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 7 30491510 30491510 + Frame_Shift_Del DEL C C - TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr7:30491510delC c.1523delG c.(1522-1524)ggtfs p.G508fs BLCA 7 30485764 30485764 + Missense_Mutation SNP C C G TCGA-GV-A3JW-01A-11D-A20D-08 TCGA-GV-A3JW-10A-01D-A20D-08 g.chr7:30485764C>G c.2446G>C c.(2446-2448)Gag>Cag p.E816Q BLCA 7 30485766 30485766 + Missense_Mutation SNP G G A TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr7:30485766G>A c.2444C>T c.(2443-2445)tCt>tTt p.S815F BLCA 7 30490888 30490888 + Silent SNP G G C TCGA-XF-AAN3-01A-11D-A42E-08 TCGA-XF-AAN3-10A-01D-A42H-08 g.chr7:30490888G>C c.2145C>G c.(2143-2145)ctC>ctG p.L715L BLCA 7 30491056 30491056 + Missense_Mutation SNP G G C TCGA-XF-AAN3-01A-11D-A42E-08 TCGA-XF-AAN3-10A-01D-A42H-08 g.chr7:30491056G>C c.1977C>G c.(1975-1977)atC>atG p.I659M BLCA 7 30491074 30491074 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr7:30491074G>C c.1959C>G c.(1957-1959)atC>atG p.I653M BLCA 7 30491189 30491189 + Missense_Mutation SNP C C T TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr7:30491189C>T c.1844G>A c.(1843-1845)aGa>aAa p.R615K BLCA 7 30491563 30491563 + Missense_Mutation SNP C C G TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr7:30491563C>G c.1470G>C c.(1468-1470)gaG>gaC p.E490D BLCA 7 30492526 30492526 + Silent SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr7:30492526G>A c.507C>T c.(505-507)ttC>ttT p.F169F BLCA 7 30496459 30496459 + Silent SNP G G T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr7:30496459G>T c.79C>A c.(79-81)Cgg>Agg p.R27R BRCA 7 30469058 30469058 + Missense_Mutation SNP C C A TCGA-AN-A0FL-01A-11W-A050-09 TCGA-AN-A0FL-10A-01W-A055-09 g.chr7:30469058C>A c.2721G>T c.(2719-2721)caG>caT p.Q907H BRCA 7 30472788 30472788 + Missense_Mutation SNP G G C TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr7:30472788G>C c.2629C>G c.(2629-2631)Caa>Gaa p.Q877E BRCA 7 30491714 30491714 + Missense_Mutation SNP C C T TCGA-BH-A0DQ-01A-11D-A099-09 TCGA-BH-A0DQ-11A-12D-A100-09 g.chr7:30491714C>T c.1319G>A c.(1318-1320)aGc>aAc p.S440N BRCA 7 30491883 30491883 + Missense_Mutation SNP G G T TCGA-A2-A04R-01A-41D-A117-09 TCGA-A2-A04R-10B-01D-A10G-09 g.chr7:30491883G>T c.1150C>A c.(1150-1152)Ctc>Atc p.L384I BRCA 7 30492497 30492498 + Frame_Shift_Del DEL CT CT - TCGA-A2-A4S0-01A-21D-A25Q-09 TCGA-A2-A4S0-10A-01D-A25Q-09 g.chr7:30492497_30492498delCT c.535_536delAG c.(535-537)agcfs p.S179fs BRCA 7 30496531 30496531 + Missense_Mutation SNP C C G TCGA-AR-A1AK-01A-21D-A12Q-09 TCGA-AR-A1AK-10A-01D-A12Q-09 g.chr7:30496531C>G c.7G>C c.(7-9)Gag>Cag p.E3Q CESC 7 30468996 30468996 + Missense_Mutation SNP T T C TCGA-EA-A411-01A-11D-A243-09 TCGA-EA-A411-10A-01D-A243-09 g.chr7:30468996T>C c.2783A>G c.(2782-2784)gAg>gGg p.E928G COAD 7 30485797 30485797 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr7:30485797C>T c.2413G>A c.(2413-2415)Gcc>Acc p.A805T COAD 7 30486604 30486604 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr7:30486604C>T c.2348G>A c.(2347-2349)tGc>tAc p.C783Y COAD 7 30486618 30486618 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr7:30486618T>G c.2334A>C c.(2332-2334)aaA>aaC p.K778N COAD 7 30487963 30487963 + Missense_Mutation SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr7:30487963T>C c.2236A>G c.(2236-2238)Aag>Gag p.K746E COAD 7 30490974 30490974 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr7:30490974C>T c.2059G>A c.(2059-2061)Gcc>Acc p.A687T COAD 7 30491556 30491556 + Missense_Mutation SNP T T C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr7:30491556T>C c.1477A>G c.(1477-1479)Atg>Gtg p.M493V COAD 7 30491959 30491959 + Silent SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr7:30491959G>A c.1074C>T c.(1072-1074)cgC>cgT p.R358R COAD 7 30491974 30491974 + Silent SNP G G T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr7:30491974G>T c.1059C>A c.(1057-1059)tcC>tcA p.S353S COAD 7 30492008 30492008 + Missense_Mutation SNP A A G TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr7:30492008A>G c.1025T>C c.(1024-1026)tTc>tCc p.F342S COAD 7 30492343 30492343 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr7:30492343G>T c.690C>A c.(688-690)ttC>ttA p.F230L COAD 7 30494853 30494853 + Missense_Mutation SNP T T G TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr7:30494853T>G c.276A>C c.(274-276)caA>caC p.Q92H COADREAD 7 30485797 30485797 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr7:30485797C>T c.2413G>A c.(2413-2415)Gcc>Acc p.A805T COADREAD 7 30486604 30486604 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr7:30486604C>T c.2348G>A c.(2347-2349)tGc>tAc p.C783Y COADREAD 7 30486618 30486618 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr7:30486618T>G c.2334A>C c.(2332-2334)aaA>aaC p.K778N COADREAD 7 30487963 30487963 + Missense_Mutation SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr7:30487963T>C c.2236A>G c.(2236-2238)Aag>Gag p.K746E COADREAD 7 30490974 30490974 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr7:30490974C>T c.2059G>A c.(2059-2061)Gcc>Acc p.A687T COADREAD 7 30491556 30491556 + Missense_Mutation SNP T T C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr7:30491556T>C c.1477A>G c.(1477-1479)Atg>Gtg p.M493V COADREAD 7 30491959 30491959 + Silent SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr7:30491959G>A c.1074C>T c.(1072-1074)cgC>cgT p.R358R COADREAD 7 30491974 30491974 + Silent SNP G G T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr7:30491974G>T c.1059C>A c.(1057-1059)tcC>tcA p.S353S COADREAD 7 30492008 30492008 + Missense_Mutation SNP A A G TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr7:30492008A>G c.1025T>C c.(1024-1026)tTc>tCc p.F342S COADREAD 7 30492330 30492330 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr7:30492330G>A c.703C>T c.(703-705)Cgc>Tgc p.R235C COADREAD 7 30492343 30492343 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr7:30492343G>T c.690C>A c.(688-690)ttC>ttA p.F230L COADREAD 7 30494853 30494853 + Missense_Mutation SNP T T G TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr7:30494853T>G c.276A>C c.(274-276)caA>caC p.Q92H DLBC 7 30491081 30491081 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr7:30491081G>A c.1952C>T c.(1951-1953)aCg>aTg p.T651M ESCA 7 30477261 30477261 + Missense_Mutation SNP T T A TCGA-VR-AA4G-01A-11D-A37C-09 TCGA-VR-AA4G-10A-01D-A37F-09 g.chr7:30477261T>A c.2465A>T c.(2464-2466)aAt>aTt p.N822I ESCA 7 30491747 30491747 + Missense_Mutation SNP G G T TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr7:30491747G>T c.1286C>A c.(1285-1287)aCt>aAt p.T429N ESCA 7 30491759 30491759 + Missense_Mutation SNP A A C TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr7:30491759A>C c.1274T>G c.(1273-1275)tTc>tGc p.F425C ESCA 7 30492172 30492172 + Silent SNP G G A TCGA-JY-A939-01A-12D-A37C-09 TCGA-JY-A939-10A-01D-A37F-09 g.chr7:30492172G>A c.861C>T c.(859-861)gaC>gaT p.D287D ESCA 7 30492190 30492190 + Missense_Mutation SNP G G T TCGA-L7-A6VZ-01A-12D-A33E-09 TCGA-L7-A6VZ-10A-01D-A33H-09 g.chr7:30492190G>T c.843C>A c.(841-843)ttC>ttA p.F281L GBM 7 30492358 30492358 + Silent SNP G G A TCGA-02-2485-01A-01D-1494-08 TCGA-02-2485-10A-01D-1494-08 g.chr7:30492358G>A c.675C>T c.(673-675)gaC>gaT p.D225D GBM 7 30492365 30492365 + Missense_Mutation SNP C C T TCGA-12-3652-01A-01D-1495-08 TCGA-12-3652-10A-01D-1495-08 g.chr7:30492365C>T c.668G>A c.(667-669)cGg>cAg p.R223Q GBM 7 30496383 30496383 + Missense_Mutation SNP G G A TCGA-32-2634-01A-01D-1495-08 TCGA-32-2634-10A-01D-1495-08 g.chr7:30496383G>A c.155C>T c.(154-156)gCc>gTc p.A52V GBMLGG 7 30491398 30491398 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:30491398C>A c.1635G>T c.(1633-1635)caG>caT p.Q545H GBMLGG 7 30492358 30492358 + Silent SNP G G A TCGA-02-2485-01A-01D-1494-08 TCGA-02-2485-10A-01D-1494-08 g.chr7:30492358G>A c.675C>T c.(673-675)gaC>gaT p.D225D GBMLGG 7 30492365 30492365 + Missense_Mutation SNP C C T TCGA-12-3652-01A-01D-1495-08 TCGA-12-3652-10A-01D-1495-08 g.chr7:30492365C>T c.668G>A c.(667-669)cGg>cAg p.R223Q GBMLGG 7 30496383 30496383 + Missense_Mutation SNP G G A TCGA-32-2634-01A-01D-1495-08 TCGA-32-2634-10A-01D-1495-08 g.chr7:30496383G>A c.155C>T c.(154-156)gCc>gTc p.A52V HNSC 7 30472736 30472736 + Missense_Mutation SNP A A G TCGA-DQ-5629-01A-01D-1870-08 TCGA-DQ-5629-10A-01D-1870-08 g.chr7:30472736A>G c.2681T>C c.(2680-2682)gTc>gCc p.V894A HNSC 7 30485798 30485798 + Silent SNP G G A TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr7:30485798G>A c.2412C>T c.(2410-2412)ctC>ctT p.L804L HNSC 7 30485828 30485828 + Silent SNP G G A TCGA-CV-7180-01A-11D-2012-08 TCGA-CV-7180-10A-01D-2013-08 g.chr7:30485828G>A c.2382C>T c.(2380-2382)aaC>aaT p.N794N HNSC 7 30486608 30486608 + Missense_Mutation SNP C C T TCGA-DQ-7596-01A-11D-2229-08 TCGA-DQ-7596-10D-01D-2229-08 g.chr7:30486608C>T c.2344G>A c.(2344-2346)Gaa>Aaa p.E782K HNSC 7 30486644 30486644 + Missense_Mutation SNP C C T TCGA-CV-6937-01A-11D-2012-08 TCGA-CV-6937-10A-01D-2013-08 g.chr7:30486644C>T c.2308G>A c.(2308-2310)Gat>Aat p.D770N HNSC 7 30491286 30491286 + Missense_Mutation SNP C C G TCGA-CV-A45X-01A-21D-A25D-08 TCGA-CV-A45X-10A-01D-A25E-08 g.chr7:30491286C>G c.1747G>C c.(1747-1749)Gat>Cat p.D583H HNSC 7 30491316 30491316 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr7:30491316G>A c.1717C>T c.(1717-1719)Ccg>Tcg p.P573S HNSC 7 30491745 30491745 + Missense_Mutation SNP C C T TCGA-CQ-7064-01A-11D-2394-08 TCGA-CQ-7064-10A-01D-2394-08 g.chr7:30491745C>T c.1288G>A c.(1288-1290)Gag>Aag p.E430K HNSC 7 30492295 30492295 + Silent SNP G G A TCGA-BA-4075-01A-01D-1434-08 TCGA-BA-4075-10A-01D-1434-08 g.chr7:30492295G>A c.738C>T c.(736-738)gaC>gaT p.D246D HNSC 7 30492447 30492447 + Missense_Mutation SNP C C T TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr7:30492447C>T c.586G>A c.(586-588)Gag>Aag p.E196K KIPAN 7 30472766 30472766 + Missense_Mutation SNP A A G TCGA-AL-3473-01A-01D-1252-08 TCGA-AL-3473-10A-01D-1252-08 g.chr7:30472766A>G c.2651T>C c.(2650-2652)gTg>gCg p.V884A KIPAN 7 30475651 30475651 + Missense_Mutation SNP T T A TCGA-B9-4116-01A-01D-1252-08 TCGA-B9-4116-10A-01D-1252-08 g.chr7:30475651T>A c.2584A>T c.(2584-2586)Agg>Tgg p.R862W KIPAN 7 30486629 30486629 + Missense_Mutation SNP A A T TCGA-B0-4823-01A-02D-1421-08 TCGA-B0-4823-11A-01D-1421-08 g.chr7:30486629A>T c.2323T>A c.(2323-2325)Tac>Aac p.Y775N KIPAN 7 30492406 30492406 + Silent SNP G G A TCGA-A4-A5XZ-01A-11D-A31X-10 TCGA-A4-A5XZ-10A-01D-A31X-10 g.chr7:30492406G>A c.627C>T c.(625-627)tcC>tcT p.S209S KIRC 7 30486629 30486629 + Missense_Mutation SNP A A T TCGA-B0-4823-01A-02D-1421-08 TCGA-B0-4823-11A-01D-1421-08 g.chr7:30486629A>T c.2323T>A c.(2323-2325)Tac>Aac p.Y775N KIRP 7 30472766 30472766 + Missense_Mutation SNP A A G TCGA-AL-3473-01A-01D-1252-08 TCGA-AL-3473-10A-01D-1252-08 g.chr7:30472766A>G c.2651T>C c.(2650-2652)gTg>gCg p.V884A KIRP 7 30475651 30475651 + Missense_Mutation SNP T T A TCGA-B9-4116-01A-01D-1252-08 TCGA-B9-4116-10A-01D-1252-08 g.chr7:30475651T>A c.2584A>T c.(2584-2586)Agg>Tgg p.R862W KIRP 7 30492406 30492406 + Silent SNP G G A TCGA-A4-A5XZ-01A-11D-A31X-10 TCGA-A4-A5XZ-10A-01D-A31X-10 g.chr7:30492406G>A c.627C>T c.(625-627)tcC>tcT p.S209S LGG 7 30491398 30491398 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:30491398C>A c.1635G>T c.(1633-1635)caG>caT p.Q545H LIHC 7 30492539 30492539 + Missense_Mutation SNP T T C TCGA-DD-AACD-01A-11D-A40R-10 TCGA-DD-AACD-10A-01D-A40U-10 g.chr7:30492539T>C c.494A>G c.(493-495)gAg>gGg p.E165G LUAD 7 30475652 30475652 + Silent SNP C C T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr7:30475652C>T c.2583G>A c.(2581-2583)gcG>gcA p.A861A LUAD 7 30490879 30490879 + Silent SNP G G A TCGA-55-A493-01A-11D-A24D-08 TCGA-55-A493-10A-01D-A24F-08 g.chr7:30490879G>A c.2154C>T c.(2152-2154)taC>taT p.Y718Y LUAD 7 30490920 30490920 + Silent SNP G G T TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr7:30490920G>T c.2113C>A c.(2113-2115)Cgg>Agg p.R705R LUAD 7 30490947 30490947 + Missense_Mutation SNP A A G TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr7:30490947A>G c.2086T>C c.(2086-2088)Tcc>Ccc p.S696P LUAD 7 30491319 30491319 + Missense_Mutation SNP C C A TCGA-95-A4VK-01A-11D-A25L-08 TCGA-95-A4VK-10A-01D-A25L-08 g.chr7:30491319C>A c.1714G>T c.(1714-1716)Ggt>Tgt p.G572C LUAD 7 30491515 30491515 + Silent SNP G G A TCGA-55-6981-01A-11D-1945-08 TCGA-55-6981-11A-01D-1945-08 g.chr7:30491515G>A c.1518C>T c.(1516-1518)ccC>ccT p.P506P LUAD 7 30492002 30492002 + Missense_Mutation SNP C C A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr7:30492002C>A c.1031G>T c.(1030-1032)cGg>cTg p.R344L LUAD 7 30492289 30492289 + Silent SNP C C A TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr7:30492289C>A c.744G>T c.(742-744)ctG>ctT p.L248L LUAD 7 30492319 30492319 + Missense_Mutation SNP C C T TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr7:30492319C>T c.714G>A c.(712-714)atG>atA p.M238I LUAD 7 30492353 30492353 + Missense_Mutation SNP C C A TCGA-50-6593-01A-11D-1753-08 TCGA-50-6593-11A-01D-1753-08 g.chr7:30492353C>A c.680G>T c.(679-681)gGg>gTg p.G227V LUAD 7 30492655 30492655 + Splice_Site SNP C C T TCGA-49-4506-01A-01D-1265-08 TCGA-49-4506-11A-01D-1265-08 g.chr7:30492655C>T c.378G>A c.(376-378)gtG>gtA p.V126V LUAD 7 30494771 30494771 + Missense_Mutation SNP C C T TCGA-69-7760-01A-11D-2167-08 TCGA-69-7760-10A-01D-2167-08 g.chr7:30494771C>T c.358G>A c.(358-360)Gtg>Atg p.V120M LUAD 7 30494868 30494868 + Silent SNP G G C TCGA-55-7913-01B-11D-2238-08 TCGA-55-7913-10A-01D-2238-08 g.chr7:30494868G>C c.261C>G c.(259-261)ctC>ctG p.L87L LUSC 7 30469038 30469038 + Missense_Mutation SNP G G T TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr7:30469038G>T c.2741C>A c.(2740-2742)gCc>gAc p.A914D LUSC 7 30475671 30475671 + Missense_Mutation SNP T T C TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr7:30475671T>C c.2564A>G c.(2563-2565)gAa>gGa p.E855G LUSC 7 30490872 30490872 + Missense_Mutation SNP G G A TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr7:30490872G>A c.2161C>T c.(2161-2163)Cgg>Tgg p.R721W LUSC 7 30491410 30491410 + Silent SNP G G A TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr7:30491410G>A c.1623C>T c.(1621-1623)ctC>ctT p.L541L LUSC 7 30492088 30492088 + Silent SNP G G A TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr7:30492088G>A c.945C>T c.(943-945)gcC>gcT p.A315A LUSC 7 30492316 30492316 + Silent SNP G G A TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr7:30492316G>A c.717C>T c.(715-717)ttC>ttT p.F239F LUSC 7 30492391 30492391 + Silent SNP C C T TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr7:30492391C>T c.642G>A c.(640-642)cgG>cgA p.R214R LUSC 7 30492415 30492415 + Silent SNP C C T TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr7:30492415C>T c.618G>A c.(616-618)gtG>gtA p.V206V LUSC 7 30496374 30496374 + Missense_Mutation SNP G G A TCGA-22-4599-01A-01D-1441-08 TCGA-22-4599-11A-01D-1441-08 g.chr7:30496374G>A c.164C>T c.(163-165)gCg>gTg p.A55V OV 7 30487962 30487962 + Missense_Mutation SNP T T G TCGA-10-0928-01A-02W-0419-10 TCGA-10-0928-11A-01W-0419-10 g.chr7:30487962T>G c.2237A>C c.(2236-2238)aAg>aCg p.K746T PAAD 7 30490965 30490965 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr7:30490965C>T c.2068G>A c.(2068-2070)Gcc>Acc p.A690T PAAD 7 30491717 30491717 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr7:30491717C>A c.1316G>T c.(1315-1317)aGc>aTc p.S439I PAAD 7 30496420 30496420 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr7:30496420G>T c.118C>A c.(118-120)Ctg>Atg p.L40M PRAD 7 30469004 30469004 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr7:30469004G>A c.2775C>T c.