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 BLCA 10 81037044 81037044 + Silent SNP C C G TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr10:81037044C>G c.387C>G c.(385-387)ctC>ctG p.L129L BLCA 10 81049571 81049571 + Silent SNP G G A TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr10:81049571G>A c.465G>A c.(463-465)caG>caA p.Q155Q BLCA 10 81050724 81050724 + Silent SNP G G A TCGA-FJ-A3Z7-01A-12D-A23M-08 TCGA-FJ-A3Z7-10A-01D-A23K-08 g.chr10:81050724G>A c.549G>A c.(547-549)ggG>ggA p.G183G BLCA 10 81051984 81051984 + Silent SNP C C T TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr10:81051984C>T c.828C>T c.(826-828)ttC>ttT p.F276F BLCA 10 81052006 81052026 + In_Frame_Del DEL GCAGCAGCGGCAGTGGCAGCA GCAGCAGCGGCAGTGGCAGCA - TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr10:81052006_81052026delGCAGCAGCGGCAGTGGCAGCA c.850_870delGCAGCAGCGGCAGTGGCAGCA c.(850-870)gcagcagcggcagtggcagcadel p.AAAAVAA284del BLCA 10 81058181 81058181 + Missense_Mutation SNP G G T TCGA-K4-A4AB-01B-12D-A289-08 TCGA-K4-A4AB-10A-01D-A289-08 g.chr10:81058181G>T c.1510G>T c.(1510-1512)Gtg>Ttg p.V504L BLCA 10 81058274 81058274 + Missense_Mutation SNP G G A TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr10:81058274G>A c.1603G>A c.(1603-1605)Gac>Aac p.D535N BLCA 10 81060560 81060560 + Missense_Mutation SNP C C T TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr10:81060560C>T c.1880C>T c.(1879-1881)tCg>tTg p.S627L BLCA 10 81061875 81061875 + Silent SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr10:81061875C>T c.2031C>T c.(2029-2031)ttC>ttT p.F677F BLCA 10 81063801 81063801 + Missense_Mutation SNP T T G TCGA-DK-AA6W-01A-12D-A391-08 TCGA-DK-AA6W-10A-01D-A394-08 g.chr10:81063801T>G c.2155T>G c.(2155-2157)Tcc>Gcc p.S719A BLCA 10 81063832 81063832 + Missense_Mutation SNP A A C TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr10:81063832A>C c.2186A>C c.(2185-2187)gAt>gCt p.D729A BLCA 10 81063878 81063878 + Silent SNP C C T TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr10:81063878C>T c.2232C>T c.(2230-2232)atC>atT p.I744I BLCA 10 81065869 81065869 + Silent SNP A A G TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr10:81065869A>G c.2436A>G c.(2434-2436)gaA>gaG p.E812E BLCA 10 81070880 81070880 + Nonsense_Mutation SNP C C G TCGA-E7-A4IJ-01A-31D-A26M-08 TCGA-E7-A4IJ-10A-01D-A26K-08 g.chr10:81070880C>G c.3035C>G c.(3034-3036)tCa>tGa p.S1012* BLCA 10 81070901 81070901 + Missense_Mutation SNP G G C TCGA-UY-A9PD-01A-11D-A38G-08 TCGA-UY-A9PD-10A-01D-A38J-08 g.chr10:81070901G>C c.3056G>C c.(3055-3057)gGa>gCa p.G1019A BLCA 10 81072474 81072474 + Missense_Mutation SNP G G A TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr10:81072474G>A c.3172G>A c.(3172-3174)Gat>Aat p.D1058N BLCA 10 81072495 81072495 + Missense_Mutation SNP G G C TCGA-ZF-AA58-01A-12D-A42E-08 TCGA-ZF-AA58-10A-01D-A42H-08 g.chr10:81072495G>C c.3193G>C c.(3193-3195)Gag>Cag p.E1065Q BRCA 10 81050733 81050733 + Missense_Mutation SNP G G T TCGA-BH-A5IZ-01A-11D-A27P-09 TCGA-BH-A5IZ-10A-01D-A27P-09 g.chr10:81050733G>T c.558G>T c.(556-558)atG>atT p.M186I BRCA 10 81058277 81058277 + Missense_Mutation SNP G G A TCGA-AN-A0XU-01A-11D-A10G-09 TCGA-AN-A0XU-10A-01D-A10G-09 g.chr10:81058277G>A c.1606G>A c.(1606-1608)Gtc>Atc p.V536I BRCA 10 81060562 81060562 + Missense_Mutation SNP G G A TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr10:81060562G>A c.1882G>A c.(1882-1884)Gtg>Atg p.V628M BRCA 10 81063837 81063837 + Missense_Mutation SNP G G T TCGA-EW-A1J2-01A-21D-A13L-09 TCGA-EW-A1J2-10A-01W-A14R-09 g.chr10:81063837G>T c.2191G>T c.(2191-2193)Gtg>Ttg p.V731L BRCA 10 81067225 81067225 + Missense_Mutation SNP T T G TCGA-C8-A134-01A-11D-A10Y-09 TCGA-C8-A134-10A-01D-A110-09 g.chr10:81067225T>G c.2732T>G c.(2731-2733)aTg>aGg p.M911R BRCA 10 81067261 81067261 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr10:81067261A>C c.2768A>C c.(2767-2769)cAc>cCc p.H923P CESC 10 81070690 81070690 + Missense_Mutation SNP G G A TCGA-JW-A5VK-01A-11D-A28B-09 TCGA-JW-A5VK-10A-01D-A28E-09 g.chr10:81070690G>A c.2845G>A c.(2845-2847)Gct>Act p.A949T CESC 10 81070929 81070929 + Silent SNP G G A TCGA-EA-A3HT-01A-61D-A21Q-09 TCGA-EA-A3HT-10A-01D-A21Q-09 g.chr10:81070929G>A c.3084G>A c.(3082-3084)gaG>gaA p.E1028E COAD 10 80976011 80976011 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:80976011A>G c.260A>G c.(259-261)aAg>aGg p.K87R COAD 10 81037001 81037001 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:81037001G>A c.344G>A c.(343-345)cGc>cAc p.R115H COAD 10 81037008 81037008 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr10:81037008C>T c.351C>T c.(349-351)agC>agT p.S117S COAD 10 81056259 81056259 + Missense_Mutation SNP A A C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr10:81056259A>C c.1262A>C c.(1261-1263)aAc>aCc p.N421T COAD 10 81057402 81057402 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:81057402C>A c.1446C>A c.(1444-1446)ttC>ttA p.F482L COAD 10 81058322 81058322 + Missense_Mutation SNP C C A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr10:81058322C>A c.1651C>A c.(1651-1653)Ctg>Atg p.L551M COAD 10 81058322 81058322 + Missense_Mutation SNP C C A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr10:81058322C>A c.1651C>A c.(1651-1653)Ctg>Atg p.L551M COAD 10 81058322 81058322 + Missense_Mutation SNP C C A TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr10:81058322C>A c.1651C>A c.(1651-1653)Ctg>Atg p.L551M COAD 10 81058853 81058853 + Silent SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr10:81058853C>T c.1713C>T c.(1711-1713)ggC>ggT p.G571G COAD 10 81058853 81058853 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr10:81058853C>T c.1713C>T c.(1711-1713)ggC>ggT p.G571G COAD 10 81060579 81060579 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr10:81060579C>T c.1899C>T c.(1897-1899)aaC>aaT p.N633N COAD 10 81063889 81063889 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr10:81063889G>A c.2243G>A c.(2242-2244)cGc>cAc p.R748H COAD 10 81066067 81066067 + Silent SNP A A C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:81066067A>C c.2634A>C c.(2632-2634)ccA>ccC p.P878P COAD 10 81070801 81070801 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr10:81070801C>T c.2956C>T c.(2956-2958)Cct>Tct p.P986S COAD 10 81070899 81070899 + Silent SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr10:81070899C>T c.3054C>T c.(3052-3054)gcC>gcT p.A1018A COADREAD 10 80976011 80976011 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:80976011A>G c.260A>G c.(259-261)aAg>aGg p.K87R COADREAD 10 81037001 81037001 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:81037001G>A c.344G>A c.(343-345)cGc>cAc p.R115H COADREAD 10 81037008 81037008 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr10:81037008C>T c.351C>T c.(349-351)agC>agT p.S117S COADREAD 10 81050780 81050780 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:81050780C>T c.605C>T c.(604-606)tCg>tTg p.S202L COADREAD 10 81056259 81056259 + Missense_Mutation SNP A A C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr10:81056259A>C c.1262A>C c.(1261-1263)aAc>aCc p.N421T COADREAD 10 81057402 81057402 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:81057402C>A c.1446C>A c.(1444-1446)ttC>ttA p.F482L COADREAD 10 81058322 81058322 + Missense_Mutation SNP C C A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr10:81058322C>A c.1651C>A c.(1651-1653)Ctg>Atg p.L551M COADREAD 10 81058322 81058322 + Missense_Mutation SNP C C A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr10:81058322C>A c.1651C>A c.(1651-1653)Ctg>Atg p.L551M COADREAD 10 81058322 81058322 + Missense_Mutation SNP C C A TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr10:81058322C>A c.1651C>A c.(1651-1653)Ctg>Atg p.L551M COADREAD 10 81058323 81058323 + Missense_Mutation SNP T T A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr10:81058323T>A c.1652T>A c.(1651-1653)cTg>cAg p.L551Q COADREAD 10 81058853 81058853 + Silent SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr10:81058853C>T c.1713C>T c.(1711-1713)ggC>ggT p.G571G COADREAD 10 81058853 81058853 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr10:81058853C>T c.1713C>T c.(1711-1713)ggC>ggT p.G571G COADREAD 10 81060579 81060579 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr10:81060579C>T c.1899C>T c.(1897-1899)aaC>aaT p.N633N COADREAD 10 81063889 81063889 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr10:81063889G>A c.2243G>A c.(2242-2244)cGc>cAc p.R748H COADREAD 10 81066067 81066067 + Silent SNP A A C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:81066067A>C c.2634A>C c.(2632-2634)ccA>ccC p.P878P COADREAD 10 81070801 81070801 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr10:81070801C>T c.2956C>T c.(2956-2958)Cct>Tct p.P986S COADREAD 10 81070899 81070899 + Silent SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr10:81070899C>T c.3054C>T c.(3052-3054)gcC>gcT p.A1018A DLBC 10 81053248 81053248 + Silent SNP G G A TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr10:81053248G>A c.1068G>A c.(1066-1068)acG>acA p.T356T ESCA 10 80968093 80968093 + Splice_Site SNP C C T TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr10:80968093C>T c.61C>T c.(61-63)Cac>Tac p.H21Y ESCA 10 81050766 81050766 + Silent SNP C C T TCGA-IC-A6RF-01A-13D-A33E-09 TCGA-IC-A6RF-10A-21D-A33H-09 g.chr10:81050766C>T c.591C>T c.(589-591)ggC>ggT p.G197G ESCA 10 81072411 81072411 + Missense_Mutation SNP C C G TCGA-LN-A7HX-01A-11D-A33E-09 TCGA-LN-A7HX-10A-01D-A33H-09 g.chr10:81072411C>G c.3109C>G c.(3109-3111)Ctc>Gtc p.L1037V GBM 10 81058831 81058831 + Missense_Mutation SNP T T G TCGA-27-2521-01A-01D-1494-08 TCGA-27-2521-10A-01D-1494-08 g.chr10:81058831T>G c.1691T>G c.(1690-1692)cTc>cGc p.L564R GBM 10 81061939 81061939 + Missense_Mutation SNP C C T TCGA-19-1790-01B-01D-1353-08 TCGA-19-1790-10B-01D-1353-08 g.chr10:81061939C>T c.2095C>T c.(2095-2097)Ctc>Ttc p.L699F GBM 10 81065892 81065892 + Missense_Mutation SNP G G T TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr10:81065892G>T c.2459G>T c.(2458-2460)tGc>tTc p.C820F GBM 10 81066012 81066012 + Missense_Mutation SNP A A C TCGA-41-4097-01A-01D-1353-08 TCGA-41-4097-10A-01D-1353-08 g.chr10:81066012A>C c.2579A>C c.(2578-2580)gAg>gCg p.E860A GBMLGG 10 80968196 80968196 + Missense_Mutation SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr10:80968196G>A c.164G>A c.(163-165)gGc>gAc p.G55D GBMLGG 10 81052006 81052026 + In_Frame_Del DEL GCAGCAGCGGCAGTGGCAGCA GCAGCAGCGGCAGTGGCAGCA - TCGA-QH-A6CU-01A-11D-A31L-08 TCGA-QH-A6CU-10A-01D-A31J-08 g.chr10:81052006_81052026delGCAGCAGCGGCAGTGGCAGCA c.850_870delGCAGCAGCGGCAGTGGCAGCA c.(850-870)gcagcagcggcagtggcagcadel p.AAAAVAA284del GBMLGG 10 81052006 81052026 + In_Frame_Del DEL GCAGCAGCGGCAGTGGCAGCA GCAGCAGCGGCAGTGGCAGCA - TCGA-TQ-A7RH-01A-12D-A34A-08 TCGA-TQ-A7RH-10A-01D-A34A-08 g.chr10:81052006_81052026delGCAGCAGCGGCAGTGGCAGCA c.850_870delGCAGCAGCGGCAGTGGCAGCA c.(850-870)gcagcagcggcagtggcagcadel p.AAAAVAA284del GBMLGG 10 81052015 81052015 + Missense_Mutation SNP G G A TCGA-DU-7009-01A-11D-2024-08 TCGA-DU-7009-10A-01D-2024-08 g.chr10:81052015G>A c.859G>A c.(859-861)Gca>Aca p.A287T GBMLGG 10 81052021 81052021 + Missense_Mutation SNP G G A TCGA-TQ-A7RN-01A-11D-A33T-08 TCGA-TQ-A7RN-10A-01D-A33W-08 g.chr10:81052021G>A c.865G>A c.(865-867)Gca>Aca p.A289T GBMLGG 10 81052057 81052057 + Missense_Mutation SNP G G A TCGA-RY-A843-01A-11D-A36O-08 TCGA-RY-A843-10A-01D-A367-08 g.chr10:81052057G>A c.901G>A c.(901-903)Gcc>Acc p.A301T GBMLGG 10 81058831 81058831 + Missense_Mutation SNP T T G TCGA-27-2521-01A-01D-1494-08 TCGA-27-2521-10A-01D-1494-08 g.chr10:81058831T>G c.1691T>G c.(1690-1692)cTc>cGc p.L564R GBMLGG 10 81060680 81060680 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:81060680C>T c.2000C>T c.(1999-2001)aCc>aTc p.T667I GBMLGG 10 81061939 81061939 + Missense_Mutation SNP C C T TCGA-19-1790-01B-01D-1353-08 TCGA-19-1790-10B-01D-1353-08 g.chr10:81061939C>T c.2095C>T c.(2095-2097)Ctc>Ttc p.L699F GBMLGG 10 81065892 81065892 + Missense_Mutation SNP G G T TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr10:81065892G>T c.2459G>T c.(2458-2460)tGc>tTc p.C820F GBMLGG 10 81066012 81066012 + Missense_Mutation SNP A A C TCGA-41-4097-01A-01D-1353-08 TCGA-41-4097-10A-01D-1353-08 g.chr10:81066012A>C c.2579A>C c.(2578-2580)gAg>gCg p.E860A GBMLGG 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-QH-A6X8-01A-12D-A32B-08 TCGA-QH-A6X8-10B-01D-A329-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del GBMLGG 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-R8-A6MO-01A-11D-A33T-08 TCGA-R8-A6MO-10C-01D-A33W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del HNSC 10 81049555 81049555 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr10:81049555C>T c.449C>T c.(448-450)tCt>tTt p.S150F HNSC 10 81050778 81050778 + Silent SNP G G C TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr10:81050778G>C c.603G>C c.(601-603)gcG>gcC p.A201A HNSC 10 81050825 81050825 + Missense_Mutation SNP C C T TCGA-QK-A64Z-01A-11D-A30E-08 TCGA-QK-A64Z-10A-01D-A30H-08 g.chr10:81050825C>T c.650C>T c.(649-651)gCg>gTg p.A217V HNSC 10 81051988 81051988 + Nonsense_Mutation SNP C C T TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr10:81051988C>T c.832C>T c.(832-834)Cag>Tag p.Q278* HNSC 10 81051996 81051996 + Silent SNP G G A TCGA-UF-A7JT-01A-11D-A34J-08 TCGA-UF-A7JT-10A-01D-A34M-08 g.chr10:81051996G>A c.840G>A c.(838-840)gcG>gcA p.A280A HNSC 10 81053160 81053160 + Missense_Mutation SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr10:81053160A>G c.980A>G c.(979-981)aAc>aGc p.N327S HNSC 10 81056307 81056307 + Missense_Mutation SNP C C T TCGA-CV-A6JT-01A-11D-A31L-08 TCGA-CV-A6JT-10A-01D-A31J-08 g.chr10:81056307C>T c.1310C>T c.(1309-1311)cCg>cTg p.P437L HNSC 10 81056365 81056365 + Silent SNP C C T TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chr10:81056365C>T c.1368C>T c.(1366-1368)tcC>tcT p.S456S HNSC 10 81058853 81058853 + Silent SNP C C T TCGA-CR-7390-01A-11D-2012-08 TCGA-CR-7390-10A-01D-2013-08 g.chr10:81058853C>T c.1713C>T c.(1711-1713)ggC>ggT p.G571G HNSC 10 81058892 81058892 + Silent SNP G G A TCGA-CX-A4AQ-01A-11D-A25D-08 TCGA-CX-A4AQ-10A-01D-A25E-08 g.chr10:81058892G>A c.1752G>A c.(1750-1752)gcG>gcA p.A584A HNSC 10 81063878 81063878 + Silent SNP C C T TCGA-CR-5248-01A-01D-2012-08 TCGA-CR-5248-10A-01D-2013-08 g.chr10:81063878C>T c.2232C>T c.(2230-2232)atC>atT p.I744I HNSC 10 81064919 81064919 + Splice_Site SNP A A G TCGA-F7-A50I-01A-11D-A28R-08 TCGA-F7-A50I-10A-01D-A28U-08 g.chr10:81064919A>G c.e20-1 HNSC 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del HNSC 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-F7-A623-01A-11D-A28R-08 TCGA-F7-A623-10A-01D-A28U-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del HNSC 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-WA-A7H4-01A-21D-A34J-08 TCGA-WA-A7H4-10A-01D-A34M-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del HNSC 10 81070805 81070805 + Missense_Mutation SNP C C T TCGA-CN-A497-01A-11D-A24D-08 TCGA-CN-A497-10A-01D-A24F-08 g.chr10:81070805C>T c.2960C>T c.(2959-2961)tCc>tTc p.S987F HNSC 10 81072426 81072426 + Missense_Mutation SNP G G A TCGA-P3-A5Q5-01A-11D-A28R-08 TCGA-P3-A5Q5-10A-01D-A28U-08 g.chr10:81072426G>A c.3124G>A c.(3124-3126)Gag>Aag p.E1042K HNSC 10 81072505 81072505 + Silent SNP G G A TCGA-BB-A5HU-01A-11D-A28R-08 TCGA-BB-A5HU-10A-01D-A28U-08 g.chr10:81072505G>A c.3203G>A c.(3202-3204)tGa>tAa p.*1068* KIPAN 10 80968102 80968102 + Missense_Mutation SNP A A T TCGA-B1-A656-01A-11D-A31X-10 TCGA-B1-A656-10A-01D-A31X-10 g.chr10:80968102A>T c.70A>T c.(70-72)Aat>Tat p.N24Y KIPAN 10 81065919 81065919 + Missense_Mutation SNP C C T TCGA-EU-5907-01A-11D-1669-08 TCGA-EU-5907-10A-01D-1669-08 g.chr10:81065919C>T c.2486C>T c.(2485-2487)tCg>tTg p.S829L KIPAN 10 81070821 81070822 + Frame_Shift_Ins INS - - C TCGA-B0-5697-01A-11D-1534-10 TCGA-B0-5697-11A-01D-1534-10 g.chr10:81070821_81070822insC c.2976_2977insC c.(2977-2979)ccgfs p.P993fs KIRC 10 81065919 81065919 + Missense_Mutation SNP C C T TCGA-EU-5907-01A-11D-1669-08 TCGA-EU-5907-10A-01D-1669-08 g.chr10:81065919C>T c.2486C>T c.