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 ACC 11 105924412 105924412 + Missense_Mutation SNP G G T TCGA-OR-A5J8-01A-11D-A29I-10 TCGA-OR-A5J8-10A-01D-A29L-10 g.chr11:105924412G>T c.1004C>A c.(1003-1005)tCt>tAt p.S335Y BLCA 11 105923824 105923824 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr11:105923824C>G c.1592G>C c.(1591-1593)tGg>tCg p.W531S BLCA 11 105923955 105923955 + Silent SNP A A G TCGA-FT-A3EE-01A-11D-A202-08 TCGA-FT-A3EE-10A-01D-A202-08 g.chr11:105923955A>G c.1461T>C c.(1459-1461)tcT>tcC p.S487S BLCA 11 105924026 105924026 + Missense_Mutation SNP C C G TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr11:105924026C>G c.1390G>C c.(1390-1392)Gag>Cag p.E464Q BLCA 11 105924178 105924178 + Missense_Mutation SNP C C G TCGA-2F-A9KR-01A-11D-A38G-08 TCGA-2F-A9KR-10A-01D-A38J-08 g.chr11:105924178C>G c.1238G>C c.(1237-1239)aGa>aCa p.R413T BLCA 11 105924564 105924564 + Silent SNP G G C TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr11:105924564G>C c.852C>G c.(850-852)ctC>ctG p.L284L BLCA 11 105924764 105924764 + Missense_Mutation SNP C C T TCGA-XF-AAMH-01A-11D-A42E-08 TCGA-XF-AAMH-10A-01D-A42H-08 g.chr11:105924764C>T c.652G>A c.(652-654)Gtt>Att p.V218I BLCA 11 105925184 105925184 + Splice_Site SNP T T C TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chr11:105925184T>C c.e3-2 BLCA 11 105929758 105929758 + Missense_Mutation SNP C C G TCGA-KQ-A41P-01A-12D-A339-08 TCGA-KQ-A41P-10F-01D-A339-08 g.chr11:105929758C>G c.67G>C c.(67-69)Gag>Cag p.E23Q BLCA 11 105929784 105929784 + Missense_Mutation SNP C C T TCGA-GV-A3JV-01A-11D-A21Z-08 TCGA-GV-A3JV-10B-01D-A21Z-08 g.chr11:105929784C>T c.41G>A c.(40-42)cGa>cAa p.R14Q BRCA 11 105929688 105929688 + Missense_Mutation SNP C C G TCGA-C8-A27B-01A-11D-A167-09 TCGA-C8-A27B-10A-01D-A167-09 g.chr11:105929688C>G c.137G>C c.(136-138)aGa>aCa p.R46T CESC 11 105923634 105923634 + Silent SNP G G A TCGA-C5-A1MN-01A-11D-A14W-08 TCGA-C5-A1MN-10A-01D-A14W-08 g.chr11:105923634G>A c.1782C>T c.(1780-1782)tgC>tgT p.C594C COAD 11 105923888 105923888 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:105923888T>C c.1528A>G c.(1528-1530)Aca>Gca p.T510A COAD 11 105923933 105923933 + Missense_Mutation SNP G G T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:105923933G>T c.1483C>A c.(1483-1485)Caa>Aaa p.Q495K COAD 11 105923981 105923981 + Missense_Mutation SNP A A G TCGA-AA-3856-01A-01W-0900-09 TCGA-AA-3856-10A-01W-0900-09 g.chr11:105923981A>G c.1435T>C c.(1435-1437)Tac>Cac p.Y479H COAD 11 105924210 105924210 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:105924210G>A c.1206C>T c.(1204-1206)ctC>ctT p.L402L COAD 11 105924396 105924396 + Silent SNP G G A TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr11:105924396G>A c.1020C>T c.(1018-1020)taC>taT p.Y340Y COAD 11 105924396 105924396 + Silent SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr11:105924396G>A c.1020C>T c.(1018-1020)taC>taT p.Y340Y COAD 11 105924396 105924396 + Silent SNP G G A TCGA-CM-6167-01A-11D-1650-10 TCGA-CM-6167-10A-01D-1650-10 g.chr11:105924396G>A c.1020C>T c.(1018-1020)taC>taT p.Y340Y COAD 11 105924397 105924397 + Missense_Mutation SNP T T A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr11:105924397T>A c.1019A>T c.(1018-1020)tAc>tTc p.Y340F COAD 11 105924837 105924837 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:105924837C>T c.579G>A c.(577-579)atG>atA p.M193I COAD 11 105924905 105924905 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:105924905C>T c.511G>A c.(511-513)Gat>Aat p.D171N COAD 11 105925136 105925136 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:105925136T>C c.280A>G c.(280-282)Acc>Gcc p.T94A COAD 11 105929634 105929634 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:105929634G>A c.191C>T c.(190-192)cCg>cTg p.P64L COAD 11 105929663 105929663 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:105929663G>T c.162C>A c.(160-162)ttC>ttA p.F54L COAD 11 105929663 105929663 + Missense_Mutation SNP G G T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:105929663G>T c.162C>A c.(160-162)ttC>ttA p.F54L COAD 11 105929664 105929664 + Missense_Mutation SNP A A T TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr11:105929664A>T c.161T>A c.(160-162)tTc>tAc p.F54Y COADREAD 11 105923757 105923757 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:105923757A>G c.1659T>C c.(1657-1659)atT>atC p.I553I COADREAD 11 105923888 105923888 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:105923888T>C c.1528A>G c.(1528-1530)Aca>Gca p.T510A COADREAD 11 105923933 105923933 + Missense_Mutation SNP G G T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:105923933G>T c.1483C>A c.(1483-1485)Caa>Aaa p.Q495K COADREAD 11 105923981 105923981 + Missense_Mutation SNP A A G TCGA-AA-3856-01A-01W-0900-09 TCGA-AA-3856-10A-01W-0900-09 g.chr11:105923981A>G c.1435T>C c.(1435-1437)Tac>Cac p.Y479H COADREAD 11 105924155 105924155 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:105924155G>T c.1261C>A c.(1261-1263)Ctc>Atc p.L421I COADREAD 11 105924210 105924210 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:105924210G>A c.1206C>T c.(1204-1206)ctC>ctT p.L402L COADREAD 11 105924350 105924350 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:105924350G>A c.1066C>T c.(1066-1068)Cga>Tga p.R356* COADREAD 11 105924396 105924396 + Silent SNP G G A TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr11:105924396G>A c.1020C>T c.(1018-1020)taC>taT p.Y340Y COADREAD 11 105924396 105924396 + Silent SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr11:105924396G>A c.1020C>T c.(1018-1020)taC>taT p.Y340Y COADREAD 11 105924396 105924396 + Silent SNP G G A TCGA-CM-6167-01A-11D-1650-10 TCGA-CM-6167-10A-01D-1650-10 g.chr11:105924396G>A c.1020C>T c.(1018-1020)taC>taT p.Y340Y COADREAD 11 105924397 105924397 + Missense_Mutation SNP T T A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr11:105924397T>A c.1019A>T c.(1018-1020)tAc>tTc p.Y340F COADREAD 11 105924837 105924837 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:105924837C>T c.579G>A c.(577-579)atG>atA p.M193I COADREAD 11 105924905 105924905 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:105924905C>T c.511G>A c.(511-513)Gat>Aat p.D171N COADREAD 11 105925136 105925136 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:105925136T>C c.280A>G c.(280-282)Acc>Gcc p.T94A COADREAD 11 105929634 105929634 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:105929634G>A c.191C>T c.(190-192)cCg>cTg p.P64L COADREAD 11 105929663 105929663 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:105929663G>T c.162C>A c.(160-162)ttC>ttA p.F54L COADREAD 11 105929663 105929663 + Missense_Mutation SNP G G T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:105929663G>T c.162C>A c.(160-162)ttC>ttA p.F54L COADREAD 11 105929664 105929664 + Missense_Mutation SNP A A T TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr11:105929664A>T c.161T>A c.(160-162)tTc>tAc p.F54Y ESCA 11 105923578 105923578 + Nonstop_Mutation SNP C C G TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr11:105923578C>G c.1838G>C c.(1837-1839)tGa>tCa p.*613S ESCA 11 105923925 105923925 + Frame_Shift_Del DEL A A - TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr11:105923925delA c.1491delT c.(1489-1491)tttfs p.F497fs ESCA 11 105929763 105929763 + Missense_Mutation SNP G G C TCGA-L5-A88W-01A-11D-A351-09 TCGA-L5-A88W-11A-11D-A351-09 g.chr11:105929763G>C c.62C>G c.(61-63)cCa>cGa p.P21R GBMLGG 11 105929784 105929784 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:105929784C>T c.41G>A c.(40-42)cGa>cAa p.R14Q HNSC 11 105923623 105923623 + Missense_Mutation SNP T T G TCGA-CN-A63V-01A-11D-A28R-08 TCGA-CN-A63V-10A-01D-A28U-08 g.chr11:105923623T>G c.1793A>C c.(1792-1794)cAg>cCg p.Q598P HNSC 11 105923675 105923675 + Missense_Mutation SNP C C G TCGA-QK-A8Z8-01A-11D-A391-08 TCGA-QK-A8Z8-10A-01D-A394-08 g.chr11:105923675C>G c.1741G>C c.(1741-1743)Gaa>Caa p.E581Q HNSC 11 105923992 105923992 + Missense_Mutation SNP C C A TCGA-CV-5439-01A-01D-1683-08 TCGA-CV-5439-11B-01D-1683-08 g.chr11:105923992C>A c.1424G>T c.(1423-1425)tGc>tTc p.C475F HNSC 11 105924349 105924349 + Missense_Mutation SNP C C T TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr11:105924349C>T c.1067G>A c.(1066-1068)cGa>cAa p.R356Q HNSC 11 105924356 105924356 + Missense_Mutation SNP A A T TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr11:105924356A>T c.1060T>A c.(1060-1062)Tgt>Agt p.C354S HNSC 11 105924371 105924371 + Missense_Mutation SNP C C T TCGA-BA-6872-01A-11D-1870-08 TCGA-BA-6872-10A-01D-1870-08 g.chr11:105924371C>T c.1045G>A c.(1045-1047)Ggt>Agt p.G349S HNSC 11 105924557 105924557 + Missense_Mutation SNP C C A TCGA-CQ-A4CG-01A-11D-A25Y-08 TCGA-CQ-A4CG-10A-01D-A25Y-08 g.chr11:105924557C>A c.859G>T c.(859-861)Gat>Tat p.D287Y HNSC 11 105924580 105924580 + Missense_Mutation SNP T T G TCGA-CR-7371-01A-11D-2012-08 TCGA-CR-7371-10A-01D-2013-08 g.chr11:105924580T>G c.836A>C c.(835-837)cAa>cCa p.Q279P HNSC 11 105924819 105924819 + Missense_Mutation SNP C C G TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr11:105924819C>G c.597G>C c.(595-597)caG>caC p.Q199H HNSC 11 105925058 105925058 + Missense_Mutation SNP C C A TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr11:105925058C>A c.358G>T c.(358-360)Gat>Tat p.D120Y KIPAN 11 105923709 105923709 + Silent SNP C C A TCGA-SX-A7SQ-01A-12D-A35Z-10 TCGA-SX-A7SQ-10A-01D-A35Z-10 g.chr11:105923709C>A c.1707G>T c.(1705-1707)gtG>gtT p.V569V KIPAN 11 105924485 105924486 + Frame_Shift_Del DEL TA TA - TCGA-BP-5195-01A-02D-1429-08 TCGA-BP-5195-11A-01D-1429-08 g.chr11:105924485_105924486delTA c.930_931delTA c.(928-933)tatacafs p.T311fs KIPAN 11 105925034 105925034 + Missense_Mutation SNP A A T TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr11:105925034A>T c.382T>A c.(382-384)Ttg>Atg p.L128M KIRC 11 105924485 105924486 + Frame_Shift_Del DEL TA TA - TCGA-BP-5195-01A-02D-1429-08 TCGA-BP-5195-11A-01D-1429-08 g.chr11:105924485_105924486delTA c.930_931delTA c.(928-933)tatacafs p.T311fs KIRP 11 105923709 105923709 + Silent SNP C C A TCGA-SX-A7SQ-01A-12D-A35Z-10 TCGA-SX-A7SQ-10A-01D-A35Z-10 g.chr11:105923709C>A c.1707G>T c.(1705-1707)gtG>gtT p.V569V KIRP 11 105925034 105925034 + Missense_Mutation SNP A A T TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr11:105925034A>T c.382T>A c.(382-384)Ttg>Atg p.L128M LGG 11 105929784 105929784 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:105929784C>T c.41G>A c.(40-42)cGa>cAa p.R14Q LIHC 11 105923599 105923600 + Missense_Mutation DNP CA CA AT TCGA-DD-AACB-01A-11D-A40R-10 TCGA-DD-AACB-10A-01D-A40U-10 g.chr11:105923599_105923600CA>AT c.1816_1817TG>AT c.(1816-1818)TGg>ATg p.W606M LIHC 11 105924774 105924774 + Missense_Mutation SNP C C T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr11:105924774C>T c.642G>A c.(640-642)atG>atA p.M214I LIHC 11 105925003 105925003 + Missense_Mutation SNP G G C TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr11:105925003G>C c.413C>G c.(412-414)tCc>tGc p.S138C LIHC 11 105925003 105925003 + Missense_Mutation SNP G G C TCGA-G3-A25S-01A-11D-A16V-10 TCGA-G3-A25S-10A-01D-A16V-10 g.chr11:105925003G>C c.413C>G c.