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 16 74922199 74922199 + Silent SNP C C A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr16:74922199C>A c.2214G>T c.(2212-2214)cgG>cgT p.R738R ACC 16 74937919 74937919 + Missense_Mutation SNP G G A TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr16:74937919G>A c.1792C>T c.(1792-1794)Cgt>Tgt p.R598C BLCA 16 74920244 74920244 + Nonsense_Mutation SNP C C A TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr16:74920244C>A c.2470G>T c.(2470-2472)Gaa>Taa p.E824* BLCA 16 74920261 74920261 + Nonsense_Mutation SNP C C T TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr16:74920261C>T c.2453G>A c.(2452-2454)tGg>tAg p.W818* BLCA 16 74921614 74921614 + Missense_Mutation SNP C C T TCGA-GU-A766-01A-11D-A32B-08 TCGA-GU-A766-10A-01D-A329-08 g.chr16:74921614C>T c.2386G>A c.(2386-2388)Gac>Aac p.D796N BLCA 16 74943792 74943792 + Silent SNP C C T TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr16:74943792C>T c.1413G>A c.(1411-1413)caG>caA p.Q471Q BLCA 16 74949825 74949825 + Silent SNP C C T TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr16:74949825C>T c.1167G>A c.(1165-1167)caG>caA p.Q389Q BLCA 16 74950088 74950088 + Missense_Mutation SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr16:74950088C>T c.1036G>A c.(1036-1038)Gag>Aag p.E346K BLCA 16 74955920 74955920 + Silent SNP A A G TCGA-E7-A677-01A-11D-A30E-08 TCGA-E7-A677-10A-01D-A30H-08 g.chr16:74955920A>G c.811T>C c.(811-813)Ttg>Ctg p.L271L BRCA 16 74943795 74943795 + Silent SNP C C A TCGA-AR-A250-01A-31D-A167-09 TCGA-AR-A250-10A-01D-A167-09 g.chr16:74943795C>A c.1410G>T c.(1408-1410)ctG>ctT p.L470L BRCA 16 74946204 74946204 + Silent SNP G G C TCGA-GI-A2C8-01A-11D-A16D-09 TCGA-GI-A2C8-11A-22D-A16D-09 g.chr16:74946204G>C c.1281C>G c.(1279-1281)gtC>gtG p.V427V BRCA 16 74972086 74972086 + Missense_Mutation SNP G G A TCGA-AO-A0J9-01A-11W-A050-09 TCGA-AO-A0J9-10A-01W-A055-09 g.chr16:74972086G>A c.613C>T c.(613-615)Cac>Tac p.H205Y BRCA 16 74972100 74972100 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr16:74972100T>G c.599A>C c.(598-600)cAc>cCc p.H200P CESC 16 74919569 74919569 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr16:74919569C>T c.2671G>A c.(2671-2673)Gac>Aac p.D891N CESC 16 74999681 74999681 + Missense_Mutation SNP C C G TCGA-DS-A0VL-01A-21D-A10S-08 TCGA-DS-A0VL-10A-01D-A10S-08 g.chr16:74999681C>G c.94G>C c.(94-96)Gtg>Ctg p.V32L COAD 16 74919552 74919552 + Splice_Site SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:74919552G>A c.2688C>T c.(2686-2688)atC>atT p.I896I COAD 16 74920199 74920199 + Nonsense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr16:74920199G>A c.2515C>T c.(2515-2517)Cga>Tga p.R839* COAD 16 74923711 74923711 + Silent SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:74923711A>C c.2085T>G c.(2083-2085)gtT>gtG p.V695V COAD 16 74943496 74943496 + Frame_Shift_Del DEL G G - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr16:74943496delG c.1545delC c.(1543-1545)cccfs p.P515fs COAD 16 74949791 74949792 + Frame_Shift_Ins INS - - CA TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr16:74949791_74949792insCA c.1200_1201insTG c.(1198-1203)gtgcaafs p.Q401fs COAD 16 74950097 74950097 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr16:74950097G>A c.1027C>T c.(1027-1029)Ccg>Tcg p.P343S COAD 16 74955897 74955897 + Silent SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:74955897G>A c.834C>T c.(832-834)ttC>ttT p.F278F COAD 16 74976691 74976691 + Frame_Shift_Del DEL T T - TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:74976691delT c.479delA c.(478-480)aatfs p.N160fs COAD 16 74983682 74983682 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:74983682G>A c.341C>T c.(340-342)gCg>gTg p.A114V COADREAD 16 74908248 74908248 + Silent SNP G G A TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr16:74908248G>A c.2784C>T c.(2782-2784)caC>caT p.H928H COADREAD 16 74919552 74919552 + Splice_Site SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:74919552G>A c.2688C>T c.(2686-2688)atC>atT p.I896I COADREAD 16 74920199 74920199 + Nonsense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr16:74920199G>A c.2515C>T c.(2515-2517)Cga>Tga p.R839* COADREAD 16 74923711 74923711 + Silent SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:74923711A>C c.2085T>G c.(2083-2085)gtT>gtG p.V695V COADREAD 16 74943496 74943496 + Frame_Shift_Del DEL G G - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr16:74943496delG c.1545delC c.(1543-1545)cccfs p.P515fs COADREAD 16 74949791 74949792 + Frame_Shift_Ins INS - - CA TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr16:74949791_74949792insCA c.1200_1201insTG c.(1198-1203)gtgcaafs p.Q401fs COADREAD 16 74950097 74950097 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr16:74950097G>A c.1027C>T c.(1027-1029)Ccg>Tcg p.P343S COADREAD 16 74955897 74955897 + Silent SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:74955897G>A c.834C>T c.(832-834)ttC>ttT p.F278F COADREAD 16 74976691 74976691 + Frame_Shift_Del DEL T T - TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:74976691delT c.479delA c.(478-480)aatfs p.N160fs COADREAD 16 74983682 74983682 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:74983682G>A c.341C>T c.(340-342)gCg>gTg p.A114V DLBC 16 74943471 74943471 + Missense_Mutation SNP T T C TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr16:74943471T>C c.1570A>G c.(1570-1572)Acg>Gcg p.T524A ESCA 16 74943462 74943462 + Missense_Mutation SNP C C T TCGA-R6-A6XQ-01B-11D-A33E-09 TCGA-R6-A6XQ-10A-01D-A33H-09 g.chr16:74943462C>T c.1579G>A c.(1579-1581)Ggg>Agg p.G527R ESCA 16 74943477 74943477 + Missense_Mutation SNP C C T TCGA-2H-A9GJ-01A-11D-A37C-09 TCGA-2H-A9GJ-11A-11D-A37F-09 g.chr16:74943477C>T c.1564G>A c.(1564-1566)Gtg>Atg p.V522M ESCA 16 74946165 74946165 + Silent SNP G G A TCGA-L5-A8NT-01A-11D-A37C-09 TCGA-L5-A8NT-11A-11D-A37F-09 g.chr16:74946165G>A c.1320C>T c.(1318-1320)aaC>aaT p.N440N ESCA 16 74990506 74990506 + Missense_Mutation SNP C C T TCGA-LN-A8HZ-01A-11D-A36J-09 TCGA-LN-A8HZ-10A-01D-A36M-09 g.chr16:74990506C>T c.107G>A c.(106-108)cGc>cAc p.R36H GBM 16 74976699 74976699 + Missense_Mutation SNP A A T TCGA-02-0055-01A-01D-1490-08 TCGA-02-0055-10A-01D-1490-08 g.chr16:74976699A>T c.471T>A c.(469-471)aaT>aaA p.N157K GBMLGG 16 74943721 74943721 + Splice_Site SNP A A G TCGA-FG-A710-01A-12D-A33T-08 TCGA-FG-A710-10A-01D-A33W-08 g.chr16:74943721A>G c.1484T>C c.(1483-1485)gTg>gCg p.V495A GBMLGG 16 74976699 74976699 + Missense_Mutation SNP A A T TCGA-02-0055-01A-01D-1490-08 TCGA-02-0055-10A-01D-1490-08 g.chr16:74976699A>T c.471T>A c.(469-471)aaT>aaA p.N157K HNSC 16 74908238 74908238 + Missense_Mutation SNP G G A TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chr16:74908238G>A c.2794C>T c.(2794-2796)Cgg>Tgg p.R932W HNSC 16 74908337 74908337 + Missense_Mutation SNP C C T TCGA-CN-A6V6-01A-12D-A34J-08 TCGA-CN-A6V6-10A-01D-A34M-08 g.chr16:74908337C>T c.2695G>A c.(2695-2697)Ggc>Agc p.G899S HNSC 16 74919617 74919617 + Missense_Mutation SNP G G C TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr16:74919617G>C c.2623C>G c.(2623-2625)Ctg>Gtg p.L875V HNSC 16 74921637 74921637 + Missense_Mutation SNP G G A TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr16:74921637G>A c.2363C>T c.(2362-2364)tCt>tTt p.S788F HNSC 16 74927630 74927631 + Frame_Shift_Ins INS - - A TCGA-F7-A61V-01A-11D-A28R-08 TCGA-F7-A61V-10A-01D-A28U-08 g.chr16:74927630_74927631insA c.1946_1947insT c.(1945-1947)atcfs p.I649fs HNSC 16 74927661 74927661 + Missense_Mutation SNP C C T TCGA-D6-A6EN-01A-11D-A31L-08 TCGA-D6-A6EN-10A-01D-A31J-08 g.chr16:74927661C>T c.1916G>A c.(1915-1917)cGa>cAa p.R639Q HNSC 16 74946248 74946248 + Missense_Mutation SNP C C G TCGA-WA-A7GZ-01A-11D-A34J-08 TCGA-WA-A7GZ-10A-01D-A34M-08 g.chr16:74946248C>G c.1237G>C c.(1237-1239)Gac>Cac p.D413H HNSC 16 74949788 74949788 + Missense_Mutation SNP T T C TCGA-F7-8489-01A-31D-2394-08 TCGA-F7-8489-10A-01D-2394-08 g.chr16:74949788T>C c.1204A>G c.(1204-1206)Atc>Gtc p.I402V HNSC 16 74949804 74949804 + Silent SNP G G C TCGA-CV-A45X-01A-21D-A25D-08 TCGA-CV-A45X-10A-01D-A25E-08 g.chr16:74949804G>C c.1188C>G c.(1186-1188)tcC>tcG p.S396S HNSC 16 74951881 74951881 + Silent SNP C C T TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr16:74951881C>T c.912G>A c.(910-912)acG>acA p.T304T HNSC 16 74951892 74951892 + Nonsense_Mutation SNP G G A TCGA-QK-A64Z-01A-11D-A30E-08 TCGA-QK-A64Z-10A-01D-A30H-08 g.chr16:74951892G>A c.901C>T c.(901-903)Caa>Taa p.Q301* HNSC 16 74957842 74957842 + Silent SNP G G C TCGA-CV-A45Q-01A-11D-A24D-08 TCGA-CV-A45Q-10A-01D-A24F-08 g.chr16:74957842G>C c.711C>G c.(709-711)gtC>gtG p.V237V HNSC 16 74972117 74972117 + Silent SNP G G A TCGA-BA-A6DJ-01A-11D-A30E-08 TCGA-BA-A6DJ-10A-01D-A30H-08 g.chr16:74972117G>A c.582C>T c.(580-582)atC>atT p.I194I HNSC 16 74972149 74972149 + Missense_Mutation SNP C C A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr16:74972149C>A c.550G>T c.(550-552)Gtg>Ttg p.V184L HNSC 16 74985406 74985406 + Silent SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:74985406G>A c.276C>T c.(274-276)gaC>gaT p.D92D HNSC 16 75018899 75018899 + Missense_Mutation SNP C C T TCGA-CQ-A4CB-01A-11D-A25D-08 TCGA-CQ-A4CB-10A-01D-A25E-08 g.chr16:75018899C>T c.17G>A c.(16-18)aGc>aAc p.S6N KICH 16 74942828 74942828 + Missense_Mutation SNP A A G TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr16:74942828A>G c.1690T>C c.(1690-1692)Tct>Cct p.S564P KICH 16 74942844 74942844 + Silent SNP T T C TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr16:74942844T>C c.1674A>G c.(1672-1674)acA>acG p.T558T KICH 16 74942865 74942865 + Silent SNP T T C TCGA-KL-8344-01A-11D-2310-10 TCGA-KL-8344-11A-01D-2310-10 g.chr16:74942865T>C c.1653A>G c.(1651-1653)gtA>gtG p.V551V KICH 16 74942865 74942865 + Silent SNP T T C TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr16:74942865T>C c.1653A>G c.(1651-1653)gtA>gtG p.V551V KICH 16 74976691 74976691 + Frame_Shift_Del DEL T T - TCGA-KN-8430-01A-11D-2310-10 TCGA-KN-8430-11A-01D-2311-10 g.chr16:74976691delT c.479delA c.(478-480)aatfs p.N160fs KIPAN 16 74942828 74942828 + Missense_Mutation SNP A A G TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr16:74942828A>G c.1690T>C c.(1690-1692)Tct>Cct p.S564P KIPAN 16 74942844 74942844 + Silent SNP T T C TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr16:74942844T>C c.1674A>G c.(1672-1674)acA>acG p.T558T KIPAN 16 74942865 74942865 + Silent SNP T T C TCGA-KL-8344-01A-11D-2310-10 TCGA-KL-8344-11A-01D-2310-10 g.chr16:74942865T>C c.1653A>G c.(1651-1653)gtA>gtG p.V551V KIPAN 16 74942865 74942865 + Silent SNP T T C TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr16:74942865T>C c.1653A>G c.(1651-1653)gtA>gtG p.V551V KIPAN 16 74976685 74976685 + Missense_Mutation SNP T T C TCGA-5P-A9K8-01A-11D-A42J-10 TCGA-5P-A9K8-10A-01D-A42M-10 g.chr16:74976685T>C c.485A>G c.(484-486)aAc>aGc p.N162S KIPAN 16 74976691 74976691 + Frame_Shift_Del DEL T T - TCGA-KN-8430-01A-11D-2310-10 TCGA-KN-8430-11A-01D-2311-10 g.chr16:74976691delT c.479delA c.(478-480)aatfs p.N160fs KIPAN 16 74990405 74990405 + Missense_Mutation SNP G G A TCGA-B3-4104-01A-01D-1458-08 TCGA-B3-4104-10A-01D-1458-08 g.chr16:74990405G>A c.208C>T c.(208-210)Cat>Tat p.H70Y KIRP 16 74976685 74976685 + Missense_Mutation SNP T T C TCGA-5P-A9K8-01A-11D-A42J-10 TCGA-5P-A9K8-10A-01D-A42M-10 g.chr16:74976685T>C c.485A>G c.(484-486)aAc>aGc p.N162S KIRP 16 74990405 74990405 + Missense_Mutation SNP G G A TCGA-B3-4104-01A-01D-1458-08 TCGA-B3-4104-10A-01D-1458-08 g.chr16:74990405G>A c.208C>T c.(208-210)Cat>Tat p.H70Y LGG 16 74943721 74943721 + Splice_Site SNP A A G TCGA-FG-A710-01A-12D-A33T-08 TCGA-FG-A710-10A-01D-A33W-08 g.chr16:74943721A>G c.1484T>C c.(1483-1485)gTg>gCg p.V495A LIHC 16 74919609 74919609 + Silent SNP C C T TCGA-DD-A73C-01A-12D-A33K-10 TCGA-DD-A73C-10A-01D-A33K-10 g.chr16:74919609C>T c.2631G>A c.(2629-2631)gaG>gaA p.E877E LIHC 16 74943789 74943789 + Silent SNP T T C TCGA-BD-A2L6-01A-11D-A20W-10 TCGA-BD-A2L6-11A-21D-A20W-10 g.chr16:74943789T>C c.1416A>G c.(1414-1416)aaA>aaG p.K472K LUAD 16 74908272 74908272 + Silent SNP G G A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr16:74908272G>A c.2760C>T c.(2758-2760)ttC>ttT p.F920F LUAD 16 74908315 74908315 + Missense_Mutation SNP C C T TCGA-J2-8194-01A-11D-2238-08 TCGA-J2-8194-10A-01D-2238-08 g.chr16:74908315C>T c.2717G>A c.(2716-2718)cGg>cAg p.R906Q LUAD 16 74920199 74920199 + Nonsense_Mutation SNP G G A TCGA-44-3396-01A-01D-1553-08 TCGA-44-3396-10A-01D-1265-08 g.chr16:74920199G>A c.2515C>T c.(2515-2517)Cga>Tga p.R839* LUAD 16 74921599 74921599 + Missense_Mutation SNP T T A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr16:74921599T>A c.2401A>T c.(2401-2403)Act>Tct p.T801S LUAD 16 74927609 74927609 + Silent SNP C C A TCGA-73-4668-01A-01D-1265-08 TCGA-73-4668-11A-01D-1265-08 g.chr16:74927609C>A c.1968G>T c.(1966-1968)ctG>ctT p.L656L LUAD 16 74927627 74927627 + Missense_Mutation SNP C C A TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr16:74927627C>A c.1950G>T c.(1948-1950)caG>caT p.Q650H LUAD 16 74927676 74927676 + Nonsense_Mutation SNP G G C TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr16:74927676G>C c.1901C>G c.(1900-1902)tCa>tGa p.S634* LUAD 16 74942824 74942824 + Missense_Mutation SNP G G T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr16:74942824G>T c.1694C>A c.(1693-1695)cCc>cAc p.P565H LUAD 16 74943460 74943460 + Silent SNP C C T TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr16:74943460C>T c.1581G>A c.(1579-1581)ggG>ggA p.G527G LUAD 16 74946198 74946198 + Missense_Mutation SNP C C A TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr16:74946198C>A c.1287G>T c.(1285-1287)atG>atT p.M429I LUAD 16 74951836 74951836 + Missense_Mutation SNP C C G TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr16:74951836C>G c.957G>C c.(955-957)caG>caC p.Q319H LUAD 16 74951893 74951893 + Silent SNP A A G TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr16:74951893A>G c.900T>C c.(898-900)taT>taC p.Y300Y LUAD 16 74957890 74957890 + Silent SNP G G A TCGA-86-7953-01A-11D-2184-08 TCGA-86-7953-10A-01D-2184-08 g.chr16:74957890G>A c.663C>T c.(661-663)taC>taT p.Y221Y LUAD 16 74972089 74972089 + Nonsense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr16:74972089C>A c.610G>T c.(610-612)Gag>Tag p.E204* LUAD 16 74976635 74976635 + Splice_Site SNP C C T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr16:74976635C>T c.e7+1 LUAD 16 74976686 74976686 + Missense_Mutation SNP T T G TCGA-55-7570-01A-11D-2036-08 TCGA-55-7570-10A-01D-2036-08 g.chr16:74976686T>G c.484A>C c.(484-486)Aac>Cac p.N162H LUAD 16 74982429 74982429 + Silent SNP G G A TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chr16:74982429G>A c.433C>T c.(433-435)Ctg>Ttg p.L145L LUSC 16 74937894 74937894 + Missense_Mutation SNP C C A TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr16:74937894C>A c.1817G>T c.(1816-1818)cGc>cTc p.R606L LUSC 16 74949878 74949878 + Missense_Mutation SNP G G A TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr16:74949878G>A c.1114C>T c.(1114-1116)Ccc>Tcc p.P372S LUSC 16 74990499 74990499 + Missense_Mutation SNP G G C TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr16:74990499G>C c.114C>G c.(112-114)ttC>ttG p.F38L PRAD 16 74950052 74950052 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:74950052G>A c.1072C>T c.(1072-1074)Cac>Tac p.H358Y PRAD 16 74955991 74955991 + Missense_Mutation SNP T T C TCGA-J4-A67M-01A-11D-A30E-08 TCGA-J4-A67M-10A-01D-A30H-08 g.chr16:74955991T>C c.740A>G c.(739-741)aAt>aGt p.N247S READ 16 74908248 74908248 + Silent SNP G G A TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr16:74908248G>A c.2784C>T c.(2782-2784)caC>caT p.H928H SARC 16 74976691 74976691 + Frame_Shift_Del DEL T T - TCGA-WK-A8XX-01A-11D-A37C-09 TCGA-WK-A8XX-10A-01D-A37F-09 g.chr16:74976691delT c.479delA c.(478-480)aatfs p.N160fs SARC 16 74983665 74983665 + Missense_Mutation SNP G G A TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chr16:74983665G>A c.358C>T c.(358-360)Ctc>Ttc p.L120F SKCM 16 74908169 74908169 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr16:74908169G>A c.2863C>T c.(2863-2865)Cgg>Tgg p.R955W SKCM 16 74908231 74908231 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr16:74908231G>A c.2801C>T c.(2800-2802)tCg>tTg p.S934L SKCM 16 74919580 74919580 + Missense_Mutation SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr16:74919580G>A c.2660C>T c.(2659-2661)tCc>tTc p.S887F SKCM 16 74922108 74922108 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr16:74922108G>A c.2305C>T c.(2305-2307)Cct>Tct p.P769S SKCM 16 74922121 74922121 + Silent SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr16:74922121G>A c.2292C>T c.(2290-2292)ccC>ccT p.P764P SKCM 16 74923628 74923628 + Missense_Mutation SNP G G A TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr16:74923628G>A c.2168C>T c.(2167-2169)cCa>cTa p.P723L SKCM 16 74927577 74927577 + Splice_Site SNP A A C TCGA-D3-A1Q4-06A-11D-A196-08 TCGA-D3-A1Q4-10A-01D-A198-08 g.chr16:74927577A>C c.2000T>G c.(1999-2001)aTa>aGa p.I667R SKCM 16 74942837 74942837 + Missense_Mutation SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr16:74942837G>A c.1681C>T c.(1681-1683)Cgg>Tgg p.R561W SKCM 16 74943437 74943437 + Missense_Mutation SNP G G A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr16:74943437G>A c.1604C>T c.(1603-1605)cCc>cTc p.P535L SKCM 16 74946209 74946209 + Missense_Mutation SNP G G A TCGA-FS-A1ZT-06A-11D-A197-08 TCGA-FS-A1ZT-10A-01D-A199-08 g.chr16:74946209G>A c.1276C>T c.(1276-1278)Cgt>Tgt p.R426C SKCM 16 74949783 74949783 + Silent SNP C C T TCGA-EE-A2GT-06A-12D-A197-08 TCGA-EE-A2GT-10A-01D-A199-08 g.chr16:74949783C>T c.1209G>A c.(1207-1209)cgG>cgA p.R403R SKCM 16 74949875 74949875 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr16:74949875G>A c.1117C>T c.(1117-1119)Cct>Tct p.P373S SKCM 16 74955968 74955968 + Missense_Mutation SNP G G A TCGA-D3-A5GL-06A-11D-A27K-08 TCGA-D3-A5GL-10A-01D-A27N-08 g.chr16:74955968G>A c.763C>T c.(763-765)Ccc>Tcc p.P255S SKCM 16 74957846 74957846 + Missense_Mutation SNP G G A TCGA-ER-A19M-06A-61D-A23B-08 TCGA-ER-A19M-10A-01D-A23B-08 g.chr16:74957846G>A c.707C>T c.(706-708)cCt>cTt p.P236L SKCM 16 74972116 74972116 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr16:74972116G>A c.583C>T c.(583-585)Cat>Tat p.H195Y SKCM 16 74972117 74972117 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:74972117G>A c.582C>T c.(580-582)atC>atT p.I194I SKCM 16 74976658 74976658 + Missense_Mutation SNP T T A TCGA-ER-A195-06A-11D-A196-08 TCGA-ER-A195-10A-01D-A198-08 g.chr16:74976658T>A c.512A>T c.(511-513)gAt>gTt p.D171V SKCM 16 74990485 74990485 + Missense_Mutation SNP T T C TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr16:74990485T>C c.128A>G c.(127-129)aAt>aGt p.N43S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 16 74942865 74942865 single base substitution T C downstream_gene_variant BLCA-CN 16 74942865 74942865 single base substitution T C exon_variant BLCA-CN 16 74942865 74942865 single base substitution T C intron_variant BLCA-CN 16 74942865 74942865 single base substitution T C synonymous_variant V100V 300A>G BLCA-CN 16 74942865 74942865 single base substitution T C synonymous_variant V551V 1653A>G BLCA-CN 16 74942865 74942865 single base substitution T C upstream_gene_variant BLCA-CN 16 74983679 74983679 single base substitution A G downstream_gene_variant BLCA-CN 16 74983679 74983679 single base substitution A G exon_variant BLCA-CN 16 74983679 74983679 single base substitution A G missense_variant V115A 344T>C BLCA-CN 16 74983679 74983679 single base substitution A G missense_variant V94A 281T>C BLCA-US 16 74920244 74920244 single base substitution C A downstream_gene_variant BLCA-US 16 74920244 74920244 single base substitution C A exon_variant BLCA-US 16 74920244 74920244 single base substitution C A stop_gained E138* 412G>T BLCA-US 16 74920244 74920244 single base substitution C A stop_gained E824* 2470G>T BLCA-US 16 74920244 74920244 single base substitution C A upstream_gene_variant BOCA-FR 16 74920931 74920931 single base substitution A G downstream_gene_variant BOCA-FR 16 74920931 74920931 single base substitution A G intron_variant BOCA-FR 16 74920931 74920931 single base substitution A G upstream_gene_variant BRCA-EU 16 74903403 74903403 single base substitution G A downstream_gene_variant BRCA-EU 16 74909044 74909044 single base substitution G A intron_variant BRCA-EU 16 74910916 74910916 single base substitution C A intron_variant BRCA-EU 16 74911317 74911324 deletion of <=200bp CTTGACAG - intron_variant BRCA-EU 16 74912057 74912057 single base substitution G C intron_variant BRCA-EU 16 74912556 74912556 deletion of <=200bp A - intron_variant BRCA-EU 16 74913543 74913543 single base substitution C T intron_variant BRCA-EU 16 74917228 74917228 single base substitution G A downstream_gene_variant BRCA-EU 16 74917228 74917228 single base substitution G A intron_variant BRCA-EU 16 74917403 74917403 single base substitution C T downstream_gene_variant BRCA-EU 16 74917403 74917403 single base substitution C T intron_variant BRCA-EU 16 74917672 74917672 single base substitution C A downstream_gene_variant BRCA-EU 16 74917672 74917672 single base substitution C A intron_variant BRCA-EU 16 74917778 74917778 single base substitution G C downstream_gene_variant BRCA-EU 16 74917778 74917778 single base substitution G C intron_variant BRCA-EU 16 74918277 74918277 single base substitution C T downstream_gene_variant BRCA-EU 16 74918277 74918277 single base substitution C T intron_variant BRCA-EU 16 74919248 74919248 single base substitution C A downstream_gene_variant BRCA-EU 16 74919248 74919248 single base substitution C A intron_variant BRCA-EU 16 74919873 74919873 single base substitution G C downstream_gene_variant BRCA-EU 16 74919873 74919873 single base substitution G C exon_variant BRCA-EU 16 74919873 74919873 single base substitution G C intron_variant BRCA-EU 16 74922297 74922297 single base substitution C T downstream_gene_variant BRCA-EU 16 74922297 74922297 single base substitution C T intron_variant BRCA-EU 16 74922297 74922297 single base substitution C T upstream_gene_variant BRCA-EU 16 74922923 74922923 single base substitution A C downstream_gene_variant BRCA-EU 16 74922923 74922923 single base substitution A C intron_variant BRCA-EU 16 74922923 74922923 single base substitution A C upstream_gene_variant BRCA-EU 16 74924019 74924019 single base substitution C T downstream_gene_variant BRCA-EU 16 74924019 74924019 single base substitution C T intron_variant BRCA-EU 16 74924019 74924019 single base substitution C T upstream_gene_variant BRCA-EU 16 74928337 74928337 single base substitution G A intron_variant BRCA-EU 16 74928337 74928337 single base substitution G A upstream_gene_variant BRCA-EU 16 74928491 74928491 single base substitution G C intron_variant BRCA-EU 16 74928491 74928491 single base substitution G C upstream_gene_variant BRCA-EU 16 74931474 74931474 single base substitution C G intron_variant BRCA-EU 16 74931474 74931474 single base substitution C G upstream_gene_variant BRCA-EU 16 74931935 74931935 single base substitution C G intron_variant BRCA-EU 16 74931935 74931935 single base substitution C G upstream_gene_variant BRCA-EU 16 74932197 74932197 single base substitution C G intron_variant BRCA-EU 16 74932197 74932197 single base substitution C G upstream_gene_variant BRCA-EU 16 74932465 74932465 single base substitution G A intron_variant BRCA-EU 16 74932465 74932465 single base substitution G A upstream_gene_variant BRCA-EU 16 74934600 74934600 single base substitution G C intron_variant BRCA-EU 16 74936531 74936531 single base substitution T C intron_variant BRCA-EU 16 74941406 74941406 single base substitution G A downstream_gene_variant BRCA-EU 16 74941406 74941406 single base substitution G A intron_variant BRCA-EU 16 74941406 74941406 single base substitution G A upstream_gene_variant BRCA-EU 16 74941954 74941954 single base substitution T G downstream_gene_variant BRCA-EU 16 74941954 74941954 single base substitution T G intron_variant BRCA-EU 16 74941954 74941954 single base substitution T G upstream_gene_variant BRCA-EU 16 74942278 74942278 single base substitution G A downstream_gene_variant BRCA-EU 16 74942278 74942278 single base substitution G A intron_variant BRCA-EU 16 74942278 74942278 single base substitution G A upstream_gene_variant BRCA-EU 16 74945393 74945393 single base substitution C T downstream_gene_variant BRCA-EU 16 74945393 74945393 single base substitution C T intron_variant BRCA-EU 16 74945393 74945393 single base substitution C T upstream_gene_variant BRCA-EU 16 74947416 74947416 single base substitution T G downstream_gene_variant BRCA-EU 16 74947416 74947416 single base substitution T G intron_variant BRCA-EU 16 74947416 74947416 single base substitution T G upstream_gene_variant BRCA-EU 16 74947951 74947951 single base substitution C T downstream_gene_variant BRCA-EU 16 74947951 74947951 single base substitution C T intron_variant BRCA-EU 16 74947951 74947951 single base substitution C T upstream_gene_variant BRCA-EU 16 74948276 74948276 single base substitution A C downstream_gene_variant BRCA-EU 16 74948276 74948276 single base substitution A C intron_variant BRCA-EU 16 74948276 74948276 single base substitution A C upstream_gene_variant BRCA-EU 16 74948609 74948609 single base substitution A G downstream_gene_variant BRCA-EU 16 74948609 74948609 single base substitution A G intron_variant BRCA-EU 16 74948609 74948609 single base substitution A G upstream_gene_variant BRCA-EU 16 74949932 74949932 single base substitution G C exon_variant BRCA-EU 16 74949932 74949932 single base substitution G C intron_variant BRCA-EU 16 74949932 74949932 single base substitution G C upstream_gene_variant BRCA-EU 16 74952140 74952140 single base substitution T A intron_variant BRCA-EU 16 74952140 74952140 single base substitution T A upstream_gene_variant BRCA-EU 16 74952724 74952724 single base substitution G A intron_variant BRCA-EU 16 74952724 74952724 single base substitution G A upstream_gene_variant BRCA-EU 16 74954548 74954548 single base substitution C T downstream_gene_variant BRCA-EU 16 74954548 74954548 single base substitution C T intron_variant BRCA-EU 16 74954548 74954548 single base substitution C T upstream_gene_variant BRCA-EU 16 74956400 74956400 single base substitution A T downstream_gene_variant BRCA-EU 16 74956400 74956400 single base substitution A T intron_variant BRCA-EU 16 74956400 74956400 single base substitution A T upstream_gene_variant BRCA-EU 16 74959056 74959056 single base substitution A C intron_variant BRCA-EU 16 74959056 74959056 single base substitution A C upstream_gene_variant BRCA-EU 16 74960167 74960167 single base substitution G A intron_variant BRCA-EU 16 74960167 74960167 single base substitution G A upstream_gene_variant BRCA-EU 16 74960759 74960759 single base substitution A C intron_variant BRCA-EU 16 74960759 74960759 single base substitution A C upstream_gene_variant BRCA-EU 16 74962014 74962014 single base substitution C T intron_variant BRCA-EU 16 74962327 74962327 single base substitution G T intron_variant BRCA-EU 16 74962979 74962979 single base substitution T C intron_variant BRCA-EU 16 74964237 74964265 deletion of <=200bp TAAATTTCTCTTTAAAAAATGGAAACAGT - intron_variant BRCA-EU 16 74964298 74964298 single base substitution C G intron_variant BRCA-EU 16 74966682 74966682 single base substitution C T intron_variant BRCA-EU 16 74966682 74966682 single base substitution C T upstream_gene_variant BRCA-EU 16 74967038 74967038 insertion of <=200bp - A intron_variant BRCA-EU 16 74967038 74967038 insertion of <=200bp - A upstream_gene_variant BRCA-EU 16 74968206 74968206 deletion of <=200bp T - downstream_gene_variant BRCA-EU 16 74968206 74968206 deletion of <=200bp T - intron_variant BRCA-EU 16 74968206 74968206 deletion of <=200bp T - upstream_gene_variant BRCA-EU 16 74969234 74969234 deletion of <=200bp A - downstream_gene_variant BRCA-EU 16 74969234 74969234 deletion of <=200bp A - intron_variant BRCA-EU 16 74969234 74969234 deletion of <=200bp A - upstream_gene_variant BRCA-EU 16 74969445 74969445 insertion of <=200bp - AA downstream_gene_variant BRCA-EU 16 74969445 74969445 insertion of <=200bp - AA intron_variant BRCA-EU 16 74969445 74969445 insertion of <=200bp - AA upstream_gene_variant BRCA-EU 16 