(2773-2775)ggC>ggT p.G925G PRAD 7 30475683 30475683 + Missense_Mutation SNP C C T TCGA-EJ-A65F-01A-21D-A30X-08 TCGA-EJ-A65F-10A-01D-A30X-08 g.chr7:30475683C>T c.2552G>A c.(2551-2553)gGc>gAc p.G851D PRAD 7 30485797 30485797 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr7:30485797C>T c.2413G>A c.(2413-2415)Gcc>Acc p.A805T PRAD 7 30491366 30491366 + Missense_Mutation SNP G G A TCGA-CH-5792-01A-11D-1576-08 TCGA-CH-5792-10A-01D-1576-08 g.chr7:30491366G>A c.1667C>T c.(1666-1668)aCg>aTg p.T556M PRAD 7 30491788 30491788 + Silent SNP G G A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr7:30491788G>A c.1245C>T c.(1243-1245)ccC>ccT p.P415P PRAD 7 30491972 30491972 + Missense_Mutation SNP G G A TCGA-J9-A8CM-01A-11D-A34U-08 TCGA-J9-A8CM-10A-01D-A34X-08 g.chr7:30491972G>A c.1061C>T c.(1060-1062)cCc>cTc p.P354L PRAD 7 30492455 30492455 + Missense_Mutation SNP T T A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr7:30492455T>A c.578A>T c.(577-579)gAg>gTg p.E193V READ 7 30492330 30492330 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr7:30492330G>A c.703C>T c.(703-705)Cgc>Tgc p.R235C SARC 7 30490912 30490912 + Silent SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr7:30490912G>A c.2121C>T c.(2119-2121)gcC>gcT p.A707A SARC 7 30490913 30490913 + Missense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr7:30490913G>A c.2120C>T c.(2119-2121)gCc>gTc p.A707V SKCM 7 30491125 30491125 + Silent SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr7:30491125G>A c.1908C>T c.(1906-1908)ccC>ccT p.P636P SKCM 7 30491343 30491343 + Missense_Mutation SNP G G A TCGA-ER-A19E-06A-11D-A197-08 TCGA-ER-A19E-10A-01D-A199-08 g.chr7:30491343G>A c.1690C>T c.(1690-1692)Ccg>Tcg p.P564S SKCM 7 30491735 30491735 + Missense_Mutation SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr7:30491735A>G c.1298T>C c.(1297-1299)cTg>cCg p.L433P SKCM 7 30491985 30491985 + Missense_Mutation SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr7:30491985G>A c.1048C>T c.(1048-1050)Cgg>Tgg p.R350W SKCM 7 30491986 30491986 + Silent SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr7:30491986G>A c.1047C>T c.(1045-1047)ctC>ctT p.L349L SKCM 7 30492007 30492007 + Silent SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr7:30492007G>A c.1026C>T c.(1024-1026)ttC>ttT p.F342F SKCM 7 30492014 30492014 + Missense_Mutation SNP C C G TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr7:30492014C>G c.1019G>C c.(1018-1020)cGc>cCc p.R340P SKCM 7 30492118 30492118 + Nonsense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr7:30492118C>T c.915G>A c.(913-915)tgG>tgA p.W305* SKCM 7 30492184 30492184 + Silent SNP G G A TCGA-EE-A2GH-06A-11D-A196-08 TCGA-EE-A2GH-10A-01D-A198-08 g.chr7:30492184G>A c.849C>T c.(847-849)ttC>ttT p.F283F SKCM 7 30492343 30492343 + Missense_Mutation SNP G G T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr7:30492343G>T c.690C>A c.(688-690)ttC>ttA p.F230L SKCM 7 30492470 30492470 + Missense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr7:30492470G>A c.563C>T c.(562-564)aCc>aTc p.T188I SKCM 7 30492619 30492619 + Silent SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr7:30492619G>A c.414C>T c.(412-414)ggC>ggT p.G138G SKCM 7 30494798 30494798 + Missense_Mutation SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr7:30494798G>A c.331C>T c.(331-333)Cct>Tct p.P111S SKCM 7 30494901 30494901 + Missense_Mutation SNP C C A TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr7:30494901C>A c.228G>T c.(226-228)caG>caT p.Q76H

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 7 30492397 30492397 single base substitution T C downstream_gene_variant ALL-US 7 30492397 30492397 single base substitution T C exon_variant ALL-US 7 30492397 30492397 single base substitution T C intron_variant ALL-US 7 30492397 30492397 single base substitution T C synonymous_variant L212L 636A>G ALL-US 7 30492397 30492397 single base substitution T C upstream_gene_variant BLCA-CN 7 30472761 30472761 single base substitution C T 3_prime_UTR_variant BLCA-CN 7 30472761 30472761 single base substitution C T exon_variant BLCA-CN 7 30472761 30472761 single base substitution C T intron_variant BLCA-CN 7 30472761 30472761 single base substitution C T missense_variant E886K 2656G>A BLCA-CN 7 30492011 30492011 single base substitution T A 3_prime_UTR_variant BLCA-CN 7 30492011 30492011 single base substitution T A downstream_gene_variant BLCA-CN 7 30492011 30492011 single base substitution T A exon_variant BLCA-CN 7 30492011 30492011 single base substitution T A missense_variant Q341L 1022A>T BLCA-CN 7 30492011 30492011 single base substitution T A upstream_gene_variant BLCA-US 7 30485764 30485764 single base substitution C G 3_prime_UTR_variant BLCA-US 7 30485764 30485764 single base substitution C G exon_variant BLCA-US 7 30485764 30485764 single base substitution C G missense_variant E816Q 2446G>C BLCA-US 7 30492526 30492526 single base substitution G A downstream_gene_variant BLCA-US 7 30492526 30492526 single base substitution G A exon_variant BLCA-US 7 30492526 30492526 single base substitution G A synonymous_variant F169F 507C>T BLCA-US 7 30492526 30492526 single base substitution G A upstream_gene_variant BRCA-EU 7 30459916 30459916 single base substitution C T downstream_gene_variant BRCA-EU 7 30460356 30460356 single base substitution G A downstream_gene_variant BRCA-EU 7 30461454 30461454 single base substitution A G downstream_gene_variant BRCA-EU 7 30461558 30461558 single base substitution G A downstream_gene_variant BRCA-EU 7 30462177 30462177 single base substitution G A downstream_gene_variant BRCA-EU 7 30463106 30463106 single base substitution T C downstream_gene_variant BRCA-EU 7 30464906 30464906 single base substitution G C 3_prime_UTR_variant BRCA-EU 7 30464906 30464906 single base substitution G C exon_variant BRCA-EU 7 30465384 30465384 single base substitution C G intron_variant BRCA-EU 7 30465951 30465951 single base substitution T G intron_variant BRCA-EU 7 30466186 30466186 single base substitution G C intron_variant BRCA-EU 7 30466522 30466522 single base substitution G A intron_variant BRCA-EU 7 30466781 30466781 single base substitution C G intron_variant BRCA-EU 7 30466824 30466824 single base substitution C T intron_variant BRCA-EU 7 30467626 30467626 single base substitution C T intron_variant BRCA-EU 7 30467992 30467992 single base substitution A T intron_variant BRCA-EU 7 30468288 30468288 insertion of <=200bp - T intron_variant BRCA-EU 7 30469257 30469257 single base substitution G A intron_variant BRCA-EU 7 30469444 30469444 single base substitution G A intron_variant BRCA-EU 7 30469722 30469722 single base substitution C G intron_variant BRCA-EU 7 30470030 30470030 single base substitution C T intron_variant BRCA-EU 7 30470927 30470928 deletion of <=200bp TC - intron_variant BRCA-EU 7 30472379 30472379 single base substitution G C intron_variant BRCA-EU 7 30472554 30472554 single base substitution G A intron_variant BRCA-EU 7 30472557 30472557 single base substitution G A intron_variant BRCA-EU 7 30472864 30472864 single base substitution G C exon_variant BRCA-EU 7 30472864 30472864 single base substitution G C intron_variant BRCA-EU 7 30474785 30474785 single base substitution C G intron_variant BRCA-EU 7 30474785 30474785 single base substitution C G upstream_gene_variant BRCA-EU 7 30475475 30475475 single base substitution A G intron_variant BRCA-EU 7 30475475 30475475 single base substitution A G upstream_gene_variant BRCA-EU 7 30475802 30475802 single base substitution G C intron_variant BRCA-EU 7 30475802 30475802 single base substitution G C upstream_gene_variant BRCA-EU 7 30476641 30476641 single base substitution T C intron_variant BRCA-EU 7 30476641 30476641 single base substitution T C upstream_gene_variant BRCA-EU 7 30476662 30476662 deletion of <=200bp A - intron_variant BRCA-EU 7 30476662 30476662 deletion of <=200bp A - upstream_gene_variant BRCA-EU 7 30479444 30479444 single base substitution A G intron_variant BRCA-EU 7 30484851 30484851 single base substitution C T intron_variant BRCA-EU 7 30488425 30488425 single base substitution G A downstream_gene_variant BRCA-EU 7 30488425 30488425 single base substitution G A intron_variant BRCA-EU 7 30488425 30488425 single base substitution G A upstream_gene_variant BRCA-EU 7 30488710 30488710 single base substitution C T downstream_gene_variant BRCA-EU 7 30488710 30488710 single base substitution C T intron_variant BRCA-EU 7 30488710 30488710 single base substitution C T upstream_gene_variant BRCA-EU 7 30490693 30490693 single base substitution C G downstream_gene_variant BRCA-EU 7 30490693 30490693 single base substitution C G intron_variant BRCA-EU 7 30490693 30490693 single base substitution C G upstream_gene_variant BRCA-EU 7 30492460 30492460 single base substitution G A downstream_gene_variant BRCA-EU 7 30492460 30492460 single base substitution G A exon_variant BRCA-EU 7 30492460 30492460 single base substitution G A synonymous_variant L191L 573C>T BRCA-EU 7 30492460 30492460 single base substitution G A upstream_gene_variant BRCA-EU 7 30492846 30492846 single base substitution G A downstream_gene_variant BRCA-EU 7 30492846 30492846 single base substitution G A intron_variant BRCA-EU 7 30492991 30492991 single base substitution C A downstream_gene_variant BRCA-EU 7 30492991 30492991 single base substitution C A intron_variant BRCA-EU 7 30494009 30494009 single base substitution G A downstream_gene_variant BRCA-EU 7 30494009 30494009 single base substitution G A intron_variant BRCA-EU 7 30494236 30494236 single base substitution A G downstream_gene_variant BRCA-EU 7 30494236 30494236 single base substitution A G intron_variant BRCA-EU 7 30495846 30495846 single base substitution C T downstream_gene_variant BRCA-EU 7 30495846 30495846 single base substitution C T intron_variant BRCA-EU 7 30496373 30496373 single base substitution C T downstream_gene_variant BRCA-EU 7 30496373 30496373 single base substitution C T exon_variant BRCA-EU 7 30496373 30496373 single base substitution C T synonymous_variant A55A 165G>A BRCA-EU 7 30497911 30497911 single base substitution T G intron_variant BRCA-EU 7 30497988 30497988 deletion of <=200bp A - intron_variant BRCA-EU 7 30498104 30498104 insertion of <=200bp - T intron_variant BRCA-EU 7 30500199 30500201 deletion of <=200bp AGG - intron_variant BRCA-EU 7 30500833 30500833 insertion of <=200bp - GCCCAG intron_variant BRCA-EU 7 30501522 30501522 deletion of <=200bp T - intron_variant BRCA-EU 7 30501923 30501923 single base substitution G T intron_variant BRCA-EU 7 30504586 30504586 single base substitution G A intron_variant BRCA-EU 7 30505599 30505599 single base substitution C G intron_variant BRCA-EU 7 30506100 30506100 single base substitution G A intron_variant BRCA-EU 7 30507315 30507318 deletion of <=200bp TTTG - intron_variant BRCA-EU 7 30507970 30507970 single base substitution G C intron_variant BRCA-EU 7 30508171 30508171 single base substitution G C intron_variant BRCA-EU 7 30508245 30508245 single base substitution T C intron_variant BRCA-EU 7 30508507 30508507 single base substitution G A intron_variant BRCA-EU 7 30509039 30509039 single base substitution C G intron_variant BRCA-EU 7 30510525 30510525 single base substitution G A intron_variant BRCA-EU 7 30511651 30511655 deletion of <=200bp AAGAC - intron_variant BRCA-EU 7 30512023 30512023 single base substitution G A intron_variant BRCA-EU 7 30512672 30512672 single base substitution C G intron_variant BRCA-EU 7 30512786 30512786 single base substitution C G intron_variant BRCA-EU 7 30513168 30513168 deletion of <=200bp T - intron_variant BRCA-EU 7 30514353 30514353 single base substitution A T intron_variant BRCA-EU 7 30514599 30514599 insertion of <=200bp - A intron_variant BRCA-EU 7 30515210 30515210 single base substitution G T intron_variant BRCA-EU 7 30516269 30516269 single base substitution A G intron_variant BRCA-EU 7 30517744 30517744 single base substitution G T intron_variant BRCA-EU 7 30518926 30518926 single base substitution G A upstream_gene_variant BRCA-EU 7 30520603 30520603 single base substitution C G upstream_gene_variant BRCA-EU 7 30520827 30520827 single base substitution G C upstream_gene_variant BRCA-EU 7 30521010 30521010 single base substitution C G upstream_gene_variant BRCA-EU 7 30521223 30521223 single base substitution C G upstream_gene_variant BRCA-FR 7 30459916 30459916 single base substitution C T downstream_gene_variant BRCA-FR 7 30466781 30466781 single base substitution C G intron_variant BRCA-FR 7 30467992 30467992 single base substitution A T intron_variant BRCA-FR 7 30495562 30495562 single base substitution G A downstream_gene_variant BRCA-FR 7 30495562 30495562 single base substitution G A intron_variant BRCA-FR 7 30497911 30497911 single base substitution T G intron_variant BRCA-FR 7 30500569 30500569 single base substitution G A intron_variant BRCA-FR 7 30520603 30520603 single base substitution C G upstream_gene_variant BRCA-UK 7 30468755 30468755 single base substitution G C intron_variant BRCA-UK 7 30492846 30492846 single base substitution G A downstream_gene_variant BRCA-UK 7 30492846 30492846 single base substitution G A intron_variant BRCA-US 7 30469058 30469058 single base substitution C A 3_prime_UTR_variant BRCA-US 7 30469058 30469058 single base substitution C A exon_variant BRCA-US 7 30469058 30469058 single base substitution C A missense_variant Q907H 2721G>T BRCA-US 7 30472788 30472788 single base substitution G C 3_prime_UTR_variant BRCA-US 7 30472788 30472788 single base substitution G C exon_variant BRCA-US 7 30472788 30472788 single base substitution G C intron_variant BRCA-US 7 30472788 30472788 single base substitution G C missense_variant Q877E 2629C>G BRCA-US 7 30491714 30491714 single base substitution C T downstream_gene_variant BRCA-US 7 30491714 30491714 single base substitution C T exon_variant BRCA-US 7 30491714 30491714 single base substitution C T missense_variant S440N 1319G>A BRCA-US 7 30491714 30491714 single base substitution C T upstream_gene_variant BRCA-US 7 30491883 30491883 single base substitution G T 3_prime_UTR_variant BRCA-US 7 30491883 30491883 single base substitution G T downstream_gene_variant BRCA-US 7 30491883 30491883 single base substitution G T exon_variant BRCA-US 7 30491883 30491883 single base substitution G T missense_variant L384I 1150C>A BRCA-US 7 30491883 30491883 single base substitution G T upstream_gene_variant BRCA-US 7 30492497 30492498 deletion of <=200bp CT - downstream_gene_variant BRCA-US 7 30492497 30492498 deletion of <=200bp CT - exon_variant BRCA-US 7 30492497 30492498 deletion of <=200bp CT - frameshift_variant S179 BRCA-US 7 30492497 30492498 deletion of <=200bp CT - upstream_gene_variant BRCA-US 7 30496531 30496531 single base substitution C G exon_variant BRCA-US 7 30496531 30496531 single base substitution C G missense_variant E3Q 7G>C BTCA-JP 7 30491915 30491915 single base substitution C T 3_prime_UTR_variant BTCA-JP 7 30491915 30491915 single base substitution C T downstream_gene_variant BTCA-JP 7 30491915 30491915 single base substitution C T exon_variant BTCA-JP 7 30491915 30491915 single base substitution C T missense_variant R373H 1118G>A BTCA-JP 7 30491915 30491915 single base substitution C T upstream_gene_variant CESC-US 7 30468996 30468996 single base substitution T C 3_prime_UTR_variant CESC-US 7 30468996 30468996 single base substitution T C exon_variant CESC-US 7 30468996 30468996 single base substitution T C missense_variant E928G 2783A>G