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 30780607 30780607 + Missense_Mutation SNP A A G TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr16:30780607A>G c.2348A>G c.(2347-2349)gAt>gGt p.D783G BLCA 16 30774487 30774487 + Missense_Mutation SNP G G A TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr16:30774487G>A c.181G>A c.(181-183)Gag>Aag p.E61K BLCA 16 30774745 30774745 + Missense_Mutation SNP G G A TCGA-DK-A6B0-01A-11D-A31L-08 TCGA-DK-A6B0-10A-01D-A31J-08 g.chr16:30774745G>A c.307G>A c.(307-309)Gaa>Aaa p.E103K BLCA 16 30774794 30774794 + Missense_Mutation SNP C C T TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr16:30774794C>T c.356C>T c.(355-357)tCt>tTt p.S119F BLCA 16 30774850 30774850 + Missense_Mutation SNP C C G TCGA-BT-A2LD-01A-12D-A20D-08 TCGA-BT-A2LD-10A-01D-A20D-08 g.chr16:30774850C>G c.412C>G c.(412-414)Ctc>Gtc p.L138V BLCA 16 30775620 30775620 + Missense_Mutation SNP C C G TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr16:30775620C>G c.563C>G c.(562-564)tCc>tGc p.S188C BLCA 16 30776275 30776275 + Silent SNP C C G TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr16:30776275C>G c.666C>G c.(664-666)ctC>ctG p.L222L BLCA 16 30777495 30777495 + Silent SNP G G A TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr16:30777495G>A c.1005G>A c.(1003-1005)ctG>ctA p.L335L BLCA 16 30778107 30778107 + Nonsense_Mutation SNP C C T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr16:30778107C>T c.1339C>T c.(1339-1341)Cag>Tag p.Q447* BLCA 16 30779568 30779568 + Missense_Mutation SNP C C G TCGA-ZF-A9R0-01A-11D-A38G-08 TCGA-ZF-A9R0-10A-01D-A38J-08 g.chr16:30779568C>G c.1696C>G c.(1696-1698)Cca>Gca p.P566A BLCA 16 30779606 30779606 + Silent SNP G G A TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr16:30779606G>A c.1734G>A c.(1732-1734)aaG>aaA p.K578K BLCA 16 30780185 30780185 + Silent SNP G G A TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr16:30780185G>A c.2124G>A c.(2122-2124)cgG>cgA p.R708R BLCA 16 30780218 30780218 + Missense_Mutation SNP G G C TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr16:30780218G>C c.2157G>C c.(2155-2157)aaG>aaC p.K719N BLCA 16 30783276 30783276 + Silent SNP C C T TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr16:30783276C>T c.2709C>T c.(2707-2709)ttC>ttT p.F903F BLCA 16 30785258 30785258 + Splice_Site SNP G G A TCGA-BT-A2LA-01A-11D-A18F-08 TCGA-BT-A2LA-11A-11D-A18F-08 g.chr16:30785258G>A c.e20-1 BLCA 16 30785347 30785347 + Missense_Mutation SNP G G T TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr16:30785347G>T c.2918G>T c.(2917-2919)cGg>cTg p.R973L BRCA 16 30774485 30774485 + Missense_Mutation SNP C C G TCGA-AC-A3OD-01A-11D-A21Q-09 TCGA-AC-A3OD-10A-01D-A21Q-09 g.chr16:30774485C>G c.179C>G c.(178-180)gCa>gGa p.A60G BRCA 16 30775646 30775646 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr16:30775646G>C c.589G>C c.(589-591)Gag>Cag p.E197Q BRCA 16 30778098 30778098 + Missense_Mutation SNP G G C TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr16:30778098G>C c.1330G>C c.(1330-1332)Gag>Cag p.E444Q BRCA 16 30778177 30778177 + Missense_Mutation SNP T T A TCGA-BH-A208-01A-11D-A159-09 TCGA-BH-A208-11A-51D-A159-09 g.chr16:30778177T>A c.1409T>A c.(1408-1410)cTg>cAg p.L470Q BRCA 16 30779332 30779332 + Missense_Mutation SNP G G T TCGA-A2-A25A-01A-12D-A16D-09 TCGA-A2-A25A-10A-01D-A16D-09 g.chr16:30779332G>T c.1547G>T c.(1546-1548)gGc>gTc p.G516V BRCA 16 30779794 30779794 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr16:30779794T>G c.1922T>G c.(1921-1923)gTg>gGg p.V641G BRCA 16 30780540 30780540 + Missense_Mutation SNP A A G TCGA-A2-A0YE-01A-11D-A10G-09 TCGA-A2-A0YE-10A-01D-A10G-09 g.chr16:30780540A>G c.2281A>G c.(2281-2283)Aca>Gca p.T761A BRCA 16 30783268 30783268 + Missense_Mutation SNP G G C TCGA-AO-A03N-01B-11D-A10M-09 TCGA-AO-A03N-10A-01D-A10M-09 g.chr16:30783268G>C c.2701G>C c.(2701-2703)Gag>Cag p.E901Q CESC 16 30776605 30776605 + Missense_Mutation SNP G G A TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr16:30776605G>A c.875G>A c.(874-876)cGa>cAa p.R292Q CESC 16 30777520 30777520 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr16:30777520G>C c.1030G>C c.(1030-1032)Gaa>Caa p.E344Q CESC 16 30778082 30778082 + Silent SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr16:30778082G>A c.1314G>A c.(1312-1314)caG>caA p.Q438Q CESC 16 30778146 30778146 + Missense_Mutation SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr16:30778146G>A c.1378G>A c.(1378-1380)Gag>Aag p.E460K CESC 16 30779455 30779455 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr16:30779455C>G c.1583C>G c.(1582-1584)tCc>tGc p.S528C CESC 16 30779514 30779514 + Missense_Mutation SNP G G C TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chr16:30779514G>C c.1642G>C c.(1642-1644)Gag>Cag p.E548Q CESC 16 30779554 30779554 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr16:30779554G>C c.1682G>C c.(1681-1683)aGa>aCa p.R561T CESC 16 30780684 30780684 + Nonsense_Mutation SNP G G T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr16:30780684G>T c.2425G>T c.(2425-2427)Gag>Tag p.E809* CESC 16 30783259 30783259 + Missense_Mutation SNP C C G TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr16:30783259C>G c.2692C>G c.(2692-2694)Cgt>Ggt p.R898G COAD 16 30773986 30773986 + Silent SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr16:30773986C>T c.120C>T c.(118-120)ggC>ggT p.G40G COAD 16 30774565 30774565 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:30774565G>T c.259G>T c.(259-261)Gat>Tat p.D87Y COAD 16 30776588 30776588 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:30776588C>T c.858C>T c.(856-858)atC>atT p.I286I COAD 16 30777733 30777733 + Missense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr16:30777733C>T c.1147C>T c.(1147-1149)Cgg>Tgg p.R383W COAD 16 30777763 30777763 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr16:30777763G>A c.1177G>A c.(1177-1179)Gcc>Acc p.A393T COAD 16 30777867 30777867 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:30777867C>T c.1281C>T c.(1279-1281)atC>atT p.I427I COAD 16 30778093 30778093 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:30778093G>A c.1325G>A c.(1324-1326)cGc>cAc p.R442H COAD 16 30778119 30778119 + Missense_Mutation SNP A A G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:30778119A>G c.1351A>G c.(1351-1353)Acg>Gcg p.T451A COAD 16 30778155 30778155 + Missense_Mutation SNP C C T TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr16:30778155C>T c.1387C>T c.(1387-1389)Cgc>Tgc p.R463C COAD 16 30779659 30779659 + Missense_Mutation SNP C C G TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:30779659C>G c.1787C>G c.(1786-1788)gCc>gGc p.A596G COAD 16 30780626 30780626 + Silent SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:30780626A>G c.2367A>G c.(2365-2367)ctA>ctG p.L789L COAD 16 30783432 30783432 + Missense_Mutation SNP G G A TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chr16:30783432G>A c.2750G>A c.(2749-2751)cGc>cAc p.R917H COAD 16 30785347 30785347 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:30785347G>A c.2918G>A c.(2917-2919)cGg>cAg p.R973Q COADREAD 16 30773986 30773986 + Silent SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr16:30773986C>T c.120C>T c.(118-120)ggC>ggT p.G40G COADREAD 16 30774565 30774565 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:30774565G>T c.259G>T c.(259-261)Gat>Tat p.D87Y COADREAD 16 30776588 30776588 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:30776588C>T c.858C>T c.(856-858)atC>atT p.I286I COADREAD 16 30777733 30777733 + Missense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr16:30777733C>T c.1147C>T c.(1147-1149)Cgg>Tgg p.R383W COADREAD 16 30777763 30777763 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr16:30777763G>A c.1177G>A c.(1177-1179)Gcc>Acc p.A393T COADREAD 16 30777867 30777867 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:30777867C>T c.1281C>T c.(1279-1281)atC>atT p.I427I COADREAD 16 30778093 30778093 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:30778093G>A c.1325G>A c.(1324-1326)cGc>cAc p.R442H COADREAD 16 30778119 30778119 + Missense_Mutation SNP A A G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:30778119A>G c.1351A>G c.(1351-1353)Acg>Gcg p.T451A COADREAD 16 30778155 30778155 + Missense_Mutation SNP C C T TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr16:30778155C>T c.1387C>T c.(1387-1389)Cgc>Tgc p.R463C COADREAD 16 30779659 30779659 + Missense_Mutation SNP C C G TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:30779659C>G c.1787C>G c.(1786-1788)gCc>gGc p.A596G COADREAD 16 30780286 30780286 + Missense_Mutation SNP G G A TCGA-AG-A02G-01A-01W-A00E-09 TCGA-AG-A02G-10A-01W-A00E-09 g.chr16:30780286G>A c.2225G>A c.(2224-2226)cGc>cAc p.R742H COADREAD 16 30780626 30780626 + Silent SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:30780626A>G c.2367A>G c.(2365-2367)ctA>ctG p.L789L COADREAD 16 30783432 30783432 + Missense_Mutation SNP G G A TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chr16:30783432G>A c.2750G>A c.(2749-2751)cGc>cAc p.R917H COADREAD 16 30785347 30785347 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:30785347G>A c.2918G>A c.(2917-2919)cGg>cAg p.R973Q DLBC 16 30778068 30778068 + Missense_Mutation SNP G G A TCGA-VB-A8QN-01A-11D-A382-10 TCGA-VB-A8QN-10A-01D-A385-10 g.chr16:30778068G>A c.1300G>A c.(1300-1302)Gag>Aag p.E434K DLBC 16 30780861 30780861 + Silent SNP C C T TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr16:30780861C>T c.2526C>T c.(2524-2526)ctC>ctT p.L842L ESCA 16 30775652 30775652 + Missense_Mutation SNP T T C TCGA-L5-A8NK-01A-21D-A37C-09 TCGA-L5-A8NK-11A-11D-A37F-09 g.chr16:30775652T>C c.595T>C c.(595-597)Tca>Cca p.S199P ESCA 16 30777483 30777483 + Splice_Site SNP G G C TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr16:30777483G>C c.e9-1 ESCA 16 30779758 30779758 + Missense_Mutation SNP C C A TCGA-L5-A8NE-01A-11D-A37C-09 TCGA-L5-A8NE-11A-11D-A37F-09 g.chr16:30779758C>A c.1886C>A c.(1885-1887)tCc>tAc p.S629Y ESCA 16 30779971 30779971 + Silent SNP C C T TCGA-JY-A6FE-01A-11D-A33E-09 TCGA-JY-A6FE-10A-01D-A33H-09 g.chr16:30779971C>T c.2011C>T c.(2011-2013)Ctg>Ttg p.L671L GBM 16 30774800 30774800 + Missense_Mutation SNP C C A TCGA-06-0686-01A-01W-0348-08 TCGA-06-0686-10A-01W-0348-08 g.chr16:30774800C>A c.362C>A c.(361-363)gCg>gAg p.A121E GBM 16 30774843 30774843 + Silent SNP G G A TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chr16:30774843G>A c.405G>A c.(403-405)ggG>ggA p.G135G GBM 16 30783282 30783282 + Silent SNP C C A TCGA-76-6280-01A-21D-1845-08 TCGA-76-6280-10A-01D-1845-08 g.chr16:30783282C>A c.2715C>A c.(2713-2715)ctC>ctA p.L905L GBMLGG 16 30774800 30774800 + Missense_Mutation SNP C C A TCGA-06-0686-01A-01W-0348-08 TCGA-06-0686-10A-01W-0348-08 g.chr16:30774800C>A c.362C>A c.(361-363)gCg>gAg p.A121E GBMLGG 16 30774843 30774843 + Silent SNP G G A TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chr16:30774843G>A c.405G>A c.(403-405)ggG>ggA p.G135G GBMLGG 16 30776312 30776312 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:30776312C>T c.703C>T c.(703-705)Cgt>Tgt p.R235C GBMLGG 16 30780680 30780680 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:30780680G>T c.2421G>T c.(2419-2421)aaG>aaT p.K807N GBMLGG 16 30783282 30783282 + Silent SNP C C A TCGA-76-6280-01A-21D-1845-08 TCGA-76-6280-10A-01D-1845-08 g.chr16:30783282C>A c.2715C>A c.(2713-2715)ctC>ctA p.L905L HNSC 16 30774767 30774767 + Missense_Mutation SNP G G A TCGA-CV-A45U-01A-12D-A24D-08 TCGA-CV-A45U-10A-01D-A24F-08 g.chr16:30774767G>A c.329G>A c.(328-330)cGa>cAa p.R110Q HNSC 16 30774800 30774800 + Missense_Mutation SNP C C T TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr16:30774800C>T c.362C>T c.(361-363)gCg>gTg p.A121V HNSC 16 30774845 30774845 + Missense_Mutation SNP C C A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr16:30774845C>A c.407C>A c.(406-408)aCt>aAt p.T136N HNSC 16 30775583 30775583 + Missense_Mutation SNP G G A TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr16:30775583G>A c.526G>A c.(526-528)Gag>Aag p.E176K HNSC 16 30776589 30776589 + Missense_Mutation SNP G G A TCGA-CV-7254-01A-11D-2012-08 TCGA-CV-7254-10A-01D-2013-08 g.chr16:30776589G>A c.859G>A c.(859-861)Gag>Aag p.E287K HNSC 16 30777510 30777510 + Missense_Mutation SNP G G C TCGA-CR-7376-01A-11D-2129-08 TCGA-CR-7376-10A-01D-2129-08 g.chr16:30777510G>C c.1020G>C c.(1018-1020)gaG>gaC p.E340D HNSC 16 30779633 30779633 + Silent SNP G G A TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr16:30779633G>A c.1761G>A c.(1759-1761)gaG>gaA p.E587E HNSC 16 30779808 30779808 + Silent SNP C C A TCGA-CV-7247-01A-11D-2012-08 TCGA-CV-7247-10A-01D-2013-08 g.chr16:30779808C>A c.1936C>A c.(1936-1938)Cgg>Agg p.R646R HNSC 16 30780713 30780713 + Silent SNP G G A TCGA-DQ-7588-01A-11D-2078-08 TCGA-DQ-7588-10B-01D-2078-08 g.chr16:30780713G>A c.2454G>A c.(2452-2454)aaG>aaA p.K818K HNSC 16 30780842 30780842 + Missense_Mutation SNP G G A TCGA-CQ-7072-01A-21D-A30E-08 TCGA-CQ-7072-10A-01D-A30H-08 g.chr16:30780842G>A c.2507G>A c.(2506-2508)cGa>cAa p.R836Q KICH 16 30777565 30777565 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr16:30777565G>A c.1075G>A c.(1075-1077)Gaa>Aaa p.E359K KIPAN 16 30773995 30773995 + Silent SNP C C A TCGA-BP-4158-01A-02D-1366-10 TCGA-BP-4158-11A-01D-1366-10 g.chr16:30773995C>A c.129C>A c.(127-129)tcC>tcA p.S43S KIPAN 16 30774777 30774777 + Missense_Mutation SNP G G T TCGA-CJ-4913-01A-01D-1429-08 TCGA-CJ-4913-11A-01D-1429-08 g.chr16:30774777G>T c.339G>T c.(337-339)gaG>gaT p.E113D KIPAN 16 30775599 30775599 + Missense_Mutation SNP T T C TCGA-GL-7773-01A-11D-2136-08 TCGA-GL-7773-10A-01D-2136-08 g.chr16:30775599T>C c.542T>C c.(541-543)cTg>cCg p.L181P KIPAN 16 30776560 30776560 + Missense_Mutation SNP C C T TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chr16:30776560C>T c.830C>T c.(829-831)aCa>aTa p.T277I KIPAN 16 30777565 30777565 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr16:30777565G>A c.1075G>A c.(1075-1077)Gaa>Aaa p.E359K KIPAN 16 30777596 30777596 + Missense_Mutation SNP G G T TCGA-CJ-4899-01A-01D-1462-08 TCGA-CJ-4899-11A-01D-1462-08 g.chr16:30777596G>T c.1106G>T c.(1105-1107)cGc>cTc p.R369L KIRC 16 30773995 30773995 + Silent SNP C C A TCGA-BP-4158-01A-02D-1366-10 TCGA-BP-4158-11A-01D-1366-10 g.chr16:30773995C>A c.129C>A c.(127-129)tcC>tcA p.S43S KIRC 16 30774777 30774777 + Missense_Mutation SNP G G T TCGA-CJ-4913-01A-01D-1429-08 TCGA-CJ-4913-11A-01D-1429-08 g.chr16:30774777G>T c.339G>T c.(337-339)gaG>gaT p.E113D KIRC 16 30776560 30776560 + Missense_Mutation SNP C C T TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chr16:30776560C>T c.830C>T c.(829-831)aCa>aTa p.T277I KIRC 16 30777596 30777596 + Missense_Mutation SNP G G T TCGA-CJ-4899-01A-01D-1462-08 TCGA-CJ-4899-11A-01D-1462-08 g.chr16:30777596G>T c.1106G>T c.(1105-1107)cGc>cTc p.R369L KIRP 16 30775599 30775599 + Missense_Mutation SNP T T C TCGA-GL-7773-01A-11D-2136-08 TCGA-GL-7773-10A-01D-2136-08 g.chr16:30775599T>C c.542T>C c.(541-543)cTg>cCg p.L181P LGG 16 30776312 30776312 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:30776312C>T c.703C>T c.(703-705)Cgt>Tgt p.R235C LGG 16 30780680 30780680 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:30780680G>T c.2421G>T c.(2419-2421)aaG>aaT p.K807N LIHC 16 30774809 30774809 + Missense_Mutation SNP C C G TCGA-2Y-A9HB-01A-11D-A38X-10 TCGA-2Y-A9HB-10A-01D-A38X-10 g.chr16:30774809C>G c.371C>G c.(370-372)gCa>gGa p.A124G LIHC 16 30779293 30779293 + Missense_Mutation SNP G G A TCGA-RC-A6M4-01A-11D-A32G-10 TCGA-RC-A6M4-10A-01D-A32G-10 g.chr16:30779293G>A c.1508G>A c.(1507-1509)cGa>cAa p.R503Q LIHC 16 30783507 30783507 + Missense_Mutation SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr16:30783507A>G c.2825A>G c.(2824-2826)tAc>tGc p.Y942C LUAD 16 30774447 30774447 + Missense_Mutation SNP G G T TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr16:30774447G>T c.141G>T c.(139-141)atG>atT p.M47I LUAD 16 30776581 30776581 + Nonsense_Mutation SNP G G A TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chr16:30776581G>A c.851G>A c.(850-852)tGg>tAg p.W284* LUAD 16 30776605 30776605 + Missense_Mutation SNP G G C TCGA-44-6145-01A-11D-1753-08 TCGA-44-6145-10A-01D-1753-08 g.chr16:30776605G>C c.875G>C c.(874-876)cGa>cCa p.R292P LUAD 16 30777537 30777537 + Silent SNP T T A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr16:30777537T>A c.1047T>A c.