(2485-2487)tCg>tTg p.S829L KIRC 10 81070821 81070822 + Frame_Shift_Ins INS - - C TCGA-B0-5697-01A-11D-1534-10 TCGA-B0-5697-11A-01D-1534-10 g.chr10:81070821_81070822insC c.2976_2977insC c.(2977-2979)ccgfs p.P993fs KIRP 10 80968102 80968102 + Missense_Mutation SNP A A T TCGA-B1-A656-01A-11D-A31X-10 TCGA-B1-A656-10A-01D-A31X-10 g.chr10:80968102A>T c.70A>T c.(70-72)Aat>Tat p.N24Y LGG 10 80968196 80968196 + Missense_Mutation SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr10:80968196G>A c.164G>A c.(163-165)gGc>gAc p.G55D LGG 10 81052006 81052026 + In_Frame_Del DEL GCAGCAGCGGCAGTGGCAGCA GCAGCAGCGGCAGTGGCAGCA - TCGA-QH-A6CU-01A-11D-A31L-08 TCGA-QH-A6CU-10A-01D-A31J-08 g.chr10:81052006_81052026delGCAGCAGCGGCAGTGGCAGCA c.850_870delGCAGCAGCGGCAGTGGCAGCA c.(850-870)gcagcagcggcagtggcagcadel p.AAAAVAA284del LGG 10 81052006 81052026 + In_Frame_Del DEL GCAGCAGCGGCAGTGGCAGCA GCAGCAGCGGCAGTGGCAGCA - TCGA-TQ-A7RH-01A-12D-A34A-08 TCGA-TQ-A7RH-10A-01D-A34A-08 g.chr10:81052006_81052026delGCAGCAGCGGCAGTGGCAGCA c.850_870delGCAGCAGCGGCAGTGGCAGCA c.(850-870)gcagcagcggcagtggcagcadel p.AAAAVAA284del LGG 10 81052015 81052015 + Missense_Mutation SNP G G A TCGA-DU-7009-01A-11D-2024-08 TCGA-DU-7009-10A-01D-2024-08 g.chr10:81052015G>A c.859G>A c.(859-861)Gca>Aca p.A287T LGG 10 81052021 81052021 + Missense_Mutation SNP G G A TCGA-TQ-A7RN-01A-11D-A33T-08 TCGA-TQ-A7RN-10A-01D-A33W-08 g.chr10:81052021G>A c.865G>A c.(865-867)Gca>Aca p.A289T LGG 10 81052057 81052057 + Missense_Mutation SNP G G A TCGA-RY-A843-01A-11D-A36O-08 TCGA-RY-A843-10A-01D-A367-08 g.chr10:81052057G>A c.901G>A c.(901-903)Gcc>Acc p.A301T LGG 10 81060680 81060680 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:81060680C>T c.2000C>T c.(1999-2001)aCc>aTc p.T667I LGG 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-QH-A6X8-01A-12D-A32B-08 TCGA-QH-A6X8-10B-01D-A329-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del LGG 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-R8-A6MO-01A-11D-A33T-08 TCGA-R8-A6MO-10C-01D-A33W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del LIHC 10 81058316 81058316 + Missense_Mutation SNP A A G TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr10:81058316A>G c.1645A>G c.(1645-1647)Agc>Ggc p.S549G LIHC 10 81064989 81064989 + Splice_Site SNP G G C TCGA-DD-AAVP-01A-11D-A40R-10 TCGA-DD-AAVP-10A-01D-A40U-10 g.chr10:81064989G>C c.e20+1 LIHC 10 81065903 81065903 + Missense_Mutation SNP C C T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr10:81065903C>T c.2470C>T c.(2470-2472)Ccg>Tcg p.P824S LUAD 10 80961439 80961439 + Missense_Mutation SNP G G C TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chr10:80961439G>C c.50G>C c.(49-51)tGc>tCc p.C17S LUAD 10 80976007 80976007 + Missense_Mutation SNP G G A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr10:80976007G>A c.256G>A c.(256-258)Gac>Aac p.D86N LUAD 10 81037046 81037046 + Missense_Mutation SNP G G A TCGA-49-6745-01A-11D-1855-08 TCGA-49-6745-11A-01D-1855-08 g.chr10:81037046G>A c.389G>A c.(388-390)aGc>aAc p.S130N LUAD 10 81050910 81050910 + Silent SNP C C T TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr10:81050910C>T c.735C>T c.(733-735)ccC>ccT p.P245P LUAD 10 81052058 81052058 + Missense_Mutation SNP C C T TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr10:81052058C>T c.902C>T c.(901-903)gCc>gTc p.A301V LUAD 10 81053264 81053264 + Missense_Mutation SNP G G T TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr10:81053264G>T c.1084G>T c.(1084-1086)Ggc>Tgc p.G362C LUAD 10 81053410 81053410 + Splice_Site SNP G G A TCGA-MP-A4SV-01A-11D-A24P-08 TCGA-MP-A4SV-10A-01D-A24P-08 g.chr10:81053410G>A c.1230G>A c.(1228-1230)gaG>gaA p.E410E LUAD 10 81056385 81056385 + Missense_Mutation SNP C C T TCGA-80-5607-01A-31D-1945-08 TCGA-80-5607-10A-01D-1946-08 g.chr10:81056385C>T c.1388C>T c.(1387-1389)aCg>aTg p.T463M LUAD 10 81058294 81058294 + Silent SNP G G T TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr10:81058294G>T c.1623G>T c.(1621-1623)ccG>ccT p.P541P LUAD 10 81058316 81058316 + Missense_Mutation SNP A A C TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr10:81058316A>C c.1645A>C c.(1645-1647)Agc>Cgc p.S549R LUAD 10 81065309 81065309 + Missense_Mutation SNP G G T TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr10:81065309G>T c.2374G>T c.(2374-2376)Ggc>Tgc p.G792C LUAD 10 81065336 81065336 + Nonsense_Mutation SNP G G T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr10:81065336G>T c.2401G>T c.(2401-2403)Gga>Tga p.G801* LUAD 10 81065350 81065350 + Silent SNP C C T TCGA-17-Z028-01A-01W-0746-08 TCGA-17-Z028-11A-01W-0746-08 g.chr10:81065350C>T c.2415C>T c.(2413-2415)gcC>gcT p.A805A LUAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-49-4505-01A-01D-1931-08 TCGA-49-4505-11A-01D-1265-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del LUSC 10 81058301 81058301 + Missense_Mutation SNP A A G TCGA-22-5471-01A-01D-1632-08 TCGA-22-5471-11A-01D-1632-08 g.chr10:81058301A>G c.1630A>G c.(1630-1632)Atc>Gtc p.I544V LUSC 10 81058846 81058847 + Frame_Shift_Del DEL GG GG - TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr10:81058846_81058847delGG c.1706_1707delGG c.(1705-1707)cggfs p.R569fs LUSC 10 81061960 81061960 + Missense_Mutation SNP A A G TCGA-66-2757-01A-01D-1522-08 TCGA-66-2757-11A-01D-1522-08 g.chr10:81061960A>G c.2116A>G c.(2116-2118)Atc>Gtc p.I706V LUSC 10 81070737 81070737 + Missense_Mutation SNP C C A TCGA-39-5019-01A-01D-1817-08 TCGA-39-5019-11A-01D-1817-08 g.chr10:81070737C>A c.2892C>A c.(2890-2892)caC>caA p.H964Q OV 10 81052045 81052045 + Missense_Mutation SNP G G A TCGA-24-2261-01A-01W-0722-08 TCGA-24-2261-11A-01W-0722-08 g.chr10:81052045G>A c.889G>A c.(889-891)Gcc>Acc p.A297T OV 10 81053247 81053247 + Missense_Mutation SNP C C T TCGA-29-1695-01A-01W-0633-09 TCGA-29-1695-10A-01W-0633-09 g.chr10:81053247C>T c.1067C>T c.(1066-1068)aCg>aTg p.T356M OV 10 81064923 81064923 + Nonsense_Mutation SNP C C A TCGA-13-1481-01A-01W-0549-09 TCGA-13-1481-10A-01W-0549-09 g.chr10:81064923C>A c.2289C>A c.(2287-2289)tgC>tgA p.C763* OV 10 81070809 81070809 + Silent SNP G G A TCGA-36-2551-01A-01D-1526-09 TCGA-36-2551-10A-01D-1526-09 g.chr10:81070809G>A c.2964G>A c.(2962-2964)caG>caA p.Q988Q PAAD 10 81037008 81037008 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:81037008C>T c.351C>T c.(349-351)agC>agT p.S117S PAAD 10 81052021 81052023 + In_Frame_Del DEL GCA GCA - TCGA-HZ-7925-01A-11D-2154-08 TCGA-HZ-7925-10A-01D-2154-08 g.chr10:81052021_81052023delGCA c.865_867delGCA c.(865-867)gcadel p.A293del PAAD 10 81056295 81056295 + Frame_Shift_Del DEL C C - TCGA-IB-8126-01A-11D-2396-08 TCGA-IB-8126-10A-01D-2396-08 g.chr10:81056295delC c.1298delC c.(1297-1299)gccfs p.A433fs PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-2J-AABK-01A-31D-A40W-08 TCGA-2J-AABK-10A-01D-A40W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-2J-AABU-01A-11D-A40W-08 TCGA-2J-AABU-10A-01D-A40W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-F2-A8YN-01A-11D-A377-08 TCGA-F2-A8YN-10A-01D-A37A-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-IB-7885-01A-11D-2154-08 TCGA-IB-7885-10A-01D-2154-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-IB-AAUP-01A-11D-A377-08 TCGA-IB-AAUP-10A-01D-A37A-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-IB-AAUQ-01A-22D-A40W-08 TCGA-IB-AAUQ-10A-01D-A40W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-LB-A7SX-01A-11D-A33T-08 TCGA-LB-A7SX-10A-01D-A33W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-YH-A8SY-01A-11D-A377-08 TCGA-YH-A8SY-10A-01D-A37A-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PAAD 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-Z5-AAPL-01A-12D-A40W-08 TCGA-Z5-AAPL-10A-01D-A40W-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del PRAD 10 81050916 81050916 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:81050916C>T c.741C>T c.(739-741)agC>agT p.S247S PRAD 10 81056320 81056320 + Silent SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:81056320C>A c.1323C>A c.(1321-1323)acC>acA p.T441T PRAD 10 81058166 81058166 + Missense_Mutation SNP C C T TCGA-EJ-7330-01A-11D-2114-08 TCGA-EJ-7330-10A-01D-2114-08 g.chr10:81058166C>T c.1495C>T c.(1495-1497)Ccc>Tcc p.P499S PRAD 10 81060603 81060603 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:81060603C>T c.1923C>T c.(1921-1923)cgC>cgT p.R641R PRAD 10 81065297 81065297 + Missense_Mutation SNP G G A TCGA-YL-A8SK-01B-21D-A377-08 TCGA-YL-A8SK-10A-01D-A37A-08 g.chr10:81065297G>A c.2362G>A c.(2362-2364)Gct>Act p.A788T READ 10 81050780 81050780 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:81050780C>T c.605C>T c.(604-606)tCg>tTg p.S202L READ 10 81058323 81058323 + Missense_Mutation SNP T T A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr10:81058323T>A c.1652T>A c.(1651-1653)cTg>cAg p.L551Q SARC 10 81070908 81070908 + Silent SNP G G A TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr10:81070908G>A c.3063G>A c.(3061-3063)caG>caA p.Q1021Q SKCM 10 80968157 80968157 + Missense_Mutation SNP C C T TCGA-EE-A29A-06A-12D-A196-08 TCGA-EE-A29A-10A-01D-A198-08 g.chr10:80968157C>T c.125C>T c.(124-126)cCa>cTa p.P42L SKCM 10 81050844 81050844 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:81050844C>T c.669C>T c.(667-669)ttC>ttT p.F223F SKCM 10 81051954 81051954 + Silent SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr10:81051954C>T c.798C>T c.(796-798)atC>atT p.I266I SKCM 10 81053203 81053203 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:81053203C>T c.1023C>T c.(1021-1023)tcC>tcT p.S341S SKCM 10 81053372 81053372 + Missense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr10:81053372C>T c.1192C>T c.(1192-1194)Ctt>Ttt p.L398F SKCM 10 81056306 81056306 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:81056306C>T c.1309C>T c.(1309-1311)Ccg>Tcg p.P437S SKCM 10 81058166 81058166 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:81058166C>T c.1495C>T c.(1495-1497)Ccc>Tcc p.P499S SKCM 10 81060555 81060555 + Silent SNP C C T TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr10:81060555C>T c.1875C>T c.(1873-1875)ccC>ccT p.P625P SKCM 10 81060673 81060673 + Nonsense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr10:81060673C>T c.1993C>T c.(1993-1995)Cag>Tag p.Q665* SKCM 10 81061875 81061875 + Silent SNP C C T TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr10:81061875C>T c.2031C>T c.(2029-2031)ttC>ttT p.F677F SKCM 10 81063817 81063817 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr10:81063817C>T c.2171C>T c.(2170-2172)aCc>aTc p.T724I SKCM 10 81065942 81065942 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:81065942C>T c.2509C>T c.(2509-2511)Cct>Tct p.P837S SKCM 10 81065958 81065958 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr10:81065958C>T c.2525C>T c.(2524-2526)tCc>tTc p.S842F SKCM 10 81066066 81066066 + Missense_Mutation SNP C C T TCGA-EE-A2GS-06A-12D-A197-08 TCGA-EE-A2GS-10A-01D-A199-08 g.chr10:81066066C>T c.2633C>T c.(2632-2634)cCa>cTa p.P878L SKCM 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del SKCM 10 81070787 81070789 + In_Frame_Del DEL CTC CTC - TCGA-EE-A2MF-06A-11D-A21A-08 TCGA-EE-A2MF-10B-01D-A21A-08 g.chr10:81070787_81070789delCTC c.2942_2944delCTC c.(2941-2946)gctcct>gct p.P986del SKCM 10 81070838 81070838 + Missense_Mutation SNP C C T TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr10:81070838C>T c.2993C>T c.(2992-2994)cCc>cTc p.P998L SKCM 10 81070875 81070875 + Silent SNP C C A TCGA-EE-A2ML-06A-11D-A197-08 TCGA-EE-A2ML-10A-01D-A199-08 g.chr10:81070875C>A c.3030C>A c.(3028-3030)ccC>ccA p.P1010P

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 10 81053188 81053188 single base substitution G A downstream_gene_variant BLCA-CN 10 81053188 81053188 single base substitution G A exon_variant BLCA-CN 10 81053188 81053188 single base substitution G A synonymous_variant P336P 1008G>A BLCA-CN 10 81066034 81066034 single base substitution C T synonymous_variant P20P 60C>T BLCA-CN 10 81066034 81066034 single base substitution C T synonymous_variant P867P 2601C>T BLCA-US 10 81037044 81037044 single base substitution C G exon_variant BLCA-US 10 81037044 81037044 single base substitution C G synonymous_variant L129L 387C>G BLCA-US 10 81049571 81049571 single base substitution G A exon_variant BLCA-US 10 81049571 81049571 single base substitution G A synonymous_variant Q155Q 465G>A BLCA-US 10 81050724 81050724 single base substitution G A exon_variant BLCA-US 10 81050724 81050724 single base substitution G A synonymous_variant G183G 549G>A BLCA-US 10 81052006 81052026 deletion of <=200bp GCAGCAGCGGCAGTGGCAGCA - downstream_gene_variant BLCA-US 10 81052006 81052026 deletion of <=200bp GCAGCAGCGGCAGTGGCAGCA - exon_variant BLCA-US 10 81052006 81052026 deletion of <=200bp GCAGCAGCGGCAGTGGCAGCA - inframe_deletion AAAAVAA284 BLCA-US 10 81063832 81063832 single base substitution A C missense_variant D729A 2186A>C BLCA-US 10 81063832 81063832 single base substitution A C upstream_gene_variant BLCA-US 10 81072474 81072474 single base substitution G A missense_variant D1058N 3172G>A BLCA-US 10 81072474 81072474 single base substitution G A missense_variant D124N 370G>A BOCA-FR 10 80917647 80917647 single base substitution C T intron_variant BOCA-FR 10 80919245 80919245 single base substitution A G intron_variant BOCA-FR 10 81001745 81001745 single base substitution G A intron_variant BOCA-FR 10 81001745 81001745 single base substitution G A upstream_gene_variant BOCA-FR 10 81027502 81027502 single base substitution G A intron_variant BOCA-FR 10 81054219 81054220 multiple base substitution (>=2bp and <=200bp) GC TT downstream_gene_variant BOCA-FR 10 81054219 81054220 multiple base substitution (>=2bp and <=200bp) GC TT exon_variant BOCA-FR 10 81054219 81054220 multiple base substitution (>=2bp and <=200bp) GC TT intron_variant BOCA-UK 10 81051926 81051926 single base substitution G C downstream_gene_variant BOCA-UK 10 81051926 81051926 single base substitution G C exon_variant BOCA-UK 10 81051926 81051926 single base substitution G C missense_variant G257A 770G>C BRCA-EU 10 80828289 80828289 single base substitution C T upstream_gene_variant BRCA-EU 10 80828467 80828467 single base substitution G C upstream_gene_variant BRCA-EU 10 80828481 80828481 single base substitution G C upstream_gene_variant BRCA-EU 10 80828718 80828718 single base substitution G C upstream_gene_variant BRCA-EU 10 80828940 80828940 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 10 80830208 80830208 single base substitution C T intron_variant BRCA-EU 10 80831114 80831114 single base substitution G C intron_variant BRCA-EU 10 80831194 80831194 single base substitution G C intron_variant BRCA-EU 10 80833786 80833786 single base substitution G T intron_variant BRCA-EU 10 80834619 80834619 single base substitution C T intron_variant BRCA-EU 10 80835814 80835814 single base substitution T G intron_variant BRCA-EU 10 80837559 80837559 single base substitution T G intron_variant BRCA-EU 10 80838219 80838219 single base substitution C G intron_variant BRCA-EU 10 80838527 80838527 single base substitution G C intron_variant BRCA-EU 10 80839014 80839014 single base substitution G A intron_variant BRCA-EU 10 80839872 80839872 single base substitution C T intron_variant BRCA-EU 10 80840895 80840895 single base substitution A T intron_variant BRCA-EU 10 80841139 80841139 single base substitution G C intron_variant BRCA-EU 10 80841247 80841247 single base substitution G A intron_variant BRCA-EU 10 80843760 80843760 single base substitution C G intron_variant BRCA-EU 10 80846350 80846350 single base substitution A C intron_variant BRCA-EU 10 80846458 80846458 single base substitution G C intron_variant BRCA-EU 10 80847784 80847784 single base substitution G A intron_variant BRCA-EU 10 80849418 80849418 single base substitution C T intron_variant BRCA-EU 10 80854674 80854674 single base substitution C A intron_variant BRCA-EU 10 80855084 80855084 single base substitution C G intron_variant BRCA-EU 10 80855596 80855596 single base