74971283 74971283 single base substitution G A downstream_gene_variant BRCA-EU 16 74971283 74971283 single base substitution G A intron_variant BRCA-EU 16 74972440 74972440 insertion of <=200bp - T downstream_gene_variant BRCA-EU 16 74972440 74972440 insertion of <=200bp - T intron_variant BRCA-EU 16 74973318 74973318 single base substitution T C downstream_gene_variant BRCA-EU 16 74973318 74973318 single base substitution T C intron_variant BRCA-EU 16 74973784 74973784 single base substitution C T downstream_gene_variant BRCA-EU 16 74973784 74973784 single base substitution C T intron_variant BRCA-EU 16 74973802 74973802 single base substitution G C downstream_gene_variant BRCA-EU 16 74973802 74973802 single base substitution G C intron_variant BRCA-EU 16 74979681 74979682 deletion of <=200bp GA - downstream_gene_variant BRCA-EU 16 74979681 74979682 deletion of <=200bp GA - intron_variant BRCA-EU 16 74981310 74981310 insertion of <=200bp - AATCAGTGTA downstream_gene_variant BRCA-EU 16 74981310 74981310 insertion of <=200bp - AATCAGTGTA intron_variant BRCA-EU 16 74984924 74984924 single base substitution G A intron_variant BRCA-EU 16 74986792 74986792 single base substitution G A downstream_gene_variant BRCA-EU 16 74986792 74986792 single base substitution G A intron_variant BRCA-EU 16 74987917 74987917 single base substitution G C downstream_gene_variant BRCA-EU 16 74987917 74987917 single base substitution G C intron_variant BRCA-EU 16 74988107 74988107 single base substitution G C downstream_gene_variant BRCA-EU 16 74988107 74988107 single base substitution G C intron_variant BRCA-EU 16 74988487 74988487 single base substitution G C downstream_gene_variant BRCA-EU 16 74988487 74988487 single base substitution G C intron_variant BRCA-EU 16 74988809 74988809 single base substitution T G downstream_gene_variant BRCA-EU 16 74988809 74988809 single base substitution T G intron_variant BRCA-EU 16 74990716 74990716 single base substitution G C intron_variant BRCA-EU 16 74991284 74991284 single base substitution G C intron_variant BRCA-EU 16 74991340 74991340 single base substitution G A intron_variant BRCA-EU 16 74992664 74992664 single base substitution A T downstream_gene_variant BRCA-EU 16 74992664 74992664 single base substitution A T intron_variant BRCA-EU 16 74993919 74993919 single base substitution G C downstream_gene_variant BRCA-EU 16 74993919 74993919 single base substitution G C intron_variant BRCA-EU 16 74994788 74994788 single base substitution A C downstream_gene_variant BRCA-EU 16 74994788 74994788 single base substitution A C intron_variant BRCA-EU 16 74996349 74996349 single base substitution C G downstream_gene_variant BRCA-EU 16 74996349 74996349 single base substitution C G intron_variant BRCA-EU 16 74997366 74997366 single base substitution C T intron_variant BRCA-EU 16 74997652 74997652 single base substitution A T intron_variant BRCA-EU 16 75000331 75000331 single base substitution T C intron_variant BRCA-EU 16 75000331 75000331 single base substitution T C upstream_gene_variant BRCA-EU 16 75001301 75001301 single base substitution C G intron_variant BRCA-EU 16 75001301 75001301 single base substitution C G upstream_gene_variant BRCA-EU 16 75002729 75002729 single base substitution C T intron_variant BRCA-EU 16 75002729 75002729 single base substitution C T upstream_gene_variant BRCA-EU 16 75005247 75005247 insertion of <=200bp - A intron_variant BRCA-EU 16 75006889 75006889 single base substitution G T intron_variant BRCA-EU 16 75007122 75007122 single base substitution A G intron_variant BRCA-EU 16 75008227 75008227 single base substitution G C intron_variant BRCA-EU 16 75008628 75008628 single base substitution G A intron_variant BRCA-EU 16 75009583 75009583 single base substitution A C intron_variant BRCA-EU 16 75009874 75009874 deletion of <=200bp C - intron_variant BRCA-EU 16 75011674 75011674 insertion of <=200bp - A intron_variant BRCA-EU 16 75014351 75014351 single base substitution A G intron_variant BRCA-EU 16 75014351 75014351 single base substitution A G upstream_gene_variant BRCA-EU 16 75015984 75015984 single base substitution T C intron_variant BRCA-EU 16 75015984 75015984 single base substitution T C upstream_gene_variant BRCA-EU 16 75016737 75016737 single base substitution C G intron_variant BRCA-EU 16 75016737 75016737 single base substitution C G upstream_gene_variant BRCA-EU 16 75017293 75017293 single base substitution C T intron_variant BRCA-EU 16 75017293 75017293 single base substitution C T upstream_gene_variant BRCA-EU 16 75017568 75017568 single base substitution C A intron_variant BRCA-EU 16 75017568 75017568 single base substitution C A upstream_gene_variant BRCA-EU 16 75019358 75019358 single base substitution C G intron_variant BRCA-EU 16 75019358 75019358 single base substitution C G upstream_gene_variant BRCA-EU 16 75020640 75020640 single base substitution C G intron_variant BRCA-EU 16 75020640 75020640 single base substitution C G upstream_gene_variant BRCA-EU 16 75021663 75021663 single base substitution C T intron_variant BRCA-EU 16 75021663 75021663 single base substitution C T upstream_gene_variant BRCA-EU 16 75022201 75022201 deletion of <=200bp A - intron_variant BRCA-EU 16 75022201 75022201 deletion of <=200bp A - upstream_gene_variant BRCA-EU 16 75023049 75023049 single base substitution C A intron_variant BRCA-EU 16 75023049 75023049 single base substitution C A upstream_gene_variant BRCA-EU 16 75023227 75023227 single base substitution T A intron_variant BRCA-EU 16 75023227 75023227 single base substitution T A upstream_gene_variant BRCA-EU 16 75023251 75023251 single base substitution G A intron_variant BRCA-EU 16 75023251 75023251 single base substitution G A upstream_gene_variant BRCA-EU 16 75023299 75023299 single base substitution G C intron_variant BRCA-EU 16 75023299 75023299 single base substitution G C upstream_gene_variant BRCA-EU 16 75023582 75023582 single base substitution A G intron_variant BRCA-EU 16 75023582 75023582 single base substitution A G upstream_gene_variant BRCA-EU 16 75024355 75024355 single base substitution C T intron_variant BRCA-EU 16 75024557 75024557 single base substitution T A intron_variant BRCA-EU 16 75026650 75026650 single base substitution T G intron_variant BRCA-EU 16 75027442 75027442 deletion of <=200bp T - intron_variant BRCA-EU 16 75027795 75027795 single base substitution C T intron_variant BRCA-EU 16 75028300 75028300 single base substitution C A intron_variant BRCA-EU 16 75033544 75033544 single base substitution C T intron_variant BRCA-EU 16 75033544 75033544 single base substitution C T upstream_gene_variant BRCA-EU 16 75037935 75037935 single base substitution T C upstream_gene_variant BRCA-FR 16 74904761 74904761 single base substitution G A downstream_gene_variant BRCA-FR 16 74913694 74913694 single base substitution T C intron_variant BRCA-FR 16 74932197 74932197 single base substitution C G intron_variant BRCA-FR 16 74932197 74932197 single base substitution C G upstream_gene_variant BRCA-FR 16 74952140 74952140 single base substitution T A intron_variant BRCA-FR 16 74952140 74952140 single base substitution T A upstream_gene_variant BRCA-FR 16 74952724 74952724 single base substitution G A intron_variant BRCA-FR 16 74952724 74952724 single base substitution G A upstream_gene_variant BRCA-FR 16 74964298 74964298 single base substitution C G intron_variant BRCA-FR 16 74973784 74973784 single base substitution C T downstream_gene_variant BRCA-FR 16 74973784 74973784 single base substitution C T intron_variant BRCA-FR 16 74975859 74975859 single base substitution C T downstream_gene_variant BRCA-FR 16 74975859 74975859 single base substitution C T intron_variant BRCA-FR 16 74990716 74990716 single base substitution G C intron_variant BRCA-FR 16 74993919 74993919 single base substitution G C downstream_gene_variant BRCA-FR 16 74993919 74993919 single base substitution G C intron_variant BRCA-FR 16 75014351 75014351 single base substitution A G intron_variant BRCA-FR 16 75014351 75014351 single base substitution A G upstream_gene_variant BRCA-FR 16 75016737 75016737 single base substitution C G intron_variant BRCA-FR 16 75016737 75016737 single base substitution C G upstream_gene_variant BRCA-FR 16 75020640 75020640 single base substitution C G intron_variant BRCA-FR 16 75020640 75020640 single base substitution C G upstream_gene_variant BRCA-FR 16 75027795 75027795 single base substitution C T intron_variant BRCA-FR 16 75029816 75029816 single base substitution A C intron_variant BRCA-FR 16 75035161 75035161 single base substitution G A upstream_gene_variant BRCA-UK 16 74910916 74910916 single base substitution C A intron_variant BRCA-UK 16 74919248 74919248 single base substitution C A downstream_gene_variant BRCA-UK 16 74919248 74919248 single base substitution C A intron_variant BRCA-UK 16 74920198 74920198 single base substitution C T downstream_gene_variant BRCA-UK 16 74920198 74920198 single base substitution C T exon_variant BRCA-UK 16 74920198 74920198 single base substitution C T missense_variant R153Q 458G>A BRCA-UK 16 74920198 74920198 single base substitution C T missense_variant R839Q 2516G>A BRCA-UK 16 74920198 74920198 single base substitution C T upstream_gene_variant BRCA-UK 16 74954548 74954548 single base substitution C T downstream_gene_variant BRCA-UK 16 74954548 74954548 single base substitution C T intron_variant BRCA-UK 16 74954548 74954548 single base substitution C T upstream_gene_variant BRCA-UK 16 75003451 75003451 single base substitution G T intron_variant BRCA-UK 16 75003451 75003451 single base substitution G T upstream_gene_variant BRCA-US 16 74943795 74943795 single base substitution C A downstream_gene_variant BRCA-US 16 74943795 74943795 single base substitution C A exon_variant BRCA-US 16 74943795 74943795 single base substitution C A synonymous_variant L19L 57G>T BRCA-US 16 74943795 74943795 single base substitution C A synonymous_variant L470L 1410G>T BRCA-US 16 74943795 74943795 single base substitution C A upstream_gene_variant BRCA-US 16 74946204 74946204 single base substitution G C downstream_gene_variant BRCA-US 16 74946204 74946204 single base substitution G C exon_variant BRCA-US 16 74946204 74946204 single base substitution G C synonymous_variant V427V 1281C>G BRCA-US 16 74946204 74946204 single base substitution G C upstream_gene_variant BRCA-US 16 74972086 74972086 single base substitution G A downstream_gene_variant BRCA-US 16 74972086 74972086 single base substitution G A exon_variant BRCA-US 16 74972086 74972086 single base substitution G A missense_variant H205Y 613C>T BRCA-US 16 74972100 74972100 single base substitution T G downstream_gene_variant BRCA-US 16 74972100 74972100 single base substitution T G exon_variant BRCA-US 16 74972100 74972100 single base substitution T G missense_variant H200P 599A>C BRCA-US 16 75033946 75033946 single base substitution A G exon_variant BRCA-US 16 75033946 75033946 single base substitution A G upstream_gene_variant BRCA-US 16 75033986 75033986 single base substitution G A exon_variant BRCA-US 16 75033986 75033986 single base substitution G A upstream_gene_variant BTCA-JP 16 74908304 74908304 single base substitution G A downstream_gene_variant BTCA-JP 16 74908304 74908304 single base substitution G A exon_variant BTCA-JP 16 74908304 74908304 single base substitution G A missense_variant R910C 2728C>T BTCA-JP 16 74922131 74922131 single base substitution A G downstream_gene_variant BTCA-JP 16 74922131 74922131 single base substitution A G exon_variant BTCA-JP 16 74922131 74922131 single base substitution A G intron_variant BTCA-JP 16 74922131 74922131 single base substitution A G missense_variant L761P 2282T>C BTCA-JP 16 74922131 74922131 single base substitution A G upstream_gene_variant BTCA-JP 16 74927685 74927685 single base substitution C T 3_prime_UTR_variant BTCA-JP 16 74927685 74927685 single base substitution C T exon_variant BTCA-JP 16 74927685 74927685 single base substitution C T missense_variant R199H 596G>A BTCA-JP 16 74927685 74927685 single base substitution C T missense_variant R33H 98G>A BTCA-JP 16 74927685 74927685 single base substitution C T missense_variant R631H 1892G>A BTCA-JP 16 74946152 74946152 single base substitution A G downstream_gene_variant BTCA-JP 16 74946152 74946152 single base substitution A G exon_variant BTCA-JP 16 74946152 74946152 single base substitution A G missense_variant F445L 1333T>C BTCA-JP 16 74946152 74946152 single base substitution A G upstream_gene_variant BTCA-JP 16 74957687 74957687 single base substitution C T downstream_gene_variant BTCA-JP 16 74957687 74957687 single base substitution C T intron_variant BTCA-JP 16 74957687 74957687 single base substitution C T upstream_gene_variant BTCA-JP 16 74976537 74976537 single base substitution C T downstream_gene_variant BTCA-JP 16 74976537 74976537 single base substitution C T intron_variant BTCA-JP 16 75033664 75033664 single base substitution C G intron_variant BTCA-JP 16 75033664 75033664 single base substitution C G upstream_gene_variant CESC-US 16 74919569 74919569 single base substitution C T downstream_gene_variant CESC-US 16 74919569 74919569 single base substitution C T exon_variant CESC-US 16 74919569 74919569 single base substitution C T missense_variant D205N 613G>A CESC-US 16 74919569 74919569 single base substitution C T missense_variant D891N 2671G>A CESC-US 16 74999681 74999681 single base substitution C G exon_variant CESC-US 16 74999681 74999681 single base substitution C G missense_variant V11L 31G>C CESC-US 16 74999681 74999681 single base substitution C G missense_variant V32L 94G>C CESC-US 16 75033937 75033937 single base substitution C T exon_variant CESC-US 16 75033937 75033937 single base substitution C T upstream_gene_variant CLLE-ES 16 74924077 74924077 single base substitution C T downstream_gene_variant CLLE-ES 16 74924077 74924077 single base substitution C T intron_variant CLLE-ES 16 74924077 74924077 single base substitution C T upstream_gene_variant CLLE-ES 16 74926098 74926098 single base substitution A C downstream_gene_variant CLLE-ES 16 74926098 74926098 single base substitution A C intron_variant CLLE-ES 16 74927688 74927688 single base substitution T C 3_prime_UTR_variant CLLE-ES 16 74927688 74927688 single base substitution T C exon_variant CLLE-ES 16 74927688 74927688 single base substitution T C missense_variant K198R 593A>G CLLE-ES 16 74927688 74927688 single base substitution T C missense_variant K32R 95A>G CLLE-ES 16 74927688 74927688 single base substitution T C missense_variant K630R 1889A>G CLLE-ES 16 74933464 74933464 single base substitution G A intron_variant CLLE-ES 16 74947149 74947149 single base substitution C A downstream_gene_variant CLLE-ES 16 74947149 74947149 single base substitution C A intron_variant CLLE-ES 16 74947149 74947149 single base substitution C A upstream_gene_variant CLLE-ES 16 74967332 74967332 single base substitution T C downstream_gene_variant CLLE-ES 16 74967332 74967332 single base substitution T C intron_variant CLLE-ES 16 74967332 74967332 single base substitution T C upstream_gene_variant CLLE-ES 16 75015933 75015933 single base substitution C T intron_variant CLLE-ES 16 75015933 75015933 single base substitution C T upstream_gene_variant CLLE-ES 16 75025403 75025403 single base substitution A G intron_variant CLLE-ES 16 75027615 75027615 single base substitution A G intron_variant CLLE-ES 16 75035373 75035373 single base substitution C A upstream_gene_variant CLLE-ES 16 75037715 75037715 single base substitution C T upstream_gene_variant COAD-US 16 74920199 74920199 single base substitution G A downstream_gene_variant COAD-US 16 74920199 74920199 single base substitution G A exon_variant COAD-US 16 74920199 74920199 single base substitution G A stop_gained R153* 457C>T COAD-US 16 74920199 74920199 single base substitution G A stop_gained R839* 2515C>T COAD-US 16 74920199 74920199 single base substitution G A upstream_gene_variant COAD-US 16 74927654 74927654 single base substitution G A 3_prime_UTR_variant COAD-US 16 74927654 74927654 single base substitution G A exon_variant COAD-US 16 74927654 74927654 single base substitution G A synonymous_variant I209I 627C>T COAD-US 16 74927654 74927654 single base substitution G A synonymous_variant I43I 129C>T COAD-US 16 74927654 74927654 single base substitution G A synonymous_variant I641I 1923C>T COAD-US 16 74943496 74943496 deletion of <=200bp G - downstream_gene_variant COAD-US 16 74943496 74943496 deletion of <=200bp G - exon_variant COAD-US 16 74943496 74943496 deletion of <=200bp G - frameshift_variant P515 COAD-US 16 74943496 74943496 deletion of <=200bp G - frameshift_variant P64 COAD-US 16 74949791 74949791 insertion of <=200bp - CA exon_variant COAD-US 16 74949791 74949791 insertion of <=200bp - CA frameshift_variant Q401L? COAD-US 16 74949791 74949791 insertion of <=200bp - CA upstream_gene_variant COAD-US 16 74950097 74950097 single base substitution G A exon_variant COAD-US 16 74950097 74950097 single base substitution G A missense_variant P343S 1027C>T COAD-US 16 74950097 74950097 single base substitution G A upstream_gene_variant COAD-US 16 74976691 74976691 deletion of <=200bp T - exon_variant COAD-US 16 74976691 74976691 deletion of <=200bp T - frameshift_variant N139 COAD-US 16 74976691 74976691 deletion of <=200bp T - frameshift_variant N160 COAD-US 16 74976691 74976691 deletion of <=200bp T - intron_variant COAD-US 16 74990473 74990473 single base substitution G T 3_prime_UTR_variant COAD-US 16 74990473 74990473 single base substitution G T exon_variant COAD-US 16 74990473 74990473 single base substitution G T missense_variant P26H 77C>A COAD-US 16 74990473 74990473 single base substitution G T missense_variant P47H 140C>A COCA-CN 16 74908080 74908080 single base substitution T C 3_prime_UTR_variant COCA-CN 16 74908080 74908080 single base substitution T C downstream_gene_variant COCA-CN 16 74908080 74908080 single base substitution T C exon_variant COCA-CN 16 74908303 74908303 single base substitution C T downstream_gene_variant COCA-CN 16 74908303 74908303 single base substitution C T exon_variant COCA-CN 16 74908303 74908303 single base substitution C T missense_variant R910H 2729G>A COCA-CN 16 74920126 74920126 single base substitution T C downstream_gene_variant COCA-CN 16 74920126 74920126 single base substitution T C exon_variant COCA-CN 16 74920126 74920126 single base substitution T C intron_variant COCA-CN 16 74922219 74922219 single base substitution T C downstream_gene_variant COCA-CN 16 74922219 74922219 single base substitution T C intron_variant COCA-CN 16 74922219 74922219 single base substitution T C splice_acceptor_variant COCA-CN 16 74922219 74922219 single base substitution T C upstream_gene_variant COCA-CN 16 74923450 74923450 single base substitution G T downstream_gene_variant COCA-CN 16 74923450 74923450 single base substitution G T intron_variant COCA-CN 16 74923450 74923450 single base substitution G T upstream_gene_variant COCA-CN 16 74933537 74933537 single base substitution C A intron_variant COCA-CN 16 74937958 74937958 single base substitution C T 3_prime_UTR_variant COCA-CN 16 74937958 74937958 single base substitution C T downstream_gene_variant COCA-CN 16 74937958 74937958 single base substitution C T exon_variant COCA-CN 16 74937958 74937958 single base substitution C T missense_variant A134T 400G>A COCA-CN 16 74937958 74937958 single base substitution C T missense_variant A585T 1753G>A COCA-CN 16 74937958 74937958 single base substitution C T upstream_gene_variant COCA-CN 16 74946161 74946161 single base substitution C T downstream_gene_variant COCA-CN 16 74946161 74946161 single base substitution C T exon_variant COCA-CN 16 74946161 74946161 single base substitution C T missense_variant A442T 1324G>A COCA-CN 16 74946161 74946161 single base substitution C T upstream_gene_variant COCA-CN 16 74950079 74950079 single base substitution G A exon_variant COCA-CN 16 74950079 74950079 single base substitution G A synonymous_variant L349L 1045C>T COCA-CN 16 74950079 74950079 single base substitution G A upstream_gene_variant COCA-CN 16 74951733 74951733 single base substitution G T intron_variant COCA-CN 16 74951733 74951733 single base substitution G T upstream_gene_variant COCA-CN 16 74976656 74976656 single base substitution C A exon_variant COCA-CN 16 74976656 74976656 single base substitution C A intron_variant COCA-CN 16 74976656 74976656 single base substitution C A missense_variant V151L 451G>T COCA-CN 16 74976656 74976656 single base substitution C A missense_variant V172L 514G>T COCA-CN 16 74983701 74983701 single base substitution G A downstream_gene_variant COCA-CN 16 74983701 74983701 single base substitution G A splice_region_variant COCA-CN 16 74983921 74983921 single base substitution G T intron_variant COCA-CN 16 74990587 74990587 single base substitution T G intron_variant COCA-CN 16 74999496 74999496 single base substitution G T intron_variant EOPC-DE 16 74975562 74975562 single base substitution C A downstream_gene_variant EOPC-DE 16 74975562 74975562 single base substitution C A intron_variant EOPC-DE 16 75028949 75028949 single base substitution T C intron_variant ESAD-UK 16 74902749 74902749 single base substitution C T downstream_gene_variant ESAD-UK 16 74905403 74905403 single base substitution G A downstream_gene_variant ESAD-UK 16 74909839 74909839 single base substitution G T intron_variant ESAD-UK 16 74915439 74915439 single base substitution T G intron_variant ESAD-UK 16 74915738 74915738 single base substitution T G intron_variant ESAD-UK 16 74916397 74916397 single base substitution G A intron_variant ESAD-UK 16 74916452 74916452 single base substitution G A intron_variant ESAD-UK 16 74917956 74917956 single base substitution C T downstream_gene_variant ESAD-UK 16 74917956 74917956 single base substitution C T intron_variant ESAD-UK 16 74923985 74923985 single base substitution G A downstream_gene_variant ESAD-UK 16 74923985 74923985 single base substitution G A intron_variant ESAD-UK 16 74923985 74923985 single base substitution G A upstream_gene_variant ESAD-UK 16 74926612 74926612 single base substitution C G downstream_gene_variant ESAD-UK 16 74926612 74926612 single base substitution C G intron_variant ESAD-UK 16 74926766 74926766 single base substitution C T downstream_gene_variant ESAD-UK 16 74926766 74926766 single base substitution C T intron_variant ESAD-UK 16 74930335 74930335 single base substitution C T intron_variant ESAD-UK 16 74930335 74930335 single base substitution C T upstream_gene_variant ESAD-UK 16 74937075 74937075 single base substitution C T intron_variant ESAD-UK 16 74937999 74937999 single base substitution C G downstream_gene_variant ESAD-UK 16 74937999 74937999 single base substitution C G exon_variant ESAD-UK 16 74937999 74937999 single base substitution C G splice_acceptor_variant ESAD-UK 16 74937999 74937999 single base substitution C G upstream_gene_variant ESAD-UK 16 74939603 74939603 single base substitution A T downstream_gene_variant ESAD-UK 16 74939603 74939603 single base substitution A T intron_variant ESAD-UK 16 74939603 74939603 single base substitution A T upstream_gene_variant ESAD-UK 16 74941228 74941228 single base substitution G T downstream_gene_variant ESAD-UK 16 74941228 74941228 single base substitution G T intron_variant ESAD-UK 16 74941228 74941228 single base substitution G T upstream_gene_variant ESAD-UK 16 74941883 74941883 single base substitution C T downstream_gene_variant ESAD-UK 16 74941883 74941883 single base substitution C T intron_variant ESAD-UK 16 74941883 74941883 single base substitution C T upstream_gene_variant ESAD-UK 16 74944911 74944911 single base substitution G A downstream_gene_variant ESAD-UK 16 74944911 74944911 single base substitution G A intron_variant ESAD-UK 16 74944911 74944911 single base substitution G A upstream_gene_variant ESAD-UK 16 74948225 74948225 single base substitution T G downstream_gene_variant ESAD-UK 16 74948225 74948225 single base substitution T G intron_variant ESAD-UK 16 74948225 74948225 single base substitution T G upstream_gene_variant ESAD-UK 16 74951480 74951480 single base substitution G A intron_variant ESAD-UK 16 74951480 74951480 single base substitution G A upstream_gene_variant ESAD-UK 16 74952456 74952456 single base substitution T C intron_variant ESAD-UK 16 74952456 74952456 single base substitution T C upstream_gene_variant ESAD-UK 16 74953122 74953122 single base substitution C T downstream_gene_variant ESAD-UK 16 74953122 74953122 single base substitution C T intron_variant ESAD-UK 16 74953122 74953122 single base substitution C T upstream_gene_variant ESAD-UK 16 74953995 74953995 single base substitution G T downstream_gene_variant ESAD-UK 16 74953995 74953995 single base substitution G T intron_variant ESAD-UK 16 74953995 74953995 single base substitution G T upstream_gene_variant ESAD-UK 16 74957603 74957603 single base substitution C T downstream_gene_variant ESAD-UK 16 74957603 74957603 single base substitution C T intron_variant ESAD-UK 16 74957603 74957603 single base substitution C T upstream_gene_variant ESAD-UK 16 74958262 74958262 single base substitution G A intron_variant ESAD-UK 16 74958262 74958262 single base substitution G A upstream_gene_variant ESAD-UK 16 74959155 74959155 single base substitution C T intron_variant ESAD-UK 16 74959155 74959155 single base substitution C T upstream_gene_variant ESAD-UK 16 74961974 74961974 single base substitution T G intron_variant ESAD-UK 16 74962678 74962678 single base substitution G A intron_variant ESAD-UK 16 74966003 74966003 deletion of <=200bp T - intron_variant ESAD-UK 16 74966003 74966003 deletion of <=200bp T - upstream_gene_variant ESAD-UK 16 74971292 74971292 single base substitution C A downstream_gene_variant ESAD-UK 16 74971292 74971292 single base substitution C A intron_variant ESAD-UK 16 74972379 74972379 single base substitution G T downstream_gene_variant ESAD-UK 16 74972379 74972379 single base substitution G T intron_variant ESAD-UK 16 74972894 74972894 single base substitution T A downstream_gene_variant ESAD-UK 16 74972894 74972894 single base substitution T A intron_variant ESAD-UK 16 74973396 74973396 deletion of <=200bp A - downstream_gene_variant ESAD-UK 16 74973396 74973396 deletion of <=200bp A - intron_variant ESAD-UK 16 74976370 74976370 single base substitution G A downstream_gene_variant ESAD-UK 16 74976370 74976370 single base substitution G A intron_variant ESAD-UK 16 74976698 74976698 single base substitution T C exon_variant ESAD-UK 16 74976698 74976698 single base substitution T C intron_variant ESAD-UK 16 74976698 74976698 single base substitution T C missense_variant K137E 409A>G ESAD-UK 16 74976698 74976698 single base substitution T C missense_variant K158E 472A>G ESAD-UK 16 74978359 74978359 single base substitution C T intron_variant ESAD-UK 16 74982229 74982229 single base substitution G A downstream_gene_variant ESAD-UK 16 74982229 74982229 single base substitution G A intron_variant ESAD-UK 16 74982595 74982595 single base substitution A G downstream_gene_variant ESAD-UK 16 74982595 74982595 single base substitution A G intron_variant ESAD-UK 16 74983482 74983482 single base substitution T G downstream_gene_variant ESAD-UK 16 74983482 74983482 single base substitution T G intron_variant ESAD-UK 16 74984112 74984112 single base substitution C T intron_variant ESAD-UK 16 74985733 74985733 single base substitution C T downstream_gene_variant ESAD-UK 16 74985733 74985733 single base substitution C T intron_variant ESAD-UK 16 74988784 74988784 single base substitution A G downstream_gene_variant ESAD-UK 16 74988784 74988784 single base substitution A G intron_variant ESAD-UK 16 74989360 74989360 single base substitution A G downstream_gene_variant ESAD-UK 16 74989360 74989360 single base substitution A G intron_variant ESAD-UK 16 74991103 74991103 single base substitution C T intron_variant ESAD-UK 16 74994098 74994098 single base substitution G A downstream_gene_variant ESAD-UK 16 74994098 74994098 single base substitution G A intron_variant ESAD-UK 16 74997144 74997144 single base substitution G A intron_variant ESAD-UK 16 74997144 74997144 single base substitution G A splice_region_variant ESAD-UK 16 74998232 74998232 single base substitution