>A maps to NM_198529.3 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr13:22088515 C>T maps to NM_152726.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr8:16948086 T>A maps to NM_181723.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr8:16935351 C>T maps to NM_181723.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:19925988 G>C maps to NM_144715.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr23:44108154 G>T did not map to a codon.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr23:44131999 T>C did not map to a codon.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr1:155104090 A>G maps to NM_004428.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:155036406 C>T maps to NM_182689.1 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:68060245 A>T did not map to a codon.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr13:107164901 C>T maps to NM_004093.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr8:132968017 C>T maps to NM_015137.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr14:23826851 C>T maps to NM_005864.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:23828917 G>A maps to NM_005864.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr4:110909738 G>T did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr23:13636138 A>T did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr23:13635855 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr23:13618145 T>C did not map to a codon.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr6:32134516 G>A maps to NM_030652.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:38418271 C>A maps to ENST00000354891 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr1:231502191 T>A maps to NM_022051.2 K416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:41306602 T>A maps to NM_053046.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr8:22548537 G>A maps to NM_004430.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:63169916 G>A maps to NM_015252.3 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr2:62934346 A>G maps to NM_015252.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr11:65349885 G>A maps to NM_001099409.1 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr11:64645858 C>T maps to NM_006795.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr19:48239720 C>A maps to NM_014601.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:42193091 C>T maps to NM_139265.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr11:34670584 G>C maps to NM_012153.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:184922366 G>A maps to NM_001966.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr9:140695436 G>A did not map to a codon.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr9:140671278 C>T maps to NM_024757.4 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr15:49170495 C>A maps to NM_014335.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr19:40023307 A>G maps to NM_152361.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr17:39846194 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:20152120 C>A did not map to a codon.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:150264606 G>C maps to NM_032025.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:37365710 G>A maps to NM_001135651.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr2:37374006 T>A maps to NM_001135651.1 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr2:88874520 A>T maps to NM_004836.5 L827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:88890365 C>T maps to NM_004836.5 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr15:40268967 C>A maps to NM_001013703.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr15:40284410 G>A maps to NM_001013703.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr15:40257896 A>G maps to NM_001013703.2 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr15:40235658 A>G maps to NM_001013703.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr1:36372682 C>T maps to NM_012199.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:36354061 G>A maps to NM_012199.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr1:36358771 T>C maps to NM_012199.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:36358771 T>C maps to NM_012199.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr8:141549417 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr8:141545587 C>A maps to NM_012154.3 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr1:36474309 T>A maps to NM_024852.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:36319143 C>T maps to NM_017629.2 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr14:67848334 T>C maps to NM_004094.4 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr23:24086217 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:24089814 C>T did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr23:24075765 A>G did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr7:2404083 A>G maps to ENST00000314800 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:109215295 A>T maps to NM_001568.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr19:10229836 G>T maps to NM_003755.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr19:10230529 A>G maps to NM_003755.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr15:44853256 A>T maps to NM_003758.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr22:38247399 T>C maps to ENST00000262832 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:78113888 A>G maps to NM_014740.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:78120724 C>G maps to NM_014740.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr12:53416355 T>C maps to ENST00000438209 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr22:31851206 A>T maps to NM_019843.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr22:31850207 G>A maps to NM_019843.3 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr3:184041028 G>T maps to NM_001194947.1 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:184038752 G>A maps to NM_001194947.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr11:10825487 A>C maps to ENST00000429377 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr11:10825558 C>A maps to ENST00000429377 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr11:10823661 C>T maps to ENST00000429377 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr1:21226400 T>C maps to NM_001198801.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr1:21221940 G>A maps to NM_001198801.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:21268371 C>T maps to NM_001198801.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:21226357 C>A maps to NM_001198801.1 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr17:7214801 T>C did not map to a codon.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr10:81272626 G>A maps to NM_001099692.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:100015353 A>C maps to NM_015904.3 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:99978206 A>T maps to NM_015904.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr18:48510775 C>A maps to NM_018696.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:12898189 A>G maps to NM_018127.6 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr17:12920218 G>A maps to NM_018127.6 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr17:12898342 C>T maps to NM_018127.6 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:852900 G>T maps to NM_001972.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr19:8038747 G>A maps to ENST00000351593 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr9:23705048 A>G maps to ENST00000359598 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr19:11565538 C>T maps to NM_001420.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:11568979 C>T maps to NM_001420.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr13:41507955 G>A maps to NM_172373.3 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr13:41525465 T>A maps to NM_172373.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr4:139983075 C>T maps to ENST00000379550 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:129201250 A>G did not map to a codon.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr22:37770866 G>A maps to NM_052906.3 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr22:37769177 G>T maps to NM_052906.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr22:37769170 C>A maps to NM_052906.3 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr23:47498681 G>A did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:205588956 C>G maps to NM_021795.2 *406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:18557589 G>A maps to NM_006532.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:44067733 C>T maps to NM_025165.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr7:37311448 T>C maps to NM_014800.9 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr7:37136305 T>C maps to NM_014800.9 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr16:67236621 T>A maps to NM_024712.3 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr16:67236113 C>T maps to NM_024712.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:67233264 C>A maps to NM_024712.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr7:73471994 T>C maps to ENST00000358929 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr1:43829742 C>T maps to NM_022821.2 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:11005703 A>C maps to NM_017770.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr18:33709980 A>T maps to ENST00000442325 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr1:79402058 T>C maps to NM_022159.3 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr4:101331486 G>T maps to NM_016242.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:101386643 G>A maps to NM_016242.3 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:153609310 C>T did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:1825567 A>C did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr16:1825397 G>T maps to NM_001010865.1 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr22:29627007 G>T did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr2:27305347 C>T maps to NM_007046.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr18:2891707 C>G maps to NM_032048.2 S528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr18:2890859 G>T maps to NM_032048.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr20:39990047 T>G maps to NM_052846.1 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr14:100375764 C>A maps to NM_001008707.1 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:46119736 G>A maps to NM_001193268.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr11:62378659 G>A maps to ENST00000278845 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:42488419 T>C maps to NM_019063.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr2:42510109 A>G maps to NM_019063.3 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr2:42472704 C>A maps to NM_019063.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr14:89153575 C>T maps to ENST00000380664 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr19:6896424 C>T maps to ENST00000381407 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr19:14755049 C>T maps to NM_032571.3 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:73145298 C>G maps to NM_004097.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr7:155251200 G>A maps to NM_001427.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr4:71495255 T>G maps to NM_031889.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr4:71510238 C>A maps to NM_031889.2 G1032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr4:71509878 C>T maps to NM_031889.2 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr11:94862592 T>G maps to NM_015036.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:130579467 A>G maps to NM_001114753.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr17:77075666 T>C maps to NM_001042573.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr1:8922982 G>A maps to NM_001428.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:129804010 G>A did not map to a codon.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr8:120569904 T>C maps to NM_006209.3 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr8:120628548 G>T maps to NM_006209.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr8:120580454 G>A maps to NM_006209.3 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:120628542 G>A maps to NM_006209.3 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr6:131958571 C>T maps to NM_005021.3 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr6:131995387 A>G maps to NM_005021.3 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr6:46133253 A>G maps to NM_021572.4 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr4:185138819 T>C maps to NM_153343.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr17:77710871 C>T maps to NM_178543.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr22:40231925 G>A maps to NM_152512.3 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr10:97607249 T>C maps to NM_001098175.1 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr9:139946005 G>T maps to NM_203468.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:40465426 T>A maps to NM_001248.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr8:23294704 G>A maps to NM_004901.3 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr14:74454757 A>G maps to NM_001249.2 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr20:25201970 T>A maps to ENST00000443525 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr9:140330188 G>A maps to NM_001033113.1 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr22:41536218 T>C maps to NM_001429.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr22:41574311 A>G maps to NM_001429.3 P2199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr22:41543892 G>A maps to NM_001429.3 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:132445442 A>C maps to ENST00000333577 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr12:132547146 G>A maps to ENST00000333577 Q2781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr12:132471270 C>A maps to ENST00000333577 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr12:132497631 C>T maps to ENST00000333577 R1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr12:132522574 G>A maps to ENST00000333577 V2083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr20:34778269 C>T maps to NM_012156.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr20:34778269 C>A maps to NM_012156.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr6:131179362 C>T maps to NM_001431.3 R977R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr18:5428359 C>T maps to NM_012307.2 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr9:112005947 A>G maps to NM_019114.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:21924624 C>T maps to ENST00000265800 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr10:32560792 A>G maps to NM_025209.2 H709H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:143097035 G>A maps to NM_005232.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:38227125 G>T maps to NM_001099439.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr1:38192871 C>A maps to NM_001099439.1 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr1:16458585 G>A maps to NM_004431.3 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:66467833 C>G maps to NM_004439.5 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:96706397 A>G maps to NM_001080448.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr6:93969180 G>C maps to NM_004440.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:22927185 A>T maps to NM_020526.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr1:22920117 C>G maps to NM_020526.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr1:22920015 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:22903098 G>T maps to NM_020526.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr1:22902867 C>T maps to NM_020526.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr1:22913108 G>A maps to NM_020526.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:22902936 G>A maps to NM_020526.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:23191445 C>T maps to ENST00000400191 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr7:100411569 C>T maps to NM_004444.4 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr7:100405124 G>C maps to NM_004444.4 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr7:142561950 C>T maps to NM_004445.3 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr7:142562310 G>T maps to NM_004445.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr7:142561392 A>T maps to NM_004445.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr1:226027664 G>A maps to NM_001136018.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr1:92518078 C>T maps to NM_173567.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr3:37032774 A>T maps to NM_014805.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:19186716 G>A maps to NM_014964.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr17:48618638 G>A maps to NM_017957.2 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr17:48619289 G>A maps to NM_017957.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr8:144940614 G>A maps to NM_031308.1 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr8:144940740 C>T maps to NM_031308.1 A2227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr8:144942849 G>A maps to NM_031308.1 L1524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr8:144943011 C>T maps to NM_031308.1 W1470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr8:144941622 C>A maps to NM_031308.1 A1933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr8:144940377 G>A maps to NM_031308.1 V2348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr1:220213564 G>A maps to NM_004446.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr19:16528866 G>A maps to ENST00000455140 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:16551693 A>G maps to ENST00000455140 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr11:723295 C>A maps to NM_022772.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:110300153 C>T maps to NM_139053.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr13:43469221 G>A maps to NM_001002264.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr17:56281633 G>A maps to NM_000502.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:96139527 G>A maps to NM_016442.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr5:96232567 G>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:37882077 C>A maps to NM_004448.2 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:37876079 A>C maps to NM_004448.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:37873628 C>T maps to NM_004448.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr5:65350721 T>A maps to ENST00000506030 V1192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr5:65288620 T>C maps to ENST00000506030 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr12:56495608 C>T maps to NM_001982.2 R1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr12:56487572 A>G maps to NM_001982.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr12:56478807 C>T maps to NM_001982.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:56491705 G>A maps to NM_001982.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:212295692 C>A maps to NM_005235.2 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr19:45916985 G>T maps to NM_202001.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:45868314 G>A maps to NM_000400.3 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:128036917 C>A maps to NM_000122.1 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr16:14041532 G>T maps to NM_005236.2 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr10:50690812 A>G maps to NM_000124.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr10:50732230 C>T maps to ENST00000515869 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr23:71426171 T>A did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:71427584 T>C did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:71427692 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:71426808 G>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:71424999 C>T did not map to a codon.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:60183306 C>T maps to NM_000082.3 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr21:39795359 C>T maps to NM_001136154.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:29502994 A>T maps to NM_016570.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr16:20802203 C>A maps to NM_080663.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr8:623547 G>A maps to NM_207332.1 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr10:101923758 A>G did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:101911986 A>G maps to NM_001100626.1 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:158182139 C>T maps to NM_001009959.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr16:23716451 C>T maps to NM_033266.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:23713535 C>T maps to NM_033266.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:124623586 C>T maps to NM_138961.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr18:19116140 G>A maps to NM_052911.2 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr13:47345583 G>A maps to NM_001984.1 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr13:47354150 A>G maps to NM_001984.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr20:13750636 A>G maps to NM_016649.3 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:53685604 A>G maps to NM_012291.4 T1884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr12:53670455 C>T maps to NM_012291.4 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr12:53685568 C>T maps to NM_012291.4 L1872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr12:53686060 G>T did not map to a codon.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr12:53685544 C>G maps to NM_012291.4 T1864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:53685529 C>T maps to NM_012291.4 Y1859Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:6512053 C>T maps to NM_031475.2 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr2:239033942 G>A maps to NM_194312.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:152265600 A>C maps to NM_001122741.1 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:152201892 A>G maps to NM_001122741.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr6:152382173 G>T maps to NM_001122741.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr16:68267895 C>G did not map to a codon.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr11:64082234 G>A maps to NM_004451.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:103499099 C>T did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr12:56524687 A>T maps to NM_001184796.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:158529818 A>G maps to NM_020728.2 Y800Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr7:158590761 T>G maps to NM_020728.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:67631298 A>G maps to NM_019002.3 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:67637128 C>T maps to NM_019002.3 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr5:137848454 G>A maps to NM_004730.2 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr4:159601751 A>G maps to NM_004453.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr12:22826446 A>G maps to NM_018638.4 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:204101335 C>T maps to NM_018208.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr11:128360460 A>T maps to NM_001143820.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:13971322 C>G maps to NM_004956.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr1:157105441 G>A maps to NM_001145312.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr1:157062695 G>T maps to NM_001004341.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr17:41610307 C>T did not map to a codon.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr17:41611246 G>A maps to NM_001079675.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:185783821 A>G maps to NM_004454.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:5721078 G>A maps to NM_153717.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:5754738 G>A maps to NM_153717.2 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:7927063 C>T maps to NM_001159944.1 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr17:74018280 G>A maps to NM_001988.2 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr17:74023228 G>A maps to NM_001988.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr17:74006473 G>A maps to NM_001988.2 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr22:29694786 A>G maps to NM_013986.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:41501705 C>T maps to NM_152596.2 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:140243597 G>A maps to NM_017820.3 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr9:140249169 G>T maps to NM_017820.3 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr1:242030290 C>T maps to NM_006027.4 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr4:56738087 A>G maps to NM_018261.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr4:56765983 A>G maps to NM_018261.3 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:446364 G>A maps to ENST00000315013 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr19:45731305 T>C maps to NM_138568.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr14:57684752 C>T maps to ENST00000340918 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr2:72411217 C>G maps to NM_015189.1 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr1:231471904 G>A maps to NM_175876.3 C529C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr8:145134931 C>T maps to NM_019037.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr4:122724129 G>A maps to NM_001034194.1 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr4:122722620 A>G maps to NM_001034194.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr4:122722614 C>T maps to NM_001034194.1 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr11:108381262 G>A maps to NM_015065.2 S1657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr11:108389043 G>T maps to NM_015065.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:108380879 C>T maps to NM_015065.2 W1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:108381025 T>G maps to NM_015065.2 T1736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:119122870 C>A maps to NM_000127.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr1:26357723 C>T maps to NM_004455.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:72182013 G>A maps to NM_000503.4 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:72129050 T>C maps to NM_000503.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr20:45618708 G>C maps to ENST00000360649 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr6:133804174 G>A maps to ENST00000452339 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:64776298 A>G maps to ENST00000370616 S2219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr17:40857162 G>A maps to ENST00000264646 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr7:148512044 G>A maps to NM_004456.3 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:148506482 C>T did not map to a codon.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr4:187208886 C>T maps to NM_000128.3 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr5:176831340 G>A maps to NM_000505.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr5:176830984 G>A maps to NM_000505.3 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr5:176831543 G>A maps to NM_000505.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr6:6225027 G>A maps to NM_000129.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:197020001 T>C maps to NM_001994.2 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr5:76028880 C>A maps to NM_001992.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr5:76128710 C>T maps to NM_005242.4 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr1:169510436 T>C maps to ENST00000367796 E1302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr1:169528478 T>C maps to ENST00000367796 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr13:113769995 T>A maps to NM_000131.3 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:154194856 G>A did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:154129669 G>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:154158319 G>A did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:154159036 A>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:154124443 A>G did not map to a codon.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr23:154157679 A>T did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:154130374 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:154157882 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:154197603 A>G did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:154132763 A>G did not map to a codon.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr23:138633385 G>T did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr23:138644197 A>C did not map to a codon.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr16:74808424 G>A maps to NM_024306.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:57313329 A>G did not map to a codon.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr23:57367783 G>A did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr23:57337125 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr23:57358083 G>A did not map to a codon.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:88427488 T>C maps to NM_001443.1 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr17:72889684 G>A maps to ENST00000310226 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr1:50941222 G>A maps to NM_007051.2 N594N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:50956259 C>T maps to NM_007051.2 E551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr15:80452757 C>T maps to NM_000137.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:1877592 G>T maps to NM_001018104.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr3:138340382 T>A did not map to a codon.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207085118 G>C maps to NM_005449.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr16:4659849 T>G maps to NM_145253.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr17:74261676 T>C maps to NM_182565.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr9:130707095 G>A maps to NM_001035254.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:14601481 G>A maps to NM_019018.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr5:14693051 C>T maps to NM_138348.4 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:81046665 A>G maps to NM_021214.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:59059733 C>T maps to NM_147189.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr11:58877130 A>C maps to NM_198947.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr12:47628908 G>T maps to NM_138371.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr12:47630057 T>A maps to NM_138371.1 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr5:153372625 G>C maps to ENST00000442256 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:57678667 G>A maps to NM_152678.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:203500480 A>C maps to NM_173511.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr22:45723919 C>T maps to NM_017911.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr12:58166554 C>T maps to NM_015433.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr9:96212844 A>G maps to NM_198841.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:170627575 C>T maps to NM_032448.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr23:133941689 G>A did not map to a codon.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr23:133941716 C>A did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr13:25743822 C>T maps to NM_152704.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:63410668 T>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:63412719 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr23:63412032 A>G did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr23:63412534 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr23:63411695 G>A did not map to a codon.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr2:131520925 C>T maps to NM_001105195.1 H427H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr2:131521381 C>A maps to NM_001105195.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:131520997 G>A maps to NM_001105195.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:131520233 C>T maps to NM_001105195.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr2:131521735 A>T maps to NM_001105195.1 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:130294040 G>A maps to NM_022833.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr9:130287412 G>A maps to NM_022833.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:184062583 C>A maps to NM_144635.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr1:16386007 T>C maps to NM_182623.2 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:16384985 G>T maps to NM_182623.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr1:16386094 G>A maps to NM_182623.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:1179847 G>C maps to NM_001014980.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr17:40737278 A>G maps to NM_178126.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr6:71235352 A>T maps to NM_001162529.1 K856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:71162229 C>G maps to NM_001162529.1 S38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:139163999 G>T maps to NM_015912.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr4:89702426 G>T maps to NM_014883.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr5:137278881 C>T maps to NM_016603.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr5:137289149 G>A maps to NM_016603.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:61112191 C>A maps to ENST00000442566 L76L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B1-A47M-01A-11D-A25F-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:187093140 A>T maps to ENST00000502894 K34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr5:177166138 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr13:108518167 G>T maps to NM_001080396.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:68748895 C>T did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr11:6239138 A>G maps to NM_032127.3 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr11:6233062 G>T maps to NM_032127.3 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:122128620 C>T maps to NM_014367.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr8:79578394 G>C maps to NM_016010.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr9:35563217 T>G maps to NM_001164310.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr9:35563220 A>G maps to NM_001164310.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr11:73120705 C>A maps to ENST00000064778 G150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr2:131813239 C>T maps to NM_001009993.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr2:187615885 T>C maps to NM_177454.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:187559028 A>G maps to NM_177454.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr10:126523419 T>C maps to NM_032182.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr10:102675795 C>T maps to NM_001136123.1 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:102683798 C>T maps to NM_001136123.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr14:45514043 A>G maps to ENST00000361462 A1375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr14:45537686 C>T maps to ENST00000361462 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr14:45468575 G>A maps to ENST00000361462 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:43616486 A>C maps to NM_001101376.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:119301392 C>T maps to NM_024581.4 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:119282963 T>G maps to NM_024581.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr6:119282963 T>G maps to NM_024581.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:30893076 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr4:91230367 G>A maps to NM_001145065.1 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr10:86132204 G>A maps to ENST00000372088 W466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr10:86130885 A>T maps to ENST00000372088 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr5:176951609 C>T maps to ENST00000442143 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:150421547 T>C maps to NM_152394.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:150421568 T>C maps to NM_152394.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:150421589 T>C maps to NM_152394.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr10:128974641 G>T maps to NM_001039762.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr4:159092385 A>G maps to NM_001128424.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:159092401 A>T maps to NM_001128424.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:159076876 C>T maps to NM_001128424.1 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:103431191 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr12:62147528 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:68788345 G>C maps to NM_182522.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193540 C>T maps to NM_020223.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193560 T>A maps to NM_020223.2 L121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr10:46272803 G>A maps to ENST00000399588 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr9:97081993 G>A maps to NM_017561.1 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:97081336 C>A maps to NM_017561.1 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr9:97082578 G>A maps to NM_017561.1 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:99700840 G>T maps to NM_001170741.1 G546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3427-01A-01D-0966-08 chr10:88946958 T>G did not map to a codon.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr10:88930274 G>C maps to ENST00000298786 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:88911775 C>G maps to ENST00000298786 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr10:88911272 A>G maps to ENST00000298786 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr18:10691259 T>A maps to NM_022068.2 K2325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr18:10697807 C>T maps to NM_022068.2 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr23:153736830 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr23:153735233 C>T did not map to a codon.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr10:120877120 C>A maps to NM_207009.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr6:82461774 G>T maps to ENST00000369756 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:82461789 T>G maps to ENST00000369756 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr6:82461831 G>A maps to ENST00000369756 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr1:27332863 G>A maps to NM_052943.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:118166326 G>T maps to NM_017709.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr23:79698229 T>C did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr23:79698410 A>T did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:34148841 G>A did not map to a codon.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr23:34148876 C>G did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr23:34148881 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr23:34148835 C>T did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr23:34148876 C>G did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr23:34148935 C>T did not map to a codon.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr23:34961786 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr23:34961453 G>A did not map to a codon.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr23:37028222 C>A did not map to a codon.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr23:37026816 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr23:37027644 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:37028374 G>A did not map to a codon.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr23:37028208 G>A did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr23:37028120 C>T did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr23:24381694 G>A did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr23:24381816 G>T did not map to a codon.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr23:24382643 C>T did not map to a codon.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr23:24381735 G>T did not map to a codon.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr2:16742256 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:130883631 C>A maps to NM_016623.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr23:153674013 T>C did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr6:136560874 G>A maps to NM_138419.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:26152902 G>T did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:114401162 C>T maps to ENST00000424269 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr11:114442139 C>A maps to NM_001077639.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr17:641268 C>A maps to NM_024792.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr16:30036623 G>A maps to NM_031478.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr23:152860112 G>C did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:190067268 A>T maps to NM_199051.1 L727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr1:190067929 G>A maps to NM_199051.1 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:190068173 C>T maps to NM_199051.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr1:190067564 G>A maps to NM_199051.1 Y628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr15:59139572 A>T maps to NM_001040450.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr6:24828488 C>T maps to NM_014722.2 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr6:24825516 T>C maps to NM_014722.2 E956E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:49219115 G>A maps to NM_080829.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr13:114514866 C>A maps to NM_182614.2 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr5:156592755 G>A maps to NM_130899.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:156590093 T>A maps to NM_130899.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:78325732 T>C maps to NM_198549.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:78248999 T>C maps to NM_198549.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr1:78269048 A>G maps to NM_198549.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr9:131804662 C>T maps to NM_032809.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr9:40704226 C>T maps to NM_001083124.1 D628D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr9:90534183 C>T maps to NM_001145124.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr9:134136483 G>A maps to NM_033387.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr2:38179039 C>T maps to NM_144713.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:38156860 A>G maps to NM_001170792.1 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr15:41037297 C>T maps to NM_018145.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr15:41043763 G>T maps to NM_018145.1 C128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr8:87486539 A>G maps to NM_016033.2 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr8:124204062 T>C maps to NM_032899.4 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr6:54791200 T>C maps to NM_001010872.1 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr20:33875699 G>A maps to NM_178468.4 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr20:37580731 C>T maps to NM_030919.2 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr20:37555363 G>A maps to NM_030919.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr20:37570603 G>A maps to NM_030919.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:49114032 G>A maps to NM_017708.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr8:144808645 T>C maps to NM_198488.3 Q995Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr8:144810121 G>A maps to NM_198488.3 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:144809116 G>C maps to NM_198488.3 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr16:5141851 C>T maps to NM_201400.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr16:5141854 T>C maps to NM_201400.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr8:12043929 G>A maps to NM_001083537.1 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:71507082 G>A maps to NM_018172.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:71504463 C>T maps to NM_018172.2 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:71507082 G>A maps to NM_018172.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr6:17608518 T>C maps to NM_016255.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr8:124787417 C>A maps to NM_144963.2 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr15:64380991 C>A maps to NM_032231.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr16:66966159 C>T maps to NM_016062.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:33810280 T>C maps to ENST00000395190 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:33813449 A>G maps to ENST00000395190 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:33813425 T>C maps to ENST00000395190 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr23:8763258 C>T did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr23:8764373 A>T did not map to a codon.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr23:8767123 C>T did not map to a codon.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr23:9000464 G>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:13061294 T>C did not map to a codon.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr23:13058889 T>C did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:89838100 C>T maps to NM_000135.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr23:14882776 C>A did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:10089632 G>A maps to NM_033084.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:22646843 C>T maps to NM_022725.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:89856163 A>T maps to NM_001113378.1 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr15:89859677 A>G maps to NM_001113378.1 K1325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr2:58386911 T>C maps to NM_001114636.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:58431303 A>G maps to NM_001114636.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:163046172 A>G maps to NM_004460.2 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr11:13734515 A>T maps to NM_032228.5 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr12:29485565 T>C maps to NM_018099.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:29469909 T>A maps to NM_018099.3 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr13:99098407 G>A maps to NM_005766.2 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr13:99083479 G>T maps to NM_005766.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr13:98865555 G>A maps to NM_005766.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:99092298 T>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:242407763 C>G maps to NM_014808.2 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:242433434 G>C maps to NM_014808.2 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:80046745 G>A maps to NM_004104.4 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:80053199 G>A maps to NM_004104.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr17:80047602 C>G did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr2:170411719 T>C maps to NM_024622.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:207655322 T>C maps to NM_014929.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr2:207639091 C>A maps to NM_014929.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:7867620 A>G maps to NM_024091.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr5:7867845 A>G maps to NM_024091.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr4:187538910 C>A maps to ENST00000260147 T2946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr4:187629280 A>C maps to ENST00000260147 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:187530417 T>A maps to ENST00000260147 I3378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:187527259 G>T maps to ENST00000260147 P3441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:187629556 G>A maps to ENST00000260147 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr4:187541478 G>A maps to ENST00000260147 Y2090Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr5:150945789 T>C maps to NM_001447.2 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr5:150897290 G>T maps to NM_001447.2 R3785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr5:150924101 G>T maps to NM_001447.2 R2196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:150911352 G>A maps to NM_001447.2 G3202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr11:92590422 G>A maps to ENST00000298047 P3803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr11:92533291 C>T maps to ENST00000298047 F2371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr11:92577386 G>T maps to ENST00000298047 L3618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr11:92534185 G>T maps to ENST00000298047 L2669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:92086238 T>C maps to ENST00000298047 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:92577150 C>T maps to ENST00000298047 R3540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr11:92543183 T>A maps to ENST00000298047 Y3141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:126411929 C>A maps to NM_024582.4 I4651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr4:126336939 A>C maps to NM_024582.4 T2274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr4:126398471 A>G maps to NM_024582.4 A4152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:126239107 T>C maps to NM_024582.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr4:126337736 A>C maps to NM_024582.4 T2326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr23:150891104 T>G did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr23:150889895 G>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:73916510 C>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr19:40330914 G>A maps to NM_001436.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr19:40330953 A>T maps to NM_001436.3 C99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:40331278 G>A maps to NM_001436.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:40331123 A>G maps to NM_001436.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr22:45929740 G>A maps to ENST00000348697 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr22:45931086 C>T maps to ENST00000348697 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr14:92349358 G>T maps to ENST00000267620 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr15:48779392 G>A maps to NM_000138.4 I1156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr15:48782116 C>A maps to NM_000138.4 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr15:48748912 C>A maps to NM_000138.4 V1781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:48703306 A>G maps to NM_000138.4 S2832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:48755318 C>T maps to NM_000138.4 A1728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:48748936 G>T maps to NM_000138.4 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr5:127645723 G>A maps to NM_001999.3 C1717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr5:127782276 G>A maps to NM_001999.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr5:127609607 A>T maps to NM_001999.3 C2588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr19:8148161 G>A maps to NM_032447.3 Y2394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:8183904 G>A maps to NM_032447.3 D1071D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr19:8193951 G>A maps to NM_032447.3 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr19:8162184 G>A maps to NM_032447.3 L1759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr19:8194140 G>C maps to NM_032447.3 S718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr19:8196480 G>A maps to NM_032447.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:8209800 G>A maps to NM_032447.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr9:97365719 T>C maps to NM_001127628.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr16:30676957 G>C did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr7:102553613 G>A maps to NM_145032.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr7:102665655 A>G maps to NM_145032.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:1702058 G>A maps to NM_152441.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr7:5541299 G>A maps to ENST00000312577 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:33415409 C>T maps to NM_012157.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr13:77581414 A>G maps to NM_012158.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:99365255 A>C maps to NM_012160.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr9:37537373 T>A maps to NM_012166.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr2:48050391 A>T maps to NM_001190274.1 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:48050457 T>G maps to NM_001190274.1 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr10:5948165 T>C maps to NM_032807.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr1:11710790 C>G maps to NM_012168.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr12:117627029 A>G did not map to a codon.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr12:117624288 C>A maps to NM_033624.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr1:224302058 C>G maps to NM_015176.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:33770353 G>A maps to NM_012175.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr16:87377236 G>C maps to NM_024735.3 Y208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr14:55818481 C>T maps to NM_152231.1 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr14:55817638 T>G maps to NM_152231.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr2:230875428 A>G maps to NM_174899.4 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr5:147781572 A>G maps to NM_205836.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr5:147778624 G>A maps to NM_205836.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr5:41927218 G>A maps to NM_012176.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr5:41934378 C>T maps to NM_012176.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr1:16577185 G>C maps to NM_018994.1 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr8:101153257 T>C maps to NM_001029860.3 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr8:101154157 A>G maps to NM_001029860.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr6:153293426 G>A maps to NM_012177.3 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr17:18653136 T>A maps to ENST00000395665 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr17:18675802 G>A maps to ENST00000395665 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr9:123527052 G>A maps to NM_012164.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr10:103454328 G>C maps to ENST00000331272 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr9:139837901 C>A maps to NM_018998.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr4:153244134 C>G maps to NM_033632.2 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:55385757 C>T maps to NM_002000.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:40419756 A>G maps to NM_003890.2 H1079H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:40376318 G>A maps to NM_003890.2 Y3995Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:40395977 G>A maps to NM_003890.2 G2473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:40366037 C>G maps to NM_003890.2 P4732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr19:40420152 G>C maps to NM_003890.2 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr19:40398045 A>G maps to NM_003890.2 C2307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr19:40376808 C>T maps to NM_003890.2 G3871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr19:40408647 G>C maps to NM_003890.2 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr19:40368732 G>C maps to NM_003890.2 L4205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:40366433 G>A maps to NM_003890.2 R4600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:161599826 T>G did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr1:161595992 C>T maps to ENST00000367964 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:161599724 C>T maps to ENST00000367964 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr5:141025712 C>A maps to ENST00000354789 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr5:141028859 G>A maps to ENST00000354789 Q132*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-PJ-A5Z9-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr1:157765909 C>T maps to NM_052938.4 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:157776892 G>A maps to NM_052938.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:157650774 G>A maps to NM_052939.3 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:157667659 G>A maps to NM_052939.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:157559027 T>C maps to NM_031282.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:161677074 C>A maps to NM_001184866.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr1:161695854 T>C maps to NM_001002901.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:155279735 A>G maps to NM_001135821.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr11:111749724 A>G maps to ENST00000428306 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:72862363 G>A maps to ENST00000442102 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr18:55233772 A>G maps to NM_001012515.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:4792819 C>A maps to NM_018708.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr15:68582266 T>C maps to NM_015322.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr5:108133966 A>G maps to NM_005246.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr8:125015548 C>T maps to NM_001039112.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:124989659 C>T maps to NM_001039112.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr8:125035808 C>T maps to NM_001039112.2 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr8:125052243 A>T maps to NM_001039112.2 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr8:125074106 C>T maps to NM_001039112.2 N1054N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr14:53385907 A>G maps to NM_001134999.1 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr11:63990879 C>T maps to NM_178443.2 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr11:63988120 C>T maps to NM_178443.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr3:186370104 T>G maps to NM_014375.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr3:186364116 A>T maps to NM_014375.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:125359541 G>A maps to NM_005103.4 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr19:35941422 C>T maps to NM_005306.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:35941486 C>T maps to NM_005306.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:155487150 G>T maps to NM_005141.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr23:54475271 C>T did not map to a codon.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr23:54475345 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr23:54491906 G>A did not map to a codon.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr12:32786520 T>G maps to NM_139241.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr3:14964674 G>C maps to NM_152536.3 L1310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr12:95546723 C>A maps to NM_018351.3 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:95603625 A>G maps to NM_018351.3 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr23:137793083 C>A did not map to a codon.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr23:137715046 G>A did not map to a codon.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr8:21903770 C>A maps to NM_003867.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:69514320 A>T maps to NM_005117.2 C120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:4554424 G>A maps to NM_020996.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr12:4554544 C>T maps to NM_020996.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr12:4553397 C>G maps to NM_020996.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr15:49776508 A>G maps to NM_002009.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr10:103534501 G>A maps to NM_033163.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr13:22275357 A>G maps to NM_002010.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr8:38314949 C>T maps to NM_001174067.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:167435949 C>A maps to NM_007045.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr10:123353229 C>T maps to ENST00000351936 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr4:1804695 C>A maps to NM_001163213.1 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr4:1803583 C>A maps to NM_000142.4 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr4:1803748 C>T maps to NM_000142.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr5:176520384 A>G maps to NM_022963.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:176522538 C>T maps to NM_213647.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr4:1019077 T>A maps to NM_021923.3 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr4:155533708 A>T maps to ENST00000407946 L18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr4:155526042 T>C maps to ENST00000407946 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:60139805 G>C did not map to a codon.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:76829077 T>C maps to NM_006682.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr7:76826153 C>T maps to NM_006682.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr7:76828960 T>C maps to NM_006682.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:76828558 G>A maps to NM_006682.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr1:27941091 T>C maps to NM_005248.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:241661271 T>G did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:241663811 G>A maps to NM_000143.3 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr23:135290018 C>T did not map to a codon.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:38463082 C>A maps to NM_004468.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:38463362 G>T maps to NM_004468.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr6:97051596 A>G maps to NM_020482.4 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr18:34192013 A>T maps to NM_025135.2 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr9:133799696 C>T maps to NM_001145106.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr11:65653800 C>T maps to NM_198897.1 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr23:15402053 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:164468065 C>T maps to NM_018086.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:76022976 A>T maps to NM_015687.2 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr3:99648840 A>G maps to NM_001042459.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr3:99568695 A>G maps to NM_001042459.1 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:54266006 G>C did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr4:54244013 C>T maps to NM_030917.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr20:42935613 C>T maps to NM_001080472.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr19:56104631 C>T maps to NM_032836.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr12:49315837 T>A maps to NM_016594.2 K179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr9:115932897 G>T maps to ENST00000446284 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr9:115931604 G>A maps to ENST00000446284 V1153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:115973832 A>G maps to ENST00000446284 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:45603574 G>A maps to NM_002013.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:2909577 T>G maps to NM_002014.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:2909051 A>G maps to NM_002014.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:33039810 C>T maps to NM_007270.3 C437C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr7:33028127 G>A maps to NM_007270.3 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:47259237 G>A maps to NM_024301.4 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:154965265 A>G maps to NM_001184891.1 *447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr1:154962042 T>G maps to NM_025207.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:154960801 G>A maps to NM_025207.4 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:154956240 T>A maps to NM_025207.4 L24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr1:152285495 G>A maps to NM_002016.1 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:152277449 G>T maps to NM_002016.1 S3304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:152277656 A>G maps to NM_002016.1 A3235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:152279671 C>A maps to NM_002016.1 G2564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr1:152278688 C>A maps to NM_002016.1 V2891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr1:152280596 A>G maps to NM_002016.1 D2255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:152284805 C>T maps to NM_002016.1 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:152324077 C>A maps to NM_001014342.2 G2062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:152330074 G>A maps to NM_001014342.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr1:152325170 T>C maps to NM_001014342.2 G1697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr11:128680489 C>T maps to NM_002017.3 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr17:18156763 A>T maps to NM_002018.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr17:18156612 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr17:18149934 G>A maps to NM_002018.2 F1008F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr8:142480801 G>A maps to NM_207414.2 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr8:142486195 G>A maps to NM_207414.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr8:142444933 T>C maps to NM_207414.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:142477561 G>A maps to NM_207414.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:71379996 C>G did not map to a codon.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr9:84607298 C>T maps to NM_001001670.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:84608501 A>T maps to NM_001001670.2 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr9:84609411 C>T maps to NM_001001670.2 Q1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr9:84608131 G>A maps to NM_001001670.2 W916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr9:84605804 C>A maps to NM_001001670.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:84605891 G>A maps to NM_001001670.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:153592961 C>G did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr23:153588775 G>A did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr23:153593803 C>G did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr23:153594982 T>G did not map to a codon.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr23:153583339 C>A did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:153588713 A>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:153578044 C>T did not map to a codon.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr3:58128450 G>A maps to NM_001164317.1 P1783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:58089734 C>T maps to NM_001164317.1 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr7:128483326 C>T maps to NM_001458.4 H865H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:63885634 G>A maps to NM_013280.4 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr14:86088730 G>T maps to NM_013231.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3427-01A-01D-0966-08 chr14:86088695 C>A maps to NM_013231.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr14:86088841 C>T maps to NM_013231.4 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr14:86089420 C>T maps to NM_013231.4 N521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr14:86088604 C>T maps to NM_013231.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr14:86088694 A>G maps to NM_013231.4 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr20:14307333 G>C maps to NM_198391.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr13:29001982 G>A maps to NM_002019.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr13:28913319 C>A maps to NM_002019.4 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr5:180047686 G>A maps to NM_182925.4 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr5:180048229 C>T maps to NM_182925.4 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr5:180050942 T>A maps to NM_182925.4 K514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr14:76045407 C>A maps to NM_017791.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr15:33358816 C>T maps to NM_001103184.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:240371660 A>C maps to ENST00000406993 G1326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:240256170 G>A maps to ENST00000406993 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr1:240371516 T>A maps to ENST00000406993 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:240255570 C>G maps to ENST00000406993 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:240371327 G>A maps to ENST00000406993 A1215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr1:240370994 G>A maps to ENST00000406993 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr17:43323618 G>T maps to NM_005892.3 E1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr17:43319769 C>T maps to NM_005892.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:153471510 T>A maps to NM_052905.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr12:50045189 A>T maps to NM_175736.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:171072966 C>T maps to NM_006894.5 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr1:146672929 G>A maps to NM_001461.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:147011650 T>A did not map to a codon.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr23:147014113 G>T did not map to a codon.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr23:147030316 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:147011710 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr23:147088241 C>T did not map to a codon.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr2:216295546 C>T maps to NM_212482.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:216271072 C>T maps to NM_212482.1 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr17:80706747 T>C maps to NM_022158.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr17:80680692 G>A maps to NM_024619.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:94009755 G>A maps to ENST00000370253 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr11:47745664 A>G maps to NM_015308.2 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr11:47788807 A>G maps to NM_015308.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr13:49719942 A>G maps to NM_001079673.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:172096212 C>T maps to NM_022763.3 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr3:172025191 C>G maps to NM_022763.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr2:27716992 A>G maps to NM_022823.2 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:159789572 G>C maps to ENST00000379346 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:159756555 G>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr4:159825695 A>G maps to ENST00000379346 *1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr4:159780274 G>A maps to ENST00000379346 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:49175929 G>A maps to NM_004476.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr11:49186292 C>T maps to NM_004476.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr11:71932760 C>T maps to NM_001113536.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr20:22562793 C>T maps to NM_021784.4 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr5:72743506 G>A maps to NM_004472.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr5:72743760 T>A maps to NM_004472.2 K143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr5:72743653 C>T maps to NM_004472.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr9:117354 A>G maps to NM_207305.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr9:70177821 T>C maps to NM_001126334.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr10:129536796 C>T maps to NM_207426.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr17:74133973 C>T maps to NM_001454.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:42744041 T>A maps to NM_001198850.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:4780486 C>T maps to ENST00000450194 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr17:80559302 C>A maps to NM_004514.3 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr17:80525989 C>T maps to NM_004514.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr12:2968316 T>C maps to NM_202002.1 E631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr14:89656757 A>G maps to NM_001085471.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:89817013 A>G did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr13:41134061 A>G maps to NM_002015.3 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr13:41134355 A>T maps to NM_002015.3 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr6:108985391 A>G maps to NM_001455.3 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr23:70320777 G>A did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:70316473 C>T did not map to a codon.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr7:114269990 G>A maps to NM_148898.3 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr7:114299728 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr23:49113205 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr6:1313356 T>C maps to NM_033260.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr23:55650702 G>C did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr20:30432838 C>T maps to NM_004118.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr19:52327624 T>A maps to NM_002030.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr4:79296890 A>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:79236853 C>T maps to NM_025074.6 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr4:79301067 C>T maps to NM_025074.6 Q1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr4:79403633 C>T maps to NM_025074.6 A2899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr9:14824064 T>G maps to ENST00000380880 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr9:14859187 T>G maps to ENST00000380880 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:14770685 G>T maps to ENST00000380880 S1662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr13:39265810 C>T maps to NM_207361.4 L1444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr13:39452996 C>G maps to NM_207361.4 T2963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr13:39451279 T>C maps to NM_207361.4 F2857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:39422802 C>G maps to NM_207361.4 S2125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr13:39266097 C>T maps to NM_207361.4 H1539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:190874220 A>G did not map to a codon.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr4:190878551 G>A did not map to a codon.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr4:190873410 T>C maps to NM_004477.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:190883027 C>T maps to NM_004477.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr4:190876209 C>G maps to NM_004477.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr4:190876306 G>A did not map to a codon.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr4:190876306 G>A did not map to a codon.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr4:190876286 G>A maps to NM_004477.2 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr4:190876306 G>A did not map to a codon.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr10:135439076 T>C maps to ENST00000443774 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr10:135438932 C>T maps to ENST00000443774 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:135439106 C>T maps to ENST00000443774 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr10:13699458 G>A maps to NM_018027.3 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr14:52174836 T>A maps to ENST00000344768 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr23:131234680 C>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:131219748 T>C did not map to a codon.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr23:131212432 T>G did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr9:37733481 A>G maps to NM_014907.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:12708336 G>T did not map to a codon.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr23:12734644 C>G did not map to a codon.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr23:12736244 G>C did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr23:12736619 C>A did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr23:12734954 G>A did not map to a codon.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr23:12701705 G>T did not map to a codon.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr23:12735001 C>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:100214267 A>G maps to NM_001013660.2 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:32836596 T>C maps to NM_023037.2 I2588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr13:32841387 C>A maps to NM_023037.2 A2676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr13:32798430 C>T maps to NM_023037.2 Q1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:48536645 A>G maps to NM_015030.1 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr4:48513001 C>G did not map to a codon.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr14:44973865 C>A maps to NM_032135.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr14:44974804 A>G maps to NM_032135.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:44975260 C>T maps to NM_032135.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79496378 G>A maps to NM_001077182.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr17:79495865 G>A maps to NM_001077182.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr17:79504051 C>A maps to NM_001077182.2 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:4306031 C>T maps to NM_024333.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr11:30253598 C>T maps to NM_001018080.1 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:49190327 G>A maps to NM_000145.3 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:40056079 C>T maps to NM_152597.4 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:186671592 C>T maps to NM_173651.2 Q5943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:186671551 C>G maps to NM_173651.2 S5929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr2:186671399 T>C maps to NM_173651.2 D5878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr2:186689202 A>G maps to NM_173651.2 L6912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:120122158 A>G maps to NM_007085.4 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr5:132939625 G>A maps to NM_015082.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr4:162307411 G>A maps to NM_020116.3 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr4:162307105 T>A maps to NM_020116.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr21:47571510 G>T maps to ENST00000397748 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr21:47558472 G>C maps to ENST00000397748 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr19:49468841 G>A maps to NM_000146.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr19:49469166 C>T maps to NM_000146.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr5:121187825 G>T maps to NM_177478.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:53922838 A>G maps to NM_001080432.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr16:71318089 T>A maps to NM_018348.5 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:37442388 A>G maps to NM_015050.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:78444625 G>A maps to ENST00000436586 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:78414968 A>G maps to ENST00000436586 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr6:143825090 G>C maps to NM_032020.4 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:91419098 G>A maps to NM_002569.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr16:31202111 A>T maps to NM_004960.3 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr16:31201623 T>C maps to NM_004960.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr8:33246864 A>G maps to ENST00000380081 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr19:5843821 T>C maps to NM_001097641.1 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr19:5843821 T>C maps to NM_001097641.1 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:71668177 T>C did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:7508977 T>C maps to NM_004860.3 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr5:39202846 T>C maps to ENST00000263405 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:46000086 G>C maps to NM_024513.2 Y1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:46009967 C>T maps to NM_024513.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr3:197501075 T>C maps to NM_032288.6 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr7:90894983 G>T maps to NM_003505.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr12:130649145 C>T maps to NM_007197.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr12:130648323 C>T maps to NM_007197.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr17:42636501 C>T maps to NM_001466.3 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr11:86662561 G>C maps to NM_012193.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr11:86662231 T>C maps to NM_012193.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr2:202901004 C>T maps to NM_003507.1 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:202900341 C>G maps to NM_003507.1 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr7:72849269 G>A maps to NM_003508.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr19:3533335 G>A maps to NM_001136198.1 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr19:3527658 C>A maps to NM_001136198.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr19:3533329 C>A maps to NM_001136198.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:3525915 G>A maps to NM_001136198.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr14:31081504 G>A maps to NM_017769.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:151183517 C>T maps to NM_198395.1 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr5:151166244 C>T maps to NM_198395.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:76570829 A>T maps to NM_203505.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr4:76573847 A>G maps to NM_203505.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr17:42148527 G>A maps to NM_138387.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr23:153763533 A>G did not map to a codon.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr23:153762611 C>A did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr17:78090844 C>T maps to NM_001079804.1 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr17:78082575 G>A maps to NM_001079804.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:77934563 G>A maps to NM_080491.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:77991911 G>A maps to NM_080491.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr23:153940886 G>C did not map to a codon.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr23:153940945 G>C did not map to a codon.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr23:153927718 G>A did not map to a codon.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr23:153908428 A>G did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr22:17449241 T>A maps to NM_001037814.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr15:50596161 C>A did not map to a codon.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:151079597 C>G maps to NM_144618.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr5:161277822 A>T maps to NM_001127648.1 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr5:161302566 C>T maps to NM_001127648.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr5:161281259 G>A maps to NM_001127648.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr4:46312217 A>T maps to ENST00000507069 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr23:151336968 G>C did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:46976324 C>T maps to NM_000809.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr15:27193283 C>A maps to NM_000810.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:161116040 T>C maps to NM_000811.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr4:47427722 C>G maps to NM_000812.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr5:160753380 C>G maps to NM_021911.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:26793189 G>C maps to NM_021912.4 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr15:26825478 A>T maps to NM_021912.4 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr23:151123278 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:151123261 A>T did not map to a codon.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr23:151123189 C>A did not map to a codon.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr4:46043109 C>T maps to NM_173536.3 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:46043271 C>T did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr5:161520981 G>T maps to NM_198903.2 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr15:27777969 C>T maps to NM_033223.4 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr15:27772597 C>T maps to NM_033223.4 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:170239018 C>T maps to NM_014211.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr23:151821522 C>A did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr23:151818947 T>C did not map to a codon.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr23:151815616 G>C did not map to a codon.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr23:151808915 C>T did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:171687569 C>T maps to NM_000817.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:171709232 A>C maps to NM_000817.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr9:92220936 T>C maps to NM_006705.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr23:49173755 G>C did not map to a codon.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr23:49173728 G>A did not map to a codon.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr23:49173750 G>A did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr23:49179736 A>T did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr4:843562 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr11:65810469 G>A maps to NM_033036.2 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr1:24122441 G>A maps to NM_001008216.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:88889079 G>A maps to NM_000512.4 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr5:153755928 C>T maps to NM_198321.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr5:153755894 T>G maps to NM_198321.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr5:153796477 G>A maps to NM_198321.3 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:153795446 C>T maps to NM_198321.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr1:230372158 C>T maps to NM_004481.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr1:230398727 T>A maps to NM_004481.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:230410255 G>C maps to NM_004481.3 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr1:230338992 A>T maps to NM_004481.3 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr1:230372422 T>C maps to NM_004481.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr12:89917615 C>T maps to NM_003774.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr12:51758020 G>C maps to NM_007210.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr12:51757966 G>A maps to NM_007210.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:51752020 G>A maps to NM_007210.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr12:51758020 G>C maps to NM_007210.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:174225145 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr12:132834319 G>A maps to NM_001122636.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:16216673 C>T maps to NM_054110.4 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr11:11400752 G>T maps to NM_198516.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr19:1398923 G>A maps to NM_138924.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3923-01A-01D-1458-08 chr16:81391530 C>A maps to NM_022041.3 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr11:62396248 A>G maps to NM_198335.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr15:42632071 G>A maps to NM_198141.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:6645957 T>C did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr19:36029206 A>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr19:36033312 T>C did not map to a codon.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr19:36033312 T>C did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr9:128086082 C>A maps to NM_015635.2 S580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr9:128099710 A>T maps to NM_015635.2 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr4:110737329 C>T maps to NM_018983.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:30662009 G>A maps to NM_002047.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr9:89560845 C>G maps to NM_002048.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr11:22707335 G>C did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr22:29704661 C>G maps to NM_152236.1 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:34077158 G>C maps to NM_139285.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:9846495 G>A maps to NM_201433.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr16:90099332 G>A did not map to a codon.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr23:48649552 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:48652220 C>T did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr23:48652277 C>G did not map to a codon.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr10:8115904 C>T maps to NM_001002295.1 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr20:61050058 G>T maps to NM_080473.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr20:61040458 G>A maps to NM_080473.4 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr7:92078079 T>A maps to NM_021167.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr7:92083892 A>G maps to NM_021167.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:30685453 C>T maps to NM_001037666.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr1:155207293 C>T maps to NM_001005742.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:155205089 A>T maps to NM_001005742.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr9:35748455 A>T maps to NM_020944.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:56046041 G>C did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr10:104120010 T>C maps to NM_004193.2 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr10:104111128 C>T maps to NM_004193.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr10:104118422 G>T maps to NM_004193.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:89528890 G>T maps to NM_002053.2 G9G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4971-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr2:237076137 G>A maps to ENST00000415226 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr4:72620173 G>A maps to ENST00000504199 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr7:127224746 G>A maps to NM_024523.5 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:109109238 C>T maps to NM_181453.3 T1480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr2:109103097 T>A maps to NM_181453.3 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr2:109099525 C>T maps to NM_181453.3 A1118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr21:34120908 T>C maps to NM_016631.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr14:55310764 C>T maps to NM_001024024.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr7:44191995 C>G maps to NM_000162.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr1:94370099 T>C maps to NM_002061.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:120599293 C>T maps to NM_006836.1 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr12:120586151 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr12:120582189 G>T maps to NM_006836.1 I1805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr12:120572148 G>C maps to NM_006836.1 A2421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr9:79117315 C>T maps to NM_001097636.1 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr9:79118094 G>T maps to NM_001097636.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr6:10529525 C>T maps to NM_145649.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:58004286 C>T maps to NM_001018090.3 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr16:81118199 C>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:74838061 A>G maps to ENST00000238018 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:48429371 G>A maps to NM_004962.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr10:48429219 G>A maps to NM_004962.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr12:56142618 C>G maps to NM_005811.3 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:18499105 A>G maps to NM_004864.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr19:18499471 G>T maps to NM_004864.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr19:18497193 C>A maps to NM_004864.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:18499141 C>A maps to NM_004864.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr19:18499237 G>T maps to NM_004864.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr12:7843114 C>A maps to NM_020634.1 E152*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KM-8439-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr2:20870530 G>A maps to NM_182828.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:20871055 C>T maps to NM_182828.2 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr10:5855179 C>A maps to NM_001494.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:69645622 C>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:76944147 G>C maps to ENST00000376217 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr11:75160646 C>T maps to NM_030792.6 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:58010242 G>T maps to NM_001111270.1 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr12:58004439 G>T maps to NM_001111270.1 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:95262645 G>A maps to NM_181702.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr5:154278062 C>T maps to NM_015465.3 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr5:154270985 G>A maps to NM_015465.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:39008931 T>G maps to NM_024775.9 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:39008787 C>T maps to NM_024775.9 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr23:14038420 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr23:14038610 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:17955657 C>T maps to NM_001130009.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr7:925700 C>T maps to ENST00000457861 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74026106 G>T maps to NM_032380.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr5:74021463 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr5:179751867 G>A maps to NM_005110.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr8:21563504 C>T maps to NM_001495.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr20:3641541 G>A maps to NM_145762.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr20:3641290 A>C maps to NM_145762.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr20:3641541 G>A maps to NM_145762.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr16:23494280 C>A maps to NM_015044.4 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:73237523 G>T maps to NM_138619.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr17:73235513 C>G maps to NM_138619.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:34934556 C>T maps to NM_024835.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr17:34935725 G>T maps to NM_024835.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr17:34942390 A>G maps to NM_024835.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr22:25007057 A>T maps to NM_005265.2 K4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr22:25010805 G>A maps to NM_005265.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr20:33450695 G>A maps to NM_178026.2 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr20:33437794 C>T maps to NM_178026.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr20:23967128 C>T maps to NM_178311.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr22:22988910 G>A maps to ENST00000215938 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:61995167 G>T maps to NM_000515.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:40344971 C>T maps to NM_032484.4 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:40342211 A>G maps to NM_032484.4 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr3:172165984 C>T maps to NM_198407.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr11:59611469 C>T maps to NM_005142.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:100279775 C>T maps to NM_022574.4 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr7:100282979 G>A maps to NM_022574.4 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:100281054 T>A maps to NM_022574.4 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:233681743 T>A did not map to a codon.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr2:233677187 T>C maps to ENST00000373566 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr2:233680349 G>A maps to ENST00000373566 W726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233659497 T>A maps to ENST00000373566 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:233671360 T>A maps to ENST00000373566 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr7:150325337 G>A maps to ENST00000438845 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr7:150174243 C>T maps to NM_175571.2 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr16:58437162 C>T maps to NM_001126129.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr19:14591228 A>G maps to NM_202470.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:78601424 T>C maps to NM_017655.4 *316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr19:3586519 A>T maps to NM_133261.2 K85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr19:46185189 C>T maps to NM_000164.2 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:27902917 T>C did not map to a codon.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr6:121769049 T>C maps to NM_000165.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr6:90604513 G>A maps to NM_032602.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr1:147231204 C>A maps to NM_005266.5 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:70444363 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr23:70444040 A>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:70443743 G>A did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr1:35250611 C>T maps to NM_001005752.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:35250434 G>A maps to NM_001005752.1 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:35226980 G>A maps to NM_153212.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr1:35227532 C>T maps to NM_153212.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:35223026 C>T maps to NM_005268.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:35223632 C>T maps to NM_005268.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr15:35044906 C>T maps to NM_020660.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr10:35896875 C>A maps to NM_153368.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:30738148 G>A did not map to a codon.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr3:141934477 C>T maps to NM_001039547.2 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:69207169 A>G maps to NM_019617.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:100656699 G>A did not map to a codon.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr11:134240283 C>T maps to NM_138342.3 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr11:134241358 A>G maps to NM_138342.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:134147735 C>A maps to NM_001080407.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr11:134188592 G>A maps to NM_001080407.2 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:6536186 C>A maps to NM_000170.2 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr16:74506245 C>T did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr16:74640707 A>C maps to NM_012201.5 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:121708839 C>T maps to NM_005270.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:121746537 C>T maps to NM_005270.4 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr7:42079818 G>T maps to NM_000168.5 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr1:53972294 G>T maps to NM_147193.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:53995547 C>T maps to NM_147193.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr9:3856039 A>G maps to NM_001042413.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr1:92712095 C>G maps to NM_053274.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr5:151208499 C>T maps to NM_001146040.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:14748580 C>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:14599356 C>G did not map to a codon.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr4:175649780 A>G maps to NM_006529.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr23:102968575 C>T did not map to a codon.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr14:96010329 C>T maps to NM_016417.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr12:56865333 A>G maps to NM_013267.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr3:52731771 G>T maps to NM_018446.2 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr12:104390595 A>G maps to NM_031302.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:104391268 G>A maps to NM_031302.3 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:48205551 C>T maps to NM_015711.3 P1521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr19:48183113 A>G maps to NM_015711.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr19:48183659 G>A maps to NM_015711.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr19:48183986 G>T maps to NM_015711.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr19:48258771 G>A maps to NM_015710.4 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:120182119 C>T did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr23:120182435 A>G did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr23:120182119 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr23:120183025 T>G did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:120183025 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:120182122 A>T did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr23:120182804 T>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr23:120182435 A>G did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:120182070 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:120182479 A>G did not map to a codon.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr5:150646945 C>T maps to NM_000405.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr2:70057233 G>A maps to NM_178439.3 E70E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5703-01A-11D-1534-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr3:49760822 A>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:3110144 A>C did not map to a codon.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr9:80049324 G>A maps to NM_004297.3 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr7:79764503 A>T maps to NM_002069.5 K10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:79842141 A>G maps to NM_002069.5 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr3:50295031 C>T maps to NM_002070.2 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr3:50290460 C>T maps to NM_002070.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:110129421 C>T maps to NM_006496.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr18:11689822 G>A maps to NM_182978.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:56377828 C>T maps to NM_138736.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr20:57429459 C>A maps to NM_080425.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr7:80091850 G>C maps to NM_001102386.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr7:100276354 C>T maps to NM_005273.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:52446238 C>T maps to NM_016194.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr15:52476834 T>G maps to NM_016194.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr11:62475842 G>T maps to NM_012202.3 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr19:2515019 T>A maps to NM_052847.2 *69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr1:38059397 G>A maps to NM_013285.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr23:54577473 G>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:54578751 A>C did not map to a codon.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr23:54577457 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr23:54585052 C>T did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr6:42931106 G>A maps to NM_018960.4 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:102179967 T>C maps to NM_024312.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr9:127690520 G>A maps to NM_002077.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr9:131021535 C>T maps to NM_004486.4 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:131028576 G>A maps to NM_004486.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr9:131021445 C>T maps to NM_004486.4 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr12:133359034 C>T maps to NM_005895.3 E1104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:37369906 A>G maps to NM_001172713.1 K2002K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr3:37360553 A>T maps to NM_001172713.1 K494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:74365098 C>A maps to NM_001038640.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr15:74370973 T>C maps to NM_001038640.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:72954854 G>A maps to NM_018652.4 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:121412703 A>G maps to ENST00000393667 D2222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:121386443 G>A maps to ENST00000393667 Q3150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr3:121415220 T>C maps to ENST00000393667 Q1383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr3:121415880 C>T maps to ENST00000393667 W1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:121415216 G>A maps to ENST00000393667 Q1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr9:88648292 G>A maps to ENST00000376023 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr9:88692458 C>T maps to ENST00000376023 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr5:32126320 C>T maps to NM_022130.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr1:150634374 A>T maps to ENST00000369003 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr1:204183025 G>T maps to NM_198447.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr1:155735258 T>C maps to ENST00000368331 E1335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:155733232 T>C maps to ENST00000368331 A1532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr1:155732097 C>A maps to ENST00000368331 R1598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr1:155764937 T>C maps to ENST00000368331 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:155723184 G>A maps to ENST00000368331 Y1884Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:155726781 C>T maps to ENST00000368331 R1828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr17:28849290 C>T maps to NM_004871.2 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:45006906 T>C maps to NM_054022.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr10:101163594 G>A maps to NM_002079.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr16:58749997 A>C maps to NM_002080.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:20327329 T>C maps to NM_001007240.1 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr16:20331780 G>A maps to NM_001007240.1 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr19:55539165 T>A maps to NM_001083899.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:145139220 G>A maps to NM_003801.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr10:113913351 G>A maps to NM_020918.4 R815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr19:33608750 C>T maps to NM_018025.2 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr17:42475997 C>T maps to NM_001002909.2 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:42477629 G>A maps to NM_001002909.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:56542172 T>A maps to NM_001127236.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:46124747 A>G maps to NM_021639.4 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr23:132834051 C>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:132437059 A>C did not map to a codon.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr23:132437028 A>C did not map to a codon.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr13:94482722 C>T maps to NM_005708.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:50503241 C>G maps to NM_005276.2 Y330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:157426663 G>A maps to NM_000408.4 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:157367410 C>T maps to NM_000408.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr14:67147885 C>T maps to NM_020806.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr23:48979946 A>T did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:48979067 G>A did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr2:27851882 C>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr12:110902938 T>C maps to NM_001164373.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr12:110897605 G>T maps to NM_001164373.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:207040929 G>A maps to NM_005279.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr23:136112590 A>T did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr23:136112679 C>T did not map to a codon.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr23:136112625 A>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:132897301 A>G did not map to a codon.