substitution G A intron_variant BRCA-EU 10 80856544 80856545 deletion of <=200bp AA - intron_variant BRCA-EU 10 80857447 80857447 single base substitution G C intron_variant BRCA-EU 10 80860328 80860328 single base substitution C T intron_variant BRCA-EU 10 80860356 80860356 single base substitution G A intron_variant BRCA-EU 10 80861480 80861480 insertion of <=200bp - G intron_variant BRCA-EU 10 80861767 80861767 single base substitution C A intron_variant BRCA-EU 10 80862815 80862815 single base substitution G A intron_variant BRCA-EU 10 80866954 80866954 single base substitution G A intron_variant BRCA-EU 10 80867115 80867115 single base substitution C T intron_variant BRCA-EU 10 80869715 80869715 single base substitution G C intron_variant BRCA-EU 10 80871165 80871165 single base substitution G C intron_variant BRCA-EU 10 80872564 80872564 single base substitution C T intron_variant BRCA-EU 10 80874898 80874898 single base substitution G A intron_variant BRCA-EU 10 80875306 80875306 single base substitution C T intron_variant BRCA-EU 10 80875326 80875326 single base substitution A T intron_variant BRCA-EU 10 80877174 80877174 single base substitution C T intron_variant BRCA-EU 10 80877731 80877731 single base substitution T C intron_variant BRCA-EU 10 80877875 80877875 single base substitution C T intron_variant BRCA-EU 10 80878677 80878677 insertion of <=200bp - A 5_prime_UTR_variant BRCA-EU 10 80878692 80878692 single base substitution T A 5_prime_UTR_variant BRCA-EU 10 80878909 80878909 single base substitution C G intron_variant BRCA-EU 10 80880436 80880436 single base substitution G A intron_variant BRCA-EU 10 80881253 80881348 deletion of <=200bp CTAGCATGACCTAGTAACTTCCTCTCCACAACTCCTTTGTAAAGTATCCTTAGGATTGTCCTTTGGAAACTTGGCCAGCAGAAAGCTCTGGGGTAC - intron_variant BRCA-EU 10 80881356 80881356 single base substitution G C intron_variant BRCA-EU 10 80882418 80882418 single base substitution C G intron_variant BRCA-EU 10 80882849 80882849 single base substitution G T intron_variant BRCA-EU 10 80883531 80883531 single base substitution C A intron_variant BRCA-EU 10 80884712 80884712 insertion of <=200bp - TCC intron_variant BRCA-EU 10 80884819 80884819 single base substitution C G intron_variant BRCA-EU 10 80885218 80885218 single base substitution C T intron_variant BRCA-EU 10 80886804 80886804 single base substitution C T intron_variant BRCA-EU 10 80887123 80887123 single base substitution A T intron_variant BRCA-EU 10 80887741 80887741 single base substitution G T intron_variant BRCA-EU 10 80890846 80890846 single base substitution G A intron_variant BRCA-EU 10 80891362 80891362 single base substitution T G intron_variant BRCA-EU 10 80891795 80891795 single base substitution G T intron_variant BRCA-EU 10 80892249 80892249 single base substitution G A intron_variant BRCA-EU 10 80892507 80892507 single base substitution C T intron_variant BRCA-EU 10 80892517 80892517 single base substitution G A intron_variant BRCA-EU 10 80893671 80893671 single base substitution T G intron_variant BRCA-EU 10 80894125 80894125 single base substitution C A intron_variant BRCA-EU 10 80894885 80894885 single base substitution A C intron_variant BRCA-EU 10 80894896 80894896 single base substitution G C intron_variant BRCA-EU 10 80894958 80894958 single base substitution G T intron_variant BRCA-EU 10 80895119 80895151 deletion of <=200bp TTGGTCAGAATTAGCCCACAAGAGAGCAGTCAT - intron_variant BRCA-EU 10 80895151 80895151 single base substitution T G intron_variant BRCA-EU 10 80895659 80895659 single base substitution C T intron_variant BRCA-EU 10 80895662 80895662 single base substitution C T intron_variant BRCA-EU 10 80896322 80896322 single base substitution G C intron_variant BRCA-EU 10 80899198 80899198 single base substitution G A intron_variant BRCA-EU 10 80899384 80899384 single base substitution G T intron_variant BRCA-EU 10 80899385 80899385 single base substitution G C intron_variant BRCA-EU 10 80899672 80899672 single base substitution G A intron_variant BRCA-EU 10 80900588 80900588 single base substitution G T intron_variant BRCA-EU 10 80901102 80901102 deletion of <=200bp A - intron_variant BRCA-EU 10 80903075 80903075 single base substitution G T intron_variant BRCA-EU 10 80903090 80903090 single base substitution G C intron_variant BRCA-EU 10 80903359 80903359 single base substitution G T intron_variant BRCA-EU 10 80904339 80904339 single base substitution C T intron_variant BRCA-EU 10 80904498 80904498 single base substitution G A intron_variant BRCA-EU 10 80905103 80905103 single base substitution C T intron_variant BRCA-EU 10 80905264 80905264 single base substitution G A intron_variant BRCA-EU 10 80906342 80906342 single base substitution C T intron_variant BRCA-EU 10 80906983 80906983 single base substitution G A intron_variant BRCA-EU 10 80907750 80907750 single base substitution C A intron_variant BRCA-EU 10 80908489 80908489 single base substitution C T intron_variant BRCA-EU 10 80909593 80909593 single base substitution G T intron_variant BRCA-EU 10 80909850 80909850 single base substitution G A intron_variant BRCA-EU 10 80909920 80909920 single base substitution G T intron_variant BRCA-EU 10 80911493 80911493 single base substitution C G intron_variant BRCA-EU 10 80914062 80914062 single base substitution T C intron_variant BRCA-EU 10 80917748 80917748 single base substitution G A intron_variant BRCA-EU 10 80918027 80918027 single base substitution C G intron_variant BRCA-EU 10 80919713 80919713 single base substitution C T intron_variant BRCA-EU 10 80919743 80919743 single base substitution C G intron_variant BRCA-EU 10 80920364 80920364 single base substitution G C intron_variant BRCA-EU 10 80922837 80922837 single base substitution G T intron_variant BRCA-EU 10 80923458 80923458 single base substitution C G intron_variant BRCA-EU 10 80923859 80923859 single base substitution A G intron_variant BRCA-EU 10 80923884 80923884 single base substitution C T intron_variant BRCA-EU 10 80924120 80924120 single base substitution G C intron_variant BRCA-EU 10 80924782 80924782 single base substitution G C intron_variant BRCA-EU 10 80925189 80925189 single base substitution G A intron_variant BRCA-EU 10 80925909 80925909 single base substitution C T intron_variant BRCA-EU 10 80926040 80926040 single base substitution C T intron_variant BRCA-EU 10 80926780 80926780 single base substitution T A intron_variant BRCA-EU 10 80927519 80927519 single base substitution C T intron_variant BRCA-EU 10 80927520 80927520 single base substitution G A intron_variant BRCA-EU 10 80927834 80927834 single base substitution C A intron_variant BRCA-EU 10 80929060 80929060 single base substitution G T intron_variant BRCA-EU 10 80929435 80929435 single base substitution G C intron_variant BRCA-EU 10 80931789 80931789 single base substitution A G intron_variant BRCA-EU 10 80932737 80932737 single base substitution G C intron_variant BRCA-EU 10 80932861 80932861 single base substitution G A intron_variant BRCA-EU 10 80932874 80932874 single base substitution C T intron_variant BRCA-EU 10 80934514 80934514 single base substitution A C intron_variant BRCA-EU 10 80935094 80935094 single base substitution T A intron_variant BRCA-EU 10 80936134 80936134 single base substitution C T intron_variant BRCA-EU 10 80937001 80937001 deletion of <=200bp A - intron_variant BRCA-EU 10 80937072 80937072 single base substitution G A intron_variant BRCA-EU 10 80937470 80937470 single base substitution G C intron_variant BRCA-EU 10 80940213 80940213 single base substitution G C intron_variant BRCA-EU 10 80940339 80940339 single base substitution C T intron_variant BRCA-EU 10 80941418 80941418 single base substitution G C intron_variant BRCA-EU 10 80941795 80941795 single base substitution C G intron_variant BRCA-EU 10 80942329 80942329 single base substitution C T intron_variant BRCA-EU 10 80943262 80943262 single base substitution G C intron_variant BRCA-EU 10 80943327 80943327 single base substitution G C intron_variant BRCA-EU 10 80944901 80944901 single base substitution C G intron_variant BRCA-EU 10 80946389 80946389 single base substitution A G intron_variant BRCA-EU 10 80947414 80947414 single base substitution G A intron_variant BRCA-EU 10 80948035 80948035 single base substitution G A intron_variant BRCA-EU 10 80951769 80951769 single base substitution G A intron_variant BRCA-EU 10 80951839 80951839 single base substitution G C intron_variant BRCA-EU 10 80953322 80953322 single base substitution G C intron_variant BRCA-EU 10 80954386 80954386 single base substitution G A intron_variant BRCA-EU 10 80954880 80954880 single base substitution C T intron_variant BRCA-EU 10 80954964 80954964 single base substitution T G intron_variant BRCA-EU 10 80956694 80956694 single base substitution G A intron_variant BRCA-EU 10 80957242 80957242 single base substitution C A intron_variant BRCA-EU 10 80957703 80957703 single base substitution C A intron_variant BRCA-EU 10 80958652 80958652 single base substitution G A intron_variant BRCA-EU 10 80958946 80958946 single base substitution C T intron_variant BRCA-EU 10 80959030 80959030 single base substitution C T intron_variant BRCA-EU 10 80960190 80960190 single base substitution T A intron_variant BRCA-EU 10 80960433 80960433 single base substitution C T intron_variant BRCA-EU 10 80962871 80962871 single base substitution G C intron_variant BRCA-EU 10 80962922 80962922 single base substitution G A intron_variant BRCA-EU 10 80963937 80963937 single base substitution C T intron_variant BRCA-EU 10 80964815 80964815 single base substitution T C intron_variant BRCA-EU 10 80964910 80964910 single base substitution G A intron_variant BRCA-EU 10 80965210 80965210 single base substitution G A intron_variant BRCA-EU 10 80965638 80965638 single base substitution G C intron_variant BRCA-EU 10 80966692 80966692 single base substitution A T intron_variant BRCA-EU 10 80968683 80968683 single base substitution G C intron_variant BRCA-EU 10 80969169 80969169 single base substitution C T intron_variant BRCA-EU 10 80969738 80969738 single base substitution G A intron_variant BRCA-EU 10 80970035 80970035 single base substitution G C intron_variant BRCA-EU 10 80970497 80970497 single base substitution C A intron_variant BRCA-EU 10 80973644 80973644 single base substitution G C intron_variant BRCA-EU 10 80973972 80973972 single base substitution G A intron_variant BRCA-EU 10 80973984 80973984 single base substitution G A intron_variant BRCA-EU 10 80975120 80975120 single base substitution G A intron_variant BRCA-EU 10 80975302 80975302 single base substitution T G intron_variant BRCA-EU 10 80978605 80978605 single base substitution G C intron_variant BRCA-EU 10 80979343 80979343 single base substitution G C intron_variant BRCA-EU 10 80979821 80979821 single base substitution G C intron_variant BRCA-EU 10 80982616 80982616 single base substitution A C intron_variant BRCA-EU 10 80984751 80984751 single base substitution G A intron_variant BRCA-EU 10 80985739 80985739 single base substitution G C intron_variant BRCA-EU 10 80986787 80986787 single base substitution G A intron_variant BRCA-EU 10 80987100 80987100 single base substitution C T intron_variant BRCA-EU 10 80987398 80987398 single base substitution G C intron_variant BRCA-EU 10 80988776 80988776 single base substitution G A intron_variant BRCA-EU 10 80990291 80990291 single base substitution C T intron_variant BRCA-EU 10 80990705 80990705 single base substitution C G intron_variant BRCA-EU 10 80991293 80991293 single base substitution G T intron_variant BRCA-EU 10 80991519 80991519 single base substitution G C intron_variant BRCA-EU 10 80991920 80991920 single base substitution G A intron_variant BRCA-EU 10 80992699 80992699 single base substitution G T intron_variant BRCA-EU 10 80992767 80992767 single base substitution C T intron_variant BRCA-EU 10 80995179 80995179 single base substitution C T intron_variant BRCA-EU 10 80995200 80995200 single base substitution C G intron_variant BRCA-EU 10 80995737 80995737 single base substitution C T intron_variant BRCA-EU 10 80996979 80996979 single base substitution G A intron_variant BRCA-EU 10 80996990 80996990 single base substitution G A intron_variant BRCA-EU 10 80997633 80997633 single base substitution C A intron_variant BRCA-EU 10 80998441 80998441 single base substitution G A intron_variant BRCA-EU 10 80998441 80998441 single base substitution G A upstream_gene_variant BRCA-EU 10 80999390 80999390 single base substitution C T intron_variant BRCA-EU 10 80999390 80999390 single base substitution C T upstream_gene_variant BRCA-EU 10 81000488 81000488 single base substitution C T intron_variant BRCA-EU 10 81000488 81000488 single base substitution C T upstream_gene_variant BRCA-EU 10 81001927 81001927 single base substitution G T intron_variant BRCA-EU 10 81001927 81001927 single base substitution G T upstream_gene_variant BRCA-EU 10 81002206 81002206 single base substitution G T intron_variant BRCA-EU 10 81002206 81002206 single base substitution G T upstream_gene_variant BRCA-EU 10 81004263 81004263 deletion of <=200bp G - intron_variant BRCA-EU 10 81004884 81004884 single base substitution C T intron_variant BRCA-EU 10 81005926 81005926 single base substitution G C intron_variant BRCA-EU 10 81006499 81006499 single base substitution A G intron_variant BRCA-EU 10 81006876 81006876 insertion of <=200bp - T intron_variant BRCA-EU 10 81007513 81007513 single base substitution C A intron_variant BRCA-EU 10 81008748 81008748 single base substitution A G intron_variant BRCA-EU 10 81008781 81008781 single base substitution G A intron_variant BRCA-EU 10 81009738 81009738 single base substitution C T intron_variant BRCA-EU 10 81009826 81009826 single base substitution G C intron_variant BRCA-EU 10 81010691 81010692 deletion of <=200bp AG - intron_variant BRCA-EU 10 81010719 81010719 single base substitution G C intron_variant BRCA-EU 10 81011102 81011102 single base substitution G A intron_variant BRCA-EU 10 81013056 81013056 single base substitution G C intron_variant BRCA-EU 10 81013886 81013886 single base substitution G A intron_variant BRCA-EU 10 81014091 81014091 single base substitution G A intron_variant BRCA-EU 10 81014449 81014449 single base substitution G A intron_variant BRCA-EU 10 81015228 81015228 single base substitution G C intron_variant BRCA-EU 10 81015979 81015979 single base substitution A C intron_variant BRCA-EU 10 81020652 81020652 single base substitution C T intron_variant BRCA-EU 10 81021197 81021197 single base substitution T A intron_variant BRCA-EU 10 81021198 81021198 single base substitution G T intron_variant BRCA-EU 10 81023317 81023317 single base substitution G A intron_variant BRCA-EU 10 81023370 81023370 single base substitution C A intron_variant BRCA-EU 10 81026716 81026716 single base substitution C T intron_variant BRCA-EU 10 81028561 81028561 single base substitution C A intron_variant BRCA-EU 10 81028992 81028992 single base substitution A G intron_variant BRCA-EU 10 81030161 81030161 single base substitution G A intron_variant BRCA-EU 10 81030805 81030805 single base substitution G T intron_variant BRCA-EU 10 81031468 81031468 single base substitution A C intron_variant BRCA-EU 10 81032905 81032905 single base substitution A G intron_variant BRCA-EU 10 81032905 81032905 single base substitution A G upstream_gene_variant BRCA-EU 10 81033661 81033661 single base substitution A T intron_variant BRCA-EU 10 81033661 81033661 single base substitution A T upstream_gene_variant BRCA-EU 10 81033726 81033726 single base substitution G A intron_variant BRCA-EU 10 81033726 81033726 single base substitution G A upstream_gene_variant BRCA-EU 10 81038349 81038349 single base substitution G A intron_variant BRCA-EU 10 81039061 81039061 single base substitution G C intron_variant BRCA-EU 10 81039226 81039226 single base substitution C G intron_variant BRCA-EU 10 81040052 81040052 single base substitution G C intron_variant