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 6470362 6470362 + Missense_Mutation SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr11:6470362C>T c.2131G>A c.(2131-2133)Gaa>Aaa p.E711K BLCA 11 6472571 6472571 + Missense_Mutation SNP T T C TCGA-XF-AAMF-01A-21D-A42E-08 TCGA-XF-AAMF-10A-01D-A42H-08 g.chr11:6472571T>C c.1631A>G c.(1630-1632)aAt>aGt p.N544S BLCA 11 6478982 6478982 + Missense_Mutation SNP A A T TCGA-XF-A9SZ-01A-11D-A391-08 TCGA-XF-A9SZ-10A-01D-A394-08 g.chr11:6478982A>T c.459T>A c.(457-459)gaT>gaA p.D153E BRCA 11 6477399 6477399 + Missense_Mutation SNP C C T TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr11:6477399C>T c.1436G>A c.(1435-1437)cGt>cAt p.R479H BRCA 11 6477399 6477399 + Missense_Mutation SNP C C T TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr11:6477399C>T c.1436G>A c.(1435-1437)cGt>cAt p.R479H BRCA 11 6477810 6477810 + Missense_Mutation SNP C C A TCGA-OK-A5Q2-01A-11D-A27P-09 TCGA-OK-A5Q2-10A-01D-A27P-09 g.chr11:6477810C>A c.1146G>T c.(1144-1146)aaG>aaT p.K382N BRCA 11 6479439 6479439 + Silent SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:6479439G>T c.219C>A c.(217-219)gtC>gtA p.V73V COAD 11 6470286 6470286 + Missense_Mutation SNP C C T TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr11:6470286C>T c.2207G>A c.(2206-2208)tGc>tAc p.C736Y COAD 11 6470394 6470394 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:6470394C>T c.2099G>A c.(2098-2100)gGc>gAc p.G700D COAD 11 6472626 6472626 + Nonsense_Mutation SNP G G A TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr11:6472626G>A c.1576C>T c.(1576-1578)Cga>Tga p.R526* COAD 11 6477355 6477355 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:6477355C>T c.1480G>A c.(1480-1482)Gca>Aca p.A494T COAD 11 6477788 6477788 + Missense_Mutation SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr11:6477788A>G c.1168T>C c.(1168-1170)Tac>Cac p.Y390H COAD 11 6477845 6477845 + Missense_Mutation SNP C C T TCGA-CM-6172-01A-11D-1650-10 TCGA-CM-6172-10A-01D-1650-10 g.chr11:6477845C>T c.1111G>A c.(1111-1113)Ggc>Agc p.G371S COAD 11 6477934 6477934 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:6477934G>A c.1022C>T c.(1021-1023)gCc>gTc p.A341V COAD 11 6478040 6478040 + Missense_Mutation SNP G G A TCGA-AA-3955-01A-02W-0995-10 TCGA-AA-3955-10A-01W-0995-10 g.chr11:6478040G>A c.916C>T c.(916-918)Cgg>Tgg p.R306W COAD 11 6478103 6478103 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:6478103C>T c.853G>A c.(853-855)Gcc>Acc p.A285T COAD 11 6478232 6478232 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:6478232G>A c.724C>T c.(724-726)Cgc>Tgc p.R242C COAD 11 6479367 6479367 + Silent SNP G G A TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr11:6479367G>A c.291C>T c.(289-291)caC>caT p.H97H COAD 11 6479469 6479469 + Silent SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:6479469C>T c.189G>A c.(187-189)cgG>cgA p.R63R COAD 11 6479490 6479490 + Silent SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr11:6479490C>T c.168G>A c.(166-168)acG>acA p.T56T COADREAD 11 6470286 6470286 + Missense_Mutation SNP C C T TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr11:6470286C>T c.2207G>A c.(2206-2208)tGc>tAc p.C736Y COADREAD 11 6470394 6470394 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:6470394C>T c.2099G>A c.(2098-2100)gGc>gAc p.G700D COADREAD 11 6470405 6470405 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:6470405G>T c.2088C>A c.(2086-2088)ttC>ttA p.F696L COADREAD 11 6472626 6472626 + Nonsense_Mutation SNP G G A TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr11:6472626G>A c.1576C>T c.(1576-1578)Cga>Tga p.R526* COADREAD 11 6477355 6477355 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:6477355C>T c.1480G>A c.(1480-1482)Gca>Aca p.A494T COADREAD 11 6477620 6477620 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:6477620G>A c.1336C>T c.(1336-1338)Cgc>Tgc p.R446C COADREAD 11 6477788 6477788 + Missense_Mutation SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr11:6477788A>G c.1168T>C c.(1168-1170)Tac>Cac p.Y390H COADREAD 11 6477845 6477845 + Missense_Mutation SNP C C T TCGA-CM-6172-01A-11D-1650-10 TCGA-CM-6172-10A-01D-1650-10 g.chr11:6477845C>T c.1111G>A c.(1111-1113)Ggc>Agc p.G371S COADREAD 11 6477934 6477934 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:6477934G>A c.1022C>T c.(1021-1023)gCc>gTc p.A341V COADREAD 11 6478040 6478040 + Missense_Mutation SNP G G A TCGA-AA-3955-01A-02W-0995-10 TCGA-AA-3955-10A-01W-0995-10 g.chr11:6478040G>A c.916C>T c.(916-918)Cgg>Tgg p.R306W COADREAD 11 6478103 6478103 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:6478103C>T c.853G>A c.(853-855)Gcc>Acc p.A285T COADREAD 11 6478232 6478232 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:6478232G>A c.724C>T c.(724-726)Cgc>Tgc p.R242C COADREAD 11 6479367 6479367 + Silent SNP G G A TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr11:6479367G>A c.291C>T c.(289-291)caC>caT p.H97H COADREAD 11 6479469 6479469 + Silent SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:6479469C>T c.189G>A c.(187-189)cgG>cgA p.R63R COADREAD 11 6479490 6479490 + Silent SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr11:6479490C>T c.168G>A c.(166-168)acG>acA p.T56T DLBC 11 6486914 6486914 + Silent SNP C C T TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr11:6486914C>T c.12G>A c.(10-12)agG>agA p.R4R ESCA 11 6477889 6477889 + Missense_Mutation SNP C C G TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chr11:6477889C>G c.1067G>C c.(1066-1068)cGc>cCc p.R356P ESCA 11 6478032 6478032 + Silent SNP C C T TCGA-Q9-A6FW-01A-31D-A31U-09 TCGA-Q9-A6FW-10A-01D-A31U-09 g.chr11:6478032C>T c.924G>A c.(922-924)tcG>tcA p.S308S ESCA 11 6478090 6478090 + Missense_Mutation SNP C C T TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chr11:6478090C>T c.866G>A c.(865-867)cGg>cAg p.R289Q ESCA 11 6478611 6478611 + Missense_Mutation SNP G G A TCGA-2H-A9GF-01A-11D-A37C-09 TCGA-2H-A9GF-11A-11D-A37F-09 g.chr11:6478611G>A c.611C>T c.(610-612)gCg>gTg p.A204V GBM 11 6470286 6470286 + Missense_Mutation SNP C C T TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr11:6470286C>T c.2207G>A c.(2206-2208)tGc>tAc p.C736Y GBM 11 6470405 6470405 + Missense_Mutation SNP G G C TCGA-15-0742-01A-01W-0348-08 TCGA-15-0742-10A-01W-0348-08 g.chr11:6470405G>C c.2088C>G c.(2086-2088)ttC>ttG p.F696L GBMLGG 11 6470286 6470286 + Missense_Mutation SNP C C T TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr11:6470286C>T c.2207G>A c.(2206-2208)tGc>tAc p.C736Y GBMLGG 11 6470405 6470405 + Missense_Mutation SNP G G C TCGA-15-0742-01A-01W-0348-08 TCGA-15-0742-10A-01W-0348-08 g.chr11:6470405G>C c.2088C>G c.(2086-2088)ttC>ttG p.F696L GBMLGG 11 6470639 6470639 + Missense_Mutation SNP C C G TCGA-S9-A7R4-01A-12D-A34J-08 TCGA-S9-A7R4-10A-01D-A34M-08 g.chr11:6470639C>G c.1979G>C c.(1978-1980)gGc>gCc p.G660A GBMLGG 11 6477399 6477399 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:6477399C>T c.1436G>A c.(1435-1437)cGt>cAt p.R479H GBMLGG 11 6478090 6478090 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:6478090C>T c.866G>A c.(865-867)cGg>cAg p.R289Q GBMLGG 11 6486802 6486804 + In_Frame_Del DEL AGA AGA - TCGA-QH-A6X3-01A-21D-A32B-08 TCGA-QH-A6X3-10B-01D-A329-08 g.chr11:6486802_6486804delAGA c.122_124delTCT c.(121-126)ttctgt>tgt p.F41del HNSC 11 6472240 6472240 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr11:6472240G>A c.1752C>T c.(1750-1752)gaC>gaT p.D584D HNSC 11 6472280 6472280 + Missense_Mutation SNP C C T TCGA-IQ-A61H-01A-11D-A30E-08 TCGA-IQ-A61H-10A-01D-A30H-08 g.chr11:6472280C>T c.1712G>A c.(1711-1713)gGa>gAa p.G571E HNSC 11 6477356 6477356 + Silent SNP G G A TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr11:6477356G>A c.1479C>T c.(1477-1479)tcC>tcT p.S493S HNSC 11 6477633 6477633 + Silent SNP G G A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr11:6477633G>A c.1323C>T c.(1321-1323)ccC>ccT p.P441P HNSC 11 6477752 6477752 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr11:6477752C>T c.1204G>A c.(1204-1206)Gtg>Atg p.V402M HNSC 11 6477901 6477901 + Missense_Mutation SNP C C G TCGA-CV-7242-01A-11D-2012-08 TCGA-CV-7242-10A-01D-2013-08 g.chr11:6477901C>G c.1055G>C c.(1054-1056)gGg>gCg p.G352A HNSC 11 6478168 6478168 + Nonsense_Mutation SNP G G T TCGA-CV-A6JN-01A-11D-A31L-08 TCGA-CV-A6JN-10A-01D-A31J-08 g.chr11:6478168G>T c.788C>A c.(787-789)tCg>tAg p.S263* KICH 11 6477762 6477762 + Silent SNP C C A TCGA-KL-8336-01A-11D-2310-10 TCGA-KL-8336-11A-01D-2310-10 g.chr11:6477762C>A c.1194G>T c.(1192-1194)ctG>ctT p.L398L KIPAN 11 6470304 6470304 + Missense_Mutation SNP G G T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr11:6470304G>T c.2189C>A c.(2188-2190)gCt>gAt p.A730D KIPAN 11 6477381 6477381 + Missense_Mutation SNP T T C TCGA-CJ-4878-01A-01D-1373-10 TCGA-CJ-4878-11A-01D-1373-10 g.chr11:6477381T>C c.1454A>G c.(1453-1455)gAa>gGa p.E485G KIPAN 11 6477762 6477762 + Silent SNP C C A TCGA-KL-8336-01A-11D-2310-10 TCGA-KL-8336-11A-01D-2310-10 g.chr11:6477762C>A c.1194G>T c.(1192-1194)ctG>ctT p.L398L KIRC 11 6477381 6477381 + Missense_Mutation SNP T T C TCGA-CJ-4878-01A-01D-1373-10 TCGA-CJ-4878-11A-01D-1373-10 g.chr11:6477381T>C c.1454A>G c.(1453-1455)gAa>gGa p.E485G KIRP 11 6470304 6470304 + Missense_Mutation SNP G G T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr11:6470304G>T c.2189C>A c.(2188-2190)gCt>gAt p.A730D LGG 11 6470639 6470639 + Missense_Mutation SNP C C G TCGA-S9-A7R4-01A-12D-A34J-08 TCGA-S9-A7R4-10A-01D-A34M-08 g.chr11:6470639C>G c.1979G>C c.(1978-1980)gGc>gCc p.G660A LGG 11 6477399 6477399 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:6477399C>T c.1436G>A c.(1435-1437)cGt>cAt p.R479H LGG 11 6478090 6478090 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:6478090C>T c.866G>A c.(865-867)cGg>cAg p.R289Q LGG 11 6486802 6486804 + In_Frame_Del DEL AGA AGA - TCGA-QH-A6X3-01A-21D-A32B-08 TCGA-QH-A6X3-10B-01D-A329-08 g.chr11:6486802_6486804delAGA c.122_124delTCT c.(121-126)ttctgt>tgt p.F41del LIHC 11 6471835 6471835 + Silent SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr11:6471835A>G c.1887T>C c.(1885-1887)gcT>gcC p.A629A LIHC 11 6472208 6472208 + Missense_Mutation SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr11:6472208T>C c.1784A>G c.(1783-1785)aAg>aGg p.K595R LIHC 11 6472512 6472512 + Missense_Mutation SNP C C T TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr11:6472512C>T c.1690G>A c.(1690-1692)Ggc>Agc p.G564S LIHC 11 6477958 6477958 + Missense_Mutation SNP C C A TCGA-BC-A10Z-01A-11D-A12Z-10 TCGA-BC-A10Z-11A-11D-A12Z-10 g.chr11:6477958C>A c.998G>T c.(997-999)cGc>cTc p.R333L LUAD 11 6472123 6472123 + Splice_Site SNP T T A TCGA-17-Z020-01A-01W-0746-08 TCGA-17-Z020-11A-01W-0746-08 g.chr11:6472123T>A c.1869A>T c.(1867-1869)gcA>gcT p.A623A LUAD 11 6472177 6472178 + Frame_Shift_Ins INS - - T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:6472177_6472178insT c.1814_1815insA c.(1813-1815)aatfs p.N605fs LUAD 11 6472225 6472225 + Missense_Mutation SNP G G C TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr11:6472225G>C c.1767C>G c.(1765-1767)atC>atG p.I589M LUAD 11 6472274 6472274 + Missense_Mutation SNP C C T TCGA-NJ-A55O-01A-11D-A25L-08 TCGA-NJ-A55O-10A-01D-A25L-08 g.chr11:6472274C>T c.1718G>A c.(1717-1719)gGc>gAc p.G573D LUAD 11 6472661 6472661 + Missense_Mutation SNP G G C TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr11:6472661G>C c.1541C>G c.(1540-1542)tCc>tGc p.S514C LUAD 11 6477334 6477334 + Missense_Mutation SNP C C T TCGA-17-Z037-01A-01W-0746-08 TCGA-17-Z037-11A-01W-0746-08 g.chr11:6477334C>T c.1501G>A c.(1501-1503)Gtg>Atg p.V501M LUAD 11 6477605 6477605 + Missense_Mutation SNP G G T TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr11:6477605G>T c.1351C>A c.(1351-1353)Cgt>Agt p.R451S LUAD 11 6477672 6477672 + Silent SNP C C T TCGA-MP-A5C7-01A-11D-A25L-08 TCGA-MP-A5C7-10A-01D-A25L-08 g.chr11:6477672C>T c.1284G>A c.(1282-1284)ccG>ccA p.P428P LUAD 11 6477718 6477718 + Missense_Mutation SNP G G C TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr11:6477718G>C c.1238C>G c.(1237-1239)cCc>cGc p.P413R LUAD 11 6477727 6477727 + Missense_Mutation SNP C C A TCGA-64-5774-01A-01D-1625-08 TCGA-64-5774-10A-01D-1625-08 g.chr11:6477727C>A c.1229G>T c.(1228-1230)cGc>cTc p.R410L LUAD 11 6478032 6478032 + Silent SNP C C T TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr11:6478032C>T c.924G>A c.(922-924)tcG>tcA p.S308S LUAD 11 6478596 6478596 + Missense_Mutation SNP T T A TCGA-67-4679-01B-01D-1753-08 TCGA-67-4679-10A-01D-1753-08 g.chr11:6478596T>A c.626A>T c.(625-627)gAg>gTg p.E209V LUAD 11 6478612 6478612 + Missense_Mutation SNP C C A TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr11:6478612C>A c.610G>T c.(610-612)Gcg>Tcg p.A204S LUAD 11 6478952 6478952 + Missense_Mutation SNP C C A TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chr11:6478952C>A c.489G>T c.(487-489)caG>caT p.Q163H LUAD 11 6479305 6479305 + Missense_Mutation SNP T T C TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr11:6479305T>C c.353A>G c.(352-354)cAt>cGt p.H118R LUSC 11 6471848 6471848 + Missense_Mutation SNP G G A TCGA-18-3415-01A-01D-0983-08 TCGA-18-3415-11A-01D-0983-08 g.chr11:6471848G>A c.1874C>T c.(1873-1875)cCc>cTc p.P625L LUSC 11 6477540 6477540 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr11:6477540G>A c.1416C>T c.(1414-1416)ctC>ctT p.L472L LUSC 11 6479499 6479499 + Missense_Mutation SNP C C G TCGA-66-2758-01A-02D-1522-08 TCGA-66-2758-11A-01D-1522-08 g.chr11:6479499C>G c.159G>C c.(157-159)caG>caC p.Q53H OV 11 6478209 6478209 + Silent SNP G G A TCGA-24-2262-01A-01W-0799-08 TCGA-24-2262-11A-01W-0799-08 g.chr11:6478209G>A c.747C>T c.(745-747)ggC>ggT p.G249G PAAD 11 6472245 6472245 + Missense_Mutation SNP C C T TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr11:6472245C>T c.1747G>A c.(1747-1749)Gta>Ata p.V583I PAAD 11 6472627 6472627 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:6472627G>A c.1575C>T c.