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 3 139077931 139077931 + Missense_Mutation SNP A A T TCGA-OR-A5K5-01A-11D-A29I-10 TCGA-OR-A5K5-10A-01D-A29L-10 g.chr3:139077931A>T c.2393T>A c.(2392-2394)tTc>tAc p.F798Y BLCA 3 139077618 139077618 + Missense_Mutation SNP C C G TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr3:139077618C>G c.2521G>C c.(2521-2523)Gac>Cac p.D841H BLCA 3 139077643 139077643 + Missense_Mutation SNP C C G TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr3:139077643C>G c.2496G>C c.(2494-2496)gaG>gaC p.E832D BLCA 3 139077648 139077648 + Missense_Mutation SNP C C T TCGA-BT-A42F-01A-11D-A23U-08 TCGA-BT-A42F-10A-01D-A23U-08 g.chr3:139077648C>T c.2491G>A c.(2491-2493)Gaa>Aaa p.E831K BLCA 3 139081296 139081296 + Nonsense_Mutation SNP G G A TCGA-DK-A6B1-01A-12D-A30E-08 TCGA-DK-A6B1-10A-01D-A30H-08 g.chr3:139081296G>A c.1948C>T c.(1948-1950)Cag>Tag p.Q650* BLCA 3 139085454 139085454 + Missense_Mutation SNP G G A TCGA-CF-A3MG-01A-11D-A20D-08 TCGA-CF-A3MG-10A-01D-A20D-08 g.chr3:139085454G>A c.1840C>T c.(1840-1842)Cca>Tca p.P614S BLCA 3 139085500 139085500 + Silent SNP G G A TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr3:139085500G>A c.1794C>T c.(1792-1794)gtC>gtT p.V598V BLCA 3 139085554 139085554 + Missense_Mutation SNP C C G TCGA-DK-A6B5-01A-11D-A31L-08 TCGA-DK-A6B5-10A-01D-A31J-08 g.chr3:139085554C>G c.1740G>C c.(1738-1740)ttG>ttC p.L580F BLCA 3 139085601 139085601 + Missense_Mutation SNP C C T TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr3:139085601C>T c.1693G>A c.(1693-1695)Ggc>Agc p.G565S BLCA 3 139087069 139087069 + Missense_Mutation SNP A A G TCGA-DK-A3IN-01A-11D-A20D-08 TCGA-DK-A3IN-10A-01D-A20D-08 g.chr3:139087069A>G c.1463T>C c.(1462-1464)cTt>cCt p.L488P BLCA 3 139092111 139092111 + Silent SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr3:139092111C>T c.1038G>A c.(1036-1038)aaG>aaA p.K346K BLCA 3 139102140 139102140 + Splice_Site SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr3:139102140C>T c.141G>A c.(139-141)caG>caA p.Q47Q BRCA 3 139077630 139077630 + Frame_Shift_Del DEL C C - TCGA-BH-A0BC-01A-22D-A099-09 TCGA-BH-A0BC-10A-01D-A099-09 g.chr3:139077630delC c.2509delG c.(2509-2511)gaafs p.E838fs BRCA 3 139077631 139077632 + Missense_Mutation DNP CA CA TG TCGA-BH-A0BC-01A-22D-A099-09 TCGA-BH-A0BC-10A-01D-A099-09 g.chr3:139077631_139077632CA>TG c.2507_2508TG>CA c.(2506-2508)aTG>aCA p.M836T BRCA 3 139092190 139092190 + Nonsense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr3:139092190G>C c.959C>G c.(958-960)tCa>tGa p.S320* BRCA 3 139092649 139092649 + Splice_Site SNP T T C TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr3:139092649T>C c.753A>G c.(751-753)ggA>ggG p.G251G CESC 3 139077085 139077085 + Missense_Mutation SNP G G A TCGA-HM-A4S6-01A-11D-A26G-09 TCGA-HM-A4S6-10A-01D-A26G-09 g.chr3:139077085G>A c.2582C>T c.(2581-2583)aCt>aTt p.T861I CHOL 3 139097937 139097937 + Missense_Mutation SNP G G T TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr3:139097937G>T c.307C>A c.(307-309)Cgc>Agc p.R103S COAD 3 139077102 139077102 + Silent SNP C C T TCGA-CM-6678-01A-11D-1835-10 TCGA-CM-6678-10A-01D-1835-10 g.chr3:139077102C>T c.2565G>A c.(2563-2565)ggG>ggA p.G855G COAD 3 139077103 139077103 + Missense_Mutation SNP C C T TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr3:139077103C>T c.2564G>A c.(2563-2565)gGg>gAg p.G855E COAD 3 139077104 139077104 + Missense_Mutation SNP C C A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr3:139077104C>A c.2563G>T c.(2563-2565)Ggg>Tgg p.G855W COAD 3 139077104 139077104 + Missense_Mutation SNP C C T TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr3:139077104C>T c.2563G>A c.(2563-2565)Ggg>Agg p.G855R COAD 3 139079943 139079943 + Missense_Mutation SNP C C G TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr3:139079943C>G c.2190G>C c.(2188-2190)atG>atC p.M730I COAD 3 139088146 139088146 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr3:139088146T>C c.1358A>G c.(1357-1359)gAc>gGc p.D453G COAD 3 139088325 139088325 + Missense_Mutation SNP A A T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr3:139088325A>T c.1267T>A c.(1267-1269)Tca>Aca p.S423T COAD 3 139092088 139092088 + Missense_Mutation SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr3:139092088T>C c.1061A>G c.(1060-1062)tAc>tGc p.Y354C COAD 3 139093358 139093358 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr3:139093358G>A c.724C>T c.(724-726)Cca>Tca p.P242S COAD 3 139094413 139094413 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr3:139094413C>T c.548G>A c.(547-549)gGa>gAa p.G183E COAD 3 139097030 139097030 + Splice_Site SNP A A C TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr3:139097030A>C c.357T>G c.(355-357)gaT>gaG p.D119E COAD 3 139097937 139097937 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:139097937G>A c.307C>T c.(307-309)Cgc>Tgc p.R103C COAD 3 139098268 139098268 + Missense_Mutation SNP C C T TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr3:139098268C>T c.182G>A c.(181-183)cGa>cAa p.R61Q COAD 3 139098272 139098272 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr3:139098272C>T c.178G>A c.(178-180)Gtt>Att p.V60I COAD 3 139102264 139102264 + Missense_Mutation SNP T T C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:139102264T>C c.17A>G c.(16-18)gAt>gGt p.D6G COADREAD 3 139077102 139077102 + Silent SNP C C T TCGA-CM-6678-01A-11D-1835-10 TCGA-CM-6678-10A-01D-1835-10 g.chr3:139077102C>T c.2565G>A c.(2563-2565)ggG>ggA p.G855G COADREAD 3 139077103 139077103 + Missense_Mutation SNP C C T TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr3:139077103C>T c.2564G>A c.(2563-2565)gGg>gAg p.G855E COADREAD 3 139077104 139077104 + Missense_Mutation SNP C C A TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr3:139077104C>A c.2563G>T c.(2563-2565)Ggg>Tgg p.G855W COADREAD 3 139077104 139077104 + Missense_Mutation SNP C C A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr3:139077104C>A c.2563G>T c.(2563-2565)Ggg>Tgg p.G855W COADREAD 3 139077104 139077104 + Missense_Mutation SNP C C A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:139077104C>A c.2563G>T c.(2563-2565)Ggg>Tgg p.G855W COADREAD 3 139077104 139077104 + Missense_Mutation SNP C C T TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr3:139077104C>T c.2563G>A c.(2563-2565)Ggg>Agg p.G855R COADREAD 3 139079943 139079943 + Missense_Mutation SNP C C G TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr3:139079943C>G c.2190G>C c.(2188-2190)atG>atC p.M730I COADREAD 3 139088146 139088146 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr3:139088146T>C c.1358A>G c.(1357-1359)gAc>gGc p.D453G COADREAD 3 139088325 139088325 + Missense_Mutation SNP A A T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr3:139088325A>T c.1267T>A c.(1267-1269)Tca>Aca p.S423T COADREAD 3 139090601 139090601 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:139090601G>A c.1169C>T c.(1168-1170)tCt>tTt p.S390F COADREAD 3 139092088 139092088 + Missense_Mutation SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr3:139092088T>C c.1061A>G c.(1060-1062)tAc>tGc p.Y354C COADREAD 3 139093358 139093358 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr3:139093358G>A c.724C>T c.(724-726)Cca>Tca p.P242S COADREAD 3 139094413 139094413 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr3:139094413C>T c.548G>A c.(547-549)gGa>gAa p.G183E COADREAD 3 139097030 139097030 + Splice_Site SNP A A C TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr3:139097030A>C c.357T>G c.(355-357)gaT>gaG p.D119E COADREAD 3 139097937 139097937 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:139097937G>A c.307C>T c.(307-309)Cgc>Tgc p.R103C COADREAD 3 139098268 139098268 + Missense_Mutation SNP C C T TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr3:139098268C>T c.182G>A c.(181-183)cGa>cAa p.R61Q COADREAD 3 139098272 139098272 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr3:139098272C>T c.178G>A c.(178-180)Gtt>Att p.V60I COADREAD 3 139102264 139102264 + Missense_Mutation SNP T T C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:139102264T>C c.17A>G c.(16-18)gAt>gGt p.D6G ESCA 3 139077077 139077077 + Missense_Mutation SNP T T C TCGA-LN-A49N-01A-11D-A247-09 TCGA-LN-A49N-10A-01D-A247-09 g.chr3:139077077T>C c.2590A>G c.(2590-2592)Att>Gtt p.I864V GBM 3 139098010 139098010 + Silent SNP G G A TCGA-06-2567-01A-01D-1494-08 TCGA-06-2567-10A-01D-1494-08 g.chr3:139098010G>A c.234C>T c.(232-234)gaC>gaT p.D78D GBMLGG 3 139079976 139079976 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139079976C>T c.2157G>A c.(2155-2157)gcG>gcA p.A719A GBMLGG 3 139085462 139085462 + Missense_Mutation SNP G G A TCGA-HW-A5KK-01A-11D-A27K-08 TCGA-HW-A5KK-10A-01D-A27N-08 g.chr3:139085462G>A c.1832C>T c.(1831-1833)cCt>cTt p.P611L GBMLGG 3 139085532 139085532 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139085532G>T c.1762C>A c.(1762-1764)Ctg>Atg p.L588M GBMLGG 3 139090653 139090653 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139090653C>A c.1117G>T c.(1117-1119)Ggg>Tgg p.G373W GBMLGG 3 139092102 139092102 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139092102G>A c.1047C>T c.(1045-1047)ggC>ggT p.G349G GBMLGG 3 139092254 139092254 + Splice_Site SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139092254G>A c.895C>T c.(895-897)Ctt>Ttt p.L299F GBMLGG 3 139098010 139098010 + Silent SNP G G A TCGA-06-2567-01A-01D-1494-08 TCGA-06-2567-10A-01D-1494-08 g.chr3:139098010G>A c.234C>T c.(232-234)gaC>gaT p.D78D HNSC 3 139077983 139077983 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr3:139077983T>C c.2341A>G c.(2341-2343)Aat>Gat p.N781D HNSC 3 139078167 139078167 + Missense_Mutation SNP G G A TCGA-CV-7238-01A-11D-2012-08 TCGA-CV-7238-10A-01D-2013-08 g.chr3:139078167G>A c.2248C>T c.(2248-2250)Cgg>Tgg p.R750W HNSC 3 139085612 139085612 + Missense_Mutation SNP A A G TCGA-CN-A49B-01A-31D-A24D-08 TCGA-CN-A49B-10A-01D-A24F-08 g.chr3:139085612A>G c.1682T>C c.(1681-1683)aTg>aCg p.M561T HNSC 3 139090585 139090585 + Silent SNP T T C TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr3:139090585T>C c.1185A>G c.(1183-1185)gcA>gcG p.A395A HNSC 3 139092255 139092255 + Splice_Site SNP C C A TCGA-CV-7418-01A-11D-2078-08 TCGA-CV-7418-10A-01D-2078-08 g.chr3:139092255C>A c.e9-1 HNSC 3 139093334 139093334 + Missense_Mutation SNP C C T TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr3:139093334C>T c.748G>A c.(748-750)Gat>Aat p.D250N HNSC 3 139093347 139093347 + Silent SNP G G A TCGA-CV-7414-01A-11D-2078-08 TCGA-CV-7414-10A-01D-2078-08 g.chr3:139093347G>A c.735C>T c.(733-735)atC>atT p.I245I HNSC 3 139096923 139096923 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr3:139096923T>C c.464A>G c.(463-465)aAc>aGc p.N155S KIPAN 3 139077639 139077639 + Missense_Mutation SNP T T G TCGA-B8-5552-01B-11D-1669-08 TCGA-B8-5552-10A-01D-1669-08 g.chr3:139077639T>G c.2500A>C c.(2500-2502)Aat>Cat p.N834H KIPAN 3 139090593 139090593 + Missense_Mutation SNP C C T TCGA-BP-4965-01A-01D-1462-08 TCGA-BP-4965-11A-01D-1462-08 g.chr3:139090593C>T c.1177G>A c.(1177-1179)Gag>Aag p.E393K KIPAN 3 139092573 139092573 + Missense_Mutation SNP C C T TCGA-G7-A8LD-01A-11D-A35Z-10 TCGA-G7-A8LD-10A-01D-A35Z-10 g.chr3:139092573C>T c.829G>A c.(829-831)Gtg>Atg p.V277M KIRC 3 139077639 139077639 + Missense_Mutation SNP T T G TCGA-B8-5552-01B-11D-1669-08 TCGA-B8-5552-10A-01D-1669-08 g.chr3:139077639T>G c.2500A>C c.(2500-2502)Aat>Cat p.N834H KIRC 3 139090593 139090593 + Missense_Mutation SNP C C T TCGA-BP-4965-01A-01D-1462-08 TCGA-BP-4965-11A-01D-1462-08 g.chr3:139090593C>T c.1177G>A c.(1177-1179)Gag>Aag p.E393K KIRP 3 139092573 139092573 + Missense_Mutation SNP C C T TCGA-G7-A8LD-01A-11D-A35Z-10 TCGA-G7-A8LD-10A-01D-A35Z-10 g.chr3:139092573C>T c.829G>A c.(829-831)Gtg>Atg p.V277M LGG 3 139079976 139079976 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139079976C>T c.2157G>A c.(2155-2157)gcG>gcA p.A719A LGG 3 139085462 139085462 + Missense_Mutation SNP G G A TCGA-HW-A5KK-01A-11D-A27K-08 TCGA-HW-A5KK-10A-01D-A27N-08 g.chr3:139085462G>A c.1832C>T c.(1831-1833)cCt>cTt p.P611L LGG 3 139085532 139085532 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139085532G>T c.1762C>A c.(1762-1764)Ctg>Atg p.L588M LGG 3 139090653 139090653 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139090653C>A c.1117G>T c.(1117-1119)Ggg>Tgg p.G373W LGG 3 139092102 139092102 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139092102G>A c.1047C>T c.(1045-1047)ggC>ggT p.G349G LGG 3 139092254 139092254 + Splice_Site SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:139092254G>A c.895C>T c.(895-897)Ctt>Ttt p.L299F LIHC 3 139077908 139077908 + Missense_Mutation SNP C C T TCGA-DD-AAEG-01A-11D-A38X-10 TCGA-DD-AAEG-10A-01D-A38X-10 g.chr3:139077908C>T c.2416G>A c.(2416-2418)Gtt>Att p.V806I LIHC 3 139096979 139096979 + Silent SNP T T C TCGA-DD-AACP-01A-11D-A40R-10 TCGA-DD-AACP-10A-01D-A40U-10 g.chr3:139096979T>C c.408A>G c.(406-408)caA>caG p.Q136Q LIHC 3 139096994 139096994 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr3:139096994delT c.393delA c.(391-393)aaafs p.K131fs LUAD 3 139087022 139087022 + Missense_Mutation SNP C C T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr3:139087022C>T c.1510G>A c.