(412-414)tCc>tGc p.S138C LUAD 11 105923631 105923631 + Missense_Mutation SNP C C A TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr11:105923631C>A c.1785G>T c.(1783-1785)caG>caT p.Q595H LUAD 11 105923999 105923999 + Missense_Mutation SNP G G A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr11:105923999G>A c.1417C>T c.(1417-1419)Ctt>Ttt p.L473F LUAD 11 105924081 105924081 + Nonsense_Mutation SNP G G C TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr11:105924081G>C c.1335C>G c.(1333-1335)taC>taG p.Y445* LUAD 11 105924167 105924167 + Frame_Shift_Del DEL C C - TCGA-44-2657-01A-01D-1105-08 TCGA-44-2657-10A-01D-1105-08 g.chr11:105924167delC c.1249delG c.(1249-1251)gacfs p.D417fs LUAD 11 105924887 105924887 + Missense_Mutation SNP C C A TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chr11:105924887C>A c.529G>T c.(529-531)Gta>Tta p.V177L LUAD 11 105925069 105925069 + Missense_Mutation SNP T T A TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chr11:105925069T>A c.347A>T c.(346-348)aAa>aTa p.K116I LUAD 11 105925172 105925172 + Missense_Mutation SNP C C T TCGA-55-7283-01A-11D-2036-08 TCGA-55-7283-10A-01D-2036-08 g.chr11:105925172C>T c.244G>A c.(244-246)Gaa>Aaa p.E82K LUAD 11 105929753 105929753 + Missense_Mutation SNP C C A TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr11:105929753C>A c.72G>T c.(70-72)aaG>aaT p.K24N LUAD 11 105929812 105929812 + Missense_Mutation SNP T T C TCGA-L4-A4E5-01A-11D-A24P-08 TCGA-L4-A4E5-10A-01D-A24P-08 g.chr11:105929812T>C c.13A>G c.(13-15)Atg>Gtg p.M5V LUSC 11 105923716 105923716 + Missense_Mutation SNP T T G TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chr11:105923716T>G c.1700A>C c.(1699-1701)gAt>gCt p.D567A LUSC 11 105923774 105923774 + Nonsense_Mutation SNP C C A TCGA-22-4599-01A-01D-1441-08 TCGA-22-4599-11A-01D-1441-08 g.chr11:105923774C>A c.1642G>T c.(1642-1644)Gga>Tga p.G548* LUSC 11 105924321 105924321 + Silent SNP T T C TCGA-34-5927-01A-11D-1817-08 TCGA-34-5927-10A-01D-1817-08 g.chr11:105924321T>C c.1095A>G c.(1093-1095)tcA>tcG p.S365S LUSC 11 105924568 105924568 + Missense_Mutation SNP C C A TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr11:105924568C>A c.848G>T c.(847-849)gGa>gTa p.G283V LUSC 11 105929622 105929622 + Missense_Mutation SNP C C A TCGA-21-1077-01A-01D-1521-08 TCGA-21-1077-11A-01D-1521-08 g.chr11:105929622C>A c.203G>T c.(202-204)tGt>tTt p.C68F OV 11 105929663 105929663 + Missense_Mutation SNP G G T TCGA-13-1497-01A-01W-0549-09 TCGA-13-1497-10A-01W-0549-09 g.chr11:105929663G>T c.162C>A c.(160-162)ttC>ttA p.F54L PAAD 11 105924236 105924236 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:105924236T>C c.1180A>G c.(1180-1182)Acc>Gcc p.T394A PAAD 11 105929591 105929591 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:105929591C>A c.e1+1 PRAD 11 105925166 105925166 + Missense_Mutation SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:105925166T>C c.250A>G c.(250-252)Aac>Gac p.N84D PRAD 11 105929646 105929646 + Missense_Mutation SNP T T C TCGA-KK-A8IG-01A-11D-A364-08 TCGA-KK-A8IG-11A-11D-A362-08 g.chr11:105929646T>C c.179A>G c.(178-180)gAt>gGt p.D60G READ 11 105923757 105923757 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:105923757A>G c.1659T>C c.(1657-1659)atT>atC p.I553I READ 11 105924155 105924155 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:105924155G>T c.1261C>A c.(1261-1263)Ctc>Atc p.L421I READ 11 105924350 105924350 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:105924350G>A c.1066C>T c.(1066-1068)Cga>Tga p.R356* SKCM 11 105923628 105923628 + Silent SNP C C T TCGA-EE-A29G-06A-12D-A196-08 TCGA-EE-A29G-10A-01D-A198-08 g.chr11:105923628C>T c.1788G>A c.(1786-1788)gtG>gtA p.V596V SKCM 11 105923920 105923920 + Missense_Mutation SNP G G T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr11:105923920G>T c.1496C>A c.(1495-1497)gCa>gAa p.A499E SKCM 11 105924005 105924005 + Missense_Mutation SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr11:105924005G>A c.1411C>T c.(1411-1413)Cca>Tca p.P471S SKCM 11 105924093 105924093 + Silent SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr11:105924093G>A c.1323C>T c.(1321-1323)ccC>ccT p.P441P SKCM 11 105924095 105924095 + Missense_Mutation SNP G G A TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr11:105924095G>A c.1321C>T c.(1321-1323)Ccc>Tcc p.P441S SKCM 11 105924522 105924522 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr11:105924522G>A c.894C>T c.(892-894)ttC>ttT p.F298F SKCM 11 105924695 105924695 + Missense_Mutation SNP C C T TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr11:105924695C>T c.721G>A c.(721-723)Gtg>Atg p.V241M SKCM 11 105925012 105925012 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr11:105925012G>A c.404C>T c.(403-405)tCc>tTc p.S135F SKCM 11 105929598 105929598 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:105929598A>C c.227T>G c.(226-228)tTt>tGt p.F76C SKCM 11 105929626 105929626 + Missense_Mutation SNP G G A TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr11:105929626G>A c.199C>T c.(199-201)Cgt>Tgt p.R67C

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 105923824 105923824 single base substitution C G downstream_gene_variant BLCA-US 11 105923824 105923824 single base substitution C G missense_variant W452S 1355G>C BLCA-US 11 105923824 105923824 single base substitution C G missense_variant W531S 1592G>C BLCA-US 11 105923955 105923955 single base substitution A G downstream_gene_variant BLCA-US 11 105923955 105923955 single base substitution A G synonymous_variant S408S 1224T>C BLCA-US 11 105923955 105923955 single base substitution A G synonymous_variant S487S 1461T>C BLCA-US 11 105924026 105924026 single base substitution C G downstream_gene_variant BLCA-US 11 105924026 105924026 single base substitution C G missense_variant E385Q 1153G>C BLCA-US 11 105924026 105924026 single base substitution C G missense_variant E464Q 1390G>C BLCA-US 11 105929784 105929784 single base substitution C T exon_variant BLCA-US 11 105929784 105929784 single base substitution C T intron_variant BLCA-US 11 105929784 105929784 single base substitution C T missense_variant R14Q 41G>A BOCA-FR 11 105917251 105917251 single base substitution G A downstream_gene_variant BRCA-EU 11 105916978 105916978 single base substitution C A downstream_gene_variant BRCA-EU 11 105917611 105917614 deletion of <=200bp AATT - downstream_gene_variant BRCA-EU 11 105918844 105918844 single base substitution G C downstream_gene_variant BRCA-EU 11 105919367 105919367 insertion of <=200bp - T downstream_gene_variant BRCA-EU 11 105919370 105919370 single base substitution T C downstream_gene_variant BRCA-EU 11 105919483 105919483 single base substitution T C downstream_gene_variant BRCA-EU 11 105920618 105920618 single base substitution C T downstream_gene_variant BRCA-EU 11 105921223 105921223 single base substitution G C downstream_gene_variant BRCA-EU 11 105922292 105922292 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 105922292 105922292 single base substitution G A downstream_gene_variant BRCA-EU 11 105922949 105922949 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 11 105922949 105922949 insertion of <=200bp - A downstream_gene_variant BRCA-EU 11 105923884 105923884 single base substitution A G downstream_gene_variant BRCA-EU 11 105923884 105923884 single base substitution A G missense_variant L432P 1295T>C BRCA-EU 11 105923884 105923884 single base substitution A G missense_variant L511P 1532T>C BRCA-EU 11 105924594 105924594 single base substitution T A downstream_gene_variant BRCA-EU 11 105924594 105924594 single base substitution T A synonymous_variant A195A 585A>T BRCA-EU 11 105924594 105924594 single base substitution T A synonymous_variant A274A 822A>T BRCA-EU 11 105925862 105925862 single base substitution G C downstream_gene_variant BRCA-EU 11 105925862 105925862 single base substitution G C intron_variant BRCA-EU 11 105928333 105928333 single base substitution T C 3_prime_UTR_variant BRCA-EU 11 105928333 105928333 single base substitution T C downstream_gene_variant BRCA-EU 11 105928333 105928333 single base substitution T C intron_variant BRCA-EU 11 105928818 105928818 single base substitution C A downstream_gene_variant BRCA-EU 11 105928818 105928818 single base substitution C A intron_variant BRCA-EU 11 105928894 105928894 single base substitution G A downstream_gene_variant BRCA-EU 11 105928894 105928894 single base substitution G A intron_variant BRCA-EU 11 105930529 105930529 single base substitution C T intron_variant BRCA-EU 11 105930529 105930529 single base substitution C T upstream_gene_variant BRCA-EU 11 105930616 105930616 single base substitution G C intron_variant BRCA-EU 11 105930616 105930616 single base substitution G C upstream_gene_variant BRCA-EU 11 105931311 105931311 single base substitution G A intron_variant BRCA-EU 11 105931311 105931311 single base substitution G A upstream_gene_variant BRCA-EU 11 105931663 105931663 single base substitution A T intron_variant BRCA-EU 11 105931663 105931663 single base substitution A T upstream_gene_variant BRCA-EU 11 105934322 105934322 single base substitution G T intron_variant BRCA-EU 11 105934322 105934322 single base substitution G T upstream_gene_variant BRCA-EU 11 105935617 105935617 single base substitution A G intron_variant BRCA-EU 11 105936454 105936454 single base substitution G A intron_variant BRCA-EU 11 105937055 105937055 single base substitution C G intron_variant BRCA-EU 11 105938442 105938442 insertion of <=200bp - A intron_variant BRCA-EU 11 105938506 105938506 single base substitution C A intron_variant BRCA-EU 11 105939066 105939066 single base substitution G A intron_variant BRCA-EU 11 105939068 105939068 single base substitution T A intron_variant BRCA-EU 11 105939623 105939623 single base substitution T G intron_variant BRCA-EU 11 105940139 105940139 single base substitution G C intron_variant BRCA-EU 11 105942751 105942751 single base substitution A T downstream_gene_variant BRCA-EU 11 105942751 105942751 single base substitution A T intron_variant BRCA-EU 11 105944618 105944618 single base substitution G A downstream_gene_variant BRCA-EU 11 105944618 105944618 single base substitution G A intron_variant BRCA-EU 11 105944841 105944841 single base substitution C A downstream_gene_variant BRCA-EU 11 105944841 105944841 single base substitution C A intron_variant BRCA-EU 11 105944843 105944843 single base substitution C A downstream_gene_variant BRCA-EU 11 105944843 105944843 single base substitution C A intron_variant BRCA-EU 11 105945771 105945771 single base substitution G A downstream_gene_variant BRCA-EU 11 105945771 105945771 single base substitution G A intron_variant BRCA-EU 11 105950189 105950189 single base substitution A C upstream_gene_variant BRCA-EU 11 105952115 105952115 single base substitution C T upstream_gene_variant BRCA-EU 11 105952180 105952180 single base substitution T C upstream_gene_variant BRCA-EU 11 105952394 105952394 single base substitution G A upstream_gene_variant BRCA-EU 11 105952765 105952765 single base substitution A G upstream_gene_variant BRCA-FR 11 105918844 105918844 single base substitution G C downstream_gene_variant BRCA-FR 11 105930616 105930616 