(1573-1575)gtC>gtT p.V525V PAAD 11 6477406 6477406 + Splice_Site SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:6477406C>T c.e7-1 PAAD 11 6477726 6477726 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:6477726G>A c.1230C>T c.(1228-1230)cgC>cgT p.R410R PAAD 11 6478037 6478037 + Nonsense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:6478037G>A c.919C>T c.(919-921)Cga>Tga p.R307* PAAD 11 6478645 6478645 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:6478645G>A c.577C>T c.(577-579)Cgc>Tgc p.R193C PAAD 11 6479076 6479076 + Splice_Site SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:6479076G>A c.365C>T c.(364-366)aCg>aTg p.T122M PAAD 11 6479370 6479370 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:6479370G>A c.288C>T c.(286-288)gcC>gcT p.A96A PCPG 11 6478231 6478231 + Missense_Mutation SNP C C T TCGA-S7-A7X1-01A-11D-A35I-08 TCGA-S7-A7X1-10A-01D-A35G-08 g.chr11:6478231C>T c.725G>A c.(724-726)cGc>cAc p.R242H PRAD 11 6478687 6478687 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:6478687C>T c.535G>A c.(535-537)Gca>Aca p.A179T PRAD 11 6479027 6479027 + Silent SNP G G A TCGA-M7-A725-01A-12D-A32B-08 TCGA-M7-A725-10A-01D-A329-08 g.chr11:6479027G>A c.414C>T c.(412-414)tgC>tgT p.C138C READ 11 6470405 6470405 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:6470405G>T c.2088C>A c.(2086-2088)ttC>ttA p.F696L READ 11 6477620 6477620 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:6477620G>A c.1336C>T c.(1336-1338)Cgc>Tgc p.R446C SARC 11 6478144 6478144 + Missense_Mutation SNP C C A TCGA-3B-A9HT-01A-11D-A38Z-09 TCGA-3B-A9HT-10A-01D-A38Z-09 g.chr11:6478144C>A c.812G>T c.(811-813)cGc>cTc p.R271L SKCM 11 6470603 6470603 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr11:6470603G>A c.2015C>T c.(2014-2016)cCc>cTc p.P672L SKCM 11 6472141 6472141 + Silent SNP G G A TCGA-D9-A6EA-06A-11D-A30X-08 TCGA-D9-A6EA-10A-01D-A30X-08 g.chr11:6472141G>A c.1851C>T c.(1849-1851)gcC>gcT p.A617A SKCM 11 6472626 6472626 + Nonsense_Mutation SNP G G A TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr11:6472626G>A c.1576C>T c.(1576-1578)Cga>Tga p.R526* SKCM 11 6472639 6472639 + Silent SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr11:6472639G>A c.1563C>T c.(1561-1563)ttC>ttT p.F521F SKCM 11 6477301 6477301 + Splice_Site SNP C C T TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr11:6477301C>T c.e7+1 SKCM 11 6477304 6477304 + Nonsense_Mutation SNP G G A TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr11:6477304G>A c.1531C>T c.(1531-1533)Cag>Tag p.Q511* SKCM 11 6477534 6477534 + Silent SNP G G A TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr11:6477534G>A c.1422C>T c.(1420-1422)ttC>ttT p.F474F SKCM 11 6477540 6477540 + Silent SNP G G A TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr11:6477540G>A c.1416C>T c.(1414-1416)ctC>ctT p.L472L SKCM 11 6477646 6477646 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:6477646G>A c.1310C>T c.(1309-1311)tCc>tTc p.S437F SKCM 11 6477676 6477676 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:6477676G>A c.1280C>T c.(1279-1281)tCc>tTc p.S427F SKCM 11 6477836 6477836 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:6477836G>A c.1120C>T c.(1120-1122)Ctt>Ttt p.L374F SKCM 11 6477849 6477849 + Silent SNP C C T TCGA-FS-A1YW-06A-11D-A197-08 TCGA-FS-A1YW-10A-01D-A199-08 g.chr11:6477849C>T c.1107G>A c.(1105-1107)ccG>ccA p.P369P SKCM 11 6477915 6477915 + Silent SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr11:6477915G>A c.1041C>T c.(1039-1041)acC>acT p.T347T SKCM 11 6478024 6478024 + Missense_Mutation SNP T T C TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chr11:6478024T>C c.932A>G c.(931-933)aAt>aGt p.N311S SKCM 11 6478607 6478607 + Silent SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr11:6478607G>A c.615C>T c.(613-615)ttC>ttT p.F205F SKCM 11 6479042 6479042 + Silent SNP G G A TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr11:6479042G>A c.399C>T c.(397-399)gcC>gcT p.A133A

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 6470362 6470362 single base substitution C T downstream_gene_variant BLCA-US 11 6470362 6470362 single base substitution C T exon_variant BLCA-US 11 6470362 6470362 single base substitution C T missense_variant E592K 1774G>A BLCA-US 11 6470362 6470362 single base substitution C T missense_variant E633K 1897G>A BLCA-US 11 6470362 6470362 single base substitution C T missense_variant E711K 2131G>A BRCA-EU 11 6466189 6466189 single base substitution A G downstream_gene_variant BRCA-EU 11 6467766 6467766 single base substitution C G downstream_gene_variant BRCA-EU 11 6467846 6467846 single base substitution A G downstream_gene_variant BRCA-EU 11 6469576 6469576 single base substitution C T downstream_gene_variant BRCA-EU 11 6469988 6469988 single base substitution A T 3_prime_UTR_variant BRCA-EU 11 6469988 6469988 single base substitution A T downstream_gene_variant BRCA-EU 11 6469988 6469988 single base substitution A T exon_variant BRCA-EU 11 6472242 6472242 single base substitution C T downstream_gene_variant BRCA-EU 11 6472242 6472242 single base substitution C T exon_variant BRCA-EU 11 6472242 6472242 single base substitution C T missense_variant D465N 1393G>A BRCA-EU 11 6472242 6472242 single base substitution C T missense_variant D506N 1516G>A BRCA-EU 11 6472242 6472242 single base substitution C T missense_variant D584N 1750G>A BRCA-EU 11 6472242 6472242 single base substitution C T upstream_gene_variant BRCA-EU 11 6473371 6473371 single base substitution G C downstream_gene_variant BRCA-EU 11 6473371 6473371 single base substitution G C exon_variant BRCA-EU 11 6473371 6473371 single base substitution G C intron_variant BRCA-EU 11 6473371 6473371 single base substitution G C upstream_gene_variant BRCA-EU 11 6474219 6474219 single base substitution C T downstream_gene_variant BRCA-EU 11 6474219 6474219 single base substitution C T exon_variant BRCA-EU 11 6474219 6474219 single base substitution C T intron_variant BRCA-EU 11 6474219 6474219 single base substitution C T upstream_gene_variant BRCA-EU 11 6474604 6474604 single base substitution T A downstream_gene_variant BRCA-EU 11 6474604 6474604 single base substitution T A intron_variant BRCA-EU 11 6474604 6474604 single base substitution T A upstream_gene_variant BRCA-EU 11 6474935 6474935 single base substitution A G downstream_gene_variant BRCA-EU 11 6474935 6474935 single base substitution A G intron_variant BRCA-EU 11 6474935 6474935 single base substitution A G upstream_gene_variant BRCA-EU 11 6477402 6477402 single base substitution C G downstream_gene_variant BRCA-EU 11 6477402 6477402 single base substitution C G exon_variant BRCA-EU 11 6477402 6477402 single base substitution C G missense_variant S359T 1076G>C BRCA-EU 11 6477402 6477402 single base substitution C G missense_variant S400T 1199G>C BRCA-EU 11 6477402 6477402 single base substitution C G missense_variant S478T 1433G>C BRCA-EU 11 6477402 6477402 single base substitution C G upstream_gene_variant BRCA-EU 11 6480038 6480038 single base substitution C G intron_variant BRCA-EU 11 6480038 6480038 single base substitution C G upstream_gene_variant BRCA-EU 11 6480201 6480201 single base substitution G A intron_variant BRCA-EU 11 6480201 6480201 single base substitution G A upstream_gene_variant BRCA-EU 11 6480328 6480328 single base substitution T G intron_variant BRCA-EU 11 6480328 6480328 single base substitution T G upstream_gene_variant BRCA-EU 11 6480445 6480445 single base substitution T C intron_variant BRCA-EU 11 6480445 6480445 single base substitution T C upstream_gene_variant BRCA-EU 11 6481232 6481232 single base substitution G A intron_variant BRCA-EU 11 6481232 6481232 single base substitution G A upstream_gene_variant BRCA-EU 11 6482160 6482160 single base substitution G A intron_variant BRCA-EU 11 6482160 6482160 single base substitution G A upstream_gene_variant BRCA-EU 11 6483336 6483336 single base substitution C G intron_variant BRCA-EU 11 6483336 6483336 single base substitution C G upstream_gene_variant BRCA-EU 11 6484785 6484785 single base substitution T C intron_variant BRCA-EU 11 6485759 6485759 single base substitution G T intron_variant BRCA-EU 11 6486111 6486111 single base substitution G A intron_variant BRCA-EU 11 6488330 6488330 single base substitution G C intron_variant BRCA-EU 11 6488693 6488693 single base substitution C T intron_variant BRCA-EU 11 6488776 6488776 single base substitution G C intron_variant BRCA-EU 11 6491981 6491981 single base substitution G C intron_variant BRCA-EU 11 6493046 6493051 deletion of <=200bp ATTGAT - intron_variant BRCA-EU 11 6493261 6493261 single base substitution C T intron_variant BRCA-EU 11 6493356 6493372 deletion of <=200bp AGGTTTAAAAAGTTAGG - intron_variant BRCA-EU 11 6493408 6493408 single base substitution C G intron_variant BRCA-EU 11 6493482 6493482 deletion of <=200bp T - intron_variant BRCA-EU 11 6493795 6493795 insertion of <=200bp - T intron_variant BRCA-EU 11 6494448 6494448 single base substitution C G 5_prime_UTR_variant BRCA-EU 11 6494448 6494448 single base substitution C G intron_variant BRCA-EU 11 6495311 6495311 deletion of <=200bp C - intron_variant BRCA-EU 11 6495311 6495311 deletion of <=200bp C - upstream_gene_variant BRCA-EU 11 6496119 6496119 single base substitution G A upstream_gene_variant BRCA-EU 11 6497914 6497914 single base substitution G A upstream_gene_variant BRCA-EU 11 6497930 6497930 single base substitution G C upstream_gene_variant BRCA-EU 11 6498108 6498108 single base substitution A G upstream_gene_variant BRCA-EU 11 6498382 6498382 single base substitution A C upstream_gene_variant BRCA-FR 11 6484785 6484785 single base substitution T C intron_variant BRCA-FR 11 6485245 6485245 single base substitution C G intron_variant BRCA-FR 11 6485759 6485759 single base substitution G T intron_variant BRCA-FR 11 6488861 6488861 single base substitution G A intron_variant BRCA-FR 11 6494448 6494448 single base substitution C G 5_prime_UTR_variant BRCA-FR 11 6494448 6494448 single base substitution C G intron_variant BRCA-UK 11 6469827 6469827 single base substitution G C downstream_gene_variant BRCA-UK 11 6470647 6470647 single base substitution G C downstream_gene_variant BRCA-UK 11 6470647 6470647 single base substitution G C exon_variant BRCA-UK 11 6470647 6470647 single base substitution G C missense_variant F538L 1614C>G BRCA-UK 11 6470647 6470647 single base substitution G C missense_variant F579L 1737C>G BRCA-UK 11 6470647 6470647 single base substitution G C missense_variant F657L 1971C>G BRCA-UK 11 6495350 6495350 single base substitution C G 5_prime_UTR_variant BRCA-UK 11 6495350 6495350 single base substitution C G upstream_gene_variant BRCA-UK 11 6495473 6495473 single base substitution G C 5_prime_UTR_variant BRCA-UK 11 6495473 6495473 single base substitution G C upstream_gene_variant BRCA-UK 11 6497526 6497526 single base substitution T G upstream_gene_variant BRCA-US 11 6477399 6477399 single base substitution C T downstream_gene_variant BRCA-US 11 6477399 6477399 single base substitution C T exon_variant BRCA-US 11 6477399 6477399 single base substitution C T missense_variant R360H 1079G>A BRCA-US 11 6477399 6477399 single base substitution C T missense_variant R401H 1202G>A BRCA-US 11 6477399 6477399 single base substitution C T missense_variant R479H 1436G>A BRCA-US 11 6477399 6477399 single base substitution C T upstream_gene_variant BRCA-US 11 6477810 6477810 single base substitution C A downstream_gene_variant BRCA-US 11 6477810 6477810 single base substitution C A exon_variant BRCA-US 11 6477810 6477810 single base substitution C A missense_variant K263N 789G>T BRCA-US 11 6477810 6477810 single base substitution C A missense_variant K304N 912G>T BRCA-US 11 6477810 6477810 single base substitution C A missense_variant K382N 1146G>T BRCA-US 11 6477810 6477810 single base substitution C A upstream_gene_variant BRCA-US 11 6479439 6479439 single base substitution G T 5_prime_UTR_variant BRCA-US 11 6479439 6479439 single base substitution G T exon_variant BRCA-US 11 6479439 6479439 single base substitution G T synonymous_variant V73V 219C>A BRCA-US 11 6479439 6479439 single base substitution G T upstream_gene_variant BRCA-US 11 6499366 6499366 single base substitution T C upstream_gene_variant BRCA-US 11 6500132 6500132 single base substitution C T upstream_gene_variant BTCA-JP 11 6471682 6471682 single base substitution G T downstream_gene_variant BTCA-JP 11 6471682 6471682 single base substitution G T exon_variant BTCA-JP 11 6471682 6471682 single base substitution G T intron_variant BTCA-JP 11 6471682 6471682 single base substitution G T upstream_gene_variant BTCA-JP 11 6500092 6500092 single base substitution C T upstream_gene_variant CESC-US 11 6498387 6498387 single base substitution G A upstream_gene_variant CESC-US 11 6498963 6498963 single base substitution G A upstream_gene_variant CESC-US 11 6500102 6500102 single base substitution C G upstream_gene_variant CLLE-ES 11 6468120 6468120 single base substitution G A downstream_gene_variant CLLE-ES 11 6471387 6471387 single base substitution G A downstream_gene_variant CLLE-ES 11 6471387 6471387 single base substitution G A exon_variant CLLE-ES 11 6471387 6471387 single base substitution G A intron_variant COAD-US 11 6477788 6477788 single base substitution A G downstream_gene_variant COAD-US 11 6477788 6477788 single base substitution A G exon_variant COAD-US 11 6477788 6477788 single base substitution A G intron_variant COAD-US 11 6477788 6477788 single base substitution A G missense_variant Y271H 811T>C COAD-US 11 6477788 6477788 single base substitution A G missense_variant Y312H 934T>C COAD-US 11 6477788 6477788 single base substitution A G missense_variant Y390H 1168T>C COAD-US 11 