Sequencing variant TCGA-B8-4619-01A-02D-1553-08 chr9:132890995 C>T maps to NM_001136557.1 Y554Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr19:6731510 C>T maps to NM_001080452.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:6733231 G>A maps to NM_001080452.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr23:135498623 A>G did not map to a codon.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr23:135431577 A>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:135431754 A>G did not map to a codon.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr23:135441580 G>A did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr23:135431433 A>C did not map to a codon.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr23:135432121 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr23:135431959 C>A did not map to a codon.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr23:135429077 T>C did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:135494442 T>C did not map to a codon.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr23:135431235 T>C did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:26532907 C>A maps to NM_001145168.1 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr6:46826441 G>A maps to NM_015234.4 T1066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:46849805 G>A maps to NM_015234.4 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr23:129518456 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr13:27332980 C>T maps to NM_005288.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr13:27333241 C>T maps to NM_005288.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr13:27333001 C>T maps to NM_005288.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr8:37696505 C>T maps to NM_032777.9 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:142691577 C>T maps to NM_198569.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:142741041 C>T maps to NM_198569.2 F1040F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:100356180 C>T maps to NM_032787.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:100354671 T>A did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:131590406 C>A maps to NM_198827.3 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:131466489 G>A maps to NM_198827.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr11:64054435 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:72368138 C>A maps to ENST00000440684 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr23:9714192 C>T did not map to a codon.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr7:1097894 A>G maps to NM_138445.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:131486933 G>A maps to NM_207364.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:154146816 G>A maps to NM_001038705.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:154055934 A>G maps to NM_001038705.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr5:94957232 A>C maps to NM_199243.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr11:67218863 G>A maps to NM_206997.1 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr11:67219268 C>A maps to NM_206997.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr11:67219406 G>A maps to NM_206997.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr2:175346285 T>C maps to NM_152529.5 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:119885980 A>G maps to NM_153002.2 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr10:25464833 G>A maps to NM_020752.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr10:25887314 C>G maps to NM_020752.2 T920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr3:169802071 T>C maps to NM_014373.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:169802563 G>A maps to NM_014373.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:150916819 G>A maps to NM_013308.3 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr17:4937585 G>T maps to NM_017986.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr17:4937402 G>T maps to NM_017986.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr23:53106302 T>G did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:53106924 A>G did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr23:78426649 A>C did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr23:78426731 C>A did not map to a codon.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr17:36495344 T>G maps to ENST00000398597 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:95271584 G>A did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:57389790 C>G maps to NM_007264.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:57389325 G>A maps to NM_007264.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr12:12815271 G>A maps to NM_006143.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:107115464 T>A maps to NM_005295.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr10:125426345 G>A maps to NM_153442.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr3:71804018 G>T maps to NM_018971.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:71804264 C>T maps to NM_018971.1 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr19:51274132 A>G maps to NM_001506.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:51273913 G>C maps to NM_001506.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:41555434 T>A did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr7:124405026 G>A maps to NM_005302.2 R2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr1:202097557 C>T maps to NM_004767.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:202097356 C>T maps to NM_004767.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr2:133175093 G>A maps to NM_001508.2 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:46094944 G>A maps to NM_005282.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr11:60621138 A>G maps to NM_004778.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:105858581 C>G maps to NM_007227.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr2:105859153 G>A maps to NM_007227.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr23:150349559 C>T did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:150348664 G>A did not map to a codon.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr1:174417938 C>T maps to NM_005684.4 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:174418157 C>A maps to NM_005684.4 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr1:110086264 T>C maps to NM_031936.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr23:19026096 C>T did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:19026232 C>G did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:54080606 A>G maps to NM_006794.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr4:8582798 C>T maps to NM_080819.2 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr4:8588870 G>A maps to NM_080819.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:54756648 G>A maps to NM_020370.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr16:57713135 C>A maps to NM_170776.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr5:89971180 C>T maps to NM_032119.3 I1744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr5:89986797 G>A maps to NM_032119.3 G2297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr5:90025456 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:89989973 A>T maps to NM_032119.3 T2467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:90149226 A>G maps to NM_032119.3 L5777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:89979467 T>C maps to NM_032119.3 D1910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr23:101911559 T>G did not map to a codon.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr23:101913004 C>T did not map to a codon.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr23:101910198 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:101910682 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:101908966 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr23:101910062 T>A did not map to a codon.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr23:101971083 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:101971024 G>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:19884047 G>A maps to NM_016235.1 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr17:72428209 C>G maps to NM_022036.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:72436052 T>A maps to NM_022036.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr12:13103069 C>T maps to NM_018654.1 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:47000238 C>T maps to NM_014696.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr16:46950589 G>T maps to NM_133443.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr16:46958368 C>T maps to NM_133443.2 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr19:35501011 G>T maps to NM_020895.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr11:123448254 G>A maps to ENST00000456860 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr3:113594421 A>G maps to NM_017577.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr3:113623085 A>G maps to NM_017577.4 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:40367066 C>T maps to NM_004810.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr12:52401015 C>A maps to NM_181711.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr7:50737541 G>A maps to NM_005311.4 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr7:50742287 G>A maps to NM_005311.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr2:11774454 C>T maps to NM_014668.3 N1730N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr2:11777870 G>A maps to NM_014668.3 P1792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr2:11706654 G>A maps to NM_014668.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr1:24666206 C>G maps to NM_021180.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:153065876 C>T maps to NM_001114183.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr4:158282179 A>C maps to NM_001083619.1 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr4:158142837 C>T maps to NM_000826.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr11:105623881 A>T maps to NM_000829.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr11:105776028 T>G did not map to a codon.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr10:87407077 G>T maps to NM_017551.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr10:87484286 T>G maps to NM_017551.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr10:87379670 C>A maps to NM_017551.2 G771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr4:94411802 G>A maps to NM_001510.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr21:30963506 C>T maps to ENST00000327783 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr11:120833223 C>T maps to NM_014619.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:120745882 C>T maps to NM_014619.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr19:42566908 C>A did not map to a codon.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:13906648 T>A maps to NM_000834.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr12:13716544 C>G maps to NM_000834.3 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:13828723 C>T maps to NM_000834.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr17:72842987 G>A maps to NM_000835.3 N691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr9:104499649 G>T maps to NM_133445.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr9:104341504 C>T maps to NM_133445.2 K968K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:1003373 G>A maps to NM_138690.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr8:145066242 A>T maps to NM_001009184.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:145066936 G>A maps to NM_001009184.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr12:66838417 G>A maps to ENST00000359742 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:66786507 A>G maps to ENST00000359742 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:14559361 G>A maps to ENST00000507975 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:48840221 C>T did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr10:121212788 G>A did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr5:176863392 G>T did not map to a codon.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr19:47424643 G>A maps to NM_004491.4 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr19:47424188 C>T maps to NM_004491.4 Q753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr19:47491244 G>C did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr6:146720022 G>T maps to NM_000838.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:34100943 G>T maps to NM_000841.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr6:34059741 C>T maps to NM_000841.1 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr5:178416291 G>C maps to NM_000843.3 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr7:126086264 G>T maps to NM_001127323.1 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr7:126173362 A>G maps to NM_001127323.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr7:126883201 G>A maps to NM_001127323.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:148730493 C>T maps to NM_152407.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr5:148730748 C>T maps to NM_152407.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr23:16168711 T>A did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr22:19137289 G>A maps to NM_005315.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr22:19137289 G>A maps to NM_005315.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:119642254 G>T maps to NM_002093.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:124074614 A>T did not map to a codon.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr23:51488137 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr23:51487801 C>T did not map to a codon.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr6:52622678 G>A maps to NM_000846.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr6:52764812 T>C maps to NM_000847.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:67352041 G>C did not map to a codon.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr22:24300633 G>T maps to NM_000854.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr13:28367052 C>T maps to NM_145657.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:144765014 A>G maps to NM_001164629.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr14:81682786 C>T maps to NM_015859.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr2:48897081 T>C maps to NM_172311.2 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr3:120495383 C>T maps to NM_005513.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:30436511 G>A maps to NM_002095.4 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30877828 C>T maps to NM_001517.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:74129237 T>C did not map to a codon.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr7:74212074 G>T maps to NM_173537.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr7:74563944 C>A maps to NM_001003795.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr16:27523214 G>A maps to NM_001520.3 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:27549610 C>T maps to NM_001520.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr16:27523127 T>C maps to NM_001520.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:27565919 G>T maps to NM_001521.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr9:135555165 A>G maps to NM_012204.2 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135553527 C>T maps to NM_012204.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135919148 G>A maps to NM_001122823.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:17448960 A>C maps to NM_133644.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr10:1043229 G>A maps to NM_012341.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr22:46719126 A>G maps to NM_016426.6 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr22:46712157 C>A maps to NM_016426.6 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr12:54857069 A>G maps to NM_144594.2 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr12:54856510 T>A did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr12:54856985 A>G maps to NM_144594.2 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr20:42355034 G>A maps to NM_176791.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr4:156638324 C>T maps to NM_001130684.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:14772232 A>C maps to NM_004963.3 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:7919109 G>A maps to NM_000180.3 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:108631734 C>A did not map to a codon.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr23:108638654 G>A did not map to a codon.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr23:108636244 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr23:108708502 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr23:108631718 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr23:108691324 C>T did not map to a codon.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr4:44700674 C>T maps to NM_021927.2 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr4:44692822 G>A maps to NM_021927.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr7:65441160 C>T maps to NM_000181.3 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr12:42512816 A>G maps to NM_173601.1 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:2772025 T>A did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr19:49485592 A>G maps to NM_002103.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:49490606 A>T maps to NM_002103.4 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:49473832 G>A maps to NM_002103.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr20:23347702 C>T maps to NM_022482.3 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr5:54329717 G>A maps to NM_002104.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr22:38201646 C>T maps to NM_005318.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr10:71868912 G>A maps to NM_018649.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr12:31944926 G>A maps to NM_001013699.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr12:31944971 A>G maps to NM_001013699.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:9305535 C>T maps to NM_004285.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr6:105192485 C>A did not map to a codon.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr6:105298825 A>G maps to NM_020771.3 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr6:105233139 C>A maps to NM_020771.3 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr3:15609988 A>G maps to NM_012260.2 N400N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr16:1869996 A>G maps to NM_005326.4 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr16:1866932 G>A maps to NM_005326.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr5:153857037 C>G maps to NM_004821.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr4:174449978 C>T maps to NM_021973.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:119923770 T>C maps to ENST00000361035 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:39887799 G>A maps to ENST00000310778 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr5:82940356 G>T maps to NM_001884.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr5:82948368 G>T maps to NM_001884.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr1:156593854 C>T maps to NM_021817.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:19371724 G>A maps to NM_023002.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:19369434 A>G maps to NM_023002.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr11:46625223 G>A maps to NM_173811.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:46637367 C>A maps to NM_173811.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr5:140073222 A>G maps to NM_012208.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:52217096 G>A maps to NM_001523.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr16:69149148 T>C maps to NM_005329.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr18:43700026 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr23:152721102 T>C did not map to a codon.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr23:152719887 T>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr5:156482503 A>C maps to NM_001173393.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr5:156479567 C>T maps to NM_001173393.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr16:230577 A>G maps to NM_005331.4 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr23:11139772 G>A did not map to a codon.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr23:153222974 G>A did not map to a codon.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr23:153215017 C>T did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr23:153223255 C>G did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr23:153215991 A>T did not map to a codon.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr23:153236255 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:153236182 G>T did not map to a codon.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr23:153220584 T>C did not map to a codon.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr23:153230056 T>C did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:121351314 G>A maps to NM_005335.4 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr5:45262589 C>T maps to NM_021072.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:45461991 G>A maps to NM_021072.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr5:45267263 G>A maps to NM_021072.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:613897 T>C maps to NM_001194.3 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:605092 G>A maps to NM_001194.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:155252387 T>C maps to NM_020897.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:73660575 G>C maps to NM_005477.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr6:55119935 C>T maps to NM_001526.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr22:50684493 A>G maps to NM_032019.5 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:13525051 T>G maps to NM_024827.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:114264644 A>C maps to ENST00000398283 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:141007713 C>A maps to NM_003883.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr2:240011716 T>C maps to NM_006037.3 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:239988462 A>T maps to NM_006037.3 I981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr2:240033258 A>G maps to NM_006037.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:48676772 A>G did not map to a codon.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr23:48681370 G>A did not map to a codon.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr23:48681738 G>A did not map to a codon.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr23:48674582 T>C did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr23:48674572 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr23:48674607 C>T did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr23:48682179 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:48185381 G>A maps to NM_015401.3 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr23:71681921 G>C did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr7:18625058 C>T maps to NM_178425.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:18975516 C>T maps to NM_178425.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr7:18705936 G>A maps to NM_178425.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr23:7035034 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr23:7023837 T>G did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:44662720 T>C maps to NM_032124.4 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr18:44639348 A>T maps to NM_032124.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:242196032 T>C maps to NM_005336.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr2:242179324 G>A maps to NM_005336.3 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr2:242203955 A>C maps to NM_005336.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:242173342 G>A maps to NM_005336.3 D1060D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr23:83724058 T>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:83599462 A>C did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:83616515 T>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:236762780 A>G did not map to a codon.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr7:796570 G>T maps to NM_017802.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr16:50128613 A>T did not map to a codon.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr16:50120248 T>G maps to NM_182922.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr16:50104087 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr14:31817064 G>A maps to ENST00000389961 A913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr14:31844039 G>A maps to ENST00000389961 R609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr2:37227888 C>T maps to NM_019024.1 K1795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:37280724 C>A maps to NM_019024.1 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:58156269 A>G maps to NM_022070.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr5:41045850 C>T maps to ENST00000296803 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr5:41064634 G>T maps to ENST00000296803 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:41045850 C>T maps to ENST00000296803 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr6:138727186 C>A maps to NM_014320.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr1:45476653 G>C maps to NM_024602.5 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:45476718 G>A maps to NM_024602.5 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr7:43484070 G>T maps to NM_015052.3 G434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr7:43503282 T>C maps to NM_015052.3 I892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:43581575 T>A maps to NM_015052.3 V1409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr7:43484309 T>C maps to NM_015052.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr7:43351594 C>A maps to NM_015052.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr2:197194347 A>T maps to NM_020760.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr3:124732418 A>G maps to NM_020733.1 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:66731857 G>A maps to NM_033647.2 K1080K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr10:96352149 A>T did not map to a codon.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr10:96354516 T>G maps to NM_018063.3 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr4:84374450 A>C maps to NM_133636.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr4:84362514 A>C maps to NM_133636.2 Y535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr4:84342847 A>G maps to NM_133636.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr17:65184579 T>C maps to NM_014877.3 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:65074430 G>A maps to NM_014877.3 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr17:65119195 A>G maps to NM_014877.3 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:65162706 T>C maps to NM_014877.3 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr17:65141856 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:65134097 G>A maps to NM_014877.3 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:65423313 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:65390504 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr23:65474913 G>T did not map to a codon.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr15:63950915 A>T maps to ENST00000261887 G3142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:64021463 C>T maps to ENST00000261887 W1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr15:64005709 C>T maps to ENST00000261887 Q1435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:63948031 G>A maps to ENST00000261887 N3331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:63966708 G>A maps to ENST00000261887 R2560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr15:28446697 A>G maps to NM_004667.4 S2540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr15:28491150 G>A maps to NM_004667.4 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr15:28414718 A>G maps to NM_004667.4 L3380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr15:28375698 G>A maps to NM_004667.4 C4204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr15:28501376 C>T maps to NM_004667.4 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr15:28482157 C>G maps to NM_004667.4 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:89575197 G>T maps to NM_014606.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:89410408 C>G maps to NM_016323.2 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr4:89425490 C>T maps to NM_016323.2 I897I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr4:89408217 A>G did not map to a codon.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr4:89408221 C>T maps to NM_016323.2 D618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr7:35678057 C>A maps to NM_022373.4 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr7:35707132 A>G maps to NM_022373.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr7:35673461 C>T did not map to a codon.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:239147554 A>G maps to NM_018645.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr17:80391634 C>A maps to NM_173620.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr17:80394585 C>T maps to NM_173620.2 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:80382346 T>C maps to NM_173620.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr8:80678001 G>A maps to NM_001040708.1 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr1:91726879 C>T maps to NM_001017975.3 K1425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:91809064 A>G maps to NM_001017975.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:210573840 G>T maps to NM_001170580.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr4:145568087 A>C maps to NM_022475.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr4:145635413 T>C maps to NM_022475.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:100119114 C>G maps to NM_001127258.1 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:100141821 G>A maps to NM_001127258.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:222715412 G>A maps to NM_024746.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:27582615 C>G maps to NM_152740.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:27672040 A>G maps to NM_152740.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr14:62200985 T>A maps to ENST00000394997 C338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr14:62211421 G>C did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:130500844 G>T maps to NM_005340.5 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr6:126288133 A>G maps to NM_138571.4 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr7:75183808 C>T maps to NM_005338.4 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr12:123343989 C>T maps to NM_003959.1 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr12:123343702 C>T maps to NM_003959.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:139258059 C>A maps to NM_022740.4 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr11:33363110 A>G maps to NM_005734.3 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:33374882 T>C maps to NM_005734.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr16:30006454 C>T maps to NM_003609.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr6:26056095 T>C maps to NM_005319.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr6:26056014 C>T maps to NM_005319.3 *214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr6:26056470 C>T maps to NM_005319.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr6:27860780 C>G maps to NM_003514.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr6:26124126 A>G maps to NM_003526.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr6:26158750 C>T maps to NM_138720.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr6:26273394 C>T maps to NM_003525.2 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:27100490 C>T maps to NM_021058.3 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr6:27114568 T>C maps to NM_080593.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:27775402 C>T maps to NM_003519.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:26021007 C>T maps to NM_003529.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1458-08 chr6:27839910 C>T maps to NM_003533.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:26104204 C>G maps to NM_003542.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149859100 C>T maps to NM_175065.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149859427 A>G maps to NM_175065.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149858562 C>T maps to NM_003517.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149858592 C>T maps to NM_003517.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr12:14923793 C>T maps to NM_175054.2 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr6:12123739 T>C maps to NM_002114.2 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr6:12125186 C>A maps to NM_002114.2 S1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr6:143094138 T>A maps to NM_006734.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr6:143081502 A>G maps to NM_006734.3 T1974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr6:143093079 C>T maps to NM_006734.3 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:41976754 G>C maps to NM_024503.3 P2196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:42048584 A>T maps to NM_024503.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr1:42049238 G>A maps to NM_024503.3 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr2:234749784 A>G maps to NM_018410.3 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:234749355 G>C maps to NM_018410.3 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:71128299 G>A maps to ENST00000439900 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr10:71048513 C>A maps to ENST00000439900 C5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr10:71103743 T>C maps to ENST00000439900 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr2:75107667 C>T maps to NM_000189.4 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr5:176308430 G>T maps to NM_002115.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr6:29911239 T>A maps to ENST00000376806 L180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr6:31323370 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:31324627 G>A maps to ENST00000428231 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:31324175 C>G maps to ENST00000428231 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr6:31323115 C>T maps to ENST00000428231 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr6:31324594 C>G maps to ENST00000428231 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr6:31238125 G>A maps to ENST00000383329 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr6:31237785 A>T maps to ENST00000383329 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr6:31237139 A>T maps to ENST00000383329 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr6:31238928 C>G maps to ENST00000383329 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr6:31238008 T>C maps to ENST00000383329 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr6:31239048 G>T maps to ENST00000383329 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr6:31239517 C>T maps to ENST00000383329 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:32714065 C>T maps to NM_020056.4 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr6:32714167 A>G maps to NM_020056.4 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr6:32632776 C>T maps to ENST00000374943 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr6:32634330 G>C maps to ENST00000374943 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr6:32557476 G>A maps to NM_002124.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr6:32549586 T>G maps to NM_002124.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:32489852 A>G maps to NM_002125.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr6:32497899 A>G did not map to a codon.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr6:32497974 A>G maps to NM_002125.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr6:32487168 C>T maps to NM_002125.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr6:32487213 T>C maps to NM_002125.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr6:32487267 A>G maps to NM_002125.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr6:30459115 T>A maps to NM_005516.5 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr6:30459404 T>C maps to NM_005516.5 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:29692859 C>T maps to NM_001098479.1 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:29692865 G>A maps to NM_001098479.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr6:29797246 C>T maps to ENST00000376828 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:29797393 G>A maps to ENST00000376828 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:29797252 G>A maps to ENST00000376828 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr6:29797246 C>T maps to ENST00000376828 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr6:29797252 G>A maps to ENST00000376828 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr6:29797429 G>T maps to ENST00000376828 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr3:148789183 C>T maps to NM_003071.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr8:28827802 C>T maps to ENST00000444075 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr11:118963205 C>A maps to NM_000190.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:186064395 C>G maps to NM_031935.2 S3439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:185985178 G>T maps to NM_031935.2 G1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:186083138 G>A maps to NM_031935.2 Q3720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:185984289 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr1:186072769 A>G maps to NM_031935.2 G3580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:186024753 T>A maps to NM_031935.2 V2364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr1:185891567 C>T maps to NM_031935.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr15:77756617 C>T maps to NM_018200.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:77759507 C>A maps to NM_018200.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:77750832 C>G maps to NM_018200.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:34210571 G>A maps to NM_145899.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr13:31036767 C>T maps to NM_002128.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:174254649 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:24151845 A>G maps to NM_000191.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr1:120307116 C>A maps to NM_005518.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:79918283 G>T maps to NM_004242.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:1082888 G>T maps to NM_012292.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr19:1067421 A>G maps to NM_012292.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr19:1084343 A>G maps to NM_012292.2 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr19:1073205 C>A maps to NM_012292.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:1081616 A>G maps to NM_012292.2 Q753Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr5:162910058 A>G maps to NM_001142556.1 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:4557883 G>T maps to NM_001127205.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr16:4557976 C>T maps to NM_001127205.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr5:173534369 C>T maps to NM_015980.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr18:61627534 C>T maps to NM_001123366.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr12:121437342 C>T maps to NM_000545.5 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:36099581 T>C maps to NM_000458.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr17:36104839 G>T maps to NM_000458.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr8:76456145 A>G maps to NM_004133.4 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr5:137088930 G>A maps to NM_006805.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:177632983 G>A maps to NM_031266.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr5:179047902 C>T maps to NM_005520.2 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr5:179043166 G>A maps to NM_005520.2 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:100668186 A>G did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr9:86587098 G>T maps to NM_031262.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:86585224 T>A maps to NM_031262.2 K405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:245022574 A>G did not map to a codon.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr1:245021519 G>A maps to NM_031844.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr1:245022135 T>C maps to NM_031844.2 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:41807609 G>C did not map to a codon.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr11:62491446 C>A maps to NM_001079559.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr11:62489599 C>A maps to NM_001079559.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr5:78672017 T>C maps to NM_004272.3 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr14:23744843 C>T maps to NM_020834.2 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr14:23744846 T>C maps to NM_020834.2 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr14:23744825 T>C maps to NM_020834.2 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr19:12881983 C>T maps to NM_013312.2 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr19:12875720 C>T maps to NM_013312.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr8:42821724 C>T maps to NM_032410.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:150689612 C>T did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr7:27211694 C>T maps to NM_018951.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr7:27169875 C>A maps to NM_002141.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr17:46608209 G>T maps to NM_002144.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:46805883 C>T maps to NM_006361.5 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr17:46628007 C>T maps to NM_002146.4 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr17:46654167 G>C maps to NM_024015.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:54383106 C>T maps to NM_017409.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr12:54394496 C>T maps to NM_006897.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr2:177033994 A>C maps to NM_006898.4 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr1:21100039 G>T maps to NM_016287.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr4:175443218 C>A did not map to a codon.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr19:35540221 A>G maps to NM_182983.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr16:72110799 G>A maps to ENST00000228226 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr23:133609297 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr10:100177389 G>A maps to NM_000195.2 D678D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:100177416 G>A maps to NM_000195.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr22:26859936 C>G maps to NM_022081.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:18327002 G>A maps to NM_181507.1 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr10:103826146 G>T maps to NM_024747.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:84243393 G>A maps to NM_006665.5 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr10:100481427 G>A maps to NM_021828.4 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:100481442 C>T maps to NM_021828.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr8:21985224 C>A maps to NM_005144.4 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr8:21974549 C>T maps to NM_005144.4 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr19:49656871 C>T maps to NM_002152.2 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr3:186395000 G>T maps to NM_000412.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:11301061 G>A maps to NM_001098211.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:22048830 C>T maps to NM_021624.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr1:152188023 C>G maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr2:20824633 T>C maps to NM_022460.3 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr2:20838371 A>G maps to NM_022460.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:20818845 C>T maps to NM_022460.3 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:87570376 T>C maps to NM_012262.3 *357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:11401503 G>A maps to NM_005114.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:26147415 G>A maps to NM_006040.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:129025736 T>A maps to NM_004807.2 *412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr2:129025927 G>A maps to NM_004807.2 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:132091224 G>C did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr23:132091341 C>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:53458522 C>T did not map to a codon.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr4:88303418 G>A maps to NM_016245.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:43837919 T>C maps to NM_016142.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr6:33172820 C>T maps to NM_014234.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr16:84158327 A>C maps to NM_031463.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr21:45053271 C>A maps to NM_007031.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:56565508 G>A maps to NM_001080439.1 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr14:102548765 G>A maps to NM_001017963.2 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr12:104341409 G>A did not map to a codon.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr10:118435937 C>T maps to NM_025015.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr10:14890640 G>A maps to NM_016299.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr6:31779707 G>A maps to NM_005527.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr6:31778273 G>T maps to NM_005527.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:65008124 G>A maps to NM_021979.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr5:132425376 T>C maps to NM_002154.3 D456D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr4:128725180 A>G maps to ENST00000438626 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:128001453 A>G maps to NM_005347.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:161495203 G>A maps to NM_002155.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:122930667 A>G maps to NM_006597.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr11:122930261 G>A maps to NM_006597.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:122931840 G>A maps to NM_006597.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr11:122930928 A>G maps to NM_006597.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:122931402 G>A maps to NM_006597.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr5:137902358 C>A maps to NM_004134.6 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr5:137903400 C>T maps to NM_004134.6 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr2:198363396 A>C did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:198365880 A>G maps to NM_002157.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr1:22168730 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr1:22190694 G>A maps to NM_005529.5 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr1:22222713 C>T maps to NM_005529.5 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr11:20403770 T>C maps to NM_001098520.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr23:135594032 A>T did not map to a codon.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr23:135581830 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr5:63257392 G>A maps to NM_000524.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr13:47470002 T>A maps to NM_000621.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:231973290 A>G maps to NM_000867.4 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:113965886 G>C did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:183756413 T>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr7:154863208 C>T maps to NM_024012.2 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr7:154862731 G>T maps to NM_024012.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:20005812 C>T maps to NM_000871.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr10:92617161 C>G maps to NM_019859.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr4:8294058 C>T maps to NM_053044.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr4:3138011 A>G maps to NM_002111.6 E919E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:3201561 C>T maps to NM_002111.6 S1824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr4:3208254 G>T maps to NM_002111.6 T1917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:3124640 T>C maps to NM_002111.6 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:3076695 T>G maps to NM_002111.6 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr4:3234984 C>G maps to NM_002111.6 L2787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:3107130 G>A maps to NM_002111.6 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:53564525 T>G did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr23:53579771 T>A did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:53674402 C>G did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:53563621 T>C did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr23:53589173 C>T did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr23:53586384 G>T did not map to a codon.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr23:53579647 G>T did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:53607788 A>G did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr23:53585979 C>T did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr23:53622277 C>A did not map to a codon.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr23:53612104 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:53564648 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr23:53675214 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr23:53595733 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:53577911 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr23:53615355 T>A did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr23:53584382 A>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:53641558 C>T did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr23:53563130 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:53615354 G>A did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr23:53586461 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:111089051 G>T maps to NM_001040107.1 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:50357590 C>T maps to NM_033158.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3923-01A-01D-1458-08 chr7:123516947 C>T maps to NM_012269.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr16:70884502 A>G maps to NM_032821.2 L4166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr16:70866801 A>G maps to NM_032821.2 P4615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr16:71163578 C>T maps to NM_032821.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr16:71025244 C>T maps to NM_032821.2 T1280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:71127827 G>A maps to NM_032821.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr11:118917417 G>A maps to NM_001130991.1 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr9:95027314 G>A maps to ENST00000375660 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr1:220316403 C>T maps to NM_018060.3 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:220318981 C>T maps to NM_018060.3 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr6:82950104 A>T maps to NM_015525.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr19:10394733 T>C maps to NM_000201.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:10444568 T>A maps to NM_002162.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr19:10407168 G>C maps to NM_003259.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr10:94291640 A>G maps to NM_004969.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:90634782 A>G did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr20:2639398 A>C maps to NM_006899.2 *386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:153059773 A>G did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr23:153055661 T>A did not map to a codon.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr8:39775605 G>A did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr8:39862888 T>C maps to NM_194294.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:148564297 A>C did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:6649693 A>G maps to NM_001193457.1 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr1:158988365 G>A maps to ENST00000295809 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:18286173 G>A maps to NM_006332.3 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:18288014 C>T maps to NM_006332.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr10:91162802 A>T maps to NM_001548.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:91143310 T>C maps to NM_001010987.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr10:91177426 A>G maps to NM_012420.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr9:21350655 G>T maps to NM_021002.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:21201942 A>T maps to NM_021057.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr21:34725062 G>A did not map to a codon.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr21:34721420 A>T maps to NM_000629.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr21:34727797 T>C maps to NM_000629.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr6:137519167 T>A maps to NM_000416.2 *490C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr6:137528119 G>A maps to NM_000416.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr21:34809268 A>T maps to ENST00000381995 *357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr21:34799206 A>T maps to ENST00000381995 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:50329825 A>G maps to ENST00000336089 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1574678 G>A maps to NM_014714.3 N1005N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1612075 G>A maps to NM_014714.3 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:27704120 A>G maps to NM_015662.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr2:27671790 A>G maps to NM_015662.1 A1473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr3:160095233 T>C maps to ENST00000326448 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr12:110565895 C>T maps to NM_014055.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr13:21163993 T>C maps to NM_175605.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr15:65667722 C>A maps to NM_004884.3 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr15:65624283 G>A maps to NM_004884.3 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr15:65628244 A>G maps to NM_004884.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65684504 T>A maps to NM_020962.1 K697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr15:99192875 G>A maps to NM_000875.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr15:99482524 C>T maps to NM_000875.3 F1131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr15:99192821 C>T maps to NM_000875.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:99454670 G>A did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr11:2154814 G>A maps to NM_001127598.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr3:185376128 A>C maps to NM_006548.4 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr6:160471665 C>T maps to NM_000876.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr7:45957038 C>G did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:217541548 C>G maps to NM_000599.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr1:201180221 G>A maps to NM_001164586.1 E2067E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr1:201180242 A>G maps to NM_001164586.1 L2074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:201166404 C>T maps to NM_001164586.1 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr22:23915500 G>A maps to NM_020070.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr19:51828627 G>A maps to NM_001101372.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:51831096 C>A maps to NM_001101372.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr23:130409966 T>C did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:130416648 C>A did not map to a codon.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr23:130409626 G>T did not map to a codon.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr23:130410025 C>T did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr23:130409463 G>A did not map to a codon.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr3:151160938 A>C maps to NM_178822.4 L1932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:151156201 T>C maps to NM_178822.4 Q2049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr3:151161388 T>A maps to NM_178822.4 A1782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:151165119 T>C maps to NM_178822.4 Q883Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:18738323 G>A maps to NM_173588.3 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr11:18729751 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr11:18738273 C>T did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr11:18738380 A>G maps to NM_173588.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:117122272 G>A maps to NM_001542.2 D1045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:117158747 A>G maps to NM_001542.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr1:117158771 C>T maps to NM_001542.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr11:133802055 G>T maps to NM_014987.1 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:133814178 C>A maps to NM_014987.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:133805657 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr11:133807379 G>A maps to NM_014987.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr11:133789677 C>T maps to NM_014987.1 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:133800912 C>T maps to NM_014987.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr12:99019896 C>A maps to NM_153687.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr9:111659235 G>A maps to NM_003640.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr23:153770606 G>T did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr23:153770611 G>C did not map to a codon.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr7:50467715 C>T maps to NM_006060.3 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr7:50444369 C>T maps to NM_006060.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr2:213872773 A>G maps to ENST00000342002 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr1:206944317 G>A maps to NM_000572.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr3:159706881 A>C maps to NM_000882.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr19:18191684 C>T maps to NM_005535.1 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:117907850 G>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:81517937 A>G maps to NM_172217.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr15:81589273 G>A maps to NM_172217.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr6:52054065 C>A maps to NM_002190.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr13:21295993 C>T maps to NM_138284.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr22:17566095 C>A maps to NM_014339.5 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:53891718 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:9959172 C>T maps to NM_153461.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr3:57136552 C>T maps to NM_017563.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr3:9957049 C>T maps to NM_153483.2 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr2:103067329 C>T maps to NM_003853.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:207014375 C>T maps to NM_153758.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:113540316 G>T maps to NM_000575.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:29973428 A>C did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:104961378 C>G did not map to a codon.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr23:104961394 G>A did not map to a codon.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr23:103903656 G>A did not map to a codon.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:102956733 T>G did not map to a codon.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:102964402 A>G did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:102849532 C>T maps to NM_003854.2 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:27459982 G>T maps to NM_181079.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:68646406 C>A maps to NM_020525.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr1:207072688 G>A maps to NM_001185156.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr14:23844832 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:14157045 C>G maps to NM_004843.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:24484204 T>C maps to NM_170743.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr10:6054845 T>G maps to NM_000417.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:6063567 G>A maps to NM_000417.2 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr12:122656991 T>C maps to NM_001014336.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:55212821 T>C maps to NM_139017.4 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr9:6251224 C>G maps to NM_033439.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:50397530 G>C maps to NM_172374.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:50393784 C>T maps to NM_172374.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr16:27374875 C>T maps to NM_000418.2 Q735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:27374338 C>T maps to NM_000418.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr16:27374116 C>T maps to NM_000418.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:27374133 G>A maps to NM_000418.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr3:3144421 A>G maps to NM_000564.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr7:22771125 T>G maps to NM_000600.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:154408587 T>C did not map to a codon.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr1:154401717 T>A maps to NM_000565.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr5:55256362 G>T maps to NM_002184.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr5:135228121 A>G maps to NM_000590.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr23:155232600 G>A did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr23:155239823 A>G did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr23:155239826 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:155239601 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr23:155233147 C>A did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:155239601 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:166944469 G>A maps to NM_199351.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr1:153637768 A>G maps to NM_004515.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr19:10799268 C>T maps to NM_017620.2 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:10794617 C>T maps to NM_017620.2 Y681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr2:239090746 A>C maps to NM_030768.2 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr19:15228698 A>T maps to NM_006844.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr19:15229992 A>G maps to NM_006844.3 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr19:15227274 G>T maps to NM_006844.3 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr7:111127298 T>A maps to NM_032549.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:111161446 G>A maps to NM_032549.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:86371414 T>G maps to NM_006839.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr2:86374839 C>T maps to NM_006839.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr17:43923234 G>A maps to NM_175882.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:82571602 G>A maps to NM_001144878.1 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr18:11999108 A>T maps to NM_014214.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr3:49065313 G>A maps to NM_000884.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660532 G>A maps to NM_001563.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660635 G>A maps to NM_001563.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:76640749 G>A maps to NM_001563.2 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr1:62550235 C>T maps to NM_176877.2 V1431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr1:62330118 A>G maps to NM_176877.2 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:62237111 A>G maps to NM_176877.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:62341006 T>A maps to NM_176877.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr1:62550316 C>T maps to NM_176877.2 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr11:61897769 C>A maps to NM_001040694.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:61906226 G>A maps to NM_001040694.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:6760400 C>T did not map to a codon.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:220437359 C>G maps to NM_002191.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr12:57828749 A>C maps to NM_005538.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr15:41279358 G>A maps to NM_017553.1 F1254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr2:74684831 C>G maps to ENST00000452361 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr2:206921630 G>A maps to NM_017759.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:99163145 G>A maps to NM_001134224.1 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr4:143159033 A>G maps to NM_003866.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr4:143007356 G>T maps to NM_003866.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:38338747 G>A maps to ENST00000373026 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:234102515 G>T maps to ENST00000359570 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr17:1400004 G>C maps to NM_016532.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:71948602 A>G maps to NM_001567.3 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr11:2168964 C>T maps to NM_001042376.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:15243189 C>T maps to NM_001031853.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:15222419 G>C maps to NM_001031853.3 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr11:15267582 G>T maps to NM_001031853.3 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr19:17932189 T>C maps to NM_005543.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr19:17932189 T>C maps to NM_005543.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr19:17932288 C>T maps to NM_005543.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:36005047 C>T maps to NM_032594.3 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr1:156821581 T>C did not map to a codon.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr1:156823586 C>T maps to NM_014215.2 G198G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7059-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:156821561 G>A maps to NM_014215.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:156823724 G>A maps to NM_014215.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:156818723 G>A maps to NM_014215.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:156814311 G>T maps to NM_014215.2 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr8:19687915 G>C did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr8:19680920 T>C maps to NM_018142.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr1:153701139 A>C maps to ENST00000428986 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:153736637 A>G maps to ENST00000428986 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:153740252 G>T maps to ENST00000428986 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr11:77612477 T>G maps to NM_033547.3 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:77614591 C>T maps to NM_033547.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:62417116 A>G maps to NM_030628.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:62417410 G>A maps to NM_030628.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr13:51939889 A>T maps to NM_012141.2 *888K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr13:51948839 G>A maps to NM_012141.2 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr8:95884141 A>G maps to NM_017864.2 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr4:128608919 T>C maps to NM_015693.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr9:103002448 C>T maps to NM_014425.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr9:103004867 C>T maps to NM_014425.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:154521108 C>G maps to NM_001130700.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:59956100 A>G maps to NM_152230.4 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr5:61779840 C>T maps to NM_001134779.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr13:98671934 C>A maps to NM_002271.4 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:98667794 A>T maps to NM_002271.4 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:30790087 C>G maps to NM_006390.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:201843414 G>A maps to NM_018085.4 K916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:237272539 C>T maps to ENST00000457693 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr3:121544944 G>A maps to NM_001023570.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr7:2632755 T>C maps to NM_152558.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr7:2645632 T>A did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr7:2629605 C>G maps to NM_152558.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr15:67664906 T>C maps to NM_001031715.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:19775435 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:75886272 A>G maps to NM_006633.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr5:75896707 C>G maps to NM_006633.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:75888709 G>A maps to NM_006633.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:12957105 C>T maps to ENST00000429247 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr3:12949879 G>T maps to ENST00000429247 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr23:53284000 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr23:53268432 C>G did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr12:275006 G>A maps to NM_001170738.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr7:123119947 A>C maps to NM_178827.4 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr23:153283527 G>A did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr23:153278781 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:153278673 G>T did not map to a codon.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr12:66597672 G>T maps to NM_007199.2 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:78758792 A>T maps to NM_004136.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr5:131821388 C>T maps to NM_002198.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:46388581 G>A maps to NM_015649.1 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr19:46388203 C>A maps to NM_015649.1 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:234744250 G>T maps to NM_182972.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr1:234744214 G>A maps to NM_182972.2 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr1:234743338 C>A maps to NM_182972.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:234742915 T>A maps to NM_182972.2 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:234743059 G>A maps to NM_182972.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr7:128587380 T>C maps to NM_001098629.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:209974722 G>A maps to NM_006147.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr11:614300 G>A maps to NM_004031.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr14:24632647 G>A maps to NM_006084.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr2:227662245 G>C maps to NM_005544.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr2:227659839 T>G maps to NM_005544.2 P1205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr13:110435913 G>A maps to NM_003749.2 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr23:107977150 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr23:107978242 C>T did not map to a codon.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr5:2748603 A>G maps to NM_033267.4 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr16:54966804 C>T maps to NM_005853.5 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr16:54966435 C>A maps to NM_005853.5 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr16:55362618 T>C maps to NM_024335.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr16:55360270 C>T maps to NM_024335.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:55360381 G>A maps to NM_024335.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:55360357 C>T maps to NM_024335.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr9:88897334 C>A maps to ENST00000452279 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr12:108960982 T>C maps to NM_213595.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:949653 A>G maps to NM_005101.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr1:156697246 C>T maps to NM_030980.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:50683583 G>T did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr5:50685529 C>T maps to NM_002202.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr5:50685732 G>A maps to NM_002202.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr14:77942315 G>A maps to NM_199296.2 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr5:128430756 T>C maps to NM_016048.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr19:55966663 G>A maps to NM_024710.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:128848935 G>A maps to ENST00000418265 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr20:33026359 A>G maps to ENST00000262650 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr20:33012329 A>C maps to ENST00000262650 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:52221112 C>G maps to NM_181501.1 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr5:52145319 G>T did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:145534207 G>A maps to NM_003637.3 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:145530385 C>T maps to NM_003637.3 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr15:68628033 C>A did not map to a codon.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr15:68661591 A>G maps to ENST00000423218 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr15:68596121 C>T maps to ENST00000423218 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr15:68624720 G>A maps to ENST00000423218 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:52366068 C>G maps to NM_002203.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:42449791 C>T did not map to a codon.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:54798565 C>G maps to NM_002205.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr12:54798983 G>T maps to NM_002205.2 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr12:54792403 G>A maps to NM_002205.2 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr2:173352129 G>A maps to ENST00000264106 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr12:56078889 C>T maps to ENST00000347027 G1166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr10:15714683 C>T maps to NM_003638.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:15688932 G>A maps to NM_003638.1 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:37523096 A>G maps to NM_002207.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:3657178 G>C maps to NM_002208.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:3649158 G>A maps to NM_002208.4 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr16:31308842 C>A maps to NM_001145808.1 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr2:187521115 A>T maps to NM_002210.3 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr2:187500899 G>A maps to NM_002210.3 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr16:31373160 G>T maps to NM_000887.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr16:31371299 G>A maps to NM_000887.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:31383748 G>A maps to NM_000887.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr16:31373394 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr10:33208865 A>G maps to ENST00000374956 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr10:33217097 G>A maps to ENST00000374956 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr17:45377873 G>C maps to NM_000212.2 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr17:73729633 G>A maps to NM_001005619.1 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:73746315 G>A maps to NM_001005619.1 W1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:73736439 G>A maps to NM_001005619.1 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:73749999 C>G maps to NM_000213.3 G1421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr17:73727412 G>T maps to NM_001005619.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr3:124536467 A>G maps to NM_002213.3 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr12:53587038 G>A maps to NM_000889.1 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr12:53594098 C>T maps to NM_000889.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr7:20371477 C>T maps to NM_002214.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:7777014 C>T maps to NM_002216.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:7791149 G>A maps to NM_002216.2 R898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr3:52858968 C>T maps to ENST00000485816 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:52858938 G>A maps to ENST00000485816 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr23:54785276 G>A did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:54777528 G>A did not map to a codon.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr23:54784435 C>T did not map to a codon.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr5:156670645 C>A maps to NM_005546.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr23:78618082 G>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr13:48833063 A>G maps to NM_021999.4 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:231741582 G>C maps to NM_030926.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:93408016 C>T maps to NM_014216.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr1:226836373 T>C maps to NM_002221.3 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr19:41243661 C>T maps to NM_025194.2 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:41223384 A>T maps to NM_025194.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr3:4706865 C>T maps to ENST00000356617 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr3:4685827 A>T maps to ENST00000356617 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr3:4730229 C>T maps to ENST00000356617 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr12:26553126 G>A maps to NM_002223.2 T2488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr12:26784954 C>T maps to NM_002223.2 E926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:26581016 T>C maps to NM_002223.2 T2258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr6:33635705 C>T maps to ENST00000374316 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr6:33639878 C>T maps to ENST00000374316 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:96993808 C>T maps to ENST00000420728 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr2:96993736 C>G maps to ENST00000420728 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr16:19127312 C>T maps to NM_001034841.3 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:19126838 A>C maps to NM_001034841.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr21:35144368 G>C maps to NM_003024.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr2:24469085 A>G maps to NM_006277.2 D1163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr2:24493590 A>G maps to NM_006277.2 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr2:24524883 T>G maps to NM_006277.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr2:24535239 A>G maps to NM_006277.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr2:24469666 A>G maps to NM_006277.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:152883241 T>G maps to NM_005547.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:152883268 A>G maps to NM_005547.2 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr2:128263301 G>T maps to NM_017969.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr2:128262647 T>C maps to NM_017969.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:150690235 C>A maps to NM_203395.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr19:49249007 C>A maps to NM_182575.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr20:10621488 C>A maps to NM_000214.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr20:10627596 G>T maps to NM_000214.2 Y625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr20:10626013 G>T maps to NM_000214.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr20:10629265 A>G maps to NM_000214.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:10653489 A>C maps to NM_000214.2 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr14:105624078 C>A maps to NM_002226.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr14:105617707 C>T maps to NM_002226.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr14:105609334 A>G maps to NM_002226.3 I1138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr1:65344793 A>T maps to NM_002227.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr9:5072559 C>T maps to NM_004972.3 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr9:5126443 G>T maps to NM_004972.3 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:5126751 T>C maps to NM_004972.3 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:17945470 G>A maps to NM_000215.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr19:17954626 G>T maps to NM_000215.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr4:6066675 C>T maps to NM_001099433.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr5:147010973 A>G did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr10:133961487 C>G maps to NM_001105521.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr14:59965597 G>C maps to ENST00000356057 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:59965573 T>C maps to ENST00000356057 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr10:64975353 G>A maps to NM_032776.1 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:64968539 A>G maps to NM_032776.1 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr1:227921678 C>T maps to NM_023007.2 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:227921192 G>A maps to NM_023007.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr17:74716492 G>A maps to NM_001081461.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr17:74721937 C>T did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:75227664 G>A maps to NM_020647.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr20:42788568 G>A maps to NM_020433.4 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:143746610 C>T maps to NM_003724.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:153949704 A>T maps to NM_006694.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr14:23444253 G>A maps to NM_032876.4 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:59247908 G>C maps to NM_002228.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr19:12903493 C>T maps to NM_002229.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr17:39927929 G>A maps to NM_021991.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr23:8504906 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr9:732500 T>C maps to NM_015158.2 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr19:11303942 A>G maps to NM_015493.6 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr1:62740523 T>G maps to NM_181712.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr16:75678247 G>A maps to NM_001130089.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:75678299 A>T maps to NM_001130089.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr3:20153264 C>T maps to NM_003884.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:20187857 C>T maps to NM_003884.4 Y685Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr3:20169034 A>G maps to NM_003884.4 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:65480306 T>A did not map to a codon.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr11:65480530 T>G did not map to a codon.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr6:149918640 A>C did not map to a codon.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr16:57775692 C>T maps to NM_005886.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr16:57785949 C>T maps to NM_005886.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr16:57788845 A>G maps to NM_005886.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr1:15428038 C>T maps to NM_201628.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:15370642 C>T maps to NM_201628.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:170371426 A>T maps to ENST00000419050 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr15:65369366 C>T maps to NM_001101362.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr11:47599122 T>C maps to NM_018095.4 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:42727130 G>A maps to NM_152393.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr13:41704757 G>A maps to NM_152903.4 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:41766947 A>T maps to NM_032138.4 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr13:41767952 G>A maps to NM_032138.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr1:111060344 C>T maps to NM_005549.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:30032893 T>C maps to NM_002233.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:156175240 G>T did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr20:48098852 C>G maps to NM_004975.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr20:47991025 G>A maps to NM_004975.2 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr11:17793894 T>C maps to NM_001112741.1 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr12:75436983 G>T maps to NM_139137.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:110774915 G>A maps to NM_004978.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:110774882 T>C maps to NM_004978.4 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:112524715 C>T maps to ENST00000315987 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr21:35821710 C>T maps to NM_000219.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr23:108868068 G>T did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr21:35743146 T>C maps to NM_172201.1 *124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr2:11053934 G>A maps to NM_002236.4 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:11053757 C>T maps to NM_002236.4 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr18:77659530 C>T maps to NM_012283.1 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr18:77659161 G>A maps to NM_012283.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:42720407 G>A maps to NM_133329.5 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr1:211093084 C>T maps to NM_172362.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr1:210857393 C>T maps to NM_172362.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:150648044 G>A maps to NM_000238.2 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr17:40330117 A>G maps to NM_012285.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr14:63447835 A>T maps to NM_139318.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr14:63473093 G>T maps to NM_139318.3 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr14:63174363 C>T maps to NM_139318.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr17:61623067 A>G maps to NM_030779.2 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:61623122 C>T maps to NM_030779.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:61613154 G>A maps to NM_030779.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:61616009 C>G maps to NM_030779.2 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr2:163256909 A>G maps to NM_033272.2 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:19389245 G>A maps to NM_144633.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:169931584 C>T maps to NM_001034837.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:95976176 C>T maps to NM_013434.4 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:17408681 T>C maps to NM_000525.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr17:21319583 C>T maps to NM_021012.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr17:21318662 G>A maps to NM_021012.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr17:21319526 C>T maps to NM_021012.4 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr17:21319742 A>G maps to NM_021012.4 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233633227 A>T maps to NM_002242.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr17:68172169 C>G maps to NM_000891.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr22:38822919 A>C maps to NM_152868.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:128781257 C>T maps to NM_000890.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr12:21918782 G>T maps to NM_004982.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr12:21918736 G>T maps to NM_004982.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr10:118957019 C>T maps to NM_181840.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:215408256 G>A maps to NM_001017425.2 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr6:39162420 C>G maps to NM_003740.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:39159333 G>A maps to NM_003740.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr6:39159434 C>T maps to NM_003740.3 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr8:140631094 G>A maps to NM_016601.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr10:78872136 C>A maps to NM_001161352.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr10:78709125 T>C did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:113822744 A>G did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:154841687 G>A maps to NM_002249.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr1:154842011 G>A maps to NM_002249.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr1:154705481 G>A maps to NM_002249.4 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:154744542 C>T maps to NM_002249.4 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:2798239 C>G maps to NM_000218.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr11:2606465 C>T maps to NM_000218.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr11:2466534 G>T maps to NM_000218.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:62078165 G>C maps to NM_172107.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:62070958 G>A maps to NM_172107.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:62065202 C>T maps to NM_172107.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr8:133141907 C>T maps to NM_004519.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr8:133141625 G>A maps to NM_004519.2 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr20:43726791 C>T maps to NM_002251.3 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:99441266 G>T maps to NM_020697.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr8:99440359 G>A maps to NM_020697.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr9:138594139 C>G maps to ENST00000298480 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:196274361 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr1:196254848 G>A maps to NM_198503.2 R879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr1:196227479 G>T maps to NM_198503.2 R1019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr8:36790509 C>A maps to NM_001031836.2 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr8:36698473 C>A maps to NM_001031836.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr9:2718620 C>T maps to NM_133497.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:2718278 C>T maps to NM_133497.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr18:24127105 C>T maps to NM_001142730.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr12:109889449 G>T maps to NM_031954.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr17:7256620 C>T maps to NM_001002914.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr13:77459422 C>G maps to NM_138444.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr13:77460121 C>G maps to NM_138444.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr11:77727893 G>T maps to NM_023930.3 C171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr16:67324886 G>C maps to NM_001100915.1 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:73058234 C>G maps to NM_015353.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr11:77885168 G>A maps to NM_001029859.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr13:45768534 G>A maps to NM_198404.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:44450333 A>T maps to NM_198353.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr4:44176968 G>C maps to NM_198353.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:25290133 C>A maps to NM_017634.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr22:38877224 G>A maps to NM_016657.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:23380288 G>A maps to NM_001009999.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr11:67017708 G>A maps to NM_012308.2 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr12:121947831 C>T maps to ENST00000377071 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr2:86693719 T>G maps to NM_001146688.1 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:137715372 T>C maps to NM_016604.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:44128740 T>C maps to NM_014663.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:5131902 G>C maps to NM_015015.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr9:7013978 G>A maps to NM_015061.3 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr11:94731984 T>A maps to NM_018039.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr12:442727 A>G maps to NM_001042603.1 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr1:202777265 G>C maps to ENST00000367264 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:202710613 T>G maps to ENST00000367264 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:202701001 A>C maps to ENST00000367264 Y1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:53222169 C>A did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr23:53223904 C>T did not map to a codon.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr23:53244974 A>G did not map to a codon.
Sequencing variant TCGA-B0-4710-01A-01W-1528-10 chr23:53222459 G>A did not map to a codon.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr23:53230751 G>A did not map to a codon.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr23:53239735 C>A did not map to a codon.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr23:53245089 C>A did not map to a codon.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr23:53228213 A>G did not map to a codon.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr23:53231126 T>A did not map to a codon.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr23:53227795 C>A did not map to a codon.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr23:53239904 G>C did not map to a codon.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr23:53224221 G>C did not map to a codon.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr23:53247142 C>G did not map to a codon.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr23:53240704 T>A did not map to a codon.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr23:53227750 G>A did not map to a codon.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr23:53228212 C>A did not map to a codon.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr23:53228203 T>G did not map to a codon.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr23:53246338 T>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:53239615 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr23:53245083 T>C did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr23:53222785 A>G did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr23:53239927 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr24:21903349 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr24:21868426 C>A did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr24:21901509 A>C did not map to a codon.