single base substitution G C intron_variant BRCA-FR 11 105930616 105930616 single base substitution G C upstream_gene_variant BRCA-FR 11 105937055 105937055 single base substitution C G intron_variant BRCA-FR 11 105940139 105940139 single base substitution G C intron_variant BRCA-FR 11 105942751 105942751 single base substitution A T downstream_gene_variant BRCA-FR 11 105942751 105942751 single base substitution A T intron_variant BRCA-KR 11 105924317 105924317 single base substitution G A downstream_gene_variant BRCA-KR 11 105924317 105924317 single base substitution G A missense_variant H288Y 862C>T BRCA-KR 11 105924317 105924317 single base substitution G A missense_variant H367Y 1099C>T BRCA-KR 11 105924568 105924568 single base substitution C G downstream_gene_variant BRCA-KR 11 105924568 105924568 single base substitution C G missense_variant G204A 611G>C BRCA-KR 11 105924568 105924568 single base substitution C G missense_variant G283A 848G>C BRCA-KR 11 105924837 105924837 single base substitution C T downstream_gene_variant BRCA-KR 11 105924837 105924837 single base substitution C T missense_variant M114I 342G>A BRCA-KR 11 105924837 105924837 single base substitution C T missense_variant M193I 579G>A BRCA-UK 11 105916978 105916978 single base substitution C A downstream_gene_variant BRCA-UK 11 105929095 105929095 single base substitution G A downstream_gene_variant BRCA-UK 11 105929095 105929095 single base substitution G A intron_variant BRCA-US 11 105929688 105929688 single base substitution C G exon_variant BRCA-US 11 105929688 105929688 single base substitution C G intron_variant BRCA-US 11 105929688 105929688 single base substitution C G missense_variant R46T 137G>C BRCA-US 11 105948464 105948464 single base substitution C G 5_prime_UTR_variant BRCA-US 11 105948464 105948464 single base substitution C G upstream_gene_variant BRCA-US 11 105948530 105948530 single base substitution C T upstream_gene_variant BRCA-US 11 105948531 105948531 single base substitution G A upstream_gene_variant BTCA-JP 11 105923886 105923886 single base substitution T C downstream_gene_variant BTCA-JP 11 105923886 105923886 single base substitution T C synonymous_variant T431T 1293A>G BTCA-JP 11 105923886 105923886 single base substitution T C synonymous_variant T510T 1530A>G BTCA-JP 11 105924779 105924779 single base substitution C T downstream_gene_variant BTCA-JP 11 105924779 105924779 single base substitution C T missense_variant E134K 400G>A BTCA-JP 11 105924779 105924779 single base substitution C T missense_variant E213K 637G>A BTCA-JP 11 105924957 105924957 single base substitution A T downstream_gene_variant BTCA-JP 11 105924957 105924957 single base substitution A T missense_variant N153K 459T>A BTCA-JP 11 105924957 105924957 single base substitution A T missense_variant N74K 222T>A CESC-US 11 105923634 105923634 single base substitution G A downstream_gene_variant CESC-US 11 105923634 105923634 single base substitution G A synonymous_variant C515C 1545C>T CESC-US 11 105923634 105923634 single base substitution G A synonymous_variant C594C 1782C>T CLLE-ES 11 105940890 105940890 single base substitution C T intron_variant CLLE-ES 11 105947727 105947737 deletion of <=200bp GCCTCTGCTCG - intron_variant CLLE-ES 11 105947727 105947737 deletion of <=200bp GCCTCTGCTCG - upstream_gene_variant CLLE-ES 11 105948641 105948641 single base substitution T A upstream_gene_variant COAD-US 11 105925136 105925136 single base substitution T C downstream_gene_variant COAD-US 11 105925136 105925136 single base substitution T C missense_variant T15A 43A>G COAD-US 11 105925136 105925136 single base substitution T C missense_variant T94A 280A>G COAD-US 11 105929626 105929626 single base substitution G A exon_variant COAD-US 11 105929626 105929626 single base substitution G A intron_variant COAD-US 11 105929626 105929626 single base substitution G A missense_variant R67C 199C>T COAD-US 11 105929634 105929634 single base substitution G A exon_variant COAD-US 11 105929634 105929634 single base substitution G A intron_variant COAD-US 11 105929634 105929634 single base substitution G A missense_variant P64L 191C>T COCA-CN 11 105923757 105923757 single base substitution A C downstream_gene_variant COCA-CN 11 105923757 105923757 single base substitution A C missense_variant I474M 1422T>G COCA-CN 11 105923757 105923757 single base substitution A C missense_variant I553M 1659T>G COCA-CN 11 105924402 105924402 single base substitution C T downstream_gene_variant COCA-CN 11 105924402 105924402 single base substitution C T synonymous_variant S259S 777G>A COCA-CN 11 105924402 105924402 single base substitution C T synonymous_variant S338S 1014G>A COCA-CN 11 105924650 105924650 single base substitution A G downstream_gene_variant COCA-CN 11 105924650 105924650 single base substitution A G missense_variant F177L 529T>C COCA-CN 11 105924650 105924650 single base substitution A G missense_variant F256L 766T>C COCA-CN 11 105925024 105925024 single base substitution A C downstream_gene_variant COCA-CN 11 105925024 105925024 single base substitution A C missense_variant F131C 392T>G COCA-CN 11 105925024 105925024 single base substitution A C missense_variant F52C 155T>G COCA-CN 11 105948546 105948546 single base substitution G A upstream_gene_variant COCA-CN 11 105950307 105950307 single base substitution G A upstream_gene_variant COCA-CN 11 105950319 105950319 single base substitution G A upstream_gene_variant EOPC-DE 11 105935907 105935907 single base substitution G A intron_variant EOPC-DE 11 105951274 105951274 single base substitution A G upstream_gene_variant EOPC-DE 11 105953095 105953095 single base substitution G A upstream_gene_variant ESAD-UK 11 105917146 105917146 single base substitution G C downstream_gene_variant ESAD-UK 11 105917378 105917378 single base substitution A C downstream_gene_variant ESAD-UK 11 105917930 105917930 single base substitution G A downstream_gene_variant ESAD-UK 11 105918046 105918046 single base substitution G C downstream_gene_variant ESAD-UK 11 105918657 105918657 single base substitution A C downstream_gene_variant ESAD-UK 11 105921360 105921360 single base substitution G T downstream_gene_variant ESAD-UK 11 105922655 105922655 single base substitution T C 3_prime_UTR_variant ESAD-UK 11 105922655 105922655 single base substitution T C downstream_gene_variant ESAD-UK 11 105923176 105923176 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 105923176 105923176 single base substitution G A downstream_gene_variant ESAD-UK 11 105924149 105924149 single base substitution C A downstream_gene_variant ESAD-UK 11 105924149 105924149 single base substitution C A missense_variant D344Y 1030G>T ESAD-UK 11 105924149 105924149 single base substitution C A missense_variant D423Y 1267G>T ESAD-UK 11 105924238 105924238 single base substitution C T downstream_gene_variant ESAD-UK 11 105924238 105924238 single base substitution C T missense_variant R314K 941G>A ESAD-UK 11 105924238 105924238 single base substitution C T missense_variant R393K 1178G>A ESAD-UK 11 105925113 105925113 single base substitution C T downstream_gene_variant ESAD-UK 11 105925113 105925113 single base substitution C T synonymous_variant K101K 303G>A ESAD-UK 11 105925113 105925113 single base substitution C T synonymous_variant K22K 66G>A ESAD-UK 11 105925185 105925185 single base substitution G T downstream_gene_variant ESAD-UK 11 105925185 105925185 single base substitution G T intron_variant ESAD-UK 11 105925609 105925609 single base substitution C G downstream_gene_variant ESAD-UK 11 105925609 105925609 single base substitution C G intron_variant ESAD-UK 11 105926425 105926425 single base substitution T C downstream_gene_variant ESAD-UK 11 105926425 105926425 single base substitution T C intron_variant ESAD-UK 11 105928088 105928088 single base substitution G C downstream_gene_variant ESAD-UK 11 105928088 105928088 single base substitution G C intron_variant ESAD-UK 11 105928290 105928290 single base substitution T C 3_prime_UTR_variant ESAD-UK 11 105928290 105928290 single base substitution T C downstream_gene_variant ESAD-UK 11 105928290 105928290 single base substitution T C intron_variant ESAD-UK 11 105929368 105929368 single base substitution C T downstream_gene_variant ESAD-UK 11 105929368 105929368 single base substitution C T intron_variant ESAD-UK 11 105930025 105930025 insertion of <=200bp - C intron_variant ESAD-UK 11 105930025 105930025 insertion of <=200bp - C upstream_gene_variant ESAD-UK 11 105931607 105931607 single base substitution T C intron_variant ESAD-UK 11 105931607 105931607 single base substitution T C upstream_gene_variant ESAD-UK 11 105932053 105932053 single base substitution G A intron_variant ESAD-UK 11 105932053 105932053 single base substitution G A upstream_gene_variant ESAD-UK 11 105932593 105932594 deletion of <=200bp TG - intron_variant ESAD-UK 11 105932593 105932594 deletion of <=200bp TG - upstream_gene_variant ESAD-UK 11 105934257 105934257 single base substitution A G intron_variant ESAD-UK 11 105934257 105934257 single base substitution A G upstream_gene_variant ESAD-UK 11 105934361 105934361 single base substitution T C intron_variant ESAD-UK 11 105934361 105934361 single base substitution T C upstream_gene_variant ESAD-UK 11 105934841 105934841 single base substitution G T intron_variant ESAD-UK 11 105935176 105935176 single base substitution C T intron_variant ESAD-UK 11 105935210 105935210 single base substitution G T intron_variant ESAD-UK 11 105936506 105936506 single base substitution G C intron_variant ESAD-UK 11 105937414 105937414 single base substitution G C intron_variant ESAD-UK 11 105937605 105937605 single base substitution C T intron_variant ESAD-UK 11 105941085 105941085 single base substitution A C intron_variant ESAD-UK 11 105941874 105941874 single base substitution T G downstream_gene_variant ESAD-UK 11 105941874 105941874 single base substitution T G intron_variant ESAD-UK 11 105942527 105942527 single base substitution G C downstream_gene_variant ESAD-UK 11 105942527 105942527 single base substitution G C intron_variant ESAD-UK 11 105943019 105943019 single base substitution A C downstream_gene_variant ESAD-UK 11 105943019 105943019 single base substitution A C intron_variant ESAD-UK 11 105943296 105943296 single base substitution A T downstream_gene_variant ESAD-UK 11 105943296 105943296 single base substitution A T intron_variant ESAD-UK 11 105943492 105943492 single base substitution T C downstream_gene_variant ESAD-UK 11 105943492 105943492 single base substitution T C intron_variant ESAD-UK 11 105943493 105943493 single base substitution T G downstream_gene_variant ESAD-UK 11 105943493 105943493 single base substitution T G intron_variant ESAD-UK 11 105944848 105944848 single base substitution C A downstream_gene_variant ESAD-UK 11 105944848 105944848 single base substitution C A intron_variant ESAD-UK 11 105948183 105948183 single base substitution C T 5_prime_UTR_variant ESAD-UK 11 105948183 105948183 single base substitution C T upstream_gene_variant ESAD-UK 11 105948208 105948208 single base substitution T C 5_prime_UTR_variant