CLLE-ES 7 30472809 30472809 single base substitution A T exon_variant CLLE-ES 7 30472809 30472809 single base substitution A T intron_variant CLLE-ES 7 30478693 30478693 single base substitution G T intron_variant CLLE-ES 7 30491907 30491907 single base substitution T C 3_prime_UTR_variant CLLE-ES 7 30491907 30491907 single base substitution T C downstream_gene_variant CLLE-ES 7 30491907 30491907 single base substitution T C exon_variant CLLE-ES 7 30491907 30491907 single base substitution T C missense_variant S376G 1126A>G CLLE-ES 7 30491907 30491907 single base substitution T C upstream_gene_variant COAD-US 7 30486618 30486618 single base substitution T G exon_variant COAD-US 7 30486618 30486618 single base substitution T G intron_variant COAD-US 7 30486618 30486618 single base substitution T G missense_variant K778N 2334A>C COAD-US 7 30490974 30490974 single base substitution C T downstream_gene_variant COAD-US 7 30490974 30490974 single base substitution C T exon_variant COAD-US 7 30490974 30490974 single base substitution C T missense_variant A687T 2059G>A COAD-US 7 30490974 30490974 single base substitution C T upstream_gene_variant COAD-US 7 30491311 30491311 single base substitution C T downstream_gene_variant COAD-US 7 30491311 30491311 single base substitution C T exon_variant COAD-US 7 30491311 30491311 single base substitution C T synonymous_variant A574A 1722G>A COAD-US 7 30491311 30491311 single base substitution C T upstream_gene_variant COAD-US 7 30491959 30491959 single base substitution G A 3_prime_UTR_variant COAD-US 7 30491959 30491959 single base substitution G A downstream_gene_variant COAD-US 7 30491959 30491959 single base substitution G A exon_variant COAD-US 7 30491959 30491959 single base substitution G A synonymous_variant R358R 1074C>T COAD-US 7 30491959 30491959 single base substitution G A upstream_gene_variant COAD-US 7 30492008 30492008 single base substitution A G 3_prime_UTR_variant COAD-US 7 30492008 30492008 single base substitution A G downstream_gene_variant COAD-US 7 30492008 30492008 single base substitution A G exon_variant COAD-US 7 30492008 30492008 single base substitution A G missense_variant F342S 1025T>C COAD-US 7 30492008 30492008 single base substitution A G upstream_gene_variant COAD-US 7 30492237 30492237 single base substitution C T downstream_gene_variant COAD-US 7 30492237 30492237 single base substitution C T exon_variant COAD-US 7 30492237 30492237 single base substitution C T missense_variant E266K 796G>A COAD-US 7 30492237 30492237 single base substitution C T synonymous_variant P220P 660G>A COAD-US 7 30492237 30492237 single base substitution C T upstream_gene_variant COAD-US 7 30492343 30492343 single base substitution G T downstream_gene_variant COAD-US 7 30492343 30492343 single base substitution G T exon_variant COAD-US 7 30492343 30492343 single base substitution G T intron_variant COAD-US 7 30492343 30492343 single base substitution G T missense_variant F230L 690C>A COAD-US 7 30492343 30492343 single base substitution G T upstream_gene_variant COAD-US 7 30492550 30492550 single base substitution G A downstream_gene_variant COAD-US 7 30492550 30492550 single base substitution G A exon_variant COAD-US 7 30492550 30492550 single base substitution G A synonymous_variant D161D 483C>T COAD-US 7 30492550 30492550 single base substitution G A upstream_gene_variant COAD-US 7 30496382 30496382 single base substitution G C downstream_gene_variant COAD-US 7 30496382 30496382 single base substitution G C exon_variant COAD-US 7 30496382 30496382 single base substitution G C synonymous_variant A52A 156C>G COCA-CN 7 30485710 30485710 single base substitution A C intron_variant COCA-CN 7 30486629 30486629 single base substitution A G exon_variant COCA-CN 7 30486629 30486629 single base substitution A G missense_variant Y775H 2323T>C COCA-CN 7 30486629 30486629 single base substitution A G splice_donor_variant COCA-CN 7 30491121 30491121 single base substitution C T downstream_gene_variant COCA-CN 7 30491121 30491121 single base substitution C T exon_variant COCA-CN 7 30491121 30491121 single base substitution C T missense_variant V638I 1912G>A COCA-CN 7 30491121 30491121 single base substitution C T upstream_gene_variant COCA-CN 7 30491725 30491725 single base substitution C T downstream_gene_variant COCA-CN 7 30491725 30491725 single base substitution C T exon_variant COCA-CN 7 30491725 30491725 single base substitution C T missense_variant M436I 1308G>A COCA-CN 7 30491725 30491725 single base substitution C T upstream_gene_variant COCA-CN 7 30492002 30492002 single base substitution C T 3_prime_UTR_variant COCA-CN 7 30492002 30492002 single base substitution C T downstream_gene_variant COCA-CN 7 30492002 30492002 single base substitution C T exon_variant COCA-CN 7 30492002 30492002 single base substitution C T missense_variant R344Q 1031G>A COCA-CN 7 30492002 30492002 single base substitution C T upstream_gene_variant EOPC-DE 7 30518566 30518566 single base substitution A G upstream_gene_variant ESAD-UK 7 30461025 30461025 single base substitution G A downstream_gene_variant ESAD-UK 7 30463712 30463712 single base substitution C T downstream_gene_variant ESAD-UK 7 30464861 30464861 single base substitution A G 3_prime_UTR_variant ESAD-UK 7 30464861 30464861 single base substitution A G exon_variant ESAD-UK 7 30465231 30465231 single base substitution C A 3_prime_UTR_variant ESAD-UK 7 30465231 30465231 single base substitution C A exon_variant ESAD-UK 7 30465540 30465540 single base substitution C T intron_variant ESAD-UK 7 30468932 30468932 single base substitution A T intron_variant ESAD-UK 7 30475684 30475684 single base substitution C T 3_prime_UTR_variant ESAD-UK 7 30475684 30475684 single base substitution C T intron_variant ESAD-UK 7 30475684 30475684 single base substitution C T missense_variant G851S 2551G>A ESAD-UK 7 30475684 30475684 single base substitution C T upstream_gene_variant ESAD-UK 7 30475698 30475698 single base substitution C G intron_variant ESAD-UK 7 30475698 30475698 single base substitution C G splice_acceptor_variant ESAD-UK 7 30475698 30475698 single base substitution C G upstream_gene_variant ESAD-UK 7 30475926 30475926 single base substitution C A intron_variant ESAD-UK 7 30475926 30475926 single base substitution C A upstream_gene_variant ESAD-UK 7 30477079 30477079 single base substitution A T intron_variant ESAD-UK 7 30477079 30477079 single base substitution A T upstream_gene_variant ESAD-UK 7 30478505 30478505 single base substitution G A intron_variant ESAD-UK 7 30485900 30485900 single base substitution C A exon_variant ESAD-UK 7 30485900 30485900 single base substitution C A intron_variant ESAD-UK 7 30491184 30491184 single base substitution G A downstream_gene_variant ESAD-UK 7 30491184 30491184 single base substitution G A exon_variant ESAD-UK 7 30491184 30491184 single base substitution G A missense_variant R617C 1849C>T ESAD-UK 7 30491184 30491184 single base substitution G A upstream_gene_variant ESAD-UK 7 30497895 30497895 single base substitution G A intron_variant ESAD-UK 7 30499887 30499887 single base substitution A C intron_variant ESAD-UK 7 30501422 30501422 single base substitution T G intron_variant ESAD-UK 7 30503530 30503530 single base substitution T A intron_variant ESAD-UK 7 30504571 30504571 single base substitution C T intron_variant ESAD-UK 7 30508759 30508759 single base substitution T G intron_variant ESAD-UK 7 30509299 30509299 single base substitution C A intron_variant ESAD-UK 7 30512799 30512799 single base substitution G A intron_variant ESAD-UK 7 30513402 30513402 single base substitution G T intron_variant ESAD-UK 7 30514288 30514288 single base substitution T G intron_variant ESAD-UK 7 30516348 30516348 single base substitution G A intron_variant ESAD-UK 7 30518178 30518178 single base substitution A T intron_variant ESAD-UK 7 30518368 30518368 single base substitution G C 5_prime_UTR_variant ESAD-UK 7 30518368 30518368 single base substitution G C upstream_gene_variant ESAD-UK 7 30520636 30520636 single base substitution G T upstream_gene_variant ESAD-UK 7 30521911 30521911 single base substitution C A upstream_gene_variant ESAD-UK 7 30522803 30522803 single base substitution G A upstream_gene_variant ESCA-CN 7 30485852 30485852 single base substitution G A exon_variant ESCA-CN 7 30485852 30485852 single base substitution G A intron_variant ESCA-CN 7 30491050 30491050 single base substitution C A downstream_gene_variant ESCA-CN 7 30491050 30491050 single base substitution C A exon_variant ESCA-CN 7 30491050 30491050 single base substitution C A missense_variant E661D 1983G>T ESCA-CN 7 30491050 30491050 single base substitution C A upstream_gene_variant GBM-US 7 30492358 30492358 single base substitution G A downstream_gene_variant GBM-US 7 30492358 30492358 single base substitution G A exon_variant GBM-US 7 30492358 30492358 single base substitution G A intron_variant GBM-US 7 30492358 30492358 single base substitution G A synonymous_variant D225D 675C>T GBM-US 7 30492358 30492358 single base substitution G A upstream_gene_variant GBM-US 7 30492365 30492365 single base substitution C T downstream_gene_variant GBM-US 7 30492365 30492365 single base substitution C T exon_variant GBM-US 7 30492365 30492365 single base substitution C T intron_variant GBM-US 7 30492365 30492365 single base substitution C T missense_variant R223Q 668G>A GBM-US 7 30492365 30492365 single base substitution C T upstream_gene_variant GBM-US 7 30496383 30496383 single base substitution G A downstream_gene_variant GBM-US 7 30496383 30496383 single base substitution G A exon_variant GBM-US 7 30496383 30496383 single base substitution G A missense_variant A52V 155C>T KIRC-US 7 30486629 30486629 single base substitution A T exon_variant KIRC-US 7 30486629 30486629 single base substitution A T missense_variant Y775N 2323T>A KIRC-US 7 30486629 30486629 single base substitution A T splice_donor_variant KIRC-US 7 30494802 30494802 insertion of <=200bp - A downstream_gene_variant KIRC-US 7 30494802 30494802 insertion of <=200bp - A exon_variant KIRC-US 7 30494802 30494802 insertion of <=200bp - A frameshift_variant F109F? KIRP-US 7 30472766 30472766 single base substitution A G 3_prime_UTR_variant KIRP-US 7 30472766 30472766 single base substitution A G exon_variant KIRP-US 7 30472766 30472766 single base substitution A G intron_variant KIRP-US 7 30472766 30472766 single base substitution A G missense_variant V884A 2651T>C KIRP-US 7 30492406 30492406 single base substitution G A downstream_gene_variant KIRP-US 7 30492406 30492406 single base substitution G A exon_variant KIRP-US 7 30492406 30492406 single base substitution G A intron_variant KIRP-US 7 30492406 30492406 single base substitution G A synonymous_variant S209S 627C>T KIRP-US 7 30492406 30492406 single base substitution G A upstream_gene_variant LAML-KR 7 30460120 30460120 single base substitution G C downstream_gene_variant LICA-FR 7 30463039 30463039 single base substitution T G downstream_gene_variant LICA-FR 7 30472794 30472794 single base substitution G C exon_variant LICA-FR 7 30472794 30472794 single base substitution G C intron_variant LICA-FR 7 30472794 30472794 single base substitution G C missense_variant L875V 2623C>G LICA-FR 7 30472794 30472794 single base substitution G C splice_region_variant LICA-FR 7 30495207 30495207 insertion of <=200bp - T downstream_gene_variant LICA-FR 7 30495207 30495207 insertion of <=200bp - T intron_variant LICA-FR 7 30495221 30495221 single base substitution C T downstream_gene_variant LICA-FR 7 30495221 30495221 single base substitution C T intron_variant LICA-FR 7 30502043 30502043 insertion of <=200bp - T intron_variant LICA-FR 7 30502565 30502565 insertion of <=200bp - A intron_variant LINC-JP 7 30463801 30463801 single base substitution T A downstream_gene_variant LINC-JP 7 30471209 30471209 single base substitution A C intron_variant LINC-JP 7 30472773 30472773 single base substitution C T 3_prime_UTR_variant LINC-JP 7 30472773 30472773 single base substitution C T exon_variant LINC-JP 7 30472773 30472773 single base substitution C T intron_variant LINC-JP 7 30472773 30472773 single base substitution C T missense_variant D882N 2644G>A LINC-JP 7 30485797 30485797 single base substitution C A 3_prime_UTR_variant LINC-JP 7 30485797 30485797 single base substitution C A exon_variant LINC-JP 7 30485797 30485797 single base substitution C A missense_variant A805S 2413G>T LINC-JP 7 30487792 30487792 single base substitution C T downstream_gene_variant LINC-JP 7 30487792 30487792 single base substitution C T intron_variant LINC-JP 7 30487792 30487792 single base substitution C T upstream_gene_variant LINC-JP 7 30487921 30487921 single base substitution A G downstream_gene_variant LINC-JP 7 30487921 30487921 single base substitution A G exon_variant LINC-JP 7 30487921 30487921 single base substitution A G missense_variant Y760H 2278T>C LINC-JP 7 30487921 30487921 single base substitution A G upstream_gene_variant LINC-JP 7 30487943 30487943 single base substitution C A downstream_gene_variant LINC-JP 7 30487943 30487943 single base substitution C A exon_variant LINC-JP 7 30487943 30487943 single base substitution C A synonymous_variant L752L 2256G>T LINC-JP 7 30487943 30487943 single base substitution C A upstream_gene_variant LINC-JP 7 30491930 30491930 single base substitution C T 3_prime_UTR_variant LINC-JP 7 30491930 30491930 single base substitution C T downstream_gene_variant LINC-JP 7 30491930 30491930 single base substitution C T exon_variant LINC-JP 7 30491930 30491930 single base substitution C T missense_variant R368Q 1103G>A LINC-JP 7 30491930 30491930 single base substitution C T upstream_gene_variant LINC-JP 7 30498980 30498980 single base substitution C T intron_variant LINC-JP 7 30503738 30503738 single base substitution A C intron_variant LINC-JP 7 30504647 30504647 single base substitution C G intron_variant LIRI-JP 7 30459775 30459775 single base substitution C T downstream_gene_variant LIRI-JP 7 30460377 30460377 single base substitution G A downstream_gene_variant LIRI-JP 7 30462760 30462760 single base substitution A G downstream_gene_variant LIRI-JP 7 30463055 30463055 single base substitution T A downstream_gene_variant LIRI-JP 7 30463178 30463178 single base substitution T C downstream_gene_variant LIRI-JP 7 30464159 30464159 single base substitution A G 3_prime_UTR_variant LIRI-JP 7 30464159 30464159 single base substitution A G downstream_gene_variant LIRI-JP 7 30464159 30464159 single base substitution A G exon_variant LIRI-JP 7 30471073 30471073 single base substitution A T intron_variant LIRI-JP 7 30473280 30473280 single base substitution G A intron_variant LIRI-JP 7 30473280 30473280 single base substitution G A upstream_gene_variant LIRI-JP 7 30488763 30488763 single base substitution C A downstream_gene_variant LIRI-JP 7 30488763 30488763 single base substitution C A intron_variant LIRI-JP 7 30488763 30488763 single base substitution C A upstream_gene_variant LIRI-JP 7 30492014 30492014 single base substitution C T 3_prime_UTR_variant LIRI-JP 7 30492014 30492014 single base substitution C T downstream_gene_variant LIRI-JP 7 30492014 30492014 single base substitution C T exon_variant LIRI-JP 7 30492014 30492014 single base substitution C T missense_variant R340H 1019G>A LIRI-JP 7 30492014 30492014 single base substitution C T upstream_gene_variant LIRI-JP 7 30493241 30493241 single base substitution G T downstream_gene_variant LIRI-JP 7 30493241 30493241 single base substitution G