6477788 6477788 single base substitution A G upstream_gene_variant COAD-US 11 6477845 6477845 single base substitution C T downstream_gene_variant COAD-US 11 6477845 6477845 single base substitution C T exon_variant COAD-US 11 6477845 6477845 single base substitution C T missense_variant G252S 754G>A COAD-US 11 6477845 6477845 single base substitution C T missense_variant G293S 877G>A COAD-US 11 6477845 6477845 single base substitution C T missense_variant G371S 1111G>A COAD-US 11 6477845 6477845 single base substitution C T upstream_gene_variant COAD-US 11 6477889 6477889 single base substitution C T downstream_gene_variant COAD-US 11 6477889 6477889 single base substitution C T exon_variant COAD-US 11 6477889 6477889 single base substitution C T missense_variant R237H 710G>A COAD-US 11 6477889 6477889 single base substitution C T missense_variant R278H 833G>A COAD-US 11 6477889 6477889 single base substitution C T missense_variant R356H 1067G>A COAD-US 11 6477889 6477889 single base substitution C T upstream_gene_variant COAD-US 11 6477934 6477934 single base substitution G A downstream_gene_variant COAD-US 11 6477934 6477934 single base substitution G A exon_variant COAD-US 11 6477934 6477934 single base substitution G A missense_variant A222V 665C>T COAD-US 11 6477934 6477934 single base substitution G A missense_variant A263V 788C>T COAD-US 11 6477934 6477934 single base substitution G A missense_variant A341V 1022C>T COAD-US 11 6477934 6477934 single base substitution G A upstream_gene_variant COAD-US 11 6478232 6478232 single base substitution G A downstream_gene_variant COAD-US 11 6478232 6478232 single base substitution G A exon_variant COAD-US 11 6478232 6478232 single base substitution G A intron_variant COAD-US 11 6478232 6478232 single base substitution G A missense_variant R123C 367C>T COAD-US 11 6478232 6478232 single base substitution G A missense_variant R242C 724C>T COAD-US 11 6478232 6478232 single base substitution G A upstream_gene_variant COAD-US 11 6479367 6479367 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 11 6479367 6479367 single base substitution G A downstream_gene_variant COAD-US 11 6479367 6479367 single base substitution G A exon_variant COAD-US 11 6479367 6479367 single base substitution G A synonymous_variant H97H 291C>T COAD-US 11 6479367 6479367 single base substitution G A upstream_gene_variant COCA-CN 11 6472239 6472239 single base substitution G A downstream_gene_variant COCA-CN 11 6472239 6472239 single base substitution G A exon_variant COCA-CN 11 6472239 6472239 single base substitution G A missense_variant R466W 1396C>T COCA-CN 11 6472239 6472239 single base substitution G A missense_variant R507W 1519C>T COCA-CN 11 6472239 6472239 single base substitution G A missense_variant R585W 1753C>T COCA-CN 11 6472239 6472239 single base substitution G A upstream_gene_variant COCA-CN 11 6477638 6477638 single base substitution C T downstream_gene_variant COCA-CN 11 6477638 6477638 single base substitution C T exon_variant COCA-CN 11 6477638 6477638 single base substitution C T intron_variant COCA-CN 11 6477638 6477638 single base substitution C T missense_variant G321S 961G>A COCA-CN 11 6477638 6477638 single base substitution C T missense_variant G362S 1084G>A COCA-CN 11 6477638 6477638 single base substitution C T missense_variant G440S 1318G>A COCA-CN 11 6477638 6477638 single base substitution C T upstream_gene_variant COCA-CN 11 6477787 6477787 single base substitution T C downstream_gene_variant COCA-CN 11 6477787 6477787 single base substitution T C exon_variant COCA-CN 11 6477787 6477787 single base substitution T C intron_variant COCA-CN 11 6477787 6477787 single base substitution T C missense_variant Y271C 812A>G COCA-CN 11 6477787 6477787 single base substitution T C missense_variant Y312C 935A>G COCA-CN 11 6477787 6477787 single base substitution T C missense_variant Y390C 1169A>G COCA-CN 11 6477787 6477787 single base substitution T C upstream_gene_variant COCA-CN 11 6478168 6478168 single base substitution G A downstream_gene_variant COCA-CN 11 6478168 6478168 single base substitution G A exon_variant COCA-CN 11 6478168 6478168 single base substitution G A intron_variant COCA-CN 11 6478168 6478168 single base substitution G A missense_variant S144L 431C>T COCA-CN 11 6478168 6478168 single base substitution G A missense_variant S263L 788C>T COCA-CN 11 6478168 6478168 single base substitution G A upstream_gene_variant COCA-CN 11 6478212 6478212 single base substitution G A downstream_gene_variant COCA-CN 11 6478212 6478212 single base substitution G A exon_variant COCA-CN 11 6478212 6478212 single base substitution G A intron_variant COCA-CN 11 6478212 6478212 single base substitution G A synonymous_variant I129I 387C>T COCA-CN 11 6478212 6478212 single base substitution G A synonymous_variant I248I 744C>T COCA-CN 11 6478212 6478212 single base substitution G A upstream_gene_variant COCA-CN 11 6478296 6478296 single base substitution G A downstream_gene_variant COCA-CN 11 6478296 6478296 single base substitution G A intron_variant COCA-CN 11 6478296 6478296 single base substitution G A upstream_gene_variant COCA-CN 11 6479024 6479024 single base substitution G A downstream_gene_variant COCA-CN 11 6479024 6479024 single base substitution G A exon_variant COCA-CN 11 6479024 6479024 single base substitution G A synonymous_variant R139R 417C>T COCA-CN 11 6479024 6479024 single base substitution G A synonymous_variant R20R 60C>T COCA-CN 11 6479024 6479024 single base substitution G A upstream_gene_variant COCA-CN 11 6484308 6484308 single base substitution G A intron_variant COCA-CN 11 6494616 6494616 single base substitution T G intron_variant COCA-CN 11 6497727 6497727 single base substitution G A upstream_gene_variant COCA-CN 11 6499967 6499967 single base substitution C T upstream_gene_variant COCA-CN 11 6500464 6500464 single base substitution C T upstream_gene_variant EOPC-DE 11 6484324 6484324 single base substitution A G intron_variant ESAD-UK 11 6464999 6464999 single base substitution C T downstream_gene_variant ESAD-UK 11 6465985 6465985 single base substitution C A downstream_gene_variant ESAD-UK 11 6466566 6466566 single base substitution T A downstream_gene_variant ESAD-UK 11 6468450 6468450 single base substitution C G downstream_gene_variant ESAD-UK 11 6471100 6471100 single base substitution C T downstream_gene_variant ESAD-UK 11 6471100 6471100 single base substitution C T exon_variant ESAD-UK 11 6471100 6471100 single base substitution C T intron_variant ESAD-UK 11 6473602 6473602 single base substitution A C downstream_gene_variant ESAD-UK 11 6473602 6473602 single base substitution A C exon_variant ESAD-UK 11 6473602 6473602 single base substitution A C intron_variant ESAD-UK 11 6473602 6473602 single base substitution A C upstream_gene_variant ESAD-UK 11 6477711 6477711 single base substitution G A downstream_gene_variant ESAD-UK 11 6477711 6477711 single base substitution G A exon_variant ESAD-UK 11 6477711 6477711 single base substitution G A intron_variant ESAD-UK 11 6477711 6477711 single base substitution G A synonymous_variant R296R 888C>T ESAD-UK 11 6477711 6477711 single base substitution G A synonymous_variant R337R 1011C>T ESAD-UK 11 6477711 6477711 single base substitution G A synonymous_variant R415R 1245C>T ESAD-UK 11 6477711 6477711 single base substitution G A upstream_gene_variant ESAD-UK 11 6478932 6478932 single base substitution C T downstream_gene_variant ESAD-UK 11 6478932 6478932 single base substitution C T exon_variant ESAD-UK 11 6478932 6478932 single base substitution C T missense_variant R170H 509G>A ESAD-UK 11 6478932 6478932 single base substitution C T missense_variant R51H 152G>A ESAD-UK 11 6478932 6478932 single base substitution C T upstream_gene_variant ESAD-UK 11 6479897 6479897 single base substitution T C intron_variant ESAD-UK 11 6479897 6479897 single base substitution T C upstream_gene_variant ESAD-UK 11 6482712 6482712 single base substitution C A intron_variant ESAD-UK 11 6482712 6482712 single base substitution C A upstream_gene_variant ESAD-UK 11 6483324 6483324 single base substitution C T intron_variant ESAD-UK 11 6483324 6483324 single base substitution C T upstream_gene_variant ESAD-UK 11 6483467 6483467 single base substitution G A intron_variant ESAD-UK 11 6483467 6483467 single base substitution G A upstream_gene_variant ESAD-UK 11 6484145 6484145 single base substitution A C intron_variant ESAD-UK 11 6484894 6484894 single base substitution C T intron_variant ESAD-UK 11 6485225 6485225 single base substitution C A intron_variant ESAD-UK 11 6485788 6485788 single base substitution C T intron_variant ESAD-UK 11 6486928 6486928 single base substitution C T 5_prime_UTR_variant ESAD-UK 11 6486928 6486928 single base substitution C T intron_variant ESAD-UK 11 6487148 6487148 single base substitution C T intron_variant ESAD-UK 11 6487549 6487549 single base substitution C T intron_variant ESAD-UK 11 6491681 6491681 single base substitution T C intron_variant ESAD-UK 11 6491967 6491967 single base substitution G A intron_variant ESAD-UK 11 6492716 6492716 single base substitution C T intron_variant ESAD-UK 11 6494418 6494418 single base substitution G C 5_prime_UTR_variant ESAD-UK 11 6494418 6494418 single base substitution G C intron_variant ESAD-UK 11 6498844 6498844 single base substitution C T upstream_gene_variant ESAD-UK 11 6500117 6500117 single base substitution T A upstream_gene_variant GBM-US 11 6470286 6470286 single base substitution C T downstream_gene_variant GBM-US 11 6470286 6470286 single base substitution C T exon_variant GBM-US 11 6470286 6470286 single base substitution C T missense_variant C617Y 1850G>A GBM-US 11 6470286 6470286 single base substitution C T missense_variant C658Y 1973G>A GBM-US 11 6470286 6470286 single base substitution C T missense_variant C736Y 2207G>A GBM-US 11 6470405 6470405 single base substitution G C downstream_gene_variant GBM-US 11 6470405 6470405 single base substitution G C exon_variant GBM-US 11 6470405 6470405 single base substitution G C missense_variant F577L 1731C>G GBM-US 11 6470405 6470405 single base substitution G C missense_variant F618L 1854C>G GBM-US 11 6470405 6470405 single base substitution G C missense_variant F696L 2088C>G KIRC-US 11 6477381 6477381 single base substitution T C downstream_gene_variant KIRC-US 11 6477381 6477381 single base substitution T C exon_variant KIRC-US 11 6477381 6477381 single base substitution T C missense_variant E366G 1097A>G KIRC-US 11 6477381 6477381 single base substitution T C missense_variant E407G 1220A>G KIRC-US 11 6477381 6477381 single base substitution T C missense_variant E485G 1454A>G KIRC-US 11 6477381 6477381 single base substitution T C upstream_gene_variant KIRC-US 11 6499971 6499971 single base substitution A T upstream_gene_variant KIRC-US 11 6500117 6500117 single base substitution T A upstream_gene_variant KIRP-US 11 6479061 6479061 single base substitution C T downstream_gene_variant KIRP-US 11 6479061 6479061 single base substitution C T exon_variant KIRP-US 11 6479061 6479061 single base substitution C T missense_variant C127Y 380G>A KIRP-US 11 6479061 6479061 single base substitution C T missense_variant C8Y 23G>A KIRP-US 11 6479061 6479061 single base substitution C T upstream_gene_variant KIRP-US 11 6486812 6486812 single base substitution C T intron_variant KIRP-US 11 6486812 6486812 single base substitution C T synonymous_variant L38L 114G>A LAML-KR 11 6499564 6499564 single base substitution G T upstream_gene_variant LICA-FR 11 6471254 6471254 single base substitution C A downstream_gene_variant LICA-FR 11 6471254 6471254 single base substitution C A exon_variant LICA-FR 11 6471254 6471254 single base substitution C A intron_variant LICA-FR 11 6476084 6476084 single base substitution T A downstream_gene_variant LICA-FR 11 6476084 6476084 single base substitution T A intron_variant LICA-FR 11 6476084 6476084 single base substitution T A upstream_gene_variant LICA-FR 11 6477923 6477923 single base substitution C G downstream_gene_variant LICA-FR 11 6477923 6477923 single base substitution C G exon_variant LICA-FR 11 6477923 6477923 single base substitution C G missense_variant V226L 676G>C LICA-FR 11 6477923 6477923 single base substitution C G missense_variant V267L 799G>C LICA-FR 11 6477923 6477923 single base substitution C G missense_variant V345L 1033G>C LICA-FR 11 6477923 6477923 single base substitution C G upstream_gene_variant LICA-FR 11 6477951 6477951 single base substitution C T downstream_gene_variant LICA-FR 11 6477951 6477951 single base substitution C T exon_variant LICA-FR 11 6477951 6477951 single base substitution C T synonymous_variant A216A 648G>A LICA-FR 11 6477951 6477951 single base substitution C T synonymous_variant A257A 771G>A LICA-FR 11 6477951 6477951 single base substitution C T synonymous_variant A335A 1005G>A LICA-FR 11 6477951 6477951 single base substitution C T upstream_gene_variant LICA-FR 11 6499281 6499281 single base substitution C G upstream_gene_variant LIHC-US 11 6471835 6471835 single base substitution A G downstream_gene_variant LIHC-US 11 6471835 6471835 single base substitution A G exon_variant LIHC-US 11 6471835 6471835 single base substitution A G synonymous_variant A510A 1530T>C LIHC-US 11 6471835 6471835 single base substitution A G synonymous_variant A551A 1653T>C LIHC-US 11 6471835 6471835 single base substitution A G synonymous_variant A629A 1887T>C LIHC-US 11 6471835 6471835 single base substitution A G upstream_gene_variant LIHC-US 11 6472512 6472512 single base substitution C T downstream_gene_variant LIHC-US 11 6472512 6472512 single base substitution C T exon_variant LIHC-US 11 6472512 6472512 single base substitution C T missense_variant G445S 1333G>A LIHC-US 11 6472512 6472512 