ESAD-UK 11 105948208 105948208 single base substitution T C upstream_gene_variant ESAD-UK 11 105948363 105948363 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 11 105948363 105948363 single base substitution G A upstream_gene_variant ESAD-UK 11 105948769 105948769 single base substitution C T upstream_gene_variant ESAD-UK 11 105949257 105949257 single base substitution A G upstream_gene_variant ESAD-UK 11 105949600 105949600 single base substitution G A upstream_gene_variant ESAD-UK 11 105949918 105949918 single base substitution G T upstream_gene_variant ESAD-UK 11 105950113 105950113 deletion of <=200bp A - upstream_gene_variant ESAD-UK 11 105950607 105950607 single base substitution C T upstream_gene_variant ESCA-CN 11 105929711 105929711 single base substitution G A exon_variant ESCA-CN 11 105929711 105929711 single base substitution G A intron_variant ESCA-CN 11 105929711 105929711 single base substitution G A synonymous_variant I38I 114C>T ESCA-CN 11 105948356 105948356 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESCA-CN 11 105948356 105948356 single base substitution G A upstream_gene_variant GACA-CN 11 105924650 105924650 single base substitution A C downstream_gene_variant GACA-CN 11 105924650 105924650 single base substitution A C missense_variant F177V 529T>G GACA-CN 11 105924650 105924650 single base substitution A C missense_variant F256V 766T>G KIRC-US 11 105924485 105924486 deletion of <=200bp TA - downstream_gene_variant KIRC-US 11 105924485 105924486 deletion of <=200bp TA - frameshift_variant YT231 KIRC-US 11 105924485 105924486 deletion of <=200bp TA - frameshift_variant YT310 KIRP-US 11 105925034 105925034 single base substitution A T downstream_gene_variant KIRP-US 11 105925034 105925034 single base substitution A T missense_variant L128M 382T>A KIRP-US 11 105925034 105925034 single base substitution A T missense_variant L49M 145T>A LAML-KR 11 105948666 105948666 single base substitution T G upstream_gene_variant LICA-FR 11 105924590 105924590 single base substitution T A downstream_gene_variant LICA-FR 11 105924590 105924590 single base substitution T A stop_gained K197* 589A>T LICA-FR 11 105924590 105924590 single base substitution T A stop_gained K276* 826A>T LICA-FR 11 105948583 105948583 single base substitution G A upstream_gene_variant LIHC-US 11 105924774 105924774 single base substitution C T downstream_gene_variant LIHC-US 11 105924774 105924774 single base substitution C T missense_variant M135I 405G>A LIHC-US 11 105924774 105924774 single base substitution C T missense_variant M214I 642G>A LIHC-US 11 105925003 105925003 single base substitution G C downstream_gene_variant LIHC-US 11 105925003 105925003 single base substitution G C missense_variant S138C 413C>G LIHC-US 11 105925003 105925003 single base substitution G C missense_variant S59C 176C>G LINC-JP 11 105921453 105921453 single base substitution C A downstream_gene_variant LINC-JP 11 105923132 105923132 single base substitution T C 3_prime_UTR_variant LINC-JP 11 105923132 105923132 single base substitution T C downstream_gene_variant LINC-JP 11 105923510 105923510 single base substitution T C 3_prime_UTR_variant LINC-JP 11 105923510 105923510 single base substitution T C downstream_gene_variant LIRI-JP 11 105916831 105916831 single base substitution G T downstream_gene_variant LIRI-JP 11 105918826 105918826 deletion of <=200bp C - downstream_gene_variant LIRI-JP 11 105918881 105918881 single base substitution A T downstream_gene_variant LIRI-JP 11 105920408 105920408 single base substitution T C downstream_gene_variant LIRI-JP 11 105922352 105922352 single base substitution C A 3_prime_UTR_variant LIRI-JP 11 105922352 105922352 single base substitution C A downstream_gene_variant LIRI-JP 11 105925729 105925729 single base substitution T C downstream_gene_variant LIRI-JP 11 105925729 105925729 single base substitution T C intron_variant LIRI-JP 11 105925743 105925743 single base substitution A T downstream_gene_variant LIRI-JP 11 105925743 105925743 single base substitution A T intron_variant LIRI-JP 11 105926067 105926067 single base substitution T C downstream_gene_variant LIRI-JP 11 105926067 105926067 single base substitution T C intron_variant LIRI-JP 11 105927347 105927347 single base substitution T C downstream_gene_variant LIRI-JP 11 105927347 105927347 single base substitution T C intron_variant LIRI-JP 11 105930913 105930913 single base substitution T C intron_variant LIRI-JP 11 105930913 105930913 single base substitution T C upstream_gene_variant LIRI-JP 11 105932155 105932155 single base substitution T C intron_variant LIRI-JP 11 105932155 105932155 single base substitution T C upstream_gene_variant LIRI-JP 11 105934110 105934110 single base substitution T C intron_variant LIRI-JP 11 105934110 105934110 single base substitution T C upstream_gene_variant LIRI-JP 11 105934571 105934571 single base substitution T C intron_variant LIRI-JP 11 105934571 105934571 single base substitution T C upstream_gene_variant LIRI-JP 11 105935164 105935164 single base substitution C A intron_variant LIRI-JP 11 105938446 105938446 single base substitution A G intron_variant LIRI-JP 11 105938651 105938651 single base substitution A T intron_variant LIRI-JP 11 105941565 105941565 single base substitution T C intron_variant LIRI-JP 11 105944731 105944731 single base substitution T A downstream_gene_variant LIRI-JP 11 105944731 105944731 single base substitution T A intron_variant LIRI-JP 11 105949592 105949592 single base substitution C T upstream_gene_variant LIRI-JP 11 105949841 105949841 single base substitution T G upstream_gene_variant LIRI-JP 11 105950293 105950293 single base substitution G A upstream_gene_variant LIRI-JP 11 105950536 105950536 single base substitution G A upstream_gene_variant LUSC-KR 11 105917065 105917065 single base substitution C A downstream_gene_variant LUSC-KR 11 105917971 105917971 single base substitution T C downstream_gene_variant LUSC-KR 11 105919483 105919483 single base substitution T A downstream_gene_variant LUSC-KR 11 105920084 105920084 single base substitution G A downstream_gene_variant LUSC-KR 11 105924210 105924210 single base substitution G A downstream_gene_variant LUSC-KR 11 105924210 105924210 single base substitution G A synonymous_variant L323L 969C>T LUSC-KR 11 105924210 105924210 single base substitution G A synonymous_variant L402L 1206C>T LUSC-KR 11 105927354 105927354 single base substitution T C downstream_gene_variant LUSC-KR 11 105927354 105927354 single base substitution T C intron_variant LUSC-KR 11 105928154 105928154 single base substitution C A 3_prime_UTR_variant LUSC-KR 11 105928154 105928154 single base substitution C A downstream_gene_variant LUSC-KR 11 105928154 105928154 single base substitution C A intron_variant LUSC-KR 11 105931039 105931039 single base substitution T C intron_variant LUSC-KR 11 105931039 105931039 single base substitution T C upstream_gene_variant LUSC-KR 11 105932404 105932404 single base substitution C A intron_variant LUSC-KR 11 105932404 105932404 single base substitution C A upstream_gene_variant LUSC-KR 11 105934376 105934376 single base substitution T C intron_variant LUSC-KR 11 105934376 105934376 single base substitution T C upstream_gene_variant LUSC-KR 11 105935592 105935592 single base substitution A T intron_variant LUSC-KR 11 105941647 105941647 single base substitution G T intron_variant LUSC-KR 11 105943161 105943161 single base substitution G A downstream_gene_variant LUSC-KR 11 105943161 105943161 single base substitution G A intron_variant LUSC-KR 11 105944255 105944255 single base substitution C T downstream_gene_variant LUSC-KR 11 105944255 105944255 single base substitution C T intron_variant LUSC-KR 11 105948113 105948113 single base substitution G A 5_prime_UTR_variant LUSC-KR 11 105948113 105948113 single base substitution G A upstream_gene_variant LUSC-KR 11 105948340 105948340 single base substitution C T 5_prime_UTR_variant LUSC-KR 11 105948340 105948340 single base substitution C T upstream_gene_variant LUSC-US 11 105923716 105923716 single base substitution T G downstream_gene_variant LUSC-US 11 105923716 105923716 single base substitution T G missense_variant D488A 1463A>C LUSC-US 11 105923716 105923716 single base substitution T G missense_variant D567A 1700A>C LUSC-US 11 105923774 105923774 single base substitution C A downstream_gene_variant LUSC-US 11 105923774 105923774 single base substitution C A stop_gained G469* 1405G>T LUSC-US 11 105923774 105923774 single base substitution C A stop_gained G548* 1642G>T LUSC-US 11 105924321 105924321 single base substitution T C downstream_gene_variant LUSC-US 11 105924321 105924321 single base substitution T C synonymous_variant S286S 858A>G LUSC-US 11 105924321 105924321 single base substitution T C synonymous_variant S365S 1095A>G LUSC-US 11 105924568 105924568 single base substitution C A downstream_gene_variant LUSC-US 11 105924568 105924568 single base substitution C A missense_variant G204V 611G>T LUSC-US 11 105924568 105924568 single base substitution C A missense_variant G283V 848G>T LUSC-US 11 105929622 105929622 single base substitution C A exon_variant LUSC-US 11 105929622 105929622 single base substitution C A intron_variant LUSC-US 11 105929622 105929622 single base substitution C A missense_variant C68F 203G>T LUSC-US 11 105948587 105948587 single base substitution G A upstream_gene_variant MALY-DE 11 105916978 105916978 single base substitution C A downstream_gene_variant MALY-DE 11 105923229 105923229 single base substitution T G 3_prime_UTR_variant MALY-DE 11 105923229 105923229 single base substitution T G downstream_gene_variant MALY-DE 11 105925704 105925704 single base substitution G A downstream_gene_variant MALY-DE 11 105925704 105925704 single base substitution G A intron_variant MALY-DE 11 105932380 105932380 single base substitution C G intron_variant MALY-DE 11 105932380 105932380 single base substitution C G upstream_gene_variant MALY-DE 11 105940322 105940322 insertion of <=200bp - A intron_variant MALY-DE 11 105944304 105944304 single base substitution G A downstream_gene_variant MALY-DE 11 105944304 105944304 single base substitution G A intron_variant MELA-AU 11 105916838 105916838 single base substitution G A downstream_gene_variant MELA-AU 11 105916980 105916980 single base substitution G A downstream_gene_variant MELA-AU 11 105917666 105917666 single base substitution G A downstream_gene_variant MELA-AU 11 105918003 105918003 single base substitution A C downstream_gene_variant MELA-AU 11 105918485 105918485 single base substitution G A downstream_gene_variant MELA-AU 11 105918688 105918688 single base substitution C T downstream_gene_variant MELA-AU 11 105918701 105918701 single base substitution A G downstream_gene_variant MELA-AU 11 105919712 105919712 single base substitution T A downstream_gene_variant MELA-AU 11 105919740 105919740 single base substitution C T downstream_gene_variant MELA-AU 11 105919799 105919799 single base substitution G A downstream_gene_variant MELA-AU 11 105919854 105919854 single base substitution G A downstream_gene_variant