Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 11 71939297 71939297 + Splice_Site SNP G G A TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chr11:71939297G>A c.246G>A c.(244-246)caG>caA p.Q82Q BLCA 11 71941240 71941240 + Missense_Mutation SNP G G C TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr11:71941240G>C c.1015G>C c.(1015-1017)Gag>Cag p.E339Q BLCA 11 71941313 71941313 + Missense_Mutation SNP G G T TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr11:71941313G>T c.1088G>T c.(1087-1089)cGc>cTc p.R363L BLCA 11 71941437 71941437 + Silent SNP G G A TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr11:71941437G>A c.1122G>A c.(1120-1122)caG>caA p.Q374Q BLCA 11 71942080 71942080 + Silent SNP G G C TCGA-4Z-AA7O-01A-31D-A391-08 TCGA-4Z-AA7O-10A-01D-A394-08 g.chr11:71942080G>C c.1344G>C c.(1342-1344)tcG>tcC p.S448S BLCA 11 71942646 71942646 + Silent SNP C C T TCGA-DK-AA6X-01A-12D-A42E-08 TCGA-DK-AA6X-10A-01D-A42H-08 g.chr11:71942646C>T c.1602C>T c.(1600-1602)atC>atT p.I534I BLCA 11 71943351 71943351 + Silent SNP C C T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr11:71943351C>T c.1683C>T c.(1681-1683)caC>caT p.H561H BLCA 11 71946178 71946178 + Missense_Mutation SNP G G C TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr11:71946178G>C c.2434G>C c.(2434-2436)Gat>Cat p.D812H BLCA 11 71946359 71946359 + Silent SNP C C G TCGA-BT-A20R-01A-12D-A16O-08 TCGA-BT-A20R-11A-11D-A16O-08 g.chr11:71946359C>G c.2523C>G c.(2521-2523)ctC>ctG p.L841L BLCA 11 71946371 71946371 + Silent SNP C C T TCGA-FD-A62N-01A-11D-A30E-08 TCGA-FD-A62N-10A-01D-A30H-08 g.chr11:71946371C>T c.2535C>T c.(2533-2535)atC>atT p.I845I BLCA 11 71946465 71946465 + Missense_Mutation SNP G G C TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr11:71946465G>C c.2629G>C c.(2629-2631)Gag>Cag p.E877Q BLCA 11 71946948 71946948 + Missense_Mutation SNP G G C TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr11:71946948G>C c.2797G>C c.(2797-2799)Gaa>Caa p.E933Q BLCA 11 71948264 71948264 + Silent SNP C C T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr11:71948264C>T c.2976C>T c.(2974-2976)gtC>gtT p.V992V BLCA 11 71948538 71948538 + Missense_Mutation SNP G G A TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr11:71948538G>A c.3250G>A c.(3250-3252)Gag>Aag p.E1084K BLCA 11 71948716 71948716 + Missense_Mutation SNP C C T TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr11:71948716C>T c.3428C>T c.(3427-3429)tCa>tTa p.S1143L BLCA 11 71949104 71949104 + Missense_Mutation SNP G G T TCGA-GC-A3BM-01A-11D-A22Z-08 TCGA-GC-A3BM-10A-01D-A22Z-08 g.chr11:71949104G>T c.3571G>T c.(3571-3573)Ggg>Tgg p.G1191W BLCA 11 71949115 71949115 + Silent SNP C C T TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr11:71949115C>T c.3582C>T c.(3580-3582)agC>agT p.S1194S BLCA 11 71949157 71949157 + Missense_Mutation SNP C C G TCGA-BT-A20R-01A-12D-A16O-08 TCGA-BT-A20R-11A-11D-A16O-08 g.chr11:71949157C>G c.3624C>G c.(3622-3624)atC>atG p.I1208M BLCA 11 71949215 71949215 + Missense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:71949215C>A c.3682C>A c.(3682-3684)Ctc>Atc p.L1228I BRCA 11 71939422 71939422 + Nonsense_Mutation SNP C C T TCGA-AN-A0FX-01A-11W-A050-09 TCGA-AN-A0FX-10A-01W-A055-09 g.chr11:71939422C>T c.277C>T c.(277-279)Cag>Tag p.Q93* BRCA 11 71939469 71939469 + Silent SNP C C T TCGA-A8-A07R-01A-21W-A050-09 TCGA-A8-A07R-10B-01D-A047-09 g.chr11:71939469C>T c.324C>T c.(322-324)ggC>ggT p.G108G BRCA 11 71940780 71940780 + Nonsense_Mutation SNP C C G TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr11:71940780C>G c.827C>G c.(826-828)tCa>tGa p.S276* BRCA 11 71941856 71941856 + Missense_Mutation SNP G G A TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr11:71941856G>A c.1214G>A c.(1213-1215)tGc>tAc p.C405Y BRCA 11 71942144 71942144 + Missense_Mutation SNP G G C TCGA-AC-A23C-01A-12D-A167-09 TCGA-AC-A23C-10A-01D-A167-09 g.chr11:71942144G>C c.1408G>C c.(1408-1410)Ggg>Cgg p.G470R BRCA 11 71942195 71942195 + Frame_Shift_Del DEL G G - TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr11:71942195delG c.1459delG c.(1459-1461)gggfs p.G488fs BRCA 11 71946992 71946992 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:71946992A>C c.2841A>C c.(2839-2841)ccA>ccC p.P947P BRCA 11 71948748 71948748 + Frame_Shift_Del DEL C C - TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr11:71948748delC c.3460delC c.(3460-3462)cccfs p.P1155fs BRCA 11 71949089 71949089 + Missense_Mutation SNP C C A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:71949089C>A c.3556C>A c.(3556-3558)Ccg>Acg p.P1186T CESC 11 71941061 71941062 + Splice_Site DNP GA GA AT TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr11:71941061_71941062GA>AT c.937_938GA>AT c.(937-939)GAg>ATg p.E313M CESC 11 71944182 71944182 + Missense_Mutation SNP C C G TCGA-EK-A2H0-01A-11D-A17W-09 TCGA-EK-A2H0-10A-01D-A17W-09 g.chr11:71944182C>G c.2015C>G c.(2014-2016)gCc>gGc p.A672G CESC 11 71944780 71944780 + Missense_Mutation SNP C C T TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr11:71944780C>T c.2204C>T c.(2203-2205)tCc>tTc p.S735F CHOL 11 71939417 71939417 + Missense_Mutation SNP G G A TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr11:71939417G>A c.272G>A c.(271-273)cGc>cAc p.R91H COAD 11 71939506 71939506 + Nonsense_Mutation SNP C C T TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr11:71939506C>T c.361C>T c.(361-363)Cga>Tga p.R121* COAD 11 71939514 71939514 + Silent SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:71939514G>A c.369G>A c.(367-369)ccG>ccA p.P123P COAD 11 71939802 71939802 + Silent SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr11:71939802G>A c.429G>A c.(427-429)ccG>ccA p.P143P COAD 11 71940985 71940985 + Missense_Mutation SNP G G T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:71940985G>T c.861G>T c.(859-861)caG>caT p.Q287H COAD 11 71941250 71941250 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:71941250G>A c.1025G>A c.(1024-1026)cGg>cAg p.R342Q COAD 11 71941447 71941447 + Missense_Mutation SNP G G T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr11:71941447G>T c.1132G>T c.(1132-1134)Ggt>Tgt p.G378C COAD 11 71941449 71941449 + Silent SNP T T C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr11:71941449T>C c.1134T>C c.(1132-1134)ggT>ggC p.G378G COAD 11 71941449 71941449 + Silent SNP T T C TCGA-F4-6805-01A-11D-1835-10 TCGA-F4-6805-10A-01D-1835-10 g.chr11:71941449T>C c.1134T>C c.(1132-1134)ggT>ggC p.G378G COAD 11 71942167 71942167 + Silent SNP C C T TCGA-AA-A01G-01A-01W-A005-10 TCGA-AA-A01G-10A-01W-A005-10 g.chr11:71942167C>T c.1431C>T c.(1429-1431)ggC>ggT p.G477G COAD 11 71942173 71942173 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr11:71942173C>T c.1437C>T c.(1435-1437)cgC>cgT p.R479R COAD 11 71942174 71942174 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:71942174G>A c.1438G>A c.(1438-1440)Gag>Aag p.E480K COAD 11 71942192 71942192 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr11:71942192C>T c.1456C>T c.(1456-1458)Cgc>Tgc p.R486C COAD 11 71943724 71943724 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr11:71943724G>A c.1767G>A c.(1765-1767)caG>caA p.Q589Q COAD 11 71944515 71944515 + Missense_Mutation SNP C C T TCGA-AA-3529-01A-02W-0831-10 TCGA-AA-3529-10A-01W-0831-10 g.chr11:71944515C>T c.2071C>T c.(2071-2073)Cgg>Tgg p.R691W COAD 11 71946427 71946427 + Missense_Mutation SNP G G A TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr11:71946427G>A c.2591G>A c.(2590-2592)gGc>gAc p.G864D COAD 11 71946427 71946427 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:71946427G>A c.2591G>A c.(2590-2592)gGc>gAc p.G864D COAD 11 71946427 71946427 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:71946427G>A c.2591G>A c.(2590-2592)gGc>gAc p.G864D COAD 11 71946900 71946900 + Missense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:71946900C>T c.2749C>T c.(2749-2751)Cgc>Tgc p.R917C COAD 11 71948238 71948238 + Missense_Mutation SNP C C A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr11:71948238C>A c.2950C>A c.(2950-2952)Cct>Act p.P984T COAD 11 71948432 71948432 + Silent SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:71948432G>A c.3144G>A c.(3142-3144)ctG>ctA p.L1048L COAD 11 71948712 71948712 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:71948712C>T c.3424C>T c.(3424-3426)Cgc>Tgc p.R1142C COAD 11 71948748 71948748 + Frame_Shift_Del DEL C C - TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:71948748delC c.3460delC c.(3460-3462)cccfs p.P1155fs COADREAD 11 71939506 71939506 + Nonsense_Mutation SNP C C T TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr11:71939506C>T c.361C>T c.(361-363)Cga>Tga p.R121* COADREAD 11 71939514 71939514 + Silent SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:71939514G>A c.369G>A c.(367-369)ccG>ccA p.P123P COADREAD 11 71939802 71939802 + Silent SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr11:71939802G>A c.429G>A c.(427-429)ccG>ccA p.P143P COADREAD 11 71940985 71940985 + Missense_Mutation SNP G G T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:71940985G>T c.861G>T c.(859-861)caG>caT p.Q287H COADREAD 11 71941250 71941250 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:71941250G>A c.1025G>A c.(1024-1026)cGg>cAg p.R342Q COADREAD 11 71941447 71941447 + Missense_Mutation SNP G G T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr11:71941447G>T c.1132G>T c.(1132-1134)Ggt>Tgt p.G378C COADREAD 11 71941449 71941449 + Silent SNP T T C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr11:71941449T>C c.1134T>C c.(1132-1134)ggT>ggC p.G378G COADREAD 11 71941449 71941449 + Silent SNP T T C TCGA-F4-6805-01A-11D-1835-10 TCGA-F4-6805-10A-01D-1835-10 g.chr11:71941449T>C c.1134T>C c.(1132-1134)ggT>ggC p.G378G COADREAD 11 71942167 71942167 + Silent SNP C C T TCGA-AA-A01G-01A-01W-A005-10 TCGA-AA-A01G-10A-01W-A005-10 g.chr11:71942167C>T c.1431C>T c.(1429-1431)ggC>ggT p.G477G COADREAD 11 71942173 71942173 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr11:71942173C>T c.1437C>T c.(1435-1437)cgC>cgT p.R479R COADREAD 11 71942174 71942174 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:71942174G>A c.1438G>A c.(1438-1440)Gag>Aag p.E480K COADREAD 11 71942192 71942192 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr11:71942192C>T c.1456C>T c.(1456-1458)Cgc>Tgc p.R486C COADREAD 11 71943724 71943724 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr11:71943724G>A c.1767G>A c.(1765-1767)caG>caA p.Q589Q COADREAD 11 71944515 71944515 + Missense_Mutation SNP C C T TCGA-AA-3529-01A-02W-0831-10 TCGA-AA-3529-10A-01W-0831-10 g.chr11:71944515C>T c.2071C>T c.(2071-2073)Cgg>Tgg p.R691W COADREAD 11 71946427 71946427 + Missense_Mutation SNP G G A TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr11:71946427G>A c.2591G>A c.(2590-2592)gGc>gAc p.G864D COADREAD 11 71946427 71946427 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:71946427G>A c.2591G>A c.(2590-2592)gGc>gAc p.G864D COADREAD 11 71946427 71946427 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:71946427G>A c.2591G>A c.(2590-2592)gGc>gAc p.G864D COADREAD 11 71946900 71946900 + Missense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:71946900C>T c.2749C>T c.(2749-2751)Cgc>Tgc p.R917C COADREAD 11 71948238 71948238 + Missense_Mutation SNP C C A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr11:71948238C>A c.2950C>A c.(2950-2952)Cct>Act p.P984T COADREAD 11 71948432 71948432 + Silent SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:71948432G>A c.3144G>A c.(3142-3144)ctG>ctA p.L1048L COADREAD 11 71948712 71948712 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:71948712C>T c.3424C>T c.(3424-3426)Cgc>Tgc p.R1142C COADREAD 11 71948748 71948748 + Frame_Shift_Del DEL C C - TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:71948748delC c.3460delC c.(3460-3462)cccfs p.P1155fs COADREAD 11 71948748 71948748 + Frame_Shift_Del DEL C C - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:71948748delC c.3460delC c.(3460-3462)cccfs p.P1155fs DLBC 11 71949157 71949157 + Silent SNP C C T TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr11:71949157C>T c.3624C>T c.(3622-3624)atC>atT p.I1208I ESCA 11 71941179 71941179 + Silent SNP G G T TCGA-IG-A4P3-01A-11D-A27G-09 TCGA-IG-A4P3-10A-01D-A27G-09 g.chr11:71941179G>T c.954G>T c.(952-954)gtG>gtT p.V318V ESCA 11 71942174 71942174 + Missense_Mutation SNP G G C TCGA-L5-A88V-01A-11D-A351-09 TCGA-L5-A88V-11A-11D-A351-09 g.chr11:71942174G>C c.1438G>C c.(1438-1440)Gag>Cag p.E480Q ESCA 11 71948432 71948433 + Frame_Shift_Ins INS - - C TCGA-V5-AASV-01A-11D-A387-09 TCGA-V5-AASV-10A-01D-A38A-09 g.chr11:71948432_71948433insC c.3144_3145insC c.(3145-3147)cccfs p.P1049fs GBM 11 71942122 71942123 + Frame_Shift_Ins INS - - C TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr11:71942122_71942123insC c.1386_1387insC c.(1387-1389)cccfs p.P463fs GBM 11 71942586 71942586 + Frame_Shift_Del DEL C C - TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chr11:71942586delC c.1542delC c.(1540-1542)gtcfs p.V514fs GBM 11 71943788 71943788 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr11:71943788C>T c.1831C>T c.(1831-1833)Cgc>Tgc p.R611C GBMLGG 11 71939482 71939482 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:71939482C>A c.337C>A c.(337-339)Ctg>Atg p.L113M GBMLGG 11 71942122 71942123 + Frame_Shift_Ins INS - - C TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr11:71942122_71942123insC c.1386_1387insC c.(1387-1389)cccfs p.P463fs GBMLGG 11 71942546 71942546 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:71942546C>T c.1502C>T c.(1501-1503)gCc>gTc p.A501V GBMLGG 11 71942586 71942586 + Frame_Shift_Del DEL C C - TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chr11:71942586delC c.1542delC c.(1540-1542)gtcfs p.V514fs GBMLGG 11 71942617 71942617 + Missense_Mutation SNP G G A TCGA-FG-7637-01A-11D-2086-08 TCGA-FG-7637-10A-01D-2086-08 g.chr11:71942617G>A c.1573G>A c.(1573-1575)Gtc>Atc p.V525I GBMLGG 11 71943759 71943759 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:71943759A>G c.1802A>G c.(1801-1803)cAc>cGc p.H601R GBMLGG 11 71943788 71943788 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr11:71943788C>T c.1831C>T c.(1831-1833)Cgc>Tgc p.R611C GBMLGG 11 71949150 71949150 + Missense_Mutation SNP G G A TCGA-DU-A6S6-01A-21D-A32B-08 TCGA-DU-A6S6-10A-01D-A329-08 g.chr11:71949150G>A c.3617G>A c.(3616-3618)cGg>cAg p.R1206Q HNSC 11 71939816 71939816 + Missense_Mutation SNP C C T TCGA-D6-A6EM-01A-21D-A31L-08 TCGA-D6-A6EM-10A-01D-A31J-08 g.chr11:71939816C>T c.443C>T c.(442-444)aCc>aTc p.T148I HNSC 11 71939892 71939892 + Splice_Site SNP G G A TCGA-D6-6823-01A-11D-1912-08 TCGA-D6-6823-10A-01D-1912-08 g.chr11:71939892G>A c.e4+1 HNSC 11 71941167 71941167 + Silent SNP G G A TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr11:71941167G>A c.942G>A c.(940-942)gtG>gtA p.V314V HNSC 11 71942179 71942179 + Nonsense_Mutation SNP G G A TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr11:71942179G>A c.1443G>A c.(1441-1443)tgG>tgA p.W481* HNSC 11 71942214 71942214 + Missense_Mutation SNP C C T TCGA-CV-6003-01A-11D-1683-08 TCGA-CV-6003-11A-01D-1683-08 g.chr11:71942214C>T c.1478C>T c.(1477-1479)aCg>aTg p.T493M HNSC 11 71943719 71943719 + Missense_Mutation SNP C C T TCGA-CN-A49C-01A-11D-A24D-08 TCGA-CN-A49C-10B-01D-A24F-08 g.chr11:71943719C>T c.1762C>T c.(1762-1764)Cgg>Tgg p.R588W HNSC 11 71946742 71946742 + Missense_Mutation SNP G G A TCGA-BA-A4IG-01A-11D-A25Y-08 TCGA-BA-A4IG-10A-01D-A25Y-08 g.chr11:71946742G>A c.2683G>A c.(2683-2685)Gag>Aag p.E895K HNSC 11 71946906 71946906 + Missense_Mutation SNP C C T TCGA-IQ-A61G-01A-11D-A30E-08 TCGA-IQ-A61G-10A-01D-A30H-08 g.chr11:71946906C>T c.2755C>T c.(2755-2757)Cca>Tca p.P919S HNSC 11 71949125 71949125 + Missense_Mutation SNP G G A TCGA-CQ-7063-01A-11D-2394-08 TCGA-CQ-7063-10A-01D-2394-08 g.chr11:71949125G>A c.3592G>A c.(3592-3594)Gag>Aag p.E1198K KIPAN 11 71939276 71939278 + In_Frame_Del DEL AGA AGA - TCGA-BP-4987-01A-01D-1462-08 TCGA-BP-4987-11A-01D-1462-08 g.chr11:71939276_71939278delAGA c.225_227delAGA c.(223-228)ggagaa>gga p.E76del KIPAN 11 71941503 71941503 + Silent SNP C C A TCGA-Y8-A8RY-01A-11D-A36X-10 TCGA-Y8-A8RY-10A-01D-A370-10 g.chr11:71941503C>A c.1188C>A c.(1186-1188)gtC>gtA p.V396V KIPAN 11 71942228 71942228 + Missense_Mutation SNP C C T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr11:71942228C>T c.1492C>T c.(1492-1494)Cgc>Tgc p.R498C KIPAN 11 71944164 71944164 + Missense_Mutation SNP G G T TCGA-IA-A40U-01A-11D-A25F-10 TCGA-IA-A40U-10A-01D-A25F-10 g.chr11:71944164G>T c.1997G>T c.(1996-1998)gGt>gTt p.G666V KIPAN 11 71948448 71948448 + Missense_Mutation SNP C C G TCGA-BP-4999-01A-01D-1462-08 TCGA-BP-4999-11A-01D-1462-08 g.chr11:71948448C>G c.3160C>G c.(3160-3162)Cca>Gca p.P1054A KIPAN 11 71948603 71948603 + Silent SNP A A G TCGA-KV-A6GD-01A-11D-A31X-10 TCGA-KV-A6GD-10A-01D-A31X-10 g.chr11:71948603A>G c.3315A>G c.(3313-3315)ccA>ccG p.P1105P KIRC 11 71939276 71939278 + In_Frame_Del DEL AGA AGA - TCGA-BP-4987-01A-01D-1462-08 TCGA-BP-4987-11A-01D-1462-08 g.chr11:71939276_71939278delAGA c.225_227delAGA c.(223-228)ggagaa>gga p.E76del KIRC 11 71948448 71948448 + Missense_Mutation SNP C C G TCGA-BP-4999-01A-01D-1462-08 TCGA-BP-4999-11A-01D-1462-08 g.chr11:71948448C>G c.3160C>G c.(3160-3162)Cca>Gca p.P1054A KIRP 11 71941503 71941503 + Silent SNP C C A TCGA-Y8-A8RY-01A-11D-A36X-10 TCGA-Y8-A8RY-10A-01D-A370-10 g.chr11:71941503C>A c.1188C>A c.(1186-1188)gtC>gtA p.V396V KIRP 11 71942228 71942228 + Missense_Mutation SNP C C T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr11:71942228C>T c.1492C>T c.(1492-1494)Cgc>Tgc p.R498C KIRP 11 71944164 71944164 + Missense_Mutation SNP G G T TCGA-IA-A40U-01A-11D-A25F-10 TCGA-IA-A40U-10A-01D-A25F-10 g.chr11:71944164G>T c.1997G>T c.(1996-1998)gGt>gTt p.G666V KIRP 11 71948603 71948603 + Silent SNP A A G TCGA-KV-A6GD-01A-11D-A31X-10 TCGA-KV-A6GD-10A-01D-A31X-10 g.chr11:71948603A>G c.3315A>G c.(3313-3315)ccA>ccG p.P1105P LGG 11 71939482 71939482 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:71939482C>A c.337C>A c.(337-339)Ctg>Atg p.L113M LGG 11 71942546 71942546 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:71942546C>T c.1502C>T c.(1501-1503)gCc>gTc p.A501V LGG 11 71942617 71942617 + Missense_Mutation SNP G G A TCGA-FG-7637-01A-11D-2086-08 TCGA-FG-7637-10A-01D-2086-08 g.chr11:71942617G>A c.1573G>A c.(1573-1575)Gtc>Atc p.V525I LGG 11 71943759 71943759 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:71943759A>G c.1802A>G c.(1801-1803)cAc>cGc p.H601R LGG 11 71949150 71949150 + Missense_Mutation SNP G G A TCGA-DU-A6S6-01A-21D-A32B-08 TCGA-DU-A6S6-10A-01D-A329-08 g.chr11:71949150G>A c.3617G>A c.(3616-3618)cGg>cAg p.R1206Q LIHC 11 71948271 71948271 + Nonsense_Mutation SNP C C T TCGA-BC-4073-01B-02D-A12Z-10 TCGA-BC-4073-10A-01D-A12Z-10 g.chr11:71948271C>T c.2983C>T c.(2983-2985)Cag>Tag p.Q995* LIHC 11 71948760 71948760 + Silent SNP C C T TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr11:71948760C>T c.3472C>T c.(3472-3474)Ctg>Ttg p.L1158L LUAD 11 71939464 71939464 + Missense_Mutation SNP C C G TCGA-44-A47G-01A-21D-A24D-08 TCGA-44-A47G-10A-01D-A24F-08 g.chr11:71939464C>G c.319C>G c.(319-321)Cag>Gag p.Q107E LUAD 11 71940249 71940249 + Missense_Mutation SNP G G T TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr11:71940249G>T c.634G>T c.(634-636)Gct>Tct p.A212S LUAD 11 71942060 71942060 + Missense_Mutation SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr11:71942060G>T c.1324G>T c.(1324-1326)Gtg>Ttg p.V442L LUAD 11 71944716 71944716 + Missense_Mutation SNP G G A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr11:71944716G>A c.2140G>A c.(2140-2142)Gtc>Atc p.V714I LUAD 11 71944745 71944745 + Silent SNP G G T TCGA-86-7711-01A-11D-2063-08 TCGA-86-7711-10A-01D-2063-08 g.chr11:71944745G>T c.2169G>T c.(2167-2169)ggG>ggT p.G723G LUAD 11 71946219 71946219 + Silent SNP C C T TCGA-67-3773-01A-01D-1040-01 TCGA-67-3773-10A-01D-1489-08 g.chr11:71946219C>T c.2475C>T c.(2473-2475)gtC>gtT p.V825V LUAD 11 71946456 71946456 + Missense_Mutation SNP G G A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr11:71946456G>A c.2620G>A c.(2620-2622)Gtg>Atg p.V874M LUAD 11 71948308 71948308 + Missense_Mutation SNP C C A TCGA-97-A4M2-01A-12D-A24P-08 TCGA-97-A4M2-10A-01D-A24P-08 g.chr11:71948308C>A c.3020C>A c.(3019-3021)gCc>gAc p.A1007D LUAD 11 71948755 71948755 + Missense_Mutation SNP G G T TCGA-78-7166-01A-12D-2063-08 TCGA-78-7166-11A-01D-2063-08 g.chr11:71948755G>T c.3467G>T c.(3466-3468)cGg>cTg p.R1156L LUAD 11 71948775 71948775 + Missense_Mutation SNP G G T TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr11:71948775G>T c.3487G>T c.(3487-3489)Ggc>Tgc p.G1163C LUAD 11 71948810 71948810 + Silent SNP G G C TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr11:71948810G>C c.3522G>C c.(3520-3522)cgG>cgC p.R1174R LUAD 11 71949145 71949145 + Missense_Mutation SNP G G T TCGA-73-4677-01A-01D-1265-08 TCGA-73-4677-11A-01D-1265-08 g.chr11:71949145G>T c.3612G>T c.(3610-3612)tgG>tgT p.W1204C LUAD 11 71949314 71949314 + Missense_Mutation SNP A A G TCGA-55-8508-01A-11D-2393-08 TCGA-55-8508-10A-01D-2393-08 g.chr11:71949314A>G c.3694A>G c.(3694-3696)Acc>Gcc p.T1232A LUAD 11 71949338 71949338 + Missense_Mutation SNP G G T TCGA-69-7763-01A-11D-2167-08 TCGA-69-7763-10A-01D-2167-08 g.chr11:71949338G>T c.3718G>T c.