BRCA-EU 10 81040730 81040730 single base substitution A G intron_variant BRCA-EU 10 81041079 81041079 single base substitution A G intron_variant BRCA-EU 10 81041774 81041774 single base substitution C T intron_variant BRCA-EU 10 81042170 81042170 single base substitution G A intron_variant BRCA-EU 10 81044084 81044097 deletion of <=200bp CCTTAAAGGGAGTA - intron_variant BRCA-EU 10 81044319 81044319 single base substitution G A intron_variant BRCA-EU 10 81044515 81044516 deletion of <=200bp TG - intron_variant BRCA-EU 10 81045341 81045341 single base substitution A G intron_variant BRCA-EU 10 81046670 81046670 single base substitution A T intron_variant BRCA-EU 10 81047800 81047800 single base substitution G C intron_variant BRCA-EU 10 81047987 81047987 single base substitution G A intron_variant BRCA-EU 10 81048517 81048517 single base substitution G C intron_variant BRCA-EU 10 81053112 81053112 single base substitution C T downstream_gene_variant BRCA-EU 10 81053112 81053112 single base substitution C T intron_variant BRCA-EU 10 81053116 81053116 single base substitution G A downstream_gene_variant BRCA-EU 10 81053116 81053116 single base substitution G A intron_variant BRCA-EU 10 81054793 81054793 single base substitution G T downstream_gene_variant BRCA-EU 10 81054793 81054793 single base substitution G T exon_variant BRCA-EU 10 81054793 81054793 single base substitution G T intron_variant BRCA-EU 10 81055765 81055765 single base substitution G C downstream_gene_variant BRCA-EU 10 81055765 81055765 single base substitution G C exon_variant BRCA-EU 10 81055765 81055765 single base substitution G C intron_variant BRCA-EU 10 81056177 81056177 single base substitution G T exon_variant BRCA-EU 10 81056177 81056177 single base substitution G T intron_variant BRCA-EU 10 81056317 81056317 single base substitution C T exon_variant BRCA-EU 10 81056317 81056317 single base substitution C T synonymous_variant L440L 1320C>T BRCA-EU 10 81057684 81057684 single base substitution G A downstream_gene_variant BRCA-EU 10 81057684 81057684 single base substitution G A intron_variant BRCA-EU 10 81058422 81058422 single base substitution G T downstream_gene_variant BRCA-EU 10 81058422 81058422 single base substitution G T intron_variant BRCA-EU 10 81059686 81059686 single base substitution C T downstream_gene_variant BRCA-EU 10 81059686 81059686 single base substitution C T intron_variant BRCA-EU 10 81061323 81061323 single base substitution T G downstream_gene_variant BRCA-EU 10 81061323 81061323 single base substitution T G intron_variant BRCA-EU 10 81061323 81061323 single base substitution T G upstream_gene_variant BRCA-EU 10 81063144 81063144 single base substitution C T intron_variant BRCA-EU 10 81063144 81063144 single base substitution C T upstream_gene_variant BRCA-EU 10 81066040 81066040 single base substitution G A synonymous_variant P22P 66G>A BRCA-EU 10 81066040 81066040 single base substitution G A synonymous_variant P869P 2607G>A BRCA-EU 10 81069551 81069551 single base substitution G A intron_variant BRCA-EU 10 81069687 81069687 single base substitution G A intron_variant BRCA-EU 10 81070143 81070143 single base substitution C T intron_variant BRCA-EU 10 81070950 81070950 single base substitution G A intron_variant BRCA-EU 10 81071318 81071318 single base substitution G A intron_variant BRCA-EU 10 81071857 81071857 single base substitution C G intron_variant BRCA-EU 10 81071879 81071879 single base substitution C G intron_variant BRCA-EU 10 81072954 81072954 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 81072954 81072954 single base substitution G A downstream_gene_variant BRCA-EU 10 81073108 81073108 single base substitution G C 3_prime_UTR_variant BRCA-EU 10 81073108 81073108 single base substitution G C downstream_gene_variant BRCA-EU 10 81073592 81073592 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 81073592 81073592 single base substitution C G downstream_gene_variant BRCA-EU 10 81074022 81074022 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 81074022 81074022 single base substitution G A downstream_gene_variant BRCA-EU 10 81074437 81074437 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 81074437 81074437 single base substitution C G downstream_gene_variant BRCA-EU 10 81074548 81074548 single base substitution T C 3_prime_UTR_variant BRCA-EU 10 81074548 81074548 single base substitution T C downstream_gene_variant BRCA-EU 10 81074651 81074651 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 81074651 81074651 single base substitution C T downstream_gene_variant BRCA-EU 10 81074683 81074683 single base substitution T G 3_prime_UTR_variant BRCA-EU 10 81074683 81074683 single base substitution T G downstream_gene_variant BRCA-EU 10 81074832 81074832 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 81074832 81074832 single base substitution C G downstream_gene_variant BRCA-EU 10 81074973 81074973 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 81074973 81074973 single base substitution C T downstream_gene_variant BRCA-EU 10 81075369 81075369 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 81075369 81075369 single base substitution C T downstream_gene_variant BRCA-EU 10 81075439 81075439 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 81075439 81075439 single base substitution G A downstream_gene_variant BRCA-EU 10 81075613 81075613 single base substitution A G 3_prime_UTR_variant BRCA-EU 10 81075613 81075613 single base substitution A G downstream_gene_variant BRCA-EU 10 81076030 81076030 single base substitution G T 3_prime_UTR_variant BRCA-EU 10 81076030 81076030 single base substitution G T downstream_gene_variant BRCA-EU 10 81076052 81076052 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 81076052 81076052 single base substitution C G downstream_gene_variant BRCA-EU 10 81076174 81076174 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 81076174 81076174 single base substitution C G downstream_gene_variant BRCA-EU 10 81076394 81076394 single base substitution T C downstream_gene_variant BRCA-EU 10 81076395 81076395 single base substitution G T downstream_gene_variant BRCA-EU 10 81076440 81076440 single base substitution G A downstream_gene_variant BRCA-EU 10 81076557 81076557 single base substitution G C downstream_gene_variant BRCA-EU 10 81076836 81076836 single base substitution C T downstream_gene_variant BRCA-EU 10 81077773 81077773 single base substitution G A downstream_gene_variant BRCA-EU 10 81079104 81079104 single base substitution G C downstream_gene_variant BRCA-EU 10 81079259 81079259 single base substitution G A downstream_gene_variant BRCA-EU 10 81079428 81079428 single base substitution G C downstream_gene_variant BRCA-EU 10 81081215 81081215 single base substitution G A downstream_gene_variant BRCA-FR 10 80831114 80831114 single base substitution G C intron_variant BRCA-FR 10 80831194 80831194 single base substitution G C intron_variant BRCA-FR 10 80846458 80846458 single base substitution G C intron_variant BRCA-FR 10 80861767 80861767 single base substitution C A intron_variant BRCA-FR 10 80861861 80861861 single base substitution C A intron_variant BRCA-FR 10 80867115 80867115 single base substitution C T intron_variant BRCA-FR 10 80874499 80874499 single base substitution C T intron_variant BRCA-FR 10 80877875 80877875 single base substitution C T intron_variant BRCA-FR 10 80888271 80888271 single base substitution A G intron_variant BRCA-FR 10 80892507 80892507 single base substitution C T intron_variant BRCA-FR 10 80899198 80899198 single base substitution G A intron_variant BRCA-FR 10 80935094 80935094 single base substitution T A intron_variant BRCA-FR 10 80940339 80940339 single base substitution C T intron_variant BRCA-FR 10 80943951 80943951 single base substitution G A intron_variant BRCA-FR 10 80954880 80954880 single base substitution C T intron_variant BRCA-FR 10 80973644 80973644 single base substitution G C intron_variant BRCA-FR 10 80981086 80981086 single base substitution C T intron_variant BRCA-FR 10 80987851 80987851 single base substitution C T intron_variant BRCA-FR 10 80988776 80988776 single base substitution G A intron_variant BRCA-FR 10 80990291 80990291 single base substitution C T intron_variant BRCA-FR 10 81005589 81005589 single base substitution G C intron_variant BRCA-FR 10 81011516 81011516 single base substitution A G intron_variant BRCA-FR 10 81013886 81013886 single base substitution G A intron_variant BRCA-FR 10 81018081 81018081 single base substitution C T intron_variant BRCA-FR 10 81018771 81018771 single base substitution A G intron_variant BRCA-FR 10 81033517 81033517 single base substitution C T intron_variant BRCA-FR 10 81033517 81033517 single base substitution C T upstream_gene_variant BRCA-FR 10 81048517 81048517 single base substitution G C intron_variant BRCA-FR 10 81053116 81053116 single base substitution G A downstream_gene_variant BRCA-FR 10 81053116 81053116 single base substitution G A intron_variant BRCA-FR 10 81076440 81076440 single base substitution G A downstream_gene_variant BRCA-FR 10 81076557 81076557 single base substitution G C downstream_gene_variant BRCA-FR 10 81079314 81079314 single base substitution C T downstream_gene_variant BRCA-UK 10 80887186 80887186 single base substitution G A intron_variant BRCA-UK 10 80887208 80887208 single base substitution G A intron_variant BRCA-UK 10 80891362 80891362 single base substitution T G intron_variant BRCA-UK 10 80915034 80915034 single base substitution G C intron_variant BRCA-UK 10 80948035 80948035 single base substitution G A intron_variant BRCA-UK 10 80952521 80952521 single base substitution C T intron_variant BRCA-UK 10 80966692 80966692 single base substitution A T intron_variant BRCA-UK 10 81001157 81001157 single base substitution G A intron_variant BRCA-UK 10 81001157 81001157 single base substitution G A upstream_gene_variant BRCA-UK 10 81014449 81014449 single base substitution G A intron_variant BRCA-UK 10 81023317 81023317 single base substitution G A intron_variant BRCA-UK 10 81028561 81028561 single base substitution C A intron_variant BRCA-UK 10 81042880 81042880 single base substitution C G intron_variant BRCA-UK 10 81046670 81046670 single base substitution A T intron_variant BRCA-UK 10 81072181 81072181 single base substitution G C intron_variant BRCA-UK 10 81073108 81073108 single base substitution G C 3_prime_UTR_variant BRCA-UK 10 81073108 81073108 single base substitution G C downstream_gene_variant BRCA-US 10 81058277 81058277 single base substitution G A downstream_gene_variant BRCA-US 10 81058277 81058277 single base substitution G A missense_variant V536I 1606G>A BRCA-US 10 81060562 81060562 single base substitution G A downstream_gene_variant BRCA-US 10 81060562 81060562 single base substitution G A missense_variant V628M 1882G>A BRCA-US 10 81063837 81063837 single base substitution G T missense_variant V731L 2191G>T BRCA-US 10 81063837 81063837 single base substitution G T upstream_gene_variant BRCA-US 10 81067225 81067225 single base substitution T G missense_variant M64R 191T>G BRCA-US 10 81067225 81067225 single base substitution T G missense_variant M911R 2732T>G BRCA-US 10 81067261 81067261 single base substitution A C missense_variant H76P 227A>C BRCA-US 10 81067261 81067261 single base substitution A C missense_variant H923P 2768A>C BRCA-US 10 81072445 81072445 insertion of <=200bp - C frameshift_variant D1048A? BRCA-US 10 81072445 81072445 insertion of <=200bp - C frameshift_variant D114A? BTCA-JP 10 80961382 80961382 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BTCA-JP 10 80976041 80976041 single base substitution C T intron_variant BTCA-JP 10 81003562 81003562 single base substitution C T intron_variant BTCA-JP 10 81045354 81045354 single base substitution T C intron_variant BTCA-JP 10 81058188 81058188 single base substitution A G downstream_gene_variant BTCA-JP 10 81058188 81058188 single base substitution A G missense_variant N506S 1517A>G CESC-US 10 81070690 81070690 single base substitution G A intron_variant CESC-US 10 81070690 81070690 single base substitution G A missense_variant A949T 2845G>A CESC-US 10 81070929 81070929 single base substitution G A intron_variant CESC-US 10 81070929 81070929 single base substitution G A synonymous_variant E1028E 3084G>A CLLE-ES 10 80878977 80878977 single base substitution A T intron_variant CLLE-ES 10 80889041 80889041 single base substitution G A intron_variant CLLE-ES 10 80911809 80911821 deletion of <=200bp CCGGGCTCTAGGG - intron_variant CLLE-ES 10 80913636 80913636 single base substitution A G intron_variant CLLE-ES 10 80924520 80924520 single base substitution G C intron_variant CLLE-ES 10 80961969 80961969 single base substitution A G intron_variant CLLE-ES 10 80971605 80971605 single base substitution C T intron_variant CLLE-ES 10 80981285 80981285 single base substitution C T intron_variant CLLE-ES 10 81008302 81008302 single base substitution G A intron_variant CLLE-ES 10 81052899 81052899 single base substitution A C downstream_gene_variant CLLE-ES 10 81052899 81052899 single base substitution A C intron_variant CLLE-ES 10 81074541 81074541 single base substitution C T 3_prime_UTR_variant CLLE-ES 10 81074541 81074541 single base substitution C T downstream_gene_variant COAD-US 10 80976011 80976011 single base substitution A G missense_variant K87R 260A>G COAD-US 10 81037001 81037001 single base substitution G A exon_variant COAD-US 10 81037001 81037001 single base substitution G A missense_variant R115H 344G>A COAD-US 10 81037008 81037008 single base substitution C T exon_variant COAD-US 10 81037008 81037008 single base substitution C T synonymous_variant S117S 351C>T COAD-US 10 81060579 81060579 single base substitution C T downstream_gene_variant COAD-US 10 81060579 81060579 single base substitution C T synonymous_variant N633N 1899C>T COAD-US 10 81066067 81066067 single base substitution A C synonymous_variant P31P 93A>C COAD-US 10 81066067 81066067 single base substitution A C synonymous_variant P878P 2634A>C COAD-US 10 81070801 81070801 single base substitution C T intron_variant COAD-US 10 81070801 81070801 single base substitution C T missense_variant P986S 2956C>T COAD-US 10 81070899 81070899 single base substitution C T intron_variant COAD-US 10 81070899 81070899 single base substitution C T synonymous_variant A1018A 3054C>T COAD-US 10 81070913 81070913 single base substitution C T intron_variant COAD-US 10 81070913 81070913 single base substitution C T missense_variant A1023V 3068C>T COAD-US 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D1048 COAD-US 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D114 COCA-CN 10 80829662 80829662 single base substitution C T intron_variant COCA-CN 10 80830551 80830551 single base substitution T C intron_variant COCA-CN 10 80835342 80835342 single base substitution A C intron_variant COCA-CN 10 80853077 80853077 single base substitution T G intron_variant COCA-CN 10 80874294 80874294 single base substitution G A intron_variant COCA-CN 10 80880199 80880199 single base substitution C T intron_variant COCA-CN 10 80889030 80889030 single base substitution C T intron_variant COCA-CN 10 80906710 80906710 single base substitution T C intron_variant COCA-CN 10 80916381 80916381 single base substitution C G intron_variant COCA-CN 10 80918487 80918487 single base substitution G C intron_variant COCA-CN 10 80961350 80961350 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 10 80964632 80964632 single base substitution G A intron_variant COCA-CN 10 80976150 80976150 single base substitution G A intron_variant COCA-CN 10 80978364 80978364 single base substitution C G intron_variant COCA-CN 10 80980626 80980626 single base substitution T C intron_variant COCA-CN 10 80982381 80982381 single base substitution G A intron_variant COCA-CN 10 80985328 80985328 single base substitution T A intron_variant COCA-CN 10 80997486 80997486 single base substitution A T intron_variant