MELA-AU 11 105920499 105920499 single base substitution T C downstream_gene_variant MELA-AU 11 105920917 105920917 single base substitution G A downstream_gene_variant MELA-AU 11 105920929 105920929 single base substitution A G downstream_gene_variant MELA-AU 11 105921768 105921768 single base substitution A G downstream_gene_variant MELA-AU 11 105922185 105922185 single base substitution A T 3_prime_UTR_variant MELA-AU 11 105922185 105922185 single base substitution A T downstream_gene_variant MELA-AU 11 105922721 105922721 single base substitution T C 3_prime_UTR_variant MELA-AU 11 105922721 105922721 single base substitution T C downstream_gene_variant MELA-AU 11 105922906 105922907 deletion of <=200bp GA - 3_prime_UTR_variant MELA-AU 11 105922906 105922907 deletion of <=200bp GA - downstream_gene_variant MELA-AU 11 105923606 105923606 single base substitution C T downstream_gene_variant MELA-AU 11 105923606 105923606 single base substitution C T missense_variant D525N 1573G>A MELA-AU 11 105923606 105923606 single base substitution C T missense_variant D604N 1810G>A MELA-AU 11 105924176 105924176 single base substitution C T downstream_gene_variant MELA-AU 11 105924176 105924176 single base substitution C T missense_variant G335R 1003G>A MELA-AU 11 105924176 105924176 single base substitution C T missense_variant G414R 1240G>A MELA-AU 11 105924234 105924235 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 105924234 105924235 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant T315I 944CC>TT MELA-AU 11 105924234 105924235 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant T394I 1181CC>TT MELA-AU 11 105925032 105925032 single base substitution C A downstream_gene_variant MELA-AU 11 105925032 105925032 single base substitution C A missense_variant L128F 384G>T MELA-AU 11 105925032 105925032 single base substitution C A missense_variant L49F 147G>T MELA-AU 11 105925616 105925616 single base substitution G A downstream_gene_variant MELA-AU 11 105925616 105925616 single base substitution G A intron_variant MELA-AU 11 105926171 105926171 single base substitution A T downstream_gene_variant MELA-AU 11 105926171 105926171 single base substitution A T intron_variant MELA-AU 11 105927412 105927412 single base substitution T G downstream_gene_variant MELA-AU 11 105927412 105927412 single base substitution T G intron_variant MELA-AU 11 105927427 105927427 single base substitution A G downstream_gene_variant MELA-AU 11 105927427 105927427 single base substitution A G intron_variant MELA-AU 11 105927492 105927492 single base substitution G A downstream_gene_variant MELA-AU 11 105927492 105927492 single base substitution G A intron_variant MELA-AU 11 105927579 105927579 single base substitution G A downstream_gene_variant MELA-AU 11 105927579 105927579 single base substitution G A intron_variant MELA-AU 11 105927827 105927827 single base substitution G A downstream_gene_variant MELA-AU 11 105927827 105927827 single base substitution G A intron_variant MELA-AU 11 105927864 105927864 single base substitution G A downstream_gene_variant MELA-AU 11 105927864 105927864 single base substitution G A intron_variant MELA-AU 11 105928248 105928248 single base substitution G A 3_prime_UTR_variant MELA-AU 11 105928248 105928248 single base substitution G A downstream_gene_variant MELA-AU 11 105928248 105928248 single base substitution G A intron_variant MELA-AU 11 105928317 105928317 single base substitution A T 3_prime_UTR_variant MELA-AU 11 105928317 105928317 single base substitution A T downstream_gene_variant MELA-AU 11 105928317 105928317 single base substitution A T intron_variant MELA-AU 11 105928322 105928322 single base substitution G A 3_prime_UTR_variant MELA-AU 11 105928322 105928322 single base substitution G A downstream_gene_variant MELA-AU 11 105928322 105928322 single base substitution G A intron_variant MELA-AU 11 105928499 105928499 single base substitution T A 3_prime_UTR_variant MELA-AU 11 105928499 105928499 single base substitution T A downstream_gene_variant MELA-AU 11 105928499 105928499 single base substitution T A intron_variant MELA-AU 11 105928758 105928758 single base substitution G A downstream_gene_variant MELA-AU 11 105928758 105928758 single base substitution G A intron_variant MELA-AU 11 105928758 105928758 single base substitution G A synonymous_variant S85S 255C>T MELA-AU 11 105928929 105928929 single base substitution G A downstream_gene_variant MELA-AU 11 105928929 105928929 single base substitution G A intron_variant MELA-AU 11 105928990 105928991 multiple base substitution (>=2bp and <=200bp) CC GT downstream_gene_variant MELA-AU 11 105928990 105928991 multiple base substitution (>=2bp and <=200bp) CC GT intron_variant MELA-AU 11 105931272 105931272 single base substitution G A intron_variant MELA-AU 11 105931272 105931272 single base substitution G A upstream_gene_variant MELA-AU 11 105931944 105931944 single base substitution G A intron_variant MELA-AU 11 105931944 105931944 single base substitution G A upstream_gene_variant MELA-AU 11 105933188 105933188 single base substitution C A intron_variant MELA-AU 11 105933188 105933188 single base substitution C A upstream_gene_variant MELA-AU 11 105933276 105933276 single base substitution G A intron_variant MELA-AU 11 105933276 105933276 single base substitution G A upstream_gene_variant MELA-AU 11 105933487 105933488 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 105933487 105933488 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 105933760 105933760 single base substitution A C intron_variant MELA-AU 11 105933760 105933760 single base substitution A C upstream_gene_variant MELA-AU 11 105934587 105934587 single base substitution G A intron_variant MELA-AU 11 105934587 105934587 single base substitution G A upstream_gene_variant MELA-AU 11 105934696 105934696 single base substitution A G intron_variant MELA-AU 11 105934696 105934696 single base substitution A G upstream_gene_variant MELA-AU 11 105934905 105934905 single base substitution G A intron_variant MELA-AU 11 105935409 105935409 single base substitution G A intron_variant MELA-AU 11 105935958 105935958 single base substitution C T intron_variant MELA-AU 11 105936055 105936055 single base substitution G A intron_variant MELA-AU 11 105936117 105936117 single base substitution G A intron_variant MELA-AU 11 105937424 105937424 single base substitution A G intron_variant MELA-AU 11 105937859 105937859 single base substitution G A intron_variant MELA-AU 11 105937882 105937882 single base substitution G A intron_variant MELA-AU 11 105938770 105938770 single base substitution G A intron_variant MELA-AU 11 105938973 105938973 single base substitution T C intron_variant MELA-AU 11 105939133 105939133 single base substitution G A intron_variant MELA-AU 11 105939470 105939470 single base substitution A T intron_variant MELA-AU 11 105939585 105939585 single base substitution G A intron_variant MELA-AU 11 105939681 105939681 single base substitution A C intron_variant MELA-AU 11 105939708 105939708 single base substitution G A intron_variant MELA-AU 11 105939778 105939778 single base substitution C T intron_variant MELA-AU 11 105940075 105940075 single base substitution G A intron_variant MELA-AU 11 105940510 105940510 single base substitution G A intron_variant MELA-AU 11 105940930 105940930 single base substitution C T intron_variant MELA-AU 11 105941774 105941774 single base substitution G A downstream_gene_variant MELA-AU 11 105941774 105941774 single base substitution G A intron_variant MELA-AU 11 105941958 105941958 single base substitution G A downstream_gene_variant MELA-AU 11 105941958 105941958 single base substitution G A intron_variant MELA-AU 11 105942356 105942356 single base substitution G A downstream_gene_variant MELA-AU 11 105942356 105942356 single base substitution G A intron_variant MELA-AU 11 105943794 105943794 single base substitution T C downstream_gene_variant MELA-AU 11 105943794 105943794 single base substitution T C intron_variant MELA-AU 11 105944488 105944488 single base substitution G A downstream_gene_variant MELA-AU 11 105944488 105944488 single base substitution G A intron_variant MELA-AU 11 105944712 105944712 single base substitution C T downstream_gene_variant MELA-AU 11 105944712 105944712 single base substitution C T intron_variant MELA-AU 11 105944848 105944848 single base substitution C A downstream_gene_variant MELA-AU 11 105944848 105944848 single base substitution C A intron_variant MELA-AU 11 105945068 105945068 single base substitution T G downstream_gene_variant MELA-AU 11 105945068 105945068 single base substitution T G intron_variant MELA-AU 11 105945682 105945682 single base substitution C T downstream_gene_variant MELA-AU 11 105945682 105945682 single base substitution C T intron_variant MELA-AU 11 105945702 105945702 single base substitution T C downstream_gene_variant MELA-AU 11 105945702 105945702 single base substitution T C intron_variant MELA-AU 11 105945768 105945768 single base substitution G A downstream_gene_variant MELA-AU 11 105945768 105945768 single base substitution G A intron_variant MELA-AU 11 105946547 105946547 single base substitution G A downstream_gene_variant MELA-AU 11 105946547 105946547 single base substitution G A intron_variant MELA-AU 11 105946860 105946860 single base substitution A C exon_variant MELA-AU 11 105946860 105946860 single base substitution A C intron_variant MELA-AU 11 105948056 105948056 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 105948056 105948056 single base substitution G A exon_variant MELA-AU 11 105948056 105948056 single base substitution G A upstream_gene_variant MELA-AU 11 105948069 105948069 single base substitution C T 5_prime_UTR_variant MELA-AU 11 105948069 105948069 single base substitution C T exon_variant MELA-AU 11 105948069 105948069 single base substitution C T upstream_gene_variant MELA-AU 11 105948671 105948671 single base substitution G A upstream_gene_variant MELA-AU 11 105950242 105950242 single base substitution C T upstream_gene_variant MELA-AU 11 105951957 105951957 single base substitution C T upstream_gene_variant MELA-AU 11 105952131 105952131 single base substitution A T upstream_gene_variant MELA-AU 11 105952311 105952311 single base substitution G A upstream_gene_variant ORCA-IN 11 105926552 105926552 single base substitution T A downstream_gene_variant ORCA-IN 11 105926552 105926552 single base substitution T A intron_variant ORCA-IN 11 105932211 105932211 single base substitution C T intron_variant ORCA-IN 11 105932211 105932211 single base substitution C T upstream_gene_variant OV-AU 11 105919330 105919330 single base substitution A G downstream_gene_variant OV-AU 11 105925843 105925843 single base substitution G C downstream_gene_variant OV-AU 11 105925843 105925843 single base substitution G C intron_variant OV-AU 11 105926146 105926146 single base substitution T A downstream_gene_variant OV-AU 11 105926146 105926146 single base substitution T A intron_variant OV-AU 11 105926676 105926676 single base substitution A G downstream_gene_variant OV-AU 11 105926676 105926676 single