(1045-1047)cgT>cgA p.R349R LUAD 16 30778076 30778076 + Silent SNP G G T TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr16:30778076G>T c.1308G>T c.(1306-1308)ggG>ggT p.G436G LUAD 16 30779731 30779731 + Missense_Mutation SNP C C G TCGA-17-Z011-01A-01W-0746-08 TCGA-17-Z011-11A-01W-0746-08 g.chr16:30779731C>G c.1859C>G c.(1858-1860)cCc>cGc p.P620R LUAD 16 30779967 30779967 + Missense_Mutation SNP G G A TCGA-69-8255-01A-11D-2284-08 TCGA-69-8255-10A-01D-2284-08 g.chr16:30779967G>A c.2007G>A c.(2005-2007)atG>atA p.M669I LUAD 16 30780669 30780669 + Missense_Mutation SNP C C T TCGA-78-7542-01A-21D-2063-08 TCGA-78-7542-11A-01D-2063-08 g.chr16:30780669C>T c.2410C>T c.(2410-2412)Cgg>Tgg p.R804W LUSC 16 30773931 30773931 + Missense_Mutation SNP T T C TCGA-18-3415-01A-01D-0983-08 TCGA-18-3415-11A-01D-0983-08 g.chr16:30773931T>C c.65T>C c.(64-66)cTg>cCg p.L22P LUSC 16 30773976 30773976 + De_novo_Start_OutOfFrame SNP G G A TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr16:30773976G>A LUSC 16 30777492 30777492 + Missense_Mutation SNP G G A TCGA-22-5477-01A-01D-1632-08 TCGA-22-5477-11A-11D-1632-08 g.chr16:30777492G>A c.1002G>A c.(1000-1002)atG>atA p.M334I LUSC 16 30779730 30779730 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr16:30779730C>T c.1858C>T c.(1858-1860)Ccc>Tcc p.P620S PAAD 16 30773901 30773902 + Frame_Shift_Ins INS - - C TCGA-XD-AAUG-01A-61D-A40W-08 TCGA-XD-AAUG-10A-01D-A40W-08 g.chr16:30773901_30773902insC c.35_36insC c.(34-39)gacgggfs p.G13fs PAAD 16 30778156 30778156 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:30778156G>A c.1388G>A c.(1387-1389)cGc>cAc p.R463H PAAD 16 30778186 30778186 + Missense_Mutation SNP A A G TCGA-HZ-A8P0-01A-11D-A36O-08 TCGA-HZ-A8P0-10A-01D-A367-08 g.chr16:30778186A>G c.1418A>G c.(1417-1419)aAc>aGc p.N473S PRAD 16 30774767 30774767 + Missense_Mutation SNP G G T TCGA-YL-A8HK-01A-11D-A364-08 TCGA-YL-A8HK-10A-01D-A362-08 g.chr16:30774767G>T c.329G>T c.(328-330)cGa>cTa p.R110L READ 16 30780286 30780286 + Missense_Mutation SNP G G A TCGA-AG-A02G-01A-01W-A00E-09 TCGA-AG-A02G-10A-01W-A00E-09 g.chr16:30780286G>A c.2225G>A c.(2224-2226)cGc>cAc p.R742H SKCM 16 30774532 30774532 + Nonsense_Mutation SNP C C T TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr16:30774532C>T c.226C>T c.(226-228)Cga>Tga p.R76* SKCM 16 30774758 30774758 + Missense_Mutation SNP C C T TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr16:30774758C>T c.320C>T c.(319-321)gCc>gTc p.A107V SKCM 16 30776312 30776312 + Missense_Mutation SNP C C T TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr16:30776312C>T c.703C>T c.(703-705)Cgt>Tgt p.R235C SKCM 16 30777523 30777523 + Silent SNP C C T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr16:30777523C>T c.1033C>T c.(1033-1035)Ctg>Ttg p.L345L SKCM 16 30777704 30777704 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr16:30777704C>T c.1118C>T c.(1117-1119)gCc>gTc p.A373V SKCM 16 30779532 30779532 + Missense_Mutation SNP C C T TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chr16:30779532C>T c.1660C>T c.(1660-1662)Cct>Tct p.P554S SKCM 16 30779532 30779532 + Missense_Mutation SNP C C T TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr16:30779532C>T c.1660C>T c.(1660-1662)Cct>Tct p.P554S SKCM 16 30779533 30779533 + Missense_Mutation SNP C C T TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr16:30779533C>T c.1661C>T c.(1660-1662)cCt>cTt p.P554L SKCM 16 30779804 30779804 + Silent SNP C C A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr16:30779804C>A c.1932C>A c.(1930-1932)acC>acA p.T644T SKCM 16 30779946 30779946 + Silent SNP C C T TCGA-D3-A5GL-06A-11D-A27K-08 TCGA-D3-A5GL-10A-01D-A27N-08 g.chr16:30779946C>T c.1986C>T c.(1984-1986)gcC>gcT p.A662A SKCM 16 30783228 30783228 + Silent SNP C C T TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr16:30783228C>T c.2661C>T c.(2659-2661)atC>atT p.I887I SKCM 16 30783229 30783229 + Nonsense_Mutation SNP C C T TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr16:30783229C>T c.2662C>T c.(2662-2664)Cag>Tag p.Q888* SKCM 16 30785434 30785434 + Silent SNP G G A TCGA-GN-A4U3-06A-11D-A32N-08 TCGA-GN-A4U3-10F-01D-A32N-08 g.chr16:30785434G>A c.3005G>A c.(3004-3006)tGa>tAa p.*1002*

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 30771541 30771541 single base substitution C G upstream_gene_variant BLCA-CN 16 30773848 30773848 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BLCA-CN 16 30773848 30773848 single base substitution C T exon_variant BLCA-CN 16 30773848 30773848 single base substitution C T intron_variant BLCA-CN 16 30773848 30773848 single base substitution C T splice_region_variant BLCA-CN 16 30773848 30773848 single base substitution C T upstream_gene_variant BLCA-CN 16 30775679 30775679 single base substitution G A downstream_gene_variant BLCA-CN 16 30775679 30775679 single base substitution G A exon_variant BLCA-CN 16 30775679 30775679 single base substitution G A intron_variant BLCA-CN 16 30775679 30775679 single base substitution G A missense_variant E208K 622G>A BLCA-CN 16 30775679 30775679 single base substitution G A missense_variant E24K 70G>A BLCA-CN 16 30775679 30775679 single base substitution G A upstream_gene_variant BLCA-CN 16 30779634 30779634 single base substitution G T downstream_gene_variant BLCA-CN 16 30779634 30779634 single base substitution G T exon_variant BLCA-CN 16 30779634 30779634 single base substitution G T missense_variant D280Y 838G>T BLCA-CN 16 30779634 30779634 single base substitution G T missense_variant D488Y 1462G>T BLCA-CN 16 30779634 30779634 single base substitution G T missense_variant D548Y 1642G>T BLCA-CN 16 30779634 30779634 single base substitution G T missense_variant D588Y 1762G>T BLCA-CN 16 30779634 30779634 single base substitution G T upstream_gene_variant BLCA-CN 16 30779775 30779775 single base substitution G A downstream_gene_variant BLCA-CN 16 30779775 30779775 single base substitution G A exon_variant BLCA-CN 16 30779775 30779775 single base substitution G A missense_variant D327N 979G>A BLCA-CN 16 30779775 30779775 single base substitution G A missense_variant D535N 1603G>A BLCA-CN 16 30779775 30779775 single base substitution G A missense_variant D595N 1783G>A BLCA-CN 16 30779775 30779775 single base substitution G A missense_variant D635N 1903G>A BLCA-CN 16 30779775 30779775 single base substitution G A upstream_gene_variant BLCA-US 16 30774850 30774850 single base substitution C G downstream_gene_variant BLCA-US 16 30774850 30774850 single base substitution C G exon_variant BLCA-US 16 30774850 30774850 single base substitution C G intron_variant BLCA-US 16 30774850 30774850 single base substitution C G missense_variant L138V 412C>G BLCA-US 16 30774850 30774850 single base substitution C G upstream_gene_variant BLCA-US 16 30775620 30775620 single base substitution C G downstream_gene_variant BLCA-US 16 30775620 30775620 single base substitution C G exon_variant BLCA-US 16 30775620 30775620 single base substitution C G intron_variant BLCA-US 16 30775620 30775620 single base substitution C G missense_variant S188C 563C>G BLCA-US 16 30775620 30775620 single base substitution C G missense_variant S4C 11C>G BLCA-US 16 30775620 30775620 single base substitution C G upstream_gene_variant BLCA-US 16 30776275 30776275 single base substitution C G downstream_gene_variant BLCA-US 16 30776275 30776275 single base substitution C G exon_variant BLCA-US 16 30776275 30776275 single base substitution C G intron_variant BLCA-US 16 30776275 30776275 single base substitution C G synonymous_variant L222L 666C>G BLCA-US 16 30776275 30776275 single base substitution C G synonymous_variant L38L 114C>G BLCA-US 16 30776275 30776275 single base substitution C G upstream_gene_variant BLCA-US 16 30777495 30777495 single base substitution G A downstream_gene_variant BLCA-US 16 30777495 30777495 single base substitution G A exon_variant BLCA-US 16 30777495 30777495 single base substitution G A intron_variant BLCA-US 16 30777495 30777495 single base substitution G A synonymous_variant L151L 453G>A BLCA-US 16 30777495 30777495 single base substitution G A synonymous_variant L335L 1005G>A BLCA-US 16 30777495 30777495 single base substitution G A upstream_gene_variant BLCA-US 16 30780185 30780185 single base substitution G A downstream_gene_variant BLCA-US 16 30780185 30780185 single base substitution G A exon_variant BLCA-US 16 30780185 30780185 single base substitution G A synonymous_variant R400R 1200G>A BLCA-US 16 30780185 30780185 single base substitution G A synonymous_variant R608R 1824G>A BLCA-US 16 30780185 30780185 single base substitution G A synonymous_variant R668R 2004G>A BLCA-US 16 30780185 30780185 single base substitution G A synonymous_variant R708R 2124G>A BLCA-US 16 30780185 30780185 single base substitution G A upstream_gene_variant BLCA-US 16 30780218 30780218 single base substitution G C downstream_gene_variant BLCA-US 16 30780218 30780218 single base substitution G C exon_variant BLCA-US 16 30780218 30780218 single base substitution G C missense_variant K411N 1233G>C BLCA-US 16 30780218 30780218 single base substitution G C missense_variant K619N 1857G>C BLCA-US 16 30780218 30780218 single base substitution G C missense_variant K679N 2037G>C BLCA-US 16 30780218 30780218 single base substitution G C missense_variant K719N 2157G>C BLCA-US 16 30780218 30780218 single base substitution G C upstream_gene_variant BRCA-EU 16 30768263 30768263 single base substitution C T upstream_gene_variant BRCA-EU 16 30769092 30769092 single base substitution C T upstream_gene_variant BRCA-EU 16 30770630 30770630 single base substitution G A upstream_gene_variant BRCA-EU 16 30770725 30770725 single base substitution C T upstream_gene_variant BRCA-EU 16 30774053 30774053 single base substitution T C intron_variant BRCA-EU 16 30774053 30774053 single base substitution T C upstream_gene_variant BRCA-EU 16 30777155 30777155 single base substitution G A downstream_gene_variant BRCA-EU 16 30777155 30777155 single base substitution G A intron_variant BRCA-EU 16 30777155 30777155 single base substitution G A upstream_gene_variant BRCA-EU 16 30777668 30777668 single base substitution T C downstream_gene_variant BRCA-EU 16 30777668 30777668 single base substitution T C intron_variant BRCA-EU 16 30777668 30777668 single base substitution T C upstream_gene_variant BRCA-EU 16 30778464 30778464 single base substitution G C downstream_gene_variant BRCA-EU 16 30778464 30778464 single base substitution G C intron_variant BRCA-EU 16 30778464 30778464 single base substitution G C upstream_gene_variant BRCA-EU 16 30778594 30778594 single base substitution G C downstream_gene_variant BRCA-EU 16 30778594 30778594 single base substitution G C intron_variant BRCA-EU 16 30778594 30778594 single base substitution G C upstream_gene_variant BRCA-EU 16 30779099 30779099 single base substitution G T downstream_gene_variant BRCA-EU 16 30779099 30779099 single base substitution G T exon_variant BRCA-EU 16 30779099 30779099 single base substitution G T intron_variant BRCA-EU 16 30779099 30779099 single base substitution G T upstream_gene_variant BRCA-EU 16 30779305 30779305 single base substitution A C downstream_gene_variant BRCA-EU 16 30779305 30779305 single base substitution A C exon_variant BRCA-EU 16 30779305 30779305 single base substitution A C missense_variant K199T 596A>C BRCA-EU 16 30779305 30779305 single base substitution A C missense_variant K407T 1220A>C BRCA-EU 16 30779305 30779305 single base substitution A C missense_variant K467T 1400A>C BRCA-EU 16 30779305 30779305 single base substitution A C missense_variant K507T 1520A>C BRCA-EU 16 30779305 30779305 single base substitution A C upstream_gene_variant BRCA-EU 16 30780337 30780337 single base substitution G C downstream_gene_variant BRCA-EU 16 30780337 30780337 single base substitution G C intron_variant BRCA-EU 16 30780337 30780337 single base substitution G C upstream_gene_variant BRCA-EU 16 30780555 30780555 single base substitution G A downstream_gene_variant BRCA-EU 16 30780555 30780555 single base substitution G A exon_variant BRCA-EU 16 30780555 30780555 single base substitution G A missense_variant E458K 1372G>A BRCA-EU 16 30780555 30780555 single base substitution G A missense_variant E666K 1996G>A BRCA-EU 16 30780555 30780555 single base substitution G A missense_variant E726K 2176G>A BRCA-EU 16 30780555 30780555 single base substitution G A missense_variant E766K 2296G>A BRCA-EU 16 30780555 30780555 single base substitution G A upstream_gene_variant BRCA-EU 16 30781114 30781114 single base substitution C T downstream_gene_variant BRCA-EU 16 30781114 30781114 single base substitution C T intron_variant BRCA-EU 16 30781114 30781114 single base substitution C T upstream_gene_variant BRCA-EU 16 30781604 30781604 deletion of <=200bp T - downstream_gene_variant BRCA-EU 16 30781604 30781604 deletion of <=200bp T - intron_variant BRCA-EU 16 30781604 30781604 deletion of <=200bp T - upstream_gene_variant BRCA-EU 16 30781889 30781889 single base substitution G A downstream_gene_variant BRCA-EU 16 30781889 30781889 single base substitution G A intron_variant BRCA-EU 16 30781889 30781889 single base substitution G A upstream_gene_variant BRCA-EU 16 30782037 30782037 single base substitution G T downstream_gene_variant BRCA-EU 16 30782037 30782037 single base substitution G T intron_variant BRCA-EU 16 30782037 30782037 single base substitution G T upstream_gene_variant BRCA-EU 16 30782044 30782044 insertion of <=200bp - T downstream_gene_variant BRCA-EU 16 30782044 30782044 insertion of <=200bp - T intron_variant BRCA-EU 16 30782044 30782044 insertion of <=200bp - T upstream_gene_variant BRCA-EU 16 30784545 30784545 single base substitution A C downstream_gene_variant BRCA-EU 16 30784545 30784545 single base substitution A C intron_variant BRCA-EU 16 30784545 30784545 single base substitution A C upstream_gene_variant BRCA-EU 16 30785863 30785863 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 30785863 30785863 single base substitution C T downstream_gene_variant BRCA-EU 16 30785863 30785863 single base substitution C T exon_variant BRCA-EU 16 30786101 30786101 single base substitution T A 3_prime_UTR_variant BRCA-EU 16 30786101 30786101 single base substitution T A downstream_gene_variant BRCA-EU 16 30786101 30786101 single base substitution T A exon_variant BRCA-EU 16 30786877 30786877 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 30786877 30786877 single base substitution C T downstream_gene_variant BRCA-EU 16 30786877 30786877 single base substitution C T exon_variant BRCA-EU 16 30787324 30787324 single base substitution G T 3_prime_UTR_variant BRCA-EU 16 30787324 30787324 single base substitution G T downstream_gene_variant BRCA-EU 16 30787324 30787324 single base substitution G T exon_variant BRCA-EU 16 30788226 30788226 single base substitution G C downstream_gene_variant BRCA-EU 16 30788264 30788264 single base substitution G A downstream_gene_variant BRCA-EU 16 30791779 30791779 single base substitution G T downstream_gene_variant BRCA-EU 16 30792359 30792359 single base substitution T G downstream_gene_variant BRCA-FR 16 30770630 30770630 single base substitution G A upstream_gene_variant BRCA-FR 16 30781114 30781114 single base substitution C T downstream_gene_variant BRCA-FR 16 30781114 30781114 single base substitution C T intron_variant BRCA-FR 16 30781114 30781114 single base substitution C T upstream_gene_variant BRCA-FR 16 30781889 30781889 single base substitution G A downstream_gene_variant BRCA-FR 16 30781889 30781889 single base substitution G A intron_variant BRCA-FR 16 30781889 30781889 single base substitution G A upstream_gene_variant BRCA-FR 16 30786495 30786495 single base substitution C T 3_prime_UTR_variant BRCA-FR 16 30786495 30786495 single base substitution C T downstream_gene_variant BRCA-FR 16 30786495 30786495 single base substitution C T exon_variant BRCA-FR 16 30788226 30788226 single base substitution G C downstream_gene_variant BRCA-FR 16 30788264 30788264 single base substitution G A downstream_gene_variant BRCA-UK 16 30770725 30770725 single base substitution C T upstream_gene_variant BRCA-UK 16 30774053 30774053 single base substitution