(1510-1512)Gga>Aga p.G504R LUAD 3 139092570 139092570 + Missense_Mutation SNP C C A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr3:139092570C>A c.832G>T c.(832-834)Gcc>Tcc p.A278S LUAD 3 139092571 139092571 + Silent SNP C C A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr3:139092571C>A c.831G>T c.(829-831)gtG>gtT p.V277V LUAD 3 139093397 139093397 + Missense_Mutation SNP C C T TCGA-50-7109-01A-11D-2036-08 TCGA-50-7109-11A-01D-2036-08 g.chr3:139093397C>T c.685G>A c.(685-687)Gcc>Acc p.A229T LUAD 3 139096946 139096946 + Missense_Mutation SNP C C G TCGA-62-8394-01A-11D-2323-08 TCGA-62-8394-10A-01D-2323-08 g.chr3:139096946C>G c.441G>C c.(439-441)caG>caC p.Q147H LUAD 3 139096978 139096978 + Missense_Mutation SNP C C G TCGA-50-5933-01A-11D-1753-08 TCGA-50-5933-11A-01D-1753-08 g.chr3:139096978C>G c.409G>C c.(409-411)Gtg>Ctg p.V137L LUAD 3 139102206 139102206 + Silent SNP A A G TCGA-17-Z032-01A-01W-0746-08 TCGA-17-Z032-11A-01W-0746-08 g.chr3:139102206A>G c.75T>C c.(73-75)ccT>ccC p.P25P LUSC 3 139080022 139080022 + Missense_Mutation SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr3:139080022G>T c.2111C>A c.(2110-2112)aCt>aAt p.T704N LUSC 3 139086994 139086994 + Missense_Mutation SNP G G A TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr3:139086994G>A c.1538C>T c.(1537-1539)gCc>gTc p.A513V LUSC 3 139102235 139102235 + Missense_Mutation SNP C C G TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr3:139102235C>G c.46G>C c.(46-48)Gat>Cat p.D16H OV 3 139077104 139077104 + Missense_Mutation SNP C C T TCGA-23-1022-01A-02W-0488-09 TCGA-23-1022-10A-01W-0488-09 g.chr3:139077104C>T c.2563G>A c.(2563-2565)Ggg>Agg p.G855R OV 3 139077948 139077949 + Frame_Shift_Del DEL TG TG - TCGA-09-2056-01B-01W-0722-08 TCGA-09-2056-11A-01W-0722-08 g.chr3:139077948_139077949delTG c.2375_2376delCA c.(2374-2376)acafs p.T792fs PAAD 3 139097937 139097937 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:139097937G>A c.307C>T c.(307-309)Cgc>Tgc p.R103C PRAD 3 139077851 139077851 + Missense_Mutation SNP G G A TCGA-HC-A6AL-01A-11D-A30E-08 TCGA-HC-A6AL-10A-01D-A30H-08 g.chr3:139077851G>A c.2473C>T c.(2473-2475)Cca>Tca p.P825S PRAD 3 139085507 139085507 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:139085507G>A c.1787C>T c.(1786-1788)aCa>aTa p.T596I PRAD 3 139088199 139088199 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:139088199G>A c.1305C>T c.(1303-1305)ggC>ggT p.G435G READ 3 139077104 139077104 + Missense_Mutation SNP C C A TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr3:139077104C>A c.2563G>T c.(2563-2565)Ggg>Tgg p.G855W READ 3 139077104 139077104 + Missense_Mutation SNP C C A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:139077104C>A c.2563G>T c.(2563-2565)Ggg>Tgg p.G855W READ 3 139090601 139090601 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:139090601G>A c.1169C>T c.(1168-1170)tCt>tTt p.S390F SARC 3 139079946 139079946 + Frame_Shift_Del DEL G G - TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr3:139079946delG c.2187delC c.(2185-2187)ttcfs p.F729fs SARC 3 139085946 139085946 + Missense_Mutation SNP C C G TCGA-DX-A8BR-01A-11D-A417-09 TCGA-DX-A8BR-10B-01D-A41A-09 g.chr3:139085946C>G c.1587G>C c.(1585-1587)tgG>tgC p.W529C SARC 3 139087001 139087001 + Missense_Mutation SNP C C G TCGA-DX-A8BR-01A-11D-A417-09 TCGA-DX-A8BR-10B-01D-A41A-09 g.chr3:139087001C>G c.1531G>C c.(1531-1533)Gaa>Caa p.E511Q SKCM 3 139076710 139076710 + Missense_Mutation SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr3:139076710C>T c.2716G>A c.(2716-2718)Gat>Aat p.D906N SKCM 3 139090653 139090653 + Missense_Mutation SNP C C A TCGA-D3-A3CB-06A-11D-A196-08 TCGA-D3-A3CB-10A-01D-A198-08 g.chr3:139090653C>A c.1117G>T c.(1117-1119)Ggg>Tgg p.G373W SKCM 3 139092233 139092233 + Missense_Mutation SNP T T C TCGA-EE-A2GB-06A-11D-A197-08 TCGA-EE-A2GB-10A-01D-A199-08 g.chr3:139092233T>C c.916A>G c.(916-918)Atg>Gtg p.M306V

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 3 139077583 139077583 single base substitution G A exon_variant BLCA-CN 3 139077583 139077583 single base substitution G A intron_variant BLCA-CN 3 139077583 139077583 single base substitution G A splice_region_variant BLCA-US 3 139071544 139071544 single base substitution G A downstream_gene_variant BLCA-US 3 139085454 139085454 single base substitution G A intron_variant BLCA-US 3 139085454 139085454 single base substitution G A missense_variant P585S 1753C>T BLCA-US 3 139085454 139085454 single base substitution G A missense_variant P614S 1840C>T BLCA-US 3 139085601 139085601 single base substitution C T intron_variant BLCA-US 3 139085601 139085601 single base substitution C T missense_variant G536S 1606G>A BLCA-US 3 139085601 139085601 single base substitution C T missense_variant G565S 1693G>A BLCA-US 3 139087069 139087069 single base substitution A G missense_variant L111P 332T>C BLCA-US 3 139087069 139087069 single base substitution A G missense_variant L459P 1376T>C BLCA-US 3 139087069 139087069 single base substitution A G missense_variant L488P 1463T>C BLCA-US 3 139092111 139092111 single base substitution C T downstream_gene_variant BLCA-US 3 139092111 139092111 single base substitution C T synonymous_variant K317K 951G>A BLCA-US 3 139092111 139092111 single base substitution C T synonymous_variant K346K 1038G>A BLCA-US 3 139092111 139092111 single base substitution C T upstream_gene_variant BOCA-UK 3 139080008 139080008 single base substitution C T intron_variant BOCA-UK 3 139080008 139080008 single base substitution C T missense_variant A680T 2038G>A BOCA-UK 3 139080008 139080008 single base substitution C T missense_variant A709T 2125G>A BOCA-UK 3 139080008 139080008 single base substitution C T upstream_gene_variant BRCA-EU 3 139071223 139071223 single base substitution A G downstream_gene_variant BRCA-EU 3 139071626 139071626 single base substitution G A downstream_gene_variant BRCA-EU 3 139072764 139072764 single base substitution A G downstream_gene_variant BRCA-EU 3 139073386 139073386 deletion of <=200bp T - downstream_gene_variant BRCA-EU 3 139073530 139073530 single base substitution C T downstream_gene_variant BRCA-EU 3 139074008 139074008 single base substitution C A downstream_gene_variant BRCA-EU 3 139075487 139075487 single base substitution G A downstream_gene_variant BRCA-EU 3 139075487 139075487 single base substitution G A intron_variant BRCA-EU 3 139076704 139076704 single base substitution G T 3_prime_UTR_variant BRCA-EU 3 139076704 139076704 single base substitution G T exon_variant BRCA-EU 3 139076704 139076704 single base substitution G T intron_variant BRCA-EU 3 139077693 139077693 single base substitution G A intron_variant BRCA-EU 3 139077693 139077693 single base substitution G A upstream_gene_variant BRCA-EU 3 139078519 139078519 single base substitution C T intron_variant BRCA-EU 3 139078519 139078519 single base substitution C T upstream_gene_variant BRCA-EU 3 139079957 139079957 single base substitution T C intron_variant BRCA-EU 3 139079957 139079957 single base substitution T C missense_variant N697D 2089A>G BRCA-EU 3 139079957 139079957 single base substitution T C missense_variant N726D 2176A>G BRCA-EU 3 139079957 139079957 single base substitution T C upstream_gene_variant BRCA-EU 3 139080144 139080144 single base substitution G C intron_variant BRCA-EU 3 139080144 139080144 single base substitution G C splice_region_variant BRCA-EU 3 139080144 139080144 single base substitution G C upstream_gene_variant BRCA-EU 3 139081085 139081085 single base substitution A G intron_variant BRCA-EU 3 139081085 139081085 single base substitution A G upstream_gene_variant BRCA-EU 3 139081982 139081982 single base substitution C T intron_variant BRCA-EU 3 139081982 139081982 single base substitution C T upstream_gene_variant BRCA-EU 3 139082238 139082238 single base substitution T C intron_variant BRCA-EU 3 139082238 139082238 single base substitution T C upstream_gene_variant BRCA-EU 3 139084473 139084473 single base substitution G A intron_variant BRCA-EU 3 139084497 139084497 single base substitution G C intron_variant BRCA-EU 3 139085885 139085885 single base substitution C T intron_variant BRCA-EU 3 139085885 139085885 single base substitution C T missense_variant E521K 1561G>A BRCA-EU 3 139085885 139085885 single base substitution C T missense_variant E550K 1648G>A BRCA-EU 3 139085915 139085915 single base substitution C G intron_variant BRCA-EU 3 139085915 139085915 single base substitution C G missense_variant V511L 1531G>C BRCA-EU 3 139085915 139085915 single base substitution C G missense_variant V540L 1618G>C BRCA-EU 3 139086061 139086061 single base substitution G A intron_variant BRCA-EU 3 139087711 139087711 single base substitution C T intron_variant BRCA-EU 3 139088721 139088721 single base substitution C G downstream_gene_variant BRCA-EU 3 139088721 139088721 single base substitution C G intron_variant BRCA-EU 3 139089205 139089205 single base substitution C G downstream_gene_variant BRCA-EU 3 139089205 139089205 single base substitution C G intron_variant BRCA-EU 3 139089301 139089301 single base substitution G T downstream_gene_variant BRCA-EU 3 139089301 139089301 single base substitution G T intron_variant BRCA-EU 3 139090283 139090283 single base substitution G T downstream_gene_variant BRCA-EU 3 139090283 139090283 single base substitution G T intron_variant BRCA-EU 3 139096239 139096239 single base substitution G A downstream_gene_variant BRCA-EU 3 139096239 139096239 single base substitution G A intron_variant BRCA-EU 3 139096952 139096952 single base substitution A T downstream_gene_variant BRCA-EU 3 139096952 139096952 single base substitution A T exon_variant BRCA-EU 3 139096952 139096952 single base substitution A T synonymous_variant V116V 348T>A BRCA-EU 3 139096952 139096952 single base substitution A T synonymous_variant V124V 372T>A BRCA-EU 3 139096952 139096952 single base substitution A T synonymous_variant V145V 435T>A BRCA-EU 3 139097187 139097187 single base substitution T G downstream_gene_variant BRCA-EU 3 139097187 139097187 single base substitution T G intron_variant BRCA-EU 3 139098204 139098204 single base substitution T C downstream_gene_variant BRCA-EU 3 139098204 139098204 single base substitution T C intron_variant BRCA-EU 3 139100603 139100603 single base substitution C G exon_variant BRCA-EU 3 139100603 139100603 single base substitution C G intron_variant BRCA-EU 3 139100957 139100957 single base substitution C T exon_variant BRCA-EU 3 139100957 139100957 single base substitution C T intron_variant BRCA-EU 3 139101198 139101198 single base substitution T C exon_variant BRCA-EU 3 139101198 139101198 single base substitution T C intron_variant BRCA-EU 3 139103316 139103316 single base substitution A T intron_variant BRCA-EU 3 139105471 139105471 single base substitution A C intron_variant BRCA-EU 3 139106726 139106726 single base substitution G C intron_variant BRCA-EU 3 139107741 139107741 deletion of <=200bp T - intron_variant BRCA-EU 3 139109331 139109331 single base substitution C G upstream_gene_variant BRCA-EU 3 139111764 139111764 insertion of <=200bp - T upstream_gene_variant BRCA-FR 3 139072392 139072392 single base substitution G A downstream_gene_variant BRCA-FR 3 139084473 139084473 single base substitution G A intron_variant BRCA-FR 3 139085100 139085100 single base substitution T A intron_variant BRCA-FR 3 139089205 139089205 single base substitution C G downstream_gene_variant BRCA-FR 3 139089205 139089205 single base substitution C G intron_variant BRCA-FR 3 139090283 139090283 single base substitution G T downstream_gene_variant BRCA-FR 3 139090283 139090283 single base substitution G T intron_variant BRCA-FR 3 139096086 139096086 single base substitution C T downstream_gene_variant BRCA-FR 3 139096086 139096086 single base substitution C T intron_variant BRCA-FR 3 139096886 139096886 single base substitution G C downstream_gene_variant BRCA-FR 3 139096886 139096886 single base substitution G C exon_variant BRCA-FR 3 139096886 139096886 single base substitution G C missense_variant I138M 414C>G BRCA-FR 3 139096886 139096886 single base substitution G C missense_variant I146M 438C>G BRCA-FR 3 139096886 139096886 single base substitution G C missense_variant I167M 501C>G BRCA-FR 3 139098204 139098204 single base substitution T C downstream_gene_variant BRCA-FR 3 139098204 139098204 single base substitution T C intron_variant BRCA-FR 3 139105648 139105648 single base substitution G C intron_variant BRCA-UK 3 139081257 139081257 single base substitution C A intron_variant BRCA-UK 3 139081257 139081257 single base substitution C A stop_gained E634* 1900G>T BRCA-UK 3 139081257 139081257 single base substitution C A stop_gained E663* 1987G>T BRCA-UK 3 139081257 139081257 single base substitution C A upstream_gene_variant BRCA-UK 3 139085594 139085594 single base substitution A G intron_variant BRCA-UK 3 139085594 139085594 single base substitution A G missense_variant I538T 1613T>C BRCA-UK 3 139085594 139085594 single base substitution