T intron_variant LIRI-JP 7 30493681 30493681 single base substitution C A downstream_gene_variant LIRI-JP 7 30493681 30493681 single base substitution C A intron_variant LIRI-JP 7 30494037 30494037 single base substitution T C downstream_gene_variant LIRI-JP 7 30494037 30494037 single base substitution T C intron_variant LIRI-JP 7 30499846 30499846 single base substitution T G intron_variant LIRI-JP 7 30499932 30499932 single base substitution T C intron_variant LIRI-JP 7 30501590 30501590 single base substitution G A intron_variant LIRI-JP 7 30503295 30503295 single base substitution C T 5_prime_UTR_variant LIRI-JP 7 30503295 30503295 single base substitution C T intron_variant LIRI-JP 7 30504185 30504185 single base substitution T C intron_variant LIRI-JP 7 30505594 30505594 single base substitution C G intron_variant LIRI-JP 7 30507458 30507458 single base substitution C A intron_variant LIRI-JP 7 30508198 30508198 single base substitution T C intron_variant LIRI-JP 7 30509059 30509059 single base substitution T C intron_variant LIRI-JP 7 30513256 30513256 single base substitution G C intron_variant LIRI-JP 7 30513513 30513513 single base substitution T C intron_variant LIRI-JP 7 30517134 30517134 single base substitution T C intron_variant LIRI-JP 7 30518193 30518193 single base substitution C G intron_variant LIRI-JP 7 30518545 30518545 single base substitution A G upstream_gene_variant LIRI-JP 7 30518896 30518896 single base substitution T A upstream_gene_variant LIRI-JP 7 30518974 30518974 single base substitution T G upstream_gene_variant LIRI-JP 7 30519685 30519685 single base substitution A G upstream_gene_variant LIRI-JP 7 30519940 30519940 single base substitution G C upstream_gene_variant LIRI-JP 7 30522131 30522131 single base substitution T C upstream_gene_variant LIRI-JP 7 30522159 30522159 single base substitution C T upstream_gene_variant LIRI-JP 7 30523145 30523145 single base substitution C T upstream_gene_variant LUSC-KR 7 30460080 30460080 single base substitution T C downstream_gene_variant LUSC-KR 7 30462979 30462979 single base substitution G A downstream_gene_variant LUSC-KR 7 30476689 30476689 single base substitution T C intron_variant LUSC-KR 7 30476689 30476689 single base substitution T C upstream_gene_variant LUSC-KR 7 30479322 30479322 single base substitution C A intron_variant LUSC-KR 7 30479350 30479350 single base substitution C G intron_variant LUSC-KR 7 30479421 30479421 single base substitution G A intron_variant LUSC-KR 7 30479661 30479661 single base substitution C G intron_variant LUSC-KR 7 30485419 30485419 single base substitution T G intron_variant LUSC-KR 7 30485710 30485710 single base substitution A C intron_variant LUSC-KR 7 30488130 30488130 single base substitution C A downstream_gene_variant LUSC-KR 7 30488130 30488130 single base substitution C A intron_variant LUSC-KR 7 30488130 30488130 single base substitution C A upstream_gene_variant LUSC-KR 7 30491311 30491311 single base substitution C T downstream_gene_variant LUSC-KR 7 30491311 30491311 single base substitution C T exon_variant LUSC-KR 7 30491311 30491311 single base substitution C T synonymous_variant A574A 1722G>A LUSC-KR 7 30491311 30491311 single base substitution C T upstream_gene_variant LUSC-KR 7 30494772 30494772 single base substitution G A downstream_gene_variant LUSC-KR 7 30494772 30494772 single base substitution G A exon_variant LUSC-KR 7 30494772 30494772 single base substitution G A synonymous_variant V119V 357C>T LUSC-KR 7 30494965 30494965 single base substitution G A downstream_gene_variant LUSC-KR 7 30494965 30494965 single base substitution G A intron_variant LUSC-KR 7 30497624 30497624 single base substitution G T intron_variant LUSC-KR 7 30504146 30504146 single base substitution C A intron_variant LUSC-KR 7 30508476 30508476 single base substitution T C intron_variant LUSC-KR 7 30509401 30509401 single base substitution C G intron_variant LUSC-KR 7 30510470 30510470 single base substitution C A intron_variant LUSC-KR 7 30512903 30512903 single base substitution A C intron_variant LUSC-KR 7 30515328 30515328 single base substitution G A intron_variant LUSC-KR 7 30517326 30517326 single base substitution C T intron_variant LUSC-KR 7 30520616 30520616 single base substitution C G upstream_gene_variant LUSC-KR 7 30523096 30523096 single base substitution G C upstream_gene_variant LUSC-US 7 30469038 30469038 single base substitution G T 3_prime_UTR_variant LUSC-US 7 30469038 30469038 single base substitution G T exon_variant LUSC-US 7 30469038 30469038 single base substitution G T missense_variant A914D 2741C>A LUSC-US 7 30475671 30475671 single base substitution T C 3_prime_UTR_variant LUSC-US 7 30475671 30475671 single base substitution T C intron_variant LUSC-US 7 30475671 30475671 single base substitution T C missense_variant E855G 2564A>G LUSC-US 7 30475671 30475671 single base substitution T C upstream_gene_variant LUSC-US 7 30490872 30490872 single base substitution G A downstream_gene_variant LUSC-US 7 30490872 30490872 single base substitution G A exon_variant LUSC-US 7 30490872 30490872 single base substitution G A missense_variant R721W 2161C>T LUSC-US 7 30490872 30490872 single base substitution G A upstream_gene_variant LUSC-US 7 30491410 30491410 single base substitution G A downstream_gene_variant LUSC-US 7 30491410 30491410 single base substitution G A exon_variant LUSC-US 7 30491410 30491410 single base substitution G A synonymous_variant L541L 1623C>T LUSC-US 7 30491410 30491410 single base substitution G A upstream_gene_variant LUSC-US 7 30492088 30492088 single base substitution G A 3_prime_UTR_variant LUSC-US 7 30492088 30492088 single base substitution G A downstream_gene_variant LUSC-US 7 30492088 30492088 single base substitution G A exon_variant LUSC-US 7 30492088 30492088 single base substitution G A synonymous_variant A315A 945C>T LUSC-US 7 30492088 30492088 single base substitution G A upstream_gene_variant LUSC-US 7 30492316 30492316 single base substitution G A downstream_gene_variant LUSC-US 7 30492316 30492316 single base substitution G A exon_variant LUSC-US 7 30492316 30492316 single base substitution G A intron_variant LUSC-US 7 30492316 30492316 single base substitution G A synonymous_variant F239F 717C>T LUSC-US 7 30492316 30492316 single base substitution G A upstream_gene_variant LUSC-US 7 30492391 30492391 single base substitution C T downstream_gene_variant LUSC-US 7 30492391 30492391 single base substitution C T exon_variant LUSC-US 7 30492391 30492391 single base substitution C T intron_variant LUSC-US 7 30492391 30492391 single base substitution C T synonymous_variant R214R 642G>A LUSC-US 7 30492391 30492391 single base substitution C T upstream_gene_variant LUSC-US 7 30492415 30492415 single base substitution C T downstream_gene_variant LUSC-US 7 30492415 30492415 single base substitution C T exon_variant LUSC-US 7 30492415 30492415 single base substitution C T intron_variant LUSC-US 7 30492415 30492415 single base substitution C T synonymous_variant V206V 618G>A LUSC-US 7 30492415 30492415 single base substitution C T upstream_gene_variant LUSC-US 7 30496374 30496374 single base substitution G A downstream_gene_variant LUSC-US 7 30496374 30496374 single base substitution G A exon_variant LUSC-US 7 30496374 30496374 single base substitution G A missense_variant A55V 164C>T MALY-DE 7 30460688 30460688 single base substitution T A downstream_gene_variant MALY-DE 7 30461824 30461824 single base substitution G A downstream_gene_variant MALY-DE 7 30465959 30465959 single base substitution T A intron_variant MALY-DE 7 30471730 30471730 single base substitution C A intron_variant MALY-DE 7 30474721 30474721 single base substitution A G intron_variant MALY-DE 7 30474721 30474721 single base substitution A G upstream_gene_variant MALY-DE 7 30478542 30478542 single base substitution T G intron_variant MALY-DE 7 30486693 30486693 single base substitution C A 3_prime_UTR_variant MALY-DE 7 30486693 30486693 single base substitution C A exon_variant MALY-DE 7 30486693 30486693 single base substitution C A intron_variant MALY-DE 7 30489732 30489732 single base substitution C A downstream_gene_variant MALY-DE 7 30489732 30489732 single base substitution C A intron_variant MALY-DE 7 30489732 30489732 single base substitution C A upstream_gene_variant MALY-DE 7 30491148 30491148 single base substitution G A downstream_gene_variant MALY-DE 7 30491148 30491148 single base substitution G A exon_variant MALY-DE 7 30491148 30491148 single base substitution G A missense_variant R629W 1885C>T MALY-DE 7 30491148 30491148 single base substitution G A upstream_gene_variant MALY-DE 7 30496325 30496325 single base substitution T A downstream_gene_variant MALY-DE 7 30496325 30496325 single base substitution T A intron_variant MALY-DE 7 30502457 30502457 single base substitution A G intron_variant MALY-DE 7 30510869 30510869 single base substitution C T intron_variant MALY-DE 7 30517129 30517129 insertion of <=200bp - TTTG intron_variant MALY-DE 7 30518259 30518259 single base substitution G C 5_prime_UTR_variant MALY-DE 7 30518259 30518259 single base substitution G C upstream_gene_variant MELA-AU 7 30459189 30459189 single base substitution C T downstream_gene_variant MELA-AU 7 30459305 30459305 single base substitution C T downstream_gene_variant MELA-AU 7 30460213 30460213 single base substitution C T downstream_gene_variant MELA-AU 7 30461058 30461058 single base substitution T G downstream_gene_variant MELA-AU 7 30461195 30461195 single base substitution G T downstream_gene_variant MELA-AU 7 30462131 30462131 single base substitution C A downstream_gene_variant MELA-AU 7 30462409 30462409 single base substitution A G downstream_gene_variant MELA-AU 7 30462611 30462612 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 7 30463606 30463606 single base substitution C T downstream_gene_variant MELA-AU 7 30463836 30463836 single base substitution G T downstream_gene_variant MELA-AU 7 30465318 30465318 single base substitution C T 3_prime_UTR_variant MELA-AU 7 30465318 30465318 single base substitution C T exon_variant MELA-AU 7 30465318 30465318 single base substitution C T missense_variant G933E 2798G>A MELA-AU 7 30466395 30466395 single base substitution C T intron_variant MELA-AU 7 30466740 30466740 single base substitution G A intron_variant MELA-AU 7 30467062 30467062 single base substitution A G intron_variant MELA-AU 7 30467935 30467935 single base substitution C T intron_variant MELA-AU 7 30468065 30468065 single base substitution C T intron_variant MELA-AU 7 30469354 30469354 single base substitution C G intron_variant MELA-AU 7 30469722 30469723 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 7 30470173 30470173 single base substitution G A intron_variant MELA-AU 7 30470787 30470787 single base substitution G A intron_variant MELA-AU 7 30471356 30471356 single base substitution A T intron_variant MELA-AU 7 30471360 30471360 single base substitution C T intron_variant MELA-AU 7 30471851 30471851 single base substitution G A intron_variant MELA-AU 7 30475267 30475267 single base substitution G A intron_variant MELA-AU 7 30475267 30475267 single base substitution G A upstream_gene_variant MELA-AU 7 30475326 30475326 single base substitution G A intron_variant MELA-AU 7 30475326 30475326 single base substitution G A upstream_gene_variant MELA-AU 7 30475333 30475333 single base substitution G T intron_variant MELA-AU 7 30475333 30475333 single base substitution G T upstream_gene_variant MELA-AU 7 30475553 30475553 single base substitution G A intron_variant MELA-AU 7 30475553 30475553 single base substitution G A upstream_gene_variant MELA-AU 7 30475668 30475668 single base substitution C T 3_prime_UTR_variant MELA-AU 7 30475668 30475668 single base substitution C T intron_variant MELA-AU 7 30475668 30475668 single base substitution C T missense_variant G856E 2567G>A MELA-AU 7 30475668 30475668 single base substitution C T upstream_gene_variant MELA-AU 7 30475705 30475705 single base substitution G A intron_variant MELA-AU 7 30475705 30475705 single base substitution G A splice_region_variant MELA-AU 7 30475705 30475705 single base substitution G A upstream_gene_variant MELA-AU 7 30475721 30475721 single base substitution G A intron_variant MELA-AU 7 30475721 30475721 single base substitution G A upstream_gene_variant MELA-AU 7 30475760 30475760 single base substitution A G intron_variant MELA-AU 7 30475760 30475760 single base substitution A G upstream_gene_variant MELA-AU 7 30475997 30475997 single base substitution G A intron_variant MELA-AU 7 30475997 30475997 single base substitution G A upstream_gene_variant MELA-AU 7 30476854 30476854 single base substitution G A intron_variant MELA-AU 7 30476854 30476854 single base substitution G A upstream_gene_variant MELA-AU 7 30477111 30477111 single base substitution G A intron_variant MELA-AU 7 30477111 30477111 single base substitution G A upstream_gene_variant MELA-AU 7 30477552 30477552 single base substitution G A intron_variant MELA-AU 7 30477552 30477552 single base substitution G A upstream_gene_variant MELA-AU 7 30477968 30477968 single base substitution G A intron_variant MELA-AU 7 30477968 30477968 single base substitution G A upstream_gene_variant MELA-AU 7 30478017 30478017 single base substitution G A intron_variant MELA-AU 7 30478017 30478017 single base substitution G A upstream_gene_variant MELA-AU 7 30478058 30478058 single base substitution G A intron_variant MELA-AU 7 30478530 30478530 single base substitution G A intron_variant MELA-AU 7 30484928 30484928 single base substitution G A intron_variant MELA-AU 7 30485118 30485118 single base substitution T G intron_variant MELA-AU 7 30485430 30485430 single base substitution G A intron_variant MELA-AU 7 30485749 30485749 single base substitution C T intron_variant MELA-AU 7 30485749 30485749 single base substitution C T splice_region_variant MELA-AU 7 30486136 30486136 single base substitution G A exon_variant MELA-AU 7 30486136 30486136 single base substitution G A intron_variant MELA-AU 7 30488118 30488118 single base substitution G A downstream_gene_variant MELA-AU 7 30488118 30488118 single base substitution G A intron_variant MELA-AU 7 30488118 30488118 single base substitution G A upstream_gene_variant MELA-AU 7 30488373 30488373 single base substitution G A downstream_gene_variant MELA-AU 7 30488373 30488373 single base substitution G A intron_variant MELA-AU 7 30488373 30488373 single base substitution G A upstream_gene_variant MELA-AU 7 30489302 30489302 single base substitution A G downstream_gene_variant MELA-AU 7 30489302 30489302 single base substitution A G intron_variant MELA-AU 7 30489302 30489302 single base substitution A G upstream_gene_variant MELA-AU 7 30489461 30489461 single base substitution G A downstream_gene_variant MELA-AU 7 30489461 30489461 single base substitution G A intron_variant MELA-AU 7 30489461 30489461 single base substitution G A upstream_gene_variant MELA-AU 7 30489898 30489898 single base substitution G A downstream_gene_variant MELA-AU 7 30489898 30489898 single base substitution G A intron_variant MELA-AU 7 30489898 30489898 single base substitution G A upstream_gene_variant MELA-AU 7 30489920 30489920 single base substitution A G downstream_gene_variant MELA-AU 7 30489920 30489920 single base substitution A G intron_variant MELA-AU 7 30489920 30489920 single base substitution A G upstream_gene_variant MELA-AU 7 30490080 30490080 single base substitution G A downstream_gene_variant