G A intron_variant ESAD-UK 16 74998905 74998905 single base substitution T G intron_variant ESAD-UK 16 75001187 75001187 single base substitution C A intron_variant ESAD-UK 16 75001187 75001187 single base substitution C A upstream_gene_variant ESAD-UK 16 75003106 75003106 single base substitution G C intron_variant ESAD-UK 16 75003106 75003106 single base substitution G C upstream_gene_variant ESAD-UK 16 75003508 75003508 single base substitution C T intron_variant ESAD-UK 16 75003508 75003508 single base substitution C T upstream_gene_variant ESAD-UK 16 75005501 75005501 single base substitution T G intron_variant ESAD-UK 16 75006821 75006821 single base substitution G C intron_variant ESAD-UK 16 75008077 75008077 deletion of <=200bp A - intron_variant ESAD-UK 16 75008755 75008755 single base substitution G A intron_variant ESAD-UK 16 75008980 75008980 single base substitution C T intron_variant ESAD-UK 16 75010918 75010918 single base substitution C T intron_variant ESAD-UK 16 75011171 75011171 single base substitution T A intron_variant ESAD-UK 16 75011455 75011455 single base substitution G A intron_variant ESAD-UK 16 75012269 75012269 single base substitution C A intron_variant ESAD-UK 16 75013419 75013419 single base substitution A C intron_variant ESAD-UK 16 75013419 75013419 single base substitution A C upstream_gene_variant ESAD-UK 16 75013957 75013957 single base substitution C T intron_variant ESAD-UK 16 75013957 75013957 single base substitution C T upstream_gene_variant ESAD-UK 16 75015106 75015106 single base substitution A T intron_variant ESAD-UK 16 75015106 75015106 single base substitution A T upstream_gene_variant ESAD-UK 16 75015135 75015135 single base substitution G A intron_variant ESAD-UK 16 75015135 75015135 single base substitution G A upstream_gene_variant ESAD-UK 16 75015169 75015169 single base substitution G A intron_variant ESAD-UK 16 75015169 75015169 single base substitution G A upstream_gene_variant ESAD-UK 16 75015839 75015839 single base substitution C T intron_variant ESAD-UK 16 75015839 75015839 single base substitution C T upstream_gene_variant ESAD-UK 16 75019069 75019069 single base substitution G T intron_variant ESAD-UK 16 75019069 75019069 single base substitution G T upstream_gene_variant ESAD-UK 16 75020350 75020350 single base substitution T G intron_variant ESAD-UK 16 75020350 75020350 single base substitution T G upstream_gene_variant ESAD-UK 16 75025768 75025768 single base substitution G C intron_variant ESAD-UK 16 75027449 75027449 single base substitution T A intron_variant ESAD-UK 16 75030167 75030167 single base substitution G C intron_variant ESAD-UK 16 75033002 75033002 single base substitution G A intron_variant ESAD-UK 16 75033002 75033002 single base substitution G A upstream_gene_variant ESAD-UK 16 75034311 75034311 single base substitution A C upstream_gene_variant ESAD-UK 16 75036370 75036370 single base substitution C T upstream_gene_variant ESAD-UK 16 75036705 75036705 single base substitution G A upstream_gene_variant ESAD-UK 16 75037961 75037961 single base substitution T C upstream_gene_variant ESCA-CN 16 74920221 74920221 single base substitution C G downstream_gene_variant ESCA-CN 16 74920221 74920221 single base substitution C G exon_variant ESCA-CN 16 74920221 74920221 single base substitution C G synonymous_variant L145L 435G>C ESCA-CN 16 74920221 74920221 single base substitution C G synonymous_variant L831L 2493G>C ESCA-CN 16 74920221 74920221 single base substitution C G upstream_gene_variant ESCA-CN 16 74942844 74942844 single base substitution T C downstream_gene_variant ESCA-CN 16 74942844 74942844 single base substitution T C exon_variant ESCA-CN 16 74942844 74942844 single base substitution T C intron_variant ESCA-CN 16 74942844 74942844 single base substitution T C synonymous_variant T107T 321A>G ESCA-CN 16 74942844 74942844 single base substitution T C synonymous_variant T558T 1674A>G ESCA-CN 16 74942844 74942844 single base substitution T C upstream_gene_variant ESCA-CN 16 74942882 74942882 single base substitution G A downstream_gene_variant ESCA-CN 16 74942882 74942882 single base substitution G A intron_variant ESCA-CN 16 74942882 74942882 single base substitution G A splice_region_variant ESCA-CN 16 74942882 74942882 single base substitution G A upstream_gene_variant ESCA-CN 16 74976690 74976690 insertion of <=200bp - T exon_variant ESCA-CN 16 74976690 74976690 insertion of <=200bp - T frameshift_variant N139N? ESCA-CN 16 74976690 74976690 insertion of <=200bp - T frameshift_variant N160N? ESCA-CN 16 74976690 74976690 insertion of <=200bp - T intron_variant GBM-US 16 74976699 74976699 single base substitution A T exon_variant GBM-US 16 74976699 74976699 single base substitution A T intron_variant GBM-US 16 74976699 74976699 single base substitution A T missense_variant N136K 408T>A GBM-US 16 74976699 74976699 single base substitution A T missense_variant N157K 471T>A LAML-KR 16 74943501 74943501 single base substitution G T downstream_gene_variant LAML-KR 16 74943501 74943501 single base substitution G T exon_variant LAML-KR 16 74943501 74943501 single base substitution G T missense_variant P514T 1540C>A LAML-KR 16 74943501 74943501 single base substitution G T missense_variant P63T 187C>A LAML-KR 16 75032885 75032885 single base substitution A G intron_variant LAML-KR 16 75032885 75032885 single base substitution A G upstream_gene_variant LIAD-FR 16 74949815 74949815 single base substitution G T exon_variant LIAD-FR 16 74949815 74949815 single base substitution G T missense_variant Q393K 1177C>A LIAD-FR 16 74949815 74949815 single base substitution G T upstream_gene_variant LICA-FR 16 74908150 74908150 single base substitution G A downstream_gene_variant LICA-FR 16 74908150 74908150 single base substitution G A exon_variant LICA-FR 16 74908150 74908150 single base substitution G A missense_variant P961L 2882C>T LICA-FR 16 74920928 74920928 single base substitution T C downstream_gene_variant LICA-FR 16 74920928 74920928 single base substitution T C intron_variant LICA-FR 16 74920928 74920928 single base substitution T C upstream_gene_variant LICA-FR 16 74970616 74970616 single base substitution C T downstream_gene_variant LICA-FR 16 74970616 74970616 single base substitution C T intron_variant LICA-FR 16 74970617 74970617 single base substitution A G downstream_gene_variant LICA-FR 16 74970617 74970617 single base substitution A G intron_variant LICA-FR 16 74970628 74970628 single base substitution G A downstream_gene_variant LICA-FR 16 74970628 74970628 single base substitution G A intron_variant LICA-FR 16 74972119 74972119 single base substitution T G downstream_gene_variant LICA-FR 16 74972119 74972119 single base substitution T G exon_variant LICA-FR 16 74972119 74972119 single base substitution T G missense_variant I194L 580A>C LICA-FR 16 75003370 75003370 single base substitution C T intron_variant LICA-FR 16 75003370 75003370 single base substitution C T upstream_gene_variant LICA-FR 16 75019873 75019873 single base substitution C T intron_variant LICA-FR 16 75019873 75019873 single base substitution C T upstream_gene_variant LICA-FR 16 75019883 75019883 single base substitution C T intron_variant LICA-FR 16 75019883 75019883 single base substitution C T upstream_gene_variant LICA-FR 16 75031728 75031728 single base substitution G A intron_variant LICA-FR 16 75031728 75031728 single base substitution G A upstream_gene_variant LICA-FR 16 75031877 75031877 single base substitution T C intron_variant LICA-FR 16 75031877 75031877 single base substitution T C upstream_gene_variant LICA-FR 16 75037151 75037151 single base substitution C T upstream_gene_variant LIHC-US 16 74919609 74919609 single base substitution C T downstream_gene_variant LIHC-US 16 74919609 74919609 single base substitution C T exon_variant LIHC-US 16 74919609 74919609 single base substitution C T synonymous_variant E191E 573G>A LIHC-US 16 74919609 74919609 single base substitution C T synonymous_variant E877E 2631G>A LINC-JP 16 74913178 74913178 single base substitution T A intron_variant LINC-JP 16 74913447 74913447 single base substitution T C intron_variant LINC-JP 16 74918669 74918669 single base substitution G A downstream_gene_variant LINC-JP 16 74918669 74918669 single base substitution G A intron_variant LINC-JP 16 74937572 74937584 deletion of <=200bp GAGTGGAGATTAC - intron_variant LINC-JP 16 74937728 74937728 single base substitution T C downstream_gene_variant LINC-JP 16 74937728 74937728 single base substitution T C intron_variant LINC-JP 16 74939282 74939282 single base substitution A G downstream_gene_variant LINC-JP 16 74939282 74939282 single base substitution A G intron_variant LINC-JP 16 74939282 74939282 single base substitution A G upstream_gene_variant LINC-JP 16 74949342 74949342 single base substitution T G downstream_gene_variant LINC-JP 16 74949342 74949342 single base substitution T G intron_variant LINC-JP 16 74949342 74949342 single base substitution T G upstream_gene_variant LINC-JP 16 74949912 74949912 single base substitution C T exon_variant LINC-JP 16 74949912 74949912 single base substitution C T intron_variant LINC-JP 16 74949912 74949912 single base substitution C T upstream_gene_variant LINC-JP 16 74950322 74950339 deletion of <=200bp GGTTAAACACCAGGGATA - intron_variant LINC-JP 16 74950322 74950339 deletion of <=200bp GGTTAAACACCAGGGATA - upstream_gene_variant LINC-JP 16 74958030 74958030 single base substitution C A intron_variant LINC-JP 16 74958030 74958030 single base substitution C A upstream_gene_variant LINC-JP 16 74966668 74966668 single base substitution T C intron_variant LINC-JP 16 74966668 74966668 single base substitution T C upstream_gene_variant LINC-JP 16 74970434 74970434 single base substitution C T downstream_gene_variant LINC-JP 16 74970434 74970434 single base substitution C T intron_variant LINC-JP 16 74974403 74974403 single base substitution A T downstream_gene_variant LINC-JP 16 74974403 74974403 single base substitution A T intron_variant LINC-JP 16 74974628 74974628 single base substitution G T downstream_gene_variant LINC-JP 16 74974628 74974628 single base substitution G T intron_variant LINC-JP 16 74976876 74976876 single base substitution T C intron_variant LINC-JP 16 74990633 74990633 single base substitution G A intron_variant LINC-JP 16 74991867 74991867 single base substitution C A downstream_gene_variant LINC-JP 16 74991867 74991867 single base substitution C A intron_variant LINC-JP 16 75014984 75014984 single base substitution C T intron_variant LINC-JP 16 75014984 75014984 single base substitution C T upstream_gene_variant LINC-JP 16 75019185 75019185 single base substitution T C intron_variant LINC-JP 16 75019185 75019185 single base substitution T C upstream_gene_variant LINC-JP 16 75021183 75021183 single base substitution C T intron_variant LINC-JP 16 75021183 75021183 single base substitution C T upstream_gene_variant LINC-JP 16 75029983 75029983 single base substitution C G intron_variant LINC-JP 16 75035227 75035227 single base substitution T G upstream_gene_variant LINC-JP 16 75037872 75037872 single base substitution C T upstream_gene_variant LIRI-JP 16 74904294 74904294 single base substitution G T downstream_gene_variant LIRI-JP 16 74906396 74906396 single base substitution T C downstream_gene_variant LIRI-JP 16 74907971 74907971 single base substitution G A 3_prime_UTR_variant LIRI-JP 16 74907971 74907971 single base substitution G A downstream_gene_variant LIRI-JP 16 74916124 74916124 single base substitution C A intron_variant LIRI-JP 16 74918078 74918078 single base substitution C A downstream_gene_variant LIRI-JP 16 74918078 74918078 single base substitution C A intron_variant LIRI-JP 16 74920632 74920632 single base substitution A G downstream_gene_variant LIRI-JP 16 74920632 74920632 single base substitution A G intron_variant LIRI-JP 16 74920632 74920632 single base substitution A G upstream_gene_variant LIRI-JP 16 74921126 74921126 single base substitution G C downstream_gene_variant LIRI-JP 16 74921126 74921126 single base substitution G C intron_variant LIRI-JP 16 74921126 74921126 single base substitution G C upstream_gene_variant LIRI-JP 16 74921688 74921688 single base substitution C A downstream_gene_variant LIRI-JP 16 74921688 74921688 single base substitution C A intron_variant LIRI-JP 16 74921688 74921688 single base substitution C A upstream_gene_variant LIRI-JP 16 74924870 74924870 single base substitution G C downstream_gene_variant LIRI-JP 16 74924870 74924870 single base substitution G C intron_variant LIRI-JP 16 74924870 74924870 single base substitution G C upstream_gene_variant LIRI-JP 16 74925372 74925372 single base substitution G T downstream_gene_variant LIRI-JP 16 74925372 74925372 single base substitution G T intron_variant LIRI-JP 16 74928985 74928985 single base substitution G A intron_variant LIRI-JP 16 74928985 74928985 single base substitution G A upstream_gene_variant LIRI-JP 16 74932071 74932071 deletion of <=200bp T - intron_variant LIRI-JP 16 74932071 74932071 deletion of <=200bp T - upstream_gene_variant LIRI-JP 16 74933627 74933627 single base substitution C T intron_variant LIRI-JP 16 74933627 74933627 single base substitution C T missense_variant R180H 539G>A LIRI-JP 16 74936252 74936252 single base substitution C T intron_variant LIRI-JP 16 74938650 74938650 single base substitution G C downstream_gene_variant LIRI-JP 16 74938650 74938650 single base substitution G C intron_variant LIRI-JP 16 74938650 74938650 single base substitution G C upstream_gene_variant LIRI-JP 16 74938750 74938750 single base substitution T C downstream_gene_variant LIRI-JP 16 74938750 74938750 single base substitution T C intron_variant LIRI-JP 16 74938750 74938750 single base substitution T C upstream_gene_variant LIRI-JP 16 74942060 74942060 single base substitution A C downstream_gene_variant LIRI-JP 16 74942060 74942060 single base substitution A C intron_variant LIRI-JP 16 74942060 74942060 single base substitution A C upstream_gene_variant LIRI-JP 16 74947420 74947420 single base substitution C A downstream_gene_variant LIRI-JP 16 74947420 74947420 single base substitution C A intron_variant LIRI-JP 16 74947420 74947420 single base substitution C A upstream_gene_variant LIRI-JP 16 74949388 74949388 single base substitution T C downstream_gene_variant LIRI-JP 16 74949388 74949388 single base substitution T C exon_variant LIRI-JP 16 74949388 74949388 single base substitution T C intron_variant LIRI-JP 16 74949388 74949388 single base substitution T C upstream_gene_variant LIRI-JP 16 74949715 74949715 single base substitution C T exon_variant LIRI-JP 16 74949715 74949715 single base substitution C T intron_variant LIRI-JP 16 74949715 74949715 single base substitution C T upstream_gene_variant LIRI-JP 16 74951922 74951922 single base substitution T C intron_variant LIRI-JP 16 74951922 74951922 single base substitution T C upstream_gene_variant LIRI-JP 16 74952024 74952024 single base substitution C A intron_variant LIRI-JP 16 74952024 74952024 single base substitution C A upstream_gene_variant LIRI-JP 16 74952819 74952819 deletion of <=200bp T - intron_variant LIRI-JP 16 74952819 74952819 deletion of <=200bp T - upstream_gene_variant LIRI-JP 16 74952946 74952946 single base substitution G T downstream_gene_variant LIRI-JP 16 74952946 74952946 single base substitution G T intron_variant LIRI-JP 16 74952946 74952946 single base substitution G T upstream_gene_variant LIRI-JP 16 74954116 74954116 single base substitution T G downstream_gene_variant LIRI-JP 16 74954116 74954116 single base substitution T G intron_variant LIRI-JP 16 74954116 74954116 single base substitution T G upstream_gene_variant LIRI-JP 16 74956983 74956983 single base substitution G C downstream_gene_variant LIRI-JP 16 74956983 74956983 single base substitution G C intron_variant LIRI-JP 16 74956983 74956983 single base substitution G C upstream_gene_variant LIRI-JP 16 74957961 74957961 single base substitution A G intron_variant LIRI-JP 16 74957961 74957961 single base substitution A G upstream_gene_variant LIRI-JP 16 74958412 74958435 deletion of <=200bp CTGTGTGAAAACCTAGGAGCCAAT - intron_variant LIRI-JP 16 74958412 74958435 deletion of <=200bp CTGTGTGAAAACCTAGGAGCCAAT - upstream_gene_variant LIRI-JP 16 74959376 74959376 single base substitution A T intron_variant LIRI-JP 16 74959376 74959376 single base substitution A T upstream_gene_variant LIRI-JP 16 74960724 74960724 single base substitution T C intron_variant LIRI-JP 16 74960724 74960724 single base substitution T C upstream_gene_variant LIRI-JP 16 74960850 74960850 single base substitution A G intron_variant LIRI-JP 16 74960850 74960850 single base substitution A G upstream_gene_variant LIRI-JP 16 74961154 74961154 single base substitution T C intron_variant LIRI-JP 16 74963391 74963391 single base substitution C A intron_variant LIRI-JP 16 74963726 74963726 single base substitution C A intron_variant LIRI-JP 16 74963801 74963801 single base substitution T C intron_variant LIRI-JP 16 74964065 74964065 single base substitution G A intron_variant LIRI-JP 16 74965375 74965375 single base substitution A C intron_variant LIRI-JP 16 74965375 74965375 single base substitution A C upstream_gene_variant LIRI-JP 16 74967381 74967381 single base substitution C T downstream_gene_variant LIRI-JP 16 74967381 74967381 single base substitution C T intron_variant LIRI-JP 16 74967381 74967381 single base substitution C T upstream_gene_variant LIRI-JP 16 74968412 74968412 single base substitution A G downstream_gene_variant LIRI-JP 16 74968412 74968412 single base substitution A G intron_variant LIRI-JP 16 74968412 74968412 single base substitution A G upstream_gene_variant LIRI-JP 16 74970885 74970885 single base substitution A C downstream_gene_variant LIRI-JP 16 74970885 74970885 single base substitution A C intron_variant LIRI-JP 16 74971014 74971014 single base substitution G A downstream_gene_variant LIRI-JP 16 74971014 74971014 single base substitution G A intron_variant LIRI-JP 16 74971750 74971750 single base substitution G C downstream_gene_variant LIRI-JP 16 74971750 74971750 single base substitution G C intron_variant LIRI-JP 16 74971881 74971881 single base substitution T C downstream_gene_variant LIRI-JP 16 74971881 74971881 single base substitution T C intron_variant LIRI-JP 16 74971904 74971904 single base substitution T C downstream_gene_variant LIRI-JP 16 74971904 74971904 single base substitution T C intron_variant LIRI-JP 16 74973540 74973540 single base substitution C A downstream_gene_variant LIRI-JP 16 74973540 74973540 single base substitution C A intron_variant LIRI-JP 16 74981546 74981546 single base substitution T C downstream_gene_variant LIRI-JP 16 74981546 74981546 single base substitution T C intron_variant LIRI-JP 16 74981708 74981708 single base substitution C A downstream_gene_variant LIRI-JP 16 74981708 74981708 single base substitution C A intron_variant LIRI-JP 16 74986263 74986263 single base substitution C T downstream_gene_variant LIRI-JP 16 74986263 74986263 single base substitution C T intron_variant LIRI-JP 16 74987176 74987176 single base substitution C A downstream_gene_variant LIRI-JP 16 74987176 74987176 single base substitution C A intron_variant LIRI-JP 16 74988969 74988969 single base substitution G A downstream_gene_variant LIRI-JP 16 74988969 74988969 single base substitution G A intron_variant LIRI-JP 16 74990021 74990021 single base substitution T C downstream_gene_variant LIRI-JP 16 74990021 74990021 single base substitution T C intron_variant LIRI-JP 16 74990167 74990167 single base substitution T G downstream_gene_variant LIRI-JP 16 74990167 74990167 single base substitution T G intron_variant LIRI-JP 16 74990388 74990388 single base substitution G C 3_prime_UTR_variant LIRI-JP 16 74990388 74990388 single base substitution G C exon_variant LIRI-JP 16 74990388 74990388 single base substitution G C missense_variant H54Q 162C>G LIRI-JP 16 74990388 74990388 single base substitution G C missense_variant H75Q 225C>G LIRI-JP 16 74990598 74990598 single base substitution T C intron_variant LIRI-JP 16 74990811 74990811 single base substitution C A intron_variant LIRI-JP 16 74991838 74991838 single base substitution A C downstream_gene_variant LIRI-JP 16 74991838 74991838 single base substitution A C intron_variant LIRI-JP 16 74991986 74991986 single base substitution T C downstream_gene_variant LIRI-JP 16 74991986 74991986 single base substitution T C intron_variant LIRI-JP 16 74995108 74995108 single base substitution A C downstream_gene_variant LIRI-JP 16 74995108 74995108 single base substitution A C intron_variant LIRI-JP 16 74996943 74996943 single base substitution C A exon_variant LIRI-JP 16 74996943 74996943 single base substitution C A intron_variant LIRI-JP 16 74997254 74997254 single base substitution T C intron_variant LIRI-JP 16 75000208 75000208 single base substitution A G intron_variant LIRI-JP 16 75000208 75000208 single base substitution A G upstream_gene_variant LIRI-JP 16 75001417 75001417 single base substitution G C intron_variant LIRI-JP 16 75001417 75001417 single base substitution G C upstream_gene_variant LIRI-JP 16 75004197 75004197 single base substitution T C intron_variant LIRI-JP 16 75004197 75004197 single base substitution T C upstream_gene_variant LIRI-JP 16 75004349 75004349 single base substitution C A intron_variant LIRI-JP 16 75004349 75004349 single base substitution C A upstream_gene_variant LIRI-JP 16 75005460 75005460 single base substitution A G intron_variant LIRI-JP 16 75006631 75006631 single base substitution T C intron_variant LIRI-JP 16 75008865 75008865 single base substitution G A intron_variant LIRI-JP 16 75009419 75009419 single base substitution G A intron_variant LIRI-JP 16 75010009 75010009 single base substitution A T intron_variant LIRI-JP 16 75012109 75012109 single base substitution T A intron_variant LIRI-JP 16 75012133 75012133 single base substitution T G intron_variant LIRI-JP 16 75012211 75012211 single base substitution T C intron_variant LIRI-JP 16 75012557 75012557 single base substitution G C intron_variant LIRI-JP 16 75013880 75013880 single base substitution G A intron_variant LIRI-JP 16 75013880 75013880 single base substitution G A upstream_gene_variant LIRI-JP 16 75016159 75016159 single base substitution T C intron_variant LIRI-JP 16 75016159 75016159 single base substitution T C upstream_gene_variant LIRI-JP 16 75016748 75016748 single base substitution T C intron_variant LIRI-JP 16 75016748 75016748 single base substitution T C upstream_gene_variant LIRI-JP 16 75017101 75017101 single base substitution T G intron_variant LIRI-JP 16 75017101 75017101 single base substitution T G upstream_gene_variant LIRI-JP 16 75019789 75019789 single base substitution A G intron_variant LIRI-JP 16 75019789 75019789 single base substitution A G upstream_gene_variant LIRI-JP 16 75020264 75020264 single base substitution T C intron_variant LIRI-JP 16 75020264 75020264 single base substitution T C upstream_gene_variant LIRI-JP 16 75023747 75023747 single base substitution A T intron_variant LIRI-JP 16 75023747 75023747 single base substitution A T upstream_gene_variant LIRI-JP 16 75028700 75028700 single base substitution G T intron_variant LIRI-JP 16 75031808 75031808 single base substitution G T intron_variant LIRI-JP 16 75031808 75031808 single base substitution G T upstream_gene_variant LIRI-JP 16 75035644 75035644 single base substitution G A upstream_gene_variant LIRI-JP 16 75037155 75037155 single base substitution C A upstream_gene_variant LUSC-KR 16 74902968 74902968 single base substitution C A downstream_gene_variant LUSC-KR 16 74908059 74908059 single base substitution C A 3_prime_UTR_variant LUSC-KR 16 74908059 74908059 single base substitution C A downstream_gene_variant LUSC-KR 16 74908059 74908059 single base substitution C A exon_variant LUSC-KR 16 74909895 74909895 single base substitution C A intron_variant LUSC-KR 16 74911722 74911722 single base substitution C T intron_variant LUSC-KR 16 74916917 74916917 single base substitution G T intron_variant LUSC-KR 16 74921393 74921393 single base substitution A C downstream_gene_variant LUSC-KR 16 74921393 74921393 single base substitution A C intron_variant LUSC-KR 16 74921393 74921393 single base substitution A C upstream_gene_variant LUSC-KR 16 74921828 74921828 single base substitution C A downstream_gene_variant LUSC-KR 16 74921828 74921828 single base substitution C A intron_variant LUSC-KR 16 74921828 74921828 single base substitution C A upstream_gene_variant LUSC-KR 16 74923530 74923530 single base substitution G A downstream_gene_variant LUSC-KR 16 74923530 74923530 single base substitution G A intron_variant LUSC-KR 16 74923530 74923530 single base substitution G A upstream_gene_variant LUSC-KR 16 74923776 74923776 single base substitution C T downstream_gene_variant LUSC-KR 16 74923776 74923776 single base substitution C T intron_variant LUSC-KR 16 74923776 74923776 single base substitution C T upstream_gene_variant LUSC-KR 16 74927107 74927107 single base substitution C A downstream_gene_variant LUSC-KR 16 74927107 74927107 single base substitution C A intron_variant LUSC-KR 16 74927917 74927917 single base substitution A T intron_variant LUSC-KR 16 74927917 74927917 single base substitution A T upstream_gene_variant LUSC-KR 16 74932282 74932282 single base substitution T G intron_variant LUSC-KR 16 74932282 74932282 single base substitution T G upstream_gene_variant LUSC-KR 16 74937707 74937707 single base substitution G A downstream_gene_variant LUSC-KR 16 74937707 74937707 single base substitution G A intron_variant LUSC-KR 16 74940428 74940428 single base substitution C T downstream_gene_variant LUSC-KR 16 74940428 74940428 single base substitution C T intron_variant LUSC-KR 16 74940428 74940428 single base substitution C T upstream_gene_variant LUSC-KR 16 74942836 74942836 single base substitution C A downstream_gene_variant LUSC-KR 16 74942836 74942836 single base substitution C A exon_variant LUSC-KR 16 74942836 74942836 single base substitution C A intron_variant LUSC-KR 16 74942836 74942836 single base substitution C A missense_variant R110L 329G>T LUSC-KR 16 74942836 74942836 single base substitution C A missense_variant R561L 1682G>T LUSC-KR 16 74942836 74942836 single base substitution C A upstream_gene_variant LUSC-KR 16 74943047 74943047 single base substitution C T downstream_gene_variant LUSC-KR 16 74943047 74943047 single base substitution C T intron_variant LUSC-KR 16 74943047 74943047 single base substitution C T upstream_gene_variant LUSC-KR 16 74945021 74945021 single base substitution C G downstream_gene_variant LUSC-KR 16 74945021 74945021 single base substitution C G intron_variant LUSC-KR 16 74945021 74945021 single base substitution C G upstream_gene_variant LUSC-KR 16 74949040 74949040 single base substitution C A downstream_gene_variant LUSC-KR 16 74949040 74949040 single base substitution C A intron_variant LUSC-KR 16 74949040 74949040 single base substitution C A upstream_gene_variant LUSC-KR 16 74950286 74950286 single base substitution A C intron_variant LUSC-KR 16 74950286 74950286 single base substitution A C upstream_gene_variant LUSC-KR 16 74958983 74958983 single base substitution C G intron_variant LUSC-KR 16 74958983 74958983 single base substitution C G upstream_gene_variant LUSC-KR 16 74959785 74959785 single base substitution A C intron_variant LUSC-KR 16 74959785 74959785 single base substitution A C upstream_gene_variant LUSC-KR 16 74979800 74979800 single base substitution C G downstream_gene_variant LUSC-KR 16 74979800 74979800 single base substitution C G intron_variant LUSC-KR 16 74981773 74981773 single base substitution A C downstream_gene_variant LUSC-KR 16 74981773 74981773 single base substitution A C intron_variant LUSC-KR 16 74985516 74985516 single base substitution T A downstream_gene_variant LUSC-KR 16 74985516 74985516 single base substitution T A intron_variant LUSC-KR 16 74991015 74991015 single base substitution G T intron_variant LUSC-KR 16 74994542 74994542 single base substitution C A downstream_gene_variant LUSC-KR 16 74994542 74994542 single base substitution C A intron_variant LUSC-KR 16 74999617 74999617 single base substitution A C intron_variant