A G missense_variant I567T 1700T>C BRCA-UK 3 139085885 139085885 single base substitution C T intron_variant BRCA-UK 3 139085885 139085885 single base substitution C T missense_variant E521K 1561G>A BRCA-UK 3 139085885 139085885 single base substitution C T missense_variant E550K 1648G>A BRCA-UK 3 139092318 139092318 single base substitution G A downstream_gene_variant BRCA-UK 3 139092318 139092318 single base substitution G A intron_variant BRCA-UK 3 139092318 139092318 single base substitution G A upstream_gene_variant BRCA-US 3 139071564 139071564 single base substitution G C downstream_gene_variant BRCA-US 3 139074558 139074558 single base substitution C G downstream_gene_variant BRCA-US 3 139074558 139074558 single base substitution C G missense_variant D106H 316G>C BRCA-US 3 139077630 139077630 deletion of <=200bp C - frameshift_variant E50 BRCA-US 3 139077630 139077630 deletion of <=200bp C - frameshift_variant E808 BRCA-US 3 139077630 139077630 deletion of <=200bp C - frameshift_variant E837 BRCA-US 3 139077630 139077630 deletion of <=200bp C - intron_variant BRCA-US 3 139077630 139077630 deletion of <=200bp C - upstream_gene_variant BRCA-US 3 139077631 139077631 single base substitution C T intron_variant BRCA-US 3 139077631 139077631 single base substitution C T missense_variant M49I 147G>A BRCA-US 3 139077631 139077631 single base substitution C T missense_variant M807I 2421G>A BRCA-US 3 139077631 139077631 single base substitution C T missense_variant M836I 2508G>A BRCA-US 3 139077631 139077631 single base substitution C T upstream_gene_variant BRCA-US 3 139077632 139077632 single base substitution A G intron_variant BRCA-US 3 139077632 139077632 single base substitution A G missense_variant M49T 146T>C BRCA-US 3 139077632 139077632 single base substitution A G missense_variant M807T 2420T>C BRCA-US 3 139077632 139077632 single base substitution A G missense_variant M836T 2507T>C BRCA-US 3 139077632 139077632 single base substitution A G upstream_gene_variant BRCA-US 3 139092190 139092190 single base substitution G C downstream_gene_variant BRCA-US 3 139092190 139092190 single base substitution G C stop_gained S291* 872C>G BRCA-US 3 139092190 139092190 single base substitution G C stop_gained S320* 959C>G BRCA-US 3 139092190 139092190 single base substitution G C upstream_gene_variant BRCA-US 3 139092649 139092649 single base substitution T C downstream_gene_variant BRCA-US 3 139092649 139092649 single base substitution T C splice_region_variant BRCA-US 3 139092649 139092649 single base substitution T C upstream_gene_variant BTCA-JP 3 139074465 139074465 single base substitution T C 3_prime_UTR_variant BTCA-JP 3 139074465 139074465 single base substitution T C downstream_gene_variant BTCA-JP 3 139077045 139077047 deletion of <=200bp TTC - exon_variant BTCA-JP 3 139077045 139077047 deletion of <=200bp TTC - inframe_deletion E845 BTCA-JP 3 139077045 139077047 deletion of <=200bp TTC - inframe_deletion E87 BTCA-JP 3 139077045 139077047 deletion of <=200bp TTC - inframe_deletion E874 BTCA-JP 3 139077045 139077047 deletion of <=200bp TTC - intron_variant BTCA-JP 3 139078212 139078212 single base substitution T A intron_variant BTCA-JP 3 139078212 139078212 single base substitution T A splice_region_variant BTCA-JP 3 139078212 139078212 single base substitution T A upstream_gene_variant BTCA-JP 3 139079893 139079896 deletion of <=200bp AATT - intron_variant BTCA-JP 3 139079893 139079896 deletion of <=200bp AATT - upstream_gene_variant BTCA-JP 3 139092056 139092056 single base substitution G A downstream_gene_variant BTCA-JP 3 139092056 139092056 single base substitution G A missense_variant R336W 1006C>T BTCA-JP 3 139092056 139092056 single base substitution G A missense_variant R365W 1093C>T BTCA-JP 3 139092056 139092056 single base substitution G A upstream_gene_variant BTCA-JP 3 139108455 139108455 single base substitution A C 5_prime_UTR_variant BTCA-JP 3 139108455 139108455 single base substitution A C exon_variant BTCA-JP 3 139108455 139108455 single base substitution A C intron_variant BTCA-JP 3 139108455 139108455 single base substitution A C upstream_gene_variant CESC-US 3 139077085 139077085 single base substitution G A exon_variant CESC-US 3 139077085 139077085 single base substitution G A intron_variant CESC-US 3 139077085 139077085 single base substitution G A missense_variant T74I 221C>T CESC-US 3 139077085 139077085 single base substitution G A missense_variant T832I 2495C>T CESC-US 3 139077085 139077085 single base substitution G A missense_variant T861I 2582C>T CLLE-ES 3 139075544 139075544 insertion of <=200bp - TA downstream_gene_variant CLLE-ES 3 139075544 139075544 insertion of <=200bp - TA intron_variant CLLE-ES 3 139095168 139095168 single base substitution A G downstream_gene_variant CLLE-ES 3 139095168 139095168 single base substitution A G intron_variant CLLE-ES 3 139095168 139095168 single base substitution A G upstream_gene_variant COAD-US 3 139092088 139092088 single base substitution T C downstream_gene_variant COAD-US 3 139092088 139092088 single base substitution T C missense_variant Y325C 974A>G COAD-US 3 139092088 139092088 single base substitution T C missense_variant Y354C 1061A>G COAD-US 3 139092088 139092088 single base substitution T C upstream_gene_variant COAD-US 3 139097030 139097030 single base substitution A C downstream_gene_variant COAD-US 3 139097030 139097030 single base substitution A C intron_variant COAD-US 3 139097030 139097030 single base substitution A C missense_variant D119E 357T>G COAD-US 3 139097030 139097030 single base substitution A C missense_variant D90E 270T>G COAD-US 3 139097030 139097030 single base substitution A C splice_region_variant COAD-US 3 139098268 139098268 single base substitution C T downstream_gene_variant COAD-US 3 139098268 139098268 single base substitution C T exon_variant COAD-US 3 139098268 139098268 single base substitution C T missense_variant R32Q 95G>A COAD-US 3 139098268 139098268 single base substitution C T missense_variant R61Q 182G>A COAD-US 3 139098272 139098272 single base substitution C T downstream_gene_variant COAD-US 3 139098272 139098272 single base substitution C T exon_variant COAD-US 3 139098272 139098272 single base substitution C T missense_variant V31I 91G>A COAD-US 3 139098272 139098272 single base substitution C T missense_variant V60I 178G>A COCA-CN 3 139069955 139069955 single base substitution A C downstream_gene_variant COCA-CN 3 139075741 139075741 single base substitution T G downstream_gene_variant COCA-CN 3 139075741 139075741 single base substitution T G intron_variant COCA-CN 3 139077663 139077663 single base substitution G T intron_variant COCA-CN 3 139077663 139077663 single base substitution G T upstream_gene_variant COCA-CN 3 139081378 139081378 single base substitution A C intron_variant COCA-CN 3 139081378 139081378 single base substitution A C upstream_gene_variant COCA-CN 3 139085389 139085389 single base substitution G T intron_variant COCA-CN 3 139086035 139086035 single base substitution C A intron_variant COCA-CN 3 139090736 139090736 single base substitution G A downstream_gene_variant COCA-CN 3 139090736 139090736 single base substitution G A intron_variant COCA-CN 3 139090736 139090736 single base substitution G A upstream_gene_variant COCA-CN 3 139090762 139090762 single base substitution G T downstream_gene_variant COCA-CN 3 139090762 139090762 single base substitution G T intron_variant COCA-CN 3 139090762 139090762 single base substitution G T upstream_gene_variant COCA-CN 3 139092227 139092227 single base substitution T C downstream_gene_variant COCA-CN 3 139092227 139092227 single base substitution T C missense_variant M279V 835A>G COCA-CN 3 139092227 139092227 single base substitution T C missense_variant M308V 922A>G COCA-CN 3 139092227 139092227 single base substitution T C upstream_gene_variant COCA-CN 3 139092646 139092646 single base substitution T G downstream_gene_variant COCA-CN 3 139092646 139092646 single base substitution T G synonymous_variant T223T 669A>C COCA-CN 3 139092646 139092646 single base substitution T G synonymous_variant T252T 756A>C COCA-CN 3 139092646 139092646 single base substitution T G upstream_gene_variant COCA-CN 3 139093335 139093335 single base substitution T C downstream_gene_variant COCA-CN 3 139093335 139093335 single base substitution T C exon_variant COCA-CN 3 139093335 139093335 single base substitution T C synonymous_variant E220E 660A>G COCA-CN 3 139093335 139093335 single base substitution T C synonymous_variant E249E 747A>G COCA-CN 3 139093335 139093335 single base substitution T C upstream_gene_variant COCA-CN 3 139093447 139093447 single base substitution G T downstream_gene_variant COCA-CN 3 139093447 139093447 single base substitution G T intron_variant COCA-CN 3 139093447 139093447 single base substitution G T upstream_gene_variant COCA-CN 3 139098025 139098025 single base substitution G T downstream_gene_variant COCA-CN 3 139098025 139098025 single base substitution G T intron_variant COCA-CN 3 139102081 139102081 single base substitution A G exon_variant COCA-CN 3 139102081 139102081 single base substitution A G intron_variant ESAD-UK 3 139071133 139071133 single base substitution A T downstream_gene_variant ESAD-UK 3 139075617 139075617 single base substitution C T downstream_gene_variant ESAD-UK 3 139075617 139075617 single base substitution C T intron_variant ESAD-UK 3 139077200 139077200 insertion of <=200bp - T exon_variant ESAD-UK 3 139077200 139077200 insertion of <=200bp - T intron_variant ESAD-UK 3 139084125 139084125 single base substitution C A intron_variant ESAD-UK 3 139085640 139085640 single base substitution G A intron_variant ESAD-UK 3 139086941 139086941 single base substitution C T intron_variant ESAD-UK 3 139089709 139089709 single base substitution G C downstream_gene_variant ESAD-UK 3 139089709 139089709 single base substitution G C intron_variant ESAD-UK 3 139092982 139092982 single base substitution T C downstream_gene_variant ESAD-UK 3 139092982 139092982 single base substitution T C intron_variant ESAD-UK 3 139092982 139092982 single base substitution T C upstream_gene_variant ESAD-UK 3 139094260 139094260 single base substitution T C downstream_gene_variant ESAD-UK 3 139094260 139094260 single base substitution T C intron_variant ESAD-UK 3 139094260 139094260 single base substitution T C upstream_gene_variant ESAD-UK 3 139095027 139095027 single base substitution A C downstream_gene_variant ESAD-UK 3 139095027 139095027 single base substitution A C intron_variant ESAD-UK 3 139095027 139095027 single base substitution A C upstream_gene_variant ESAD-UK 3 139095103 139095103 insertion of <=200bp - ATAA downstream_gene_variant ESAD-UK 3 139095103 139095103 insertion of <=200bp - ATAA intron_variant ESAD-UK 3 139095103 139095103 insertion of <=200bp - ATAA upstream_gene_variant ESAD-UK 3 139096715 139096715 single base substitution A G downstream_gene_variant ESAD-UK 3 139096715 139096715 single base substitution A G intron_variant ESAD-UK 3 139097374 139097374 single base substitution G A downstream_gene_variant ESAD-UK 3 139097374 139097374 single base substitution G A intron_variant ESAD-UK 3 139097884 139097884 single base substitution C G downstream_gene_variant ESAD-UK 3 139097884 139097884 single base substitution C G splice_region_variant ESAD-UK 3 139099147 139099147 single base substitution C A exon_variant ESAD-UK 3 139099147 139099147 single base substitution C A intron_variant ESAD-UK 3 139099569 139099569 single base substitution G A exon_variant ESAD-UK 3 139099569 139099569 single base substitution G A intron_variant ESAD-UK 3 139102487 139102487 single base substitution C T intron_variant ESAD-UK 3 139107870 139107870 single base substitution C T intron_variant ESAD-UK 3 139110476 139110476 single base substitution T A upstream_gene_variant ESAD-UK 3 139111766 139111766 single base substitution T C upstream_gene_variant ESAD-UK 3 139112658 139112658 single base substitution A T upstream_gene_variant ESAD-UK 3 139112819 139112819 single base substitution G A upstream_gene_variant GBM-US 3 139098010 139098010 single base substitution G A downstream_gene_variant GBM-US 3 139098010 139098010 single base substitution G A exon_variant GBM-US 3 139098010 139098010 single base substitution G A synonymous_variant D49D 147C>T GBM-US 3 139098010 139098010 single base substitution G A synonymous_variant D78D 234C>T KIRC-US 3 139074556 139074556 single base substitution A G downstream_gene_variant KIRC-US 3 139074556 139074556 single base substitution A G synonymous_variant D106D 318T>C KIRC-US 3 139077639 139077639 single base substitution T G intron_variant KIRC-US 3 139077639 139077639 single base substitution T G missense_variant N47H 139A>C KIRC-US 3 139077639 139077639 single base substitution T G missense_variant N805H 2413A>C KIRC-US 3 139077639 139077639 single base substitution T G missense_variant N834H 2500A>C KIRC-US 3 139077639 139077639 single base substitution T G upstream_gene_variant KIRC-US 3 139085577 139085577 single base