MELA-AU 7 30490080 30490080 single base substitution G A intron_variant MELA-AU 7 30490080 30490080 single base substitution G A upstream_gene_variant MELA-AU 7 30490313 30490313 single base substitution G A downstream_gene_variant MELA-AU 7 30490313 30490313 single base substitution G A intron_variant MELA-AU 7 30490313 30490313 single base substitution G A upstream_gene_variant MELA-AU 7 30490757 30490757 single base substitution A C downstream_gene_variant MELA-AU 7 30490757 30490757 single base substitution A C intron_variant MELA-AU 7 30490757 30490757 single base substitution A C upstream_gene_variant MELA-AU 7 30491125 30491125 single base substitution G A downstream_gene_variant MELA-AU 7 30491125 30491125 single base substitution G A exon_variant MELA-AU 7 30491125 30491125 single base substitution G A synonymous_variant P636P 1908C>T MELA-AU 7 30491125 30491125 single base substitution G A upstream_gene_variant MELA-AU 7 30491497 30491497 single base substitution G A downstream_gene_variant MELA-AU 7 30491497 30491497 single base substitution G A exon_variant MELA-AU 7 30491497 30491497 single base substitution G A synonymous_variant S512S 1536C>T MELA-AU 7 30491497 30491497 single base substitution G A upstream_gene_variant MELA-AU 7 30492207 30492207 single base substitution G A downstream_gene_variant MELA-AU 7 30492207 30492207 single base substitution G A exon_variant MELA-AU 7 30492207 30492207 single base substitution G A missense_variant P276S 826C>T MELA-AU 7 30492207 30492207 single base substitution G A synonymous_variant S230S 690C>T MELA-AU 7 30492207 30492207 single base substitution G A upstream_gene_variant MELA-AU 7 30492274 30492274 single base substitution C T downstream_gene_variant MELA-AU 7 30492274 30492274 single base substitution C T exon_variant MELA-AU 7 30492274 30492274 single base substitution C T missense_variant C208Y 623G>A MELA-AU 7 30492274 30492274 single base substitution C T synonymous_variant L253L 759G>A MELA-AU 7 30492274 30492274 single base substitution C T upstream_gene_variant MELA-AU 7 30492340 30492340 single base substitution G A downstream_gene_variant MELA-AU 7 30492340 30492340 single base substitution G A exon_variant MELA-AU 7 30492340 30492340 single base substitution G A intron_variant MELA-AU 7 30492340 30492340 single base substitution G A synonymous_variant F231F 693C>T MELA-AU 7 30492340 30492340 single base substitution G A upstream_gene_variant MELA-AU 7 30492343 30492343 single base substitution G T downstream_gene_variant MELA-AU 7 30492343 30492343 single base substitution G T exon_variant MELA-AU 7 30492343 30492343 single base substitution G T intron_variant MELA-AU 7 30492343 30492343 single base substitution G T missense_variant F230L 690C>A MELA-AU 7 30492343 30492343 single base substitution G T upstream_gene_variant MELA-AU 7 30492407 30492407 single base substitution G A downstream_gene_variant MELA-AU 7 30492407 30492407 single base substitution G A exon_variant MELA-AU 7 30492407 30492407 single base substitution G A intron_variant MELA-AU 7 30492407 30492407 single base substitution G A missense_variant S209F 626C>T MELA-AU 7 30492407 30492407 single base substitution G A upstream_gene_variant MELA-AU 7 30493018 30493018 single base substitution G A downstream_gene_variant MELA-AU 7 30493018 30493018 single base substitution G A intron_variant MELA-AU 7 30493266 30493266 single base substitution G A downstream_gene_variant MELA-AU 7 30493266 30493266 single base substitution G A intron_variant MELA-AU 7 30493625 30493625 single base substitution G A downstream_gene_variant MELA-AU 7 30493625 30493625 single base substitution G A intron_variant MELA-AU 7 30493657 30493657 single base substitution G A downstream_gene_variant MELA-AU 7 30493657 30493657 single base substitution G A intron_variant MELA-AU 7 30494046 30494046 single base substitution G A downstream_gene_variant MELA-AU 7 30494046 30494046 single base substitution G A intron_variant MELA-AU 7 30494236 30494236 single base substitution A T downstream_gene_variant MELA-AU 7 30494236 30494236 single base substitution A T intron_variant MELA-AU 7 30494741 30494741 single base substitution G A downstream_gene_variant MELA-AU 7 30494741 30494741 single base substitution G A intron_variant MELA-AU 7 30495063 30495063 single base substitution T A downstream_gene_variant MELA-AU 7 30495063 30495063 single base substitution T A intron_variant MELA-AU 7 30495508 30495508 single base substitution G A downstream_gene_variant MELA-AU 7 30495508 30495508 single base substitution G A intron_variant MELA-AU 7 30495522 30495522 single base substitution C A downstream_gene_variant MELA-AU 7 30495522 30495522 single base substitution C A intron_variant MELA-AU 7 30495809 30495809 single base substitution G A downstream_gene_variant MELA-AU 7 30495809 30495809 single base substitution G A intron_variant MELA-AU 7 30497097 30497097 single base substitution G A intron_variant MELA-AU 7 30497285 30497285 single base substitution G A intron_variant MELA-AU 7 30497382 30497382 single base substitution T C intron_variant MELA-AU 7 30497633 30497633 single base substitution C T intron_variant MELA-AU 7 30497723 30497723 single base substitution G A intron_variant MELA-AU 7 30498051 30498051 single base substitution T A intron_variant MELA-AU 7 30498267 30498267 single base substitution G A intron_variant MELA-AU 7 30498650 30498650 single base substitution G A intron_variant MELA-AU 7 30499128 30499128 single base substitution G A intron_variant MELA-AU 7 30500000 30500000 single base substitution G A intron_variant MELA-AU 7 30500236 30500236 single base substitution G A intron_variant MELA-AU 7 30500415 30500415 single base substitution T C intron_variant MELA-AU 7 30500610 30500610 single base substitution G A intron_variant MELA-AU 7 30500662 30500662 single base substitution C T intron_variant MELA-AU 7 30501303 30501303 single base substitution C T intron_variant MELA-AU 7 30501446 30501446 single base substitution C T intron_variant MELA-AU 7 30501656 30501656 single base substitution G A intron_variant MELA-AU 7 30501786 30501786 single base substitution C A intron_variant MELA-AU 7 30502129 30502129 single base substitution G A intron_variant MELA-AU 7 30503080 30503080 single base substitution C T intron_variant MELA-AU 7 30503157 30503157 single base substitution G A intron_variant MELA-AU 7 30503222 30503222 single base substitution C T intron_variant MELA-AU 7 30503222 30503222 single base substitution C T splice_region_variant MELA-AU 7 30504740 30504740 single base substitution C T intron_variant MELA-AU 7 30505065 30505065 single base substitution T G intron_variant MELA-AU 7 30505248 30505248 single base substitution C A intron_variant MELA-AU 7 30505720 30505720 single base substitution G A intron_variant MELA-AU 7 30506202 30506202 single base substitution G A intron_variant MELA-AU 7 30506203 30506203 single base substitution G A intron_variant MELA-AU 7 30506668 30506668 single base substitution G A intron_variant MELA-AU 7 30506900 30506900 single base substitution G A intron_variant MELA-AU 7 30506999 30506999 single base substitution G A intron_variant MELA-AU 7 30507113 30507113 single base substitution G A intron_variant MELA-AU 7 30507725 30507725 single base substitution T A intron_variant MELA-AU 7 30507903 30507903 single base substitution G A intron_variant MELA-AU 7 30509257 30509257 single base substitution G A intron_variant MELA-AU 7 30509291 30509291 single base substitution C T intron_variant MELA-AU 7 30509562 30509562 single base substitution C T intron_variant MELA-AU 7 30509989 30509989 single base substitution G A intron_variant MELA-AU 7 30510053 30510053 single base substitution G A intron_variant MELA-AU 7 30510269 30510269 single base substitution A C intron_variant MELA-AU 7 30511094 30511094 single base substitution G A intron_variant MELA-AU 7 30511312 30511312 single base substitution G A intron_variant MELA-AU 7 30511617 30511617 single base substitution G A intron_variant MELA-AU 7 30511801 30511801 single base substitution A G intron_variant MELA-AU 7 30511881 30511881 single base substitution C A intron_variant MELA-AU 7 30512627 30512627 single base substitution G A intron_variant MELA-AU 7 30512647 30512647 single base substitution G A intron_variant MELA-AU 7 30513279 30513279 single base substitution A G intron_variant MELA-AU 7 30513392 30513401 deletion of <=200bp GCAGGGGTGG - intron_variant MELA-AU 7 30513919 30513919 single base substitution G A intron_variant MELA-AU 7 30514078 30514078 single base substitution C T intron_variant MELA-AU 7 30514736 30514736 single base substitution G A intron_variant MELA-AU 7 30515058 30515058 single base substitution G A intron_variant MELA-AU 7 30515362 30515362 single base substitution A G intron_variant MELA-AU 7 30515968 30515968 single base substitution C T intron_variant MELA-AU 7 30516362 30516362 single base substitution C A intron_variant MELA-AU 7 30516902 30516902 single base substitution G A intron_variant MELA-AU 7 30517253 30517253 single base substitution C T intron_variant MELA-AU 7 30520198 30520198 single base substitution A G upstream_gene_variant MELA-AU 7 30520217 30520217 single base substitution C T upstream_gene_variant MELA-AU 7 30520261 30520261 single base substitution C T upstream_gene_variant MELA-AU 7 30521553 30521553 single base substitution A C upstream_gene_variant MELA-AU 7 30521626 30521626 single base substitution C T upstream_gene_variant MELA-AU 7 30521747 30521747 single base substitution C T upstream_gene_variant MELA-AU 7 30521778 30521778 single base substitution C T upstream_gene_variant MELA-AU 7 30522400 30522400 single base substitution C T upstream_gene_variant MELA-AU 7 30522744 30522744 single base substitution C T upstream_gene_variant MELA-AU 7 30523116 30523116 single base substitution T G upstream_gene_variant MELA-AU 7 30523140 30523140 single base substitution G A upstream_gene_variant MELA-AU 7 30523364 30523364 single base substitution G A upstream_gene_variant ORCA-IN 7 30462085 30462085 single base substitution G C downstream_gene_variant ORCA-IN 7 30486651 30486651 single base substitution C G 3_prime_UTR_variant ORCA-IN 7 30486651 30486651 single base substitution C G exon_variant ORCA-IN 7 30486651 30486651 single base substitution C G missense_variant Q767H 2301G>C ORCA-IN 7 30489141 30489141 single base substitution G A downstream_gene_variant ORCA-IN 7 30489141 30489141 single base substitution G A intron_variant ORCA-IN 7 30489141 30489141 single base substitution G A upstream_gene_variant ORCA-IN 7 30491787 30491787 single base substitution C A 3_prime_UTR_variant ORCA-IN 7 30491787 30491787 single base substitution C A downstream_gene_variant ORCA-IN 7 30491787 30491787 single base substitution C A exon_variant ORCA-IN 7 30491787 30491787 single base substitution C A missense_variant D416Y 1246G>T ORCA-IN 7 30491787 30491787 single base substitution C A upstream_gene_variant OV-AU 7 30491108 30491108 single base substitution C A downstream_gene_variant OV-AU 7 30491108 30491108 single base substitution C A exon_variant OV-AU 7 30491108 30491108 single base substitution C A missense_variant S642I 1925G>T OV-AU 7 30491108 30491108 single base substitution C A upstream_gene_variant OV-AU 7 30497943 30497943 single base substitution G T intron_variant OV-AU 7 30501966 30501966 single base substitution G C intron_variant OV-AU 7 30506112 30506112 single base substitution A C intron_variant OV-AU 7 30519122 30519122 single base substitution T G upstream_gene_variant PACA-AU 7 30466621 30466621 single base substitution G A intron_variant PACA-AU 7 30467162 30467162 single base substitution A G intron_variant PACA-AU 7 30467990 30467990 single base substitution T A intron_variant PACA-AU 7 30469133 30469133 single base substitution G A intron_variant PACA-AU 7 30475631 30475631 single base substitution C T 3_prime_UTR_variant PACA-AU 7 30475631 30475631 single base substitution C T intron_variant PACA-AU 7 30475631 30475631 single base substitution C T synonymous_variant T868T 2604G>A PACA-AU 7 30475631 30475631 single base substitution C T upstream_gene_variant PACA-AU 7 30476048 30476048 single base substitution C T intron_variant PACA-AU 7 30476048 30476048 single base substitution C T upstream_gene_variant PACA-AU 7 30485971 30485971 single base substitution G C exon_variant PACA-AU 7 30485971 30485971 single base substitution G C intron_variant PACA-AU 7 30494480 30494480 single base substitution T C downstream_gene_variant PACA-AU 7 30494480 30494480 single base substitution T C intron_variant PACA-AU 7 30496208 30496208 single base substitution T G downstream_gene_variant PACA-AU 7 30496208 30496208 single base substitution T G intron_variant PACA-AU 7 30508653 30508653 single base substitution G A intron_variant PACA-AU 7 30510016 30510016 single base substitution A G intron_variant PACA-AU 7 30515521 30515521 single base substitution C T 5_prime_UTR_variant PACA-AU 7 30515521 30515521 single base substitution C T intron_variant PACA-AU 7 30517858 30517858 single base substitution T G intron_variant PACA-AU 7 30518836 30518836 single base substitution A T upstream_gene_variant PACA-AU 7 30522184 30522184 single base substitution G A upstream_gene_variant PACA-AU 7 30523308 30523308 single base substitution T A upstream_gene_variant PACA-CA 7 30463391 30463391 single base substitution G T downstream_gene_variant PACA-CA 7 30465235 30465235 single base substitution T C 3_prime_UTR_variant PACA-CA 7 30465235 30465235 single base substitution T C exon_variant PACA-CA 7 30468647 30468647 single base substitution T C intron_variant PACA-CA 7 30471530 30471530 single base substitution G A intron_variant PACA-CA 7 30472802 30472802 deletion of <=200bp A - exon_variant PACA-CA 7 30472802 30472802 deletion of <=200bp A - intron_variant PACA-CA 7 30472802 30472802 deletion of <=200bp A - splice_region_variant PACA-CA 7 30489403 30489403 single base substitution C T downstream_gene_variant PACA-CA 7 30489403 30489403 single base substitution C T intron_variant PACA-CA 7 30489403 30489403 single base substitution C T upstream_gene_variant PACA-CA 7 30489673 30489673 single base substitution G A downstream_gene_variant PACA-CA 7 30489673 30489673 single base substitution G A intron_variant PACA-CA 7 30489673 30489673 single base substitution G A upstream_gene_variant PACA-CA 7 30491095 30491095 single base substitution C A downstream_gene_variant PACA-CA 7 30491095 30491095 single base substitution C A exon_variant PACA-CA 7 30491095 30491095 single base substitution C A synonymous_variant V646V 1938G>T PACA-CA 7 30491095 30491095 single base substitution C A upstream_gene_variant PACA-CA 7 30491788 30491788 single base substitution G A 3_prime_UTR_variant PACA-CA 7 30491788 30491788 single base substitution G A downstream_gene_variant PACA-CA 7 30491788 30491788 single base substitution G A exon_variant PACA-CA 7 30491788 30491788 single base substitution G A synonymous_variant P415P 1245C>T PACA-CA 7 30491788 30491788 single base substitution G A upstream_gene_variant PACA-CA 7 30492153 30492153 single base substitution C T downstream_gene_variant PACA-CA 7 30492153 30492153 single base substitution C T exon_variant PACA-CA 7 30492153 30492153 single base substitution C T missense_variant D294N 880G>A PACA-CA 7 30492153 30492153 single base substitution C T stop_gained W248* 744G>A PACA-CA 7 30492153 30492153 single base