base substitution A G intron_variant OV-AU 11 105927273 105927273 single base substitution G A downstream_gene_variant OV-AU 11 105927273 105927273 single base substitution G A intron_variant OV-AU 11 105928200 105928200 single base substitution T A 3_prime_UTR_variant OV-AU 11 105928200 105928200 single base substitution T A downstream_gene_variant OV-AU 11 105928200 105928200 single base substitution T A intron_variant OV-AU 11 105937651 105937651 single base substitution A T intron_variant OV-AU 11 105938968 105938968 single base substitution C G intron_variant OV-AU 11 105944847 105944847 single base substitution C A downstream_gene_variant OV-AU 11 105944847 105944847 single base substitution C A intron_variant OV-AU 11 105945182 105945182 single base substitution C T downstream_gene_variant OV-AU 11 105945182 105945182 single base substitution C T intron_variant OV-AU 11 105948128 105948128 single base substitution C G 5_prime_UTR_variant OV-AU 11 105948128 105948128 single base substitution C G upstream_gene_variant OV-AU 11 105949948 105949948 single base substitution G C upstream_gene_variant OV-US 11 105929663 105929663 single base substitution G T exon_variant OV-US 11 105929663 105929663 single base substitution G T intron_variant OV-US 11 105929663 105929663 single base substitution G T missense_variant F54L 162C>A PACA-AU 11 105918134 105918134 single base substitution A G downstream_gene_variant PACA-AU 11 105922212 105922212 single base substitution G A 3_prime_UTR_variant PACA-AU 11 105922212 105922212 single base substitution G A downstream_gene_variant PACA-AU 11 105925422 105925422 deletion of <=200bp A - downstream_gene_variant PACA-AU 11 105925422 105925422 deletion of <=200bp A - intron_variant PACA-AU 11 105931520 105931520 single base substitution G C intron_variant PACA-AU 11 105931520 105931520 single base substitution G C upstream_gene_variant PACA-AU 11 105933115 105933115 single base substitution T A intron_variant PACA-AU 11 105933115 105933115 single base substitution T A upstream_gene_variant PACA-AU 11 105934580 105934580 single base substitution C T intron_variant PACA-AU 11 105934580 105934580 single base substitution C T upstream_gene_variant PACA-AU 11 105937474 105937474 single base substitution A C intron_variant PACA-AU 11 105937486 105937486 single base substitution T C intron_variant PACA-AU 11 105937875 105937875 single base substitution C A intron_variant PACA-AU 11 105939531 105939531 single base substitution T C intron_variant PACA-AU 11 105940840 105940840 single base substitution A C intron_variant PACA-AU 11 105941845 105941845 single base substitution T G downstream_gene_variant PACA-AU 11 105941845 105941845 single base substitution T G intron_variant PACA-AU 11 105942957 105942957 single base substitution T A downstream_gene_variant PACA-AU 11 105942957 105942957 single base substitution T A intron_variant PACA-AU 11 105944631 105944631 single base substitution T A downstream_gene_variant PACA-AU 11 105944631 105944631 single base substitution T A intron_variant PACA-AU 11 105944847 105944847 single base substitution C A downstream_gene_variant PACA-AU 11 105944847 105944847 single base substitution C A intron_variant PACA-AU 11 105947745 105947745 single base substitution G A intron_variant PACA-AU 11 105947745 105947745 single base substitution G A upstream_gene_variant PACA-CA 11 105917488 105917488 single base substitution C T downstream_gene_variant PACA-CA 11 105919023 105919023 single base substitution G A downstream_gene_variant PACA-CA 11 105919245 105919245 single base substitution A T downstream_gene_variant PACA-CA 11 105920830 105920830 single base substitution C G downstream_gene_variant PACA-CA 11 105924602 105924602 single base substitution T C downstream_gene_variant PACA-CA 11 105924602 105924602 single base substitution T C missense_variant M193V 577A>G PACA-CA 11 105924602 105924602 single base substitution T C missense_variant M272V 814A>G PACA-CA 11 105927368 105927368 single base substitution T C downstream_gene_variant PACA-CA 11 105927368 105927368 single base substitution T C intron_variant PACA-CA 11 105929312 105929312 single base substitution G A downstream_gene_variant PACA-CA 11 105929312 105929312 single base substitution G A intron_variant PACA-CA 11 105932941 105932941 single base substitution G A intron_variant PACA-CA 11 105932941 105932941 single base substitution G A upstream_gene_variant PACA-CA 11 105936286 105936286 single base substitution G T intron_variant PACA-CA 11 105937743 105937743 single base substitution C T intron_variant PACA-CA 11 105942722 105942722 single base substitution T C downstream_gene_variant PACA-CA 11 105942722 105942722 single base substitution T C intron_variant PACA-CA 11 105943792 105943792 single base substitution G A downstream_gene_variant PACA-CA 11 105943792 105943792 single base substitution G A intron_variant PACA-CA 11 105945517 105945517 single base substitution A G downstream_gene_variant PACA-CA 11 105945517 105945517 single base substitution A G intron_variant PACA-CA 11 105951675 105951675 single base substitution C A upstream_gene_variant PBCA-DE 11 105926253 105926258 deletion of <=200bp AATAGA - downstream_gene_variant PBCA-DE 11 105926253 105926258 deletion of <=200bp AATAGA - intron_variant PBCA-DE 11 105928956 105928956 deletion of <=200bp A - downstream_gene_variant PBCA-DE 11 105928956 105928956 deletion of <=200bp A - intron_variant PBCA-DE 11 105929524 105929524 single base substitution G T exon_variant PBCA-DE 11 105929524 105929524 single base substitution G T intron_variant PBCA-DE 11 105930004 105930004 single base substitution T A intron_variant PBCA-DE 11 105930004 105930004 single base substitution T A upstream_gene_variant PBCA-DE 11 105930629 105930629 single base substitution C T intron_variant PBCA-DE 11 105930629 105930629 single base substitution C T upstream_gene_variant PBCA-DE 11 105932603 105932603 insertion of <=200bp - TA intron_variant PBCA-DE 11 105932603 105932603 insertion of <=200bp - TA upstream_gene_variant PBCA-DE 11 105949321 105949321 single base substitution G A upstream_gene_variant PBCA-DE 11 105949739 105949739 single base substitution G A upstream_gene_variant PBCA-DE 11 105952952 105952952 single base substitution T A upstream_gene_variant PRAD-CA 11 105929387 105929387 single base substitution G T downstream_gene_variant PRAD-CA 11 105929387 105929387 single base substitution G T intron_variant PRAD-UK 11 105920075 105920075 single base substitution A G downstream_gene_variant PRAD-UK 11 105925694 105925694 single base substitution C T downstream_gene_variant PRAD-UK 11 105925694 105925694 single base substitution C T intron_variant PRAD-UK 11 105933251 105933258 deletion of <=200bp TTTTTCAA - intron_variant PRAD-UK 11 105933251 105933258 deletion of <=200bp TTTTTCAA - upstream_gene_variant PRAD-UK 11 105940538 105940538 single base substitution C G intron_variant PRAD-UK 11 105944564 105944564 single base substitution T G downstream_gene_variant PRAD-UK 11 105944564 105944564 single base substitution T G intron_variant PRAD-UK 11 105951140 105951140 insertion of <=200bp - AAAT upstream_gene_variant READ-US 11 105923822 105923822 single base substitution T C downstream_gene_variant READ-US 11 105923822 105923822 single base substitution T C missense_variant K453E 1357A>G READ-US 11 105923822 105923822 single base substitution T C missense_variant K532E 1594A>G READ-US 11 105924639 105924639 single base substitution C A downstream_gene_variant READ-US 11 105924639 105924639 single base substitution C A missense_variant E180D 540G>T READ-US 11 105924639 105924639 single base substitution C A missense_variant E259D 777G>T READ-US 11 105948598 105948598 single base substitution C T upstream_gene_variant READ-US 11 105950309 105950309 single base substitution A C upstream_gene_variant RECA-EU 11 105928760 105928760 single base substitution A T downstream_gene_variant RECA-EU 11 105928760 105928760 single base substitution A T intron_variant RECA-EU 11 105928760 105928760 single base substitution A T missense_variant S85T 253T>A RECA-EU 11 105936374 105936374 single base substitution T C intron_variant RECA-EU 11 105939054 105939054 single base substitution C T intron_variant SKCA-BR 11 105918170 105918170 single base substitution A G downstream_gene_variant SKCA-BR 11 105918733 105918733 single base substitution T C downstream_gene_variant SKCA-BR 11 105919854 105919854 single base substitution G A downstream_gene_variant SKCA-BR 11 105920675 105920675 single base substitution T C downstream_gene_variant SKCA-BR 11 105922687 105922687 single base substitution G A 3_prime_UTR_variant SKCA-BR 11 105922687 105922687 single base substitution G A downstream_gene_variant SKCA-BR 11 105926331 105926331 single base substitution C T downstream_gene_variant SKCA-BR 11 105926331 105926331 single base substitution C T intron_variant SKCA-BR 11 105927625 105927625 single base substitution A G downstream_gene_variant SKCA-BR 11 105927625 105927625 single base substitution A G intron_variant SKCA-BR 11 105928360 105928360 single base substitution G A 3_prime_UTR_variant SKCA-BR 11 105928360 105928360 single base substitution G A downstream_gene_variant SKCA-BR 11 105928360 105928360 single base substitution G A intron_variant SKCA-BR 11 105929992 105929992 single base substitution A T intron_variant SKCA-BR 11 105929992 105929992 single base substitution A T upstream_gene_variant SKCA-BR 11 105931673 105931673 insertion of <=200bp - GA intron_variant SKCA-BR 11 105931673 105931673 insertion of <=200bp - GA upstream_gene_variant SKCA-BR 11 105936664 105936664 single base substitution G A intron_variant SKCA-BR 11 105936705 105936705 single base substitution A T intron_variant SKCA-BR 11 105937191 105937191 single base substitution A C intron_variant SKCA-BR 11 105952169 105952169 single base substitution A G upstream_gene_variant SKCA-BR 11 105952308 105952308 single base substitution A T upstream_gene_variant SKCM-US 11 105923628 105923628 single base substitution C T downstream_gene_variant SKCM-US 11 105923628 105923628 single base substitution C T synonymous_variant V517V 1551G>A SKCM-US 11 105923628 105923628 single base substitution C T synonymous_variant V596V 1788G>A SKCM-US 11 105923920 105923920 single base substitution G T downstream_gene_variant SKCM-US 11 105923920 105923920 single base substitution G T missense_variant A420E 1259C>A SKCM-US 11 105923920 105923920 single base substitution G T missense_variant A499E 1496C>A SKCM-US 11 105924005 105924005 single base substitution G A downstream_gene_variant SKCM-US 11 105924005 105924005 single base substitution G A missense_variant P392S 1174C>T SKCM-US 11 105924005 105924005 single base substitution G A missense_variant P471S 1411C>T SKCM-US 11 105924093 105924093 single base substitution G A downstream_gene_variant SKCM-US 11 105924093 105924093 single base substitution G A synonymous_variant P362P 1086C>T SKCM-US 11 105924093 105924093 single base substitution G A synonymous_variant P441P 1323C>T SKCM-US 11 105924095 105924095 