LUSC-KR 16 74999625 74999625 single base substitution A T intron_variant LUSC-KR 16 75006181 75006181 single base substitution G A intron_variant LUSC-KR 16 75006413 75006413 single base substitution G T intron_variant LUSC-KR 16 75008727 75008727 single base substitution C T intron_variant LUSC-KR 16 75010385 75010385 single base substitution G C intron_variant LUSC-KR 16 75011357 75011357 single base substitution C A intron_variant LUSC-KR 16 75022102 75022102 single base substitution A T intron_variant LUSC-KR 16 75022102 75022102 single base substitution A T upstream_gene_variant LUSC-KR 16 75030036 75030036 single base substitution A T intron_variant LUSC-KR 16 75033624 75033624 single base substitution T C intron_variant LUSC-KR 16 75033624 75033624 single base substitution T C upstream_gene_variant LUSC-KR 16 75034037 75034037 single base substitution G T exon_variant LUSC-KR 16 75034037 75034037 single base substitution G T upstream_gene_variant LUSC-KR 16 75038537 75038537 single base substitution G T upstream_gene_variant LUSC-US 16 74937894 74937894 single base substitution C A 3_prime_UTR_variant LUSC-US 16 74937894 74937894 single base substitution C A downstream_gene_variant LUSC-US 16 74937894 74937894 single base substitution C A exon_variant LUSC-US 16 74937894 74937894 single base substitution C A missense_variant R155L 464G>T LUSC-US 16 74937894 74937894 single base substitution C A missense_variant R606L 1817G>T LUSC-US 16 74937894 74937894 single base substitution C A missense_variant R8L 23G>T LUSC-US 16 74949878 74949878 single base substitution G A exon_variant LUSC-US 16 74949878 74949878 single base substitution G A missense_variant P372S 1114C>T LUSC-US 16 74949878 74949878 single base substitution G A upstream_gene_variant LUSC-US 16 74990499 74990499 single base substitution G C 3_prime_UTR_variant LUSC-US 16 74990499 74990499 single base substitution G C exon_variant LUSC-US 16 74990499 74990499 single base substitution G C missense_variant F17L 51C>G LUSC-US 16 74990499 74990499 single base substitution G C missense_variant F38L 114C>G MALY-DE 16 74903767 74903767 single base substitution C A downstream_gene_variant MALY-DE 16 74904126 74904126 single base substitution G A downstream_gene_variant MALY-DE 16 74909517 74909517 single base substitution C T intron_variant MALY-DE 16 74918027 74918027 single base substitution C T downstream_gene_variant MALY-DE 16 74918027 74918027 single base substitution C T intron_variant MALY-DE 16 74923677 74923677 single base substitution G A 3_prime_UTR_variant MALY-DE 16 74923677 74923677 single base substitution G A downstream_gene_variant MALY-DE 16 74923677 74923677 single base substitution G A exon_variant MALY-DE 16 74923677 74923677 single base substitution G A intron_variant MALY-DE 16 74923677 74923677 single base substitution G A missense_variant L275F 823C>T MALY-DE 16 74923677 74923677 single base substitution G A missense_variant L707F 2119C>T MALY-DE 16 74923677 74923677 single base substitution G A upstream_gene_variant MALY-DE 16 74928469 74928469 single base substitution G A intron_variant MALY-DE 16 74928469 74928469 single base substitution G A upstream_gene_variant MALY-DE 16 74932722 74932722 single base substitution T A intron_variant MALY-DE 16 74932722 74932722 single base substitution T A upstream_gene_variant MALY-DE 16 74939864 74939864 single base substitution G A downstream_gene_variant MALY-DE 16 74939864 74939864 single base substitution G A intron_variant MALY-DE 16 74939864 74939864 single base substitution G A upstream_gene_variant MALY-DE 16 74948230 74948236 deletion of <=200bp TCAAATG - downstream_gene_variant MALY-DE 16 74948230 74948236 deletion of <=200bp TCAAATG - intron_variant MALY-DE 16 74948230 74948236 deletion of <=200bp TCAAATG - upstream_gene_variant MALY-DE 16 74953668 74953668 single base substitution T G downstream_gene_variant MALY-DE 16 74953668 74953668 single base substitution T G intron_variant MALY-DE 16 74953668 74953668 single base substitution T G upstream_gene_variant MALY-DE 16 74961783 74961783 single base substitution C T intron_variant MALY-DE 16 74969465 74969465 single base substitution T G downstream_gene_variant MALY-DE 16 74969465 74969465 single base substitution T G intron_variant MALY-DE 16 74969465 74969465 single base substitution T G upstream_gene_variant MALY-DE 16 74975957 74975957 single base substitution G A downstream_gene_variant MALY-DE 16 74975957 74975957 single base substitution G A intron_variant MALY-DE 16 74982344 74982344 single base substitution G A downstream_gene_variant MALY-DE 16 74982344 74982344 single base substitution G A intron_variant MALY-DE 16 74983890 74983890 single base substitution G A intron_variant MALY-DE 16 74993243 74993243 single base substitution C T downstream_gene_variant MALY-DE 16 74993243 74993243 single base substitution C T intron_variant MALY-DE 16 74993243 74993243 single base substitution C T splice_region_variant MALY-DE 16 74996351 74996351 single base substitution G A downstream_gene_variant MALY-DE 16 74996351 74996351 single base substitution G A intron_variant MALY-DE 16 74997926 74997926 insertion of <=200bp - A intron_variant MALY-DE 16 75010363 75010363 single base substitution C T intron_variant MALY-DE 16 75010959 75010959 single base substitution A C intron_variant MALY-DE 16 75020940 75020940 single base substitution G A intron_variant MALY-DE 16 75020940 75020940 single base substitution G A upstream_gene_variant MALY-DE 16 75022078 75022078 single base substitution T G intron_variant MALY-DE 16 75022078 75022078 single base substitution T G upstream_gene_variant MALY-DE 16 75022405 75022405 single base substitution C T intron_variant MALY-DE 16 75022405 75022405 single base substitution C T upstream_gene_variant MALY-DE 16 75027002 75027002 deletion of <=200bp A - intron_variant MALY-DE 16 75028812 75028812 deletion of <=200bp A - intron_variant MALY-DE 16 75030647 75030647 single base substitution C T intron_variant MELA-AU 16 74902685 74902685 single base substitution G A downstream_gene_variant MELA-AU 16 74902772 74902772 single base substitution G A downstream_gene_variant MELA-AU 16 74902781 74902781 single base substitution A G downstream_gene_variant MELA-AU 16 74903033 74903034 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 74904491 74904491 single base substitution G A downstream_gene_variant MELA-AU 16 74905071 74905071 single base substitution G A downstream_gene_variant MELA-AU 16 74905142 74905142 single base substitution G A downstream_gene_variant MELA-AU 16 74905310 74905311 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 74905395 74905395 single base substitution G A downstream_gene_variant MELA-AU 16 74905506 74905506 insertion of <=200bp - A downstream_gene_variant MELA-AU 16 74905635 74905635 single base substitution C G downstream_gene_variant MELA-AU 16 74905704 74905704 single base substitution C G downstream_gene_variant MELA-AU 16 74906177 74906178 multiple base substitution (>=2bp and <=200bp) CC GA downstream_gene_variant MELA-AU 16 74906287 74906287 single base substitution G A downstream_gene_variant MELA-AU 16 74906319 74906319 single base substitution A C downstream_gene_variant MELA-AU 16 74907067 74907067 single base substitution C G downstream_gene_variant MELA-AU 16 74908042 74908042 single base substitution A C 3_prime_UTR_variant MELA-AU 16 74908042 74908042 single base substitution A C downstream_gene_variant MELA-AU 16 74908042 74908042 single base substitution A C exon_variant MELA-AU 16 74908679 74908679 single base substitution G A intron_variant MELA-AU 16 74909125 74909125 single base substitution G A intron_variant MELA-AU 16 74909505 74909505 single base substitution C T intron_variant MELA-AU 16 74909515 74909515 single base substitution A G intron_variant MELA-AU 16 74909824 74909824 single base substitution C T intron_variant MELA-AU 16 74910754 74910754 single base substitution G A intron_variant MELA-AU 16 74911194 74911194 single base substitution G A intron_variant MELA-AU 16 74911211 74911211 single base substitution G A intron_variant MELA-AU 16 74911440 74911440 single base substitution G A intron_variant MELA-AU 16 74911605 74911605 single base substitution G A intron_variant MELA-AU 16 74911662 74911662 single base substitution C T intron_variant MELA-AU 16 74911732 74911732 single base substitution C T intron_variant MELA-AU 16 74912102 74912102 single base substitution A G intron_variant MELA-AU 16 74912497 74912497 single base substitution C T intron_variant MELA-AU 16 74912718 74912718 single base substitution G A intron_variant MELA-AU 16 74913431 74913431 single base substitution G A intron_variant MELA-AU 16 74913601 74913601 single base substitution G A intron_variant MELA-AU 16 74913602 74913602 single base substitution G A intron_variant MELA-AU 16 74913984 74913984 single base substitution G A intron_variant MELA-AU 16 74914141 74914141 single base substitution C T intron_variant MELA-AU 16 74914156 74914197 deletion of <=200bp TAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATT - intron_variant MELA-AU 16 74914427 74914427 single base substitution G A intron_variant MELA-AU 16 74915042 74915042 single base substitution G A intron_variant MELA-AU 16 74915133 74915133 single base substitution T C intron_variant MELA-AU 16 74915151 74915151 single base substitution G A intron_variant MELA-AU 16 74915505 74915505 single base substitution G A intron_variant MELA-AU 16 74915842 74915842 single base substitution C T intron_variant MELA-AU 16 74916763 74916763 single base substitution G A intron_variant MELA-AU 16 74917541 74917541 single base substitution G A downstream_gene_variant MELA-AU 16 74917541 74917541 single base substitution G A intron_variant MELA-AU 16 74917675 74917675 single base substitution C T downstream_gene_variant MELA-AU 16 74917675 74917675 single base substitution C T intron_variant MELA-AU 16 74917937 74917937 single base substitution G A downstream_gene_variant MELA-AU 16 74917937 74917937 single base substitution G A intron_variant MELA-AU 16 74918767 74918767 single base substitution C T downstream_gene_variant MELA-AU 16 74918767 74918767 single base substitution C T intron_variant MELA-AU 16 74919163 74919163 single base substitution C T downstream_gene_variant MELA-AU 16 74919163 74919163 single base substitution C T intron_variant MELA-AU 16 74919580 74919580 single base substitution G A downstream_gene_variant MELA-AU 16 74919580 74919580 single base substitution G A exon_variant MELA-AU 16 74919580 74919580 single base substitution G A missense_variant S201F 602C>T MELA-AU 16 74919580 74919580 single base substitution G A missense_variant S887F 2660C>T MELA-AU 16 74920397 74920397 single base substitution G A downstream_gene_variant MELA-AU 16 74920397 74920397 single base substitution G A intron_variant MELA-AU 16 74920397 74920397 single base substitution G A upstream_gene_variant MELA-AU 16 74920409 74920409 single base substitution G A downstream_gene_variant MELA-AU 16 74920409 74920409 single base substitution G A intron_variant MELA-AU 16 74920409 74920409 single base substitution G A upstream_gene_variant MELA-AU 16 74920833 74920833 insertion of <=200bp - T downstream_gene_variant MELA-AU 16 74920833 74920833 insertion of <=200bp - T intron_variant MELA-AU 16 74920833 74920833 insertion of <=200bp - T upstream_gene_variant MELA-AU 16 74920898 74920898 single base substitution G A downstream_gene_variant MELA-AU 16 74920898 74920898 single base substitution G A intron_variant MELA-AU 16 74920898 74920898 single base substitution G A upstream_gene_variant MELA-AU 16 74920993 74920993 single base substitution G A downstream_gene_variant MELA-AU 16 74920993 74920993 single base substitution G A intron_variant MELA-AU 16 74920993 74920993 single base substitution G A upstream_gene_variant MELA-AU 16 74920999 74920999 single base substitution A T downstream_gene_variant MELA-AU 16 74920999 74920999 single base substitution A T intron_variant MELA-AU 16 74920999 74920999 single base substitution A T upstream_gene_variant MELA-AU 16 74921332 74921332 single base substitution G A downstream_gene_variant MELA-AU 16 74921332 74921332 single base substitution G A intron_variant MELA-AU 16 74921332 74921332 single base substitution G A upstream_gene_variant MELA-AU 16 74921367 74921367 single base substitution G A downstream_gene_variant MELA-AU 16 74921367 74921367 single base substitution G A intron_variant MELA-AU 16 74921367 74921367 single base substitution G A upstream_gene_variant MELA-AU 16 74921485 74921485 deletion of <=200bp A - downstream_gene_variant MELA-AU 16 74921485 74921485 deletion of <=200bp A - intron_variant MELA-AU 16 74921485 74921485 deletion of <=200bp A - upstream_gene_variant MELA-AU 16 74921516 74921516 single base substitution G A downstream_gene_variant MELA-AU 16 74921516 74921516 single base substitution G A intron_variant MELA-AU 16 74921516 74921516 single base substitution G A upstream_gene_variant MELA-AU 16 74921538 74921539 multiple base substitution (>=2bp and <=200bp) AG TA downstream_gene_variant MELA-AU 16 74921538 74921539 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 16 74921538 74921539 multiple base substitution (>=2bp and <=200bp) AG TA upstream_gene_variant MELA-AU 16 74921625 74921625 single base substitution G A downstream_gene_variant MELA-AU 16 74921625 74921625 single base substitution G A missense_variant S106F 317C>T MELA-AU 16 74921625 74921625 single base substitution G A missense_variant S792F 2375C>T MELA-AU 16 74921625 74921625 single base substitution G A upstream_gene_variant MELA-AU 16 74921805 74921805 single base substitution C T downstream_gene_variant MELA-AU 16 74921805 74921805 single base substitution C T intron_variant MELA-AU 16 74921805 74921805 single base substitution C T upstream_gene_variant MELA-AU 16 74921814 74921814 single base substitution G A downstream_gene_variant MELA-AU 16 74921814 74921814 single base substitution G A intron_variant MELA-AU 16 74921814 74921814 single base substitution G A upstream_gene_variant MELA-AU 16 74922038 74922038 single base substitution C T downstream_gene_variant MELA-AU 16 74922038 74922038 single base substitution C T intron_variant MELA-AU 16 74922038 74922038 single base substitution C T upstream_gene_variant MELA-AU 16 74922114 74922114 single base substitution G A downstream_gene_variant MELA-AU 16 74922114 74922114 single base substitution G A exon_variant MELA-AU 16 74922114 74922114 single base substitution G A intron_variant MELA-AU 16 74922114 74922114 single base substitution G A missense_variant P767S 2299C>T MELA-AU 16 74922114 74922114 single base substitution G A upstream_gene_variant MELA-AU 16 74922629 74922629 single base substitution C T downstream_gene_variant MELA-AU 16 74922629 74922629 single base substitution C T intron_variant MELA-AU 16 74922629 74922629 single base substitution C T upstream_gene_variant MELA-AU 16 74922920 74922920 single base substitution G A downstream_gene_variant MELA-AU 16 74922920 74922920 single base substitution G A intron_variant MELA-AU 16 74922920 74922920 single base substitution G A upstream_gene_variant MELA-AU 16 74922947 74922948 multiple base substitution (>=2bp and <=200bp) CC TA downstream_gene_variant MELA-AU 16 74922947 74922948 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU 16 74922947 74922948 multiple base substitution (>=2bp and <=200bp) CC TA upstream_gene_variant MELA-AU 16 74922977 74922977 single base substitution G A downstream_gene_variant MELA-AU 16 74922977 74922977 single base substitution G A intron_variant MELA-AU 16 74922977 74922977 single base substitution G A upstream_gene_variant MELA-AU 16 74923143 74923143 single base substitution A C downstream_gene_variant MELA-AU 16 74923143 74923143 single base substitution A C intron_variant MELA-AU 16 74923143 74923143 single base substitution A C upstream_gene_variant MELA-AU 16 74923354 74923354 single base substitution C T downstream_gene_variant MELA-AU 16 74923354 74923354 single base substitution C T intron_variant MELA-AU 16 74923354 74923354 single base substitution C T upstream_gene_variant MELA-AU 16 74923467 74923467 single base substitution G A downstream_gene_variant MELA-AU 16 74923467 74923467 single base substitution G A intron_variant MELA-AU 16 74923467 74923467 single base substitution G A upstream_gene_variant MELA-AU 16 74923472 74923472 single base substitution G A downstream_gene_variant MELA-AU 16 74923472 74923472 single base substitution G A intron_variant MELA-AU 16 74923472 74923472 single base substitution G A upstream_gene_variant MELA-AU 16 74924319 74924319 single base substitution G A downstream_gene_variant MELA-AU 16 74924319 74924319 single base substitution G A intron_variant MELA-AU 16 74924319 74924319 single base substitution G A upstream_gene_variant MELA-AU 16 74924905 74924905 single base substitution G A downstream_gene_variant MELA-AU 16 74924905 74924905 single base substitution G A intron_variant MELA-AU 16 74924905 74924905 single base substitution G A upstream_gene_variant MELA-AU 16 74924906 74924906 single base substitution G A downstream_gene_variant MELA-AU 16 74924906 74924906 single base substitution G A intron_variant MELA-AU 16 74924906 74924906 single base substitution G A upstream_gene_variant MELA-AU 16 74925260 74925260 single base substitution G A downstream_gene_variant MELA-AU 16 74925260 74925260 single base substitution G A intron_variant MELA-AU 16 74925260 74925260 single base substitution G A upstream_gene_variant MELA-AU 16 74925289 74925289 single base substitution G A downstream_gene_variant MELA-AU 16 74925289 74925289 single base substitution G A intron_variant MELA-AU 16 74925289 74925289 single base substitution G A upstream_gene_variant MELA-AU 16 74925716 74925716 single base substitution G A downstream_gene_variant MELA-AU 16 74925716 74925716 single base substitution G A intron_variant MELA-AU 16 74926126 74926126 single base substitution G A downstream_gene_variant MELA-AU 16 74926126 74926126 single base substitution G A intron_variant MELA-AU 16 74926368 74926368 single base substitution G A downstream_gene_variant MELA-AU 16 74926368 74926368 single base substitution G A intron_variant MELA-AU 16 74926532 74926532 single base substitution T G downstream_gene_variant MELA-AU 16 74926532 74926532 single base substitution T G intron_variant MELA-AU 16 74926673 74926673 single base substitution G A downstream_gene_variant MELA-AU 16 74926673 74926673 single base substitution G A intron_variant MELA-AU 16 74926737 74926737 single base substitution C T downstream_gene_variant MELA-AU 16 74926737 74926737 single base substitution C T intron_variant MELA-AU 16 74926813 74926813 single base substitution T C downstream_gene_variant MELA-AU 16 74926813 74926813 single base substitution T C intron_variant MELA-AU 16 74926858 74926858 single base substitution G A downstream_gene_variant MELA-AU 16 74926858 74926858 single base substitution G A intron_variant MELA-AU 16 74927062 74927062 single base substitution G A downstream_gene_variant MELA-AU 16 74927062 74927062 single base substitution G A intron_variant MELA-AU 16 74927206 74927206 single base substitution G A downstream_gene_variant MELA-AU 16 74927206 74927206 single base substitution G A intron_variant MELA-AU 16 74927728 74927728 single base substitution G A exon_variant MELA-AU 16 74927728 74927728 single base substitution G A intron_variant MELA-AU 16 74927752 74927752 single base substitution A T exon_variant MELA-AU 16 74927752 74927752 single base substitution A T intron_variant MELA-AU 16 74928033 74928033 single base substitution G A intron_variant MELA-AU 16 74928033 74928033 single base substitution G A upstream_gene_variant MELA-AU 16 74929295 74929295 single base substitution G A intron_variant MELA-AU 16 74929295 74929295 single base substitution G A upstream_gene_variant MELA-AU 16 74929475 74929475 single base substitution G A intron_variant MELA-AU 16 74929475 74929475 single base substitution G A upstream_gene_variant MELA-AU 16 74930070 74930070 single base substitution G C intron_variant MELA-AU 16 74930070 74930070 single base substitution G C upstream_gene_variant MELA-AU 16 74930501 74930501 single base substitution C T intron_variant MELA-AU 16 74930501 74930501 single base substitution C T upstream_gene_variant MELA-AU 16 74930546 74930546 single base substitution A T intron_variant MELA-AU 16 74930546 74930546 single base substitution A T upstream_gene_variant MELA-AU 16 74930999 74930999 single base substitution G A intron_variant MELA-AU 16 74930999 74930999 single base substitution G A upstream_gene_variant MELA-AU 16 74931000 74931000 single base substitution G A intron_variant MELA-AU 16 74931000 74931000 single base substitution G A upstream_gene_variant MELA-AU 16 74932249 74932249 single base substitution G A intron_variant MELA-AU 16 74932249 74932249 single base substitution G A upstream_gene_variant MELA-AU 16 74932444 74932444 single base substitution G A intron_variant MELA-AU 16 74932444 74932444 single base substitution G A upstream_gene_variant MELA-AU 16 74932465 74932465 single base substitution G A intron_variant MELA-AU 16 74932465 74932465 single base substitution G A upstream_gene_variant MELA-AU 16 74932704 74932704 single base substitution G A intron_variant MELA-AU 16 74932704 74932704 single base substitution G A upstream_gene_variant MELA-AU 16 74932896 74932896 single base substitution G A intron_variant MELA-AU 16 74933549 74933550 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 16 74933630 74933630 single base substitution C T intron_variant MELA-AU 16 74933630 74933630 single base substitution C T missense_variant R179Q 536G>A MELA-AU 16 74934048 74934048 single base substitution G A intron_variant MELA-AU 16 74934277 74934277 single base substitution T A intron_variant MELA-AU 16 74934697 74934697 single base substitution T C intron_variant MELA-AU 16 74934932 74934932 single base substitution G A intron_variant MELA-AU 16 74935355 74935355 single base substitution G A intron_variant MELA-AU 16 74935468 74935468 single base substitution G A intron_variant MELA-AU 16 74935815 74935815 single base substitution G A intron_variant MELA-AU 16 74936199 74936199 single base substitution G A intron_variant MELA-AU 16 74936766 74936766 single base substitution G A intron_variant MELA-AU 16 74936796 74936796 single base substitution G A intron_variant MELA-AU 16 74936805 74936805 single base substitution G A intron_variant MELA-AU 16 74936908 74936908 single base substitution G A intron_variant MELA-AU 16 74936997 74936997 single base substitution G A intron_variant MELA-AU 16 74937274 74937274 single base substitution G A intron_variant MELA-AU 16 74937590 74937590 single base substitution G A intron_variant MELA-AU 16 74937694 74937694 single base substitution G A downstream_gene_variant MELA-AU 16 74937694 74937694 single base substitution G A intron_variant MELA-AU 16 74937731 74937731 single base substitution G A downstream_gene_variant MELA-AU 16 74937731 74937731 single base substitution G A intron_variant MELA-AU 16 74937933 74937933 single base substitution G A 3_prime_UTR_variant MELA-AU 16 74937933 74937933 single base substitution G A downstream_gene_variant MELA-AU 16 74937933 74937933 single base substitution G A exon_variant MELA-AU 16 74937933 74937933 single base substitution G A missense_variant A142V 425C>T MELA-AU 16 74937933 74937933 single base substitution G A missense_variant A593V 1778C>T MELA-AU 16 74937933 74937933 single base substitution G A upstream_gene_variant MELA-AU 16 74938013 74938013 single base substitution G A downstream_gene_variant MELA-AU 16 74938013 74938013 single base substitution G A exon_variant MELA-AU 16 74938013 74938013 single base substitution G A intron_variant MELA-AU 16 74938013 74938013 single base substitution G A upstream_gene_variant MELA-AU 16 74938308 74938308 single base substitution A G downstream_gene_variant MELA-AU 16 74938308 74938308 single base substitution A G intron_variant MELA-AU 16 74938308 74938308 single base substitution A G upstream_gene_variant MELA-AU 16 74938721 74938721 single base substitution G A downstream_gene_variant MELA-AU 16 74938721 74938721 single base substitution G A intron_variant MELA-AU 16 74938721 74938721 single base substitution G A upstream_gene_variant MELA-AU 16 74938857 74938857 single base substitution G A downstream_gene_variant MELA-AU 16 74938857 74938857 single base substitution G A intron_variant MELA-AU 16 74938857 74938857 single base substitution G A upstream_gene_variant MELA-AU 16 74938926 74938926 single base substitution G A downstream_gene_variant MELA-AU 16 74938926 74938926 single base substitution G A intron_variant MELA-AU 16 74938926 74938926 single base substitution G A upstream_gene_variant MELA-AU 16 74939567 74939567 single base substitution G A downstream_gene_variant MELA-AU 16 74939567 74939567 single base substitution G A intron_variant MELA-AU 16 74939567 74939567 single base substitution G A upstream_gene_variant MELA-AU 16 74939849 74939849 single base substitution C T downstream_gene_variant MELA-AU 16 74939849 74939849 single base substitution C T intron_variant MELA-AU 16 74939849 74939849 single base substitution C T upstream_gene_variant MELA-AU 16 74940450 74940450 single base substitution A T downstream_gene_variant MELA-AU 16 74940450 74940450 single base substitution A T intron_variant MELA-AU 16 74940450 74940450 single base substitution A T upstream_gene_variant MELA-AU 16 74940537 74940537 single base substitution G A downstream_gene_variant MELA-AU 16 74940537 74940537 single base substitution G A intron_variant MELA-AU 16 74940537 74940537 single base substitution G A upstream_gene_variant MELA-AU 16 74940973 74940973 single base substitution G A downstream_gene_variant MELA-AU 16 74940973 74940973 single base substitution G A intron_variant MELA-AU 16 74940973 74940973 single base substitution G A upstream_gene_variant MELA-AU 16 74941171 74941171 single base substitution T A downstream_gene_variant MELA-AU 16 74941171 74941171 single base substitution T A intron_variant MELA-AU 16 74941171 74941171 single base substitution T A upstream_gene_variant MELA-AU 16 74941406 74941406 single base substitution G A downstream_gene_variant MELA-AU 16 74941406 74941406 single base substitution G A intron_variant MELA-AU 16 74941406 74941406 single base substitution G A upstream_gene_variant MELA-AU 16 74941990 74941990 single base substitution G A downstream_gene_variant MELA-AU 16 74941990 74941990 single base substitution G A intron_variant MELA-AU 16 74941990 74941990 single base substitution G A upstream_gene_variant MELA-AU 16 74942210 74942210 single base substitution G A downstream_gene_variant MELA-AU 16 74942210 74942210 single base substitution G A intron_variant MELA-AU 16 74942210 74942210 single base substitution G A upstream_gene_variant MELA-AU 16 74942363 74942363 single base substitution A C downstream_gene_variant MELA-AU 16 74942363 74942363 single base substitution A C intron_variant MELA-AU 16 74942363 74942363 single base substitution A C upstream_gene_variant MELA-AU 16 74942558 74942558 single base substitution T G downstream_gene_variant MELA-AU 16 74942558 74942558 single base substitution T G intron_variant MELA-AU 16 74942558 74942558 single base substitution T G upstream_gene_variant MELA-AU 16 74942870 74942870 single base substitution G A downstream_gene_variant MELA-AU 16 74942870 74942870 single base substitution G A exon_variant MELA-AU 16 74942870 74942870 single base substitution G A intron_variant MELA-AU 16 74942870 74942870 single base substitution G A synonymous_variant L550L 1648C>T MELA-AU 16 74942870 74942870 single base substitution G A synonymous_variant L99L 295C>T MELA-AU 16 74942870 74942870 single base substitution G A upstream_gene_variant MELA-AU 16 74943409 74943409 single base substitution G A downstream_gene_variant MELA-AU 16 74943409 74943409 single base substitution G A exon_variant MELA-AU 16 74943409 74943409 single base substitution G A synonymous_variant F544F 1632C>T MELA-AU 16 74943409 74943409 single base substitution