(3718-3720)Ggg>Tgg p.G1240W LUSC 11 71939479 71939479 + Missense_Mutation SNP G G C TCGA-56-5898-01A-11D-1632-08 TCGA-56-5898-10A-01D-1632-08 g.chr11:71939479G>C c.334G>C c.(334-336)Gcc>Ccc p.A112P LUSC 11 71940529 71940529 + Nonsense_Mutation SNP C C G TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr11:71940529C>G c.680C>G c.(679-681)tCa>tGa p.S227* LUSC 11 71942192 71942192 + Missense_Mutation SNP C C T TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr11:71942192C>T c.1456C>T c.(1456-1458)Cgc>Tgc p.R486C LUSC 11 71946722 71946722 + Frame_Shift_Del DEL G G - TCGA-66-2768-01A-01D-1522-08 TCGA-66-2768-11A-01D-1522-08 g.chr11:71946722delG c.2663delG c.(2662-2664)tggfs p.W888fs OV 11 71939237 71939237 + Silent SNP T T C TCGA-20-1685-01A-01W-0633-09 TCGA-20-1685-10A-01W-0633-09 g.chr11:71939237T>C c.186T>C c.(184-186)taT>taC p.Y62Y OV 11 71941250 71941250 + Missense_Mutation SNP G G A TCGA-04-1343-01A-01W-0488-09 TCGA-04-1343-10A-01W-0489-09 g.chr11:71941250G>A c.1025G>A c.(1024-1026)cGg>cAg p.R342Q OV 11 71945599 71945599 + Silent SNP C C G TCGA-61-1740-01A-01W-0639-09 TCGA-61-1740-11A-01W-0639-09 g.chr11:71945599C>G c.2355C>G c.(2353-2355)gcC>gcG p.A785A PAAD 11 71941873 71941873 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:71941873A>G c.1231A>G c.(1231-1233)Atg>Gtg p.M411V PAAD 11 71948167 71948167 + Splice_Site SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:71948167G>T c.e26-1 PRAD 11 71946489 71946489 + Missense_Mutation SNP C C T TCGA-V1-A9ZK-01A-11D-A41K-08 TCGA-V1-A9ZK-10A-01D-A41N-08 g.chr11:71946489C>T c.2653C>T c.(2653-2655)Ctc>Ttc p.L885F READ 11 71948748 71948748 + Frame_Shift_Del DEL C C - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:71948748delC c.3460delC c.(3460-3462)cccfs p.P1155fs SARC 11 71943350 71943350 + Missense_Mutation SNP A A T TCGA-WK-A8XS-01A-11D-A37C-09 TCGA-WK-A8XS-10E-01D-A37F-09 g.chr11:71943350A>T c.1682A>T c.(1681-1683)cAc>cTc p.H561L SKCM 11 71939239 71939240 + Frame_Shift_Del DEL AG AG - TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr11:71939239_71939240delAG c.188_189delAG c.(187-189)cagfs p.Q63fs SKCM 11 71939529 71939529 + Silent SNP C C T TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr11:71939529C>T c.384C>T c.(382-384)gaC>gaT p.D128D SKCM 11 71939530 71939530 + Missense_Mutation SNP C C T TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr11:71939530C>T c.385C>T c.(385-387)Cgg>Tgg p.R129W SKCM 11 71939791 71939791 + Missense_Mutation SNP C C T TCGA-DA-A1I2-06A-21D-A19A-08 TCGA-DA-A1I2-10A-01D-A19A-08 g.chr11:71939791C>T c.418C>T c.(418-420)Ccg>Tcg p.P140S SKCM 11 71940600 71940600 + Nonsense_Mutation SNP C C T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr11:71940600C>T c.751C>T c.(751-753)Cag>Tag p.Q251* SKCM 11 71940997 71940997 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:71940997C>T c.873C>T c.(871-873)tcC>tcT p.S291S SKCM 11 71941316 71941316 + Splice_Site SNP G G C TCGA-D9-A3Z3-06A-11D-A23B-08 TCGA-D9-A3Z3-10A-01D-A23B-08 g.chr11:71941316G>C c.e9+1 SKCM 11 71941504 71941504 + Missense_Mutation SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:71941504A>G c.1189A>G c.(1189-1191)Agt>Ggt p.S397G SKCM 11 71941854 71941854 + Silent SNP C C T TCGA-FS-A1ZS-06A-12D-A197-08 TCGA-FS-A1ZS-10A-01D-A199-08 g.chr11:71941854C>T c.1212C>T c.(1210-1212)ttC>ttT p.F404F SKCM 11 71942074 71942074 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:71942074C>T c.1338C>T c.(1336-1338)ttC>ttT p.F446F SKCM 11 71942105 71942105 + Missense_Mutation SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr11:71942105G>A c.1369G>A c.(1369-1371)Gag>Aag p.E457K SKCM 11 71942228 71942228 + Missense_Mutation SNP C C T TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr11:71942228C>T c.1492C>T c.(1492-1494)Cgc>Tgc p.R498C SKCM 11 71944134 71944134 + Missense_Mutation SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr11:71944134C>T c.1967C>T c.(1966-1968)tCc>tTc p.S656F SKCM 11 71944756 71944756 + Missense_Mutation SNP T T C TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr11:71944756T>C c.2180T>C c.(2179-2181)gTt>gCt p.V727A SKCM 11 71945360 71945360 + Missense_Mutation SNP T T C TCGA-EE-A2GB-06A-11D-A197-08 TCGA-EE-A2GB-10A-01D-A199-08 g.chr11:71945360T>C c.2248T>C c.(2248-2250)Ttt>Ctt p.F750L SKCM 11 71945395 71945395 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:71945395C>T c.2283C>T c.(2281-2283)agC>agT p.S761S SKCM 11 71946225 71946225 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:71946225C>T c.2481C>T c.(2479-2481)tcC>tcT p.S827S SKCM 11 71946393 71946393 + Silent SNP C C T TCGA-FS-A4FD-06A-11D-A25O-08 TCGA-FS-A4FD-10B-01D-A25O-08 g.chr11:71946393C>T c.2557C>T c.(2557-2559)Ctg>Ttg p.L853L SKCM 11 71946398 71946398 + Silent SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:71946398C>T c.2562C>T c.(2560-2562)acC>acT p.T854T SKCM 11 71946430 71946430 + Missense_Mutation SNP A A T TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr11:71946430A>T c.2594A>T c.(2593-2595)aAt>aTt p.N865I SKCM 11 71946937 71946937 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr11:71946937C>T c.2786C>T c.(2785-2787)tCc>tTc p.S929F SKCM 11 71946938 71946938 + Silent SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr11:71946938C>T c.2787C>T c.(2785-2787)tcC>tcT p.S929S SKCM 11 71946982 71946982 + Missense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr11:71946982C>T c.2831C>T c.(2830-2832)cCc>cTc p.P944L SKCM 11 71948209 71948209 + Frame_Shift_Del DEL C C - TCGA-ER-A3EV-06A-11D-A20D-08 TCGA-ER-A3EV-10A-01D-A20D-08 g.chr11:71948209delC c.2921delC c.(2920-2922)gccfs p.A974fs SKCM 11 71948210 71948210 + Silent SNP C C T TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr11:71948210C>T c.2922C>T c.(2920-2922)gcC>gcT p.A974A SKCM 11 71948326 71948326 + Missense_Mutation SNP C C T TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr11:71948326C>T c.3038C>T c.(3037-3039)aCc>aTc p.T1013I SKCM 11 71948480 71948480 + Silent SNP C C T TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr11:71948480C>T c.3192C>T c.(3190-3192)ttC>ttT p.F1064F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 11 71932542 71932542 single base substitution C T upstream_gene_variant BLCA-US 11 71932735 71932735 single base substitution G C upstream_gene_variant BLCA-US 11 71943351 71943351 single base substitution C T downstream_gene_variant BLCA-US 11 71943351 71943351 single base substitution C T exon_variant BLCA-US 11 71943351 71943351 single base substitution C T synonymous_variant H319H 957C>T BLCA-US 11 71943351 71943351 single base substitution C T synonymous_variant H561H 1683C>T BLCA-US 11 71943351 71943351 single base substitution C T upstream_gene_variant BLCA-US 11 71946359 71946359 single base substitution C G downstream_gene_variant BLCA-US 11 71946359 71946359 single base substitution C G exon_variant BLCA-US 11 71946359 71946359 single base substitution C G intron_variant BLCA-US 11 71946359 71946359 single base substitution C G synonymous_variant L599L 1797C>G BLCA-US 11 71946359 71946359 single base substitution C G synonymous_variant L841L 2523C>G BLCA-US 11 71946359 71946359 single base substitution C G upstream_gene_variant BLCA-US 11 71949087 71949087 single base substitution C A downstream_gene_variant BLCA-US 11 71949087 71949087 single base substitution C A intron_variant BLCA-US 11 71949087 71949087 single base substitution C A missense_variant A1185D 3554C>A BLCA-US 11 71949087 71949087 single base substitution C A missense_variant A46D 137C>A BLCA-US 11 71949087 71949087 single base substitution C A missense_variant A943D 2828C>A BLCA-US 11 71949104 71949104 single base substitution G T downstream_gene_variant BLCA-US 11 71949104 71949104 single base substitution G T intron_variant BLCA-US 11 71949104 71949104 single base substitution G T missense_variant G1191W 3571G>T BLCA-US 11 71949104 71949104 single base substitution G T missense_variant G52W 154G>T BLCA-US 11 71949104 71949104 single base substitution G T missense_variant G949W 2845G>T BLCA-US 11 71949115 71949115 single base substitution C T downstream_gene_variant BLCA-US 11 71949115 71949115 single base substitution C T intron_variant BLCA-US 11 71949115 71949115 single base substitution C T synonymous_variant S1194S 3582C>T BLCA-US 11 71949115 71949115 single base substitution C T synonymous_variant S55S 165C>T BLCA-US 11 71949115 71949115 single base substitution C T synonymous_variant S952S 2856C>T BLCA-US 11 71949157 71949157 single base substitution C G downstream_gene_variant BLCA-US 11 71949157 71949157 single base substitution C G intron_variant BLCA-US 11 71949157 71949157 single base substitution C G missense_variant I1208M 3624C>G BLCA-US 11 71949157 71949157 single base substitution C G missense_variant I69M 207C>G BLCA-US 11 71949157 71949157 single base substitution C G missense_variant I966M 2898C>G BLCA-US 11 71950871 71950871 single base substitution G A downstream_gene_variant BRCA-EU 11 71929956 71929956 single base substitution C T upstream_gene_variant BRCA-EU 11 71930399 71930399 deletion of <=200bp T - upstream_gene_variant BRCA-EU 11 71932432 71932432 single base substitution G A upstream_gene_variant BRCA-EU 11 71933232 71933232 single base substitution C G upstream_gene_variant BRCA-EU 11 71934218 71934218 single base substitution G A upstream_gene_variant BRCA-EU 11 71935435 71935435 single base substitution C G intron_variant BRCA-EU 11 71935435 71935435 single base substitution C G upstream_gene_variant BRCA-EU 11 71939096 71939096 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 11 71939096 71939096 single base substitution G A downstream_gene_variant BRCA-EU 11 71939096 71939096 single base substitution G A intron_variant BRCA-EU 11 71939096 71939096 single base substitution G A upstream_gene_variant BRCA-EU 11 71939802 71939802 single base substitution G A 5_prime_UTR_variant BRCA-EU 11 71939802 71939802 single base substitution G A downstream_gene_variant BRCA-EU 11 71939802 71939802 single base substitution G A synonymous_variant P143P 429G>A BRCA-EU 11 71939802 71939802 single base substitution G A upstream_gene_variant BRCA-EU 11 71941613 71941613 single base substitution C T downstream_gene_variant BRCA-EU 11 71941613 71941613 single base substitution C T intron_variant BRCA-EU 11 71941613 71941613 single base substitution C T upstream_gene_variant BRCA-EU 11 71942131 71942131 single base substitution C A downstream_gene_variant BRCA-EU 11 71942131 71942131 single base substitution C A exon_variant BRCA-EU 11 71942131 71942131 single base substitution C A missense_variant D223E 669C>A BRCA-EU 11 71942131 71942131 single base substitution C A missense_variant D465E 1395C>A BRCA-EU 11 71942131 71942131 single base substitution C A upstream_gene_variant BRCA-EU 11 71942207 71942207 single base substitution G T downstream_gene_variant BRCA-EU 11 71942207 71942207 single base substitution G T exon_variant BRCA-EU 11 71942207 71942207 single base substitution G T stop_gained E249* 745G>T BRCA-EU 11 71942207 71942207 single base substitution G T stop_gained E491* 1471G>T BRCA-EU 11 71942207 71942207 single base substitution G T upstream_gene_variant BRCA-EU 11 71942499 71942499 single base substitution G C downstream_gene_variant BRCA-EU 11 71942499 71942499 single base substitution G C exon_variant BRCA-EU 11 71942499 71942499 single base substitution G C intron_variant BRCA-EU 11 71942499 71942499 single base substitution G C upstream_gene_variant BRCA-EU 11 71942733 71942733 single base substitution G C downstream_gene_variant BRCA-EU 11 71942733 71942733 single base substitution G C intron_variant BRCA-EU 11 71942733 71942733 single base substitution G C upstream_gene_variant BRCA-EU 11 71943332 71943332 single base substitution T C downstream_gene_variant BRCA-EU 11 71943332 71943332 single base substitution T C exon_variant BRCA-EU 11 71943332 71943332 single base substitution T C missense_variant F313S 938T>C BRCA-EU 11 71943332 71943332 single base substitution T C missense_variant F555S 1664T>C BRCA-EU 11 71943332 71943332 single base substitution T C upstream_gene_variant BRCA-EU 11 71943934 71943934 single base substitution A G downstream_gene_variant BRCA-EU 11 71943934 71943934 single base substitution A G exon_variant BRCA-EU 11 71943934 71943934 single base substitution A G missense_variant I381V 1141A>G BRCA-EU 11 71943934 71943934 single base substitution A G missense_variant I623V 1867A>G BRCA-EU 11 71943934 71943934 single base substitution A G upstream_gene_variant BRCA-EU 11 71946373 71946373 single base substitution G C downstream_gene_variant BRCA-EU 11 71946373 71946373 single base substitution G C exon_variant BRCA-EU 11 71946373 71946373 single base substitution G C intron_variant BRCA-EU 11 71946373 71946373 single base substitution G C missense_variant G604A 1811G>C BRCA-EU 11 71946373 71946373 single base substitution G C missense_variant G846A 2537G>C BRCA-EU 11 71946373 71946373 single base substitution G C upstream_gene_variant BRCA-EU 11 71947511 71947511 single base substitution G C downstream_gene_variant BRCA-EU 11 71947511 71947511 single base substitution G C intron_variant BRCA-EU 11 71947511 71947511 single base substitution G C upstream_gene_variant BRCA-EU 11 71948992 71948992 single base substitution T C downstream_gene_variant BRCA-EU 11 71948992 71948992 single base substitution T C intron_variant BRCA-EU 11 71949199 71949199 single base substitution G A downstream_gene_variant BRCA-EU 11 71949199 71949199 single base substitution G A intron_variant BRCA-EU 11 71949199 71949199 single base substitution G A stop_gained W1222* 3666G>A BRCA-EU 11 71949199 71949199 single base substitution G A stop_gained W83* 249G>A BRCA-EU 11 71949199 71949199 single base substitution G A stop_gained W980* 2940G>A BRCA-EU 11 71949200 71949200 single base substitution G C downstream_gene_variant BRCA-EU 11 71949200 71949200 single base substitution G C intron_variant BRCA-EU 11 71949200 71949200 single base substitution G C missense_variant D1223H 3667G>C BRCA-EU 11 71949200 71949200 single base substitution G C missense_variant D84H 250G>C BRCA-EU 11 71949200 71949200 single base substitution G C missense_variant D981H 2941G>C BRCA-EU 11 71949396 71949396 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 71949396 71949396 single base substitution G C downstream_gene_variant BRCA-EU 11 71949396 71949396 single base substitution G C intron_variant BRCA-EU 11 71949396 71949396 single base substitution G C stop_lost *1017S 3050G>C BRCA-EU 11 71949396 71949396 single base substitution G C stop_lost *1259S 3776G>C BRCA-EU 11 71949396 71949396 single base substitution G C stop_lost *149S 446G>C BRCA-EU 11 71949417 71949417 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 71949417 71949417 single base substitution C G downstream_gene_variant BRCA-EU 11 71949417 71949417 single base substitution C G intron_variant BRCA-EU 11 71951518 71951518 single base substitution T G downstream_gene_variant BRCA-EU 11 71954215 71954215 single base substitution G C downstream_gene_variant BRCA-EU 11 71955139 71955139 single base substitution C G downstream_gene_variant BRCA-FR 11 71933579 71933579 single base substitution G A upstream_gene_variant BRCA-FR 11 71937790 71937790 single base substitution G A downstream_gene_variant BRCA-FR 11 71937790 71937790 single base substitution G A intron_variant BRCA-FR 11 71937790 71937790 single base substitution G A upstream_gene_variant BRCA-FR 11 71942605 71942605 single base substitution C T downstream_gene_variant BRCA-FR 11 71942605 71942605 single base substitution C T exon_variant BRCA-FR 11 71942605 71942605 single base substitution C T missense_variant R279C 835C>T BRCA-FR 11 71942605 71942605 single base substitution C T missense_variant R521C 1561C>T BRCA-FR 11 71942605 71942605 single base substitution C T upstream_gene_variant BRCA-FR 11 71953705 71953705 single base substitution C A downstream_gene_variant BRCA-FR 11 71954215 71954215 single base substitution G C downstream_gene_variant BRCA-KR 11 71946297 71946297 single base substitution G C downstream_gene_variant BRCA-KR 11 71946297 71946297 single base substitution G C intron_variant BRCA-KR 11 71946297 71946297 single base substitution G C upstream_gene_variant BRCA-UK 11 71932638 71932638 single base substitution C T upstream_gene_variant BRCA-UK 11 71935908 71935908 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-UK 11 71935908 71935908 single base substitution C T upstream_gene_variant BRCA-UK 11 71942499 71942499 single base substitution G C downstream_gene_variant BRCA-UK 11 71942499 71942499 single base substitution G C exon_variant BRCA-UK 11 71942499 71942499 single base substitution G C intron_variant BRCA-UK 11 71942499 71942499 single base substitution G C upstream_gene_variant BRCA-UK 11 71943044 71943044 single base substitution C T downstream_gene_variant BRCA-UK 11 71943044 71943044 single base substitution C T intron_variant BRCA-UK 11 71943044 71943044 single base substitution C T upstream_gene_variant BRCA-UK 11 71951149 71951149 single base substitution C G downstream_gene_variant BRCA-US 11 71939422 71939422 single base substitution C T 5_prime_UTR_variant BRCA-US 11 71939422 71939422 single base substitution C T downstream_gene_variant BRCA-US 11 71939422 71939422 single base substitution C T exon_variant BRCA-US 11 71939422 71939422 single base substitution C T stop_gained Q93* 277C>T BRCA-US 11 71939422 71939422 single base substitution C T upstream_gene_variant BRCA-US 11 71939469 71939469 single base substitution C T 5_prime_UTR_variant BRCA-US 11 71939469 71939469 single base substitution C T downstream_gene_variant BRCA-US 11 71939469 71939469 single base substitution C T exon_variant BRCA-US 11 71939469 71939469 single base substitution C T synonymous_variant G108G 324C>T BRCA-US 11 71939469 71939469 single base substitution C T upstream_gene_variant BRCA-US 11 71940780 71940780 single base substitution C G downstream_gene_variant BRCA-US 11 71940780 71940780 single base substitution C G intron_variant BRCA-US 11 71940780 71940780 single base substitution C G stop_gained S276* 827C>G BRCA-US 11 71940780 71940780 single base substitution C G stop_gained S34* 101C>G BRCA-US 11 71940780 71940780 single base substitution C G synonymous_variant ?34 BRCA-US 11 71940780 71940780 single base substitution C G upstream_gene_variant BRCA-US 11 71941856 71941856 single base substitution G A downstream_gene_variant BRCA-US 11 71941856 71941856 single base substitution G A exon_variant BRCA-US 11 71941856 71941856 single base substitution G A missense_variant C163Y 488G>A BRCA-US 11 71941856 71941856 single base substitution G A missense_variant C405Y 1214G>A BRCA-US 11 71941856 71941856 single base substitution G A upstream_gene_variant BRCA-US 11 71942144 71942144 single base substitution G C downstream_gene_variant BRCA-US 11 71942144 71942144 single base substitution G C exon_variant BRCA-US 11 71942144 71942144 single base substitution G C missense_variant G228R 682G>C BRCA-US 11 71942144 71942144 single base substitution G C missense_variant G470R 1408G>C BRCA-US 11 71942144 71942144 single base substitution G C upstream_gene_variant BRCA-US 11 71942195 71942195 deletion of <=200bp G - downstream_gene_variant BRCA-US 11 71942195 71942195 deletion of <=200bp G - exon_variant BRCA-US 11 71942195 71942195 deletion of <=200bp G - frameshift_variant G245 BRCA-US 11 71942195 71942195 deletion of <=200bp G - frameshift_variant G487 BRCA-US 11 71942195 71942195 deletion of <=200bp G - upstream_gene_variant BRCA-US 11 71946992 71946992 single base substitution A C downstream_gene_variant BRCA-US 11 71946992 71946992 single base substitution A C intron_variant BRCA-US 11 71946992 71946992 single base substitution A C synonymous_variant P705P 2115A>C BRCA-US 11 71946992 71946992 single base substitution A C synonymous_variant P947P 2841A>C BRCA-US 11 71946992 71946992 single base substitution A C upstream_gene_variant BRCA-US 11 71948208 71948208 insertion of <=200bp - C downstream_gene_variant BRCA-US 11 71948208 71948208 insertion of <=200bp - C frameshift_variant A732R? BRCA-US 11 71948208 71948208 insertion of <=200bp - C frameshift_variant A974R? BRCA-US 11 71948208 71948208 insertion of <=200bp - C intron_variant BRCA-US 11 71948208 71948208 insertion of <=200bp - C upstream_gene_variant BRCA-US 11 71948748 71948748 deletion of <=200bp C - downstream_gene_variant BRCA-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P1154 BRCA-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P15 BRCA-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P167 BRCA-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P912 BRCA-US 11 71948748 71948748 deletion of <=200bp C - intron_variant BRCA-US 11 71949089 71949089 single base substitution C A downstream_gene_variant BRCA-US 11 71949089 71949089 single base substitution C A intron_variant BRCA-US 11 71949089 71949089 single base substitution C A missense_variant P1186T 3556C>A BRCA-US 11 71949089 71949089 single base substitution C A missense_variant P47T 139C>A BRCA-US 11 71949089 71949089 single base substitution C A missense_variant P944T 2830C>A BTCA-JP 11 71940699 71940699 deletion of <=200bp C - downstream_gene_variant