T C intron_variant BRCA-UK 16 30774053 30774053 single base substitution T C upstream_gene_variant BRCA-US 16 30768802 30768802 single base substitution T C upstream_gene_variant BRCA-US 16 30770365 30770365 single base substitution A T upstream_gene_variant BRCA-US 16 30771679 30771679 single base substitution C T upstream_gene_variant BRCA-US 16 30772925 30772925 single base substitution G A upstream_gene_variant BRCA-US 16 30774485 30774485 single base substitution C G exon_variant BRCA-US 16 30774485 30774485 single base substitution C G intron_variant BRCA-US 16 30774485 30774485 single base substitution C G missense_variant A60G 179C>G BRCA-US 16 30774485 30774485 single base substitution C G upstream_gene_variant BRCA-US 16 30775646 30775646 single base substitution G C downstream_gene_variant BRCA-US 16 30775646 30775646 single base substitution G C exon_variant BRCA-US 16 30775646 30775646 single base substitution G C intron_variant BRCA-US 16 30775646 30775646 single base substitution G C missense_variant E13Q 37G>C BRCA-US 16 30775646 30775646 single base substitution G C missense_variant E197Q 589G>C BRCA-US 16 30775646 30775646 single base substitution G C upstream_gene_variant BRCA-US 16 30778098 30778098 single base substitution G C downstream_gene_variant BRCA-US 16 30778098 30778098 single base substitution G C exon_variant BRCA-US 16 30778098 30778098 single base substitution G C missense_variant E136Q 406G>C BRCA-US 16 30778098 30778098 single base substitution G C missense_variant E344Q 1030G>C BRCA-US 16 30778098 30778098 single base substitution G C missense_variant E404Q 1210G>C BRCA-US 16 30778098 30778098 single base substitution G C missense_variant E444Q 1330G>C BRCA-US 16 30778098 30778098 single base substitution G C upstream_gene_variant BRCA-US 16 30778177 30778177 single base substitution T A downstream_gene_variant BRCA-US 16 30778177 30778177 single base substitution T A exon_variant BRCA-US 16 30778177 30778177 single base substitution T A missense_variant L162Q 485T>A BRCA-US 16 30778177 30778177 single base substitution T A missense_variant L370Q 1109T>A BRCA-US 16 30778177 30778177 single base substitution T A missense_variant L430Q 1289T>A BRCA-US 16 30778177 30778177 single base substitution T A missense_variant L470Q 1409T>A BRCA-US 16 30778177 30778177 single base substitution T A upstream_gene_variant BRCA-US 16 30779332 30779332 single base substitution G T downstream_gene_variant BRCA-US 16 30779332 30779332 single base substitution G T exon_variant BRCA-US 16 30779332 30779332 single base substitution G T missense_variant G208V 623G>T BRCA-US 16 30779332 30779332 single base substitution G T missense_variant G416V 1247G>T BRCA-US 16 30779332 30779332 single base substitution G T missense_variant G476V 1427G>T BRCA-US 16 30779332 30779332 single base substitution G T missense_variant G516V 1547G>T BRCA-US 16 30779332 30779332 single base substitution G T upstream_gene_variant BRCA-US 16 30779794 30779794 single base substitution T G downstream_gene_variant BRCA-US 16 30779794 30779794 single base substitution T G exon_variant BRCA-US 16 30779794 30779794 single base substitution T G missense_variant V333G 998T>G BRCA-US 16 30779794 30779794 single base substitution T G missense_variant V541G 1622T>G BRCA-US 16 30779794 30779794 single base substitution T G missense_variant V601G 1802T>G BRCA-US 16 30779794 30779794 single base substitution T G missense_variant V641G 1922T>G BRCA-US 16 30779794 30779794 single base substitution T G upstream_gene_variant BRCA-US 16 30780540 30780540 single base substitution A G downstream_gene_variant BRCA-US 16 30780540 30780540 single base substitution A G exon_variant BRCA-US 16 30780540 30780540 single base substitution A G missense_variant T453A 1357A>G BRCA-US 16 30780540 30780540 single base substitution A G missense_variant T661A 1981A>G BRCA-US 16 30780540 30780540 single base substitution A G missense_variant T721A 2161A>G BRCA-US 16 30780540 30780540 single base substitution A G missense_variant T761A 2281A>G BRCA-US 16 30780540 30780540 single base substitution A G upstream_gene_variant BRCA-US 16 30783268 30783268 single base substitution G C downstream_gene_variant BRCA-US 16 30783268 30783268 single base substitution G C exon_variant BRCA-US 16 30783268 30783268 single base substitution G C missense_variant E593Q 1777G>C BRCA-US 16 30783268 30783268 single base substitution G C missense_variant E801Q 2401G>C BRCA-US 16 30783268 30783268 single base substitution G C missense_variant E861Q 2581G>C BRCA-US 16 30783268 30783268 single base substitution G C missense_variant E901Q 2701G>C BRCA-US 16 30783268 30783268 single base substitution G C upstream_gene_variant BTCA-JP 16 30777750 30777750 single base substitution C A downstream_gene_variant BTCA-JP 16 30777750 30777750 single base substitution C A exon_variant BTCA-JP 16 30777750 30777750 single base substitution C A intron_variant BTCA-JP 16 30777750 30777750 single base substitution C A stop_gained Y348* 1044C>A BTCA-JP 16 30777750 30777750 single base substitution C A stop_gained Y388* 1164C>A BTCA-JP 16 30777750 30777750 single base substitution C A upstream_gene_variant BTCA-JP 16 30780294 30780294 single base substitution G A downstream_gene_variant BTCA-JP 16 30780294 30780294 single base substitution G A exon_variant BTCA-JP 16 30780294 30780294 single base substitution G A missense_variant G437S 1309G>A BTCA-JP 16 30780294 30780294 single base substitution G A missense_variant G645S 1933G>A BTCA-JP 16 30780294 30780294 single base substitution G A missense_variant G705S 2113G>A BTCA-JP 16 30780294 30780294 single base substitution G A missense_variant G745S 2233G>A BTCA-JP 16 30780294 30780294 single base substitution G A upstream_gene_variant BTCA-JP 16 30780528 30780528 single base substitution G C downstream_gene_variant BTCA-JP 16 30780528 30780528 single base substitution G C exon_variant BTCA-JP 16 30780528 30780528 single base substitution G C missense_variant E449Q 1345G>C BTCA-JP 16 30780528 30780528 single base substitution G C missense_variant E657Q 1969G>C BTCA-JP 16 30780528 30780528 single base substitution G C missense_variant E717Q 2149G>C BTCA-JP 16 30780528 30780528 single base substitution G C missense_variant E757Q 2269G>C BTCA-JP 16 30780528 30780528 single base substitution G C upstream_gene_variant BTCA-JP 16 30785342 30785342 single base substitution C T downstream_gene_variant BTCA-JP 16 30785342 30785342 single base substitution C T exon_variant BTCA-JP 16 30785342 30785342 single base substitution C T synonymous_variant C663C 1989C>T BTCA-JP 16 30785342 30785342 single base substitution C T synonymous_variant C871C 2613C>T BTCA-JP 16 30785342 30785342 single base substitution C T synonymous_variant C931C 2793C>T BTCA-JP 16 30785342 30785342 single base substitution C T synonymous_variant C971C 2913C>T BTCA-JP 16 30785342 30785342 single base substitution C T upstream_gene_variant BTCA-JP 16 30786210 30786210 single base substitution C T 3_prime_UTR_variant BTCA-JP 16 30786210 30786210 single base substitution C T downstream_gene_variant BTCA-JP 16 30786210 30786210 single base substitution C T exon_variant CESC-US 16 30768370 30768370 single base substitution A C upstream_gene_variant CESC-US 16 30776605 30776605 single base substitution G A downstream_gene_variant CESC-US 16 30776605 30776605 single base substitution G A exon_variant CESC-US 16 30776605 30776605 single base substitution G A intron_variant CESC-US 16 30776605 30776605 single base substitution G A missense_variant R108Q 323G>A CESC-US 16 30776605 30776605 single base substitution G A missense_variant R292Q 875G>A CESC-US 16 30776605 30776605 single base substitution G A upstream_gene_variant CESC-US 16 30777520 30777520 single base substitution G C downstream_gene_variant CESC-US 16 30777520 30777520 single base substitution G C exon_variant CESC-US 16 30777520 30777520 single base substitution G C intron_variant CESC-US 16 30777520 30777520 single base substitution G C missense_variant E160Q 478G>C CESC-US 16 30777520 30777520 single base substitution G C missense_variant E344Q 1030G>C CESC-US 16 30777520 30777520 single base substitution G C upstream_gene_variant CESC-US 16 30778082 30778082 single base substitution G A downstream_gene_variant CESC-US 16 30778082 30778082 single base substitution G A exon_variant CESC-US 16 30778082 30778082 single base substitution G A synonymous_variant Q130Q 390G>A CESC-US 16 30778082 30778082 single base substitution G A synonymous_variant Q338Q 1014G>A CESC-US 16 30778082 30778082 single base substitution G A synonymous_variant Q398Q 1194G>A CESC-US 16 30778082 30778082 single base substitution G A synonymous_variant Q438Q 1314G>A CESC-US 16 30778082 30778082 single base substitution G A upstream_gene_variant CESC-US 16 30778146 30778146 single base substitution G A downstream_gene_variant CESC-US 16 30778146 30778146 single base substitution G A exon_variant CESC-US 16 30778146 30778146 single base substitution G A missense_variant E152K 454G>A CESC-US 16 30778146 30778146 single base substitution G A missense_variant E360K 1078G>A CESC-US 16 30778146 30778146 single base substitution G A missense_variant E420K 1258G>A CESC-US 16 30778146 30778146 single base substitution G A missense_variant E460K 1378G>A CESC-US 16 30778146 30778146 single base substitution G A upstream_gene_variant CESC-US 16 30779455 30779455 single base substitution C G downstream_gene_variant CESC-US 16 30779455 30779455 single base substitution C G exon_variant CESC-US 16 30779455 30779455 single base substitution C G missense_variant S220C 659C>G CESC-US 16 30779455 30779455 single base substitution C G missense_variant S428C 1283C>G CESC-US 16 30779455 30779455 single base substitution C G missense_variant S488C 1463C>G CESC-US 16 30779455 30779455 single base substitution C G missense_variant S528C 1583C>G CESC-US 16 30779455 30779455 single base substitution C G upstream_gene_variant CESC-US 16 30779514 30779514 single base substitution G C downstream_gene_variant CESC-US 16 30779514 30779514 single base substitution G C exon_variant CESC-US 16 30779514 30779514 single base substitution G C missense_variant E240Q 718G>C CESC-US 16 30779514 30779514 single base substitution G C missense_variant E448Q 1342G>C CESC-US 16 30779514 30779514 single base substitution G C missense_variant E508Q 1522G>C CESC-US 16 30779514 30779514 single base substitution G C missense_variant E548Q 1642G>C CESC-US 16 30779514 30779514 single base substitution G C upstream_gene_variant CESC-US 16 30779554 30779554 single base substitution G C downstream_gene_variant CESC-US 16 30779554 30779554 single base substitution G C exon_variant CESC-US 16 30779554 30779554 single base substitution G C missense_variant R253T 758G>C CESC-US 16 30779554 30779554 single base substitution G C missense_variant R461T 1382G>C CESC-US 16 30779554 30779554 single base substitution G C missense_variant R521T 1562G>C CESC-US 16 30779554 30779554 single base substitution G C missense_variant R561T 1682G>C CESC-US 16 30779554 30779554 single base substitution G C upstream_gene_variant CESC-US 16 30780684 30780684 single base substitution G T downstream_gene_variant CESC-US 16 30780684 30780684 single base substitution G T exon_variant CESC-US 16 30780684 30780684 single base substitution G T stop_gained E501* 1501G>T CESC-US 16 30780684 30780684 single base substitution G T stop_gained E709* 2125G>T CESC-US 16 30780684 30780684 single base substitution G T stop_gained E769* 2305G>T CESC-US 16 30780684 30780684 single base substitution G T stop_gained E809* 2425G>T CESC-US 16 30780684 30780684 single base substitution G T upstream_gene_variant CESC-US 16 30783259 30783259 single base substitution C G downstream_gene_variant CESC-US 16 30783259 30783259 single base substitution C G exon_variant CESC-US 16 30783259 30783259 single base substitution C G missense_variant R590G 1768C>G CESC-US 16 30783259 30783259 single base substitution C G missense_variant R798G 2392C>G CESC-US 16 30783259 30783259 single base substitution C G missense_variant R858G 2572C>G CESC-US 16 30783259 30783259 single base substitution C G missense_variant R898G 2692C>G CESC-US 16 30783259 30783259 single base substitution C G upstream_gene_variant COAD-US 16 30771609 30771609 single base substitution A G upstream_gene_variant COAD-US 16 30777733 30777733 single base substitution C T downstream_gene_variant COAD-US 16 30777733 30777733 single base substitution C T exon_variant COAD-US 16 30777733 30777733 single base substitution C T intron_variant COAD-US 16 30777733 30777733 single base substitution C T missense_variant R343W 1027C>T COAD-US 16 30777733 30777733 single base substitution C T missense_variant R383W 1147C>T COAD-US 16 30777733 30777733 single base substitution C T upstream_gene_variant COAD-US 16 30777763 30777763 single base substitution G A downstream_gene_variant COAD-US 16 30777763 30777763 single base substitution G A exon_variant COAD-US 16 30777763 30777763 single base substitution G A intron_variant COAD-US 16 30777763 30777763 single base substitution G A missense_variant A353T 1057G>A COAD-US 16 30777763 30777763 single base substitution G A missense_variant A393T 1177G>A COAD-US 16 30777763 30777763 single base substitution G A missense_variant A85T 253G>A COAD-US 16 30777763 30777763 single base substitution G A upstream_gene_variant COAD-US 16 30777867 30777867 single base substitution C T downstream_gene_variant COAD-US 16 30777867 30777867 single base substitution C T exon_variant COAD-US 16 30777867 30777867 single base substitution C T intron_variant COAD-US 16 30777867 30777867 single base substitution C T synonymous_variant I119I 357C>T COAD-US 16 30777867 30777867 single base substitution C T synonymous_variant I387I 1161C>T COAD-US 16 30777867 30777867 single base substitution C T synonymous_variant I427I 1281C>T COAD-US 16 30777867 30777867 single base substitution C T upstream_gene_variant COAD-US 16 30778119 30778119 single base substitution A G downstream_gene_variant COAD-US 16 30778119 30778119 single base substitution A G exon_variant COAD-US 16 30778119 30778119 single base substitution A G missense_variant T143A 427A>G COAD-US 16 30778119 30778119 single base substitution A G missense_variant T351A 1051A>G COAD-US 16 30778119 30778119 single base substitution A G missense_variant T411A 1231A>G COAD-US 16 30778119 30778119 single base substitution A G missense_variant T451A 1351A>G COAD-US 16 30778119 30778119 single base substitution A G upstream_gene_variant COAD-US 16 30778155 30778155 single base substitution C T downstream_gene_variant COAD-US 16 30778155 30778155 single base substitution C T exon_variant COAD-US 16 30778155 30778155 single base substitution C T missense_variant R155C 463C>T COAD-US 16 30778155 30778155 single base substitution C T missense_variant R363C 1087C>T COAD-US 16 30778155 30778155 single base substitution C T missense_variant R423C 1267C>T COAD-US 16 30778155 30778155 single base substitution C T missense_variant R463C 1387C>T COAD-US 16 30778155 30778155 single base substitution C T upstream_gene_variant COAD-US 16 30779547 30779547 single base substitution G A downstream_gene_variant COAD-US 16 30779547 30779547 single base substitution G A exon_variant COAD-US 16 30779547 30779547 single base substitution G A missense_variant D251N 751G>A COAD-US 16 30779547 30779547 single base substitution G A missense_variant D459N 1375G>A COAD-US 16 30779547 30779547 single base substitution G A missense_variant D519N 1555G>A COAD-US 16 30779547 30779547 single base substitution G A missense_variant D559N 1675G>A COAD-US 16 30779547 30779547 single base substitution G A upstream_gene_variant COAD-US 16 30780626 30780626 single base substitution A G downstream_gene_variant COAD-US 16 30780626 30780626 single base substitution A G exon_variant COAD-US 16 30780626 30780626 single base substitution A G synonymous_variant L481L 1443A>G COAD-US 16 30780626 30780626 single base substitution A G synonymous_variant L689L 2067A>G COAD-US 16 30780626 30780626 single base substitution A G synonymous_variant L749L 2247A>G COAD-US 16 30780626 