substitution C T upstream_gene_variant PACA-CA 7 30492774 30492774 single base substitution C T downstream_gene_variant PACA-CA 7 30492774 30492774 single base substitution C T intron_variant PACA-CA 7 30500431 30500431 single base substitution G C intron_variant PACA-CA 7 30512272 30512272 single base substitution C T intron_variant PACA-CA 7 30514448 30514448 single base substitution G T intron_variant PACA-CA 7 30517426 30517426 single base substitution C T intron_variant PACA-CA 7 30518328 30518328 single base substitution G C 5_prime_UTR_variant PACA-CA 7 30518328 30518328 single base substitution G C upstream_gene_variant PAEN-AU 7 30517373 30517373 single base substitution G T intron_variant PAEN-IT 7 30472895 30472895 single base substitution A C exon_variant PAEN-IT 7 30472895 30472895 single base substitution A C intron_variant PAEN-IT 7 30476514 30476514 single base substitution C G intron_variant PAEN-IT 7 30476514 30476514 single base substitution C G upstream_gene_variant PAEN-IT 7 30477588 30477588 single base substitution C T intron_variant PAEN-IT 7 30477588 30477588 single base substitution C T upstream_gene_variant PBCA-DE 7 30461508 30461508 deletion of <=200bp T - downstream_gene_variant PBCA-DE 7 30467992 30467992 single base substitution A T intron_variant PBCA-DE 7 30472441 30472441 deletion of <=200bp C - intron_variant PBCA-DE 7 30477255 30477255 single base substitution A G 3_prime_UTR_variant PBCA-DE 7 30477255 30477255 single base substitution A G intron_variant PBCA-DE 7 30477255 30477255 single base substitution A G missense_variant V824A 2471T>C PBCA-DE 7 30477255 30477255 single base substitution A G upstream_gene_variant PBCA-DE 7 30485564 30485564 single base substitution G C intron_variant PBCA-DE 7 30490848 30490848 single base substitution G A downstream_gene_variant PBCA-DE 7 30490848 30490848 single base substitution G A exon_variant PBCA-DE 7 30490848 30490848 single base substitution G A missense_variant R729C 2185C>T PBCA-DE 7 30490848 30490848 single base substitution G A upstream_gene_variant PBCA-DE 7 30491702 30491702 single base substitution C T downstream_gene_variant PBCA-DE 7 30491702 30491702 single base substitution C T exon_variant PBCA-DE 7 30491702 30491702 single base substitution C T missense_variant R444Q 1331G>A PBCA-DE 7 30491702 30491702 single base substitution C T upstream_gene_variant PBCA-DE 7 30500720 30500720 single base substitution A C intron_variant PBCA-DE 7 30507617 30507617 single base substitution C A intron_variant PBCA-DE 7 30523073 30523073 single base substitution C T upstream_gene_variant PRAD-CA 7 30514088 30514088 single base substitution C T intron_variant PRAD-CA 7 30519286 30519286 single base substitution G A upstream_gene_variant PRAD-UK 7 30469818 30469818 single base substitution G T intron_variant PRAD-UK 7 30475756 30475756 deletion of <=200bp T - intron_variant PRAD-UK 7 30475756 30475756 deletion of <=200bp T - upstream_gene_variant PRAD-UK 7 30498641 30498641 single base substitution C A intron_variant PRAD-UK 7 30503577 30503577 single base substitution C A intron_variant PRAD-UK 7 30506112 30506112 deletion of <=200bp A - intron_variant PRAD-UK 7 30511194 30511194 single base substitution A T intron_variant PRAD-UK 7 30521557 30521557 single base substitution C A upstream_gene_variant PRAD-US 7 30475683 30475683 single base substitution C T 3_prime_UTR_variant PRAD-US 7 30475683 30475683 single base substitution C T intron_variant PRAD-US 7 30475683 30475683 single base substitution C T missense_variant G851D 2552G>A PRAD-US 7 30475683 30475683 single base substitution C T upstream_gene_variant PRAD-US 7 30491366 30491366 single base substitution G A downstream_gene_variant PRAD-US 7 30491366 30491366 single base substitution G A exon_variant PRAD-US 7 30491366 30491366 single base substitution G A missense_variant T556M 1667C>T PRAD-US 7 30491366 30491366 single base substitution G A upstream_gene_variant PRAD-US 7 30491788 30491788 single base substitution G A 3_prime_UTR_variant PRAD-US 7 30491788 30491788 single base substitution G A downstream_gene_variant PRAD-US 7 30491788 30491788 single base substitution G A exon_variant PRAD-US 7 30491788 30491788 single base substitution G A synonymous_variant P415P 1245C>T PRAD-US 7 30491788 30491788 single base substitution G A upstream_gene_variant RECA-EU 7 30463258 30463258 single base substitution G T downstream_gene_variant RECA-EU 7 30464682 30464682 single base substitution G A 3_prime_UTR_variant RECA-EU 7 30464682 30464682 single base substitution G A downstream_gene_variant RECA-EU 7 30464682 30464682 single base substitution G A exon_variant SKCA-BR 7 30461437 30461437 single base substitution G A downstream_gene_variant SKCA-BR 7 30464908 30464908 single base substitution T G 3_prime_UTR_variant SKCA-BR 7 30464908 30464908 single base substitution T G exon_variant SKCA-BR 7 30464961 30464961 single base substitution T C 3_prime_UTR_variant SKCA-BR 7 30464961 30464961 single base substitution T C exon_variant SKCA-BR 7 30466640 30466640 single base substitution T A intron_variant SKCA-BR 7 30469270 30469270 single base substitution T C intron_variant SKCA-BR 7 30469406 30469406 single base substitution G A intron_variant SKCA-BR 7 30471139 30471139 single base substitution G A intron_variant SKCA-BR 7 30472091 30472091 single base substitution T C intron_variant SKCA-BR 7 30479230 30479230 single base substitution G A intron_variant SKCA-BR 7 30479289 30479289 single base substitution T G intron_variant SKCA-BR 7 30479444 30479444 single base substitution A G intron_variant SKCA-BR 7 30485199 30485199 single base substitution A C intron_variant SKCA-BR 7 30485584 30485584 single base substitution T A intron_variant SKCA-BR 7 30489905 30489905 single base substitution G A downstream_gene_variant SKCA-BR 7 30489905 30489905 single base substitution G A intron_variant SKCA-BR 7 30489905 30489905 single base substitution G A upstream_gene_variant SKCA-BR 7 30493725 30493725 single base substitution G A downstream_gene_variant SKCA-BR 7 30493725 30493725 single base substitution G A intron_variant SKCA-BR 7 30498525 30498525 single base substitution G T intron_variant SKCA-BR 7 30500423 30500423 single base substitution C T intron_variant SKCA-BR 7 30503725 30503725 single base substitution A G intron_variant SKCA-BR 7 30503738 30503738 single base substitution A C intron_variant SKCA-BR 7 30504359 30504359 single base substitution G A intron_variant SKCA-BR 7 30505273 30505273 insertion of <=200bp - CT intron_variant SKCA-BR 7 30511264 30511264 single base substitution G A intron_variant SKCA-BR 7 30511870 30511870 single base substitution A C intron_variant SKCA-BR 7 30511896 30511896 single base substitution A C intron_variant SKCA-BR 7 30513209 30513209 single base substitution G A intron_variant SKCA-BR 7 30514919 30514919 single base substitution G A intron_variant SKCA-BR 7 30515901 30515901 single base substitution C T intron_variant SKCA-BR 7 30515945 30515945 single base substitution C T intron_variant SKCA-BR 7 30516080 30516080 single base substitution C T intron_variant SKCA-BR 7 30516687 30516687 single base substitution G A intron_variant SKCA-BR 7 30517211 30517211 single base substitution A G intron_variant SKCA-BR 7 30517297 30517297 insertion of <=200bp - AT intron_variant SKCA-BR 7 30518443 30518443 single base substitution C A upstream_gene_variant SKCA-BR 7 30519365 30519365 single base substitution G C upstream_gene_variant SKCA-BR 7 30520278 30520278 single base substitution G A upstream_gene_variant SKCA-BR 7 30520561 30520561 single base substitution C T upstream_gene_variant SKCA-BR 7 30520706 30520706 single base substitution A G upstream_gene_variant SKCA-BR 7 30521097 30521097 single base substitution C T upstream_gene_variant SKCM-US 7 30491125 30491125 single base substitution G A downstream_gene_variant SKCM-US 7 30491125 30491125 single base substitution G A exon_variant SKCM-US 7 30491125 30491125 single base substitution G A synonymous_variant P636P 1908C>T SKCM-US 7 30491125 30491125 single base substitution G A upstream_gene_variant SKCM-US 7 30491343 30491343 single base substitution G A downstream_gene_variant SKCM-US 7 30491343 30491343 single base substitution G A exon_variant SKCM-US 7 30491343 30491343 single base substitution G A missense_variant P564S 1690C>T SKCM-US 7 30491343 30491343 single base substitution G A upstream_gene_variant SKCM-US 7 30491516 30491516 single base substitution G A downstream_gene_variant SKCM-US 7 30491516 30491516 single base substitution G A exon_variant SKCM-US 7 30491516 30491516 single base substitution G A missense_variant P506L 1517C>T SKCM-US 7 30491516 30491516 single base substitution G A upstream_gene_variant SKCM-US 7 30491735 30491735 single base substitution A G downstream_gene_variant SKCM-US 7 30491735 30491735 single base substitution A G exon_variant SKCM-US 7 30491735 30491735 single base substitution A G missense_variant L433P 1298T>C SKCM-US 7 30491735 30491735 single base substitution A G upstream_gene_variant SKCM-US 7 30492007 30492007 single base substitution G A 3_prime_UTR_variant SKCM-US 7 30492007 30492007 single base substitution G A downstream_gene_variant SKCM-US 7 30492007 30492007 single base substitution G A exon_variant SKCM-US 7 30492007 30492007 single base substitution G A synonymous_variant F342F 1026C>T SKCM-US 7 30492007 30492007 single base substitution G A upstream_gene_variant SKCM-US 7 30492014 30492014 single base substitution C G 3_prime_UTR_variant SKCM-US 7 30492014 30492014 single base substitution C G downstream_gene_variant SKCM-US 7 30492014 30492014 single base substitution C G exon_variant SKCM-US 7 30492014 30492014 single base substitution C G missense_variant R340P 1019G>C SKCM-US 7 30492014 30492014 single base substitution C G upstream_gene_variant SKCM-US 7 30492118 30492118 single base substitution C T 3_prime_UTR_variant SKCM-US 7 30492118 30492118 single base substitution C T downstream_gene_variant SKCM-US 7 30492118 30492118 single base substitution C T exon_variant SKCM-US 7 30492118 30492118 single base substitution C T stop_gained W305* 915G>A SKCM-US 7 30492118 30492118 single base substitution C T upstream_gene_variant SKCM-US 7 30492184 30492184 single base substitution G A downstream_gene_variant SKCM-US 7 30492184 30492184 single base substitution G A exon_variant SKCM-US 7 30492184 30492184 single base substitution G A missense_variant S238L 713C>T SKCM-US 7 30492184 30492184 single base substitution G A synonymous_variant F283F 849C>T SKCM-US 7 30492184 30492184 single base substitution G A upstream_gene_variant SKCM-US 7 30492343 30492343 single base substitution G T downstream_gene_variant SKCM-US 7 30492343 30492343 single base substitution G T exon_variant SKCM-US 7 30492343 30492343 single base substitution G T intron_variant SKCM-US 7 30492343 30492343 single base substitution G T missense_variant F230L 690C>A SKCM-US 7 30492343 30492343 single base substitution G T upstream_gene_variant SKCM-US 7 30492470 30492470 single base substitution G A downstream_gene_variant SKCM-US 7 30492470 30492470 single base substitution G A exon_variant SKCM-US 7 30492470 30492470 single base substitution G A missense_variant T188I 563C>T SKCM-US 7 30492470 30492470 single base substitution G A upstream_gene_variant SKCM-US 7 30492619 30492619 single base substitution G A downstream_gene_variant SKCM-US 7 30492619 30492619 single base substitution G A exon_variant SKCM-US 7 30492619 30492619 single base substitution G A synonymous_variant G138G 414C>T SKCM-US 7 30494798 30494798 single base substitution G A downstream_gene_variant SKCM-US 7 30494798 30494798 single base substitution G A exon_variant SKCM-US 7 30494798 30494798 single base substitution G A missense_variant P111S 331C>T SKCM-US 7 30494901 30494901 single base substitution C A downstream_gene_variant SKCM-US 7 30494901 30494901 single base substitution C A exon_variant SKCM-US 7 30494901 30494901 single base substitution C A missense_variant Q76H 228G>T SKCM-US 7 30496450 30496450 single base substitution G A exon_variant SKCM-US 7 30496450 30496450 single base substitution G A synonymous_variant L30L 88C>T STAD-US 7 30465314 30465314 single base substitution G A 3_prime_UTR_variant STAD-US 7 30465314 30465314 single base substitution G A exon_variant STAD-US 7 30465314 30465314 single base substitution G A synonymous_variant N934N 2802C>T STAD-US 7 30485816 30485816 single base substitution A G 3_prime_UTR_variant STAD-US 7 30485816 30485816 single base substitution A G exon_variant STAD-US 7 30485816 30485816 single base substitution A G synonymous_variant S798S 2394T>C STAD-US 7 30490868 30490868 single base substitution T C downstream_gene_variant STAD-US 7 30490868 30490868 single base substitution T C exon_variant STAD-US 7 30490868 30490868 single base substitution T C missense_variant E722G 2165A>G STAD-US 7 30490868 30490868 single base substitution T C upstream_gene_variant STAD-US 7 30490931 30490931 single base substitution T C downstream_gene_variant STAD-US 7 30490931 30490931 single base substitution T C exon_variant STAD-US 7 30490931 30490931 single base substitution T C missense_variant H701R 2102A>G STAD-US 7 30490931 30490931 single base substitution T C upstream_gene_variant STAD-US 7 30491122 30491122 single base substitution G A downstream_gene_variant STAD-US 7 30491122 30491122 single base substitution G A exon_variant STAD-US 7 30491122 30491122 single base substitution G A synonymous_variant R637R 1911C>T STAD-US 7 30491122 30491122 single base substitution G A upstream_gene_variant STAD-US 7 30491130 30491130 single base substitution G T downstream_gene_variant STAD-US 7 30491130 30491130 single base substitution G T exon_variant STAD-US 7 30491130 30491130 single base substitution G T missense_variant L635M 1903C>A STAD-US 7 30491130 30491130 single base substitution G T upstream_gene_variant STAD-US 7 30491486 30491486 deletion of <=200bp A - downstream_gene_variant STAD-US 7 30491486 30491486 deletion of <=200bp A - exon_variant STAD-US 7 30491486 30491486 deletion of <=200bp A - frameshift_variant F516 STAD-US 7 30491486 30491486 deletion of <=200bp A - upstream_gene_variant STAD-US 7 30491514 30491514 single base substitution C T downstream_gene_variant STAD-US 7 30491514 30491514 single base substitution C T exon_variant STAD-US 7 30491514 30491514 single base substitution C T missense_variant G507R 1519G>A STAD-US 7 30491514 30491514 single base substitution C T upstream_gene_variant STAD-US 7 30491602 30491602 single base substitution G C downstream_gene_variant STAD-US 7 30491602 30491602 single base substitution G C exon_variant STAD-US 7 30491602 30491602 single base substitution G C synonymous_variant V477V 1431C>G STAD-US 7 30491602 30491602 single base substitution G C upstream_gene_variant STAD-US 7 30491688 30491688 single base substitution G A downstream_gene_variant STAD-US 7 30491688 30491688 single base substitution G A exon_variant STAD-US 7 30491688 30491688 single base substitution G A missense_variant P449S 1345C>T STAD-US 7 30491688 30491688 single base substitution G A upstream_gene_variant STAD-US 7 30492144 30492144 single base substitution G A 3_prime_UTR_variant STAD-US 7 30492144 30492144 single base substitution G A downstream_gene_variant STAD-US 7 30492144 30492144 single base substitution G A exon_variant STAD-US 7 30492144 30492144 single base substitution G A missense_variant R297C 889C>T