BTCA-JP 11 71940699 71940699 deletion of <=200bp C - intron_variant BTCA-JP 11 71940699 71940699 deletion of <=200bp C - splice_region_variant BTCA-JP 11 71940699 71940699 deletion of <=200bp C - upstream_gene_variant BTCA-JP 11 71941220 71941220 single base substitution T A downstream_gene_variant BTCA-JP 11 71941220 71941220 single base substitution T A missense_variant F332Y 995T>A BTCA-JP 11 71941220 71941220 single base substitution T A missense_variant F60Y 179T>A BTCA-JP 11 71941220 71941220 single base substitution T A missense_variant F90Y 269T>A BTCA-JP 11 71941220 71941220 single base substitution T A upstream_gene_variant BTCA-JP 11 71946688 71946688 single base substitution C T downstream_gene_variant BTCA-JP 11 71946688 71946688 single base substitution C T intron_variant BTCA-JP 11 71946688 71946688 single base substitution C T upstream_gene_variant BTCA-JP 11 71946770 71946770 single base substitution C T downstream_gene_variant BTCA-JP 11 71946770 71946770 single base substitution C T exon_variant BTCA-JP 11 71946770 71946770 single base substitution C T intron_variant BTCA-JP 11 71946770 71946770 single base substitution C T missense_variant S662F 1985C>T BTCA-JP 11 71946770 71946770 single base substitution C T missense_variant S904F 2711C>T BTCA-JP 11 71946770 71946770 single base substitution C T upstream_gene_variant BTCA-JP 11 71946779 71946779 single base substitution G A downstream_gene_variant BTCA-JP 11 71946779 71946779 single base substitution G A exon_variant BTCA-JP 11 71946779 71946779 single base substitution G A intron_variant BTCA-JP 11 71946779 71946779 single base substitution G A missense_variant R665Q 1994G>A BTCA-JP 11 71946779 71946779 single base substitution G A missense_variant R907Q 2720G>A BTCA-JP 11 71946779 71946779 single base substitution G A upstream_gene_variant BTCA-JP 11 71948484 71948484 deletion of <=200bp C - downstream_gene_variant BTCA-JP 11 71948484 71948484 deletion of <=200bp C - frameshift_variant P1066 BTCA-JP 11 71948484 71948484 deletion of <=200bp C - frameshift_variant P79 BTCA-JP 11 71948484 71948484 deletion of <=200bp C - frameshift_variant P824 BTCA-JP 11 71948484 71948484 deletion of <=200bp C - intron_variant BTCA-JP 11 71948484 71948484 deletion of <=200bp C - upstream_gene_variant BTCA-JP 11 71948754 71948754 single base substitution C T downstream_gene_variant BTCA-JP 11 71948754 71948754 single base substitution C T intron_variant BTCA-JP 11 71948754 71948754 single base substitution C T missense_variant R1156W 3466C>T BTCA-JP 11 71948754 71948754 single base substitution C T missense_variant R169W 505C>T BTCA-JP 11 71948754 71948754 single base substitution C T missense_variant R17W 49C>T BTCA-JP 11 71948754 71948754 single base substitution C T missense_variant R914W 2740C>T CESC-US 11 71941061 71941061 single base substitution G A downstream_gene_variant CESC-US 11 71941061 71941061 single base substitution G A missense_variant E313K 937G>A CESC-US 11 71941061 71941061 single base substitution G A missense_variant E41K 121G>A CESC-US 11 71941061 71941061 single base substitution G A missense_variant E71K 211G>A CESC-US 11 71941061 71941061 single base substitution G A upstream_gene_variant CESC-US 11 71941062 71941062 single base substitution A T downstream_gene_variant CESC-US 11 71941062 71941062 single base substitution A T missense_variant E313V 938A>T CESC-US 11 71941062 71941062 single base substitution A T missense_variant E41V 122A>T CESC-US 11 71941062 71941062 single base substitution A T missense_variant E71V 212A>T CESC-US 11 71941062 71941062 single base substitution A T upstream_gene_variant CESC-US 11 71944182 71944182 single base substitution C G downstream_gene_variant CESC-US 11 71944182 71944182 single base substitution C G exon_variant CESC-US 11 71944182 71944182 single base substitution C G missense_variant A430G 1289C>G CESC-US 11 71944182 71944182 single base substitution C G missense_variant A672G 2015C>G CESC-US 11 71944182 71944182 single base substitution C G upstream_gene_variant CESC-US 11 71944780 71944780 single base substitution C T downstream_gene_variant CESC-US 11 71944780 71944780 single base substitution C T exon_variant CESC-US 11 71944780 71944780 single base substitution C T missense_variant S493F 1478C>T CESC-US 11 71944780 71944780 single base substitution C T missense_variant S735F 2204C>T CESC-US 11 71944780 71944780 single base substitution C T upstream_gene_variant CLLE-ES 11 71951908 71951908 single base substitution G A downstream_gene_variant COAD-US 11 71932236 71932236 single base substitution G A upstream_gene_variant COAD-US 11 71932615 71932615 single base substitution G A upstream_gene_variant COAD-US 11 71939506 71939506 single base substitution C T 5_prime_UTR_variant COAD-US 11 71939506 71939506 single base substitution C T downstream_gene_variant COAD-US 11 71939506 71939506 single base substitution C T exon_variant COAD-US 11 71939506 71939506 single base substitution C T stop_gained R121* 361C>T COAD-US 11 71939506 71939506 single base substitution C T upstream_gene_variant COAD-US 11 71941250 71941250 single base substitution G A downstream_gene_variant COAD-US 11 71941250 71941250 single base substitution G A missense_variant R100Q 299G>A COAD-US 11 71941250 71941250 single base substitution G A missense_variant R342Q 1025G>A COAD-US 11 71941250 71941250 single base substitution G A missense_variant R70Q 209G>A COAD-US 11 71941250 71941250 single base substitution G A upstream_gene_variant COAD-US 11 71942174 71942174 single base substitution G A downstream_gene_variant COAD-US 11 71942174 71942174 single base substitution G A exon_variant COAD-US 11 71942174 71942174 single base substitution G A missense_variant E238K 712G>A COAD-US 11 71942174 71942174 single base substitution G A missense_variant E480K 1438G>A COAD-US 11 71942174 71942174 single base substitution G A upstream_gene_variant COAD-US 11 71943704 71943704 single base substitution C T downstream_gene_variant COAD-US 11 71943704 71943704 single base substitution C T exon_variant COAD-US 11 71943704 71943704 single base substitution C T missense_variant L341F 1021C>T COAD-US 11 71943704 71943704 single base substitution C T missense_variant L583F 1747C>T COAD-US 11 71943704 71943704 single base substitution C T upstream_gene_variant COAD-US 11 71943724 71943724 single base substitution G A downstream_gene_variant COAD-US 11 71943724 71943724 single base substitution G A exon_variant COAD-US 11 71943724 71943724 single base substitution G A synonymous_variant Q347Q 1041G>A COAD-US 11 71943724 71943724 single base substitution G A synonymous_variant Q589Q 1767G>A COAD-US 11 71943724 71943724 single base substitution G A upstream_gene_variant COAD-US 11 71946900 71946900 single base substitution C T downstream_gene_variant COAD-US 11 71946900 71946900 single base substitution C T exon_variant COAD-US 11 71946900 71946900 single base substitution C T intron_variant COAD-US 11 71946900 71946900 single base substitution C T missense_variant R675C 2023C>T COAD-US 11 71946900 71946900 single base substitution C T missense_variant R917C 2749C>T COAD-US 11 71946900 71946900 single base substitution C T upstream_gene_variant COAD-US 11 71948432 71948432 single base substitution G A downstream_gene_variant COAD-US 11 71948432 71948432 single base substitution G A intron_variant COAD-US 11 71948432 71948432 single base substitution G A synonymous_variant L1048L 3144G>A COAD-US 11 71948432 71948432 single base substitution G A synonymous_variant L61L 183G>A COAD-US 11 71948432 71948432 single base substitution G A synonymous_variant L806L 2418G>A COAD-US 11 71948432 71948432 single base substitution G A upstream_gene_variant COAD-US 11 71948712 71948712 single base substitution C T downstream_gene_variant COAD-US 11 71948712 71948712 single base substitution C T intron_variant COAD-US 11 71948712 71948712 single base substitution C T missense_variant R1142C 3424C>T COAD-US 11 71948712 71948712 single base substitution C T missense_variant R155C 463C>T COAD-US 11 71948712 71948712 single base substitution C T missense_variant R3C 7C>T COAD-US 11 71948712 71948712 single base substitution C T missense_variant R900C 2698C>T COAD-US 11 71948748 71948748 deletion of <=200bp C - downstream_gene_variant COAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P1154 COAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P15 COAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P167 COAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P912 COAD-US 11 71948748 71948748 deletion of <=200bp C - intron_variant COAD-US 11 71952252 71952252 single base substitution G A downstream_gene_variant COAD-US 11 71952331 71952331 single base substitution G T downstream_gene_variant COCA-CN 11 71932683 71932683 single base substitution C G upstream_gene_variant COCA-CN 11 71940112 71940112 single base substitution A C 5_prime_UTR_variant COCA-CN 11 71940112 71940112 single base substitution A C downstream_gene_variant COCA-CN 11 71940112 71940112 single base substitution A C intron_variant COCA-CN 11 71940112 71940112 single base substitution A C upstream_gene_variant COCA-CN 11 71940124 71940124 single base substitution C T 5_prime_UTR_variant COCA-CN 11 71940124 71940124 single base substitution C T downstream_gene_variant COCA-CN 11 71940124 71940124 single base substitution C T intron_variant COCA-CN 11 71940124 71940124 single base substitution C T upstream_gene_variant COCA-CN 11 71941117 71941117 single base substitution G A downstream_gene_variant COCA-CN 11 71941117 71941117 single base substitution G A intron_variant COCA-CN 11 71941117 71941117 single base substitution G A upstream_gene_variant COCA-CN 11 71943770 71943770 single base substitution T G downstream_gene_variant COCA-CN 11 71943770 71943770 single base substitution T G exon_variant COCA-CN 11 71943770 71943770 single base substitution T G missense_variant F363V 1087T>G COCA-CN 11 71943770 71943770 single base substitution T G missense_variant F605V 1813T>G COCA-CN 11 71943770 71943770 single base substitution T G upstream_gene_variant COCA-CN 11 71946165 71946165 single base substitution A G downstream_gene_variant COCA-CN 11 71946165 71946165 single base substitution A G exon_variant COCA-CN 11 71946165 71946165 single base substitution A G intron_variant COCA-CN 11 71946165 71946165 single base substitution A G synonymous_variant K565K 1695A>G COCA-CN 11 71946165 71946165 single base substitution A G synonymous_variant K807K 2421A>G COCA-CN 11 71946165 71946165 single base substitution A G upstream_gene_variant COCA-CN 11 71946468 71946468 single base substitution C T downstream_gene_variant COCA-CN 11 71946468 71946468 single base substitution C T exon_variant COCA-CN 11 71946468 71946468 single base substitution C T intron_variant COCA-CN 11 71946468 71946468 single base substitution C T missense_variant R636C 1906C>T COCA-CN 11 71946468 71946468 single base substitution C T missense_variant R878C 2632C>T COCA-CN 11 71946468 71946468 single base substitution C T upstream_gene_variant COCA-CN 11 71948207 71948207 single base substitution G A downstream_gene_variant COCA-CN 11 71948207 71948207 single base substitution G A intron_variant COCA-CN 11 71948207 71948207 single base substitution G A synonymous_variant A731A 2193G>A COCA-CN 11 71948207 71948207 single base substitution G A synonymous_variant A973A 2919G>A COCA-CN 11 71948207 71948207 single base substitution G A upstream_gene_variant COCA-CN 11 71948512 71948512 single base substitution C A downstream_gene_variant COCA-CN 11 71948512 71948512 single base substitution C A intron_variant COCA-CN 11 71948512 71948512 single base substitution C A missense_variant P1075Q 3224C>A COCA-CN 11 71948512 71948512 single base substitution C A missense_variant P833Q 2498C>A COCA-CN 11 71948512 71948512 single base substitution C A missense_variant P88Q 263C>A COCA-CN 11 71948512 71948512 single base substitution C A upstream_gene_variant EOPC-DE 11 71952967 71952967 single base substitution A C downstream_gene_variant ESAD-UK 11 71931051 71931051 single base substitution A T upstream_gene_variant ESAD-UK 11 71932414 71932414 single base substitution T G upstream_gene_variant ESAD-UK 11 71934360 71934360 single base substitution G C upstream_gene_variant ESAD-UK 11 71936427 71936427 single base substitution T C downstream_gene_variant ESAD-UK 11 71936427 71936427 single base substitution T C intron_variant ESAD-UK 11 71936427 71936427 single base substitution T C upstream_gene_variant ESAD-UK 11 71937369 71937369 single base substitution C T downstream_gene_variant ESAD-UK 11 71937369 71937369 single base substitution C T intron_variant ESAD-UK 11 71937369 71937369 single base substitution C T upstream_gene_variant ESAD-UK 11 71937868 71937868 single base substitution G A downstream_gene_variant ESAD-UK 11 71937868 71937868 single base substitution G A intron_variant ESAD-UK 11 71937868 71937868 single base substitution G A upstream_gene_variant ESAD-UK 11 71938444 71938444 single base substitution G A downstream_gene_variant ESAD-UK 11 71938444 71938444 single base substitution G A intron_variant ESAD-UK 11 71938444 71938444 single base substitution G A upstream_gene_variant ESAD-UK 11 71938840 71938840 single base substitution C G downstream_gene_variant ESAD-UK 11 71938840 71938840 single base substitution C G intron_variant ESAD-UK 11 71938840 71938840 single base substitution C G upstream_gene_variant ESAD-UK 11 71940064 71940064 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 11 71940064 71940064 single base substitution C G downstream_gene_variant ESAD-UK 11 71940064 71940064 single base substitution C G intron_variant ESAD-UK 11 71940064 71940064 single base substitution C G upstream_gene_variant ESAD-UK 11 71941274 71941274 single base substitution G A downstream_gene_variant ESAD-UK 11 71941274 71941274 single base substitution G A missense_variant R108Q 323G>A ESAD-UK 11 71941274 71941274 single base substitution G A missense_variant R350Q 1049G>A ESAD-UK 11 71941274 71941274 single base substitution G A missense_variant R78Q 233G>A ESAD-UK 11 71941274 71941274 single base substitution G A upstream_gene_variant ESAD-UK 11 71946472 71946472 single base substitution T C downstream_gene_variant ESAD-UK 11 71946472 71946472 single base substitution T C exon_variant ESAD-UK 11 71946472 71946472 single base substitution T C intron_variant ESAD-UK 11 71946472 71946472 single base substitution T C missense_variant L637P 1910T>C ESAD-UK 11 71946472 71946472 single base substitution T C missense_variant L879P 2636T>C ESAD-UK 11 71946472 71946472 single base substitution T C upstream_gene_variant ESAD-UK 11 71949695 71949695 single base substitution G T 3_prime_UTR_variant ESAD-UK 11 71949695 71949695 single base substitution G T downstream_gene_variant ESAD-UK 11 71949695 71949695 single base substitution G T intron_variant ESAD-UK 11 71950557 71950557 single base substitution C A downstream_gene_variant ESAD-UK 11 71951406 71951406 single base substitution G A downstream_gene_variant ESAD-UK 11 71951839 71951839 single base substitution G A downstream_gene_variant ESAD-UK 11 71952441 71952441 single base substitution G A downstream_gene_variant ESAD-UK 11 71954362 71954362 single base substitution C T downstream_gene_variant ESAD-UK 11 71954473 71954473 single base substitution A G downstream_gene_variant ESAD-UK 11 71954898 71954898 single base substitution C T downstream_gene_variant ESCA-CN 11 71941212 71941212 single base substitution A G downstream_gene_variant ESCA-CN 11 71941212 71941212 single base substitution A G synonymous_variant S329S 987A>G ESCA-CN 11 71941212 71941212 single base substitution A G synonymous_variant S57S 171A>G ESCA-CN 11 71941212 71941212 single base substitution A G synonymous_variant S87S 261A>G ESCA-CN 11 71941212 71941212 single base substitution A G upstream_gene_variant ESCA-CN 11 71941812 71941812 single base substitution C T downstream_gene_variant ESCA-CN 11 71941812 71941812 single base substitution C T exon_variant ESCA-CN 11 71941812 71941812 single base substitution C T intron_variant ESCA-CN 11 71941812 71941812 single base substitution C T upstream_gene_variant ESCA-CN 11 71942104 71942104 single base substitution C T downstream_gene_variant ESCA-CN 11 71942104 71942104 single base substitution C T exon_variant ESCA-CN 11 71942104 71942104 single base substitution C T synonymous_variant D214D 642C>T ESCA-CN 11 71942104 71942104 single base substitution C T synonymous_variant D456D 1368C>T ESCA-CN 11 71942104 71942104 single base substitution C T upstream_gene_variant GBM-US 11 71942122 71942122 insertion of <=200bp - C downstream_gene_variant GBM-US 11 71942122 71942122 insertion of <=200bp - C exon_variant GBM-US 11 71942122 71942122 insertion of <=200bp - C frameshift_variant I220I? GBM-US 11 71942122 71942122 insertion of <=200bp - C frameshift_variant I462I? GBM-US 11 71942122 71942122 insertion of <=200bp - C upstream_gene_variant GBM-US 11 71942586 71942586 deletion of <=200bp C - downstream_gene_variant GBM-US 11 71942586 71942586 deletion of <=200bp C - exon_variant GBM-US 11 71942586 71942586 deletion of <=200bp C - frameshift_variant V272 GBM-US 11 71942586 71942586 deletion of <=200bp C - frameshift_variant V514 GBM-US 11 71942586 71942586 deletion of <=200bp C - upstream_gene_variant GBM-US 11 71943788 71943788 single base substitution C T downstream_gene_variant GBM-US 11 71943788 71943788 single base substitution C T exon_variant GBM-US 11 71943788 71943788 single base substitution C T missense_variant R369C 1105C>T GBM-US 11 71943788 71943788 single base substitution C T missense_variant R611C 1831C>T GBM-US 11 71943788 71943788 single base substitution C T upstream_gene_variant KIRC-US 11 71939276 71939278 deletion of <=200bp AGA - 5_prime_UTR_variant KIRC-US 11 71939276 71939278 deletion of <=200bp AGA - downstream_gene_variant KIRC-US 11 71939276 71939278 deletion of <=200bp AGA - exon_variant KIRC-US 11 71939276 71939278 deletion of <=200bp AGA - inframe_deletion GE75G KIRC-US 11 71939276 71939278 deletion of <=200bp AGA - upstream_gene_variant KIRC-US 11 71948448 71948448 single base substitution C G downstream_gene_variant KIRC-US 11 71948448 71948448 single base substitution C G intron_variant KIRC-US 11 71948448 71948448 single base substitution C G missense_variant P1054A 3160C>G KIRC-US 11 71948448 71948448 single base substitution C G missense_variant P67A 199C>G KIRC-US 11 71948448 71948448 single base substitution C G missense_variant P812A 2434C>G KIRC-US 11 71948448 71948448 single base substitution C G upstream_gene_variant KIRP-US 11 71931920 71931920 single base substitution C A upstream_gene_variant KIRP-US 11 71931977 71931977 single base substitution A C upstream_gene_variant KIRP-US 11 71944164 71944164 single base substitution G T downstream_gene_variant KIRP-US 11 71944164 71944164 single base substitution G T exon_variant KIRP-US 11 71944164 71944164 single base substitution G T missense_variant G424V 1271G>T KIRP-US 11 71944164 71944164 single base substitution G T missense_variant G666V 1997G>T KIRP-US 11 71944164 71944164 single base substitution G T upstream_gene_variant KIRP-US 11 71948376 71948376 single base substitution C T downstream_gene_variant KIRP-US 11 71948376 71948376 single base substitution C T intron_variant KIRP-US 11 71948376 71948376 single base substitution C T missense_variant R1030W 3088C>T KIRP-US 11 71948376 71948376 single base substitution C T missense_variant R43W 127C>T KIRP-US 11 71948376 71948376 single base substitution C T missense_variant R788W 2362C>T KIRP-US 11 71948376 71948376 single base substitution C T upstream_gene_variant KIRP-US 11 71948603 71948603 single base substitution A G downstream_gene_variant KIRP-US 11 71948603 71948603 single base substitution A G intron_variant KIRP-US 11 71948603 71948603 single base substitution A G synonymous_variant P1105P 3315A>G KIRP-US 11 71948603 71948603 single base substitution A G synonymous_variant P118P 354A>G KIRP-US 11 71948603 71948603 single base substitution A G synonymous_variant P863P 2589A>G KIRP-US 11 71948603 71948603 single base substitution A G upstream_gene_variant LAML-KR 11 71949206 71949206 single base substitution C A downstream_gene_variant LAML-KR 11 71949206 71949206 single base substitution C A intron_variant LAML-KR 11 71949206 71949206 single base substitution C A missense_variant L1225M 3673C>A LAML-KR 11 71949206 71949206 single base substitution C A missense_variant L86M 256C>A LAML-KR 11 71949206 71949206 single base substitution C A missense_variant L983M 2947C>A LGG-US 11 71942617 71942617 single base substitution G A downstream_gene_variant LGG-US 11 71942617 71942617 single base substitution G A exon_variant LGG-US 11 71942617 71942617 single base substitution G A missense_variant V283I 847G>A LGG-US 11 71942617 71942617 single base substitution G A missense_variant V525I 1573G>A LGG-US 11 71942617 71942617 single base substitution G A upstream_gene_variant LICA-CN 11 71932645 71932645 single base substitution T A upstream_gene_variant LICA-CN 11 71941838 71941838 single base