30780626 single base substitution A G synonymous_variant L789L 2367A>G COAD-US 16 30780626 30780626 single base substitution A G upstream_gene_variant COAD-US 16 30785347 30785347 single base substitution G A downstream_gene_variant COAD-US 16 30785347 30785347 single base substitution G A exon_variant COAD-US 16 30785347 30785347 single base substitution G A missense_variant R665Q 1994G>A COAD-US 16 30785347 30785347 single base substitution G A missense_variant R873Q 2618G>A COAD-US 16 30785347 30785347 single base substitution G A missense_variant R933Q 2798G>A COAD-US 16 30785347 30785347 single base substitution G A missense_variant R973Q 2918G>A COAD-US 16 30785347 30785347 single base substitution G A upstream_gene_variant COCA-CN 16 30773926 30773926 single base substitution G T exon_variant COCA-CN 16 30773926 30773926 single base substitution G T intron_variant COCA-CN 16 30773926 30773926 single base substitution G T missense_variant K20N 60G>T COCA-CN 16 30773926 30773926 single base substitution G T upstream_gene_variant COCA-CN 16 30775714 30775714 single base substitution C A downstream_gene_variant COCA-CN 16 30775714 30775714 single base substitution C A intron_variant COCA-CN 16 30775714 30775714 single base substitution C A splice_region_variant COCA-CN 16 30775714 30775714 single base substitution C A upstream_gene_variant COCA-CN 16 30776332 30776332 single base substitution G A downstream_gene_variant COCA-CN 16 30776332 30776332 single base substitution G A exon_variant COCA-CN 16 30776332 30776332 single base substitution G A intron_variant COCA-CN 16 30776332 30776332 single base substitution G A synonymous_variant Q241Q 723G>A COCA-CN 16 30776332 30776332 single base substitution G A synonymous_variant Q57Q 171G>A COCA-CN 16 30776332 30776332 single base substitution G A upstream_gene_variant COCA-CN 16 30778156 30778156 single base substitution G A downstream_gene_variant COCA-CN 16 30778156 30778156 single base substitution G A exon_variant COCA-CN 16 30778156 30778156 single base substitution G A missense_variant R155H 464G>A COCA-CN 16 30778156 30778156 single base substitution G A missense_variant R363H 1088G>A COCA-CN 16 30778156 30778156 single base substitution G A missense_variant R423H 1268G>A COCA-CN 16 30778156 30778156 single base substitution G A missense_variant R463H 1388G>A COCA-CN 16 30778156 30778156 single base substitution G A upstream_gene_variant COCA-CN 16 30779336 30779336 single base substitution G T downstream_gene_variant COCA-CN 16 30779336 30779336 single base substitution G T missense_variant K209N 627G>T COCA-CN 16 30779336 30779336 single base substitution G T missense_variant K417N 1251G>T COCA-CN 16 30779336 30779336 single base substitution G T missense_variant K477N 1431G>T COCA-CN 16 30779336 30779336 single base substitution G T missense_variant K517N 1551G>T COCA-CN 16 30779336 30779336 single base substitution G T splice_region_variant COCA-CN 16 30779336 30779336 single base substitution G T upstream_gene_variant COCA-CN 16 30779626 30779626 single base substitution C T downstream_gene_variant COCA-CN 16 30779626 30779626 single base substitution C T exon_variant COCA-CN 16 30779626 30779626 single base substitution C T missense_variant S277F 830C>T COCA-CN 16 30779626 30779626 single base substitution C T missense_variant S485F 1454C>T COCA-CN 16 30779626 30779626 single base substitution C T missense_variant S545F 1634C>T COCA-CN 16 30779626 30779626 single base substitution C T missense_variant S585F 1754C>T COCA-CN 16 30779626 30779626 single base substitution C T upstream_gene_variant EOPC-DE 16 30768503 30768503 single base substitution T A upstream_gene_variant ESAD-UK 16 30770633 30770633 single base substitution G A upstream_gene_variant ESAD-UK 16 30770807 30770807 single base substitution C T upstream_gene_variant ESAD-UK 16 30776300 30776300 single base substitution C T downstream_gene_variant ESAD-UK 16 30776300 30776300 single base substitution C T exon_variant ESAD-UK 16 30776300 30776300 single base substitution C T intron_variant ESAD-UK 16 30776300 30776300 single base substitution C T stop_gained R231* 691C>T ESAD-UK 16 30776300 30776300 single base substitution C T stop_gained R47* 139C>T ESAD-UK 16 30776300 30776300 single base substitution C T upstream_gene_variant ESAD-UK 16 30779099 30779099 single base substitution G A downstream_gene_variant ESAD-UK 16 30779099 30779099 single base substitution G A exon_variant ESAD-UK 16 30779099 30779099 single base substitution G A intron_variant ESAD-UK 16 30779099 30779099 single base substitution G A upstream_gene_variant ESAD-UK 16 30779868 30779868 single base substitution G A downstream_gene_variant ESAD-UK 16 30779868 30779868 single base substitution G A intron_variant ESAD-UK 16 30779868 30779868 single base substitution G A upstream_gene_variant ESAD-UK 16 30781439 30781439 insertion of <=200bp - AATG downstream_gene_variant ESAD-UK 16 30781439 30781439 insertion of <=200bp - AATG intron_variant ESAD-UK 16 30781439 30781439 insertion of <=200bp - AATG upstream_gene_variant ESAD-UK 16 30782099 30782099 single base substitution C G downstream_gene_variant ESAD-UK 16 30782099 30782099 single base substitution C G intron_variant ESAD-UK 16 30782099 30782099 single base substitution C G upstream_gene_variant ESAD-UK 16 30783306 30783306 single base substitution G A downstream_gene_variant ESAD-UK 16 30783306 30783306 single base substitution G A intron_variant ESAD-UK 16 30783306 30783306 single base substitution G A upstream_gene_variant ESAD-UK 16 30784281 30784281 single base substitution G A downstream_gene_variant ESAD-UK 16 30784281 30784281 single base substitution G A intron_variant ESAD-UK 16 30784281 30784281 single base substitution G A upstream_gene_variant ESAD-UK 16 30787934 30787934 single base substitution G T downstream_gene_variant ESAD-UK 16 30788709 30788709 single base substitution C A downstream_gene_variant ESAD-UK 16 30790939 30790939 single base substitution G A downstream_gene_variant GBM-US 16 30770347 30770347 single base substitution G C upstream_gene_variant GBM-US 16 30774800 30774800 single base substitution C A downstream_gene_variant GBM-US 16 30774800 30774800 single base substitution C A exon_variant GBM-US 16 30774800 30774800 single base substitution C A intron_variant GBM-US 16 30774800 30774800 single base substitution C A missense_variant A121E 362C>A GBM-US 16 30774800 30774800 single base substitution C A upstream_gene_variant GBM-US 16 30774843 30774843 single base substitution G A downstream_gene_variant GBM-US 16 30774843 30774843 single base substitution G A exon_variant GBM-US 16 30774843 30774843 single base substitution G A intron_variant GBM-US 16 30774843 30774843 single base substitution G A synonymous_variant G135G 405G>A GBM-US 16 30774843 30774843 single base substitution G A upstream_gene_variant GBM-US 16 30783282 30783282 single base substitution C A downstream_gene_variant GBM-US 16 30783282 30783282 single base substitution C A exon_variant GBM-US 16 30783282 30783282 single base substitution C A synonymous_variant L597L 1791C>A GBM-US 16 30783282 30783282 single base substitution C A synonymous_variant L805L 2415C>A GBM-US 16 30783282 30783282 single base substitution C A synonymous_variant L865L 2595C>A GBM-US 16 30783282 30783282 single base substitution C A synonymous_variant L905L 2715C>A GBM-US 16 30783282 30783282 single base substitution C A upstream_gene_variant KIRC-US 16 30768957 30768957 single base substitution C T upstream_gene_variant KIRC-US 16 30773995 30773995 single base substitution C A exon_variant KIRC-US 16 30773995 30773995 single base substitution C A intron_variant KIRC-US 16 30773995 30773995 single base substitution C A synonymous_variant S43S 129C>A KIRC-US 16 30773995 30773995 single base substitution C A upstream_gene_variant KIRC-US 16 30774777 30774777 single base substitution G T downstream_gene_variant KIRC-US 16 30774777 30774777 single base substitution G T exon_variant KIRC-US 16 30774777 30774777 single base substitution G T intron_variant KIRC-US 16 30774777 30774777 single base substitution G T missense_variant E113D 339G>T KIRC-US 16 30774777 30774777 single base substitution G T upstream_gene_variant KIRC-US 16 30776560 30776560 single base substitution C T downstream_gene_variant KIRC-US 16 30776560 30776560 single base substitution C T exon_variant KIRC-US 16 30776560 30776560 single base substitution C T intron_variant KIRC-US 16 30776560 30776560 single base substitution C T missense_variant T277I 830C>T KIRC-US 16 30776560 30776560 single base substitution C T missense_variant T93I 278C>T KIRC-US 16 30776560 30776560 single base substitution C T upstream_gene_variant KIRC-US 16 30777596 30777596 single base substitution G T downstream_gene_variant KIRC-US 16 30777596 30777596 single base substitution G T exon_variant KIRC-US 16 30777596 30777596 single base substitution G T intron_variant KIRC-US 16 30777596 30777596 single base substitution G T missense_variant R369L 1106G>T KIRC-US 16 30777596 30777596 single base substitution G T upstream_gene_variant KIRP-US 16 30775599 30775599 single base substitution T C 5_prime_UTR_variant KIRP-US 16 30775599 30775599 single base substitution T C downstream_gene_variant KIRP-US 16 30775599 30775599 single base substitution T C exon_variant KIRP-US 16 30775599 30775599 single base substitution T C intron_variant KIRP-US 16 30775599 30775599 single base substitution T C missense_variant L181P 542T>C KIRP-US 16 30775599 30775599 single base substitution T C upstream_gene_variant KIRP-US 16 30776526 30776526 single base substitution A T downstream_gene_variant KIRP-US 16 30776526 30776526 single base substitution A T exon_variant KIRP-US 16 30776526 30776526 single base substitution A T intron_variant KIRP-US 16 30776526 30776526 single base substitution A T missense_variant T266S 796A>T KIRP-US 16 30776526 30776526 single base substitution A T missense_variant T82S 244A>T KIRP-US 16 30776526 30776526 single base substitution A T upstream_gene_variant LICA-CN 16 30774514 30774514 single base substitution G T exon_variant LICA-CN 16 30774514 30774514 single base substitution G T intron_variant LICA-CN 16 30774514 30774514 single base substitution G T stop_gained E70* 208G>T LICA-CN 16 30774514 30774514 single base substitution G T upstream_gene_variant LICA-CN 16 30774862 30774862 single base substitution G T downstream_gene_variant LICA-CN 16 30774862 30774862 single base substitution G T exon_variant LICA-CN 16 30774862 30774862 single base substitution G T intron_variant LICA-CN 16 30774862 30774862 single base substitution G T missense_variant G142W 424G>T LICA-CN 16 30774862 30774862 single base substitution G T upstream_gene_variant LICA-FR 16 30775606 30775606 single base substitution C T 5_prime_UTR_variant LICA-FR 16 30775606 30775606 single base substitution C T downstream_gene_variant LICA-FR 16 30775606 30775606 single base substitution C T exon_variant LICA-FR 16 30775606 30775606 single base substitution C T intron_variant LICA-FR 16 30775606 30775606 single base substitution C T synonymous_variant G183G 549C>T LICA-FR 16 30775606 30775606 single base substitution C T upstream_gene_variant LICA-FR 16 30780014 30780014 single base substitution A C downstream_gene_variant LICA-FR 16 30780014 30780014 single base substitution A C exon_variant LICA-FR 16 30780014 30780014 single base substitution A C missense_variant D377A 1130A>C LICA-FR 16 30780014 30780014 single base substitution A C missense_variant D585A 1754A>C LICA-FR 16 30780014 30780014 single base substitution A C missense_variant D645A 1934A>C LICA-FR 16 30780014 30780014 single base substitution A C missense_variant D685A 2054A>C LICA-FR 16 30780014 30780014 single base substitution A C upstream_gene_variant LIHC-US 16 30768227 30768227 single base substitution C T upstream_gene_variant LIHC-US 16 30771751 30771751 single base substitution A T upstream_gene_variant LINC-JP 16 30768493 30768499 deletion of <=200bp CTCTGGC - upstream_gene_variant LINC-JP 16 30779676 30779676 single base substitution C T downstream_gene_variant LINC-JP 16 30779676 30779676 single base substitution C T exon_variant LINC-JP 16 30779676 30779676 single base substitution C T missense_variant R294W 880C>T LINC-JP 16 30779676 30779676 single base substitution C T missense_variant R502W 1504C>T LINC-JP 16 30779676 30779676 single base substitution C T missense_variant R562W 1684C>T LINC-JP 16 30779676 30779676 single base substitution C T missense_variant R602W 1804C>T LINC-JP 16 30779676 30779676 single base substitution C T upstream_gene_variant LIRI-JP 16 30772260 30772260 single base substitution C T upstream_gene_variant LIRI-JP 16 30775238 30775238 single base substitution A T downstream_gene_variant LIRI-JP 16 30775238 30775238 single base substitution A T intron_variant LIRI-JP 16 30775238 30775238 single base substitution A T upstream_gene_variant LIRI-JP 16 30775575 30775575 single base substitution G A downstream_gene_variant LIRI-JP 16 30775575 30775575 single base substitution G A exon_variant LIRI-JP 16 30775575 30775575 single base substitution G A intron_variant LIRI-JP 16 30775575 30775575 single base substitution G A missense_variant S173N 518G>A LIRI-JP 16 30775575 30775575 single base substitution G A upstream_gene_variant LIRI-JP 16 30775915 30775915 single base substitution G A downstream_gene_variant LIRI-JP 16 30775915 30775915 single base substitution G A intron_variant LIRI-JP 16 30775915 30775915 single base substitution G A upstream_gene_variant LIRI-JP 16 30776723 30776723 single base substitution G T downstream_gene_variant LIRI-JP 16 30776723 30776723 single base substitution G T intron_variant LIRI-JP 16 30776723 30776723 single base substitution G T upstream_gene_variant LIRI-JP 16 30779821 30779821 single base substitution A T downstream_gene_variant LIRI-JP 16 30779821 30779821 single base substitution A T exon_variant LIRI-JP 16 30779821 30779821 single base substitution A T missense_variant E342V 1025A>T LIRI-JP 16 30779821 30779821 single base substitution A T missense_variant E550V 1649A>T LIRI-JP 16 30779821 30779821 single base substitution A T missense_variant E610V 1829A>T LIRI-JP 16 30779821 30779821 single base substitution A T missense_variant E650V 1949A>T LIRI-JP 16 30779821 30779821 single base substitution A T upstream_gene_variant LIRI-JP 16 30781796 30781796 single base substitution T C downstream_gene_variant LIRI-JP 16 30781796 30781796 single base substitution T C intron_variant LIRI-JP 16 30781796 30781796 single base substitution T C upstream_gene_variant LIRI-JP 16 30784937 30784937 single base substitution C T intron_variant LIRI-JP 16 30784937 30784937 single base substitution C T upstream_gene_variant LIRI-JP 16 30789281 30789281 single base substitution G A downstream_gene_variant LIRI-JP 16 30789735 30789735 single base substitution T A downstream_gene_variant LIRI-JP 16 30789746 30789746 single base substitution T C downstream_gene_variant LIRI-JP 16 30790274 30790274 single base substitution A G downstream_gene_variant LIRI-JP 16 30792205 30792205 single base substitution G T downstream_gene_variant LUSC-KR 16 30768286 30768286 single base substitution G C upstream_gene_variant LUSC-KR 16 30773798 30773798 single base substitution G C intron_variant LUSC-KR 16 30773798 30773798 single base substitution G C splice_region_variant LUSC-KR 16 30773798 30773798 single base substitution G C upstream_gene_variant LUSC-KR 16 30775787 30775787 single base substitution C G downstream_gene_variant LUSC-KR 16 30775787 30775787 single base substitution C G intron_variant LUSC-KR 16 30775787 30775787 single base substitution C G upstream_gene_variant LUSC-KR 16 30780424 30780424 single base substitution C T downstream_gene_variant LUSC-KR 16 30780424 30780424 single base substitution C T intron_variant LUSC-KR 16 30780424 30780424 single base substitution C T upstream_gene_variant LUSC-KR 16 30781829 30781829 single base substitution G T downstream_gene_variant LUSC-KR 16 30781829 30781829 single base substitution G T intron_variant LUSC-KR 16 30781829 30781829 single base substitution G T upstream_gene_variant