substitution G C intron_variant KIRC-US 3 139085577 139085577 single base substitution G C missense_variant L544V 1630C>G KIRC-US 3 139085577 139085577 single base substitution G C missense_variant L573V 1717C>G LAML-KR 3 139092116 139092116 single base substitution C T downstream_gene_variant LAML-KR 3 139092116 139092116 single base substitution C T missense_variant V316I 946G>A LAML-KR 3 139092116 139092116 single base substitution C T missense_variant V345I 1033G>A LAML-KR 3 139092116 139092116 single base substitution C T upstream_gene_variant LGG-US 3 139085462 139085462 single base substitution G A intron_variant LGG-US 3 139085462 139085462 single base substitution G A missense_variant P582L 1745C>T LGG-US 3 139085462 139085462 single base substitution G A missense_variant P611L 1832C>T LICA-CN 3 139102264 139102264 single base substitution T G 5_prime_UTR_variant LICA-CN 3 139102264 139102264 single base substitution T G exon_variant LICA-CN 3 139102264 139102264 single base substitution T G missense_variant D6A 17A>C LICA-FR 3 139072052 139072052 single base substitution T G downstream_gene_variant LICA-FR 3 139079018 139079018 single base substitution G A intron_variant LICA-FR 3 139079018 139079018 single base substitution G A upstream_gene_variant LICA-FR 3 139079401 139079401 single base substitution A T intron_variant LICA-FR 3 139079401 139079401 single base substitution A T upstream_gene_variant LICA-FR 3 139083860 139083877 deletion of <=200bp AATAAGATTTTAAAAGAG - intron_variant LICA-FR 3 139085480 139085480 single base substitution A G intron_variant LICA-FR 3 139085480 139085480 single base substitution A G missense_variant M576T 1727T>C LICA-FR 3 139085480 139085480 single base substitution A G missense_variant M605T 1814T>C LICA-FR 3 139087932 139087932 single base substitution A T intron_variant LICA-FR 3 139090585 139090585 single base substitution T C downstream_gene_variant LICA-FR 3 139090585 139090585 single base substitution T C synonymous_variant A18A 54A>G LICA-FR 3 139090585 139090585 single base substitution T C synonymous_variant A366A 1098A>G LICA-FR 3 139090585 139090585 single base substitution T C synonymous_variant A395A 1185A>G LICA-FR 3 139098846 139098851 deletion of <=200bp TTTTTT - downstream_gene_variant LICA-FR 3 139098846 139098851 deletion of <=200bp TTTTTT - intron_variant LICA-FR 3 139110784 139110784 single base substitution T C upstream_gene_variant LICA-FR 3 139112805 139112805 single base substitution C G upstream_gene_variant LINC-JP 3 139069897 139069897 single base substitution A G downstream_gene_variant LINC-JP 3 139081433 139081433 single base substitution C T intron_variant LINC-JP 3 139081433 139081433 single base substitution C T upstream_gene_variant LINC-JP 3 139092726 139092726 single base substitution T C downstream_gene_variant LINC-JP 3 139092726 139092726 single base substitution T C intron_variant LINC-JP 3 139092726 139092726 single base substitution T C upstream_gene_variant LINC-JP 3 139094347 139094347 single base substitution C A downstream_gene_variant LINC-JP 3 139094347 139094347 single base substitution C A exon_variant LINC-JP 3 139094347 139094347 single base substitution C A missense_variant G176V 527G>T LINC-JP 3 139094347 139094347 single base substitution C A missense_variant G205V 614G>T LINC-JP 3 139094347 139094347 single base substitution C A upstream_gene_variant LINC-JP 3 139094348 139094348 single base substitution C A downstream_gene_variant LINC-JP 3 139094348 139094348 single base substitution C A exon_variant LINC-JP 3 139094348 139094348 single base substitution C A missense_variant G176C 526G>T LINC-JP 3 139094348 139094348 single base substitution C A missense_variant G205C 613G>T LINC-JP 3 139094348 139094348 single base substitution C A upstream_gene_variant LINC-JP 3 139094360 139094360 single base substitution A G downstream_gene_variant LINC-JP 3 139094360 139094360 single base substitution A G exon_variant LINC-JP 3 139094360 139094360 single base substitution A G missense_variant Y172H 514T>C LINC-JP 3 139094360 139094360 single base substitution A G missense_variant Y201H 601T>C LINC-JP 3 139094360 139094360 single base substitution A G upstream_gene_variant LINC-JP 3 139105148 139105148 single base substitution G T intron_variant LIRI-JP 3 139069779 139069779 single base substitution A G downstream_gene_variant LIRI-JP 3 139070016 139070016 single base substitution A T downstream_gene_variant LIRI-JP 3 139070237 139070237 single base substitution G T downstream_gene_variant LIRI-JP 3 139070315 139070315 insertion of <=200bp - A downstream_gene_variant LIRI-JP 3 139070912 139070912 single base substitution G A downstream_gene_variant LIRI-JP 3 139071022 139071022 single base substitution T G downstream_gene_variant LIRI-JP 3 139071827 139071827 single base substitution T A downstream_gene_variant LIRI-JP 3 139072946 139072946 single base substitution T C downstream_gene_variant LIRI-JP 3 139073187 139073187 single base substitution A G downstream_gene_variant LIRI-JP 3 139075502 139075502 single base substitution A G downstream_gene_variant LIRI-JP 3 139075502 139075502 single base substitution A G intron_variant LIRI-JP 3 139075727 139075727 single base substitution T G downstream_gene_variant LIRI-JP 3 139075727 139075727 single base substitution T G intron_variant LIRI-JP 3 139077133 139077133 single base substitution T C exon_variant LIRI-JP 3 139077133 139077133 single base substitution T C intron_variant LIRI-JP 3 139077312 139077312 single base substitution A T exon_variant LIRI-JP 3 139077312 139077312 single base substitution A T intron_variant LIRI-JP 3 139078184 139078189 deletion of <=200bp AGCTCT - disruptive_inframe_deletion LEL713L LIRI-JP 3 139078184 139078189 deletion of <=200bp AGCTCT - disruptive_inframe_deletion LEL742L LIRI-JP 3 139078184 139078189 deletion of <=200bp AGCTCT - intron_variant LIRI-JP 3 139078184 139078189 deletion of <=200bp AGCTCT - upstream_gene_variant LIRI-JP 3 139078471 139078471 single base substitution A C intron_variant LIRI-JP 3 139078471 139078471 single base substitution A C upstream_gene_variant LIRI-JP 3 139080182 139080182 single base substitution C T intron_variant LIRI-JP 3 139080182 139080182 single base substitution C T upstream_gene_variant LIRI-JP 3 139080687 139080687 single base substitution T C intron_variant LIRI-JP 3 139080687 139080687 single base substitution T C upstream_gene_variant LIRI-JP 3 139082254 139082254 single base substitution A T intron_variant LIRI-JP 3 139082254 139082254 single base substitution A T upstream_gene_variant LIRI-JP 3 139082278 139082278 single base substitution A C intron_variant LIRI-JP 3 139082278 139082278 single base substitution A C upstream_gene_variant LIRI-JP 3 139083268 139083268 single base substitution A T intron_variant LIRI-JP 3 139084144 139084144 single base substitution T C intron_variant LIRI-JP 3 139085264 139085264 single base substitution T G intron_variant LIRI-JP 3 139086528 139086528 single base substitution G C intron_variant LIRI-JP 3 139086689 139086689 single base substitution T C intron_variant LIRI-JP 3 139088235 139088235 single base substitution G C downstream_gene_variant LIRI-JP 3 139088235 139088235 single base substitution G C intron_variant LIRI-JP 3 139091565 139091565 single base substitution A T downstream_gene_variant LIRI-JP 3 139091565 139091565 single base substitution A T intron_variant LIRI-JP 3 139091565 139091565 single base substitution A T upstream_gene_variant LIRI-JP 3 139093924 139093924 single base substitution A G downstream_gene_variant LIRI-JP 3 139093924 139093924 single base substitution A G intron_variant LIRI-JP 3 139093924 139093924 single base substitution A G upstream_gene_variant LIRI-JP 3 139097100 139097100 single base substitution T G downstream_gene_variant LIRI-JP 3 139097100 139097100 single base substitution T G intron_variant LIRI-JP 3 139100633 139100634 deletion of <=200bp AA - exon_variant LIRI-JP 3 139100633 139100634 deletion of <=200bp AA - intron_variant LIRI-JP 3 139103716 139103716 single base substitution T C intron_variant LIRI-JP 3 139105260 139105260 single base substitution C T intron_variant LIRI-JP 3 139107763 139107763 single base substitution T C intron_variant LIRI-JP 3 139109113 139109113 single base substitution G C upstream_gene_variant LIRI-JP 3 139111409 139111409 single base substitution A G upstream_gene_variant LIRI-JP 3 139113179 139113179 single base substitution G T upstream_gene_variant LUSC-KR 3 139077201 139077201 single base substitution T G exon_variant LUSC-KR 3 139077201 139077201 single base substitution T G intron_variant LUSC-KR 3 139080303 139080303 single base substitution G C intron_variant LUSC-KR 3 139080303 139080303 single base substitution G C upstream_gene_variant LUSC-KR 3 139084819 139084819 single base substitution C T intron_variant LUSC-KR 3 139085475 139085475 single base substitution C G intron_variant LUSC-KR 3 139085475 139085475 single base substitution C G missense_variant D578H 1732G>C LUSC-KR 3 139085475 139085475 single base substitution C G missense_variant D607H 1819G>C LUSC-KR 3 139097433 139097433 single base substitution C A downstream_gene_variant LUSC-KR 3 139097433 139097433 single base substitution C A intron_variant LUSC-KR 3 139106649 139106649 single base substitution A G intron_variant LUSC-KR 3 139108289 139108289 single base substitution G A intron_variant LUSC-KR 3 139111677 139111677 single base substitution G T upstream_gene_variant LUSC-KR 3 139111678 139111678 single base substitution G T upstream_gene_variant LUSC-KR 3 139113342 139113342 single base substitution G A upstream_gene_variant LUSC-US 3 139080022 139080022 single base substitution G T intron_variant LUSC-US 3 139080022 139080022 single base substitution G T missense_variant T675N 2024C>A LUSC-US 3 139080022 139080022 single base substitution G T missense_variant T704N 2111C>A LUSC-US 3 139080022 139080022 single base substitution G T upstream_gene_variant LUSC-US 3 139086994 139086994 single base substitution G A missense_variant A136V 407C>T LUSC-US 3 139086994 139086994 single base substitution G A missense_variant A484V 1451C>T LUSC-US 3 139086994 139086994 single base substitution G A missense_variant A513V 1538C>T LUSC-US 3 139102235 139102235 single base substitution C G 5_prime_UTR_variant LUSC-US 3 139102235 139102235 single base substitution C G exon_variant LUSC-US 3 139102235 139102235 single base substitution C G missense_variant D16H 46G>C MALY-DE 3 139071745 139071745 single base substitution T A downstream_gene_variant MALY-DE 3 139074856 139074856 single base substitution C A downstream_gene_variant MALY-DE 3 139074856 139074856 single base substitution C A intron_variant MALY-DE 3 139076702 139076702 single base substitution C T 3_prime_UTR_variant MALY-DE 3 139076702 139076702 single base substitution C T exon_variant MALY-DE 3 139076702 139076702 single base substitution C T intron_variant MALY-DE 3 139089206 139089207 deletion of <=200bp AA - downstream_gene_variant MALY-DE 3 139089206 139089207 deletion of <=200bp AA - intron_variant MALY-DE 3 139107091 139107091 single base substitution C T intron_variant MALY-DE 3 139109907 139109907 single base substitution T C upstream_gene_variant MALY-DE 3 139110546 139110546 single base substitution A C upstream_gene_variant MALY-DE 3 139110551 139110551 single base substitution A G upstream_gene_variant MELA-AU 3 139070697 139070697 single base substitution C T downstream_gene_variant MELA-AU 3 139071190 139071190 single base substitution C T downstream_gene_variant MELA-AU 3 139071303 139071303 single base substitution T G downstream_gene_variant MELA-AU 3 139072215 139072215 single base substitution G T downstream_gene_variant MELA-AU 3 139073148 139073148 single base substitution T G downstream_gene_variant MELA-AU 3 139076547 139076547 single base substitution C T 3_prime_UTR_variant MELA-AU 3 139076547 139076547 single base substitution C T downstream_gene_variant MELA-AU 3 139076547 139076547 single base substitution C T intron_variant MELA-AU 3 139077552 139077552 single base substitution C A exon_variant MELA-AU 3 139077552 139077552 single base substitution C A intron_variant MELA-AU 3 139079168 139079169 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 139079168 139079169 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 3 139080714 139080714 single base substitution C G intron_variant MELA-AU 3 139080714 139080714 single base substitution C G upstream_gene_variant MELA-AU 3 139081892 139081892 single base substitution C T intron_variant MELA-AU 3 139081892 139081892 single base substitution C T upstream_gene_variant MELA-AU 3 139082329 139082329 single base substitution T G intron_variant MELA-AU 3 139082329 139082329 single base substitution T G upstream_gene_variant MELA-AU 3 139082637 139082638 multiple base substitution (>=2bp and <=200bp) CT AA intron_variant MELA-AU 3 139082637 139082638 multiple base substitution (>=2bp and <=200bp) CT AA upstream_gene_variant MELA-AU 