substitution A C downstream_gene_variant LICA-CN 11 71941838 71941838 single base substitution A C exon_variant LICA-CN 11 71941838 71941838 single base substitution A C splice_acceptor_variant LICA-CN 11 71941838 71941838 single base substitution A C upstream_gene_variant LICA-CN 11 71943290 71943290 single base substitution A T downstream_gene_variant LICA-CN 11 71943290 71943290 single base substitution A T exon_variant LICA-CN 11 71943290 71943290 single base substitution A T missense_variant K299M 896A>T LICA-CN 11 71943290 71943290 single base substitution A T missense_variant K541M 1622A>T LICA-CN 11 71943290 71943290 single base substitution A T upstream_gene_variant LICA-CN 11 71943360 71943360 single base substitution G A downstream_gene_variant LICA-CN 11 71943360 71943360 single base substitution G A exon_variant LICA-CN 11 71943360 71943360 single base substitution G A synonymous_variant S322S 966G>A LICA-CN 11 71943360 71943360 single base substitution G A synonymous_variant S564S 1692G>A LICA-CN 11 71943360 71943360 single base substitution G A upstream_gene_variant LICA-FR 11 71932559 71932559 single base substitution C A upstream_gene_variant LICA-FR 11 71939414 71939414 single base substitution G A 5_prime_UTR_variant LICA-FR 11 71939414 71939414 single base substitution G A downstream_gene_variant LICA-FR 11 71939414 71939414 single base substitution G A exon_variant LICA-FR 11 71939414 71939414 single base substitution G A missense_variant R90H 269G>A LICA-FR 11 71939414 71939414 single base substitution G A upstream_gene_variant LICA-FR 11 71940705 71940705 single base substitution A G downstream_gene_variant LICA-FR 11 71940705 71940705 single base substitution A G intron_variant LICA-FR 11 71940705 71940705 single base substitution A G splice_acceptor_variant LICA-FR 11 71940705 71940705 single base substitution A G upstream_gene_variant LICA-FR 11 71944155 71944155 single base substitution A G downstream_gene_variant LICA-FR 11 71944155 71944155 single base substitution A G exon_variant LICA-FR 11 71944155 71944155 single base substitution A G missense_variant Y421C 1262A>G LICA-FR 11 71944155 71944155 single base substitution A G missense_variant Y663C 1988A>G LICA-FR 11 71944155 71944155 single base substitution A G upstream_gene_variant LICA-FR 11 71946372 71946372 single base substitution G T downstream_gene_variant LICA-FR 11 71946372 71946372 single base substitution G T exon_variant LICA-FR 11 71946372 71946372 single base substitution G T intron_variant LICA-FR 11 71946372 71946372 single base substitution G T missense_variant G604C 1810G>T LICA-FR 11 71946372 71946372 single base substitution G T missense_variant G846C 2536G>T LICA-FR 11 71946372 71946372 single base substitution G T upstream_gene_variant LICA-FR 11 71948527 71948527 single base substitution G A downstream_gene_variant LICA-FR 11 71948527 71948527 single base substitution G A intron_variant LICA-FR 11 71948527 71948527 single base substitution G A missense_variant R1080H 3239G>A LICA-FR 11 71948527 71948527 single base substitution G A missense_variant R838H 2513G>A LICA-FR 11 71948527 71948527 single base substitution G A missense_variant R93H 278G>A LICA-FR 11 71948527 71948527 single base substitution G A upstream_gene_variant LICA-FR 11 71948663 71948663 single base substitution G A downstream_gene_variant LICA-FR 11 71948663 71948663 single base substitution G A intron_variant LICA-FR 11 71948663 71948663 single base substitution G A synonymous_variant Q1125Q 3375G>A LICA-FR 11 71948663 71948663 single base substitution G A synonymous_variant Q138Q 414G>A LICA-FR 11 71948663 71948663 single base substitution G A synonymous_variant Q883Q 2649G>A LICA-FR 11 71948663 71948663 single base substitution G A upstream_gene_variant LIHC-US 11 71932083 71932083 single base substitution T A upstream_gene_variant LIHC-US 11 71943737 71943737 single base substitution G T downstream_gene_variant LIHC-US 11 71943737 71943737 single base substitution G T exon_variant LIHC-US 11 71943737 71943737 single base substitution G T missense_variant D352Y 1054G>T LIHC-US 11 71943737 71943737 single base substitution G T missense_variant D594Y 1780G>T LIHC-US 11 71943737 71943737 single base substitution G T upstream_gene_variant LIHC-US 11 71944787 71944787 single base substitution A G downstream_gene_variant LIHC-US 11 71944787 71944787 single base substitution A G splice_region_variant LIHC-US 11 71944787 71944787 single base substitution A G upstream_gene_variant LIHC-US 11 71948271 71948271 single base substitution C T downstream_gene_variant LIHC-US 11 71948271 71948271 single base substitution C T intron_variant LIHC-US 11 71948271 71948271 single base substitution C T stop_gained Q753* 2257C>T LIHC-US 11 71948271 71948271 single base substitution C T stop_gained Q8* 22C>T LIHC-US 11 71948271 71948271 single base substitution C T stop_gained Q995* 2983C>T LIHC-US 11 71948271 71948271 single base substitution C T upstream_gene_variant LIHC-US 11 71948760 71948760 single base substitution C T downstream_gene_variant LIHC-US 11 71948760 71948760 single base substitution C T intron_variant LIHC-US 11 71948760 71948760 single base substitution C T synonymous_variant L1158L 3472C>T LIHC-US 11 71948760 71948760 single base substitution C T synonymous_variant L171L 511C>T LIHC-US 11 71948760 71948760 single base substitution C T synonymous_variant L19L 55C>T LIHC-US 11 71948760 71948760 single base substitution C T synonymous_variant L916L 2746C>T LINC-JP 11 71931686 71931686 single base substitution G T upstream_gene_variant LINC-JP 11 71940261 71940261 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 11 71940261 71940261 single base substitution C T downstream_gene_variant LINC-JP 11 71940261 71940261 single base substitution C T missense_variant R216W 646C>T LINC-JP 11 71940261 71940261 single base substitution C T upstream_gene_variant LINC-JP 11 71940532 71940532 single base substitution G T 5_prime_UTR_variant LINC-JP 11 71940532 71940532 single base substitution G T downstream_gene_variant LINC-JP 11 71940532 71940532 single base substitution G T missense_variant G228V 683G>T LINC-JP 11 71940532 71940532 single base substitution G T upstream_gene_variant LINC-JP 11 71942126 71942126 single base substitution C A downstream_gene_variant LINC-JP 11 71942126 71942126 single base substitution C A exon_variant LINC-JP 11 71942126 71942126 single base substitution C A missense_variant H222N 664C>A LINC-JP 11 71942126 71942126 single base substitution C A missense_variant H464N 1390C>A LINC-JP 11 71942126 71942126 single base substitution C A upstream_gene_variant LINC-JP 11 71946908 71946908 single base substitution A G downstream_gene_variant LINC-JP 11 71946908 71946908 single base substitution A G exon_variant LINC-JP 11 71946908 71946908 single base substitution A G intron_variant LINC-JP 11 71946908 71946908 single base substitution A G synonymous_variant P677P 2031A>G LINC-JP 11 71946908 71946908 single base substitution A G synonymous_variant P919P 2757A>G LINC-JP 11 71946908 71946908 single base substitution A G upstream_gene_variant LINC-JP 11 71948289 71948289 single base substitution C T downstream_gene_variant LINC-JP 11 71948289 71948289 single base substitution C T intron_variant LINC-JP 11 71948289 71948289 single base substitution C T missense_variant P1001S 3001C>T LINC-JP 11 71948289 71948289 single base substitution C T missense_variant P14S 40C>T LINC-JP 11 71948289 71948289 single base substitution C T missense_variant P759S 2275C>T LINC-JP 11 71948289 71948289 single base substitution C T upstream_gene_variant LINC-JP 11 71952356 71952356 single base substitution C G downstream_gene_variant LINC-JP 11 71952357 71952357 insertion of <=200bp - G downstream_gene_variant LINC-JP 11 71952367 71952367 single base substitution C G downstream_gene_variant LINC-JP 11 71952368 71952368 single base substitution A C downstream_gene_variant LIRI-JP 11 71933557 71933557 single base substitution G T upstream_gene_variant LIRI-JP 11 71937369 71937369 single base substitution C T downstream_gene_variant LIRI-JP 11 71937369 71937369 single base substitution C T intron_variant LIRI-JP 11 71937369 71937369 single base substitution C T upstream_gene_variant LIRI-JP 11 71937468 71937468 single base substitution A T downstream_gene_variant LIRI-JP 11 71937468 71937468 single base substitution A T intron_variant LIRI-JP 11 71937468 71937468 single base substitution A T upstream_gene_variant LIRI-JP 11 71938929 71938929 single base substitution G T 5_prime_UTR_variant LIRI-JP 11 71938929 71938929 single base substitution G T downstream_gene_variant LIRI-JP 11 71938929 71938929 single base substitution G T intron_variant LIRI-JP 11 71938929 71938929 single base substitution G T upstream_gene_variant LIRI-JP 11 71942303 71942303 single base substitution A G downstream_gene_variant LIRI-JP 11 71942303 71942303 single base substitution A G exon_variant LIRI-JP 11 71942303 71942303 single base substitution A G intron_variant LIRI-JP 11 71942303 71942303 single base substitution A G upstream_gene_variant LIRI-JP 11 71944602 71944602 single base substitution G A downstream_gene_variant LIRI-JP 11 71944602 71944602 single base substitution G A exon_variant LIRI-JP 11 71944602 71944602 single base substitution G A intron_variant LIRI-JP 11 71944602 71944602 single base substitution G A upstream_gene_variant LIRI-JP 11 71945747 71945747 single base substitution G C downstream_gene_variant LIRI-JP 11 71945747 71945747 single base substitution G C intron_variant LIRI-JP 11 71945747 71945747 single base substitution G C upstream_gene_variant LIRI-JP 11 71948586 71948586 deletion of <=200bp C - downstream_gene_variant LIRI-JP 11 71948586 71948586 deletion of <=200bp C - frameshift_variant P1100 LIRI-JP 11 71948586 71948586 deletion of <=200bp C - frameshift_variant P113 LIRI-JP 11 71948586 71948586 deletion of <=200bp C - frameshift_variant P858 LIRI-JP 11 71948586 71948586 deletion of <=200bp C - intron_variant LIRI-JP 11 71948586 71948586 deletion of <=200bp C - upstream_gene_variant LIRI-JP 11 71949612 71949612 deletion of <=200bp G - 3_prime_UTR_variant LIRI-JP 11 71949612 71949612 deletion of <=200bp G - downstream_gene_variant LIRI-JP 11 71949612 71949612 deletion of <=200bp G - intron_variant LIRI-JP 11 71953846 71953846 single base substitution G A downstream_gene_variant LUSC-KR 11 71930887 71930887 single base substitution T C upstream_gene_variant LUSC-KR 11 71931172 71931172 single base substitution C A upstream_gene_variant LUSC-KR 11 71931173 71931173 single base substitution C T upstream_gene_variant LUSC-KR 11 71938348 71938348 single base substitution T C downstream_gene_variant LUSC-KR 11 71938348 71938348 single base substitution T C intron_variant LUSC-KR 11 71938348 71938348 single base substitution T C upstream_gene_variant LUSC-KR 11 71942389 71942389 single base substitution G T downstream_gene_variant LUSC-KR 11 71942389 71942389 single base substitution G T exon_variant LUSC-KR 11 71942389 71942389 single base substitution G T intron_variant LUSC-KR 11 71942389 71942389 single base substitution G T upstream_gene_variant LUSC-US 11 71939479 71939479 single base substitution G C 5_prime_UTR_variant LUSC-US 11 71939479 71939479 single base substitution G C downstream_gene_variant LUSC-US 11 71939479 71939479 single base substitution G C exon_variant LUSC-US 11 71939479 71939479 single base substitution G C missense_variant A112P 334G>C LUSC-US 11 71939479 71939479 single base substitution G C upstream_gene_variant LUSC-US 11 71940529 71940529 single base substitution C G 5_prime_UTR_variant LUSC-US 11 71940529 71940529 single base substitution C G downstream_gene_variant LUSC-US 11 71940529 71940529 single base substitution C G stop_gained S227* 680C>G LUSC-US 11 71940529 71940529 single base substitution C G upstream_gene_variant LUSC-US 11 71942192 71942192 single base substitution C T downstream_gene_variant LUSC-US 11 71942192 71942192 single base substitution C T exon_variant LUSC-US 11 71942192 71942192 single base substitution C T missense_variant R244C 730C>T LUSC-US 11 71942192 71942192 single base substitution C T missense_variant R486C 1456C>T LUSC-US 11 71942192 71942192 single base substitution C T upstream_gene_variant LUSC-US 11 71946722 71946722 deletion of <=200bp G - downstream_gene_variant LUSC-US 11 71946722 71946722 deletion of <=200bp G - exon_variant LUSC-US 11 71946722 71946722 deletion of <=200bp G - frameshift_variant W646 LUSC-US 11 71946722 71946722 deletion of <=200bp G - frameshift_variant W888 LUSC-US 11 71946722 71946722 deletion of <=200bp G - intron_variant LUSC-US 11 71946722 71946722 deletion of <=200bp G - upstream_gene_variant LUSC-US 11 71952160 71952160 single base substitution C T downstream_gene_variant MALY-DE 11 71930228 71930228 single base substitution G C upstream_gene_variant MALY-DE 11 71933751 71933751 single base substitution A G upstream_gene_variant MALY-DE 11 71950404 71950406 deletion of <=200bp CAC - downstream_gene_variant MALY-DE 11 71954846 71954846 single base substitution G A downstream_gene_variant MELA-AU 11 71929875 71929875 single base substitution C T upstream_gene_variant MELA-AU 11 71929953 71929953 single base substitution C T upstream_gene_variant MELA-AU 11 71929969 71929969 single base substitution C T upstream_gene_variant MELA-AU 11 71930258 71930258 single base substitution C T upstream_gene_variant MELA-AU 11 71930272 71930272 single base substitution G A upstream_gene_variant MELA-AU 11 71930290 71930290 single base substitution C T upstream_gene_variant MELA-AU 11 71930327 71930327 single base substitution C T upstream_gene_variant MELA-AU 11 71930340 71930340 single base substitution T A upstream_gene_variant MELA-AU 11 71930587 71930587 single base substitution G A upstream_gene_variant MELA-AU 11 71930896 71930896 single base substitution T A upstream_gene_variant MELA-AU 11 71931076 71931076 single base substitution G A upstream_gene_variant MELA-AU 11 71931156 71931156 single base substitution G A upstream_gene_variant MELA-AU 11 71931451 71931451 single base substitution C T upstream_gene_variant MELA-AU 11 71931758 71931758 single base substitution G A upstream_gene_variant MELA-AU 11 71931845 71931845 single base substitution G A upstream_gene_variant MELA-AU 11 71931895 71931895 single base substitution C T upstream_gene_variant MELA-AU 11 71932004 71932004 single base substitution G A upstream_gene_variant MELA-AU 11 71932191 71932191 single base substitution G A upstream_gene_variant MELA-AU 11 71932260 71932260 single base substitution C T upstream_gene_variant MELA-AU 11 71932679 71932679 single base substitution A G upstream_gene_variant MELA-AU 11 71932798 71932798 single base substitution C T upstream_gene_variant MELA-AU 11 71933795 71933795 single base substitution C T upstream_gene_variant MELA-AU 11 71933883 71933883 single base substitution A G upstream_gene_variant MELA-AU 11 71934331 71934331 single base substitution G A upstream_gene_variant MELA-AU 11 71934414 71934414 single base substitution C T upstream_gene_variant MELA-AU 11 71934421 71934421 single base substitution G A upstream_gene_variant MELA-AU 11 71934435 71934435 single base substitution C T upstream_gene_variant MELA-AU 11 71934500 71934500 single base substitution C T upstream_gene_variant MELA-AU 11 71935356 71935356 single base substitution C G intron_variant MELA-AU 11 71935356 71935356 single base substitution C G upstream_gene_variant MELA-AU 11 71935593 71935593 single base substitution G C intron_variant MELA-AU 11 71935593 71935593 single base substitution G C upstream_gene_variant MELA-AU 11 71937712 71937712 single base substitution G A downstream_gene_variant MELA-AU 11 71937712 71937712 single base substitution G A intron_variant MELA-AU 11 71937712 71937712 single base substitution G A upstream_gene_variant MELA-AU 11 71937834 71937834 single base substitution C T downstream_gene_variant MELA-AU 11 71937834 71937834 single base substitution C T intron_variant MELA-AU 11 71937834 71937834 single base substitution C T upstream_gene_variant MELA-AU 11 71938700 71938700 single base substitution C T downstream_gene_variant MELA-AU 11 71938700 71938700 single base substitution C T intron_variant MELA-AU 11 71938700 71938700 single base substitution C T upstream_gene_variant MELA-AU 11 71938880 71938880 single base substitution A T downstream_gene_variant MELA-AU 11 71938880 71938880 single base substitution A T intron_variant MELA-AU 11 71938880 71938880 single base substitution A T upstream_gene_variant MELA-AU 11 71939581 71939581 single base substitution C T downstream_gene_variant MELA-AU 11 71939581 71939581 single base substitution C T exon_variant MELA-AU 11 71939581 71939581 single base substitution C T intron_variant MELA-AU 11 71939581 71939581 single base substitution C T upstream_gene_variant MELA-AU 11 71939987 71939987 single base substitution G A 5_prime_UTR_variant MELA-AU 11 71939987 71939987 single base substitution G A downstream_gene_variant MELA-AU 11 71939987 71939987 single base substitution G A intron_variant MELA-AU 11 71939987 71939987 single base substitution G A upstream_gene_variant MELA-AU 11 71939999 71939999 single base substitution C T 5_prime_UTR_variant MELA-AU 11 71939999 71939999 single base substitution C T downstream_gene_variant MELA-AU 11 71939999 71939999 single base substitution C T intron_variant MELA-AU 11 71939999 71939999 single base substitution C T upstream_gene_variant MELA-AU 11 71940312 71940313 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 71940312 71940313 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 71940312 71940313 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 71940401 71940401 single base substitution C T downstream_gene_variant MELA-AU 11 71940401 71940401 single base substitution C T intron_variant MELA-AU 11 71940401 71940401 single base substitution C T upstream_gene_variant MELA-AU 11 71940504 71940504 single base substitution C T downstream_gene_variant MELA-AU 11 71940504 71940504 single base substitution C T splice_region_variant MELA-AU 11 71940504 71940504 single base substitution C T upstream_gene_variant MELA-AU 11 71940636 71940636 single base substitution C T downstream_gene_variant MELA-AU 11 71940636 71940636 single base substitution C T intron_variant MELA-AU 11 71940636 71940636 single base substitution C T upstream_gene_variant MELA-AU 11 71940958 71940958 single base substitution T C downstream_gene_variant MELA-AU 11 71940958 71940958 single base substitution T C intron_variant MELA-AU 11 71940958 71940958 single base substitution T C upstream_gene_variant MELA-AU 11 71941835 71941835 single base substitution C T downstream_gene_variant MELA-AU 11 71941835 71941835 single base substitution C T exon_variant MELA-AU 11 71941835 71941835 single base substitution C T splice_region_variant MELA-AU 11 71941835 71941835 single base substitution C T upstream_gene_variant MELA-AU 11 71942541 71942541 single base substitution G T downstream_gene_variant MELA-AU 11 71942541 71942541 single base substitution G T exon_variant MELA-AU 11 71942541 71942541 single base substitution G T splice_acceptor_variant MELA-AU 11 71942541 71942541 single base substitution G T upstream_gene_variant MELA-AU 11 71942543 71942543 single base substitution T A downstream_gene_variant MELA-AU 11 71942543 71942543 single base substitution T A exon_variant MELA-AU 11 71942543 71942543 single base substitution T A missense_variant I258N 773T>A MELA-AU 11 71942543 71942543 single base substitution T A missense_variant I500N 1499T>A MELA-AU 11 71942543 71942543 single base substitution T A splice_region_variant MELA-AU 11 71942543 71942543 single base substitution T A upstream_gene_variant MELA-AU 11 71942980 71942981 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 71942980 71942981 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 71942980 71942981 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 71943125 71943125 single base substitution C T downstream_gene_variant MELA-AU 11 71943125 71943125 single base substitution C T intron_variant MELA-AU 11 71943125 71943125 single base substitution C T upstream_gene_variant MELA-AU 11 71943847 71943847 single base substitution G A downstream_gene_variant MELA-AU 11 71943847 71943847 single base substitution G A intron_variant MELA-AU 11 71943847 71943847 single base substitution G A upstream_gene_variant MELA-AU 11 71944153 71944153 single base substitution C T downstream_gene_variant MELA-AU 11 71944153 71944153 single base substitution C T exon_variant MELA-AU 11 71944153 71944153 single base substitution C T synonymous_variant R420R 1260C>T MELA-AU 11 71944153 71944153 single base substitution C T synonymous_variant R662R 1986C>T MELA-AU 11 71944153 71944153 single base substitution C T upstream_gene_variant MELA-AU 11 71944627 71944627 single base substitution C T downstream_gene_variant MELA-AU 11 71944627 71944627 single base substitution C T exon_variant MELA-AU 11 71944627 71944627 single base substitution C T intron_variant MELA-AU 11 71944627 71944627 single base substitution C T upstream_gene_variant