STAD-US 7 30492144 30492144 single base substitution G A upstream_gene_variant STAD-US 7 30492160 30492160 single base substitution C T downstream_gene_variant STAD-US 7 30492160 30492160 single base substitution C T exon_variant STAD-US 7 30492160 30492160 single base substitution C T missense_variant R246Q 737G>A STAD-US 7 30492160 30492160 single base substitution C T synonymous_variant S291S 873G>A STAD-US 7 30492160 30492160 single base substitution C T upstream_gene_variant STAD-US 7 30492371 30492371 single base substitution G A downstream_gene_variant STAD-US 7 30492371 30492371 single base substitution G A exon_variant STAD-US 7 30492371 30492371 single base substitution G A intron_variant STAD-US 7 30492371 30492371 single base substitution G A missense_variant T221M 662C>T STAD-US 7 30492371 30492371 single base substitution G A upstream_gene_variant STAD-US 7 30492472 30492472 single base substitution G T downstream_gene_variant STAD-US 7 30492472 30492472 single base substitution G T exon_variant STAD-US 7 30492472 30492472 single base substitution G T synonymous_variant T187T 561C>A STAD-US 7 30492472 30492472 single base substitution G T upstream_gene_variant STAD-US 7 30492520 30492520 single base substitution A G downstream_gene_variant STAD-US 7 30492520 30492520 single base substitution A G exon_variant STAD-US 7 30492520 30492520 single base substitution A G synonymous_variant N171N 513T>C STAD-US 7 30492520 30492520 single base substitution A G upstream_gene_variant STAD-US 7 30492568 30492570 deletion of <=200bp CAG - downstream_gene_variant STAD-US 7 30492568 30492570 deletion of <=200bp CAG - exon_variant STAD-US 7 30492568 30492570 deletion of <=200bp CAG - inframe_deletion L155 STAD-US 7 30492568 30492570 deletion of <=200bp CAG - upstream_gene_variant STAD-US 7 30492600 30492603 deletion of <=200bp GCAC - downstream_gene_variant STAD-US 7 30492600 30492603 deletion of <=200bp GCAC - exon_variant STAD-US 7 30492600 30492603 deletion of <=200bp GCAC - frameshift_variant VL144 STAD-US 7 30494838 30494838 single base substitution G A downstream_gene_variant STAD-US 7 30494838 30494838 single base substitution G A exon_variant STAD-US 7 30494838 30494838 single base substitution G A synonymous_variant Y97Y 291C>T STAD-US 7 30496526 30496526 single base substitution C A exon_variant STAD-US 7 30496526 30496526 single base substitution C A missense_variant Q4H 12G>T THCA-SA 7 30496410 30496410 single base substitution T A exon_variant THCA-SA 7 30496410 30496410 single base substitution T A missense_variant N43I 128A>T THCA-US 7 30491380 30491380 single base substitution C A downstream_gene_variant THCA-US 7 30491380 30491380 single base substitution C A exon_variant THCA-US 7 30491380 30491380 single base substitution C A synonymous_variant A551A 1653G>T THCA-US 7 30491380 30491380 single base substitution C A upstream_gene_variant UCEC-US 7 30465278 30465278 single base substitution A G 3_prime_UTR_variant UCEC-US 7 30465278 30465278 single base substitution A G exon_variant UCEC-US 7 30465278 30465278 single base substitution A G synonymous_variant D946D 2838T>C UCEC-US 7 30472754 30472754 single base substitution A G 3_prime_UTR_variant UCEC-US 7 30472754 30472754 single base substitution A G exon_variant UCEC-US 7 30472754 30472754 single base substitution A G intron_variant UCEC-US 7 30472754 30472754 single base substitution A G missense_variant L888S 2663T>C UCEC-US 7 30475652 30475652 single base substitution C T 3_prime_UTR_variant UCEC-US 7 30475652 30475652 single base substitution C T intron_variant UCEC-US 7 30475652 30475652 single base substitution C T synonymous_variant A861A 2583G>A UCEC-US 7 30475652 30475652 single base substitution C T upstream_gene_variant UCEC-US 7 30477216 30477216 single base substitution C T 3_prime_UTR_variant UCEC-US 7 30477216 30477216 single base substitution C T intron_variant UCEC-US 7 30477216 30477216 single base substitution C T missense_variant R837Q 2510G>A UCEC-US 7 30477216 30477216 single base substitution C T upstream_gene_variant UCEC-US 7 30486650 30486650 single base substitution T C 3_prime_UTR_variant UCEC-US 7 30486650 30486650 single base substitution T C exon_variant UCEC-US 7 30486650 30486650 single base substitution T C missense_variant I768V 2302A>G UCEC-US 7 30487912 30487912 single base substitution A G downstream_gene_variant UCEC-US 7 30487912 30487912 single base substitution A G splice_donor_variant UCEC-US 7 30487912 30487912 single base substitution A G upstream_gene_variant UCEC-US 7 30490878 30490878 single base substitution C T downstream_gene_variant UCEC-US 7 30490878 30490878 single base substitution C T exon_variant UCEC-US 7 30490878 30490878 single base substitution C T missense_variant G719S 2155G>A UCEC-US 7 30490878 30490878 single base substitution C T upstream_gene_variant UCEC-US 7 30491063 30491063 single base substitution C T downstream_gene_variant UCEC-US 7 30491063 30491063 single base substitution C T exon_variant UCEC-US 7 30491063 30491063 single base substitution C T missense_variant R657H 1970G>A UCEC-US 7 30491063 30491063 single base substitution C T upstream_gene_variant UCEC-US 7 30491197 30491197 single base substitution G A downstream_gene_variant UCEC-US 7 30491197 30491197 single base substitution G A exon_variant UCEC-US 7 30491197 30491197 single base substitution G A synonymous_variant A612A 1836C>T UCEC-US 7 30491197 30491197 single base substitution G A upstream_gene_variant UCEC-US 7 30491310 30491310 single base substitution G A downstream_gene_variant UCEC-US 7 30491310 30491310 single base substitution G A exon_variant UCEC-US 7 30491310 30491310 single base substitution G A missense_variant R575W 1723C>T UCEC-US 7 30491310 30491310 single base substitution G A upstream_gene_variant UCEC-US 7 30491341 30491341 single base substitution C T downstream_gene_variant UCEC-US 7 30491341 30491341 single base substitution C T exon_variant UCEC-US 7 30491341 30491341 single base substitution C T synonymous_variant P564P 1692G>A UCEC-US 7 30491341 30491341 single base substitution C T upstream_gene_variant UCEC-US 7 30491780 30491780 single base substitution G A 3_prime_UTR_variant UCEC-US 7 30491780 30491780 single base substitution G A downstream_gene_variant UCEC-US 7 30491780 30491780 single base substitution G A exon_variant UCEC-US 7 30491780 30491780 single base substitution G A missense_variant T418M 1253C>T UCEC-US 7 30491780 30491780 single base substitution G A upstream_gene_variant UCEC-US 7 30494808 30494808 single base substitution G A downstream_gene_variant UCEC-US 7 30494808 30494808 single base substitution G A exon_variant UCEC-US 7 30494808 30494808 single base substitution G A synonymous_variant I107I 321C>T UCEC-US 7 30494880 30494880 single base substitution G A downstream_gene_variant UCEC-US 7 30494880 30494880 single base substitution G A exon_variant UCEC-US 7 30494880 30494880 single base substitution G A synonymous_variant S83S 249C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-A4-A5XZ-01 COSM3995548 c.627C>T p.S209S Substitution - coding silent 7:30452790-30452790 - TCGA-FW-A5DX-01 COSM3637885 c.1908C>T p.P636P Substitution - coding silent 7:30451509-30451509 - TCGA-BR-6452-01 COSM3880543 c.1345C>T p.P449S Substitution - Missense 7:30452072-30452072 - TCGA-EJ-A65F-01 COSM4640798 c.2552G>A p.G851D Substitution - Missense 7:30436067-30436067 - LIM1899 COSM4640798 c.2552G>A p.G851D Substitution - Missense 7:30436067-30436067 - TCGA-AG-A002-01 COSM262424 c.703C>T p.R235C Substitution - Missense 7:30452714-30452714 - TCGA-02-2485-01 COSM3411972 c.675C>T p.D225D Substitution - coding silent 7:30452742-30452742 - CSCC-56-T COSM4457007 c.102C>T p.I34I Substitution - coding silent 7:30456820-30456820 - TCGA-ER-A19E-06 COSM3637886 c.1690C>T p.P564S Substitution - Missense 7:30451727-30451727 - DLD1 COSM4626011 c.2185C>T p.R729C Substitution - Missense 7:30451232-30451232 - CSCC-7-T COSM4509015 c.794C>T p.P265L Substitution - Missense 7:30452623-30452623 - S02375 COSM5696679 c.1166C>T p.S389F Substitution - Missense 7:30452251-30452251 - TCGA-DM-A1D4-01 COSM1450333 c.1025T>C p.F342S Substitution - Missense 7:30452392-30452392 - TCGA-AM-5820-01 COSM3762624 c.483C>T p.D161D Substitution - coding silent 7:30452934-30452934 - AOCS-065-3-6 COSM4164294 c.1925G>T p.S642I Substitution - Missense 7:30451492-30451492 - PT37 COSM5919387 c.1360C>T p.H454Y Substitution - Missense 7:30452057-30452057 - OSCC-GB_01060111 COSM4882974 c.1246G>T p.D416Y Substitution - Missense 7:30452171-30452171 - TCGA-EE-A2GH-06 COSM3637891 c.849C>T p.F283F Substitution - coding silent 7:30452568-30452568 - TCGA-61-1736-01 COSM115748 c.1733T>C p.L578P Substitution - Missense 7:30451684-30451684 - TCGA-22-4599-01 COSM746232 c.164C>T p.A55V Substitution - Missense 7:30456758-30456758 - PCSI0001 COSM1158422 c.880G>A p.D294N Substitution - Missense 7:30452537-30452537 - 37M COSM5583853 c.1401C>T p.A467A Substitution - coding silent 7:30452016-30452016 - TCGA-66-2759-01 COSM746236 c.717C>T p.F239F Substitution - coding silent 7:30452700-30452700 - TCGA-D1-A168-01 COSM1089067 c.1836C>T p.A612A Substitution - coding silent 7:30451581-30451581 - 19M COSM5579109 c.1095C>T p.F365F Substitution - coding silent 7:30452322-30452322 - T207 COSM4707456 c.2066C>T p.S689L Substitution - Missense 7:30451351-30451351 - ESO-887 COSM1259274 c.2202-1G>C p.? Unknown 7:30448382-30448382 - TCGA-CM-6162-01 COSM1450332 c.1074C>T p.R358R Substitution - coding silent 7:30452343-30452343 - HCC123 COSM1622772 c.2413G>T p.A805S Substitution - Missense 7:30446181-30446181 - TCGA-BR-6452-01 COSM3880537 c.2165A>G p.E722G Substitution - Missense 7:30451252-30451252 - TCGA-BR-7723-01 COSM3880539 c.1911C>T p.R637R Substitution - coding silent 7:30451506-30451506 - 509LT COSM4386041 c.2283G>T p.L761F Substitution - Missense 7:30448300-30448300 - TCGA-HU-A4GT-01 COSM3880548 c.513T>C p.N171N Substitution - coding silent 7:30452904-30452904 - EV003-R6 COSM4410690 c.2635_2637GAA>AAC p.E879N Substitution - Missense 7:30433164-30433166 - TP_2061 COSM3637890 c.915G>A p.W305* Substitution - Nonsense 7:30452502-30452502 - TCGA-EB-A44O-01 COSM3637887 c.1517C>T p.P506L Substitution - Missense 7:30451900-30451900 - HCC107T COSM1622774 c.1103G>A p.R368Q Substitution - Missense 7:30452314-30452314 - CSCC-49-T COSM4513174 c.929C>T p.P310L Substitution - Missense 7:30452488-30452488 - TCGA-AP-A054-01 COSM1089065 c.2155G>A p.G719S Substitution - Missense 7:30451262-30451262 - sysucc-1317T COSM3028184 c.1912G>A p.V638I Substitution - Missense 7:30451505-30451505 - S02292 COSM5702197 c.820_821CG>TT p.R274F Substitution - Missense 7:30452596-30452597 - TCGA-AP-A056-01 COSM1089064 c.2285+2T>C p.? Unknown 7:30448296-30448296 - HCT15 COSM4626011 c.2185C>T p.R729C Substitution - Missense 7:30451232-30451232 - B34 COSM1755243 c.2656G>A p.E886K Substitution - Missense 7:30433145-30433145 - BZ37 COSM3028176 c.2154C>T p.Y718Y Substitution - coding silent 7:30451263-30451263 - 009-0026-02TD COSM145681 c.1126A>G p.S376G Substitution - Missense 7:30452291-30452291 - C008 COSM5523288 c.1929C>T p.F643F Substitution - coding silent 7:30451488-30451488 - BCM325T COSM4798948 c.2623C>G p.L875V Substitution - Missense 7:30433178-30433178 - TCGA-CD-8529-01 COSM3880538 c.2102A>G p.H701R Substitution - Missense 7:30451315-30451315 - Au2 COSM5600059 c.1829C>T p.A610V Substitution - Missense 7:30451588-30451588 - 1092 COSM1159739 c.2381_2382insA p.N794fs*6 Insertion - Frameshift 7:30446212-30446213 - ESCC_38 COSM5629182 c.2271T>A p.I757I Substitution - coding silent 7:30448312-30448312 - LIM2099 COSM3637895 c.88C>T p.L30L Substitution - coding silent 7:30456834-30456834 - TCGA-CA-6717-01 COSM1450328 c.2334A>C p.K778N Substitution - Missense 7:30447002-30447002 - PD22355a COSM3028227 c.165G>A p.A55A Substitution - coding silent 7:30456757-30456757 - TCGA-HU-A4GU-01 COSM3880540 c.1903C>A p.L635M Substitution - Missense 7:30451514-30451514 - ZZUFHECRKL-G011T COSM5445265 c.1983G>T p.E661D Substitution - Missense 7:30451434-30451434 - TCGA-B0-5812-01 COSM485256 c.394C>A p.Q132K Substitution - Missense 7:30453023-30453023 - Gp2D COSM3028204 c.931delC p.L311fs*65 Deletion - Frameshift 7:30452486-30452486 - T613 COSM3411972 c.675C>T p.D225D Substitution - coding silent 7:30452742-30452742 - TCGA-AM-5820-01 COSM3762623 c.1722G>A p.A574A Substitution - coding silent 7:30451695-30451695 - TCGA-A5-A0GB-01 COSM1089069 c.1692G>A p.P564P Substitution - coding silent 7:30451725-30451725 - SJMB017 COSM255348 c.2012C>T p.A671V Substitution - Missense 7:30451405-30451405 - ESCC_157 COSM5550380 c.2080G>A p.A694T Substitution - Missense 7:30451337-30451337 - 2492703 COSM262424 c.703C>T p.R235C Substitution - Missense 7:30452714-30452714 - 223 COSM4425560 c.570C>A p.I190I Substitution - coding silent 7:30452847-30452847 - SNUH_G76_S1 COSM3736441 c.796G>A p.E266K Substitution - Missense 7:30452621-30452621 - 2492701 COSM5600059 c.1829C>T p.A610V Substitution - Missense 7:30451588-30451588 - TCGA-QB-A6FS-06 COSM3923469 c.228G>T p.Q76H Substitution - Missense 7:30455285-30455285 - TCGA-EE-A2MI-06 COSM3637894 c.331C>T p.P111S Substitution - Missense 7:30455182-30455182 - TCGA-A5-A0VP-01 COSM1089066 c.1970G>A p.R657H Substitution - Missense 7:30451447-30451447 - 229 COSM4426340 c.605G>A p.G202D Substitution - Missense 7:30452812-30452812 - 2492703 COSM5600059 c.1829C>T p.A610V Substitution - Missense 7:30451588-30451588 - TCGA-A2-A4S0-01 COSM5835395 c.535_536delAG p.S179fs*14 Deletion - Frameshift 7:30452881-30452882 - T3080 COSM4707457 c.1031G>A p.R344Q Substitution - Missense 7:30452386-30452386 - I2L-P24Ta-Tumor-Biopsy COSM5358260 c.2155G>C p.G719R Substitution - Missense 7:30451262-30451262 - 2166 COSM5011735 c.580C>A p.Q194K Substitution - Missense 7:30452837-30452837 - TCGA-CA-6717-01 COSM1450334 c.690C>A p.F230L Substitution - Missense 7:30452727-30452727 - TCGA-AR-A1AK-01 COSM452955 c.7G>C p.E3Q Substitution - Missense 7:30456915-30456915 - pfg019T COSM1643324 c.2622-7delT p.? Unknown 7:30433186-30433186 - TCGA-AA-3492-01 COSM1450330 c.2059G>A p.A687T Substitution - Missense 7:30451358-30451358 - HCC32 COSM1622771 c.2644G>A p.D882N Substitution - Missense 7:30433157-30433157 - CSCC-27-T COSM3995548 c.627C>T p.S209S Substitution - coding silent 7:30452790-30452790 - TCGA-GN-A26C-01 COSM3637895 c.88C>T p.L30L Substitution - coding silent 7:30456834-30456834 - BN01T COSM1622773 c.2278T>C p.Y760H Substitution - Missense 7:30448305-30448305 - TCGA-AM-5820-01 COSM3736441 c.796G>A p.E266K Substitution - Missense 7:30452621-30452621 - TCGA-33-4583-01 COSM746242 c.2741C>A p.A914D Substitution - Missense 7:30429422-30429422 - ESCC_42 COSM5629770 c.1036A>G p.K346E Substitution - Missense 7:30452381-30452381 - 545 COSM5612723 c.2603C>T p.T868M Substitution - Missense 7:30436016-30436016 - TCGA-BR-4361-01 COSM3880544 c.889C>T p.R297C Substitution - Missense 7:30452528-30452528 - RK261_C01 COSM4778327 c.1019G>A p.R340H Substitution - Missense 7:30452398-30452398 - TCGA-EE-A2M5-06 COSM3637885 c.1908C>T p.P636P Substitution - coding silent 7:30451509-30451509 - cSCCP7 COSM139699 c.1646C>T p.P549L Substitution - Missense 7:30451771-30451771 - SJMB017 COSM255348 c.2012C>T p.A671V Substitution - Missense 7:30451405-30451405 - CSCC-55-T COSM4463142 c.1278C>T p.L426L Substitution - coding silent 7:30452139-30452139 - SC_9094 COSM5551295 c.1779C>T p.C593C Substitution - coding silent 7:30451638-30451638 - HCC123T COSM1622772 c.2413G>T p.A805S Substitution - Missense 7:30446181-30446181 - Pat_60_B