G A synonymous_variant F93F 279C>T MELA-AU 16 74943411 74943411 single base substitution A T downstream_gene_variant MELA-AU 16 74943411 74943411 single base substitution A T exon_variant MELA-AU 16 74943411 74943411 single base substitution A T missense_variant F544I 1630T>A MELA-AU 16 74943411 74943411 single base substitution A T missense_variant F93I 277T>A MELA-AU 16 74943458 74943458 single base substitution G A downstream_gene_variant MELA-AU 16 74943458 74943458 single base substitution G A exon_variant MELA-AU 16 74943458 74943458 single base substitution G A missense_variant S528L 1583C>T MELA-AU 16 74943458 74943458 single base substitution G A missense_variant S77L 230C>T MELA-AU 16 74943744 74943744 single base substitution G A downstream_gene_variant MELA-AU 16 74943744 74943744 single base substitution G A exon_variant MELA-AU 16 74943744 74943744 single base substitution G A synonymous_variant L36L 108C>T MELA-AU 16 74943744 74943744 single base substitution G A synonymous_variant L487L 1461C>T MELA-AU 16 74943744 74943744 single base substitution G A upstream_gene_variant MELA-AU 16 74944052 74944052 single base substitution G A downstream_gene_variant MELA-AU 16 74944052 74944052 single base substitution G A intron_variant MELA-AU 16 74944052 74944052 single base substitution G A upstream_gene_variant MELA-AU 16 74944205 74944205 single base substitution G A downstream_gene_variant MELA-AU 16 74944205 74944205 single base substitution G A intron_variant MELA-AU 16 74944205 74944205 single base substitution G A upstream_gene_variant MELA-AU 16 74944728 74944728 single base substitution T A downstream_gene_variant MELA-AU 16 74944728 74944728 single base substitution T A intron_variant MELA-AU 16 74944728 74944728 single base substitution T A upstream_gene_variant MELA-AU 16 74945062 74945062 single base substitution A T downstream_gene_variant MELA-AU 16 74945062 74945062 single base substitution A T intron_variant MELA-AU 16 74945062 74945062 single base substitution A T upstream_gene_variant MELA-AU 16 74945616 74945616 single base substitution C T downstream_gene_variant MELA-AU 16 74945616 74945616 single base substitution C T intron_variant MELA-AU 16 74945616 74945616 single base substitution C T upstream_gene_variant MELA-AU 16 74945643 74945643 single base substitution G A downstream_gene_variant MELA-AU 16 74945643 74945643 single base substitution G A intron_variant MELA-AU 16 74945643 74945643 single base substitution G A upstream_gene_variant MELA-AU 16 74945714 74945714 single base substitution G A downstream_gene_variant MELA-AU 16 74945714 74945714 single base substitution G A intron_variant MELA-AU 16 74945714 74945714 single base substitution G A upstream_gene_variant MELA-AU 16 74945741 74945741 single base substitution G A downstream_gene_variant MELA-AU 16 74945741 74945741 single base substitution G A intron_variant MELA-AU 16 74945741 74945741 single base substitution G A upstream_gene_variant MELA-AU 16 74946014 74946014 single base substitution C T downstream_gene_variant MELA-AU 16 74946014 74946014 single base substitution C T exon_variant MELA-AU 16 74946014 74946014 single base substitution C T intron_variant MELA-AU 16 74946014 74946014 single base substitution C T upstream_gene_variant MELA-AU 16 74946121 74946121 single base substitution G A downstream_gene_variant MELA-AU 16 74946121 74946121 single base substitution G A exon_variant MELA-AU 16 74946121 74946121 single base substitution G A missense_variant S455F 1364C>T MELA-AU 16 74946121 74946121 single base substitution G A missense_variant S4F 11C>T MELA-AU 16 74946121 74946121 single base substitution G A upstream_gene_variant MELA-AU 16 74946154 74946154 single base substitution G A downstream_gene_variant MELA-AU 16 74946154 74946154 single base substitution G A exon_variant MELA-AU 16 74946154 74946154 single base substitution G A missense_variant S444F 1331C>T MELA-AU 16 74946154 74946154 single base substitution G A upstream_gene_variant MELA-AU 16 74946361 74946361 single base substitution G T downstream_gene_variant MELA-AU 16 74946361 74946361 single base substitution G T intron_variant MELA-AU 16 74946361 74946361 single base substitution G T upstream_gene_variant MELA-AU 16 74946534 74946534 single base substitution G A downstream_gene_variant MELA-AU 16 74946534 74946534 single base substitution G A intron_variant MELA-AU 16 74946534 74946534 single base substitution G A upstream_gene_variant MELA-AU 16 74947910 74947910 single base substitution A G downstream_gene_variant MELA-AU 16 74947910 74947910 single base substitution A G intron_variant MELA-AU 16 74947910 74947910 single base substitution A G upstream_gene_variant MELA-AU 16 74947952 74947952 single base substitution G A downstream_gene_variant MELA-AU 16 74947952 74947952 single base substitution G A intron_variant MELA-AU 16 74947952 74947952 single base substitution G A upstream_gene_variant MELA-AU 16 74948712 74948712 single base substitution G A downstream_gene_variant MELA-AU 16 74948712 74948712 single base substitution G A intron_variant MELA-AU 16 74948712 74948712 single base substitution G A upstream_gene_variant MELA-AU 16 74948788 74948788 single base substitution C T downstream_gene_variant MELA-AU 16 74948788 74948788 single base substitution C T intron_variant MELA-AU 16 74948788 74948788 single base substitution C T upstream_gene_variant MELA-AU 16 74948900 74948900 single base substitution C T downstream_gene_variant MELA-AU 16 74948900 74948900 single base substitution C T intron_variant MELA-AU 16 74948900 74948900 single base substitution C T upstream_gene_variant MELA-AU 16 74950100 74950100 single base substitution G A exon_variant MELA-AU 16 74950100 74950100 single base substitution G A synonymous_variant L342L 1024C>T MELA-AU 16 74950100 74950100 single base substitution G A upstream_gene_variant MELA-AU 16 74950249 74950250 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 74950249 74950250 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 74951134 74951134 single base substitution A T intron_variant MELA-AU 16 74951134 74951134 single base substitution A T upstream_gene_variant MELA-AU 16 74951243 74951243 single base substitution G A intron_variant MELA-AU 16 74951243 74951243 single base substitution G A upstream_gene_variant MELA-AU 16 74952210 74952210 single base substitution G A intron_variant MELA-AU 16 74952210 74952210 single base substitution G A upstream_gene_variant MELA-AU 16 74952273 74952273 single base substitution G A intron_variant MELA-AU 16 74952273 74952273 single base substitution G A upstream_gene_variant MELA-AU 16 74952352 74952352 single base substitution G A intron_variant MELA-AU 16 74952352 74952352 single base substitution G A upstream_gene_variant MELA-AU 16 74952584 74952584 single base substitution G A intron_variant MELA-AU 16 74952584 74952584 single base substitution G A upstream_gene_variant MELA-AU 16 74952734 74952734 single base substitution G A intron_variant MELA-AU 16 74952734 74952734 single base substitution G A upstream_gene_variant MELA-AU 16 74953001 74953001 single base substitution G A downstream_gene_variant MELA-AU 16 74953001 74953001 single base substitution G A intron_variant MELA-AU 16 74953001 74953001 single base substitution G A upstream_gene_variant MELA-AU 16 74953320 74953320 single base substitution C T downstream_gene_variant MELA-AU 16 74953320 74953320 single base substitution C T intron_variant MELA-AU 16 74953320 74953320 single base substitution C T upstream_gene_variant MELA-AU 16 74954026 74954026 single base substitution A G downstream_gene_variant MELA-AU 16 74954026 74954026 single base substitution A G intron_variant MELA-AU 16 74954026 74954026 single base substitution A G upstream_gene_variant MELA-AU 16 74954204 74954204 single base substitution G A downstream_gene_variant MELA-AU 16 74954204 74954204 single base substitution G A intron_variant MELA-AU 16 74954204 74954204 single base substitution G A upstream_gene_variant MELA-AU 16 74954975 74954975 single base substitution A T downstream_gene_variant MELA-AU 16 74954975 74954975 single base substitution A T intron_variant MELA-AU 16 74954975 74954975 single base substitution A T upstream_gene_variant MELA-AU 16 74954983 74954983 single base substitution T A downstream_gene_variant MELA-AU 16 74954983 74954983 single base substitution T A intron_variant MELA-AU 16 74954983 74954983 single base substitution T A upstream_gene_variant MELA-AU 16 74955190 74955190 single base substitution C T downstream_gene_variant MELA-AU 16 74955190 74955190 single base substitution C T intron_variant MELA-AU 16 74955779 74955779 single base substitution A G downstream_gene_variant MELA-AU 16 74955779 74955779 single base substitution A G intron_variant MELA-AU 16 74956448 74956448 single base substitution G A downstream_gene_variant MELA-AU 16 74956448 74956448 single base substitution G A intron_variant MELA-AU 16 74956448 74956448 single base substitution G A upstream_gene_variant MELA-AU 16 74957361 74957361 single base substitution G A downstream_gene_variant MELA-AU 16 74957361 74957361 single base substitution G A intron_variant MELA-AU 16 74957361 74957361 single base substitution G A upstream_gene_variant MELA-AU 16 74957566 74957566 single base substitution G A downstream_gene_variant MELA-AU 16 74957566 74957566 single base substitution G A intron_variant MELA-AU 16 74957566 74957566 single base substitution G A upstream_gene_variant MELA-AU 16 74957618 74957618 single base substitution G A downstream_gene_variant MELA-AU 16 74957618 74957618 single base substitution G A intron_variant MELA-AU 16 74957618 74957618 single base substitution G A upstream_gene_variant MELA-AU 16 74958164 74958164 single base substitution G A intron_variant MELA-AU 16 74958164 74958164 single base substitution G A upstream_gene_variant MELA-AU 16 74958377 74958377 single base substitution G A intron_variant MELA-AU 16 74958377 74958377 single base substitution G A upstream_gene_variant MELA-AU 16 74958620 74958620 single base substitution A G intron_variant MELA-AU 16 74958620 74958620 single base substitution A G upstream_gene_variant MELA-AU 16 74959485 74959485 single base substitution T A intron_variant MELA-AU 16 74959485 74959485 single base substitution T A upstream_gene_variant MELA-AU 16 74959710 74959710 single base substitution T C intron_variant MELA-AU 16 74959710 74959710 single base substitution T C upstream_gene_variant MELA-AU 16 74960148 74960148 single base substitution G A intron_variant MELA-AU 16 74960148 74960148 single base substitution G A upstream_gene_variant MELA-AU 16 74960149 74960149 single base substitution G A intron_variant MELA-AU 16 74960149 74960149 single base substitution G A upstream_gene_variant MELA-AU 16 74960279 74960279 single base substitution G A intron_variant MELA-AU 16 74960279 74960279 single base substitution G A upstream_gene_variant MELA-AU 16 74960294 74960294 single base substitution G A intron_variant MELA-AU 16 74960294 74960294 single base substitution G A upstream_gene_variant MELA-AU 16 74960455 74960455 single base substitution G A intron_variant MELA-AU 16 74960455 74960455 single base substitution G A upstream_gene_variant MELA-AU 16 74961360 74961360 single base substitution C T intron_variant MELA-AU 16 74961469 74961469 single base substitution G A intron_variant MELA-AU 16 74961939 74961939 single base substitution G A intron_variant MELA-AU 16 74962860 74962860 single base substitution C T intron_variant MELA-AU 16 74962875 74962875 single base substitution T A intron_variant MELA-AU 16 74962997 74962997 single base substitution G A intron_variant MELA-AU 16 74964235 74964235 single base substitution C T intron_variant MELA-AU 16 74964326 74964326 single base substitution G A intron_variant MELA-AU 16 74964425 74964425 single base substitution G C intron_variant MELA-AU 16 74964550 74964550 single base substitution G A intron_variant MELA-AU 16 74964559 74964559 single base substitution G A intron_variant MELA-AU 16 74964853 74964853 single base substitution G A intron_variant MELA-AU 16 74964853 74964853 single base substitution G A upstream_gene_variant MELA-AU 16 74967163 74967164 multiple base substitution (>=2bp and <=200bp) GG TA downstream_gene_variant MELA-AU 16 74967163 74967164 multiple base substitution (>=2bp and <=200bp) GG TA intron_variant MELA-AU 16 74967163 74967164 multiple base substitution (>=2bp and <=200bp) GG TA upstream_gene_variant MELA-AU 16 74967271 74967271 single base substitution C T downstream_gene_variant MELA-AU 16 74967271 74967271 single base substitution C T intron_variant MELA-AU 16 74967271 74967271 single base substitution C T upstream_gene_variant MELA-AU 16 74967305 74967305 single base substitution C T downstream_gene_variant MELA-AU 16 74967305 74967305 single base substitution C T intron_variant MELA-AU 16 74967305 74967305 single base substitution C T upstream_gene_variant MELA-AU 16 74967472 74967472 single base substitution C T downstream_gene_variant MELA-AU 16 74967472 74967472 single base substitution C T intron_variant MELA-AU 16 74967472 74967472 single base substitution C T upstream_gene_variant MELA-AU 16 74969189 74969189 single base substitution G A downstream_gene_variant MELA-AU 16 74969189 74969189 single base substitution G A intron_variant MELA-AU 16 74969189 74969189 single base substitution G A upstream_gene_variant MELA-AU 16 74969406 74969406 single base substitution G A downstream_gene_variant MELA-AU 16 74969406 74969406 single base substitution G A intron_variant MELA-AU 16 74969406 74969406 single base substitution G A upstream_gene_variant MELA-AU 16 74970109 74970109 single base substitution T A downstream_gene_variant MELA-AU 16 74970109 74970109 single base substitution T A intron_variant MELA-AU 16 74970130 74970130 single base substitution G A downstream_gene_variant MELA-AU 16 74970130 74970130 single base substitution G A intron_variant MELA-AU 16 74970578 74970578 single base substitution G C downstream_gene_variant MELA-AU 16 74970578 74970578 single base substitution G C intron_variant MELA-AU 16 74970643 74970643 single base substitution G A downstream_gene_variant MELA-AU 16 74970643 74970643 single base substitution G A intron_variant MELA-AU 16 74970766 74970766 single base substitution C T downstream_gene_variant MELA-AU 16 74970766 74970766 single base substitution C T intron_variant MELA-AU 16 74971260 74971260 single base substitution G A downstream_gene_variant MELA-AU 16 74971260 74971260 single base substitution G A intron_variant MELA-AU 16 74971480 74971480 single base substitution A G downstream_gene_variant MELA-AU 16 74971480 74971480 single base substitution A G intron_variant MELA-AU 16 74971758 74971758 single base substitution G A downstream_gene_variant MELA-AU 16 74971758 74971758 single base substitution G A intron_variant MELA-AU 16 74972116 74972116 single base substitution G A downstream_gene_variant MELA-AU 16 74972116 74972116 single base substitution G A exon_variant MELA-AU 16 74972116 74972116 single base substitution G A missense_variant H195Y 583C>T MELA-AU 16 74972349 74972349 single base substitution C G downstream_gene_variant MELA-AU 16 74972349 74972349 single base substitution C G intron_variant MELA-AU 16 74972680 74972680 single base substitution C T downstream_gene_variant MELA-AU 16 74972680 74972680 single base substitution C T intron_variant MELA-AU 16 74973844 74973844 single base substitution C T downstream_gene_variant MELA-AU 16 74973844 74973844 single base substitution C T intron_variant MELA-AU 16 74973858 74973859 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 74973858 74973859 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 74973887 74973887 deletion of <=200bp A - downstream_gene_variant MELA-AU 16 74973887 74973887 deletion of <=200bp A - intron_variant MELA-AU 16 74973895 74973895 single base substitution G A downstream_gene_variant MELA-AU 16 74973895 74973895 single base substitution G A intron_variant MELA-AU 16 74973976 74973976 single base substitution G A downstream_gene_variant MELA-AU 16 74973976 74973976 single base substitution G A intron_variant MELA-AU 16 74974378 74974378 single base substitution G A downstream_gene_variant MELA-AU 16 74974378 74974378 single base substitution G A intron_variant MELA-AU 16 74974697 74974697 single base substitution G A downstream_gene_variant MELA-AU 16 74974697 74974697 single base substitution G A intron_variant MELA-AU 16 74974818 74974819 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 74974818 74974819 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 74974939 74974939 single base substitution T A downstream_gene_variant MELA-AU 16 74974939 74974939 single base substitution T A intron_variant MELA-AU 16 74975006 74975006 single base substitution G A downstream_gene_variant MELA-AU 16 74975006 74975006 single base substitution G A intron_variant MELA-AU 16 74975096 74975096 single base substitution G A downstream_gene_variant MELA-AU 16 74975096 74975096 single base substitution G A intron_variant MELA-AU 16 74975354 74975354 single base substitution G A downstream_gene_variant MELA-AU 16 74975354 74975354 single base substitution G A intron_variant MELA-AU 16 74975406 74975406 single base substitution A G downstream_gene_variant MELA-AU 16 74975406 74975406 single base substitution A G intron_variant MELA-AU 16 74975726 74975726 single base substitution G A downstream_gene_variant MELA-AU 16 74975726 74975726 single base substitution G A intron_variant MELA-AU 16 74975979 74975979 single base substitution G A downstream_gene_variant MELA-AU 16 74975979 74975979 single base substitution G A intron_variant MELA-AU 16 74976267 74976267 single base substitution C T downstream_gene_variant MELA-AU 16 74976267 74976267 single base substitution C T intron_variant MELA-AU 16 74976597 74976597 single base substitution G A downstream_gene_variant MELA-AU 16 74976597 74976597 single base substitution G A intron_variant MELA-AU 16 74976940 74976940 single base substitution G A intron_variant MELA-AU 16 74977779 74977779 single base substitution C G intron_variant MELA-AU 16 74977867 74977867 single base substitution G A intron_variant MELA-AU 16 74978027 74978027 single base substitution G A intron_variant MELA-AU 16 74978345 74978345 single base substitution C G intron_variant MELA-AU 16 74978663 74978663 single base substitution G A intron_variant MELA-AU 16 74978964 74978964 single base substitution G A downstream_gene_variant MELA-AU 16 74978964 74978964 single base substitution G A intron_variant MELA-AU 16 74979712 74979712 single base substitution A G downstream_gene_variant MELA-AU 16 74979712 74979712 single base substitution A G intron_variant MELA-AU 16 74980536 74980536 single base substitution C T downstream_gene_variant MELA-AU 16 74980536 74980536 single base substitution C T intron_variant MELA-AU 16 74980932 74980932 single base substitution G A downstream_gene_variant MELA-AU 16 74980932 74980932 single base substitution G A intron_variant MELA-AU 16 74980976 74980976 single base substitution G A downstream_gene_variant MELA-AU 16 74980976 74980976 single base substitution G A intron_variant MELA-AU 16 74981727 74981727 single base substitution G C downstream_gene_variant MELA-AU 16 74981727 74981727 single base substitution G C intron_variant MELA-AU 16 74981993 74981993 single base substitution G A downstream_gene_variant MELA-AU 16 74981993 74981993 single base substitution G A intron_variant MELA-AU 16 74982037 74982037 single base substitution A T downstream_gene_variant MELA-AU 16 74982037 74982037 single base substitution A T intron_variant MELA-AU 16 74982230 74982230 single base substitution G A downstream_gene_variant MELA-AU 16 74982230 74982230 single base substitution G A intron_variant MELA-AU 16 74982344 74982344 single base substitution G A downstream_gene_variant MELA-AU 16 74982344 74982344 single base substitution G A intron_variant MELA-AU 16 74983327 74983327 single base substitution G A downstream_gene_variant MELA-AU 16 74983327 74983327 single base substitution G A intron_variant MELA-AU 16 74983731 74983731 single base substitution G A downstream_gene_variant MELA-AU 16 74983731 74983731 single base substitution G A intron_variant MELA-AU 16 74983872 74983872 single base substitution G A intron_variant MELA-AU 16 74984783 74984783 single base substitution G A intron_variant MELA-AU 16 74984869 74984869 single base substitution C T intron_variant MELA-AU 16 74984982 74984982 single base substitution C T intron_variant MELA-AU 16 74985254 74985254 single base substitution A C intron_variant MELA-AU 16 74985734 74985734 single base substitution G A downstream_gene_variant MELA-AU 16 74985734 74985734 single base substitution G A intron_variant MELA-AU 16 74987614 74987614 single base substitution G A downstream_gene_variant MELA-AU 16 74987614 74987614 single base substitution G A intron_variant MELA-AU 16 74988115 74988115 single base substitution G A downstream_gene_variant MELA-AU 16 74988115 74988115 single base substitution G A intron_variant MELA-AU 16 74988233 74988233 single base substitution G A downstream_gene_variant MELA-AU 16 74988233 74988233 single base substitution G A intron_variant MELA-AU 16 74989447 74989447 single base substitution G A downstream_gene_variant MELA-AU 16 74989447 74989447 single base substitution G A intron_variant MELA-AU 16 74990358 74990358 single base substitution C A downstream_gene_variant MELA-AU 16 74990358 74990358 single base substitution C A intron_variant MELA-AU 16 74990584 74990584 single base substitution A G intron_variant MELA-AU 16 74991199 74991199 single base substitution G A intron_variant MELA-AU 16 74991284 74991284 single base substitution G A intron_variant MELA-AU 16 74991476 74991476 single base substitution G A intron_variant MELA-AU 16 74991551 74991551 single base substitution G A intron_variant MELA-AU 16 74991990 74991990 single base substitution G A downstream_gene_variant MELA-AU 16 74991990 74991990 single base substitution G A intron_variant MELA-AU 16 74992061 74992061 single base substitution G A downstream_gene_variant MELA-AU 16 74992061 74992061 single base substitution G A intron_variant MELA-AU 16 74992676 74992676 single base substitution G A downstream_gene_variant MELA-AU 16 74992676 74992676 single base substitution G A intron_variant MELA-AU 16 74992773 74992773 single base substitution C T downstream_gene_variant MELA-AU 16 74992773 74992773 single base substitution C T intron_variant MELA-AU 16 74993328 74993328 single base substitution G A 3_prime_UTR_variant MELA-AU 16 74993328 74993328 single base substitution G A downstream_gene_variant MELA-AU 16 74993328 74993328 single base substitution G A intron_variant MELA-AU 16 74993332 74993332 single base substitution G A 3_prime_UTR_variant MELA-AU 16 74993332 74993332 single base substitution G A downstream_gene_variant MELA-AU 16 74993332 74993332 single base substitution G A intron_variant MELA-AU 16 74993367 74993367 single base substitution G A 3_prime_UTR_variant MELA-AU 16 74993367 74993367 single base substitution G A downstream_gene_variant MELA-AU 16 74993367 74993367 single base substitution G A intron_variant MELA-AU 16 74993543 74993543 single base substitution G A downstream_gene_variant MELA-AU 16 74993543 74993543 single base substitution G A intron_variant MELA-AU 16 74993957 74993957 single base substitution G T downstream_gene_variant MELA-AU 16 74993957 74993957 single base substitution G T intron_variant MELA-AU 16 74994532 74994532 single base substitution A G downstream_gene_variant MELA-AU 16 74994532 74994532 single base substitution A G intron_variant MELA-AU 16 74994792 74994792 single base substitution A T downstream_gene_variant MELA-AU 16 74994792 74994792 single base substitution A T intron_variant MELA-AU 16 74995820 74995820 single base substitution G A downstream_gene_variant MELA-AU 16 74995820 74995820 single base substitution G A intron_variant MELA-AU 16 74997477 74997477 single base substitution G T intron_variant MELA-AU 16 74997478 74997478 single base substitution G A intron_variant MELA-AU 16 74997827 74997827 single base substitution G A intron_variant MELA-AU 16 74997829 74997829 single base substitution G A intron_variant MELA-AU 16 74997863 74997863 single base substitution G A intron_variant MELA-AU 16 74998305 74998305 single base substitution G A intron_variant MELA-AU 16 74998631 74998631 single base substitution G A intron_variant MELA-AU 16 74998632 74998632 single base substitution G A intron_variant MELA-AU 16 74998640 74998640 single base substitution G A intron_variant MELA-AU 16 74998729 74998729 single base substitution G A intron_variant MELA-AU 16 74999343 74999343 single base substitution A G intron_variant MELA-AU 16 74999373 74999373 single base substitution C T intron_variant MELA-AU 16 75000805 75000805 single base substitution G A intron_variant MELA-AU 16 75000805 75000805 single base substitution G A upstream_gene_variant MELA-AU 16 75001422 75001422 single base substitution G A intron_variant MELA-AU 16 75001422 75001422 single base substitution G A upstream_gene_variant MELA-AU 16 75001423 75001423 single base substitution G A intron_variant MELA-AU 16 75001423 75001423 single base substitution G A upstream_gene_variant MELA-AU 16 75001571 75001571 single base substitution A G intron_variant MELA-AU 16 75001571 75001571 single base substitution A G upstream_gene_variant MELA-AU 16 75001621 75001621 single base substitution G A intron_variant MELA-AU 16 75001621 75001621 single base substitution G A upstream_gene_variant MELA-AU 16 75001963 75001963 single base substitution G A intron_variant MELA-AU 16 75001963 75001963 single base substitution G A upstream_gene_variant MELA-AU 16 75002102 75002102 single base substitution G A intron_variant MELA-AU 16 75002102 75002102 single base substitution G A upstream_gene_variant MELA-AU 16 75002529 75002529 single base substitution G A intron_variant MELA-AU 16 75002529 75002529 single base substitution G A upstream_gene_variant MELA-AU 16 75002754 75002754 single base substitution G A intron_variant MELA-AU 16 75002754 75002754 single base substitution G A upstream_gene_variant MELA-AU 16 75003197 75003197 single base substitution G A intron_variant MELA-AU 16 75003197 75003197 single base substitution G A upstream_gene_variant MELA-AU 16 75003495 75003495 single base substitution G A intron_variant MELA-AU 16 75003495 75003495 single base substitution G A upstream_gene_variant MELA-AU 16 75003953 75003953 single base substitution C T intron_variant MELA-AU 16 75003953 75003953 single base substitution C T upstream_gene_variant MELA-AU 16 75004434 75004434 single base substitution C T intron_variant MELA-AU 16 75004434 75004434 single base substitution C T upstream_gene_variant MELA-AU 16 75004692 75004692 single base substitution A T intron_variant MELA-AU 16 75004692 75004692 single base substitution A T upstream_gene_variant MELA-AU 16 75004876 75004876 single base substitution G A intron_variant MELA-AU 16 75004926 75004926 single base substitution G A intron_variant MELA-AU 16 75005465 75005465 single base substitution G A intron_variant MELA-AU 16 75005601 75005601 single base substitution G A intron_variant MELA-AU 16 75005835 75005835 single base substitution G A intron_variant MELA-AU 16 75006135 75006135 single base substitution G A intron_variant MELA-AU 16 75007216 75007216 single base substitution G A intron_variant MELA-AU 16 75008044 75008044 single base substitution G A intron_variant MELA-AU 16 75008081 75008081 single base substitution A G intron_variant MELA-AU 16 75008923 75008923 single base substitution G A intron_variant MELA-AU 16 75009153 75009153 single base substitution G A intron_variant MELA-AU 16 75009754 75009754 single base substitution G A intron_variant MELA-AU 16 75010814 75010814 single base substitution A G intron_variant MELA-AU 16 75011088 75011088 single base substitution C T intron_variant MELA-AU 16 75011673 75011673 single base substitution G A intron_variant MELA-AU 16 75014325 75014325 single base substitution C T intron_variant MELA-AU 16 75014325 75014325 single