3 139083382 139083382 single base substitution G A intron_variant MELA-AU 3 139083413 139083413 single base substitution G A intron_variant MELA-AU 3 139083605 139083605 single base substitution T G intron_variant MELA-AU 3 139084332 139084332 single base substitution C T intron_variant MELA-AU 3 139084440 139084440 single base substitution G A intron_variant MELA-AU 3 139085864 139085864 single base substitution A C intron_variant MELA-AU 3 139085864 139085864 single base substitution A C missense_variant L528V 1582T>G MELA-AU 3 139085864 139085864 single base substitution A C missense_variant L557V 1669T>G MELA-AU 3 139086389 139086389 single base substitution C T intron_variant MELA-AU 3 139088336 139088336 single base substitution T C downstream_gene_variant MELA-AU 3 139088336 139088336 single base substitution T C missense_variant K390R 1169A>G MELA-AU 3 139088336 139088336 single base substitution T C missense_variant K419R 1256A>G MELA-AU 3 139088336 139088336 single base substitution T C missense_variant K42R 125A>G MELA-AU 3 139088575 139088575 single base substitution G A downstream_gene_variant MELA-AU 3 139088575 139088575 single base substitution G A intron_variant MELA-AU 3 139088664 139088664 single base substitution G A downstream_gene_variant MELA-AU 3 139088664 139088664 single base substitution G A intron_variant MELA-AU 3 139089933 139089934 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 3 139089933 139089934 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 139092170 139092170 single base substitution G A downstream_gene_variant MELA-AU 3 139092170 139092170 single base substitution G A synonymous_variant L298L 892C>T MELA-AU 3 139092170 139092170 single base substitution G A synonymous_variant L327L 979C>T MELA-AU 3 139092170 139092170 single base substitution G A upstream_gene_variant MELA-AU 3 139092233 139092233 single base substitution T C downstream_gene_variant MELA-AU 3 139092233 139092233 single base substitution T C missense_variant M277V 829A>G MELA-AU 3 139092233 139092233 single base substitution T C missense_variant M306V 916A>G MELA-AU 3 139092233 139092233 single base substitution T C upstream_gene_variant MELA-AU 3 139092319 139092319 single base substitution A C downstream_gene_variant MELA-AU 3 139092319 139092319 single base substitution A C intron_variant MELA-AU 3 139092319 139092319 single base substitution A C upstream_gene_variant MELA-AU 3 139092321 139092321 single base substitution T A downstream_gene_variant MELA-AU 3 139092321 139092321 single base substitution T A intron_variant MELA-AU 3 139092321 139092321 single base substitution T A upstream_gene_variant MELA-AU 3 139092954 139092954 single base substitution T C downstream_gene_variant MELA-AU 3 139092954 139092954 single base substitution T C intron_variant MELA-AU 3 139092954 139092954 single base substitution T C upstream_gene_variant MELA-AU 3 139093049 139093049 single base substitution A T downstream_gene_variant MELA-AU 3 139093049 139093049 single base substitution A T intron_variant MELA-AU 3 139093049 139093049 single base substitution A T upstream_gene_variant MELA-AU 3 139093658 139093658 single base substitution G A downstream_gene_variant MELA-AU 3 139093658 139093658 single base substitution G A intron_variant MELA-AU 3 139093658 139093658 single base substitution G A upstream_gene_variant MELA-AU 3 139094077 139094077 single base substitution C T downstream_gene_variant MELA-AU 3 139094077 139094077 single base substitution C T intron_variant MELA-AU 3 139094077 139094077 single base substitution C T upstream_gene_variant MELA-AU 3 139094091 139094091 single base substitution G A downstream_gene_variant MELA-AU 3 139094091 139094091 single base substitution G A intron_variant MELA-AU 3 139094091 139094091 single base substitution G A upstream_gene_variant MELA-AU 3 139094286 139094286 single base substitution A C downstream_gene_variant MELA-AU 3 139094286 139094286 single base substitution A C intron_variant MELA-AU 3 139094286 139094286 single base substitution A C upstream_gene_variant MELA-AU 3 139094813 139094813 single base substitution G A downstream_gene_variant MELA-AU 3 139094813 139094813 single base substitution G A intron_variant MELA-AU 3 139094813 139094813 single base substitution G A upstream_gene_variant MELA-AU 3 139095593 139095593 single base substitution A T downstream_gene_variant MELA-AU 3 139095593 139095593 single base substitution A T intron_variant MELA-AU 3 139095593 139095593 single base substitution A T upstream_gene_variant MELA-AU 3 139095915 139095915 single base substitution A T downstream_gene_variant MELA-AU 3 139095915 139095915 single base substitution A T intron_variant MELA-AU 3 139095921 139095921 single base substitution A G downstream_gene_variant MELA-AU 3 139095921 139095921 single base substitution A G intron_variant MELA-AU 3 139096189 139096189 single base substitution C T downstream_gene_variant MELA-AU 3 139096189 139096189 single base substitution C T intron_variant MELA-AU 3 139096239 139096239 single base substitution G A downstream_gene_variant MELA-AU 3 139096239 139096239 single base substitution G A intron_variant MELA-AU 3 139097264 139097264 single base substitution A G downstream_gene_variant MELA-AU 3 139097264 139097264 single base substitution A G intron_variant MELA-AU 3 139097532 139097532 single base substitution G A downstream_gene_variant MELA-AU 3 139097532 139097532 single base substitution G A intron_variant MELA-AU 3 139097554 139097554 single base substitution A G downstream_gene_variant MELA-AU 3 139097554 139097554 single base substitution A G intron_variant MELA-AU 3 139097979 139097979 single base substitution G T downstream_gene_variant MELA-AU 3 139097979 139097979 single base substitution G T exon_variant MELA-AU 3 139097979 139097979 single base substitution G T missense_variant L60M 178C>A MELA-AU 3 139097979 139097979 single base substitution G T missense_variant L89M 265C>A MELA-AU 3 139098638 139098638 single base substitution G A downstream_gene_variant MELA-AU 3 139098638 139098638 single base substitution G A exon_variant MELA-AU 3 139098638 139098638 single base substitution G A intron_variant MELA-AU 3 139099290 139099290 single base substitution C T exon_variant MELA-AU 3 139099290 139099290 single base substitution C T intron_variant MELA-AU 3 139099310 139099310 single base substitution G A exon_variant MELA-AU 3 139099310 139099310 single base substitution G A intron_variant MELA-AU 3 139099565 139099565 single base substitution G A exon_variant MELA-AU 3 139099565 139099565 single base substitution G A intron_variant MELA-AU 3 139099929 139099929 single base substitution A G exon_variant MELA-AU 3 139099929 139099929 single base substitution A G intron_variant MELA-AU 3 139099977 139099977 single base substitution C G exon_variant MELA-AU 3 139099977 139099977 single base substitution C G intron_variant MELA-AU 3 139100604 139100604 single base substitution G A exon_variant MELA-AU 3 139100604 139100604 single base substitution G A intron_variant MELA-AU 3 139100916 139100916 single base substitution G A exon_variant MELA-AU 3 139100916 139100916 single base substitution G A intron_variant MELA-AU 3 139101290 139101290 single base substitution T C exon_variant MELA-AU 3 139101290 139101290 single base substitution T C intron_variant MELA-AU 3 139101588 139101588 single base substitution G A exon_variant MELA-AU 3 139101588 139101588 single base substitution G A intron_variant MELA-AU 3 139101807 139101807 single base substitution G A exon_variant MELA-AU 3 139101807 139101807 single base substitution G A intron_variant MELA-AU 3 139102349 139102349 single base substitution T C intron_variant MELA-AU 3 139102695 139102695 single base substitution G A intron_variant MELA-AU 3 139103315 139103315 single base substitution G A intron_variant MELA-AU 3 139104584 139104584 single base substitution T C intron_variant MELA-AU 3 139104696 139104696 single base substitution A T intron_variant MELA-AU 3 139104920 139104920 single base substitution G A intron_variant MELA-AU 3 139105304 139105304 single base substitution G A intron_variant MELA-AU 3 139105751 139105751 single base substitution G A intron_variant MELA-AU 3 139105905 139105905 single base substitution T C intron_variant MELA-AU 3 139108393 139108393 single base substitution G A 5_prime_UTR_variant MELA-AU 3 139108393 139108393 single base substitution G A exon_variant MELA-AU 3 139108393 139108393 single base substitution G A intron_variant MELA-AU 3 139108422 139108422 single base substitution C T 5_prime_UTR_variant MELA-AU 3 139108422 139108422 single base substitution C T exon_variant MELA-AU 3 139108422 139108422 single base substitution C T intron_variant MELA-AU 3 139108422 139108422 single base substitution C T upstream_gene_variant MELA-AU 3 139108501 139108501 single base substitution G A 5_prime_UTR_variant MELA-AU 3 139108501 139108501 single base substitution G A upstream_gene_variant MELA-AU 3 139108573 139108573 single base substitution C T 5_prime_UTR_variant MELA-AU 3 139108573 139108573 single base substitution C T upstream_gene_variant MELA-AU 3 139108574 139108574 single base substitution C T 5_prime_UTR_variant MELA-AU 3 139108574 139108574 single base substitution C T upstream_gene_variant MELA-AU 3 139108579 139108579 single base substitution C T upstream_gene_variant MELA-AU 3 139108594 139108594 single base substitution C T upstream_gene_variant MELA-AU 3 139108845 139108846 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 3 139109410 139109410 single base substitution C T upstream_gene_variant MELA-AU 3 139110711 139110711 single base substitution C T upstream_gene_variant MELA-AU 3 139111252 139111252 single base substitution G A upstream_gene_variant MELA-AU 3 139111778 139111778 single base substitution G C upstream_gene_variant MELA-AU 3 139112044 139112044 single base substitution T C upstream_gene_variant MELA-AU 3 139112051 139112051 single base substitution C T upstream_gene_variant MELA-AU 3 139112357 139112357 single base substitution A G upstream_gene_variant MELA-AU 3 139112663 139112663 deletion of <=200bp A - upstream_gene_variant MELA-AU 3 139113260 139113260 single base substitution C A upstream_gene_variant ORCA-IN 3 139069846 139069846 single base substitution G C downstream_gene_variant ORCA-IN 3 139078716 139078716 single base substitution G A intron_variant ORCA-IN 3 139078716 139078716 single base substitution G A upstream_gene_variant ORCA-IN 3 139084453 139084453 single base substitution G A intron_variant ORCA-IN 3 139099813 139099813 single base substitution G A exon_variant ORCA-IN 3 139099813 139099813 single base substitution G A intron_variant ORCA-IN 3 139105141 139105141 single base substitution C T intron_variant ORCA-IN 3 139110629 139110629 single base substitution G A upstream_gene_variant OV-AU 3 139070841 139070841 single base substitution G C downstream_gene_variant OV-AU 3 139079141 139079141 single base substitution G A intron_variant OV-AU 3 139079141 139079141 single base substitution G A upstream_gene_variant OV-AU 3 139081931 139081931 single base substitution A C intron_variant OV-AU 3 139081931 139081931 single base substitution A C upstream_gene_variant OV-AU 3 139107335 139107335 single base substitution T G intron_variant OV-AU 3 139110672 139110672 single base substitution A T upstream_gene_variant OV-AU 3 139111155 139111155 single base substitution C A upstream_gene_variant OV-US 3 139077104 139077104 single base substitution C T exon_variant OV-US 3 139077104 139077104 single base substitution C T intron_variant OV-US 3 139077104 139077104 single base substitution C T missense_variant G68R 202G>A OV-US 3 139077104 139077104 single base substitution C T missense_variant G826R 2476G>A OV-US 3 139077104 139077104 single base substitution C T missense_variant G855R 2563G>A PACA-AU 3 139070201 139070201 single base substitution C A downstream_gene_variant PACA-AU 3 139080854 139080860 deletion of <=200bp GGGGGTT - intron_variant PACA-AU 3 139080854 139080860 deletion of <=200bp GGGGGTT - upstream_gene_variant PACA-AU 3 139080967 139080967 single base substitution C T intron_variant PACA-AU 3 139080967 139080967 single base substitution C T upstream_gene_variant PACA-AU 3 139081452 139081452 single base substitution C T intron_variant PACA-AU 3 139081452 139081452 single base substitution C T upstream_gene_variant PACA-AU 3 139084672 139084672 single base substitution A C intron_variant PACA-AU 3 139087623 139087623 single base substitution C A intron_variant PACA-AU 3 139088333 139088333 single base substitution T C downstream_gene_variant PACA-AU 3 139088333 139088333 single base substitution T C missense_variant E391G 1172A>G PACA-AU 3 139088333 139088333 single base substitution T C missense_variant E420G 1259A>G PACA-AU 3 139088333 139088333 single base substitution T C missense_variant E43G 128A>G PACA-AU 3 139097856 139097856 single base substitution A G downstream_gene_variant PACA-AU 3 139097856 139097856 