single base substitution C T missense_variant G486S 1456G>A LIHC-US 11 6472512 6472512 single base substitution C T missense_variant G564S 1690G>A LIHC-US 11 6472512 6472512 single base substitution C T upstream_gene_variant LIHC-US 11 6477958 6477958 single base substitution C A downstream_gene_variant LIHC-US 11 6477958 6477958 single base substitution C A exon_variant LIHC-US 11 6477958 6477958 single base substitution C A missense_variant R214L 641G>T LIHC-US 11 6477958 6477958 single base substitution C A missense_variant R255L 764G>T LIHC-US 11 6477958 6477958 single base substitution C A missense_variant R333L 998G>T LIHC-US 11 6477958 6477958 single base substitution C A upstream_gene_variant LINC-JP 11 6471439 6471439 single base substitution A G downstream_gene_variant LINC-JP 11 6471439 6471439 single base substitution A G exon_variant LINC-JP 11 6471439 6471439 single base substitution A G intron_variant LINC-JP 11 6478603 6478603 single base substitution C T downstream_gene_variant LINC-JP 11 6478603 6478603 single base substitution C T exon_variant LINC-JP 11 6478603 6478603 single base substitution C T missense_variant D207N 619G>A LINC-JP 11 6478603 6478603 single base substitution C T missense_variant D88N 262G>A LINC-JP 11 6478603 6478603 single base substitution C T upstream_gene_variant LINC-JP 11 6493857 6493857 single base substitution A T intron_variant LINC-JP 11 6498403 6498403 single base substitution C T upstream_gene_variant LINC-JP 11 6499259 6499259 single base substitution C T upstream_gene_variant LINC-JP 11 6500651 6500651 single base substitution G A upstream_gene_variant LIRI-JP 11 6465027 6465027 single base substitution C T downstream_gene_variant LIRI-JP 11 6466750 6466750 single base substitution A T downstream_gene_variant LIRI-JP 11 6467446 6467446 single base substitution C T downstream_gene_variant LIRI-JP 11 6467984 6467984 single base substitution C T downstream_gene_variant LIRI-JP 11 6471620 6471620 single base substitution G C downstream_gene_variant LIRI-JP 11 6471620 6471620 single base substitution G C exon_variant LIRI-JP 11 6471620 6471620 single base substitution G C intron_variant LIRI-JP 11 6471621 6471621 single base substitution C A downstream_gene_variant LIRI-JP 11 6471621 6471621 single base substitution C A exon_variant LIRI-JP 11 6471621 6471621 single base substitution C A intron_variant LIRI-JP 11 6472700 6472700 single base substitution T C downstream_gene_variant LIRI-JP 11 6472700 6472700 single base substitution T C exon_variant LIRI-JP 11 6472700 6472700 single base substitution T C intron_variant LIRI-JP 11 6472700 6472700 single base substitution T C upstream_gene_variant LIRI-JP 11 6483871 6483871 single base substitution G A intron_variant LIRI-JP 11 6483871 6483871 single base substitution G A upstream_gene_variant LIRI-JP 11 6488297 6488297 single base substitution G T intron_variant LIRI-JP 11 6490611 6490611 single base substitution A C intron_variant LIRI-JP 11 6492118 6492118 single base substitution A C intron_variant LIRI-JP 11 6492309 6492309 single base substitution G C intron_variant LIRI-JP 11 6494561 6494561 single base substitution G A intron_variant LIRI-JP 11 6495655 6495655 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 11 6495655 6495655 single base substitution G A upstream_gene_variant LIRI-JP 11 6495967 6495967 single base substitution A G upstream_gene_variant LIRI-JP 11 6497802 6497802 single base substitution A G upstream_gene_variant LIRI-JP 11 6497845 6497845 single base substitution A T upstream_gene_variant LIRI-JP 11 6499377 6499377 single base substitution C A upstream_gene_variant LIRI-JP 11 6500060 6500060 single base substitution C T upstream_gene_variant LUSC-KR 11 6466426 6466426 single base substitution C G downstream_gene_variant LUSC-KR 11 6469468 6469468 single base substitution C G downstream_gene_variant LUSC-KR 11 6470770 6470770 single base substitution C A downstream_gene_variant LUSC-KR 11 6470770 6470770 single base substitution C A exon_variant LUSC-KR 11 6470770 6470770 single base substitution C A intron_variant LUSC-KR 11 6472176 6472176 single base substitution C A downstream_gene_variant LUSC-KR 11 6472176 6472176 single base substitution C A exon_variant LUSC-KR 11 6472176 6472176 single base substitution C A missense_variant G487C 1459G>T LUSC-KR 11 6472176 6472176 single base substitution C A missense_variant G528C 1582G>T LUSC-KR 11 6472176 6472176 single base substitution C A missense_variant G606C 1816G>T LUSC-KR 11 6472176 6472176 single base substitution C A upstream_gene_variant LUSC-KR 11 6481988 6481988 single base substitution C A intron_variant LUSC-KR 11 6481988 6481988 single base substitution C A upstream_gene_variant LUSC-KR 11 6487018 6487018 single base substitution T C intron_variant LUSC-KR 11 6487737 6487737 single base substitution T C intron_variant LUSC-KR 11 6487840 6487840 single base substitution C T intron_variant LUSC-KR 11 6489559 6489559 single base substitution T C intron_variant LUSC-KR 11 6489572 6489572 single base substitution A G intron_variant LUSC-KR 11 6492872 6492872 single base substitution G A intron_variant LUSC-KR 11 6496023 6496023 single base substitution C G upstream_gene_variant LUSC-KR 11 6496928 6496928 single base substitution G T upstream_gene_variant LUSC-KR 11 6497772 6497772 single base substitution T G upstream_gene_variant LUSC-KR 11 6498980 6498980 single base substitution C T upstream_gene_variant LUSC-KR 11 6498993 6498993 single base substitution C A upstream_gene_variant LUSC-KR 11 6500264 6500264 single base substitution C T upstream_gene_variant LUSC-US 11 6471848 6471848 single base substitution G A downstream_gene_variant LUSC-US 11 6471848 6471848 single base substitution G A exon_variant LUSC-US 11 6471848 6471848 single base substitution G A missense_variant P506L 1517C>T LUSC-US 11 6471848 6471848 single base substitution G A missense_variant P547L 1640C>T LUSC-US 11 6471848 6471848 single base substitution G A missense_variant P625L 1874C>T LUSC-US 11 6471848 6471848 single base substitution G A upstream_gene_variant LUSC-US 11 6477540 6477540 single base substitution G A downstream_gene_variant LUSC-US 11 6477540 6477540 single base substitution G A exon_variant LUSC-US 11 6477540 6477540 single base substitution G A intron_variant LUSC-US 11 6477540 6477540 single base substitution G A synonymous_variant L353L 1059C>T LUSC-US 11 6477540 6477540 single base substitution G A synonymous_variant L394L 1182C>T LUSC-US 11 6477540 6477540 single base substitution G A synonymous_variant L472L 1416C>T LUSC-US 11 6477540 6477540 single base substitution G A upstream_gene_variant LUSC-US 11 6479499 6479499 single base substitution C G 5_prime_UTR_variant LUSC-US 11 6479499 6479499 single base substitution C G exon_variant LUSC-US 11 6479499 6479499 single base substitution C G missense_variant Q53H 159G>C LUSC-US 11 6479499 6479499 single base substitution C G upstream_gene_variant LUSC-US 11 6499300 6499300 single base substitution G T upstream_gene_variant LUSC-US 11 6500011 6500011 single base substitution C A upstream_gene_variant MALY-DE 11 6467734 6467734 single base substitution A G downstream_gene_variant MALY-DE 11 6473948 6473948 single base substitution G A downstream_gene_variant MALY-DE 11 6473948 6473948 single base substitution G A exon_variant MALY-DE 11 6473948 6473948 single base substitution G A intron_variant MALY-DE 11 6473948 6473948 single base substitution G A upstream_gene_variant MALY-DE 11 6482753 6482753 deletion of <=200bp C - intron_variant MALY-DE 11 6482753 6482753 deletion of <=200bp C - upstream_gene_variant MALY-DE 11 6490085 6490085 insertion of <=200bp - TGAATGAA intron_variant MALY-DE 11 6497496 6497496 single base substitution C A upstream_gene_variant MALY-DE 11 6498724 6498724 single base substitution G A upstream_gene_variant MELA-AU 11 6465488 6465489 deletion of <=200bp TA - downstream_gene_variant MELA-AU 11 6466190 6466190 single base substitution G A downstream_gene_variant MELA-AU 11 6467104 6467104 single base substitution G T downstream_gene_variant MELA-AU 11 6468078 6468078 single base substitution G A downstream_gene_variant MELA-AU 11 6468243 6468243 single base substitution G A downstream_gene_variant MELA-AU 11 6468644 6468644 single base substitution G T downstream_gene_variant MELA-AU 11 6468890 6468890 single base substitution G A downstream_gene_variant MELA-AU 11 6469551 6469552 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 6469893 6469893 single base substitution G A 3_prime_UTR_variant MELA-AU 11 6469893 6469893 single base substitution G A downstream_gene_variant MELA-AU 11 6469893 6469893 single base substitution G A exon_variant MELA-AU 11 6470043 6470043 single base substitution G A 3_prime_UTR_variant MELA-AU 11 6470043 6470043 single base substitution G A downstream_gene_variant MELA-AU 11 6470043 6470043 single base substitution G A exon_variant MELA-AU 11 6470597 6470597 single base substitution C T downstream_gene_variant MELA-AU 11 6470597 6470597 single base substitution C T exon_variant MELA-AU 11 6470597 6470597 single base substitution C T missense_variant G555E 1664G>A MELA-AU 11 6470597 6470597 single base substitution C T missense_variant G596E 1787G>A MELA-AU 11 6470597 6470597 single base substitution C T missense_variant G674E 2021G>A MELA-AU 11 6470705 6470705 single base substitution G A downstream_gene_variant MELA-AU 11 6470705 6470705 single base substitution G A exon_variant MELA-AU 11 6470705 6470705 single base substitution G A intron_variant MELA-AU 11 6470818 6470818 single base substitution C G downstream_gene_variant MELA-AU 11 6470818 6470818 single base substitution C G exon_variant MELA-AU 11 6470818 6470818 single base substitution C G intron_variant MELA-AU 11 6470999 6470999 single base substitution G A downstream_gene_variant MELA-AU 11 6470999 6470999 single base substitution G A exon_variant MELA-AU 11 6470999 6470999 single base substitution G A intron_variant MELA-AU 11 6471472 6471472 single base substitution C T downstream_gene_variant MELA-AU 11 6471472 6471472 single base substitution C T exon_variant MELA-AU 11 6471472 6471472 single base substitution C T intron_variant MELA-AU 11 6472246 6472247 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 6472246 6472247 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 11 6472246 6472247 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant A463V 1388CC>TT MELA-AU 11 6472246 6472247 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant A504V 1511CC>TT MELA-AU 11 6472246 6472247 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant A582V 1745CC>TT MELA-AU 11 6472246 6472247 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 6472853 6472853 single base substitution G C downstream_gene_variant MELA-AU 11 6472853 6472853 single base substitution G C exon_variant MELA-AU 11 6472853 6472853 single base substitution G C intron_variant MELA-AU 11 6472853 6472853 single base substitution G C upstream_gene_variant MELA-AU 11 6472964 6472964 single base substitution G A downstream_gene_variant MELA-AU 11 6472964 6472964 single base substitution G A exon_variant MELA-AU 11 6472964 6472964 single base substitution G A intron_variant MELA-AU 11 6472964 6472964 single base substitution G A upstream_gene_variant MELA-AU 11 6473564 6473564 single base substitution G T downstream_gene_variant MELA-AU 11 6473564 6473564 single base substitution G T exon_variant MELA-AU 11 6473564 6473564 single base substitution G T intron_variant MELA-AU 11 6473564 6473564 single base substitution G T upstream_gene_variant MELA-AU 11 6474717 6474717 single base substitution G A downstream_gene_variant MELA-AU 11 6474717 6474717 single base substitution G A intron_variant MELA-AU 11 6474717 6474717 single base substitution G A upstream_gene_variant MELA-AU 11 6475522 6475522 single base substitution G A downstream_gene_variant MELA-AU 11 6475522 6475522 single base substitution G A intron_variant MELA-AU 11 6475522 6475522 single base substitution G A upstream_gene_variant MELA-AU 11 6475932 6475932 single base substitution G A downstream_gene_variant MELA-AU 11 6475932 6475932 single base substitution G A intron_variant MELA-AU 11 6475932 6475932 single base substitution G A upstream_gene_variant MELA-AU 11 6476044 6476045 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 6476044 6476045 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 6476044 6476045 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 6476554 6476554 single base substitution G A downstream_gene_variant MELA-AU 11 6476554 6476554 single base substitution G A intron_variant MELA-AU 11 6476554 6476554 single base substitution G A upstream_gene_variant MELA-AU 11 6476669 6476669 single base substitution A G downstream_gene_variant MELA-AU 11 6476669 6476669 single base substitution A G intron_variant MELA-AU 11 6476669 6476669 single base substitution A G upstream_gene_variant MELA-AU 11 6476799 6476799 single base substitution C A downstream_gene_variant MELA-AU 11 6476799 6476799 single base substitution C A intron_variant MELA-AU 11 6476799 6476799 single base substitution C A upstream_gene_variant MELA-AU 11 6477758 6477758 single base substitution G A downstream_gene_variant MELA-AU 11 6477758 6477758 single base substitution G A exon_variant MELA-AU 11 6477758 6477758 single base substitution G A intron_variant MELA-AU 11 6477758 6477758 single base substitution G A missense_variant L281F 841C>T MELA-AU 11 6477758 6477758 single base substitution G A missense_variant L322F 964C>T MELA-AU 11 6477758 6477758 single base substitution G A missense_variant L400F 1198C>T MELA-AU 11 6477758 6477758 single base substitution G A upstream_gene_variant MELA-AU 11 6478095 