MELA-AU 11 71944715 71944715 single base substitution C T downstream_gene_variant MELA-AU 11 71944715 71944715 single base substitution C T exon_variant MELA-AU 11 71944715 71944715 single base substitution C T synonymous_variant I471I 1413C>T MELA-AU 11 71944715 71944715 single base substitution C T synonymous_variant I713I 2139C>T MELA-AU 11 71944715 71944715 single base substitution C T upstream_gene_variant MELA-AU 11 71944781 71944781 single base substitution C T downstream_gene_variant MELA-AU 11 71944781 71944781 single base substitution C T exon_variant MELA-AU 11 71944781 71944781 single base substitution C T synonymous_variant S493S 1479C>T MELA-AU 11 71944781 71944781 single base substitution C T synonymous_variant S735S 2205C>T MELA-AU 11 71944781 71944781 single base substitution C T upstream_gene_variant MELA-AU 11 71945103 71945103 single base substitution C T downstream_gene_variant MELA-AU 11 71945103 71945103 single base substitution C T intron_variant MELA-AU 11 71945103 71945103 single base substitution C T upstream_gene_variant MELA-AU 11 71945360 71945360 single base substitution T C downstream_gene_variant MELA-AU 11 71945360 71945360 single base substitution T C exon_variant MELA-AU 11 71945360 71945360 single base substitution T C missense_variant F508L 1522T>C MELA-AU 11 71945360 71945360 single base substitution T C missense_variant F750L 2248T>C MELA-AU 11 71945360 71945360 single base substitution T C upstream_gene_variant MELA-AU 11 71946061 71946061 single base substitution C T downstream_gene_variant MELA-AU 11 71946061 71946061 single base substitution C T intron_variant MELA-AU 11 71946061 71946061 single base substitution C T upstream_gene_variant MELA-AU 11 71946564 71946564 single base substitution A C downstream_gene_variant MELA-AU 11 71946564 71946564 single base substitution A C intron_variant MELA-AU 11 71946564 71946564 single base substitution A C upstream_gene_variant MELA-AU 11 71947027 71947028 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 71947027 71947028 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 71947027 71947028 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P717L 2150CC>TT MELA-AU 11 71947027 71947028 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P959L 2876CC>TT MELA-AU 11 71947027 71947028 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 71947033 71947033 single base substitution G A downstream_gene_variant MELA-AU 11 71947033 71947033 single base substitution G A intron_variant MELA-AU 11 71947033 71947033 single base substitution G A splice_region_variant MELA-AU 11 71947033 71947033 single base substitution G A upstream_gene_variant MELA-AU 11 71947752 71947752 single base substitution C T downstream_gene_variant MELA-AU 11 71947752 71947752 single base substitution C T intron_variant MELA-AU 11 71947752 71947752 single base substitution C T upstream_gene_variant MELA-AU 11 71948187 71948187 single base substitution C T downstream_gene_variant MELA-AU 11 71948187 71948187 single base substitution C T intron_variant MELA-AU 11 71948187 71948187 single base substitution C T missense_variant P725S 2173C>T MELA-AU 11 71948187 71948187 single base substitution C T missense_variant P967S 2899C>T MELA-AU 11 71948187 71948187 single base substitution C T upstream_gene_variant MELA-AU 11 71948315 71948315 single base substitution C T downstream_gene_variant MELA-AU 11 71948315 71948315 single base substitution C T intron_variant MELA-AU 11 71948315 71948315 single base substitution C T synonymous_variant V1009V 3027C>T MELA-AU 11 71948315 71948315 single base substitution C T synonymous_variant V22V 66C>T MELA-AU 11 71948315 71948315 single base substitution C T synonymous_variant V767V 2301C>T MELA-AU 11 71948315 71948315 single base substitution C T upstream_gene_variant MELA-AU 11 71948330 71948330 single base substitution G A downstream_gene_variant MELA-AU 11 71948330 71948330 single base substitution G A intron_variant MELA-AU 11 71948330 71948330 single base substitution G A synonymous_variant K1014K 3042G>A MELA-AU 11 71948330 71948330 single base substitution G A synonymous_variant K27K 81G>A MELA-AU 11 71948330 71948330 single base substitution G A synonymous_variant K772K 2316G>A MELA-AU 11 71948330 71948330 single base substitution G A upstream_gene_variant MELA-AU 11 71949042 71949042 single base substitution T C downstream_gene_variant MELA-AU 11 71949042 71949042 single base substitution T C intron_variant MELA-AU 11 71949266 71949266 single base substitution C T downstream_gene_variant MELA-AU 11 71949266 71949266 single base substitution C T intron_variant MELA-AU 11 71949266 71949266 single base substitution C T missense_variant P106S 316C>T MELA-AU 11 71949278 71949278 single base substitution C T downstream_gene_variant MELA-AU 11 71949278 71949278 single base substitution C T intron_variant MELA-AU 11 71949278 71949278 single base substitution C T missense_variant L110F 328C>T MELA-AU 11 71949670 71949670 single base substitution A G 3_prime_UTR_variant MELA-AU 11 71949670 71949670 single base substitution A G downstream_gene_variant MELA-AU 11 71949670 71949670 single base substitution A G intron_variant MELA-AU 11 71952067 71952067 single base substitution C T downstream_gene_variant MELA-AU 11 71952121 71952121 single base substitution C T downstream_gene_variant MELA-AU 11 71952173 71952173 single base substitution C T downstream_gene_variant MELA-AU 11 71952542 71952542 single base substitution G A downstream_gene_variant MELA-AU 11 71952613 71952613 single base substitution A C downstream_gene_variant MELA-AU 11 71953143 71953143 single base substitution C T downstream_gene_variant MELA-AU 11 71953171 71953171 single base substitution C T downstream_gene_variant MELA-AU 11 71953345 71953345 single base substitution C T downstream_gene_variant MELA-AU 11 71953518 71953518 single base substitution C T downstream_gene_variant MELA-AU 11 71953519 71953520 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 71953610 71953610 single base substitution C T downstream_gene_variant MELA-AU 11 71953824 71953824 single base substitution C T downstream_gene_variant MELA-AU 11 71954007 71954007 single base substitution G A downstream_gene_variant MELA-AU 11 71954039 71954039 single base substitution C T downstream_gene_variant MELA-AU 11 71954150 71954150 single base substitution G A downstream_gene_variant MELA-AU 11 71954309 71954309 single base substitution C T downstream_gene_variant MELA-AU 11 71954380 71954380 single base substitution C T downstream_gene_variant MELA-AU 11 71954411 71954411 single base substitution C T downstream_gene_variant MELA-AU 11 71954436 71954436 single base substitution G A downstream_gene_variant MELA-AU 11 71954503 71954503 single base substitution C T downstream_gene_variant MELA-AU 11 71954637 71954637 single base substitution G A downstream_gene_variant ORCA-IN 11 71931952 71931952 single base substitution C A upstream_gene_variant ORCA-IN 11 71932301 71932301 single base substitution C A upstream_gene_variant ORCA-IN 11 71933767 71933767 single base substitution C G upstream_gene_variant ORCA-IN 11 71939521 71939521 single base substitution C A 5_prime_UTR_variant ORCA-IN 11 71939521 71939521 single base substitution C A downstream_gene_variant ORCA-IN 11 71939521 71939521 single base substitution C A exon_variant ORCA-IN 11 71939521 71939521 single base substitution C A missense_variant P126T 376C>A ORCA-IN 11 71939521 71939521 single base substitution C A upstream_gene_variant ORCA-IN 11 71939535 71939535 single base substitution T A 5_prime_UTR_variant ORCA-IN 11 71939535 71939535 single base substitution T A downstream_gene_variant ORCA-IN 11 71939535 71939535 single base substitution T A exon_variant ORCA-IN 11 71939535 71939535 single base substitution T A missense_variant D130E 390T>A ORCA-IN 11 71939535 71939535 single base substitution T A upstream_gene_variant ORCA-IN 11 71945431 71945431 single base substitution C T 3_prime_UTR_variant ORCA-IN 11 71945431 71945431 single base substitution C T downstream_gene_variant ORCA-IN 11 71945431 71945431 single base substitution C T exon_variant ORCA-IN 11 71945431 71945431 single base substitution C T synonymous_variant C531C 1593C>T ORCA-IN 11 71945431 71945431 single base substitution C T synonymous_variant C773C 2319C>T ORCA-IN 11 71945431 71945431 single base substitution C T upstream_gene_variant ORCA-IN 11 71945809 71945809 single base substitution A G downstream_gene_variant ORCA-IN 11 71945809 71945809 single base substitution A G intron_variant ORCA-IN 11 71945809 71945809 single base substitution A G upstream_gene_variant OV-AU 11 71934421 71934421 single base substitution G C upstream_gene_variant OV-AU 11 71948484 71948484 insertion of <=200bp - C downstream_gene_variant OV-AU 11 71948484 71948484 insertion of <=200bp - C frameshift_variant P1066P? OV-AU 11 71948484 71948484 insertion of <=200bp - C frameshift_variant P79P? OV-AU 11 71948484 71948484 insertion of <=200bp - C frameshift_variant P824P? OV-AU 11 71948484 71948484 insertion of <=200bp - C intron_variant OV-AU 11 71948484 71948484 insertion of <=200bp - C upstream_gene_variant OV-AU 11 71950152 71950152 single base substitution G C downstream_gene_variant OV-AU 11 71952700 71952700 single base substitution C G downstream_gene_variant OV-AU 11 71954773 71954773 single base substitution G A downstream_gene_variant OV-US 11 71941250 71941250 single base substitution G A downstream_gene_variant OV-US 11 71941250 71941250 single base substitution G A missense_variant R100Q 299G>A OV-US 11 71941250 71941250 single base substitution G A missense_variant R342Q 1025G>A OV-US 11 71941250 71941250 single base substitution G A missense_variant R70Q 209G>A OV-US 11 71941250 71941250 single base substitution G A upstream_gene_variant PACA-AU 11 71945760 71945761 deletion of <=200bp AG - downstream_gene_variant PACA-AU 11 71945760 71945761 deletion of <=200bp AG - intron_variant PACA-AU 11 71945760 71945761 deletion of <=200bp AG - upstream_gene_variant PACA-AU 11 71949045 71949045 insertion of <=200bp - G downstream_gene_variant PACA-AU 11 71949045 71949045 insertion of <=200bp - G intron_variant PACA-AU 11 71949091 71949091 single base substitution G A downstream_gene_variant PACA-AU 11 71949091 71949091 single base substitution G A intron_variant PACA-AU 11 71949091 71949091 single base substitution G A synonymous_variant P1186P 3558G>A PACA-AU 11 71949091 71949091 single base substitution G A synonymous_variant P47P 141G>A PACA-AU 11 71949091 71949091 single base substitution G A synonymous_variant P944P 2832G>A PACA-AU 11 71952253 71952253 single base substitution C T downstream_gene_variant PACA-AU 11 71952376 71952376 single base substitution T G downstream_gene_variant PACA-AU 11 71953667 71953667 single base substitution C A downstream_gene_variant PACA-AU 11 71954076 71954076 deletion of <=200bp A - downstream_gene_variant PACA-CA 11 71930611 71930611 single base substitution C T upstream_gene_variant PACA-CA 11 71932044 71932044 single base substitution T G upstream_gene_variant PACA-CA 11 71938846 71938846 single base substitution T A downstream_gene_variant PACA-CA 11 71938846 71938846 single base substitution T A intron_variant PACA-CA 11 71938846 71938846 single base substitution T A upstream_gene_variant PACA-CA 11 71939460 71939460 insertion of <=200bp - A 5_prime_UTR_variant PACA-CA 11 71939460 71939460 insertion of <=200bp - A downstream_gene_variant PACA-CA 11 71939460 71939460 insertion of <=200bp - A exon_variant PACA-CA 11 71939460 71939460 insertion of <=200bp - A frameshift_variant P105P? PACA-CA 11 71939460 71939460 insertion of <=200bp - A upstream_gene_variant PACA-CA 11 71940308 71940308 single base substitution C A downstream_gene_variant PACA-CA 11 71940308 71940308 single base substitution C A intron_variant PACA-CA 11 71940308 71940308 single base substitution C A upstream_gene_variant PACA-CA 11 71948748 71948748 deletion of <=200bp C - downstream_gene_variant PACA-CA 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P1154 PACA-CA 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P15 PACA-CA 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P167 PACA-CA 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P912 PACA-CA 11 71948748 71948748 deletion of <=200bp C - intron_variant PAEN-AU 11 71936226 71936253 deletion of <=200bp GCTCCTTGCGGGCTGGCGTGGACCGGGA - downstream_gene_variant PAEN-AU 11 71936226 71936253 deletion of <=200bp GCTCCTTGCGGGCTGGCGTGGACCGGGA - intron_variant PAEN-AU 11 71936226 71936253 deletion of <=200bp GCTCCTTGCGGGCTGGCGTGGACCGGGA - upstream_gene_variant PAEN-AU 11 71939464 71939464 single base substitution C T 5_prime_UTR_variant PAEN-AU 11 71939464 71939464 single base substitution C T downstream_gene_variant PAEN-AU 11 71939464 71939464 single base substitution C T exon_variant PAEN-AU 11 71939464 71939464 single base substitution C T stop_gained Q107* 319C>T PAEN-AU 11 71939464 71939464 single base substitution C T upstream_gene_variant PBCA-DE 11 71932121 71932121 single base substitution A C upstream_gene_variant PBCA-DE 11 71934695 71934695 single base substitution G A upstream_gene_variant PBCA-DE 11 71935746 71935746 single base substitution A G intron_variant PBCA-DE 11 71935746 71935746 single base substitution A G upstream_gene_variant PBCA-DE 11 71936253 71936253 single base substitution A G downstream_gene_variant PBCA-DE 11 71936253 71936253 single base substitution A G intron_variant PBCA-DE 11 71936253 71936253 single base substitution A G upstream_gene_variant PRAD-UK 11 71930827 71930827 single base substitution C G upstream_gene_variant PRAD-UK 11 71931006 71931006 single base substitution C T upstream_gene_variant PRAD-UK 11 71938178 71938178 single base substitution G A downstream_gene_variant PRAD-UK 11 71938178 71938178 single base substitution G A intron_variant PRAD-UK 11 71938178 71938178 single base substitution G A upstream_gene_variant PRAD-UK 11 71942996 71942996 single base substitution G A downstream_gene_variant PRAD-UK 11 71942996 71942996 single base substitution G A intron_variant PRAD-UK 11 71942996 71942996 single base substitution G A upstream_gene_variant PRAD-UK 11 71954860 71954860 single base substitution G A downstream_gene_variant PRAD-US 11 71932028 71932028 single base substitution G A upstream_gene_variant READ-US 11 71932241 71932241 single base substitution G T upstream_gene_variant READ-US 11 71948748 71948748 deletion of <=200bp C - downstream_gene_variant READ-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P1154 READ-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P15 READ-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P167 READ-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P912 READ-US 11 71948748 71948748 deletion of <=200bp C - intron_variant READ-US 11 71955012 71955012 single base substitution C T downstream_gene_variant RECA-EU 11 71932414 71932414 single base substitution T C upstream_gene_variant RECA-EU 11 71937415 71937415 single base substitution G T downstream_gene_variant RECA-EU 11 71937415 71937415 single base substitution G T intron_variant RECA-EU 11 71937415 71937415 single base substitution G T upstream_gene_variant RECA-EU 11 71939664 71939664 single base substitution G T downstream_gene_variant RECA-EU 11 71939664 71939664 single base substitution G T exon_variant RECA-EU 11 71939664 71939664 single base substitution G T intron_variant RECA-EU 11 71939664 71939664 single base substitution G T upstream_gene_variant SKCA-BR 11 71929981 71929981 single base substitution G A upstream_gene_variant SKCA-BR 11 71930261 71930261 single base substitution G A upstream_gene_variant SKCA-BR 11 71931261 71931261 single base substitution G A upstream_gene_variant SKCA-BR 11 71932793 71932793 single base substitution G A upstream_gene_variant SKCA-BR 11 71935784 71935784 single base substitution T C intron_variant SKCA-BR 11 71935784 71935784 single base substitution T C upstream_gene_variant SKCA-BR 11 71936019 71936019 single base substitution T C 5_prime_UTR_variant SKCA-BR 11 71936019 71936019 single base substitution T C upstream_gene_variant SKCA-BR 11 71939402 71939402 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 11 71939402 71939402 single base substitution G C downstream_gene_variant SKCA-BR 11 71939402 71939402 single base substitution G C exon_variant SKCA-BR 11 71939402 71939402 single base substitution G C missense_variant G86A 257G>C SKCA-BR 11 71939402 71939402 single base substitution G C upstream_gene_variant SKCA-BR 11 71939473 71939473 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 11 71939473 71939473 single base substitution G C downstream_gene_variant SKCA-BR 11 71939473 71939473 single base substitution G C exon_variant SKCA-BR 11 71939473 71939473 single base substitution G C missense_variant V110L 328G>C SKCA-BR 11 71939473 71939473 single base substitution G C upstream_gene_variant SKCA-BR 11 71939548 71939548 single base substitution T C downstream_gene_variant SKCA-BR 11 71939548 71939548 single base substitution T C exon_variant SKCA-BR 11 71939548 71939548 single base substitution T C intron_variant SKCA-BR 11 71939548 71939548 single base substitution T C splice_region_variant SKCA-BR 11 71939548 71939548 single base substitution T C upstream_gene_variant SKCA-BR 11 71940258 71940258 single base substitution T G 5_prime_UTR_variant SKCA-BR 11 71940258 71940258 single base substitution T G downstream_gene_variant SKCA-BR 11 71940258 71940258 single base substitution T G missense_variant C215G 643T>G SKCA-BR 11 71940258 71940258 single base substitution T G upstream_gene_variant SKCA-BR 11 71940696 71940696 single base substitution C T downstream_gene_variant SKCA-BR 11 71940696 71940696 single base substitution C T intron_variant SKCA-BR 11 71940696 71940696 single base substitution C T upstream_gene_variant SKCA-BR 11 71944132 71944132 single base substitution C T downstream_gene_variant SKCA-BR 11 71944132 71944132 single base substitution C T exon_variant SKCA-BR 11 71944132 71944132 single base substitution C T synonymous_variant I413I 1239C>T SKCA-BR 11 71944132 71944132 single base substitution C T synonymous_variant I655I 1965C>T SKCA-BR 11 71944132 71944132 single base substitution C T upstream_gene_variant SKCA-BR 11 71945104 71945104 single base substitution C T downstream_gene_variant SKCA-BR 11 71945104 71945104 single base substitution C T intron_variant SKCA-BR 11 71945104 71945104 single base substitution C T upstream_gene_variant SKCA-BR 11 71945463 71945463 single base substitution T G downstream_gene_variant SKCA-BR 11 71945463 71945463 single base substitution T G intron_variant SKCA-BR 11 71945463 71945463 single base substitution T G upstream_gene_variant SKCA-BR 11 71945776 71945778 deletion of <=200bp AGT - downstream_gene_variant SKCA-BR 11 71945776 71945778 deletion of <=200bp AGT - intron_variant SKCA-BR 11 71945776 71945778 deletion of <=200bp AGT - upstream_gene_variant SKCA-BR 11 71950928 71950928 single base substitution G C downstream_gene_variant SKCA-BR 11 71954542 71954542 single base substitution G C downstream_gene_variant SKCM-US 11 71932097 71932097 single base substitution C T upstream_gene_variant SKCM-US 11 71939239 71939240 deletion of <=200bp AG - 5_prime_UTR_variant SKCM-US 11 71939239 71939240 deletion of <=200bp AG - downstream_gene_variant SKCM-US 11 71939239 71939240 deletion of <=200bp AG - exon_variant SKCM-US 11 71939239 71939240 deletion of <=200bp AG - frameshift_variant Q63 SKCM-US 11 71939239 71939240 deletion of <=200bp AG - upstream_gene_variant SKCM-US 11 71939791 71939791 single base substitution C T 5_prime_UTR_variant SKCM-US 11 71939791 71939791 single base substitution C T downstream_gene_variant SKCM-US 11 71939791 71939791 single base substitution C T missense_variant P140S 418C>T SKCM-US 11 71939791 71939791 single base substitution C T upstream_gene_variant SKCM-US 11 71940600 71940600 single base substitution C T downstream_gene_variant SKCM-US 11 71940600 71940600 single base substitution C T stop_gained Q251* 751C>T SKCM-US 11 71940600 71940600 single base substitution C T stop_gained Q9* 25C>T SKCM-US 11 71940600 71940600 single base substitution C T upstream_gene_variant SKCM-US 11 71940997 71940997 single base substitution C T downstream_gene_variant SKCM-US 11 71940997 71940997 single base substitution C T synonymous_variant S19S 57C>T SKCM-US 11 71940997 71940997 single base substitution C T synonymous_variant S291S 873C>T SKCM-US 11 71940997 71940997 single base substitution C T synonymous_variant S49S 147C>T SKCM-US 11 71940997 71940997 single base substitution C T upstream_gene_variant SKCM-US 11 71941316 71941316 single base substitution G C downstream_gene_variant SKCM-US 11 71941316 71941316 single base substitution G C splice_donor_variant SKCM-US 11 71941316 71941316 single base substitution G C upstream_gene_variant SKCM-US 11 71941504 71941504 single base substitution A G downstream_gene_variant SKCM-US 11 71941504 71941504 single base substitution A G missense_variant S125G 373A>G SKCM-US 11 71941504 71941504 single base substitution A G missense_variant S155G 