base substitution C T upstream_gene_variant MELA-AU 16 75014770 75014770 single base substitution G A intron_variant MELA-AU 16 75014770 75014770 single base substitution G A upstream_gene_variant MELA-AU 16 75014986 75014986 single base substitution G C intron_variant MELA-AU 16 75014986 75014986 single base substitution G C upstream_gene_variant MELA-AU 16 75015362 75015362 single base substitution G A intron_variant MELA-AU 16 75015362 75015362 single base substitution G A upstream_gene_variant MELA-AU 16 75015779 75015779 single base substitution C T intron_variant MELA-AU 16 75015779 75015779 single base substitution C T upstream_gene_variant MELA-AU 16 75016015 75016015 single base substitution G A intron_variant MELA-AU 16 75016015 75016015 single base substitution G A upstream_gene_variant MELA-AU 16 75016125 75016125 single base substitution T C intron_variant MELA-AU 16 75016125 75016125 single base substitution T C upstream_gene_variant MELA-AU 16 75017033 75017033 single base substitution G A intron_variant MELA-AU 16 75017033 75017033 single base substitution G A upstream_gene_variant MELA-AU 16 75017404 75017404 single base substitution G A intron_variant MELA-AU 16 75017404 75017404 single base substitution G A upstream_gene_variant MELA-AU 16 75017511 75017512 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 75017511 75017512 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 75018789 75018789 single base substitution G A intron_variant MELA-AU 16 75018789 75018789 single base substitution G A upstream_gene_variant MELA-AU 16 75019090 75019090 single base substitution C T intron_variant MELA-AU 16 75019090 75019090 single base substitution C T upstream_gene_variant MELA-AU 16 75019337 75019337 single base substitution C T intron_variant MELA-AU 16 75019337 75019337 single base substitution C T upstream_gene_variant MELA-AU 16 75019352 75019352 single base substitution T G intron_variant MELA-AU 16 75019352 75019352 single base substitution T G upstream_gene_variant MELA-AU 16 75019851 75019851 single base substitution C T intron_variant MELA-AU 16 75019851 75019851 single base substitution C T upstream_gene_variant MELA-AU 16 75020144 75020144 single base substitution G A intron_variant MELA-AU 16 75020144 75020144 single base substitution G A upstream_gene_variant MELA-AU 16 75020431 75020431 single base substitution G A intron_variant MELA-AU 16 75020431 75020431 single base substitution G A upstream_gene_variant MELA-AU 16 75020540 75020540 single base substitution G A intron_variant MELA-AU 16 75020540 75020540 single base substitution G A upstream_gene_variant MELA-AU 16 75020634 75020634 single base substitution C T intron_variant MELA-AU 16 75020634 75020634 single base substitution C T upstream_gene_variant MELA-AU 16 75020687 75020687 single base substitution C T intron_variant MELA-AU 16 75020687 75020687 single base substitution C T upstream_gene_variant MELA-AU 16 75020688 75020688 single base substitution C T intron_variant MELA-AU 16 75020688 75020688 single base substitution C T upstream_gene_variant MELA-AU 16 75020725 75020725 single base substitution T C intron_variant MELA-AU 16 75020725 75020725 single base substitution T C upstream_gene_variant MELA-AU 16 75020854 75020854 single base substitution C T intron_variant MELA-AU 16 75020854 75020854 single base substitution C T upstream_gene_variant MELA-AU 16 75020918 75020918 single base substitution G A intron_variant MELA-AU 16 75020918 75020918 single base substitution G A upstream_gene_variant MELA-AU 16 75021043 75021043 single base substitution G A intron_variant MELA-AU 16 75021043 75021043 single base substitution G A upstream_gene_variant MELA-AU 16 75021780 75021780 single base substitution C T intron_variant MELA-AU 16 75021780 75021780 single base substitution C T upstream_gene_variant MELA-AU 16 75021840 75021840 single base substitution C T intron_variant MELA-AU 16 75021840 75021840 single base substitution C T upstream_gene_variant MELA-AU 16 75021844 75021844 single base substitution C T intron_variant MELA-AU 16 75021844 75021844 single base substitution C T upstream_gene_variant MELA-AU 16 75021989 75021989 single base substitution G A intron_variant MELA-AU 16 75021989 75021989 single base substitution G A upstream_gene_variant MELA-AU 16 75022358 75022359 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 75022358 75022359 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 75022838 75022838 single base substitution G A intron_variant MELA-AU 16 75022838 75022838 single base substitution G A upstream_gene_variant MELA-AU 16 75023327 75023327 single base substitution C T intron_variant MELA-AU 16 75023327 75023327 single base substitution C T upstream_gene_variant MELA-AU 16 75023474 75023474 single base substitution G A intron_variant MELA-AU 16 75023474 75023474 single base substitution G A upstream_gene_variant MELA-AU 16 75023562 75023562 single base substitution G A intron_variant MELA-AU 16 75023562 75023562 single base substitution G A upstream_gene_variant MELA-AU 16 75025113 75025113 single base substitution C T intron_variant MELA-AU 16 75025399 75025399 single base substitution G A intron_variant MELA-AU 16 75026912 75026912 single base substitution C T intron_variant MELA-AU 16 75027326 75027326 single base substitution G A intron_variant MELA-AU 16 75027616 75027616 single base substitution C T intron_variant MELA-AU 16 75027773 75027773 single base substitution G A intron_variant MELA-AU 16 75027821 75027821 single base substitution G A intron_variant MELA-AU 16 75027839 75027839 single base substitution G T intron_variant MELA-AU 16 75028000 75028000 single base substitution C T intron_variant MELA-AU 16 75028007 75028007 single base substitution C T intron_variant MELA-AU 16 75028544 75028544 single base substitution C T intron_variant MELA-AU 16 75028685 75028685 single base substitution A G intron_variant MELA-AU 16 75029120 75029120 single base substitution G A intron_variant MELA-AU 16 75029282 75029282 single base substitution T C intron_variant MELA-AU 16 75030134 75030134 single base substitution C T intron_variant MELA-AU 16 75030715 75030715 single base substitution G A intron_variant MELA-AU 16 75030746 75030746 single base substitution C T intron_variant MELA-AU 16 75031187 75031187 single base substitution A C intron_variant MELA-AU 16 75031187 75031187 single base substitution A C upstream_gene_variant MELA-AU 16 75031189 75031189 single base substitution C T intron_variant MELA-AU 16 75031189 75031189 single base substitution C T upstream_gene_variant MELA-AU 16 75031314 75031314 single base substitution G A intron_variant MELA-AU 16 75031314 75031314 single base substitution G A upstream_gene_variant MELA-AU 16 75031410 75031410 single base substitution C A intron_variant MELA-AU 16 75031410 75031410 single base substitution C A upstream_gene_variant MELA-AU 16 75032660 75032660 single base substitution C T intron_variant MELA-AU 16 75032660 75032660 single base substitution C T upstream_gene_variant MELA-AU 16 75033419 75033419 single base substitution C T intron_variant MELA-AU 16 75033419 75033419 single base substitution C T upstream_gene_variant MELA-AU 16 75035204 75035204 single base substitution C T upstream_gene_variant MELA-AU 16 75035495 75035495 single base substitution T C upstream_gene_variant MELA-AU 16 75035852 75035852 single base substitution A C upstream_gene_variant MELA-AU 16 75036095 75036095 single base substitution T A upstream_gene_variant MELA-AU 16 75036122 75036122 single base substitution C T upstream_gene_variant MELA-AU 16 75036814 75036814 single base substitution C T upstream_gene_variant MELA-AU 16 75036819 75036819 single base substitution C T upstream_gene_variant MELA-AU 16 75036982 75036982 single base substitution G C upstream_gene_variant MELA-AU 16 75037246 75037246 single base substitution G A upstream_gene_variant MELA-AU 16 75037391 75037391 single base substitution C T upstream_gene_variant MELA-AU 16 75037811 75037811 single base substitution C T upstream_gene_variant MELA-AU 16 75038944 75038944 single base substitution C T upstream_gene_variant ORCA-IN 16 74912575 74912575 deletion of <=200bp T - intron_variant ORCA-IN 16 74913526 74913526 single base substitution C T intron_variant ORCA-IN 16 74937934 74937934 single base substitution C A 3_prime_UTR_variant ORCA-IN 16 74937934 74937934 single base substitution C A downstream_gene_variant ORCA-IN 16 74937934 74937934 single base substitution C A exon_variant ORCA-IN 16 74937934 74937934 single base substitution C A missense_variant A142S 424G>T ORCA-IN 16 74937934 74937934 single base substitution C A missense_variant A593S 1777G>T ORCA-IN 16 74937934 74937934 single base substitution C A upstream_gene_variant ORCA-IN 16 74937967 74937967 single base substitution C A downstream_gene_variant ORCA-IN 16 74937967 74937967 single base substitution C A exon_variant ORCA-IN 16 74937967 74937967 single base substitution C A missense_variant G131C 391G>T ORCA-IN 16 74937967 74937967 single base substitution C A missense_variant G582C 1744G>T ORCA-IN 16 74937967 74937967 single base substitution C A upstream_gene_variant ORCA-IN 16 74950145 74950145 single base substitution C G exon_variant ORCA-IN 16 74950145 74950145 single base substitution C G missense_variant D327H 979G>C ORCA-IN 16 74950145 74950145 single base substitution C G upstream_gene_variant ORCA-IN 16 74952130 74952130 single base substitution A G intron_variant ORCA-IN 16 74952130 74952130 single base substitution A G upstream_gene_variant ORCA-IN 16 74959440 74959440 single base substitution T A intron_variant ORCA-IN 16 74959440 74959440 single base substitution T A upstream_gene_variant ORCA-IN 16 74961341 74961341 single base substitution C T intron_variant ORCA-IN 16 74966627 74966627 single base substitution T C intron_variant ORCA-IN 16 74966627 74966627 single base substitution T C upstream_gene_variant ORCA-IN 16 74968239 74968239 single base substitution C A downstream_gene_variant ORCA-IN 16 74968239 74968239 single base substitution C A intron_variant ORCA-IN 16 74968239 74968239 single base substitution C A upstream_gene_variant ORCA-IN 16 75004783 75004783 deletion of <=200bp T - intron_variant ORCA-IN 16 75006412 75006412 single base substitution C T intron_variant ORCA-IN 16 75011319 75011319 single base substitution G A intron_variant ORCA-IN 16 75023791 75023791 single base substitution C G intron_variant ORCA-IN 16 75023791 75023791 single base substitution C G upstream_gene_variant ORCA-IN 16 75027116 75027116 single base substitution G A intron_variant OV-AU 16 74906290 74906290 single base substitution G A downstream_gene_variant OV-AU 16 74907616 74907616 single base substitution A T 3_prime_UTR_variant OV-AU 16 74907616 74907616 single base substitution A T downstream_gene_variant OV-AU 16 74936948 74936948 single base substitution C A intron_variant OV-AU 16 74940248 74940248 single base substitution T G downstream_gene_variant OV-AU 16 74940248 74940248 single base substitution T G intron_variant OV-AU 16 74940248 74940248 single base substitution T G upstream_gene_variant OV-AU 16 74941556 74941556 single base substitution T C downstream_gene_variant OV-AU 16 74941556 74941556 single base substitution T C intron_variant OV-AU 16 74941556 74941556 single base substitution T C upstream_gene_variant OV-AU 16 74944011 74944011 single base substitution G A downstream_gene_variant OV-AU 16 74944011 74944011 single base substitution G A intron_variant OV-AU 16 74944011 74944011 single base substitution G A upstream_gene_variant OV-AU 16 74944582 74944582 single base substitution T C downstream_gene_variant OV-AU 16 74944582 74944582 single base substitution T C intron_variant OV-AU 16 74944582 74944582 single base substitution T C upstream_gene_variant OV-AU 16 74950402 74950402 single base substitution G C intron_variant OV-AU 16 74950402 74950402 single base substitution G C upstream_gene_variant OV-AU 16 74956993 74956993 single base substitution A C downstream_gene_variant OV-AU 16 74956993 74956993 single base substitution A C intron_variant OV-AU 16 74956993 74956993 single base substitution A C upstream_gene_variant OV-AU 16 74969722 74969722 single base substitution C T downstream_gene_variant OV-AU 16 74969722 74969722 single base substitution C T intron_variant OV-AU 16 74980351 74980351 single base substitution G A downstream_gene_variant OV-AU 16 74980351 74980351 single base substitution G A intron_variant OV-AU 16 74992597 74992597 single base substitution T C downstream_gene_variant OV-AU 16 74992597 74992597 single base substitution T C intron_variant OV-AU 16 74994779 74994779 single base substitution C G downstream_gene_variant OV-AU 16 74994779 74994779 single base substitution C G intron_variant OV-AU 16 74997652 74997652 single base substitution A T intron_variant OV-AU 16 74999678 74999678 single base substitution G T exon_variant OV-AU 16 74999678 74999678 single base substitution G T missense_variant L12I 34C>A OV-AU 16 74999678 74999678 single base substitution G T missense_variant L33I 97C>A OV-AU 16 75005721 75005721 single base substitution C T intron_variant OV-AU 16 75017668 75017668 single base substitution G A intron_variant OV-AU 16 75017668 75017668 single base substitution G A upstream_gene_variant OV-AU 16 75017907 75017907 single base substitution G A intron_variant OV-AU 16 75017907 75017907 single base substitution G A upstream_gene_variant OV-AU 16 75020942 75020942 single base substitution C A intron_variant OV-AU 16 75020942 75020942 single base substitution C A upstream_gene_variant OV-AU 16 75023424 75023424 single base substitution A G intron_variant OV-AU 16 75023424 75023424 single base substitution A G upstream_gene_variant OV-AU 16 75028353 75028353 single base substitution T C intron_variant OV-AU 16 75030948 75030948 single base substitution G C exon_variant OV-AU 16 75030948 75030948 single base substitution G C intron_variant OV-AU 16 75036516 75036516 single base substitution G A upstream_gene_variant PACA-AU 16 74906910 74906910 single base substitution C A downstream_gene_variant PACA-AU 16 74907213 74907213 single base substitution G A downstream_gene_variant PACA-AU 16 74910311 74910311 single base substitution A G intron_variant PACA-AU 16 74911248 74911248 single base substitution C T intron_variant PACA-AU 16 74914276 74914276 single base substitution C T intron_variant PACA-AU 16 74922354 74922354 single base substitution A G downstream_gene_variant PACA-AU 16 74922354 74922354 single base substitution A G intron_variant PACA-AU 16 74922354 74922354 single base substitution A G upstream_gene_variant PACA-AU 16 74923356 74923356 single base substitution C G downstream_gene_variant PACA-AU 16 74923356 74923356 single base substitution C G intron_variant PACA-AU 16 74923356 74923356 single base substitution C G upstream_gene_variant PACA-AU 16 74931147 74931147 single base substitution C G intron_variant PACA-AU 16 74931147 74931147 single base substitution C G upstream_gene_variant PACA-AU 16 74932521 74932521 single base substitution G A intron_variant PACA-AU 16 74932521 74932521 single base substitution G A upstream_gene_variant PACA-AU 16 74937890 74937890 single base substitution G A 3_prime_UTR_variant PACA-AU 16 74937890 74937890 single base substitution G A downstream_gene_variant PACA-AU 16 74937890 74937890 single base substitution G A exon_variant PACA-AU 16 74937890 74937890 single base substitution G A synonymous_variant S156S 468C>T PACA-AU 16 74937890 74937890 single base substitution G A synonymous_variant S607S 1821C>T PACA-AU 16 74937890 74937890 single base substitution G A synonymous_variant S9S 27C>T PACA-AU 16 74940505 74940505 single base substitution G C downstream_gene_variant PACA-AU 16 74940505 74940505 single base substitution G C intron_variant PACA-AU 16 74940505 74940505 single base substitution G C upstream_gene_variant PACA-AU 16 74943469 74943469 single base substitution C T downstream_gene_variant PACA-AU 16 74943469 74943469 single base substitution C T exon_variant PACA-AU 16 74943469 74943469 single base substitution C T synonymous_variant T524T 1572G>A PACA-AU 16 74943469 74943469 single base substitution C T synonymous_variant T73T 219G>A PACA-AU 16 74950338 74950338 single base substitution T A intron_variant PACA-AU 16 74950338 74950338 single base substitution T A upstream_gene_variant PACA-AU 16 74952396 74952396 single base substitution T C intron_variant PACA-AU 16 74952396 74952396 single base substitution T C upstream_gene_variant PACA-AU 16 74954983 74954983 single base substitution T A downstream_gene_variant PACA-AU 16 74954983 74954983 single base substitution T A intron_variant PACA-AU 16 74954983 74954983 single base substitution T A upstream_gene_variant PACA-AU 16 74981715 74981715 single base substitution T A downstream_gene_variant PACA-AU 16 74981715 74981715 single base substitution T A intron_variant PACA-AU 16 74988035 74988035 single base substitution G A downstream_gene_variant PACA-AU 16 74988035 74988035 single base substitution G A intron_variant PACA-AU 16 74988390 74988390 single base substitution C T downstream_gene_variant PACA-AU 16 74988390 74988390 single base substitution C T intron_variant PACA-AU 16 74991908 74991908 single base substitution G A downstream_gene_variant PACA-AU 16 74991908 74991908 single base substitution G A intron_variant PACA-AU 16 74994452 74994452 single base substitution G T downstream_gene_variant PACA-AU 16 74994452 74994452 single base substitution G T intron_variant PACA-AU 16 74994935 74994960 deletion of <=200bp GCTCACGTCTATAATCCCAGCATTTT - downstream_gene_variant PACA-AU 16 74994935 74994960 deletion of <=200bp GCTCACGTCTATAATCCCAGCATTTT - intron_variant PACA-AU 16 74996330 74996330 single base substitution C T downstream_gene_variant PACA-AU 16 74996330 74996330 single base substitution C T intron_variant PACA-AU 16 75002785 75002785 single base substitution G A intron_variant PACA-AU 16 75002785 75002785 single base substitution G A upstream_gene_variant PACA-AU 16 75008711 75008711 single base substitution T C intron_variant PACA-AU 16 75015146 75015146 single base substitution C T intron_variant PACA-AU 16 75015146 75015146 single base substitution C T upstream_gene_variant PACA-AU 16 75016396 75016396 single base substitution G T intron_variant PACA-AU 16 75016396 75016396 single base substitution G T upstream_gene_variant PACA-AU 16 75020856 75020856 single base substitution C A intron_variant PACA-AU 16 75020856 75020856 single base substitution C A upstream_gene_variant PACA-AU 16 75021697 75021697 single base substitution T A intron_variant PACA-AU 16 75021697 75021697 single base substitution T A upstream_gene_variant PACA-AU 16 75024709 75024709 single base substitution G A intron_variant PACA-AU 16 75024711 75024711 single base substitution G A intron_variant PACA-AU 16 75025552 75025552 single base substitution T C intron_variant PACA-AU 16 75028149 75028149 single base substitution T A intron_variant PACA-AU 16 75032885 75032885 single base substitution A G intron_variant PACA-AU 16 75032885 75032885 single base substitution A G upstream_gene_variant PACA-AU 16 75035173 75035173 single base substitution C T upstream_gene_variant PACA-AU 16 75036484 75036484 single base substitution C G upstream_gene_variant PACA-AU 16 75037584 75037584 single base substitution C T upstream_gene_variant PACA-CA 16 74905274 74905274 single base substitution T A downstream_gene_variant PACA-CA 16 74905494 74905494 single base substitution C A downstream_gene_variant PACA-CA 16 74905734 74905734 single base substitution C A downstream_gene_variant PACA-CA 16 74907181 74907181 single base substitution T G downstream_gene_variant PACA-CA 16 74912362 74912362 single base substitution G A intron_variant PACA-CA 16 74912363 74912363 single base substitution C T intron_variant PACA-CA 16 74923979 74923979 single base substitution A C downstream_gene_variant PACA-CA 16 74923979 74923979 single base substitution A C intron_variant PACA-CA 16 74923979 74923979 single base substitution A C upstream_gene_variant PACA-CA 16 74925454 74925454 single base substitution A G downstream_gene_variant PACA-CA 16 74925454 74925454 single base substitution A G intron_variant PACA-CA 16 74925464 74925464 single base substitution T A downstream_gene_variant PACA-CA 16 74925464 74925464 single base substitution T A intron_variant PACA-CA 16 74925485 74925485 single base substitution C G downstream_gene_variant PACA-CA 16 74925485 74925485 single base substitution C G intron_variant PACA-CA 16 74927657 74927657 single base substitution C A 3_prime_UTR_variant PACA-CA 16 74927657 74927657 single base substitution C A exon_variant PACA-CA 16 74927657 74927657 single base substitution C A missense_variant Q208H 624G>T PACA-CA 16 74927657 74927657 single base substitution C A missense_variant Q42H 126G>T PACA-CA 16 74927657 74927657 single base substitution C A missense_variant Q640H 1920G>T PACA-CA 16 74930636 74930636 single base substitution A T intron_variant PACA-CA 16 74930636 74930636 single base substitution A T upstream_gene_variant PACA-CA 16 74934612 74934612 single base substitution G T intron_variant PACA-CA 16 74935009 74935009 deletion of <=200bp A - intron_variant PACA-CA 16 74935155 74935155 insertion of <=200bp - A intron_variant PACA-CA 16 74935964 74935964 single base substitution G T intron_variant PACA-CA 16 74936171 74936171 single base substitution G A intron_variant PACA-CA 16 74938452 74938452 single base substitution G A downstream_gene_variant PACA-CA 16 74938452 74938452 single base substitution G A intron_variant PACA-CA 16 74938452 74938452 single base substitution G A upstream_gene_variant PACA-CA 16 74940612 74940612 single base substitution T C downstream_gene_variant PACA-CA 16 74940612 74940612 single base substitution T C intron_variant PACA-CA 16 74940612 74940612 single base substitution T C upstream_gene_variant PACA-CA 16 74942014 74942014 single base substitution G A downstream_gene_variant PACA-CA 16 74942014 74942014 single base substitution G A intron_variant PACA-CA 16 74942014 74942014 single base substitution G A upstream_gene_variant PACA-CA 16 74942865 74942865 single base substitution T C downstream_gene_variant PACA-CA 16 74942865 74942865 single base substitution T C exon_variant PACA-CA 16 74942865 74942865 single base substitution T C intron_variant PACA-CA 16 74942865 74942865 single base substitution T C synonymous_variant V100V 300A>G PACA-CA 16 74942865 74942865 single base substitution T C synonymous_variant V551V 1653A>G PACA-CA 16 74942865 74942865 single base substitution T C upstream_gene_variant PACA-CA 16 74945531 74945531 single base substitution G A downstream_gene_variant PACA-CA 16 74945531 74945531 single base substitution G A intron_variant PACA-CA 16 74945531 74945531 single base substitution G A upstream_gene_variant PACA-CA 16 74947606 74947606 single base substitution A G downstream_gene_variant PACA-CA 16 74947606 74947606 single base substitution A G intron_variant PACA-CA 16 74947606 74947606 single base substitution A G upstream_gene_variant PACA-CA 16 74949786 74949786 single base substitution G C exon_variant PACA-CA 16 74949786 74949786 single base substitution G C missense_variant I402M 1206C>G PACA-CA 16 74949786 74949786 single base substitution G C upstream_gene_variant PACA-CA 16 74956464 74956464 insertion of <=200bp - C downstream_gene_variant PACA-CA 16 74956464 74956464 insertion of <=200bp - C intron_variant PACA-CA 16 74956464 74956464 insertion of <=200bp - C upstream_gene_variant PACA-CA 16 74958739 74958739 single base substitution G A intron_variant PACA-CA 16 74958739 74958739 single base substitution G A upstream_gene_variant PACA-CA 16 74965976 74965976 single base substitution C T intron_variant PACA-CA 16 74965976 74965976 single base substitution C T upstream_gene_variant PACA-CA 16 74969894 74969894 single base substitution C A downstream_gene_variant PACA-CA 16 74969894 74969894 single base substitution C A intron_variant PACA-CA 16 74970061 74970061 single base substitution T G downstream_gene_variant PACA-CA 16 74970061 74970061 single base substitution T G intron_variant PACA-CA 16 74972883 74972883 single base substitution G C downstream_gene_variant PACA-CA 16 74972883 74972883 single base substitution G C intron_variant PACA-CA 16 74973591 74973591 single base substitution G C downstream_gene_variant PACA-CA 16 74973591 74973591 single base substitution G C intron_variant PACA-CA 16 74975318 74975318 single base substitution G A downstream_gene_variant PACA-CA 16 74975318 74975318 single base substitution G A intron_variant PACA-CA 16 74976610 74976610 single base substitution T G downstream_gene_variant PACA-CA 16 74976610 74976610 single base substitution T G intron_variant PACA-CA 16 74977586 74977586 single base substitution A G intron_variant PACA-CA 16 74978409 74978409 single base substitution G A intron_variant PACA-CA 16 74979876 74979876 single base substitution C T downstream_gene_variant PACA-CA 16 74979876 74979876 single base substitution C T intron_variant PACA-CA 16 74981290 74981290 insertion of <=200bp - A downstream_gene_variant PACA-CA 16 74981290 74981290 insertion of <=200bp - A intron_variant PACA-CA 16 74982558 74982558 single base substitution A G downstream_gene_variant PACA-CA 16 74982558 74982558 single base substitution A G intron_variant PACA-CA 16 74987694 74987694 single base substitution T C downstream_gene_variant PACA-CA 16 74987694 74987694 single base substitution T C intron_variant PACA-CA 16 74990741 74990741 single base substitution C T intron_variant PACA-CA 16 74991909 74991909 single base substitution C T downstream_gene_variant PACA-CA 16 74991909 74991909 single base substitution C T intron_variant PACA-CA 16 75002693 75002693 insertion of <=200bp - A intron_variant PACA-CA 16 75002693 75002693 insertion of <=200bp - A upstream_gene_variant PACA-CA 16 75004291 75004291 single base substitution A C intron_variant PACA-CA 16 75004291 75004291 single base substitution A C upstream_gene_variant PACA-CA 16 75005236 75005236 deletion of <=200bp A - intron_variant PACA-CA 16 75008462 75008462 single base substitution G A intron_variant PACA-CA 16 75010040 75010040 single base substitution G A intron_variant PACA-CA 16 75021617 75021617 single base substitution G A intron_variant PACA-CA 16 75021617 75021617 single base substitution G A upstream_gene_variant PACA-CA 16 75022614 75022614 single base substitution C T intron_variant PACA-CA 16 75022614 75022614 single base substitution C T upstream_gene_variant PACA-CA 16 75025295 75025295 single base substitution A T intron_variant PACA-CA 16 75026190 75026190 single base substitution C A intron_variant PACA-CA 16 75026234 75026234 single base substitution G T intron_variant PACA-CA 16 75031452 75031452 single base substitution G A intron_variant PACA-CA 16 75031452 75031452 single base substitution G A upstream_gene_variant PACA-CA 16 75032234 75032234 single base substitution C A intron_variant PACA-CA 16 75032234 75032234 single base substitution C A upstream_gene_variant PACA-CA 16 75032974 75032974 single base substitution G T intron_variant PACA-CA 16 75032974 75032974 single base substitution G T upstream_gene_variant PACA-CA 16 75035208 75035208 single base substitution T C upstream_gene_variant PACA-CA 16 75036042 75036042 single base substitution G T upstream_gene_variant PACA-CA 16 75037034 75037034 insertion of <=200bp - T upstream_gene_variant PAEN-AU 16 74904485 74904485 single base substitution C T downstream_gene_variant PAEN-AU 16 74930845 74930845 single base substitution T C intron_variant PAEN-AU 16 74930845 74930845 single base substitution T C upstream_gene_variant PAEN-AU 16 74981937 74981937 single base substitution C T downstream_gene_variant PAEN-AU 16 74981937 74981937 single base substitution C T intron_variant PAEN-AU 16 74991454 74991454 single base substitution G T intron_variant PAEN-IT 16 74914300 74914300 single base substitution G A intron_variant PAEN-IT 16 74941103 74941103 single base substitution T C downstream_gene_variant PAEN-IT 16 74941103 74941103 single base substitution T C