6478095 single base substitution C T downstream_gene_variant MELA-AU 11 6478095 6478095 single base substitution C T exon_variant MELA-AU 11 6478095 6478095 single base substitution C T intron_variant MELA-AU 11 6478095 6478095 single base substitution C T synonymous_variant P168P 504G>A MELA-AU 11 6478095 6478095 single base substitution C T synonymous_variant P287P 861G>A MELA-AU 11 6478095 6478095 single base substitution C T upstream_gene_variant MELA-AU 11 6478535 6478535 single base substitution G A downstream_gene_variant MELA-AU 11 6478535 6478535 single base substitution G A exon_variant MELA-AU 11 6478535 6478535 single base substitution G A intron_variant MELA-AU 11 6478535 6478535 single base substitution G A synonymous_variant A110A 330C>T MELA-AU 11 6478535 6478535 single base substitution G A synonymous_variant A229A 687C>T MELA-AU 11 6478535 6478535 single base substitution G A upstream_gene_variant MELA-AU 11 6478607 6478607 single base substitution G A downstream_gene_variant MELA-AU 11 6478607 6478607 single base substitution G A exon_variant MELA-AU 11 6478607 6478607 single base substitution G A synonymous_variant F205F 615C>T MELA-AU 11 6478607 6478607 single base substitution G A synonymous_variant F86F 258C>T MELA-AU 11 6478607 6478607 single base substitution G A upstream_gene_variant MELA-AU 11 6478724 6478724 single base substitution C T downstream_gene_variant MELA-AU 11 6478724 6478724 single base substitution C T intron_variant MELA-AU 11 6478724 6478724 single base substitution C T upstream_gene_variant MELA-AU 11 6479024 6479024 single base substitution G C downstream_gene_variant MELA-AU 11 6479024 6479024 single base substitution G C exon_variant MELA-AU 11 6479024 6479024 single base substitution G C synonymous_variant R139R 417C>G MELA-AU 11 6479024 6479024 single base substitution G C synonymous_variant R20R 60C>G MELA-AU 11 6479024 6479024 single base substitution G C upstream_gene_variant MELA-AU 11 6479168 6479168 single base substitution G A downstream_gene_variant MELA-AU 11 6479168 6479168 single base substitution G A intron_variant MELA-AU 11 6479168 6479168 single base substitution G A upstream_gene_variant MELA-AU 11 6480001 6480001 single base substitution G A intron_variant MELA-AU 11 6480001 6480001 single base substitution G A upstream_gene_variant MELA-AU 11 6480002 6480002 single base substitution G A intron_variant MELA-AU 11 6480002 6480002 single base substitution G A upstream_gene_variant MELA-AU 11 6480297 6480297 single base substitution C T intron_variant MELA-AU 11 6480297 6480297 single base substitution C T upstream_gene_variant MELA-AU 11 6481381 6481381 single base substitution G A intron_variant MELA-AU 11 6481381 6481381 single base substitution G A upstream_gene_variant MELA-AU 11 6481489 6481489 single base substitution G A intron_variant MELA-AU 11 6481489 6481489 single base substitution G A upstream_gene_variant MELA-AU 11 6481702 6481702 single base substitution G A intron_variant MELA-AU 11 6481702 6481702 single base substitution G A upstream_gene_variant MELA-AU 11 6481710 6481710 single base substitution G A intron_variant MELA-AU 11 6481710 6481710 single base substitution G A upstream_gene_variant MELA-AU 11 6481772 6481773 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 6481772 6481773 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 6481780 6481780 single base substitution G A intron_variant MELA-AU 11 6481780 6481780 single base substitution G A upstream_gene_variant MELA-AU 11 6482577 6482577 single base substitution C T intron_variant MELA-AU 11 6482577 6482577 single base substitution C T upstream_gene_variant MELA-AU 11 6482753 6482753 single base substitution C T intron_variant MELA-AU 11 6482753 6482753 single base substitution C T upstream_gene_variant MELA-AU 11 6483367 6483367 single base substitution G A intron_variant MELA-AU 11 6483367 6483367 single base substitution G A upstream_gene_variant MELA-AU 11 6484472 6484472 single base substitution A T intron_variant MELA-AU 11 6484824 6484824 single base substitution G A intron_variant MELA-AU 11 6485002 6485002 single base substitution G A intron_variant MELA-AU 11 6485109 6485109 single base substitution G A intron_variant MELA-AU 11 6485153 6485153 single base substitution G A intron_variant MELA-AU 11 6485308 6485308 single base substitution G A intron_variant MELA-AU 11 6486052 6486052 single base substitution A G intron_variant MELA-AU 11 6486759 6486759 single base substitution G A intron_variant MELA-AU 11 6486869 6486869 single base substitution G A intron_variant MELA-AU 11 6486869 6486869 single base substitution G A synonymous_variant F19F 57C>T MELA-AU 11 6486889 6486889 single base substitution G A intron_variant MELA-AU 11 6486889 6486889 single base substitution G A stop_gained Q13* 37C>T MELA-AU 11 6487721 6487721 single base substitution C T intron_variant MELA-AU 11 6487844 6487844 single base substitution T C intron_variant MELA-AU 11 6487849 6487849 single base substitution G A intron_variant MELA-AU 11 6487967 6487967 single base substitution C T intron_variant MELA-AU 11 6488065 6488065 single base substitution C T intron_variant MELA-AU 11 6488523 6488523 single base substitution G A intron_variant MELA-AU 11 6488678 6488678 single base substitution G A intron_variant MELA-AU 11 6489277 6489277 single base substitution G A intron_variant MELA-AU 11 6489617 6489617 single base substitution G A intron_variant MELA-AU 11 6489966 6489966 single base substitution G A intron_variant MELA-AU 11 6491263 6491263 single base substitution G A intron_variant MELA-AU 11 6491840 6491840 single base substitution G A intron_variant MELA-AU 11 6492692 6492692 single base substitution G A intron_variant MELA-AU 11 6493399 6493399 single base substitution T A intron_variant MELA-AU 11 6493649 6493650 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU 11 6493790 6493790 single base substitution G A intron_variant MELA-AU 11 6495663 6495663 single base substitution G C 5_prime_UTR_variant MELA-AU 11 6495663 6495663 single base substitution G C upstream_gene_variant MELA-AU 11 6495674 6495674 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 6495674 6495674 single base substitution G A upstream_gene_variant MELA-AU 11 6496147 6496148 multiple base substitution (>=2bp and <=200bp) GG AC upstream_gene_variant MELA-AU 11 6496466 6496466 single base substitution G A upstream_gene_variant MELA-AU 11 6496973 6496973 single base substitution A G upstream_gene_variant MELA-AU 11 6497039 6497039 single base substitution T A upstream_gene_variant MELA-AU 11 6497980 6497980 single base substitution G A upstream_gene_variant MELA-AU 11 6498157 6498157 single base substitution A G upstream_gene_variant MELA-AU 11 6498891 6498891 single base substitution G A upstream_gene_variant MELA-AU 11 6498909 6498909 single base substitution T C upstream_gene_variant MELA-AU 11 6498918 6498918 single base substitution G A upstream_gene_variant MELA-AU 11 6498979 6498979 single base substitution G A upstream_gene_variant MELA-AU 11 6499451 6499451 single base substitution G A upstream_gene_variant MELA-AU 11 6499512 6499512 single base substitution G A upstream_gene_variant MELA-AU 11 6499896 6499896 single base substitution G A upstream_gene_variant MELA-AU 11 6500456 6500456 single base substitution G A upstream_gene_variant ORCA-IN 11 6468378 6468378 single base substitution C G downstream_gene_variant ORCA-IN 11 6473022 6473022 single base substitution C T downstream_gene_variant ORCA-IN 11 6473022 6473022 single base substitution C T exon_variant ORCA-IN 11 6473022 6473022 single base substitution C T intron_variant ORCA-IN 11 6473022 6473022 single base substitution C T upstream_gene_variant ORCA-IN 11 6499846 6499846 single base substitution A G upstream_gene_variant OV-AU 11 6473739 6473739 single base substitution C G downstream_gene_variant OV-AU 11 6473739 6473739 single base substitution C G exon_variant OV-AU 11 6473739 6473739 single base substitution C G intron_variant OV-AU 11 6473739 6473739 single base substitution C G upstream_gene_variant OV-AU 11 6494306 6494306 single base substitution G T intron_variant OV-AU 11 6494306 6494306 single base substitution G T splice_region_variant OV-AU 11 6499952 6499952 single base substitution G C upstream_gene_variant PACA-AU 11 6465488 6465488 insertion of <=200bp - TA downstream_gene_variant PACA-AU 11 6465750 6465750 single base substitution G A downstream_gene_variant PACA-AU 11 6472757 6472757 deletion of <=200bp C - downstream_gene_variant PACA-AU 11 6472757 6472757 deletion of <=200bp C - exon_variant PACA-AU 11 6472757 6472757 deletion of <=200bp C - intron_variant PACA-AU 11 6472757 6472757 deletion of <=200bp C - upstream_gene_variant PACA-AU 11 6476169 6476169 single base substitution C T downstream_gene_variant PACA-AU 11 6476169 6476169 single base substitution C T intron_variant PACA-AU 11 6476169 6476169 single base substitution C T upstream_gene_variant PACA-AU 11 6478812 6478812 single base substitution G A downstream_gene_variant PACA-AU 11 6478812 6478812 single base substitution G A intron_variant PACA-AU 11 6478812 6478812 single base substitution G A upstream_gene_variant PACA-AU 11 6483475 6483475 single base substitution G C intron_variant PACA-AU 11 6483475 6483475 single base substitution G C upstream_gene_variant PACA-AU 11 6486315 6486315 single base substitution T C intron_variant PACA-AU 11 6486747 6486747 single base substitution T C intron_variant PACA-AU 11 6487680 6487680 deletion of <=200bp G - intron_variant PACA-AU 11 6491724 6491724 single base substitution C T intron_variant PACA-CA 11 6465226 6465226 single base substitution A G downstream_gene_variant PACA-CA 11 6466465 6466465 single base substitution T G downstream_gene_variant PACA-CA 11 6469609 6469609 single base substitution T C downstream_gene_variant PACA-CA 11 6471603 6471603 single base substitution T G downstream_gene_variant PACA-CA 11 6471603 6471603 single base substitution T G exon_variant PACA-CA 11 6471603 6471603 single base substitution T G intron_variant PACA-CA 11 6477698 6477698 single base substitution G A downstream_gene_variant PACA-CA 11 6477698 6477698 single base substitution G A exon_variant PACA-CA 11 6477698 6477698 single base substitution G A intron_variant PACA-CA 11 6477698 6477698 single base substitution G A missense_variant R301C 901C>T PACA-CA 11 6477698 6477698 single base substitution G A missense_variant R342C 1024C>T PACA-CA 11 6477698 6477698 single base substitution G A missense_variant R420C 1258C>T PACA-CA 11 6477698 6477698 single base substitution G A upstream_gene_variant PACA-CA 11 6477850 6477850 single base substitution G A downstream_gene_variant PACA-CA 11 6477850 6477850 single base substitution G A exon_variant PACA-CA 11 6477850 6477850 single base substitution G A missense_variant P250L 749C>T PACA-CA 11 6477850 6477850 single base substitution G A missense_variant P291L 872C>T PACA-CA 11 6477850 6477850 single base substitution G A missense_variant P369L 1106C>T PACA-CA 11 6477850 6477850 single base substitution G A upstream_gene_variant PACA-CA 11 6479011 6479011 single base substitution G A downstream_gene_variant PACA-CA 11 6479011 6479011 single base substitution G A exon_variant PACA-CA 11 6479011 6479011 single base substitution G A missense_variant R144C 430C>T PACA-CA 11 6479011 6479011 single base substitution G A missense_variant R25C 73C>T PACA-CA 11 6479011 6479011 single base substitution G A upstream_gene_variant PACA-CA 11 6479660 6479660 single base substitution G A intron_variant PACA-CA 11 6479660 6479660 single base substitution G A upstream_gene_variant PACA-CA 11 6479994 6479994 single base substitution G C intron_variant PACA-CA 11 6479994 6479994 single base substitution G C upstream_gene_variant PACA-CA 11 6482742 6482742 single base substitution C T intron_variant PACA-CA 11 6482742 6482742 single base substitution C T upstream_gene_variant PACA-CA 11 6485002 6485002 single base substitution G C intron_variant PACA-CA 11 6486945 6486945 insertion of <=200bp - T 5_prime_UTR_variant PACA-CA 11 6486945 6486945 insertion of <=200bp - T intron_variant PACA-CA 11 6494926 6494926 single base substitution G C intron_variant PACA-CA 11 6495573 6495573 single base substitution G T 5_prime_UTR_variant PACA-CA 11 6495573 6495573 single base substitution G T upstream_gene_variant PACA-CA 11 6496767 6496767 single base substitution T A upstream_gene_variant PACA-CA 11 6497111 6497111 single base substitution G T upstream_gene_variant PAEN-AU 11 6473756 6473756 single base substitution A C downstream_gene_variant PAEN-AU 11 6473756 6473756 single base substitution A C exon_variant PAEN-AU 11 6473756 6473756 single base substitution A C intron_variant PAEN-AU 11 6473756 6473756 single base substitution A C upstream_gene_variant PAEN-AU 11 6481567 6481567 single base substitution G A intron_variant PAEN-AU 11 6481567 6481567 single base substitution G A upstream_gene_variant PAEN-AU 11 6487824 6487824 single base substitution T G intron_variant PAEN-AU 11 6496008 6496008 single base substitution T A upstream_gene_variant PBCA-DE 11 6464915 6464915 single base substitution C T downstream_gene_variant PBCA-DE 11 6465488 6465489 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 11 6472245 6472245 single base substitution C T downstream_gene_variant PBCA-DE 11 6472245 6472245 single base substitution C T exon_variant PBCA-DE 11 6472245 6472245 single base substitution C T missense_variant V464I 1390G>A PBCA-DE 11 6472245 6472245 single base substitution C T missense_variant V505I 1513G>A PBCA-DE 11 6472245 6472245 single base substitution C T missense_variant V583I 1747G>A PBCA-DE 11 6472245 6472245 single base substitution C T