463A>G SKCM-US 11 71941504 71941504 single base substitution A G missense_variant S397G 1189A>G SKCM-US 11 71941504 71941504 single base substitution A G upstream_gene_variant SKCM-US 11 71941854 71941854 single base substitution C T downstream_gene_variant SKCM-US 11 71941854 71941854 single base substitution C T exon_variant SKCM-US 11 71941854 71941854 single base substitution C T synonymous_variant F162F 486C>T SKCM-US 11 71941854 71941854 single base substitution C T synonymous_variant F404F 1212C>T SKCM-US 11 71941854 71941854 single base substitution C T upstream_gene_variant SKCM-US 11 71942074 71942074 single base substitution C T downstream_gene_variant SKCM-US 11 71942074 71942074 single base substitution C T exon_variant SKCM-US 11 71942074 71942074 single base substitution C T synonymous_variant F204F 612C>T SKCM-US 11 71942074 71942074 single base substitution C T synonymous_variant F446F 1338C>T SKCM-US 11 71942074 71942074 single base substitution C T upstream_gene_variant SKCM-US 11 71942105 71942105 single base substitution G A downstream_gene_variant SKCM-US 11 71942105 71942105 single base substitution G A exon_variant SKCM-US 11 71942105 71942105 single base substitution G A missense_variant E215K 643G>A SKCM-US 11 71942105 71942105 single base substitution G A missense_variant E457K 1369G>A SKCM-US 11 71942105 71942105 single base substitution G A upstream_gene_variant SKCM-US 11 71942228 71942228 single base substitution C T downstream_gene_variant SKCM-US 11 71942228 71942228 single base substitution C T exon_variant SKCM-US 11 71942228 71942228 single base substitution C T missense_variant R256C 766C>T SKCM-US 11 71942228 71942228 single base substitution C T missense_variant R498C 1492C>T SKCM-US 11 71942228 71942228 single base substitution C T upstream_gene_variant SKCM-US 11 71944134 71944134 single base substitution C T downstream_gene_variant SKCM-US 11 71944134 71944134 single base substitution C T exon_variant SKCM-US 11 71944134 71944134 single base substitution C T missense_variant S414F 1241C>T SKCM-US 11 71944134 71944134 single base substitution C T missense_variant S656F 1967C>T SKCM-US 11 71944134 71944134 single base substitution C T upstream_gene_variant SKCM-US 11 71944715 71944715 single base substitution C T downstream_gene_variant SKCM-US 11 71944715 71944715 single base substitution C T exon_variant SKCM-US 11 71944715 71944715 single base substitution C T synonymous_variant I471I 1413C>T SKCM-US 11 71944715 71944715 single base substitution C T synonymous_variant I713I 2139C>T SKCM-US 11 71944715 71944715 single base substitution C T upstream_gene_variant SKCM-US 11 71944756 71944756 single base substitution T C downstream_gene_variant SKCM-US 11 71944756 71944756 single base substitution T C exon_variant SKCM-US 11 71944756 71944756 single base substitution T C missense_variant V485A 1454T>C SKCM-US 11 71944756 71944756 single base substitution T C missense_variant V727A 2180T>C SKCM-US 11 71944756 71944756 single base substitution T C upstream_gene_variant SKCM-US 11 71945360 71945360 single base substitution T C downstream_gene_variant SKCM-US 11 71945360 71945360 single base substitution T C exon_variant SKCM-US 11 71945360 71945360 single base substitution T C missense_variant F508L 1522T>C SKCM-US 11 71945360 71945360 single base substitution T C missense_variant F750L 2248T>C SKCM-US 11 71945360 71945360 single base substitution T C upstream_gene_variant SKCM-US 11 71945395 71945395 single base substitution C T 3_prime_UTR_variant SKCM-US 11 71945395 71945395 single base substitution C T downstream_gene_variant SKCM-US 11 71945395 71945395 single base substitution C T exon_variant SKCM-US 11 71945395 71945395 single base substitution C T synonymous_variant S519S 1557C>T SKCM-US 11 71945395 71945395 single base substitution C T synonymous_variant S761S 2283C>T SKCM-US 11 71945395 71945395 single base substitution C T upstream_gene_variant SKCM-US 11 71946225 71946225 single base substitution C T downstream_gene_variant SKCM-US 11 71946225 71946225 single base substitution C T exon_variant SKCM-US 11 71946225 71946225 single base substitution C T intron_variant SKCM-US 11 71946225 71946225 single base substitution C T synonymous_variant S585S 1755C>T SKCM-US 11 71946225 71946225 single base substitution C T synonymous_variant S827S 2481C>T SKCM-US 11 71946225 71946225 single base substitution C T upstream_gene_variant SKCM-US 11 71946393 71946393 single base substitution C T downstream_gene_variant SKCM-US 11 71946393 71946393 single base substitution C T exon_variant SKCM-US 11 71946393 71946393 single base substitution C T intron_variant SKCM-US 11 71946393 71946393 single base substitution C T synonymous_variant L611L 1831C>T SKCM-US 11 71946393 71946393 single base substitution C T synonymous_variant L853L 2557C>T SKCM-US 11 71946393 71946393 single base substitution C T upstream_gene_variant SKCM-US 11 71946398 71946398 single base substitution C T downstream_gene_variant SKCM-US 11 71946398 71946398 single base substitution C T exon_variant SKCM-US 11 71946398 71946398 single base substitution C T intron_variant SKCM-US 11 71946398 71946398 single base substitution C T synonymous_variant T612T 1836C>T SKCM-US 11 71946398 71946398 single base substitution C T synonymous_variant T854T 2562C>T SKCM-US 11 71946398 71946398 single base substitution C T upstream_gene_variant SKCM-US 11 71946430 71946430 single base substitution A T downstream_gene_variant SKCM-US 11 71946430 71946430 single base substitution A T exon_variant SKCM-US 11 71946430 71946430 single base substitution A T intron_variant SKCM-US 11 71946430 71946430 single base substitution A T missense_variant N623I 1868A>T SKCM-US 11 71946430 71946430 single base substitution A T missense_variant N865I 2594A>T SKCM-US 11 71946430 71946430 single base substitution A T upstream_gene_variant SKCM-US 11 71946982 71946982 single base substitution C T downstream_gene_variant SKCM-US 11 71946982 71946982 single base substitution C T exon_variant SKCM-US 11 71946982 71946982 single base substitution C T intron_variant SKCM-US 11 71946982 71946982 single base substitution C T missense_variant P702L 2105C>T SKCM-US 11 71946982 71946982 single base substitution C T missense_variant P944L 2831C>T SKCM-US 11 71946982 71946982 single base substitution C T upstream_gene_variant SKCM-US 11 71948209 71948209 deletion of <=200bp C - downstream_gene_variant SKCM-US 11 71948209 71948209 deletion of <=200bp C - frameshift_variant A732 SKCM-US 11 71948209 71948209 deletion of <=200bp C - frameshift_variant A974 SKCM-US 11 71948209 71948209 deletion of <=200bp C - intron_variant SKCM-US 11 71948209 71948209 deletion of <=200bp C - upstream_gene_variant SKCM-US 11 71948210 71948210 single base substitution C T downstream_gene_variant SKCM-US 11 71948210 71948210 single base substitution C T intron_variant SKCM-US 11 71948210 71948210 single base substitution C T synonymous_variant A732A 2196C>T SKCM-US 11 71948210 71948210 single base substitution C T synonymous_variant A974A 2922C>T SKCM-US 11 71948210 71948210 single base substitution C T upstream_gene_variant SKCM-US 11 71948326 71948326 single base substitution C T downstream_gene_variant SKCM-US 11 71948326 71948326 single base substitution C T intron_variant SKCM-US 11 71948326 71948326 single base substitution C T missense_variant T1013I 3038C>T SKCM-US 11 71948326 71948326 single base substitution C T missense_variant T26I 77C>T SKCM-US 11 71948326 71948326 single base substitution C T missense_variant T771I 2312C>T SKCM-US 11 71948326 71948326 single base substitution C T upstream_gene_variant SKCM-US 11 71948480 71948480 single base substitution C T downstream_gene_variant SKCM-US 11 71948480 71948480 single base substitution C T intron_variant SKCM-US 11 71948480 71948480 single base substitution C T synonymous_variant F1064F 3192C>T SKCM-US 11 71948480 71948480 single base substitution C T synonymous_variant F77F 231C>T SKCM-US 11 71948480 71948480 single base substitution C T synonymous_variant F822F 2466C>T SKCM-US 11 71948480 71948480 single base substitution C T upstream_gene_variant SKCM-US 11 71950911 71950911 single base substitution C T downstream_gene_variant STAD-US 11 71931995 71931995 single base substitution T G upstream_gene_variant STAD-US 11 71932561 71932561 single base substitution T G upstream_gene_variant STAD-US 11 71932594 71932594 single base substitution C A upstream_gene_variant STAD-US 11 71932697 71932697 single base substitution C T upstream_gene_variant STAD-US 11 71939254 71939254 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 71939254 71939254 single base substitution C T downstream_gene_variant STAD-US 11 71939254 71939254 single base substitution C T exon_variant STAD-US 11 71939254 71939254 single base substitution C T missense_variant T68M 203C>T STAD-US 11 71939254 71939254 single base substitution C T upstream_gene_variant STAD-US 11 71939260 71939260 single base substitution G A 5_prime_UTR_variant STAD-US 11 71939260 71939260 single base substitution G A downstream_gene_variant STAD-US 11 71939260 71939260 single base substitution G A exon_variant STAD-US 11 71939260 71939260 single base substitution G A missense_variant R70H 209G>A STAD-US 11 71939260 71939260 single base substitution G A upstream_gene_variant STAD-US 11 71939414 71939414 single base substitution G A 5_prime_UTR_variant STAD-US 11 71939414 71939414 single base substitution G A downstream_gene_variant STAD-US 11 71939414 71939414 single base substitution G A exon_variant STAD-US 11 71939414 71939414 single base substitution G A missense_variant R90H 269G>A STAD-US 11 71939414 71939414 single base substitution G A upstream_gene_variant STAD-US 11 71939801 71939801 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 71939801 71939801 single base substitution C T downstream_gene_variant STAD-US 11 71939801 71939801 single base substitution C T missense_variant P143L 428C>T STAD-US 11 71939801 71939801 single base substitution C T upstream_gene_variant STAD-US 11 71942042 71942042 single base substitution G A downstream_gene_variant STAD-US 11 71942042 71942042 single base substitution G A exon_variant STAD-US 11 71942042 71942042 single base substitution G A missense_variant V194I 580G>A STAD-US 11 71942042 71942042 single base substitution G A missense_variant V436I 1306G>A STAD-US 11 71942042 71942042 single base substitution G A upstream_gene_variant STAD-US 11 71942175 71942175 single base substitution A G downstream_gene_variant STAD-US 11 71942175 71942175 single base substitution A G exon_variant STAD-US 11 71942175 71942175 single base substitution A G missense_variant E238G 713A>G STAD-US 11 71942175 71942175 single base substitution A G missense_variant E480G 1439A>G STAD-US 11 71942175 71942175 single base substitution A G upstream_gene_variant STAD-US 11 71942235 71942235 single base substitution T C downstream_gene_variant STAD-US 11 71942235 71942235 single base substitution T C exon_variant STAD-US 11 71942235 71942235 single base substitution T C splice_donor_variant STAD-US 11 71942235 71942235 single base substitution T C upstream_gene_variant STAD-US 11 71942618 71942618 single base substitution T C downstream_gene_variant STAD-US 11 71942618 71942618 single base substitution T C exon_variant STAD-US 11 71942618 71942618 single base substitution T C missense_variant V283A 848T>C STAD-US 11 71942618 71942618 single base substitution T C missense_variant V525A 1574T>C STAD-US 11 71942618 71942618 single base substitution T C upstream_gene_variant STAD-US 11 71943988 71943988 single base substitution C T downstream_gene_variant STAD-US 11 71943988 71943988 single base substitution C T exon_variant STAD-US 11 71943988 71943988 single base substitution C T missense_variant R399W 1195C>T STAD-US 11 71943988 71943988 single base substitution C T missense_variant R641W 1921C>T STAD-US 11 71943988 71943988 single base substitution C T upstream_gene_variant STAD-US 11 71946233 71946233 single base substitution G A downstream_gene_variant STAD-US 11 71946233 71946233 single base substitution G A exon_variant STAD-US 11 71946233 71946233 single base substitution G A intron_variant STAD-US 11 71946233 71946233 single base substitution G A missense_variant G588D 1763G>A STAD-US 11 71946233 71946233 single base substitution G A missense_variant G830D 2489G>A STAD-US 11 71946233 71946233 single base substitution G A upstream_gene_variant STAD-US 11 71946494 71946494 single base substitution C T downstream_gene_variant STAD-US 11 71946494 71946494 single base substitution C T intron_variant STAD-US 11 71946494 71946494 single base substitution C T splice_region_variant STAD-US 11 71946494 71946494 single base substitution C T upstream_gene_variant STAD-US 11 71946764 71946764 deletion of <=200bp C - downstream_gene_variant STAD-US 11 71946764 71946764 deletion of <=200bp C - exon_variant STAD-US 11 71946764 71946764 deletion of <=200bp C - frameshift_variant A660 STAD-US 11 71946764 71946764 deletion of <=200bp C - frameshift_variant A902 STAD-US 11 71946764 71946764 deletion of <=200bp C - intron_variant STAD-US 11 71946764 71946764 deletion of <=200bp C - upstream_gene_variant STAD-US 11 71948209 71948209 deletion of <=200bp C - downstream_gene_variant STAD-US 11 71948209 71948209 deletion of <=200bp C - frameshift_variant A732 STAD-US 11 71948209 71948209 deletion of <=200bp C - frameshift_variant A974 STAD-US 11 71948209 71948209 deletion of <=200bp C - intron_variant STAD-US 11 71948209 71948209 deletion of <=200bp C - upstream_gene_variant STAD-US 11 71948209 71948209 insertion of <=200bp - C downstream_gene_variant STAD-US 11 71948209 71948209 insertion of <=200bp - C frameshift_variant A732A? STAD-US 11 71948209 71948209 insertion of <=200bp - C frameshift_variant A974A? STAD-US 11 71948209 71948209 insertion of <=200bp - C intron_variant STAD-US 11 71948209 71948209 insertion of <=200bp - C upstream_gene_variant STAD-US 11 71948327 71948327 single base substitution C T downstream_gene_variant STAD-US 11 71948327 71948327 single base substitution C T intron_variant STAD-US 11 71948327 71948327 single base substitution C T synonymous_variant T1013T 3039C>T STAD-US 11 71948327 71948327 single base substitution C T synonymous_variant T26T 78C>T STAD-US 11 71948327 71948327 single base substitution C T synonymous_variant T771T 2313C>T STAD-US 11 71948327 71948327 single base substitution C T upstream_gene_variant STAD-US 11 71948467 71948467 single base substitution A T downstream_gene_variant STAD-US 11 71948467 71948467 single base substitution A T intron_variant STAD-US 11 71948467 71948467 single base substitution A T missense_variant D1060V 3179A>T STAD-US 11 71948467 71948467 single base substitution A T missense_variant D73V 218A>T STAD-US 11 71948467 71948467 single base substitution A T missense_variant D818V 2453A>T STAD-US 11 71948467 71948467 single base substitution A T upstream_gene_variant STAD-US 11 71948484 71948484 deletion of <=200bp C - downstream_gene_variant STAD-US 11 71948484 71948484 deletion of <=200bp C - frameshift_variant P1066 STAD-US 11 71948484 71948484 deletion of <=200bp C - frameshift_variant P79 STAD-US 11 71948484 71948484 deletion of <=200bp C - frameshift_variant P824 STAD-US 11 71948484 71948484 deletion of <=200bp C - intron_variant STAD-US 11 71948484 71948484 deletion of <=200bp C - upstream_gene_variant STAD-US 11 71948520 71948520 single base substitution C T downstream_gene_variant STAD-US 11 71948520 71948520 single base substitution C T intron_variant STAD-US 11 71948520 71948520 single base substitution C T missense_variant R1078W 3232C>T STAD-US 11 71948520 71948520 single base substitution C T missense_variant R836W 2506C>T STAD-US 11 71948520 71948520 single base substitution C T missense_variant R91W 271C>T STAD-US 11 71948520 71948520 single base substitution C T upstream_gene_variant STAD-US 11 71948521 71948521 single base substitution G A downstream_gene_variant STAD-US 11 71948521 71948521 single base substitution G A intron_variant STAD-US 11 71948521 71948521 single base substitution G A missense_variant R1078Q 3233G>A STAD-US 11 71948521 71948521 single base substitution G A missense_variant R836Q 2507G>A STAD-US 11 71948521 71948521 single base substitution G A missense_variant R91Q 272G>A STAD-US 11 71948521 71948521 single base substitution G A upstream_gene_variant STAD-US 11 71948719 71948719 single base substitution C T downstream_gene_variant STAD-US 11 71948719 71948719 single base substitution C T intron_variant STAD-US 11 71948719 71948719 single base substitution C T missense_variant A1144V 3431C>T STAD-US 11 71948719 71948719 single base substitution C T missense_variant A157V 470C>T STAD-US 11 71948719 71948719 single base substitution C T missense_variant A5V 14C>T STAD-US 11 71948719 71948719 single base substitution C T missense_variant A902V 2705C>T STAD-US 11 71948748 71948748 deletion of <=200bp C - downstream_gene_variant STAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P1154 STAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P15 STAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P167 STAD-US 11 71948748 71948748 deletion of <=200bp C - frameshift_variant P912 STAD-US 11 71948748 71948748 deletion of <=200bp C - intron_variant STAD-US 11 71950893 71950893 single base substitution T C downstream_gene_variant STAD-US 11 71952153 71952153 single base substitution C T downstream_gene_variant STAD-US 11 71952170 71952170 single base substitution G A downstream_gene_variant STAD-US 11 71952253 71952253 single base substitution C T downstream_gene_variant STAD-US 11 71954983 71954983 single base substitution G A downstream_gene_variant THCA-SA 11 71950934 71950934 single base substitution A C downstream_gene_variant THCA-US 11 71943766 71943766 single base substitution C T downstream_gene_variant THCA-US 11 71943766 71943766 single base substitution C T exon_variant THCA-US 11 71943766 71943766 single base substitution C T synonymous_variant F361F 1083C>T THCA-US 11 71943766 71943766 single base substitution C T synonymous_variant F603F 1809C>T THCA-US 11 71943766 71943766 single base substitution C T upstream_gene_variant THCA-US 11 71950915 71950915 single base substitution C T downstream_gene_variant UCEC-US 11 71932640 71932640 single base substitution G A upstream_gene_variant UCEC-US 11 71939285 71939285 single base substitution C A 5_prime_UTR_variant UCEC-US 11 71939285 71939285 single base substitution C A downstream_gene_variant UCEC-US 11 71939285 71939285 single base substitution C A exon_variant UCEC-US 11 71939285 71939285 single base substitution C A missense_variant F78L 234C>A UCEC-US 11 71939285 71939285 single base substitution C A upstream_gene_variant UCEC-US 11 71939397 71939397 single base substitution G A 5_prime_UTR_variant UCEC-US 11 71939397 71939397 single base substitution G A downstream_gene_variant UCEC-US 11 71939397 71939397 single base substitution G A exon_variant UCEC-US 11 71939397 71939397 single base substitution G A synonymous_variant S84S 252G>A UCEC-US 11 71939397 71939397 single base substitution G A upstream_gene_variant UCEC-US 11 71939417 71939417 single base substitution G A 5_prime_UTR_variant UCEC-US 11 71939417 71939417 single base substitution G A downstream_gene_variant UCEC-US 11 71939417 71939417 single base substitution G A exon_variant UCEC-US 11 71939417 71939417 single base substitution G A missense_variant R91H 272G>A UCEC-US 11 71939417 71939417 single base substitution G A upstream_gene_variant UCEC-US 11 71939864 71939864 single base substitution A C 5_prime_UTR_variant UCEC-US 11 71939864 71939864 single base substitution A C downstream_gene_variant UCEC-US 11 71939864 71939864 single base substitution A C missense_variant E164A 491A>C UCEC-US 11 71939864 71939864 single base substitution A C upstream_gene_variant UCEC-US 11 71940250 71940250 single base substitution C T 5_prime_UTR_variant UCEC-US 11 71940250 71940250 single base substitution C T downstream_gene_variant UCEC-US 11 71940250 71940250 single base substitution C T missense_variant A212V 635C>T UCEC-US 11 71940250 71940250 single base substitution C T upstream_gene_variant UCEC-US 11 71940256 71940256 single base substitution C A 5_prime_UTR_variant UCEC-US 11 71940256 71940256 single base substitution C A downstream_gene_variant UCEC-US 11 71940256 71940256 single base substitution C A stop_gained S214* 641C>A UCEC-US 11 71940256 71940256 single base substitution C A upstream_gene_variant UCEC-US 11 71940583 71940583 single base substitution C A downstream_gene_variant UCEC-US 11 71940583 71940583 single base substitution C A missense_variant T245N 734C>A UCEC-US 11 71940583 71940583 single base substitution C A missense_variant T3N 8C>A UCEC-US 11 71940583 71940583 single base substitution C A upstream_gene_variant UCEC-US 11 71941405 71941405 single base substitution G C downstream_gene_variant UCEC-US 11 71941405 71941405 single base substitution G C splice_acceptor_variant UCEC-US 11 71941405 71941405 single base substitution G C upstream_gene_variant UCEC-US 11 71942080 71942080 single base