intron_variant PAEN-IT 16 74941103 74941103 single base substitution T C upstream_gene_variant PAEN-IT 16 74950927 74950927 single base substitution T C intron_variant PAEN-IT 16 74950927 74950927 single base substitution T C upstream_gene_variant PAEN-IT 16 75014959 75014959 single base substitution C T intron_variant PAEN-IT 16 75014959 75014959 single base substitution C T upstream_gene_variant PBCA-DE 16 74908791 74908791 insertion of <=200bp - T intron_variant PBCA-DE 16 74920409 74920409 single base substitution G A downstream_gene_variant PBCA-DE 16 74920409 74920409 single base substitution G A intron_variant PBCA-DE 16 74920409 74920409 single base substitution G A upstream_gene_variant PBCA-DE 16 74933587 74933587 single base substitution G A intron_variant PBCA-DE 16 74947364 74947364 insertion of <=200bp - A downstream_gene_variant PBCA-DE 16 74947364 74947364 insertion of <=200bp - A intron_variant PBCA-DE 16 74947364 74947364 insertion of <=200bp - A upstream_gene_variant PBCA-DE 16 74960783 74960783 single base substitution A G intron_variant PBCA-DE 16 74960783 74960783 single base substitution A G upstream_gene_variant PBCA-DE 16 74961524 74961524 single base substitution T A intron_variant PBCA-DE 16 74962323 74962323 single base substitution C T intron_variant PBCA-DE 16 74969579 74969579 single base substitution C T downstream_gene_variant PBCA-DE 16 74969579 74969579 single base substitution C T intron_variant PBCA-DE 16 74969579 74969579 single base substitution C T upstream_gene_variant PBCA-DE 16 74974819 74974819 single base substitution G T downstream_gene_variant PBCA-DE 16 74974819 74974819 single base substitution G T intron_variant PBCA-DE 16 74979756 74979756 single base substitution G T downstream_gene_variant PBCA-DE 16 74979756 74979756 single base substitution G T intron_variant PBCA-DE 16 74986666 74986667 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 16 74986666 74986667 deletion of <=200bp TA - intron_variant PBCA-DE 16 74989781 74989781 single base substitution G T downstream_gene_variant PBCA-DE 16 74989781 74989781 single base substitution G T intron_variant PBCA-DE 16 74990379 74990379 single base substitution C T downstream_gene_variant PBCA-DE 16 74990379 74990379 single base substitution C T exon_variant PBCA-DE 16 74990379 74990379 single base substitution C T synonymous_variant A57A 171G>A PBCA-DE 16 74990379 74990379 single base substitution C T synonymous_variant A78A 234G>A PBCA-DE 16 74995048 74995048 insertion of <=200bp - TAT downstream_gene_variant PBCA-DE 16 74995048 74995048 insertion of <=200bp - TAT intron_variant PBCA-DE 16 74995053 74995053 deletion of <=200bp C - downstream_gene_variant PBCA-DE 16 74995053 74995053 deletion of <=200bp C - intron_variant PBCA-DE 16 75004946 75004946 deletion of <=200bp A - intron_variant PBCA-DE 16 75011431 75011431 insertion of <=200bp - A intron_variant PBCA-DE 16 75014708 75014708 insertion of <=200bp - A intron_variant PBCA-DE 16 75014708 75014708 insertion of <=200bp - A upstream_gene_variant PBCA-DE 16 75019991 75019991 single base substitution C T intron_variant PBCA-DE 16 75019991 75019991 single base substitution C T upstream_gene_variant PBCA-DE 16 75024711 75024711 single base substitution G A intron_variant PBCA-DE 16 75028812 75028812 insertion of <=200bp - A intron_variant PRAD-CA 16 74914301 74914301 single base substitution C T intron_variant PRAD-CA 16 74914590 74914590 single base substitution T G intron_variant PRAD-CA 16 74915786 74915786 single base substitution G A intron_variant PRAD-CA 16 74926671 74926671 single base substitution G T downstream_gene_variant PRAD-CA 16 74926671 74926671 single base substitution G T intron_variant PRAD-CA 16 74929301 74929301 single base substitution C T intron_variant PRAD-CA 16 74929301 74929301 single base substitution C T upstream_gene_variant PRAD-CA 16 74937197 74937197 single base substitution G A intron_variant PRAD-CA 16 74947064 74947064 single base substitution C A downstream_gene_variant PRAD-CA 16 74947064 74947064 single base substitution C A intron_variant PRAD-CA 16 74947064 74947064 single base substitution C A upstream_gene_variant PRAD-CA 16 74961370 74961370 single base substitution C T intron_variant PRAD-CA 16 74965120 74965120 single base substitution T G intron_variant PRAD-CA 16 74965120 74965120 single base substitution T G upstream_gene_variant PRAD-CA 16 75020347 75020347 single base substitution G A intron_variant PRAD-CA 16 75020347 75020347 single base substitution G A upstream_gene_variant PRAD-UK 16 74910637 74910637 insertion of <=200bp - GCCC intron_variant PRAD-UK 16 74954850 74954850 single base substitution C T downstream_gene_variant PRAD-UK 16 74954850 74954850 single base substitution C T intron_variant PRAD-UK 16 74954850 74954850 single base substitution C T upstream_gene_variant PRAD-UK 16 74960266 74960266 single base substitution C A intron_variant PRAD-UK 16 74960266 74960266 single base substitution C A upstream_gene_variant PRAD-UK 16 74974901 74974901 single base substitution C T downstream_gene_variant PRAD-UK 16 74974901 74974901 single base substitution C T intron_variant PRAD-UK 16 74976688 74976688 single base substitution G T exon_variant PRAD-UK 16 74976688 74976688 single base substitution G T intron_variant PRAD-UK 16 74976688 74976688 single base substitution G T missense_variant A140D 419C>A PRAD-UK 16 74976688 74976688 single base substitution G T missense_variant A161D 482C>A PRAD-UK 16 75006757 75006757 single base substitution C G intron_variant PRAD-UK 16 75018183 75018183 insertion of <=200bp - A intron_variant PRAD-UK 16 75035128 75035128 single base substitution T C upstream_gene_variant PRAD-UK 16 75035949 75035949 single base substitution C T upstream_gene_variant PRAD-US 16 74955991 74955991 single base substitution T C downstream_gene_variant PRAD-US 16 74955991 74955991 single base substitution T C exon_variant PRAD-US 16 74955991 74955991 single base substitution T C missense_variant N247S 740A>G PRAD-US 16 74955991 74955991 single base substitution T C upstream_gene_variant READ-US 16 74908248 74908248 single base substitution G A downstream_gene_variant READ-US 16 74908248 74908248 single base substitution G A exon_variant READ-US 16 74908248 74908248 single base substitution G A synonymous_variant H928H 2784C>T READ-US 16 74949816 74949816 single base substitution C T exon_variant READ-US 16 74949816 74949816 single base substitution C T synonymous_variant Q392Q 1176G>A READ-US 16 74949816 74949816 single base substitution C T upstream_gene_variant RECA-EU 16 74903074 74903074 single base substitution T C downstream_gene_variant RECA-EU 16 74903857 74903857 single base substitution C T downstream_gene_variant RECA-EU 16 74909402 74909402 single base substitution C T intron_variant RECA-EU 16 74910704 74910704 single base substitution T C intron_variant RECA-EU 16 74920247 74920247 single base substitution G C downstream_gene_variant RECA-EU 16 74920247 74920247 single base substitution G C exon_variant RECA-EU 16 74920247 74920247 single base substitution G C missense_variant P137A 409C>G RECA-EU 16 74920247 74920247 single base substitution G C missense_variant P823A 2467C>G RECA-EU 16 74920247 74920247 single base substitution G C upstream_gene_variant RECA-EU 16 74928720 74928720 single base substitution T A intron_variant RECA-EU 16 74928720 74928720 single base substitution T A upstream_gene_variant RECA-EU 16 74937520 74937520 single base substitution G A intron_variant RECA-EU 16 74945048 74945048 single base substitution C A downstream_gene_variant RECA-EU 16 74945048 74945048 single base substitution C A intron_variant RECA-EU 16 74945048 74945048 single base substitution C A upstream_gene_variant RECA-EU 16 74947664 74947664 single base substitution C T downstream_gene_variant RECA-EU 16 74947664 74947664 single base substitution C T intron_variant RECA-EU 16 74947664 74947664 single base substitution C T upstream_gene_variant RECA-EU 16 74950756 74950756 single base substitution C A intron_variant RECA-EU 16 74950756 74950756 single base substitution C A upstream_gene_variant RECA-EU 16 74955235 74955235 single base substitution A T downstream_gene_variant RECA-EU 16 74955235 74955235 single base substitution A T intron_variant RECA-EU 16 74968363 74968363 single base substitution G A downstream_gene_variant RECA-EU 16 74968363 74968363 single base substitution G A intron_variant RECA-EU 16 74968363 74968363 single base substitution G A upstream_gene_variant RECA-EU 16 74972030 74972030 single base substitution C T downstream_gene_variant RECA-EU 16 74972030 74972030 single base substitution C T intron_variant RECA-EU 16 74980614 74980614 single base substitution C G downstream_gene_variant RECA-EU 16 74980614 74980614 single base substitution C G intron_variant RECA-EU 16 74980943 74980943 single base substitution A T downstream_gene_variant RECA-EU 16 74980943 74980943 single base substitution A T intron_variant RECA-EU 16 74981188 74981188 single base substitution A C downstream_gene_variant RECA-EU 16 74981188 74981188 single base substitution A C intron_variant RECA-EU 16 74982085 74982085 single base substitution C A downstream_gene_variant RECA-EU 16 74982085 74982085 single base substitution C A intron_variant RECA-EU 16 75009692 75009692 single base substitution G C intron_variant RECA-EU 16 75011810 75011810 single base substitution T C intron_variant RECA-EU 16 75012000 75012000 single base substitution T A intron_variant RECA-EU 16 75019183 75019183 single base substitution G A intron_variant RECA-EU 16 75019183 75019183 single base substitution G A upstream_gene_variant RECA-EU 16 75031115 75031115 single base substitution G C intron_variant RECA-EU 16 75031115 75031115 single base substitution G C upstream_gene_variant RECA-EU 16 75031116 75031116 single base substitution T A intron_variant RECA-EU 16 75031116 75031116 single base substitution T A upstream_gene_variant RECA-EU 16 75031877 75031877 single base substitution T C intron_variant RECA-EU 16 75031877 75031877 single base substitution T C upstream_gene_variant RECA-EU 16 75034794 75034794 single base substitution C T upstream_gene_variant SKCA-BR 16 74904927 74904927 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 16 74906464 74906464 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 16 74911440 74911440 single base substitution G A intron_variant SKCA-BR 16 74911502 74911502 single base substitution G A intron_variant SKCA-BR 16 74919547 74919547 single base substitution T C downstream_gene_variant SKCA-BR 16 74919547 74919547 single base substitution T C intron_variant SKCA-BR 16 74919547 74919547 single base substitution T C splice_region_variant SKCA-BR 16 74922108 74922108 single base substitution G A downstream_gene_variant SKCA-BR 16 74922108 74922108 single base substitution G A intron_variant SKCA-BR 16 74922108 74922108 single base substitution G A missense_variant P769S 2305C>T SKCA-BR 16 74922108 74922108 single base substitution G A upstream_gene_variant SKCA-BR 16 74923062 74923062 single base substitution G A downstream_gene_variant SKCA-BR 16 74923062 74923062 single base substitution G A intron_variant SKCA-BR 16 74923062 74923062 single base substitution G A upstream_gene_variant SKCA-BR 16 74928035 74928035 single base substitution G A intron_variant SKCA-BR 16 74928035 74928035 single base substitution G A upstream_gene_variant SKCA-BR 16 74932258 74932258 single base substitution G T intron_variant SKCA-BR 16 74932258 74932258 single base substitution G T upstream_gene_variant SKCA-BR 16 74932663 74932663 single base substitution G A intron_variant SKCA-BR 16 74932663 74932663 single base substitution G A upstream_gene_variant SKCA-BR 16 74936364 74936364 single base substitution G A intron_variant SKCA-BR 16 74940744 74940744 single base substitution G A downstream_gene_variant SKCA-BR 16 74940744 74940744 single base substitution G A intron_variant SKCA-BR 16 74940744 74940744 single base substitution G A upstream_gene_variant SKCA-BR 16 74940951 74940951 single base substitution G A downstream_gene_variant SKCA-BR 16 74940951 74940951 single base substitution G A intron_variant SKCA-BR 16 74940951 74940951 single base substitution G A upstream_gene_variant SKCA-BR 16 74944734 74944734 single base substitution G A downstream_gene_variant SKCA-BR 16 74944734 74944734 single base substitution G A intron_variant SKCA-BR 16 74944734 74944734 single base substitution G A upstream_gene_variant SKCA-BR 16 74948491 74948492 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 16 74948491 74948492 deletion of <=200bp TA - intron_variant SKCA-BR 16 74948491 74948492 deletion of <=200bp TA - upstream_gene_variant SKCA-BR 16 74950771 74950771 single base substitution G A intron_variant SKCA-BR 16 74950771 74950771 single base substitution G A upstream_gene_variant SKCA-BR 16 74951733 74951733 single base substitution G A intron_variant SKCA-BR 16 74951733 74951733 single base substitution G A upstream_gene_variant SKCA-BR 16 74953966 74953968 deletion of <=200bp CAA - downstream_gene_variant SKCA-BR 16 74953966 74953968 deletion of <=200bp CAA - intron_variant SKCA-BR 16 74953966 74953968 deletion of <=200bp CAA - upstream_gene_variant SKCA-BR 16 74954024 74954024 single base substitution C A downstream_gene_variant SKCA-BR 16 74954024 74954024 single base substitution C A intron_variant SKCA-BR 16 74954024 74954024 single base substitution C A upstream_gene_variant SKCA-BR 16 74961579 74961579 insertion of <=200bp - AACAC intron_variant SKCA-BR 16 74961579 74961579 insertion of <=200bp - AAC intron_variant SKCA-BR 16 74961806 74961806 single base substitution C T intron_variant SKCA-BR 16 74963506 74963506 single base substitution G A intron_variant SKCA-BR 16 74965864 74965864 single base substitution C T intron_variant SKCA-BR 16 74965864 74965864 single base substitution C T upstream_gene_variant SKCA-BR 16 74981171 74981171 single base substitution A C downstream_gene_variant SKCA-BR 16 74981171 74981171 single base substitution A C intron_variant SKCA-BR 16 74981184 74981184 single base substitution T A downstream_gene_variant SKCA-BR 16 74981184 74981184 single base substitution T A intron_variant SKCA-BR 16 74981386 74981386 single base substitution A T downstream_gene_variant SKCA-BR 16 74981386 74981386 single base substitution A T intron_variant SKCA-BR 16 74983872 74983872 single base substitution G A intron_variant SKCA-BR 16 74986382 74986382 single base substitution G A downstream_gene_variant SKCA-BR 16 74986382 74986382 single base substitution G A intron_variant SKCA-BR 16 74986563 74986563 single base substitution G A downstream_gene_variant SKCA-BR 16 74986563 74986563 single base substitution G A intron_variant SKCA-BR 16 74990712 74990712 single base substitution G A intron_variant SKCA-BR 16 74992474 74992474 single base substitution G T downstream_gene_variant SKCA-BR 16 74992474 74992474 single base substitution G T intron_variant SKCA-BR 16 74993765 74993765 single base substitution A G downstream_gene_variant SKCA-BR 16 74993765 74993765 single base substitution A G intron_variant SKCA-BR 16 74998265 74998265 single base substitution G A intron_variant SKCA-BR 16 75001755 75001757 deletion of <=200bp CAA - intron_variant SKCA-BR 16 75001755 75001757 deletion of <=200bp CAA - upstream_gene_variant SKCA-BR 16 75002079 75002079 single base substitution G A intron_variant SKCA-BR 16 75002079 75002079 single base substitution G A upstream_gene_variant SKCA-BR 16 75002440 75002440 single base substitution G A intron_variant SKCA-BR 16 75002440 75002440 single base substitution G A upstream_gene_variant SKCA-BR 16 75002694 75002694 single base substitution A T intron_variant SKCA-BR 16 75002694 75002694 single base substitution A T upstream_gene_variant SKCA-BR 16 75004926 75004926 single base substitution G A intron_variant SKCA-BR 16 75005521 75005521 single base substitution G C intron_variant SKCA-BR 16 75006020 75006020 single base substitution C T intron_variant SKCA-BR 16 75006719 75006720 deletion of <=200bp TA - intron_variant SKCA-BR 16 75006719 75006726 deletion of <=200bp TAAAAAAA - intron_variant SKCA-BR 16 75011699 75011699 single base substitution G A intron_variant SKCA-BR 16 75012288 75012288 single base substitution G C intron_variant SKCA-BR 16 75013396 75013396 insertion of <=200bp - CA intron_variant SKCA-BR 16 75013396 75013396 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 16 75013612 75013612 single base substitution T C intron_variant SKCA-BR 16 75013612 75013612 single base substitution T C upstream_gene_variant SKCA-BR 16 75018102 75018102 single base substitution G A intron_variant SKCA-BR 16 75018954 75018954 single base substitution T C 5_prime_UTR_variant SKCA-BR 16 75018954 75018954 single base substitution T C intron_variant SKCA-BR 16 75018954 75018954 single base substitution T C upstream_gene_variant SKCA-BR 16 75018958 75018958 single base substitution A C 5_prime_UTR_variant SKCA-BR 16 75018958 75018958 single base substitution A C intron_variant SKCA-BR 16 75018958 75018958 single base substitution A C upstream_gene_variant SKCA-BR 16 75019069 75019069 single base substitution G A intron_variant SKCA-BR 16 75019069 75019069 single base substitution G A upstream_gene_variant SKCA-BR 16 75020961 75020961 insertion of <=200bp - CG intron_variant SKCA-BR 16 75020961 75020961 insertion of <=200bp - CG upstream_gene_variant SKCA-BR 16 75021160 75021160 insertion of <=200bp - AT intron_variant SKCA-BR 16 75021160 75021160 insertion of <=200bp - AT upstream_gene_variant SKCA-BR 16 75023328 75023328 single base substitution C T intron_variant SKCA-BR 16 75023328 75023328 single base substitution C T upstream_gene_variant SKCA-BR 16 75027652 75027652 single base substitution C T intron_variant SKCA-BR 16 75027691 75027691 single base substitution G A intron_variant SKCA-BR 16 75028742 75028742 single base substitution T G intron_variant SKCA-BR 16 75032879 75032879 single base substitution A G intron_variant SKCA-BR 16 75032879 75032879 single base substitution A G upstream_gene_variant SKCA-BR 16 75032885 75032885 single base substitution A G intron_variant SKCA-BR 16 75032885 75032885 single base substitution A G upstream_gene_variant SKCA-BR 16 75033134 75033134 single base substitution A G intron_variant SKCA-BR 16 75033134 75033134 single base substitution A G upstream_gene_variant SKCA-BR 16 75033786 75033786 single base substitution A C intron_variant SKCA-BR 16 75033786 75033786 single base substitution A C upstream_gene_variant SKCA-BR 16 75036422 75036422 single base substitution T G upstream_gene_variant SKCA-BR 16 75037582 75037582 single base substitution T C upstream_gene_variant SKCA-BR 16 75038966 75038966 single base substitution C T upstream_gene_variant SKCM-US 16 74908169 74908169 single base substitution G A downstream_gene_variant SKCM-US 16 74908169 74908169 single base substitution G A exon_variant SKCM-US 16 74908169 74908169 single base substitution G A missense_variant R955W 2863C>T SKCM-US 16 74919580 74919580 single base substitution G A downstream_gene_variant SKCM-US 16 74919580 74919580 single base substitution G A exon_variant SKCM-US 16 74919580 74919580 single base substitution G A missense_variant S201F 602C>T SKCM-US 16 74919580 74919580 single base substitution G A missense_variant S887F 2660C>T SKCM-US 16 74922108 74922108 single base substitution G A downstream_gene_variant SKCM-US 16 74922108 74922108 single base substitution G A intron_variant SKCM-US 16 74922108 74922108 single base substitution G A missense_variant P769S 2305C>T SKCM-US 16 74922108 74922108 single base substitution G A upstream_gene_variant SKCM-US 16 74922121 74922121 single base substitution G A downstream_gene_variant SKCM-US 16 74922121 74922121 single base substitution G A exon_variant SKCM-US 16 74922121 74922121 single base substitution G A intron_variant SKCM-US 16 74922121 74922121 single base substitution G A synonymous_variant P764P 2292C>T SKCM-US 16 74922121 74922121 single base substitution G A upstream_gene_variant SKCM-US 16 74923603 74923603 single base substitution G A downstream_gene_variant SKCM-US 16 74923603 74923603 single base substitution G A exon_variant SKCM-US 16 74923603 74923603 single base substitution G A intron_variant SKCM-US 16 74923603 74923603 single base substitution G A splice_region_variant SKCM-US 16 74923603 74923603 single base substitution G A synonymous_variant S299S 897C>T SKCM-US 16 74923603 74923603 single base substitution G A upstream_gene_variant SKCM-US 16 74923628 74923628 single base substitution G A 3_prime_UTR_variant SKCM-US 16 74923628 74923628 single base substitution G A downstream_gene_variant SKCM-US 16 74923628 74923628 single base substitution G A exon_variant SKCM-US 16 74923628 74923628 single base substitution G A intron_variant SKCM-US 16 74923628 74923628 single base substitution G A missense_variant P291L 872C>T SKCM-US 16 74923628 74923628 single base substitution G A missense_variant P723L 2168C>T SKCM-US 16 74923628 74923628 single base substitution G A upstream_gene_variant SKCM-US 16 74923643 74923643 single base substitution G A 3_prime_UTR_variant SKCM-US 16 74923643 74923643 single base substitution G A downstream_gene_variant SKCM-US 16 74923643 74923643 single base substitution G A exon_variant SKCM-US 16 74923643 74923643 single base substitution G A intron_variant SKCM-US 16 74923643 74923643 single base substitution G A missense_variant P286L 857C>T SKCM-US 16 74923643 74923643 single base substitution G A missense_variant P718L 2153C>T SKCM-US 16 74923643 74923643 single base substitution G A upstream_gene_variant SKCM-US 16 74927577 74927577 single base substitution A C downstream_gene_variant SKCM-US 16 74927577 74927577 single base substitution A C missense_variant I235R 704T>G SKCM-US 16 74927577 74927577 single base substitution A C missense_variant I667R 2000T>G SKCM-US 16 74927577 74927577 single base substitution A C missense_variant I69R 206T>G SKCM-US 16 74927577 74927577 single base substitution A C splice_region_variant SKCM-US 16 74942837 74942837 single base substitution G A downstream_gene_variant SKCM-US 16 74942837 74942837 single base substitution G A exon_variant SKCM-US 16 74942837 74942837 single base substitution G A intron_variant SKCM-US 16 74942837 74942837 single base substitution G A missense_variant R110W 328C>T SKCM-US 16 74942837 74942837 single base substitution G A missense_variant R561W 1681C>T SKCM-US 16 74942837 74942837 single base substitution G A upstream_gene_variant SKCM-US 16 74943437 74943437 single base substitution G A downstream_gene_variant SKCM-US 16 74943437 74943437 single base substitution G A exon_variant SKCM-US 16 74943437 74943437 single base substitution G A missense_variant P535L 1604C>T SKCM-US 16 74943437 74943437 single base substitution G A missense_variant P84L 251C>T SKCM-US 16 74946186 74946186 single base substitution G A downstream_gene_variant SKCM-US 16 74946186 74946186 single base substitution G A exon_variant SKCM-US 16 74946186 74946186 single base substitution G A synonymous_variant F433F 1299C>T SKCM-US 16 74946186 74946186 single base substitution G A upstream_gene_variant SKCM-US 16 74946209 74946209 single base substitution G A downstream_gene_variant SKCM-US 16 74946209 74946209 single base substitution G A exon_variant SKCM-US 16 74946209 74946209 single base substitution G A missense_variant R426C 1276C>T SKCM-US 16 74946209 74946209 single base substitution G A upstream_gene_variant SKCM-US 16 74949783 74949783 single base substitution C T exon_variant SKCM-US 16 74949783 74949783 single base substitution C T synonymous_variant R403R 1209G>A SKCM-US 16 74949783 74949783 single base substitution C T upstream_gene_variant SKCM-US 16 74949875 74949875 single base substitution G A exon_variant SKCM-US 16 74949875 74949875 single base substitution G A missense_variant P373S 1117C>T SKCM-US 16 74949875 74949875 single base substitution G A upstream_gene_variant SKCM-US 16 74957846 74957846 single base substitution G A downstream_gene_variant SKCM-US 16 74957846 74957846 single base substitution G A exon_variant SKCM-US 16 74957846 74957846 single base substitution G A missense_variant P236L 707C>T SKCM-US 16 74957846 74957846 single base substitution G A upstream_gene_variant SKCM-US 16 74972116 74972116 single base substitution G A downstream_gene_variant SKCM-US 16 74972116 74972116 single base substitution G A exon_variant SKCM-US 16 74972116 74972116 single base substitution G A missense_variant H195Y 583C>T SKCM-US 16 74972117 74972117 single base substitution G A downstream_gene_variant SKCM-US 16 74972117 74972117 single base substitution G A exon_variant SKCM-US 16 74972117 74972117 single base substitution G A synonymous_variant I194I 582C>T SKCM-US 16 74976658 74976658 single base substitution T A exon_variant SKCM-US 16 74976658 74976658 single base substitution T A intron_variant SKCM-US 16 74976658 74976658 single base substitution T A missense_variant D150V 449A>T SKCM-US 16 74976658 74976658 single base substitution T A missense_variant D171V 512A>T SKCM-US 16 74990485 74990485 single base substitution T C 3_prime_UTR_variant SKCM-US 16 74990485 74990485 single base substitution T C exon_variant SKCM-US 16 74990485 74990485 single base substitution T C missense_variant N22S 65A>G SKCM-US 16 74990485 74990485 single base substitution T C missense_variant N43S 128A>G SKCM-US 16 75033985 75033985 single base substitution C T exon_variant SKCM-US 16 75033985 75033985 single base substitution C T upstream_gene_variant STAD-US 16 74908279 74908279 single base substitution T C downstream_gene_variant STAD-US 16 74908279 74908279 single base substitution T C exon_variant STAD-US 16 74908279 74908279 single base substitution T C missense_variant K918R 2753A>G STAD-US 16 74908338 74908338 single base substitution G A exon_variant STAD-US 16 74908338 74908338 single base substitution G A synonymous_variant F212F 636C>T STAD-US 16 74908338 74908338 single base substitution G A synonymous_variant F898F 2694C>T STAD-US 16 74937943 74937943 single base substitution G A 3_prime_UTR_variant STAD-US 16 74937943 74937943 single base substitution G A downstream_gene_variant STAD-US 16 74937943 74937943 single base substitution G A exon_variant STAD-US 16 74937943 74937943 single base substitution G A missense_variant R139C 415C>T STAD-US 16 74937943 74937943 single base substitution G A missense_variant R590C 1768C>T STAD-US 16 74937943 74937943 single base substitution G A upstream_gene_variant STAD-US 16 74943405 74943405 single base substitution C A downstream_gene_variant STAD-US 16 74943405 74943405 single base substitution C A exon_variant STAD-US 16 74943405 74943405 single base substitution C A stop_gained G546* 1636G>T STAD-US 16 74943405 74943405 single base substitution C A stop_gained G95* 283G>T STAD-US 16 74943480 74943480 single base substitution G A downstream_gene_variant STAD-US 16 74943480 74943480 single base substitution G A exon_variant STAD-US 16 74943480 74943480 single base substitution G A missense_variant R521W 1561C>T STAD-US 16 74943480 74943480 single base substitution G A missense_variant R70W 208C>T STAD-US 16 74943527 74943527 single base substitution G A downstream_gene_variant STAD-US 16 74943527 74943527 single base substitution G A exon_variant STAD-US 16 74943527 74943527 single base substitution G A missense_variant P505L 1514C>T STAD-US 16 74943527 74943527 single base substitution G A missense_variant P54L 161C>T STAD-US 16 74943527 74943527 single base substitution G A upstream_gene_variant STAD-US 16 74950079 74950079 single base substitution G T exon_variant STAD-US 16 74950079 74950079 single base substitution G T missense_variant L349M 1045C>A STAD-US 16 74950079 74950079 single base substitution G T upstream_gene_variant STAD-US 16 74976648 74976648 single base substitution T C exon_variant STAD-US 16 74976648 74976648 single base substitution T C intron_variant STAD-US 16 74976648 74976648 single base substitution T C missense_variant I153M 459A>G STAD-US 16 74976648 74976648 single base substitution T C missense_variant I174M 522A>G STAD-US 16 74976652 74976652 single