COCA-CN 10 81002310 81002310 single base substitution T C intron_variant COCA-CN 10 81002310 81002310 single base substitution T C upstream_gene_variant COCA-CN 10 81003522 81003522 single base substitution G A intron_variant COCA-CN 10 81032272 81032272 single base substitution G A intron_variant COCA-CN 10 81032272 81032272 single base substitution G A upstream_gene_variant COCA-CN 10 81050508 81050508 single base substitution G A intron_variant COCA-CN 10 81050704 81050704 single base substitution C A intron_variant COCA-CN 10 81051440 81051440 single base substitution C T downstream_gene_variant COCA-CN 10 81051440 81051440 single base substitution C T intron_variant COCA-CN 10 81056211 81056211 single base substitution T G exon_variant COCA-CN 10 81056211 81056211 single base substitution T G intron_variant COCA-CN 10 81056286 81056286 single base substitution A G exon_variant COCA-CN 10 81056286 81056286 single base substitution A G missense_variant Q430R 1289A>G COCA-CN 10 81057335 81057335 single base substitution C T downstream_gene_variant COCA-CN 10 81057335 81057335 single base substitution C T intron_variant COCA-CN 10 81058122 81058122 single base substitution C T downstream_gene_variant COCA-CN 10 81058122 81058122 single base substitution C T intron_variant COCA-CN 10 81060474 81060474 single base substitution T C downstream_gene_variant COCA-CN 10 81060474 81060474 single base substitution T C intron_variant COCA-CN 10 81060585 81060585 single base substitution G A downstream_gene_variant COCA-CN 10 81060585 81060585 single base substitution G A synonymous_variant T635T 1905G>A COCA-CN 10 81060724 81060724 single base substitution C T downstream_gene_variant COCA-CN 10 81060724 81060724 single base substitution C T intron_variant COCA-CN 10 81065337 81065337 single base substitution G A missense_variant G801E 2402G>A COCA-CN 10 81065337 81065337 single base substitution G A upstream_gene_variant COCA-CN 10 81067040 81067040 single base substitution C T intron_variant COCA-CN 10 81073763 81073763 single base substitution G C 3_prime_UTR_variant COCA-CN 10 81073763 81073763 single base substitution G C downstream_gene_variant COCA-CN 10 81075077 81075077 single base substitution C A 3_prime_UTR_variant COCA-CN 10 81075077 81075077 single base substitution C A downstream_gene_variant EOPC-DE 10 80835342 80835342 single base substitution A C intron_variant EOPC-DE 10 80842885 80842885 single base substitution T C intron_variant EOPC-DE 10 80851784 80851784 single base substitution G C intron_variant EOPC-DE 10 80889098 80889098 single base substitution G A intron_variant EOPC-DE 10 80942855 80942855 single base substitution G C intron_variant EOPC-DE 10 81046319 81046319 single base substitution G C intron_variant EOPC-DE 10 81079238 81079238 single base substitution T C downstream_gene_variant ESAD-UK 10 80826668 80826668 single base substitution G A upstream_gene_variant ESAD-UK 10 80828041 80828041 single base substitution A G upstream_gene_variant ESAD-UK 10 80828614 80828614 single base substitution T G upstream_gene_variant ESAD-UK 10 80828702 80828702 single base substitution C A upstream_gene_variant ESAD-UK 10 80832307 80832307 single base substitution C G intron_variant ESAD-UK 10 80838030 80838030 single base substitution G T intron_variant ESAD-UK 10 80840221 80840221 single base substitution A G intron_variant ESAD-UK 10 80841986 80841986 single base substitution A G intron_variant ESAD-UK 10 80842051 80842051 single base substitution T A intron_variant ESAD-UK 10 80842389 80842389 insertion of <=200bp - CCTC intron_variant ESAD-UK 10 80845608 80845608 single base substitution G A intron_variant ESAD-UK 10 80846104 80846104 single base substitution A G intron_variant ESAD-UK 10 80847639 80847639 single base substitution T G intron_variant ESAD-UK 10 80847697 80847697 deletion of <=200bp C - intron_variant ESAD-UK 10 80847886 80847886 single base substitution C T intron_variant ESAD-UK 10 80848090 80848090 single base substitution T A intron_variant ESAD-UK 10 80850976 80850976 deletion of <=200bp C - intron_variant ESAD-UK 10 80855797 80855797 single base substitution C T intron_variant ESAD-UK 10 80856394 80856394 single base substitution G A intron_variant ESAD-UK 10 80858425 80858425 single base substitution G T intron_variant ESAD-UK 10 80861301 80861301 single base substitution C T intron_variant ESAD-UK 10 80862231 80862232 deletion of <=200bp GT - intron_variant ESAD-UK 10 80863573 80863573 single base substitution C T intron_variant ESAD-UK 10 80866906 80866906 single base substitution C T intron_variant ESAD-UK 10 80867603 80867603 single base substitution A C intron_variant ESAD-UK 10 80869431 80869431 single base substitution C G intron_variant ESAD-UK 10 80874406 80874406 single base substitution C T intron_variant ESAD-UK 10 80876290 80876290 single base substitution A T intron_variant ESAD-UK 10 80877392 80877392 single base substitution A G intron_variant ESAD-UK 10 80878791 80878791 single base substitution A G intron_variant ESAD-UK 10 80879203 80879203 single base substitution A G intron_variant ESAD-UK 10 80881323 80881323 single base substitution T G intron_variant ESAD-UK 10 80884016 80884016 single base substitution A G intron_variant ESAD-UK 10 80891972 80891972 single base substitution G A intron_variant ESAD-UK 10 80892739 80892739 single base substitution A T intron_variant ESAD-UK 10 80895272 80895272 single base substitution C A intron_variant ESAD-UK 10 80895762 80895762 single base substitution T C intron_variant ESAD-UK 10 80900570 80900570 single base substitution C T intron_variant ESAD-UK 10 80901990 80901990 single base substitution G A intron_variant ESAD-UK 10 80903681 80903681 single base substitution G A intron_variant ESAD-UK 10 80903880 80903880 single base substitution G A intron_variant ESAD-UK 10 80903928 80903931 deletion of <=200bp CCTA - intron_variant ESAD-UK 10 80905024 80905024 single base substitution C G intron_variant ESAD-UK 10 80905178 80905178 single base substitution A T intron_variant ESAD-UK 10 80908371 80908371 single base substitution C T intron_variant ESAD-UK 10 80909211 80909211 single base substitution T G intron_variant ESAD-UK 10 80911649 80911649 single base substitution C T intron_variant ESAD-UK 10 80912738 80912738 single base substitution G A intron_variant ESAD-UK 10 80915150 80915150 single base substitution C T intron_variant ESAD-UK 10 80915984 80915984 single base substitution G A intron_variant ESAD-UK 10 80922133 80922133 single base substitution G T intron_variant ESAD-UK 10 80924523 80924523 single base substitution T G intron_variant ESAD-UK 10 80924607 80924607 single base substitution A G intron_variant ESAD-UK 10 80929042 80929042 single base substitution G A intron_variant ESAD-UK 10 80929403 80929403 single base substitution C A intron_variant ESAD-UK 10 80929599 80929599 single base substitution G C intron_variant ESAD-UK 10 80930746 80930746 single base substitution C T intron_variant ESAD-UK 10 80931865 80931865 single base substitution A C intron_variant ESAD-UK 10 80933059 80933059 insertion of <=200bp - T intron_variant ESAD-UK 10 80933442 80933442 single base substitution G A intron_variant ESAD-UK 10 80934562 80934562 single base substitution G A intron_variant ESAD-UK 10 80934704 80934704 single base substitution T A intron_variant ESAD-UK 10 80939838 80939838 single base substitution G A intron_variant ESAD-UK 10 80940088 80940088 single base substitution A G intron_variant ESAD-UK 10 80946633 80946633 single base substitution C T intron_variant ESAD-UK 10 80953726 80953726 single base substitution A C intron_variant ESAD-UK 10 80953879 80953879 single base substitution C T intron_variant ESAD-UK 10 80955029 80955029 single base substitution C T intron_variant ESAD-UK 10 80955374 80955374 single base substitution A C intron_variant ESAD-UK 10 80955481 80955481 single base substitution T G intron_variant ESAD-UK 10 80960761 80960761 single base substitution G A intron_variant ESAD-UK 10 80961553 80961553 single base substitution G A intron_variant ESAD-UK 10 80968159 80968159 single base substitution C T missense_variant R43W 127C>T ESAD-UK 10 80968338 80968338 single base substitution G C intron_variant ESAD-UK 10 80968352 80968352 single base substitution G T intron_variant ESAD-UK 10 80969855 80969855 single base substitution G A intron_variant ESAD-UK 10 80971016 80971016 single base substitution C T intron_variant ESAD-UK 10 80971561 80971561 single base substitution A G intron_variant ESAD-UK 10 80973466 80973466 single base substitution A G intron_variant ESAD-UK 10 80974421 80974421 single base substitution C T intron_variant ESAD-UK 10 80975336 80975336 single base substitution G T intron_variant ESAD-UK 10 80975865 80975865 single base substitution G T intron_variant ESAD-UK 10 80975911 80975911 single base substitution C T intron_variant ESAD-UK 10 80976212 80976212 single base substitution G A intron_variant ESAD-UK 10 80976270 80976270 single base substitution G A intron_variant ESAD-UK 10 80981000 80981000 single base substitution C A intron_variant ESAD-UK 10 80991091 80991091 single base substitution G A intron_variant ESAD-UK 10 80992667 80992667 single base substitution A T intron_variant ESAD-UK 10 80993017 80993017 single base substitution C T intron_variant ESAD-UK 10 80994950 80994950 single base substitution G A intron_variant ESAD-UK 10 80998130 80998130 single base substitution C T intron_variant ESAD-UK 10 80999969 80999969 single base substitution C T intron_variant ESAD-UK 10 80999969 80999969 single base substitution C T upstream_gene_variant ESAD-UK 10 81000059 81000059 single base substitution G A intron_variant ESAD-UK 10 81000059 81000059 single base substitution G A upstream_gene_variant ESAD-UK 10 81000068 81000068 single base substitution G T intron_variant ESAD-UK 10 81000068 81000068 single base substitution G T upstream_gene_variant ESAD-UK 10 81001314 81001314 single base substitution T C intron_variant ESAD-UK 10 81001314 81001314 single base substitution T C upstream_gene_variant ESAD-UK 10 81001934 81001934 single base substitution G A intron_variant ESAD-UK 10 81001934 81001934 single base substitution G A upstream_gene_variant ESAD-UK 10 81002027 81002027 single base substitution A G intron_variant ESAD-UK 10 81002027 81002027 single base substitution A G upstream_gene_variant ESAD-UK 10 81002474 81002474 single base substitution C A intron_variant ESAD-UK 10 81002474 81002474 single base substitution C A upstream_gene_variant ESAD-UK 10 81002488 81002488 single base substitution G A intron_variant ESAD-UK 10 81002488 81002488 single base substitution G A upstream_gene_variant ESAD-UK 10 81002967 81002967 single base substitution G A intron_variant ESAD-UK 10 81002967 81002967 single base substitution G A upstream_gene_variant ESAD-UK 10 81003225 81003225 single base substitution G A intron_variant ESAD-UK 10 81003225 81003225 single base substitution G A upstream_gene_variant ESAD-UK 10 81003326 81003326 single base substitution C T intron_variant ESAD-UK 10 81003326 81003326 single base substitution C T upstream_gene_variant ESAD-UK 10 81003462 81003462 single base substitution G A exon_variant ESAD-UK 10 81003462 81003462 single base substitution G A intron_variant ESAD-UK 10 81004466 81004466 single base substitution G A intron_variant ESAD-UK 10 81008570 81008570 single base substitution G A intron_variant ESAD-UK 10 81008890 81008890 single base substitution C A intron_variant ESAD-UK 10 81009120 81009120 single base substitution C T intron_variant ESAD-UK 10 81009132 81009132 single base substitution C G intron_variant ESAD-UK 10 81009136 81009136 single base substitution G T intron_variant ESAD-UK 10 81009394 81009394 single base substitution A T intron_variant ESAD-UK 10 81009474 81009474 single base substitution T C intron_variant ESAD-UK 10 81010419 81010419 single base substitution A G intron_variant ESAD-UK 10 81013860 81013860 single base substitution T A intron_variant ESAD-UK 10 81013982 81013982 single base substitution C A intron_variant ESAD-UK 10 81014168 81014168 single base substitution G T intron_variant ESAD-UK 10 81018714 81018714 single base substitution G A intron_variant ESAD-UK 10 81020151 81020151 single base substitution A G intron_variant ESAD-UK 10 81020214 81020214 single base substitution G A intron_variant ESAD-UK 10 81020830 81020830 single base substitution C T intron_variant ESAD-UK 10 81025034 81025034 single base substitution G A intron_variant ESAD-UK 10 81025844 81025844 single base substitution C T intron_variant ESAD-UK 10 81026766 81026766 single base substitution C T intron_variant ESAD-UK 10 81027162 81027162 single base substitution A G intron_variant ESAD-UK 10 81031710 81031710 single base substitution T G intron_variant ESAD-UK 10 81031712 81031712 single base substitution G T intron_variant ESAD-UK 10 81034164 81034164 single base substitution G A intron_variant ESAD-UK 10 81034164 81034164 single base substitution G A upstream_gene_variant ESAD-UK 10 81035941 81035941 single base substitution A T intron_variant ESAD-UK 10 81035941 81035941 single base substitution A T upstream_gene_variant ESAD-UK 10 81036259 81036259 single base substitution G C intron_variant ESAD-UK 10 81036259 81036259 single base substitution G C upstream_gene_variant ESAD-UK 10 81039057 81039057 single base substitution C T intron_variant ESAD-UK 10 81041317 81041317 single base substitution A G intron_variant ESAD-UK 10 81042067 81042067 single base substitution G A intron_variant ESAD-UK 10 81043183 81043183 single base substitution C T intron_variant ESAD-UK 10 81044832 81044832 single base substitution G A intron_variant ESAD-UK 10 81046238 81046238 single base substitution C T intron_variant ESAD-UK 10 81046379 81046379 single base substitution C T intron_variant ESAD-UK 10 81053253 81053253 single base substitution C T downstream_gene_variant ESAD-UK 10 81053253 81053253 single base substitution C T exon_variant ESAD-UK 10 81053253 81053253 single base substitution C T missense_variant S358L 1073C>T ESAD-UK 10 81053883 81053883 single base substitution G T downstream_gene_variant ESAD-UK 10 81053883 81053883 single base substitution G T exon_variant ESAD-UK 10 81053883 81053883 single base substitution G T intron_variant ESAD-UK 10 81056299 81056299 single base substitution C A exon_variant ESAD-UK 10 81056299 81056299 single base substitution C A synonymous_variant P434P 1302C>A ESAD-UK 10 81057227 81057227 single base substitution G A downstream_gene_variant ESAD-UK 10 81057227 81057227 single base substitution G A intron_variant ESAD-UK 10 81057611 81057611 single base substitution A C downstream_gene_variant ESAD-UK 10 81057611 81057611 single base substitution A C intron_variant ESAD-UK 10 81058983 81058983 single base substitution G A downstream_gene_variant ESAD-UK 10 81058983 81058983 single base substitution G A intron_variant ESAD-UK 10 81061167 81061167 single base substitution C T downstream_gene_variant ESAD-UK 10 81061167 81061167 single base substitution C T intron_variant ESAD-UK 10 81061167 81061167 single base substitution C T upstream_gene_variant ESAD-UK 10 81061737 81061737 single base substitution G C intron_variant ESAD-UK 10 81061737 81061737 single base substitution G C upstream_gene_variant ESAD-UK 10 81061860 81061860 single base substitution G A splice_region_variant ESAD-UK 10 81061860 81061860 single base substitution G A upstream_gene_variant ESAD-UK 10 81065737 81065737 single base substitution G A intron_variant ESAD-UK 10 81065737 81065737 single base substitution G A upstream_gene_variant ESAD-UK 10 81066425 81066425 single base substitution G C intron_variant ESAD-UK 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D1048 ESAD-UK 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D114 ESAD-UK 10 81073432 81073432 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 