Sequencing variant TCGA-B0-5075-01A-01D-1392-10 chr23:44732885 C>T did not map to a codon.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr23:44928975 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:44949020 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr23:44733230 A>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:44870204 G>C did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:7748925 C>A maps to NM_001080424.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:7755371 T>G maps to NM_001080424.1 A1423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr17:7750210 A>C maps to NM_001080424.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:10610565 G>T maps to NM_203500.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr19:10610394 A>G maps to NM_203500.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:10610177 G>A maps to NM_203500.1 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:142640922 C>T maps to NM_000420.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr7:142658017 G>A maps to NM_000420.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr2:27322320 C>T maps to NM_006488.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr2:27317802 G>A did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr19:6420476 G>C maps to NM_003685.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:19545820 C>T maps to NM_015047.1 K986K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr17:26948414 A>G did not map to a codon.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:26965109 A>G maps to NM_014680.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:48309112 T>C maps to NM_001080394.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr16:71956528 C>T maps to NM_014761.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr16:71956528 C>T maps to NM_014761.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr16:85706124 C>T maps to NM_014615.2 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:85689999 C>T maps to NM_014615.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr16:85696692 C>T maps to NM_014615.2 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr16:85701800 C>T maps to NM_014615.2 H1062H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr17:73485345 G>A did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr17:73487467 G>T maps to ENST00000375248 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr3:197427933 G>A maps to NM_014687.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:197410177 C>T maps to NM_014687.1 K660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr3:197408101 G>A maps to NM_014687.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:6860176 G>A maps to NM_014743.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr4:6862717 C>T maps to NM_014743.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr6:42832829 G>T maps to NM_015349.1 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr6:42832808 G>A maps to NM_015349.1 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr14:105356096 T>G did not map to a codon.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr14:105349387 A>C maps to ENST00000453495 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr14:105349471 C>T maps to ENST00000453495 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:105354292 A>G maps to ENST00000453495 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:34832920 G>A maps to NM_014686.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:34818400 C>T maps to NM_014686.3 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr9:114184458 A>T maps to NM_001080398.1 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr9:114182376 C>G maps to NM_001080398.1 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:35593086 T>C maps to NM_014672.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr20:36634746 T>C maps to NM_014657.1 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr20:36642155 G>T maps to NM_014657.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr20:36631057 G>T maps to NM_014657.1 S875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr20:36612010 T>A maps to NM_014657.1 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr7:4830446 C>A maps to ENST00000450194 P1405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr7:4825313 C>T maps to ENST00000450194 H1088H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:46146070 G>A maps to NM_001142397.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:15711250 G>A maps to NM_014647.3 H954H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:22623803 C>T maps to ENST00000446597 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr12:22646272 T>A did not map to a codon.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr16:27732991 T>C maps to NM_015202.2 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:42460951 C>T maps to NM_015058.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr13:42273323 G>A maps to NM_015058.1 F1149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr13:42461383 G>T maps to NM_015058.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr14:58937441 G>T did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:46666906 C>T maps to NM_001142673.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr17:2596081 G>A maps to NM_015229.3 Q1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr12:55356979 G>A maps to NM_001098815.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr17:6531559 G>A maps to NM_014804.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr17:6515463 C>T maps to NM_014804.2 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:39880151 A>T maps to NM_015038.1 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr6:96997452 A>G maps to NM_015323.4 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr18:8813134 C>T maps to ENST00000456698 N1240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:19431718 G>C maps to NM_015329.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr19:19454739 G>A maps to NM_015329.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:36396612 G>A maps to NM_001100425.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:155903552 C>G maps to NM_014949.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:154542028 C>A maps to NM_001131007.1 S1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr5:5462476 G>T maps to NM_015325.1 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr5:5489407 G>T maps to NM_015325.1 E2256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr6:84884490 T>C maps to NM_014895.2 K660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr18:29487428 A>T maps to NM_014939.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr18:29496395 C>T maps to NM_014939.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr18:29437669 G>A maps to NM_014939.3 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr18:29410857 G>A maps to NM_014939.3 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr18:29511427 T>C maps to NM_014939.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr15:79749415 C>T maps to NM_015206.2 N309N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:79748656 C>T maps to NM_015206.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:105527568 C>G maps to NM_015275.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr12:105504981 C>T maps to NM_015275.1 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr4:123156096 G>T maps to NM_015312.3 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:123150304 T>C maps to NM_015312.3 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:123150306 C>A maps to NM_015312.3 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr4:123270438 G>A maps to NM_015312.3 G4469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr4:123264652 C>G maps to NM_015312.3 G4147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr3:44794949 T>C maps to NM_020696.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:141365047 A>T maps to NM_001080392.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:81181039 A>T did not map to a codon.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr15:81224217 A>T maps to NM_018689.1 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr15:81216981 C>T maps to NM_018689.1 N741N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr23:118222878 T>C did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr23:118217055 G>C did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr23:118219439 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr23:118219356 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:118223093 A>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr4:57182199 G>A maps to NM_020722.1 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:57182388 C>T maps to NM_020722.1 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr4:57182676 G>A maps to NM_020722.1 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr10:24832824 G>A maps to NM_019590.3 E1542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr10:24834979 C>A maps to NM_019590.3 L1853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:24835171 T>C maps to NM_019590.3 H1917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:138584305 C>T maps to NM_020340.4 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:138584326 C>T maps to NM_020340.4 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr17:44248411 T>C maps to NM_015443.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr10:72293730 C>G maps to NM_014431.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:70775349 G>A maps to NM_015634.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr2:97278653 A>G maps to ENST00000421845 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:97267382 T>C maps to ENST00000421845 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr2:97278027 C>T maps to ENST00000421845 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:97285434 G>T maps to ENST00000421845 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr1:109740266 C>T maps to NM_020775.3 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:109735385 C>T maps to NM_020775.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:113684199 G>A maps to NM_020817.1 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr14:93994954 T>C maps to ENST00000393153 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr14:94088744 C>T maps to ENST00000393153 D1744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr14:94004417 G>T maps to ENST00000393153 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr14:94088411 C>A maps to ENST00000393153 S1633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr14:94129060 G>A did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr14:94156609 T>C maps to ENST00000393153 H2472H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr14:94160697 T>C maps to ENST00000393153 C2557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr8:95503872 T>C maps to NM_015496.3 S1691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:95541375 G>A maps to NM_015496.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr4:186085306 C>A maps to NM_020827.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr9:5763717 C>T maps to ENST00000414202 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr9:5763501 G>A maps to ENST00000414202 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr10:30318484 G>A maps to NM_020848.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr18:59854884 T>G maps to NM_020854.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr18:59895744 A>G maps to NM_020854.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr18:59888684 C>T maps to NM_020854.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr9:100092961 G>A maps to ENST00000375206 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr9:100128908 C>T maps to ENST00000375206 C1361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr4:1369833 G>A maps to NM_020894.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr7:138602904 A>G maps to NM_001164665.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:138602634 C>T maps to NM_001164665.1 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr7:138603069 G>T maps to NM_001164665.1 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr16:84516269 C>T maps to NM_020947.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr16:84529459 C>A maps to NM_020947.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr18:43492337 G>A maps to NM_020964.2 V1300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:18377008 C>T maps to NM_001145304.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr2:176835533 T>C did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:77580237 C>T maps to NM_033426.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:1897856 C>A maps to ENST00000434971 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr1:1897856 C>A maps to ENST00000434971 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr20:36869595 C>A maps to NM_001029864.1 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr20:36870193 C>T maps to NM_001029864.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr9:20758087 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr9:20758139 G>A maps to NM_017794.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr6:111587970 T>A maps to NM_153369.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr3:113376124 C>T maps to NM_001009899.2 Q1468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr3:113376679 G>T maps to NM_001009899.2 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:113377558 T>C maps to NM_001009899.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376121 C>T maps to NM_001009899.2 Q1469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376127 C>T maps to NM_001009899.2 Q1467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:73961091 C>T did not map to a codon.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr23:73962034 G>T did not map to a codon.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr23:73960855 C>A did not map to a codon.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr23:73964284 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr23:73962407 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr23:73961520 T>A did not map to a codon.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr23:73962313 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr23:73963361 T>C did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr9:5968195 T>A maps to NM_001017969.2 K679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr9:5968931 A>G maps to NM_001017969.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr2:8919169 G>T maps to NM_020738.2 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr2:8891617 G>C maps to NM_020738.2 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr2:8953447 A>C maps to NM_020738.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr2:8871659 G>A maps to NM_020738.2 L1502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr10:94399585 A>G maps to NM_004523.3 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:17898398 C>T maps to NM_022113.4 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr8:28991586 C>T maps to NM_015254.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr8:29037679 G>A maps to NM_015254.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr8:29035050 A>G maps to NM_015254.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr3:44816878 G>T maps to NM_020242.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:16359621 G>A maps to NM_024704.4 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr1:21014270 C>T maps to NM_020816.2 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:28116198 T>C maps to NM_031217.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr17:43009010 G>A maps to ENST00000438933 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr17:43009570 C>T maps to ENST00000438933 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr17:72340955 C>A maps to NM_153209.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr17:72340926 C>A maps to NM_153209.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr2:241662860 C>T maps to ENST00000373308 W1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr2:241706373 C>A maps to ENST00000373308 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr2:241686666 G>A maps to ENST00000373308 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr1:10318552 C>T maps to ENST00000377086 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr1:10364567 T>C maps to NM_183416.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:10352149 A>G maps to ENST00000377086 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr17:4916955 C>T maps to NM_006612.5 H500H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:4908296 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr17:4924145 C>T maps to NM_006612.5 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr5:137520632 C>T maps to NM_005733.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr12:39726835 G>C maps to ENST00000395670 S854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr12:39695436 C>A maps to ENST00000395670 V1593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:200943294 G>A maps to NM_017596.2 Y1601Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:200960790 G>T maps to NM_017596.2 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:200959171 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:200973947 C>A maps to NM_017596.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr6:168443301 G>A maps to NM_030615.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr14:104643366 G>A maps to NM_015656.1 R1414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr14:104643408 A>G maps to NM_015656.1 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr14:104642340 A>G maps to NM_015656.1 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr14:104643720 C>A maps to NM_015656.1 A1532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:245583032 C>T maps to NM_018012.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:86485504 T>A maps to NM_017576.1 K896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr5:61649099 A>G did not map to a codon.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr5:61653553 C>T maps to NM_001098511.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:51901647 C>T maps to NM_032559.4 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr20:30897807 G>C maps to NM_004798.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:69624619 A>G did not map to a codon.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr23:69637741 C>T did not map to a codon.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr23:69622532 T>C did not map to a codon.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr23:69595152 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:69637855 T>C did not map to a codon.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr23:69622482 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr23:69561757 C>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:69595070 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:69595075 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr5:154394372 C>T maps to NM_001099293.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:154395500 G>A maps to NM_001099293.1 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr5:154394948 T>C maps to NM_001099293.1 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:57965900 C>T maps to NM_004984.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:57976895 G>A maps to NM_004984.2 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:57957253 C>T maps to NM_004984.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:32320042 A>G maps to NM_004521.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:149835495 C>T maps to NM_004522.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:149850957 G>C maps to NM_004522.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr2:149799206 G>A maps to NM_004522.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr1:170004686 G>A maps to NM_014970.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr6:33374603 G>T maps to NM_002263.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr16:57806197 T>C maps to NM_005550.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr10:7829794 C>T maps to NM_012311.2 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:7811177 C>T did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:55286794 T>C maps to ENST00000291633 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:55239155 G>A maps to NM_153443.3 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:158059419 T>G did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr1:158056510 G>A maps to ENST00000368173 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:36353425 A>G maps to NM_199180.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36349604 G>A did not map to a codon.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr11:126299166 C>T maps to NM_032531.3 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr19:918607 C>T maps to NM_032551.4 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr4:55570035 C>G maps to NM_000222.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr13:33635591 T>C maps to NM_004795.3 D792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr4:39435919 G>T maps to NM_175737.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:39435930 G>T maps to NM_175737.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr4:39448541 C>G maps to NM_175737.3 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr14:104129225 C>T maps to ENST00000445352 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr19:45849908 A>G maps to NM_177417.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:43042367 G>T maps to NM_201523.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr7:130418524 G>A maps to NM_138693.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:44595404 C>G maps to NM_173484.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr23:56295818 G>C did not map to a codon.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr23:56310907 G>A did not map to a codon.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr23:56310755 T>G did not map to a codon.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr23:56291624 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr23:56292016 T>C did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr9:73027802 A>G maps to NM_001206.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr9:73027904 G>A maps to NM_001206.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr9:73027945 C>A maps to NM_001206.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr9:73027889 T>C maps to NM_001206.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr7:129761892 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr14:50249622 T>G maps to NM_014315.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:87764192 T>C maps to NM_017566.3 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:87760466 C>T maps to NM_017566.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:27933685 G>A maps to NM_020782.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:27934039 C>T maps to NM_020782.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr1:18807867 G>A maps to NM_152375.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:50987533 T>C maps to NM_138433.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:205306598 G>T maps to NM_018203.1 C327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr3:49210261 C>T maps to NM_173546.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr13:70681441 C>A maps to NM_020866.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr17:40004450 A>C maps to NM_152467.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:202866047 G>A maps to NM_021633.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:117043341 T>C did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:117053556 T>C did not map to a codon.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr23:24006421 C>A did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:24007139 G>T did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:173703124 A>T maps to NM_014458.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:20796431 G>C maps to NM_032775.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr5:136974756 G>A maps to NM_017415.2 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:136963989 G>A maps to NM_017415.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr23:21675433 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr23:21674906 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:21675167 G>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:86773062 C>G did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr23:86890698 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:86887409 A>G did not map to a codon.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr23:86921521 G>T did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr3:183211911 G>T maps to NM_130446.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:183217549 G>T maps to NM_130446.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:88099692 G>A maps to NM_020803.3 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr4:88106696 A>G maps to NM_020803.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:51518765 G>T maps to NM_001077500.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr19:51584904 G>T maps to NM_022046.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr19:51378100 C>A maps to NM_005551.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr19:51378100 C>A maps to NM_005551.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr19:51412532 G>A maps to NM_004917.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:51503867 C>T maps to NM_144505.1 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr2:48687266 G>T maps to NM_001135629.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr12:9754097 T>C maps to NM_002258.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr7:139164444 C>T maps to NM_198508.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:10541381 G>A maps to NM_007360.3 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr1:241723980 C>G maps to NM_003679.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:135013086 C>T maps to ENST00000368572 Q964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr10:135012531 G>A maps to ENST00000368572 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr10:135000147 T>C maps to ENST00000368572 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:123087701 G>A maps to NM_014708.4 T1671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:160249254 A>G maps to NM_002268.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr3:160227601 C>A maps to NM_002268.3 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr6:117013532 A>G maps to NM_002269.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr17:45747172 C>T maps to NM_002265.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr17:45727755 G>A maps to NM_002265.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr1:152732828 C>A maps to NM_001025231.1 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr17:8274813 T>G maps to NM_213597.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:91855962 T>C maps to NM_194456.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:91851359 T>C maps to NM_194456.1 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:75895545 T>C maps to NM_007043.6 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr17:38977370 T>A did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:38978228 G>A maps to NM_000421.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr17:39658937 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr17:39658759 G>A maps to NM_153490.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr17:39658843 T>C maps to NM_153490.2 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr17:39775938 C>T maps to NM_000422.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr17:39680197 G>A maps to NM_002276.4 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr12:53039078 G>T maps to NM_000423.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:53045389 A>G maps to NM_000423.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr12:53045839 C>A maps to NM_000423.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr12:53043742 G>A maps to NM_000423.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr17:39086292 G>A maps to NM_015515.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:39092458 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr17:38859816 G>A maps to NM_019016.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:38926070 C>A maps to NM_181539.4 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr17:39619146 G>A maps to NM_002278.3 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr17:39623193 G>A maps to NM_002278.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr17:39535272 G>A maps to NM_021013.3 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:39635601 C>T maps to NM_002280.4 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr17:39579095 G>A maps to NM_003770.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr17:39595538 A>G maps to NM_006771.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr12:53207989 G>A maps to NM_002272.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:53207944 G>T maps to NM_002272.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52910638 G>A maps to NM_000424.3 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:52913573 G>T maps to NM_000424.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52882314 G>A maps to NM_005554.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:52886555 G>A maps to NM_005554.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr12:52845664 G>T maps to NM_005555.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr12:52843580 A>G maps to NM_005555.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr12:52863662 C>T maps to NM_173086.4 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52867038 G>A maps to NM_173086.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:52867104 G>A maps to NM_173086.4 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:52629133 G>T maps to NM_005556.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr12:53012200 G>T maps to NM_175068.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr12:53009993 C>T maps to NM_175068.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:52967396 C>A maps to NM_175053.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr12:53162772 A>G maps to NM_015848.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:53169329 C>T maps to NM_015848.4 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:53097169 G>T maps to NM_175078.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr12:53242513 C>T maps to NM_173352.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:53225245 C>A maps to NM_175834.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr12:53216798 C>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:52574311 T>C maps to NM_182507.2 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52681794 G>A maps to NM_002281.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52681803 G>A maps to NM_002281.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52682213 C>T maps to NM_002281.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr12:52797690 G>A maps to NM_033033.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr12:52774145 C>T did not map to a codon.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr12:52777474 G>A maps to NM_033045.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr12:52756640 G>T maps to NM_002283.3 C358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr12:52760937 G>A maps to NM_002283.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr12:52699043 C>G maps to NM_002284.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr17:39197637 A>G maps to NM_030967.2 C4C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr17:39197484 A>G maps to NM_030967.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr17:39190638 G>A maps to NM_030966.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr17:39191010 G>C maps to NM_030966.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:39183128 A>G maps to NM_031957.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr21:45959196 G>A maps to NM_198691.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr21:46057624 T>C maps to NM_181688.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:46057372 C>T maps to NM_181688.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr21:46057633 T>C maps to NM_181688.1 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr21:46057624 T>C maps to NM_181688.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr21:46057633 T>C maps to NM_181688.1 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr21:46117130 C>T maps to NM_198699.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr21:45970771 A>G maps to NM_198693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr21:45971080 C>T maps to NM_198693.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr21:45970771 A>G maps to NM_198693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr21:45978022 G>A maps to NM_198696.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr21:45978007 G>A maps to NM_198696.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr21:46000293 C>T maps to NM_198694.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr21:46011525 T>A maps to NM_198688.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr21:46012290 A>G maps to NM_198688.2 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr21:46032304 T>C maps to NM_198695.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr21:46047393 C>A maps to NM_198690.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr21:31768457 C>T maps to NM_181599.2 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr21:31859595 G>T maps to NM_181608.1 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:31709824 G>A maps to NM_001077711.1 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr17:39334329 G>T maps to ENST00000458321 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr17:39324138 T>G maps to NM_033187.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39324103 A>G maps to NM_033187.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:39316568 G>T maps to NM_032524.1 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:39305509 G>A maps to NM_033188.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr17:39254246 A>T maps to NM_031960.2 C30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr17:39254123 C>G maps to NM_031960.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr17:39254126 A>G maps to NM_031960.2 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr17:39261864 C>A maps to NM_001146041.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:39261741 C>T maps to NM_001146041.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr17:39262095 C>T maps to ENST00000377731 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr11:1606137 T>G maps to NM_001005922.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr11:1606128 A>C maps to NM_001005922.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr11:1605897 C>T maps to NM_001005922.1 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr11:1605978 A>G maps to NM_001005922.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr11:71276701 C>T maps to NM_001012710.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr11:71276875 A>G maps to ENST00000422553 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr11:71293817 C>T maps to ENST00000376535 G22G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KN-8435-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:1643254 G>A maps to ENST00000359229 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:1642702 A>G maps to NM_001012709.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:1643005 G>C maps to ENST00000359229 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:1643278 C>T maps to ENST00000359229 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr11:1643254 G>A maps to ENST00000359229 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr11:1643254 G>A maps to ENST00000359229 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:1651126 C>T maps to NM_001001480.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr11:71238684 G>A maps to NM_001012503.1 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr11:71249604 C>T maps to NM_021046.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr11:71260167 C>A maps to NM_005553.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:39411912 C>T maps to ENST00000431129 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr17:25919597 G>T maps to ENST00000268763 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:118293233 T>C maps to ENST00000339824 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr14:56137505 T>A maps to NM_001079521.1 T1109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr14:56103976 A>G maps to NM_001079521.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:56079009 C>A maps to NM_001079521.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr14:56107680 C>T maps to NM_001079521.1 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:134323199 C>A maps to NM_178554.4 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr23:153131182 G>A did not map to a codon.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr23:153129372 C>A did not map to a codon.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr23:153131184 C>A did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr23:153130646 G>A did not map to a codon.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr23:153130542 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:50713787 T>C maps to NM_024884.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:41621937 G>A maps to NM_031488.4 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr6:130415458 G>T maps to NM_032438.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr12:55026039 C>A maps to NM_033277.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr15:63419761 C>A maps to NM_032857.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr1:201354879 T>G maps to NM_005558.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:201358385 G>A maps to NM_005558.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:54872526 C>A maps to NM_002287.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:54872808 C>T maps to NM_002287.3 L26L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KN-8426-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:54875935 C>T maps to NM_002287.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:55019388 G>T maps to NM_002288.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr12:48961739 T>C maps to NM_002289.2 *143W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr18:6992668 G>A maps to NM_005559.2 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr18:7008501 C>T maps to NM_005559.2 V1369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr18:6949183 C>A maps to NM_005559.2 V2824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr18:7026066 C>T maps to NM_005559.2 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:7025997 A>G maps to NM_005559.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr18:7036006 C>T maps to NM_005559.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr18:7042147 G>A maps to NM_005559.2 H419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:129766959 C>T maps to NM_000426.3 A2141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:129796547 T>C did not map to a codon.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr18:21406682 C>A maps to ENST00000416669 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr18:21441743 C>A maps to ENST00000416669 V1521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:21451429 G>T maps to ENST00000416669 V1603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:21474919 C>T maps to ENST00000416669 G1839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr18:21508089 T>C maps to ENST00000416669 F2729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:112454682 G>C maps to NM_001105206.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr6:112513052 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:112457350 G>A maps to NM_001105206.1 Q1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr6:112480082 C>G did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr20:60895845 G>A maps to NM_005560.3 S2199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr20:60908163 G>A maps to NM_005560.3 I1088I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr20:60904898 C>G maps to NM_005560.3 L1351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr20:60921135 C>T did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:60891784 C>T maps to NM_005560.3 L2566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr7:107596065 A>G maps to NM_002291.2 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr7:107605112 G>A maps to NM_002291.2 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr3:49160287 G>A maps to NM_002292.3 L1474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr3:49158998 C>T maps to NM_002292.3 Q1709Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr1:209807971 G>A maps to NM_000228.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:209799285 C>T maps to NM_000228.2 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:209796912 G>A maps to NM_000228.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr1:209799336 C>T maps to NM_000228.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr1:183197725 G>A maps to NM_005562.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr1:183204763 T>G maps to NM_005562.2 Y785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr9:133928344 C>T maps to ENST00000355048 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr9:133942551 C>T maps to ENST00000355048 Y851Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr9:133942464 C>A maps to ENST00000355048 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr9:133942398 C>T maps to ENST00000355048 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr9:133914404 G>A maps to ENST00000355048 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr9:133914284 G>A maps to ENST00000355048 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:113964010 C>T maps to NM_005561.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr23:119581774 C>A did not map to a codon.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr23:119562464 A>G did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:119581841 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr3:182871517 A>G maps to NM_014398.3 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr2:20237322 T>G maps to NM_014713.4 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr22:33670591 G>A maps to NM_133642.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr22:33679189 G>A maps to NM_133642.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr4:129012652 T>C maps to NM_018078.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr12:50869376 G>C maps to ENST00000429001 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:50847397 T>C maps to ENST00000429001 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:858886 A>G maps to NM_015155.1 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr15:71128825 T>C maps to NM_018357.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:113578402 T>C maps to ENST00000509061 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr5:145557189 C>T maps to NM_020117.9 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr23:64744050 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:64749563 C>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr1:150940936 C>T maps to NM_181746.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:150939612 G>T maps to NM_181746.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr1:150938647 A>G maps to NM_181746.2 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr19:8316055 C>T maps to NM_024552.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr6:150001248 A>G maps to NM_004690.2 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:150005369 G>T maps to NM_004690.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:149997826 C>G maps to NM_004690.2 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr13:21557680 C>A maps to NM_014572.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr11:111431065 G>A maps to ENST00000375615 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr20:36989401 T>G maps to NM_004139.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr20:36978014 C>T maps to NM_004139.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr1:225599095 T>A maps to NM_194442.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:74725149 C>T maps to NM_001009812.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr6:80203391 C>A maps to NM_181714.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr6:80197554 C>T maps to NM_181714.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr1:152785008 C>T maps to NM_178349.1 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:152777876 G>A maps to NM_178351.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:152552160 G>A maps to NM_032563.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr2:30756118 T>A maps to NM_182551.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr15:43621543 G>T maps to NM_014793.4 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr9:138413981 G>A maps to NM_002297.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr10:98715213 A>G maps to NM_001170765.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr13:46730640 C>T maps to NM_002298.4 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr2:136566909 G>A maps to NM_002299.2 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:136558374 G>A maps to NM_002299.2 V1556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:136555629 T>G maps to NM_002299.2 R1649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr10:88466359 A>C maps to NM_007078.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr11:18424450 C>T maps to NM_001165414.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr15:59499807 T>A maps to NM_033195.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr19:11210911 C>A maps to NM_000527.4 C27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr1:54477873 C>T maps to NM_001010978.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr4:109084819 G>A maps to NM_016269.4 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:226075313 G>A maps to ENST00000419724 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:226075305 G>T maps to ENST00000419724 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:226127229 G>A maps to NM_003240.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:226128689 G>A maps to NM_003240.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:54966578 C>T maps to ENST00000431846 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr15:52254682 T>C maps to NM_138792.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr3:189689770 G>T maps to NM_018192.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:189711952 A>G maps to NM_018192.3 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:65895650 C>A maps to NM_017526.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr8:29994915 T>G maps to NM_001128208.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:51450185 G>A maps to ENST00000448283 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:63273899 G>C maps to NM_001142535.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:20355184 G>A maps to ENST00000324290 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr10:95557391 T>C maps to NM_005097.2 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:95549894 T>C maps to NM_005097.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:25005582 C>T maps to NM_018176.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:27402258 C>G did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:202273685 G>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:206785683 C>T maps to NM_006893.2 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr23:111914247 T>A did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:9547648 G>A did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:35299576 C>T maps to NM_005568.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr9:139091692 C>T maps to NM_014564.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:113909128 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:113901231 T>C maps to NM_022363.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr4:39472862 T>C maps to NM_006859.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:38510728 T>C maps to NM_002310.5 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr19:55106238 G>A maps to NM_006863.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr19:55107717 C>T maps to NM_006863.1 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:55085834 C>A maps to NM_001130917.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr19:55085804 C>A maps to NM_001130917.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr19:55086975 C>T maps to NM_001130917.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr19:55086954 C>T maps to NM_001130917.1 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr19:55086948 A>G maps to NM_001130917.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:54822786 A>C maps to NM_021250.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr19:54744776 C>T maps to ENST00000245620 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr19:54744734 G>A maps to ENST00000245620 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:55144005 C>A maps to ENST00000427581 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:55148075 G>A maps to ENST00000427581 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:54783676 C>T maps to ENST00000391747 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:54778569 C>T maps to ENST00000391747 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:54725772 T>C maps to NM_001081450.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:54721108 C>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:54725991 G>A maps to NM_001081450.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr19:54724410 C>T maps to NM_001081450.1 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:54721051 G>T maps to NM_001081450.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:55176301 T>A did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr19:54760025 G>A maps to NM_001081442.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr12:50571221 T>C maps to NM_001113546.1 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr12:50571731 C>T maps to NM_001113546.1 W466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr12:50589646 C>T maps to NM_001113546.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:73535229 G>A maps to NM_002314.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr22:31674309 C>A maps to ENST00000438187 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr12:81239679 G>C maps to NM_004664.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr12:81239637 A>T maps to NM_004664.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr9:27948986 A>C maps to NM_152570.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr9:27950498 G>A maps to NM_152570.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:2290212 C>T maps to NM_001101391.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr15:101110264 T>A maps to NM_001040616.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr15:58838058 C>T maps to NM_000236.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr15:58837950 C>T maps to NM_000236.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr19:42930773 C>T maps to NM_005357.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr19:42930827 C>T maps to NM_005357.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:42907052 G>A maps to NM_005357.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr18:47095826 C>T maps to NM_006033.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr21:15579136 T>C maps to NM_198996.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr21:15561569 G>A maps to NM_198996.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr21:15554118 C>T maps to NM_198996.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr10:90497390 G>T did not map to a codon.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:96443095 C>A maps to NM_153234.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr17:18144991 C>T maps to NM_004140.3 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr17:18135883 C>T maps to NM_004140.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:73565070 C>A maps to NM_001031803.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:66522753 G>A maps to NM_032338.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr18:57026428 C>T maps to NM_005570.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:156518212 A>G maps to ENST00000354505 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr12:49495926 A>G maps to NM_018113.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr12:49495052 G>T maps to NM_018113.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr3:8579023 G>A maps to NM_014583.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr3:197748372 C>A maps to NM_001136049.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr1:156105084 C>T maps to NM_170707.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:156105093 C>G maps to NM_170707.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:156107473 A>C maps to NM_170707.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr5:126158525 C>T maps to NM_005573.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:2444466 T>A maps to NM_032737.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr1:87805217 G>C did not map to a codon.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr7:123302917 T>C maps to NM_207163.1 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr3:69169079 T>C maps to NM_198271.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr7:97823181 C>G maps to NM_014916.3 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr19:48994715 T>G maps to NM_001080434.1 T1420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:49001438 C>A maps to NM_001080434.1 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr3:100170597 C>T maps to ENST00000489752 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:96350726 C>A maps to NM_005575.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr4:54362297 G>A maps to NM_001126328.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr4:54343068 T>C maps to NM_001126328.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr13:28143268 G>A maps to NM_153371.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr16:22545905 C>T maps to NM_001135865.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr22:24373818 T>C maps to NM_001144931.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr7:28319098 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr1:13183479 A>G maps to NM_001136561.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr1:13183398 A>G maps to NM_001136561.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr1:13183836 G>A maps to NM_001136561.2 H12H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:11350387 C>T maps to ENST00000252453 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:20851090 C>T maps to NM_030941.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr16:48286155 G>A maps to NM_031490.2 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr16:48385616 T>C maps to NM_031490.2 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr23:118109100 G>T did not map to a codon.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr23:118140160 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:118108849 G>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:118151558 G>A did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr5:121409740 G>T maps to NM_002317.5 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:121413455 G>C maps to NM_002317.5 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr15:74239563 G>A maps to NM_005576.2 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:74761482 G>A maps to NM_032603.2 H633H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr10:100022770 C>T maps to NM_032211.6 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr6:161032705 C>A maps to NM_005577.2 G831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr6:161027524 C>T maps to NM_005577.2 E923E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr6:160952769 T>C maps to NM_005577.2 R2038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:78011130 G>T did not map to a codon.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr23:78011221 G>T did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr23:78011380 C>T did not map to a codon.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr23:78010585 A>G did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr23:78010715 C>A did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:1488542 A>T maps to NM_024830.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr12:7090782 A>C maps to NM_005768.5 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr12:7125632 C>T maps to NM_005768.5 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr1:82408995 T>C maps to ENST00000370717 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr4:62812746 C>T maps to ENST00000506720 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr4:62542579 T>G maps to ENST00000506720 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:11925179 C>T maps to ENST00000396099 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:11960559 A>G maps to ENST00000396099 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr2:11922577 C>T maps to ENST00000396099 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr20:39987125 C>T maps to NM_022896.1 F785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr20:39984631 T>C maps to NM_022896.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:19811709 C>T maps to NM_000237.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr1:99767413 T>C maps to NM_014839.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr4:151827109 A>T maps to NM_006726.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:151829519 G>A maps to NM_006726.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr4:151842426 A>G maps to NM_006726.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr23:114357117 T>C did not map to a codon.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr23:114400840 C>A did not map to a codon.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr23:114398271 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:114357117 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:114357119 A>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:114357359 C>T did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr7:100174728 C>A maps to NM_002319.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr11:804238 C>T maps to NM_145886.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr19:36435682 C>A maps to NM_024509.1 S550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:66627367 T>A maps to NM_024036.4 L537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:42360767 C>T maps to NM_152447.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:133812164 T>C maps to NM_144648.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:66460689 C>A maps to NM_015541.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:113657325 C>A maps to NM_014813.1 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr1:113633958 T>C maps to NM_014813.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr1:113652930 G>A maps to NM_014813.1 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr12:59274492 G>A maps to NM_153377.3 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr12:59271293 C>A maps to NM_153377.3 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:59274639 C>T maps to NM_153377.3 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr12:59276666 T>C maps to NM_153377.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:57605025 C>T maps to NM_002332.2 C4328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr12:57600463 G>A maps to NM_002332.2 A3933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr12:57588206 C>A maps to NM_002332.2 T2663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr12:57548477 C>T maps to NM_002332.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr12:57590880 T>A maps to NM_002332.2 Y3003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr6:150174137 C>A did not map to a codon.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr8:105507334 A>T maps to NM_013437.4 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:141773378 T>G maps to NM_018557.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr2:141812721 A>T maps to NM_018557.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr2:141571373 A>G maps to NM_018557.2 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr2:141259354 G>A maps to NM_018557.2 G2917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr2:141607701 G>A maps to NM_018557.2 N1636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr2:170012841 G>T maps to NM_004525.2 V4031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr2:170028540 T>C maps to NM_004525.2 S3749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:170030630 T>C maps to NM_004525.2 K3604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr2:170062050 G>A maps to NM_004525.2 V2551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr2:169993943 G>C maps to NM_004525.2 Y4526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:170055305 A>G maps to NM_004525.2 P2856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr2:169995116 A>C maps to NM_004525.2 P4496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr2:170060530 C>A maps to NM_004525.2 E2656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr2:170072852 A>G maps to NM_004525.2 T1912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr2:170026248 G>A maps to NM_004525.2 S3820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr2:170029717 G>A maps to NM_004525.2 L3677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:170129473 G>A maps to NM_004525.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr2:169999256 T>C maps to NM_004525.2 R4345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:170136008 T>A maps to NM_004525.2 K480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr19:33697007 C>T maps to NM_002333.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr19:33697545 C>T maps to NM_002333.3 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr11:46914587 G>T maps to ENST00000256991 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr11:46880581 G>A maps to ENST00000256991 D1935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr11:46895080 G>A maps to ENST00000256991 D1476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:46911058 G>A maps to ENST00000256991 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr11:68216348 C>T maps to NM_002335.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr11:68125160 C>A maps to NM_002335.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:68197136 C>T maps to NM_002335.2 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr12:12274104 A>G maps to NM_002336.2 H1599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr12:12303826 G>C maps to NM_002336.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:12302075 C>T maps to NM_002336.2 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:53723083 T>G maps to NM_004631.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:53792605 G>T maps to NM_004631.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr4:3519767 A>G maps to NM_002337.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:44145521 C>T maps to NM_133259.3 W971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:44176771 T>A maps to NM_133259.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr2:44207046 A>G maps to NM_133259.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr2:44203319 T>A maps to NM_133259.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:145745729 A>G maps to NM_014665.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr6:25509936 C>T maps to NM_017640.5 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr6:25285101 G>T maps to NM_017640.5 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr10:50121786 G>A maps to NM_001006939.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr9:26997768 T>G maps to NM_022901.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:7023219 A>C maps to NM_006992.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr12:7023183 C>A maps to NM_006992.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:18507173 C>T maps to NM_145256.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:196387839 C>T maps to NM_198565.1 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr16:67404968 C>T maps to NM_018296.5 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:62855781 A>T maps to NM_199340.2 I1494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr7:127670480 C>T maps to NM_022143.4 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:46751889 T>G maps to ENST00000254454 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:122669245 T>C maps to NM_001098519.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:122674784 A>T maps to NM_001098519.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr12:122672369 C>T maps to NM_001098519.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr17:79986135 C>T maps to NM_144999.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51021775 C>T maps to NM_001080457.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:40136543 C>G maps to NM_020929.1 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr16:84211445 A>G maps to NM_178452.4 *726W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr16:84211398 T>C maps to NM_178452.4 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr11:56954875 G>A maps to NM_001005210.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:551240 G>C maps to NM_198075.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:150033985 C>G maps to NM_023942.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr4:52861444 G>A maps to NM_001024611.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr1:70504368 G>A maps to NM_020794.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr1:70518806 T>C maps to NM_020794.2 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr1:70505475 G>A maps to NM_020794.2 R1285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr9:131670919 G>T maps to NM_001127244.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr9:131669448 T>A maps to NM_001127244.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr1:90049714 C>T maps to NM_015350.2 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr1:90049486 T>C maps to NM_015350.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr1:90048979 A>G maps to NM_015350.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr1:90048544 A>G maps to NM_015350.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:90179187 T>C maps to NM_032270.4 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:7964516 C>T maps to NM_025061.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr19:7964009 T>G maps to NM_025061.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr8:86057650 G>T maps to NM_033402.4 E1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:85449851 G>T maps to NM_001079910.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr1:74575230 C>T maps to NM_001105659.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:169555370 A>G maps to NM_001080460.1 K545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr15:101529602 A>G maps to NM_024652.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr15:101595296 G>T maps to NM_024652.3 E1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr15:101595283 C>A maps to NM_024652.3 S1396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr15:101593135 G>T maps to NM_024652.3 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr15:101601456 G>A maps to NM_024652.3 Q1587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr15:101597209 A>T maps to NM_024652.3 R1494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr15:101528944 G>A maps to NM_024652.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:40758850 A>G maps to NM_198578.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr12:40728899 A>G maps to NM_198578.3 K1963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:40689346 C>A maps to NM_198578.3 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr5:138209475 T>G maps to NM_015564.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr9:130241214 C>T maps to NM_001005374.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr7:102106462 G>T maps to NM_152892.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:42117588 C>T maps to ENST00000411445 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:35757259 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:35758027 C>A maps to NM_205834.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr21:47626683 T>G did not map to a codon.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr12:21242949 A>G maps to ENST00000381541 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:96421287 A>G maps to NM_000895.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr14:24785138 C>T maps to NM_181657.3 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr2:33534504 C>T maps to ENST00000354476 I1163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr2:33622347 C>G maps to ENST00000354476 V1662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr14:74970232 G>A maps to NM_000428.2 C1553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr14:74972835 C>T maps to NM_000428.2 V1364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr14:75019016 C>G maps to NM_000428.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr11:65318873 G>A maps to NM_001130144.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:65319016 A>T did not map to a codon.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr19:41120305 G>A maps to ENST00000308370 R989R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr19:41132931 G>T maps to ENST00000308370 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:41129531 C>T maps to ENST00000308370 R1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:46477691 C>T maps to NM_002343.3 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:46492032 A>G maps to NM_002343.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr15:41798199 G>T maps to NM_002344.5 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr7:139097304 C>A maps to NM_016019.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr7:139086942 A>T maps to NM_016019.2 K106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr12:91502696 G>C maps to NM_002345.3 Y20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr12:91502420 G>A maps to NM_002345.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr23:114541170 T>A did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:31675741 G>A maps to ENST00000375834 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr2:160697358 C>A maps to NM_001198759.1 E1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr2:99901198 C>A maps to NM_174898.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr19:13211727 C>T maps to NM_005583.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr2:133403818 C>T maps to ENST00000409034 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr19:43969648 G>A maps to NM_014400.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:43965541 T>C maps to NM_014400.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr19:42341276 G>A maps to NM_173506.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr19:44301841 G>T maps to NM_001031749.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr1:219347282 A>G maps to NM_138794.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr6:5260905 T>A maps to NM_001164840.1 K21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr15:100269537 C>T maps to NM_152449.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr1:235969774 C>T maps to NM_000081.2 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr1:235884145 A>G maps to NM_000081.2 Y3125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr1:235971938 G>A maps to NM_000081.2 Q727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:235964395 C>T maps to NM_000081.2 G1238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:235884163 G>A maps to NM_000081.2 L3119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr10:29580864 T>A maps to NM_032517.4 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr8:20107280 C>T maps to NM_021020.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:20107304 G>A maps to NM_021020.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr12:9096394 A>G did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr13:36049372 G>A maps to NM_005584.4 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:39908527 C>G maps to ENST00000361689 S4357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr1:39908130 C>A maps to ENST00000361689 A4273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:39888511 C>T maps to ENST00000361689 A3301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:39951258 C>T maps to ENST00000361689 A5362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr11:63767185 A>G maps to NM_014067.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr20:15967709 G>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:16021923 G>A did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr7:2255570 C>T maps to NM_003550.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr1:166962001 C>T maps to NM_032858.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr16:79633709 A>G maps to NM_005360.4 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr19:35800934 G>T maps to NM_002361.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:151303632 G>T did not map to a codon.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr23:151303309 G>T did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr23:151303810 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr23:148797542 C>A did not map to a codon.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr23:151092615 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr23:151283745 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr23:151870044 G>A did not map to a codon.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr23:27840134 C>A did not map to a codon.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr23:27840419 G>A did not map to a codon.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr23:35820493 C>T did not map to a codon.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr23:35821145 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr23:30236764 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr23:30236765 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr23:30236764 G>T did not map to a codon.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr23:30237264 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr23:30254276 A>T did not map to a codon.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr23:30254881 G>C did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:30260476 G>C did not map to a codon.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr23:30260746 C>G did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:30261229 C>A did not map to a codon.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:26212242 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:26212892 C>A did not map to a codon.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr23:26212261 C>T did not map to a codon.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:140996269 G>C did not map to a codon.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr23:140994210 C>T did not map to a codon.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr23:140994461 A>C did not map to a codon.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr23:140995586 G>C did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr23:140993824 G>C did not map to a codon.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr23:140993715 G>C did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr23:140994793 G>C did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr23:140993876 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr23:140993863 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr23:140993372 G>A did not map to a codon.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr23:140995290 G>A did not map to a codon.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr23:140994356 C>A did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr23:140994319 G>T did not map to a codon.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr23:140994086 C>A did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr23:140994351 C>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:140993911 C>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:140994380 C>G did not map to a codon.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr23:140994009 C>T did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr23:140953291 C>T did not map to a codon.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr23:51638669 G>A did not map to a codon.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr23:51640357 A>G did not map to a codon.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr23:51638327 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:51637858 A>G did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr23:54839918 A>G did not map to a codon.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr23:54841821 G>C did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:54841946 C>T did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr23:54837699 G>A did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr23:75649862 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:75650468 G>T did not map to a codon.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr23:75648790 C>T did not map to a codon.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr23:75004669 C>A did not map to a codon.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr23:75003526 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:23889370 A>T maps to NM_019066.4 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr3:65425593 C>T maps to NM_001033057.1 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr3:65425590 T>C maps to NM_001033057.1 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr3:65425593 C>T maps to NM_001033057.1 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:65425596 C>T maps to NM_001033057.1 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:78131030 C>A maps to NM_012301.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr7:79082435 C>A maps to NM_012301.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr1:114157262 T>A maps to NM_001142782.1 Y353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:10766046 G>T maps to NM_018048.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr23:77096798 C>G did not map to a codon.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr23:77150868 G>T did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr23:77150837 C>A did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr6:10802229 A>T maps to NM_005906.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:110873285 G>A maps to NM_005434.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr18:56414968 C>T maps to NM_006785.2 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr9:139748705 C>T maps to ENST00000392881 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:139748711 C>T maps to ENST00000392881 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:179160184 C>T maps to NM_014757.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:179192886 G>A maps to NM_014757.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr5:179201811 C>G maps to NM_014757.4 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr5:179201052 G>A maps to NM_014757.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:179193184 G>T maps to NM_014757.4 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:179192793 G>A maps to NM_014757.4 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr11:95825220 C>T maps to NM_032427.1 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825247 C>T maps to NM_032427.1 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:95825355 T>C maps to NM_032427.1 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:95825394 C>T maps to NM_032427.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr11:95825796 A>G maps to NM_032427.1 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr11:95825400 C>T maps to NM_032427.1 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:95825361 C>T maps to NM_032427.1 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr11:95825361 C>T maps to NM_032427.1 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr11:95825361 C>T maps to NM_032427.1 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:140811125 C>T maps to ENST00000509479 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr4:140811128 T>C maps to ENST00000509479 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr4:140811101 C>T maps to ENST00000509479 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr23:149639658 A>T did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:149639326 G>A did not map to a codon.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr23:149613801 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr23:149638088 A>C did not map to a codon.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr23:149638777 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr19:49216784 C>T maps to NM_001130915.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:117984947 G>A did not map to a codon.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr9:140002044 C>T maps to NM_016219.3 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr15:91449979 C>A maps to NM_006122.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr12:12483329 T>A maps to NM_018050.2 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:12483848 G>T maps to NM_018050.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:43571200 C>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:43590944 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr23:43515618 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr23:43571992 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:43702914 C>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:43655116 C>T did not map to a codon.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr15:43821932 T>A maps to ENST00000382031 A2945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr5:71495733 G>A maps to NM_005909.3 S2184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr5:71493193 C>T maps to NM_005909.3 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr5:71495394 G>A maps to NM_005909.3 K2071K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr5:71494890 C>A maps to NM_005909.3 G1903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:71495627 C>G maps to NM_005909.3 S2149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr20:33147237 G>T maps to NM_181509.1 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:17836822 C>T maps to NM_018174.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:17837416 G>A maps to NM_018174.4 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:210561003 C>T maps to NM_002374.3 D1370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr17:21215482 C>T maps to NM_145109.2 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:12016634 T>C maps to ENST00000415385 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr17:11998977 C>T maps to ENST00000415385 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:7976337 A>G maps to ENST00000425613 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr5:56160678 T>G maps to NM_005921.1 L318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr5:56152548 T>A maps to NM_005921.1 L202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:56177036 T>A maps to NM_005921.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr5:56170959 G>T maps to NM_005921.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr19:40719457 C>T maps to NM_002446.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr11:65375919 C>A did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:185191374 G>A maps to NM_004721.3 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr3:185195184 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:185146746 C>T maps to NM_004721.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr23:19410162 C>T did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr23:19389074 A>C did not map to a codon.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr23:19398324 G>C did not map to a codon.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr23:19398360 G>C did not map to a codon.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr17:61762879 C>T maps to NM_203351.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr6:161523806 T>C maps to NM_005922.2 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:161470013 C>A maps to NM_005922.2 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:161413040 G>A maps to NM_005922.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr6:136879990 T>C maps to NM_005923.3 L1337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:137113271 G>A maps to NM_005923.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr6:91228281 C>A did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:91226400 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr14:71267588 G>A maps to NM_033141.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr3:47957987 C>T maps to ENST00000426837 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr2:39519947 C>A maps to NM_003618.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:39526943 T>C did not map to a codon.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr2:102490652 C>A maps to NM_145686.2 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:102493543 C>A maps to NM_145686.2 I1043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr2:102486843 C>G maps to NM_145686.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:102493591 C>G maps to NM_145686.2 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:36644626 G>A did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:36642064 G>A maps to NM_018067.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr23:20081683 G>A did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr23:20074910 T>C did not map to a codon.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr23:135312675 A>G did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr23:135314178 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr23:135328305 T>A did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr23:135314168 T>C did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr22:22142569 G>A maps to NM_138957.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr22:50695075 C>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr6:36040749 C>A maps to NM_139012.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr8:144801160 A>T did not map to a codon.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr8:144801566 G>C maps to NM_139021.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr18:48190483 C>T maps to NM_002747.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr17:19284304 C>G maps to NM_139034.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr17:19284373 C>T maps to NM_139034.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:45925698 C>T maps to NM_005456.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:1815159 G>A maps to NM_015133.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr9:128246856 T>G maps to NM_001006617.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:50685440 C>G maps to NM_004635.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr15:42113792 C>A maps to NM_001128608.1 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:27248499 C>T maps to NM_012326.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr2:27245100 G>A maps to NM_012326.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:44101443 C>G maps to NM_001123066.3 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:60802311 C>A maps to NM_152598.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr17:60813346 T>A maps to NM_152598.2 K628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:8503276 C>T maps to NM_016496.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:45953839 A>G maps to NM_145021.4 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr10:45959706 T>A maps to NM_145021.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:58149445 C>T maps to NM_138396.4 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr12:58152574 C>T maps to NM_138396.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr2:119731957 G>A maps to NM_006770.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr11:63670172 G>T maps to NM_001039469.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr11:63671475 C>G maps to NM_001039469.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr14:103941507 G>A maps to ENST00000335102 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:57894295 C>T maps to NM_004990.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr12:57894253 G>C maps to NM_004990.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr2:198571442 G>A maps to NM_138395.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr16:71663302 C>T maps to NM_001017967.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr6:29454617 T>A maps to NM_052967.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr3:186937984 G>A maps to NM_001879.5 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr19:12975919 G>T maps to NM_014975.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:46290208 T>C maps to NM_015112.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr19:18234142 C>A maps to NM_015016.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:66432457 C>G maps to NM_001164664.1 L820L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5098-01A-01D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr5:66459284 C>T maps to NM_001164664.1 H1426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr5:66459740 G>A maps to NM_001164664.1 P1578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr2:85769803 T>C maps to NM_005911.4 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr2:85768974 T>C maps to NM_005911.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr8:99028777 T>C maps to ENST00000254898 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:99019719 C>T maps to ENST00000254898 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr20:43927152 G>A maps to ENST00000372754 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr5:138643266 T>C maps to ENST00000394800 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr14:65544755 T>C did not map to a codon.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr18:47799981 A>T maps to ENST00000424334 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr18:47800702 C>T maps to ENST00000424334 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr18:47803543 A>C maps to ENST00000424334 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr18:47799226 T>A maps to ENST00000424334 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr3:129152726 A>G maps to NM_003925.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:149227851 T>G maps to ENST00000404807 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:149248039 A>C maps to ENST00000404807 P1613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:149226186 G>A maps to ENST00000404807 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:57920769 T>G maps to NM_052897.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr12:57918127 G>T maps to NM_052897.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:57918526 C>A maps to NM_052897.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:152163261 C>T maps to NM_021038.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:131540268 T>A did not map to a codon.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr6:20212417 G>T maps to NM_001080480.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr6:20144500 G>A maps to NM_001080480.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr2:9048797 A>C maps to NM_138799.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr18:74700844 C>T maps to NM_001025101.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr17:49281221 A>G maps to ENST00000389496 N226N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr16:84101411 C>T maps to NM_003791.2 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr16:84094305 G>C maps to NM_003791.2 V895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr18:13885199 G>T maps to NM_000529.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr20:54824369 C>A maps to ENST00000371389 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr18:13826627 C>T maps to NM_005913.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr18:13826447 G>A maps to NM_005913.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:119182660 T>A did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:119185944 C>T maps to NM_006500.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:103349336 C>T did not map to a codon.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr23:103349893 G>A did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:112458402 A>T maps to NM_001085377.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:182759358 C>G maps to NM_020166.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr2:71351337 C>A maps to NM_032601.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr23:138713617 T>A did not map to a codon.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr23:138684575 C>T did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr23:138698452 A>G did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:138695405 A>G did not map to a codon.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr13:113728834 G>A maps to NM_001112732.1 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr3:182897462 C>T maps to NM_015078.2 Q1041Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:183013204 G>A maps to NM_015078.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:183028732 T>C maps to NM_015078.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:150551616 C>T maps to NM_021960.4 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr3:127337929 G>T maps to NM_004526.2 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr3:127323459 C>T maps to NM_004526.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr6:52129391 G>A maps to ENST00000419835 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr21:47692475 T>A maps to NM_003906.3 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr8:48874106 T>A maps to NM_182746.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr8:48889310 G>T maps to NM_182746.1 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr8:48882494 C>T maps to NM_182746.1 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:99690936 C>A maps to NM_005916.3 G646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr20:5933142 A>C maps to NM_032485.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:119245293 T>C did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:85491699 A>G maps to NM_018298.9 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:85491893 G>C maps to NM_018298.9 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr8:6266848 T>A maps to NM_024596.3 Y24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr8:6266850 C>G maps to NM_024596.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:6302562 T>C maps to NM_024596.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:94253678 C>T did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:94841733 C>T maps to NM_018349.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr23:119739389 A>T did not map to a codon.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr6:30680149 T>C maps to NM_014641.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr6:30672174 C>G maps to NM_014641.2 R1595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr6:30681949 T>C maps to NM_014641.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr6:37606074 C>T maps to ENST00000297153 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:37622224 G>T maps to ENST00000297153 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr14:47613332 A>T maps to NM_001113498.2 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:63826355 C>G maps to NM_005917.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:68720391 G>A maps to NM_020128.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:68696604 T>A maps to NM_017440.4 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:90402312 G>C maps to NM_014611.1 S3479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr6:90459293 G>A maps to NM_014611.1 Q1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr11:86198483 T>G did not map to a codon.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr1:37975130 G>A maps to NM_022756.4 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr3:168802757 C>T maps to NM_004991.3 W1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr23:153296885 G>C did not map to a codon.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr23:153296614 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:153296437 C>T did not map to a codon.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr17:37565878 G>A maps to NM_004774.3 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr17:37579983 A>T maps to NM_004774.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr23:70345893 G>A did not map to a codon.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr23:70342187 A>G did not map to a codon.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr23:70341180 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:70352800 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr23:70360568 T>C did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:70349197 G>T did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr3:150874117 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr3:150877785 C>T maps to NM_053002.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr17:60129920 T>C maps to NM_005121.2 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:116549249 G>T maps to NM_015335.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:116428912 C>T maps to NM_015335.4 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr23:40586007 T>C did not map to a codon.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr23:40568602 T>G did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr23:40573154 T>C did not map to a codon.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr23:40570474 A>T did not map to a codon.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr23:40526074 A>C did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:20920815 G>A maps to NM_001003891.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr22:20921041 T>C maps to NM_001003891.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr22:20920818 G>A maps to NM_001003891.1 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr19:871134 A>G maps to NM_005481.2 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr1:28660958 C>T maps to NM_017638.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr9:136212035 G>C maps to NM_133640.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:131931275 G>T maps to ENST00000403834 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:38182476 C>T maps to NM_014815.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:38187789 C>G did not map to a codon.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:50338352 C>T maps to NM_030973.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr19:50333062 T>C maps to NM_030973.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr9:134889740 A>G maps to NM_004269.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:134889752 A>G maps to NM_004269.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr9:134955075 A>G maps to NM_004269.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr13:48669205 C>G maps to NM_014166.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr13:48669154 C>T maps to NM_014166.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr5:88025095 A>G maps to NM_002397.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr16:3293875 G>A maps to NM_000243.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr16:3304653 T>C maps to NM_000243.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr5:126754855 A>T maps to NM_032446.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:126778708 T>G maps to NM_032446.2 Y794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:126705694 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:66214757 G>A maps to NM_032445.2 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr9:123476114 G>A maps to ENST00000426959 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:123476126 G>A maps to ENST00000426959 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr22:42191443 C>A maps to NM_152513.3 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr22:42154471 A>C maps to NM_152513.3 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr2:66667008 G>T maps to ENST00000407092 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr9:36583633 A>G maps to NM_014791.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr9:36665414 A>G maps to NM_014791.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr11:64577152 G>A maps to NM_130804.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:15725808 G>A maps to NM_005924.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr15:81295652 G>A maps to NM_022566.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:81295559 C>T maps to NM_022566.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr15:81294773 G>C maps to NM_022566.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:81282036 G>A maps to NM_015154.1 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr15:90321561 C>T maps to NM_001039958.1 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr7:116339926 G>T maps to NM_001127500.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr7:116411637 C>G maps to NM_001127500.1 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr7:116411694 A>G maps to NM_001127500.1 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr4:99955421 G>T maps to NM_015143.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr12:95888730 A>T did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:58165806 G>A maps to ENST00000408972 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr10:126477650 A>G maps to NM_212554.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr1:171753286 C>T maps to NM_015935.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr1:171753604 A>G maps to NM_015935.4 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:60501295 A>G maps to NM_181725.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr14:21966491 C>T maps to NM_019852.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr14:21967448 C>G did not map to a codon.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr18:2544670 T>A maps to NM_022840.3 K388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr18:2547513 G>C maps to NM_022840.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr2:170677783 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:56076035 G>A maps to NM_152637.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr16:21611122 G>C maps to NM_016025.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr16:21611191 C>G maps to NM_016025.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:1555891 G>A maps to NM_001174118.1 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:44105506 C>T maps to NM_005926.2 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr15:44109599 T>G maps to NM_005926.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr5:153432672 C>T maps to NM_005927.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr15:89449934 G>A maps to NM_005928.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr8:8748227 G>T maps to NM_004225.2 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:8655001 C>A did not map to a codon.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr3:196733605 G>T maps to NM_005929.5 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:179094913 T>G maps to NM_033540.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:179096585 C>A maps to NM_033540.2 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr22:37875490 C>T maps to NM_002405.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr3:158545108 A>T maps to NM_022736.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr4:2934200 C>G maps to NM_001146069.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:74738355 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:74772620 C>T maps to NM_024311.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr17:74765927 T>C maps to NM_024311.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:40434357 A>G maps to NM_001136493.1 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr1:40430906 C>T maps to NM_001136493.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr8:145735860 C>A maps to NM_138431.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr12:53647797 C>T maps to NM_001170790.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:53647587 C>G maps to NM_001170790.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr2:191334580 G>T maps to NM_017694.3 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr17:8701340 G>A maps to NM_152599.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr15:41988560 A>G maps to ENST00000219905 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr15:42034894 A>G maps to ENST00000219905 T1628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr15:42057123 C>T maps to ENST00000219905 N2644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:141762387 C>T maps to ENST00000475668 A1381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr7:141732689 T>C maps to ENST00000475668 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:141759732 A>G maps to ENST00000475668 K1342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr7:141752122 C>A maps to ENST00000475668 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:141731532 T>G maps to ENST00000475668 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4804-01A-02D-1373-10 chr22:39883402 G>C maps to NM_001098270.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr22:39884299 C>T maps to NM_001098270.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr5:179225512 G>A maps to NM_054013.3 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr12:86373525 C>T maps to ENST00000393205 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:135012081 G>A maps to NM_002410.3 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr5:138724268 C>T maps to NM_016459.3 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr10:103552625 A>G maps to NM_012215.3 Y715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr10:103563516 A>G maps to NM_012215.3 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr16:4727554 G>A maps to NM_015246.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr18:19379922 A>G maps to NM_020774.2 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr11:12278354 C>T maps to NM_014632.2 P993P. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:12225945 G>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr22:18389488 C>T maps to NM_015241.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr22:18389488 C>T maps to NM_015241.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr22:18304889 A>G maps to NM_015241.2 R1118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr22:18376627 G>A maps to NM_015241.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr11:12316357 T>C maps to NM_032867.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr11:12316165 T>G maps to NM_032867.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:12316189 C>T maps to NM_032867.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:1477989 C>G did not map to a codon.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr7:1480279 C>T maps to NM_182924.3 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr7:1480285 G>A maps to NM_182924.3 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:38664686 G>T did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:38664367 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr23:38664278 A>G did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr1:67394624 T>C maps to NM_020948.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:67423740 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:12089879 C>T maps to NM_021933.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr1:12081815 G>T maps to NM_021933.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr3:97673273 G>T maps to NM_153182.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:4800539 T>G maps to NM_153827.4 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr7:7635994 G>T maps to NM_019005.3 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:50926722 G>T maps to NM_017584.5 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr3:69928531 A>T maps to ENST00000448226 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr10:129906187 C>A maps to NM_002417.4 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr10:129913432 A>C maps to NM_002417.4 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr10:129899863 T>C maps to NM_002417.4 E3121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr2:122488642 G>A maps to NM_032390.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr20:10393757 G>A maps to NM_170784.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr22:40813488 G>A maps to NM_020831.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr22:40814635 C>T maps to NM_020831.3 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr16:14304163 A>G maps to NM_014048.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:2041089 G>T maps to NM_199054.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr17:56285342 A>G maps to NM_017777.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:56290441 C>T maps to NM_017777.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr22:50518346 G>A maps to NM_015166.3 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:6859056 C>T maps to NM_005439.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:75516129 T>A maps to NM_001040108.1 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr16:74716658 G>T maps to NM_152649.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr16:74725179 G>A maps to NM_152649.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr11:118352712 G>A maps to NM_001197104.1 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr11:118372560 T>A maps to NM_001197104.1 L2165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr11:118375277 G>T maps to NM_001197104.1 E2891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr11:118370616 T>A maps to NM_001197104.1 P2049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr12:49444843 G>T maps to NM_003482.3 C874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr12:49442447 T>C maps to NM_003482.3 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr12:49420871 G>C maps to NM_003482.3 A4959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr12:49445197 A>G maps to NM_003482.3 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49425838 G>A maps to NM_003482.3 Q4217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49426525 G>A maps to NM_003482.3 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr12:49444337 C>T maps to NM_003482.3 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr12:49442447 T>C maps to NM_003482.3 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:49443746 G>A maps to NM_003482.3 I1208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:49425038 C>T maps to NM_003482.3 L4483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr12:49431829 A>T maps to NM_003482.3 A3103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr12:49433379 C>G maps to NM_003482.3 L2689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr7:151842347 G>T maps to ENST00000355193 T4745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr7:151945348 T>A maps to ENST00000355193 K724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr7:151877174 G>A maps to ENST00000355193 Q2396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:151884404 A>T maps to ENST00000355193 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr7:151879015 G>A maps to ENST00000355193 Q1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr7:151860718 G>A maps to ENST00000355193 Q3315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr7:151882664 G>T maps to ENST00000355193 S1687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr7:151970835 G>A maps to ENST00000355193 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr7:151851227 G>T maps to ENST00000355193 S4105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr7:151848092 C>G did not map to a codon.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr7:151932922 G>A maps to ENST00000355193 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr7:151945348 T>A maps to ENST00000355193 K724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:151921113 A>T maps to ENST00000355193 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:36229180 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36210430 C>T maps to NM_014727.1 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr7:104719410 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:104750954 G>T maps to NM_182931.2 P1292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr19:6216489 G>C maps to NM_005934.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr19:6218034 C>T maps to NM_005934.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr10:22023040 A>C maps to NM_004641.3 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:168271096 A>G maps to ENST00000400822 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr6:168273012 A>T maps to ENST00000400822 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr6:168297598 C>T maps to ENST00000400822 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:168276026 A>C maps to ENST00000400822 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr6:168344079 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr13:49796386 C>G maps to NM_001507.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr16:2258564 C>T maps to NM_022372.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr17:40721609 A>G maps to NM_170607.2 L208L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6134-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:40720855 T>C maps to NM_170607.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr12:122616845 C>T maps to NM_014938.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr7:73020309 G>A maps to NM_032951.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr16:83940608 G>T maps to NM_012213.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr3:154862149 C>A maps to NM_007289.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:154855892 T>A maps to NM_007289.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:154858035 A>G maps to NM_007289.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr3:154898166 G>A maps to NM_007289.2 Q724Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr1:2540841 C>T maps to NM_033467.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr23:135047253 A>T did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr11:102650296 G>A maps to NM_002425.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr22:24122847 G>T maps to NM_005940.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr11:102737124 A>C maps to ENST00000326227 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:58074477 C>A maps to NM_002428.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr16:55519325 G>A maps to NM_004530.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr16:3100413 C>T maps to NM_022468.4 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr17:34093632 G>A maps to NM_024302.3 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr17:34093554 G>A maps to NM_024302.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:102713446 G>T maps to NM_002422.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr11:102709282 T>G maps to NM_002422.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr11:102394121 G>A maps to NM_002423.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:44641957 G>A maps to NM_004994.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:88703694 G>A maps to NM_024756.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr10:99220743 G>A maps to ENST00000422291 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr10:99223687 A>G maps to ENST00000422291 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr10:99229885 C>T maps to ENST00000422291 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr10:99222419 C>T maps to ENST00000422291 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr22:28192793 C>T maps to NM_002430.2 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr22:28194899 T>C maps to NM_002430.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr22:28194899 T>C maps to NM_002430.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr22:28194911 T>C maps to NM_002430.2 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr22:28194926 C>T maps to NM_002430.2 Q535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr22:28193288 C>T maps to NM_002430.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr14:61434958 T>C maps to NM_002431.3 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:61434985 T>C maps to NM_002431.