upstream_gene_variant PBCA-DE 11 6472288 6472288 single base substitution G C downstream_gene_variant PBCA-DE 11 6472288 6472288 single base substitution G C splice_region_variant PBCA-DE 11 6472288 6472288 single base substitution G C upstream_gene_variant PBCA-DE 11 6477669 6477669 single base substitution G A downstream_gene_variant PBCA-DE 11 6477669 6477669 single base substitution G A exon_variant PBCA-DE 11 6477669 6477669 single base substitution G A intron_variant PBCA-DE 11 6477669 6477669 single base substitution G A synonymous_variant D310D 930C>T PBCA-DE 11 6477669 6477669 single base substitution G A synonymous_variant D351D 1053C>T PBCA-DE 11 6477669 6477669 single base substitution G A synonymous_variant D429D 1287C>T PBCA-DE 11 6477669 6477669 single base substitution G A upstream_gene_variant PBCA-DE 11 6488991 6488994 deletion of <=200bp TCTG - intron_variant PBCA-DE 11 6498601 6498601 single base substitution T C upstream_gene_variant PRAD-CA 11 6466813 6466813 single base substitution C T downstream_gene_variant PRAD-CA 11 6480956 6480956 single base substitution G A intron_variant PRAD-CA 11 6480956 6480956 single base substitution G A upstream_gene_variant PRAD-CA 11 6494786 6494786 single base substitution T C intron_variant PRAD-UK 11 6494517 6494517 single base substitution C A intron_variant PRAD-UK 11 6495058 6495058 single base substitution C T 5_prime_UTR_variant PRAD-UK 11 6495058 6495058 single base substitution C T exon_variant PRAD-UK 11 6495058 6495058 single base substitution C T intron_variant READ-US 11 6470271 6470271 single base substitution C T downstream_gene_variant READ-US 11 6470271 6470271 single base substitution C T exon_variant READ-US 11 6470271 6470271 single base substitution C T missense_variant R622H 1865G>A READ-US 11 6470271 6470271 single base substitution C T missense_variant R663H 1988G>A READ-US 11 6470271 6470271 single base substitution C T missense_variant R741H 2222G>A READ-US 11 6477620 6477620 single base substitution G A downstream_gene_variant READ-US 11 6477620 6477620 single base substitution G A exon_variant READ-US 11 6477620 6477620 single base substitution G A intron_variant READ-US 11 6477620 6477620 single base substitution G A missense_variant R327C 979C>T READ-US 11 6477620 6477620 single base substitution G A missense_variant R368C 1102C>T READ-US 11 6477620 6477620 single base substitution G A missense_variant R446C 1336C>T READ-US 11 6477620 6477620 single base substitution G A upstream_gene_variant READ-US 11 6478170 6478170 single base substitution G T downstream_gene_variant READ-US 11 6478170 6478170 single base substitution G T exon_variant READ-US 11 6478170 6478170 single base substitution G T intron_variant READ-US 11 6478170 6478170 single base substitution G T synonymous_variant G143G 429C>A READ-US 11 6478170 6478170 single base substitution G T synonymous_variant G262G 786C>A READ-US 11 6478170 6478170 single base substitution G T upstream_gene_variant RECA-EU 11 6472329 6472329 single base substitution C G downstream_gene_variant RECA-EU 11 6472329 6472329 single base substitution C G intron_variant RECA-EU 11 6472329 6472329 single base substitution C G upstream_gene_variant RECA-EU 11 6486445 6486445 single base substitution A G intron_variant SKCA-BR 11 6466091 6466091 single base substitution A C downstream_gene_variant SKCA-BR 11 6466837 6466837 single base substitution A C downstream_gene_variant SKCA-BR 11 6468149 6468149 single base substitution A G downstream_gene_variant SKCA-BR 11 6468619 6468619 single base substitution T C downstream_gene_variant SKCA-BR 11 6469379 6469379 single base substitution G C downstream_gene_variant SKCA-BR 11 6469662 6469662 single base substitution T G downstream_gene_variant SKCA-BR 11 6470698 6470698 single base substitution G A downstream_gene_variant SKCA-BR 11 6470698 6470698 single base substitution G A exon_variant SKCA-BR 11 6470698 6470698 single base substitution G A intron_variant SKCA-BR 11 6475939 6475939 single base substitution A T downstream_gene_variant SKCA-BR 11 6475939 6475939 single base substitution A T intron_variant SKCA-BR 11 6475939 6475939 single base substitution A T upstream_gene_variant SKCA-BR 11 6477332 6477332 single base substitution C T downstream_gene_variant SKCA-BR 11 6477332 6477332 single base substitution C T exon_variant SKCA-BR 11 6477332 6477332 single base substitution C T synonymous_variant V382V 1146G>A SKCA-BR 11 6477332 6477332 single base substitution C T synonymous_variant V423V 1269G>A SKCA-BR 11 6477332 6477332 single base substitution C T synonymous_variant V501V 1503G>A SKCA-BR 11 6477332 6477332 single base substitution C T upstream_gene_variant SKCA-BR 11 6481512 6481512 single base substitution A G intron_variant SKCA-BR 11 6481512 6481512 single base substitution A G upstream_gene_variant SKCA-BR 11 6482985 6482985 single base substitution G A intron_variant SKCA-BR 11 6482985 6482985 single base substitution G A upstream_gene_variant SKCA-BR 11 6486425 6486425 single base substitution G A intron_variant SKCA-BR 11 6495866 6495866 single base substitution A T upstream_gene_variant SKCA-BR 11 6500575 6500575 single base substitution G A upstream_gene_variant SKCM-US 11 6470603 6470603 single base substitution G A downstream_gene_variant SKCM-US 11 6470603 6470603 single base substitution G A exon_variant SKCM-US 11 6470603 6470603 single base substitution G A missense_variant P553L 1658C>T SKCM-US 11 6470603 6470603 single base substitution G A missense_variant P594L 1781C>T SKCM-US 11 6470603 6470603 single base substitution G A missense_variant P672L 2015C>T SKCM-US 11 6472141 6472141 single base substitution G A downstream_gene_variant SKCM-US 11 6472141 6472141 single base substitution G A exon_variant SKCM-US 11 6472141 6472141 single base substitution G A synonymous_variant A498A 1494C>T SKCM-US 11 6472141 6472141 single base substitution G A synonymous_variant A539A 1617C>T SKCM-US 11 6472141 6472141 single base substitution G A synonymous_variant A617A 1851C>T SKCM-US 11 6472141 6472141 single base substitution G A upstream_gene_variant SKCM-US 11 6472626 6472626 single base substitution G A downstream_gene_variant SKCM-US 11 6472626 6472626 single base substitution G A exon_variant SKCM-US 11 6472626 6472626 single base substitution G A stop_gained R407* 1219C>T SKCM-US 11 6472626 6472626 single base substitution G A stop_gained R448* 1342C>T SKCM-US 11 6472626 6472626 single base substitution G A stop_gained R526* 1576C>T SKCM-US 11 6472626 6472626 single base substitution G A upstream_gene_variant SKCM-US 11 6472639 6472639 single base substitution G A downstream_gene_variant SKCM-US 11 6472639 6472639 single base substitution G A exon_variant SKCM-US 11 6472639 6472639 single base substitution G A synonymous_variant F402F 1206C>T SKCM-US 11 6472639 6472639 single base substitution G A synonymous_variant F443F 1329C>T SKCM-US 11 6472639 6472639 single base substitution G A synonymous_variant F521F 1563C>T SKCM-US 11 6472639 6472639 single base substitution G A upstream_gene_variant SKCM-US 11 6477301 6477301 single base substitution C T downstream_gene_variant SKCM-US 11 6477301 6477301 single base substitution C T splice_donor_variant SKCM-US 11 6477301 6477301 single base substitution C T upstream_gene_variant SKCM-US 11 6477304 6477304 single base substitution G A downstream_gene_variant SKCM-US 11 6477304 6477304 single base substitution G A splice_region_variant SKCM-US 11 6477304 6477304 single base substitution G A stop_gained Q392* 1174C>T SKCM-US 11 6477304 6477304 single base substitution G A stop_gained Q433* 1297C>T SKCM-US 11 6477304 6477304 single base substitution G A stop_gained Q511* 1531C>T SKCM-US 11 6477304 6477304 single base substitution G A upstream_gene_variant SKCM-US 11 6477533 6477533 single base substitution G A downstream_gene_variant SKCM-US 11 6477533 6477533 single base substitution G A exon_variant SKCM-US 11 6477533 6477533 single base substitution G A intron_variant SKCM-US 11 6477533 6477533 single base substitution G A missense_variant R356C 1066C>T SKCM-US 11 6477533 6477533 single base substitution G A missense_variant R397C 1189C>T SKCM-US 11 6477533 6477533 single base substitution G A missense_variant R475C 1423C>T SKCM-US 11 6477533 6477533 single base substitution G A upstream_gene_variant SKCM-US 11 6477534 6477534 single base substitution G A downstream_gene_variant SKCM-US 11 6477534 6477534 single base substitution G A exon_variant SKCM-US 11 6477534 6477534 single base substitution G A intron_variant SKCM-US 11 6477534 6477534 single base substitution G A synonymous_variant F355F 1065C>T SKCM-US 11 6477534 6477534 single base substitution G A synonymous_variant F396F 1188C>T SKCM-US 11 6477534 6477534 single base substitution G A synonymous_variant F474F 1422C>T SKCM-US 11 6477534 6477534 single base substitution G A upstream_gene_variant SKCM-US 11 6477540 6477540 single base substitution G A downstream_gene_variant SKCM-US 11 6477540 6477540 single base substitution G A exon_variant SKCM-US 11 6477540 6477540 single base substitution G A intron_variant SKCM-US 11 6477540 6477540 single base substitution G A synonymous_variant L353L 1059C>T SKCM-US 11 6477540 6477540 single base substitution G A synonymous_variant L394L 1182C>T SKCM-US 11 6477540 6477540 single base substitution G A synonymous_variant L472L 1416C>T SKCM-US 11 6477540 6477540 single base substitution G A upstream_gene_variant SKCM-US 11 6477646 6477646 single base substitution G A downstream_gene_variant SKCM-US 11 6477646 6477646 single base substitution G A exon_variant SKCM-US 11 6477646 6477646 single base substitution G A intron_variant SKCM-US 11 6477646 6477646 single base substitution G A missense_variant S318F 953C>T SKCM-US 11 6477646 6477646 single base substitution G A missense_variant S359F 1076C>T SKCM-US 11 6477646 6477646 single base substitution G A missense_variant S437F 1310C>T SKCM-US 11 6477646 6477646 single base substitution G A upstream_gene_variant SKCM-US 11 6477676 6477676 single base substitution G A downstream_gene_variant SKCM-US 11 6477676 6477676 single base substitution G A exon_variant SKCM-US 11 6477676 6477676 single base substitution G A intron_variant SKCM-US 11 6477676 6477676 single base substitution G A missense_variant S308F 923C>T SKCM-US 11 6477676 6477676 single base substitution G A missense_variant S349F 1046C>T SKCM-US 11 6477676 6477676 single base substitution G A missense_variant S427F 1280C>T SKCM-US 11 6477676 6477676 single base substitution G A upstream_gene_variant SKCM-US 11 6477836 6477836 single base substitution G A downstream_gene_variant SKCM-US 11 6477836 6477836 single base substitution G A exon_variant SKCM-US 11 6477836 6477836 single base substitution G A missense_variant L255F 763C>T SKCM-US 11 6477836 6477836 single base substitution G A missense_variant L296F 886C>T SKCM-US 11 6477836 6477836 single base substitution G A missense_variant L374F 1120C>T SKCM-US 11 6477836 6477836 single base substitution G A upstream_gene_variant SKCM-US 11 6477849 6477849 single base substitution C T downstream_gene_variant SKCM-US 11 6477849 6477849 single base substitution C T exon_variant SKCM-US 11 6477849 6477849 single base substitution C T synonymous_variant P250P 750G>A SKCM-US 11 6477849 6477849 single base substitution C T synonymous_variant P291P 873G>A SKCM-US 11 6477849 6477849 single base substitution C T synonymous_variant P369P 1107G>A SKCM-US 11 6477849 6477849 single base substitution C T upstream_gene_variant SKCM-US 11 6477915 6477915 single base substitution G A downstream_gene_variant SKCM-US 11 6477915 6477915 single base substitution G A exon_variant SKCM-US 11 6477915 6477915 single base substitution G A synonymous_variant T228T 684C>T SKCM-US 11 6477915 6477915 single base substitution G A synonymous_variant T269T 807C>T SKCM-US 11 6477915 6477915 single base substitution G A synonymous_variant T347T 1041C>T SKCM-US 11 6477915 6477915 single base substitution G A upstream_gene_variant SKCM-US 11 6478024 6478024 single base substitution T C downstream_gene_variant SKCM-US 11 6478024 6478024 single base substitution T C exon_variant SKCM-US 11 6478024 6478024 single base substitution T C missense_variant N192S 575A>G SKCM-US 11 6478024 6478024 single base substitution T C missense_variant N233S 698A>G SKCM-US 11 6478024 6478024 single base substitution T C missense_variant N311S 932A>G SKCM-US 11 6478024 6478024 single base substitution T C upstream_gene_variant SKCM-US 11 6478607 6478607 single base substitution G A downstream_gene_variant SKCM-US 11 6478607 6478607 single base substitution G A exon_variant SKCM-US 11 6478607 6478607 single base substitution G A synonymous_variant F205F 615C>T SKCM-US 11 6478607 6478607 single base substitution G A synonymous_variant F86F 258C>T SKCM-US 11 6478607 6478607 single base substitution G A upstream_gene_variant SKCM-US 11 6479042 6479042 single base substitution G A downstream_gene_variant SKCM-US 11 6479042 6479042 single base substitution G A exon_variant SKCM-US 11 6479042 6479042 single base substitution G A synonymous_variant A133A 399C>T SKCM-US 11 6479042 6479042 single base substitution G A synonymous_variant A14A 42C>T SKCM-US 11 6479042 6479042 single base substitution G A upstream_gene_variant SKCM-US 11 6499989 6499989 single base substitution G A upstream_gene_variant SKCM-US 11 6500164 6500164 single base substitution C T upstream_gene_variant STAD-US 11 6471805 6471805 single base substitution C T downstream_gene_variant STAD-US 11 6471805 6471805 single base substitution C T exon_variant STAD-US 11 6471805 6471805 single base substitution C T synonymous_variant T520T 1560G>A STAD-US 11 6471805 6471805 single base substitution