LUSC-KR 16 30781830 30781830 single base substitution C A downstream_gene_variant LUSC-KR 16 30781830 30781830 single base substitution C A intron_variant LUSC-KR 16 30781830 30781830 single base substitution C A upstream_gene_variant LUSC-KR 16 30792334 30792334 single base substitution C G downstream_gene_variant LUSC-US 16 30770363 30770363 single base substitution C G upstream_gene_variant LUSC-US 16 30771025 30771025 single base substitution C G upstream_gene_variant LUSC-US 16 30771646 30771646 single base substitution G T upstream_gene_variant LUSC-US 16 30773931 30773931 single base substitution T C exon_variant LUSC-US 16 30773931 30773931 single base substitution T C intron_variant LUSC-US 16 30773931 30773931 single base substitution T C missense_variant L22P 65T>C LUSC-US 16 30773931 30773931 single base substitution T C upstream_gene_variant LUSC-US 16 30773976 30773976 single base substitution G A exon_variant LUSC-US 16 30773976 30773976 single base substitution G A intron_variant LUSC-US 16 30773976 30773976 single base substitution G A missense_variant R37H 110G>A LUSC-US 16 30773976 30773976 single base substitution G A upstream_gene_variant LUSC-US 16 30777492 30777492 single base substitution G A downstream_gene_variant LUSC-US 16 30777492 30777492 single base substitution G A exon_variant LUSC-US 16 30777492 30777492 single base substitution G A intron_variant LUSC-US 16 30777492 30777492 single base substitution G A missense_variant M150I 450G>A LUSC-US 16 30777492 30777492 single base substitution G A missense_variant M334I 1002G>A LUSC-US 16 30777492 30777492 single base substitution G A upstream_gene_variant LUSC-US 16 30779730 30779730 single base substitution C T downstream_gene_variant LUSC-US 16 30779730 30779730 single base substitution C T exon_variant LUSC-US 16 30779730 30779730 single base substitution C T missense_variant P312S 934C>T LUSC-US 16 30779730 30779730 single base substitution C T missense_variant P520S 1558C>T LUSC-US 16 30779730 30779730 single base substitution C T missense_variant P580S 1738C>T LUSC-US 16 30779730 30779730 single base substitution C T missense_variant P620S 1858C>T LUSC-US 16 30779730 30779730 single base substitution C T upstream_gene_variant MALY-DE 16 30768503 30768503 single base substitution T A upstream_gene_variant MALY-DE 16 30770700 30770700 single base substitution C T upstream_gene_variant MALY-DE 16 30772474 30772474 single base substitution A G upstream_gene_variant MALY-DE 16 30777220 30777220 single base substitution T C downstream_gene_variant MALY-DE 16 30777220 30777220 single base substitution T C intron_variant MALY-DE 16 30777220 30777220 single base substitution T C upstream_gene_variant MALY-DE 16 30788507 30788507 single base substitution G T downstream_gene_variant MELA-AU 16 30768117 30768117 single base substitution C T upstream_gene_variant MELA-AU 16 30768124 30768125 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 30768207 30768207 single base substitution T C upstream_gene_variant MELA-AU 16 30770084 30770084 single base substitution C A upstream_gene_variant MELA-AU 16 30770260 30770260 single base substitution C T upstream_gene_variant MELA-AU 16 30770425 30770425 single base substitution G A upstream_gene_variant MELA-AU 16 30770818 30770818 single base substitution C T upstream_gene_variant MELA-AU 16 30771108 30771108 single base substitution C T upstream_gene_variant MELA-AU 16 30772247 30772247 single base substitution A G upstream_gene_variant MELA-AU 16 30773207 30773207 single base substitution G C 5_prime_UTR_variant MELA-AU 16 30773207 30773207 single base substitution G C upstream_gene_variant MELA-AU 16 30773502 30773502 single base substitution C T 5_prime_UTR_variant MELA-AU 16 30773502 30773502 single base substitution C T intron_variant MELA-AU 16 30773502 30773502 single base substitution C T upstream_gene_variant MELA-AU 16 30773586 30773587 multiple base substitution (>=2bp and <=200bp) CC AT 5_prime_UTR_variant MELA-AU 16 30773586 30773587 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 16 30773586 30773587 multiple base substitution (>=2bp and <=200bp) CC AT upstream_gene_variant MELA-AU 16 30773595 30773595 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 16 30773595 30773595 single base substitution C T intron_variant MELA-AU 16 30773595 30773595 single base substitution C T upstream_gene_variant MELA-AU 16 30774192 30774192 single base substitution C T intron_variant MELA-AU 16 30774192 30774192 single base substitution C T upstream_gene_variant MELA-AU 16 30774430 30774430 single base substitution C T intron_variant MELA-AU 16 30774430 30774430 single base substitution C T upstream_gene_variant MELA-AU 16 30774731 30774731 single base substitution C T intron_variant MELA-AU 16 30774731 30774731 single base substitution C T splice_region_variant MELA-AU 16 30774731 30774731 single base substitution C T upstream_gene_variant MELA-AU 16 30775545 30775545 single base substitution T A downstream_gene_variant MELA-AU 16 30775545 30775545 single base substitution T A exon_variant MELA-AU 16 30775545 30775545 single base substitution T A intron_variant MELA-AU 16 30775545 30775545 single base substitution T A stop_gained L163* 488T>A MELA-AU 16 30775545 30775545 single base substitution T A upstream_gene_variant MELA-AU 16 30775559 30775559 single base substitution G T downstream_gene_variant MELA-AU 16 30775559 30775559 single base substitution G T exon_variant MELA-AU 16 30775559 30775559 single base substitution G T intron_variant MELA-AU 16 30775559 30775559 single base substitution G T missense_variant A168S 502G>T MELA-AU 16 30775559 30775559 single base substitution G T upstream_gene_variant MELA-AU 16 30775778 30775778 single base substitution C T downstream_gene_variant MELA-AU 16 30775778 30775778 single base substitution C T intron_variant MELA-AU 16 30775778 30775778 single base substitution C T upstream_gene_variant MELA-AU 16 30776035 30776035 single base substitution C T downstream_gene_variant MELA-AU 16 30776035 30776035 single base substitution C T intron_variant MELA-AU 16 30776035 30776035 single base substitution C T upstream_gene_variant MELA-AU 16 30776402 30776402 single base substitution G A downstream_gene_variant MELA-AU 16 30776402 30776402 single base substitution G A intron_variant MELA-AU 16 30776402 30776402 single base substitution G A upstream_gene_variant MELA-AU 16 30776439 30776439 single base substitution G A downstream_gene_variant MELA-AU 16 30776439 30776439 single base substitution G A intron_variant MELA-AU 16 30776439 30776439 single base substitution G A upstream_gene_variant MELA-AU 16 30776707 30776707 single base substitution C T downstream_gene_variant MELA-AU 16 30776707 30776707 single base substitution C T intron_variant MELA-AU 16 30776707 30776707 single base substitution C T upstream_gene_variant MELA-AU 16 30777419 30777419 single base substitution G T downstream_gene_variant MELA-AU 16 30777419 30777419 single base substitution G T intron_variant MELA-AU 16 30777419 30777419 single base substitution G T upstream_gene_variant MELA-AU 16 30777422 30777422 single base substitution G T downstream_gene_variant MELA-AU 16 30777422 30777422 single base substitution G T intron_variant MELA-AU 16 30777422 30777422 single base substitution G T upstream_gene_variant MELA-AU 16 30777616 30777616 single base substitution A G downstream_gene_variant MELA-AU 16 30777616 30777616 single base substitution A G intron_variant MELA-AU 16 30777616 30777616 single base substitution A G upstream_gene_variant MELA-AU 16 30777665 30777665 single base substitution C T downstream_gene_variant MELA-AU 16 30777665 30777665 single base substitution C T intron_variant MELA-AU 16 30777665 30777665 single base substitution C T upstream_gene_variant MELA-AU 16 30777705 30777705 single base substitution C T downstream_gene_variant MELA-AU 16 30777705 30777705 single base substitution C T exon_variant MELA-AU 16 30777705 30777705 single base substitution C T intron_variant MELA-AU 16 30777705 30777705 single base substitution C T synonymous_variant A333A 999C>T MELA-AU 16 30777705 30777705 single base substitution C T synonymous_variant A373A 1119C>T MELA-AU 16 30777705 30777705 single base substitution C T upstream_gene_variant MELA-AU 16 30778910 30778910 single base substitution G A downstream_gene_variant MELA-AU 16 30778910 30778910 single base substitution G A intron_variant MELA-AU 16 30778910 30778910 single base substitution G A upstream_gene_variant MELA-AU 16 30779107 30779107 single base substitution C T downstream_gene_variant MELA-AU 16 30779107 30779107 single base substitution C T exon_variant MELA-AU 16 30779107 30779107 single base substitution C T intron_variant MELA-AU 16 30779107 30779107 single base substitution C T upstream_gene_variant MELA-AU 16 30779226 30779226 single base substitution C G downstream_gene_variant MELA-AU 16 30779226 30779226 single base substitution C G exon_variant MELA-AU 16 30779226 30779226 single base substitution C G missense_variant R173G 517C>G MELA-AU 16 30779226 30779226 single base substitution C G missense_variant R381G 1141C>G MELA-AU 16 30779226 30779226 single base substitution C G missense_variant R441G 1321C>G MELA-AU 16 30779226 30779226 single base substitution C G missense_variant R481G 1441C>G MELA-AU 16 30779226 30779226 single base substitution C G upstream_gene_variant MELA-AU 16 30779621 30779621 single base substitution C T downstream_gene_variant MELA-AU 16 30779621 30779621 single base substitution C T exon_variant MELA-AU 16 30779621 30779621 single base substitution C T synonymous_variant V275V 825C>T MELA-AU 16 30779621 30779621 single base substitution C T synonymous_variant V483V 1449C>T MELA-AU 16 30779621 30779621 single base substitution C T synonymous_variant V543V 1629C>T MELA-AU 16 30779621 30779621 single base substitution C T synonymous_variant V583V 1749C>T MELA-AU 16 30779621 30779621 single base substitution C T upstream_gene_variant MELA-AU 16 30780027 30780027 single base substitution C T downstream_gene_variant MELA-AU 16 30780027 30780027 single base substitution C T exon_variant MELA-AU 16 30780027 30780027 single base substitution C T synonymous_variant L381L 1143C>T MELA-AU 16 30780027 30780027 single base substitution C T synonymous_variant L589L 1767C>T MELA-AU 16 30780027 30780027 single base substitution C T synonymous_variant L649L 1947C>T MELA-AU 16 30780027 30780027 single base substitution C T synonymous_variant L689L 2067C>T MELA-AU 16 30780027 30780027 single base substitution C T upstream_gene_variant MELA-AU 16 30780335 30780335 single base substitution C T downstream_gene_variant MELA-AU 16 30780335 30780335 single base substitution C T intron_variant MELA-AU 16 30780335 30780335 single base substitution C T upstream_gene_variant MELA-AU 16 30781652 30781652 single base substitution C T downstream_gene_variant MELA-AU 16 30781652 30781652 single base substitution C T intron_variant MELA-AU 16 30781652 30781652 single base substitution C T upstream_gene_variant MELA-AU 16 30782266 30782266 single base substitution C T downstream_gene_variant MELA-AU 16 30782266 30782266 single base substitution C T intron_variant MELA-AU 16 30782266 30782266 single base substitution C T upstream_gene_variant MELA-AU 16 30782859 30782859 single base substitution A G downstream_gene_variant MELA-AU 16 30782859 30782859 single base substitution A G intron_variant MELA-AU 16 30782859 30782859 single base substitution A G upstream_gene_variant MELA-AU 16 30782913 30782913 single base substitution G A downstream_gene_variant MELA-AU 16 30782913 30782913 single base substitution G A intron_variant MELA-AU 16 30782913 30782913 single base substitution G A upstream_gene_variant MELA-AU 16 30783952 30783952 single base substitution G A downstream_gene_variant MELA-AU 16 30783952 30783952 single base substitution G A intron_variant MELA-AU 16 30783952 30783952 single base substitution G A upstream_gene_variant MELA-AU 16 30784304 30784305 multiple base substitution (>=2bp and <=200bp) TC GT downstream_gene_variant MELA-AU 16 30784304 30784305 multiple base substitution (>=2bp and <=200bp) TC GT intron_variant MELA-AU 16 30784304 30784305 multiple base substitution (>=2bp and <=200bp) TC GT upstream_gene_variant MELA-AU 16 30785363 30785364 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 30785363 30785364 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 16 30785363 30785364 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant AR670AC MELA-AU 16 30785363 30785364 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant AR878AC MELA-AU 16 30785363 30785364 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant AR938AC MELA-AU 16 30785363 30785364 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant AR978AC MELA-AU 16 30785363 30785364 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 30786446 30786446 single base substitution C T 3_prime_UTR_variant MELA-AU 16 30786446 30786446 single base substitution C T downstream_gene_variant MELA-AU 16 30786446 30786446 single base substitution C T exon_variant MELA-AU 16 30786628 30786628 single base substitution G A 3_prime_UTR_variant MELA-AU 16 30786628 30786628 single base substitution G A downstream_gene_variant MELA-AU 16 30786628 30786628 single base substitution G A exon_variant MELA-AU 16 30787762 30787763 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 30789041 30789041 single base substitution G A downstream_gene_variant MELA-AU 16 30789144 30789144 single base substitution C T downstream_gene_variant MELA-AU 16 30789184 30789184 single base substitution T A downstream_gene_variant MELA-AU 16 30789273 30789273 single base substitution G A downstream_gene_variant MELA-AU 16 30789901 30789901 single base substitution T A downstream_gene_variant MELA-AU 16 30790561 30790561 single base substitution T A downstream_gene_variant MELA-AU 16 30791434 30791435 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 30792033 30792033 single base substitution C T downstream_gene_variant ORCA-IN 16 30768311 30768311 single base substitution G T upstream_gene_variant ORCA-IN 16 30771680 30771680 single base substitution G C upstream_gene_variant ORCA-IN 16 30772950 30772950 single base substitution C A upstream_gene_variant ORCA-IN 16 30777100 30777100 single base substitution G A downstream_gene_variant ORCA-IN 16 30777100 30777100 single base substitution G A intron_variant ORCA-IN 16 30777100 30777100 single base substitution G A upstream_gene_variant ORCA-IN 16 30778759 30778759 single base substitution G A downstream_gene_variant ORCA-IN 16 30778759 30778759 single base substitution G A intron_variant ORCA-IN 16 30778759 30778759 single base substitution G A upstream_gene_variant ORCA-IN 16 30779464 30779464 single base substitution A G downstream_gene_variant ORCA-IN 16 30779464 30779464 single base substitution A G exon_variant ORCA-IN 16 30779464 30779464 single base substitution A G missense_variant N223S 668A>G ORCA-IN 16 30779464 30779464 single base substitution A G missense_variant N431S 1292A>G ORCA-IN 16 30779464 30779464 single base substitution A G missense_variant N491S 1472A>G ORCA-IN 16 30779464 30779464 single base substitution A G missense_variant N531S 1592A>G ORCA-IN 16 30779464 30779464 single base substitution A G upstream_gene_variant ORCA-IN 16 30783429 30783429 single base substitution G A downstream_gene_variant ORCA-IN 16 30783429 30783429 single base substitution G A exon_variant ORCA-IN 16 30783429 30783429 single base substitution G A missense_variant R608Q 1823G>A ORCA-IN 16 30783429 30783429 single base substitution G A missense_variant R816Q 2447G>A ORCA-IN 16 30783429 30783429 single base substitution G A missense_variant R876Q 2627G>A ORCA-IN 16 30783429 30783429 single base substitution G A missense_variant R916Q 2747G>A ORCA-IN 16 30783429 30783429 single base substitution G A upstream_gene_variant ORCA-IN 16 30785347 30785347 deletion of <=200bp G - downstream_gene_variant ORCA-IN 16 30785347 30785347 deletion of <=200bp G - exon_variant ORCA-IN 16 30785347 30785347 deletion of <=200bp G - frameshift_variant R665 ORCA-IN 16 30785347 30785347 