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr15:56735642 A>C maps to NM_018365.2 Y332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr11:1501648 C>T maps to NM_001172223.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr11:1491712 C>A maps to NM_001172223.1 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr11:1492591 G>T maps to NM_001172223.1 Y141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:47078804 G>A maps to NM_145279.4 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:39893449 A>T maps to ENST00000425303 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr20:49576092 C>T maps to NM_014484.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr11:75438649 G>T maps to NM_025098.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:49946455 G>A maps to NM_032355.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:77228769 C>A maps to NM_014940.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr12:62918363 C>A maps to ENST00000393630 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr12:62954343 A>T maps to ENST00000393630 V1162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr21:37721694 T>C maps to ENST00000290384 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr23:106186436 T>A did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr23:106201625 A>G did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr1:2268197 C>T maps to NM_024848.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:220971316 G>A maps to NM_022746.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr1:220960438 G>T maps to NM_022746.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:220964856 G>A maps to NM_022746.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr23:14891809 G>A did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr1:113241048 A>G maps to NM_020963.3 K819K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr22:50558940 C>T maps to NM_018995.2 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr22:50552902 C>T maps to NM_018995.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr9:13183482 A>G maps to ENST00000319217 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr11:58978850 T>A maps to NM_001039396.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:58978385 A>T maps to NM_001039396.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:56355332 C>T maps to ENST00000340482 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr23:154033609 G>T did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:154010063 C>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:67787026 T>C maps to NM_022474.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr14:67779287 T>C maps to NM_022474.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr11:30557622 A>T maps to NM_001584.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:30601905 A>G maps to NM_001584.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:17080726 G>A did not map to a codon.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr17:17078668 C>A maps to NM_015134.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr16:15501818 A>G maps to NM_001128423.1 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr11:118106269 A>G maps to NM_198275.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:118106269 A>G maps to NM_198275.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr11:118111081 G>A maps to NM_198275.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr21:33684177 C>G maps to ENST00000445271 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:18122709 G>A maps to NM_002438.2 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr17:60766322 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:60753773 C>A maps to NM_006039.3 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr11:94169017 G>A maps to NM_005591.3 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:94219121 G>T maps to NM_005591.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr11:68747867 C>G maps to NM_198923.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr11:18195247 C>T maps to NM_054032.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr11:18195096 C>T maps to NM_054032.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:13875776 C>T maps to NM_001031727.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr18:48345980 T>C maps to NM_001127176.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr18:48331526 A>G maps to NM_001127176.1 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr8:55049857 C>G maps to NM_014175.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr6:160218316 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr6:160218372 T>C maps to NM_014161.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:104153052 G>A maps to NM_019051.2 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:6602136 A>C maps to NM_016497.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr2:74699715 C>T maps to NM_053050.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr1:151735550 C>T maps to NM_031420.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr1:36926349 G>A maps to NM_031280.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr6:43642985 A>T maps to ENST00000372118 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:139062899 G>A maps to NM_020191.2 W11*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4981-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr5:44809453 A>G maps to NM_016640.3 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr7:140710229 A>C maps to NM_053035.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:1822946 C>G maps to ENST00000432952 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:1822946 C>G maps to ENST00000432952 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:95773988 C>A maps to NM_031902.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr11:10624762 C>G maps to NM_001098579.1 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:10647665 C>G maps to NM_001098579.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:59837675 G>A did not map to a codon.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr11:59949128 T>C maps to NM_152852.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr5:80074599 C>T maps to NM_002439.3 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr5:80037367 G>C did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:80040401 G>A maps to NM_002439.3 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr5:79968624 C>G maps to NM_002439.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr1:76262747 T>C maps to NM_002440.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr6:31729358 A>G maps to ENST00000375742 Q733Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:48010557 C>A maps to NM_000179.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr12:120791102 G>A maps to NM_002442.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr3:135913892 G>A maps to NM_018133.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr2:234775438 T>A did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr16:815129 G>A maps to NM_013404.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr16:816774 C>G maps to NM_013404.4 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:818455 G>A maps to NM_013404.4 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr16:823127 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr9:35753712 G>A maps to NM_001044264.1 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr23:64958994 G>A did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:64936757 G>C did not map to a codon.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr23:64959701 C>T did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:16021616 A>G maps to ENST00000445506 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr8:16026113 G>T maps to ENST00000445506 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr8:16035393 C>T did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr8:9912061 C>T maps to NM_012331.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr3:49725085 G>A maps to NM_020998.3 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49723816 G>A maps to NM_020998.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr3:49924838 C>G maps to NM_002447.2 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49940430 G>A maps to NM_002447.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr5:174156376 A>T maps to NM_002449.4 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:62366079 C>G maps to NM_004739.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr11:47644273 A>G maps to NM_014342.3 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr11:47653264 T>C did not map to a codon.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr8:98731380 T>C maps to NM_178812.3 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr8:98703399 A>C maps to NM_178812.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:107371721 T>C maps to NM_025198.3 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr1:38323149 C>A maps to NM_005955.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:38288351 G>T maps to NM_005955.2 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr15:65295423 A>C maps to NM_139242.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr16:86565765 G>T maps to NM_001159377.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:86565820 G>A maps to NM_001159377.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:55473594 G>A maps to NM_002453.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr23:149764980 A>G did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr23:149900041 A>C did not map to a codon.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr23:149901023 G>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:31251263 G>C maps to NM_017762.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:149901784 G>C maps to NM_001145862.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr1:149908473 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:149901021 T>A maps to NM_001145862.1 *710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr15:31206243 C>T maps to NM_014967.4 Y587Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr22:30403924 T>C maps to NM_021090.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr22:30408371 T>C maps to NM_021090.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr22:30413917 G>T maps to NM_021090.3 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:30416248 C>T maps to NM_021090.3 C867C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr22:30419454 C>T maps to NM_153050.2 D1108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr22:30418650 T>C maps to NM_021090.3 S1130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr8:17157529 G>A maps to NM_004686.4 D608D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr23:63548771 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr23:63568631 T>A did not map to a codon.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr23:63488823 G>A did not map to a codon.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr8:11142462 C>T maps to NM_015458.3 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr11:92714907 G>C maps to NM_005959.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:92702958 C>A maps to NM_005959.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:11217288 A>G maps to NM_004958.3 Y1463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr1:11168293 C>T maps to NM_004958.3 E2526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:11273602 G>C maps to NM_004958.3 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr1:11190693 G>A maps to NM_004958.3 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr1:11189850 C>T maps to NM_004958.3 Q1886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:11270888 G>A maps to NM_004958.3 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr6:153323723 G>A maps to NM_019041.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr5:7895896 C>A maps to NM_024010.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr5:7897259 G>T maps to NM_024010.2 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr5:7878201 G>T maps to NM_024010.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr5:7878350 A>C maps to NM_024010.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr8:125603468 G>T maps to NM_014751.4 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr4:100521757 C>T maps to ENST00000511045 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr8:17612772 G>A maps to NM_001001924.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr13:29599345 G>T maps to NM_001033602.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr1:155160210 G>T maps to ENST00000425082 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr3:124632010 A>G maps to NM_033049.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr3:124635227 C>T maps to NM_033049.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:26582749 C>T maps to NM_001135091.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:9077785 G>T maps to NM_024690.2 I3220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr19:9091028 T>C maps to NM_024690.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr19:9064630 G>A maps to NM_024690.2 P7605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr19:8996450 G>A maps to NM_024690.2 C13707C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr19:9077023 G>A maps to NM_024690.2 L3474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr19:8998752 G>T maps to NM_024690.2 T13610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:9047433 A>G maps to NM_024690.2 D11399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:9074344 T>C maps to NM_024690.2 T4367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr19:9067639 A>G maps to NM_024690.2 S6602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr19:9085837 C>A maps to NM_024690.2 E1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr19:9061084 G>T maps to NM_024690.2 I8787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:8976795 T>C maps to NM_024690.2 P14090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr19:9046548 A>G maps to NM_024690.2 P11694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr19:8999461 C>T maps to NM_024690.2 L13571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr19:9054241 A>G maps to NM_024690.2 S10460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr19:9018538 C>T maps to NM_024690.2 L12545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr19:9005604 A>T maps to NM_024690.2 T13267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr19:9018475 G>A maps to NM_024690.2 S12566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr19:9012857 G>A maps to NM_024690.2 T12862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:8966764 C>T maps to NM_024690.2 S14396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:8999440 G>A maps to NM_024690.2 I13578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr19:9025603 A>G maps to NM_024690.2 L12284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr19:9006369 A>G maps to NM_024690.2 Y13216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:9012815 G>A maps to NM_024690.2 G12876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:9012818 T>A maps to NM_024690.2 P12875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr19:9012839 G>A maps to NM_024690.2 Y12868Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr19:8999413 G>A maps to NM_024690.2 D13587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:9088826 T>C maps to NM_024690.2 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:9058715 G>C maps to NM_024690.2 S9577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr7:100686873 T>G maps to NM_001040105.1 S4059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr7:100692246 G>A maps to NM_001040105.1 T4219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:100675713 G>C maps to NM_001040105.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:100681164 T>C maps to NM_001040105.1 Y2156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:100684572 G>A maps to NM_001040105.1 T3292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr7:100681509 T>C maps to NM_001040105.1 T2271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr7:100681950 C>A maps to NM_001040105.1 S2418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr11:1092237 C>T maps to ENST00000441003 Q1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr11:1093325 C>A maps to ENST00000441003 G1715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1093409 C>A maps to ENST00000441003 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1093391 C>T maps to ENST00000441003 T1737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1093115 C>T maps to ENST00000441003 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:1093253 C>T maps to ENST00000441003 T1691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:1092965 C>A maps to ENST00000441003 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:1093271 A>C maps to ENST00000441003 T1697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:1093568 A>C maps to ENST00000441003 T1796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr11:1082314 C>T maps to ENST00000441003 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr11:1092094 G>A maps to ENST00000441003 W1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:1099776 T>C maps to ENST00000441003 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:1098667 G>A maps to ENST00000441003 V2346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr11:1092629 T>C maps to ENST00000441003 T1483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr11:1092458 C>A maps to ENST00000441003 T1426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:1093157 T>C maps to ENST00000441003 T1659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:1093451 G>A maps to ENST00000441003 P1757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr11:1093574 G>T maps to ENST00000441003 T1798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr11:1093568 A>C maps to ENST00000441003 T1796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr11:1093046 T>C maps to ENST00000441003 T1622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr11:1075669 C>T maps to ENST00000441003 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr11:1092953 G>A maps to ENST00000441003 T1591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:1092623 C>A maps to ENST00000441003 T1481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr11:1093310 C>A maps to ENST00000441003 T1710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr3:195453060 C>A maps to ENST00000447234 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr6:30954812 T>C maps to NM_001010909.2 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr6:30954602 G>A maps to NM_001010909.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr6:30955118 A>T maps to NM_001010909.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr6:30955157 C>T maps to NM_001010909.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr6:30954920 C>G maps to NM_001010909.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:195538679 C>T maps to NM_018406.5 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr11:1268537 G>A maps to ENST00000447027 S3479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:1264223 C>A maps to ENST00000447027 T2041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr11:1268528 G>A maps to ENST00000447027 S3476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:1281624 T>G did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr11:1253367 C>A maps to ENST00000447027 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:1264091 C>T maps to ENST00000447027 R1997R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr11:1270382 G>A maps to ENST00000447027 T4094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr11:1270400 G>A maps to ENST00000447027 T4100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:1028223 A>G did not map to a codon.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr11:1029577 G>A maps to NM_005961.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr11:1017613 G>A maps to NM_005961.2 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr11:1017646 G>T maps to NM_005961.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:1027278 G>A maps to NM_005961.2 N740N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr11:1025855 G>T maps to NM_005961.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr11:1018030 G>A maps to NM_005961.2 P1590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr11:1016683 G>A maps to NM_005961.2 H2039H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr11:1017529 G>A maps to NM_005961.2 H1757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr11:1018393 C>T maps to NM_005961.2 Q1469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr11:1016605 T>C maps to NM_005961.2 T2065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr11:1018168 C>G maps to NM_005961.2 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr11:1016242 A>G maps to NM_005961.2 H2186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr11:1018339 T>C maps to NM_005961.2 P1487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr11:1016737 A>T maps to NM_005961.2 T2021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr11:1017466 G>T maps to NM_005961.2 T1778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr11:1016644 G>C maps to NM_005961.2 L2052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr11:1017199 G>C maps to NM_005961.2 A1867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr11:1016884 A>C maps to NM_005961.2 P1972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr11:1016776 G>A maps to NM_005961.2 H2008H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr11:1017067 C>T maps to NM_005961.2 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr12:55250593 T>A maps to NM_058173.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr23:105450812 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr9:103348312 A>C maps to NM_001018116.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr5:176734854 G>C maps to ENST00000423571 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr4:2254185 G>A maps to NM_006454.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:3235383 G>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr23:3238718 A>G did not map to a codon.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr23:3228208 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr23:3235732 G>A did not map to a codon.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr1:1290407 A>G maps to NM_032348.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr19:54377172 C>T maps to NM_001020818.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr17:4442823 T>A maps to NM_001105538.1 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:4451583 C>T maps to NM_001105538.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:67477039 T>A maps to NM_001080416.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:42328635 C>T maps to NM_002466.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr20:42340165 G>T maps to NM_002466.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr12:102046969 G>T maps to NM_002465.2 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr12:102043095 G>T maps to NM_002465.2 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr19:50939281 G>T maps to NM_004533.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr11:47356592 G>A maps to ENST00000399249 Q969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:77669614 T>C maps to NM_015057.4 E3359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr13:77730191 C>A did not map to a codon.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr13:77799636 A>G maps to NM_015057.4 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr17:48600412 A>T maps to NM_032133.4 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:40363240 G>A maps to NM_001033082.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:16082257 A>G maps to NM_005378.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr3:38180514 C>T maps to NM_001172567.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:81101548 G>T maps to NM_002469.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:81101619 T>A maps to NM_002469.2 L41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:8424547 G>A maps to ENST00000360416 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:8416921 C>T maps to ENST00000360416 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr16:15872667 C>T maps to NM_001040114.1 T260T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KN-8428-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:15818056 G>A maps to NM_001143979.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr17:10261144 C>T did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:10258305 C>G maps to NM_003802.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr17:10219053 G>A maps to NM_003802.2 Q1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr17:10225009 C>A maps to NM_003802.2 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:10253891 C>T maps to NM_003802.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:10267724 C>T maps to NM_003802.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr17:10247204 G>T maps to NM_003802.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:10227378 A>T maps to NM_003802.2 L965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:10267835 G>A maps to NM_003802.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr19:50783388 C>T maps to NM_001145809.1 H1376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:50812920 C>G maps to NM_001145809.1 T1995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr19:50762504 C>T maps to NM_001145809.1 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr19:50713654 G>C maps to NM_001145809.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr3:108205347 G>C maps to NM_014981.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr3:108224620 T>C maps to NM_014981.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:108110609 G>A maps to NM_014981.1 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr17:10447216 A>T did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:10433385 G>A maps to NM_017534.5 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr17:10435068 C>A maps to NM_017534.5 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:10426830 G>A maps to NM_017534.5 I1818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr17:10543474 G>A maps to NM_002470.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:10554907 G>A maps to NM_002470.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr17:10353951 C>T maps to NM_017533.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:10348582 C>A maps to NM_017533.2 E1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr17:10369588 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:10366487 G>A maps to NM_017533.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr14:23891450 C>A maps to NM_000257.2 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr14:23894488 A>T did not map to a codon.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr14:23894067 T>C maps to NM_000257.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr14:23885476 C>T maps to NM_000257.2 L1563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr14:23886717 G>A maps to NM_000257.2 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr14:23886723 C>T maps to NM_000257.2 R1447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr14:23898981 A>G did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr20:33577861 C>T maps to NM_020884.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr20:33587602 G>T maps to NM_020884.3 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr20:33567236 G>T maps to NM_020884.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr20:33575920 C>A maps to NM_020884.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr20:33575695 C>T maps to NM_020884.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr17:10299726 G>A maps to NM_002472.2 Q1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr17:10312635 A>T maps to NM_002472.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr17:10300167 A>T maps to NM_002472.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr22:36693019 C>T maps to NM_002473.4 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr22:36702091 G>T maps to NM_002473.4 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr7:101265478 G>T maps to NM_138403.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:101259534 G>A maps to NM_138403.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr4:674307 C>T maps to NM_002477.1 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr20:35177591 C>T maps to NM_006097.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr3:123411690 G>A maps to NM_053025.3 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr20:30408124 C>T maps to NM_033118.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:46766186 C>T maps to NM_182493.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr6:2678596 A>G maps to NM_001012418.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr6:2689125 G>T maps to NM_001012418.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr5:16701662 G>A maps to NM_012334.2 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:16764478 G>T maps to NM_012334.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:16701575 G>A maps to NM_012334.2 C976C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr5:16674990 A>G maps to NM_012334.2 I1645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:16877716 C>G did not map to a codon.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr17:18044109 C>T maps to ENST00000205890 P1790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:18022776 G>A maps to ENST00000205890 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr13:109793008 C>T maps to NM_015011.1 H1461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr13:109535456 T>C maps to NM_015011.1 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr13:109793008 C>T maps to NM_015011.1 H1461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:27437603 G>T maps to NM_078471.3 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr22:26423001 C>G maps to ENST00000407587 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr22:26400726 C>T maps to ENST00000407587 Q2128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr22:26164740 A>T maps to ENST00000407587 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:26422671 C>T maps to ENST00000407587 P2246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr12:57440665 G>A maps to NM_005379.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr2:192228922 C>A maps to NM_001130158.1 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr2:192250810 G>T did not map to a codon.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr2:192141692 A>G maps to NM_001130158.1 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr17:1370771 A>C did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:59515312 C>G maps to NM_004998.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:59501014 G>A maps to NM_004998.2 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr12:109826582 C>T maps to NM_001101421.3 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr10:26377304 G>T maps to NM_017433.4 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr10:26385321 T>C maps to NM_017433.4 N525N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr10:26286158 G>T maps to NM_017433.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr15:52720649 C>G maps to ENST00000358212 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr15:52606370 T>C maps to ENST00000358212 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr15:52613682 A>G maps to ENST00000358212 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr18:47518663 G>C maps to NM_001080467.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:47500736 C>T maps to NM_001080467.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr18:47463680 G>A maps to NM_001080467.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr18:47500799 G>T maps to NM_001080467.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr15:52505430 T>C maps to NM_018728.3 Q1365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr15:52521377 A>T maps to NM_018728.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:52571771 C>A maps to NM_018728.3 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr15:52562049 G>A maps to NM_018728.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr15:52510727 A>G maps to NM_018728.3 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:52500780 G>T maps to NM_018728.3 L1452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr6:76570738 G>C did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr11:76890089 G>T did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:76867020 C>T maps to NM_000260.3 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:76891502 G>A maps to NM_000260.3 K890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr11:76903187 C>T maps to NM_000260.3 N1339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:72190907 A>G maps to ENST00000424560 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:72192124 T>G maps to ENST00000424560 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr15:72190901 G>T maps to ENST00000424560 G1314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:17322845 G>A maps to NM_004145.3 T2067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:171605340 G>C maps to NM_000261.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr17:12642617 C>T maps to NM_001146312.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr10:95076525 G>C maps to NM_013451.3 P1881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:95168569 T>G maps to NM_013451.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr18:3089565 T>C maps to NM_003803.3 E1346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:2005805 C>A maps to NM_003970.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr8:2033422 C>T maps to NM_003970.2 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr8:2020500 G>A maps to NM_003970.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr1:24434559 T>C maps to ENST00000330966 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:137222570 T>A maps to NM_006790.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr19:46394099 C>T maps to NM_001012643.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:59125679 A>G maps to NM_001085487.1 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr16:31141807 C>T maps to NM_182958.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr10:76788757 A>G maps to NM_012330.2 E1392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr20:62850363 G>A maps to NM_004535.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr20:62851190 C>T maps to NM_004535.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:1946772 C>T maps to ENST00000399161 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:1805512 T>C maps to ENST00000399161 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr2:1926643 G>A maps to ENST00000399161 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:59082639 G>A maps to NM_198055.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr16:48596216 G>A maps to NM_153029.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:48576973 G>A maps to NM_153029.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr4:40122526 C>T maps to NM_018177.3 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:33095587 T>C did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:21306118 T>C maps to NM_174928.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:153198017 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr23:153196256 C>T did not map to a codon.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr4:140280991 C>T maps to NM_057175.3 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:112498997 A>G maps to NM_024953.3 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr12:112516502 G>A maps to NM_024953.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64813974 G>A maps to ENST00000340252 Y592Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:64822096 C>A maps to ENST00000340252 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr12:57485519 T>G maps to NM_005967.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr12:57485372 G>T maps to NM_005967.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr12:57110096 G>A maps to NM_001113203.1 L1739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:57112265 A>G maps to NM_001113203.1 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:57114974 T>C maps to NM_001113203.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:59668190 C>T maps to NM_199290.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:59668145 A>G maps to NM_199290.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:66857504 T>C did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr4:164050357 A>G maps to NM_138386.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr4:164050120 G>A maps to NM_138386.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr4:164061508 T>C maps to NM_138386.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr22:42456378 G>A maps to NM_000262.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:40695934 C>T maps to NM_000263.3 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr16:5081818 C>A maps to NM_016256.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr17:42083123 T>C maps to NM_153006.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:101881860 T>C maps to NM_052867.2 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr7:105904029 T>C maps to NM_005746.2 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr12:7947297 C>T maps to NM_024865.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr12:7947570 C>T maps to NM_024865.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:13988493 A>G maps to NM_001098622.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr23:72433896 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr23:72432979 T>G did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr23:92927723 C>T did not map to a codon.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr23:92927544 T>C did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr4:89618836 T>C maps to NM_153757.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr7:102769016 C>T maps to ENST00000455523 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr8:144660317 G>T maps to ENST00000276844 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr8:144658710 G>A maps to ENST00000276844 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:80443513 C>T maps to ENST00000374611 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr17:80436688 C>T maps to ENST00000374611 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:46083163 A>G maps to NM_002482.3 K729K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr8:18080419 T>C maps to NM_001160176.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:73868602 G>A maps to NM_003960.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr2:73928330 C>T maps to NM_016347.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr17:72769712 A>G did not map to a codon.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr1:201772832 A>G maps to ENST00000367296 K1210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr1:201751583 C>T maps to ENST00000367296 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr1:201781617 G>T maps to ENST00000367296 E1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr1:201618542 C>T maps to ENST00000367296 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr11:19954836 G>A maps to ENST00000396087 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr11:20124910 G>A maps to ENST00000396087 L2235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr11:19735258 C>A maps to ENST00000396087 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:78604233 C>T maps to NM_014903.4 C2343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr12:78574709 A>G maps to NM_014903.4 T1837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr12:78400325 C>G maps to NM_014903.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr12:78401105 C>T maps to NM_014903.4 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:78591181 G>C did not map to a codon.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr2:15326914 A>T maps to NM_015909.2 L2221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:15691632 A>G maps to NM_015909.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr13:35758116 G>T maps to ENST00000400445 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr13:36046543 G>T maps to ENST00000400445 V2152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr13:35733739 A>C maps to ENST00000400445 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr13:36167553 A>G maps to ENST00000400445 R2422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:35733451 A>G maps to ENST00000400445 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:203972838 G>A maps to NM_001114132.1 W597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr2:204002983 A>T maps to NM_001114132.1 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr3:47050125 C>A maps to NM_015175.1 A2665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr3:47038047 G>A maps to NM_015175.1 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47032942 G>T maps to NM_015175.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr3:47037323 C>G maps to NM_015175.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr3:47041770 G>A maps to NM_015175.1 G1394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr1:16907913 C>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:145367813 A>G maps to NM_001039703.4 P3470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:145301801 C>G maps to NM_001039703.4 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr1:145296485 G>A maps to NM_001039703.4 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr1:145299778 C>T maps to NM_001039703.4 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:148025785 G>A maps to ENST00000310701 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr1:148004721 C>T maps to ENST00000310701 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:148017562 A>G maps to ENST00000310701 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:148010986 T>C maps to ENST00000310701 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:21808125 G>A maps to NM_032264.2 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr1:21798205 A>G maps to NM_032264.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr1:21806630 G>T maps to NM_032264.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr1:21795328 C>G maps to NM_032264.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr1:21808098 A>G maps to NM_032264.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:144813823 G>C maps to NM_001037675.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:144828609 T>G maps to NM_001037675.2 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr17:41349124 T>C did not map to a codon.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr8:102705064 C>T maps to NM_032041.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr11:113133586 T>C maps to ENST00000397960 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr21:22652946 A>G maps to NM_004540.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:22658661 A>T maps to NM_004540.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:19329805 G>A maps to NM_004386.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:19338432 A>C maps to NM_004386.2 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr12:6638742 C>A maps to NM_014865.3 R1213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:6637491 T>C maps to NM_014865.3 A1099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr4:17819615 C>G maps to NM_022346.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr7:158447310 G>T maps to NM_017760.5 R908R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr22:50956418 C>T maps to NM_001185011.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr22:50961540 G>A maps to NM_001185011.1 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr9:100409779 C>T maps to NM_002486.4 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:39687742 C>T maps to NM_001001414.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr19:39688860 C>T maps to NM_001001414.1 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr7:74197913 G>A maps to NM_000265.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr7:74193717 C>T maps to NM_000265.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr1:183532671 T>A maps to NM_001127651.2 K359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr2:183791546 A>G maps to NM_205842.1 D1095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr12:54893216 A>T maps to NM_005337.4 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr2:133540312 G>A maps to NM_207363.2 S1357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:50185654 G>A maps to NM_001037806.3 Y1324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr2:232321357 T>C maps to NM_005381.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:24991158 C>T maps to NM_003743.4 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:24930396 G>A maps to NM_003743.4 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:71050556 T>C maps to NM_006540.2 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:71126195 A>C maps to NM_006540.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr20:46252828 T>C did not map to a codon.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr20:46279838 G>A maps to NM_181659.2 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr20:46279862 G>A maps to NM_181659.2 Q1263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr20:46279826 G>A maps to NM_181659.2 Q1251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr20:46254224 G>A maps to NM_181659.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr10:51585172 G>A maps to NM_001145260.1 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr10:51586275 A>T maps to NM_001145260.1 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr20:33337537 A>G maps to NM_014071.2 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr20:33328812 C>A maps to NM_014071.2 T1749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:126210642 G>A maps to NM_181782.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:15971430 T>G maps to ENST00000395857 T1522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr17:16021255 A>G maps to ENST00000395857 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:15964733 A>G maps to ENST00000395857 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr17:15952283 T>G maps to ENST00000395857 P2152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr17:15974761 G>A maps to ENST00000395857 V1387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:16089948 G>C maps to ENST00000395857 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr17:16068463 G>A maps to ENST00000395857 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:124887101 C>T maps to NM_006312.4 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:124839983 G>A maps to NM_006312.4 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:124829473 G>A maps to NM_006312.4 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:124848290 A>G maps to NM_006312.4 N954N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr12:124819112 T>G maps to NM_006312.4 A2161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr6:41304035 T>C maps to NM_004828.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:41303623 C>T maps to NM_004828.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr18:2616500 C>T maps to NM_006101.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:8350136 T>C maps to ENST00000402554 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr17:8370301 T>C maps to ENST00000402554 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:141517332 G>T maps to NM_030571.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr13:80094985 G>A maps to NM_019080.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr15:23932262 C>T maps to NM_002487.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr15:23931881 G>A maps to NM_002487.2 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr23:43809266 C>A did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:149921205 C>T maps to NM_001543.4 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:115767017 G>A maps to NM_022569.1 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr23:119005936 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:5897009 T>A did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr19:5897009 T>A did not map to a codon.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr22:42482195 G>A maps to NM_002490.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:41689068 G>A maps to NM_016013.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49059934 C>A maps to NM_199069.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr6:97344646 A>G maps to NM_014165.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:47002142 T>G did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:179322635 G>A maps to NM_002492.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr3:179336310 T>C did not map to a codon.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr9:32571038 T>C maps to NM_002493.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:14677077 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr8:125562075 T>A maps to NM_005005.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr2:206994914 T>C maps to ENST00000455934 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:161183706 C>A maps to NM_004550.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:47605942 G>A maps to NM_004551.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr11:47602126 G>T maps to NM_004551.2 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr21:44323940 A>G maps to NM_021075.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr21:44317077 T>C maps to NM_021075.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:152534240 G>C maps to NM_001164507.1 G1204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr2:152348618 A>C maps to NM_001164507.1 T8350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:152397246 C>T maps to NM_001164507.1 L6917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr2:152471014 G>T maps to NM_001164507.1 S3792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:152552136 A>T maps to NM_001164507.1 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr2:152548581 T>C maps to NM_001164507.1 Q699Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr2:152372971 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:152397300 T>C maps to NM_001164507.1 E6899E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:152512858 C>T maps to NM_001164507.1 E2101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:152390039 G>T maps to NM_001164508.1 A7111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:152382498 G>A maps to NM_001164507.1 V7378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr10:21309108 G>A maps to NM_213569.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr10:21124509 C>A maps to ENST00000430741 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:21097514 G>A maps to ENST00000430741 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr15:56208588 A>G maps to ENST00000508342 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:56208024 G>A maps to ENST00000508342 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr18:55992364 G>A maps to NM_001144967.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr18:56033229 G>A did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr18:56056372 T>C maps to NM_001144967.1 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr6:11185613 C>T maps to NM_006403.3 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:29885428 T>C maps to NM_021076.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr8:24771575 C>T maps to NM_005382.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:71873191 G>A maps to NM_173808.2 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr4:178243704 C>G maps to NM_018248.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:178283612 T>A maps to NM_018248.2 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr13:52707348 C>A maps to NM_002498.2 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr13:52649896 T>C maps to NM_199289.1 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr13:52686430 T>C maps to NM_199289.1 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:75558058 G>A maps to NM_033116.4 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr11:21250959 C>T maps to NM_006157.3 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:44917250 C>T maps to NM_001145107.1 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:212619209 G>A maps to NM_013349.4 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr15:73575303 G>A did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr15:73590936 T>C maps to NM_002499.3 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:156642563 A>G maps to NM_006617.1 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr6:31829195 G>A maps to NM_000434.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:233898966 C>T maps to NM_005383.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:74717077 A>T maps to NM_006656.5 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:7228700 G>A maps to NM_032442.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:182543428 C>A maps to NM_002500.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr12:55421029 G>C maps to NM_021191.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:31377934 G>A maps to NM_022728.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr4:113436043 T>G maps to NM_024019.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr17:29687576 G>T maps to NM_001042492.2 G2745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:29533388 G>A maps to NM_001042492.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr22:30035202 T>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr22:30051665 G>A did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr22:30069349 T>C maps to NM_181832.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr22:30000102 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr22:30038222 C>A maps to NM_181832.2 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr22:30050708 A>T maps to NM_181832.2 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr22:30050714 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr22:30067835 C>T maps to NM_181832.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:30051665 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr22:30057328 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:204955081 G>A maps to ENST00000367172 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:204985553 G>T maps to ENST00000367172 E1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:69727577 C>T maps to NM_138713.2 Q1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr18:77211776 C>T maps to NM_172387.1 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr18:77171060 T>G maps to NM_172387.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr16:68200895 A>T maps to NM_173165.2 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr16:68225472 C>T maps to NM_173165.2 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr16:68224815 T>A maps to NM_173165.2 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr14:24845236 C>T maps to NM_001136022.1 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr17:46134731 A>T maps to ENST00000362042 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr17:46128662 C>A maps to ENST00000362042 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr2:178096051 C>A maps to NM_006164.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr1:61554263 T>C maps to NM_001145512.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr19:13192530 C>T maps to ENST00000397661 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:13186459 C>T maps to ENST00000397661 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr10:104156716 C>T maps to NM_001077494.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:35872503 A>G maps to NM_020529.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr8:145661995 C>T maps to NM_013432.4 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr8:145661319 G>A maps to NM_013432.4 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:145668061 C>T maps to NM_013432.4 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:129747270 G>A maps to NM_006165.3 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr20:34262294 C>T maps to NM_021100.4 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:41218905 T>G maps to ENST00000308733 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr1:115829227 C>A maps to NM_002506.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr17:47588005 G>T maps to NM_002507.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr3:25824815 C>T maps to NM_018297.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr3:25773884 A>T maps to NM_018297.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:25770622 C>T did not map to a codon.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr15:90815013 A>G maps to NM_001033088.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr4:103822297 C>T maps to NM_139173.3 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr4:103826787 T>G maps to NM_139173.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:103826768 G>A maps to NM_139173.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr4:103971408 A>G maps to NM_178833.4 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:177580731 G>T maps to NM_017838.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:17745771 G>A did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr23:17745607 C>G did not map to a codon.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr23:17746841 C>T did not map to a codon.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr23:17745493 G>C did not map to a codon.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr23:17745122 C>A did not map to a codon.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr23:71360503 A>G did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr23:71359244 A>C did not map to a codon.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr23:71358470 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:71360544 C>T did not map to a codon.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr23:71360545 G>A did not map to a codon.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr3:49466657 C>T maps to NM_032316.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49463423 C>G maps to NM_032316.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr1:236212061 G>A maps to NM_002508.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr1:236143953 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:236195869 A>G maps to NM_002508.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr14:52534719 G>C maps to NM_007361.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr14:51259501 A>C maps to NM_020921.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr14:51237586 C>A maps to NM_020921.3 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:51219340 T>A maps to NM_020921.3 T1615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr14:51196405 C>T maps to NM_020921.3 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr15:23048906 C>G maps to NM_144599.4 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:48037861 T>C maps to NM_207330.1 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:99215363 A>T maps to NM_024759.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr5:156899850 C>T maps to NM_001099287.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr5:37006526 G>A maps to NM_133433.3 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr5:37064852 A>G maps to NM_133433.3 K2758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr5:37051933 C>T maps to NM_133433.3 N2336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr5:37048672 T>A maps to NM_133433.3 L2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr5:37020559 G>T did not map to a codon.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr5:36985237 A>G maps to NM_133433.3 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:107531255 T>A maps to NM_018376.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr3:52504924 T>A did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:52505968 C>T maps to NM_007184.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:124979432 C>T maps to NM_001040214.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr6:124979411 G>A maps to NM_001040214.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:61878937 G>A maps to NM_152864.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr23:119059314 C>A did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr23:119077351 G>T did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr23:119072772 C>T did not map to a codon.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr6:28227517 G>A maps to NM_001007531.1 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr16:50583387 C>T maps to NM_033119.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:23942483 G>A maps to NM_020345.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr23:118724875 T>A did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr23:118723544 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr23:118724239 T>G did not map to a codon.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr3:42679499 T>G maps to NM_005385.3 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:21376575 G>T maps to NM_033176.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:21376974 G>A maps to NM_033176.1 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr5:172659919 C>G maps to NM_004387.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr5:172659919 C>G maps to NM_004387.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:13545663 G>A maps to NM_001189.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr3:173998402 T>G maps to NM_014932.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr3:173322837 C>T maps to NM_014932.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr17:7319144 G>C maps to NM_020795.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr23:70387071 C>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:70387443 G>C did not map to a codon.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr23:6069115 T>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:5827147 G>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:5810996 A>G did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr24:16952766 C>T did not map to a codon.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:26449739 T>C maps to NM_016231.4 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:26490599 A>G maps to NM_016231.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr16:3614349 C>T maps to ENST00000448023 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:3598163 T>C maps to ENST00000448023 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr17:5462473 C>T maps to NM_033004.3 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:5436263 G>A maps to NM_033004.3 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr19:56320979 G>C maps to NM_145007.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr19:54313325 G>A maps to ENST00000391773 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr19:54312935 G>A maps to ENST00000391773 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr11:7064162 C>G maps to NM_176822.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr19:55497590 G>T maps to NM_017852.3 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr19:55489136 C>T maps to NM_017852.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:247588674 C>T maps to NM_004895.4 Q644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:56363604 A>G maps to NM_134444.4 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:56515288 A>G maps to NM_153447.4 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr19:56565045 G>A maps to NM_153447.4 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:56539071 C>T maps to NM_153447.4 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr11:281410 C>T maps to NM_138329.1 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr11:281107 G>C maps to NM_138329.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:55452314 C>T maps to ENST00000446217 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr19:55451067 C>T maps to ENST00000446217 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr19:55450707 G>A maps to ENST00000446217 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:55450842 G>A maps to ENST00000446217 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr19:56473594 A>G maps to NM_176811.2 Q735Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr19:56459315 C>T maps to NM_176811.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:56487642 C>T maps to NM_176811.2 N950N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr19:56243987 A>T maps to NM_176820.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr19:56243851 G>A maps to NM_176820.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr6:142409627 C>T maps to NM_002511.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr6:142396952 G>A maps to NM_002511.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:160945095 T>C maps to ENST00000472947 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr16:1820991 T>A maps to NM_002513.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr3:48336156 T>C maps to NM_005793.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:48338259 C>T maps to NM_005793.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr16:4511891 G>A maps to NM_020677.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr16:4519368 C>T maps to NM_020677.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr17:43173563 A>C maps to NM_021079.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr2:232393299 G>C maps to NM_006056.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:43609437 T>A maps to NM_182977.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr5:43619221 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:43613076 A>G maps to NM_182977.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr16:69776453 G>A maps to NM_014062.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr16:69786143 C>T maps to NM_014062.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:880467 C>T maps to NM_015658.3 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:96116289 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:96121494 T>C maps to NM_022451.9 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr12:132633360 G>T maps to NM_024078.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:30492405 G>A maps to NM_006092.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:54672234 G>A maps to NM_005450.4 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr9:33467190 C>A maps to NM_022917.4 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr9:95062257 G>C maps to NM_017948.5 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:6610593 G>A maps to NM_024654.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr10:103917062 A>G maps to ENST00000405356 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr7:156752789 T>G maps to NM_138400.1 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr7:156742604 A>G maps to NM_138400.1 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr7:156742688 G>A maps to NM_138400.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr16:18528573 A>G maps to NM_001004060.1 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr16:18522872 C>T maps to NM_001004060.1 T1072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr23:70511742 T>G did not map to a codon.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr23:70516748 T>G did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr4:2948136 A>G did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr4:2952918 T>C maps to NM_003703.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:2950031 G>A maps to NM_003703.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr12:6669890 G>T maps to ENST00000382421 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:203155145 T>C maps to NM_015934.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:117710300 G>C maps to ENST00000338101 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:26087757 G>A maps to NM_000625.4 F967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr7:150698929 G>A maps to NM_000603.4 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr7:150697630 C>T maps to NM_000603.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr19:50063189 C>G did not map to a codon.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr9:139396755 C>A maps to NM_017617.3 R1784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr9:139399348 G>A maps to NM_017617.3 R1598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:139418247 G>A maps to NM_017617.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:120506374 G>T maps to NM_024408.2 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr1:120539836 T>C maps to NM_024408.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr1:120497757 G>A maps to NM_024408.2 C708C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:120491749 C>A did not map to a codon.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr1:120548024 G>A maps to NM_024408.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:120462210 A>G maps to NM_024408.2 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr19:15302554 C>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr19:15303026 G>T maps to NM_000435.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr19:15289962 G>T maps to NM_000435.2 Y1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:15300135 A>G maps to NM_000435.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr19:15285051 T>C maps to NM_000435.2 P1521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr6:32170157 C>T maps to NM_004557.3 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr6:32188641 T>C maps to NM_004557.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr6:32188965 G>A maps to NM_004557.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:32191690 T>C maps to NM_004557.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:32169042 C>T maps to NM_004557.3 R1330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:79913364 G>A maps to NM_178493.5 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr19:46443969 G>A maps to NM_002516.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr23:100117450 A>C did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:100103735 T>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:100099032 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr23:100105316 A>T did not map to a codon.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr6:155776181 G>A maps to NM_015718.2 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr11:89088167 G>A maps to NM_016931.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr11:89223700 A>G maps to NM_016931.3 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:69328248 C>T maps to NM_024505.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr15:69320700 C>T maps to NM_024505.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr9:140320782 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:34145547 C>T maps to NM_001164749.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:66192163 T>C maps to NM_178864.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr11:66189603 G>A maps to NM_178864.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:66191470 C>A maps to NM_178864.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr11:108040714 C>G maps to NM_002519.2 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:108032023 A>G maps to NM_002519.2 S1263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:79860377 A>G maps to NM_148896.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr7:44579791 A>C maps to NM_013389.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr20:57282246 A>C maps to NM_024663.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:45669319 A>G did not map to a codon.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr17:45656825 A>G maps to NM_006310.3 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:45668144 A>G maps to NM_006310.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:45669356 A>T maps to NM_006310.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:73012853 C>G maps to NM_004885.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr3:132416206 C>A did not map to a codon.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr3:132418234 A>T maps to ENST00000393156 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:5935028 G>A maps to NM_015102.2 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr1:179521758 C>A maps to NM_014625.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr1:11918767 G>A maps to NM_002521.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:153651703 A>G maps to NM_000906.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr1:153659770 C>A maps to NM_000906.3 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:35792785 T>C maps to NM_003995.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr9:35792437 A>G maps to NM_003995.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr3:50387110 A>G maps to NM_006545.4 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr3:50386815 C>G did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:34724246 A>G maps to NM_207172.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:73884464 G>A maps to NM_012428.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr7:98256631 C>T maps to NM_002523.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:2070177 C>A maps to NM_001099456.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr7:24324864 A>G maps to NM_000905.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:27240350 G>A maps to NM_021969.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:38253600 A>G maps to NM_021724.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:47283270 G>C maps to NM_005693.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr3:119528961 C>A maps to NM_022002.2 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr3:119528964 G>A maps to NM_022002.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr12:95422175 T>C maps to NM_003297.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:19313199 C>T maps to ENST00000420605 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr15:72104833 C>T maps to NM_014249.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:92923830 G>A maps to NM_005654.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr19:17346353 G>A maps to NM_005234.3 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr5:142779612 A>C maps to NM_001024094.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr4:149356734 T>G maps to ENST00000511528 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr12:52448381 G>A maps to ENST00000360284 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52449896 G>A maps to ENST00000360284 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr9:102590585 G>T maps to NM_173200.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr9:127262608 C>A maps to NM_004959.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr1:200014590 C>A maps to NM_205860.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr10:115381804 G>A maps to ENST00000369358 F872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr2:27663339 C>A maps to ENST00000379863 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr2:27663324 C>T maps to ENST00000379863 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:27656878 T>C maps to ENST00000379863 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr8:144920928 G>A maps to NM_178564.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr7:107808821 G>A maps to ENST00000379032 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:52256296 C>A maps to NM_002525.2 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:52306074 T>C maps to NM_002525.2 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr5:139232129 G>A maps to NM_013982.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:139251391 G>T maps to NM_013982.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr21:16338034 G>A maps to NM_003489.3 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:16337669 A>G maps to NM_003489.3 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:105167296 A>G did not map to a codon.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr23:105132389 C>G did not map to a codon.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr23:105197101 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr23:105132299 A>C did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr10:33543117 G>A maps to NM_003873.5 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:206580919 T>C maps to NM_201266.1 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr2:206640997 C>T maps to NM_018534.3 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr2:50149351 T>A maps to ENST00000404971 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:50574024 G>C maps to NM_138735.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr11:64427891 T>G maps to NM_015080.3 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr11:64417941 G>A maps to NM_015080.3 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:64428552 A>T maps to NM_015080.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr14:80130118 A>G did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:176696647 C>T maps to NM_022455.4 N1783N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr5:176636689 G>A maps to NM_022455.4 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr5:176637817 A>C maps to NM_022455.4 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr5:176637985 C>T maps to NM_022455.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr5:176720944 C>T maps to NM_022455.4 F2192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr5:176631294 T>C did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:176639041 T>C maps to NM_022455.4 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:44806263 G>A maps to NM_006178.2 Q624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr8:59506789 C>G did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr8:59514095 T>C did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr5:6600167 G>A maps to NM_017755.5 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr2:18765440 C>T maps to ENST00000455492 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:18745214 G>A maps to ENST00000455492 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr7:33055307 G>A maps to NM_001002010.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr12:104179175 C>A maps to NM_001031701.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:2093637 C>T maps to NM_002528.5 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr19:49167833 A>G did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:49167944 A>C maps to NM_145807.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr1:107691259 G>A maps to NM_001113226.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr9:135102353 C>A maps to NM_032536.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135073708 G>A maps to NM_032536.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:156843560 C>T maps to NM_002529.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:156851383 C>T maps to NM_002529.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr15:88727493 G>A maps to NM_001012338.1 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr20:61386086 G>T maps to NM_002531.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr5:162881023 G>T maps to NM_145266.4 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr23:51075923 T>C did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:51075839 C>T did not map to a codon.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr23:51075900 G>A did not map to a codon.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:51239273 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:102891794 A>C maps to NM_031438.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr5:102891743 G>A maps to NM_031438.2 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:102895829 A>G maps to NM_031438.2 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr13:48619889 A>G maps to NM_018283.1 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr12:93793100 T>C maps to NM_199040.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr4:88379167 T>C maps to NM_024047.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:27613673 G>T maps to NM_020772.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr14:73746100 A>G maps to NM_001005743.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr14:73759583 T>C did not map to a codon.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr19:41173897 T>C maps to NM_004756.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr1:229602503 C>A did not map to a codon.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr1:229643912 C>G maps to NM_018230.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:229631731 G>T maps to NM_018230.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr6:17706531 G>C maps to ENST00000430136 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr6:17637569 A>G maps to ENST00000430136 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr11:47819409 A>C maps to NM_015231.1 A1070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:47837536 A>G maps to NM_015231.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:131755474 G>A did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr9:131730828 A>G maps to NM_015354.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr7:135277918 C>A maps to NM_015135.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:135290918 A>G maps to NM_015135.2 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr7:135307640 C>T maps to NM_015135.2 R1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:13399892 G>A maps to NM_024923.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr1:154027277 T>A maps to NM_207308.2 K1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr1:154031094 T>A maps to NM_207308.2 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr1:154067512 C>T maps to NM_207308.2 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:154033033 T>C maps to NM_207308.2 E944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:134004847 G>T maps to ENST00000451030 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr9:134072981 C>G maps to ENST00000451030 G1368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr22:45574341 A>G maps to NM_007172.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr22:45574341 A>G maps to NM_007172.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:50412017 C>T maps to NM_012346.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:50412995 C>T maps to NM_012346.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3923-01A-01D-1458-08 chr23:106397334 A>C did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr17:5290384 G>A maps to NM_002532.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr17:5322724 G>T maps to NM_002532.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:56792501 T>C maps to NM_014669.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr11:3700798 G>A maps to NM_016320.4 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:41669494 C>T maps to NM_016359.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr1:224468832 G>A maps to NM_002533.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:224491541 G>A maps to NM_002533.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr19:16910758 G>A maps to ENST00000438489 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr19:16875872 C>T maps to ENST00000438489 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr19:16910779 G>T maps to ENST00000438489 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr23:101581403 A>G did not map to a codon.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr23:101615562 C>A did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr23:101615545 C>T did not map to a codon.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr23:102337710 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:102332663 C>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:102337710 C>T did not map to a codon.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr23:101095847 C>A did not map to a codon.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr23:101092584 T>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr23:101096013 T>A did not map to a codon.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr19:17571477 T>G maps to NM_138454.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr12:57619418 G>A maps to NM_007224.3 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr12:57619418 G>A maps to NM_007224.3 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr12:57618902 G>A maps to NM_007224.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr23:108780249 G>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:108779192 A>C did not map to a codon.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr14:24878973 A>T maps to NM_025081.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:24879315 C>T maps to NM_025081.2 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr23:41333523 G>C did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr23:41333571 G>A did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr11:120096480 G>T maps to NM_178507.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr12:113448225 C>T maps to NM_016817.2 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr12:113405907 C>G maps to NM_006187.2 Y1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:113376451 C>T maps to NM_006187.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:121465529 C>A maps to NM_003733.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:192550346 T>G maps to NM_001031716.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr1:228467537 C>G maps to NM_001098623.1 L2471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr1:228559758 T>C maps to NM_001098623.1 L7094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:228528241 C>T maps to NM_001098623.1 P5817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:228403480 G>C maps to NM_001098623.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:228473854 G>C maps to NM_001098623.1 R3027R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr1:228504668 G>A maps to NM_001098623.1 A4515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:228469851 G>T maps to NM_001098623.1 E2806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:220420910 G>A maps to NM_015311.2 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:220431630 G>T maps to NM_015311.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:220428158 C>A maps to NM_015311.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:28090199 T>A did not map to a codon.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr19:17337969 G>A maps to NM_024578.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr5:68840910 C>G maps to NM_002538.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr7:5922121 A>T did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:128720993 C>T did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:128678969 T>G did not map to a codon.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr9:131256863 C>T maps to NM_153435.1 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr9:131256883 A>G maps to NM_153435.1 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr9:131256868 T>C maps to NM_153435.1 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr1:86851138 A>C did not map to a codon.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:199996 T>C maps to NM_053280.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:123637523 G>T did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr23:123630880 C>G did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr23:123838861 C>A did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr23:123517772 G>T did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:123515036 T>G did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr23:123839010 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:123518586 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr23:124030082 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr23:123554561 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr23:123517591 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr23:123680910 A>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr23:123519704 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:123680888 T>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr4:183713662 C>T maps to NM_001080477.1 V1946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr4:183714514 C>T maps to NM_001080477.1 D2230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr4:183714118 C>G maps to NM_001080477.1 L2098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr11:78412935 G>A maps to NM_001098816.2 N1574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr11:78565191 G>A maps to NM_001098816.2 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr23:13754639 T>C did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:44747233 T>C maps to ENST00000444676 N965N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr7:44747513 C>T maps to ENST00000444676 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr7:44664055 G>T maps to ENST00000444676 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr7:44687317 C>A maps to ENST00000444676 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:56485679 T>C did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr20:61442845 G>A maps to NM_007346.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr3:9792670 G>C maps to NM_016821.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:70782730 C>T did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr23:70775920 C>A did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:70784540 G>A did not map to a codon.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr23:70776830 C>T did not map to a codon.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr23:70756093 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr23:70756091 A>G did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr10:74673123 T>C maps to NM_152635.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3427-01A-01D-0966-08 chr19:9965170 C>T maps to NM_058164.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:102269841 C>T maps to ENST00000338858 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr13:53624773 A>G maps to NM_006418.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr13:53624867 C>T maps to NM_006418.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:127572162 C>T maps to NM_182487.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr1:161953695 G>A maps to ENST00000451379 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:161989777 C>G maps to ENST00000451379 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr11:76814079 C>T maps to NM_006189.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr18:55143924 G>A maps to NM_004852.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr3:193355796 C>G maps to NM_130837.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr23:67273542 C>T did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:67283720 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr23:67413750 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:153496171 C>A did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr7:128413771 G>T maps to NM_001708.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:128415146 C>T maps to NM_001708.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr6:47754338 C>A maps to ENST00000489301 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr6:154412360 C>A maps to NM_001145279.1 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr1:203465246 C>T maps to NM_014359.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr10:13160993 C>T maps to NM_021980.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr11:6897949 T>G maps to NM_207186.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr11:6867587 T>C maps to ENST00000379831 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr6:29407842 C>T maps to NM_013941.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr14:22038053 G>A maps to NM_001005465.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr11:123886794 C>T maps to NM_001004462.1 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr11:123887006 C>T maps to NM_001004462.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr11:123886664 G>A maps to NM_001004462.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr11:123909171 G>A maps to NM_001004463.1 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:123909513 G>C maps to NM_001004463.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr11:123909162 G>C maps to NM_001004463.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr11:123894276 G>A maps to NM_001001953.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr19:15918526 G>A maps to NM_013940.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:15839671 C>T maps to NM_013939.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr19:15839689 C>T maps to NM_013939.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr19:15852603 C>T maps to NM_013938.1 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr19:16059969 G>A maps to NM_001004465.1 W51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr1:159505524 A>G maps to NM_001004469.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:159505239 A>C maps to NM_001004469.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158576302 C>T maps to NM_001004478.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr14:20666033 C>T maps to NM_001005503.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr14:20711759 A>T maps to NM_001004479.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr9:107367524 G>A maps to NM_001004481.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr9:107367648 G>C maps to NM_001004481.1 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr9:107367737 G>C maps to NM_001004481.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr9:107331657 C>T maps to NM_001004483.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:35869822 C>T maps to NM_001004487.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:125391499 G>A maps to NM_001004450.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr17:2995984 G>T maps to NM_002548.2 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr17:3030488 G>A maps to ENST00000381953 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr19:15198106 C>T maps to NM_001004713.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr9:125486285 T>C maps to NM_001005235.1 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:125315954 C>T maps to NM_001004457.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr11:57982413 G>A maps to NM_001004458.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr11:57970966 G>A maps to NM_001004459.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:143807470 C>T maps to NM_001005480.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:143806680 A>G maps to NM_001005480.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:143748123 G>A maps to NM_012365.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr7:99474476 A>G maps to NM_001005276.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr11:6806546 C>T maps to NM_001004489.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr11:6789369 G>T maps to NM_001004490.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr11:74800062 G>C maps to NM_001005285.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:74800083 G>A maps to NM_001005285.1 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr1:247614531 G>A maps to NM_001004492.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr6:27879248 G>A maps to NM_033057.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr6:29054172 A>G maps to NM_001005226.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr16:3406080 G>A maps to NM_012368.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr1:247695756 G>A maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:247694871 T>A maps to NM_198074.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr11:6942588 C>T maps to NM_001004684.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr7:143657716 C>T maps to NM_012369.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr7:143633179 G>A maps to NM_001004685.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr1:247751787 T>C maps to NM_001001915.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr1:247752395 C>T maps to NM_001001915.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr1:247752194 T>C maps to NM_001001915.1 D178D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4982-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr1:248202411 C>T maps to NM_001004686.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:248112584 G>A maps to NM_001001963.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:248343457 C>A maps to NM_001004688.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr1:248343934 T>C maps to NM_001004688.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:248309354 G>A maps to NM_001004690.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:248458379 G>A maps to NM_001004692.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:248458418 G>C maps to NM_001004692.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:248813270 C>A maps to NM_001001824.1 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr1:248436252 G>C maps to NM_001004695.1 Y288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:248436861 G>T maps to NM_001004695.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr1:248801632 A>G maps to NM_001001827.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr1:248525733 T>C maps to NM_001004696.1 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:248525255 C>A maps to NM_001004696.1 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr1:248525307 A>G maps to NM_001004696.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr1:248551307 T>C maps to NM_001005471.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:248084573 C>A maps to NM_001005522.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr1:248059808 G>A maps to NM_001001957.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr1:248059094 G>T maps to NM_001001957.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:248059781 G>A maps to NM_001001957.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:3195480 G>A maps to ENST00000397187 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:51412338 A>T maps to NM_001005272.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr11:50003857 G>A maps to NM_001005270.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr11:50003263 G>T maps to NM_001005270.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:49974075 C>A maps to NM_001001955.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr11:48347235 C>T maps to NM_001004702.1 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr11:48346848 T>A maps to NM_001004702.1 Y119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr11:48346512 T>C maps to NM_001004702.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr11:123810586 C>T maps to NM_001001965.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr11:59282456 C>T maps to NM_001004711.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr14:22133739 C>T maps to NM_001001912.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:102346641 G>T maps to NM_001005326.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr14:20483199 A>T maps to NM_001004712.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:20345256 C>A maps to NM_001005501.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr14:20389304 T>C maps to NM_001005483.1 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr14:20389391 C>T maps to NM_001005483.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr14:20248759 C>A maps to NM_001005500.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr15:22369271 G>T maps to NM_001004719.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr15:22383137 C>G maps to NM_001005241.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr11:55406261 C>A maps to NM_001004124.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr11:55418711 C>T maps to NM_001004059.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:4929157 C>T maps to NM_001004749.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr11:5322936 C>T maps to NM_033179.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr11:5323104 C>G maps to NM_033179.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr11:4674481 T>G maps to NM_152430.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:4936272 G>A maps to NM_001005238.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr11:4903716 C>T maps to NM_001004759.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:4904095 A>C maps to NM_001004759.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr11:4903764 C>T maps to NM_001004759.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr11:5221675 G>C maps to NM_001004760.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:5152921 T>C maps to NM_001005160.2 *317W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:6191109 G>A maps to NM_001004052.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:5510049 T>C maps to NM_001005163.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr11:5068544 C>T maps to NM_001001916.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr11:5068522 A>T maps to NM_001001916.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:5068081 C>T maps to NM_001001916.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr11:5068156 C>T maps to NM_001001916.2 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr11:5068192 T>C maps to NM_001001916.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr11:5068655 C>T maps to NM_001001916.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr11:4510759 G>A maps to NM_001005171.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr11:4566710 C>T maps to NM_001004137.1 D97D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AK-3425-01A-02D-1361-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:6048448 A>G maps to NM_001001917.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr11:5969271 C>A maps to NM_001003443.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:5969445 C>A maps to NM_001003443.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr11:6024123 G>A maps to NM_001005179.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr11:59211420 C>T maps to NM_001004728.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr11:56756939 T>A maps to NM_001005323.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr11:56431823 C>A maps to NM_001004730.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:56431746 G>T maps to NM_001004730.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr11:55761255 A>G maps to NM_003697.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr11:55762020 G>A maps to NM_003697.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr3:97852335 G>A maps to NM_001005338.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr3:97851891 G>A maps to NM_001005338.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr3:97868390 T>C maps to NM_001005514.1 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr3:97887842 A>G maps to NM_001005515.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr3:97983601 T>C maps to NM_001005479.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:97983655 A>G maps to NM_001005479.1 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr3:98188527 G>A maps to NM_001004736.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr11:55579067 C>T maps to NM_001004738.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr11:56380810 T>C maps to NM_001004740.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr11:56237918 G>A maps to NM_001004742.1 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr11:56258041 G>A maps to NM_001005282.1 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:56258309 C>T maps to NM_001005282.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr11:7818171 G>A maps to NM_153444.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr11:55999587 T>C maps to NM_001004746.1 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr12:55725603 G>T maps to NM_054104.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr12:55759682 A>G maps to NM_001005497.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158735809 G>A maps to NM_001005185.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr11:123814284 C>T maps to NM_001005187.1 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:158517502 A>T maps to NM_001005189.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:14991894 G>A maps to NM_030901.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr19:9296954 A>G maps to NM_175883.2 L166L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5119-01A-02D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr19:9237029 C>A maps to NM_001001958.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr19:9236855 C>T maps to NM_001001958.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr11:124252981 C>T maps to NM_001005468.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:124310918 C>T maps to NM_012378.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:124310504 G>A maps to NM_012378.1 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr11:124135726 C>T maps to ENST00000341493 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:124095996 C>A maps to NM_001007249.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:56057617 T>C maps to NM_001005199.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:55904465 C>T maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:142724165 C>G maps to NM_001001658.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:141619430 C>T maps to NM_001001656.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr11:56468234 C>T maps to NM_001013358.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:57886019 G>A maps to NM_001005211.1 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr12:55523605 A>G maps to NM_001005243.1 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:52849238 G>A maps to NM_004153.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr2:201790561 C>A maps to NM_006190.4 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr2:148693264 A>T maps to NM_181742.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr7:103807321 C>T maps to NM_002553.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr12:56213244 C>T maps to NM_014182.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr22:31091333 G>A maps to NM_030758.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr22:31266428 C>T maps to NM_030758.3 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr3:31774805 G>T maps to NM_017784.4 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr3:125286404 A>C maps to NM_022776.4 L234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr18:21898606 G>C maps to NM_080597.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr18:21819190 C>A maps to NM_080597.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr18:21914247 T>C maps to NM_080597.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr7:24931998 T>C maps to NM_015550.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr11:3143329 T>C did not map to a codon.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr11:3150288 C>T maps to NM_020896.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr11:3109494 G>A maps to NM_020896.3 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:179253840 C>G maps to ENST00000392505 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr2:179255927 G>A maps to ENST00000392505 K835K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr2:179255816 T>G maps to ENST00000392505 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr17:45891938 G>C maps to NM_145798.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr17:45894651 G>A maps to NM_145798.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:36915922 C>T maps to ENST00000356637 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr14:20916147 A>G maps to NM_017807.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr2:190618647 T>C maps to NM_022353.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:83994294 G>A maps to NM_013370.3 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4804-01A-02D-1373-10 chr5:38886146 T>G maps to NM_003999.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr4:109571837 C>T maps to ENST00000512478 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:195955791 G>A did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:38260573 C>A did not map to a codon.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr23:38211975 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr23:38262962 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:21734299 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr2:26717854 C>T maps to NM_194248.2 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr4:4190682 G>A maps to NM_177998.1 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:72942795 G>A maps to NM_178233.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr11:63764640 C>A maps to ENST00000422031 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr1:20233087 A>G maps to NM_015207.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:20233030 T>C maps to NM_015207.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr23:69282741 G>T did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr15:31779680 G>A maps to ENST00000382902 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:31818595 G>A maps to ENST00000382902 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr1:149920965 A>G maps to NM_020205.2 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr1:149920956 A>G maps to NM_020205.2 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr2:63283087 C>A maps to NM_014562.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr14:57271022 C>A maps to NM_021728.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr20:18005498 C>T maps to NM_021220.2 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr5:41807504 T>A maps to NM_000436.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr5:41794777 C>G did not map to a codon.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr2:42990998 C>A maps to NM_148962.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:107718928 T>C maps to NM_001198533.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr3:25835879 T>G maps to NM_017897.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr3:8809351 G>T maps to NM_000916.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr3:8809675 G>A maps to NM_000916.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr12:133198302 C>A maps to NM_170683.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr11:57118270 C>T maps to NM_002559.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr12:121655011 C>T maps to NM_002560.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr12:121660765 G>A maps to NM_002560.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:121648005 C>T maps to NM_002560.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr23:78216452 C>T did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr11:72945650 C>T maps to NM_176071.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr23:1585210 A>C did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr23:1585212 A>G did not map to a codon.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr23:1585027 C>A did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr10:74806680 A>C did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:74834564 C>G did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:74810905 G>A maps to NM_000917.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr5:131546091 G>T maps to NM_001142599.1 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr5:131543564 G>A maps to NM_001142599.1 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr8:101725344 T>G maps to NM_002568.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr8:101725326 T>C maps to NM_002568.3 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr8:101724673 A>G maps to NM_002568.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr8:101719225 C>G did not map to a codon.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr8:101721898 C>A maps to NM_002568.3 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr20:43541487 T>C maps to NM_001124756.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr13:25671754 G>A maps to NM_030979.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr13:25672006 A>G maps to NM_030979.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr13:25672006 A>G maps to NM_030979.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr13:25670500 G>A maps to NM_030979.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr13:25670548 C>G maps to NM_030979.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr13:25670872 A>G maps to NM_030979.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr13:25671205 A>G maps to NM_030979.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr13:25670872 A>G maps to NM_030979.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:40029529 C>T maps to NM_001135653.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:90691459 A>C did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr23:90691349 C>T did not map to a codon.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr23:90691443 C>G did not map to a codon.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr14:23790863 G>A maps to NM_004643.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:66008915 T>A maps to NM_018026.2 Y816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:105833602 C>T maps to ENST00000458164 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr6:34499374 A>C did not map to a codon.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:17609567 G>A maps to NM_016233.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:17727909 C>T maps to NM_207421.3 F687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr19:39880355 A>G maps to NM_019088.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:2577359 T>C maps to NM_000430.3 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:81897571 G>A maps to NM_018440.3 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr23:49454062 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:103246687 A>G maps to NM_000277.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr12:103240686 C>A maps to NM_000277.1 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr5:43555943 A>T maps to NM_006451.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr5:138700257 A>G maps to NM_001033112.1 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr3:196529977 C>T maps to NM_002577.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr3:196530012 A>G maps to NM_002577.4 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr3:196530021 C>T maps to NM_002577.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr23:110366369 T>C did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr23:110406198 T>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:110366493 G>A did not map to a codon.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr16:23647614 G>T maps to NM_024675.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr4:169433374 G>A maps to NM_001166108.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:169837135 T>C maps to NM_001166108.1 D936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr12:56720444 T>C maps to NM_001127460.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:56720459 T>C maps to NM_001127460.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr13:28840990 A>G maps to NM_175854.7 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:91371797 T>C maps to NM_148977.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:93911575 C>G maps to NM_015368.3 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50617543 G>A maps to NM_052839.3 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:135193908 C>T maps to NM_152911.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr16:50261848 C>T maps to NM_001040284.2 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr5:6749687 C>A maps to NM_006999.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr19:39591390 T>G maps to NM_001004318.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr14:97009230 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr7:4899653 G>A maps to NM_020144.4 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr2:60987313 T>C maps to NM_022894.3 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr9:118950339 C>T maps to NM_002581.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr1:176738771 G>C maps to NM_020318.2 G1451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:176525850 G>A maps to NM_020318.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:176709218 A>C maps to NM_020318.2 S1346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr4:108608292 A>C maps to NM_005443.4 L151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr10:89501011 C>T maps to NM_001015880.1 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr15:69689887 C>T maps to NM_017705.