C T synonymous_variant T561T 1683G>A STAD-US 11 6471805 6471805 single base substitution C T synonymous_variant T639T 1917G>A STAD-US 11 6471805 6471805 single base substitution C T upstream_gene_variant STAD-US 11 6472626 6472626 single base substitution G A downstream_gene_variant STAD-US 11 6472626 6472626 single base substitution G A exon_variant STAD-US 11 6472626 6472626 single base substitution G A stop_gained R407* 1219C>T STAD-US 11 6472626 6472626 single base substitution G A stop_gained R448* 1342C>T STAD-US 11 6472626 6472626 single base substitution G A stop_gained R526* 1576C>T STAD-US 11 6472626 6472626 single base substitution G A upstream_gene_variant STAD-US 11 6477697 6477697 single base substitution C T downstream_gene_variant STAD-US 11 6477697 6477697 single base substitution C T exon_variant STAD-US 11 6477697 6477697 single base substitution C T intron_variant STAD-US 11 6477697 6477697 single base substitution C T missense_variant R301H 902G>A STAD-US 11 6477697 6477697 single base substitution C T missense_variant R342H 1025G>A STAD-US 11 6477697 6477697 single base substitution C T missense_variant R420H 1259G>A STAD-US 11 6477697 6477697 single base substitution C T upstream_gene_variant STAD-US 11 6477741 6477741 single base substitution G A downstream_gene_variant STAD-US 11 6477741 6477741 single base substitution G A exon_variant STAD-US 11 6477741 6477741 single base substitution G A intron_variant STAD-US 11 6477741 6477741 single base substitution G A synonymous_variant Y286Y 858C>T STAD-US 11 6477741 6477741 single base substitution G A synonymous_variant Y327Y 981C>T STAD-US 11 6477741 6477741 single base substitution G A synonymous_variant Y405Y 1215C>T STAD-US 11 6477741 6477741 single base substitution G A upstream_gene_variant STAD-US 11 6478040 6478040 single base substitution G A downstream_gene_variant STAD-US 11 6478040 6478040 single base substitution G A exon_variant STAD-US 11 6478040 6478040 single base substitution G A missense_variant R187W 559C>T STAD-US 11 6478040 6478040 single base substitution G A missense_variant R228W 682C>T STAD-US 11 6478040 6478040 single base substitution G A missense_variant R306W 916C>T STAD-US 11 6478040 6478040 single base substitution G A upstream_gene_variant STAD-US 11 6478559 6478559 single base substitution G A downstream_gene_variant STAD-US 11 6478559 6478559 single base substitution G A exon_variant STAD-US 11 6478559 6478559 single base substitution G A synonymous_variant S102S 306C>T STAD-US 11 6478559 6478559 single base substitution G A synonymous_variant S221S 663C>T STAD-US 11 6478559 6478559 single base substitution G A upstream_gene_variant STAD-US 11 6486843 6486843 single base substitution C T intron_variant STAD-US 11 6486843 6486843 single base substitution C T missense_variant R28Q 83G>A STAD-US 11 6499032 6499032 single base substitution C A upstream_gene_variant STAD-US 11 6499103 6499103 single base substitution G A upstream_gene_variant STAD-US 11 6500092 6500092 single base substitution C T upstream_gene_variant THCA-US 11 6499070 6499070 single base substitution G C upstream_gene_variant THCA-US 11 6500468 6500468 single base substitution G A upstream_gene_variant UCEC-US 11 6470405 6470405 single base substitution G A downstream_gene_variant UCEC-US 11 6470405 6470405 single base substitution G A exon_variant UCEC-US 11 6470405 6470405 single base substitution G A synonymous_variant F577F 1731C>T UCEC-US 11 6470405 6470405 single base substitution G A synonymous_variant F618F 1854C>T UCEC-US 11 6470405 6470405 single base substitution G A synonymous_variant F696F 2088C>T UCEC-US 11 6470616 6470616 single base substitution G A downstream_gene_variant UCEC-US 11 6470616 6470616 single base substitution G A exon_variant UCEC-US 11 6470616 6470616 single base substitution G A stop_gained Q549* 1645C>T UCEC-US 11 6470616 6470616 single base substitution G A stop_gained Q590* 1768C>T UCEC-US 11 6470616 6470616 single base substitution G A stop_gained Q668* 2002C>T UCEC-US 11 6470629 6470629 single base substitution G A downstream_gene_variant UCEC-US 11 6470629 6470629 single base substitution G A exon_variant UCEC-US 11 6470629 6470629 single base substitution G A synonymous_variant G544G 1632C>T UCEC-US 11 6470629 6470629 single base substitution G A synonymous_variant G585G 1755C>T UCEC-US 11 6470629 6470629 single base substitution G A synonymous_variant G663G 1989C>T UCEC-US 11 6472143 6472143 single base substitution C T downstream_gene_variant UCEC-US 11 6472143 6472143 single base substitution C T exon_variant UCEC-US 11 6472143 6472143 single base substitution C T missense_variant A498T 1492G>A UCEC-US 11 6472143 6472143 single base substitution C T missense_variant A539T 1615G>A UCEC-US 11 6472143 6472143 single base substitution C T missense_variant A617T 1849G>A UCEC-US 11 6472143 6472143 single base substitution C T upstream_gene_variant UCEC-US 11 6477399 6477399 single base substitution C T downstream_gene_variant UCEC-US 11 6477399 6477399 single base substitution C T exon_variant UCEC-US 11 6477399 6477399 single base substitution C T missense_variant R360H 1079G>A UCEC-US 11 6477399 6477399 single base substitution C T missense_variant R401H 1202G>A UCEC-US 11 6477399 6477399 single base substitution C T missense_variant R479H 1436G>A UCEC-US 11 6477399 6477399 single base substitution C T upstream_gene_variant UCEC-US 11 6478552 6478552 single base substitution C T downstream_gene_variant UCEC-US 11 6478552 6478552 single base substitution C T exon_variant UCEC-US 11 6478552 6478552 single base substitution C T missense_variant E105K 313G>A UCEC-US 11 6478552 6478552 single base substitution C T missense_variant E224K 670G>A UCEC-US 11 6478552 6478552 single base substitution C T splice_donor_variant UCEC-US 11 6478552 6478552 single base substitution C T upstream_gene_variant UCEC-US 11 6478579 6478579 single base substitution G A downstream_gene_variant UCEC-US 11 6478579 6478579 single base substitution G A exon_variant UCEC-US 11 6478579 6478579 single base substitution G A missense_variant R215C 643C>T UCEC-US 11 6478579 6478579 single base substitution G A missense_variant R96C 286C>T UCEC-US 11 6478579 6478579 single base substitution G A upstream_gene_variant UCEC-US 11 6478674 6478674 single base substitution A G downstream_gene_variant UCEC-US 11 6478674 6478674 single base substitution A G exon_variant UCEC-US 11 6478674 6478674 single base substitution A G missense_variant V183A 548T>C UCEC-US 11 6478674 6478674 single base substitution A G missense_variant V64A 191T>C UCEC-US 11 6478674 6478674 single base substitution A G upstream_gene_variant UCEC-US 11 6478950 6478950 single base substitution C T downstream_gene_variant UCEC-US 11 6478950 6478950 single base substitution C T exon_variant UCEC-US 11 6478950 6478950 single base substitution C T missense_variant R164H 491G>A UCEC-US 11 6478950 6478950 single base substitution C T missense_variant R45H 134G>A UCEC-US 11 6478950 6478950 single base substitution C T upstream_gene_variant UCEC-US 11 6479055 6479055 single base substitution G T downstream_gene_variant UCEC-US 11 6479055 6479055 single base substitution G T exon_variant UCEC-US 11 6479055 6479055 single base substitution G T missense_variant A10D 29C>A UCEC-US 11 6479055 6479055 single base substitution G T missense_variant A129D 386C>A UCEC-US 11 6479055 6479055 single base substitution G T upstream_gene_variant UCEC-US 11 6479075 6479075 single base substitution C T downstream_gene_variant UCEC-US 11 6479075 6479075 single base substitution C T splice_region_variant UCEC-US 11 6479075 6479075 single base substitution C T upstream_gene_variant UCEC-US 11 6479471 6479471 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 11 6479471 6479471 single base substitution G A exon_variant UCEC-US 11 6479471 6479471 single base substitution G A missense_variant R63W 187C>T UCEC-US 11 6479471 6479471 single base substitution G A upstream_gene_variant UCEC-US 11 6479526 6479526 single base substitution T G missense_variant R44S 132A>C UCEC-US 11 6479526 6479526 single base substitution T G splice_region_variant UCEC-US 11 6479526 6479526 single base substitution T G upstream_gene_variant UCEC-US 11 6486844 6486844 single base substitution G A intron_variant UCEC-US 11 6486844 6486844 single base substitution G A missense_variant R28W 82C>T UCEC-US 11 6499012 6499012 single base substitution C A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PR-09-3687 COSM247981 c.2169G>A p.S723S Substitution - coding silent 11:6449094-6449094 - ESO-717 COSM1242952 c.1988G>C p.G663A Substitution - Missense 11:6449400-6449400 - 3N52-VS-3T52 COSM4983392 c.1458C>T p.F486F Substitution - coding silent 11:6456147-6456147 - TCGA-B5-A11E-01 COSM930292 c.643C>T p.R215C Substitution - Missense 11:6457349-6457349 - 2492703 COSM5600720 c.1281C>T p.S427S Substitution - coding silent 11:6456445-6456445 - TCGA-EI-6507-01 COSM1561682 c.1336C>T p.R446C Substitution - Missense 11:6456390-6456390 - TCGA-15-0742-01 COSM3398033 c.2088C>G p.F696L Substitution - Missense 11:6449175-6449175 - TCGA-FW-A3R5-06 COSM3869883 c.1280C>T p.S427F Substitution - Missense 11:6456446-6456446 - Au2 COSM5600720 c.1281C>T p.S427S Substitution - coding silent 11:6456445-6456445 - TCGA-AA-3672-01 COSM267636 c.189G>A p.R63R Substitution - coding silent 11:6458239-6458239 - TCGA-B9-4115-01 COSM3986346 c.114G>A p.L38L Substitution - coding silent 11:6465582-6465582 - T3021 COSM930320 c.82C>T p.R28W Substitution - Missense 11:6465614-6465614 - sysucc-311T COSM5477753 c.417C>T p.R139R Substitution - coding silent 11:6457794-6457794 - Mx43 COSM32979 c.1576C>T p.R526* Substitution - Nonsense 11:6451396-6451396 - TCGA-G2-A2EO-01 COSM1298398 c.2131G>A p.E711K Substitution - Missense 11:6449132-6449132 - 2492724 COSM5724918 c.1564C>T p.R522C Substitution - Missense 11:6451408-6451408 - TCGA-AX-A0J1-01 COSM930278 c.2002C>T p.Q668* Substitution - Nonsense 11:6449386-6449386 - PD4127a COSM165129 c.1971C>G p.F657L Substitution - Missense 11:6449417-6449417 - TCGA-CJ-4878-01 COSM3359316 c.1454A>G p.E485G Substitution - Missense 11:6456151-6456151 - TCGA-DW-7840-01 COSM3986344 c.380G>A p.C127Y Substitution - Missense 11:6457831-6457831 - CHEWS006 COSM4574642 c.1845T>C p.R615R Substitution - coding silent 11:6450917-6450917 - TCGA-BG-A0LX-01 COSM930290 c.1110C>T p.D370D Substitution - coding silent 11:6456616-6456616 - BN24 COSM1604994 c.619G>A p.D207N Substitution - Missense 11:6457373-6457373 - TCGA-ES-A2HS-01 COSM4910355 c.1690G>A p.G564S Substitution - Missense 11:6451282-6451282 - TCGA-D9-A6EA-06 COSM4398151 c.1851C>T p.A617A Substitution - coding silent 11:6450911-6450911 - TCGA-02-0083-01 COSM35585 c.1111G>A p.G371S Substitution - Missense 11:6456615-6456615 - TCGA-DD-A119-01 COSM4919844 c.1887T>C p.A629A Substitution - coding silent 11:6450605-6450605 - TCGA-CM-5861-01 COSM1355812 c.1168T>C p.Y390H Substitution - Missense 11:6456558-6456558 - LUAD-S00488 COSM394928 c.2144G>T p.G715V Substitution - Missense 11:6449119-6449119 - 19M COSM5579765 c.1832G>A p.R611H Substitution - Missense 11:6450930-6450930 - BCM723T COSM4956358 c.1005G>A p.A335A Substitution - coding silent 11:6456721-6456721 - TCGA-EE-A3AB-06 COSM3451669 c.1422C>T p.F474F Substitution - coding silent 11:6456304-6456304 - Ad1 COSM4440773 c.759C>A p.S253R Substitution - Missense 11:6456967-6456967 - 05-P8068 COSM4574648 c.12G>A p.R4R Substitution - coding silent 11:6465684-6465684 - CSCC-38-T COSM4470794 c.1682C>T p.S561F Substitution - Missense 11:6451290-6451290 - ccRCC-97 COSM1664680 c.705A>T p.Q235H Substitution - Missense 11:6457021-6457021 - LUAD-S01346 COSM397432 c.2081A>T p.Q694L Substitution - Missense 11:6449307-6449307 - SNU-C4 COSM4615465 c.1421delT p.F474fs*29 Deletion - Frameshift 11:6456305-6456305 - TCGA-AP-A0LM-01 COSM930320 c.82C>T p.R28W Substitution - Missense 11:6465614-6465614 - Pat_32_A COSM5839207 c.1088G>A p.R363H Substitution - Missense 11:6456638-6456638 - PDA_019 COSM4998990 c.343T>G p.C115G Substitution - Missense 11:6458085-6458085 - TCGA-RP-A695-06 COSM4896217 c.399C>T p.A133A Substitution - coding silent 11:6457812-6457812 - 2492700 COSM5600720 c.1281C>T p.S427S Substitution - coding silent 11:6456445-6456445 - 2492701 COSM5715436 c.1824G>A p.L608L Substitution - coding silent 11:6450938-6450938 - UACC-62 COSM1675797 c.1543A>C p.N515H Substitution - Missense 11:6451429-6451429 - U343 COSM5712562 c.1326C>A p.G442G Substitution - coding silent 11:6456400-6456400 - TCGA-AN-A046-01 COSM3810005 c.219C>A p.V73V Substitution - coding silent 11:6458209-6458209 - TCGA-FS-A1YW-06 COSM3451671 c.1107G>A p.P369P Substitution - coding silent 11:6456619-6456619 - PT08_1 COSM5893613 c.311C>T p.P104L Substitution - Missense 11:6458117-6458117 - 2492701 COSM5600720 c.1281C>T p.S427S Substitution - coding silent 11:6456445-6456445 - TCGA-AP-A056-01 COSM930277 c.2088C>T p.F696F Substitution - coding silent 11:6449175-6449175 - TARGET-30-PASTKC COSM1288618 c.795G>A p.P265P Substitution - coding silent 11:6456931-6456931 - TCGA-06-0122-01 COSM35477 c.2207G>A p.C736Y Substitution - Missense 11:6449056-6449056 - 2492725 COSM5724918 c.1564C>T p.R522C Substitution - Missense 11:6451408-6451408 - 9227_T COSM5042351 c.938G>A p.G313D Substitution - Missense 11:6456788-6456788 - PTC-77C COSM2164905 c.330C>G p.G110G Substitution - coding silent 11:6458098-6458098 - CHC1211T COSM4954957 c.1033G>C p.V345L Substitution - Missense 11:6456693-6456693 - TCGA-AP-A0LM-01 COSM930298 c.187C>T p.R63W Substitution - Missense 11:6458241-6458241 - 545 COSM5612778 c.1297C>T p.R433C Substitution - Missense 11:6456429-6456429 - TCGA-AA-3955-01 COSM297087 c.916C>T p.R306W Substitution - Missense 11:6456810-6456810 - TCGA-D9-A4Z3-01 COSM3451668 c.1423C>T