substitution G A downstream_gene_variant UCEC-US 11 71942080 71942080 single base substitution G A exon_variant UCEC-US 11 71942080 71942080 single base substitution G A synonymous_variant S206S 618G>A UCEC-US 11 71942080 71942080 single base substitution G A synonymous_variant S448S 1344G>A UCEC-US 11 71942080 71942080 single base substitution G A upstream_gene_variant UCEC-US 11 71942192 71942192 single base substitution C T downstream_gene_variant UCEC-US 11 71942192 71942192 single base substitution C T exon_variant UCEC-US 11 71942192 71942192 single base substitution C T missense_variant R244C 730C>T UCEC-US 11 71942192 71942192 single base substitution C T missense_variant R486C 1456C>T UCEC-US 11 71942192 71942192 single base substitution C T upstream_gene_variant UCEC-US 11 71942194 71942194 single base substitution C T downstream_gene_variant UCEC-US 11 71942194 71942194 single base substitution C T exon_variant UCEC-US 11 71942194 71942194 single base substitution C T synonymous_variant R244R 732C>T UCEC-US 11 71942194 71942194 single base substitution C T synonymous_variant R486R 1458C>T UCEC-US 11 71942194 71942194 single base substitution C T upstream_gene_variant UCEC-US 11 71942581 71942581 single base substitution C A downstream_gene_variant UCEC-US 11 71942581 71942581 single base substitution C A exon_variant UCEC-US 11 71942581 71942581 single base substitution C A missense_variant L271M 811C>A UCEC-US 11 71942581 71942581 single base substitution C A missense_variant L513M 1537C>A UCEC-US 11 71942581 71942581 single base substitution C A upstream_gene_variant UCEC-US 11 71942633 71942633 insertion of <=200bp - G downstream_gene_variant UCEC-US 11 71942633 71942633 insertion of <=200bp - G exon_variant UCEC-US 11 71942633 71942633 insertion of <=200bp - G frameshift_variant V288G? UCEC-US 11 71942633 71942633 insertion of <=200bp - G frameshift_variant V530G? UCEC-US 11 71942633 71942633 insertion of <=200bp - G upstream_gene_variant UCEC-US 11 71943379 71943379 single base substitution C T downstream_gene_variant UCEC-US 11 71943379 71943379 single base substitution C T exon_variant UCEC-US 11 71943379 71943379 single base substitution C T missense_variant R329W 985C>T UCEC-US 11 71943379 71943379 single base substitution C T missense_variant R571W 1711C>T UCEC-US 11 71943379 71943379 single base substitution C T upstream_gene_variant UCEC-US 11 71943739 71943739 single base substitution C T downstream_gene_variant UCEC-US 11 71943739 71943739 single base substitution C T exon_variant UCEC-US 11 71943739 71943739 single base substitution C T synonymous_variant D352D 1056C>T UCEC-US 11 71943739 71943739 single base substitution C T synonymous_variant D594D 1782C>T UCEC-US 11 71943739 71943739 single base substitution C T upstream_gene_variant UCEC-US 11 71944186 71944186 single base substitution G A downstream_gene_variant UCEC-US 11 71944186 71944186 single base substitution G A exon_variant UCEC-US 11 71944186 71944186 single base substitution G A stop_gained W431* 1293G>A UCEC-US 11 71944186 71944186 single base substitution G A stop_gained W673* 2019G>A UCEC-US 11 71944186 71944186 single base substitution G A upstream_gene_variant UCEC-US 11 71944516 71944516 single base substitution G A downstream_gene_variant UCEC-US 11 71944516 71944516 single base substitution G A exon_variant UCEC-US 11 71944516 71944516 single base substitution G A missense_variant R449Q 1346G>A UCEC-US 11 71944516 71944516 single base substitution G A missense_variant R691Q 2072G>A UCEC-US 11 71944516 71944516 single base substitution G A upstream_gene_variant UCEC-US 11 71944765 71944765 deletion of <=200bp C - downstream_gene_variant UCEC-US 11 71944765 71944765 deletion of <=200bp C - exon_variant UCEC-US 11 71944765 71944765 deletion of <=200bp C - frameshift_variant T488 UCEC-US 11 71944765 71944765 deletion of <=200bp C - frameshift_variant T730 UCEC-US 11 71944765 71944765 deletion of <=200bp C - upstream_gene_variant UCEC-US 11 71944788 71944788 single base substitution G A downstream_gene_variant UCEC-US 11 71944788 71944788 single base substitution G A missense_variant G496R 1486G>A UCEC-US 11 71944788 71944788 single base substitution G A missense_variant G738R 2212G>A UCEC-US 11 71944788 71944788 single base substitution G A splice_region_variant UCEC-US 11 71944788 71944788 single base substitution G A upstream_gene_variant UCEC-US 11 71945645 71945645 single base substitution C T 3_prime_UTR_variant UCEC-US 11 71945645 71945645 single base substitution C T downstream_gene_variant UCEC-US 11 71945645 71945645 single base substitution C T exon_variant UCEC-US 11 71945645 71945645 single base substitution C T missense_variant R559C 1675C>T UCEC-US 11 71945645 71945645 single base substitution C T missense_variant R801C 2401C>T UCEC-US 11 71945645 71945645 single base substitution C T upstream_gene_variant UCEC-US 11 71946494 71946494 single base substitution C T downstream_gene_variant UCEC-US 11 71946494 71946494 single base substitution C T intron_variant UCEC-US 11 71946494 71946494 single base substitution C T splice_region_variant UCEC-US 11 71946494 71946494 single base substitution C T upstream_gene_variant UCEC-US 11 71948243 71948243 single base substitution C A downstream_gene_variant UCEC-US 11 71948243 71948243 single base substitution C A intron_variant UCEC-US 11 71948243 71948243 single base substitution C A synonymous_variant A743A 2229C>A UCEC-US 11 71948243 71948243 single base substitution C A synonymous_variant A985A 2955C>A UCEC-US 11 71948243 71948243 single base substitution C A upstream_gene_variant UCEC-US 11 71948267 71948267 single base substitution G A downstream_gene_variant UCEC-US 11 71948267 71948267 single base substitution G A intron_variant UCEC-US 11 71948267 71948267 single base substitution G A synonymous_variant P6P 18G>A UCEC-US 11 71948267 71948267 single base substitution G A synonymous_variant P751P 2253G>A UCEC-US 11 71948267 71948267 single base substitution G A synonymous_variant P993P 2979G>A UCEC-US 11 71948267 71948267 single base substitution G A upstream_gene_variant UCEC-US 11 71948292 71948292 deletion of <=200bp C - downstream_gene_variant UCEC-US 11 71948292 71948292 deletion of <=200bp C - frameshift_variant P1002 UCEC-US 11 71948292 71948292 deletion of <=200bp C - frameshift_variant P15 UCEC-US 11 71948292 71948292 deletion of <=200bp C - frameshift_variant P760 UCEC-US 11 71948292 71948292 deletion of <=200bp C - intron_variant UCEC-US 11 71948292 71948292 deletion of <=200bp C - upstream_gene_variant UCEC-US 11 71948375 71948375 single base substitution C T downstream_gene_variant UCEC-US 11 71948375 71948375 single base substitution C T intron_variant UCEC-US 11 71948375 71948375 single base substitution C T synonymous_variant H1029H 3087C>T UCEC-US 11 71948375 71948375 single base substitution C T synonymous_variant H42H 126C>T UCEC-US 11 71948375 71948375 single base substitution C T synonymous_variant H787H 2361C>T UCEC-US 11 71948375 71948375 single base substitution C T upstream_gene_variant UCEC-US 11 71949110 71949110 single base substitution G A downstream_gene_variant UCEC-US 11 71949110 71949110 single base substitution G A intron_variant UCEC-US 11 71949110 71949110 single base substitution G A missense_variant A1193T 3577G>A UCEC-US 11 71949110 71949110 single base substitution G A missense_variant A54T 160G>A UCEC-US 11 71949110 71949110 single base substitution G A missense_variant A951T 2851G>A UCEC-US 11 71949201 71949201 single base substitution A G downstream_gene_variant UCEC-US 11 71949201 71949201 single base substitution A G intron_variant UCEC-US 11 71949201 71949201 single base substitution A G missense_variant D1223G 3668A>G UCEC-US 11 71949201 71949201 single base substitution A G missense_variant D84G 251A>G UCEC-US 11 71949201 71949201 single base substitution A G missense_variant D981G 2942A>G

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AP-A056-01 COSM195548 c.1456C>T p.R486C Substitution - Missense 11:72231148-72231148 + 2492714 COSM5606636 c.1969T>G p.F657V Substitution - Missense 11:72233092-72233092 + HCT116 COSM1356794 c.3144G>A p.L1048L Substitution - coding silent 11:72237388-72237388 + 2290929 COSM2016143 c.1497+5delG p.? Unknown 11:72231194-72231194 + TCGA-A8-A09Z-01 COSM3810363 c.1214G>A p.C405Y Substitution - Missense 11:72230812-72230812 + MOLT-4 COSM1676277 c.2617C>T p.R873W Substitution - Missense 11:72235409-72235409 + TCGA-B5-A11E-01 COSM931659 c.272G>A p.R91H Substitution - Missense 11:72228373-72228373 + TCGA-EE-A2MC-06 COSM3452999 c.2594A>T p.N865I Substitution - Missense 11:72235386-72235386 + TCGA-D9-A6EC-06 COSM4403012 c.1189A>G p.S397G Substitution - Missense 11:72230460-72230460 + PT15_1 COSM5897795 c.2950C>T p.P984S Substitution - Missense 11:72237194-72237194 + LUAD-RT-S01818 COSM383807 c.1938C>G p.V646V Substitution - coding silent 11:72232961-72232961 + SNUH_G16_S1 COSM3998573 c.1894C>A p.L632I Substitution - Missense 11:72232917-72232917 + T2940 COSM4613274 c.2921delC p.P976fs*155 Deletion - Frameshift 11:72237165-72237165 + 2521252 COSM5889146 c.1109C>T p.S370F Substitution - Missense 11:72230380-72230380 + Au8 COSM5606636 c.1969T>G p.F657V Substitution - Missense 11:72233092-72233092 + HCC35T COSM1605186 c.683G>T p.G228V Substitution - Missense 11:72229488-72229488 + TCGA-CK-4952-01 COSM1356793 c.2749C>T p.R917C Substitution - Missense 11:72235856-72235856 + T3174 COSM4692630 c.542T>C p.V181A Substitution - Missense 11:72229113-72229113 + TCGA-EE-A2MI-06 COSM3452990 c.1369G>A p.E457K Substitution - Missense 11:72231061-72231061 + TCGA-AA-3966-01 COSM272808 c.2950C>A p.P984T Substitution - Missense 11:72237194-72237194 + TCGA-CM-4746-01 COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + CSCC-31-T COSM4458630 c.1093C>T p.R365C Substitution - Missense 11:72230364-72230364 + TCGA-EE-A3AG-06 COSM3453001 c.3038C>T p.T1013I Substitution - Missense 11:72237282-72237282 + CRC-11T COSM2016176 c.2632C>T p.R878C Substitution - Missense 11:72235424-72235424 + S00827 COSM312002 c.1009G>T p.D337Y Substitution - Missense 11:72230190-72230190 + SW620 COSM2016152 c.1743G>T p.R581R Substitution - coding silent 11:72232656-72232656 + PD11753a COSM195545 c.429G>A p.P143P Substitution - coding silent 11:72228758-72228758 + TCGA-04-1343-01 COSM75017 c.1025G>A p.R342Q Substitution - Missense 11:72230206-72230206 + WSU-HN12 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + RH30SJ_ COSM2016192 c.3316G>A p.A1106T Substitution - Missense 11:72237560-72237560 + ccRCC-29 COSM1662277 c.1141T>A p.F381I Substitution - Missense 11:72230412-72230412 + SNU-175 COSM4200697 c.1479G>A p.T493T Substitution - coding silent 11:72231171-72231171 + TCGA-D1-A17U-01 COSM931677 c.2401C>T p.R801C Substitution - Missense 11:72234601-72234601 + 103452 COSM94504 c.3550G>C p.E1184Q Substitution - Missense 11:72237794-72237794 + sysucc-274T COSM5475573 c.519-10C>T p.? Unknown 11:72229080-72229080 + S0049 COSM5882127 c.856C>G p.L286V Substitution - Missense 11:72229936-72229936 + ESO-173 COSM1254858 c.2624C>T p.P875L Substitution - Missense 11:72235416-72235416 + ZZUFHECRKL-G062T COSM3998571 c.1368C>T p.D456D Substitution - coding silent 11:72231060-72231060 + T3021 COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + TCGA-AP-A059-01 COSM931667 c.1458C>T p.R486R Substitution - coding silent 11:72231150-72231150 + CHC892T COSM4795383 c.3375G>A p.Q1125Q Substitution - coding silent 11:72237619-72237619 + TCGA-BT-A20R-01 COSM1298577 c.2523C>G p.L841L Substitution - coding silent 11:72235315-72235315 + 587316 COSM1210738 c.2918C>T p.A973V Substitution - Missense 11:72237162-72237162 + TCGA-AZ-6601-01 COSM1356791 c.1438G>A p.E480K Substitution - Missense 11:72231130-72231130 + TCGA-BT-A20R-01 COSM1298578 c.3624C>G p.I1208M Substitution - Missense 11:72238113-72238113 + MZ7-mel COSM13661 c.2591G>A p.G864D Substitution - Missense 11:72235383-72235383 + 93VU147T COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + TCGA-AD-5900-01 COSM1356794 c.3144G>A p.L1048L Substitution - coding silent 11:72237388-72237388 + YURIDA COSM1704345 c.2336A>G p.K779R Substitution - Missense 11:72234536-72234536 + TCGA-CU-A0YO-01 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + CHC1704T COSM4036452 c.269G>A p.R90H Substitution - Missense 11:72228370-72228370 + ZZUFHECRKL-G062T COSM4146291 c.987A>G p.S329S Substitution - coding silent 11:72230168-72230168 + 2492713 COSM5606636 c.1969T>G p.F657V Substitution - Missense 11:72233092-72233092 + LUAD-S01409 COSM346322 c.418C>A p.P140T Substitution - Missense 11:72228747-72228747 + 8057513 COSM3383803 c.3558G>A p.P1186P Substitution - coding silent 11:72238047-72238047 + T2269 COSM4692631 c.546G>A p.S182S Substitution - coding silent 11:72229117-72229117 + PD4953a COSM5771532 c.1867A>G p.I623V Substitution - Missense 11:72232890-72232890 + GCT27 COSM5749488 c.2522T>C p.L841P Substitution - Missense 11:72235314-72235314 + S02344 COSM5693328 c.2504-2A>G p.? Unknown 11:72235294-72235294 + CHC451T COSM4957299 c.1988A>G p.Y663C Substitution - Missense 11:72233111-72233111 + TCGA-KV-A6GD-01 COSM3986439 c.3315A>G p.P1105P Substitution - coding silent 11:72237559-72237559 + TCGA-AG-A014-01 COSM5072832 c.2757A>T p.P919P Substitution - coding silent 11:72235864-72235864 + TCGA-BG-A0M4-01 COSM931671 c.1712G>A p.R571Q Substitution - Missense 11:72232336-72232336 + SC_9081 COSM931674 c.2072G>A p.R691Q Substitution - Missense 11:72233472-72233472 + 1517_PT COSM5753799 c.2609T>C p.M870T Substitution - Missense 11:72235401-72235401 + TCGA-BR-4184-01 COSM2016112 c.209G>A p.R70H Substitution - Missense 11:72228216-72228216 + T228 COSM4692633 c.1230C>A p.L410L Substitution - coding silent 11:72230828-72230828 + TCGA-CC-A7IK-01 COSM4924974 c.3472C>T p.L1158L Substitution - coding silent 11:72237716-72237716 + TCGA-B5-A11J-01 COSM931670 c.1711C>T p.R571W Substitution - Missense 11:72232335-72232335 + TCGA-BR-7707-01 COSM2016112 c.209G>A p.R70H Substitution - Missense 11:72228216-72228216 + PTC-10C COSM3998572 c.1893C>A p.L631L Substitution - coding silent 11:72232916-72232916 + HCT8 COSM4633415 c.2730G>T p.Q910H Substitution - Missense 11:72235745-72235745 + MO_1337 COSM5566018 c.2003G>T p.R668L Substitution - Missense 11:72233126-72233126 + TCGA-CK-5916-01 COSM3687800 c.1747C>T p.L583F Substitution - Missense 11:72232660-72232660 + TCGA-A8-A08H-01 COSM265407 c.2920_2921insC p.P977fs*7 Insertion - Frameshift 11:72237164-72237165 + Au3 COSM5601637 c.3237C>T p.G1079G Substitution - coding silent 11:72237481-72237481 + PTC-7C COSM4146291 c.987A>G p.S329S Substitution - coding silent 11:72230168-72230168 + 7285 COSM5616553 c.498C>A p.P166P Substitution - coding silent 11:72228827-72228827 + T36 COSM1676277 c.2617C>T p.R873W Substitution - Missense 11:72235409-72235409 + HCC055T COSM5823835 c.1198-2A>C p.? Unknown 11:72230794-72230794 + T368 COSM4692637 c.1470G>T p.K490N Substitution - Missense 11:72231162-72231162 + TCGA-66-2785-01 COSM690800 c.680C>G p.S227* Substitution - Nonsense 11:72229485-72229485 + TCGA-BC-4073-01 COSM4937040 c.2983C>T p.Q995* Substitution - Nonsense 11:72237227-72237227 + BICR_22 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + HCC129T COSM5817082 c.1692G>A p.S564S Substitution - coding silent 11:72232316-72232316 + TCGA-EE-A2MI-06 COSM3452994 c.2180T>C p.V727A Substitution - Missense 11:72233712-72233712 + HN_62506 COSM128242 c.255G>A p.Q85Q Substitution - coding silent 11:72228356-72228356 + TCGA-AP-A059-01 COSM931668 c.1537C>A p.L513M Substitution - Missense 11:72231537-72231537 + C086 COSM5532750 c.3255C>T p.A1085A Substitution - coding silent 11:72237499-72237499 + Au3 COSM5601636 c.456C>T p.A152A Substitution - coding silent 11:72228785-72228785 + CSCC-32-T COSM1254859 c.476C>T p.P159L Substitution - Missense 11:72228805-72228805 + TCGA-AN-A0AK-01 COSM5205807 c.1459delG p.G488fs*43 Deletion - Frameshift 11:72231151-72231151 + WA16 COSM240237 c.1115G>A p.R372H Substitution - Missense 11:72230386-72230386 + TCGA-CC-A3MC-01 COSM4919516 c.2211A>G p.K737K Substitution - coding silent 11:72233743-72233743 + IPMN11 COSM248775 c.1498-1G>A p.? Unknown 11:72231497-72231497 + TCGA-IR-A3LK-01 COSM4817712 c.937G>A p.E313K Substitution - Missense 11:72230017-72230017 + TCGA-ER-A193-06 COSM3452996 c.2283C>T p.S761S Substitution - coding silent 11:72234351-72234351 + CHC892T COSM4795383 c.3375G>A p.Q1125Q Substitution - coding silent 11:72237619-72237619 + 8051716 COSM4135704 c.319C>T p.Q107* Substitution - Nonsense 11:72228420-72228420 + LUAD-B00523 COSM331730 c.2412C>T p.P804P Substitution - coding silent 11:72234612-72234612 + TARGET-30-PAPVFD COSM1236636 c.1435C>T p.R479C Substitution - Missense 11:72231127-72231127 + TCGA-BR-8361-01 COSM4036461 c.3179A>T p.D1060V Substitution - Missense 11:72237423-72237423 + ESO-0149 COSM1254856 c.1202G>A p.R401Q Substitution - Missense 11:72230800-72230800 + CHC798T COSM4958316 c.3239G>A p.R1080H Substitution - Missense 11:72237483-72237483 + SCC-9 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + TCGA-D1-A103-01 COSM931676 c.2212G>A p.G738R Substitution - Missense 11:72233744-72233744 + TCGA-DA-A1I2-06 COSM3452986 c.418C>T p.P140S Substitution - Missense 11:72228747-72228747 + TCGA-AN-A0FX-01 COSM429800 c.277C>T p.Q93* Substitution - Nonsense 11:72228378-72228378 + PT55 COSM5942386 c.2570C>T p.S857F Substitution - Missense 11:72235362-72235362 + TCGA-D1-A160-01 COSM931664 c.734C>A p.T245N Substitution - Missense 11:72229539-72229539 + TCGA-B5-A11E-01 COSM931682 c.3087C>T p.H1029H Substitution - coding silent 11:72237331-72237331 + RKO COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + TCGA-20-1685-01 COSM1322189 c.186T>C p.Y62Y Substitution - coding silent 11:72228193-72228193 + TCGA-B5-A11Y-01 COSM931678 c.2658C>T p.Y886Y Substitution - coding silent 11:72235450-72235450 + TCGA-B7-5816-01 COSM4036456 c.1497+2T>C p.? Unknown 11:72231191-72231191 + 98 COSM5016366 c.1288delA p.T430fs*13 Deletion - Frameshift 11:72230886-72230886 + TCGA-BP-4999-01 COSM467383 c.3160C>G p.P1054A Substitution - Missense 11:72237404-72237404 + TCGA-CD-5801-01 COSM4036453 c.428C>T p.P143L Substitution - Missense 11:72228757-72228757 + T3658 COSM4613274 c.2921delC p.P976fs*155 Deletion - Frameshift 11:72237165-72237165 + HCC133 COSM1605189 c.3001C>T p.P1001S Substitution - Missense 11:72237245-72237245 + TCGA-AN-A0AK-01 COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + LUAD-B02077 COSM334994 c.593G>T p.R198M Substitution - Missense 11:72229164-72229164 + TCGA-D9-A6EC-06 COSM4404392 c.2562C>T p.T854T Substitution - coding silent 11:72235354-72235354 + TCGA-A8-A0A6-01 COSM3810364 c.2841A>C p.P947P Substitution - coding silent 11:72235948-72235948 + CHC1704T COSM4036452 c.269G>A p.R90H Substitution - Missense 11:72228370-72228370 + TCGA-G3-A7M9-01 COSM4922726 c.1780G>T p.D594Y Substitution - Missense 11:72232693-72232693 + SNU-175 COSM2016134 c.1083C>T p.H361H Substitution - coding silent 11:72230264-72230264 + TCGA-A8-A09I-01 COSM265407 c.2920_2921insC p.P977fs*7 Insertion - Frameshift 11:72237164-72237165 + HCC35 COSM1605186 c.683G>T p.G228V Substitution - Missense 11:72229488-72229488 + HCC66T COSM1605185 c.646C>T p.R216W Substitution - Missense 11:72229217-72229217 + LUAD-S01331 COSM396394 c.3575G>T p.R1192L Substitution - Missense 11:72238064-72238064 + I2L-P19Ta-Tumor-Organoid COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + TCGA-CG-4305-01 COSM4036452 c.269G>A p.R90H Substitution - Missense 11:72228370-72228370 + TCGA-AZ-6601-01 COSM1356795 c.3424C>T p.R1142C Substitution - Missense 11:72237668-72237668 + Pat_26_B COSM5839542 c.2771C>T p.A924V Substitution - Missense 11:72235878-72235878 + NB2221T COSM1236636 c.1435C>T p.R479C Substitution - Missense 11:72231127-72231127 + TCGA-AP-A0LE-01 COSM931674 c.2072G>A p.R691Q Substitution - Missense 11:72233472-72233472 + CHC451T COSM4957299 c.1988A>G p.Y663C Substitution - Missense 11:72233111-72233111 + TCGA-FS-A1ZS-06 COSM3452989 c.1212C>T p.F404F Substitution - coding silent 11:72230810-72230810 + STC263 COSM5051124 c.3226G>C p.V1076L Substitution - Missense 11:72237470-72237470 + TCGA-BR-6452-01 COSM4036455 c.1439A>G p.E480G Substitution - Missense 11:72231131-72231131 + TCGA-EJ-7125-01 COSM3670890 c.2780C>A p.P927Q Substitution - Missense 11:72235887-72235887 + TCGA-A6-6781-01 COSM75017 c.1025G>A p.R342Q Substitution - Missense 11:72230206-72230206 + TCGA-AP-A059-01 COSM931679 c.2955C>A p.A985A Substitution - coding silent 11:72237199-72237199 + TCGA-AP-A0LO-01 COSM931661 c.608A>C p.H203P Substitution - Missense 11:72229179-72229179 + LIM2405 COSM4036462 c.3232C>T p.R1078W Substitution - Missense 11:72237476-72237476 + T2932 COSM4613274 c.2921delC p.P976fs*155 Deletion - Frameshift 11:72237165-72237165 + CSCC-55-T COSM4517448 c.3464_3465CC>TT p.P1155L Substitution - Missense 11:72237708-72237709 + BD124T COSM5492838 c.754-8delC p.? Unknown 11:72229655-72229655 + PD6722a COSM5778890 c.3776G>C p.