COSM255348 c.2012C>T p.A671V Substitution - Missense 7:30451405-30451405 - TCGA-AG-3726-01 COSM5066940 c.2480_2482delAAG p.E827delE Deletion - In frame 7:30437628-30437630 - T25 COSM3762624 c.483C>T p.D161D Substitution - coding silent 7:30452934-30452934 - SC_9081 COSM5562728 c.1827C>T p.P609P Substitution - coding silent 7:30451590-30451590 - TCGA-18-4083-01 COSM746235 c.642G>A p.R214R Substitution - coding silent 7:30452775-30452775 - ESO-717 COSM1242573 c.1718C>T p.P573L Substitution - Missense 7:30451699-30451699 - TCGA-12-3652-01 COSM3028213 c.668G>A p.R223Q Substitution - Missense 7:30452749-30452749 - ESO-0292 COSM1241495 c.977C>T p.A326V Substitution - Missense 7:30452440-30452440 - BCM325T COSM4798948 c.2623C>G p.L875V Substitution - Missense 7:30433178-30433178 - 91T COSM109281 c.811T>C p.F271L Substitution - Missense 7:30452606-30452606 - HCC13 COSM1259273 c.2256G>T p.L752L Substitution - coding silent 7:30448327-30448327 - TCGA-66-2773-01 COSM746237 c.945C>T p.A315A Substitution - coding silent 7:30452472-30452472 - TCGA-D1-A165-01 COSM1089071 c.621C>A p.G207G Substitution - coding silent 7:30452796-30452796 - TCGA-66-2756-01 COSM746241 c.2564A>G p.E855G Substitution - Missense 7:30436055-30436055 - SNUH_G76_S1 COSM3762624 c.483C>T p.D161D Substitution - coding silent 7:30452934-30452934 - MO_1337 COSM5554269 c.1735T>C p.F579L Substitution - Missense 7:30451682-30451682 - TCGA-10-0928-01 COSM78182 c.2237A>C p.K746T Substitution - Missense 7:30448346-30448346 - LUAD-S00488 COSM395376 c.1145C>T p.P382L Substitution - Missense 7:30452272-30452272 - PT33 COSM5908772 c.1048C>T p.R350W Substitution - Missense 7:30452369-30452369 - TCGA-CG-4306-01 COSM3880546 c.662C>T p.T221M Substitution - Missense 7:30452755-30452755 - 674 COSM1159752 c.2831A>G p.Y944C Substitution - Missense 7:30425669-30425669 - HCC32T COSM1622771 c.2644G>A p.D882N Substitution - Missense 7:30433157-30433157 - TCGA-B5-A11E-01 COSM1089063 c.2302A>G p.I768V Substitution - Missense 7:30447034-30447034 - TCGA-BG-A0MO-01 COSM1089060 c.2838T>C p.D946D Substitution - coding silent 7:30425662-30425662 - EV003-R9 COSM4410690 c.2635_2637GAA>AAC p.E879N Substitution - Missense 7:30433164-30433166 - Gp5D COSM3028204 c.931delC p.L311fs*65 Deletion - Frameshift 7:30452486-30452486 - TCGA-GV-A3JW-01 COSM1313027 c.2446G>C p.E816Q Substitution - Missense 7:30446148-30446148 - T42 COSM5345333 c.1016C>T p.P339L Substitution - Missense 7:30452401-30452401 - 8016470 COSM3394708 c.2604G>A p.T868T Substitution - coding silent 7:30436015-30436015 - Au2 COSM262424 c.703C>T p.R235C Substitution - Missense 7:30452714-30452714 - TCGA-AN-A0FL-01 COSM452953 c.2721G>T p.Q907H Substitution - Missense 7:30429442-30429442 - ICGC_MB2 COSM216062 c.2471T>C p.V824A Substitution - Missense 7:30437639-30437639 - TCGA-32-2634-01 COSM3411973 c.155C>T p.A52V Substitution - Missense 7:30456767-30456767 - HCC13T COSM1259273 c.2256G>T p.L752L Substitution - coding silent 7:30448327-30448327 - TCGA-AL-3473-01 COSM3995547 c.2651T>C p.V884A Substitution - Missense 7:30433150-30433150 - TCGA-G9-6365-01 COSM3674916 c.1314C>A p.P438P Substitution - coding silent 7:30452103-30452103 - TCGA-B5-A11H-01 COSM1089068 c.1723C>T p.R575W Substitution - Missense 7:30451694-30451694 - PAPNNX COSM5004554 c.1850G>A p.R617H Substitution - Missense 7:30451567-30451567 - sysucc-1370T COSM5472398 c.1308G>A p.M436I Substitution - Missense 7:30452109-30452109 - 2492702 COSM5600059 c.1829C>T p.A610V Substitution - Missense 7:30451588-30451588 - STC232 COSM5062422 c.2361G>A p.T787T Substitution - coding silent 7:30446975-30446975 - AOCS-065-1-9 COSM4164294 c.1925G>T p.S642I Substitution - Missense 7:30451492-30451492 - TCGA-CD-A4MI-01 COSM3880549 c.291C>T p.Y97Y Substitution - coding silent 7:30455222-30455222 - TCGA-BH-A0DQ-01 COSM452954 c.1319G>A p.S440N Substitution - Missense 7:30452098-30452098 - LUAD-D01751 COSM338373 c.57C>T p.H19H Substitution - coding silent 7:30456865-30456865 - PCSI_0001_Pa_X COSM1158422 c.880G>A p.D294N Substitution - Missense 7:30452537-30452537 - TCGA-BR-8370-01 COSM3880545 c.873G>A p.S291S Substitution - coding silent 7:30452544-30452544 - TCGA-A2-A04R-01 COSM3832627 c.1150C>A p.L384I Substitution - Missense 7:30452267-30452267 - PTC-7C COSM4162168 c.238G>T p.E80* Substitution - Nonsense 7:30455275-30455275 - TCGA-D9-A6EC-06 COSM4402644 c.1298T>C p.L433P Substitution - Missense 7:30452119-30452119 - LIM2551 COSM4644796 c.468G>T p.E156D Substitution - Missense 7:30452949-30452949 - 6115123 COSM5550380 c.2080G>A p.A694T Substitution - Missense 7:30451337-30451337 - SJRHB049 COSM3738301 c.1916A>G p.Q639R Substitution - Missense 7:30451501-30451501 - TCGA-KK-A59V-01 COSM4806723 c.1245C>T p.P415P Substitution - coding silent 7:30452172-30452172 - PCSI_0015_Pa_P_526 COSM4963295 c.1938G>T p.V646V Substitution - coding silent 7:30451479-30451479 - BN01 COSM1622773 c.2278T>C p.Y760H Substitution - Missense 7:30448305-30448305 - TCGA-BR-4368-01 COSM3880541 c.1519G>A p.G507R Substitution - Missense 7:30451898-30451898 - TCGA-B0-4823-01 COSM485255 c.2323T>A p.Y775N Substitution - Missense 7:30447013-30447013 - TCGA-CG-4305-01 COSM3880550 c.12G>T p.Q4H Substitution - Missense 7:30456910-30456910 - TCGA-DK-A2I4-01 COSM3778379 c.507C>T p.F169F Substitution - coding silent 7:30452910-30452910 - B23-Tumor COSM1755244 c.1022A>T p.Q341L Substitution - Missense 7:30452395-30452395 - TCGA-D8-A1JA-01 COSM3832626 c.2629C>G p.Q877E Substitution - Missense 7:30433172-30433172 - 2492700 COSM262424 c.703C>T p.R235C Substitution - Missense 7:30452714-30452714 - LUAD-D02085 COSM363428 c.678A>C p.A226A Substitution - coding silent 7:30452739-30452739 - BD124T COSM3028198 c.1118G>A p.R373H Substitution - Missense 7:30452299-30452299 - 2492701 COSM262424 c.703C>T p.R235C Substitution - Missense 7:30452714-30452714 - 05-P8014 COSM4587353 c.2805G>A p.L935L Substitution - coding silent 7:30425695-30425695 - 3402_T COSM3950393 c.1A>C p.M1L Substitution - Missense 7:30456921-30456921 - TCGA-D7-A4YT-01 COSM3880542 c.1431C>G p.V477V Substitution - coding silent 7:30451986-30451986 - HCC107 COSM1622774 c.1103G>A p.R368Q Substitution - Missense 7:30452314-30452314 - 079T COSM1730765 c.586G>A p.E196K Substitution - Missense 7:30452831-30452831 - 1N38-VS-1T38 COSM4975186 c.2740G>T p.A914S Substitution - Missense 7:30429423-30429423 - TCGA-66-2773-01 COSM746238 c.1623C>T p.L541L Substitution - coding silent 7:30451794-30451794 - SC_9008 COSM5551289 c.1674C>T p.C558C Substitution - coding silent 7:30451743-30451743 - TCGA-D1-A167-01 COSM1089070 c.1253C>T p.T418M Substitution - Missense 7:30452164-30452164 - 2492702 COSM262424 c.703C>T p.R235C Substitution - Missense 7:30452714-30452714 - SNUH_G76_S1 COSM3762623 c.1722G>A p.A574A Substitution - coding silent 7:30451695-30451695 - TCGA-AP-A0LM-01 COSM1089072 c.321C>T p.I107I Substitution - coding silent 7:30455192-30455192 - CSCC-44-T COSM4501766 c.597C>T p.F199F Substitution - coding silent 7:30452820-30452820 - CSCC-16-T COSM4485893 c.298C>T p.L100F Substitution - Missense 7:30455215-30455215 - TCGA-BJ-A0ZH-01 COSM3028190 c.1653G>T p.A551A Substitution - coding silent 7:30451764-30451764 - SNUH_G76_S1 COSM3762625 c.156C>G p.A52A Substitution - coding silent 7:30456766-30456766 - TCGA-GN-A266-06 COSM3637889 c.1019G>C p.R340P Substitution - Missense 7:30452398-30452398 - TCGA-BR-8361-01 COSM3880536 c.2394T>C p.S798S Substitution - coding silent 7:30446200-30446200 - I2L-P24Ta-Tumor-Organoid COSM5358260 c.2155G>C p.G719R Substitution - Missense 7:30451262-30451262 - CSCC-31-T COSM4564367 c.1149_1150CC>TT p.L384F Substitution - Missense 7:30452267-30452268 - T3091 COSM4707454 c.2817G>T p.E939D Substitution - Missense 7:30425683-30425683 - ESCC_80 COSM5635810 c.916G>A p.E306K Substitution - Missense 7:30452501-30452501 - T3094 COSM4707455 c.2248G>A p.E750K Substitution - Missense 7:30448335-30448335 - TCGA-AM-5820-01 COSM3762625 c.156C>G p.A52A Substitution - coding silent 7:30456766-30456766 - TCGA-AP-A0LM-01 COSM1089073 c.249C>T p.S83S Substitution - coding silent 7:30455264-30455264 - pfg016T COSM1643324 c.2622-7delT p.? Unknown 7:30433186-30433186 - TCGA-34-5231-01 COSM746234 c.618G>A p.V206V Substitution - coding silent 7:30452799-30452799 - STC291 COSM5062423 c.1721C>T p.A574V Substitution - Missense 7:30451696-30451696 - 009 COSM145681 c.1126A>G p.S376G Substitution - Missense 7:30452291-30452291 - GC_299T1-GC_299N COSM4772511 c.2067G>A p.S689S Substitution - coding silent 7:30451350-30451350 - B34-Tumor COSM1755243 c.2656G>A p.E886K Substitution - Missense 7:30433145-30433145 - 61 COSM5737895 c.1446G>T p.E482D Substitution - Missense 7:30451971-30451971 - ASHPC_0029_Pa_P COSM4806723 c.1245C>T p.P415P Substitution - coding silent 7:30452172-30452172 - TCGA-43-6143-01 COSM746240 c.2161C>T p.R721W Substitution - Missense 7:30451256-30451256 - TCGA-EA-A411-01 COSM4838076 c.2783A>G p.E928G Substitution - Missense 7:30429380-30429380 - B23 COSM1755244 c.1022A>T p.Q341L Substitution - Missense 7:30452395-30452395 - PASFXA COSM5005991 c.636A>G p.L212L Substitution - coding silent 7:30452781-30452781 - 07-058 COSM3736441 c.796G>A p.E266K Substitution - Missense 7:30452621-30452621 - CSCC-18-T COSM4505466 c.693C>T p.F231F Substitution - coding silent 7:30452724-30452724 - OSCC-GB_00740111 COSM4890972 c.2301G>C p.Q767H Substitution - Missense 7:30447035-30447035 - 2492700 COSM5600059 c.1829C>T p.A610V Substitution - Missense 7:30451588-30451588 - LIM2551 COSM4644795 c.2307C>T p.T769T Substitution - coding silent 7:30447029-30447029 - TCGA-HU-A4GT-01 COSM3880547 c.561C>A p.T187T Substitution - coding silent 7:30452856-30452856 - TCGA-EE-A2A2-06 COSM3637892 c.563C>T p.T188I Substitution - Missense 7:30452854-30452854 - TCGA-D1-A15W-01 COSM601040 c.2583G>A p.A861A Substitution - coding silent 7:30436036-30436036 - LOVO COSM3028199 c.1098C>T p.P366P Substitution - coding silent 7:30452319-30452319 - I2L-P24Tb-Tumor-Organoid COSM5358260 c.2155G>C p.G719R Substitution - Missense 7:30451262-30451262 - PT52 COSM5939712 c.2369+8G>A p.? Unknown 7:30446959-30446959 - YUFLA COSM1698474 c.1261C>G p.L421V Substitution - Missense 7:30452156-30452156 - PTC-28C COSM3736441 c.796G>A p.E266K Substitution - Missense 7:30452621-30452621 - TCGA-AP-A059-01 COSM1089062 c.2510G>A p.R837Q Substitution - Missense 7:30437600-30437600 - PAPNNX COSM5004505 c.80G>A p.R27Q Substitution - Missense 7:30456842-30456842 - CHEWS031 COSM4587354 c.2258C>T p.T753I Substitution - Missense 7:30448325-30448325 - TCGA-CH-5792-01 COSM1131601 c.1667C>T p.T556M Substitution - Missense 7:30451750-30451750 - TCGA-D9-A1JW-06 COSM3637893 c.414C>T p.G138G Substitution - coding silent 7:30453003-30453003 - C80 COSM4619876 c.205C>T p.R69C Substitution - Missense 7:30455308-30455308 - 587316 COSM1217545 c.2092G>A p.V698I Substitution - Missense 7:30451325-30451325 - ESO-114 COSM1259273 c.2256G>T p.L752L Substitution - coding silent 7:30448327-30448327 - TCGA-EE-A2GI-06 COSM3637888 c.1026C>T p.F342F Substitution - coding silent 7:30452391-30452391 - ESCC_42 COSM5650015 c.1036_1038delAAG p.K346delK Deletion - In frame 7:30452379-30452381 - PT13 COSM5895922 c.1309C>T p.Q437* Substitution - Nonsense 7:30452108-30452108 - ICGC_MB57 COSM3765347 c.1331G>A p.R444Q Substitution - Missense 7:30452086-30452086 - ICGC_MB57 COSM3765347 c.1331G>A p.R444Q Substitution - Missense 7:30452086-30452086 - I2L-P24Tb-Tumor-Biopsy COSM5358260 c.2155G>C p.G719R Substitution - Missense 7:30451262-30451262 - TCGA-EE-A182-06 COSM3637890 c.915G>A p.W305* Substitution - Nonsense 7:30452502-30452502 - HCT116 COSM3028202 c.1025T>A p.F342Y Substitution - Missense 7:30452392-30452392 - TCGA-AP-A0LE-01 COSM1089061 c.2663T>C p.L888S Substitution - Missense 7:30433138-30433138 - TCGA-AP-A051-01 COSM1089066 c.1970G>A p.R657H Substitution - Missense 7:30451447-30451447 - TCGA-EE-A20C-06 COSM1450334 c.690C>A p.F230L Substitution - Missense 7:30452727-30452727 - TCGA-CG-5728-01 COSM3880535 c.2802C>T p.N934N Substitution - coding silent 7:30425698-30425698 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.405153 7p15-p14 605980

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - A Frameshift p.H136Sfs*5 c.405_406insT 7 30492627 COREAD - A Frameshift p.S110Ffs*15 c.328dupT 7 30494801 HNSC - A Frameshift p.S110Lfs*15 c.326dupT 7 30494803 RCCC A G 3-UTRSNV . c.2859+1098T>C 7 30464159 HC A G Missense p.L578P c.1733T>C 7 30491300 OV A G Missense p.L888S c.2663T>C 7 30472754 UCEC A G Missense p.V824A c.2471T>C 7 30477255 MB A G Missense p.V894A c.2681T>C 7 30472736 HNSC A G Synonymous p.D946D c.2838T>C 7 30465278 UCEC A - IntronicDeletion . c.2622-7delT 7 30472802 STAD A T Missense p.Y775N c.2323T>A 7 30486629 RCCC C A Missense p.G227V c.680G>T 7 30492353 LUAD C A Missense p.Q4H c.12G>T 7 30496526 STAD C A Missense p.Q907H c.2721G>T 7 30469058 BRCA C A Missense p.R368L c.1103G>T 7 30491930 LUAD C A Synonymous p.A551A c.1653G>T 7 30491380 THCA C A Synonymous p.L752L c.2256G>T 7 30487943 ESCA C A Synonymous p.V390V c.1170G>T 7 30491863 LUAD C G Missense p.E3Q c.7G>C 7 30496531 BRCA C G Missense p.E816Q c.2446G>C 7 30485764 BLCA C G SpliceAcceptorSNV . c.2202-1G>C 7 30487998 ESCA C T IntronicSNV . c.1-5996G>A 7 30502533 PIA C T Missense p.A485T c.1453G>A 7 30491580 STAD C T Missense p.D770N c.2308G>A 7 30486644 HNSC C T Missense p.E196K c.586G>A 7 30492447 HNSC C T Missense p.G507R c.1519G>A 7 30491514 STAD C T Missense p.G719S c.2155G>A 7 30490878 UCEC C T Missense p.R223Q c.668G>A 7 30492365 GBM C T Missense p.R657H c.1970G>A 7 30491063 UCEC C T Missense p.S440N c.1319G>A 7 30491714 BRCA C T Nonsense p.W305* c.915G>A 7 30492118 CM C T Synonymous p.A861A c.2583G>A 7 30475652 LUAD C T Synonymous p.A861A c.2583G>A 7 30475652 UCEC C T Synonymous p.P564P c.1692G>A 7 30491341 UCEC C T Synonymous p.R214R c.642G>A 7 30492391 LUSC C T Synonymous p.V126V c.378G>A 7 30492655 LUAD C T Synonymous p.V206V c.618G>A 7 30492415 LUSC G A Missense p.A52V c.155C>T 7 30496383 GBM G A Missense p.A551V c.1652C>T 7 30491381 CM G A Missense p.A55V c.164C>T 7 30496374 LUSC G A Missense p.P111S c.331C>T 7 30494798 CM G A Missense p.P564S c.1690C>T 7 30491343 CM G A Missense p.P573L c.1718C>T 7 30491315 CM G A Missense p.R235C c.703C>T 7 30492330 CM G A Missense p.R575W c.1723C>T 7 30491310 UCEC G A Missense p.R721W c.2161C>T 7 30490872 LUSC G A Missense p.T188I c.563C>T 7 30492470 CM G A Missense p.T221M c.662C>T 7 30492371 STAD G A Missense p.T556M c.1667C>T 7 30491366 PRAD G A Synonymous p.A315A c.945C>T 7 30492088 LUSC G A Synonymous p.A612A c.1836C>T 7 30491197 UCEC G A Synonymous p.D225D c.675C>T 7 30492358 GBM G A Synonymous p.D246D c.738C>T 7 30492295 HNSC G A Synonymous p.F169F c.507C>T 7 30492526 BLCA G A Synonymous p.F239F c.717C>T 7 30492316 LUSC G A Synonymous p.F283F c.849C>T 7 30492184 CM G A Synonymous p.F342F c.1026C>T 7 30492007 CM G A Synonymous p.G138G c.414C>T 7 30492619 CM G A Synonymous p.L30L c.88C>T 7 30496450 CM G A Synonymous p.L541L c.1623C>T 7 30491410 LUSC G A Synonymous p.L804L c.2412C>T 7 30485798 HNSC G A Synonymous p.N794N c.2382C>T 7 30485828 HNSC G A Synonymous p.N934N c.2802C>T 7 30465314 STAD G A Synonymous p.P366P c.1098C>T 7 30491935 CM G A Synonymous p.P636P c.1908C>T 7 30491125 CM G T Missense p.A914D c.2741C>A 7 30469038 LUSC G T Missense p.F230L c.690C>A 7 30492343 CM G T Synonymous p.P438P c.1314C>A 7 30491719 PRAD G T Synonymous p.R705R c.2113C>A 7 30490920 LUAD T C Missense p.E855G c.2564A>G 7 30475671 LUSC T C Missense p.N381S c.1142A>G 7 30491891 CM T C Missense p.S376G c.1126A>G 7 30491907 CLL T G Missense p.K746T c.2237A>C 7 30487962 OV