p.R475C Substitution - Missense 11:6456303-6456303 - CRC-34T COSM5460749 c.1753C>T p.R585W Substitution - Missense 11:6451009-6451009 - HCT15 COSM2164864 c.1380C>T p.G460G Substitution - coding silent 11:6456346-6456346 - T3505 COSM4736025 c.1392G>A p.K464K Substitution - coding silent 11:6456334-6456334 - PTC-28C COSM4146086 c.603C>T p.I201I Substitution - coding silent 11:6457389-6457389 - P37 COSM1736231 c.385G>T p.A129S Substitution - Missense 11:6457826-6457826 - LUAD_E00522 COSM352405 c.2136A>G p.P712P Substitution - coding silent 11:6449127-6449127 - TCGA-D7-6524-01 COSM4035310 c.663C>T p.S221S Substitution - coding silent 11:6457329-6457329 - sysucc-1128T COSM1243696 c.788C>T p.S263L Substitution - Missense 11:6456938-6456938 - TCGA-EE-A3AC-06 COSM3451672 c.1041C>T p.T347T Substitution - coding silent 11:6456685-6456685 - 587378 COSM1230311 c.479C>T p.A160V Substitution - Missense 11:6457732-6457732 - SNU-C4 COSM2164864 c.1380C>T p.G460G Substitution - coding silent 11:6456346-6456346 - TCGA-D1-A161-01 COSM930291 c.670G>A p.E224K Substitution - Missense 11:6457322-6457322 - TCGA-BH-A18G-01 COSM930289 c.1436G>A p.R479H Substitution - Missense 11:6456169-6456169 - TCGA-24-2262-01 COSM80675 c.747C>T p.G249G Substitution - coding silent 11:6456979-6456979 - TCGA-18-3409-01 COSM689630 c.1416C>T p.L472L Substitution - coding silent 11:6456310-6456310 - TCGA-CM-6172-01 COSM35585 c.1111G>A p.G371S Substitution - Missense 11:6456615-6456615 - TCGA-BS-A0TG-01 COSM930295 c.491G>A p.R164H Substitution - Missense 11:6457720-6457720 - TCGA-EE-A20C-06 COSM2164888 c.615C>T p.F205F Substitution - coding silent 11:6457377-6457377 - CHC1211T COSM4954957 c.1033G>C p.V345L Substitution - Missense 11:6456693-6456693 - TCGA-66-2758-01 COSM689629 c.159G>C p.Q53H Substitution - Missense 11:6458269-6458269 - TCGA-EE-A183-06 COSM3451666 c.1533+1G>A p.? Unknown 11:6456071-6456071 - J33_T COSM3953638 c.1816G>T p.G606C Substitution - Missense 11:6450946-6450946 - TCGA-CL-4957-01 COSM3416112 c.786C>A p.G262G Substitution - coding silent 11:6456940-6456940 - TCGA-D1-A103-01 COSM930279 c.1989C>T p.G663G Substitution - coding silent 11:6449399-6449399 - TCGA-BC-A10Z-01 COSM4936280 c.998G>T p.R333L Substitution - Missense 11:6456728-6456728 - PTC-70C COSM2164905 c.330C>G p.G110G Substitution - coding silent 11:6458098-6458098 - TCGA-EI-6882-01 COSM2164817 c.2222G>A p.R741H Substitution - Missense 11:6449041-6449041 - 53M COSM5595481 c.204C>T p.L68L Substitution - coding silent 11:6458224-6458224 - T207 COSM4736027 c.919C>G p.R307G Substitution - Missense 11:6456807-6456807 - TCGA-EE-A2GD-06 COSM3451673 c.932A>G p.N311S Substitution - Missense 11:6456794-6456794 - I2L-P19Tb-Tumor-Organoid COSM5360777 c.984G>T p.T328T Substitution - coding silent 11:6456742-6456742 - TCGA-18-3415-01 COSM689631 c.1874C>T p.P625L Substitution - Missense 11:6450618-6450618 - 90405 COSM330242 c.1125G>A p.P375P Substitution - coding silent 11:6456601-6456601 - TCGA-BR-6452-01 COSM4035323 c.83G>A p.R28Q Substitution - Missense 11:6465613-6465613 - PT33 COSM5909183 c.1430-7C>T p.? Unknown 11:6456182-6456182 - EGC15 COSM5051009 c.1794C>T p.C598C Substitution - coding silent 11:6450968-6450968 - T3240 COSM2164907 c.270G>A p.Q90Q Substitution - coding silent 11:6458158-6458158 - TCGA-EE-A2MI-06 COSM3451658 c.1563C>T p.F521F Substitution - coding silent 11:6451409-6451409 - TCGA-F4-6856-01 COSM1355813 c.1022C>T p.A341V Substitution - Missense 11:6456704-6456704 - LC_C6 COSM1188151 c.1963T>A p.F655I Substitution - Missense 11:6449425-6449425 - TCGA-BR-4184-01 COSM32979 c.1576C>T p.R526* Substitution - Nonsense 11:6451396-6451396 - PCSI_0080_Pa_P_526 COSM3376014 c.1106C>T p.P369L Substitution - Missense 11:6456620-6456620 - TCGA-EE-A2MC-06 COSM32979 c.1576C>T p.R526* Substitution - Nonsense 11:6451396-6451396 - pfg181T COSM4749313 c.1811C>A p.P604H Substitution - Missense 11:6450951-6450951 - I2L-P19Tb-Tumor-Biopsy COSM5360777 c.984G>T p.T328T Substitution - coding silent 11:6456742-6456742 - cSCCP2 COSM137556 c.746G>A p.G249D Substitution - Missense 11:6456980-6456980 - PTC-515C COSM2164905 c.330C>G p.G110G Substitution - coding silent 11:6458098-6458098 - PT45 COSM5927656 c.298G>A p.E100K Substitution - Missense 11:6458130-6458130 - BCM723T COSM4956358 c.1005G>A p.A335A Substitution - coding silent 11:6456721-6456721 - ME001T COSM221770 c.1310C>A p.S437Y Substitution - Missense 11:6456416-6456416 - 2492702 COSM5715436 c.1824G>A p.L608L Substitution - coding silent 11:6450938-6450938 - CSCC-18-T COSM4456565 c.1014C>T p.G338G Substitution - coding silent 11:6456712-6456712 - ESO-081 COSM1243696 c.788C>T p.S263L Substitution - Missense 11:6456938-6456938 - TCGA-FS-A1ZW-06 COSM689630 c.1416C>T p.L472L Substitution - coding silent 11:6456310-6456310 - CSCC-29-T COSM4471652 c.1732C>T p.P578S Substitution - Missense 11:6451030-6451030 - TCGA-CG-4306-01 COSM4035308 c.1259G>A p.R420H Substitution - Missense 11:6456467-6456467 - CHEWS012 COSM4574645 c.420C>G p.A140A Substitution - coding silent 11:6457791-6457791 - T3021 COSM2164864 c.1380C>T p.G460G Substitution - coding silent 11:6456346-6456346 - TCGA-CG-5733-01 COSM297087 c.916C>T p.R306W Substitution - Missense 11:6456810-6456810 - C086 COSM5540805 c.173C>T p.S58F Substitution - Missense 11:6458255-6458255 - 9 COSM5732521 c.1706A>G p.K569R Substitution - Missense 11:6451056-6451056 - I2L-P31-Tumor-Organoid COSM5126475 c.416G>A p.R139H Substitution - Missense 11:6457795-6457795 - PR-00-1165 COSM247980 c.1565G>A p.R522H Substitution - Missense 11:6451407-6451407 - TCGA-FW-A3R5-06 COSM3869884 c.1120C>T p.L374F Substitution - Missense 11:6456606-6456606 - T1154 COSM4736024 c.1594C>A p.Q532K Substitution - Missense 11:6451378-6451378 - TCGA-EE-A2GI-06 COSM3451654 c.2015C>T p.P672L Substitution - Missense 11:6449373-6449373 - CSCC-31-T COSM2164842 c.1831C>T p.R611C Substitution - Missense 11:6450931-6450931 - TCGA-AP-A0LM-01 COSM930297 c.366G>A p.T122T Substitution - coding silent 11:6457845-6457845 - TCGA-D8-A1J8-01 COSM930289 c.1436G>A p.R479H Substitution - Missense 11:6456169-6456169 - 2492726 COSM5724918 c.1564C>T p.R522C Substitution - Missense 11:6451408-6451408 - TCGA-AA-A010-01 COSM285939 c.2099G>A p.G700D Substitution - Missense 11:6449164-6449164 - TCGA-DA-A1I4-06 COSM3451667 c.1531C>T p.Q511* Substitution - Nonsense 11:6456074-6456074 - TCGA-OK-A5Q2-01 COSM3810003 c.1146G>T p.K382N Substitution - Missense 11:6456580-6456580 - T3724 COSM4736026 c.1102G>A p.G368S Substitution - Missense 11:6456624-6456624 - BK0033 COSM4186959 c.517T>A p.L173M Substitution - Missense 11:6457475-6457475 - TCGA-BR-4370-01 COSM4035309 c.1215C>T p.Y405Y Substitution - coding silent 11:6456511-6456511 - CSCC-30-T COSM4535348 c.217G>A p.V73I Substitution - Missense 11:6458211-6458211 - TCGA-AP-A051-01 COSM930299 c.132A>C p.R44S Substitution - Missense 11:6458296-6458296 - sysucc-1370T COSM5469710 c.1318G>A p.G440S Substitution - Missense 11:6456408-6456408 - 3N31-VS-3T31 COSM4980613 c.1869A>T p.A623A Substitution - coding silent 11:6450893-6450893 - 234 COSM3731089 c.974C>T p.T325M Substitution - Missense 11:6456752-6456752 - Gp2D COSM4611699 c.1108_1109insG p.D370fs*18 Insertion - Frameshift 11:6456617-6456618 - BN24T COSM1604994 c.619G>A p.D207N Substitution - Missense 11:6457373-6457373 - LP6005334-DNA_F03 COSM5036034 c.509G>A p.R170H Substitution - Missense 11:6457702-6457702 - TCGA-BS-A0UF-01 COSM930294 c.548T>C p.V183A Substitution - Missense 11:6457444-6457444 - ESO-083 COSM1268528 c.1610C>G p.T537R Substitution - Missense 11:6451362-6451362 - RKO COSM4647409 c.1284G>A p.P428P Substitution - coding silent 11:6456442-6456442 - Hs-578-T COSM1675797 c.1543A>C p.N515H Substitution - Missense 11:6451429-6451429 - T4 COSM5341665 c.1181C>A p.T394K Substitution - Missense 11:6456545-6456545 - T3225 COSM4736028 c.490C>T p.R164C Substitution - Missense 11:6457721-6457721 - 2492700 COSM5715436 c.1824G>A p.L608L Substitution - coding silent 11:6450938-6450938 - PCSI_0080_Pa_X COSM3376014 c.1106C>T p.P369L Substitution - Missense 11:6456620-6456620 - PT35 COSM5913293 c.2083-8T>A p.? Unknown 11:6449188-6449188 - 2492702 COSM5600720 c.1281C>T p.S427S Substitution - coding silent 11:6456445-6456445 - pfg182T COSM3451670 c.1310C>T p.S437F Substitution - Missense 11:6456416-6456416 - 2492703 COSM5715436 c.1824G>A p.L608L Substitution - coding silent 11:6450938-6450938 - HCC2998 COSM2164888 c.615C>T p.F205F Substitution - coding silent 11:6457377-6457377 - Pat_60_A COSM5839206 c.1472G>A p.G491D Substitution - Missense 11:6456133-6456133 - TCGA-B5-A11H-01 COSM930284 c.1849G>A p.A617T Substitution - Missense 11:6450913-6450913 - TCGA-ER-A193-06 COSM3451670 c.1310C>T p.S437F Substitution - Missense 11:6456416-6456416 - TCGA-BR-8361-01 COSM4035304 c.1917G>A p.T639T Substitution - coding silent 11:6450575-6450575 - Au4 COSM5605180 c.861G>A p.P287P Substitution - coding silent 11:6456865-6456865 - PTC-1C COSM2164905 c.330C>G p.G110G Substitution - coding silent 11:6458098-6458098 - PTC-7C COSM4146085 c.2168C>T p.S723L Substitution - Missense 11:6449095-6449095 - CSCC-55-T COSM4548587 c.450G>T p.L150L Substitution - coding silent 11:6457761-6457761 - CSCC-27-T COSM4480652 c.243C>T p.F81F Substitution - coding silent 11:6458185-6458185 - SC_9029 COSM5561200 c.2070C>T p.N690N Substitution - coding silent 11:6449318-6449318 - CHEWS008 COSM4574644 c.726C>T p.R242R Substitution - coding silent 11:6457000-6457000 - TCGA-CM-6680-01 COSM1355824 c.291C>T p.H97H Substitution - coding silent 11:6458137-6458137 - DLD1 COSM2164864 c.1380C>T p.G460G Substitution - coding silent 11:6456346-6456346 - 587342 COSM1230312 c.635T>C p.L212P Substitution - Missense 11:6457357-6457357 - Pat_45_A COSM5839208 c.953C>T p.T318M Substitution - Missense 11:6456773-6456773 - sysucc-274T COSM5475557 c.1169A>G p.Y390C Substitution - Missense 11:6456557-6456557 - TCGA-CK-5913-01 COSM3752620 c.1067G>A p.R356H Substitution - Missense 11:6456659-6456659 - M14 COSM1675797 c.1543A>C p.N515H Substitution - Missense 11:6451429-6451429 - CP66-MEL COSM24051 c.1629C>T p.T543T Substitution - coding silent 11:6451343-6451343 - PT38 COSM5922932 c.516-7C>T p.? Unknown 11:6457483-6457483 - S00936 COSM316137 c.1579G>T p.G527* Substitution - Nonsense 11:6451393-6451393 - C086 COSM5540806 c.1806C>T p.F602F Substitution - coding silent 11:6450956-6450956 - TCGA-AZ-6601-01 COSM1355814 c.724C>T p.R242C Substitution - Missense 11:6457002-6457002 - UM-SCC-47 COSM4600082 c.365C>T p.T122M Substitution - Missense 11:6457846-6457846 - ASHPC_0025_Pa_P COSM4808169 c.430C>T p.R144C Substitution - Missense 11:6457781-6457781 - TCGA-A5-A0VP-01 COSM930289 c.1436G>A p.R479H Substitution - Missense 11:6456169-6456169 - HCT15 COSM4632571 c.1229G>A p.R410H Substitution - Missense 11:6456497-6456497 - TCGA-D1-A103-01 COSM930296 c.386C>A p.A129D Substitution - Missense 11:6457825-6457825 - Pat_01_B COSM5839203 c.1582C>T p.R528C Substitution - Missense 11:6451390-6451390 - PCSI_0104_Pa_P_526 COSM4961767 c.1258C>T p.R420C Substitution - Missense 11:6456468-6456468 - TCGA-06-0122 COSM35477 c.2207G>A p.C736Y Substitution - Missense 11:6449056-6449056 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.591981;Hs.591983;Hs.591992 11p15.5 602355;605493 2401087|CGAP|BC096827|A/G|coding|Pro375Pro|1355|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A T IntronicSNV . c.1941+145T>A 11 6471636 CM C A Missense p.R410L c.1229G>T 11 6477727 LUAD C A Nonsense p.G527* c.1579G>T 11 6472623 SCLC C G Missense p.G352A c.1055G>C 11 6477901 HNSC C G Missense p.Q53H c.159G>C 11 6479499 LUSC C G Synonymous p.L219L c.657G>C 11 6478565 LUAD C T Missense p.A617T c.1849G>A 11 6472143 UCEC C T Missense p.C736Y c.2207G>A 11 6470286 GBM C T Missense p.D94N c.280G>A 11 6479378 RCCC C T Missense p.E224K c.670G>A 11 6478552 UCEC C T Missense p.E711K c.2131G>A 11 6470362 BLCA C T Missense p.R164H c.491G>A 11 6478950 UCEC C T Missense p.R420H c.1259G>A 11 6477697 STAD C T Missense p.R479H c.1436G>A 11 6477399 UCEC C T Missense p.V501M c.1501G>A 11 6477334 LUAD C T Nonsense p.R526* c.1576C>T 11 6472626 COREAD C T SpliceDonorSNV . c.1533+1G>A 11 6477301 CM C T Synonymous p.P265P c.795G>A 11 6478161 NB C T Synonymous p.P369P c.1107G>A 11 6477849 CM G A 5-UTRSNV . c.1-8730C>T 11 6495655 HC G A IntronicSNV . c.1534-37C>T 11 6472705 CM G A IntronicSNV . c.1534-61C>T 11 6472729 CM G A IntronicSNV . c.1534-82C>T 11 6472750 CM G A IntronicSNV . c.1941+21C>T 11 6471760 CM G A IntronicSNV . c.1942-59C>T 11 6470735 CM G A Missense p.P625L c.1874C>T 11 6471848 LUSC G A Missense p.P672L c.2015C>T 11 6470603 CM G A Missense p.P672S c.2014C>T 11 6470604 CM G A Missense p.R306W c.916C>T 11 6478040 COREAD G A Missense p.R306W c.916C>T 11 6478040 STAD G A Missense p.S437F c.1310C>T 11 6477646 CM G A Missense p.T357I c.1070C>T 11 6477886 STAD G A Nonsense p.Q511* c.1531C>T 11 6477304 CM G A Nonsense p.R526* c.1576C>T 11 6472626 CM G A Synonymous p.F205F c.615C>T 11 6478607 CM G A Synonymous p.F474F c.1422C>T 11 6477534 CM G A Synonymous p.F521F c.1563C>T 11 6472639 CM G A Synonymous p.G249G c.747C>T 11 6478209 OV G A Synonymous p.L219L c.655C>T 11 6478567 CM G A Synonymous p.L472L c.1416C>T 11 6477540 CM G A Synonymous p.S221S c.663C>T 11 6478559 STAD G A Synonymous p.T347T c.1041C>T 11 6477915 CM G A Synonymous p.Y405Y c.1215C>T 11 6477741 STAD G C Missense p.F657L c.1971C>G 11 6470647 BRCA G C Missense p.F696L c.2088C>G 11 6470405 GBM G C Missense p.S514C c.1541C>G 11 6472661 LUAD G C Missense p.T537R c.1610C>G 11 6472592 ESCA G T Missense p.P369Q c.1106C>A 11 6477850 LUAD G T Missense p.S437Y c.1310C>A 11 6477646 CM T A Missense p.E209V c.626A>T 11 6478596 LUAD T A Synonymous p.A623A c.1869A>T 11 6472123 LUAD T C IntronicSNV . c.1534-32A>G 11 6472700 HC T C Missense p.E485G c.1454A>G 11 6477381 RCCC T C Missense p.N311S c.932A>G 11 6478024 CM