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr6:52268835 T>A maps to ENST00000361841 C280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr2:206037068 G>A maps to ENST00000406610 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr20:49367022 T>C maps to NM_032521.2 *373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr20:49367003 T>C maps to NM_032521.2 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:162864431 C>T maps to NM_004562.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr6:161781135 T>C maps to NM_004562.2 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr6:162394347 C>A maps to NM_004562.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr4:75937686 G>C maps to NM_015393.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:14678280 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr16:14711479 G>A maps to NM_002582.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr1:226566973 T>A maps to NM_001618.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:226561929 A>G maps to NM_001618.3 Y689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr1:226564844 G>C maps to NM_001618.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr7:139724548 G>C maps to NM_022750.2 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:122418639 A>T maps to NM_017554.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:122414351 G>A maps to NM_017554.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:122437695 A>G maps to NM_017554.2 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:122420028 C>T maps to NM_017554.2 H876H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:122436992 C>G maps to NM_017554.2 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr3:122354764 C>T maps to NM_001113523.1 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr13:25029239 T>C maps to NM_006437.3 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr13:25044067 G>A maps to NM_006437.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr13:25020899 C>T did not map to a codon.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr13:25075849 T>C maps to NM_006437.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr13:25067775 T>C maps to NM_006437.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr13:25016007 C>T maps to NM_006437.3 E1214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr15:72542433 C>T did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:72552950 G>T maps to NM_020214.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr5:50093024 T>G maps to ENST00000505697 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr3:122277191 G>T maps to NM_031458.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr3:122247558 G>C maps to NM_031458.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr1:55224825 C>T maps to NM_152268.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr11:12518074 G>T maps to NM_018222.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:44564536 C>T maps to NM_001003828.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:150828199 G>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:150780185 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr23:150842544 G>T did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr23:150817085 G>A did not map to a codon.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr23:150791420 T>C did not map to a codon.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr2:242063381 G>C maps to ENST00000358649 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr2:223066657 C>T maps to NM_181457.3 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr2:223066807 C>A maps to NM_181459.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:223066672 C>T maps to NM_181459.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr11:31816304 C>T maps to NM_001604.4 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:113984804 G>A maps to NM_003466.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr3:52685755 A>G did not map to a codon.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr3:52682445 T>A maps to ENST00000296302 K243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:52643560 G>A maps to ENST00000296302 Q779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr3:52678739 A>G maps to ENST00000296302 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr3:52621463 G>A maps to ENST00000296302 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr3:52621463 G>A maps to ENST00000296302 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr3:52668806 G>C maps to ENST00000296302 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:52637739 G>T maps to ENST00000296302 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr3:52620673 G>A maps to ENST00000296302 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr3:52643327 C>T did not map to a codon.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr3:52678734 G>T maps to ENST00000296302 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr3:52643827 T>A maps to ENST00000296302 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr3:52676062 T>A did not map to a codon.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr3:52662983 C>A maps to ENST00000296302 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr3:52649436 G>A maps to ENST00000296302 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr3:52668816 C>A maps to ENST00000296302 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr3:52692234 G>A maps to ENST00000296302 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr3:52643897 A>T maps to ENST00000296302 Y666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:52649429 T>A maps to ENST00000296302 K621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr3:52692332 T>A did not map to a codon.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr3:52613208 C>A maps to ENST00000296302 E1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr3:52678805 C>T did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr3:52702513 C>T maps to ENST00000296302 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:52584625 G>A maps to ENST00000296302 Q1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr3:52712579 G>A maps to ENST00000296302 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr3:52621463 G>A maps to ENST00000296302 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr3:52651291 C>A maps to ENST00000296302 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr3:52696147 C>A did not map to a codon.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:52702611 T>A maps to ENST00000296302 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr3:52623109 C>A maps to ENST00000296302 E981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr3:52712579 G>A maps to ENST00000296302 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr3:52643347 G>A maps to ENST00000296302 R850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr3:52643347 G>A maps to ENST00000296302 R850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr3:52663034 G>A maps to ENST00000296302 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:52623266 A>G maps to ENST00000296302 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr3:52595786 A>C maps to ENST00000296302 Y1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr3:52668654 G>A maps to ENST00000296302 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr3:52637710 G>A maps to ENST00000296302 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr3:52712613 C>A did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr3:52643767 G>A maps to ENST00000296302 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr3:52584608 A>T maps to ENST00000296302 Y1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52651554 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:52702661 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr3:52643503 T>A maps to ENST00000296302 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr3:52620673 G>A maps to ENST00000296302 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr3:52613193 C>A maps to ENST00000296302 E1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr3:52643359 C>A maps to ENST00000296302 E846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr3:52661376 T>A maps to ENST00000296302 K485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr3:52621445 C>A maps to ENST00000296302 E1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:52597492 G>A maps to ENST00000296302 Q1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:52610714 C>G did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr3:52663051 C>A did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:52682458 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr3:52696198 C>A maps to ENST00000296302 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr3:52637554 G>A maps to ENST00000296302 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr3:52712614 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr3:52643532 G>T maps to ENST00000296302 S788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr3:52598157 G>T maps to ENST00000296302 Y1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr3:52692297 G>A maps to ENST00000296302 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr3:52661324 G>C maps to ENST00000296302 S502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr9:128724471 C>T maps to ENST00000373487 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:154920115 A>C did not map to a codon.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr11:66619325 G>A maps to NM_022172.2 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr11:66636399 C>A maps to NM_022172.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:66636375 G>T maps to NM_022172.2 Y321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:70314949 A>G maps to NM_006196.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr13:100925448 G>A did not map to a codon.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr5:141243420 G>A maps to NM_032420.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr5:141233714 G>A maps to NM_032420.2 C1202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr5:141242927 T>A maps to NM_032420.2 K990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr4:134071549 C>A maps to NM_032961.1 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr4:134071516 C>A maps to NM_032961.1 Y74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:91137906 C>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:91090851 G>T did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:91133612 G>A did not map to a codon.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr23:91134174 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:91873324 C>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:91456391 C>T did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:91133624 C>A did not map to a codon.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr23:91090724 G>T did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr23:91134111 C>T did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:91873699 C>T did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr24:4966254 G>T did not map to a codon.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr24:4967266 C>T did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr10:55617002 C>A maps to NM_001142763.1 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr10:55849760 A>G maps to NM_001142763.1 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:55626410 G>A maps to NM_001142763.1 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:55583105 G>C maps to NM_001142763.1 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr13:58299307 G>A maps to NM_001040429.2 Q1120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:138450854 G>A maps to NM_019035.3 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr23:99661615 G>C did not map to a codon.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr23:99662749 G>A did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr23:99661924 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr13:61987112 C>A maps to NM_022843.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr13:61989198 T>G maps to NM_022843.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr4:30725279 A>T maps to NM_001173523.1 K746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr13:67800363 G>A maps to NM_203487.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr5:140362134 C>A maps to NM_018909.2 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr5:140248768 G>A maps to NM_018902.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr5:140250598 C>T maps to NM_018902.3 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140250127 C>T maps to NM_018902.3 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr5:140256583 G>A maps to NM_018903.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr5:140255596 T>G maps to NM_018903.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr5:140257018 C>T maps to NM_018903.2 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:140176264 C>A maps to NM_018905.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr5:140174869 G>A maps to NM_018905.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr5:140182764 C>A maps to NM_018906.2 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:140188709 C>T maps to NM_018907.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr5:140188640 C>T maps to NM_018907.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:140202643 C>T maps to NM_018908.2 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr5:140202182 G>T maps to NM_018908.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:140202961 G>A maps to NM_018908.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr5:140202820 C>G maps to NM_018908.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr5:140201425 C>T maps to NM_018908.2 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr5:140208908 T>C maps to NM_018909.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr5:140215596 G>A maps to NM_018910.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:140222315 G>C maps to NM_018911.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr5:140221436 C>T maps to NM_018911.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140223200 G>A maps to NM_018911.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140222342 G>A maps to NM_018911.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr5:140222357 G>A maps to NM_018911.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr5:140230077 G>A maps to NM_031857.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr5:140229360 G>A maps to NM_031857.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr5:140228472 A>G maps to NM_031857.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140229540 C>T maps to NM_031857.1 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:140307712 A>G maps to NM_018898.3 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr5:140347847 G>A maps to NM_018899.5 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr5:140432179 C>T maps to NM_013340.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr5:140579544 G>C maps to NM_018931.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:140595248 T>C maps to NM_018933.2 S518S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-5168-01A-01D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr5:140594886 G>T maps to NM_018933.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr5:140605206 G>C maps to NM_018934.2 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:140625664 T>C maps to NM_018935.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr5:140563510 C>T maps to NM_020957.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:140563806 C>A maps to NM_020957.1 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr5:140563753 T>G maps to NM_020957.1 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr5:140480793 C>T maps to NM_018937.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr5:140481573 C>T maps to NM_018937.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr5:140481177 T>C maps to NM_018937.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr5:140480871 C>T maps to NM_018937.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:140503001 C>A maps to NM_018938.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr5:140531289 C>T maps to NM_018939.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr5:140532189 C>A maps to NM_018939.2 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:140531175 C>T maps to NM_018939.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:140554719 T>A maps to NM_018940.2 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr5:140553990 G>A maps to NM_018940.2 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr5:140559267 G>T maps to NM_019120.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr5:140559546 G>A maps to NM_019120.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr5:140569000 T>C maps to NM_019119.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:140712437 A>G maps to NM_018912.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:140711927 G>A maps to NM_018912.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr5:140890568 C>T maps to NM_018915.2 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr5:140712347 G>A maps to NM_018912.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr5:140794505 C>T maps to NM_018913.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr5:140800832 G>A maps to NM_018914.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:140802437 G>C maps to NM_018914.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140811804 G>A maps to NM_003735.2 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr5:140720916 G>A maps to NM_018915.2 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr5:140718868 G>T maps to NM_018915.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr5:140720556 C>T maps to NM_018915.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:140724209 A>T maps to NM_018916.3 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:140724919 G>T maps to NM_018916.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr5:140725546 C>T maps to NM_018916.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr5:140736272 C>T maps to NM_018917.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:140745639 C>T maps to NM_018918.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr5:140745222 A>G maps to NM_018918.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:140753887 C>T maps to NM_018919.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:140762924 G>A maps to NM_018920.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr5:140762930 C>T maps to NM_018920.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr5:140764004 C>T maps to NM_018920.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr5:140773213 A>G maps to NM_032088.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr5:140772926 C>T maps to NM_032088.1 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr5:140741741 G>A maps to NM_018923.2 E680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr5:140751664 G>A maps to NM_018924.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr5:140750549 A>T maps to NM_018924.2 K197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140750095 G>A maps to NM_018924.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr5:140798208 C>T maps to NM_018927.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:140856909 G>A maps to NM_002588.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr5:140857473 C>T maps to NM_002588.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:140865324 C>G maps to NM_018928.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr5:140870295 C>T maps to NM_018929.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:82877723 A>G maps to NM_015885.3 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:82879803 A>T maps to NM_015885.3 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr11:82877717 T>C maps to NM_015885.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr11:82877726 A>G maps to NM_015885.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr2:74732305 C>T maps to NM_032673.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr17:36895855 C>T maps to NM_007144.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr13:113854791 A>G maps to ENST00000246505 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr20:56140433 C>T maps to NM_002591.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr20:56136505 C>T maps to NM_002591.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:56140805 C>A maps to NM_002591.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:82784462 C>T maps to NM_033026.5 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr7:82580447 C>T maps to NM_033026.5 T3152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr7:82763634 A>G maps to NM_033026.5 N1077N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr7:82532015 A>G maps to NM_033026.5 P4493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr7:82785210 G>T maps to NM_033026.5 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr6:150094280 A>G maps to NM_005389.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr8:52773606 C>A maps to NM_052937.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr8:52733015 T>C maps to NM_052937.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr8:52732958 G>A maps to NM_052937.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr21:47832896 C>T maps to NM_006031.5 D2047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr21:47850086 G>A maps to NM_006031.5 Q2618Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr14:71479736 G>A maps to NM_014982.2 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr14:71571969 A>T maps to NM_014982.2 G2038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr14:71462625 T>C maps to NM_014982.2 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr1:233150460 G>T maps to NM_014801.3 C1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr11:65384726 C>T maps to NM_032223.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr7:100204167 C>A maps to NM_002593.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:142607734 T>G maps to NM_013363.3 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr5:95746663 G>A maps to NM_000439.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr20:17434532 C>T maps to NM_002594.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr19:1482901 G>A maps to NM_017573.3 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr9:78774009 C>T maps to NM_001190482.1 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr15:101983759 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:101933521 G>A maps to NM_002570.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr15:101865151 A>G maps to NM_002570.3 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:117077796 G>A maps to NM_004716.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:117097975 C>A maps to NM_004716.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr1:55527081 C>T maps to NM_174936.3 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr1:55505642 T>C maps to NM_174936.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:195974372 G>A maps to NM_005017.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79865646 A>G did not map to a codon.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr17:79866842 G>T maps to NM_001184917.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr10:105164924 C>T maps to NM_014976.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr10:105160257 A>G maps to NM_014976.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:170893453 C>T maps to NM_002598.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr19:34904639 A>C did not map to a codon.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:34895340 G>T maps to NM_032346.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:112655818 A>G maps to NM_014456.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr3:33855049 G>A did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr9:125582791 G>A maps to NM_005388.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr4:56448341 T>C maps to NM_152401.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr4:56435976 T>C maps to NM_152401.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr11:771045 A>G maps to NM_182612.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:178936707 G>A maps to NM_016953.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr3:57542939 T>C maps to NM_177966.5 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr12:54962994 G>A maps to NM_000924.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr12:54963141 C>T maps to NM_000924.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:54971105 G>A maps to NM_000924.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr7:31877506 C>T maps to NM_001191057.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr12:20792853 T>A maps to NM_000921.3 Y738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr12:20522511 G>A maps to NM_000921.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:10568585 C>T maps to NM_001111307.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr19:10565502 A>C did not map to a codon.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr19:18327664 C>A maps to NM_000923.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:144906485 G>A maps to NM_014644.4 Q791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr1:144864283 C>G maps to NM_014644.4 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr1:144864283 C>G maps to NM_014644.4 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr1:144931264 G>A maps to NM_001002811.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr1:144856851 C>T maps to NM_014644.4 A2211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr4:120442143 A>G maps to NM_001083.3 H617H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr4:120486566 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr4:120446850 C>A did not map to a codon.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:149240510 C>A maps to NM_000440.2 G844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:649740 C>G maps to NM_000283.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr10:95400271 G>A maps to NM_006204.3 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr6:136500188 G>A maps to NM_018945.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:76645326 C>T maps to NM_003719.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr22:39621820 C>A maps to NM_002608.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr5:149499608 G>A maps to NM_002609.3 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr5:149506121 G>C maps to NM_002609.3 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:19369446 C>G did not map to a codon.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:58416620 G>A maps to NM_000925.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr11:35016593 C>T maps to NM_003477.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr16:336869 T>A maps to NM_006849.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr16:334731 C>T maps to NM_006849.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr15:44060740 G>A maps to NM_005313.4 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:148702374 C>T maps to NM_004911.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr2:10924425 G>A maps to ENST00000381611 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr2:10927528 A>T maps to ENST00000381611 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr16:20380852 G>T maps to NM_174924.1 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:20376784 G>A maps to NM_174924.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr17:48184156 G>C did not map to a codon.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr23:24537119 A>C did not map to a codon.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:131607571 C>T maps to NM_003687.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131602210 C>T maps to NM_003687.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr8:94934632 C>T maps to NM_001161778.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr16:70180076 T>C maps to NM_017990.3 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr16:70161180 C>T maps to NM_017990.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr4:39905678 G>A maps to NM_001100399.1 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr13:33281136 A>T maps to ENST00000400481 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr13:33316757 G>A maps to ENST00000400481 W835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr13:33306262 A>T maps to ENST00000400481 K717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:15126716 G>T did not map to a codon.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr16:15126792 G>T maps to NM_015027.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr16:15130100 C>A maps to NM_015027.2 S779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr20:1961112 A>T maps to NM_024411.4 Y207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr23:69506936 G>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:31983431 C>G maps to NM_178140.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:32090570 C>T maps to NM_178140.2 I2339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr5:32052784 C>T maps to NM_178140.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:32108144 G>A maps to NM_178140.2 L2808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr5:32089796 C>T maps to NM_178140.2 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:153070050 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr10:119044854 G>A maps to NM_173791.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr10:119049790 C>A maps to NM_173791.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr10:119044692 T>C maps to NM_173791.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:119134717 G>T maps to NM_173791.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:145761287 T>C maps to NM_002614.3 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr1:47653016 G>A maps to NM_005764.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr3:73673577 G>C maps to NM_015009.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr3:73673577 G>C maps to NM_015009.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:73657757 C>G maps to NM_015009.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:41585334 C>T maps to NM_001164595.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:160181402 C>A maps to ENST00000368075 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr6:4128066 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:32100868 T>C maps to NM_012392.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:32100954 C>A maps to NM_012392.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr1:32101117 G>A maps to NM_012392.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr19:57329186 G>A maps to NM_006210.2 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr19:57327460 G>T maps to NM_006210.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr19:57327001 A>G maps to NM_006210.2 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr19:57327328 T>C maps to NM_006210.2 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr19:57325906 T>G maps to NM_006210.2 V1301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr2:64323336 T>C maps to NM_020651.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr14:56757029 G>T maps to NM_021255.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr17:4576619 C>T maps to ENST00000301396 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:4575450 T>C maps to ENST00000301396 E1089E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:4575081 C>T maps to ENST00000301396 E1212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr17:4575432 C>T maps to ENST00000301396 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:17425655 G>T maps to NM_148172.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr8:57354187 C>T maps to NM_001135690.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr19:33882245 G>A maps to NM_000285.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:8047042 T>G maps to NM_002616.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:8044490 G>A maps to NM_002616.2 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:239184525 A>C maps to NM_022817.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr2:239185782 T>C maps to NM_022817.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr2:239162230 G>A maps to NM_022817.2 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr2:239186361 C>T maps to NM_022817.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr1:7886602 C>A maps to ENST00000377532 S674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:7845602 A>C maps to ENST00000377532 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:7854050 T>C maps to ENST00000377532 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:92151472 A>G maps to NM_000466.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:92119226 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:2341813 A>C maps to NM_153818.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:145522546 C>T maps to NM_003846.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr1:10678474 G>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:10535060 T>C did not map to a codon.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr22:18566232 T>G maps to NM_017929.5 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr12:7362623 T>G maps to NM_001131023.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr6:42946219 C>A maps to NM_000287.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr17:8169633 C>T maps to NM_012393.2 C928C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr20:52830987 A>G maps to NM_002623.3 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr23:54982602 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr10:6257232 C>T maps to NM_004566.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr3:48577176 C>A maps to NM_004567.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr3:48576037 G>T maps to NM_004567.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr21:45743722 C>T maps to NM_002626.4 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr12:48526704 C>T maps to NM_001166686.1 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr12:48538848 C>A maps to NM_001166686.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr10:3172123 A>G maps to NM_002627.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr10:99192202 C>T maps to NM_002629.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr11:3846651 G>A maps to NM_014489.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr17:37829070 C>T maps to NM_033419.3 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr6:28251757 C>T maps to NM_032507.3 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr10:50725061 A>T maps to ENST00000515869 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr1:230461072 G>A maps to ENST00000321327 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr6:41711089 G>T maps to NM_002630.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr1:10477168 C>A maps to NM_002631.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr14:75416058 C>T did not map to a codon.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr23:77373614 T>A did not map to a codon.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr23:77369582 T>A did not map to a codon.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr6:49754597 G>A maps to NM_138733.4 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr19:15586418 C>T maps to NM_052890.3 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr19:15587342 G>T maps to NM_052890.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr1:153271693 G>A maps to NM_052891.1 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:153279660 G>C maps to NM_052891.1 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr11:74085549 G>A maps to NM_173582.3 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr6:83881748 C>T maps to ENST00000416472 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr15:99511853 A>T maps to NM_001102612.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:100999186 C>T maps to NM_000926.4 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:118370496 C>T did not map to a codon.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr17:76396756 G>A did not map to a codon.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr6:13206173 G>A maps to NM_030948.1 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr6:13230365 C>A maps to NM_030948.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:144086446 G>C maps to NM_001100164.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr20:58322873 G>A maps to NM_080672.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr20:58318177 G>C maps to NM_080672.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:28800468 C>A maps to NM_023923.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr1:28785763 C>A maps to NM_023923.3 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:7079387 G>A maps to NM_001144831.1 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr6:33382564 T>C maps to NM_024165.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:170117954 C>A maps to NM_018288.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr6:170115863 A>G maps to NM_018288.3 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr6:170115872 T>A maps to NM_018288.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr5:133887863 T>C maps to ENST00000448712 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:46917972 A>C did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:46913819 A>G did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:46918437 A>G did not map to a codon.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr23:46887436 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr23:46887396 A>C did not map to a codon.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr20:34487449 A>T maps to NM_016436.4 K481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr11:45955638 C>A maps to ENST00000257821 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr11:46001379 T>C maps to ENST00000257821 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr23:133547904 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr23:133551238 G>C did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr3:52454990 A>G maps to ENST00000454052 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr23:54043170 T>C did not map to a codon.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr23:54044119 G>T did not map to a codon.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr23:54019190 C>A did not map to a codon.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr23:54048717 T>C did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr23:53966768 C>G did not map to a codon.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr23:54049205 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:54012316 G>A did not map to a codon.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr6:79708067 G>A maps to NM_017934.5 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:71829513 C>T did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr23:71831022 C>A did not map to a codon.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr23:71813084 G>C did not map to a codon.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr23:71830969 C>A did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:71822084 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr23:71802267 C>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:71886082 G>A did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:71925083 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:71802351 G>A did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr23:18972369 A>G did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr23:18970643 T>A did not map to a codon.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr23:18926099 C>T did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:18919657 C>A did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr12:76424936 T>C maps to NM_007350.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr12:76424987 C>T maps to NM_007350.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:76424939 C>T maps to NM_007350.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:111685551 T>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr18:60612365 T>C maps to NM_194449.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr18:60646513 G>A maps to NM_194449.2 P1668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr16:71689234 C>T maps to NM_015020.2 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr17:47302351 G>T maps to NM_001143804.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:170557974 T>A maps to NM_001008489.3 L165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:41748006 T>G maps to NM_003924.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr11:608266 C>A maps to ENST00000264555 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:608821 G>A maps to ENST00000264555 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr7:77469586 C>G maps to ENST00000427986 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr7:77569447 A>G maps to ENST00000427986 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr8:22079279 G>T maps to NM_014759.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr10:60936660 C>A maps to NM_032439.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr10:60994151 A>C maps to NM_032439.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr6:36922578 C>T maps to NM_153370.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:25235820 C>A maps to NM_018323.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr22:21104190 A>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr22:21073054 G>A maps to NM_058004.2 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr22:21119516 C>T maps to NM_058004.2 W757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr22:21088356 G>A maps to NM_058004.2 H1284H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:21082094 C>T maps to NM_058004.2 P1522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:151274727 G>A maps to NM_002651.2 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr1:151288135 G>A maps to NM_002651.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr15:68445965 C>T maps to NM_016166.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:68479998 T>C maps to NM_016166.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr19:4013123 G>A maps to NM_015897.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr13:73482728 C>T maps to NM_006346.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr13:73572976 A>G maps to NM_006346.2 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr11:85733456 T>C maps to ENST00000393343 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr15:65114483 G>A maps to ENST00000333425 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr4:520920 G>A maps to NM_001127178.1 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr18:59821798 C>G maps to NM_176787.4 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr9:35095478 G>A maps to NM_032634.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:35089136 A>C maps to NM_032634.2 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr21:38444808 C>A maps to NM_153681.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr16:624547 C>T maps to NM_148920.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:207105905 C>A maps to NM_002644.3 G635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:207106512 T>C did not map to a codon.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207105816 C>G maps to NM_002644.3 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr20:44054402 A>C maps to NM_015937.4 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr20:44049023 G>C maps to NM_015937.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr20:44050026 C>T maps to NM_015937.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr20:44045232 A>G maps to NM_015937.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr20:33225753 C>T maps to NM_080476.4 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27121058 C>T maps to NM_017837.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr3:196674754 C>T maps to NM_025163.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:196675119 A>T maps to NM_025163.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:49950352 A>G maps to NM_017916.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:111938615 G>A maps to NM_138789.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr10:98405299 G>A maps to NM_152309.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:17118794 A>G maps to NM_002645.2 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr11:17121507 A>G maps to NM_002645.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr1:204399129 T>G maps to NM_002646.3 G1439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr12:18649022 T>C maps to NM_004570.4 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:18762520 G>A maps to NM_004570.4 E1339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr12:18446880 C>T maps to NM_004570.4 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr3:178921333 T>A maps to NM_006218.2 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:138456587 T>C maps to NM_006219.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:67576766 T>G maps to ENST00000396611 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:67588177 A>G maps to ENST00000396611 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:18279616 G>A maps to NM_005027.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr3:130454820 T>C maps to NM_014602.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr17:8792002 C>G maps to NM_001142633.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:209190804 C>A maps to NM_015040.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:99972036 C>T maps to NM_013439.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr7:99956459 G>A maps to ENST00000413850 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr6:37139028 C>G maps to ENST00000373507 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr7:142832379 A>G maps to NM_002652.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:23003186 G>A maps to NM_005028.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:36927420 G>A maps to NM_003559.4 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:36943163 G>A maps to NM_003559.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr17:36935737 C>A maps to NM_003559.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr12:57995052 C>T maps to NM_024779.4 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:57995121 C>G maps to NM_024779.4 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr19:3651894 C>A maps to NM_012398.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:130684386 C>T maps to NM_001135219.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr17:10728776 G>A maps to NM_001101387.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:65665780 T>C did not map to a codon.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr11:67269465 T>C maps to NM_004910.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr11:67267650 G>A maps to NM_004910.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:67265786 G>A maps to NM_004910.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr12:123488977 C>T maps to NM_020845.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr12:123479958 C>T maps to NM_020845.2 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr17:6381330 G>A maps to NM_031220.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr17:6375989 C>T maps to NM_031220.3 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr17:6386892 G>A maps to NM_031220.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr10:3209165 A>C maps to ENST00000380989 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr10:3208556 A>G maps to ENST00000380989 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr12:130839158 G>T maps to NM_004764.4 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:94341804 C>T maps to NM_152431.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr23:68382202 G>A did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr23:68382324 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr23:68382877 G>A did not map to a codon.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr23:68382227 T>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:108714548 A>G maps to NM_014819.4 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr16:2168071 G>A maps to NM_001009944.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr16:2153594 G>A maps to NM_001009944.2 D2821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr16:2168404 G>A maps to NM_001009944.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr16:2142547 G>A maps to NM_001009944.2 Y3734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr16:2168071 G>A maps to NM_001009944.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr16:2139967 G>A maps to NM_001009944.2 T4224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr7:47968828 C>T maps to NM_138295.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3443-01A-01D-0966-08 chr16:81190481 G>A maps to NM_052892.3 D1369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr16:81232573 T>C maps to NM_052892.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr4:88986630 C>T maps to NM_000297.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr10:102089624 C>T did not map to a codon.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr5:137257414 T>G maps to ENST00000230643 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr5:137230169 T>G maps to ENST00000230643 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr22:46654830 A>G maps to NM_006071.1 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr22:46654193 G>A maps to NM_006071.1 Q1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr22:46653501 C>T maps to NM_006071.1 W1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:51930864 A>G maps to NM_138694.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr6:51524621 A>G maps to NM_138694.3 T3434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr6:51747998 C>A maps to NM_138694.3 L2414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:51882413 G>A maps to NM_138694.3 F1798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr6:51612745 G>T maps to NM_138694.3 S3223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:51889789 G>A maps to NM_138694.3 V1606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr8:110420392 G>C maps to ENST00000426474 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr8:110464466 T>A maps to ENST00000426474 A2155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr8:110464466 T>A maps to ENST00000426474 A2155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr8:110530495 T>A maps to ENST00000426474 V3931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr8:110488891 C>G maps to ENST00000426474 Y2971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:110451258 G>A maps to ENST00000426474 K1298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr8:110456095 G>T maps to ENST00000426474 G1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr8:110460594 T>C maps to ENST00000426474 N2000N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr8:110477388 C>T maps to ENST00000426474 D2776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:110530423 T>C maps to ENST00000426474 T3907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr19:14580587 G>A maps to NM_213560.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr1:89298944 T>C maps to NM_006256.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr9:131480825 A>C did not map to a codon.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr21:44427620 A>G maps to NM_004571.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr12:32949146 G>A maps to NM_004572.3 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:159490675 G>T maps to NM_003628.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr16:68283193 C>T maps to NM_012320.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr1:20304928 G>A maps to NM_001161728.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:20466688 C>T maps to NM_022819.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:20470068 G>A maps to NM_022819.3 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr1:186839571 G>A maps to NM_024420.2 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr15:42386651 C>T maps to NM_178034.3 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr15:42363001 G>A maps to NM_178034.3 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr15:42446346 G>A maps to ENST00000397272 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr15:42434286 C>T maps to ENST00000397272 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:20416293 G>A maps to NM_000929.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr22:38516842 G>A maps to NM_003560.2 Y555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:38536029 G>A maps to NM_003560.2 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr2:160813102 A>G maps to NM_007366.4 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr9:26925950 C>A maps to NM_001031689.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr23:133700598 T>A did not map to a codon.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr21:42551342 G>C maps to NM_182832.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr10:81904025 G>C maps to NM_001012973.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr20:30784296 C>T maps to NM_002657.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr10:75673066 C>T maps to NM_002658.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr2:28812900 T>C maps to NM_153021.4 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:28841244 C>T maps to NM_153021.4 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr2:28752199 C>A maps to NM_153021.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr2:28752600 G>A maps to NM_153021.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr12:14656714 A>G maps to NM_024829.5 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr20:8703022 C>T maps to NM_015192.2 D512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr20:8713924 C>T maps to NM_015192.2 N643N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr20:8698473 G>T maps to NM_015192.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr20:8608960 T>G maps to NM_015192.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:40594159 T>A maps to NM_004573.2 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr15:40594519 T>A maps to NM_004573.2 K135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:64024201 C>A maps to NM_000932.2 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64034707 C>T maps to NM_000932.2 Q1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr11:64029900 G>A maps to NM_000932.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr11:64026684 C>T maps to NM_000932.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr20:9374305 G>T maps to NM_001172646.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr2:219487601 G>C did not map to a codon.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr2:219501272 G>A maps to ENST00000432688 Q786Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr10:95791805 G>T maps to ENST00000371380 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr10:95849075 A>G maps to NM_001165979.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr20:39798839 C>T maps to NM_002660.2 A913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr20:39796505 G>T maps to NM_002660.2 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr20:39802103 G>A maps to NM_002660.2 V1108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr16:81934321 C>G maps to NM_002661.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr3:155212208 G>A maps to ENST00000340059 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:155199833 A>G maps to ENST00000340059 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:2426374 C>T maps to NM_014638.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:2415963 C>T maps to NM_014638.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:2418422 G>A maps to NM_014638.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr3:17053309 G>C maps to NM_001144382.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr3:111432756 C>T maps to ENST00000312791 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr12:18858243 A>T maps to ENST00000266505 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:171394618 G>A maps to NM_002662.3 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:171395428 G>A maps to NM_002662.3 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr19:40873737 G>A maps to NM_012268.2 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr19:40876045 A>T maps to NM_012268.2 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:242253368 G>A maps to NM_152666.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr8:145004391 G>A maps to NM_201380.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr8:144991468 G>A maps to NM_201380.2 Q4311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr8:144991469 C>T maps to NM_201380.2 E4310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr8:145001216 C>T maps to NM_201380.2 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:144998456 C>T maps to NM_201380.2 L2017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr8:144995867 A>G maps to NM_201380.2 N2844N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr8:144999884 C>G maps to NM_201380.2 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr8:144991672 C>A maps to NM_201380.2 E4243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr8:144995792 C>T maps to NM_201380.2 A2869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:144997532 C>G maps to NM_201380.2 L2325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr8:144996110 C>T maps to NM_201380.2 L2763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:144995546 G>A maps to NM_201380.2 G2951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr8:144997655 C>T maps to NM_201380.2 A2284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr8:144996262 G>A maps to NM_201380.2 L2713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr10:124189324 T>A maps to NM_021622.4 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:124172504 C>T maps to NM_021622.4 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr8:38827143 C>A maps to NM_021623.1 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr2:179368496 C>T maps to NM_019091.3 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:49362922 A>C maps to NM_020904.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr12:19410395 T>C maps to ENST00000429027 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr1:204242840 T>C maps to ENST00000367191 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr11:16838610 G>A maps to ENST00000448080 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr11:16816508 C>T maps to ENST00000448080 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr11:16876456 C>T maps to ENST00000448080 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr7:30094388 T>C maps to ENST00000440706 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr14:65210036 G>A maps to ENST00000394691 S1092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr14:65204094 T>C did not map to a codon.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr16:67318758 G>A maps to NM_001129729.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:163210 A>G maps to NM_052909.3 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr1:6532595 C>G maps to NM_198681.2 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr1:6531589 T>C maps to NM_198681.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:6436887 G>A maps to NM_001144856.1 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr12:93134669 T>C maps to NM_001004330.2 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr14:68038959 C>A maps to NM_020715.2 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr14:68047713 T>A maps to NM_020715.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr14:68052684 C>A maps to NM_020715.2 Y1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:43973090 A>T maps to NM_172069.3 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:40821476 C>A maps to NM_024927.4 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr17:43523002 C>G maps to NM_014798.2 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:16053892 C>T maps to ENST00000420314 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr2:208795800 C>A maps to NM_001080475.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr15:65157276 G>A maps to NM_025201.4 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:65157909 C>T maps to NM_025201.4 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr6:161135848 G>T maps to NM_000301.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr6:161139401 T>A maps to NM_000301.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr6:161152840 A>G maps to NM_000301.3 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr6:161155094 C>T maps to NM_000301.3 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:161139488 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr9:19126157 C>A maps to NM_001122.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr19:4510614 G>A maps to NM_001080400.1 D1105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr19:4511490 A>G maps to NM_001080400.1 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:4511772 G>A maps to NM_001080400.1 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr19:4511493 G>A maps to NM_001080400.1 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:4512513 G>C maps to NM_001080400.1 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr20:21142792 T>A maps to NM_018474.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr4:128813595 T>C maps to NM_014264.4 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:145803002 A>T maps to NM_182943.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:155465647 T>C maps to NM_002669.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:155470081 T>C maps to NM_002669.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr23:114874763 A>G did not map to a codon.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr23:114864222 A>G did not map to a codon.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr23:114880822 G>C did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:114883785 G>C did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:146167109 C>T maps to ENST00000497985 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44534918 G>A maps to NM_006227.2 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr20:44539885 C>T maps to NM_006227.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr17:37265508 G>A maps to NM_020405.4 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:126708216 C>T maps to NM_032242.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr3:126707666 C>T maps to NM_032242.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr3:126733640 C>A maps to NM_032242.3 Y948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:153700939 C>T did not map to a codon.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr23:153699963 A>G did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr23:153699460 T>A did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr23:153692791 G>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:153696320 G>A did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr3:48447206 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:48459372 C>A maps to NM_001130082.1 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr22:50724517 G>T maps to NM_012401.2 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50720399 G>A maps to NM_012401.2 D1076D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50726134 G>A maps to NM_012401.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr22:50716443 T>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:153037077 G>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:153037466 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:153037417 G>A did not map to a codon.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr23:153035377 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:129324249 C>G maps to NM_015103.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:129276045 G>T maps to NM_015103.2 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:129286539 C>T did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr3:129281630 A>G maps to NM_015103.2 L1608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:89859123 T>A maps to NM_001010853.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr20:56227615 C>T maps to NM_020182.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr1:156209391 A>C maps to NM_007221.3 *206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr16:72158691 C>A maps to NM_031293.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:74325642 G>A maps to NM_033238.2 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:74327952 G>A maps to NM_033239.2 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:74315582 C>T maps to NM_033238.2 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:74327977 C>T maps to NM_033239.2 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr7:6042191 A>G maps to NM_000535.5 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr7:6042152 T>A maps to NM_000535.5 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:152937047 G>C did not map to a codon.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr23:152936764 C>A did not map to a codon.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr23:152936427 G>A did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr23:152937463 A>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:152938462 C>G did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:152938522 C>A did not map to a codon.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr10:118305650 G>C did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr10:118357346 T>C maps to NM_006229.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr14:74180282 A>G maps to NM_006029.4 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:26365720 C>T maps to NM_007257.5 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr23:152226010 A>G did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr23:152226514 T>C did not map to a codon.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr23:152159502 C>T did not map to a codon.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr23:152159196 G>A did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr17:37826359 A>G maps to NM_002686.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr14:39650382 C>T maps to NM_002687.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr14:39645317 T>C maps to NM_002687.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr2:68400545 T>C maps to NM_020143.2 L230L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr23:7889833 G>T did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:7615222 G>A maps to NM_001166111.1 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr19:7614965 C>T maps to NM_001166111.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:7619509 G>A maps to NM_001166111.1 Q855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:7606948 C>T maps to NM_001166111.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:7615902 G>A maps to NM_001166111.1 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:89793800 T>C maps to NM_006813.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr12:89885861 A>G maps to NM_172240.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74981181 G>C maps to NM_001099271.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:14044011 G>A maps to NM_024825.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr7:131241088 C>T maps to NM_001018111.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr7:131194327 C>T maps to NM_001018111.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr7:131194124 C>T maps to NM_001018111.2 W341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr3:127379563 A>G maps to NM_015720.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:127379598 T>A maps to NM_015720.2 L243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr21:46689907 G>A maps to NM_133635.4 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:166818811 G>T maps to NM_017542.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr1:166816821 C>G maps to NM_017542.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:151381039 G>A maps to NM_015100.3 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151377514 G>A maps to NM_015100.3 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:24744125 T>A did not map to a codon.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr23:24735483 G>A did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:24906192 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:24750525 T>A did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr11:65048557 G>A maps to NM_002689.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr19:50905746 G>A maps to ENST00000391817 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr19:50905131 C>T maps to ENST00000391817 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr22:42992338 G>T maps to ENST00000415122 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:42987961 G>A maps to ENST00000415122 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:133235891 A>G maps to ENST00000455752 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr14:50136256 G>A maps to NM_002692.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:62487032 G>A maps to NM_007215.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr18:51820611 A>G maps to NM_007195.2 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr7:44113447 T>C maps to NM_013284.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:44121935 C>A maps to NM_013284.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr4:2175732 A>G maps to NM_181808.2 H441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr3:121207745 T>A maps to ENST00000393672 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:121263751 T>C maps to ENST00000393672 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr2:86325786 G>A maps to NM_015425.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr9:37500906 C>T maps to NM_022490.1 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr17:7415173 G>T maps to NM_000937.4 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr17:7416180 G>A maps to NM_000937.4 W1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7404999 G>A maps to NM_000937.4 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr4:57873144 C>T maps to NM_000938.1 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr4:57891053 A>G maps to NM_000938.1 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr16:57503111 G>A maps to NM_032940.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:57503975 G>A maps to NM_032940.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr3:184082990 C>T maps to NM_006232.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:840427 G>A maps to NM_021128.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr20:18448194 G>A maps to NM_006466.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:72416769 G>A maps to ENST00000434423 K1249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr7:75055732 G>C maps to ENST00000257665 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr7:53103957 C>T maps to NM_182595.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr13:29238706 G>T did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr9:134385343 C>G maps to NM_007171.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr9:134385418 C>G maps to NM_007171.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr14:77765101 G>A maps to NM_013382.5 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr7:76255327 C>T maps to NM_012230.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr7:94993299 C>A maps to NM_000940.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:99152323 G>T maps to NM_015029.2 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr7:100304815 G>A maps to NM_005837.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr3:119378937 G>A maps to NM_022135.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:75615289 T>C maps to NM_000941.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr23:48378841 T>G did not map to a codon.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr13:38162096 G>A maps to NM_006475.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr7:124503401 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr7:124493108 C>T maps to NM_015450.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr8:43152261 G>A maps to NM_001005365.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr18:14542887 A>G maps to ENST00000444806 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr2:132021814 G>A maps to NM_001083538.1 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr2:130832596 G>A maps to NM_001099771.2 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr2:130872870 C>T maps to NM_001099771.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr14:19553652 C>T maps to NM_001005356.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:16287579 G>T maps to NM_001136213.1 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr14:20019956 G>A maps to ENST00000439503 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr3:87311218 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr1:167365545 G>A maps to NM_002697.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:82764045 G>T did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr23:82763422 T>C did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr4:147561257 T>C maps to NM_004575.2 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr5:145719655 G>T maps to NM_002700.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:93076681 A>T maps to NM_153216.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:39446254 C>T maps to NM_007252.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr8:38125964 G>C maps to NM_001102559.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr9:4662476 C>A maps to NM_203453.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:35392131 A>C maps to NM_006238.4 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:12447396 G>C maps to NM_015869.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr3:12422836 G>A maps to NM_015869.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr4:23816121 T>A maps to NM_013261.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:23814444 T>C maps to NM_013261.3 E648E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:149212385 G>A maps to NM_133263.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr4:74853009 T>C maps to NM_002704.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr23:18836211 C>T did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:18822153 G>T did not map to a codon.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr4:76787407 T>C maps to NM_006239.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr4:76797628 G>A maps to NM_006239.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr11:70218603 T>C maps to NM_003626.2 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr11:70200405 G>T did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr12:81661719 A>G maps to NM_003625.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr12:81719629 T>C maps to NM_003625.2 E856E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:203025586 C>A maps to ENST00000367238 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr12:27835399 T>C maps to NM_003622.3 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr12:27799071 C>T maps to NM_003622.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr12:27824428 T>C maps to NM_003622.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr12:27787952 T>C maps to NM_003622.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:64454354 T>C did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:122359695 T>A maps to NM_000943.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr1:43124122 G>A maps to NM_006347.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:149855819 T>C maps to NM_139126.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr16:4953993 C>A maps to NM_002705.4 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr16:4935160 G>A maps to NM_002705.4 N1165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:4940316 G>A maps to NM_002705.4 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:60749543 G>T maps to NM_177952.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr2:44457730 T>C maps to NM_002706.4 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr2:44429132 T>A maps to NM_002706.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr2:44436368 T>C maps to NM_002706.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr2:44429129 A>G maps to NM_002706.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:58740445 G>T maps to NM_003620.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:56833489 G>A maps to NM_014906.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr3:52282682 C>T maps to NM_144641.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:46002035 C>T maps to NM_001080401.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr1:161140728 G>A maps to NM_001122764.1 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:161139814 G>T did not map to a codon.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr6:30570686 T>A maps to NM_002714.2 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr6:30569884 G>A maps to NM_002714.2 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr12:80214665 A>G maps to NM_001143885.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr1:204380313 C>A maps to NM_032833.3 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:204379051 A>G maps to NM_032833.3 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr1:204379182 C>A maps to NM_032833.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr8:145722669 C>T maps to NM_032902.5 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr20:37536821 G>T maps to NM_015568.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr7:113518386 A>G maps to NM_002711.3 H920H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr7:113559038 C>A maps to NM_002711.3 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr8:8998707 G>A maps to NM_024607.2 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr23:49142979 G>T did not map to a codon.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr23:49143161 G>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr7:94539703 T>C maps to NM_001166160.1 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr7:94540663 C>T maps to NM_001166160.1 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr5:133533530 G>A maps to NM_002715.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr8:30643765 T>G maps to NM_001009552.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr8:30651535 G>T maps to NM_001009552.1 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr19:52729233 A>G maps to NM_014225.5 *590W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr11:111624211 G>T maps to NM_181699.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr8:26196503 G>T did not map to a codon.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr5:146077635 G>A maps to ENST00000394414 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr4:6349696 C>T maps to NM_181876.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr10:133748060 T>G did not map to a codon.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr3:135745813 C>T maps to NM_002718.4 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:135825107 T>C maps to NM_002718.4 A1091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:102323021 G>A did not map to a codon.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr6:42975941 C>T maps to NM_006245.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr18:9570185 T>A maps to NM_001042388.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr14:94697033 C>A maps to NM_058237.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr19:46878880 T>C maps to NM_006247.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr9:127915853 G>A maps to NM_001123355.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:244868991 A>G maps to NM_016076.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr10:103907138 A>C maps to NM_015062.3 R1464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr19:8563523 C>A maps to NM_032152.4 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr22:22893220 A>C maps to NM_206954.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:12854435 G>C maps to NM_023013.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr1:12854405 G>A maps to NM_023013.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr1:12854400 G>T maps to NM_023013.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr1:12885126 G>A maps to NM_001146344.1 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:12835788 C>T maps to NM_001080830.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr1:12837663 C>T maps to NM_001080830.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:12837357 G>A maps to NM_001080830.1 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:13497725 A>C maps to NM_001045480.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr1:13474979 G>A maps to NM_001099850.1 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:12919094 A>C maps to NM_023014.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:12921593 C>G maps to NM_023014.1 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr1:12939547 G>C maps to ENST00000376192 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr1:12977625 A>G maps to NM_001012277.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr1:12980073 T>A maps to NM_001012277.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr12:11506355 G>A maps to NM_005039.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr12:11506646 T>C maps to NM_005039.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr12:11506382 C>T maps to NM_005039.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr12:11508459 A>G maps to NM_005039.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr12:11546615 A>G maps to NM_006248.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr12:11546261 G>A maps to NM_006248.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:11546447 G>A maps to NM_006248.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr12:11546633 G>A maps to NM_006248.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr12:11546873 T>C maps to NM_006248.3 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr12:11546624 A>G maps to NM_006248.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:11420474 A>G maps to NM_006249.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr15:91523520 C>T maps to NM_003981.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr11:82560213 T>C maps to NM_199418.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:106553249 G>A maps to NM_001198.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:129794866 A>G maps to NM_020228.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr11:129817094 C>T maps to NM_020228.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr11:129817184 G>A maps to NM_020228.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr9:133543579 C>A maps to NM_021619.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr6:100057183 G>A did not map to a codon.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr6:100057080 C>T maps to ENST00000359773 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr8:70978468 C>A did not map to a codon.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:70981666 A>G maps to NM_024504.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr21:43298958 C>G maps to NM_022115.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr21:43241556 C>T maps to NM_022115.3 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:3334450 C>T maps to NM_022114.3 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr1:14075879 C>T maps to NM_012231.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr1:14106782 A>G maps to NM_012231.4 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:14107223 G>A maps to NM_012231.4 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr1:14107868 T>C maps to NM_012231.4 C1193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr4:121631519 G>T maps to NM_018699.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr16:90127012 C>A maps to NM_001098173.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr5:23526897 C>T maps to NM_020227.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr5:23521145 G>A maps to NM_020227.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:12911997 T>C maps to NM_005809.4 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:12911039 A>G maps to NM_005809.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr6:105800845 C>T did not map to a codon.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:44554021 T>A maps to NM_001171603.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr2:44556212 A>C maps to NM_001171603.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566371 G>A maps to NM_001171603.1 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566450 A>G maps to NM_001171603.1 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr20:47271872 G>A maps to NM_020820.3 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr20:47258751 C>A maps to NM_020820.3 R1243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr20:47258947 G>A maps to NM_020820.3 N1227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:47361657 G>A maps to NM_020820.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr8:68939494 T>C maps to NM_024870.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:72360283 G>A maps to NM_005041.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr1:186278972 T>A maps to NM_005807.3 L1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr1:186277943 C>G maps to NM_005807.3 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr12:11035695 C>T did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:62191641 T>C maps to NM_001037335.2 V2513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr20:62193087 C>G maps to NM_001037335.2 L2234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr20:62195725 G>A maps to NM_001037335.2 D1483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr20:62194102 A>G maps to NM_001037335.2 P2024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr20:62195086 A>G maps to NM_001037335.2 S1696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr20:62197378 G>A maps to NM_001037335.2 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:42858292 G>A maps to NM_153026.2 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr23:49034678 A>G did not map to a codon.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr6:41752689 C>T maps to NM_013397.5 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr12:57139903 C>T maps to NM_000946.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr6:57185309 C>T maps to NM_000947.2 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr6:57467162 G>C maps to NM_000947.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr6:57372298 G>A maps to NM_000947.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr6:57498974 T>C maps to NM_000947.2 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr14:94245648 A>G maps to NM_178013.3 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr14:94245651 C>T maps to NM_178013.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:40775605 C>T did not map to a codon.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr1:84670171 G>C maps to ENST00000370680 *265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr1:84663464 T>C maps to NM_182948.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:71628288 G>A maps to NM_002732.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr9:71628294 G>A maps to NM_002732.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:151262971 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:66526490 G>A maps to NM_212472.1 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:106799966 T>A maps to NM_002736.2 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr17:64800058 T>C maps to NM_002737.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr17:64731698 C>T maps to NM_002737.2 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr16:24185868 G>C maps to NM_002738.6 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:23848698 C>T maps to NM_002738.6 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr3:53219627 C>T maps to NM_212539.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr3:53223225 C>A maps to NM_212539.1 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr3:53219627 C>T maps to NM_212539.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr3:53215261 C>T maps to NM_212539.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr3:53220040 A>T maps to NM_212539.1 K362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:46203637 G>A maps to NM_005400.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr2:46211701 C>A maps to NM_005400.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr19:54395810 G>A maps to NM_002739.3 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:170002333 T>C maps to NM_002740.5 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:2066776 C>T maps to NM_002744.4 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr19:47181734 G>A maps to ENST00000449438 N752N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:37501594 A>C maps to NM_005813.3 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr8:48744422 G>T maps to NM_006904.6 L2738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr8:48694797 C>T maps to NM_006904.6 W3804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:48826504 G>A maps to NM_006904.6 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:82061796 A>T maps to NM_006259.1 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr2:179307991 A>T did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:3544549 G>C did not map to a codon.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr23:3631166 A>G did not map to a codon.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr10:120353898 C>A maps to NM_004248.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr19:50187292 C>T maps to NM_001536.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr19:50185318 C>T maps to NM_001536.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr4:148578941 C>T did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr21:48083429 G>A maps to NM_206962.1 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:107599741 C>T maps to NM_018137.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr16:68373379 T>C maps to NM_019023.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr16:68386312 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr20:33762616 A>T maps to NM_006404.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:36290975 C>T maps to NM_021232.1 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr3:71830710 G>A maps to NM_001126128.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr4:71275488 C>T maps to NM_021225.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr4:16020104 G>A maps to NM_006017.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr5:177421250 C>T maps to NM_006261.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:93646099 C>T maps to NM_000313.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr3:93624945 C>A maps to NM_000313.3 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr3:93643108 C>A did not map to a codon.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr1:214171380 C>T maps to NM_002763.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr1:214171242 T>A maps to NM_002763.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:214171102 C>T maps to NM_002763.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr11:60658694 G>A maps to NM_014502.4 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr11:60671328 A>T maps to NM_014502.4 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:150312942 C>T maps to NM_004698.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr19:54625913 A>C maps to NM_015629.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr14:45579917 A>G maps to NM_017922.3 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr14:45571776 T>C maps to NM_017922.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:153573941 G>A maps to ENST00000410080 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr20:62648173 T>C maps to NM_012469.3 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr20:62642792 C>T maps to NM_012469.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr20:62642771 G>C maps to NM_012469.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr12:49690228 C>T maps to ENST00000451891 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr23:106885677 G>A did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr23:12817353 G>A did not map to a codon.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr23:12827406 G>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:12840842 C>G did not map to a codon.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr19:50118188 C>T maps to NM_020719.1 F1649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:50097990 G>C maps to NM_020719.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:53837460 A>G maps to NM_018457.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr16:30666136 G>A maps to NM_024031.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr19:42814765 C>T maps to NM_199285.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr2:240982051 C>G maps to NM_001080835.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr2:240981514 A>G maps to NM_001080835.1 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr3:138724462 G>A maps to NM_001134659.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr16:863366 C>T maps to NM_001013638.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr22:45132784 T>C maps to NM_001198721.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr23:150868603 A>T did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr23:150869295 C>A did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:150869197 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr3:9989479 G>C maps to NM_207351.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr7:142458496 C>A maps to ENST00000486171 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:142458541 A>G maps to ENST00000486171 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:142458550 C>T maps to ENST00000486171 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr7:142459666 G>A maps to ENST00000486171 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:142460777 T>C maps to ENST00000486171 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr4:119273491 A>T maps to NM_003619.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr6:27216900 A>C maps to NM_005865.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr7:142481270 A>C maps to ENST00000311757 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr16:2867458 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr9:33798078 T>C maps to NM_007343.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr9:33796656 C>T maps to NM_007343.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr9:33796800 G>A did not map to a codon.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:33796800 G>A did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr9:33796800 G>A did not map to a codon.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr9:33797880 G>A maps to NM_007343.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr9:33798015 C>T maps to NM_007343.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr9:33796659 T>C maps to NM_007343.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr6:84233612 C>T maps to NM_153362.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr6:84233684 G>A maps to NM_153362.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:228004908 G>T did not map to a codon.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr3:46754549 C>T maps to NM_013270.4 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:31098020 C>T maps to NM_001039503.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr16:58314589 G>A maps to NM_001080492.1 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:10396086 C>A maps to NM_198464.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr8:10396086 C>G maps to NM_198464.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr8:10390472 G>A maps to NM_198464.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:56032871 G>A maps to NM_173814.4 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:841047 C>T maps to NM_002777.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr9:79325302 G>T maps to NM_015225.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:79325025 G>A maps to NM_015225.2 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr9:79324115 G>C maps to NM_015225.2 S1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr9:79324153 A>T maps to NM_015225.2 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:79322500 T>C maps to NM_015225.2 Q1563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr19:40900147 G>T maps to NM_181882.2 R1371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr19:40903259 C>T maps to NM_181882.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr8:143763546 C>A maps to ENST00000301258 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:139193772 T>C maps to NM_032289.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr5:139217289 G>A maps to NM_032289.2 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:139197068 C>T maps to NM_032289.2 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr5:139189306 G>A maps to NM_032289.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr8:18725290 T>G maps to ENST00000440756 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr8:18725566 T>C maps to ENST00000440756 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:113940962 T>G maps to NM_012455.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:113942577 C>T maps to NM_012455.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr14:73685984 A>G maps to NM_000021.3 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:43376180 G>A maps to NM_006905.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr19:43383679 G>T maps to NM_006905.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr19:43585216 A>T maps to ENST00000449000 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr19:43585273 A>G maps to ENST00000449000 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr19:43243170 A>T maps to NM_021016.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr19:43237191 G>T maps to NM_021016.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr19:43709646 G>A maps to ENST00000449000 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:43689068 C>A maps to ENST00000270059 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr19:43439633 C>A maps to NM_002783.2 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr19:43773526 C>A maps to NM_002784.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr8:87060712 G>T maps to ENST00000276616 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr11:14536020 C>A maps to NM_148976.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr7:42964386 C>A maps to NM_002787.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr14:58714514 A>G maps to NM_002788.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr14:35777198 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr18:23714009 G>A maps to NM_144662.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:151372077 G>A maps to NM_002796.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:151372468 G>A maps to NM_002796.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr6:32808789 T>A maps to NM_148919.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr14:90730103 T>G maps to NM_002802.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr7:103004702 G>T maps to NM_002803.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr7:103008446 C>T maps to NM_002803.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:40726132 G>T maps to NM_016556.2 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr19:40480500 C>T maps to NM_006503.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr19:40486338 T>C maps to NM_006503.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:40478460 A>G maps to NM_006503.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr17:61907490 A>G did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr17:61908393 A>G did not map to a codon.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:231937036 T>A maps to NM_002807.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:65362548 G>C maps to NM_002816.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr11:251909 C>T maps to NM_002817.3 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr11:250864 G>A maps to NM_002817.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:162227814 T>C maps to NM_005805.4 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:184019769 C>T maps to NM_002808.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr3:184019769 C>T maps to NM_002808.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:123591453 T>C maps to NM_005047.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr3:64004273 C>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr14:24613238 C>T did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr2:54176407 A>G maps to NM_014614.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr20:1144991 C>T maps to NM_006814.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr13:20279799 A>G did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr10:124742524 C>T maps to NM_153336.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr10:124740204 A>G maps to NM_153336.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr15:77328194 A>G maps to NM_003978.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr18:43572168 C>A did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr1:28477381 C>A maps to NM_001164721.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:28477259 G>A maps to NM_001164721.1 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr19:808432 C>T maps to NM_002819.4 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:99022429 G>A maps to NM_001198879.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr7:99022963 C>T maps to NM_001198879.1 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:99022813 G>A maps to NM_001198879.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr2:86359529 A>G maps to NM_017952.5 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr9:98239879 T>C maps to NM_000264.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr9:98211563 G>A maps to NM_000264.3 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr9:98209385 C>G maps to NM_000264.3 P1384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr1:45288275 A>T maps to NM_003738.4 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr23:23410646 G>C did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr23:23411324 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr1:11562883 G>T maps to NM_020780.1 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr1:11579863 C>T maps to NM_020780.1 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr10:27702369 G>A maps to NM_001034842.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr10:89725042 G>A did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr10:89717761 A>T maps to NM_000314.4 K263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr10:89624274 C>T maps to NM_000314.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr10:89725041 A>G did not map to a codon.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr10:89712005 C>T maps to NM_000314.4 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr10:89690805 T>A maps to NM_000314.4 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5568-01A-01D-1534-10 chr10:89711909 T>G maps to NM_000314.4 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:89693002 A>T maps to NM_000314.4 K163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr10:16547024 T>C maps to NM_030664.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr14:52741642 C>T maps to NM_000953.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:40681715 C>T maps to NM_000958.2 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:78959186 G>A maps to NM_000959.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr1:78958514 C>A maps to NM_000959.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:78958514 C>A maps to NM_000959.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr20:48130812 C>T maps to NM_000961.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:114332439 A>G maps to NM_001146108.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr9:125140797 G>T maps to NM_000962.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr1:186646027 G>A maps to NM_000963.2 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr1:186645101 G>T maps to NM_000963.2 Y395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr3:46939562 G>T did not map to a codon.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr8:141745399 G>T maps to NM_005607.4 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr8:141712776 G>T maps to NM_005607.4 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:141745381 C>T maps to NM_005607.4 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr6:43044270 T>G maps to NM_002821.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:43112986 G>A maps to NM_002821.3 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr1:32377373 C>T maps to NM_080391.3 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr8:142437879 T>C maps to NM_032611.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr9:96857596 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr11:47593081 C>A maps to NM_175732.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr20:49196425 G>T maps to NM_002827.2 G351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:112893797 A>G maps to ENST00000392596 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr12:112892408 T>C maps to ENST00000392596 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr7:77256020 G>A did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr7:77256099 T>G maps to NM_002835.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr4:87684096 T>A maps to NM_080685.2 S1257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr4:87679431 G>A maps to NM_080685.2 W1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr4:87662969 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:87691258 C>T maps to NM_080685.2 V1575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:214556992 G>A maps to NM_005401.4 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:131116983 C>T maps to NM_014369.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr14:88983530 C>T maps to NM_007039.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:88945932 C>T maps to NM_007039.3 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:114402064 A>G maps to NM_015967.5 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr3:47452809 G>A maps to NM_015466.2 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:112185014 A>G maps to NM_002829.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr9:112151593 G>C maps to NM_002829.3 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr9:112172525 G>A maps to NM_002829.3 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr9:112151593 G>C maps to NM_002829.3 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr2:120720266 G>T maps to NM_002830.2 E786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr11:18787396 G>T maps to NM_032781.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr20:2998528 C>T maps to NM_002836.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr20:3016488 G>T maps to NM_002836.3 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr12:71029652 G>T maps to NM_001109754.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr12:70965010 C>T maps to NM_001109754.1 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:71002987 G>A maps to NM_001109754.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:198704381 G>A did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:198678921 C>T maps to ENST00000271610 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr9:8500874 A>T maps to NM_002839.3 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:8507426 C>G maps to NM_002839.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr9:8484278 G>A maps to NM_002839.3 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:8485822 C>T maps to NM_002839.3 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:129859260 C>A maps to NM_006504.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr10:129866454 C>T maps to NM_006504.4 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:44086830 C>T maps to NM_002840.3 Y1861Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:44063473 C>T maps to NM_002840.3 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:44063521 C>T maps to NM_002840.3 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:44083551 C>T maps to NM_002840.3 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr19:55713577 C>T maps to NM_002842.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr6:128643198 C>T maps to ENST00000368210 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr18:8113696 T>A maps to NM_001105244.1 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr18:8379244 G>A maps to NM_001105244.1 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr18:8378411 G>T maps to NM_001105244.1 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr18:8314789 C>T maps to NM_001105244.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:220164915 A>G maps to NM_002846.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr7:157985187 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:157414138 G>A maps to NM_002847.3 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr12:71078028 C>A maps to NM_002849.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr12:71139698 G>T maps to NM_002849.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:5220166 T>A did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:5214699 G>T maps to NM_002850.3 R1456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:5214436 G>A maps to NM_002850.3 Q1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr19:5219379 C>G maps to NM_002850.3 G1288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr20:40710578 G>A maps to ENST00000373198 D1427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr20:41306677 A>T maps to ENST00000373198 Y327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr20:41385108 G>A maps to ENST00000373198 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr20:41100969 G>A maps to ENST00000373198 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr20:40713329 G>T maps to ENST00000373198 V1398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr20:40730778 G>A maps to ENST00000373198 N1255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:29585158 C>T maps to NM_005704.4 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr7:121651685 G>A maps to NM_002851.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:121651530 C>T maps to NM_002851.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr7:121681009 G>A maps to NM_002851.2 V1926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr7:121652843 T>C maps to NM_002851.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:130476384 C>T maps to NM_001002913.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr17:57775084 C>T maps to ENST00000409433 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr8:144898830 G>C maps to NM_078480.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr8:144899130 C>A maps to NM_078480.1 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr8:144898884 G>A maps to NM_078480.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr8:144902838 T>C maps to NM_078480.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:45162148 C>T maps to NM_006505.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr11:119510666 G>T maps to NM_203285.1 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:45381870 T>C maps to NM_002856.2 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:45391602 A>G maps to NM_001042724.1 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr3:110852893 G>A maps to NM_015480.1 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:110830988 G>A maps to NM_015480.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:110837734 T>A maps to NM_015480.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:161049404 C>T maps to NM_030916.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:159520918 G>A maps to NM_001130864.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:134218415 C>T maps to NM_138499.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr2:1664725 G>A maps to NM_012293.1 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr2:1667442 C>A maps to NM_012293.1 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:1653136 C>T maps to NM_012293.1 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr8:52359591 C>A maps to NM_144651.4 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr8:52361652 G>C maps to NM_144651.4 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:120650284 A>G maps to NM_001080855.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:120653398 G>A maps to NM_001080855.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr16:31213522 G>T maps to NM_013258.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr3:191179037 G>A maps to NM_001083308.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr14:51375669 G>A maps to NM_002863.4 Y727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr11:64522810 G>A maps to NM_005609.2 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr15:55841137 T>C maps to NM_015617.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr15:55838991 A>G maps to NM_015617.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:158912062 T>G maps to NM_152501.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr12:9317896 G>A maps to NM_002864.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:9305861 G>T maps to NM_002864.2 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr12:9321468 A>G maps to NM_002864.2 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr12:9344840 C>T maps to NM_002864.2 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr16:29706447 G>T maps to NM_014298.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr17:74278088 G>A maps to NM_032134.1 I1207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr17:74288034 G>A maps to NM_032134.1 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:32953740 C>T maps to NM_001076786.1 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr11:32953289 C>A maps to NM_001076786.1 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr11:32954929 C>A maps to NM_001076786.1 S580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:32955023 C>T maps to NM_001076786.1 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr11:32953803 C>T maps to NM_001076786.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:180135638 C>A maps to NM_002826.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr19:10823282 C>T maps to NM_031209.2 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:10818002 C>T maps to NM_031209.2 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:113795753 A>G maps to ENST00000485050 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr2:136402958 C>T maps to ENST00000409606 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:136473265 T>A did not map to a codon.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr12:57648627 C>G maps to ENST00000438036 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:57674167 T>C maps to ENST00000438036 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr20:42969921 C>T maps to NM_178491.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:37729418 C>A maps to NM_001002814.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:570231 C>T maps to NM_014700.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:568987 G>A maps to NM_014700.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:238494740 C>A maps to NM_022449.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:66039635 G>A maps to NM_030981.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr6:57075109 T>A maps to NM_016277.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr5:176728944 A>G maps to NM_130781.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr5:176728924 C>T did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr15:55516127 T>A maps to NM_183235.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr6:146865252 C>T maps to NM_006834.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr23:129306269 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr23:129306193 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr17:27041907 G>A maps to NM_001144943.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr11:87908438 G>A maps to NM_022337.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr23:154490260 C>T did not map to a codon.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr23:154490259 G>C did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr19:18309635 G>C maps to NM_002866.4 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr1:52385646 C>T maps to NM_002867.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr5:57913492 G>A maps to NM_138453.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:135920122 A>G maps to ENST00000283060 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr1:220346066 A>G maps to ENST00000358951 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr23:69502406 G>T did not map to a codon.