81073432 81073432 single base substitution G A downstream_gene_variant ESAD-UK 10 81080167 81080167 single base substitution C T downstream_gene_variant ESCA-CN 10 81051960 81051960 single base substitution G A downstream_gene_variant ESCA-CN 10 81051960 81051960 single base substitution G A exon_variant ESCA-CN 10 81051960 81051960 single base substitution G A synonymous_variant P268P 804G>A ESCA-CN 10 81053560 81053560 single base substitution G A downstream_gene_variant ESCA-CN 10 81053560 81053560 single base substitution G A exon_variant ESCA-CN 10 81053560 81053560 single base substitution G A intron_variant ESCA-CN 10 81065774 81065774 single base substitution G T intron_variant ESCA-CN 10 81065774 81065774 single base substitution G T upstream_gene_variant ESCA-CN 10 81073763 81073763 single base substitution G C 3_prime_UTR_variant ESCA-CN 10 81073763 81073763 single base substitution G C downstream_gene_variant ESCA-CN 10 81074222 81074222 single base substitution C G 3_prime_UTR_variant ESCA-CN 10 81074222 81074222 single base substitution C G downstream_gene_variant GBM-US 10 81058831 81058831 single base substitution T G downstream_gene_variant GBM-US 10 81058831 81058831 single base substitution T G missense_variant L564R 1691T>G GBM-US 10 81061939 81061939 single base substitution C T missense_variant L699F 2095C>T GBM-US 10 81061939 81061939 single base substitution C T upstream_gene_variant GBM-US 10 81066012 81066012 single base substitution A C missense_variant E13A 38A>C GBM-US 10 81066012 81066012 single base substitution A C missense_variant E860A 2579A>C KIRC-US 10 81065919 81065919 single base substitution C T missense_variant S829L 2486C>T KIRC-US 10 81065919 81065919 single base substitution C T upstream_gene_variant KIRC-US 10 81070821 81070821 insertion of <=200bp - C frameshift_variant Q992H? KIRC-US 10 81070821 81070821 insertion of <=200bp - C intron_variant KIRP-US 10 80968102 80968102 single base substitution A T missense_variant N24Y 70A>T KIRP-US 10 81037038 81037038 single base substitution C G exon_variant KIRP-US 10 81037038 81037038 single base substitution C G synonymous_variant P127P 381C>G LAML-KR 10 80838490 80838490 single base substitution G T intron_variant LAML-KR 10 80910809 80910809 single base substitution C T intron_variant LAML-KR 10 80935361 80935361 single base substitution G A intron_variant LAML-KR 10 81025750 81025750 single base substitution A C intron_variant LAML-KR 10 81052039 81052039 single base substitution G A downstream_gene_variant LAML-KR 10 81052039 81052039 single base substitution G A exon_variant LAML-KR 10 81052039 81052039 single base substitution G A missense_variant A295T 883G>A LAML-KR 10 81053021 81053021 single base substitution A G downstream_gene_variant LAML-KR 10 81053021 81053021 single base substitution A G intron_variant LAML-KR 10 81054136 81054136 single base substitution G A downstream_gene_variant LAML-KR 10 81054136 81054136 single base substitution G A exon_variant LAML-KR 10 81054136 81054136 single base substitution G A intron_variant LAML-KR 10 81054710 81054710 single base substitution T G downstream_gene_variant LAML-KR 10 81054710 81054710 single base substitution T G exon_variant LAML-KR 10 81054710 81054710 single base substitution T G intron_variant LAML-KR 10 81060752 81060752 single base substitution G A downstream_gene_variant LAML-KR 10 81060752 81060752 single base substitution G A intron_variant LAML-KR 10 81061724 81061724 single base substitution G A intron_variant LAML-KR 10 81061724 81061724 single base substitution G A upstream_gene_variant LAML-KR 10 81065201 81065201 single base substitution G A intron_variant LAML-KR 10 81065201 81065201 single base substitution G A upstream_gene_variant LGG-US 10 81052015 81052015 single base substitution G A downstream_gene_variant LGG-US 10 81052015 81052015 single base substitution G A exon_variant LGG-US 10 81052015 81052015 single base substitution G A missense_variant A287T 859G>A LGG-US 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D1048 LGG-US 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D114 LICA-CN 10 81065963 81065963 single base substitution C T missense_variant R844W 2530C>T LICA-CN 10 81065963 81065963 single base substitution C T upstream_gene_variant LICA-FR 10 80832364 80832364 single base substitution A C intron_variant LICA-FR 10 80833596 80833596 insertion of <=200bp - AG intron_variant LICA-FR 10 80842677 80842706 deletion of <=200bp GGGCAGAGTCTGGGGTCCTTTTGTGCCTCC - intron_variant LICA-FR 10 80875992 80875992 single base substitution A C intron_variant LICA-FR 10 80887112 80887112 single base substitution C G intron_variant LICA-FR 10 80908976 80908976 deletion of <=200bp T - intron_variant LICA-FR 10 80918170 80918170 single base substitution A C intron_variant LICA-FR 10 80935357 80935357 single base substitution G A intron_variant LICA-FR 10 80936915 80936915 single base substitution G T intron_variant LICA-FR 10 80978342 80978342 insertion of <=200bp - GT intron_variant LICA-FR 10 81005039 81005039 single base substitution G A intron_variant LICA-FR 10 81044385 81044385 single base substitution C G intron_variant LICA-FR 10 81063825 81063825 single base substitution G A missense_variant G727R 2179G>A LICA-FR 10 81063825 81063825 single base substitution G A upstream_gene_variant LINC-JP 10 80833119 80833119 single base substitution A G intron_variant LINC-JP 10 80838474 80838474 single base substitution G T intron_variant LINC-JP 10 80850815 80850815 single base substitution A G intron_variant LINC-JP 10 80889429 80889429 single base substitution A G intron_variant LINC-JP 10 80917383 80917383 single base substitution C G intron_variant LINC-JP 10 80948269 80948269 single base substitution A G intron_variant LINC-JP 10 80961258 80961258 single base substitution T A intron_variant LINC-JP 10 80976074 80976074 single base substitution G A intron_variant LINC-JP 10 80986642 80986642 single base substitution A T intron_variant LINC-JP 10 81005111 81005111 single base substitution C T intron_variant LINC-JP 10 81016872 81016872 single base substitution C T intron_variant LINC-JP 10 81036523 81036523 single base substitution G A intron_variant LINC-JP 10 81036523 81036523 single base substitution G A upstream_gene_variant LINC-JP 10 81055753 81055753 single base substitution T G downstream_gene_variant LINC-JP 10 81055753 81055753 single base substitution T G exon_variant LINC-JP 10 81055753 81055753 single base substitution T G intron_variant LINC-JP 10 81058832 81058832 single base substitution C T downstream_gene_variant LINC-JP 10 81058832 81058832 single base substitution C T synonymous_variant L564L 1692C>T LINC-JP 10 81063799 81063799 single base substitution C T missense_variant A718V 2153C>T LINC-JP 10 81063799 81063799 single base substitution C T upstream_gene_variant LINC-JP 10 81064930 81064930 single base substitution C G missense_variant L766V 2296C>G LINC-JP 10 81064930 81064930 single base substitution C G upstream_gene_variant LINC-JP 10 81066111 81066111 single base substitution G A intron_variant LINC-JP 10 81067025 81067025 single base substitution C A intron_variant LINC-JP 10 81067094 81067094 single base substitution C A intron_variant LINC-JP 10 81067202 81067202 single base substitution C T synonymous_variant H56H 168C>T LINC-JP 10 81067202 81067202 single base substitution C T synonymous_variant H903H 2709C>T LINC-JP 10 81073028 81073037 deletion of <=200bp CCACCCACCA - 3_prime_UTR_variant LINC-JP 10 81073028 81073037 deletion of <=200bp CCACCCACCA - downstream_gene_variant LINC-JP 10 81073663 81073663 single base substitution A G 3_prime_UTR_variant LINC-JP 10 81073663 81073663 single base substitution A G downstream_gene_variant LINC-JP 10 81073771 81073771 deletion of <=200bp G - 3_prime_UTR_variant LINC-JP 10 81073771 81073771 deletion of <=200bp G - downstream_gene_variant LIRI-JP 10 80825529 80825529 single base substitution T C upstream_gene_variant LIRI-JP 10 80826328 80826328 single base substitution G T upstream_gene_variant LIRI-JP 10 80834032 80834032 single base substitution C T intron_variant LIRI-JP 10 80834935 80834935 single base substitution G A intron_variant LIRI-JP 10 80834991 80834991 single base substitution A G intron_variant LIRI-JP 10 80841727 80841727 single base substitution C T intron_variant LIRI-JP 10 80842191 80842191 single base substitution A G intron_variant LIRI-JP 10 80845545 80845546 deletion of <=200bp CT - intron_variant LIRI-JP 10 80846568 80846568 single base substitution T C intron_variant LIRI-JP 10 80847555 80847555 single base substitution A C intron_variant LIRI-JP 10 80848283 80848283 single base substitution G A intron_variant LIRI-JP 10 80851912 80851912 single base substitution T C intron_variant LIRI-JP 10 80853749 80853749 single base substitution C G intron_variant LIRI-JP 10 80853805 80853805 single base substitution C G intron_variant LIRI-JP 10 80853965 80853965 single base substitution C G intron_variant LIRI-JP 10 80855457 80855457 single base substitution A G intron_variant LIRI-JP 10 80858792 80858792 single base substitution C A intron_variant LIRI-JP 10 80859327 80859327 single base substitution G A intron_variant LIRI-JP 10 80864952 80864952 single base substitution T G intron_variant LIRI-JP 10 80866385 80866385 single base substitution G A intron_variant LIRI-JP 10 80868196 80868196 single base substitution G T intron_variant LIRI-JP 10 80868543 80868543 single base substitution G C intron_variant LIRI-JP 10 80869662 80869662 single base substitution C A intron_variant LIRI-JP 10 80870783 80870783 single base substitution A G intron_variant LIRI-JP 10 80871656 80871656 single base substitution G A intron_variant LIRI-JP 10 80872125 80872125 single base substitution G A intron_variant LIRI-JP 10 80872269 80872269 single base substitution C T intron_variant LIRI-JP 10 80874416 80874416 single base substitution C T intron_variant LIRI-JP 10 80876589 80876589 single base substitution C G intron_variant LIRI-JP 10 80880417 80880417 single base substitution G A intron_variant LIRI-JP 10 80883528 80883528 single base substitution A G intron_variant LIRI-JP 10 80888317 80888318 deletion of <=200bp GT - intron_variant LIRI-JP 10 80888932 80888932 single base substitution G T intron_variant LIRI-JP 10 80889637 80889637 single base substitution C G intron_variant LIRI-JP 10 80891969 80891969 single base substitution G A intron_variant LIRI-JP 10 80892792 80892792 single base substitution G T intron_variant LIRI-JP 10 80895149 80895149 single base substitution C T intron_variant LIRI-JP 10 80895194 80895194 single base substitution G A intron_variant LIRI-JP 10 80896778 80896778 single base substitution A G intron_variant LIRI-JP 10 80899719 80899719 single base substitution G T intron_variant LIRI-JP 10 80899720 80899720 single base substitution C T intron_variant LIRI-JP 10 80900492 80900492 single base substitution T G intron_variant LIRI-JP 10 80900689 80900689 single base substitution A G intron_variant LIRI-JP 10 80907431 80907431 single base substitution C A intron_variant LIRI-JP 10 80911115 80911115 single base substitution C G intron_variant LIRI-JP 10 80919939 80919939 single base substitution G A intron_variant LIRI-JP 10 80920790 80920790 single base substitution C A intron_variant LIRI-JP 10 80921322 80921322 single base substitution G T intron_variant LIRI-JP 10 80923315 80923315 single base substitution C T intron_variant LIRI-JP 10 80924251 80924251 single base substitution G T intron_variant LIRI-JP 10 80925852 80925852 single base substitution C T intron_variant LIRI-JP 10 80929490 80929490 single base substitution C A intron_variant LIRI-JP 10 80933607 80933607 single base substitution A G intron_variant LIRI-JP 10 80935972 80935972 single base substitution G A intron_variant LIRI-JP 10 80937680 80937680 single base substitution T G intron_variant LIRI-JP 10 80938323 80938323 single base substitution C A intron_variant LIRI-JP 10 80940444 80940444 single base substitution A G intron_variant LIRI-JP 10 80941738 80941738 single base substitution G A intron_variant LIRI-JP 10 80943479 80943479 single base substitution G A intron_variant LIRI-JP 10 80943598 80943598 single base substitution T A intron_variant LIRI-JP 10 80943634 80943634 single base substitution G A intron_variant LIRI-JP 10 80943867 80943867 single base substitution G A intron_variant LIRI-JP 10 80945353 80945353 single base substitution T A intron_variant LIRI-JP 10 80951301 80951301 single base substitution A G intron_variant LIRI-JP 10 80953083 80953083 single base substitution A C intron_variant LIRI-JP 10 80955284 80955293 deletion of <=200bp TTGTAGCGAC - intron_variant LIRI-JP 10 80956725 80956725 single base substitution C T intron_variant LIRI-JP 10 80956927 80956927 single base substitution A T intron_variant LIRI-JP 10 80958643 80958643 single base substitution T C intron_variant LIRI-JP 10 80960592 80960597 deletion of <=200bp CATGTG - intron_variant LIRI-JP 10 80964648 80964648 single base substitution A G intron_variant LIRI-JP 10 80964650 80964650 single base substitution G A intron_variant LIRI-JP 10 80966392 80966392 single base substitution G A intron_variant LIRI-JP 10 80966618 80966618 single base substitution T C intron_variant LIRI-JP 10 80968172 80968172 single base substitution G A missense_variant R47Q 140G>A LIRI-JP 10 80968663 80968663 single base substitution A T intron_variant LIRI-JP 10 80969944 80969944 single base substitution A G intron_variant LIRI-JP 10 80970496 80970496 single base substitution G A intron_variant LIRI-JP 10 80972402 80972402 single base substitution A C intron_variant LIRI-JP 10 80973849 80973849 single base substitution C A intron_variant LIRI-JP 10 80973927 80973927 single base substitution A G intron_variant LIRI-JP 10 80974914 80974914 single base substitution C G intron_variant LIRI-JP 10 80976031 80976031 single base substitution G T missense_variant A94S 280G>T LIRI-JP 10 80978368 80978368 single base substitution C G intron_variant LIRI-JP 10 80979065 80979065 single base substitution C T intron_variant LIRI-JP 10 80979437 80979437 single base substitution A T intron_variant LIRI-JP 10 80980268 80980268 single base substitution C T intron_variant LIRI-JP 10 80980549 80980549 single base substitution T G intron_variant LIRI-JP 10 80983362 80983362 single base substitution T C intron_variant LIRI-JP 10 80984958 80984958 single base substitution A T intron_variant LIRI-JP 10 80989548 80989548 single base substitution A G intron_variant LIRI-JP 10 80989682 80989682 single base substitution C T intron_variant LIRI-JP 10 80990794 80990794 single base substitution T G intron_variant LIRI-JP 10 80991182 80991182 single base substitution G A intron_variant LIRI-JP 10 80999088 80999088 single base substitution C G intron_variant LIRI-JP 10 80999088 80999088 single base substitution C G upstream_gene_variant LIRI-JP 10 81004976 81004976 single base substitution C G intron_variant LIRI-JP 10 81008212 81008212 single base substitution T G intron_variant LIRI-JP 10 81009191 81009191 single base substitution C T intron_variant LIRI-JP 10 81011240 81011240 single base substitution A G intron_variant LIRI-JP 10 81015057 81015057 single base substitution G A intron_variant LIRI-JP 10 81016117 81016117 single base substitution T C intron_variant LIRI-JP 10 81019659 81019659 single base substitution G A intron_variant LIRI-JP 10 81019918 81019918 single base substitution G A intron_variant LIRI-JP 10 81022246 81022246 single base substitution C G intron_variant LIRI-JP 10 81024026 81024026 single base substitution C A intron_variant LIRI-JP 10 81024030 81024030 single base substitution C T intron_variant LIRI-JP 10 81024266 81024266 single base substitution T A intron_variant LIRI-JP 10 81024510 81024510 single base substitution G T intron_variant LIRI-JP 10 81028542 81028542 single base substitution A G intron_variant