single base substitution G A downstream_gene_variant SKCM-US 11 105924095 105924095 single base substitution G A missense_variant P362S 1084C>T SKCM-US 11 105924095 105924095 single base substitution G A missense_variant P441S 1321C>T SKCM-US 11 105924522 105924522 single base substitution G A downstream_gene_variant SKCM-US 11 105924522 105924522 single base substitution G A synonymous_variant F219F 657C>T SKCM-US 11 105924522 105924522 single base substitution G A synonymous_variant F298F 894C>T SKCM-US 11 105924695 105924695 single base substitution C T downstream_gene_variant SKCM-US 11 105924695 105924695 single base substitution C T missense_variant V162M 484G>A SKCM-US 11 105924695 105924695 single base substitution C T missense_variant V241M 721G>A SKCM-US 11 105924856 105924856 single base substitution G A downstream_gene_variant SKCM-US 11 105924856 105924856 single base substitution G A missense_variant S108F 323C>T SKCM-US 11 105924856 105924856 single base substitution G A missense_variant S187F 560C>T SKCM-US 11 105925012 105925012 single base substitution G A downstream_gene_variant SKCM-US 11 105925012 105925012 single base substitution G A missense_variant S135F 404C>T SKCM-US 11 105925012 105925012 single base substitution G A missense_variant S56F 167C>T SKCM-US 11 105929598 105929598 single base substitution A C exon_variant SKCM-US 11 105929598 105929598 single base substitution A C intron_variant SKCM-US 11 105929598 105929598 single base substitution A C missense_variant F76C 227T>G SKCM-US 11 105929626 105929626 single base substitution G A exon_variant SKCM-US 11 105929626 105929626 single base substitution G A intron_variant SKCM-US 11 105929626 105929626 single base substitution G A missense_variant R67C 199C>T SKCM-US 11 105929663 105929663 single base substitution G A exon_variant SKCM-US 11 105929663 105929663 single base substitution G A intron_variant SKCM-US 11 105929663 105929663 single base substitution G A synonymous_variant F54F 162C>T SKCM-US 11 105948468 105948468 single base substitution G C 5_prime_UTR_variant SKCM-US 11 105948468 105948468 single base substitution G C upstream_gene_variant SKCM-US 11 105950416 105950416 single base substitution C T upstream_gene_variant STAD-US 11 105923985 105923985 deletion of <=200bp A - downstream_gene_variant STAD-US 11 105923985 105923985 deletion of <=200bp A - frameshift_variant F398 STAD-US 11 105923985 105923985 deletion of <=200bp A - frameshift_variant F477 STAD-US 11 105924271 105924271 single base substitution T A downstream_gene_variant STAD-US 11 105924271 105924271 single base substitution T A missense_variant D303V 908A>T STAD-US 11 105924271 105924271 single base substitution T A missense_variant D382V 1145A>T STAD-US 11 105924490 105924490 single base substitution T C downstream_gene_variant STAD-US 11 105924490 105924490 single base substitution T C missense_variant Q230R 689A>G STAD-US 11 105924490 105924490 single base substitution T C missense_variant Q309R 926A>G STAD-US 11 105924527 105924527 single base substitution T C downstream_gene_variant STAD-US 11 105924527 105924527 single base substitution T C missense_variant I218V 652A>G STAD-US 11 105924527 105924527 single base substitution T C missense_variant I297V 889A>G STAD-US 11 105924893 105924893 single base substitution G C downstream_gene_variant STAD-US 11 105924893 105924893 single base substitution G C missense_variant H175D 523C>G STAD-US 11 105924893 105924893 single base substitution G C missense_variant H96D 286C>G STAD-US 11 105929633 105929633 single base substitution C T exon_variant STAD-US 11 105929633 105929633 single base substitution C T intron_variant STAD-US 11 105929633 105929633 single base substitution C T synonymous_variant P64P 192G>A STAD-US 11 105929644 105929644 single base substitution C T exon_variant STAD-US 11 105929644 105929644 single base substitution C T intron_variant STAD-US 11 105929644 105929644 single base substitution C T missense_variant E61K 181G>A THCA-SA 11 105922826 105922826 single base substitution G A 3_prime_UTR_variant THCA-SA 11 105922826 105922826 single base substitution G A downstream_gene_variant THCA-SA 11 105947285 105947285 single base substitution C T 5_prime_UTR_variant THCA-SA 11 105947285 105947285 single base substitution C T exon_variant THCA-SA 11 105947285 105947285 single base substitution C T intron_variant THCA-US 11 105924439 105924439 single base substitution T C downstream_gene_variant THCA-US 11 105924439 105924439 single base substitution T C missense_variant Q247R 740A>G THCA-US 11 105924439 105924439 single base substitution T C missense_variant Q326R 977A>G UCEC-US 11 105924013 105924013 single base substitution G A downstream_gene_variant UCEC-US 11 105924013 105924013 single base substitution G A missense_variant A389V 1166C>T UCEC-US 11 105924013 105924013 single base substitution G A missense_variant A468V 1403C>T UCEC-US 11 105924071 105924071 single base substitution C T downstream_gene_variant UCEC-US 11 105924071 105924071 single base substitution C T missense_variant A370T 1108G>A UCEC-US 11 105924071 105924071 single base substitution C T missense_variant A449T 1345G>A UCEC-US 11 105924350 105924350 single base substitution G A downstream_gene_variant UCEC-US 11 105924350 105924350 single base substitution G A stop_gained R277* 829C>T UCEC-US 11 105924350 105924350 single base substitution G A stop_gained R356* 1066C>T UCEC-US 11 105924395 105924395 single base substitution C T downstream_gene_variant UCEC-US 11 105924395 105924395 single base substitution C T missense_variant G262R 784G>A UCEC-US 11 105924395 105924395 single base substitution C T missense_variant G341R 1021G>A UCEC-US 11 105924443 105924443 single base substitution G A downstream_gene_variant UCEC-US 11 105924443 105924443 single base substitution G A missense_variant P246S 736C>T UCEC-US 11 105924443 105924443 single base substitution G A missense_variant P325S 973C>T UCEC-US 11 105924472 105924472 single base substitution T C downstream_gene_variant UCEC-US 11 105924472 105924472 single base substitution T C missense_variant N236S 707A>G UCEC-US 11 105924472 105924472 single base substitution T C missense_variant N315S 944A>G UCEC-US 11 105924550 105924550 single base substitution C T downstream_gene_variant UCEC-US 11 105924550 105924550 single base substitution C T missense_variant R210Q 629G>A UCEC-US 11 105924550 105924550 single base substitution C T missense_variant R289Q 866G>A UCEC-US 11 105924646 105924646 single base substitution T G downstream_gene_variant UCEC-US 11 105924646 105924646 single base substitution T G missense_variant N178T 533A>C UCEC-US 11 105924646 105924646 single base substitution T G missense_variant N257T 770A>C UCEC-US 11 105924846 105924846 single base substitution G T downstream_gene_variant UCEC-US 11 105924846 105924846 single base substitution G T missense_variant F111L 333C>A UCEC-US 11 105924846 105924846 single base substitution G T missense_variant F190L 570C>A UCEC-US 11 105924871 105924871 single base substitution G A downstream_gene_variant UCEC-US 11 105924871 105924871 single base substitution G A missense_variant S103F 308C>T UCEC-US 11 105924871 105924871 single base substitution G A missense_variant S182F 545C>T UCEC-US 11 105924879 105924879 single base substitution A G downstream_gene_variant UCEC-US 11 105924879 105924879 single base substitution A G synonymous_variant H100H 300T>C UCEC-US 11 105924879 105924879 single base substitution A G synonymous_variant H179H 537T>C UCEC-US 11 105924880 105924880 single base substitution T A downstream_gene_variant UCEC-US 11 105924880 105924880 single base substitution T A missense_variant H100L 299A>T UCEC-US 11 105924880 105924880 single base substitution T A missense_variant H179L 536A>T UCEC-US 11 105929686 105929686 single base substitution C T exon_variant UCEC-US 11 105929686 105929686 single base substitution C T intron_variant UCEC-US 11 105929686 105929686 single base substitution C T missense_variant E47K 139G>A UCEC-US 11 105950229 105950229 single base substitution G T upstream_gene_variant UCEC-US 11 105950307 105950307 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-D1-A17Q-01 COSM922541 c.139G>A p.E47K Substitution - Missense 11:106058959-106058959 - 2492701 COSM5599740 c.743A>G p.E248G Substitution - Missense 11:106053946-106053946 - ESO-118 COSM1255206 c.81C>T p.N27N Substitution - coding silent 11:106059017-106059017 - 381_T COSM3979048 c.249A>T p.V83V Substitution - coding silent 11:106054440-106054440 - KYSE-30 COSM4183639 c.1132C>G p.P378A Substitution - Missense 11:106053557-106053557 - TCGA-EE-A3AF-06 COSM3442968 c.1323C>T p.P441P Substitution - coding silent 11:106053366-106053366 - S02403 COSM5700339 c.1244C>T p.S415F Substitution - Missense 11:106053445-106053445 - 587226 COSM1211374 c.1067G>A p.R356Q Substitution - Missense 11:106053622-106053622 - GC1_T COSM3748515 c.766T>G p.F256V Substitution - Missense 11:106053923-106053923 - TCGA-EP-A2KA-01 COSM4917265 c.642G>A p.M214I Substitution - Missense 11:106054047-106054047 - WM3211 COSM3727137 c.953C>T p.S318F Substitution - Missense 11:106053736-106053736 - CHC1616T COSM4803678 c.826A>T p.K276* Substitution - Nonsense 11:106053863-106053863 - CSCC-7-T COSM4547250 c.418G>A p.A140T Substitution - Missense 11:106054271-106054271 - sysucc-311T COSM5477406 c.1659T>G p.I553M Substitution - Missense 11:106053030-106053030 - Gp5D COSM2109587 c.423C>T p.C141C Substitution - coding silent 11:106054266-106054266 - 587222 COSM1211375 c.568T>G p.F190V Substitution - Missense 11:106054121-106054121 - TCGA-21-1077-01 COSM685669 c.203G>T p.C68F Substitution - Missense 11:106058895-106058895 - TCGA-AA-3672-01 COSM266741 c.1483C>A p.Q495K Substitution - Missense 11:106053206-106053206 - TCGA-AP-A0LM-01 COSM922531 c.1345G>A p.A449T Substitution - Missense 11:106053344-106053344 - TCGA-FT-A3EE-01 COSM3791134 c.1461T>C p.S487S Substitution - coding silent 11:106053228-106053228 - RMH008-R5 COSM2109564 c.1600G>A p.E534K Substitution - Missense 11:106053089-106053089 - BD236T COSM4694116 c.1530A>G p.T510T Substitution - coding silent 11:106053159-106053159 - CSCC-35-T COSM4569578 c.185T>A p.I62K Substitution - Missense 11:106058913-106058913 - TCGA-AG-A002-01 COSM261487 c.1659T>C p.I553I Substitution - coding silent 11:106053030-106053030 - TCGA-AA-3856-01 COSM295883 c.1435T>C p.Y479H Substitution - Missense 11:106053254-106053254 - RMH008-R6 COSM2109564 c.1600G>A p.E534K Substitution - Missense 11:106053089-106053089 - YUKLAB COSM1704519 c.486T>A p.D162E Substitution - Missense 11:106054203-106054203 - TCGA-EE-A3AE-06 COSM3442966 c.1496C>A p.A499E Substitution - Missense 11:106053193-106053193 - TCGA-F5-6814-01 COSM3415463 c.777G>T p.E259D Substitution - Missense 11:106053912-106053912 - TCGA-DI-A0WH-01 COSM922533 c.973C>T p.P325S Substitution - Missense 11:106053716-106053716 - 2492703 COSM5599740 c.743A>G p.E248G Substitution - Missense 11:106053946-106053946 - Gp5D COSM2109586 c.478A>G p.I160V Substitution - Missense 11:106054211-106054211 - TCGA-EE-A2MJ-06 COSM3442971 c.404C>T p.S135F Substitution - Missense 11:106054285-106054285 - TCGA-AA-A00N-01 COSM275631 c.1528A>G p.T510A Substitution - Missense 11:106053161-106053161 - Gp2D COSM2109586 c.478A>G p.I160V Substitution - Missense 11:106054211-106054211 - sysucc-311T COSM5477407 c.1014G>A p.S338S Substitution - coding silent 11:106053675-106053675 - TCGA-G3-A25S-01 COSM4927024 c.413C>G p.S138C Substitution - Missense 11:106054276-106054276 - TCGA-BR-8360-01 COSM4017484 c.889A>G p.I297V Substitution - Missense 11:106053800-106053800 - T636 COSM4694116 c.1530A>G p.T510T Substitution - coding silent 11:106053159-106053159 - TCGA-EE-A181-06 COSM3442973 c.162C>T p.F54F Substitution - coding silent 11:106058936-106058936 - TCGA-AX-A05Z-01 COSM922530 c.1403C>T p.A468V Substitution - Missense 11:106053286-106053286 - LUAD_E00522 COSM352331 c.48A>G p.T16T Substitution - coding silent 11:106059050-106059050 - LUAD-S01315 COSM343926 c.1632A>T p.A544A Substitution - coding silent 11:106053057-106053057 - TCGA-GV-A3JV-01 COSM1297591 c.41G>A p.R14Q Substitution - Missense 11:106059057-106059057 - TCGA-B5-A11E-01 COSM922536 c.770A>C p.N257T Substitution - Missense 11:106053919-106053919 - TCGA-AA-3663-01 COSM1350610 c.280A>G p.T94A Substitution - Missense 11:106054409-106054409 - TCGA-AZ-4315-01 COSM1350611 c.191C>T p.P64L Substitution - Missense 11:106058907-106058907 - WA16 COSM237583 c.975G>A p.P325P Substitution - coding silent 11:106053714-106053714 - PCSI_0083_Pa_P COSM3375623 c.814A>G p.M272V Substitution - Missense 11:106053875-106053875 - KPOPBR-05-T COSM1350609 c.579G>A p.M193I Substitution - Missense 11:106054110-106054110 - ATL010 COSM5703852 c.1837T>C p.