Sequencing variant TCGA-AS-3777-01A-01D-0966-08 chr3:128840236 C>A maps to NM_198490.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:128813981 G>A maps to ENST00000418265 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:133553467 C>T maps to NM_016577.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:130738209 G>A maps to NM_032144.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr15:63547743 C>G maps to NM_016530.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr19:42461227 G>T maps to NM_006423.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr16:28922428 C>T maps to NM_024816.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr9:125760993 G>A maps to NM_012197.3 W441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr9:125782627 T>C maps to NM_012197.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:125751641 C>T maps to NM_012197.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:24734892 C>T maps to NM_182836.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr1:76255647 G>A maps to NM_004582.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:114391750 G>A maps to ENST00000409875 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr3:120428687 G>A maps to NM_173825.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr7:6442070 G>C maps to NM_018890.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr19:13058666 G>A maps to NM_005053.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:131953818 A>G maps to NM_005732.3 A1074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr5:131894989 T>C maps to NM_005732.3 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:131976366 T>C maps to NM_005732.3 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr15:40993341 A>T maps to NM_002875.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:17699550 G>T maps to NM_001099218.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr2:17698605 A>G maps to NM_001099218.2 N359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr2:17697414 T>A maps to NM_001099218.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:1036423 A>G maps to NM_134424.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:1023069 T>C maps to NM_134424.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr8:95403998 G>A maps to NM_012415.2 C549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr1:46743872 G>A maps to NM_003579.3 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:51667681 C>T maps to NM_015106.2 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:51697405 C>T maps to NM_015106.2 D1458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr3:51690164 C>T maps to NM_015106.2 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:110969391 A>G maps to NM_152442.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:4841356 G>A maps to NM_018059.4 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr7:4839089 G>A maps to NM_018059.4 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:4876099 G>A maps to NM_018059.4 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr6:150210679 G>A maps to NM_139165.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr6:150211276 A>G maps to NM_139165.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr6:150342041 T>A maps to NM_130900.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:36614944 G>A maps to NM_000536.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr5:34757613 C>G maps to NM_001145521.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:34757667 C>T maps to NM_001145521.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr5:34824235 G>C maps to NM_001145521.1 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr5:34824214 A>G maps to NM_001145521.1 E756E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:17819165 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr23:17819212 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr23:17819772 C>T did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr14:36096962 G>A maps to NM_194301.2 Q1558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr14:36143765 G>A maps to NM_194301.2 Q1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:36143778 A>C maps to NM_194301.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr20:20486075 A>G maps to NM_020343.3 F1677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:20491912 A>T maps to NM_020343.3 L1638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:20475758 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr20:37150281 G>A maps to NM_020336.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr20:37126160 T>C did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr9:135985693 C>A maps to NM_006266.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr16:67840334 C>T maps to NM_020850.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr5:170336744 G>T maps to NM_022897.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr2:109384149 A>G maps to NM_006267.4 R2385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr2:109392303 T>C maps to NM_006267.4 I2803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:109379712 T>C maps to NM_006267.4 N906N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr5:36301484 G>A maps to NM_001161429.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr9:6014374 G>A maps to NM_012416.2 S411S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B0-4836-01A-01D-1373-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:21936723 G>C maps to NM_001145658.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr1:21936672 G>A maps to NM_001145658.1 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:21952820 G>T maps to NM_001145658.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:134505711 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr12:48143586 C>T maps to NM_001098531.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr2:173894948 C>T maps to NM_007023.3 N872N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr5:130841086 T>G maps to ENST00000514667 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr5:130897688 C>T maps to ENST00000514667 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:38346942 C>T maps to ENST00000456989 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:204305854 C>T maps to ENST00000374493 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr2:204305221 T>A maps to ENST00000374493 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr2:204305989 A>G maps to ENST00000374493 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr11:47463273 G>T maps to NM_005055.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:47469614 C>A maps to NM_005055.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr17:38510747 C>T maps to NM_001145301.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:38512459 G>T maps to NM_001145301.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr12:53621179 G>C maps to NM_000966.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr7:150037575 C>A maps to NM_002889.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:167937679 G>T maps to NM_002887.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr5:167919716 C>T maps to NM_002887.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr5:167927654 A>T maps to NM_002887.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr3:141278762 A>G maps to ENST00000452898 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr13:114782718 G>T maps to ENST00000389544 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr1:178421770 C>T maps to ENST00000263528 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr9:85624581 A>T maps to NM_152573.2 Y311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:43696216 C>T maps to ENST00000374459 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:82368696 A>G maps to NM_152545.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr5:179538532 T>C maps to NM_175062.3 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr15:79264228 G>A maps to NM_002891.4 Y1236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:79264260 G>A maps to NM_002891.4 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:38904045 A>T maps to ENST00000405332 C434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr19:49224072 G>C maps to NM_017805.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr12:65004519 A>G maps to NM_178169.2 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:45485140 C>T maps to NM_032023.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:563218 C>T maps to NM_003475.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr12:86199471 C>A maps to NM_005447.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr19:10431798 G>T maps to NM_133452.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr13:49051535 A>G maps to NM_000321.2 E903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr8:53570006 C>T maps to NM_014781.4 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr8:53569321 G>A maps to NM_014781.4 Q1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr8:53554924 G>A maps to NM_014781.4 S1441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr1:33138432 C>T maps to NM_005610.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr16:24580911 A>G maps to NM_006910.4 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr16:24573317 T>G maps to NM_006910.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr16:24583714 A>G maps to NM_006910.4 K1776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:16864058 A>G did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr18:20562276 G>A maps to ENST00000360790 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr16:53495737 G>T maps to NM_005611.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr23:47041265 G>A did not map to a codon.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr21:15599584 C>T maps to NM_144770.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr8:94746442 A>C maps to NM_203390.2 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr8:94747483 A>G maps to NM_203390.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr11:66392255 C>T maps to NM_006328.3 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr11:66392879 C>T maps to NM_006328.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr1:110888164 T>C maps to NM_022768.4 F956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:110882977 T>C maps to NM_022768.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr6:155145480 A>G maps to NM_014892.3 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr10:6143319 C>T maps to NM_001145547.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr12:114364984 T>C maps to NM_016196.3 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr12:114397158 C>T maps to NM_016196.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:114385204 G>A maps to NM_016196.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:23374813 C>G did not map to a codon.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr6:17292139 C>T maps to NM_001143942.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr14:73550236 A>G maps to NM_021239.2 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:79945131 C>T maps to ENST00000438737 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr7:127975594 A>C did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr7:127964663 C>T maps to NM_018077.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr7:127979813 G>A maps to NM_018077.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr7:127961368 T>A maps to NM_018077.2 K505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr23:48434993 T>G did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr23:48434951 T>G did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr23:48434801 C>T did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr7:155537938 T>G maps to NM_053043.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr7:155465596 A>T maps to NM_053043.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr20:34312530 T>C maps to NM_184234.1 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr20:34292610 A>G maps to NM_184234.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:36128156 G>A maps to NM_024321.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36120478 G>A maps to NM_024321.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:238722325 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:238733022 C>T maps to NM_001080504.2 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:178977554 C>T maps to ENST00000456670 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr2:178990776 C>G maps to ENST00000456670 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr4:40440589 G>A maps to NM_001098634.1 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:66444484 G>A maps to NM_031492.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr3:50147867 T>C maps to NM_005778.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr3:50155813 T>A maps to NM_005778.2 Y791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:50005641 C>T maps to NM_005777.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:36206006 A>G maps to NM_001082578.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr3:29925684 T>G maps to NM_001003793.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr23:135960072 C>T did not map to a codon.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr23:135957715 A>G did not map to a codon.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr23:135957698 C>T did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr23:135956573 C>G did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr23:135960229 C>T did not map to a codon.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr23:135956461 G>C did not map to a codon.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr23:135956466 C>T did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:129546640 A>T did not map to a codon.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:89448939 A>G maps to NM_019610.5 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr1:89449134 T>C maps to NM_019610.5 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr1:89448840 T>C maps to NM_019610.5 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr1:89448867 A>T maps to NM_019610.5 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr1:89449140 A>G maps to NM_019610.5 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr4:26426099 C>T maps to NM_005349.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr4:26426304 C>T maps to NM_005349.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr20:43940943 C>T maps to NM_014276.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr8:30361882 A>G maps to NM_001008712.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr9:125620199 A>G did not map to a codon.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr1:24861634 T>C maps to NM_013441.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:50115836 G>A maps to NM_018191.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:50134122 G>C maps to NM_018191.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr13:49086879 T>C maps to NM_001268.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr1:17739592 C>T maps to NM_018715.2 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr1:17743002 T>A maps to NM_018715.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr1:17743002 T>A maps to NM_018715.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:17748728 G>A maps to NM_018715.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:91500667 G>A maps to NM_033544.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr11:66613412 A>C maps to NM_005133.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr4:76439475 T>C maps to NM_015436.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr9:4849484 A>G maps to NM_005772.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr11:63681730 A>T did not map to a codon.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr1:211486236 T>A maps to NM_001136223.1 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr17:9808161 G>A maps to NM_002903.2 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr17:9808239 G>A maps to NM_002903.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:31922208 T>C maps to ENST00000375425 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr14:68157016 G>A maps to NM_016026.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr14:68191258 C>T maps to NM_152443.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr12:57345980 C>T maps to NM_003708.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:56118169 A>T maps to NM_002905.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:10132217 C>A maps to NM_015725.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr17:34249623 C>T maps to NM_145654.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr11:110150411 C>A maps to ENST00000405097 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr17:73657710 A>T maps to NM_004259.5 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:137776731 C>T maps to ENST00000378339 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:61147173 A>C did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:65423174 A>G maps to NM_021975.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr5:141019627 G>A maps to NM_173828.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr7:103130249 G>T maps to ENST00000428762 L3234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:103234872 G>C maps to ENST00000428762 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr7:103159948 T>C maps to ENST00000428762 L2561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr23:153209148 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr23:153205588 A>G did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:153200790 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr7:150069171 C>A maps to NM_001099695.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr6:139233901 C>T maps to ENST00000367663 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:139235872 G>T maps to ENST00000367663 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr23:17092278 C>G did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:8415615 G>T maps to NM_012102.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr1:8424202 C>T maps to NM_012102.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:8421202 T>C maps to NM_012102.3 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr10:43601999 G>C maps to NM_020975.4 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr10:43608352 C>T maps to NM_020975.4 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr2:85573122 C>A maps to NM_017750.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr2:100019182 T>G maps to NM_016316.2 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr6:111711295 G>A maps to NM_002912.3 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:111701284 C>A maps to NM_002912.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr11:114314630 T>C maps to NM_015523.3 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr4:39324977 T>C maps to ENST00000381897 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:39325031 C>T maps to ENST00000381897 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr4:39297337 C>T maps to ENST00000381897 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr7:73661053 A>G maps to NM_181471.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr3:186508150 C>T maps to NM_181573.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr12:118462709 C>A maps to NM_007370.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr17:33348595 G>A maps to NM_001017368.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr22:29837975 C>A maps to NM_021026.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr22:32587022 C>G maps to NM_001098527.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr22:32587082 G>C maps to NM_001098527.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr22:32589042 C>T maps to NM_001098527.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr6:112671197 T>C maps to NM_001013734.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr3:53126087 T>A did not map to a codon.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr3:53139766 G>A maps to NM_052859.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:198508983 C>T maps to NM_144629.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:175914296 A>G maps to NM_022457.5 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:175996825 T>C did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr19:14104646 T>C maps to NM_002918.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr19:5997190 G>A maps to NM_000635.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:107154994 T>A maps to ENST00000357881 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:151315360 G>T maps to NM_000449.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr1:151317011 C>A maps to NM_000449.3 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr6:117248668 C>T maps to NM_173560.3 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:117241585 C>T maps to NM_173560.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr6:117241540 T>C maps to NM_173560.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr6:117248565 G>T maps to NM_173560.3 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr15:56390305 A>G maps to NM_022841.5 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr15:56388044 A>T maps to NM_022841.5 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr15:56388707 T>C maps to NM_022841.5 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:101284213 C>T maps to NM_017819.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr4:100478513 C>T maps to NM_001134666.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:109695056 A>T did not map to a codon.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr23:109694659 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:109694571 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr23:109696888 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr23:109696416 A>G did not map to a codon.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr23:109696031 A>G did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr23:109695934 T>G did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:109696983 G>T did not map to a codon.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr23:109698464 A>G did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr23:71349972 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr23:71351147 C>A did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:71351212 T>C did not map to a codon.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr23:71350155 T>C did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:183885723 G>A maps to NM_015149.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr22:24041047 A>T maps to ENST00000382833 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr5:98115299 A>T maps to NM_001012761.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr5:73144820 T>C maps to NM_001080479.2 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr5:73136426 T>C maps to NM_001080479.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:73161822 C>T maps to NM_001080479.2 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr9:35751269 G>A maps to ENST00000456972 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr2:88125233 T>C maps to NM_001078170.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr2:88125233 T>C maps to NM_001078170.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:107032392 G>A maps to ENST00000304514 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:107073431 G>A maps to ENST00000304514 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:3441323 T>C maps to NM_198229.2 P1419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr4:3432132 G>T did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:3417848 G>A did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:176798988 C>T maps to ENST00000398128 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr6:153332801 A>T maps to NM_012419.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr1:192150458 A>G maps to NM_130782.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:192128418 C>T maps to NM_130782.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr8:54764572 T>C maps to NM_170587.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr8:101054050 G>A maps to NM_015668.3 Y639Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr9:116246491 T>C maps to NM_144488.4 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr1:240969478 G>A maps to ENST00000407727 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr6:49587013 C>T maps to NM_000324.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr2:227771559 T>C maps to NM_001167608.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:75517558 C>T maps to NM_001040456.1 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr22:29656764 C>A maps to NM_012265.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr16:109254 C>T maps to NM_022450.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr17:30621398 T>G maps to NM_138328.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr17:30643270 C>T maps to NM_138328.2 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:30632399 C>T maps to NM_138328.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:90022630 G>A maps to NM_016321.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:25628089 G>A maps to ENST00000357542 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr2:20647606 C>A maps to NM_004040.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr10:62637690 G>A maps to NM_014836.4 C567C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:113244308 C>G maps to NM_175744.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr14:63735886 G>C did not map to a codon.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:720685 G>A maps to NM_138769.1 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5568-01A-01D-1534-10 chr16:720317 C>T maps to NM_138769.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:119249700 T>C did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr19:33493760 A>G maps to NM_033103.4 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr19:33493829 G>A maps to NM_033103.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr11:208889 G>T maps to NM_021932.4 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:107209025 G>T maps to ENST00000392837 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:12847384 G>T did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:38954923 A>C maps to ENST00000296782 Y883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:130892348 A>C maps to NM_015347.4 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:130919338 G>A maps to NM_015347.4 D714D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:73000564 G>A did not map to a codon.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr6:72960118 T>A maps to NM_014989.4 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr6:72960945 T>A maps to NM_014989.4 L858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr6:72974722 A>G maps to NM_014989.4 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr6:73102465 A>G maps to NM_014989.4 G1524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:104513248 T>C maps to NM_001100117.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:41092245 G>T maps to NM_014747.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:41107441 C>T maps to NM_014747.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:66100154 T>C maps to NM_004292.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:66101540 G>A maps to NM_004292.2 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr11:66102087 G>A maps to NM_004292.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:19956189 C>T maps to ENST00000255006 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:19955385 C>T maps to ENST00000255006 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr14:93118452 C>A maps to NM_024832.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:39360339 G>C maps to NM_001195833.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr7:105182934 T>C maps to NM_021930.4 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr6:7410656 G>A maps to NM_031480.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr18:21043936 T>C maps to NM_003831.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr6:3113550 T>A maps to NM_003804.3 L665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr6:3081328 T>C maps to NM_003804.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr8:90802424 G>A maps to NM_003821.5 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr14:24805464 G>T maps to NM_006871.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr14:24808451 C>T maps to NM_006871.3 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr14:24808387 A>G maps to NM_006871.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr21:43166866 G>C maps to ENST00000352483 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr6:84563844 C>T maps to NM_001009994.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:40627265 G>C maps to NM_012421.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr1:40705014 A>G maps to NM_012421.3 T1547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr23:73812619 T>G did not map to a codon.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr23:73811840 T>C did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:73811736 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:73811738 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:73811736 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:73811738 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr23:73812507 C>G did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:73811694 A>G did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:73811738 A>G did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:73811754 C>G did not map to a codon.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr23:73811760 G>T did not map to a codon.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr23:73811736 T>A did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:73811994 G>T did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr19:14139175 C>T maps to NM_080864.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr16:67680180 C>T maps to NM_001013838.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr16:67683207 C>T maps to NM_001013838.1 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:151751271 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr6:151726968 G>T maps to NM_017909.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr6:151744762 T>C maps to NM_017909.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:86947924 G>A maps to NM_022780.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr2:86980657 C>T maps to NM_022780.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr5:177574746 C>T maps to NM_022762.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr14:21024784 A>G maps to NM_001110361.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:182550455 G>A maps to NM_021133.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:182544562 A>G maps to NM_021133.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:182551375 G>A maps to NM_021133.3 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr5:31423044 C>A maps to NM_013235.4 E1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:49251931 C>T maps to NM_014470.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr12:120972754 G>A maps to ENST00000458409 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr2:86832537 A>C maps to NM_005667.3 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr23:119004754 G>A did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr23:106031217 T>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:105970390 T>G did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:105970573 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr23:106034464 G>A did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr3:149678839 C>T maps to NM_007282.4 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr5:179382656 A>G maps to NM_018434.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr17:29311738 A>T maps to NM_032322.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr8:125498659 T>G maps to NM_007218.3 L257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr8:125487508 C>T maps to NM_007218.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr5:158603686 A>G maps to NM_144726.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr5:158630640 C>T maps to NM_144726.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr7:122342195 G>C maps to NM_198085.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr2:101898369 C>T maps to NM_173647.3 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:74158076 C>A maps to NM_052916.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:88765420 C>A maps to NM_178841.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:196214404 G>T maps to NM_152617.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr11:74546694 A>T maps to NM_001098638.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr13:25419106 G>C maps to ENST00000381927 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr13:25352541 T>C maps to ENST00000381927 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr13:25439114 T>C maps to ENST00000381927 H1409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr1:20141318 G>C maps to NM_019062.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:101299910 C>T maps to NM_183419.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:185060811 T>C maps to NM_007212.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr4:1075244 G>A maps to NM_001131034.3 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:78337080 C>G maps to NM_020914.4 A3894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:78293015 C>G maps to NM_020914.4 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr17:78321743 A>G maps to NM_020914.4 A3252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr17:78328248 T>C maps to NM_020914.4 L3628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:78321575 C>T maps to NM_020914.4 R3196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr17:78355390 C>G maps to NM_020914.4 G4663G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KL-8330-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:78318716 G>A maps to NM_020914.4 P2243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:78320903 C>T maps to NM_020914.4 L2972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr7:5752485 G>T maps to NM_207111.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:5781126 G>C maps to NM_207111.2 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:125397822 A>G maps to NM_152553.2 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr6:125366367 C>G maps to NM_152553.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr13:79190196 A>G maps to NM_024546.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:219532705 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr2:219536684 C>G maps to NM_022453.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr14:24619564 C>T maps to NM_017999.4 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr14:24617486 A>G maps to NM_017999.4 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr7:156450263 C>T maps to NM_001184997.1 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:156437190 A>G did not map to a codon.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr6:30043170 G>C maps to NM_025236.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr16:30773994 C>A maps to NM_014771.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr17:56448328 G>T maps to NM_017763.4 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:90342857 A>C maps to NM_001031709.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr2:241514016 C>T maps to NM_018226.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr2:241516159 G>A maps to NM_018226.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:241516156 C>T maps to NM_018226.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr16:2314217 G>C maps to NM_080594.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr3:78706389 G>T maps to NM_002941.3 Y824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:78735004 G>A maps to NM_002941.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:78666911 G>A maps to NM_002941.3 S1385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:78685207 G>A maps to NM_002941.3 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr3:77651361 T>C maps to ENST00000332191 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:77526692 C>T maps to ENST00000332191 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr3:77571940 C>T maps to ENST00000332191 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:124741006 C>A maps to NM_022370.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:124765530 G>A maps to NM_019055.5 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr18:18600157 G>A maps to NM_005406.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr18:18546994 G>A maps to NM_005406.2 Q1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr18:18535178 G>A maps to NM_005406.2 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr2:11361379 T>C maps to NM_004850.3 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr3:125702159 G>A maps to NM_001012337.1 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr1:64643610 A>G maps to NM_005012.2 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:94487338 C>G maps to NM_004560.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr1:151801926 C>A maps to ENST00000392697 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:151789697 G>A maps to ENST00000392697 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr6:117674151 C>A did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr6:117681073 T>C maps to NM_002944.2 R1182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr6:117647552 C>T maps to NM_002944.2 Q1797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:117706857 T>A maps to NM_002944.2 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:55534828 A>G maps to NM_006269.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr8:10470572 C>T maps to NM_178857.5 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr8:10468847 C>T maps to NM_178857.5 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr8:10467236 G>T maps to NM_178857.5 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr23:46713305 C>G did not map to a codon.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr23:46696622 G>T did not map to a codon.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr7:33136130 G>A maps to NM_203288.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:96139816 A>T did not map to a codon.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:96139634 G>A did not map to a codon.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr15:41823329 C>T maps to NM_015540.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr12:48063951 T>G maps to NM_024604.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr1:68903914 G>C maps to NM_000329.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr1:84945168 C>A maps to NM_025065.6 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr23:38180283 T>G did not map to a codon.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr23:38145179 C>T did not map to a codon.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr23:38182652 G>A did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:38145450 T>C did not map to a codon.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr23:38144798 C>A did not map to a codon.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr23:38145699 T>C did not map to a codon.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr23:38145703 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr14:21793035 C>T maps to NM_020366.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr14:21793466 G>A maps to NM_020366.3 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr14:21771588 C>T maps to NM_020366.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr14:21796726 C>T maps to NM_020366.3 Q1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:21769355 C>G maps to NM_020366.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:21769307 C>T maps to NM_020366.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr17:171081 G>A maps to NM_006987.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:89036069 C>T maps to NM_144563.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr23:153627910 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr6:35436590 C>T maps to NM_007104.4 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr9:130213581 G>A maps to NM_000976.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:49118704 C>T did not map to a codon.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr17:37360843 G>A maps to NM_000981.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:6246872 A>T maps to NM_000983.3 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr3:170585833 G>T maps to NM_001099645.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr3:170584195 A>G maps to NM_001099645.1 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr3:101404667 T>C maps to NM_000986.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:52027875 G>T maps to NM_000992.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:52029444 G>A maps to NM_000992.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr22:39711443 A>T maps to NM_000967.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr22:39713524 G>A maps to NM_000967.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr22:39711371 A>C did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:217364691 T>A maps to NM_000998.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:1995883 C>T maps to NM_005061.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr1:93307321 G>C did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:93299159 C>A maps to NM_000969.3 Y44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr9:136216908 T>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr9:136216908 T>A did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr3:128350831 T>A maps to NM_002950.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr20:35842246 G>A maps to NM_002951.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:30314293 C>T maps to ENST00000412529 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr18:33606994 C>T maps to NM_018170.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:150415710 T>C maps to NM_015203.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:150390093 T>C maps to NM_015203.3 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:150445628 C>A maps to NM_015203.3 S1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr2:154334998 C>T maps to NM_019845.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:45056016 C>T maps to NM_203400.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:33240469 G>A maps to NM_022551.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr6:33240436 T>C maps to NM_022551.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr8:56986628 G>A maps to NM_001146227.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr10:79814396 C>T maps to NM_001142285.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:26873741 G>A maps to NM_001006665.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr23:20206636 T>C did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr23:20194423 C>T did not map to a codon.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr23:20195137 T>C did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:20222170 G>A did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr23:20187575 C>T did not map to a codon.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr11:64127743 A>G maps to NM_003942.2 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr23:83320076 A>G did not map to a codon.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr23:83361950 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr17:58022844 C>T maps to NM_003161.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:213244384 T>C did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr1:213341273 C>T maps to NM_012424.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:152128053 T>C maps to NM_001122965.1 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr1:152127951 T>C maps to NM_001122965.1 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:78858926 C>T maps to NM_020761.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr15:40865742 G>T maps to NM_152260.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr11:126080884 T>A maps to NM_032795.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr16:66958809 A>G maps to NM_004165.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:55744772 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:39305248 A>G maps to NM_022157.2 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr20:17600276 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr20:17641023 G>T maps to ENST00000377813 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr6:7246993 C>T maps to NM_001003699.3 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr6:7231265 T>A maps to NM_001003699.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr2:10262858 G>A maps to NM_001165931.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr10:99145672 C>T maps to NM_015179.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr10:99148127 C>A maps to NM_015179.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr10:99120375 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr10:99125880 T>C maps to NM_015179.3 E1167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr10:99116858 G>A maps to NM_015179.3 R1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr21:45096682 T>C maps to NM_015056.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr21:45107949 C>G maps to NM_015056.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr22:42910735 C>T maps to NM_015703.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr22:42910783 C>T maps to NM_015703.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr11:6623148 T>C maps to NM_015324.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr3:51968674 G>A maps to NM_004704.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:51971259 G>T maps to NM_004704.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr23:18660195 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr23:18690180 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:48559511 C>A maps to NM_018346.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr2:7023568 G>A maps to NM_080657.4 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr1:15987647 T>C maps to NM_006511.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr11:77378303 C>T maps to NM_016578.3 R1328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr11:77412359 A>T maps to NM_016578.3 C638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:77412779 T>C maps to NM_016578.3 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr21:43897416 G>A maps to NM_080860.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr7:5984720 C>T maps to NM_173565.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr7:5972411 C>G did not map to a codon.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr6:159420741 A>T maps to NM_031924.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:46317978 G>A maps to NM_030785.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr19:46318401 A>G maps to NM_030785.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:46308229 G>A maps to NM_030785.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:38079541 C>T maps to NM_001038633.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr8:108970371 T>C maps to NM_178565.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:62322287 T>C maps to ENST00000482936 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr15:41769653 A>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:74668861 G>T maps to NM_001015055.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr10:63958098 T>C maps to NM_145307.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr10:63957975 A>C maps to NM_145307.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr14:101351020 C>T maps to NM_001134888.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr14:101350370 C>T maps to NM_001134888.2 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr19:45996517 G>A maps to NM_005619.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr11:63517658 C>A maps to ENST00000377819 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr6:107069325 C>A maps to NM_032730.4 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:1840902 G>T maps to NM_178568.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr18:67871412 C>T maps to NM_173630.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr18:67872494 C>A maps to NM_173630.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr10:70141060 A>G maps to NM_017987.4 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr10:70140990 G>A maps to NM_017987.4 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr4:71648806 G>T did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:218954704 C>T maps to NM_198483.3 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr2:218935327 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr21:36259169 G>T maps to NM_001754.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr8:92982924 G>A maps to NM_175634.2 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr8:93004068 T>G maps to NM_175634.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr1:25256116 C>A maps to NM_001031680.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:155292769 A>C maps to NM_001105203.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr1:155291905 C>A maps to NM_001105203.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr9:35560974 G>A maps to NM_001135999.1 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr9:35547729 A>T maps to NM_001135999.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:127816144 G>T maps to NM_003707.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr19:49517739 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr21:30380356 A>G maps to NM_016940.2 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:155912174 G>A maps to NM_181885.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr9:137300035 C>T maps to NM_002957.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr19:38946384 C>T maps to NM_000540.2 N595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:39039029 T>C maps to NM_000540.2 R4084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr19:38985139 G>A maps to NM_000540.2 A2141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr19:39008077 G>T maps to NM_000540.2 G3255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:39058442 C>T maps to NM_000540.2 P4515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:38948846 C>G maps to NM_000540.2 Y694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:237947722 C>T maps to NM_001035.2 S4237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:237796990 A>G maps to NM_001035.2 E2223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:237895426 C>A maps to NM_001035.2 R3673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:237778052 G>A maps to NM_001035.2 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:237538045 T>C maps to NM_001035.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr15:33988669 T>C maps to NM_001036.3 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr15:34113724 T>G maps to NM_001036.3 G3639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr15:33954437 C>T maps to NM_001036.3 C1569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr15:33873833 C>T maps to NM_001036.3 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr15:34152845 C>T maps to NM_001036.3 R4784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr1:153509894 G>A maps to ENST00000359215 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:153391769 T>C maps to NM_176823.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr19:10334662 T>G maps to NM_004230.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr19:3179455 C>T maps to NM_003775.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr19:10625363 C>T maps to NM_001166215.1 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr13:23915482 T>G maps to NM_014363.4 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr13:23906941 G>A maps to NM_014363.4 F3691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr19:5613493 C>T maps to NM_014649.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr2:234240286 G>A maps to NM_000541.4 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr23:134978475 A>C did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:134990741 A>G did not map to a codon.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr23:134992604 G>A did not map to a codon.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr23:134991923 G>T did not map to a codon.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr16:51174806 G>C maps to ENST00000251020 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr16:51171322 T>C maps to ENST00000251020 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr16:51172850 A>G maps to ENST00000251020 H1094H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:51173804 C>T maps to ENST00000251020 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr14:21992202 C>T maps to NM_005407.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr18:76753525 G>A maps to NM_171999.2 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr18:76753964 G>A maps to NM_171999.2 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr20:50405585 G>A maps to NM_020436.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr20:50407914 C>A maps to NM_020436.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr20:62607108 C>T maps to NM_080621.4 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr17:48191586 A>G maps to NM_174920.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr14:55203898 G>A maps to NM_015589.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr14:55218222 G>T maps to NM_015589.4 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr6:147830099 G>A maps to NM_001030060.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr7:92734735 A>G maps to NM_017654.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr7:92731888 C>T maps to NM_017654.3 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr7:92734660 G>A maps to NM_017654.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr7:92763472 T>C maps to NM_152703.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr7:92763421 G>A maps to NM_152703.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr20:35547820 G>T maps to NM_015474.3 C266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr19:55752902 A>T maps to ENST00000443936 L379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:55743011 T>G maps to ENST00000443936 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr11:68312470 T>C maps to NM_001164160.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr11:68315578 T>A maps to NM_001164160.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:68377389 T>A maps to NM_001164160.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr9:136573486 G>A maps to NM_007101.3 Y464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr9:136550313 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:65744158 C>T maps to NM_005146.4 N593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr12:108920273 G>A maps to NM_014706.3 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:148808751 C>G maps to NM_015278.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr1:100575994 A>G maps to NM_194292.1 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:100572513 A>C maps to NM_194292.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:200193630 T>A maps to NM_001172509.1 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:200245088 G>A maps to NM_001172509.1 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr23:84363715 G>C did not map to a codon.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr14:51131953 C>A maps to NM_021818.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:66456177 G>C maps to NM_016038.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr7:66453384 T>C maps to NM_016038.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr22:50903271 T>C maps to ENST00000337034 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr11:9875240 A>C maps to NM_030962.3 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr11:9809225 C>T maps to NM_030962.3 W1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr19:1132139 G>A maps to NM_001100122.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:1116910 C>T maps to NM_014963.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr19:1108865 G>A maps to NM_014963.2 G1176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr19:36018433 C>T maps to NM_001166034.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr9:127789179 T>G maps to NM_173690.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr15:75143006 T>G maps to NM_005697.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:1924168 G>A maps to NM_079834.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr6:28541172 G>A maps to NM_052923.1 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr6:28543056 T>C maps to NM_052923.1 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr6:28542930 A>T maps to NM_052923.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:47455553 T>A maps to NM_012235.2 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:47456624 C>T maps to NM_012235.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:77087750 A>T maps to ENST00000324767 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:27516083 C>T maps to NM_016240.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr8:27779571 G>A maps to NM_173833.5 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:27779544 C>T maps to NM_173833.5 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr4:77084505 G>A maps to NM_005506.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr4:77095295 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:83557888 G>C maps to NM_001037582.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr14:31122775 A>T maps to ENST00000311943 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr2:224462647 C>T maps to NM_003469.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr15:51993376 A>G maps to NM_013243.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr11:61977949 G>T maps to NM_002407.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr6:25701538 T>C maps to NM_006998.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr3:159606613 A>T maps to NM_001197113.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:239006932 C>T maps to NM_016510.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:41503103 G>A maps to NM_001031694.2 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr23:17768308 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr23:17763602 G>T did not map to a codon.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr3:38798547 G>T maps to NM_006514.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:38802743 A>G maps to NM_006514.2 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr3:38783880 G>T maps to NM_006514.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr3:38739265 G>A maps to NM_006514.2 S1815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:38739682 G>T maps to NM_006514.2 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr3:38888541 G>T maps to ENST00000302328 P1673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:38962723 G>T maps to ENST00000302328 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:166898838 T>C maps to NM_001165963.1 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:166915108 C>T maps to NM_001165963.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr2:166847874 T>C maps to NM_001165963.1 T1970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:166153544 A>T maps to NM_001040142.1 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr2:166170261 T>G maps to NM_001040142.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:166201261 C>G maps to NM_001040142.1 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr2:165947166 G>C maps to NM_006922.3 V1832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:166012355 G>T maps to NM_006922.3 Y363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:165987816 G>T maps to NM_006922.3 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr11:123513373 G>A maps to NM_018400.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr17:62024486 G>T maps to NM_000334.4 S1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr17:62029158 G>T maps to NM_000334.4 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:62021159 G>A maps to NM_000334.4 N1321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045581 C>T maps to NM_000334.4 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045584 C>T maps to NM_000334.4 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:38647615 G>T maps to NM_001099404.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:167060899 C>T maps to ENST00000303354 K1492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:23360138 C>G maps to ENST00000307331 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr4:141302256 A>G maps to NM_001153484.1 *160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr17:55058512 C>G maps to NM_021626.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr8:144874054 C>T maps to NM_182706.3 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr8:144890885 G>A maps to NM_182706.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr17:45918191 A>G maps to NM_138355.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr2:175289229 G>A maps to NM_024583.4 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:656173 G>A maps to NM_033129.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr22:43625096 G>A maps to NM_173050.2 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr22:43614318 C>T maps to NM_173050.2 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr11:9048917 C>A maps to ENST00000457346 R898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr6:35212547 C>T maps to ENST00000394681 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:35213119 G>A maps to ENST00000394681 K855K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr6:35182248 C>T maps to ENST00000394681 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr11:65293510 C>T maps to NM_020680.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:65305493 G>A maps to NM_020680.3 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr12:100704844 G>A maps to NM_017988.4 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr12:100731224 C>T maps to NM_017988.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:169831810 G>A maps to NM_181093.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:169824949 A>T maps to NM_181093.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr4:76897075 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:76877178 C>T maps to NM_018115.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr2:20402565 G>C maps to NM_001006946.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr2:20403633 C>T maps to NM_001006946.1 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr2:20403726 C>T maps to NM_001006946.1 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:31347252 G>T maps to NM_014654.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr14:50256252 C>T maps to NM_004713.3 Q886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr14:50312884 G>C maps to NM_004713.3 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr1:243581286 T>C maps to NM_006642.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:243419489 G>A maps to NM_006642.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr7:4011188 G>T maps to NM_152744.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr7:4014045 G>A maps to NM_152744.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr7:4152924 C>T maps to NM_152744.3 R1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr7:4056808 C>T maps to NM_152744.3 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr17:71415435 G>T maps to NM_001144952.1 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr17:71429904 C>T maps to NM_001144952.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr17:71420173 G>A maps to NM_001144952.1 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr17:71375626 C>A maps to NM_001144952.1 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr8:57219233 C>T did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:82032716 C>A maps to NM_145168.2 *394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr12:113865885 T>A maps to NM_138432.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:10346827 G>A maps to ENST00000343726 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr17:75209463 C>T maps to NM_001039573.2 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr22:30856106 G>T maps to NM_174975.4 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr22:30888521 G>T maps to NM_174977.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr9:139360546 G>T maps to NM_014866.1 Y1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr1:177927419 A>C maps to NM_033127.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr3:42602762 C>T maps to NM_032970.2 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr14:39511998 A>C maps to NM_006364.2 Y659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr5:134002686 G>A did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr10:75520025 C>T maps to NM_198597.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr10:75519463 G>A maps to NM_198597.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:119666216 T>A did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr4:119718965 C>T did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr4:83788376 A>G maps to ENST00000505472 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr4:83774803 G>A maps to ENST00000505472 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:127774578 C>T maps to ENST00000464451 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr3:127785927 C>T maps to ENST00000464451 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:169706124 C>T maps to NM_003262.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr6:108227976 A>G maps to NM_007214.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:49293278 A>C maps to NM_001193489.1 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:49304925 A>T maps to NM_001193489.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr15:49301546 A>C maps to NM_001193489.1 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:49320718 G>T maps to NM_001193489.1 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:13868445 G>T maps to NM_025229.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr1:169701066 T>C maps to NM_000450.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr1:151337663 C>G did not map to a codon.
Alternatively spliced codon TCGA-B0-5694-01A-11D-1534-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr1:151342243 A>C maps to ENST00000435071 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr1:151339306 C>T maps to ENST00000435071 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151339348 G>A maps to ENST00000435071 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:169677786 A>T maps to NM_000655.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr22:50649113 C>T maps to NM_031454.1 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr1:169565277 A>G maps to NM_003005.3 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr12:109017990 G>A maps to ENST00000228463 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr7:83640553 A>G maps to NM_006080.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr7:83590704 C>T maps to NM_006080.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:83739848 G>A maps to NM_006080.2 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr3:50310780 C>T maps to NM_004636.2 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr7:80458055 G>A maps to NM_006379.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr7:83023611 C>G did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr7:82996991 G>A maps to NM_012431.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr7:82997338 T>A maps to NM_012431.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:156146589 A>G maps to NM_022367.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:90768608 C>T maps to NM_198925.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr9:92017851 C>T maps to NM_006378.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr9:91994190 A>G maps to NM_006378.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:92007356 A>T maps to NM_006378.3 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr2:74902020 G>T maps to NM_004263.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr10:102732886 G>A maps to NM_017893.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr5:9226980 C>T maps to NM_003966.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:9119219 A>T maps to NM_003966.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr5:115803360 C>G maps to ENST00000257414 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr5:115822557 G>A maps to ENST00000257414 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:151109385 C>T maps to NM_001178061.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:151112137 T>C maps to NM_001178061.1 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr1:151105697 C>T maps to NM_001178061.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr15:48063501 G>A maps to NM_153618.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr20:43837137 T>C maps to NM_003007.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr17:7470322 G>A did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr6:76421099 A>T maps to NM_015571.2 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr3:101060581 C>A maps to NM_020654.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr15:72432090 C>T maps to NM_145204.3 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr16:30455758 G>T maps to ENST00000478753 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr4:77941775 T>G maps to ENST00000510515 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:242283309 C>A maps to ENST00000391972 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr22:42383240 G>A maps to NM_145733.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr22:42383653 G>T maps to NM_145733.2 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr17:56603080 C>A maps to NM_004574.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr22:19710007 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:19709429 C>T maps to NM_002688.5 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr23:118797594 T>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:35912376 G>A did not map to a codon.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr6:158565366 A>G maps to NM_032861.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:158565366 A>G maps to NM_032861.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr6:158541584 T>C maps to NM_032861.3 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr6:122777746 A>G maps to NM_020755.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr15:44087391 C>A maps to ENST00000319327 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr14:94756789 C>T maps to NM_001100607.1 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr14:95029882 C>T maps to NM_006215.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:105280774 A>G did not map to a codon.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr23:105278360 C>A did not map to a codon.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr14:94936171 T>C maps to NM_175739.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr6:2836101 C>T maps to NM_030666.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr18:61600418 C>T maps to NM_005024.1 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr18:61264229 G>A maps to NM_012397.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr18:61264229 G>A maps to NM_012397.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr18:61310790 G>C maps to NM_002974.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:2948771 C>A maps to ENST00000316782 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr6:2955760 G>C maps to ENST00000316782 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr18:61471601 A>G maps to NM_001040147.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:21140327 G>A maps to NM_000185.3 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:100780345 G>C maps to NM_000602.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr7:100780309 C>T maps to NM_000602.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr2:224866440 C>T maps to NM_001136530.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr2:224862979 G>A maps to NM_001136530.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:1673259 C>A maps to NM_002615.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr17:1648686 C>T maps to NM_000934.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr3:167508175 C>T maps to NM_005025.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr3:167170763 G>A maps to NM_006217.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:64863636 A>G maps to NM_014755.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr1:210412916 G>A maps to NM_019605.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr1:210415006 A>C maps to NM_019605.3 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr18:42281355 C>T maps to NM_015559.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr18:42531245 A>G maps to NM_015559.2 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr18:42533243 C>T maps to NM_015559.2 D1313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr16:30977376 C>G maps to NM_014712.1 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr16:30991932 C>T maps to NM_014712.1 D1512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr3:47079268 T>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr3:47098859 C>T maps to NM_014159.6 Q2138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr3:47155364 C>A did not map to a codon.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr3:47163944 G>T maps to NM_014159.6 C727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr3:47162786 A>C maps to NM_014159.6 Y1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr3:47127736 C>T maps to NM_014159.6 W1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr3:47164612 C>A maps to NM_014159.6 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr3:47164497 G>T maps to NM_014159.6 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr3:47129721 C>A maps to NM_014159.6 E1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr3:47143033 G>A maps to NM_014159.6 N1643N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr3:47163796 C>A maps to NM_014159.6 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr3:47164446 G>T maps to NM_014159.6 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr3:47155364 C>T did not map to a codon.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr3:47079154 C>G did not map to a codon.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr3:47142964 A>C maps to NM_014159.6 Y1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr3:47161670 C>G did not map to a codon.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr3:47125379 C>A maps to NM_014159.6 E1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr3:47061275 T>A maps to NM_014159.6 K2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47143046 T>C did not map to a codon.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:47127735 C>T maps to NM_014159.6 W1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr3:47164729 T>A maps to NM_014159.6 K466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr3:47098902 A>T maps to NM_014159.6 L2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:47162023 G>A maps to NM_014159.6 Q1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:47098444 G>A maps to NM_014159.6 Q2277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr3:47163208 T>A maps to NM_014159.6 R973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr3:47084093 G>A maps to NM_014159.6 R2399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr3:47164504 G>T maps to NM_014159.6 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr14:99932085 A>G maps to NM_032233.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr14:99929880 C>T maps to NM_032233.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr21:37418116 T>C maps to NM_017438.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr21:37416206 C>T maps to NM_017438.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr21:37418056 C>T maps to NM_017438.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr21:37408417 G>C maps to NM_017438.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr3:9512541 T>C maps to ENST00000407969 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr3:9486833 A>C maps to ENST00000407969 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr16:58549931 T>C maps to NM_001160305.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr9:135158713 T>C maps to ENST00000372169 L2161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr9:135173489 G>A maps to ENST00000372169 L1920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr17:27287869 C>T maps to NM_178860.4 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr22:26688759 G>T maps to NM_021115.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:26702083 G>A maps to NM_021115.4 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr11:64533400 A>C maps to NM_004630.3 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr22:30740939 T>A maps to NM_005877.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr19:2245451 C>A maps to NM_007165.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:2248400 G>A maps to NM_007165.4 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:198285206 T>C maps to NM_012433.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr2:198257041 A>C maps to NM_012433.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr11:65820517 G>A maps to NM_006842.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr11:65829381 C>A maps to NM_006842.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr16:70605580 G>A maps to NM_012426.4 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:19420930 C>T maps to NM_172231.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr22:32000341 C>T maps to NM_001007467.1 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr10:7239536 C>A maps to NM_001018039.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:7214000 G>A maps to NM_001018039.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr7:37955989 C>A maps to ENST00000223214 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr10:99531062 T>C maps to NM_003015.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr17:56083836 G>T maps to NM_006924.4 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr19:19136451 G>A maps to NM_001017392.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr19:19121012 G>A maps to NM_001017392.3 Y663Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr21:33043797 T>A maps to NM_020706.2 K1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr21:33044134 A>G maps to NM_020706.2 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr21:33057762 A>G maps to NM_020706.2 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:45572383 T>G did not map to a codon.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr23:1713016 A>G did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr23:1712875 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr23:1718089 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr23:1712781 G>A did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr23:1719997 C>T did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:99848472 A>T maps to NM_032870.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr6:99858628 C>T maps to NM_032870.2 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr17:74732440 T>C maps to NM_003016.4 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:74732523 G>A maps to NM_003016.4 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr12:46328262 T>C maps to NM_004719.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:46318585 T>A maps to NM_004719.2 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr1:29475062 G>C maps to NM_005626.4 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr10:81371397 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:81702147 G>C maps to NM_003019.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr10:81702177 G>A maps to NM_003019.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr17:48245012 C>T maps to NM_000023.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:156186310 C>T maps to NM_000337.5 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr7:94257636 T>A maps to NM_001099401.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr13:23869611 G>T maps to NM_000231.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr3:153870722 T>A did not map to a codon.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr1:67101649 C>T maps to NM_032291.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:8235102 A>T maps to NM_001080826.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr15:77406688 G>A maps to NM_024776.2 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr15:77407252 G>A maps to NM_024776.2 L1496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr15:77472612 A>T maps to NM_024776.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:201438488 T>G maps to NM_152524.5 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr10:72617448 T>C did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr22:25251634 T>A maps to NM_001039948.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr22:40800333 C>T maps to NM_015705.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr22:40803847 G>C did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr22:40804934 A>G did not map to a codon.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr22:40802518 C>T maps to NM_015705.4 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr22:40802190 G>T maps to NM_015705.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:111885275 G>A maps to NM_005475.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr1:162368718 T>G maps to NM_053282.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr8:19252098 C>T maps to NM_022071.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr15:78385102 G>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:80532506 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:38051327 C>A maps to NM_018957.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr2:235950114 G>A maps to NM_014521.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15298470 G>A maps to NM_004844.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:249106347 G>C maps to NM_030645.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr19:4363419 G>A maps to NM_003025.2 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:17787381 A>G maps to NM_003026.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:19560044 C>A did not map to a codon.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr23:19587267 A>T did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:19626145 G>T did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr23:19854347 C>T did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr4:170043336 A>G maps to NM_020870.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr4:170028337 A>G maps to NM_020870.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr5:145428751 C>T maps to NM_152550.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:110053414 G>T maps to NM_001099289.1 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr4:8229880 A>T maps to NM_018986.3 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:8230106 C>T maps to NM_018986.3 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr5:148407014 A>G maps to NM_024577.3 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr19:51219978 G>A maps to ENST00000391814 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:51215206 G>A maps to ENST00000391814 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:70349009 G>A maps to ENST00000338508 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr11:70338535 G>T maps to ENST00000338508 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:51117230 C>T maps to NM_001080420.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr17:7534019 C>T maps to NM_001040.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr1:154938021 A>C maps to NM_001130040.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr19:434717 G>A maps to NM_012435.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr9:91680465 A>C maps to NM_016848.5 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:4290584 C>T maps to NM_020209.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr19:4280224 G>A maps to NM_020209.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr7:155596097 G>A maps to NM_000193.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr13:26625046 G>A maps to NM_001007538.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr13:26625046 G>A maps to NM_001007538.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr1:201860696 G>T did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr3:48510781 C>T maps to NM_016479.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr17:18243555 G>T maps to NM_004169.3 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr12:57627118 C>A maps to NM_005412.5 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr10:112764371 A>G maps to NM_007373.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:3514080 G>T maps to NM_013276.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:132161118 C>T maps to NM_001172700.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr23:9900829 G>T did not map to a codon.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr23:9863547 C>T did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr23:9905225 A>G did not map to a codon.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr23:9900607 A>C did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr4:77662124 C>T maps to NM_020859.3 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr23:50556988 G>A did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:50350751 T>C did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr23:50350697 C>T did not map to a codon.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr23:50350757 C>T did not map to a codon.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr23:50376677 T>A did not map to a codon.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr23:50341292 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr23:50350750 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr23:50350697 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr23:50350697 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr23:50350757 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr23:50556985 G>A did not map to a codon.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr23:50376363 A>G did not map to a codon.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr3:164741458 G>A maps to NM_001041.3 Q1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr16:48396057 T>A maps to NM_001006610.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr3:150460185 G>C maps to NM_005067.5 Y239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr20:3677900 G>C maps to NM_023068.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr20:3669218 T>C maps to NM_023068.3 P1706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr20:3679975 G>A maps to NM_023068.3 H553H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr19:51919242 G>A maps to NM_033130.4 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:50461597 G>A maps to NM_052884.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr19:50453229 C>T maps to NM_052884.2 K698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr19:52001299 C>A maps to NM_053003.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr19:52000157 G>A maps to NM_053003.2 N525N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr19:52132740 G>A maps to ENST00000222107 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51646039 G>A maps to NM_014385.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr19:51958702 G>A maps to NM_014442.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr21:44840176 G>A maps to NM_173354.3 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:111590500 C>T maps to NM_015191.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr5:138378409 T>A did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr12:56348042 A>G maps to NM_006928.3 C647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr15:75702578 A>G maps to NM_001145357.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr15:75673956 T>A maps to NM_001145357.1 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:75692464 C>T maps to NM_001145357.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:75664532 G>A maps to NM_001145357.1 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr15:75705129 G>A maps to NM_001145357.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:16982118 G>A maps to NM_015260.1 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr14:72169178 G>A maps to NM_015556.1 T1201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr14:72055086 T>C maps to NM_015556.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr1:232650233 T>G maps to NM_020808.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr1:232651060 C>A maps to NM_020808.3 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr1:232607211 T>A maps to NM_020808.3 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:232649813 A>T maps to NM_020808.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr19:38572297 A>G maps to NM_015073.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr20:1902131 A>T maps to ENST00000400068 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr20:1895841 T>C maps to ENST00000400068 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr20:1460663 G>T maps to NM_001122962.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr20:1460669 T>C maps to NM_001122962.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr20:1615979 C>A maps to NM_018556.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr20:1617068 A>G maps to NM_018556.3 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:224194 G>A maps to NM_012239.5 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:79870324 G>A maps to NM_016538.2 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:105222012 C>T maps to NM_006427.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr2:45171736 C>A maps to NM_005413.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr13:21746644 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr13:21732195 A>G maps to NM_145061.5 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr13:21742125 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:46239836 C>G maps to NM_003726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr7:26894414 A>G maps to NM_003930.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr1:2234821 G>A maps to NM_003036.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:2238152 G>A maps to NM_003036.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr3:170078220 G>A maps to NM_005414.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr6:31930532 G>A maps to NM_006929.4 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr5:54645467 A>G maps to NM_015360.4 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr5:54618205 T>C maps to NM_015360.4 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr5:54701365 T>A maps to NM_015360.4 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr20:35262936 G>A maps to NM_032214.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr13:103718248 A>T maps to NM_000452.2 Y117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr23:153716012 C>G did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:48518685 C>G maps to NM_000338.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr5:127477608 T>G maps to NM_001046.2 L570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr5:127488498 T>G did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:127477531 T>A maps to NM_001046.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr16:56906658 A>G maps to NM_000339.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr16:67979423 C>A maps to NM_005072.4 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44670174 C>T maps to NM_001134771.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr20:44669097 C>T maps to NM_001134771.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr15:34546784 A>G maps to NM_133647.1 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr5:1064224 C>G maps to NM_006598.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr5:1073765 C>T maps to NM_006598.2 E741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr5:1094289 C>T maps to NM_006598.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr5:1093743 C>A maps to NM_006598.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:124930169 C>T maps to NM_001195483.1 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr7:100459531 C>T maps to NM_020246.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr7:122757653 G>A maps to NM_022444.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:122765635 A>G maps to NM_022444.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr17:26817925 T>G did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr20:45192088 G>A maps to NM_022829.5 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr7:135370371 C>T maps to NM_012450.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr7:135390993 G>A maps to NM_012450.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:135370356 C>A maps to NM_012450.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:6597516 C>G did not map to a codon.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr17:6594202 G>A maps to NM_177550.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr17:6606362 G>T maps to NM_177550.3 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr18:43319598 G>A maps to NM_001146037.1 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr18:43249306 C>T maps to NM_007163.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr18:43212330 G>T maps to NM_007163.3 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr3:121613337 G>A maps to NM_021082.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr3:121659850 C>A maps to NM_021082.3 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:60709587 A>C maps to NM_016582.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr11:60711235 G>A maps to NM_016582.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr1:113460276 G>A maps to NM_003051.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:6946082 C>T did not map to a codon.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr17:6941492 C>T maps to NM_201566.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr17:6942203 C>G maps to NM_201566.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr2:230910734 G>A maps to NM_152527.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr2:230914570 C>G maps to NM_152527.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr23:73745645 T>C did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr23:73641568 T>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:73744293 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:80194626 G>C maps to NM_001042423.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:110921781 A>C maps to NM_004696.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr17:73096900 A>T maps to ENST00000450736 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr17:73096579 C>T maps to ENST00000450736 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr17:66270211 C>A did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:66267172 A>G maps to NM_004694.4 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr22:38476982 G>A maps to NM_013356.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr10:61413931 C>T maps to NM_194298.2 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr6:25830752 T>C maps to NM_005074.3 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr6:25811998 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr6:25913556 A>C maps to NM_005835.2 L426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr6:25850133 A>G maps to NM_001098486.1 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr6:25779370 A>T maps to NM_005495.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:22397593 C>A maps to NM_020346.2 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr19:49934325 G>A maps to NM_020309.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:100796247 T>C maps to NM_139319.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr10:119029904 G>T maps to NM_003054.4 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:119003519 G>T maps to NM_003054.4 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr21:46951438 G>A maps to NM_194255.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr21:46951555 A>G maps to NM_194255.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:169446749 G>A maps to NM_006996.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr11:35338966 A>G maps to NM_004171.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:65217142 C>A maps to NM_003038.4 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:15063792 C>T maps to NM_005071.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr1:53608094 C>T maps to NM_006671.4 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:53555557 G>A maps to NM_006671.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr2:113418128 G>A maps to NM_005415.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr2:113420442 G>T maps to NM_005415.3 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:113404572 A>G maps to NM_005415.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr8:42294727 C>T maps to NM_006749.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:63065115 A>T maps to NM_001039752.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr11:63057714 C>G maps to NM_001039752.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr11:64326671 C>T maps to NM_018484.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr11:64326665 C>T maps to NM_018484.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr11:64360345 C>A maps to NM_144585.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:38316202 T>C maps to NM_004256.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:38316609 C>A maps to NM_004256.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr1:116534698 G>C maps to NM_018420.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:110746233 C>A maps to NM_033125.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr11:64991020 G>A maps to ENST00000438990 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr6:3324227 G>A maps to ENST00000436008 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:160769795 C>T maps to ENST00000392145 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131647951 A>C maps to NM_003059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr5:131630692 C>T maps to NM_003059.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:131729503 G>A did not map to a codon.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr11:62744738 A>G maps to NM_004790.3 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr6:43266248 G>A maps to ENST00000372585 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr6:43272448 C>T maps to ENST00000372585 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr11:63175622 T>A maps to NM_080866.2 L443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr20:4864397 T>G maps to NM_203327.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr20:4839998 G>A maps to NM_203327.1 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:220030022 A>G maps to NM_001144890.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr15:65942808 A>G maps to NM_004727.2 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr20:19679324 G>C did not map to a codon.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr14:92958091 C>T maps to NM_153646.3 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr12:113737764 T>G maps to NM_024959.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr12:113742185 G>A maps to NM_024959.2 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:19164389 G>A maps to NM_005984.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr7:95818644 C>T maps to NM_001160210.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr23:129499646 A>C did not map to a codon.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr23:129483275 G>T did not map to a codon.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr17:73279617 G>A maps to NM_021734.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:140683029 G>A maps to NM_031947.2 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:140683387 C>T maps to NM_031947.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr3:48900023 C>T maps to NM_000387.4 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr14:37194882 C>G did not map to a codon.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr3:66428111 A>C did not map to a codon.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr14:100758954 G>A maps to NM_001039355.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr14:100759045 C>A maps to NM_001039355.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:39431017 C>T maps to NM_017875.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr17:42399918 C>T maps to NM_001143780.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr7:87483611 T>C maps to NM_018843.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr1:156169865 G>T maps to NM_014655.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr1:156169880 C>A maps to NM_014655.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr23:118603863 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr23:118604408 C>T did not map to a codon.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr23:118603863 G>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:118603719 T>G did not map to a codon.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr23:118603755 T>A did not map to a codon.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr23:118603728 G>A did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr23:1505636 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:1506260 G>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:983982 T>C maps to NM_213613.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:983646 C>T maps to NM_213613.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:982689 A>G maps to NM_213613.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:78215585 C>T maps to NM_173626.3 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:149361288 T>C maps to NM_000112.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr7:107315387 A>T did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr7:107334907 C>T maps to NM_000441.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr7:107329536 G>A maps to NM_000441.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr7:103029856 G>A maps to ENST00000354356 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:103018051 C>A maps to ENST00000354356 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:103029510 A>G maps to ENST00000354356 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:103017285 G>T maps to ENST00000354356 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:48668740 T>C did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr3:48669761 G>A maps to NM_022911.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr6:35922940 G>A maps to NM_052961.3 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr6:35949920 C>T maps to NM_052961.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr6:35922961 G>A maps to NM_052961.3 Y733Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr6:35930386 A>G maps to NM_052961.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:50528291 G>A maps to NM_003645.3 *621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr1:153750665 G>T maps to ENST00000271857 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:128321006 C>T maps to NM_001017372.1 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr15:85451986 G>T maps to NM_004213.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:85476452 G>A maps to NM_004213.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr15:45559672 C>A maps to NM_004212.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:86895779 G>A maps to NM_022127.2 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr6:44197390 C>T maps to ENST00000313248 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr10:73121851 G>A maps to NM_018344.5 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr7:5342509 C>T maps to NM_153247.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr7:5338713 T>C maps to NM_153247.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:43394676 G>T maps to NM_006516.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:45355543 C>T maps to NM_030777.3 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr22:24226510 C>T maps to NM_030807.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:8083894 A>T maps to NM_006931.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:8074167 A>G maps to NM_006931.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr20:62373330 T>A maps to NM_020062.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr20:62374340 T>C maps to NM_020062.3 *388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr1:9118228 A>T maps to NM_003039.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr9:136340533 G>A maps to NM_017585.3 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr9:130167741 A>G maps to NM_014580.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr4:42077745 T>C maps to NM_006345.3 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:37356312 C>T maps to NM_080552.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr3:155547593 C>T maps to NM_004733.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr5:176825283 C>A maps to NM_003052.4 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr4:25664145 A>G maps to NM_006424.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr4:25667855 C>A maps to NM_006424.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr9:140126521 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr6:88210967 T>C maps to NM_006416.4 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr23:48762074 G>A did not map to a codon.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr23:48762339 C>T did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:139947278 T>A maps to NM_080670.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr5:139946852 T>C maps to NM_080670.2 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:47781477 T>A maps to ENST00000415270 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:44224153 C>T maps to NM_178148.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr6:44224428 C>T maps to NM_178148.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr6:8413925 T>C maps to NM_001142540.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr6:8417151 A>T maps to NM_001142540.1 L317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr6:8422802 C>G maps to NM_001142540.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr1:67486081 A>C maps to NM_015139.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:67519573 C>A maps to NM_015139.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr12:69140525 G>A maps to NM_018656.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:234458835 C>T maps to NM_173508.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:234454500 T>A maps to NM_173508.2 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:114512804 A>C maps to NM_025181.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr5:150838430 G>A maps to NM_078483.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr5:150867781 C>T maps to NM_078483.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr5:150701631 A>G maps to NM_181776.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:150660716 G>T maps to NM_001145017.1 Y375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:92917686 C>A did not map to a codon.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr12:46623009 T>C maps to NM_030674.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr12:46633472 A>G maps to NM_030674.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr17:79268691 C>T maps to NM_001037984.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr17:79220706 G>A maps to NM_001037984.1 D740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:79220315 C>T maps to NM_001037984.1 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr17:79257256 C>A maps to NM_001037984.1 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr17:79219502 G>A maps to NM_001037984.1 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr12:46760865 G>A maps to NM_018976.4 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:46760916 T>C maps to NM_018976.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr16:58713826 C>T maps to NM_018231.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:84063152 A>G maps to NM_001080442.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr16:84050800 C>A maps to NM_001080442.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr1:153934707 G>T maps to NM_014437.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr1:153932642 C>T maps to NM_014437.3 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:196545177 G>T maps to NM_001127257.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr10:18250700 G>A maps to NM_001145195.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr11:47433930 G>A maps to NM_001128225.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr19:2732985 T>C maps to NM_144564.4 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56630208 C>G maps to NM_001135195.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr18:33689576 G>A maps to NM_012319.3 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr6:33170810 C>T maps to NM_006979.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:33169432 T>C maps to NM_006979.2 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr14:69866097 C>T maps to NM_018375.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr2:44547378 A>G maps to NM_000341.3 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr2:44507852 A>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:44508524 G>C did not map to a codon.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr11:62652669 C>T maps to NM_001012661.1 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:62648665 G>A maps to NM_001012661.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr1:205767923 G>A maps to NM_173854.4 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:57268328 C>T did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr11:57182148 G>A maps to ENST00000428603 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr9:108128707 C>T maps to NM_080546.3 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr1:95286512 A>G maps to NM_001114106.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:95330397 T>A maps to NM_001114106.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr1:8390935 C>T maps to ENST00000377479 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:142238283 G>A maps to NM_001080431.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr13:29278213 A>G maps to NM_001135919.1 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr13:29275083 T>G maps to NM_001135919.1 *464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr17:19582220 T>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:42335910 T>A maps to NM_000342.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr17:42333124 G>A maps to NM_000342.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr2:162696377 A>G maps to NM_001178015.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:162815016 A>G maps to NM_001178015.1 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr20:3210300 G>A maps to NM_001174090.1 N580N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr7:150763998 T>C maps to NM_003040.3 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr2:220497111 T>C maps to NM_201574.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr2:220497000 C>T maps to NM_201574.2 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr4:72313419 C>T maps to NM_001098484.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:72429511 T>A maps to NM_001098484.2 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr3:27451005 C>T maps to ENST00000454389 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:18863862 C>T maps to NM_152351.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr17:18916792 C>T maps to NM_152351.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:18923132 C>T maps to NM_152351.3 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr17:18918395 G>C maps to NM_152351.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:26725401 A>G maps to NM_178498.3 H206H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr11:26718742 A>G maps to NM_178498.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr21:35467805 G>C maps to NM_006933.4 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr21:35468405 C>G maps to NM_006933.4 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:27427729 G>C maps to NM_021095.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:108604762 T>A maps to NM_021815.2 L51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr12:101560444 G>T maps to NM_145913.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:101588896 C>T maps to NM_145913.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr1:48694800 C>T maps to NM_001135181.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:10960100 C>T maps to NM_014229.1 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr12:318975 G>C maps to NM_003044.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr23:115573955 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr23:115568960 G>C did not map to a codon.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr12:85279277 A>G maps to NM_182767.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:49797186 C>T maps to NM_014037.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:110709685 C>T maps to NM_001010898.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr5:1219217 C>T maps to NM_001003841.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr16:55734211 T>C maps to NM_001043.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:55705979 C>T maps to NM_001043.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:55690629 G>A maps to NM_001043.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr3:14508106 A>G maps to NM_001134367.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:152960546 C>T did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr23:152958792 T>C did not map to a codon.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr23:152957539 A>G did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr23:152954166 C>A did not map to a codon.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr23:152956788 T>A did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr23:152956938 A>G did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr23:152956888 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:44467232 G>C maps to NM_201649.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr13:30098299 G>A maps to NM_003045.4 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr13:30096466 C>T maps to NM_003045.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr19:33702228 G>A maps to NM_019849.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr8:87229701 A>G maps to NM_138817.2 Y392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr8:87242197 C>T maps to NM_138817.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr8:87226721 T>A maps to NM_138817.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr3:170185028 G>A maps to NM_020949.2 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:170198276 G>A maps to NM_020949.2 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:17419588 G>A maps to NM_001164771.1 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr8:17412116 G>A maps to NM_001164771.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:17401958 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr8:17409423 G>A maps to NM_001164771.1 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr23:70147813 A>C did not map to a codon.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr23:70147193 G>A did not map to a codon.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr23:70148385 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr23:70147707 A>C did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr23:70145692 A>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:70147757 A>G did not map to a codon.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr22:21385633 G>A maps to NM_004173.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr22:21385822 C>T maps to NM_004173.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr22:21385372 G>C maps to NM_004173.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr16:87885387 G>A maps to NM_003486.5 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr16:87871507 G>A maps to NM_003486.5 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr16:68328655 C>A maps to NM_003983.4 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr16:68325150 G>A maps to NM_003983.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr14:23243679 T>C maps to NM_001126106.1 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr14:23635684 C>A maps to NM_012244.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:40342425 G>A maps to NM_021097.2 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr19:47969449 G>T maps to NM_015063.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr14:70527577 C>T maps to NM_183002.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27428599 C>T maps to NM_003047.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:27440752 G>C maps to NM_003047.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr3:111983129 T>C maps to NM_183061.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr5:482712 G>A maps to NM_004174.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:475167 G>A maps to NM_004174.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:72745285 A>T maps to NM_004252.3 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr2:103120166 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr2:103148952 G>T maps to NM_001011552.3 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr16:67290935 C>T maps to NM_004594.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:135098842 T>A did not map to a codon.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr23:135080341 A>C did not map to a codon.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr23:135080322 T>C did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr23:46522059 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:46491074 A>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:46529081 A>G did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:48431565 T>C maps to ENST00000417961 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr12:21471821 G>T maps to NM_134431.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr12:21454186 T>A maps to NM_134431.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr12:21355423 G>T did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:21032478 G>T maps to NM_019844.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr12:20905249 C>T maps to NM_017435.4 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:133692537 G>C maps to NM_005630.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr11:74915492 C>T maps to NM_007256.4 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr20:61300315 G>T maps to NM_016354.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr20:61300282 G>A maps to NM_016354.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr5:101631680 G>A maps to NM_180991.4 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:101592956 G>C maps to NM_180991.4 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:101834203 C>A maps to NM_173488.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr5:101811426 G>A maps to NM_173488.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr17:33679557 T>C maps to NM_152270.3 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr17:33679779 G>A maps to NM_152270.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr17:33690265 C>T maps to NM_152270.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:33749974 C>A maps to NM_018042.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr17:33802319 A>G maps to ENST00000361112 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr17:33591511 C>A maps to NM_144975.3 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:33586029 T>G maps to NM_144975.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr4:20535254 T>A maps to ENST00000273739 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr4:20490576 G>A maps to ENST00000273739 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr4:20543096 T>C maps to ENST00000273739 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr4:20512748 T>C maps to ENST00000273739 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr5:168098201 C>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:168096803 G>A maps to NM_003062.2 G1440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr23:144904213 C>T did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr23:144905974 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:144904632 G>C did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr23:144904237 C>T did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr23:144906353 A>G did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr3:164905804 C>G maps to NM_014926.2 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr23:142718801 G>C did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:142716869 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr13:88329823 A>G maps to NM_015567.1 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr13:86369854 C>T maps to NM_032229.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr13:86369823 C>A maps to NM_032229.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr13:86370303 G>A maps to NM_032229.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr13:86368848 G>A maps to NM_032229.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr10:105780243 A>G did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr3:57743530 A>G maps to ENST00000428312 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr20:57611523 A>C did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr20:57611628 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr20:57613689 C>T did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr15:59191918 C>A maps to NM_024755.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr18:45368210 G>T maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr15:67473651 C>T maps to NM_005902.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:67358663 C>T maps to NM_005902.3 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr18:46474802 A>G maps to NM_005904.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:40872507 T>A maps to NM_022733.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:40839875 T>A maps to NM_022733.2 C28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr23:128614735 C>T did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr9:2116049 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:2110311 C>T maps to NM_003070.3 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr9:2039760 A>G maps to NM_003070.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr9:2056811 T>A maps to NM_003070.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr9:2039817 A>G maps to NM_003070.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:2191374 C>T maps to NM_003070.3 S1568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:11143963 A>G did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:11144468 C>A maps to NM_001128849.1 G1267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:11134285 C>G maps to NM_001128849.1 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr19:11129631 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr19:11145750 C>A maps to NM_001128849.1 S1371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr19:11113808 G>T maps to NM_001128849.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3923-01A-01D-1458-08 chr4:144457700 A>G maps to NM_003601.2 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr4:144445523 C>T maps to NM_003601.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr2:217279801 C>G maps to NM_014140.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr2:217285019 A>T did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr2:217342997 A>G maps to NM_014140.3 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr22:24159113 C>A maps to NM_003073.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr22:24175873 C>T maps to NM_003073.3 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:47677512 T>C maps to NM_003074.3 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr3:47823125 C>T maps to NM_003074.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr12:56567524 A>G maps to NM_003075.3 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr12:56558429 A>C maps to NM_003075.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr12:56558429 A>C maps to NM_003075.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr23:53430708 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:53407984 A>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:53440301 C>G did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr10:112342363 A>G maps to NM_005445.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:160119802 T>C maps to NM_005496.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr9:72892385 C>T maps to NM_015110.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr2:17922876 A>G did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:2718193 C>T maps to NM_015295.2 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr14:91925214 T>A did not map to a codon.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:55813756 T>A maps to NM_001122964.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:55844409 C>T maps to NM_001122964.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr2:55804448 A>T did not map to a codon.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr16:18849888 A>G maps to ENST00000389467 N2356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr16:18864920 G>T maps to ENST00000389467 I1584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr16:18844470 G>A maps to ENST00000389467 F2861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr16:18844383 A>T maps to ENST00000389467 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr1:156243167 T>A maps to NM_015327.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:2195863 A>T maps to NM_017575.4 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr7:128849217 C>G maps to NM_005631.4 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr7:128848597 A>T did not map to a codon.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:109764750 G>T maps to NM_003080.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:109764876 A>G maps to NM_003080.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr23:22002496 G>T did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr22:31484746 G>C maps to ENST00000454496 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:4500238 C>T maps to NM_001114974.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr7:98639740 G>C maps to NM_020429.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr17:62542418 A>T maps to NM_022739.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr2:88383882 C>T maps to NM_198274.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:48600832 C>T maps to NM_005985.3 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr15:42822002 C>T maps to NM_003825.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr20:10258334 G>A maps to NM_130811.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:84302943 C>A maps to NM_014841.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr9:139272474 G>T maps to NM_003086.2 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr9:139273026 C>G maps to NM_003086.2 G1084G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr9:139272501 T>C maps to NM_003086.2 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr4:90743426 A>G maps to NM_001146055.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr5:121758632 T>C maps to ENST00000379533 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr7:127341300 T>C maps to NM_014390.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr2:241991874 G>A maps to NM_001080437.1 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr2:242026824 A>T maps to NM_001080437.1 R1380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr3:43389697 C>T maps to NM_017719.4 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr2:96959207 A>G maps to NM_014014.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:96943381 A>G maps to NM_014014.3 A1942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr6:7605679 G>A maps to NM_152551.3 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr20:16717905 C>T maps to NM_198220.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr20:32026770 G>A maps to NM_003098.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr8:121587443 G>A maps to NM_021021.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr8:121823810 G>C maps to NM_021021.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr8:51705387 G>T maps to NM_018967.2 *518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr2:1094046 T>G maps to NM_018968.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr3:63649636 A>T maps to NM_001080537.1 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:25207296 C>T maps to NM_022804.2 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr14:78217739 A>G maps to NM_012245.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr14:78184795 A>G maps to NM_012245.2 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr15:64426981 G>A maps to NM_003099.3 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:70280927 G>T did not map to a codon.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr6:86303400 C>T maps to NM_153816.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr6:86258078 A>T maps to NM_153816.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr5:53814576 T>A maps to NM_052870.2 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr5:53815389 C>T maps to NM_052870.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr11:130785009 T>G maps to NM_014758.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:130785819 T>A maps to NM_014758.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr5:122154606 T>G maps to NM_003100.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr16:50707451 G>T maps to NM_182854.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151641044 T>C maps to ENST00000458013 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:12618620 C>T maps to NM_001080530.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:75949417 C>T maps to NM_153271.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:35062275 A>T maps to NM_152233.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr7:2314822 C>T maps to NM_013321.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:158330821 T>G maps to NM_016224.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr12:53517644 C>T maps to NM_003578.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr17:76354729 C>T maps to NM_003955.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr17:36523826 A>G maps to NM_014598.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr17:36508825 C>A maps to NM_014598.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:36521269 G>A maps to NM_014598.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr6:160113747 G>T maps to NM_000636.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr21:34929510 T>C maps to NM_138927.1 C2070C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr21:34922736 T>A maps to NM_138927.1 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:186508840 C>T maps to ENST00000355634 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr10:108366995 A>G maps to NM_001013031.1 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:7725500 C>T maps to NM_020777.2 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3374-01A-01D-0966-08 chr10:106976770 C>T maps to NM_014978.1 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr10:107015521 G>T maps to NM_014978.1 G1100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:109884660 T>C maps to NM_002959.4 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:39285888 G>T maps to NM_005633.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:39285903 C>T maps to NM_005633.3 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr2:39284008 T>C did not map to a codon.