deletion of <=200bp G - frameshift_variant R873 ORCA-IN 16 30785347 30785347 deletion of <=200bp G - frameshift_variant R933 ORCA-IN 16 30785347 30785347 deletion of <=200bp G - frameshift_variant R973 ORCA-IN 16 30785347 30785347 deletion of <=200bp G - upstream_gene_variant OV-AU 16 30770896 30770896 single base substitution G A upstream_gene_variant OV-AU 16 30771142 30771142 single base substitution G T upstream_gene_variant OV-AU 16 30773374 30773374 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant OV-AU 16 30773374 30773374 single base substitution T C splice_donor_variant OV-AU 16 30773374 30773374 single base substitution T C upstream_gene_variant OV-AU 16 30780543 30780543 single base substitution G C downstream_gene_variant OV-AU 16 30780543 30780543 single base substitution G C exon_variant OV-AU 16 30780543 30780543 single base substitution G C missense_variant G454R 1360G>C OV-AU 16 30780543 30780543 single base substitution G C missense_variant G662R 1984G>C OV-AU 16 30780543 30780543 single base substitution G C missense_variant G722R 2164G>C OV-AU 16 30780543 30780543 single base substitution G C missense_variant G762R 2284G>C OV-AU 16 30780543 30780543 single base substitution G C upstream_gene_variant PACA-AU 16 30776567 30776567 single base substitution G T downstream_gene_variant PACA-AU 16 30776567 30776567 single base substitution G T exon_variant PACA-AU 16 30776567 30776567 single base substitution G T intron_variant PACA-AU 16 30776567 30776567 single base substitution G T synonymous_variant V279V 837G>T PACA-AU 16 30776567 30776567 single base substitution G T synonymous_variant V95V 285G>T PACA-AU 16 30776567 30776567 single base substitution G T upstream_gene_variant PACA-AU 16 30785812 30785812 single base substitution G A 3_prime_UTR_variant PACA-AU 16 30785812 30785812 single base substitution G A downstream_gene_variant PACA-AU 16 30785812 30785812 single base substitution G A exon_variant PACA-AU 16 30789247 30789247 single base substitution C G downstream_gene_variant PACA-CA 16 30770140 30770140 single base substitution G C upstream_gene_variant PACA-CA 16 30779357 30779357 single base substitution G A downstream_gene_variant PACA-CA 16 30779357 30779357 single base substitution G A intron_variant PACA-CA 16 30779357 30779357 single base substitution G A upstream_gene_variant PACA-CA 16 30781438 30781438 insertion of <=200bp - AATG downstream_gene_variant PACA-CA 16 30781438 30781438 insertion of <=200bp - AATG intron_variant PACA-CA 16 30781438 30781438 insertion of <=200bp - AATG upstream_gene_variant PACA-CA 16 30786674 30786674 single base substitution G A 3_prime_UTR_variant PACA-CA 16 30786674 30786674 single base substitution G A downstream_gene_variant PACA-CA 16 30786674 30786674 single base substitution G A exon_variant PACA-CA 16 30789495 30789495 single base substitution C T downstream_gene_variant PACA-CA 16 30790541 30790541 single base substitution G A downstream_gene_variant PAEN-AU 16 30782030 30782030 single base substitution T G downstream_gene_variant PAEN-AU 16 30782030 30782030 single base substitution T G intron_variant PAEN-AU 16 30782030 30782030 single base substitution T G upstream_gene_variant PAEN-IT 16 30782870 30782870 single base substitution G A downstream_gene_variant PAEN-IT 16 30782870 30782870 single base substitution G A intron_variant PAEN-IT 16 30782870 30782870 single base substitution G A upstream_gene_variant PBCA-DE 16 30768503 30768503 single base substitution T A upstream_gene_variant PBCA-DE 16 30779490 30779490 single base substitution G A downstream_gene_variant PBCA-DE 16 30779490 30779490 single base substitution G A exon_variant PBCA-DE 16 30779490 30779490 single base substitution G A missense_variant V232I 694G>A PBCA-DE 16 30779490 30779490 single base substitution G A missense_variant V440I 1318G>A PBCA-DE 16 30779490 30779490 single base substitution G A missense_variant V500I 1498G>A PBCA-DE 16 30779490 30779490 single base substitution G A missense_variant V540I 1618G>A PBCA-DE 16 30779490 30779490 single base substitution G A upstream_gene_variant PBCA-DE 16 30783489 30783491 deletion of <=200bp AGG - downstream_gene_variant PBCA-DE 16 30783489 30783491 deletion of <=200bp AGG - exon_variant PBCA-DE 16 30783489 30783491 deletion of <=200bp AGG - inframe_deletion QE628Q PBCA-DE 16 30783489 30783491 deletion of <=200bp AGG - inframe_deletion QE836Q PBCA-DE 16 30783489 30783491 deletion of <=200bp AGG - inframe_deletion QE896Q PBCA-DE 16 30783489 30783491 deletion of <=200bp AGG - inframe_deletion QE936Q PBCA-DE 16 30783489 30783491 deletion of <=200bp AGG - upstream_gene_variant PBCA-DE 16 30784588 30784588 single base substitution G A downstream_gene_variant PBCA-DE 16 30784588 30784588 single base substitution G A intron_variant PBCA-DE 16 30784588 30784588 single base substitution G A upstream_gene_variant PRAD-CA 16 30780015 30780015 single base substitution T C downstream_gene_variant PRAD-CA 16 30780015 30780015 single base substitution T C exon_variant PRAD-CA 16 30780015 30780015 single base substitution T C synonymous_variant D377D 1131T>C PRAD-CA 16 30780015 30780015 single base substitution T C synonymous_variant D585D 1755T>C PRAD-CA 16 30780015 30780015 single base substitution T C synonymous_variant D645D 1935T>C PRAD-CA 16 30780015 30780015 single base substitution T C synonymous_variant D685D 2055T>C PRAD-CA 16 30780015 30780015 single base substitution T C upstream_gene_variant PRAD-CA 16 30790586 30790586 single base substitution C A downstream_gene_variant PRAD-UK 16 30774279 30774279 single base substitution G T intron_variant PRAD-UK 16 30774279 30774279 single base substitution G T upstream_gene_variant PRAD-UK 16 30774280 30774280 single base substitution C T intron_variant PRAD-UK 16 30774280 30774280 single base substitution C T upstream_gene_variant READ-US 16 30774490 30774490 single base substitution C T exon_variant READ-US 16 30774490 30774490 single base substitution C T intron_variant READ-US 16 30774490 30774490 single base substitution C T missense_variant R62W 184C>T READ-US 16 30774490 30774490 single base substitution C T upstream_gene_variant RECA-EU 16 30770443 30770443 single base substitution G A upstream_gene_variant RECA-EU 16 30770444 30770444 single base substitution A T upstream_gene_variant RECA-EU 16 30772578 30772578 single base substitution G A upstream_gene_variant RECA-EU 16 30772579 30772579 single base substitution C G upstream_gene_variant RECA-EU 16 30774052 30774052 single base substitution C T intron_variant RECA-EU 16 30774052 30774052 single base substitution C T upstream_gene_variant RECA-EU 16 30778594 30778594 single base substitution G A downstream_gene_variant RECA-EU 16 30778594 30778594 single base substitution G A intron_variant RECA-EU 16 30778594 30778594 single base substitution G A upstream_gene_variant RECA-EU 16 30785152 30785152 single base substitution G C exon_variant RECA-EU 16 30785152 30785152 single base substitution G C intron_variant RECA-EU 16 30785152 30785152 single base substitution G C upstream_gene_variant SKCA-BR 16 30773054 30773054 single base substitution T G upstream_gene_variant SKCA-BR 16 30776747 30776747 single base substitution T C downstream_gene_variant SKCA-BR 16 30776747 30776747 single base substitution T C intron_variant SKCA-BR 16 30776747 30776747 single base substitution T C missense_variant L123P 368T>C SKCA-BR 16 30776747 30776747 single base substitution T C missense_variant L307P 920T>C SKCA-BR 16 30776747 30776747 single base substitution T C splice_region_variant SKCA-BR 16 30776747 30776747 single base substitution T C upstream_gene_variant SKCA-BR 16 30777505 30777505 single base substitution T C downstream_gene_variant SKCA-BR 16 30777505 30777505 single base substitution T C exon_variant SKCA-BR 16 30777505 30777505 single base substitution T C intron_variant SKCA-BR 16 30777505 30777505 single base substitution T C synonymous_variant L155L 463T>C SKCA-BR 16 30777505 30777505 single base substitution T C synonymous_variant L339L 1015T>C SKCA-BR 16 30777505 30777505 single base substitution T C upstream_gene_variant SKCA-BR 16 30778272 30778272 single base substitution C T downstream_gene_variant SKCA-BR 16 30778272 30778272 single base substitution C T intron_variant SKCA-BR 16 30778272 30778272 single base substitution C T upstream_gene_variant SKCA-BR 16 30782449 30782449 single base substitution G A downstream_gene_variant SKCA-BR 16 30782449 30782449 single base substitution G A intron_variant SKCA-BR 16 30782449 30782449 single base substitution G A upstream_gene_variant SKCA-BR 16 30787701 30787701 single base substitution G A downstream_gene_variant SKCA-BR 16 30788677 30788677 single base substitution A C downstream_gene_variant SKCA-BR 16 30788691 30788691 single base substitution T C downstream_gene_variant SKCM-US 16 30776312 30776312 single base substitution C T downstream_gene_variant SKCM-US 16 30776312 30776312 single base substitution C T exon_variant SKCM-US 16 30776312 30776312 single base substitution C T intron_variant SKCM-US 16 30776312 30776312 single base substitution C T missense_variant R235C 703C>T SKCM-US 16 30776312 30776312 single base substitution C T missense_variant R51C 151C>T SKCM-US 16 30776312 30776312 single base substitution C T upstream_gene_variant SKCM-US 16 30777523 30777523 single base substitution C T downstream_gene_variant SKCM-US 16 30777523 30777523 single base substitution C T exon_variant SKCM-US 16 30777523 30777523 single base substitution C T intron_variant SKCM-US 16 30777523 30777523 single base substitution C T synonymous_variant L161L 481C>T SKCM-US 16 30777523 30777523 single base substitution C T synonymous_variant L345L 1033C>T SKCM-US 16 30777523 30777523 single base substitution C T upstream_gene_variant SKCM-US 16 30777704 30777704 single base substitution C T downstream_gene_variant SKCM-US 16 30777704 30777704 single base substitution C T exon_variant SKCM-US 16 30777704 30777704 single base substitution C T intron_variant SKCM-US 16 30777704 30777704 single base substitution C T missense_variant A333V 998C>T SKCM-US 16 30777704 30777704 single base substitution C T missense_variant A373V 1118C>T SKCM-US 16 30777704 30777704 single base substitution C T upstream_gene_variant SKCM-US 16 30779532 30779532 single base substitution C T downstream_gene_variant SKCM-US 16 30779532 30779532 single base substitution C T exon_variant SKCM-US 16 30779532 30779532 single base substitution C T missense_variant P246S 736C>T SKCM-US 16 30779532 30779532 single base substitution C T missense_variant P454S 1360C>T SKCM-US 16 30779532 30779532 single base substitution C T missense_variant P514S 1540C>T SKCM-US 16 30779532 30779532 single base substitution C T missense_variant P554S 1660C>T SKCM-US 16 30779532 30779532 single base substitution C T upstream_gene_variant SKCM-US 16 30779804 30779804 single base substitution C A downstream_gene_variant SKCM-US 16 30779804 30779804 single base substitution C A exon_variant SKCM-US 16 30779804 30779804 single base substitution C A synonymous_variant T336T 1008C>A SKCM-US 16 30779804 30779804 single base substitution C A synonymous_variant T544T 1632C>A SKCM-US 16 30779804 30779804 single base substitution C A synonymous_variant T604T 1812C>A SKCM-US 16 30779804 30779804 single base substitution C A synonymous_variant T644T 1932C>A SKCM-US 16 30779804 30779804 single base substitution C A upstream_gene_variant STAD-US 16 30768156 30768156 single base substitution G A upstream_gene_variant STAD-US 16 30768205 30768205 single base substitution G A upstream_gene_variant STAD-US 16 30768236 30768236 single base substitution C T upstream_gene_variant STAD-US 16 30768297 30768297 single base substitution A G upstream_gene_variant STAD-US 16 30768315 30768315 single base substitution T C upstream_gene_variant STAD-US 16 30768329 30768329 deletion of <=200bp C - upstream_gene_variant STAD-US 16 30768336 30768336 single base substitution G T upstream_gene_variant STAD-US 16 30768881 30768881 single base substitution G A upstream_gene_variant STAD-US 16 30768894 30768894 single base substitution C T upstream_gene_variant STAD-US 16 30768963 30768963 single base substitution A G upstream_gene_variant STAD-US 16 30771925 30771925 deletion of <=200bp A - upstream_gene_variant STAD-US 16 30777494 30777494 single base substitution T A downstream_gene_variant STAD-US 16 30777494 30777494 single base substitution T A exon_variant STAD-US 16 30777494 30777494 single base substitution T A intron_variant STAD-US 16 30777494 30777494 single base substitution T A missense_variant L151Q 452T>A STAD-US 16 30777494 30777494 single base substitution T A missense_variant L335Q 1004T>A STAD-US 16 30777494 30777494 single base substitution T A upstream_gene_variant STAD-US 16 30777709 30777709 single base substitution C T downstream_gene_variant STAD-US 16 30777709 30777709 single base substitution C T exon_variant STAD-US 16 30777709 30777709 single base substitution C T intron_variant STAD-US 16 30777709 30777709 single base substitution C T missense_variant R335W 1003C>T STAD-US 16 30777709 30777709 single base substitution C T missense_variant R375W 1123C>T STAD-US 16 30777709 30777709 single base substitution C T upstream_gene_variant STAD-US 16 30779227 30779227 single base substitution G A downstream_gene_variant STAD-US 16 30779227 30779227 single base substitution G A exon_variant STAD-US 16 30779227 30779227 single base substitution G A missense_variant R173H 518G>A STAD-US 16 30779227 30779227 single base substitution G A missense_variant R381H 1142G>A STAD-US 16 30779227 30779227 single base substitution G A missense_variant R441H 1322G>A STAD-US 16 30779227 30779227 single base substitution G A missense_variant R481H 1442G>A STAD-US 16 30779227 30779227 single base substitution G A upstream_gene_variant STAD-US 16 30779269 30779269 single base substitution A G downstream_gene_variant STAD-US 16 30779269 30779269 single base substitution A G exon_variant STAD-US 16 30779269 30779269 single base substitution A G missense_variant H187R 560A>G STAD-US 16 30779269 30779269 single base substitution A G missense_variant H395R 1184A>G STAD-US 16 30779269 30779269 single base substitution A G missense_variant H455R 1364A>G STAD-US 16 30779269 30779269 single base substitution A G missense_variant H495R 1484A>G STAD-US 16 30779269 30779269 single base substitution A G upstream_gene_variant STAD-US 16 30779279 30779279 single base substitution A G downstream_gene_variant STAD-US 16 30779279 30779279 single base substitution A G exon_variant STAD-US 16 30779279 30779279 single base substitution A G synonymous_variant K190K 570A>G STAD-US 16 30779279 30779279 single base substitution A G synonymous_variant K398K 1194A>G STAD-US 16 30779279 30779279 single base substitution A G synonymous_variant K458K 1374A>G STAD-US 16 30779279 30779279 single base substitution A G synonymous_variant K498K 1494A>G STAD-US 16 30779279 30779279 single base substitution A G upstream_gene_variant STAD-US 16 30779423 30779423 single base substitution G C downstream_gene_variant STAD-US 16 30779423 30779423 single base substitution G C splice_acceptor_variant STAD-US 16 30779423 30779423 single base substitution G C upstream_gene_variant STAD-US 16 30779458 30779458 deletion of <=200bp C - downstream_gene_variant STAD-US 16 30779458 30779458 deletion of <=200bp C - exon_variant STAD-US 16 30779458 30779458 deletion of <=200bp C - frameshift_variant T221 STAD-US 16 30779458 30779458 deletion of <=200bp C - frameshift_variant T429 STAD-US 16 30779458 30779458 deletion of <=200bp C - frameshift_variant T489 STAD-US 16 30779458 30779458 deletion of <=200bp C - frameshift_variant T529 STAD-US 16 30779458 30779458 deletion of <=200bp C - upstream_gene_variant STAD-US 16 30780556 30780556 single base substitution A G downstream_gene_variant STAD-US 16 30780556 30780556 single base substitution A G exon_variant STAD-US 16 30780556 30780556 single base substitution A G missense_variant E458G 1373A>G STAD-US 16 30780556 30780556 single base substitution A G missense_variant E666G 1997A>G STAD-US 16 30780556 30780556 single base substitution