single base substitution A G intron_variant PACA-AU 3 139106151 139106151 single base substitution T C intron_variant PACA-AU 3 139107335 139107335 single base substitution T G intron_variant PACA-AU 3 139107716 139107717 deletion of <=200bp CT - intron_variant PACA-AU 3 139113177 139113177 single base substitution A G upstream_gene_variant PACA-CA 3 139071179 139071179 single base substitution T A downstream_gene_variant PACA-CA 3 139076604 139076604 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 3 139076604 139076604 insertion of <=200bp - T downstream_gene_variant PACA-CA 3 139076604 139076604 insertion of <=200bp - T intron_variant PACA-CA 3 139081456 139081456 single base substitution C G intron_variant PACA-CA 3 139081456 139081456 single base substitution C G upstream_gene_variant PACA-CA 3 139089806 139089806 single base substitution T A downstream_gene_variant PACA-CA 3 139089806 139089806 single base substitution T A intron_variant PACA-CA 3 139090464 139090464 single base substitution A T downstream_gene_variant PACA-CA 3 139090464 139090464 single base substitution A T intron_variant PACA-CA 3 139095589 139095589 single base substitution A T downstream_gene_variant PACA-CA 3 139095589 139095589 single base substitution A T intron_variant PACA-CA 3 139095589 139095589 single base substitution A T upstream_gene_variant PACA-CA 3 139095593 139095593 single base substitution A T downstream_gene_variant PACA-CA 3 139095593 139095593 single base substitution A T intron_variant PACA-CA 3 139095593 139095593 single base substitution A T upstream_gene_variant PACA-CA 3 139099867 139099873 deletion of <=200bp GTAGATT - exon_variant PACA-CA 3 139099867 139099873 deletion of <=200bp GTAGATT - intron_variant PACA-CA 3 139100280 139100280 single base substitution T C exon_variant PACA-CA 3 139100280 139100280 single base substitution T C intron_variant PACA-CA 3 139106446 139106446 single base substitution G T intron_variant PACA-CA 3 139108519 139108519 single base substitution A T 5_prime_UTR_variant PACA-CA 3 139108519 139108519 single base substitution A T upstream_gene_variant PACA-CA 3 139111492 139111492 single base substitution C G upstream_gene_variant PACA-CA 3 139112662 139112662 single base substitution T C upstream_gene_variant PAEN-AU 3 139094011 139094011 insertion of <=200bp - A downstream_gene_variant PAEN-AU 3 139094011 139094011 insertion of <=200bp - A intron_variant PAEN-AU 3 139094011 139094011 insertion of <=200bp - A upstream_gene_variant PAEN-AU 3 139096167 139096167 single base substitution T C downstream_gene_variant PAEN-AU 3 139096167 139096167 single base substitution T C intron_variant PAEN-IT 3 139086423 139086423 single base substitution C T intron_variant PAEN-IT 3 139089247 139089247 single base substitution C G downstream_gene_variant PAEN-IT 3 139089247 139089247 single base substitution C G intron_variant PAEN-IT 3 139096200 139096200 single base substitution A G downstream_gene_variant PAEN-IT 3 139096200 139096200 single base substitution A G intron_variant PAEN-IT 3 139112540 139112540 single base substitution T G upstream_gene_variant PBCA-DE 3 139086093 139086093 single base substitution T C intron_variant PBCA-DE 3 139091616 139091616 single base substitution G C downstream_gene_variant PBCA-DE 3 139091616 139091616 single base substitution G C intron_variant PBCA-DE 3 139091616 139091616 single base substitution G C upstream_gene_variant PBCA-DE 3 139102271 139102271 single base substitution G A 5_prime_UTR_variant PBCA-DE 3 139102271 139102271 single base substitution G A exon_variant PBCA-DE 3 139102271 139102271 single base substitution G A stop_gained R4* 10C>T PBCA-DE 3 139107248 139107248 deletion of <=200bp G - intron_variant PRAD-CA 3 139086811 139086811 single base substitution T G intron_variant PRAD-CA 3 139095593 139095593 single base substitution A T downstream_gene_variant PRAD-CA 3 139095593 139095593 single base substitution A T intron_variant PRAD-CA 3 139095593 139095593 single base substitution A T upstream_gene_variant PRAD-CA 3 139099679 139099679 single base substitution C T exon_variant PRAD-CA 3 139099679 139099679 single base substitution C T intron_variant PRAD-UK 3 139072968 139072968 insertion of <=200bp - GAGCTTACTGCAAACCACAG downstream_gene_variant PRAD-UK 3 139086830 139086830 single base substitution G C intron_variant PRAD-UK 3 139088753 139088753 single base substitution A G downstream_gene_variant PRAD-UK 3 139088753 139088753 single base substitution A G intron_variant PRAD-UK 3 139090797 139090797 single base substitution A G downstream_gene_variant PRAD-UK 3 139090797 139090797 single base substitution A G intron_variant PRAD-UK 3 139090797 139090797 single base substitution A G upstream_gene_variant PRAD-UK 3 139098822 139098822 single base substitution C A downstream_gene_variant PRAD-UK 3 139098822 139098822 single base substitution C A intron_variant PRAD-UK 3 139098823 139098823 single base substitution T A downstream_gene_variant PRAD-UK 3 139098823 139098823 single base substitution T A intron_variant PRAD-US 3 139077851 139077851 single base substitution G A intron_variant PRAD-US 3 139077851 139077851 single base substitution G A missense_variant P38S 112C>T PRAD-US 3 139077851 139077851 single base substitution G A missense_variant P796S 2386C>T PRAD-US 3 139077851 139077851 single base substitution G A missense_variant P825S 2473C>T PRAD-US 3 139077851 139077851 single base substitution G A upstream_gene_variant READ-US 3 139092543 139092543 single base substitution C T downstream_gene_variant READ-US 3 139092543 139092543 single base substitution C T missense_variant A258T 772G>A READ-US 3 139092543 139092543 single base substitution C T missense_variant A287T 859G>A READ-US 3 139092543 139092543 single base substitution C T upstream_gene_variant READ-US 3 139097009 139097009 single base substitution C G downstream_gene_variant READ-US 3 139097009 139097009 single base substitution C G exon_variant READ-US 3 139097009 139097009 single base substitution C G intron_variant READ-US 3 139097009 139097009 single base substitution C G missense_variant W126C 378G>C READ-US 3 139097009 139097009 single base substitution C G missense_variant W97C 291G>C RECA-EU 3 139072252 139072252 single base substitution A C downstream_gene_variant RECA-EU 3 139072339 139072339 single base substitution C A downstream_gene_variant RECA-EU 3 139086730 139086730 single base substitution T A intron_variant RECA-EU 3 139087804 139087804 single base substitution A C intron_variant RECA-EU 3 139093660 139093660 single base substitution A G downstream_gene_variant RECA-EU 3 139093660 139093660 single base substitution A G intron_variant RECA-EU 3 139093660 139093660 single base substitution A G upstream_gene_variant RECA-EU 3 139106959 139106959 single base substitution A T intron_variant RECA-EU 3 139106960 139106960 single base substitution A T intron_variant SKCA-BR 3 139087639 139087639 single base substitution C G intron_variant SKCA-BR 3 139088001 139088001 single base substitution G A intron_variant SKCA-BR 3 139096093 139096093 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 3 139096093 139096093 insertion of <=200bp - AT intron_variant SKCA-BR 3 139098850 139098850 insertion of <=200bp - TC downstream_gene_variant SKCA-BR 3 139098850 139098850 insertion of <=200bp - TC intron_variant SKCA-BR 3 139101461 139101461 single base substitution G A exon_variant SKCA-BR 3 139101461 139101461 single base substitution G A intron_variant SKCA-BR 3 139104889 139104889 single base substitution C G intron_variant SKCA-BR 3 139107139 139107139 single base substitution T C intron_variant SKCA-BR 3 139107793 139107793 single base substitution A C intron_variant SKCA-BR 3 139107827 139107827 single base substitution A C intron_variant SKCA-BR 3 139108593 139108593 single base substitution C T upstream_gene_variant SKCA-BR 3 139112204 139112204 single base substitution C T upstream_gene_variant SKCM-US 3 139076710 139076710 single base substitution C T exon_variant SKCM-US 3 139076710 139076710 single base substitution C T intron_variant SKCM-US 3 139076710 139076710 single base substitution C T missense_variant D177N 529G>A SKCM-US 3 139076710 139076710 single base substitution C T missense_variant D877N 2629G>A SKCM-US 3 139076710 139076710 single base substitution C T missense_variant D906N 2716G>A SKCM-US 3 139090653 139090653 single base substitution C A downstream_gene_variant SKCM-US 3 139090653 139090653 single base substitution C A missense_variant G344W 1030G>T SKCM-US 3 139090653 139090653 single base substitution C A missense_variant G373W 1117G>T SKCM-US 3 139090653 139090653 single base substitution C A upstream_gene_variant SKCM-US 3 139092233 139092233 single base substitution T C downstream_gene_variant SKCM-US 3 139092233 139092233 single base substitution T C missense_variant M277V 829A>G SKCM-US 3 139092233 139092233 single base substitution T C missense_variant M306V 916A>G SKCM-US 3 139092233 139092233 single base substitution T C upstream_gene_variant SKCM-US 3 139094319 139094319 single base substitution C G downstream_gene_variant SKCM-US 3 139094319 139094319 single base substitution C G exon_variant SKCM-US 3 139094319 139094319 single base substitution C G missense_variant W185C 555G>C SKCM-US 3 139094319 139094319 single base substitution C G missense_variant W214C 642G>C SKCM-US 3 139094319 139094319 single base substitution C G upstream_gene_variant STAD-US 3 139074577 139074577 single base substitution G A downstream_gene_variant STAD-US 3 139074577 139074577 single base substitution G A synonymous_variant G99G 297C>T STAD-US 3 139074583 139074583 single base substitution C T downstream_gene_variant STAD-US 3 139074583 139074583 single base substitution C T synonymous_variant P97P 291G>A STAD-US 3 139077618 139077618 single base substitution C A intron_variant STAD-US 3 139077618 139077618 single base substitution C A missense_variant D54Y 160G>T STAD-US 3 139077618 139077618 single base substitution C A missense_variant D812Y 2434G>T STAD-US 3 139077618 139077618 single base substitution C A missense_variant D841Y 2521G>T STAD-US 3 139077618 139077618 single base substitution C A upstream_gene_variant STAD-US 3 139077910 139077910 single base substitution A G intron_variant STAD-US 3 139077910 139077910 single base substitution A G missense_variant F18S 53T>C STAD-US 3 139077910 139077910 single base substitution A G missense_variant F776S 2327T>C STAD-US 3 139077910 139077910 single base substitution A G missense_variant F805S 2414T>C STAD-US 3 139077910 139077910 single base substitution A G upstream_gene_variant STAD-US 3 139077962 139077962 single base substitution G T intron_variant STAD-US 3 139077962 139077962 single base substitution G T missense_variant L1I 1C>A STAD-US 3 139077962 139077962 single base substitution G T missense_variant L759I 2275C>A STAD-US 3 139077962 139077962 single base substitution G T missense_variant L788I 2362C>A STAD-US 3 139077962 139077962 single base substitution G T upstream_gene_variant STAD-US 3 139078162 139078162 single base substitution C A intron_variant STAD-US 3 139078162 139078162 single base substitution C A synonymous_variant L722L 2166G>T STAD-US 3 139078162 139078162 single base substitution C A synonymous_variant L751L 2253G>T STAD-US 3 139078162 139078162 single base substitution C A upstream_gene_variant STAD-US 3 139080026 139080026 single base substitution C T intron_variant STAD-US 3 139080026 139080026 single base substitution C T missense_variant A674T 2020G>A STAD-US 3 139080026 139080026 single base substitution C T missense_variant A703T 2107G>A STAD-US 3 139080026 139080026 single base substitution C T upstream_gene_variant STAD-US 3 139080062 139080062 single base substitution G A intron_variant STAD-US 3 139080062 139080062 single base substitution G A missense_variant H662Y 1984C>T STAD-US 3 139080062 139080062 single base substitution G A missense_variant H691Y 2071C>T STAD-US 3 139080062 139080062 single base substitution G A upstream_gene_variant STAD-US 3 139081286 139081286 single base substitution T C intron_variant STAD-US 3 139081286 139081286 single base substitution T C missense_variant E624G 1871A>G STAD-US 3 139081286 139081286 single base substitution T C missense_variant E653G 1958A>G STAD-US 3 139081286 139081286 single base substitution T C upstream_gene_variant STAD-US 3 139085471 139085471 single base substitution T G intron_variant STAD-US 3 139085471 139085471 single base substitution T G missense_variant K579T 1736A>C STAD-US 3 139085471 139085471 single base substitution T G missense_variant K608T 1823A>C STAD-US 3 139085492 139085492 single base substitution C A intron_variant STAD-US 3 139085492 139085492 single base substitution C A missense_variant R572M 1715G>T STAD-US 3 139085492 139085492 single base substitution C A missense_variant R601M 1802G>T STAD-US 3 139090584 139090584 single base substitution A G downstream_gene_variant STAD-US 3 139090584 139090584 single base