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr14:50597306 T>A maps to NM_006939.2 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr14:50626455 T>A maps to NM_006939.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:38374015 C>T maps to NM_006941.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr20:307248 G>A maps to NM_006943.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr3:137483859 A>T maps to NM_004189.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr5:157078492 G>A maps to NM_178424.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr12:23998949 T>A maps to NM_006940.4 K150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr11:16133397 A>G maps to NM_001145819.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:1034953 T>C maps to NM_014587.3 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr12:53776831 T>G maps to NM_138473.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:231077476 T>G maps to NM_080424.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr17:46000416 C>G maps to NM_003110.5 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr7:21468914 G>A maps to NM_003112.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr7:21469334 T>C maps to NM_003112.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:171572791 G>A maps to NM_001003845.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:45925060 G>A maps to NM_199262.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr12:53722358 C>T maps to NM_001173467.1 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:20824952 G>C maps to NM_182700.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:20824955 C>G maps to NM_182700.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr7:20824613 C>T maps to NM_182700.4 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr8:101196264 A>G maps to NM_003114.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr8:7308687 G>T maps to NM_016512.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr1:118624113 G>A maps to NM_206996.2 N638N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr17:4863166 A>T maps to NM_004890.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr17:4871030 A>C maps to NM_004890.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr17:4864113 T>C maps to NM_004890.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:49067111 G>T maps to ENST00000376407 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr7:123599587 C>A maps to NM_001174046.1 Y365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr23:140785695 T>C did not map to a codon.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr23:140785754 C>T did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:32289268 C>G maps to NM_014946.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:217975147 G>T maps to NM_138796.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:48628384 G>A maps to NM_022827.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr17:48629512 G>T maps to NM_022827.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr4:123868399 G>T maps to NM_145207.2 G491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr15:45706845 T>C maps to NM_024063.2 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:145096166 T>G maps to NM_198572.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:44329697 G>A maps to NM_145026.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr4:177248329 C>T maps to NM_021928.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr17:8660583 G>C maps to NM_001128076.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr17:8658872 C>T maps to NM_001128076.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr7:101991205 G>A maps to NM_001146210.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr7:101988945 G>A maps to NM_001146210.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr5:35774016 A>G maps to NM_024867.3 E1324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr2:220338226 C>A maps to NM_005876.4 G1383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:220338576 C>A maps to NM_005876.4 R1467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220349150 C>T maps to NM_005876.4 S2322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr2:220350134 G>T maps to NM_005876.4 S2559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:220354241 G>A maps to NM_005876.4 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:7324266 C>A maps to NM_199339.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:16199599 C>T maps to NM_015001.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:16258647 T>C maps to NM_015001.2 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:16260462 T>G maps to NM_015001.2 V2576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:16256118 C>T maps to NM_015001.2 D1128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr15:69237965 A>G maps to NM_145658.3 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr15:69238205 A>G maps to NM_145658.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr15:44888370 G>A maps to NM_025137.3 C1448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr15:44877929 A>T maps to NM_025137.3 S1675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:44951364 A>T maps to NM_025137.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr15:44881588 G>A maps to NM_025137.3 V1589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:36909382 T>C maps to NM_001142294.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:89613083 G>T maps to NM_003119.2 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr19:49129224 G>A maps to NM_020126.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr2:228883286 A>G maps to NM_001142644.1 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr2:228882778 C>A maps to NM_001142644.1 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:228860229 G>C maps to NM_001142644.1 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr19:50926245 C>A maps to NM_003121.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr12:101880232 C>A maps to ENST00000299272 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr23:57162316 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr23:57020875 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr5:147661755 C>T maps to NM_001040129.2 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:41146020 C>T maps to NM_181642.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:38774303 G>T maps to NM_021102.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr19:38782513 G>A maps to NM_021102.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr18:12454458 T>C maps to NM_001128626.1 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr18:12463348 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr16:28993799 C>T maps to NM_032038.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr17:4389783 C>T maps to NM_182538.4 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr17:4381895 G>C maps to NM_182538.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr1:32279572 G>A maps to NM_144569.4 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr1:32259421 G>T maps to NM_144569.4 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:136328173 G>A maps to NM_004598.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr5:136448174 C>A maps to NM_004598.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:14063069 C>T maps to NM_006108.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:139308571 A>G maps to NM_001001664.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:234959666 C>A maps to NM_006944.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr15:38632096 G>T did not map to a codon.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr15:38591663 C>T maps to NM_152594.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:152957849 C>T maps to NM_005987.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:153004964 C>T maps to NM_003125.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr12:56863102 G>A maps to NM_207344.3 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:56862410 C>T maps to NM_207344.3 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:9416576 G>A maps to NM_025106.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr12:6981773 C>A maps to NM_032641.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr1:158609797 C>G did not map to a codon.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:158647557 G>T maps to NM_003126.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:158596632 C>T maps to NM_003126.2 W1943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:131339497 T>C maps to NM_001130438.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr9:131371419 C>T maps to NM_001130438.2 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr9:131374048 G>A maps to NM_001130438.2 R1610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:131370208 G>T maps to NM_001130438.2 G1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:131386740 G>A maps to NM_001130438.2 K1989K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr14:65240105 C>T maps to ENST00000389723 K1674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr14:65240096 T>C maps to ENST00000389723 A1677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr14:65289683 G>A maps to ENST00000389723 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr14:65245964 C>T did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:54851999 C>T maps to NM_003128.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr2:54883107 G>T maps to NM_003128.2 E2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr2:54855277 G>C maps to NM_003128.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr2:54870208 T>C maps to NM_003128.2 H1316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:66466956 C>T maps to NM_006946.2 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:66483324 G>A maps to NM_006946.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr11:66483387 G>A maps to NM_006946.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr11:66463960 C>A maps to NM_006946.2 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:41029411 C>T maps to NM_020971.2 H1241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:41072216 G>A maps to NM_020971.2 A2096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr15:42147093 C>T maps to ENST00000320955 L3168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr15:42147763 G>A maps to ENST00000320955 S3067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr15:42175213 C>T maps to ENST00000320955 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr15:42143072 G>A maps to ENST00000320955 R3634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr9:94821489 G>A maps to NM_006415.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:94877625 A>T maps to NM_006415.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:94808321 C>T maps to NM_006415.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr14:78045380 G>A maps to NM_004863.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr11:18636131 T>G maps to NM_194285.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr5:79616822 G>A maps to NM_032567.3 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr15:45962136 A>G maps to NM_021199.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:179248067 C>T maps to NM_003900.4 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr2:45616664 G>C maps to NM_018079.4 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr20:36024601 C>A maps to ENST00000373558 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr16:30718523 G>T maps to NM_006662.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr16:30734515 C>T maps to NM_006662.2 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr16:30750867 A>G maps to NM_006662.2 V3169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr16:30740444 T>C maps to NM_006662.2 R1939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr16:30734025 C>T maps to NM_006662.2 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr16:30749421 A>T maps to NM_006662.2 P2687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:30735226 A>C maps to NM_006662.2 A1494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr16:30734927 T>C maps to NM_006662.2 L1395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:30744760 A>G maps to NM_006662.2 E2096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:76024630 C>T maps to NM_080744.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr17:17722890 A>G maps to NM_001005291.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr6:43146556 G>A maps to NM_003131.2 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr12:64377782 C>T maps to NM_020762.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:64521383 C>G maps to NM_020762.2 S807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr12:64436721 T>A maps to NM_020762.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr16:4247842 G>A maps to ENST00000330063 N549N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:74042205 C>T maps to NM_014230.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr4:57366825 G>C maps to NM_006947.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr6:35856614 T>C maps to ENST00000361690 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr6:35838124 T>C maps to ENST00000361690 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr23:153047252 A>G did not map to a codon.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr23:99922294 A>G did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:99919924 T>G did not map to a codon.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr1:24995883 C>G maps to NM_005839.3 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr16:2816399 G>A maps to NM_016333.3 R1957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr16:2815940 C>T maps to NM_016333.3 S1804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr16:2807886 T>C maps to NM_016333.3 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr16:2817281 A>T maps to NM_016333.3 P2251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:2817458 T>C maps to NM_016333.3 S2310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr16:2816399 G>A maps to NM_016333.3 R1957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:100485328 T>C maps to NM_015908.5 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr7:100478986 A>G maps to NM_015908.5 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:100484813 C>T maps to NM_015908.5 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr20:633660 A>G maps to NM_080725.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr18:23637607 T>A maps to ENST00000415083 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:54870253 C>T maps to NM_145716.2 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:54707863 G>T maps to NM_145716.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr2:182765605 A>T maps to NM_001130445.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:182765432 T>C maps to NM_001130445.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr2:182780850 T>C maps to NM_001130445.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:182757371 G>A maps to NM_001130445.1 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr17:28120928 G>A maps to NM_033389.2 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr12:26348667 C>G maps to NM_005086.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:149502568 C>A maps to NM_198455.2 G2795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr7:149502985 A>G maps to NM_198455.2 P2831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:149516804 G>A did not map to a codon.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr7:149485495 G>A maps to NM_198455.2 W1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr7:149497463 C>T maps to NM_198455.2 Q2409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr7:149512018 C>G maps to NM_198455.2 S3526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr7:149480235 C>T maps to NM_198455.2 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr7:149518181 C>T maps to NM_198455.2 C4179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:155979423 A>G maps to ENST00000368312 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:57100281 C>A maps to NM_003146.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:65338204 C>T maps to NM_006396.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr3:187386908 G>T maps to NM_001048.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr22:37603326 G>A maps to NM_001051.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr20:23016317 C>A maps to NM_001052.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr16:1129326 G>A maps to NM_001053.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:1480324 C>T maps to NM_014188.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:48123288 G>A did not map to a codon.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr1:85117600 G>C maps to NM_001166417.1 S490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr1:85117617 G>T maps to NM_001166417.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr23:48213476 G>T did not map to a codon.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr23:48053634 G>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:48054485 G>T did not map to a codon.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr23:52681936 T>C did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr8:53028900 C>T maps to NM_014682.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr8:53025805 T>C maps to NM_014682.2 K1032K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:70432187 G>A maps to NM_006927.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr1:44386569 T>A maps to NM_174963.2 Y405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:44365369 T>C maps to NM_174963.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:44303968 G>A maps to NM_174963.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:126283515 T>C maps to ENST00000356132 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr11:126283464 C>T maps to ENST00000356132 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr3:186761060 G>A maps to NM_003032.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:107460217 C>G maps to NM_001142351.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr17:74622131 C>T maps to NM_018414.3 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr7:116759715 T>C maps to ENST00000323984 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:113126669 T>C maps to NM_017744.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr12:22440139 G>A maps to NM_003034.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr18:55027489 T>A maps to NM_015879.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr5:100192025 G>T maps to NM_005668.4 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr10:17495607 C>T maps to NM_001004470.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52554290 C>A maps to NM_015136.2 C1828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:52552012 C>T maps to NM_015136.2 V1585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:104030937 G>C maps to NM_017564.9 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr12:104071250 C>T maps to NM_017564.9 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr12:104062491 C>A maps to NM_017564.9 C719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr17:37369245 A>C did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:37368583 C>T maps to NM_198993.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:37373421 G>A maps to NM_198993.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr3:136062773 G>A maps to NM_005862.2 Q1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr3:136062786 G>T maps to NM_005862.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr3:136170988 C>T maps to NM_005862.2 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:123197833 C>A did not map to a codon.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr23:123191776 C>G did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:123197874 C>T did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr23:123185065 C>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr23:123176468 C>T did not map to a codon.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr23:123197043 C>T did not map to a codon.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr23:123179197 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr23:123200036 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr23:123179153 T>G did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr23:123184075 A>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:123202455 C>T did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr17:37816463 G>T maps to NM_006804.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr17:37815806 G>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr17:37817258 G>T maps to NM_006804.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr7:38256829 T>A maps to NM_032016.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr12:56744655 G>A maps to NM_005419.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr12:56745116 G>A maps to NM_005419.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr12:56750312 G>A maps to NM_005419.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56742946 C>T maps to NM_005419.3 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr17:40476789 G>A maps to NM_139276.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr17:40371846 C>T maps to NM_012448.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr17:40359717 A>G maps to NM_012448.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:47741018 T>A maps to NM_017453.2 K239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr8:74464270 A>G maps to NM_001164380.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr8:74515975 T>C maps to NM_001164380.1 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr8:23702338 G>T maps to NM_003155.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:89854551 C>T maps to NM_152999.3 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr1:47717421 G>A maps to NM_001048166.1 R1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr11:63965324 G>A did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:171471933 T>G maps to NM_005990.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr19:1220428 C>T maps to NM_000455.4 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr19:1220428 C>T maps to NM_000455.4 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr2:220465990 C>T maps to NM_052902.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220470427 G>T maps to NM_052902.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr2:220473922 C>T maps to NM_052902.2 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr2:197002268 C>A maps to NM_004226.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr7:23821076 G>T maps to NM_031414.3 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr7:23827687 T>C maps to NM_031414.3 N859N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr7:23825128 A>G maps to NM_031414.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr10:134121100 C>T maps to NM_173575.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:134036391 C>T maps to NM_173575.2 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr20:2097951 T>A maps to NM_080836.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:219556969 C>G maps to NM_015690.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:27461269 A>G did not map to a codon.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr20:62275106 G>T did not map to a codon.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr20:62275588 G>A maps to NM_015894.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr8:27099959 G>A maps to NM_030795.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr15:74281092 A>G maps to NM_004809.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr2:48809433 G>A maps to NM_172311.2 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:81744520 G>A maps to NM_033104.2 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr10:70645315 G>A maps to NM_001130161.2 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr4:184930538 C>A maps to NM_020225.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:74483210 T>C maps to ENST00000449139 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr7:134928141 C>T maps to NM_182489.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr2:202343186 G>A maps to NM_018571.5 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr2:202344885 C>T maps to NM_018571.5 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr2:37126773 G>A maps to NM_003162.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr2:37094994 A>G maps to NM_003162.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr14:31376114 A>T maps to NM_001083893.1 L619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr19:47228596 C>G maps to NM_001039877.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr19:47234129 C>T maps to NM_001039877.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr11:125479361 C>A maps to NM_152713.3 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:732018 G>T did not map to a codon.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr19:13260324 T>C maps to NM_003765.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:102730747 G>A maps to NM_017919.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr3:93733630 C>T maps to NM_001001850.1 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr3:93733336 C>T maps to NM_001001850.1 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr16:31045792 G>A maps to NM_004604.3 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:62592561 C>A maps to NM_003164.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr1:180945771 T>C maps to NM_005819.4 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr9:130413897 G>T maps to NM_003165.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr6:147637420 G>A maps to NM_001127715.1 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr6:147685199 C>T maps to NM_001127715.1 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr6:147646105 C>A maps to NM_001127715.1 S605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr3:121097678 C>T maps to NM_014980.2 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr12:10772766 G>C maps to NM_018423.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:84652565 A>G maps to NM_003849.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr2:84660488 C>T maps to NM_003849.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:84652538 C>T maps to NM_003849.3 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr10:104352444 C>A maps to NM_016169.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr13:53231665 G>C did not map to a codon.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr13:53239771 G>A maps to NM_001130912.1 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr8:70536393 C>T maps to NM_001128206.1 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr8:70533275 C>T maps to NM_001128206.1 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:46365621 G>A maps to NM_001161841.1 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr16:28607131 G>A maps to NM_001054.3 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:28603674 C>T maps to NM_001054.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr2:108910185 G>T maps to ENST00000437390 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr2:108910185 G>T maps to ENST00000437390 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr4:70707774 T>C maps to NM_005420.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr19:48385433 A>G maps to NM_003167.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr19:49096054 C>G maps to NM_177973.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:39138451 G>A maps to ENST00000405018 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:21821860 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:21834650 G>A maps to NM_007192.3 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr19:39965286 C>T maps to NM_003169.3 Q985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr17:27023952 T>C maps to NM_003170.3 D1354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:27014485 G>T maps to NM_003170.3 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:27028051 C>T maps to NM_003170.3 Q1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr10:70967646 C>A maps to NM_003171.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr9:136233528 G>A maps to NM_033161.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr9:136231847 T>C maps to NM_033161.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:24581139 C>A maps to NM_019601.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr22:24579609 G>T maps to NM_019601.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr1:223408419 G>A maps to NM_001037175.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr1:223401080 C>G did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:223465988 G>A maps to NM_017982.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr23:48557407 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:67925895 G>A maps to NM_017635.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr17:30302575 A>T maps to NM_015355.2 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:149883491 G>A maps to NM_014849.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr9:113241932 C>T maps to ENST00000374463 E823E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr10:29759269 G>A maps to NM_021738.2 H1926H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr7:138333762 G>T maps to NM_001139456.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr8:110587761 G>A maps to NM_001099744.1 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr8:110598353 G>A maps to NM_001099744.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr19:13011344 A>G maps to NM_001105578.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr19:39694579 G>T maps to NM_001080468.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:115489893 G>T maps to NM_003176.2 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:102125408 T>C maps to ENST00000449403 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr12:102125402 T>C maps to ENST00000449403 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr9:93624626 G>A did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr9:93606287 T>C maps to NM_003177.5 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr9:93636535 G>A maps to NM_003177.5 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:46319802 G>T maps to NM_004819.2 I1097I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:47432307 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:12192766 C>T maps to NM_133625.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr6:86324827 A>G maps to NM_006372.4 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr6:152779923 G>A maps to NM_182961.2 Q846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:152542149 G>A maps to NM_182961.2 Q7230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:152599303 G>A maps to NM_182961.2 L6165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:152470617 G>A maps to NM_182961.2 R8212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr6:152642497 G>A maps to NM_182961.2 R5371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr14:64496674 A>G maps to NM_182914.2 T2259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr14:64683101 C>G maps to NM_182914.2 P6513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr14:64545254 G>C maps to NM_182914.2 G3698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr14:64447731 G>A maps to NM_182914.2 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr14:64633997 G>A maps to NM_182914.2 L5551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr14:64519116 T>G maps to NM_182914.2 L2829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr6:33408547 G>A maps to NM_006772.2 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr22:39777741 C>G maps to NM_004711.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr21:34066597 A>T maps to NM_003895.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr21:34011315 G>A maps to NM_003895.3 Q1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr21:34099146 G>A maps to NM_003895.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr6:158449968 A>T maps to NM_003898.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:158450004 C>T maps to NM_003898.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr6:158497794 A>G maps to NM_003898.3 K810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr6:158507980 G>A maps to NM_003898.3 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3427-01A-01D-0966-08 chr14:70855303 G>A maps to NM_018373.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:99672332 G>T maps to ENST00000336292 V1255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr15:99670373 T>C maps to ENST00000336292 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:99671286 A>T maps to ENST00000336292 K907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr4:119948177 C>T maps to NM_133477.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr4:119947952 T>A maps to NM_133477.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:119951252 C>T maps to NM_133477.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:49050638 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:49049789 T>C did not map to a codon.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr12:33579107 C>T maps to NM_198992.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr11:66807535 G>A maps to NM_001177880.1 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr11:66813239 G>T maps to NM_001177880.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:210267874 T>C maps to NM_001146261.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr10:46963838 C>T did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr10:46962002 G>C maps to NM_031912.3 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr14:62462754 G>A maps to NM_031914.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr14:62463093 A>C maps to NM_031914.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr16:19195339 G>A maps to NM_016524.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:19236098 T>C maps to NM_016524.2 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr1:202566076 C>T maps to NM_177402.4 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr19:51140595 G>T maps to NM_001160329.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr18:40850386 T>C maps to NM_020783.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr19:55686304 G>A maps to NM_003180.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr19:55690358 G>A maps to NM_003180.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:61295624 G>A maps to NM_004200.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr11:1858202 C>A maps to NM_138567.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr11:7324615 G>A maps to NM_175733.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr11:7439308 C>T maps to NM_175733.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr11:85409118 T>A maps to ENST00000359152 K1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr11:85438960 G>T maps to ENST00000359152 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr6:159184434 C>A maps to ENST00000297239 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr6:159173010 G>A maps to ENST00000297239 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:99945080 T>C did not map to a codon.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr23:37984721 C>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:64898664 C>T maps to NM_172230.2 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr6:132910009 C>T maps to NM_003967.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr6:132910003 G>T maps to NM_003967.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:132910126 A>G maps to NM_003967.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr6:132892287 T>A maps to NM_175067.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:132859484 C>T maps to NM_175057.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr22:39826037 C>A maps to NM_006116.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr22:39814794 G>A maps to NM_006116.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr23:30849593 G>A did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr12:57409499 C>A maps to NM_013251.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr12:57409488 A>T maps to NM_013251.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr10:123987405 T>C maps to NM_206862.2 H2593H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr10:123845032 G>A maps to NM_206862.2 Q1006Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr4:1729914 A>G maps to NM_006342.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr4:1738985 G>A maps to NM_006342.1 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr4:1729794 A>G maps to NM_006342.1 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:1746486 G>A maps to NM_006342.1 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr10:71166877 G>A maps to NM_001057.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr10:71166859 G>T maps to NM_001057.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr4:104512714 G>A maps to NM_001059.2 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:166833058 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr17:35836945 C>A maps to NM_001166105.1 Y397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr4:7056534 C>T maps to NM_152293.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr23:70613247 G>A did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:70618523 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:70643917 T>C did not map to a codon.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr23:70603944 A>G did not map to a codon.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr23:70602416 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr23:70607245 C>T did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr23:70627427 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:6632969 G>A maps to NM_006284.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:34147196 T>C maps to NM_139215.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr17:34171884 C>A maps to NM_139215.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:10051036 C>T maps to NM_005680.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr16:84215641 G>T maps to NM_005679.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:32633309 G>A maps to NM_153809.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr10:8051124 G>T maps to NM_031923.2 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr18:23969873 T>C maps to ENST00000418698 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr1:229738592 C>A maps to NM_014409.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr7:99707630 G>A maps to ENST00000472509 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr23:100531460 A>C did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr23:100524197 G>A did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr23:100532701 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr23:100547951 G>T did not map to a codon.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr23:100531436 C>T did not map to a codon.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr23:100531442 T>A did not map to a codon.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr23:100531445 A>C did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:77387114 T>C did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr23:77395086 G>A did not map to a codon.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr6:159456930 A>G maps to NM_054114.3 C708C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:111719761 C>A maps to NM_001008272.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr11:747519 C>T maps to NM_006755.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:763427 T>G maps to NM_006755.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr2:159992708 C>G maps to NM_033394.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:160086334 C>A maps to NM_033394.2 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:160080759 G>A maps to NM_033394.2 E1232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:61497779 A>G maps to ENST00000389520 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:118588924 G>A maps to NM_016281.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr6:32805898 G>A maps to ENST00000452392 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr4:16165152 G>T maps to NM_153365.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr1:234599595 T>C maps to NM_005646.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr15:102261431 T>A maps to NM_152334.2 K155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:6639490 C>T maps to NM_138697.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:19166251 C>G maps to NM_152232.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr1:19181060 G>A maps to NM_152232.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr1:1267927 G>A maps to NM_152228.1 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:1269264 G>A maps to NM_152228.1 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr5:9629742 C>G maps to NM_019599.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:9629373 G>A maps to NM_019599.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr5:9629358 G>A maps to NM_019599.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr12:11286819 A>T maps to ENST00000422992 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr12:11286735 G>C maps to NM_001097643.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr12:11183808 A>G maps to NM_176885.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:11183796 C>T maps to NM_176885.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:143175819 C>T maps to NM_176883.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr12:11139224 C>A maps to NM_176890.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr12:11138583 C>T maps to NM_176890.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr7:143140756 C>G maps to NM_177437.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr20:13561620 C>T maps to NM_017714.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr8:125527985 C>T did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr7:27856558 A>T maps to ENST00000409980 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:27856086 T>C maps to ENST00000409980 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr7:27788295 T>G maps to ENST00000409980 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr7:27839639 A>G maps to ENST00000409980 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr23:153649047 C>G did not map to a codon.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr23:153649067 G>T did not map to a codon.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr16:30380670 C>T maps to NM_015527.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr16:30370550 G>A maps to NM_015527.3 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr10:96291126 A>G maps to NM_015188.1 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr10:96290994 T>C maps to NM_015188.1 D679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr9:131570109 T>C maps to NM_018201.3 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr12:72288465 A>T maps to NM_022771.4 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:77915894 C>A maps to NM_019020.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:50391042 G>A maps to NM_024682.2 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr4:26640456 G>A did not map to a codon.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr4:26741523 T>C maps to NM_018317.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:26585818 T>C maps to NM_018317.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr9:100991263 C>T maps to NM_018421.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr9:100963823 C>T maps to NM_018421.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:419912 G>T maps to ENST00000246077 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:420957 G>A maps to ENST00000246077 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr15:74174088 G>A did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr22:47507401 A>G did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:100042460 T>A maps to ENST00000394144 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr16:2546379 C>A maps to ENST00000434757 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr16:2550435 G>T maps to ENST00000434757 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr23:48418767 C>A did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr23:48403329 G>C did not map to a codon.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr23:48418658 G>A did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr23:48418348 C>A did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:18541948 A>G maps to NM_001039397.2 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr17:28887639 T>C maps to NM_015594.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr13:75923414 C>A maps to ENST00000431480 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr13:75936706 T>A maps to ENST00000431480 K179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr3:17279708 G>A maps to NM_001134381.1 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr3:17550056 A>G maps to NM_001134381.1 Y2Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr3:17415992 C>T maps to NM_001134381.1 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:101706725 G>C maps to NM_001102426.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:101670696 G>A maps to NM_001102426.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr23:106092529 G>A did not map to a codon.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr23:106117007 G>T did not map to a codon.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr23:106093256 G>A did not map to a codon.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr23:106109182 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:106109169 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:106070528 G>A did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr4:141590819 G>T maps to NM_015130.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr4:141590873 G>A maps to NM_015130.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr4:141600355 C>T maps to NM_015130.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr4:141580760 G>C maps to NM_015130.2 Y634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:141600811 G>A maps to NM_015130.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:179326224 C>T maps to NM_198868.2 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr6:42713802 G>A maps to NM_003192.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:80885834 G>C maps to NM_005993.4 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr17:80772757 G>A maps to NM_005993.4 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr17:80863899 C>A maps to NM_005993.4 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr17:80765529 G>A maps to NM_005993.4 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:106967780 G>A maps to NM_001163436.1 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:107163638 G>A maps to NM_001163436.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:107154197 A>G maps to NM_001163436.1 C512C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr23:9677736 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr23:9660210 A>G did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:9683002 C>T did not map to a codon.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr7:72985070 C>A maps to NM_012453.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:2026054 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr6:170871096 G>A maps to NM_003194.4 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr6:170871084 G>A maps to NM_003194.4 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr14:55895568 G>A maps to NM_199047.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr2:162273244 T>G maps to NM_006593.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr1:168269665 C>T maps to NM_005149.2 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:79286339 T>G did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr23:79286335 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr17:59544912 G>C maps to ENST00000393853 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:114841565 G>A maps to NM_000192.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr12:114836386 T>G maps to NM_000192.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:37821722 G>A did not map to a codon.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr20:62698281 G>C maps to NM_003195.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr1:23751093 G>A maps to NM_003196.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr1:23743878 G>A maps to NM_003196.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr23:101382230 C>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:101382405 T>C did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr23:102864441 A>G did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr23:102864046 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr23:102864333 G>A did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:102841990 A>G did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr23:102841695 A>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:102841928 A>T did not map to a codon.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr23:102842228 T>C did not map to a codon.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr23:102529083 T>C did not map to a codon.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr23:101396081 A>G did not map to a codon.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr23:102508843 G>A did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr18:44560192 G>A maps to NM_016427.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:44554923 C>T maps to NM_145653.3 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr5:145838724 C>T maps to NM_006706.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr5:145862190 A>G maps to NM_006706.3 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr5:145878249 G>A did not map to a codon.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr5:145838658 C>T maps to NM_006706.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr5:145838640 C>T maps to NM_006706.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr10:132932682 T>C maps to NM_174937.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr15:57458627 C>A maps to NM_207036.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:31127383 C>T maps to NM_007109.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr22:42606196 G>A maps to NM_005650.1 C1705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr22:42609901 G>T maps to NM_005650.1 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:27373230 A>T maps to NM_175769.2 K155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr19:1623967 C>T maps to NM_003200.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr19:1622115 G>A maps to NM_003200.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:1621855 G>A maps to NM_003200.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:52921811 A>G maps to ENST00000398339 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr18:52937098 G>A maps to ENST00000398339 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:85361149 C>G maps to NM_031283.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:152082278 C>T maps to NM_007113.2 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr1:152084845 G>T maps to NM_007113.2 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:152059686 C>T maps to NM_001008536.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr11:59622264 A>G maps to NM_001062.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr11:59622279 A>G maps to NM_001062.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr22:31018989 T>A maps to NM_000355.3 L381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr6:160200277 C>T maps to NM_030752.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr6:167789487 C>T maps to NM_004610.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr6:167595370 T>C maps to NM_001145121.1 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr6:167592605 T>A maps to NM_001145121.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr6:35087005 A>T maps to NM_001093728.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:35086063 T>G maps to NM_001093728.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr6:35086048 A>G maps to NM_001093728.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr6:35086230 G>A maps to NM_001093728.1 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr12:104376607 G>A maps to NM_003211.4 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:104359838 G>C did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr12:104376607 G>A maps to NM_003211.4 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:90429931 G>A maps to NM_018319.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr10:115962899 A>T maps to NM_198795.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr10:115973102 A>T did not map to a codon.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr10:115973823 T>C maps to NM_198795.1 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:154493834 G>A maps to NM_001098475.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr13:61103272 A>G maps to NM_001146070.1 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr13:61102843 T>C maps to NM_001146070.1 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr6:46658405 C>G maps to NM_001010870.2 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr6:46656687 G>T maps to NM_001010870.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr6:46660118 C>T maps to NM_001010870.2 C1418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:100227198 T>G maps to NM_014290.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr1:151751218 A>G maps to NM_001083965.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr4:48148399 A>T maps to NM_003215.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr4:48139498 A>G maps to NM_003215.2 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr7:97874214 A>G maps to ENST00000379795 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr7:97847036 C>T maps to ENST00000379795 E1119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr14:102910131 G>A maps to NM_014844.3 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr14:102916036 G>A maps to NM_014844.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr14:102901085 C>T maps to NM_014844.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr4:65147224 A>G maps to NM_001010874.4 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr4:65274892 G>A maps to NM_001010874.4 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:121016493 G>T maps to NM_005422.2 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr11:120989264 G>A maps to NM_005422.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:120980197 C>T maps to NM_005422.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr10:114044311 C>T maps to NM_058222.1 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr10:114046094 G>A maps to NM_058222.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:27183559 T>C maps to NM_000459.3 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr9:27109632 C>T maps to NM_000459.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:6703553 C>A did not map to a codon.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr1:36553612 G>T maps to NM_014466.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:36552573 C>T maps to NM_014466.2 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr2:95540715 G>A maps to NM_144705.2 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr2:95539320 A>G maps to NM_144705.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr2:95539854 T>G did not map to a codon.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:95539854 T>G did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr16:1552945 G>T maps to NM_016111.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr16:1550654 C>T maps to NM_016111.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr14:20840923 T>C maps to NM_007110.4 K2348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr14:20846266 G>C maps to NM_007110.4 A1879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr14:20847177 G>A maps to NM_007110.4 D1738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:20845480 G>A maps to NM_007110.4 L2016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr5:1272326 C>A maps to NM_198253.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr12:117513077 A>G maps to ENST00000392545 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr9:35608910 G>C maps to NM_006285.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr10:70450817 A>G maps to NM_030625.2 G1886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr10:70450815 G>T maps to NM_030625.2 G1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr4:106156074 A>T maps to ENST00000513237 K347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:106157460 G>T maps to ENST00000513237 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:74275020 C>T maps to ENST00000409262 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:74320720 G>T maps to ENST00000409262 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:74327958 C>T maps to ENST00000409262 D1255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr9:103109628 T>G maps to NM_017746.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:103064526 G>A maps to NM_017746.3 N912N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr23:69942474 G>A did not map to a codon.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr23:69774532 T>G did not map to a codon.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr23:69811637 C>A did not map to a codon.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr23:69825331 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr23:69898663 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr23:69871374 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr23:69871298 C>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:70080717 G>A did not map to a codon.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr23:104464655 C>T did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr23:104463696 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr23:104464106 A>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:104463684 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr17:56651591 T>C maps to ENST00000240361 E1159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:56638927 T>A maps to ENST00000240361 P1416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:30694448 T>C maps to NM_031271.3 Q2734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr17:62291517 G>A maps to NM_018469.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr17:62228233 G>A maps to NM_018469.3 D1083D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:62291322 G>A maps to NM_018469.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr20:55208517 G>A maps to NM_003222.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:50740508 G>T maps to NM_172238.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr1:246707836 T>C maps to NM_022366.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr23:132351936 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr23:132352094 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:132351882 G>A did not map to a codon.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr23:132351242 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr23:48895569 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr23:48900724 C>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:48888985 G>A did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:41658861 G>A maps to ENST00000343317 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:41655520 C>A maps to ENST00000343317 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr6:41658460 G>A maps to ENST00000343317 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:100224940 C>A maps to NM_003227.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr7:100238671 G>A maps to NM_003227.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr7:100218518 C>G maps to NM_003227.3 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr8:134107430 C>A maps to NM_003235.4 V2461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr8:134128948 C>T maps to NM_003235.4 Y2617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr1:92193362 A>G maps to NM_003243.4 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr2:105915064 C>T maps to NM_004257.4 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr23:89177556 C>A did not map to a codon.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr14:24731315 G>A maps to NM_000359.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr20:2306575 T>C maps to NM_003245.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr15:43552388 G>A maps to NM_201631.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr8:56717518 C>T maps to NM_024831.6 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr16:67876819 G>A maps to NM_020457.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:67877044 T>C maps to NM_020457.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:72068027 T>G maps to NM_031435.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr2:242545862 C>A maps to NM_015963.5 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr4:83839152 C>T maps to NM_024672.4 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:39886355 C>A maps to NM_003246.2 Y1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr15:39887563 T>C maps to NM_003246.2 D1169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr15:39882094 C>G maps to NM_003246.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:39880742 T>G maps to NM_003246.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr6:169649024 G>T maps to NM_003247.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr6:169634862 C>T maps to NM_003247.2 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr6:169648850 G>C maps to NM_003247.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:155175048 C>T maps to NM_007112.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:155172113 G>A maps to NM_007112.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr5:79351851 A>T maps to NM_003248.4 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:79366536 C>T maps to NM_003248.4 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr2:88485425 G>T maps to NM_018271.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:216575 G>A maps to NM_005131.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:122756984 T>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr23:122755200 T>A did not map to a codon.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr23:122769987 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr23:122770006 A>G did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:122801089 A>G did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr23:122759901 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:122757674 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr5:175388334 T>C maps to NM_032361.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr17:38243107 T>A did not map to a codon.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr1:36755252 C>T maps to NM_005119.3 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr15:72039332 C>T maps to NM_024817.2 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr15:72040773 C>T maps to NM_024817.2 C752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:11675887 G>A maps to ENST00000423059 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:138400115 C>T maps to ENST00000272643 C1289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr2:39964199 C>G did not map to a codon.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr11:119290971 C>G maps to NM_006288.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr21:32513435 C>T maps to NM_003253.2 E1258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:32638550 G>A maps to NM_003253.2 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr21:32639201 G>T maps to NM_003253.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr6:155566797 G>A maps to ENST00000456144 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr6:155451457 T>C maps to ENST00000456144 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:155450719 C>T maps to ENST00000456144 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr19:4816505 C>A maps to NM_182919.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:134785314 G>C maps to NM_001099221.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:90035226 G>T maps to NM_145715.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr8:144680423 G>T maps to NM_032862.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr12:56814822 C>G maps to NM_003920.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr23:48751505 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:48751201 T>C did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr10:51592503 T>C maps to NM_006327.2 *210W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr19:7999039 C>T maps to NM_006351.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr17:76921134 G>A maps to NM_003255.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr6:54212216 T>C maps to NM_014464.3 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:24709983 G>C maps to NM_001099274.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:168168188 G>A maps to NM_152902.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr15:30008819 A>G maps to NM_003257.3 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr15:30026550 T>C maps to NM_003257.3 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:30019081 T>G maps to NM_003257.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:3730390 C>G maps to NM_014428.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr23:153524231 G>C did not map to a codon.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr23:153556231 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:27052950 G>T maps to NM_138463.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr4:166929188 C>T maps to ENST00000507499 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr4:166996129 T>C maps to ENST00000507499 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr10:98273268 G>A maps to NM_012465.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr10:98182330 G>T maps to NM_012465.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:35711015 C>T maps to NM_006289.3 K1361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr15:62978976 A>G maps to NM_015059.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr4:187004361 T>C maps to NM_003265.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr9:120475389 T>C maps to NM_138554.3 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4760-01A-02D-1421-08 chr9:120475350 G>C maps to NM_138554.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:223286360 G>A maps to NM_003268.5 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr1:223284111 G>T maps to NM_003268.5 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr23:12906240 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr23:12906680 C>A did not map to a codon.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr23:12904429 T>C did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:12905177 T>C did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr23:12939544 C>A did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr23:12938992 G>T did not map to a codon.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr23:12937361 T>C did not map to a codon.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr23:12937472 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr23:12938125 T>A did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr2:74742181 C>G maps to NM_016170.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:170736389 G>A maps to NM_021025.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr8:38853912 G>A maps to NM_078473.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:149093474 G>A maps to ENST00000383054 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr3:196053865 C>T maps to NM_138461.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:196051158 G>A maps to NM_138461.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr2:228228664 A>T maps to NM_024795.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr15:83805261 T>A maps to NM_023003.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr19:19380553 G>C maps to NM_001001524.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr19:19381022 G>A maps to NM_001001524.2 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:27152582 T>A maps to NM_016551.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr12:27156168 C>T maps to NM_016551.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr8:105360796 C>A maps to NM_030788.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr8:105361634 G>A maps to NM_030788.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr10:98312747 A>T maps to NM_020123.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr10:98307652 T>C maps to NM_020123.3 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:30730876 C>T maps to NM_014742.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr2:219140332 G>A maps to NM_022152.4 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr12:66546146 T>C maps to ENST00000286424 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr9:75355126 T>C did not map to a codon.
Sequencing variant TCGA-AK-3465-01A-01D-0966-08 chr20:2592910 C>T maps to NM_080751.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:2560636 C>T maps to NM_080751.2 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr15:81633741 A>G maps to ENST00000454937 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:54669260 G>T maps to NM_001145303.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr16:19073097 A>T did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr16:19051690 C>A maps to NM_024847.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr17:76127731 G>A maps to NM_152468.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:76133811 C>T maps to NM_152468.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr17:76133426 T>G maps to NM_152468.4 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:129546960 G>A maps to NM_001017395.3 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr12:94975435 A>G maps to NM_020698.2 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:20082230 G>A maps to NM_181719.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:140021511 G>A maps to ENST00000252100 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr16:68893911 A>C maps to NM_024562.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr16:68953055 C>A maps to NM_024562.1 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr16:68877597 G>T maps to NM_024562.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr12:124069275 G>A maps to NM_006815.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr1:93620446 T>A did not map to a codon.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr9:103235852 G>T maps to NM_003692.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:193056716 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:42089523 C>T maps to NM_032376.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:41365848 C>T maps to NM_145041.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr11:60689309 A>T maps to NM_024092.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:60689598 C>T maps to NM_024092.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr3:10011438 G>A maps to NM_018447.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr3:10005821 T>C maps to NM_018447.2 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr3:10005827 G>A maps to NM_018447.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr12:44782259 A>G maps to NM_032256.1 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:44338121 T>C maps to NM_032256.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:75617586 G>T maps to NM_031925.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr7:75617797 G>C maps to NM_031925.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr7:98457931 G>A maps to NM_001134450.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:98413328 T>A maps to NM_015348.1 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr2:98373847 T>C did not map to a codon.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr11:60701217 T>C did not map to a codon.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr12:126135243 C>T maps to NM_052907.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr12:125834193 T>C maps to NM_052907.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:126138172 C>T maps to NM_052907.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr12:129558539 G>T maps to NM_133448.2 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:130184818 C>G maps to NM_133448.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:36230749 G>C maps to NM_024660.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr19:36230812 C>T maps to NM_024660.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr2:85828226 G>T maps to NM_001031738.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr2:85828148 G>T maps to NM_001031738.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr19:55824238 C>T maps to NM_001085488.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr4:38990525 G>T maps to NM_024943.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:87494938 G>A maps to NM_153354.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr23:109247113 C>A did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr23:109352335 C>G did not map to a codon.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:216965264 A>T maps to NM_138390.3 *298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr2:62728553 G>T maps to NM_198276.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr2:62728622 C>G did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:150500796 C>A maps to NM_018487.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr7:1589782 G>A maps to NM_001097620.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:1588278 G>A maps to NM_001097620.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr23:148690435 C>A did not map to a codon.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr23:153247609 G>T did not map to a codon.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr20:48760153 C>T maps to NM_199203.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:48744629 C>T maps to NM_199203.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr20:48713265 T>C maps to NM_199203.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr7:15433777 T>C maps to NM_001004320.1 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr17:26686414 C>T maps to ENST00000457710 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr9:74305108 C>T maps to NM_013390.2 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr9:140099455 C>A maps to NM_053045.1 *137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr16:67262756 T>A maps to NM_014187.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr16:67261755 C>T maps to NM_014187.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr16:29982730 G>A maps to NM_194280.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:27648816 C>T maps to NM_032125.2 V43V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4960-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:15682859 A>G did not map to a codon.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr23:15657839 A>G did not map to a codon.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr14:61747643 A>G maps to NM_001017970.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr23:102968788 A>T did not map to a codon.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr23:102967203 G>C did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:108536276 C>A maps to NM_018112.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:32557362 G>C maps to NM_018056.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:185212512 A>G maps to NM_080652.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr3:185214711 T>C maps to NM_080652.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:129724697 A>G maps to NM_138788.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr23:34657471 C>T did not map to a codon.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr17:57915759 T>C did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:64174891 T>G maps to NM_014254.1 L88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:45120713 G>T maps to NM_024587.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr1:226037700 C>T maps to NM_014698.2 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:94821183 G>A maps to NM_153704.5 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr8:56652729 T>C maps to ENST00000434581 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:46156751 C>T maps to NM_016486.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr8:74893387 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr8:109796775 G>A maps to NM_153015.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr11:18722526 C>T maps to NM_153347.1 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr15:42512317 T>A maps to ENST00000389834 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr20:24523930 G>A maps to NM_024893.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr19:41888744 C>T maps to NM_001098821.1 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:26653713 C>T maps to NM_014573.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr17:31260287 C>A maps to NM_015544.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr3:69072459 T>C maps to NM_007114.2 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:69096706 T>C maps to NM_007114.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:69101210 G>A maps to NM_007114.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr17:28651877 G>C maps to NM_206832.1 S199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr19:4294618 A>C maps to NM_144615.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr9:100326389 G>A maps to NM_003275.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr15:52074919 C>T maps to NM_014548.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr15:52098675 C>T maps to NM_014548.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr1:151146998 T>A maps to NM_013353.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:33135654 C>T maps to NM_001039770.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr4:68777128 C>T maps to NM_182606.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr4:68719844 G>A maps to NM_004262.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:68930481 A>G maps to NM_207407.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr4:68995526 C>T did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:68930402 C>A maps to NM_207407.2 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr11:117772954 T>C maps to ENST00000413475 *567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr11:117785149 G>A maps to ENST00000413475 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:117789316 T>C maps to ENST00000413475 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr11:117789301 C>T maps to ENST00000413475 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr21:19725218 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr21:19685346 T>G maps to NM_002772.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr21:19716369 G>T maps to NM_002772.2 Y393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr21:19751609 C>T maps to NM_002772.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr21:19744528 G>A maps to NM_002772.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr21:19770213 G>T maps to NM_002772.2 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr21:43803191 G>A maps to ENST00000380399 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:117984052 G>T maps to NM_019894.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr22:37469599 G>A maps to ENST00000381792 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:2416796 G>A maps to NM_182973.1 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr19:2422195 G>A maps to NM_182973.1 Q799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr19:2418066 C>T maps to NM_182973.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:2408352 G>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:2410352 G>A maps to NM_182973.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:2425066 C>T maps to NM_182973.1 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr12:29670367 A>G maps to NM_001193451.1 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr12:83290129 G>A maps to NM_152588.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr12:83526101 A>G maps to NM_152588.1 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr12:83525987 G>C did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr17:42265112 T>C did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr17:42266746 G>A maps to NM_001076674.1 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr17:42268153 C>T maps to NM_001076674.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr18:66367640 C>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:117848832 C>A maps to NM_002160.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr9:117803274 G>T maps to NM_002160.2 I1779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr9:117803268 G>A maps to NM_002160.2 A1781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr9:117848653 G>A maps to NM_002160.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr17:26667401 C>T maps to NM_021137.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr6:138201232 C>T maps to NM_006290.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr8:119938823 C>T maps to NM_002546.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr12:6439821 G>T maps to NM_001065.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr6:47254096 G>A maps to NM_014452.3 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr6:47251932 G>A maps to NM_014452.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr17:7464140 G>A maps to NM_003808.3 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3453-01A-01D-0966-08 chr19:6534881 C>T maps to NM_003811.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:150444533 C>G maps to NM_006058.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr5:150422133 G>C maps to NM_006058.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:7287557 T>C maps to NM_003985.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr3:195594609 C>T maps to NM_001010938.1 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr8:9413532 G>T maps to NM_003747.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr11:57087710 G>A maps to NM_033396.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:57076185 C>T maps to NM_033396.2 G1333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr1:74819042 T>A maps to NM_001112808.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr1:74954919 C>G maps to NM_001112808.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:11362954 G>A maps to NM_005425.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:72183031 T>G maps to NM_002270.3 L429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:12825696 C>T maps to NM_001136196.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr1:175323626 A>T maps to NM_003285.2 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr1:175334170 C>T maps to NM_003285.2 E854E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:175355201 G>A maps to NM_003285.2 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr7:5372498 C>T maps to NM_001080495.2 K1967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr7:5396760 C>A maps to NM_001080495.2 G1660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr7:5348897 G>A maps to NM_001080495.2 A2830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:5415787 G>A maps to NM_001080495.2 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr7:5391570 C>T maps to NM_001080495.2 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr7:5396873 G>A maps to NM_001080495.2 Q1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr7:5352658 G>T maps to NM_001080495.2 S2621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr7:5428641 G>A maps to NM_001080495.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr22:40552183 A>G maps to ENST00000454349 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:40717183 C>T maps to ENST00000454349 R1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:218712983 G>C maps to NM_022648.4 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr2:218713667 C>G maps to NM_022648.4 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:218678432 T>A maps to NM_022648.4 P1508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:218713274 C>T maps to NM_022648.4 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:218678510 C>G maps to NM_022648.4 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:47384597 G>T maps to NM_022748.11 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:32017811 G>A maps to ENST00000375244 G3134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr6:32047062 G>A maps to ENST00000375244 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr6:31977380 T>C maps to NM_032470.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr6:32052211 C>T maps to ENST00000375244 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:32016287 C>T maps to ENST00000375244 A3299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr17:48941285 T>C maps to NM_005749.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr22:35719145 T>C maps to ENST00000451197 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr17:53026925 A>G maps to NM_005486.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr17:53014034 T>C maps to NM_005486.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr17:17772712 G>A maps to NM_001082968.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr17:17769631 G>T maps to NM_001082968.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr20:39708802 A>G maps to NM_003286.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:144411528 G>A maps to NM_052963.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:18212207 A>G maps to NM_004618.3 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr17:18196162 G>A maps to NM_004618.3 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr3:133331388 C>T maps to NM_007027.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr3:133368473 A>G maps to NM_007027.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:179833915 C>A maps to NM_022347.3 *132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr1:179815211 A>C maps to NM_145034.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:179057116 G>A maps to NM_022371.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr8:60031453 A>T maps to NM_014729.2 Y31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr20:42635212 C>T maps to ENST00000348077 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr20:42574587 G>A maps to ENST00000348077 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:52478205 C>T maps to ENST00000407228 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:52478214 C>T maps to ENST00000407228 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr17:7579698 C>A did not map to a codon.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr17:7579395 G>A maps to NM_001126112.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr17:7577497 C>A did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr17:7577593 A>T maps to NM_001126112.1 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr17:7577017 C>T did not map to a codon.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr17:7577063 T>A maps to NM_001126112.1 K292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr17:7579698 C>A did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr15:43748160 G>C maps to NM_001141980.1 S882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:43724400 G>A maps to NM_001141980.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr15:43733776 A>G maps to NM_001141980.1 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43771710 T>C maps to NM_001141980.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr15:43748190 G>T maps to NM_001141980.1 S872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr15:43748236 G>A maps to NM_001141980.1 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr1:223994598 T>C maps to NM_001031685.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:223984098 A>G maps to NM_001031685.2 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr1:223983852 T>A maps to NM_001031685.2 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr1:223983954 C>T maps to NM_001031685.2 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr17:27896079 G>A maps to NM_138349.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:24305871 G>A maps to NM_147184.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr3:189608581 T>C maps to NM_003722.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:189612035 G>C maps to NM_003722.4 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr3:189604290 G>A maps to NM_003722.4 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:189526149 C>T maps to NM_003722.4 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:3624322 C>T maps to NM_005427.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr12:113727989 C>A maps to NM_001143819.1 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr12:113704161 G>T did not map to a codon.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:68853398 G>A did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr6:125569530 T>C did not map to a codon.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr11:18050850 G>A maps to ENST00000341556 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr12:6976717 C>T maps to NM_001159287.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:1500517 C>T maps to NM_000547.5 F789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr13:103275382 C>T maps to ENST00000376052 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr13:103328695 A>G maps to ENST00000376052 R1210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr5:678107 G>T maps to NM_007030.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr16:67424232 C>G maps to NM_016140.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr1:186302398 T>C maps to NM_003292.2 T1770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:186324771 T>A maps to NM_003292.2 K673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr1:186327743 G>A maps to NM_003292.2 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:186310210 T>G maps to NM_003292.2 A1323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr1:186286644 G>T maps to NM_003292.2 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:186316561 A>G maps to NM_003292.2 D935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr1:3545079 C>T maps to NM_182752.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr16:1291268 C>T maps to ENST00000461509 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1291623 C>G maps to ENST00000461509 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr16:1291181 C>T maps to ENST00000461509 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr16:1278743 C>T maps to ENST00000445910 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr16:1279703 A>G maps to ENST00000445910 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr16:1279709 G>A maps to ENST00000445910 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr16:1306664 A>G maps to NM_012217.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1306953 C>G maps to NM_012217.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:65705942 C>G maps to NM_003596.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr7:65705727 C>T maps to NM_003596.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr7:23547079 C>T maps to NM_013293.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr9:139794875 C>G maps to ENST00000359662 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr17:27075314 C>A maps to NM_004295.3 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr1:211545689 C>A maps to ENST00000427925 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:211545848 G>A maps to ENST00000427925 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr12:112580007 A>G maps to NM_006700.2 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:42218378 G>A maps to NM_001042646.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:202262966 G>A maps to NM_015049.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr3:36873054 C>T maps to NM_014831.2 L2629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr3:36872706 C>T maps to NM_014831.2 A2745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr16:3712966 G>A maps to NM_016292.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:7834022 G>A maps to NM_001166621.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr21:45502924 G>A maps to NM_003274.4 E660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr21:45502875 G>A maps to NM_003274.4 W644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr23:13732605 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr23:13738009 C>T did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr8:141310713 C>T did not map to a codon.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:141415690 A>G maps to NM_031466.5 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr10:17195590 T>C maps to NM_004412.5 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr6:123545247 C>T maps to NM_006073.2 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr6:123539745 T>G maps to NM_006073.2 *730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr11:118531942 G>A maps to ENST00000264029 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr6:41129013 C>T maps to NM_018965.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:41162230 C>T maps to ENST00000373108 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr6:41165976 A>G maps to ENST00000373108 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr6:41166021 A>G maps to ENST00000373108 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr6:41166024 G>A maps to ENST00000373108 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr6:42232447 G>A maps to NM_033502.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:152710188 G>T did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr8:110131437 G>A maps to NM_003301.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr8:110131431 C>T maps to NM_003301.4 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr8:110100373 T>A maps to NM_003301.4 Y211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:126445605 G>A maps to NM_025195.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr8:126448322 T>C maps to NM_025195.2 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:12858615 C>A maps to NM_021643.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr6:30139747 C>T maps to NM_033229.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr17:15539559 C>T maps to ENST00000455584 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr4:154197263 C>T maps to NM_015271.3 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr11:4411234 G>A maps to NM_003141.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr11:5717666 C>T maps to NM_006074.4 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:5717509 C>T maps to NM_006074.4 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr7:138145433 G>A maps to NM_015905.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr11:119996483 C>G maps to NM_012101.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:119988940 G>A maps to NM_012101.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:6486811 C>T maps to NM_033278.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr11:6477761 C>A maps to NM_033278.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr9:119460980 T>C maps to NM_012210.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr5:114499349 T>A maps to NM_018700.3 K55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:114515695 G>A maps to NM_018700.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr17:57181740 A>G maps to NM_015294.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr17:57078980 G>A maps to NM_015294.3 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:25967010 G>C maps to NM_006355.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr7:99514381 G>A maps to NM_033017.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr5:180651529 T>A maps to NM_033549.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr3:140401924 C>T maps to NM_152616.4 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr3:140401753 G>A maps to NM_152616.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr1:117660995 C>T maps to NM_025188.3 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:89537574 G>C maps to NM_020358.2 Y21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr11:89537460 G>T maps to NM_020358.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr11:5687232 T>C maps to NM_033034.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr7:72734196 T>C maps to NM_178125.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr5:180687082 G>T maps to NM_032765.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr8:67047248 C>A maps to NM_184085.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:33625314 C>T maps to NM_018207.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:4624491 G>A maps to NM_018073.5 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:45048564 G>C did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr3:32860207 C>T maps to NM_001039111.1 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:32932840 G>A maps to NM_001039111.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:75028468 A>G maps to ENST00000430211 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:75028468 A>G maps to ENST00000430211 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr10:104415048 G>A maps to NM_030912.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr10:104404880 C>T maps to NM_030912.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:189026065 C>T maps to ENST00000326754 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr22:38151616 G>T maps to NM_001039141.2 E1880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr22:38109336 C>T maps to NM_001039141.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr22:38120428 T>C maps to NM_001039141.2 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr22:38122447 C>T maps to NM_001039141.2 S1295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr19:6744908 C>T maps to ENST00000313244 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:6744587 C>T maps to ENST00000313244 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr14:92470020 T>C maps to NM_004239.3 K1433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr2:230675715 G>A maps to ENST00000389044 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:230654395 C>T maps to ENST00000389044 P1515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr2:230650535 C>A maps to ENST00000389044 A1650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr2:230642130 G>T maps to ENST00000389044 S1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:908119 C>T maps to NM_004237.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr5:916036 C>T maps to NM_004237.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr15:64692968 T>C maps to NM_016213.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr15:64717796 T>C maps to NM_016213.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr7:100466247 C>T maps to NM_003302.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:13220781 G>A maps to NM_001136035.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr23:100265617 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr23:100297050 T>C did not map to a codon.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr2:29073073 T>C maps to NM_017910.3 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3427-01A-01D-0966-08 chr3:3170804 A>T maps to NM_182916.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:3179091 G>C maps to NM_182916.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr23:54948718 T>G did not map to a codon.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr23:54950146 G>C did not map to a codon.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr23:54957275 T>A did not map to a codon.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr23:54953022 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr23:54957280 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr23:54957275 T>A did not map to a codon.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr23:54955457 C>T did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:54955087 A>G did not map to a codon.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr8:72975791 A>C maps to NM_007332.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr8:72958840 G>A maps to NM_007332.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr4:122853761 G>A maps to NM_001130698.1 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:122853524 G>A maps to NM_001130698.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr4:122872718 G>A maps to NM_001130698.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr13:38357440 A>C maps to NM_003306.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr13:38266298 C>T maps to NM_003306.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:38237840 G>T maps to NM_003306.1 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:33623073 A>C maps to NM_015638.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:33622950 G>T maps to NM_015638.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr23:111090367 A>C did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:135561910 T>A maps to NM_020389.2 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr15:31318394 C>T maps to NM_002420.4 K1170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr15:31355417 G>A maps to NM_002420.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:31295001 C>A maps to NM_002420.4 G1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr21:45798893 C>A maps to ENST00000397932 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr21:45798893 C>A maps to ENST00000397932 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr21:45825793 C>T maps to ENST00000397932 I888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr9:73477849 C>A maps to ENST00000419692 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr19:49674875 C>T maps to NM_017636.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:49703679 G>T maps to NM_017636.3 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:49714006 G>T maps to NM_017636.3 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:2432684 C>T maps to ENST00000452833 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr11:2435945 A>G maps to ENST00000452833 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr9:77436727 C>A maps to NM_017662.4 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr9:77377716 C>T maps to NM_017662.4 R1290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr17:3486631 C>T maps to ENST00000399756 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr7:142626640 G>A maps to NM_019841.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:142606702 G>A maps to NM_019841.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr7:98507680 T>C maps to ENST00000359863 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr9:131077878 G>A maps to NM_015679.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr7:141952103 A>T maps to NM_001001317.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr16:2126067 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:2122848 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr16:2134518 C>G maps to NM_000548.3 A1432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:150128648 C>T maps to NM_014779.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr3:150127404 C>T maps to NM_014779.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr23:106957761 C>G did not map to a codon.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr1:184023904 C>A maps to NM_052965.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr3:12545141 C>T maps to NM_025265.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr17:73519836 C>G maps to NM_207346.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr12:58190296 G>A maps to NM_001172696.1 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:99720472 C>A maps to NM_025244.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:99689478 A>C did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr11:65715208 C>T maps to NM_152762.2 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr18:72999467 C>A maps to NM_005786.4 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr18:72999254 G>A maps to NM_005786.4 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr18:72997838 A>C maps to NM_005786.4 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr20:51870957 A>T maps to NM_173485.5 K321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr19:31770506 G>A maps to NM_020856.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr19:31768040 C>T maps to NM_020856.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:76506752 C>T maps to NM_015516.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr5:110407686 C>T maps to NM_033035.4 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr8:143412302 G>A maps to ENST00000445818 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr1:231700332 C>A maps to NM_005999.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr5:176084584 G>A maps to NM_012171.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr5:176084596 G>A maps to NM_012171.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:115601515 G>A maps to NM_005725.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr12:58140427 G>C maps to NM_005981.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr7:128804349 C>A maps to NM_178562.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr12:71526583 G>A maps to NM_004616.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr23:53114043 C>A did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr23:53115407 G>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:54482520 G>A maps to NM_001003937.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr17:2228034 A>G maps to NM_018128.4 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr9:100380107 G>A maps to NM_139246.4 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr6:43221355 G>T maps to NM_032538.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:43226955 C>G maps to NM_032538.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr5:159437681 T>C maps to NM_003314.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:113230093 G>T maps to NM_017868.3 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr2:3391615 C>T maps to NM_016030.5 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:3483102 G>A maps to NM_016030.5 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:3392362 G>C maps to NM_016030.5 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr11:43427494 A>C maps to NM_018259.5 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:75037056 G>A maps to NM_145170.3 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr17:15930769 C>T maps to NM_017775.2 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr5:34880313 T>C maps to NM_144725.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr1:156552876 C>T maps to NM_001105669.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr1:156553239 C>T maps to NM_001105669.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:138822684 G>A maps to NM_024926.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:33002959 G>A maps to NM_017735.4 W564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:74718486 G>A maps to NM_022492.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr8:109462082 A>G maps to NM_014673.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:109489021 C>T maps to NM_014673.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:109462687 A>T maps to NM_014673.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr5:94803694 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr5:94876455 T>G maps to NM_014639.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr1:51755791 C>A did not map to a codon.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr9:15211316 C>T maps to NM_152574.2 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr18:21710335 G>A maps to NM_001135993.1 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr14:20774051 T>C maps to NM_138376.2 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:20763922 G>A maps to NM_138376.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:47221560 C>A maps to ENST00000394850 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:47300863 C>T maps to ENST00000394850 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr14:91044470 G>A maps to NM_001010854.1 H763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr14:89307273 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr14:89338025 G>T maps to NM_144596.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:89307766 A>G did not map to a codon.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr19:40723223 A>G maps to NM_152479.5 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:117633171 A>T maps to NM_003594.3 K839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:43442516 C>G maps to NM_012263.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr22:43459836 G>A maps to NM_012263.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr9:124751434 C>T maps to NM_194252.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr22:43569807 G>T maps to NM_015140.3 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr22:43565505 C>T maps to NM_015140.3 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr6:167753862 T>C maps to NM_031949.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:9868879 T>C maps to NM_001025930.3 Y501Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr2:219612346 C>T maps to NM_014640.4 S759S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B4-5844-01A-11D-1669-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr2:179399167 C>T maps to NM_133378.4 R31490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr2:179593687 A>G maps to NM_133378.4 S5115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr2:179466063 G>A maps to NM_133378.4 R15986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:179411555 A>G maps to NM_133378.4 D28965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:179449123 T>C maps to NM_133378.4 E19150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:179481862 G>T maps to NM_133378.4 T13385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr2:179395675 C>T maps to NM_133378.4 R32654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:179587902 G>A maps to NM_133378.4 N6033N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr2:179400234 G>A maps to NM_133378.4 R31135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr2:179404240 G>A maps to NM_133378.4 R30283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:179435408 C>T maps to NM_133378.4 Q22582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:179634826 C>T maps to NM_133378.4 V2867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr2:179605551 G>A maps to NM_133437.3 G3965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr2:179467027 G>T maps to NM_133378.4 I15799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr2:179439167 A>C maps to NM_133378.4 Y21329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr2:179447817 T>A maps to NM_133378.4 L19336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr2:179595295 T>C maps to NM_133378.4 T4744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr2:179614715 A>G maps to ENST00000375038 D4139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr2:179464024 C>T maps to NM_133378.4 W16264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:179665290 G>T maps to NM_133378.4 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr2:179405008 T>A maps to NM_133378.4 G30060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr2:179658187 T>C maps to NM_133378.4 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr2:179437361 T>A maps to NM_133378.4 L21931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr2:179664359 C>T maps to NM_133378.4 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr2:179484438 T>C maps to NM_133378.4 R12967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr2:179504808 G>A maps to NM_133378.4 L11016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr2:179598117 A>T maps to NM_133378.4 L4057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr2:179428025 T>C maps to NM_133378.4 E25043E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr2:179634603 C>A maps to NM_133378.4 E2902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:179452052 C>T maps to NM_133378.4 G18727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:179575503 G>A maps to NM_133378.4 G8196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:179611916 T>C maps to ENST00000375038 L5072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr2:179424710 T>A maps to NM_133378.4 T26148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:179479673 C>T maps to NM_133378.4 E13652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr2:179631233 G>A maps to NM_133378.4 R3193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr2:179591820 T>C maps to NM_133378.4 V5513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr2:179516237 A>T maps to NM_133378.4 V10729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr2:179433485 G>A maps to NM_133378.4 A23223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr2:179667068 C>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:179433842 G>C maps to NM_133378.4 Y23104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:179419673 A>G maps to NM_133378.4 D26936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:179425265 A>G maps to NM_133378.4 Y25963Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr2:179567315 C>A maps to NM_133378.4 E8856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:179599139 A>G maps to NM_133378.4 F3893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:179598481 C>A maps to NM_133378.4 G3968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr2:179615957 C>T maps to ENST00000375038 T3725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr2:179480473 A>G maps to NM_133378.4 D13550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:179401231 C>T maps to NM_133378.4 K30846K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr2:179497286 T>C maps to NM_133378.4 E11914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr2:179644741 A>C maps to NM_133378.4 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:179578855 C>T maps to NM_133378.4 T7599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:179426291 A>G maps to NM_133378.4 Y25621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:54937847 A>G did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:72209749 C>T maps to NM_032646.5 Y8Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr17:72249929 C>T maps to NM_032646.5 Y494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr17:72233485 G>T maps to NM_032646.5 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr7:2698600 C>T maps to NM_025250.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:2691877 T>C did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr12:49522586 G>A maps to NM_006082.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr12:49666781 T>C maps to NM_032704.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr13:19751675 G>A maps to NM_006001.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr13:19751291 T>C maps to NM_006001.1 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr13:19751300 C>T maps to NM_006001.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:132236968 G>A maps to NM_080386.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr2:132236920 G>A maps to NM_080386.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr22:18609611 C>A maps to NM_018943.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:30691480 T>A maps to NM_178014.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr6:30692125 C>A maps to NM_178014.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr20:57599036 G>A maps to NM_030773.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr9:140137359 T>C maps to NM_006088.5 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr9:140137407 C>A maps to NM_006088.5 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr19:6501364 G>A maps to NM_006087.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr10:93803 C>T maps to NM_177987.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr10:94010 G>T maps to NM_177987.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:94004 G>A maps to NM_177987.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr17:40765979 C>T maps to NM_001070.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:40765684 C>T maps to NM_001070.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr10:135106636 C>T maps to NM_006659.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr22:50665214 C>T maps to NM_020461.3 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr22:50660935 G>A maps to NM_020461.3 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr16:28857317 G>A maps to NM_003321.4 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr1:151552138 A>G maps to NM_020127.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr6:158923757 G>C maps to NM_020245.3 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr8:15531299 C>T maps to NM_006765.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr17:1198810 C>T maps to NM_172367.2 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr7:19738025 T>C maps to NM_001002926.1 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr7:19738223 G>A maps to NM_001002926.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr7:19738031 C>T maps to NM_001002926.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr7:19738031 C>T maps to NM_001002926.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:32646098 T>C maps to NM_175852.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:139563746 T>C maps to ENST00000358430 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:16804660 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr9:113013694 T>C maps to NM_003329.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr16:11785335 T>C maps to ENST00000356957 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4177-01A-02D-1421-08 chr16:11829974 C>A maps to ENST00000356957 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:52492990 C>A maps to NM_015913.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr14:52922173 G>C maps to NM_020784.2 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr18:9887669 A>G maps to NM_001098529.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr18:9887807 C>T maps to NM_001098529.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr6:7889003 A>C maps to NM_030810.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr6:7883468 G>A maps to NM_030810.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr18:77733687 G>T maps to NM_006701.2 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:19870862 A>T maps to NM_006440.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr19:10475697 G>A maps to NM_003331.4 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr19:10468694 G>A maps to NM_003331.4 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:10473018 C>A maps to NM_003331.4 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr22:50965101 C>T maps to ENST00000395681 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr15:41864762 G>A did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr15:41862435 A>G did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr15:41865310 T>C did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr15:41854917 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:41854917 T>G did not map to a codon.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr9:12698512 C>T maps to NM_000550.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr10:71906009 C>G maps to NM_173555.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr10:71905694 A>G maps to NM_173555.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr7:66582491 C>T maps to NM_018264.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr7:66474574 C>T maps to NM_018264.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr7:66479412 T>C maps to NM_018264.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr7:66532333 C>T maps to NM_018264.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:70987422 C>T maps to NM_018003.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr15:70991968 G>A maps to NM_018003.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:47069021 T>G did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr23:47062341 G>A did not map to a codon.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr23:47062168 A>G did not map to a codon.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr23:47058253 A>G did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr4:68534338 T>C maps to NM_018227.5 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr4:68547885 G>A maps to NM_018227.5 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:138839742 T>C maps to NM_016172.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr9:34241772 C>G maps to NM_001171201.1 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr9:33960822 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr9:33989091 C>T maps to NM_018449.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:154227751 C>T maps to NM_014847.3 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr17:16285910 A>G maps to NM_018955.2 *230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:16285475 C>G maps to NM_018955.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr12:125397654 C>A maps to NM_021009.5 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr12:125397894 A>G maps to NM_021009.5 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr23:118716564 A>G did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:83728804 G>T maps to NM_198920.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr10:60128478 G>T did not map to a codon.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr10:60124535 T>A maps to NM_003338.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr4:103723779 G>A maps to NM_181890.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr23:142967629 C>T did not map to a codon.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr17:74392602 G>A maps to NM_022066.3 D805D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr17:74392797 G>A maps to NM_022066.3 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr17:74392557 G>T maps to NM_022066.3 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr17:74398735 C>T maps to NM_022066.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr1:154522940 C>T maps to NM_017582.6 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr19:55913034 A>G maps to NM_014501.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr15:25615994 A>G maps to NM_000462.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr12:109935724 T>C maps to NM_183415.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:156963037 T>A maps to NM_014671.2 L79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:118250227 C>T maps to NM_004788.2 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:10177625 C>A maps to NM_001105562.2 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:11346094 G>C maps to NM_013319.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr5:158696066 C>G maps to NM_145049.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr16:4924864 G>A maps to NM_016936.3 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr16:4924284 C>G maps to NM_016936.3 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr7:138967975 G>A maps to NM_173569.3 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr7:138958745 T>A maps to NM_173569.3 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:138960857 A>G maps to NM_173569.3 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr20:3102445 G>T maps to NM_014948.2 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr20:3090942 G>A maps to NM_014948.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr3:33481334 G>T maps to NM_001128161.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr9:86276809 G>C maps to NM_013438.4 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:5529516 A>G maps to NM_017481.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr11:5528856 G>A maps to NM_017481.2 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr11:5537652 G>A maps to NM_145053.4 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:43299482 C>A did not map to a codon.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr15:43307884 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr15:43281100 C>A maps to NM_174916.2 G1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:42657390 G>A maps to NM_015255.2 E1703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr6:42604790 C>T maps to NM_015255.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr2:170885901 T>A maps to ENST00000442603 I1529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr2:170684547 G>A maps to ENST00000442603 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr1:19505690 T>C maps to ENST00000375267 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr1:19480420 G>T maps to ENST00000375267 G2157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr1:19455527 G>A maps to ENST00000375267 Q2983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:19407976 G>A maps to ENST00000375267 D5033D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr1:19447689 C>T maps to ENST00000375267 E3378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:19471345 G>A maps to ENST00000375267 Y2667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr8:103266716 G>T maps to NM_015902.4 S2738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:103341597 A>G maps to NM_015902.4 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr8:103300467 T>C maps to NM_015902.4 G1580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr8:103277496 G>A maps to NM_015902.4 R2478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:99327794 G>A maps to NM_024954.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr17:42287518 C>T maps to NM_014233.2 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr1:26609137 A>C did not map to a codon.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:26608864 A>G maps to NM_183008.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:136505918 T>C maps to NM_014607.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr9:134404930 G>A maps to NM_031432.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr1:165859455 A>T maps to NM_012474.4 K39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:62571653 G>A maps to NM_017859.3 H472H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr10:5415961 C>T maps to NM_053049.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:141481157 T>C maps to NM_021833.4 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr11:73686107 C>A maps to NM_003355.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr2:128927879 G>T maps to NM_020120.3 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:128878019 G>A maps to NM_020120.3 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr2:128927888 G>T maps to NM_020120.3 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:128918713 C>A maps to NM_020120.3 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr2:234637942 G>A maps to NM_019093.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr2:234526874 C>A maps to NM_019076.4 C174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr2:234580966 A>G maps to NM_021027.2 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr4:69817430 G>A maps to NM_024743.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:69816983 A>G maps to NM_024743.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr4:69795704 T>G maps to NM_024743.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr4:69692198 C>T maps to NM_001075.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr4:70346628 C>G did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr4:70361486 T>C maps to NM_021139.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:69972924 T>C maps to NM_001074.2 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:69978198 A>G maps to NM_001074.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr4:69978238 C>T maps to NM_001074.2 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr4:115544545 T>G maps to NM_003360.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr6:34826413 C>T maps to NM_017754.3 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:34825519 C>T maps to NM_017754.3 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr12:100433379 C>T maps to NM_015054.1 R1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:6460651 C>T maps to NM_152896.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr5:176402396 G>A maps to ENST00000377219 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr5:176332368 A>G maps to ENST00000377219 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr5:176382975 T>C maps to ENST00000377219 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr6:150290453 G>T maps to NM_025218.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr6:150267505 A>G did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:132405712 C>G maps to NM_003565.2 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr12:132395296 C>T maps to NM_003565.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:75132965 T>C maps to NM_001099436.1 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr15:75132622 C>T maps to NM_001099436.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr21:43533906 G>T maps to NM_173568.3 E905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr19:17756597 G>A maps to ENST00000428389 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr19:17760371 G>A maps to ENST00000428389 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr19:17767188 G>T maps to ENST00000428389 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr9:35243361 G>C did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr9:35310689 G>T maps to ENST00000396787 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:35396916 C>T maps to ENST00000396787 R1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr15:54557622 T>A maps to ENST00000260323 V1249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr17:73830528 C>T maps to ENST00000412096 E725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr17:73832899 A>T maps to ENST00000412096 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:73831765 G>T maps to ENST00000412096 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr17:33510468 C>T maps to NM_173167.2 D801D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr17:33498339 G>C did not map to a codon.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr17:33477187 G>A maps to NM_173167.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr17:33513508 A>G maps to NM_173167.2 E909E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr5:176305474 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr5:176297518 T>C maps to NM_133369.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr5:176305474 G>A did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr10:73055665 C>T maps to NM_170744.3 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr6:41001861 C>T maps to NM_173561.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr8:35541183 C>T maps to ENST00000416672 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr12:109541416 G>A did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr17:73814862 C>T maps to NM_001080419.1 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr17:73814847 A>C maps to NM_001080419.1 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr17:73818636 A>T maps to NM_001080419.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr22:24906777 A>G maps to NM_016327.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr10:12071444 G>A maps to NM_015542.2 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr13:115067469 A>G maps to NM_023011.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr23:118974622 C>T did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:118977250 T>C did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:118985466 C>G did not map to a codon.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr2:158958550 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:158971731 A>G maps to NM_001135098.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:74520733 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr23:74517349 T>A did not map to a codon.