*613R Nonstop extension 11:106052852-106052852 - TCGA-DA-A1I0-06 COSM3442972 c.199C>T p.R67C Substitution - Missense 11:106058899-106058899 - TCGA-AX-A05Z-01 COSM922537 c.570C>A p.F190L Substitution - Missense 11:106054119-106054119 - TCGA-G2-A2EO-01 COSM1297589 c.1592G>C p.W531S Substitution - Missense 11:106053097-106053097 - TCGA-CZ-5470-01 COSM466247 c.1751C>A p.P584Q Substitution - Missense 11:106052938-106052938 - ATL071 COSM5703853 c.916G>T p.G306* Substitution - Nonsense 11:106053773-106053773 - SC_9047 COSM237583 c.975G>A p.P325P Substitution - coding silent 11:106053714-106053714 - TCGA-BG-A0LX-01 COSM922533 c.973C>T p.P325S Substitution - Missense 11:106053716-106053716 - TCGA-AP-A0LM-01 COSM922538 c.545C>T p.S182F Substitution - Missense 11:106054144-106054144 - RMH008-R8 COSM2109564 c.1600G>A p.E534K Substitution - Missense 11:106053089-106053089 - SS6003119 COSM3716764 c.234-3C>A p.? Unknown 11:106054458-106054458 - TCGA-RP-A694-06 COSM4893681 c.1321C>T p.P441S Substitution - Missense 11:106053368-106053368 - TCGA-13-1497-01 COSM75064 c.162C>A p.F54L Substitution - Missense 11:106058936-106058936 - TCGA-BR-6452-01 COSM4017482 c.1145A>T p.D382V Substitution - Missense 11:106053544-106053544 - Br27P COSM40210 c.1020C>T p.Y340Y Substitution - coding silent 11:106053669-106053669 - TCGA-D1-A103-01 COSM922532 c.1021G>A p.G341R Substitution - Missense 11:106053668-106053668 - 61 COSM5739432 c.539A>G p.H180R Substitution - Missense 11:106054150-106054150 - LUAD-B01811 COSM333785 c.606_607GG>TT p.L202>? Complex 11:106054082-106054083 - TCGA-AA-A00J-01 COSM298356 c.511G>A p.D171N Substitution - Missense 11:106054178-106054178 - TCGA-E8-A242-01 COSM3368192 c.977A>G p.Q326R Substitution - Missense 11:106053712-106053712 - KPOPBR-05-T COSM5963231 c.848G>C p.G283A Substitution - Missense 11:106053841-106053841 - 2492700 COSM5599740 c.743A>G p.E248G Substitution - Missense 11:106053946-106053946 - TCGA-EE-A29G-06 COSM3442965 c.1788G>A p.V596V Substitution - coding silent 11:106052901-106052901 - 587376 COSM167764 c.1066C>T p.R356* Substitution - Nonsense 11:106053623-106053623 - 718T COSM4382047 c.1614G>C p.E538D Substitution - Missense 11:106053075-106053075 - TCGA-AM-5820-01 COSM3442972 c.199C>T p.R67C Substitution - Missense 11:106058899-106058899 - GC_350T-GC_350N COSM4772024 c.261_264delAAGA p.R88fs*15 Deletion - Frameshift 11:106054425-106054428 - TCGA-HU-A4HD-01 COSM4017486 c.181G>A p.E61K Substitution - Missense 11:106058917-106058917 - TCGA-B5-A0JR-01 COSM922539 c.537T>C p.H179H Substitution - coding silent 11:106054152-106054152 - SJHGG003_A COSM4968862 c.1537A>G p.I513V Substitution - Missense 11:106053152-106053152 - ESCC_134 COSM5642701 c.162C>G p.F54L Substitution - Missense 11:106058936-106058936 - TCGA-D9-A6EC-06 COSM4403635 c.227T>G p.F76C Substitution - Missense 11:106058871-106058871 - 61 COSM5739431 c.924T>A p.N308K Substitution - Missense 11:106053765-106053765 - SNU-175 COSM2109567 c.1511C>A p.A504D Substitution - Missense 11:106053178-106053178 - LP6007520-DNA_A01 COSM4413166 c.1267G>T p.D423Y Substitution - Missense 11:106053422-106053422 - YUHAMA COSM5371550 c.62C>T p.P21L Substitution - Missense 11:106059036-106059036 - TCGA-22-4599-01 COSM685672 c.1642G>T p.G548* Substitution - Nonsense 11:106053047-106053047 - CHC1616T COSM4803678 c.826A>T p.K276* Substitution - Nonsense 11:106053863-106053863 - TCGA-66-2763-01 COSM685673 c.1700A>C p.D567A Substitution - Missense 11:106052989-106052989 - 587376 COSM1211376 c.925C>A p.Q309K Substitution - Missense 11:106053764-106053764 - TCGA-A5-A0G9-01 COSM922535 c.866G>A p.R289Q Substitution - Missense 11:106053823-106053823 - PCSI_0083_Pa_P_526 COSM3375623 c.814A>G p.M272V Substitution - Missense 11:106053875-106053875 - TCGA-DA-A1HY-06 COSM3442967 c.1411C>T p.P471S Substitution - Missense 11:106053278-106053278 - ME049T COSM230238 c.1075C>T p.R359* Substitution - Nonsense 11:106053614-106053614 - CSCC-27-T COSM4464580 c.1340C>T p.P447L Substitution - Missense 11:106053349-106053349 - LUAD-S01315 COSM343927 c.114C>T p.I38I Substitution - coding silent 11:106058984-106058984 - 2492702 COSM5599740 c.743A>G p.E248G Substitution - Missense 11:106053946-106053946 - UMC11 COSM2109584 c.649A>T p.K217* Substitution - Nonsense 11:106054040-106054040 - TCGA-34-5927-01 COSM685671 c.1095A>G p.S365S Substitution - coding silent 11:106053594-106053594 - RMH008-R7 COSM2109564 c.1600G>A p.E534K Substitution - Missense 11:106053089-106053089 - Au2 COSM5599740 c.743A>G p.E248G Substitution - Missense 11:106053946-106053946 - TCGA-33-4583-01 COSM685670 c.848G>T p.G283V Substitution - Missense 11:106053841-106053841 - RMH008-R4 COSM2109564 c.1600G>A p.E534K Substitution - Missense 11:106053089-106053089 - LN229 COSM5712606 c.1091A>T p.E364V Substitution - Missense 11:106053598-106053598 - EGC15 COSM5050482 c.1246C>T p.R416W Substitution - Missense 11:106053443-106053443 - TCGA-EI-6917-01 COSM3415462 c.1594A>G p.K532E Substitution - Missense 11:106053095-106053095 - TCGA-G2-A3IE-01 COSM1297590 c.1390G>C p.E464Q Substitution - Missense 11:106053299-106053299 - TCGA-BR-4257-01 COSM4017483 c.926A>G p.Q309R Substitution - Missense 11:106053763-106053763 - 1N45-VS-1T45 COSM4975760 c.871T>C p.S291P Substitution - Missense 11:106053818-106053818 - TCGA-CD-8531-01 COSM4017485 c.523C>G p.H175D Substitution - Missense 11:106054166-106054166 - 42 COSM5733945 c.128_132delAGAAT p.Q43fs*2 Deletion - Frameshift 11:106058966-106058970 - TCGA-GF-A6C9-06 COSM4899849 c.894C>T p.F298F Substitution - coding silent 11:106053795-106053795 - TCGA-C8-A27B-01 COSM1474968 c.137G>C p.R46T Substitution - Missense 11:106058961-106058961 - TCGA-AA-A00N-01 COSM275632 c.1206C>T p.L402L Substitution - coding silent 11:106053483-106053483 - KPOPBR-07-T COSM5964110 c.1099C>T p.H367Y Substitution - Missense 11:106053590-106053590 - ESCC-003T COSM343927 c.114C>T p.I38I Substitution - coding silent 11:106058984-106058984 - S00945 COSM312140 c.1586G>T p.C529F Substitution - Missense 11:106053103-106053103 - PT37 COSM5920137 c.1339C>T p.P447S Substitution - Missense 11:106053350-106053350 - TCGA-B5-A11N-01 COSM167764 c.1066C>T p.R356* Substitution - Nonsense 11:106053623-106053623 - TCGA-BR-8081-01 COSM2109589 c.192G>A p.P64P Substitution - coding silent 11:106058906-106058906 - 3N09-VS-3T09 COSM4979163 c.1313G>A p.S438N Substitution - Missense 11:106053376-106053376 - BD59T COSM5498581 c.637G>A p.E213K Substitution - Missense 11:106054052-106054052 - PCSI_0083_Pa_X COSM3375623 c.814A>G p.M272V Substitution - Missense 11:106053875-106053875 - 718LT COSM4382047 c.1614G>C p.E538D Substitution - Missense 11:106053075-106053075 - TCGA-A5-A0GJ-01 COSM922540 c.536A>T p.H179L Substitution - Missense 11:106054153-106054153 - Gp2D COSM2109587 c.423C>T p.C141C Substitution - coding silent 11:106054266-106054266 - S02273 COSM1211374 c.1067G>A p.R356Q Substitution - Missense 11:106053622-106053622 - TCGA-EB-A5UN-06 COSM3442969 c.721G>A p.V241M Substitution - Missense 11:106053968-106053968 - TCGA-HE-A5NL-01 COSM3985876 c.382T>A p.L128M Substitution - Missense 11:106054307-106054307 - ESO-130 COSM1255207 c.794C>A p.T265K Substitution - Missense 11:106053895-106053895 - HCT15 COSM2109591 c.88G>T p.V30L Substitution - Missense 11:106059010-106059010 - TCGA-EB-A4IS-01 COSM3442970 c.560C>T p.S187F Substitution - Missense 11:106054129-106054129 - TCGA-D1-A103-01 COSM922534 c.944A>G p.N315S Substitution - Missense 11:106053745-106053745 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.101949 11q22.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.Y479H c.1435T>C 11 105923981 COREAD A G Synonymous p.H179H c.537T>C 11 105924879 UCEC A G Synonymous p.P429P c.1287T>C 11 105924129 HNSC A G Synonymous p.Y560Y c.1680T>C 11 105923736 BRCA A T Missense p.C354S c.1060T>A 11 105924356 HNSC C A 3-UTRSNV . c.1836+1228G>T 11 105922352 HC C A Missense p.C475F c.1424G>T 11 105923992 HNSC C A Missense p.C529F c.1586G>T 11 105923830 SCLC C A Missense p.C68F c.203G>T 11 105929622 LUSC C A Missense p.G283V c.848G>T 11 105924568 LUSC C A Nonsense p.G548* c.1642G>T 11 105923774 LUSC C - Frameshift p.D417Tfs*6 c.1249delG 11 105924167 LUAD C G Missense p.E464Q c.1390G>C 11 105924026 BLCA C G Missense p.R46T c.137G>C 11 105929688 BRCA C G Missense p.W531S c.1592G>C 11 105923824 BLCA C T IntronicSNV . c.233+1060G>A 11 105928532 MB C T Missense p.A71T c.211G>A 11 105929614 CM C T Missense p.G349S c.1045G>A 11 105924371 HNSC C T Missense p.R14Q c.41G>A 11 105929784 BLCA C T Missense p.R289Q c.866G>A 11 105924550 UCEC C T Synonymous p.V596V c.1788G>A 11 105923628 CM C T Synonymous p.Y340Y c.1020C>T 11 105924396 GBM G A Missense p.P325S c.973C>T 11 105924443 UCEC G A Missense p.P471S c.1411C>T 11 105924005 CM G A Missense p.R67C c.199C>T 11 105929626 CM G A Missense p.S135F c.404C>T 11 105925012 CM G A Synonymous p.N27N c.81C>T 11 105929744 ESCA G A Synonymous p.P441P c.1323C>T 11 105924093 CM G T IntronicSNV . c.233+68C>A 11 105929524 MB G T Missense p.A499E c.1496C>A 11 105923920 CM G T Missense p.F54L c.162C>A 11 105929663 OV G T Missense p.T265K c.794C>A 11 105924622 ESCA TA - Frameshift p.T311Ifs*4 c.930_931delTA 11 105924485 RCCC T A Missense p.H179L c.536A>T 11 105924880 UCEC T C Missense p.Q309R c.926A>G 11 105924490 STAD T C Missense p.Q326R c.977A>G 11 105924439 THCA T C Synonymous p.S365S c.1095A>G 11 105924321 LUSC T G 3-UTRSNV . c.1836+351A>C 11 105923229 DLBCL T G Missense p.D567A c.1700A>C 11 105923716 LUSC T G Missense p.Q279P c.836A>C 11 105924580 HNSC