A G missense_variant E726G 2177A>G STAD-US 16 30780556 30780556 single base substitution A G missense_variant E766G 2297A>G STAD-US 16 30780556 30780556 single base substitution A G upstream_gene_variant STAD-US 16 30780692 30780692 single base substitution C T downstream_gene_variant STAD-US 16 30780692 30780692 single base substitution C T exon_variant STAD-US 16 30780692 30780692 single base substitution C T synonymous_variant G503G 1509C>T STAD-US 16 30780692 30780692 single base substitution C T synonymous_variant G711G 2133C>T STAD-US 16 30780692 30780692 single base substitution C T synonymous_variant G771G 2313C>T STAD-US 16 30780692 30780692 single base substitution C T synonymous_variant G811G 2433C>T STAD-US 16 30780692 30780692 single base substitution C T upstream_gene_variant STAD-US 16 30783165 30783165 single base substitution C T downstream_gene_variant STAD-US 16 30783165 30783165 single base substitution C T exon_variant STAD-US 16 30783165 30783165 single base substitution C T synonymous_variant A558A 1674C>T STAD-US 16 30783165 30783165 single base substitution C T synonymous_variant A766A 2298C>T STAD-US 16 30783165 30783165 single base substitution C T synonymous_variant A826A 2478C>T STAD-US 16 30783165 30783165 single base substitution C T synonymous_variant A866A 2598C>T STAD-US 16 30783165 30783165 single base substitution C T upstream_gene_variant STAD-US 16 30783174 30783174 single base substitution G C downstream_gene_variant STAD-US 16 30783174 30783174 single base substitution G C exon_variant STAD-US 16 30783174 30783174 single base substitution G C synonymous_variant L561L 1683G>C STAD-US 16 30783174 30783174 single base substitution G C synonymous_variant L769L 2307G>C STAD-US 16 30783174 30783174 single base substitution G C synonymous_variant L829L 2487G>C STAD-US 16 30783174 30783174 single base substitution G C synonymous_variant L869L 2607G>C STAD-US 16 30783174 30783174 single base substitution G C upstream_gene_variant STAD-US 16 30785346 30785346 single base substitution C T downstream_gene_variant STAD-US 16 30785346 30785346 single base substitution C T exon_variant STAD-US 16 30785346 30785346 single base substitution C T missense_variant R665W 1993C>T STAD-US 16 30785346 30785346 single base substitution C T missense_variant R873W 2617C>T STAD-US 16 30785346 30785346 single base substitution C T missense_variant R933W 2797C>T STAD-US 16 30785346 30785346 single base substitution C T missense_variant R973W 2917C>T STAD-US 16 30785346 30785346 single base substitution C T upstream_gene_variant THCA-SA 16 30785824 30785824 single base substitution C T 3_prime_UTR_variant THCA-SA 16 30785824 30785824 single base substitution C T downstream_gene_variant THCA-SA 16 30785824 30785824 single base substitution C T exon_variant UCEC-US 16 30768183 30768183 single base substitution G A upstream_gene_variant UCEC-US 16 30768328 30768328 single base substitution G A upstream_gene_variant UCEC-US 16 30768961 30768961 single base substitution G T upstream_gene_variant UCEC-US 16 30770761 30770761 single base substitution C T upstream_gene_variant UCEC-US 16 30774876 30774876 single base substitution G C downstream_gene_variant UCEC-US 16 30774876 30774876 single base substitution G C exon_variant UCEC-US 16 30774876 30774876 single base substitution G C intron_variant UCEC-US 16 30774876 30774876 single base substitution G C synonymous_variant L146L 438G>C UCEC-US 16 30774876 30774876 single base substitution G C upstream_gene_variant UCEC-US 16 30777583 30777583 single base substitution C T downstream_gene_variant UCEC-US 16 30777583 30777583 single base substitution C T exon_variant UCEC-US 16 30777583 30777583 single base substitution C T intron_variant UCEC-US 16 30777583 30777583 single base substitution C T missense_variant R365W 1093C>T UCEC-US 16 30777583 30777583 single base substitution C T upstream_gene_variant UCEC-US 16 30779624 30779624 single base substitution C A downstream_gene_variant UCEC-US 16 30779624 30779624 single base substitution C A exon_variant UCEC-US 16 30779624 30779624 single base substitution C A synonymous_variant P276P 828C>A UCEC-US 16 30779624 30779624 single base substitution C A synonymous_variant P484P 1452C>A UCEC-US 16 30779624 30779624 single base substitution C A synonymous_variant P544P 1632C>A UCEC-US 16 30779624 30779624 single base substitution C A synonymous_variant P584P 1752C>A UCEC-US 16 30779624 30779624 single base substitution C A upstream_gene_variant UCEC-US 16 30779996 30779996 single base substitution C T downstream_gene_variant UCEC-US 16 30779996 30779996 single base substitution C T exon_variant UCEC-US 16 30779996 30779996 single base substitution C T missense_variant A371V 1112C>T UCEC-US 16 30779996 30779996 single base substitution C T missense_variant A579V 1736C>T UCEC-US 16 30779996 30779996 single base substitution C T missense_variant A639V 1916C>T UCEC-US 16 30779996 30779996 single base substitution C T missense_variant A679V 2036C>T UCEC-US 16 30779996 30779996 single base substitution C T upstream_gene_variant UCEC-US 16 30780031 30780031 single base substitution G A downstream_gene_variant UCEC-US 16 30780031 30780031 single base substitution G A exon_variant UCEC-US 16 30780031 30780031 single base substitution G A missense_variant A383T 1147G>A UCEC-US 16 30780031 30780031 single base substitution G A missense_variant A591T 1771G>A UCEC-US 16 30780031 30780031 single base substitution G A missense_variant A651T 1951G>A UCEC-US 16 30780031 30780031 single base substitution G A missense_variant A691T 2071G>A UCEC-US 16 30780031 30780031 single base substitution G A upstream_gene_variant UCEC-US 16 30780216 30780218 deletion of <=200bp AAG - downstream_gene_variant UCEC-US 16 30780216 30780218 deletion of <=200bp AAG - exon_variant UCEC-US 16 30780216 30780218 deletion of <=200bp AAG - inframe_deletion K411 UCEC-US 16 30780216 30780218 deletion of <=200bp AAG - inframe_deletion K619 UCEC-US 16 30780216 30780218 deletion of <=200bp AAG - inframe_deletion K679 UCEC-US 16 30780216 30780218 deletion of <=200bp AAG - inframe_deletion K719 UCEC-US 16 30780216 30780218 deletion of <=200bp AAG - upstream_gene_variant UCEC-US 16 30780224 30780224 single base substitution C T downstream_gene_variant UCEC-US 16 30780224 30780224 single base substitution C T exon_variant UCEC-US 16 30780224 30780224 single base substitution C T synonymous_variant I413I 1239C>T UCEC-US 16 30780224 30780224 single base substitution C T synonymous_variant I621I 1863C>T UCEC-US 16 30780224 30780224 single base substitution C T synonymous_variant I681I 2043C>T UCEC-US 16 30780224 30780224 single base substitution C T synonymous_variant I721I 2163C>T UCEC-US 16 30780224 30780224 single base substitution C T upstream_gene_variant UCEC-US 16 30780244 30780244 single base substitution G A downstream_gene_variant UCEC-US 16 30780244 30780244 single base substitution G A exon_variant UCEC-US 16 30780244 30780244 single base substitution G A missense_variant R420Q 1259G>A UCEC-US 16 30780244 30780244 single base substitution G A missense_variant R628Q 1883G>A UCEC-US 16 30780244 30780244 single base substitution G A missense_variant R688Q 2063G>A UCEC-US 16 30780244 30780244 single base substitution G A missense_variant R728Q 2183G>A UCEC-US 16 30780244 30780244 single base substitution G A upstream_gene_variant UCEC-US 16 30780579 30780579 single base substitution C T downstream_gene_variant UCEC-US 16 30780579 30780579 single base substitution C T exon_variant UCEC-US 16 30780579 30780579 single base substitution C T missense_variant R466W 1396C>T UCEC-US 16 30780579 30780579 single base substitution C T missense_variant R674W 2020C>T UCEC-US 16 30780579 30780579 single base substitution C T missense_variant R734W 2200C>T UCEC-US 16 30780579 30780579 single base substitution C T missense_variant R774W 2320C>T UCEC-US 16 30780579 30780579 single base substitution C T upstream_gene_variant UCEC-US 16 30780688 30780688 single base substitution T C downstream_gene_variant UCEC-US 16 30780688 30780688 single base substitution T C exon_variant UCEC-US 16 30780688 30780688 single base substitution T C missense_variant L502S 1505T>C UCEC-US 16 30780688 30780688 single base substitution T C missense_variant L710S 2129T>C UCEC-US 16 30780688 30780688 single base substitution T C missense_variant L770S 2309T>C UCEC-US 16 30780688 30780688 single base substitution T C missense_variant L810S 2429T>C UCEC-US 16 30780688 30780688 single base substitution T C upstream_gene_variant UCEC-US 16 30783270 30783270 single base substitution G T downstream_gene_variant UCEC-US 16 30783270 30783270 single base substitution G T exon_variant UCEC-US 16 30783270 30783270 single base substitution G T missense_variant E593D 1779G>T UCEC-US 16 30783270 30783270 single base substitution G T missense_variant E801D 2403G>T UCEC-US 16 30783270 30783270 single base substitution G T missense_variant E861D 2583G>T UCEC-US 16 30783270 30783270 single base substitution G T missense_variant E901D 2703G>T UCEC-US 16 30783270 30783270 single base substitution G T upstream_gene_variant UCEC-US 16 30783428 30783428 single base substitution C T downstream_gene_variant UCEC-US 16 30783428 30783428 single base substitution C T exon_variant UCEC-US 16 30783428 30783428 single base substitution C T missense_variant R608W 1822C>T UCEC-US 16 30783428 30783428 single base substitution C T missense_variant R816W 2446C>T UCEC-US 16 30783428 30783428 single base substitution C T missense_variant R876W 2626C>T UCEC-US 16 30783428 30783428 single base substitution C T missense_variant R916W 2746C>T UCEC-US 16 30783428 30783428 single base substitution C T upstream_gene_variant UCEC-US 16 30783493 30783493 single base substitution G T downstream_gene_variant UCEC-US 16 30783493 30783493 single base substitution G T exon_variant UCEC-US 16 30783493 30783493 single base substitution G T missense_variant E629D 1887G>T UCEC-US 16 30783493 30783493 single base substitution G T missense_variant E837D 2511G>T UCEC-US 16 30783493 30783493 single base substitution G T missense_variant E897D 2691G>T UCEC-US 16 30783493 30783493 single base substitution G T missense_variant E937D 2811G>T UCEC-US 16 30783493 30783493 single base substitution G T upstream_gene_variant UCEC-US 16 30785346 30785346 single base substitution C T downstream_gene_variant UCEC-US 16 30785346 30785346 single base substitution C T exon_variant UCEC-US 16 30785346 30785346 single base substitution C T missense_variant R665W 1993C>T UCEC-US 16 30785346 30785346 single base substitution C T missense_variant R873W 2617C>T UCEC-US 16 30785346 30785346 single base substitution C T missense_variant R933W 2797C>T UCEC-US 16 30785346 30785346 single base substitution C T missense_variant R973W 2917C>T UCEC-US 16 30785346 30785346 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LUAD-RT-S01699 COSM378221 c.37G>T p.G13W Substitution - Missense 16:30762582-30762582 + LIM2551 COSM4643977 c.71G>C p.R24P Substitution - Missense 16:30762616-30762616 + TCGA-AC-A3OD-01 COSM3817830 c.179C>G p.A60G Substitution - Missense 16:30763164-30763164 + CSCC-10-T COSM4477335 c.2143C>T p.R715* Substitution - Nonsense 16:30768883-30768883 + TCGA-E6-A1LZ-01 COSM969973 c.474C>A p.L158L Substitution - coding silent 16:30764210-30764210 + LUAD-VUMN6 COSM347868 c.1360C>G p.Q454E Substitution - Missense 16:30766807-30766807 + 587286 COSM1224012 c.1205C>G p.S402C Substitution - Missense 16:30766470-30766470 + TCGA-CJ-4913-01 COSM471648 c.339G>T p.E113D Substitution - Missense 16:30763456-30763456 + ESO-081 COSM1243572 c.2072C>T p.A691V Substitution - Missense 16:30768711-30768711 + TCGA-A2-A0T5-01 COSM3817834 c.1922T>G p.V641G Substitution - Missense 16:30768473-30768473 + B80 COSM1749564 c.1903G>A p.D635N Substitution - Missense 16:30768454-30768454 + CSCC-31-T COSM4480810 c.2456C>T p.S819F Substitution - Missense 16:30769394-30769394 + MAVER-1 COSM1740271 c.2794G>A p.D932N Substitution - Missense 16:30772155-30772155 + H23 COSM1196310 c.1547G>C p.G516A Substitution - Missense 16:30768011-30768011 + LUAD-LIP77 COSM342205 c.2275G>A p.D759N Substitution - Missense 16:30769213-30769213 + MO_1232 COSM5560967 c.1039A>G p.N347D Substitution - Missense 16:30766208-30766208 + TCGA-28-5218-01 COSM3402280 c.405G>A p.G135G Substitution - coding silent 16:30763522-30763522 + 01-P8014 COSM3113147 c.627C>T p.L209L Substitution - coding silent 16:30764363-30764363 + H2009 COSM1193715 c.1231G>A p.E411K Substitution - Missense 16:30766496-30766496 + TCGA-AM-5821-01 COSM3690936 c.1675G>A p.D559N Substitution - Missense 16:30768226-30768226 + 8047913 COSM3387386 c.837G>T p.V279V Substitution - coding silent 16:30765246-30765246 + UD-SCC-2 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-G2-A3IE-01 COSM1301895 c.2157G>C p.K719N Substitution - Missense 16:30768897-30768897 + 3402_T COSM460556 c.875G>A p.R292Q Substitution - Missense 16:30765284-30765284 + CCK81 COSM3113161 c.963delG p.G323fs*13 Deletion - Frameshift 16:30765469-30765469 + SW620 COSM3113140 c.291C>T p.Y97Y Substitution - coding silent 16:30763276-30763276 + H2122 COSM1197272 c.1555C>T p.R519W Substitution - Missense 16:30768106-30768106 + UM-SCC-47 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-AD-6889-01 COSM1377496 c.1281C>T p.I427I Substitution - coding silent 16:30766546-30766546 + SCC-25 COSM4590572 c.1844A>G p.Q615R Substitution - Missense sysucc-1640T COSM5765549 c.723G>A p.Q241Q Substitution - coding silent 16:30765011-30765011 + PTC-14C COSM4128996 c.1958A>G p.K653R Substitution - Missense 16:30768509-30768509 + TCGA-HU-A4GQ-01 COSM4060238 c.1123C>T p.R375W Substitution - Missense 16:30766388-30766388 + B86 COSM1749563 c.622G>A p.E208K Substitution - Missense 16:30764358-30764358 + 93VU147T COSM4590572 c.1844A>G p.Q615R Substitution - Missense LS411 COSM3113186 c.2182C>T p.R728W Substitution - Missense 16:30768922-30768922 + TCGA-CD-A4MG-01 COSM4060240 c.1484A>G p.H495R Substitution - Missense 16:30767948-30767948 + LOVO COSM3113154 c.799T>C p.S267P Substitution - Missense 16:30765208-30765208 + S02289 COSM4752036 c.691C>T p.R231* Substitution - Nonsense 16:30764979-30764979 + ORL-48 COSM4590572 c.1844A>G p.Q615R Substitution - Missense GB11 COSM1744287 c.1045C>T p.R349C Substitution - Missense 16:30766214-30766214 + TCGA-EQ-A4SO-01 COSM4060242 c.1552-1G>C p.? Unknown 16:30768102-30768102 + ICGC_MB6 COSM215643 c.1618G>A p.V540I Substitution - Missense 16:30768169-30768169 + 19M COSM5579468 c.810C>T p.T270T Substitution - coding silent 16:30765219-30765219 + ESCC_158 COSM5646675 c.1525C>T p.R509* Substitution - Nonsense 16:30767989-30767989 + WSU-HN30 COSM4590572 c.1844A>G p.Q615R Substitution - Missense 1N28-VS-1T28 COSM4973769 c.2555G>A p.R852H Substitution - Missense 16:30769569-30769569 + TCGA-H4-A2HQ-01 COSM1301894 c.2124G>A p.R708R Substitution - coding silent 16:30768864-30768864 + XHDG20 COSM4768868 c.1734G>C p.K578N Substitution - Missense 16:30768285-30768285 + TCGA-IR-A3LK-01 COSM4817380 c.1682G>C p.R561T Substitution - Missense 16:30768233-30768233 + TCGA-BT-A3PH-01 COSM1301893 c.1005G>A p.L335L Substitution - coding silent 16:30766174-30766174 + WSU-HN12 COSM4590572 c.1844A>G p.Q615R Substitution - Missense HCC2998 COSM3113174 c.1500C>T p.D500D Substitution - coding silent 16:30767964-30767964 + TCGA-A2-A25A-01 COSM1478804 c.1547G>T p.G516V Substitution - Missense 16:30768011-30768011 + TCGA-BG-A0M8-01 COSM970002 c.2895C>T p.H965H Substitution - coding silent 16:30774003-30774003 + QC2-15-T2 COSM5652505 c.1481A>G p.N494S Substitution - Missense 16:30767945-30767945 + 205T COSM1726805 c.557A>C p.E186A Substitution - Missense 16:30764293-30764293 + TCGA-HF-7132-01 COSM970004 c.2917C>T p.R973W Substitution - Missense 16:30774025-30774025 + TCGA-AP-A051-01 COSM969978 c.1093C>T p.R365W Substitution - Missense 16:30766262-30766262 + TCGA-BR-7703-01 COSM4060237 c.1004T>A p.L335Q Substitution - Missense 16:30766173-30766173 + TCGA-AC-A23H-01 COSM3817831 c.589G>C p.E197Q Substitution - Missense 16:30764325-30764325 + WSU-HN13 COSM4590572 c.1844A>G p.Q615R Substitution - Missense WSU-HN6 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-AD-6964-01 COSM1377499 c.2367A>G