*1259S Nonstop extension 11:72238352-72238352 + 262LT COSM4386404 c.3020C>G p.A1007G Substitution - Missense 11:72237264-72237264 + RW7213 COSM1298576 c.1683C>T p.H561H Substitution - coding silent 11:72232307-72232307 + PD23558a COSM5777572 c.1395C>A p.D465E Substitution - Missense 11:72231087-72231087 + HCA7 COSM3452991 c.1492C>T p.R498C Substitution - Missense 11:72231184-72231184 + T3724 COSM4692634 c.1317delA p.N441fs*2 Deletion - Frameshift 11:72231009-72231009 + TCGA-A5-A0VP-01 COSM931683 c.3577G>A p.A1193T Substitution - Missense 11:72238066-72238066 + TCGA-A5-A0VP-01 COSM931680 c.2979G>A p.P993P Substitution - coding silent 11:72237223-72237223 + ESO-1145 COSM1254857 c.3571G>A p.G1191R Substitution - Missense 11:72238060-72238060 + PD11340a COSM5772908 c.3667G>C p.D1223H Substitution - Missense 11:72238156-72238156 + TCGA-B6-A0IM-01 COSM265407 c.2920_2921insC p.P977fs*7 Insertion - Frameshift 11:72237164-72237165 + NCI-H716 COSM2016118 c.432_433insTCTG p.G146fs*20 Insertion - Frameshift 11:72228761-72228762 + PTC-10C COSM3998573 c.1894C>A p.L632I Substitution - Missense 11:72232917-72232917 + 587350 COSM1210739 c.3394G>A p.E1132K Substitution - Missense 11:72237638-72237638 + UM-SCC-2 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + 30374 COSM5044226 c.189G>T p.Q63H Substitution - Missense 11:72228196-72228196 + TCGA-EE-A2A2-06 COSM3452987 c.751C>T p.Q251* Substitution - Nonsense 11:72229556-72229556 + TCGA-FW-A3R5-06 COSM3870147 c.873C>T p.S291S Substitution - coding silent 11:72229953-72229953 + 8066081 COSM3383803 c.3558G>A p.P1186P Substitution - coding silent 11:72238047-72238047 + SNUH_G16_S1 COSM3998574 c.2504-7T>C p.? Unknown 11:72235289-72235289 + TCGA-D9-A3Z3-06 COSM3452988 c.1090+1G>C p.? Unknown 11:72230272-72230272 + MO_1118 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + CSCC-31-T COSM4517179 c.2923_2924CC>TT p.P975F Substitution - Missense 11:72237167-72237168 + T3021 COSM4692636 c.1459G>T p.G487W Substitution - Missense 11:72231151-72231151 + TCGA-IA-A40U-01 COSM3986437 c.1997G>T p.G666V Substitution - Missense 11:72233120-72233120 + MO_1215 COSM5557883 c.799A>G p.K267E Substitution - Missense 11:72229708-72229708 + sysucc-882T COSM5446956 c.2421A>G p.K807K Substitution - coding silent 11:72235121-72235121 + OSCC-GB_01390111 COSM5954541 c.2319C>T p.C773C Substitution - coding silent 11:72234387-72234387 + TCGA-BS-A0TE-01 COSM931673 c.2019G>A p.W673* Substitution - Nonsense 11:72233142-72233142 + HCC31 COSM1605188 c.2757A>G p.P919P Substitution - coding silent 11:72235864-72235864 + CHC1704T COSM4804079 c.2536G>T p.G846C Substitution - Missense 11:72235328-72235328 + TCGA-EK-A2H0-01 COSM4818931 c.2015C>G p.A672G Substitution - Missense 11:72233138-72233138 + Pat_14_B COSM5318929 c.2140G>A p.V714I Substitution - Missense 11:72233672-72233672 + TCGA-61-1740-01 COSM1322188 c.2355C>G p.A785A Substitution - coding silent 11:72234555-72234555 + PT15_1 COSM5897796 c.1952-6C>T p.? Unknown 11:72233069-72233069 + BD236T COSM2016189 c.3196delC p.S1068fs*63 Deletion - Frameshift 11:72237440-72237440 + TCGA-AG-A02N-01 COSM265407 c.2920_2921insC p.P977fs*7 Insertion - Frameshift 11:72237164-72237165 + YUPAER COSM5373542 c.1149G>A p.K383K Substitution - coding silent 11:72230420-72230420 + YURAY COSM5373544 c.2996C>T p.P999L Substitution - Missense 11:72237240-72237240 + TCGA-BR-6452-01 COSM931678 c.2658C>T p.Y886Y Substitution - coding silent 11:72235450-72235450 + S02277 COSM2016161 c.1945C>T p.R649* Substitution - Nonsense 11:72232968-72232968 + ME016T COSM224988 c.1754T>C p.L585P Substitution - Missense 11:72232667-72232667 + ESCC_45 COSM5630253 c.872C>G p.S291C Substitution - Missense 11:72229952-72229952 + OSCC-GB_01060111 COSM4882771 c.376C>A p.P126T Substitution - Missense 11:72228477-72228477 + CN-AML-CR-35-Dx COSM5428204 c.3673C>A p.L1225M Substitution - Missense 11:72238162-72238162 + CAL33 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + TCGA-GC-A3BM-01 COSM3791903 c.3571G>T p.G1191W Substitution - Missense 11:72238060-72238060 + TCGA-CG-5721-01 COSM4036458 c.1921C>T p.R641W Substitution - Missense 11:72232944-72232944 + HCC53 COSM1605187 c.1390C>A p.H464N Substitution - Missense 11:72231082-72231082 + 2492712 COSM5606636 c.1969T>G p.F657V Substitution - Missense 11:72233092-72233092 + pfg181T COSM4757263 c.3368T>C p.V1123A Substitution - Missense 11:72237612-72237612 + PD11340a COSM5772907 c.3666G>A p.W1222* Substitution - Nonsense 11:72238155-72238155 + YUQUEST COSM5373543 c.2855C>T p.P952L Substitution - Missense 11:72235962-72235962 + I2L-P19Ta-Tumor-Biopsy COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + SCC-25 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + TCGA-FW-A3R5-06 COSM3870148 c.1338C>T p.F446F Substitution - coding silent 11:72231030-72231030 + CSCC-18-T COSM4480360 c.2411C>T p.P804L Substitution - Missense 11:72234611-72234611 + CSCC-27-T COSM4484636 c.2833C>T p.P945S Substitution - Missense 11:72235940-72235940 + S02289 COSM5685923 c.3362G>C p.C1121S Substitution - Missense 11:72237606-72237606 + TCGA-B5-A11Q-01 COSM931675 c.2189delC p.S731fs*27 Deletion - Frameshift 11:72233721-72233721 + CSCC-27-T COSM4507792 c.756C>T p.N252N Substitution - coding silent 11:72229665-72229665 + C086 COSM5532749 c.3256C>T p.R1086C Substitution - Missense 11:72237500-72237500 + 2492711 COSM5606636 c.1969T>G p.F657V Substitution - Missense 11:72233092-72233092 + HN_62755 COSM128243 c.685C>T p.L229L Substitution - coding silent 11:72229490-72229490 + CHEWS009 COSM4574772 c.3271C>T p.P1091S Substitution - Missense 11:72237515-72237515 + TCGA-EE-A2MC-06 COSM3453002 c.3192C>T p.F1064F Substitution - coding silent 11:72237436-72237436 + LS174T COSM2016162 c.1953T>G p.S651R Substitution - Missense 11:72233076-72233076 + D01 COSM5543939 c.317A>G p.N106S Substitution - Missense 11:72228418-72228418 + HCC133T COSM1605189 c.3001C>T p.P1001S Substitution - Missense 11:72237245-72237245 + YUPAER COSM5373545 c.3747C>T p.L1249L Substitution - coding silent 11:72238323-72238323 + CHC1738T COSM4805222 c.754-2A>G p.? Unknown 11:72229661-72229661 + TCGA-G4-6626-01 COSM1356787 c.361C>T p.R121* Substitution - Nonsense 11:72228462-72228462 + CRC-02T COSM5454004 c.3224C>A p.P1075Q Substitution - Missense 11:72237468-72237468 + T3498 COSM4200699 c.2920G>C p.A974P Substitution - Missense 11:72237164-72237164 + TCGA-AP-A0LM-01 COSM931666 c.1344G>A p.S448S Substitution - coding silent 11:72231036-72231036 + pfg164T COSM4757262 c.1511C>T p.S504L Substitution - Missense 11:72231511-72231511 + TCGA-FG-7637-01 COSM3967818 c.1573G>A p.V525I Substitution - Missense 11:72231573-72231573 + LUAD_E00565 COSM388994 c.2397T>C p.S799S Substitution - coding silent 11:72234597-72234597 + SNUH_G16_S1 COSM3998571 c.1368C>T p.D456D Substitution - coding silent 11:72231060-72231060 + TCGA-EI-6507-01 COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + T3149 COSM4692640 c.3529A>G p.I1177V Substitution - Missense 11:72237773-72237773 + CHC1738T COSM4805222 c.754-2A>G p.? Unknown 11:72229661-72229661 + TCGA-B5-A0JY-01 COSM931660 c.491A>C p.E164A Substitution - Missense 11:72228820-72228820 + CHC798T COSM4958316 c.3239G>A p.R1080H Substitution - Missense 11:72237483-72237483 + ACINAR28 COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + TCGA-AC-A23H-01 COSM3810365 c.3556C>A p.P1186T Substitution - Missense 11:72238045-72238045 + TCGA-EE-A2GB-06 COSM3452995 c.2248T>C p.F750L Substitution - Missense 11:72234316-72234316 + TCGA-BT-A3PJ-01 COSM3791904 c.3582C>T p.S1194S Substitution - coding silent 11:72238071-72238071 + ESCC_64 COSM5633444 c.3443G>A p.G1148D Substitution - Missense 11:72237687-72237687 + CLL066 COSM1289632 c.1688C>A p.T563N Substitution - Missense 11:72232312-72232312 + T95 COSM4692635 c.1324G>A p.V442M Substitution - Missense 11:72231016-72231016 + T3091 COSM4692641 c.3545C>T p.A1182V Substitution - Missense 11:72237789-72237789 + TCGA-56-5898-01 COSM690801 c.334G>C p.A112P Substitution - Missense 11:72228435-72228435 + TCGA-CD-8536-01 COSM4036462 c.3232C>T p.R1078W Substitution - Missense 11:72237476-72237476 + TCGA-A5-A0GI-01 COSM931681 c.3004delC p.S1003fs*128 Deletion - Frameshift 11:72237248-72237248 + TCGA-FS-A4FD-06 COSM3452998 c.2557C>T p.L853L Substitution - coding silent 11:72235349-72235349 + CLN2 COSM5024812 c.1700A>G p.E567G Substitution - Missense 11:72232324-72232324 + HCC31T COSM1605188 c.2757A>G p.P919P Substitution - coding silent 11:72235864-72235864 + TCGA-AP-A0LE-01 COSM931684 c.3668A>G p.D1223G Substitution - Missense 11:72238157-72238157 + CSCC-35-T COSM4539479 c.2690G>A p.G897E Substitution - Missense 11:72235705-72235705 + PTC-14C COSM931661 c.608A>C p.H203P Substitution - Missense 11:72229179-72229179 + CSCC-44-T COSM4538886 c.2614G>A p.V872M Substitution - Missense 11:72235406-72235406 + 70 COSM5744377 c.2543C>T p.T848M Substitution - Missense 11:72235335-72235335 + SC_9054 COSM5560209 c.2988G>T p.L996L Substitution - coding silent 11:72237232-72237232 + ESO-S41 COSM1254859 c.476C>T p.P159L Substitution - Missense 11:72228805-72228805 + CHEWS031 COSM4574773 c.3696C>G p.T1232T Substitution - coding silent 11:72238272-72238272 + PD13763a COSM5773486 c.1471G>T p.E491* Substitution - Nonsense 11:72231163-72231163 + TCGA-A8-A07R-01 COSM429801 c.324C>T p.G108G Substitution - coding silent 11:72228425-72228425 + HCC66 COSM1605185 c.646C>T p.R216W Substitution - Missense 11:72229217-72229217 + HCC025T COSM5803656 c.1622A>T p.K541M Substitution - Missense 11:72232246-72232246 + 8057501 COSM3383803 c.3558G>A p.P1186P Substitution - coding silent 11:72238047-72238047 + MO_1337 COSM5567664 c.1343C>A p.S448* Substitution - Nonsense 11:72231035-72231035 + 587376 COSM1210741 c.2934G>T p.K978N Substitution - Missense 11:72237178-72237178 + TCGA-BS-A0UV-01 COSM931657 c.234C>A p.F78L Substitution - Missense 11:72228241-72228241 + SNUH_G22_S1 COSM3998570 c.754-9T>C p.? Unknown 11:72229654-72229654 + ESCC_11 COSM5649633 c.634G>C p.A212P Substitution - Missense 11:72229205-72229205 + TCGA-F1-A448-01 COSM4036459 c.2489G>A p.G830D Substitution - Missense 11:72235189-72235189 + HCT15 COSM2016145 c.1505T>C p.M502T Substitution - Missense 11:72231505-72231505 + SNUH_G16_S1 COSM3998572 c.1893C>A p.L631L Substitution - coding silent 11:72232916-72232916 + TCGA-EM-A1YC-01 COSM3368553 c.1809C>T p.F603F Substitution - coding silent 11:72232722-72232722 + HCC53T COSM1605187 c.1390C>A p.H464N Substitution - Missense 11:72231082-72231082 + TCGA-AD-6964-01 COSM1356792 c.1767G>A p.Q589Q Substitution - coding silent 11:72232680-72232680 + TCGA-06-5858-01 COSM3398118 c.1831C>T p.R611C Substitution - Missense 11:72232744-72232744 + TCGA-FS-A1ZZ-06 COSM3452992 c.1967C>T p.S656F Substitution - Missense 11:72233090-72233090 + cSCCP5 COSM138006 c.619C>T p.L207F Substitution - Missense 11:72229190-72229190 + TCGA-ER-A193-06 COSM3452997 c.2481C>T p.S827S Substitution - coding silent 11:72235181-72235181 + OSCC-GB_00620111 COSM4881222 c.390T>A p.D130E Substitution - Missense 11:72228491-72228491 + T3512 COSM3452987 c.751C>T p.Q251* Substitution - Nonsense 11:72229556-72229556 + TCGA-AP-A051-01 COSM931672 c.1782C>T p.D594D Substitution - coding silent 11:72232695-72232695 + TCGA-A5-A0G9-01 COSM931669 c.1589_1590insG p.K531fs*21 Insertion - Frameshift 11:72231589-72231590 + PT19_1 COSM5899621 c.1300+8C>T p.? Unknown 11:72230906-72230906 + T3064 COSM195549 c.2071C>T p.R691W Substitution - Missense 11:72233471-72233471 + WSU-HN8 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + TCGA-22-1016-01 COSM195548 c.1456C>T p.R486C Substitution - Missense 11:72231148-72231148 + CHC1704T COSM4804079 c.2536G>T p.G846C Substitution - Missense 11:72235328-72235328 + TCGA-C8-A26Y-01 COSM3810362 c.827C>G p.S276* Substitution - Nonsense 11:72229736-72229736 + 98 COSM5016365 c.1284_1285delAG p.I428fs*37 Deletion - Frameshift 11:72230882-72230883 + CP66-MEL COSM13660 c.1133G>A p.G378D Substitution - Missense 11:72230404-72230404 + LUAD-S01404 COSM398684 c.2780C>T p.P927L Substitution - Missense 11:72235887-72235887 + DN14012 COSM5961224 c.1561C>T p.R521C Substitution - Missense 11:72231561-72231561 + T96 COSM4692632 c.950A>T p.D317V Substitution - Missense 11:72230131-72230131 + TCGA-DA-A1I0-06 COSM3452991 c.1492C>T p.R498C Substitution - Missense 11:72231184-72231184 + 40 COSM4966101 c.2741C>A p.S914* Substitution - Nonsense 11:72235848-72235848 + BD57T COSM5510534 c.2720G>A p.R907Q Substitution - Missense 11:72235735-72235735 + LUAD-RT-S01818 COSM383806 c.1720C>T p.Q574* Substitution - Nonsense 11:72232633-72232633 + TCGA-EE-A3AA-06 COSM3452993 c.2139C>T p.I713I Substitution - coding silent 11:72233671-72233671 + TCGA-G2-A2ES-01 COSM1298576 c.1683C>T p.H561H Substitution - coding silent 11:72232307-72232307 + TCGA-HU-A4GT-01 COSM4036464 c.3431C>T p.A1144V Substitution - Missense 11:72237675-72237675 + PD9595a COSM5800110 c.2537G>C p.G846A Substitution - Missense 11:72235329-72235329 + TCGA-HU-A4GU-01 COSM4036454 c.1306G>A p.V436I Substitution - Missense 11:72230998-72230998 + TCGA-GF-A6C9-06 COSM4902293 c.2831C>T p.P944L Substitution - Missense 11:72235938-72235938 + cSCCP8 COSM140665 c.251C>T p.S84L Substitution - Missense 11:72228352-72228352 + S0029 COSM5882128 c.1762C>T p.R588W Substitution - Missense 11:72232675-72232675 + PT48 COSM5932785 c.2239T>C p.Y747H Substitution - Missense 11:72234307-72234307 + T3203 COSM4692638 c.2813C>T p.P938L Substitution - Missense 11:72235920-72235920 + TCGA-EK-A2RJ-01 COSM4831918 c.2204C>T p.S735F Substitution - Missense 11:72233736-72233736 + LS180 COSM2016162 c.1953T>G p.S651R Substitution - Missense 11:72233076-72233076 + TCGA-B1-5398-01 COSM3986438 c.3088C>T p.R1030W Substitution - Missense 11:72237332-72237332 + Pat_41_B COSM5839543 c.3127G>A p.E1043K Substitution - Missense 11:72237371-72237371 + T2932 COSM4692639 c.3484T>C p.Y1162H Substitution - Missense 11:72237728-72237728 + TCGA-IR-A3LK-01 COSM4817414 c.938A>T p.E313V Substitution - Missense 11:72230018-72230018 + TCGA-BR-6452-01 COSM4036457 c.1574T>C p.V525A Substitution - Missense 11:72231574-72231574 + TCGA-FI-A2EW-01 COSM931663 c.641C>A p.S214* Substitution - Nonsense 11:72229212-72229212 + I2L-P5-Tumor-Organoid COSM5360982 c.253C>T p.Q85* Substitution - Nonsense 11:72228354-72228354 + WA52 COSM240238 c.1322_1323insA p.N441fs*25 Insertion - Frameshift 11:72231014-72231015 + pfg212T COSM4613274 c.2921delC p.P976fs*155 Deletion - Frameshift 11:72237165-72237165 + 66 COSM1356796 c.3460delC p.R1156fs*46 Deletion - Frameshift 11:72237704-72237704 + BD174T COSM5521377 c.3466C>T p.R1156W Substitution - Missense 11:72237710-72237710 + TCGA-AP-A0LM-01 COSM931658 c.252G>A p.S84S Substitution - coding silent 11:72228353-72228353 + TCGA-BR-4368-01 COSM4036463 c.3233G>A p.R1078Q Substitution - Missense 11:72237477-72237477 + TCGA-BG-A0LX-01 COSM931665 c.1091-1G>C p.? Unknown 11:72230361-72230361 + 8066067 COSM3383803 c.3558G>A p.P1186P Substitution - coding silent 11:72238047-72238047 + 587376 COSM1210740 c.1040G>A p.R347Q Substitution - Missense 11:72230221-72230221 + TCGA-CG-4306-01 COSM4036451 c.203C>T p.T68M Substitution - Missense 11:72228210-72228210 + PR-09-3687 COSM245038 c.3554C>A p.A1185D Substitution - Missense 11:72238043-72238043 + TCGA-AC-A23C-01 COSM1475876 c.1408G>C p.G470R Substitution - Missense 11:72231100-72231100 + S00827 COSM312002 c.1009G>T p.D337Y Substitution - Missense 11:72230190-72230190 + LIM2405 COSM4613274 c.2921delC p.P976fs*155 Deletion - Frameshift 11:72237165-72237165 + 1N01-VS-1T01 COSM4972357 c.753G>C p.Q251H Substitution - Missense 11:72229558-72229558 + 2492730 COSM5728789 c.518+1G>A p.? Unknown 11:72228848-72228848 + CSB1 COSM5027442 c.3032C>T p.S1011F Substitution - Missense 11:72237276-72237276 + TCGA-F1-6177-01 COSM4036460 c.3039C>T p.T1013T Substitution - coding silent 11:72237283-72237283 + Pat_26_A COSM5839542 c.2771C>T p.A924V Substitution - Missense 11:72235878-72235878 + SC_9058 COSM5559374 c.102G>C p.L34L Substitution - coding silent 11:72225086-72225086 + CSCC-11-T COSM3453000 c.2922C>T p.A974A Substitution - coding silent 11:72237166-72237166 + TCGA-GF-A3OT-06 COSM3453000 c.2922C>T p.A974A Substitution - coding silent 11:72237166-72237166 + TCGA-BS-A0UM-01 COSM931662 c.635C>T p.A212V Substitution - Missense 11:72229206-72229206 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.523875 11q13 600829

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AGA - InFrameDeletion p.E76delE c.228_230delAGA 11 71939276 RCCC AG - Frameshift p.K64Afs*10 c.189_190delGA 11 71939239 CM A G IntronicSNV . c.1497+70A>G 11 71942303 HC A G Missense p.D1223G c.3668A>G 11 71949201 UCEC A G Missense p.E936G c.2807A>G 11 71946958 BRCA A T Missense p.N865I c.2594A>T 11 71946430 CM C A Missense p.T245N c.734C>A 11 71940583 UCEC C A Missense p.T563N c.1688C>A 11 71943356 CLL C A Nonsense p.S214* c.641C>A 11 71940256 UCEC C A Synonymous p.P166P c.498C>A 11 71939871 NSCLC CC TT Missense p.R129W c.384_385delinsTT 11 71939529 CM CC TT Missense p.S929F c.2786_2787delinsTT 11 71946937 CM C - Frameshift p.K515Sfs*16 c.1542delC 11 71942586 GBM C - Frameshift p.P976Hfs*155 c.2927delC 11 71948209 CM - C Frameshift p.P977Tfs*7 c.2927dupC 11 71948209 LUAD C - Frameshift p.R1156Gfs*46 c.3466delC 11 71948748 STAD C - Frameshift p.S1003Rfs*128 c.3006delC 11 71948292 UCEC C - Frameshift p.S731Pfs*27 c.2190delC 11 71944765 UCEC C G Missense p.A196G c.587C>G 11 71940202 CM C G Missense p.H518Q c.1554C>G 11 71942598 CM C G Missense p.I1208M c.3624C>G 11 71949157 BLCA C G Missense p.P1054A c.3160C>G 11 71948448 RCCC C G Synonymous p.L841L c.2523C>G 11 71946359 BLCA C T IntronicSNV . c.1713-124C>T 11 71943546 CM C T IntronicSNV . c.1713-79C>T 11 71943591 CM C T Missense p.A212V c.635C>T 11 71940250 UCEC C T Missense p.P1154L c.3461C>T 11 71948749 CM C T Missense p.P140S c.418C>T 11 71939791 CM C T Missense p.P143L c.428C>T 11 71939801 STAD C T Missense p.P159L c.476C>T 11 71939849 ESCA C T Missense p.P720L c.2159C>T 11 71944735 CM C T Missense p.P875L c.2624C>T 11 71946460 ESCA C T Missense p.P976S c.2926C>T 11 71948214 CM C T Missense p.R479C c.1435C>T 11 71942171 NB C T Missense p.R486C c.1456C>T 11 71942192 LUSC C T Missense p.R498C c.1492C>T 11 71942228 CM C T Missense p.R571W c.1711C>T 11 71943379 UCEC C T Missense p.R691W c.2071C>T 11 71944515 COREAD C T Missense p.R801C c.2401C>T 11 71945645 UCEC C T Missense p.S1011F c.3032C>T 11 71948320 BRCA C T Missense p.S656F c.1967C>T 11 71944134 CM C T Missense p.T1013I c.3038C>T 11 71948326 CM C T Missense p.T493M c.1478C>T 11 71942214 HNSC C T Missense p.T68M c.203C>T 11 71939254 STAD C T Nonsense p.Q251* c.751C>T 11 71940600 CM C T Nonsense p.Q93* c.277C>T 11 71939422 BRCA C T Synonymous p.A1085A c.3255C>T 11 71948543 CM C T Synonymous p.A1136A c.3408C>T 11 71948696 CM C T Synonymous p.F1064F c.3192C>T 11 71948480 CM C T Synonymous p.F404F c.1212C>T 11 71941854 CM C T Synonymous p.F427F c.1281C>T 11 71941923 CM C T Synonymous p.F603F c.1809C>T 11 71943766 THCA C T Synonymous p.G108G c.324C>T 11 71939469 BRCA C T Synonymous p.G477G c.1431C>T 11 71942167 COREAD C T Synonymous p.H561H c.1683C>T 11 71943351 BLCA C T Synonymous p.I713I c.2139C>T 11 71944715 CM C T Synonymous p.L229L c.685C>T 11 71940534 HNSC C T Synonymous p.L585L c.1753C>T 11 71943710 LUAD C T Synonymous p.L590L c.1770C>T 11 71943727 BRCA C T Synonymous p.L853L c.2557C>T 11 71946393 CM C T Synonymous p.S1194S c.3582C>T 11 71949115 BLCA C T Synonymous p.S761S c.2283C>T 11 71945395 CM C T Synonymous p.S827S c.2481C>T 11 71946225 CM C T Synonymous p.T1013T c.3039C>T 11 71948327 STAD C T Synonymous p.V825V c.2475C>T 11 71946219 LUAD C T Synonymous p.Y497Y c.1491C>T 11 71942227 CM C T Synonymous p.Y770Y c.2310C>T 11 71945422 CM C T Synonymous p.Y886Y c.2658C>T 11 71946494 UCEC G - 3-UTRDeletion . c.3774+217delC 11 71949611 HC G A IntronicSNV . c.2123-55G>A 11 71944644 CM G A IntronicSNV . c.3686+10G>A 11 71949229 CM G A Missense p.A1193T c.3577G>A 11 71949110 UCEC G A Missense p.E457K c.1369G>A 11 71942105 CM G A Missense p.G1191R c.3571G>A 11 71949104 ESCA G A Missense p.G340D c.1019G>A 11 71941244 BRCA G A Missense p.R1078Q c.3233G>A 11 71948521 STAD G A Missense p.R342Q c.1025G>A 11 71941250 OV G A Missense p.R401Q c.1202G>A 11 71941844 ESCA G A Missense p.R691Q c.2072G>A 11 71944516 UCEC G A Missense p.R70H c.209G>A 11 71939260 STAD G A Missense p.R90H c.269G>A 11 71939414 STAD G A Missense p.V525I c.1573G>A 11 71942617 LGG G A Missense p.V546I c.1636G>A 11 71943304 BRCA G A Missense p.V874M c.2620G>A 11 71946456 LUAD G A Nonsense p.W481* c.1443G>A 11 71942179 HNSC G A Nonsense p.W673* c.2019G>A 11 71944186 UCEC G A SpliceDonorSNV . c.518+1G>A 11 71939892 HNSC G A Synonymous p.G470G c.1410G>A 11 71942146 CM G A Synonymous p.P993P c.2979G>A 11 71948267 UCEC G A Synonymous p.Q85Q c.255G>A 11 71939400 HNSC G C Missense p.A112P c.334G>C 11 71939479 LUSC G C Missense p.G1111R c.3331G>C 11 71948619 CM G C Missense p.G470R c.1408G>C 11 71942144 BRCA G C SpliceAcceptorSNV . c.1091-1G>C 11 71941405 UCEC G C Synonymous p.R1174R c.3522G>C 11 71948810 LUAD - G Frameshift p.K531Efs*21 c.1590dupG 11 71942634 UCEC G - Frameshift p.W888*fs*1 c.2664delG 11 71946722 LUSC G T Missense p.A212S c.634G>T 11 71940249 LUAD G T Missense p.D337Y c.1009G>T 11 71941234 SCLC G T Missense p.W1204C c.3612G>T 11 71949145 LUAD T C Missense p.F750L c.2248T>C 11 71945360 CM T C Missense p.L585P c.1754T>C 11 71943711 CM T C Missense p.V727A c.2180T>C 11 71944756 CM T C Missense p.W1222R c.3664T>C 11 71949197 CM T C SpliceDonorSNV . c.1497+2T>C 11 71942235 STAD T G IntronicSNV . c.519-52T>G 11 71940082 CM