LIRI-JP 10 81028596 81028596 single base substitution G T intron_variant LIRI-JP 10 81031628 81031628 single base substitution C G intron_variant LIRI-JP 10 81032499 81032499 single base substitution G T intron_variant LIRI-JP 10 81032499 81032499 single base substitution G T upstream_gene_variant LIRI-JP 10 81033318 81033318 single base substitution T G intron_variant LIRI-JP 10 81033318 81033318 single base substitution T G upstream_gene_variant LIRI-JP 10 81034322 81034322 single base substitution G C intron_variant LIRI-JP 10 81034322 81034322 single base substitution G C upstream_gene_variant LIRI-JP 10 81034384 81034389 deletion of <=200bp CGTGGC - intron_variant LIRI-JP 10 81034384 81034389 deletion of <=200bp CGTGGC - upstream_gene_variant LIRI-JP 10 81040319 81040319 single base substitution A G intron_variant LIRI-JP 10 81041253 81041253 single base substitution G A intron_variant LIRI-JP 10 81041781 81041781 single base substitution C T intron_variant LIRI-JP 10 81044460 81044460 single base substitution A G intron_variant LIRI-JP 10 81046586 81046586 single base substitution A G intron_variant LIRI-JP 10 81047114 81047114 single base substitution G T intron_variant LIRI-JP 10 81049251 81049251 single base substitution A G intron_variant LIRI-JP 10 81053741 81053741 single base substitution A G downstream_gene_variant LIRI-JP 10 81053741 81053741 single base substitution A G exon_variant LIRI-JP 10 81053741 81053741 single base substitution A G intron_variant LIRI-JP 10 81054698 81054700 deletion of <=200bp GAG - downstream_gene_variant LIRI-JP 10 81054698 81054700 deletion of <=200bp GAG - exon_variant LIRI-JP 10 81054698 81054700 deletion of <=200bp GAG - intron_variant LIRI-JP 10 81056295 81056295 single base substitution C T exon_variant LIRI-JP 10 81056295 81056295 single base substitution C T missense_variant A433V 1298C>T LIRI-JP 10 81056685 81056685 single base substitution A T exon_variant LIRI-JP 10 81056685 81056685 single base substitution A T intron_variant LIRI-JP 10 81059026 81059026 single base substitution G A downstream_gene_variant LIRI-JP 10 81059026 81059026 single base substitution G A intron_variant LIRI-JP 10 81059403 81059403 single base substitution A G downstream_gene_variant LIRI-JP 10 81059403 81059403 single base substitution A G intron_variant LIRI-JP 10 81061364 81061364 single base substitution G A downstream_gene_variant LIRI-JP 10 81061364 81061364 single base substitution G A intron_variant LIRI-JP 10 81061364 81061364 single base substitution G A upstream_gene_variant LIRI-JP 10 81062173 81062173 single base substitution A T intron_variant LIRI-JP 10 81062173 81062173 single base substitution A T upstream_gene_variant LIRI-JP 10 81067274 81067274 single base substitution G A missense_variant M80I 240G>A LIRI-JP 10 81067274 81067274 single base substitution G A missense_variant M927I 2781G>A LIRI-JP 10 81067484 81067484 single base substitution G A intron_variant LIRI-JP 10 81068161 81068161 single base substitution A C intron_variant LIRI-JP 10 81068579 81068579 insertion of <=200bp - A intron_variant LIRI-JP 10 81073055 81073055 single base substitution G T 3_prime_UTR_variant LIRI-JP 10 81073055 81073055 single base substitution G T downstream_gene_variant LIRI-JP 10 81073056 81073056 single base substitution C T 3_prime_UTR_variant LIRI-JP 10 81073056 81073056 single base substitution C T downstream_gene_variant LIRI-JP 10 81075158 81075158 insertion of <=200bp - T 3_prime_UTR_variant LIRI-JP 10 81075158 81075158 insertion of <=200bp - T downstream_gene_variant LIRI-JP 10 81075434 81075434 single base substitution C T 3_prime_UTR_variant LIRI-JP 10 81075434 81075434 single base substitution C T downstream_gene_variant LIRI-JP 10 81076293 81076293 single base substitution T C downstream_gene_variant LUSC-KR 10 80824480 80824480 single base substitution T G upstream_gene_variant LUSC-KR 10 80836172 80836172 single base substitution T G intron_variant LUSC-KR 10 80840555 80840555 single base substitution G A intron_variant LUSC-KR 10 80849340 80849340 single base substitution G T intron_variant LUSC-KR 10 80863037 80863037 single base substitution G T intron_variant LUSC-KR 10 80864357 80864357 single base substitution T C intron_variant LUSC-KR 10 80874271 80874271 single base substitution T C intron_variant LUSC-KR 10 80878887 80878887 single base substitution G T intron_variant LUSC-KR 10 80883151 80883151 single base substitution A G intron_variant LUSC-KR 10 80885639 80885639 single base substitution G T intron_variant LUSC-KR 10 80886595 80886595 single base substitution G A intron_variant LUSC-KR 10 80891454 80891454 single base substitution C T intron_variant LUSC-KR 10 80892562 80892562 single base substitution G T intron_variant LUSC-KR 10 80906714 80906714 single base substitution T C intron_variant LUSC-KR 10 80906749 80906749 single base substitution A T intron_variant LUSC-KR 10 80924493 80924493 single base substitution C T intron_variant LUSC-KR 10 80924781 80924781 single base substitution A G intron_variant LUSC-KR 10 80928427 80928427 single base substitution G A intron_variant LUSC-KR 10 80934868 80934868 single base substitution G T intron_variant LUSC-KR 10 80940271 80940271 single base substitution G A intron_variant LUSC-KR 10 80946369 80946369 single base substitution A G intron_variant LUSC-KR 10 80951540 80951540 single base substitution G T intron_variant LUSC-KR 10 80955854 80955854 single base substitution G C intron_variant LUSC-KR 10 80975400 80975400 single base substitution G A intron_variant LUSC-KR 10 80981994 80981994 single base substitution A G intron_variant LUSC-KR 10 80989793 80989793 single base substitution G T intron_variant LUSC-KR 10 80991150 80991150 single base substitution A G intron_variant LUSC-KR 10 80999646 80999646 single base substitution A C intron_variant LUSC-KR 10 80999646 80999646 single base substitution A C upstream_gene_variant LUSC-KR 10 81008166 81008166 single base substitution G A intron_variant LUSC-KR 10 81008863 81008863 single base substitution G C intron_variant LUSC-KR 10 81012734 81012734 single base substitution A C intron_variant LUSC-KR 10 81022768 81022768 single base substitution G A intron_variant LUSC-KR 10 81023613 81023613 single base substitution A T intron_variant LUSC-KR 10 81026873 81026873 single base substitution G C intron_variant LUSC-KR 10 81032249 81032249 single base substitution G T intron_variant LUSC-KR 10 81032249 81032249 single base substitution G T upstream_gene_variant LUSC-KR 10 81039311 81039311 single base substitution G T intron_variant LUSC-KR 10 81041459 81041459 single base substitution T C intron_variant LUSC-KR 10 81046954 81046954 single base substitution G A intron_variant LUSC-KR 10 81047530 81047530 single base substitution G A intron_variant LUSC-KR 10 81047941 81047941 single base substitution A T intron_variant LUSC-KR 10 81047953 81047953 single base substitution G A intron_variant LUSC-KR 10 81048849 81048849 single base substitution G A intron_variant LUSC-KR 10 81049128 81049128 single base substitution G A intron_variant LUSC-KR 10 81050781 81050781 single base substitution G A exon_variant LUSC-KR 10 81050781 81050781 single base substitution G A synonymous_variant S202S 606G>A LUSC-KR 10 81060097 81060097 single base substitution G A downstream_gene_variant LUSC-KR 10 81060097 81060097 single base substitution G A intron_variant LUSC-KR 10 81060730 81060730 single base substitution C T downstream_gene_variant LUSC-KR 10 81060730 81060730 single base substitution C T intron_variant LUSC-KR 10 81060946 81060946 single base substitution C G downstream_gene_variant LUSC-KR 10 81060946 81060946 single base substitution C G intron_variant LUSC-KR 10 81062107 81062107 single base substitution G A intron_variant LUSC-KR 10 81062107 81062107 single base substitution G A upstream_gene_variant LUSC-KR 10 81065014 81065014 single base substitution G T intron_variant LUSC-KR 10 81065014 81065014 single base substitution G T upstream_gene_variant LUSC-KR 10 81071455 81071455 single base substitution G T intron_variant LUSC-KR 10 81072632 81072632 single base substitution G A 3_prime_UTR_variant LUSC-KR 10 81072632 81072632 single base substitution G A downstream_gene_variant LUSC-KR 10 81073764 81073764 single base substitution G A 3_prime_UTR_variant LUSC-KR 10 81073764 81073764 single base substitution G A downstream_gene_variant LUSC-US 10 81058301 81058301 single base substitution A G downstream_gene_variant LUSC-US 10 81058301 81058301 single base substitution A G missense_variant I544V 1630A>G LUSC-US 10 81058846 81058847 deletion of <=200bp GG - downstream_gene_variant LUSC-US 10 81058846 81058847 deletion of <=200bp GG - frameshift_variant R569 LUSC-US 10 81061960 81061960 single base substitution A G missense_variant I706V 2116A>G LUSC-US 10 81061960 81061960 single base substitution A G upstream_gene_variant LUSC-US 10 81070737 81070737 single base substitution C A intron_variant LUSC-US 10 81070737 81070737 single base substitution C A missense_variant H964Q 2892C>A MALY-DE 10 80828605 80828605 single base substitution A G upstream_gene_variant MALY-DE 10 80831073 80831073 single base substitution T A intron_variant MALY-DE 10 80834081 80834081 single base substitution C G intron_variant MALY-DE 10 80834413 80834413 single base substitution G C intron_variant MALY-DE 10 80836035 80836035 single base substitution T G intron_variant MALY-DE 10 80836996 80836996 single base substitution G A intron_variant MALY-DE 10 80853047 80853074 deletion of <=200bp TTTATTTATTTATTTATTTATTTATTTA - intron_variant MALY-DE 10 80856510 80856510 single base substitution C A intron_variant MALY-DE 10 80859310 80859310 single base substitution G A intron_variant MALY-DE 10 80869449 80869449 single base substitution C T intron_variant MALY-DE 10 80879708 80879746 deletion of <=200bp GAAAGGGGCCTGTCCCACTCTCTGCTCCGTGGAGAAACA - intron_variant MALY-DE 10 80887247 80887247 single base substitution A G intron_variant MALY-DE 10 80897206 80897206 single base substitution C T intron_variant MALY-DE 10 80898966 80898966 single base substitution C T intron_variant MALY-DE 10 80904667 80904667 single base substitution G T intron_variant MALY-DE 10 80915579 80915579 single base substitution C T intron_variant MALY-DE 10 80918767 80918767 single base substitution G A intron_variant MALY-DE 10 80925853 80925853 single base substitution T C intron_variant MALY-DE 10 80934970 80934970 single base substitution A C intron_variant MALY-DE 10 80937337 80937337 single base substitution G C intron_variant MALY-DE 10 80943305 80943305 single base substitution G A intron_variant MALY-DE 10 80975762 80975762 single base substitution A G intron_variant MALY-DE 10 80989539 80989539 single base substitution C T intron_variant MALY-DE 10 80989806 80989806 single base substitution C T intron_variant MALY-DE 10 80990395 80990395 insertion of <=200bp - T intron_variant MALY-DE 10 80990397 80990401 deletion of <=200bp CAGAC - intron_variant MALY-DE 10 80995987 80995987 single base substitution C A intron_variant MALY-DE 10 81004419 81004419 single base substitution T A intron_variant MALY-DE 10 81008582 81008583 deletion of <=200bp TG - intron_variant MALY-DE 10 81008692 81008692 single base substitution C T intron_variant MALY-DE 10 81024089 81024089 single base substitution C T intron_variant MALY-DE 10 81044232 81044232 single base substitution C T intron_variant MALY-DE 10 81047175 81047175 single base substitution T A intron_variant MALY-DE 10 81047880 81047880 single base substitution T G intron_variant MALY-DE 10 81071891 81071891 single base substitution C T intron_variant MALY-DE 10 81079085 81079085 single base substitution A G downstream_gene_variant MELA-AU 10 80823864 80823864 single base substitution G A upstream_gene_variant MELA-AU 10 80824657 80824657 single base substitution G A upstream_gene_variant MELA-AU 10 80825418 80825418 single base substitution G A upstream_gene_variant MELA-AU 10 80825819 80825819 single base substitution G A upstream_gene_variant MELA-AU 10 80826388 80826388 single base substitution A G upstream_gene_variant MELA-AU 10 80826398 80826398 single base substitution G A upstream_gene_variant MELA-AU 10 80827214 80827214 single base substitution G A upstream_gene_variant MELA-AU 10 80827353 80827353 single base substitution G A upstream_gene_variant MELA-AU 10 80828355 80828355 single base substitution G A upstream_gene_variant MELA-AU 10 80831548 80831548 single base substitution G A intron_variant MELA-AU 10 80833372 80833372 single base substitution C T intron_variant MELA-AU 10 80833853 80833853 single base substitution C T intron_variant MELA-AU 10 80833937 80833937 single base substitution G C intron_variant MELA-AU 10 80834186 80834186 single base substitution C T intron_variant MELA-AU 10 80835357 80835357 single base substitution C T intron_variant MELA-AU 10 80837980 80837980 single base substitution T C intron_variant MELA-AU 10 80838062 80838062 single base substitution G A intron_variant MELA-AU 10 80838118 80838118 single base substitution C T intron_variant MELA-AU 10 80840822 80840822 single base substitution C T intron_variant MELA-AU 10 80841048 80841048 single base substitution C T intron_variant MELA-AU 10 80841197 80841197 single base substitution G A intron_variant MELA-AU 10 80841208 80841208 single base substitution G A intron_variant MELA-AU 10 80841376 80841376 single base substitution C T intron_variant MELA-AU 10 80841382 80841383 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 80841551 80841551 single base substitution C T intron_variant MELA-AU 10 80842060 80842060 single base substitution C T intron_variant MELA-AU 10 80842120 80842120 single base substitution C T intron_variant MELA-AU 10 80842283 80842283 single base substitution G A intron_variant MELA-AU 10 80843986 80843986 single base substitution G A intron_variant MELA-AU 10 80845496 80845496 single base substitution A T intron_variant MELA-AU 10 80845960 80845960 single base substitution G A intron_variant MELA-AU 10 80847279 80847279 single base substitution C T intron_variant MELA-AU 10 80847323 80847323 single base substitution C T intron_variant MELA-AU 10 80847722 80847722 single base substitution C T intron_variant MELA-AU 10 80848062 80848063 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80848345 80848345 single base substitution C T intron_variant MELA-AU 10 80848463 80848463 single base substitution T C intron_variant MELA-AU 10 80848976 80848976 single base substitution C T intron_variant MELA-AU 10 80850078 80850078 single base substitution T C intron_variant MELA-AU 10 80851315 80851315 single base substitution G T intron_variant MELA-AU 10 80852025 80852025 single base substitution C A intron_variant MELA-AU 10 80852066 80852066 single base substitution C T intron_variant MELA-AU 10 80852163 80852163 single base substitution C T intron_variant MELA-AU 10 80852289 80852289 single base substitution C T intron_variant MELA-AU 10 80852305 80852305 single base substitution C T intron_variant MELA-AU 10 80853749 80853749 single base substitution C T intron_variant MELA-AU 10 80854806 80854806 single base substitution C A intron_variant MELA-AU 10 80857450 80857450 single base substitution T G intron_variant MELA-AU 10 80859352 80859352 single base substitution C T intron_variant MELA-AU 10 80860436 80860436 single base substitution G A intron_variant MELA-AU 10 80860594 80860594 single base substitution C T intron_variant MELA-AU 10 80860628 80860628 single base substitution C T intron_variant MELA-AU 10 80862395 80862395 single base substitution G A intron_variant MELA-AU 10 80863524 80863524 single base substitution C T intron_variant MELA-AU 10 80865648 80865648 single base substitution C T intron_variant MELA-AU 10 80866180 80866180 single base substitution A T intron_variant MELA-AU 10 80866568 80866568 single base substitution T C intron_variant