p.L789L Substitution - coding silent 16:30769305-30769305 + TCGA-BT-A2LD-01 COSM1301890 c.412C>G p.L138V Substitution - Missense 16:30763529-30763529 + S02194 COSM5674815 c.304G>C p.D102H Substitution - Missense 16:30763421-30763421 + TCGA-FS-A1ZK-06 COSM3508941 c.1118C>T p.A373V Substitution - Missense 16:30766383-30766383 + TCGA-AZ-4315-01 COSM1377497 c.1351A>G p.T451A Substitution - Missense 16:30766798-30766798 + TCGA-AP-A0LM-01 COSM969990 c.2183G>A p.R728Q Substitution - Missense 16:30768923-30768923 + TCGA-A2-A0YE-01 COSM3817835 c.2281A>G p.T761A Substitution - Missense 16:30769219-30769219 + TCGA-AD-6890-01 COSM1377498 c.1387C>T p.R463C Substitution - Missense 16:30766834-30766834 + B80-Tumor COSM1749564 c.1903G>A p.D635N Substitution - Missense 16:30768454-30768454 + UM-SCC-4 COSM4590572 c.1844A>G p.Q615R Substitution - Missense H322T COSM1194921 c.2173G>A p.D725N Substitution - Missense 16:30768913-30768913 + 555TS COSM673749 c.1319delA p.K440fs*47 Deletion - Frameshift 16:30766766-30766766 + LUAD-NYU201 COSM371324 c.2255A>C p.E752A Substitution - Missense 16:30769193-30769193 + TCGA-B5-A11J-01 COSM969994 c.2429T>C p.L810S Substitution - Missense 16:30769367-30769367 + SCC-9 COSM4590572 c.1844A>G p.Q615R Substitution - Missense OSCC-GB_01250111 COSM5954656 c.1592A>G p.N531S Substitution - Missense 16:30768143-30768143 + YUROG COSM5384756 c.1358C>T p.A453V Substitution - Missense 16:30766805-30766805 + LIM2405 COSM4642008 c.283A>G p.N95D Substitution - Missense 16:30763268-30763268 + 2492713 COSM5719004 c.1387C>A p.R463S Substitution - Missense 16:30766834-30766834 + CSCC-38-T COSM4564035 c.243_244GA>AT p.K82* Substitution - Nonsense 16:30763228-30763229 + TCGA-AO-A03N-01 COSM435134 c.2701G>C p.E901Q Substitution - Missense 16:30771947-30771947 + 587332 COSM1224013 c.301-2A>G p.? Unknown 16:30763416-30763416 + CSCC-7-T COSM4468705 c.1559C>T p.A520V Substitution - Missense 16:30768110-30768110 + CSCC-19-T COSM1377496 c.1281C>T p.I427I Substitution - coding silent 16:30766546-30766546 + PDA_025 COSM4999273 c.2590G>A p.V864I Substitution - Missense 16:30771836-30771836 + TCGA-18-3409-01 COSM703241 c.1858C>T p.P620S Substitution - Missense 16:30768409-30768409 + UPCI:SCC090 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-BR-A452-01 COSM4060239 c.1442G>A p.R481H Substitution - Missense 16:30767906-30767906 + TCGA-GV-A3JZ-01 COSM1301891 c.563C>G p.S188C Substitution - Missense 16:30764299-30764299 + T2197 COSM4722205 c.328C>T p.R110* Substitution - Nonsense 16:30763445-30763445 + P04-1084 COSM247083 c.1786G>T p.A596S Substitution - Missense 16:30768337-30768337 + TCGA-C5-A1MH-01 COSM4820797 c.1642G>C p.E548Q Substitution - Missense 16:30768193-30768193 + TCGA-EI-6917-01 COSM3420944 c.184C>T p.R62W Substitution - Missense 16:30763169-30763169 + PTC-7C COSM4128997 c.2774T>G p.V925G Substitution - Missense 16:30772135-30772135 + TCGA-BH-A208-01 COSM1478803 c.1409T>A p.L470Q Substitution - Missense 16:30766856-30766856 + TCGA-C8-A26Y-01 COSM3817833 c.1330G>C p.E444Q Substitution - Missense 16:30766777-30766777 + BHY COSM4590572 c.1844A>G p.Q615R Substitution - Missense CHC1595T COSM4801749 c.549C>T p.G183G Substitution - coding silent 16:30764285-30764285 + PD6418a COSM5791464 c.1520A>C p.K507T Substitution - Missense 16:30767984-30767984 + NCI-H23 COSM1196310 c.1547G>C p.G516A Substitution - Missense 16:30768011-30768011 + CSCC-11-T COSM4452748 c.210A>T p.E70D Substitution - Missense 16:30763195-30763195 + SNU-C4 COSM4652717 c.2749C>T p.R917C Substitution - Missense 16:30772110-30772110 + PTC-10C COSM4128995 c.1055A>C p.E352A Substitution - Missense 16:30766224-30766224 + HCC076T COSM5822074 c.208G>T p.E70* Substitution - Nonsense 16:30763193-30763193 + CHC1700T COSM4800476 c.2054A>C p.D685A Substitution - Missense 16:30768693-30768693 + HCC089T COSM5247540 c.424G>T p.G142W Substitution - Missense 16:30763541-30763541 + CHC1700T COSM4800476 c.2054A>C p.D685A Substitution - Missense 16:30768693-30768693 + I2L-P19Ta-Tumor-Organoid COSM5363407 c.2745G>A p.L915L Substitution - coding silent 16:30772106-30772106 + TCGA-BP-4158-01 COSM3361732 c.129C>A p.S43S Substitution - coding silent 16:30762674-30762674 + TCGA-DI-A0WH-01 COSM969980 c.1752C>A p.P584P Substitution - coding silent 16:30768303-30768303 + Br27P COSM40555 c.1252G>A p.A418T Substitution - Missense 16:30766517-30766517 + WA30 COSM236854 c.2857A>G p.T953A Substitution - Missense 16:30773965-30773965 + T3011 COSM4722206 c.1208T>C p.L403P Substitution - Missense 16:30766473-30766473 + TCGA-AA-A010-01 COSM284637 c.259G>T p.D87Y Substitution - Missense 16:30763244-30763244 + TCGA-06-0686-01 COSM3402279 c.362C>A p.A121E Substitution - Missense 16:30763479-30763479 + TCGA-GV-A3JZ-01 COSM1301892 c.666C>G p.L222L Substitution - coding silent 16:30764954-30764954 + SCC-15 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-BR-4184-01 COSM4060244 c.2433C>T p.G811G Substitution - coding silent 16:30769371-30769371 + TCGA-AS-3777-01 COSM1493628 c.2425G>A p.E809K Substitution - Missense 16:30769363-30769363 + UM-SCC-11B COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-DR-A0ZM-01 COSM460556 c.875G>A p.R292Q Substitution - Missense 16:30765284-30765284 + WSU-HN8 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-AP-A059-01 COSM969984 c.2071G>A p.A691T Substitution - Missense 16:30768710-30768710 + TCGA-AD-6889-01 COSM1377500 c.2918G>A p.R973Q Substitution - Missense 16:30774026-30774026 + LOVO COSM3113170 c.1441C>T p.R481C Substitution - Missense 16:30767905-30767905 + TCGA-CG-5723-01 COSM4060241 c.1494A>G p.K498K Substitution - coding silent 16:30767958-30767958 + TCGA-AY-6197-01 COSM1377494 c.1147C>T p.R383W Substitution - Missense 16:30766412-30766412 + TCGA-18-3415-01 COSM703244 c.65T>C p.L22P Substitution - Missense 16:30762610-30762610 + TCGA-AP-A051-01 COSM969988 c.2163C>T p.I721I Substitution - coding silent 16:30768903-30768903 + Detroit_562 COSM4590572 c.1844A>G p.Q615R Substitution - Missense BZ15 COSM5758338 c.1497G>C p.G499G Substitution - coding silent 16:30767961-30767961 + TCGA-Q1-A73O-01 COSM4836085 c.2692C>G p.R898G Substitution - Missense 16:30771938-30771938 + U343 COSM5712730 c.1289T>G p.M430R Substitution - Missense 16:30766554-30766554 + TCGA-76-6280-01 COSM3402281 c.2715C>A p.L905L Substitution - coding silent 16:30771961-30771961 + 2521244 COSM5887440 c.2203G>A p.E735K Substitution - Missense 16:30768943-30768943 + 4095_T COSM3957481 c.1552-6T>G p.? Unknown 16:30768097-30768097 + 587234 COSM1224014 c.1501G>A p.A501T Substitution - Missense 16:30767965-30767965 + AOCS-079-1-1 COSM3948483 c.2284G>C p.G762R Substitution - Missense 16:30769222-30769222 + TCGA-CD-8536-01 COSM4060245 c.2598C>T p.A866A Substitution - coding silent 16:30771844-30771844 + CPCG0334-F1 COSM4880565 c.2055T>C p.D685D Substitution - coding silent 16:30768694-30768694 + TCGA-EB-A5UL-06 COSM3508942 c.1660C>T p.P554S Substitution - Missense 16:30768211-30768211 + TCGA-AG-A02G-01 COSM265388 c.2225G>A p.R742H Substitution - Missense 16:30768965-30768965 + TCGA-CJ-4640-01 COSM1135785 c.830C>T p.T277I Substitution - Missense 16:30765239-30765239 + T155 COSM969982 c.2036C>T p.A679V Substitution - Missense 16:30768675-30768675 + U2940 COSM5621723 c.2768G>A p.R923K Substitution - Missense 16:30772129-30772129 + ESO-0292 COSM1241682 c.1735A>G p.K579E Substitution - Missense 16:30768286-30768286 + OSCC-GB_00150111 COSM3711921 c.2747G>A p.R916Q Substitution - Missense 16:30772108-30772108 + LIM2551 COSM4643979 c.2796C>T p.D932D Substitution - coding silent 16:30772157-30772157 + CHC1595T COSM4801749 c.549C>T p.G183G Substitution - coding silent 16:30764285-30764285 + pfg097T COSM4752036 c.691C>T p.R231* Substitution - Nonsense 16:30764979-30764979 + TCGA-D1-A17U-01 COSM969986 c.2155_2157delAAG p.K720delK Deletion - In frame 16:30768895-30768897 + TCGA-BR-4368-01 COSM4060243 c.2297A>G p.E766G Substitution - Missense 16:30769235-30769235 + 36773720 COSM1644960 c.550C>G p.R184G Substitution - Missense 16:30764286-30764286 + B86-Tumor COSM1749563 c.622G>A p.E208K Substitution - Missense 16:30764358-30764358 + BICR_22 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-B9-4114-01 COSM3988431 c.796A>T p.T266S Substitution - Missense 16:30765205-30765205 + 2492729 COSM5726261 c.1717A>G p.T573A Substitution - Missense 16:30768268-30768268 + BN24 COSM1293579 c.1804C>T p.R602W Substitution - Missense 16:30768355-30768355 + SJHGG058_A COSM4971120 c.1979+10_1979+14delTGTTC p.? Unknown 16:30768540-30768544 + TCGA-D3-A3C7-06 COSM3508940 c.1033C>T p.L345L Substitution - coding silent 16:30766202-30766202 + S01861 COSM5671099 c.43delT p.S15fs*8 Deletion - Frameshift 16:30762588-30762588 + SC_9008 COSM5565427 c.874C>T p.R292* Substitution - Nonsense 16:30765283-30765283 + CSCC-31-T COSM4487613 c.320C>G p.A107G Substitution - Missense 16:30763437-30763437 + TCGA-GL-7773-01 COSM3988430 c.542T>C p.L181P Substitution - Missense 16:30764278-30764278 + SNU-175 COSM3113162 c.1072G>A p.A358T Substitution - Missense 16:30766241-30766241 + BN24T COSM1293579 c.1804C>T p.R602W Substitution - Missense 16:30768355-30768355 + BD121T COSM5138270 c.2913C>T p.C971C Substitution - coding silent 16:30774021-30774021 + YUKAT COSM5384757 c.1528G>A p.E510K Substitution - Missense 16:30767992-30767992 + Pat_32_A COSM5850752 c.2648G>A p.R883Q Substitution - Missense 16:30771894-30771894 + UM-SCC-17B COSM4590572 c.1844A>G p.Q615R Substitution - Missense sysucc-274T COSM5475868 c.1388G>A p.R463H Substitution - Missense 16:30766835-30766835 + TCGA-AP-A051-01 COSM969982 c.2036C>T p.A679V Substitution - Missense 16:30768675-30768675 + RK076_C01 COSM3701082 c.1949A>T p.E650V Substitution - Missense 16:30768500-30768500 + TCGA-Q1-A73O-01 COSM4834671 c.2425G>T p.E809* Substitution - Nonsense 16:30769363-30769363 + TCGA-EE-A29S-06 COSM3508939 c.703C>T p.R235C Substitution - Missense 16:30764991-30764991 + TCGA-AA-A010-01 COSM284638 c.858C>T p.I286I Substitution - coding silent 16:30765267-30765267 + TCGA-BS-A0TJ-01 COSM970000 c.2811G>T p.E937D Substitution - Missense 16:30772172-30772172 + SNU-C2B COSM3113194 c.2937C>T p.R979R Substitution - coding silent 16:30774045-30774045 + 477 COSM4438695 c.1106G>A p.R369H Substitution - Missense 16:30766275-30766275 + TCGA-AP-A0LM-01 COSM969996 c.2703G>T p.E901D Substitution - Missense 16:30771949-30771949 + LUAD-S01346 COSM397514 c.2838G>A p.L946L Substitution - coding silent 16:30773946-30773946 + 2492729 COSM5726260 c.1155G>A p.T385T Substitution - coding silent 16:30766420-30766420 + CRC-02T COSM5454442 c.1754C>T p.S585F Substitution - Missense 16:30768305-30768305 + TCGA-B5-A11N-01 COSM970004 c.2917C>T p.R973W Substitution - Missense 16:30774025-30774025 + TCGA-AA-3818-01 COSM270867 c.2750G>A p.R917H Substitution - Missense 16:30772111-30772111 + TCGA-BG-A187-01 COSM969971 c.438G>C p.L146L Substitution - coding silent 16:30763555-30763555 + RK023_C01 COSM1629873 c.518G>A p.S173N Substitution - Missense 16:30764254-30764254 + NOKSI COSM4590572 c.1844A>G p.Q615R Substitution - Missense SW480 COSM3113140 c.291C>T p.Y97Y Substitution - coding silent 16:30763276-30763276 + TCGA-22-5477-01 COSM703242 c.1002G>A p.M334I Substitution - Missense 16:30766171-30766171 + TCGA-CJ-4899-01 COSM471649 c.1106G>T p.R369L Substitution - Missense 16:30766275-30766275 + ESCC_46 COSM5630512 c.2725C>T p.Q909* Substitution - Nonsense 16:30771971-30771971 + pfg019T COSM1640463 c.2961C>T p.N987N Substitution - coding silent 16:30774069-30774069 + LIM2551 COSM4643978 c.2030A>C p.K677T Substitution - Missense 16:30768669-30768669 + SW1116 COSM3113159 c.897C>A p.H299Q Substitution - Missense 16:30765306-30765306 + TCGA-BT-A2LA-01 COSM1301896 c.2830-1G>A p.? Unknown 16:30773937-30773937 + CAL33 COSM4590572 c.1844A>G p.Q615R Substitution - Missense TCGA-D1-A15X-01 COSM969998 c.2746C>T p.R916W Substitution - Missense 16:30772107-30772107 + TCGA-DS-A1OD-01 COSM1293579 c.1804C>T p.R602W Substitution - Missense 16:30768355-30768355 + LUAD-QCHM7 COSM377149 c.1207C>G p.L403V Substitution - Missense 16:30766472-30766472 + YUGOE COSM1709085 c.1133C>T p.P378L Substitution - Missense 16:30766398-30766398 + HCT116 COSM3113191 c.2650C>T p.L884L Substitution - coding silent 16:30771896-30771896 + sysucc-783T COSM5484016 c.1551G>T p.K517N Substitution - Missense 16:30768015-30768015 + TCGA-JW-A5VL-01 COSM4847321 c.1378G>A p.E460K Substitution - Missense 16:30766825-30766825 + CSCC-17-T COSM4531398 c.1784G>A p.G595E Substitution - Missense 16:30768335-30768335 + TCGA-EE-A29D-06 COSM3508943 c.1932C>A p.T644T Substitution - coding silent 16:30768483-30768483 + 15T COSM3711921 c.2747G>A p.R916Q Substitution - Missense 16:30772108-30772108 + C709 COSM4443883 c.277A>G p.I93V Substitution - Missense 16:30763262-30763262 + sysucc-311T COSM5479102 c.60G>T p.K20N Substitution - Missense 16:30762605-30762605 + BD57T COSM5510806 c.2233G>A p.G745S Substitution - Missense 16:30768973-30768973 + TCGA-66-2789-01 COSM703243 c.110G>A p.R37H Substitution - Missense 16:30762655-30762655 + UM-SCC-2 COSM4590572 c.1844A>G p.Q615R Substitution - Missense ESO-582 COSM1264400 c.1706G>A p.G569D Substitution - Missense 16:30768257-30768257 + TCGA-DC-6154-01 COSM5076862 c.464G>A p.R155Q Substitution - Missense 16:30764200-30764200 + CAL27 COSM4590572 c.1844A>G p.Q615R Substitution - Missense PTC-7C COSM1640463 c.2961C>T p.N987N Substitution - coding silent 16:30774069-30774069 + TCGA-D1-A167-01 COSM969992 c.2320C>T p.R774W Substitution - Missense 16:30769258-30769258 + TCGA-A6-6781-01 COSM1377495 c.1177G>A p.A393T Substitution - Missense 16:30766442-30766442 + B80-Tumor COSM3932331 c.1762G>T p.D588Y Substitution - Missense 16:30768313-30768313 + SWE-2A COSM1178163 c.993G>A p.K331K Substitution - coding silent 16:30765499-30765499 + TCGA-CG-4437-01 COSM4060246 c.2607G>C p.L869L Substitution - coding silent 16:30771853-30771853 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.65238 16p11.2-p11.1 607700

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAG - InFrameDeletion p.K720delK c.2159_2161delAGA 16 30780216 UCEC A G Missense p.E766G c.2297A>G 16 30780556 STAD C A Missense p.A121E c.362C>A 16 30774800 GBM C A Synonymous p.L905L c.2715C>A 16 30783282 GBM C A Synonymous p.P584P c.1752C>A 16 30779624 UCEC C A Synonymous p.R646R c.1936C>A 16 30779808 HNSC CC TT Missense p.P554F c.1660_1661delinsTT 16 30779532 CM CC TT Missense p.Q888* c.2661_2662delinsTT 16 30783228 CM C - Frameshift p.N531Tfs*47 c.1590delC 16 30779458 STAD C G Missense p.L138V c.412C>G 16 30774850 BLCA C G Missense p.P620R c.1859C>G 16 30779731 LUAD C G Missense p.S188C c.563C>G 16 30775620 BLCA C G Synonymous p.L222L c.666C>G 16 30776275 BLCA C T Missense p.A373V c.1118C>T 16 30777704 CM C T Missense p.R235C c.703C>T 16 30776312 CM C T Missense p.T277I c.830C>T 16 30776560 RCCC C T Synonymous p.L345L c.1033C>T 16 30777523 CM C T Synonymous p.N987N c.2961C>T 16 30785390 STAD G A Missense p.A418T c.1252G>A 16 30777838 GBM G A Missense p.E287K c.859G>A 16 30776589 HNSC G A Missense p.E465K c.1393G>A 16 30778161 CM G A Missense p.G569D c.1706G>A 16 30779578 ESCA G A Missense p.M334I c.1002G>A 16 30777492 LUSC G A Missense p.R37H c.110G>A 16 30773976 LUSC G A Missense p.R742H c.2225G>A 16 30780286 COREAD G A Missense p.R917H c.2750G>A 16 30783432 COREAD G A Missense p.S173N c.518G>A 16 30775575 HC G A Missense p.V540I c.1618G>A 16 30779490 MB G A SpliceAcceptorSNV . c.2830-1G>A 16 30785258 BLCA G A Synonymous p.E587E c.1761G>A 16 30779633 HNSC G A Synonymous p.G135G c.405G>A 16 30774843 GBM G A Synonymous p.K818K c.2454G>A 16 30780713 HNSC G A Synonymous p.L335L c.1005G>A 16 30777495 BLCA G A Synonymous p.R708R c.2124G>A 16 30780185 BLCA G C Missense p.E340D c.1020G>C 16 30777510 HNSC G C Missense p.E901Q c.2701G>C 16 30783268 BRCA G C Missense p.K719N c.2157G>C 16 30780218 BLCA G C Missense p.R292P c.875G>C 16 30776605 LUAD G C Synonymous p.L146L c.438G>C 16 30774876 UCEC G C Synonymous p.L869L c.2607G>C 16 30783174 STAD G T Missense p.E113D c.339G>T 16 30774777 RCCC G T Missense p.E937D c.2811G>T 16 30783493 UCEC G T Missense p.G516V c.1547G>T 16 30779332 BRCA G T Missense p.R369L c.1106G>T 16 30777596 RCCC T A Missense p.L470Q c.1409T>A 16 30778177 BRCA T C Missense p.L22P c.65T>C 16 30773931 LUSC T C Missense p.L810S c.2429T>C 16 30780688 UCEC