base substitution C A exon_variant STAD-US 16 74976652 74976652 single base substitution C A intron_variant STAD-US 16 74976652 74976652 single base substitution C A missense_variant R152L 455G>T STAD-US 16 74976652 74976652 single base substitution C A missense_variant R173L 518G>T STAD-US 16 74976691 74976691 deletion of <=200bp T - exon_variant STAD-US 16 74976691 74976691 deletion of <=200bp T - frameshift_variant N139 STAD-US 16 74976691 74976691 deletion of <=200bp T - frameshift_variant N160 STAD-US 16 74976691 74976691 deletion of <=200bp T - intron_variant STAD-US 16 74985388 74985388 single base substitution G A downstream_gene_variant STAD-US 16 74985388 74985388 single base substitution G A exon_variant STAD-US 16 74985388 74985388 single base substitution G A synonymous_variant G77G 231C>T STAD-US 16 74985388 74985388 single base substitution G A synonymous_variant G98G 294C>T STAD-US 16 74990459 74990459 single base substitution G A 3_prime_UTR_variant STAD-US 16 74990459 74990459 single base substitution G A exon_variant STAD-US 16 74990459 74990459 single base substitution G A stop_gained R31* 91C>T STAD-US 16 74990459 74990459 single base substitution G A stop_gained R52* 154C>T STAD-US 16 75033951 75033951 single base substitution C G exon_variant STAD-US 16 75033951 75033951 single base substitution C G upstream_gene_variant THCA-US 16 74919593 74919593 single base substitution A C downstream_gene_variant THCA-US 16 74919593 74919593 single base substitution A C exon_variant THCA-US 16 74919593 74919593 single base substitution A C missense_variant L197V 589T>G THCA-US 16 74919593 74919593 single base substitution A C missense_variant L883V 2647T>G THCA-US 16 74990380 74990380 single base substitution G A downstream_gene_variant THCA-US 16 74990380 74990380 single base substitution G A exon_variant THCA-US 16 74990380 74990380 single base substitution G A missense_variant A57V 170C>T THCA-US 16 74990380 74990380 single base substitution G A missense_variant A78V 233C>T UCEC-US 16 74908203 74908203 single base substitution G A downstream_gene_variant UCEC-US 16 74908203 74908203 single base substitution G A exon_variant UCEC-US 16 74908203 74908203 single base substitution G A synonymous_variant H943H 2829C>T UCEC-US 16 74923615 74923615 single base substitution C A downstream_gene_variant UCEC-US 16 74923615 74923615 single base substitution C A exon_variant UCEC-US 16 74923615 74923615 single base substitution C A intron_variant UCEC-US 16 74923615 74923615 single base substitution C A missense_variant Q295H 885G>T UCEC-US 16 74923615 74923615 single base substitution C A missense_variant Q727H 2181G>T UCEC-US 16 74923615 74923615 single base substitution C A upstream_gene_variant UCEC-US 16 74927608 74927608 single base substitution G A 3_prime_UTR_variant UCEC-US 16 74927608 74927608 single base substitution G A exon_variant UCEC-US 16 74927608 74927608 single base substitution G A missense_variant P225S 673C>T UCEC-US 16 74927608 74927608 single base substitution G A missense_variant P59S 175C>T UCEC-US 16 74927608 74927608 single base substitution G A missense_variant P657S 1969C>T UCEC-US 16 74927661 74927661 single base substitution C T 3_prime_UTR_variant UCEC-US 16 74927661 74927661 single base substitution C T exon_variant UCEC-US 16 74927661 74927661 single base substitution C T missense_variant R207Q 620G>A UCEC-US 16 74927661 74927661 single base substitution C T missense_variant R41Q 122G>A UCEC-US 16 74927661 74927661 single base substitution C T missense_variant R639Q 1916G>A UCEC-US 16 74937847 74937847 single base substitution G A downstream_gene_variant UCEC-US 16 74937847 74937847 single base substitution G A missense_variant R171W 511C>T UCEC-US 16 74937847 74937847 single base substitution G A missense_variant R24W 70C>T UCEC-US 16 74937847 74937847 single base substitution G A missense_variant R622W 1864C>T UCEC-US 16 74937847 74937847 single base substitution G A splice_region_variant UCEC-US 16 74937909 74937909 single base substitution C T 3_prime_UTR_variant UCEC-US 16 74937909 74937909 single base substitution C T downstream_gene_variant UCEC-US 16 74937909 74937909 single base substitution C T exon_variant UCEC-US 16 74937909 74937909 single base substitution C T missense_variant S150N 449G>A UCEC-US 16 74937909 74937909 single base substitution C T missense_variant S3N 8G>A UCEC-US 16 74937909 74937909 single base substitution C T missense_variant S601N 1802G>A UCEC-US 16 74937956 74937956 single base substitution C T 3_prime_UTR_variant UCEC-US 16 74937956 74937956 single base substitution C T downstream_gene_variant UCEC-US 16 74937956 74937956 single base substitution C T exon_variant UCEC-US 16 74937956 74937956 single base substitution C T synonymous_variant A134A 402G>A UCEC-US 16 74937956 74937956 single base substitution C T synonymous_variant A585A 1755G>A UCEC-US 16 74937956 74937956 single base substitution C T upstream_gene_variant UCEC-US 16 74943405 74943405 single base substitution C T downstream_gene_variant UCEC-US 16 74943405 74943405 single base substitution C T exon_variant UCEC-US 16 74943405 74943405 single base substitution C T missense_variant G546R 1636G>A UCEC-US 16 74943405 74943405 single base substitution C T missense_variant G95R 283G>A UCEC-US 16 74943479 74943479 single base substitution C T downstream_gene_variant UCEC-US 16 74943479 74943479 single base substitution C T exon_variant UCEC-US 16 74943479 74943479 single base substitution C T missense_variant R521Q 1562G>A UCEC-US 16 74943479 74943479 single base substitution C T missense_variant R70Q 209G>A UCEC-US 16 74943481 74943481 single base substitution C T downstream_gene_variant UCEC-US 16 74943481 74943481 single base substitution C T exon_variant UCEC-US 16 74943481 74943481 single base substitution C T synonymous_variant A520A 1560G>A UCEC-US 16 74943481 74943481 single base substitution C T synonymous_variant A69A 207G>A UCEC-US 16 74949884 74949884 single base substitution C A exon_variant UCEC-US 16 74949884 74949884 single base substitution C A stop_gained E370* 1108G>T UCEC-US 16 74949884 74949884 single base substitution C A upstream_gene_variant UCEC-US 16 74950046 74950046 single base substitution C T exon_variant UCEC-US 16 74950046 74950046 single base substitution C T missense_variant A360T 1078G>A UCEC-US 16 74950046 74950046 single base substitution C T upstream_gene_variant UCEC-US 16 74950050 74950050 single base substitution G A exon_variant UCEC-US 16 74950050 74950050 single base substitution G A synonymous_variant H358H 1074C>T UCEC-US 16 74950050 74950050 single base substitution G A upstream_gene_variant UCEC-US 16 74990458 74990458 single base substitution C T 3_prime_UTR_variant UCEC-US 16 74990458 74990458 single base substitution C T exon_variant UCEC-US 16 74990458 74990458 single base substitution C T missense_variant R31Q 92G>A UCEC-US 16 74990458 74990458 single base substitution C T missense_variant R52Q 155G>A UCEC-US 16 74990506 74990506 single base substitution C T missense_variant R15H 44G>A UCEC-US 16 74990506 74990506 single base substitution C T missense_variant R36H 107G>A UCEC-US 16 74990506 74990506 single base substitution C T splice_region_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CSCC-7-T COSM4459521 c.1129C>T p.L377L Substitution - coding silent 16:74915965-74915965 - PD3998a COSM165579 c.2516G>A p.R839Q Substitution - Missense 16:74886300-74886300 - 587376 COSM1232616 c.1232C>T p.A411V Substitution - Missense 16:74912355-74912355 - CHC1192T COSM4803473 c.2882C>T p.P961L Substitution - Missense 16:74874252-74874252 - NB-1931 COSM1288943 c.233C>T p.A78V Substitution - Missense 16:74956482-74956482 - WSU-HN12 COSM4591959 c.947T>G p.V316G Substitution - Missense 16:74917948-74917948 - OSCC-GB_00560111 COSM4883635 c.1777G>T p.A593S Substitution - Missense 16:74904036-74904036 - YUPLA COSM4062787 c.1768C>T p.R590C Substitution - Missense 16:74904045-74904045 - TCGA-EQ-8122-01 COSM4062794 c.154C>T p.R52* Substitution - Nonsense 16:74956561-74956561 - TCGA-AX-A0J1-01 COSM973677 c.1074C>T p.H358H Substitution - coding silent 16:74916152-74916152 - Pat_27_B COSM5851478 c.2801C>T p.S934L Substitution - Missense 16:74874333-74874333 - TCGA-A6-4105-01 COSM1379768 c.1200_1201insTG p.Q401fs*32 Insertion - Frameshift 16:74915893-74915894 - TCGA-EE-A2GR-06 COSM3512203 c.1117C>T p.P373S Substitution - Missense 16:74915977-74915977 - TCGA-CK-5913-01 COSM559097 c.2515C>T p.R839* Substitution - Nonsense 16:74886301-74886301 - GC_370T-GC_370N COSM3932443 c.1653A>G p.V551V Substitution - coding silent 16:74908967-74908967 - TCGA-FY-A3I5-01 COSM1288943 c.233C>T p.A78V Substitution - Missense 16:74956482-74956482 - T3202 COSM1379770 c.479delA p.N160fs*28 Deletion - Frameshift 16:74942793-74942793 - 93VU147T COSM4590555 c.950A>G p.D317G Substitution - Missense 16:74917945-74917945 - TCGA-BR-8591-01 COSM4062793 c.294C>T p.G98G Substitution - coding silent 16:74951490-74951490 - ORL-48 COSM4597030 c.2641G>C p.E881Q Substitution - Missense 16:74885701-74885701 - pfg016T COSM1640554 c.1593C>T p.D531D Substitution - coding silent 16:74909550-74909550 - SC_9081 COSM73283 c.2420C>T p.A807V Substitution - Missense 16:74886396-74886396 - T84 COSM1288943 c.233C>T p.A78V Substitution - Missense 16:74956482-74956482 - TCGA-AA-A010-01 COSM286510 c.2085T>G p.V695V Substitution - coding silent 16:74889813-74889813 - CSCC-56-T COSM4477895 c.2194C>T p.L732L Substitution - coding silent 16:74889704-74889704 - ESCC_BICR_028T COSM5431723 c.2493G>C p.L831L Substitution - coding silent 16:74886323-74886323 - TCGA-AX-A0J0-01 COSM973669 c.1864C>T p.R622W Substitution - Missense 16:74903949-74903949 - TCGA-FS-A1ZT-06 COSM3512201 c.1276C>T p.R426C Substitution - Missense 16:74912311-74912311 - TCGA-FP-A4BE-01 COSM4062791 c.1045C>A p.L349M Substitution - Missense 16:74916181-74916181 - GC_370T-GC_370N COSM4773229 c.1643-7C>T p.? Unknown 16:74908984-74908984 - PT48 COSM4773229 c.1643-7C>T p.? Unknown 16:74908984-74908984 - TCGA-22-5472-01 COSM704136 c.1817G>T p.R606L Substitution - Missense 16:74903996-74903996 - BICR_22 COSM4590555 c.950A>G p.D317G Substitution - Missense 16:74917945-74917945 - TCGA-AP-A0LN-01 COSM973673 c.1562G>A p.R521Q Substitution - Missense 16:74909581-74909581 - WSU-HN13 COSM4591959 c.947T>G p.V316G Substitution - Missense 16:74917948-74917948 - TCGA-G4-6628-01 COSM1379770 c.479delA p.N160fs*28 Deletion - Frameshift 16:74942793-74942793 - 272 COSM146103 c.1889A>G p.K630R Substitution - Missense 16:74893790-74893790 - TCGA-DS-A0VL-01 COSM460457 c.94G>C p.V32L Substitution - Missense 16:74965783-74965783 - TCGA-AO-A0J9-01 COSM435774 c.613C>T p.H205Y Substitution - Missense 16:74938188-74938188 - TCGA-FR-A3YN-06 COSM3512196 c.2168C>T p.P723L Substitution - Missense 16:74889730-74889730 - TCGA-EK-A3GK-01 COSM4853288 c.2671G>A p.D891N Substitution - Missense 16:74885671-74885671 - S02289 COSM5685991 c.304C>G p.Q102E Substitution - Missense 16:74951480-74951480 - TCGA-BF-A1Q0-01 COSM3512200 c.1299C>T p.F433F Substitution - coding silent 16:74912288-74912288 - SC_9081 COSM5551408 c.2904C>T p.C968C Substitution - coding silent 16:74874230-74874230 - BZ23 COSM1379770 c.479delA p.N160fs*28 Deletion - Frameshift 16:74942793-74942793 - CSCC-7-T COSM4468436 c.1543C>T p.P515S Substitution - Missense 16:74909600-74909600 - TCGA-AP-A0LM-01 COSM973668 c.1916G>A p.R639Q Substitution - Missense 16:74893763-74893763 - TCGA-AY-6197-01 COSM1379767 c.1545delC p.L516fs*7 Deletion - Frameshift 16:74909598-74909598 - TCGA-AP-A0LM-01 COSM973671 c.1755G>A p.A585A Substitution - coding silent 16:74904058-74904058 - LIM2405 COSM4642057 c.1273C>T p.H425Y Substitution - Missense 16:74912314-74912314 - TCGA-EE-A2M5-06 COSM3512193 c.2660C>T p.S887F Substitution - Missense 16:74885682-74885682 - RKO COSM1379770 c.479delA p.N160fs*28 Deletion - Frameshift 16:74942793-74942793 - TCGA-EB-A553-01 COSM3512197 c.2153C>T p.P718L Substitution - Missense 16:74889745-74889745 - YUSCA COSM5385383 c.604G>A p.D202N Substitution - Missense 16:74938197-74938197 - LS174T COSM2690988 c.2126C>T p.P709L Substitution - Missense 16:74889772-74889772 - OSCC-GB_00620111 COSM4881524 c.1744G>T p.G582C Substitution - Missense 16:74904069-74904069 - SNU-175 COSM2691031 c.673C>T p.R225W Substitution - Missense 16:74923982-74923982 - MO_1012 COSM5550470 c.2237C>T p.A746V Substitution - Missense 16:74888278-74888278 - D9 COSM5007823 c.1826A>G p.K609R Substitution - Missense 16:74903987-74903987 - TCGA-F1-6177-01 COSM4062787 c.1768C>T p.R590C Substitution - Missense 16:74904045-74904045 - ZZUFHECRKL-G021T COSM4773229 c.1643-7C>T p.? Unknown 16:74908984-74908984 - HCC2998 COSM1679274 c.1340T>G p.F447C Substitution - Missense 16:74912247-74912247 - TCGA-DD-A73C-01 COSM4916697 c.2631G>A p.E877E Substitution - coding silent 16:74885711-74885711 - TCGA-D3-A1Q4-06 COSM3512198 c.2000T>G p.I667R Substitution - Missense 16:74893679-74893679 - 345480 COSM3726271 c.2214G>T p.R738R Substitution - coding silent 16:74888301-74888301 - BD72T COSM5513216 c.2728C>T p.R910C Substitution - Missense 16:74874406-74874406 - TCGA-BS-A0TE-01 COSM973672 c.1636G>A p.G546R Substitution - Missense 16:74909507-74909507 - TCGA-FP-A4BE-01 COSM4062792 c.518G>T p.R173L Substitution - Missense 16:74942754-74942754 - XPA27PT1 COSM1579874 c.1769G>A p.R590H Substitution - Missense 16:74904044-74904044 - XPA27PT2 COSM1579874 c.1769G>A p.R590H Substitution - Missense 16:74904044-74904044 - PT27 COSM5906036 c.2885C>T p.T962I Substitution - Missense 16:74874249-74874249 - ESCC_BICR_010T COSM5100714 c.479_480insA p.N160fs*3 Insertion - Frameshift 16:74942792-74942793 - BD114T COSM5504222 c.2282T>C p.L761P Substitution - Missense 16:74888233-74888233 - P100 COSM559097 c.2515C>T p.R839* Substitution - Nonsense 16:74886301-74886301 - EGC15 COSM5055093 c.2798delG p.G933fs*7 Deletion - Frameshift 16:74874336-74874336 - TCGA-ER-A195-06 COSM3512207 c.512A>T p.D171V Substitution - Missense 16:74942760-74942760 - TCGA-IP-7968-01 COSM4062790 c.1514C>T p.P505L Substitution - Missense 16:74909629-74909629 - TCGA-AP-A059-01 COSM973666 c.2181G>T p.Q727H Substitution - Missense 16:74889717-74889717 - T3091 COSM4741002 c.782delA p.N261fs*11 Deletion - Frameshift 16:74922051-74922051 - TCGA-HU-A4GN-01 COSM4062786 c.2694C>T p.F898F Substitution - coding silent 16:74874440-74874440 - TCGA-AP-A059-01 COSM973676 c.1078G>A p.A360T Substitution - Missense 16:74916148-74916148 - TCGA-EM-A2P2-01 COSM3370555 c.2647T>G p.L883V Substitution - Missense 16:74885695-74885695 - PT08_1 COSM5893892 c.764C>T p.P255L Substitution - Missense 16:74922069-74922069 - 8032817 COSM3387598 c.1572G>A p.T524T Substitution - coding silent 16:74909571-74909571 - 6115122 COSM5566931 c.250C>T p.R84* Substitution - Nonsense 16:74951534-74951534 - TCGA-ER-A19M-06 COSM3512204 c.707C>T p.P236L Substitution - Missense 16:74923948-74923948 - ESO-682 COSM1270412 c.879G>A p.Q293Q Substitution - coding silent 16:74921954-74921954 - pfg129T COSM2691024 c.943C>T p.R315W Substitution - Missense 16:74917952-74917952 - TCGA-AZ-4615-01 COSM3691175 c.140C>A p.P47H Substitution - Missense 16:74956575-74956575 - CAL33 COSM4590555 c.950A>G p.D317G Substitution - Missense 16:74917945-74917945 - CAL27 COSM4590555 c.950A>G p.D317G Substitution - Missense 16:74917945-74917945 - WSU-HN6 COSM4602056 c.1949A>T p.Q650L Substitution - Missense 16:74893730-74893730 - B52 COSM1749778 c.344T>C p.V115A Substitution - Missense 16:74949781-74949781 - TCGA-BS-A0UF-01 COSM973678 c.155G>A p.R52Q Substitution - Missense 16:74956560-74956560 - S00827 COSM5659508 c.1865G>C p.R622P Substitution - Missense 16:74903948-74903948 - TCGA-AP-A059-01 COSM973674 c.1560G>A p.A520A Substitution - coding silent 16:74909583-74909583 - TCGA-AX-A0J0-01 COSM973675 c.1108G>T p.E370* Substitution - Nonsense 16:74915986-74915986 - TCGA-AF-2690-01 COSM3421158 c.1176G>A p.Q392Q Substitution - coding silent 16:74915918-74915918 - TCGA-AX-A0J1-01 COSM973679 c.107G>A p.R36H Substitution - Missense 16:74956608-74956608 - 8057528 COSM3387597 c.1821C>T p.S607S Substitution - coding silent 16:74903992-74903992 - C086 COSM5541718 c.2507C>T p.P836L Substitution - Missense 16:74886309-74886309 - XHDG04 COSM4768313 c.2465C>T p.S822L Substitution - Missense 16:74886351-74886351 - CSCC-41-T COSM4464400 c.1331C>T p.S444F Substitution - Missense 16:74912256-74912256 - CHC1040T COSM4799593 c.580A>C p.I194L Substitution - Missense 16:74938221-74938221 - TCGA-02-0055-01 COSM3748005 c.471T>A p.N157K Substitution - Missense 16:74942801-74942801 - WSU-HN12 COSM4590555 c.950A>G p.D317G Substitution - Missense 16:74917945-74917945 - LUAD-5V8LT COSM401653 c.1091A>T p.E364V Substitution - Missense 16:74916135-74916135 - TCGA-G2-A2EO-01 COSM1302246 c.2470G>T p.E824* Substitution - Nonsense 16:74886346-74886346 - TCGA-EE-A3J5-06 COSM3512199 c.1681C>T p.R561W Substitution - Missense 16:74908939-74908939 - CAL27 COSM4591959 c.947T>G p.V316G Substitution - Missense 16:74917948-74917948 - T368 COSM1379770 c.479delA p.N160fs*28 Deletion - Frameshift 16:74942793-74942793 - SCC-9 COSM4591959 c.947T>G p.V316G Substitution - Missense 16:74917948-74917948 - CRC-02T COSM5454485 c.327-5C>T p.? Unknown 16:74949803-74949803 - C0023T COSM4151411 c.2467C>G p.P823A Substitution - Missense 16:74886349-74886349 - T2938 COSM4741003 c.528T>C p.D176D Substitution - coding silent 16:74942744-74942744 - CHC1040T COSM4799593 c.580A>C p.I194L Substitution - Missense 16:74938221-74938221 - B65-Tumor COSM3932443 c.1653A>G p.V551V Substitution - coding silent 16:74908967-74908967 - 0034_CRUK_PC_0034_T1_DNA COSM5422081 c.482C>A p.A161D Substitution - Missense 16:74942790-74942790 - STC252 COSM5055094 c.1028C>A p.P343Q Substitution - Missense 16:74916198-74916198 - TCGA-22-5473-01 COSM704135 c.1114C>T p.P372S Substitution - Missense 16:74915980-74915980 - LUAD-F00368 COSM341073 c.1780C>T p.P594S Substitution - Missense 16:74904033-74904033 - TCGA-BR-4280-01 COSM4062785 c.2753A>G p.K918R Substitution - Missense 16:74874381-74874381 - CHC1192T COSM4803473 c.2882C>T p.P961L Substitution - Missense 16:74874252-74874252 - sysucc-1397T COSM5473780 c.1324G>A p.A442T Substitution - Missense 16:74912263-74912263 - BRC18 COSM5028172 c.691C>T p.L231F Substitution - Missense 16:74923964-74923964 - TCGA-CG-4444-01 COSM4062789 c.1561C>T p.R521W Substitution - Missense 16:74909582-74909582 - 23_tFL COSM4170773 c.2489G>T p.S830I Substitution - Missense 16:74886327-74886327 - TCGA-EE-A2MR-06 COSM3512206 c.582C>T p.I194I Substitution - coding silent 16:74938219-74938219 - OSCC-GB_00950111 COSM4882006 c.979G>C p.D327H Substitution - Missense 16:74916247-74916247 - ESCC_114 COSM4062789 c.1561C>T p.R521W Substitution - Missense 16:74909582-74909582 - WSU-HN13 COSM4590555 c.950A>G p.D317G Substitution - Missense 16:74917945-74917945 - TCGA-AR-A250-01 COSM1479097 c.1410G>T p.L470L Substitution - coding silent 16:74909897-74909897 - sysucc-809T COSM5468192 c.2729G>A p.R910H Substitution - Missense 16:74874405-74874405 - CSCC-6-T COSM4447473 c.54+3G>A p.? Unknown 16:74984961-74984961 - YUDUTY COSM1709395 c.200G>A p.W67* Substitution - Nonsense 16:74956515-74956515 - 202_T COSM3957824 c.2696G>T p.G899V Substitution - Missense 16:74874438-74874438 - tumor_4102009 COSM3356859 c.2119C>T p.L707F Substitution - Missense 16:74889779-74889779 - CSCC-62-T COSM4564917 c.1544_1545CC>TT p.P515L Substitution - Missense 16:74909598-74909599 - CSCC-55-T COSM4521377 c.1108G>A p.E370K Substitution - Missense 16:74915986-74915986 - T2969 COSM4741001 c.1323C>T p.A441A Substitution - coding silent 16:74912264-74912264 - DF01 COSM4062790 c.1514C>T p.P505L Substitution - Missense 16:74909629-74909629 - TCGA-FP-A4BE-01 COSM4062794 c.154C>T p.R52* Substitution - Nonsense 16:74956561-74956561 - RK102_C01 COSM3701124 c.225C>G p.H75Q Substitution - Missense 16:74956490-74956490 - ESCC_11 COSM5624336 c.1681C>A p.R561R Substitution - coding silent 16:74908939-74908939 - TCGA-A5-A0GP-01 COSM973665 c.2829C>T p.H943H Substitution - coding silent 16:74874305-74874305 - TCGA-39-5031-01 COSM704133 c.114C>G p.F38L Substitution - Missense 16:74956601-74956601 - LUAD-S01413 COSM347055 c.216C>G p.S72R Substitution - Missense 16:74956499-74956499 - TCGA-EE-A2GO-06 COSM3888959 c.2305C>T p.P769S Substitution - Missense 16:74888210-74888210 - EGC3 COSM1379770 c.479delA p.N160fs*28 Deletion - Frameshift 16:74942793-74942793 - TCGA-EE-A3JB-06 COSM4898381 c.1604C>T p.P535L Substitution - Missense 16:74909539-74909539 - AOCS-108-1-7 COSM4141902 c.97C>A p.L33I Substitution - Missense 16:74965780-74965780 - CHC1439T COSM3667939 c.1177C>A p.Q393K Substitution - Missense 16:74915917-74915917 - 93VU147T COSM4591959 c.947T>G p.V316G Substitution - Missense 16:74917948-74917948 - S02354 COSM5695561 c.2265_2288del24 p.Q755_N763>H Complex - deletion inframe 16:74888227-74888250 - 2492729 COSM3512202 c.1209G>A p.R403R Substitution - coding silent 16:74915885-74915885 - J76_T COSM3957825 c.1682G>T p.R561L Substitution - Missense 16:74908938-74908938 - 587336 COSM1232615 c.1891C>T p.R631C Substitution - Missense 16:74893788-74893788 - 61 COSM5740738 c.2617T>C p.W873R Substitution - Missense 16:74885725-74885725 - TCGA-24-2271-01 COSM73283 c.2420C>T p.A807V Substitution - Missense 16:74886396-74886396 - BZ19 COSM5758489 c.1578C>T p.Y526Y Substitution - coding silent 16:74909565-74909565 - PCSI_0120_Pa_P COSM3932443 c.1653A>G p.V551V Substitution - coding silent 16:74908967-74908967 - SCC-25 COSM4590555 c.950A>G p.D317G Substitution - Missense 16:74917945-74917945 - P117 COSM1379770 c.479delA p.N160fs*28 Deletion - Frameshift 16:74942793-74942793 - TCGA-B5-A11U-01 COSM973670 c.1802G>A p.S601N Substitution - Missense 16:74904011-74904011 - sysucc-880T COSM5462586 c.2196-2A>G p.? Unknown 16:74888321-74888321 - TCGA-EE-A2GT-06 COSM3512202 c.1209G>A p.R403R Substitution - coding silent 16:74915885-74915885 - TCGA-J4-A67M-01 COSM3782992 c.740A>G p.N247S Substitution - Missense 16:74922093-74922093 - PT36 COSM5916551 c.205C>T p.P69S Substitution - Missense 16:74956510-74956510 - Case6 COSM1579528 c.1409T>C p.L470P Substitution - Missense 16:74909898-74909898 - TCGA-EE-A181-06 COSM3512195 c.2193C>T p.S731S Substitution - coding silent 16:74889705-74889705 - LS180 COSM2690988 c.2126C>T p.P709L Substitution - Missense 16:74889772-74889772 - CN-AML-CR-23-Dx COSM5428104 c.1540C>A p.P514T Substitution - Missense 16:74909603-74909603 - ZZUFHECRKL-G021T COSM5228501 c.1674A>G p.T558T Substitution - coding silent 16:74908946-74908946 - TCGA-ER-A193-06 COSM3512208 c.128A>G p.N43S Substitution - Missense 16:74956587-74956587 - TCGA-AP-A0LE-01 COSM973667 c.1969C>T p.P657S Substitution - Missense 16:74893710-74893710 - TCGA-A2-A0T5-01 COSM3818550 c.599A>C p.H200P Substitution - Missense 16:74938202-74938202 - 1342576 COSM51297 c.1677G>A p.M559I Substitution - Missense 16:74908943-74908943 - TCGA-CG-4306-01 COSM2691037 c.522A>G p.I174M Substitution - Missense 16:74942750-74942750 - TCGA-CH-5738-01 COSM1128877 c.2284C>A p.P762T Substitution - Missense 16:74888231-74888231 - TCGA-EE-A20C-06 COSM3512205 c.583C>T p.H195Y Substitution - Missense 16:74938218-74938218 - CSCC-47-T COSM4473401 c.1847C>T p.S616F Substitution - Missense 16:74903966-74903966 - T1154 COSM4741004 c.374C>A p.S125Y Substitution - Missense 16:74949751-74949751 - I2L-P27-Tumor-Biopsy COSM5363588 c.686A>G p.N229S Substitution - Missense 16:74923969-74923969 - TCGA-GI-A2C8-01 COSM1479098 c.1281C>G p.V427V Substitution - coding silent 16:74912306-74912306 - TCGA-AZ-4615-01 COSM3691174 c.1923C>T p.I641I Substitution - coding silent 16:74893756-74893756 - TCGA-EE-A3J5-06 COSM3512194 c.2292C>T p.P764P Substitution - coding silent 16:74888223-74888223 - TCGA-EE-A29E-06 COSM3512192 c.2863C>T p.R955W Substitution - Missense 16:74874271-74874271 - TCGA-G9-6351-01 COSM3672323 c.2619G>T p.W873C Substitution - Missense 16:74885723-74885723 - SCC-25 COSM4591959 c.947T>G p.V316G Substitution - Missense 16:74917948-74917948 - HCC2998 COSM1679274 c.1340T>G p.F447C Substitution - Missense 16:74912247-74912247 - C91 COSM435774 c.613C>T p.H205Y Substitution - Missense 16:74938188-74938188 - KM12 COSM2691039 c.507C>T p.D169D Substitution - coding silent 16:74942765-74942765 - BICR_22 COSM4591959 c.947T>G p.V316G Substitution - Missense 16:74917948-74917948 - B52-Tumor COSM1749778 c.344T>C p.V115A Substitution - Missense 16:74949781-74949781 - 631064 COSM326875 c.1241G>C p.R414T Substitution - Missense 16:74912346-74912346 - TCGA-HU-A4H8-01 COSM4062788 c.1636G>T p.G546* Substitution - Nonsense 16:74909507-74909507 - T2999 COSM4741000 c.1459C>T p.L487F Substitution - Missense 16:74909848-74909848 - sysucc-966T COSM5487051 c.514G>T p.V172L Substitution - Missense 16:74942758-74942758 - TCGA-F5-6813-01 COSM1563500 c.2784C>T p.H928H Substitution - coding silent 16:74874350-74874350 - 272-01-2TD COSM146103 c.1889A>G p.K630R Substitution - Missense 16:74893790-74893790 - TCGA-A6-6781-01 COSM1379769 c.1027C>T p.P343S Substitution - Missense 16:74916199-74916199 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.280936;Hs.280951 16q23.1

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.I667R c.2000T>G 16 74927577 CM A C Missense p.L883V c.2647T>G 16 74919593 THCA A G Synonymous p.Y300Y c.900T>C 16 74951893 LUAD A T Missense p.N157K c.471T>A 16 74976699 GBM C A IntronicSNV . c.1225-889G>T 16 74947149 CLL C A Missense p.M429I c.1287G>T 16 74946198 LUAD C A Missense p.Q650H c.1950G>T 16 74927627 LUAD C A Missense p.R606L c.1817G>T 16 74937894 LUSC C A Missense p.R932L c.2795G>T 16 74908237 CM C A Nonsense p.E824* c.2470G>T 16 74920244 BLCA C A SpliceDonorSNV . c.1866+1G>T 16 74937844 BRCA C A Synonymous p.L470L c.1410G>T 16 74943795 BRCA C A Synonymous p.L656L c.1968G>T 16 74927609 LUAD C G Missense p.Q319H c.957G>C 16 74951836 LUAD C G Missense p.R414T c.1241G>C 16 74946244 SCLC C T IntronicSNV . c.2546+48G>A 16 74920120 CM C T Missense p.A412T c.1234G>A 16 74946251 CM C T Missense p.G546R c.1636G>A 16 74943405 UCEC C T Missense p.G633R c.1897G>A 16 74927680 CM C T Missense p.R521Q c.1562G>A 16 74943479 UCEC C T Missense p.R839Q c.2516G>A 16 74920198 BRCA C T Missense p.S601N c.1802G>A 16 74937909 UCEC C T SpliceDonorSNV . c.534+1G>A 16 74976635 LUAD C T Synonymous p.G829G c.2487G>A 16 74920227 CM C T Synonymous p.Q293Q c.879G>A 16 74955852 ESCA C T Synonymous p.R403R c.1209G>A 16 74949783 CM C T Synonymous p.T304T c.912G>A 16 74951881 HNSC G A 3-UTRSNV . c.2922+139C>T 16 74907971 HC G A IntronicSNV . c.1389+110C>T 16 74945986 CM G A IntronicSNV . c.1485+62C>T 16 74943658 CM G A IntronicSNV . c.327-29C>T 16 74983725 NSCLC G A Missense p.A78V c.233C>T 16 74990380 THCA G A Missense p.A807V c.2420C>T 16 74920294 OV G A Missense p.H195Y c.583C>T 16 74972116 CM G A Missense p.L231F c.691C>T 16 74957862 BRCA G A Missense p.P372S c.1114C>T 16 74949878 LUSC G A Missense p.P373S c.1117C>T 16 74949875 CM G A Missense p.P535L c.1604C>T 16 74943437 CM G A Missense p.P657S c.1969C>T 16 74927608 UCEC G A Missense p.P769S c.2305C>T 16 74922108 CM G A Missense p.R426C c.1276C>T 16 74946209 CM G A Missense p.R521W c.1561C>T 16 74943480 STAD G A Missense p.R561W c.1681C>T 16 74942837 CM G A Missense p.R590C c.1768C>T 16 74937943 STAD G A Missense p.S613F c.1838C>T 16 74937873 CM G A Missense p.S887F c.2660C>T 16 74919580 CM G A Nonsense p.R839* c.2515C>T 16 74920199 LUAD G A Synonymous p.D531D c.1593C>T 16 74943448 STAD G A Synonymous p.F433F c.1299C>T 16 74946186 CM G A Synonymous p.H943H c.2829C>T 16 74908203 UCEC G A Synonymous p.I41I c.123C>T 16 74990490 CM G A Synonymous p.I584I c.1752C>T 16 74937959 CM G A Synonymous p.L145L c.433C>T 16 74982429 LUAD G A Synonymous p.P764P c.2292C>T 16 74922121 CM G A Synonymous p.P836P c.2508C>T 16 74920206 CM G A Synonymous p.S731S c.2193C>T 16 74923603 CM G C Missense p.F38L c.114C>G 16 74990499 LUSC G C Missense p.R307G c.919C>G 16 74951874 CM G C Synonymous p.P180P c.540C>G 16 74972159 CM G C Synonymous p.V427V c.1281C>G 16 74946204 BRCA G T Missense p.R837S c.2509C>A 16 74920205 LUAD T A Missense p.D171V c.512A>T 16 74976658 CM T C Missense p.I174M c.522A>G 16 74976648 STAD T C Missense p.K630R c.1889A>G 16 74927688 CLL T C Missense p.K918R c.2753A>G 16 74908279 STAD T C Missense p.N247S c.740A>G 16 74955991 PRAD T C Missense p.N43S c.128A>G 16 74990485 CM - T IntronicInsertion . c.1390-53dupA 16 74943868 CM