Sequencing variant TCGA-B0-5117-01A-01D-1421-08 chr22:30163416 G>A maps to ENST00000406782 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:97244061 T>A maps to NM_006294.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr16:21982910 T>C maps to NM_003366.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr16:21982910 T>C maps to NM_003366.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:229771820 G>A maps to NM_014777.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr7:43918275 G>C maps to NM_001077663.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:45479705 C>T maps to NM_000374.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:17542426 G>T maps to NM_153676.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr11:17523512 A>C maps to NM_153676.3 Y733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr11:17544963 A>C did not map to a codon.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr11:17531373 C>T maps to NM_153676.3 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr1:216219776 G>T maps to ENST00000366943 V2107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr1:215820888 C>T maps to ENST00000366943 W4922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr1:216061914 T>C maps to ENST00000366943 P2692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr1:216405368 T>C maps to ENST00000366943 Q973Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr1:215799122 T>G maps to ENST00000366943 *5227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:215848922 G>T maps to ENST00000366943 Y4110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:215820885 G>T maps to ENST00000366943 I4923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr19:17366334 G>A maps to NM_031941.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:17366409 G>A maps to NM_031941.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr4:76722352 G>A maps to NM_003715.2 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr16:84797725 G>A maps to NM_005153.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:84778425 C>T maps to NM_005153.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:84797743 G>A maps to NM_005153.2 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr23:47100844 T>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr23:47102997 T>C did not map to a codon.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr23:47092431 A>G did not map to a codon.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr13:27680063 G>T maps to NM_182488.3 Y49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:179426710 C>A maps to NM_003940.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:179478996 C>T maps to NM_003940.2 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:62795033 T>A maps to ENST00000280377 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr8:11995986 G>A maps to NM_201402.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr22:18640564 C>T maps to NM_017414.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr22:18640564 C>A maps to NM_017414.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr3:49153189 A>G maps to ENST00000434032 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr17:20931912 G>A maps to ENST00000455117 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:55612676 A>G maps to NM_015306.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr1:55638067 G>A maps to NM_015306.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr1:55642116 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:55642114 A>T maps to NM_015306.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr21:17246742 C>T maps to ENST00000285681 F931F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr21:17138431 C>G maps to ENST00000285681 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr23:132160270 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:132160220 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr23:132161105 G>A did not map to a codon.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr11:113701631 C>A maps to NM_020886.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:113679908 G>T maps to NM_020886.2 Y680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr19:57640817 G>T maps to NM_020903.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr19:57642745 T>C maps to NM_020903.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:23083423 G>T maps to NM_020718.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr1:78177500 A>G maps to NM_015017.3 C810C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:78194349 T>C maps to NM_015017.3 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr2:61454344 A>C maps to NM_014709.3 V2484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:61441706 G>A maps to NM_014709.3 L2724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr2:61571100 T>C maps to NM_014709.3 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr2:61566796 A>G maps to NM_014709.3 H840H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr2:61575327 G>A maps to NM_014709.3 C654C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr2:61493233 C>T maps to NM_014709.3 K1834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr2:61415631 G>T maps to NM_014709.3 R3416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr11:77921085 C>T maps to NM_020798.2 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr17:76795061 A>C maps to NM_025090.3 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:219350460 T>C maps to NM_020935.2 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr4:144106647 G>A maps to NM_032557.5 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:85875074 T>G maps to NM_006590.2 L529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr3:49321433 T>A maps to NM_003363.3 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr3:49337920 G>A maps to NM_003363.3 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:49362338 T>C maps to NM_003363.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:234431844 A>G maps to NM_018218.2 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:234468566 G>A maps to NM_018218.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr7:6190119 C>T maps to ENST00000404835 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr17:9559805 A>G maps to NM_153210.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr17:9604522 C>A maps to NM_153210.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr6:99930672 T>C maps to NM_001080481.1 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:99894084 T>C maps to NM_001080481.1 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr1:22109369 G>A maps to NM_032236.5 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:22073614 A>G maps to NM_032236.5 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr6:41773625 G>A maps to ENST00000373009 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:41767667 G>A maps to ENST00000373009 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr15:50833302 G>A maps to ENST00000456636 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr15:50835959 G>A maps to ENST00000456636 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr23:55513336 C>T did not map to a codon.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr23:55513237 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr23:55514570 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr23:55513641 C>A did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr23:55514284 C>G did not map to a codon.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr4:120182904 T>C maps to NM_019050.2 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr17:5066235 C>A maps to NM_004505.2 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:5044783 T>C maps to NM_004505.2 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr15:50763850 A>G maps to NM_005154.3 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr23:41091720 C>G did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr23:40999923 C>A did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:41043809 C>T did not map to a codon.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr23:41047252 A>G did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr23:41088594 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr23:41025292 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr23:41077773 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr23:41025334 A>G did not map to a codon.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr23:41002592 T>G did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr23:41029422 G>A did not map to a codon.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr23:41010225 G>T did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:41022127 T>C did not map to a codon.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr24:14952323 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr24:14847583 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr24:14847618 A>C did not map to a codon.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr24:14850171 A>T did not map to a codon.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr23:129045755 A>T did not map to a codon.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr23:129054542 A>T did not map to a codon.
Sequencing variant TCGA-BP-4795-01A-02D-1421-08 chr23:129058771 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr23:129045743 C>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:52603704 G>C maps to NM_021645.5 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:72864378 T>A maps to NM_032175.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr17:30207664 T>C maps to NM_018428.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr6:144844256 A>T maps to NM_007124.2 R1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr6:144768772 A>T maps to NM_007124.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr6:144811220 G>A maps to NM_007124.2 E1383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr11:75852291 A>T maps to NM_003369.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr23:47518229 G>A did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:116226630 C>A maps to NM_001172412.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:116226587 C>T maps to NM_001172412.1 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr1:160385971 G>C maps to NM_020335.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr18:9954093 T>A maps to NM_003574.5 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:31760033 G>A maps to NM_006295.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:31745373 C>T maps to NM_006295.2 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr6:30890911 C>T maps to NM_001167734.1 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30883014 G>A did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:4432542 A>C maps to NM_138440.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr16:4431909 C>T maps to NM_138440.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr16:4431372 G>C maps to NM_138440.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:4432671 T>C maps to NM_138440.2 C598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr16:4432542 A>C maps to NM_138440.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:46021016 C>T maps to NM_003370.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr19:46024607 T>G maps to NM_003370.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr19:6853973 T>G maps to NM_005428.2 Y783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr19:6853049 C>T maps to NM_005428.2 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr10:118893698 C>T maps to NM_001112704.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr2:71160066 G>A maps to NM_012476.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr5:82850837 G>A maps to NM_004385.4 W3239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr5:82834254 T>C maps to NM_004385.4 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr5:82835014 G>T maps to NM_004385.4 E2065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr5:82815672 T>G maps to NM_004385.4 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:82786053 G>T maps to NM_004385.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr5:82841437 G>T maps to NM_004385.4 V3116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr5:82815684 G>A maps to NM_004385.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr9:35061686 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr9:35062135 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:35061056 A>G maps to NM_007126.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr8:67576660 T>G maps to NM_025054.4 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr8:67546927 T>C maps to NM_025054.4 E1159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr23:7811789 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr23:8138164 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr23:8138181 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr23:8138169 C>G did not map to a codon.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr23:6451842 G>A did not map to a codon.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr23:8434367 G>C did not map to a codon.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr23:8434370 A>G did not map to a codon.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr23:8434220 G>C did not map to a codon.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr6:43742100 A>G maps to NM_001025366.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr6:43746625 A>G maps to NM_001025366.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr17:56058036 G>T maps to NM_007146.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr17:56060481 C>T maps to NM_007146.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr12:95676228 A>G maps to NM_017599.3 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr23:135638637 A>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:87017992 C>T maps to NM_016206.2 R228R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A3-3331-01A-01W-0886-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr3:10188320 G>C did not map to a codon.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr3:10183793 G>A maps to NM_000551.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr3:10183871 G>C did not map to a codon.
Sequencing variant TCGA-AK-3445-01A-02W-1359-10 chr3:10183816 C>T maps to NM_000551.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02W-1359-10 chr3:10183872 T>C did not map to a codon.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr3:10188196 G>T did not map to a codon.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr3:10188320 G>T did not map to a codon.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr3:10191469 G>A did not map to a codon.
Sequencing variant TCGA-B0-4824-01A-01W-1359-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr3:10188196 G>C did not map to a codon.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr3:10191469 G>A did not map to a codon.
Sequencing variant TCGA-B0-4845-01A-01W-1359-10 chr3:10183793 G>A maps to NM_000551.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr3:10191571 G>T maps to NM_000551.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr3:10191468 A>G did not map to a codon.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr3:10191469 G>C did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr3:10188196 G>T did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr3:10183866 C>A maps to NM_000551.2 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr3:10191469 G>T did not map to a codon.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr3:10191571 G>T maps to NM_000551.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr3:10191481 A>T maps to NM_000551.2 K159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr3:10191468 A>G did not map to a codon.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr3:10188289 C>T maps to NM_000551.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr3:10191562 G>T maps to NM_000551.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr3:10191535 A>T maps to NM_000551.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr3:10188320 G>T did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02W-1382-10 chr3:10183816 C>T maps to NM_000551.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:10191531 C>A maps to NM_000551.2 Y175*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-4349-01A-01W-1362-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4355-01A-01W-1362-10 chr3:10183747 C>T maps to NM_000551.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01W-1362-10 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-4782-01A-02D-2099-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4789-01A-01W-1369-10 chr3:10183816 C>T maps to NM_000551.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1392-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr3:10188320 G>T did not map to a codon.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr3:10183743 C>T maps to NM_000551.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:10183793 G>A maps to NM_000551.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1392-10 chr3:10183810 G>T maps to NM_000551.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr3:10183738 G>T maps to NM_000551.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:10191484 G>T maps to NM_000551.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01W-1369-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:10183747 C>T maps to NM_000551.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:10191647 G>T maps to NM_000551.2 *214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:10191487 C>T maps to NM_000551.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr3:10188204 T>C maps to NM_000551.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:10188289 C>T maps to NM_000551.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02W-1584-10 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr3:10191589 C>T maps to NM_000551.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:10188321 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5455-01A-01W-1528-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr3:10191592 A>T maps to NM_000551.2 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:156268770 C>T maps to NM_001004319.2 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr3:38038587 C>T maps to NM_015873.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr3:38040854 C>T maps to NM_015873.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:17278344 T>G maps to NM_003380.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:42577628 C>T maps to NM_004624.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:158828653 T>C maps to ENST00000402066 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:53762786 C>T maps to NM_173856.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:53762719 T>C maps to NM_173856.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr19:53770837 G>A maps to NM_173857.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr6:133065438 C>T maps to NM_004665.2 *521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:51452312 T>G did not map to a codon.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr3:51455598 A>C maps to ENST00000273612 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:51457621 C>G maps to ENST00000273612 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:51475087 C>T did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr9:79985484 C>T maps to ENST00000376646 G2967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr9:79955423 T>A maps to ENST00000376646 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr9:79936444 C>T maps to ENST00000376646 F1871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr8:100847773 A>G maps to NM_017890.3 P3275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr8:100871684 C>A maps to NM_017890.3 S3699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr8:100514006 T>G maps to NM_017890.3 R1321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr8:100832148 G>A maps to NM_017890.3 R2956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:62155702 C>A maps to NM_020821.2 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr15:62243163 G>A maps to NM_020821.2 L1506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:62261605 G>A maps to NM_020821.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:62219325 A>G maps to NM_020821.2 P2160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr1:12381876 C>T maps to NM_015378.2 C2520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr1:12403072 C>T maps to NM_015378.2 P2950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr1:12566927 T>A maps to NM_015378.2 I4272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:12327037 T>C maps to NM_015378.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr1:12321994 G>T maps to NM_015378.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr1:12304649 T>C maps to NM_015378.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr15:41194908 G>T maps to NM_020857.2 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr15:41191987 A>C maps to NM_020857.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr11:134115447 C>T maps to NM_052875.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr12:122723268 G>T maps to NM_022916.4 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr13:52990210 G>T maps to NM_016075.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr11:60899491 T>G maps to NM_017966.4 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr15:42462023 G>T maps to ENST00000348544 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr15:42500324 C>T maps to ENST00000348544 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr18:61058288 T>C maps to NM_004869.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:33231656 C>T did not map to a codon.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr17:617868 G>A maps to NM_001128159.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr2:64196096 T>A maps to NM_016516.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:64199371 T>A maps to NM_016516.2 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:184603939 C>T maps to ENST00000437079 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:58358986 C>T maps to NM_001130480.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr23:107304758 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr23:107319362 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr12:118506260 C>T maps to NM_019086.5 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr12:118506353 T>C maps to NM_019086.5 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:118506350 C>T maps to NM_019086.5 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr23:65252419 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr23:65244922 C>T did not map to a codon.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr1:159827559 C>T maps to NM_001013661.1 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr2:17773469 A>G maps to NM_003385.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr19:54561797 A>T maps to NM_198481.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr20:36572444 G>A maps to NM_080607.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:68118140 C>T maps to NM_006370.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr17:26697200 G>T maps to NM_000638.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr16:22122216 C>T maps to NM_173615.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr2:98907041 G>A maps to NM_144992.4 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr11:123988557 A>G maps to NM_014622.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:49815192 C>T maps to NM_198570.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4869-01A-02D-1429-08 chr7:49842425 C>A maps to NM_198570.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:49815180 C>T maps to NM_198570.3 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:215440517 G>T maps to NM_001080500.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr11:61026691 C>A maps to NM_152718.2 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:6138618 G>A maps to NM_000552.3 H952H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr12:6094832 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:6180475 A>G maps to NM_000552.3 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:6180484 G>T maps to NM_000552.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr12:6091107 C>T maps to NM_000552.3 P2377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6097-01A-11D-1669-08 chr12:6161869 C>T maps to NM_000552.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:6078502 G>A maps to NM_000552.3 R2535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr10:88230844 A>T maps to ENST00000342368 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr14:100801316 A>C maps to NM_173701.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr14:100809695 A>G maps to NM_173701.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr23:48544488 A>T did not map to a codon.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr23:48545246 C>T did not map to a codon.
Sequencing variant TCGA-B4-5835-01A-11D-1669-08 chr1:27745563 T>C maps to NM_006990.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:27739178 A>G maps to NM_006990.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:27736339 A>G maps to NM_006990.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:17010 T>C maps to NM_182905.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr7:123329153 T>C maps to NM_003941.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:14943405 A>G maps to NM_016312.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:41657032 C>T maps to NM_007187.3 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr7:71175759 C>A maps to NM_022479.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr7:70800581 T>G maps to NM_022479.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr7:73249147 A>C maps to NM_152559.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr7:73280190 T>C maps to NM_182504.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr13:52293352 G>C maps to NM_052950.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr4:85724466 A>T maps to NM_014991.4 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr4:85664901 G>A maps to NM_014991.4 Y2008Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr4:85675020 T>C maps to NM_014991.4 Q1856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr14:55411061 A>G maps to NM_007086.3 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr4:10099337 A>G maps to NM_017491.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr10:122622313 G>A maps to NM_018117.11 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr10:122661796 G>T maps to NM_018117.11 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr10:122664156 G>A did not map to a codon.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr23:48462750 A>C did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr23:48458030 G>T did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:48462760 G>A did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:9501595 C>A maps to NM_145054.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr4:177050012 T>C did not map to a codon.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:994288 C>T maps to NM_024100.3 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr19:990273 T>A maps to NM_024100.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr19:984532 T>C maps to NM_024100.3 N60N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr19:984553 C>G maps to NM_024100.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:991961 C>T maps to NM_024100.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:102675937 T>C maps to ENST00000454394 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr14:102689210 T>A maps to NM_181291.1 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr14:100847488 T>A maps to NM_001161476.1 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr1:224586647 G>T maps to NM_025160.6 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr2:128471383 G>A maps to NM_018383.4 H1027H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:128526505 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:128477699 T>A maps to NM_018383.4 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr2:20138114 C>G maps to NM_001006657.1 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr2:20189770 G>A maps to NM_001006657.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr10:1149774 A>C maps to ENST00000416775 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:117526749 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr3:39108072 A>T maps to NM_020839.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr9:137006662 G>A maps to NM_052821.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr3:113114595 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:140049031 T>C maps to NM_017706.4 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr16:74942864 T>C maps to NM_030581.3 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr16:74942843 T>C maps to NM_030581.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr16:74942864 T>C maps to NM_030581.3 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr3:122133766 T>C maps to NM_019069.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:122133532 A>T maps to NM_019069.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr19:36575624 G>T maps to NM_001083961.1 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr1:85564292 A>G maps to NM_145172.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr1:241875145 T>C maps to NM_144625.4 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr1:241875160 G>A maps to NM_144625.4 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr12:122413566 T>C maps to NM_144668.4 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr12:122406015 C>T maps to NM_144668.4 C904C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr2:228754593 G>T maps to NM_178821.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr18:54424322 A>G maps to NM_015285.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:37381725 C>T maps to NM_018034.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr5:37721278 A>G maps to NM_018034.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr15:54025232 C>T maps to NM_182758.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr11:62601146 C>A did not map to a codon.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr2:190324064 G>A maps to NM_032168.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr1:111990199 T>A did not map to a codon.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr1:67340462 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:3564111 G>A maps to NM_017818.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:3547643 G>A maps to NM_017818.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:1633710 G>A maps to NM_001163809.1 K1235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr7:151092873 G>A maps to ENST00000426624 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:33666432 G>A maps to NM_173479.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr14:64066629 G>A maps to NM_080666.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:707222 T>G did not map to a codon.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:707786 C>T maps to NM_145294.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr7:134873247 C>T maps to NM_014149.3 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr7:134889160 A>G maps to NM_014149.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr1:27609918 C>T maps to ENST00000319394 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr11:9610145 C>T maps to NM_003390.3 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr16:681283 C>T maps to NM_053284.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:683831 C>A maps to NM_053284.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr4:6303444 G>A maps to NM_006005.3 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:6303093 C>T maps to NM_006005.3 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr8:38205402 G>T maps to NM_023034.1 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr17:38416824 G>A maps to NM_133264.4 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:38420805 A>G maps to NM_133264.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr7:29923571 T>C maps to NM_001080529.1 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr17:66440667 C>T maps to NM_017983.5 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr20:43348734 C>A maps to NM_003881.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr1:68614298 G>A maps to NM_024911.6 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr1:68697907 T>C maps to NM_024911.6 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:988848 A>C maps to NM_018979.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr9:96055158 C>T maps to ENST00000297954 P1841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr9:96002137 C>T maps to ENST00000297954 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:96051601 C>T maps to ENST00000297954 T1559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr9:95997111 C>T maps to ENST00000297954 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr9:95991991 C>G maps to ENST00000297954 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr23:54276545 G>T did not map to a codon.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr23:54321068 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr23:54319686 A>T did not map to a codon.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr23:54319392 A>T did not map to a codon.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr23:54276506 G>A did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:44845985 C>T maps to NM_030753.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr12:1755045 C>T maps to NM_032642.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr12:1742018 G>A maps to NM_032642.2 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr3:13921262 G>T maps to NM_004625.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr6:2784576 G>A maps to NM_020135.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:6012934 C>G maps to NM_015253.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr6:160176078 C>A maps to NM_004906.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:184129217 C>T maps to ENST00000448232 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr23:10085337 C>T did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr23:10062248 A>T did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr23:10085673 T>C did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:10066561 A>C did not map to a codon.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr8:87424055 T>C maps to NM_007013.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr8:87464826 A>G maps to NM_007013.3 E771E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr19:7694392 G>A maps to NM_020196.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr2:31598320 G>A maps to NM_000379.3 C509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:31621475 G>A maps to NM_000379.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr23:123025167 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr23:123020287 A>G did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:123020209 G>T did not map to a codon.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr2:167760330 C>T maps to NM_152381.5 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr2:168101916 A>T maps to NM_152381.5 K1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr2:168105253 C>A maps to NM_152381.5 S2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:168105758 G>A maps to NM_152381.5 R2619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:168100983 C>T maps to NM_152381.5 Q1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:168100184 C>T maps to NM_152381.5 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr23:37553616 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr23:37586900 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:17280835 G>T maps to NM_175878.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:56436131 C>T maps to NM_052898.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr8:56015737 C>T maps to NM_052898.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:56435873 C>G maps to NM_052898.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr8:11058308 G>A maps to NM_173683.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr20:30584473 G>A maps to NM_001011718.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:28290010 C>T maps to NM_018053.2 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr9:100437765 C>T maps to NM_000380.3 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr3:14193900 A>T maps to NM_004628.4 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr23:128886125 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr23:128895979 A>G did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr23:128886137 C>A did not map to a codon.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr23:128895242 G>T did not map to a codon.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr23:128886302 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-B2-4098-01A-02D-1386-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:43541218 G>C maps to NM_020750.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr6:43492325 T>C maps to NM_020750.2 E1120E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CZ-5459-01A-01D-1501-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr6:43493657 A>G maps to NM_020750.2 D995D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr16:28115914 G>T maps to NM_015171.2 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr16:28128692 G>A maps to NM_015171.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr12:64808727 C>A maps to NM_007235.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:82406898 G>T maps to NM_022406.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr22:42054276 C>T maps to NM_001469.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr12:58347426 C>T maps to NM_033276.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr3:142037708 A>G maps to NM_019001.3 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr20:21321459 A>T maps to NM_012255.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:38404483 C>G maps to NM_005108.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:17202724 C>A maps to NM_022166.3 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:17294473 G>A maps to NM_022166.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr16:17221642 C>T maps to NM_022166.3 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr16:17202836 A>G maps to NM_022166.3 N865N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:17202635 G>A maps to NM_022166.3 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:102100587 T>C maps to NM_001130145.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr11:101984952 T>C maps to NM_001130145.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:102100554 G>T maps to NM_001130145.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5834-01A-11D-1669-08 chr1:33252022 T>C maps to NM_003680.3 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:43166451 G>A maps to NM_004559.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr22:21982829 C>T maps to NM_001017964.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr3:183490250 G>C maps to NM_018023.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr12:69756581 T>G maps to NM_006530.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:32517398 A>G maps to NM_032312.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr14:75248650 C>T maps to NM_019589.2 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:75248110 G>A maps to NM_019589.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr14:75266223 T>A maps to NM_019589.2 S1408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr14:75279328 A>G did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr14:75248500 A>T maps to NM_019589.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr14:75301974 G>A maps to NM_019589.2 W2101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr14:75265324 C>T maps to NM_019589.2 R1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:207222970 A>G maps to NM_018566.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr4:69202907 C>T maps to NM_001031732.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr4:69188620 C>A maps to NM_001031732.2 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr5:112899758 T>C maps to NM_022828.3 A882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr20:61845284 A>G maps to NM_017798.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:61833791 T>C maps to NM_017798.3 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr8:64099318 G>A maps to ENST00000339066 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr20:43533771 G>A maps to NM_139323.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr17:1257622 A>G maps to NM_006761.4 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr22:32352659 C>T maps to NM_003405.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:155630356 G>A maps to ENST00000368339 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr23:21875587 G>A did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:100344176 C>T maps to ENST00000349350 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:100349674 T>C maps to ENST00000349350 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr7:100334191 C>T maps to ENST00000349350 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr3:166958708 T>A did not map to a codon.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr3:167045871 A>G maps to ENST00000307529 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:167039951 T>C maps to ENST00000307529 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:56185304 G>A maps to NM_030776.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr8:81411970 T>C maps to NM_001105539.1 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:81412102 T>C maps to NM_001105539.1 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5181-01A-01D-1429-08 chr3:101378746 A>T maps to NM_014415.3 S642S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KL-8343-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:31868725 G>A maps to NM_181842.2 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr11:113934294 G>T maps to NM_001018011.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr3:114070435 T>C maps to NM_001164342.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:62519738 G>A maps to NM_024784.3 Y516Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr23:119387853 T>A did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr23:119387345 C>T did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr23:119389134 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:129642635 C>T maps to ENST00000319119 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr3:141163201 G>T maps to NM_001080412.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr3:141163045 C>T maps to NM_001080412.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr1:22839531 C>T maps to NM_014870.3 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr1:197169166 G>T maps to NM_194314.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:129595384 G>T maps to NM_014007.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr11:130131509 C>A maps to ENST00000397753 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr11:130131236 G>T maps to ENST00000397753 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr11:130131060 A>G maps to ENST00000397753 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:130131042 A>T maps to ENST00000397753 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr11:130131007 A>T maps to ENST00000397753 L254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr20:62407315 C>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr20:62407207 G>A maps to NM_025224.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr1:6640755 T>A maps to NM_005341.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:6646762 G>A maps to NM_005341.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr1:6641320 G>T maps to NM_005341.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr4:4303968 C>T maps to NM_145291.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:4322598 C>A maps to NM_145291.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:4322721 C>T maps to NM_145291.3 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr18:45567043 G>A maps to NM_001039360.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr18:45555828 T>C maps to NM_001039360.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr1:33116037 G>T maps to NM_178547.2 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:203819760 C>T maps to NM_014827.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr13:46584526 A>G maps to ENST00000242848 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr2:187367290 A>T maps to NM_018471.2 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:88694028 G>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:88653022 G>T maps to ENST00000452588 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr16:88644134 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr16:88697619 G>A maps to ENST00000452588 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:88653084 C>T maps to ENST00000452588 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr8:144522388 G>A maps to NM_015117.2 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr8:144550432 G>C maps to NM_015117.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr8:144550601 G>A maps to NM_015117.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:144522451 G>T maps to NM_015117.2 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr19:47575242 T>A maps to NM_015168.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr2:113069432 G>A maps to NM_198581.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr2:113089833 A>G maps to NM_198581.2 P1113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr16:11873153 A>G maps to NM_014153.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr22:41742094 G>A maps to ENST00000351589 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr7:138764441 G>A maps to ENST00000464606 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr23:64137702 G>A did not map to a codon.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr23:64137683 C>T did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr5:132342535 T>G maps to ENST00000509437 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:52902540 G>T maps to NM_001009881.2 R1350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr23:117960297 G>T did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr23:73524499 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr23:111698753 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr18:60242637 T>C maps to NM_017742.4 Y1108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr10:81146145 G>A maps to NM_153367.3 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr23:77913713 C>A did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:77913358 G>A did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr23:77913570 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:80600584 G>A maps to NM_032280.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr7:100017326 T>A maps to NM_017984.3 K70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr3:28533616 G>A did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr3:28533651 G>A maps to NM_001040432.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr2:207169575 C>G maps to NM_020923.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:207171573 G>A maps to NM_020923.1 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr16:67428939 T>A maps to NM_013304.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr16:67428939 T>A maps to NM_013304.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:19170817 C>A maps to NM_019028.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr12:77216265 A>G maps to NM_015336.2 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:27176924 G>A maps to NM_032283.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr8:17067899 A>G maps to NM_016353.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr16:85010784 G>A maps to NM_001145548.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr22:20127298 C>A maps to NM_013373.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr23:128948749 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr23:128975881 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr23:128962963 C>T did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr23:128963039 G>T did not map to a codon.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr23:128945409 C>T did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:145156026 G>A maps to NM_014795.3 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr9:131514949 A>C did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:220072713 C>T maps to NM_138802.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr2:220073737 G>A maps to NM_138802.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:220072989 C>A maps to NM_138802.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr9:74971942 G>A maps to ENST00000437241 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr8:135521986 G>A maps to NM_020863.3 R1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:72017887 A>T maps to NM_144982.4 L1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:72993579 G>A maps to NM_006885.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr16:72984697 G>A maps to NM_006885.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:72821092 G>T maps to NM_006885.3 T3694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr16:72992625 C>T maps to NM_006885.3 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr16:72830805 A>T maps to NM_006885.3 G1925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:72991476 G>A maps to NM_006885.3 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992634 T>C maps to NM_006885.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992637 C>T maps to NM_006885.3 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:72822643 C>T maps to NM_006885.3 S3177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:77775450 T>A maps to NM_024721.4 P3167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr8:77776701 G>A maps to NM_024721.4 K3584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr8:77768348 T>C maps to NM_024721.4 L3064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr8:77776068 T>C maps to NM_024721.4 A3373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr8:77616433 G>A maps to NM_024721.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr15:42743698 A>G maps to NM_022473.1 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr15:42749283 A>G maps to NM_022473.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr15:42742411 G>A maps to NM_022473.1 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:42742930 C>T maps to NM_022473.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr15:42734361 T>C maps to NM_022473.1 Q1201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr19:44833538 A>T maps to ENST00000412927 Y274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr19:36832151 T>C maps to NM_020917.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:4995908 T>C maps to NM_153018.2 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr19:39898402 T>C maps to NM_003407.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:69256348 C>G maps to NM_004926.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr20:50769884 C>T maps to NM_018197.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr16:68598498 T>C maps to NM_133458.2 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:58384896 C>A maps to NM_053023.4 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr11:58381763 A>G maps to NM_053023.4 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr11:58346867 G>A maps to NM_053023.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr11:64854836 C>A maps to NM_006782.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4965-01A-01D-1462-08 chr16:88599109 G>A maps to NM_153813.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr8:106646500 C>T maps to NM_012082.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr8:106813473 C>T maps to NM_012082.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr8:106810964 T>C maps to NM_012082.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr8:106811084 C>A maps to NM_012082.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:3813947 G>T maps to NM_015174.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr23:24228653 G>A did not map to a codon.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr23:24197790 G>A did not map to a codon.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr24:2829143 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr24:2829188 G>A did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr24:2843188 G>C did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr24:2829114 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:41105575 C>T maps to NM_001077268.1 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr15:41099909 A>G maps to NM_001077268.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr14:68274333 G>T maps to NM_015346.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:68282658 C>A maps to NM_015346.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr14:68256096 A>G maps to NM_015346.3 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr14:68268850 G>T maps to NM_015346.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr4:2307124 G>A maps to NM_020972.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:52703735 T>A maps to NM_004799.2 L216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr16:2882102 G>A maps to NM_145252.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:62366739 T>A maps to NM_032527.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr20:62340423 T>G maps to NM_032527.4 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr8:124267673 A>G maps to NM_007222.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr8:123964181 T>A maps to NM_014943.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:123964436 C>T maps to NM_014943.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr20:39832046 C>A maps to NM_015035.3 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:147128793 G>T maps to NM_003412.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:147109012 C>A maps to NM_001168379.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5843-01A-11D-1669-08 chr13:100617840 T>C maps to NM_033132.3 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr13:100623584 C>T maps to NM_033132.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:58096318 G>A did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr19:57646762 C>T maps to NM_052882.1 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:57647365 A>G maps to NM_052882.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr7:99631798 G>A maps to NM_003439.1 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:99621200 A>G maps to NM_003439.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr16:25264265 C>T did not map to a codon.
Sequencing variant TCGA-BP-4994-01A-01D-1462-08 chr16:25268246 C>A maps to NM_001012981.4 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr6:28329174 A>G maps to NM_024493.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr6:28333713 G>A maps to NM_024493.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:101152940 A>T did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr5:140085214 G>T maps to NM_144723.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:178785386 C>A maps to NM_022470.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr22:30134341 C>A maps to NM_019103.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr22:30134341 C>A maps to NM_019103.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:81037037 C>G maps to NM_020338.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr7:44796727 G>A maps to NM_031449.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:44805817 C>G maps to NM_031449.3 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:40733504 A>G maps to NM_005857.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr1:40735724 C>T maps to NM_005857.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:40724032 G>C maps to NM_005857.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:35578966 G>A maps to NM_024772.3 K512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr1:35576004 T>C maps to NM_024772.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:35580007 C>A maps to NM_024772.3 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:35569919 G>C maps to NM_024772.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr23:70467239 G>T did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr23:70465235 T>C did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:70468026 T>C did not map to a codon.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr23:70472955 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:35853065 T>C maps to NM_005095.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr1:35870745 G>A maps to NM_005095.2 W1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:35865107 A>G maps to NM_005095.2 G1153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr13:20398871 T>C maps to NM_001142684.1 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr13:20398976 A>G maps to NM_001142684.1 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr13:20413048 G>T maps to NM_001142684.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr1:35454279 T>C maps to NM_007167.3 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr3:50380355 C>T maps to NM_015896.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:50379016 C>T maps to NM_015896.2 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr10:225961 T>C maps to NM_006624.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr17:4645275 T>C maps to NM_001136046.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr17:4647402 G>T did not map to a codon.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr19:21910450 A>C maps to NM_173531.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr19:19789580 G>C maps to NM_033204.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr7:64168952 C>T maps to NM_016220.3 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr7:6731606 C>T maps to ENST00000330442 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:247322363 G>A maps to NM_003431.2 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr5:43161422 A>G maps to ENST00000509156 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr19:58948570 C>T maps to NM_003433.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:58945193 T>A maps to NM_003433.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:19822256 T>G maps to NM_021030.2 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr4:367074 C>T maps to NM_003441.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr4:367200 C>A maps to NM_003441.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:219509114 A>T maps to NM_001105537.1 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:219503379 G>T maps to NM_001105537.1 T1582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:9519249 T>G maps to NM_003442.5 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr19:53577474 C>T maps to NM_001102603.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:44612086 T>C maps to NM_018651.2 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:97063237 C>T maps to NM_194320.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:57931171 A>G maps to NM_006959.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr19:44980906 T>C maps to NM_013256.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr19:35232371 A>G maps to ENST00000392232 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr23:47836676 G>C did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr6:27420476 G>A maps to NM_007149.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr6:27420045 G>C maps to NM_007149.2 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr23:152132416 A>T did not map to a codon.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr23:152128270 G>C did not map to a codon.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr23:152086677 C>T did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr23:152091353 G>T did not map to a codon.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr16:71512808 C>A maps to NM_006961.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:28116331 G>A maps to NM_006298.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr6:28200338 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:44684293 C>T maps to NM_006991.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr19:12243968 A>T maps to NM_021143.2 C344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:123598247 C>T maps to NM_003455.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr19:22154067 T>C maps to NM_007153.3 E1256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:22155690 A>G maps to NM_007153.3 H715H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:22155714 G>A maps to NM_007153.3 N707N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr11:6977425 C>A maps to NM_013250.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr14:21560705 C>G maps to NM_001102454.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:44470617 A>C maps to NM_013359.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr19:44469418 C>T maps to NM_013359.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr19:44570595 G>A maps to NM_013361.4 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:44570871 C>T maps to NM_013361.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr19:44635910 A>C maps to NM_013362.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr19:44680230 G>A maps to NM_001032372.1 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr19:44740520 T>C maps to NM_182490.1 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr19:44739324 A>T maps to NM_182490.1 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:5009700 A>G maps to NM_014519.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:5009511 A>G maps to NM_014519.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr19:44792843 T>C maps to NM_004234.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr18:74587547 C>A maps to NM_007345.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:74622685 C>T maps to NM_007345.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr18:74620407 G>A maps to NM_007345.3 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr18:74680293 G>T maps to NM_007345.3 *1846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr8:146107412 G>A maps to NM_021061.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:145947049 A>T maps to NM_138367.1 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:24309779 A>G maps to NM_203282.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:24310236 A>T maps to NM_203282.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr19:58453893 T>A maps to NM_005773.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:22270899 C>A maps to NM_033468.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:22271295 G>A maps to NM_033468.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr19:37005750 A>G maps to NM_001166038.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr19:37006029 G>A maps to NM_001166038.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:3334015 C>T maps to NM_005741.4 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr19:57724078 C>T maps to NM_003417.4 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:58724016 G>C maps to NM_133502.1 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr23:152612539 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr23:152613053 G>A did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr16:89789583 G>A maps to NM_001113525.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr22:22842484 C>T maps to NM_080764.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr23:129363021 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr15:56924220 A>C maps to NM_017661.2 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:200376814 T>C maps to NM_012482.3 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:200378263 C>T maps to NM_012482.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr19:44352475 G>T maps to NM_181845.1 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:44586258 G>A did not map to a codon.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr19:44890684 T>G maps to NM_152354.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr17:15620444 C>T maps to NM_020652.2 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr6:87970403 G>T maps to NM_015021.1 E2353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:43413769 T>C maps to NM_020727.4 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr7:99668972 G>C maps to NM_032924.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:35435240 G>A maps to NM_001099438.1 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr5:150276422 T>C maps to NM_001172831.1 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr5:150276452 T>C maps to NM_001172831.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr19:35175868 A>G maps to ENST00000221282 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr19:35175649 G>A maps to ENST00000221282 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr6:43306338 G>C maps to NM_014345.2 T1799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5712-01A-11D-1669-08 chr6:43316103 G>A maps to NM_014345.2 S1010S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr6:43305843 C>T maps to NM_014345.2 K1964K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr6:43333134 A>C maps to NM_014345.2 L148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr16:58031773 G>A maps to NM_020807.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr16:58030678 G>A maps to NM_020807.1 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr19:53385206 A>G maps to NM_207333.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:53384826 A>G maps to NM_207333.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr6:26638478 A>G maps to NM_024639.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr6:28294514 T>G maps to NM_030899.4 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr19:58639915 C>A maps to NM_024620.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr19:14829356 C>T maps to NM_032433.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr20:44578918 G>C maps to NM_022095.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr20:25655967 C>T maps to NM_015655.2 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr10:38301274 C>T maps to NM_006954.1 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr10:43088521 G>A maps to NM_006955.1 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr20:32379289 C>T maps to ENST00000375200 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr20:32376705 G>T maps to ENST00000375200 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:176471534 G>C did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53643806 A>G maps to NM_001172674.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53644103 G>C maps to NM_001172674.1 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53644115 A>G maps to NM_001172674.1 C656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr19:52469414 C>G maps to NM_021632.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr5:178139393 T>C maps to NM_005649.2 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr5:178139384 C>T maps to NM_005649.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr5:178293301 C>T maps to NM_058230.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr10:64415146 A>T maps to NM_199452.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr5:71756852 G>T maps to NM_152625.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:71739939 G>C maps to NM_152625.1 Y626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:71739708 C>T maps to NM_152625.1 R703R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KL-8340-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr12:6777080 C>T maps to ENST00000407384 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr12:54764719 T>C maps to NM_001130967.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr2:180310275 C>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:180308132 A>G maps to NM_152520.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr2:180383278 G>A maps to NM_152520.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:180309602 T>A maps to NM_152520.4 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr6:27368215 C>T maps to NM_001076781.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr8:28214211 A>G maps to NM_018660.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr8:28206649 A>G maps to NM_018660.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:28209092 C>A maps to NM_018660.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr18:32822820 G>A maps to NM_001135178.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr18:72346772 T>C maps to NM_017757.2 V1266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr19:53611976 T>A maps to NM_001164309.1 K441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr19:53619569 G>T maps to NM_001164309.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:58084257 A>G maps to NM_017879.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr19:58084872 A>T maps to NM_017879.1 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr19:58084929 G>A maps to NM_017879.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr19:58439173 A>T maps to NM_133460.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr19:58439305 G>A maps to NM_133460.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr16:49670776 C>T maps to NM_015069.2 E762E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr16:49672051 A>T maps to NM_015069.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:49671193 G>A maps to NM_015069.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr7:148801993 C>G maps to NM_001001661.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr7:148800799 A>G maps to NM_001001661.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:21992037 A>G maps to NM_003423.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr19:21992280 A>C maps to NM_003423.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr19:21992280 A>C maps to NM_003423.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr19:21216890 G>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:12126006 C>A maps to NM_001080411.1 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:23693622 G>A maps to NM_001077195.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr10:31134378 T>C maps to NM_182755.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr10:31134198 C>T maps to NM_182755.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr10:31138700 A>G maps to NM_182755.2 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr19:11979299 G>T maps to NM_152262.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr19:11892093 T>C maps to NM_152355.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:11892621 T>C maps to NM_152355.2 H661H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr3:44489836 C>T maps to NM_181489.5 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:44492833 T>C maps to NM_181489.5 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:58991384 G>A maps to NM_017908.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr23:134483226 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr19:44418056 G>A maps to NM_003425.3 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr19:44418081 G>A maps to NM_003425.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:44418133 G>C maps to NM_003425.3 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5832-01A-11D-1669-08 chr6:57013118 C>T maps to NM_001031623.2 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5162-01A-01D-1421-08 chr6:56997883 C>A maps to NM_001031623.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr9:109734320 C>T maps to NM_021224.4 Q2155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:109691640 G>A maps to NM_021224.4 E1816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr19:53352379 C>T maps to NM_001008801.1 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:53352379 C>T maps to NM_001008801.1 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:57037031 A>G maps to NM_020813.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr19:50550198 G>T maps to NM_015428.1 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:50548035 C>T maps to NM_015428.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr9:114304000 A>G maps to NM_133464.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr9:95610603 A>G maps to NM_031486.1 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:44112495 C>T maps to NM_145312.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr19:22836215 C>A maps to NM_020855.2 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:21606000 A>G maps to NM_001076678.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:247463961 G>C maps to NM_032752.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:58867602 C>A maps to NM_198458.1 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr16:4812664 G>A maps to NM_021646.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:19905759 G>C maps to NM_001099269.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:32873420 T>A maps to NM_014910.4 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr9:99521469 C>A maps to NM_014930.1 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5836-01A-11D-1669-08 chr10:135123288 G>A maps to NM_145806.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:27840356 A>G maps to NM_032434.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr20:62596014 C>T maps to NM_020713.1 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr18:14105185 T>C maps to NM_145287.3 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:14105674 T>C maps to NM_145287.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:22805628 G>C maps to NM_015461.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr18:22930910 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr19:37879643 G>A maps to NM_032453.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr19:52918812 T>C maps to NM_032423.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:58118341 A>T maps to NM_020880.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr18:56585626 C>T maps to NM_018181.4 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr18:56587465 T>C maps to NM_018181.4 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:52941907 C>T maps to NM_001143939.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:30936490 G>A maps to NM_014717.1 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:30936334 T>C maps to NM_014717.1 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr19:38103227 T>C maps to NM_152606.3 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr19:57838031 C>G maps to NM_213598.3 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr19:58772268 T>C maps to NM_014480.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr19:58198815 T>C maps to ENST00000356715 Y391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr19:7083598 T>C maps to NM_024341.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:7075687 C>G maps to NM_024341.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:9578113 A>C maps to NM_152476.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5838-01A-11D-1669-08 chr19:12429409 A>C maps to NM_145276.2 *477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:37916857 C>T maps to NM_152484.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:2915554 C>T maps to NM_173480.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:38056036 G>A maps to NM_016536.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr8:125987896 A>G maps to NM_152412.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:52376954 A>G maps to NM_032679.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:58290701 T>C maps to NM_017652.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr19:58371201 C>T maps to NM_032828.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:26496650 T>C maps to NM_015871.4 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr17:5086702 G>T maps to NM_032530.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr16:2050420 T>C maps to ENST00000431526 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr16:2052324 C>T maps to ENST00000431526 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:2052643 C>T maps to ENST00000431526 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:35250174 C>A maps to NM_001007248.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5084-01A-01D-1462-08 chr19:58490862 A>C maps to NM_025027.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr19:58490169 A>G maps to NM_025027.3 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr5:124079965 C>G maps to NM_020747.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr5:124079839 C>T maps to NM_020747.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:64966234 G>T maps to NM_015042.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr15:64967098 C>A maps to NM_015042.1 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr15:64968214 C>A maps to NM_015042.1 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:52857565 C>T maps to NM_001161425.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01W-0886-08 chr19:52496684 G>A maps to ENST00000354939 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:52496291 C>A maps to ENST00000354939 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:52505117 T>G maps to ENST00000354939 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr19:52619875 T>G maps to NM_178523.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr3:40528384 A>T maps to NM_001145082.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr3:40529518 C>G maps to NM_001145082.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:40553891 G>C did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr3:40574133 T>A maps to NM_001098414.1 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr19:12256408 C>T maps to ENST00000439556 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:20807269 A>G maps to NM_001076675.2 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:55993789 A>G maps to NM_033113.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:55994239 C>T maps to NM_033113.2 H556H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:30794424 G>A maps to NM_001080417.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr2:71653714 T>A maps to NM_014497.3 V1572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:71607374 T>C maps to NM_014497.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:91406115 G>A maps to NM_201269.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:91403568 G>T maps to NM_201269.1 S1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:31090722 G>A maps to NM_014699.3 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr16:31092684 C>T maps to NM_014699.3 T1680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:31089678 T>C maps to NM_014699.3 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:11594520 G>A maps to NM_138783.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr3:88190086 A>T maps to NM_018293.2 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr7:99170285 G>A maps to NM_001083956.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:99158260 C>T maps to NM_001083956.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr9:40775034 C>T maps to NM_033160.5 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:53668283 T>A maps to NM_024733.3 K487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr19:53668434 G>T maps to NM_024733.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:56952704 T>C maps to ENST00000342634 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr16:31072730 A>C maps to NM_001172669.1 G529G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KN-8437-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr16:31073369 C>G maps to ENST00000417110 L186L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KO-8410-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A3-3331-01A-01W-0886-08 chr1:247200915 T>C maps to NM_033213.3 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr1:247202839 C>T did not map to a codon.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr19:22363630 G>A maps to NM_001001411.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr19:22363588 C>T maps to NM_001001411.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr19:22363630 G>A maps to NM_001001411.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr19:22363609 A>G maps to NM_001001411.2 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:22363171 G>A maps to NM_001001411.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:22363447 A>T maps to NM_001001411.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:53740494 G>A maps to NM_182609.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr1:227842448 A>T maps to NM_178549.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr7:63981784 A>G maps to NM_178558.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr1:41012840 T>C maps to NM_152373.3 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:151259372 C>G maps to NM_020832.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:151263417 C>A maps to NM_020832.1 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:43317093 C>A maps to ENST00000442768 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr1:249150135 A>G maps to NM_001136036.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr8:144378276 G>C maps to NM_030895.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr19:9407409 G>A maps to NM_198535.1 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5083-01A-02D-1421-08 chr22:24087078 G>A maps to NM_021916.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr19:12060407 T>C maps to NM_144566.1 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr19:53086656 C>T maps to NM_001172655.1 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr8:81577133 G>T maps to NM_001033723.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr8:144776492 C>T maps to NM_173831.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:12574913 G>A maps to ENST00000428311 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr15:90616472 C>G maps to NM_198526.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr23:84510341 G>A did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr23:84526277 T>C did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr7:55991393 T>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:437055 A>G maps to NM_133474.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr4:289863 C>T maps to ENST00000419098 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr4:289887 G>A maps to ENST00000419098 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr16:30545835 C>A maps to NM_023931.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr23:134427882 C>T did not map to a codon.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr23:134427941 T>G did not map to a codon.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr19:53959770 C>T maps to NM_001008401.3 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr19:12088186 G>A maps to NM_001012753.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr19:12087920 G>C maps to NM_001012753.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:30569337 G>T maps to NM_033410.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr19:53911473 A>G maps to NM_001040185.1 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr16:30419388 G>A maps to NM_001142305.1 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr19:58018036 A>T maps to NM_198542.1 K192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr19:58016676 A>G maps to NM_198542.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:58264680 C>T maps to NM_173632.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr7:149129496 C>T maps to ENST00000440594 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:149129442 C>T maps to ENST00000440594 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr16:89294594 C>T maps to NM_182531.2 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:89294016 C>T maps to NM_182531.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr19:40540305 G>A maps to NM_001005851.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr19:40540305 G>A maps to NM_001005851.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:99580431 T>A maps to NM_001001662.1 K625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr9:99580321 G>A maps to NM_001001662.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr16:30596804 C>T maps to NM_152458.6 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr7:148769509 A>T maps to NM_152411.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr7:148768359 G>T maps to NM_152411.3 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr19:56614565 G>C maps to NM_001002836.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr7:99084909 T>C maps to NM_213603.2 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr7:99084963 G>A maps to NM_213603.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr9:130207130 T>C maps to NM_007135.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3440-01A-01D-0966-08 chr9:130207139 A>G maps to NM_007135.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr9:130206350 T>C maps to NM_007135.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr19:38027919 G>A maps to NM_001013659.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:12502557 C>T maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:12502923 A>T maps to NM_001080821.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr19:12502159 G>T maps to NM_001080821.2 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr19:58805701 C>G maps to NM_021089.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:58805587 G>A maps to NM_021089.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:185801067 A>G maps to NM_194250.1 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr19:57765249 A>T maps to NM_001023563.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:57765509 T>G maps to NM_001023563.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr19:53057179 T>C maps to NM_001039886.3 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr19:53057357 A>T maps to NM_001039886.3 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:47774691 A>G did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:47774818 A>G did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:58385872 T>C maps to NM_001144989.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr19:53454064 G>A maps to NM_001031665.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr4:146824029 C>T maps to ENST00000508784 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr19:37382714 A>G maps to NM_001171979.1 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:33288776 C>A maps to NM_052857.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:33289280 T>C maps to NM_052857.3 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3313-01A-01D-0966-08 chr20:57768698 G>A maps to NM_178457.1 Q875Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr20:57766295 C>T maps to NM_178457.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr20:57769661 G>A maps to NM_178457.1 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr20:57782031 A>G maps to NM_178457.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:57769703 C>T maps to NM_178457.1 H1210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:52660095 G>A maps to NM_001102657.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr19:52659378 A>T maps to NM_001102657.1 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr19:52659396 G>A maps to NM_001102657.1 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr19:52660630 C>T maps to NM_001102657.1 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr19:52660554 A>G maps to NM_001102657.1 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:52570737 C>A maps to NM_001136499.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr19:53856495 A>G maps to NM_138374.1 E856E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr7:149544911 C>A maps to NM_001099220.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr19:52877550 G>A did not map to a codon.
Sequencing variant TCGA-B0-5098-01A-01D-1421-08 chr19:22574542 A>G maps to NM_001098626.1 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr19:22952717 C>A did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr20:47887949 C>T maps to NM_021035.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr7:100867048 A>T maps to NM_006349.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5844-01A-11D-1669-08 chr1:86146556 G>C maps to NM_017953.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr22:29445938 C>G maps to NM_032173.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr19:5455975 C>T maps to NM_181710.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:238053764 A>T maps to NM_021186.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:238045722 T>A maps to NM_021186.3 *541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr7:50070787 A>T maps to NM_007009.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr3:102157366 T>C maps to NM_175056.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr10:126671766 G>A maps to NM_017580.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr10:126670373 A>G maps to NM_017580.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:15841259 C>G did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr23:15838365 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr19:58549264 G>T maps to NM_182572.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:3142578 C>T maps to NM_032805.1 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr19:58596699 G>A maps to NM_001145542.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr15:85147433 A>T maps to NM_181877.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:33960784 C>T maps to NM_145238.3 I947I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B0-5109-01A-02D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:43653717 T>C maps to NM_152455.3 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr15:43653849 A>G maps to NM_152455.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr15:43661268 T>C maps to NM_152455.3 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr19:56732943 T>C maps to NM_024303.1 *497W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr2:187693067 A>C maps to NM_182521.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr20:44506357 G>A maps to NM_080752.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr19:13919689 C>A maps to NM_023072.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4900-01A-01D-1462-08 chr19:13941545 C>T maps to NM_023072.2 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:13936442 G>A maps to NM_023072.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr1:45484290 G>A maps to NM_020883.1 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr6:116981932 A>C maps to NM_145062.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr15:66824727 C>T maps to NM_017975.3 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr23:57618844 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:57618702 G>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr23:57620758 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:57618714 C>T did not map to a codon.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr3:126160624 G>A maps to NM_025112.4 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:53262038 T>C maps to NM_024646.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr7:143078855 C>T maps to NM_001010972.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr17:3921210 C>T maps to NM_015113.3 R2520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr17:4005689 A>G maps to NM_015113.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr17:3977516 C>T maps to NM_015113.3 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:3919675 C>A maps to NM_015113.3 G2696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr17:3981270 C>T maps to NM_015113.3 W965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:78045310 T>C maps to NM_015534.4 K661K. Only missense variants will be evaluated by CHASM.