substitution A G missense_variant W19R 55T>C STAD-US 3 139090584 139090584 single base substitution A G missense_variant W367R 1099T>C STAD-US 3 139090584 139090584 single base substitution A G missense_variant W396R 1186T>C STAD-US 3 139092574 139092574 single base substitution G A downstream_gene_variant STAD-US 3 139092574 139092574 single base substitution G A synonymous_variant C247C 741C>T STAD-US 3 139092574 139092574 single base substitution G A synonymous_variant C276C 828C>T STAD-US 3 139092574 139092574 single base substitution G A upstream_gene_variant STAD-US 3 139093415 139093415 single base substitution G A downstream_gene_variant STAD-US 3 139093415 139093415 single base substitution G A exon_variant STAD-US 3 139093415 139093415 single base substitution G A stop_gained Q194* 580C>T STAD-US 3 139093415 139093415 single base substitution G A stop_gained Q223* 667C>T STAD-US 3 139093415 139093415 single base substitution G A upstream_gene_variant STAD-US 3 139094430 139094430 single base substitution T C downstream_gene_variant STAD-US 3 139094430 139094430 single base substitution T C exon_variant STAD-US 3 139094430 139094430 single base substitution T C synonymous_variant P148P 444A>G STAD-US 3 139094430 139094430 single base substitution T C synonymous_variant P177P 531A>G STAD-US 3 139094430 139094430 single base substitution T C upstream_gene_variant STAD-US 3 139096964 139096964 single base substitution G A downstream_gene_variant STAD-US 3 139096964 139096964 single base substitution G A exon_variant STAD-US 3 139096964 139096964 single base substitution G A synonymous_variant H112H 336C>T STAD-US 3 139096964 139096964 single base substitution G A synonymous_variant H120H 360C>T STAD-US 3 139096964 139096964 single base substitution G A synonymous_variant H141H 423C>T UCEC-US 3 139069829 139069829 single base substitution G A downstream_gene_variant UCEC-US 3 139071596 139071596 single base substitution G T downstream_gene_variant UCEC-US 3 139071620 139071620 single base substitution G T downstream_gene_variant UCEC-US 3 139074617 139074617 single base substitution A G downstream_gene_variant UCEC-US 3 139074617 139074617 single base substitution A G intron_variant UCEC-US 3 139074622 139074622 single base substitution A C downstream_gene_variant UCEC-US 3 139074622 139074622 single base substitution A C intron_variant UCEC-US 3 139075836 139075836 single base substitution C T downstream_gene_variant UCEC-US 3 139075836 139075836 single base substitution C T intron_variant UCEC-US 3 139076709 139076709 single base substitution T C exon_variant UCEC-US 3 139076709 139076709 single base substitution T C intron_variant UCEC-US 3 139076709 139076709 single base substitution T C missense_variant D177G 530A>G UCEC-US 3 139076709 139076709 single base substitution T C missense_variant D877G 2630A>G UCEC-US 3 139076709 139076709 single base substitution T C missense_variant D906G 2717A>G UCEC-US 3 139076716 139076716 single base substitution A C exon_variant UCEC-US 3 139076716 139076716 single base substitution A C intron_variant UCEC-US 3 139076716 139076716 single base substitution A C missense_variant L175V 523T>G UCEC-US 3 139076716 139076716 single base substitution A C missense_variant L875V 2623T>G UCEC-US 3 139076716 139076716 single base substitution A C missense_variant L904V 2710T>G UCEC-US 3 139077103 139077103 single base substitution C T exon_variant UCEC-US 3 139077103 139077103 single base substitution C T intron_variant UCEC-US 3 139077103 139077103 single base substitution C T missense_variant G68E 203G>A UCEC-US 3 139077103 139077103 single base substitution C T missense_variant G826E 2477G>A UCEC-US 3 139077103 139077103 single base substitution C T missense_variant G855E 2564G>A UCEC-US 3 139077108 139077108 single base substitution A G exon_variant UCEC-US 3 139077108 139077108 single base substitution A G intron_variant UCEC-US 3 139077108 139077108 single base substitution A G synonymous_variant L66L 198T>C UCEC-US 3 139077108 139077108 single base substitution A G synonymous_variant L824L 2472T>C UCEC-US 3 139077108 139077108 single base substitution A G synonymous_variant L853L 2559T>C UCEC-US 3 139079976 139079976 single base substitution C T intron_variant UCEC-US 3 139079976 139079976 single base substitution C T synonymous_variant A690A 2070G>A UCEC-US 3 139079976 139079976 single base substitution C T synonymous_variant A719A 2157G>A UCEC-US 3 139079976 139079976 single base substitution C T upstream_gene_variant UCEC-US 3 139080051 139080051 single base substitution C A intron_variant UCEC-US 3 139080051 139080051 single base substitution C A missense_variant Q665H 1995G>T UCEC-US 3 139080051 139080051 single base substitution C A missense_variant Q694H 2082G>T UCEC-US 3 139080051 139080051 single base substitution C A upstream_gene_variant UCEC-US 3 139081249 139081249 single base substitution C T intron_variant UCEC-US 3 139081249 139081249 single base substitution C T splice_region_variant UCEC-US 3 139081249 139081249 single base substitution C T upstream_gene_variant UCEC-US 3 139081313 139081313 single base substitution C T intron_variant UCEC-US 3 139081313 139081313 single base substitution C T missense_variant R615H 1844G>A UCEC-US 3 139081313 139081313 single base substitution C T missense_variant R644H 1931G>A UCEC-US 3 139081313 139081313 single base substitution C T upstream_gene_variant UCEC-US 3 139085575 139085575 single base substitution A C intron_variant UCEC-US 3 139085575 139085575 single base substitution A C synonymous_variant L544L 1632T>G UCEC-US 3 139085575 139085575 single base substitution A C synonymous_variant L573L 1719T>G UCEC-US 3 139085939 139085939 single base substitution C T missense_variant D503N 1507G>A UCEC-US 3 139085939 139085939 single base substitution C T missense_variant D532N 1594G>A UCEC-US 3 139085939 139085939 single base substitution C T splice_region_variant UCEC-US 3 139088134 139088134 single base substitution A C downstream_gene_variant UCEC-US 3 139088134 139088134 single base substitution A C missense_variant L428R 1283T>G UCEC-US 3 139088134 139088134 single base substitution A C missense_variant L457R 1370T>G UCEC-US 3 139088134 139088134 single base substitution A C missense_variant L80R 239T>G UCEC-US 3 139090575 139090575 single base substitution C T downstream_gene_variant UCEC-US 3 139090575 139090575 single base substitution C T missense_variant D22N 64G>A UCEC-US 3 139090575 139090575 single base substitution C T missense_variant D370N 1108G>A UCEC-US 3 139090575 139090575 single base substitution C T missense_variant D399N 1195G>A UCEC-US 3 139092642 139092642 single base substitution G A downstream_gene_variant UCEC-US 3 139092642 139092642 single base substitution G A missense_variant R225C 673C>T UCEC-US 3 139092642 139092642 single base substitution G A missense_variant R254C 760C>T UCEC-US 3 139092642 139092642 single base substitution G A upstream_gene_variant UCEC-US 3 139097029 139097029 single base substitution C A downstream_gene_variant UCEC-US 3 139097029 139097029 single base substitution C A intron_variant UCEC-US 3 139097029 139097029 single base substitution C A missense_variant D120Y 358G>T UCEC-US 3 139097029 139097029 single base substitution C A missense_variant D91Y 271G>T UCEC-US 3 139097029 139097029 single base substitution C A splice_region_variant UCEC-US 3 139102214 139102214 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 139102214 139102214 single base substitution G A exon_variant UCEC-US 3 139102214 139102214 single base substitution G A synonymous_variant L23L 67C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-34-2600-01 COSM728143 c.46G>C p.D16H Substitution - Missense 3:139383393-139383393 - PT23_1 COSM5902632 c.516G>T p.L172F Substitution - Missense 3:139375603-139375603 - UM-SCC-2 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - ME032T COSM227240 c.2206G>A p.G736S Substitution - Missense 3:139361085-139361085 - Patient1 COSM1166834 c.680G>A p.G227E Substitution - Missense 3:139374560-139374560 - PD24199a COSM5796999 c.435T>A p.V145V Substitution - coding silent 3:139378110-139378110 - TCGA-HC-A6AL-01 COSM3673852 c.2473C>T p.P825S Substitution - Missense 3:139359009-139359009 - TCGA-D5-6924-01 COSM1419487 c.182G>A p.R61Q Substitution - Missense 3:139379426-139379426 - UM-SCC-17B COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - TCGA-G5-6233-01 COSM3427144 c.378G>C p.W126C Substitution - Missense 3:139378167-139378167 - TCGA-D1-A17Q-01 COSM1039105 c.1719T>G p.L573L Substitution - coding silent 3:139366733-139366733 - PD11762a COSM5779855 c.1618G>C p.V540L Substitution - Missense 3:139367073-139367073 - pfg029T COSM1642104 c.2525T>G p.F842C Substitution - Missense 3:139358772-139358772 - KM12 COSM1670598 c.1523A>G p.D508G Substitution - Missense 3:139368167-139368167 - TCGA-B5-A0JY-01 COSM1039111 c.358G>T p.D120Y Substitution - Missense 3:139378187-139378187 - C10 COSM4616583 c.445G>A p.V149M Substitution - Missense 3:139378100-139378100 - TCGA-AX-A0J0-01 COSM1039107 c.1370T>G p.L457R Substitution - Missense 3:139369292-139369292 - HCC077T COSM5810412 c.17A>C p.D6A Substitution - Missense 3:139383422-139383422 - TCGA-G2-A2EO-01 COSM1308654 c.1038G>A p.K346K Substitution - coding silent 3:139373269-139373269 - TCGA-D3-A3CB-06 COSM3588071 c.1117G>T p.G373W Substitution - Missense 3:139371811-139371811 - TCGA-DK-A1A5-01 COSM419796 c.1693G>A p.G565S Substitution - Missense 3:139366759-139366759 - YUDAB COSM1693516 c.1802_1803GG>AC p.R601N Substitution - Missense 3:139366649-139366650 - CN-AML-08-T COSM5425829 c.1033G>A p.V345I Substitution - Missense 3:139373274-139373274 - pfg003T COSM1642105 c.2483C>T p.T828M Substitution - Missense 3:139358999-139358999 - HCC2998 COSM1670599 c.10C>T p.R4* Substitution - Nonsense 3:139383429-139383429 - TCGA-B5-A0JR-01 COSM1039102 c.2082G>T p.Q694H Substitution - Missense 3:139361209-139361209 - SC_9081 COSM1642106 c.1266delA p.K422fs*23 Deletion - Frameshift 3:139369484-139369484 - TCGA-DK-A3IN-01 COSM3774591 c.1463T>C p.L488P Substitution - Missense 3:139368227-139368227 - 587376 COSM1202068 c.49C>T p.R17* Substitution - Nonsense 3:139383390-139383390 - PD4005a COSM3664611 c.1648G>A p.E550K Substitution - Missense 3:139367043-139367043 - BD223T COSM5496481 c.2211-8A>T p.? Unknown 3:139359370-139359370 - HCT8 COSM4634915 c.2608G>A p.A870T Substitution - Missense 3:139358217-139358217 - BN13 COSM1616985 c.601T>C p.Y201H Substitution - Missense 3:139375518-139375518 - TCGA-BR-8487-01 COSM4113987 c.828C>T p.C276C Substitution - coding silent 3:139373732-139373732 - TCGA-A5-A0GB-01 COSM1039096 c.2717A>G p.D906G Substitution - Missense 3:139357867-139357867 - TCGA-BH-A0BC-01 COSM3846367 c.2507T>C p.M836T Substitution - Missense 3:139358790-139358790 - UPCI:SCC090 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - BD236T COSM3124305 c.1093C>T p.R365W Substitution - Missense 3:139373214-139373214 - TCGA-AA-A010-01 COSM280078 c.724C>T p.P242S Substitution - Missense 3:139374516-139374516 - YUKAT COSM5398269 c.1441A>G p.T481A Substitution - Missense 3:139368249-139368249 - TCGA-BR-4184-01 COSM4113982 c.2071C>T p.H691Y Substitution - Missense 3:139361220-139361220 - TCGA-AP-A059-01 COSM1039099 c.2559T>C p.L853L Substitution - coding silent 3:139358266-139358266 - TCGA-23-1022-01 COSM74236 c.2563G>A p.G855R Substitution - Missense 3:139358262-139358262 - LP6005334-DNA_G01 COSM5034906 c.355+5G>C p.? Unknown 3:139379042-139379042 - NOKSI COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - I2L-P7-Tumor-Organoid COSM5355523 c.1027C>T p.L343L Substitution - coding silent 3:139373280-139373280 - TCGA-BG-A18B-01 COSM1039100 c.2553+2T>G p.? Unknown 3:139358742-139358742 - J30_T COSM3944930 c.1819G>C p.D607H Substitution - Missense 3:139366633-139366633 - TCGA-BH-A0BC-01 COSM5834553 c.2509delG p.E837fs*44 Deletion - Frameshift 3:139358788-139358788 - TCGA-BF-A1Q0-01 COSM3588073 c.642G>C p.W214C Substitution - Missense 3:139375477-139375477 - T1743 COSM4674176 c.2156C>T p.A719V Substitution - Missense 3:139361135-139361135 - TCGA-HU-8604-01 COSM4113980 c.2253G>T p.L751L Substitution - coding silent 3:139359320-139359320 - 66 COSM1039104 c.1931G>A p.R644H Substitution - Missense 3:139362471-139362471 - TCGA-DA-A1IC-06 COSM3588069 c.2716G>A p.D906N Substitution - Missense 3:139357868-139357868 - T3024 COSM4674175 c.2431G>A p.V811M Substitution - Missense 3:139359051-139359051 - PD8965a COSM5785725 c.2176A>G p.N726D Substitution - Missense 3:139361115-139361115 - HCC113 COSM1616983 c.614G>T p.G205V Substitution - Missense 3:139375505-139375505 - PD6358a COSM1637064 c.2125G>A p.A709T Substitution - Missense 3:139361166-139361166 - TCGA-AA-3492-01 COSM1419484 c.1061A>G p.Y354C Substitution - Missense 3:139373246-139373246 - Pat_76_A COSM5863635 c.346A>G p.T116A Substitution - Missense 3:139379056-139379056 - TCGA-CD-A4MG-01 COSM4113983 c.1958A>G p.E653G Substitution - Missense 3:139362444-139362444 - TCGA-AZ-6598-01 COSM1419488 c.178G>A p.V60I Substitution - Missense 3:139379430-139379430 - CAL27 COSM3124284 c.1913C>T p.S638F Substitution - Missense 3:139362489-139362489 - PD4120a COSM160159 c.1987G>T p.E663* Substitution - Nonsense 3:139362415-139362415 - TCGA-AK-3445-01 COSM3365016 c.1717C>G p.L573V Substitution - Missense 3:139366735-139366735 - LUAD_E01086 COSM354777 c.1908A>C p.T636T Substitution - coding silent 3:139362494-139362494 - B9-Tumor COSM4005277 c.2553+3C>T p.? Unknown 3:139358741-139358741 - CHC1201T COSM4801676 c.1814T>C p.M605T Substitution - Missense 3:139366638-139366638 - TCGA-AP-A0LP-01 COSM1039101 c.2157G>A p.A719A Substitution - coding silent 3:139361134-139361134 - TCGA-BR-4361-01 COSM4113989 c.531A>G p.P177P Substitution - coding silent 3:139375588-139375588 - TCGA-BH-A0BC-01 COSM368853 c.2508G>A p.M836I Substitution - Missense 3:139358789-139358789 - LUAD-S01409 COSM346698 c.383G>T p.W128L Substitution - Missense 3:139378162-139378162 - LUAD-LIP77 COSM342459 c.939G>C p.K313N Substitution - Missense 3:139373368-139373368 - T3152 COSM4674177 c.1733A>G p.K578R Substitution - Missense 3:139366719-139366719 - sysucc-311T COSM5465730 c.747A>G p.E249E Substitution - coding silent 3:139374493-139374493 - WSU-HN12 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - TCGA-CG-5721-01 COSM4113978 c.2414T>C p.F805S Substitution - Missense 3:139359068-139359068 - UM-SCC-11B COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - ESO-913 COSM1248970 c.2067C>T p.C689C Substitution - coding silent 3:139361224-139361224 - TCGA-BR-8368-01 COSM4113979 c.2362C>A p.L788I Substitution - Missense 3:139359120-139359120 - WSU-HN8 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - C91 COSM4444887 c.1938G>T p.E646D Substitution - Missense 3:139362464-139362464 - TCGA-06-2567 COSM2153042 c.234C>T p.D78D Substitution - coding silent 3:139379168-139379168 - 587284 COSM1202067 c.884T>A p.I295N Substitution - Missense 3:139373676-139373676 - TCGA-66-2754-01 COSM728144 c.1538C>T p.A513V Substitution - Missense 3:139368152-139368152 - T3498 COSM4674179 c.647A>G p.Y216C Substitution - Missense 3:139375472-139375472 - SNUH_G16_S1 COSM4002477 c.342T>C p.I114I Substitution - coding silent 3:139379060-139379060 - 7 COSM327400 c.2078C>T p.A693V Substitution - Missense 3:139361213-139361213 - TCGA-AX-A0J1-01 COSM1039110 c.760C>T p.R254C Substitution - Missense 3:139373800-139373800 - TCGA-BR-7707-01 COSM4113985 c.1802G>T p.R601M Substitution - Missense 3:139366650-139366650 - 93VU147T COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - TCGA-06-2567-01 COSM2153042 c.234C>T p.D78D Substitution - coding silent 3:139379168-139379168 - TCGA-85-6561-01 COSM728145 c.2111C>A p.T704N Substitution - Missense 3:139361180-139361180 - VACO4S COSM3124316 c.111C>T p.G37G Substitution - coding silent 3:139383328-139383328 - TCGA-AA-3819-01 COSM294011 c.2190G>C p.M730I Substitution - Missense 3:139361101-139361101 - WSU-HN6 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - WSU-HN13 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - 587278 COSM1202066 c.2061G>T p.Q687H Substitution - Missense 3:139361230-139361230 - LUAD-YINHD COSM350740 c.160G>A p.E54K Substitution - Missense 3:139379448-139379448 - TCGA-CG-4306-01 COSM4113988 c.667C>T p.Q223* Substitution - Nonsense 3:139374573-139374573 - CAL33 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - TCGA-B8-5552-01 COSM479498 c.2500A>C p.N834H Substitution - Missense 3:139358797-139358797 - DN1401F COSM5961123 c.501C>G p.I167M Substitution - Missense 3:139378044-139378044 - HCC113T COSM1616983 c.614G>T p.G205V Substitution - Missense 3:139375505-139375505 - TCGA-A5-A0GP-01 COSM1039097 c.2710T>G p.L904V Substitution - Missense 3:139357874-139357874 - 8016470 COSM3392089 c.1259A>G p.E420G Substitution - Missense 3:139369491-139369491 - BRC5 COSM5026046 c.655A>G p.K219E Substitution - Missense 3:139374585-139374585 - CSCC-55-T COSM4452175 c.1634A>T p.Y545F Substitution - Missense 3:139367057-139367057 - TCGA-HR-A2OH-01 COSM3588070 c.1424A>G p.E475G Substitution - Missense 3:139368266-139368266 - TCGA-CG-4306-01 COSM4113977 c.2521G>T p.D841Y Substitution - Missense 3:139358776-139358776 - TCGA-AA-A00N-01 COSM274634 c.307C>T p.R103C Substitution - Missense 3:139379095-139379095 - TCGA-AP-A051-01 COSM1039098 c.2564G>A p.G855E Substitution - Missense 3:139358261-139358261 - TCGA-BR-8680-01 COSM4113984 c.1823A>C p.K608T Substitution - Missense 3:139366629-139366629 - ESO-717 COSM1242151 c.1603A>G p.I535V Substitution - Missense 3:139367088-139367088 - 8665_CLM COSM5756171 c.1258G>A p.E420K Substitution - Missense 3:139369492-139369492 - PT37 COSM5918036 c.1930C>T p.R644C Substitution - Missense 3:139362472-139362472 - CCK81 COSM3124292 c.1664C>T p.A555V Substitution - Missense 3:139367027-139367027 - BD6T COSM5498866 c.2620_2622delGAA p.E874delE Deletion - In frame 3:139358203-139358205 - sysucc-882T COSM5447537 c.756A>C p.T252T Substitution - coding silent 3:139373804-139373804 - TCGA-AP-A0LM-01 COSM1039108 c.1195G>A p.D399N Substitution - Missense 3:139371733-139371733 - 4132_T COSM3944931 c.1359C>G p.D453E Substitution - Missense 3:139369303-139369303 - TCGA-CM-6166-01 COSM1419486 c.357T>G p.D119E Substitution - Missense 3:139378188-139378188 - CHC2321T COSM3669089 c.1185A>G p.A395A Substitution - coding silent 3:139371743-139371743 - LUAD-NYU1051S COSM368853 c.2508G>A p.M836I Substitution - Missense 3:139358789-139358789 - PD4132a COSM160158 c.1700T>C p.I567T Substitution - Missense 3:139366752-139366752 - TCGA-EE-A2GB-06 COSM3588072 c.916A>G p.M306V Substitution - Missense 3:139373391-139373391 - HCC2998 COSM1670599 c.10C>T p.R4* Substitution - Nonsense 3:139383429-139383429 - WSU-HN30 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - TCGA-C8-A3M7-01 COSM3846369 c.753A>G p.G251G Substitution - coding silent 3:139373807-139373807 - TCGA-09-2056-01 COSM68976 c.2375_2376delCA p.T792fs*3 Deletion - Frameshift 3:139359106-139359107 - 234 COSM3730450 c.528A>G p.S176S Substitution - coding silent 3:139375591-139375591 - CSCC-31-T COSM4472082 c.175C>T p.P59S Substitution - Missense 3:139379433-139379433 - TCGA-BR-4201-01 COSM4113981 c.2107G>A p.A703T Substitution - Missense 3:139361184-139361184 - CAL27 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - SCC-25 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - TCGA-CZ-5458-01 COSM479499 c.509G>T p.W170L Substitution - Missense 3:139375610-139375610 - TCGA-BR-8368-01 COSM4113986 c.1186T>C p.W396R Substitution - Missense 3:139371742-139371742 - pfg016T COSM1642106 c.1266delA p.K422fs*23 Deletion - Frameshift 3:139369484-139369484 - SE35PT COSM1580047 c.2474C>G p.P825R Substitution - Missense 3:139359008-139359008 - 12 COSM1419483 c.1267T>A p.S423T Substitution - Missense 3:139369483-139369483 - PD4005a COSM3664611 c.1648G>A p.E550K Substitution - Missense 3:139367043-139367043 - BN13T COSM1616985 c.601T>C p.Y201H Substitution - Missense 3:139375518-139375518 - TCGA-B5-A11E-01 COSM1039104 c.1931G>A p.R644H Substitution - Missense 3:139362471-139362471 - SCC-15 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - pfg019T COSM1642106 c.1266delA p.K422fs*23 Deletion - Frameshift 3:139369484-139369484 - LIM2551 COSM1642106 c.1266delA p.K422fs*23 Deletion - Frameshift 3:139369484-139369484 - ICGC_MB82 COSM1670599 c.10C>T p.R4* Substitution - Nonsense 3:139383429-139383429 - TCGA-AC-A23H-01 COSM3846368 c.959C>G p.S320* Substitution - Nonsense 3:139373348-139373348 - TCGA-D1-A17M-01 COSM1039109 c.829G>T p.V277L Substitution - Missense 3:139373731-139373731 - TCGA-CF-A3MG-01 COSM1308653 c.1840C>T p.P614S Substitution - Missense 3:139366612-139366612 - sysucc-1317T COSM5449793 c.922A>G p.M308V Substitution - Missense 3:139373385-139373385 - P04-1421 COSM243814 c.476C>T p.A159V Substitution - Missense 3:139378069-139378069 - KM12 COSM1670598 c.1523A>G p.D508G Substitution - Missense 3:139368167-139368167 - TCGA-BP-4965-01 COSM1495348 c.1177G>A p.E393K Substitution - Missense 3:139371751-139371751 - CHC2321T COSM3669089 c.1185A>G p.A395A Substitution - coding silent 3:139371743-139371743 - CHC1201T COSM4801676 c.1814T>C p.M605T Substitution - Missense 3:139366638-139366638 - T1182 COSM4674178 c.1305C>T p.G435G Substitution - coding silent 3:139369357-139369357 - SCC-9 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - TCGA-HM-A4S6-01 COSM4854963 c.2582C>T p.T861I Substitution - Missense 3:139358243-139358243 - PD4005a COSM3664611 c.1648G>A p.E550K Substitution - Missense 3:139367043-139367043 - TCGA-AP-A0LM-01 COSM1039112 c.67C>T p.L23L Substitution - coding silent 3:139383372-139383372 - TCGA-A5-A0GP-01 COSM1039106 c.1594G>A p.D532N Substitution - Missense 3:139367097-139367097 - HCC113T COSM1616984 c.613G>T p.G205C Substitution - Missense 3:139375506-139375506 - HCC113 COSM1616984 c.613G>T p.G205C Substitution - Missense 3:139375506-139375506 - YULAXER COSM1693518 c.676G>A p.E226K Substitution - Missense 3:139374564-139374564 - Pat_76_B COSM5863635 c.346A>G p.T116A Substitution - Missense 3:139379056-139379056 - 61 COSM5736772 c.2573C>A p.A858D Substitution - Missense 3:139358252-139358252 - PD7321a COSM5769176 c.1996-7C>G p.? Unknown 3:139361302-139361302 - CN-AML-NR-08-Dx COSM5425829 c.1033G>A p.V345I Substitution - Missense 3:139373274-139373274 - TCGA-D7-A4YY-01 COSM4113990 c.423C>T p.H141H Substitution - coding silent 3:139378122-139378122 - TCGA-EI-6917-01 COSM3427143 c.859G>A p.A287T Substitution - Missense 3:139373701-139373701 - UD-SCC-2 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - BICR_22 COSM4590949 c.594C>A p.D198E Substitution - Missense 3:139375525-139375525 - PT37 COSM5918037 c.1268C>T p.S423L Substitution - Missense 3:139369482-139369482 - 2171675 COSM4423388 c.2248C>T p.R750W Substitution - Missense 3:139359325-139359325 - S02397 COSM5699269 c.510G>C p.W170C Substitution - Missense 3:139375609-139375609 - TCGA-AX-A0J1-01 COSM1039103 c.1995G>A p.E665E Substitution - coding silent 3:139362407-139362407 - YUROG COSM5398268 c.2090G>A p.G697E Substitution - Missense 3:139361201-139361201 - TCGA-HW-A5KK-01 COSM3974190 c.1832C>T p.P611L Substitution - Missense 3:139366620-139366620 - YULAN COSM1693517 c.1084C>T p.P362S Substitution - Missense 3:139373223-139373223 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.681540;Hs.681541;Hs.681543;Hs.681546;Hs.681547;Hs.681548;Hs.681549;Hs.681550;Hs.681552;Hs.681553;Hs.681554;Hs.681555;Hs.681556;Hs.681557;Hs.681558;Hs.681559;Hs.681560;Hs.681562;Hs.681563;Hs.681564;Hs.681565;Hs.681567;Hs.681569;Hs.681572;Hs.681573;Hs.681574;Hs.681575;Hs.681576;Hs.681578;Hs.681579;Hs.681581;Hs.681582;Hs.681583;Hs.681585;Hs.681586;Hs.681587;Hs.681588;Hs.681589;Hs.681590;Hs.681592;Hs.681593;Hs.681594;Hs.681595;Hs.681598;Hs.681599;Hs.681600;Hs.681601;Hs.681602;Hs.681603;Hs.681604;Hs.681605;Hs.681606;Hs.681607;Hs.681608;Hs.681609;Hs.681610;Hs.681611;Hs.681612;Hs.681613;Hs.681614;Hs.681615;Hs.681616 3q23 606990

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F842C c.2525T>G 3 139077614 STAD A C Missense p.L904V c.2710T>G 3 139076716 UCEC A - Frameshift p.F388Lfs*18 c.1164delT 3 139090606 RCCC A G Missense p.I567T c.1700T>C 3 139085594 BRCA A G Missense p.L488P c.1463T>C 3 139087069 BLCA C A Missense p.D841Y c.2521G>T 3 139077618 STAD C A Missense p.G373W c.1117G>T 3 139090653 CM C A Missense p.Q694H c.2082G>T 3 139080051 UCEC C A Nonsense p.E663* c.1987G>T 3 139081257 BRCA C A SpliceAcceptorSNV . c.895-1G>T 3 139092255 HNSC C G Missense p.D16H c.46G>C 3 139102235 LUSC C G Missense p.K19N c.57G>C 3 139102224 STAD C G Missense p.M730I c.2190G>C 3 139079943 COREAD C G Missense p.V137L c.409G>C 3 139096978 LUAD C G Missense p.W214C c.642G>C 3 139094319 CM C T Missense p.A703T c.2107G>A 3 139080026 STAD C T Missense p.D250N c.748G>A 3 139093334 HNSC C T Missense p.D532N c.1594G>A 3 139085939 UCEC C T Missense p.D906N c.2716G>A 3 139076710 CM C T Missense p.G565S c.1693G>A 3 139085601 BLCA C T Missense p.G736S c.2206G>A 3 139079927 CM C T Missense p.G855R c.2563G>A 3 139077104 OV C T Synonymous p.A719A c.2157G>A 3 139079976 UCEC C T Synonymous p.K346K c.1038G>A 3 139092111 BLCA G A Missense p.A513V c.1538C>T 3 139086994 LUSC G A Missense p.P614S c.1840C>T 3 139085454 BLCA G A Missense p.P825S c.2473C>T 3 139077851 PRAD G A Missense p.R750W c.2248C>T 3 139078167 HNSC G A Missense p.T828M c.2483C>T 3 139077841 STAD G A Nonsense p.Q223* c.667C>T 3 139093415 STAD G A Nonsense p.R4* c.10C>T 3 139102271 MB G A Synonymous p.C134C c.402C>T 3 139096985 STAD G A Synonymous p.C689C c.2067C>T 3 139080066 ESCA G A Synonymous p.D78D c.234C>T 3 139098010 GBM G A Synonymous p.I245I c.735C>T 3 139093347 HNSC G A Synonymous p.L818L c.2452C>T 3 139077872 BRCA G C Missense p.L573V c.1717C>G 3 139085577 RCCC G T 5-UTRSNV . c.1-51C>A 3 139108443 ESCA G T Missense p.T704N c.2111C>A 3 139080022 LUSC T C Missense p.D906G c.2717A>G 3 139076709 UCEC T C Missense p.E475G c.1424A>G 3 139087108 CM T C Missense p.K219E c.655A>G 3 139093427 BRCA T C Missense p.M306V c.916A>G 3 139092233 CM T - Frameshift p.K422Nfs*23 c.1266delA 3 139088326 STAD TG - Frameshift p.T792Rfs*3 c.2375_2376delCA 3 139077948 OV T G Missense p.N834H c.2500A>C 3 139077639 RCCC