MELA-AU 10 80866709 80866709 single base substitution C T intron_variant MELA-AU 10 80867083 80867083 single base substitution C T intron_variant MELA-AU 10 80867378 80867378 single base substitution C T intron_variant MELA-AU 10 80867969 80867969 single base substitution C T intron_variant MELA-AU 10 80868414 80868414 single base substitution C T intron_variant MELA-AU 10 80868622 80868622 single base substitution C T intron_variant MELA-AU 10 80869777 80869777 single base substitution A G intron_variant MELA-AU 10 80871179 80871180 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80871465 80871465 single base substitution C T intron_variant MELA-AU 10 80871872 80871872 single base substitution C T intron_variant MELA-AU 10 80871973 80871973 single base substitution C T intron_variant MELA-AU 10 80872101 80872101 single base substitution T C intron_variant MELA-AU 10 80873033 80873033 single base substitution G A intron_variant MELA-AU 10 80873464 80873464 single base substitution C T intron_variant MELA-AU 10 80873602 80873602 single base substitution C T intron_variant MELA-AU 10 80873957 80873957 single base substitution T C intron_variant MELA-AU 10 80874008 80874008 single base substitution C T intron_variant MELA-AU 10 80874082 80874082 single base substitution C T intron_variant MELA-AU 10 80874421 80874421 single base substitution C T intron_variant MELA-AU 10 80874525 80874525 single base substitution C T intron_variant MELA-AU 10 80874612 80874613 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 80877080 80877080 single base substitution C T intron_variant MELA-AU 10 80878001 80878001 single base substitution C T intron_variant MELA-AU 10 80878324 80878324 single base substitution C T intron_variant MELA-AU 10 80878758 80878758 single base substitution G C 5_prime_UTR_variant MELA-AU 10 80879204 80879204 single base substitution T A intron_variant MELA-AU 10 80879386 80879387 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 10 80880359 80880359 single base substitution C T intron_variant MELA-AU 10 80880816 80880816 single base substitution C T intron_variant MELA-AU 10 80880946 80880946 single base substitution C T intron_variant MELA-AU 10 80881658 80881658 single base substitution C T intron_variant MELA-AU 10 80881966 80881966 single base substitution C T intron_variant MELA-AU 10 80882361 80882361 single base substitution C T intron_variant MELA-AU 10 80883158 80883158 single base substitution C T intron_variant MELA-AU 10 80883621 80883621 single base substitution C T intron_variant MELA-AU 10 80884334 80884334 single base substitution C T intron_variant MELA-AU 10 80884829 80884829 single base substitution A G intron_variant MELA-AU 10 80885283 80885283 single base substitution C T intron_variant MELA-AU 10 80885726 80885726 single base substitution C T intron_variant MELA-AU 10 80886294 80886294 single base substitution C T intron_variant MELA-AU 10 80886555 80886555 single base substitution C T intron_variant MELA-AU 10 80886878 80886878 single base substitution A G intron_variant MELA-AU 10 80889320 80889320 single base substitution C T intron_variant MELA-AU 10 80889325 80889325 single base substitution C T intron_variant MELA-AU 10 80890708 80890708 single base substitution C T intron_variant MELA-AU 10 80892274 80892274 single base substitution C T intron_variant MELA-AU 10 80892744 80892744 single base substitution C T intron_variant MELA-AU 10 80892933 80892933 single base substitution C T intron_variant MELA-AU 10 80892940 80892940 single base substitution C T intron_variant MELA-AU 10 80893180 80893180 single base substitution C T intron_variant MELA-AU 10 80893890 80893890 single base substitution C T intron_variant MELA-AU 10 80894055 80894055 single base substitution C A intron_variant MELA-AU 10 80894778 80894778 single base substitution T C intron_variant MELA-AU 10 80895057 80895057 single base substitution C T intron_variant MELA-AU 10 80896040 80896040 single base substitution C T intron_variant MELA-AU 10 80896570 80896570 single base substitution G T intron_variant MELA-AU 10 80896689 80896689 single base substitution G T intron_variant MELA-AU 10 80898883 80898883 single base substitution C T intron_variant MELA-AU 10 80898990 80898990 single base substitution A G intron_variant MELA-AU 10 80900436 80900436 single base substitution C T intron_variant MELA-AU 10 80900498 80900498 single base substitution C T intron_variant MELA-AU 10 80900740 80900740 single base substitution C T intron_variant MELA-AU 10 80900970 80900970 single base substitution C T intron_variant MELA-AU 10 80900972 80900972 single base substitution C T intron_variant MELA-AU 10 80901054 80901054 single base substitution C T intron_variant MELA-AU 10 80901256 80901256 single base substitution C T intron_variant MELA-AU 10 80901943 80901943 single base substitution A G intron_variant MELA-AU 10 80902073 80902073 single base substitution G A intron_variant MELA-AU 10 80902864 80902864 single base substitution C T intron_variant MELA-AU 10 80903087 80903087 single base substitution C T intron_variant MELA-AU 10 80903209 80903209 single base substitution C A intron_variant MELA-AU 10 80903450 80903450 single base substitution G A intron_variant MELA-AU 10 80904148 80904148 single base substitution C T intron_variant MELA-AU 10 80904762 80904762 single base substitution C T intron_variant MELA-AU 10 80904962 80904962 single base substitution C T intron_variant MELA-AU 10 80906175 80906175 single base substitution C T intron_variant MELA-AU 10 80906224 80906224 single base substitution C T intron_variant MELA-AU 10 80907577 80907577 single base substitution G A intron_variant MELA-AU 10 80908313 80908313 single base substitution C T intron_variant MELA-AU 10 80910712 80910712 single base substitution C T intron_variant MELA-AU 10 80911089 80911089 single base substitution C T intron_variant MELA-AU 10 80911312 80911312 single base substitution G T intron_variant MELA-AU 10 80911396 80911396 single base substitution C T intron_variant MELA-AU 10 80911437 80911437 single base substitution C T intron_variant MELA-AU 10 80911490 80911490 single base substitution G A intron_variant MELA-AU 10 80912788 80912788 single base substitution C T intron_variant MELA-AU 10 80913226 80913226 single base substitution C T intron_variant MELA-AU 10 80913277 80913277 single base substitution C T intron_variant MELA-AU 10 80913526 80913526 single base substitution C T intron_variant MELA-AU 10 80913883 80913883 single base substitution G A intron_variant MELA-AU 10 80913900 80913900 single base substitution C T intron_variant MELA-AU 10 80913987 80913987 single base substitution C T intron_variant MELA-AU 10 80914501 80914501 single base substitution G A intron_variant MELA-AU 10 80914779 80914779 single base substitution C T intron_variant MELA-AU 10 80914858 80914858 single base substitution C T intron_variant MELA-AU 10 80915915 80915915 single base substitution G A intron_variant MELA-AU 10 80916472 80916472 single base substitution C T intron_variant MELA-AU 10 80917327 80917327 single base substitution C T intron_variant MELA-AU 10 80918027 80918027 single base substitution C T intron_variant MELA-AU 10 80918833 80918833 single base substitution C T intron_variant MELA-AU 10 80918842 80918842 single base substitution G A intron_variant MELA-AU 10 80919121 80919121 single base substitution G A intron_variant MELA-AU 10 80920537 80920537 single base substitution C T intron_variant MELA-AU 10 80921017 80921017 single base substitution C T intron_variant MELA-AU 10 80921035 80921035 single base substitution C T intron_variant MELA-AU 10 80921438 80921438 single base substitution C T intron_variant MELA-AU 10 80921833 80921833 single base substitution G A 5_prime_UTR_variant MELA-AU 10 80922684 80922684 single base substitution G A intron_variant MELA-AU 10 80923408 80923408 single base substitution C T intron_variant MELA-AU 10 80923583 80923583 single base substitution C T intron_variant MELA-AU 10 80923656 80923656 single base substitution C T intron_variant MELA-AU 10 80923711 80923711 single base substitution C T intron_variant MELA-AU 10 80924491 80924491 single base substitution T C intron_variant MELA-AU 10 80924929 80924929 single base substitution C T intron_variant MELA-AU 10 80925331 80925331 single base substitution C T intron_variant MELA-AU 10 80925492 80925492 single base substitution C T intron_variant MELA-AU 10 80925522 80925522 single base substitution G A intron_variant MELA-AU 10 80925736 80925736 single base substitution T A intron_variant MELA-AU 10 80926230 80926230 single base substitution C T intron_variant MELA-AU 10 80926499 80926499 single base substitution C T intron_variant MELA-AU 10 80926849 80926849 single base substitution C T intron_variant MELA-AU 10 80928111 80928111 single base substitution C T intron_variant MELA-AU 10 80928143 80928144 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80929031 80929032 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80929252 80929252 single base substitution T C intron_variant MELA-AU 10 80929430 80929430 single base substitution G T intron_variant MELA-AU 10 80929452 80929452 single base substitution A G intron_variant MELA-AU 10 80929521 80929521 single base substitution C T intron_variant MELA-AU 10 80930723 80930723 single base substitution C T intron_variant MELA-AU 10 80930802 80930802 single base substitution C T intron_variant MELA-AU 10 80930991 80930991 single base substitution C G intron_variant MELA-AU 10 80931409 80931409 single base substitution C T intron_variant MELA-AU 10 80931959 80931959 single base substitution C T intron_variant MELA-AU 10 80932525 80932525 single base substitution C T intron_variant MELA-AU 10 80932545 80932545 single base substitution C T intron_variant MELA-AU 10 80932619 80932619 single base substitution G A intron_variant MELA-AU 10 80933879 80933879 single base substitution C T intron_variant MELA-AU 10 80934393 80934393 single base substitution C T intron_variant MELA-AU 10 80934868 80934868 single base substitution G A intron_variant MELA-AU 10 80935482 80935482 single base substitution T G intron_variant MELA-AU 10 80935530 80935530 single base substitution C T intron_variant MELA-AU 10 80935885 80935885 single base substitution C T intron_variant MELA-AU 10 80936205 80936205 single base substitution C T intron_variant MELA-AU 10 80936221 80936221 single base substitution C T intron_variant MELA-AU 10 80936501 80936501 single base substitution C T intron_variant MELA-AU 10 80937115 80937115 single base substitution G A intron_variant MELA-AU 10 80937528 80937528 single base substitution C T intron_variant MELA-AU 10 80938311 80938311 single base substitution C A intron_variant MELA-AU 10 80938506 80938506 single base substitution G A intron_variant MELA-AU 10 80938659 80938659 single base substitution C T intron_variant MELA-AU 10 80938756 80938756 single base substitution C T intron_variant MELA-AU 10 80939337 80939337 single base substitution G A intron_variant MELA-AU 10 80939819 80939819 single base substitution C T intron_variant MELA-AU 10 80940233 80940233 single base substitution C T intron_variant MELA-AU 10 80940348 80940348 single base substitution C T intron_variant MELA-AU 10 80940640 80940640 single base substitution C T intron_variant MELA-AU 10 80941563 80941564 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80941697 80941697 single base substitution G A intron_variant MELA-AU 10 80942337 80942337 single base substitution C T intron_variant MELA-AU 10 80942502 80942502 single base substitution C T intron_variant MELA-AU 10 80942621 80942621 single base substitution C T intron_variant MELA-AU 10 80943412 80943412 single base substitution C T intron_variant MELA-AU 10 80943826 80943827 multiple base substitution (>=2bp and <=200bp) TG GT intron_variant MELA-AU 10 80943973 80943973 single base substitution C T intron_variant MELA-AU 10 80944181 80944181 single base substitution C T intron_variant MELA-AU 10 80944315 80944315 single base substitution C T intron_variant MELA-AU 10 80944450 80944450 single base substitution A G intron_variant MELA-AU 10 80944527 80944527 single base substitution C T intron_variant MELA-AU 10 80944836 80944836 single base substitution G T intron_variant MELA-AU 10 80945007 80945007 single base substitution G A intron_variant MELA-AU 10 80945033 80945033 single base substitution C T intron_variant MELA-AU 10 80945130 80945132 deletion of <=200bp TCT - intron_variant MELA-AU 10 80945636 80945636 single base substitution C T intron_variant MELA-AU 10 80945739 80945740 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80945826 80945826 single base substitution T G intron_variant MELA-AU 10 80946023 80946023 deletion of <=200bp T - intron_variant MELA-AU 10 80946898 80946898 single base substitution C T intron_variant MELA-AU 10 80947228 80947228 single base substitution C T intron_variant MELA-AU 10 80947490 80947490 single base substitution C T intron_variant MELA-AU 10 80947948 80947949 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80948611 80948611 single base substitution C T intron_variant MELA-AU 10 80948922 80948922 single base substitution C T intron_variant MELA-AU 10 80948923 80948923 single base substitution C T intron_variant MELA-AU 10 80949911 80949911 single base substitution C T intron_variant MELA-AU 10 80950114 80950114 single base substitution C T intron_variant MELA-AU 10 80951176 80951176 single base substitution C T intron_variant MELA-AU 10 80951216 80951216 single base substitution C T intron_variant MELA-AU 10 80951312 80951312 single base substitution G A intron_variant MELA-AU 10 80951465 80951465 single base substitution C T intron_variant MELA-AU 10 80951545 80951545 single base substitution C T intron_variant MELA-AU 10 80954952 80954952 single base substitution G A intron_variant MELA-AU 10 80955166 80955166 single base substitution C T intron_variant MELA-AU 10 80955222 80955222 single base substitution G T intron_variant MELA-AU 10 80956107 80956107 single base substitution C T intron_variant MELA-AU 10 80956206 80956206 single base substitution C T intron_variant MELA-AU 10 80956369 80956370 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80956370 80956370 single base substitution C T intron_variant MELA-AU 10 80957519 80957519 single base substitution C T intron_variant MELA-AU 10 80957622 80957622 single base substitution T A intron_variant MELA-AU 10 80957777 80957777 single base substitution G T intron_variant MELA-AU 10 80957898 80957899 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80958166 80958166 single base substitution T C intron_variant MELA-AU 10 80958395 80958395 single base substitution C A intron_variant MELA-AU 10 80958826 80958826 single base substitution C T intron_variant MELA-AU 10 80959257 80959257 single base substitution C T intron_variant MELA-AU 10 80959646 80959646 single base substitution C T intron_variant MELA-AU 10 80959731 80959731 single base substitution C T intron_variant MELA-AU 10 80959805 80959805 single base substitution C T intron_variant MELA-AU 10 80960225 80960225 single base substitution C T intron_variant MELA-AU 10 80960375 80960375 single base substitution C T intron_variant MELA-AU 10 80960439 80960439 single base substitution C T intron_variant MELA-AU 10 80963382 80963382 single base substitution C T intron_variant MELA-AU 10 80964161 80964161 single base substitution C T intron_variant MELA-AU 10 80964266 80964266 single base substitution A G intron_variant MELA-AU 10 80965172 80965172 single base substitution C T intron_variant MELA-AU 10 80966060 80966060 single base substitution C T intron_variant MELA-AU 10 80966575 80966575 single base substitution G A intron_variant MELA-AU 10 80966906 80966906 single base substitution C T intron_variant MELA-AU 10 80967181 80967181 single base substitution C T intron_variant MELA-AU 10 80967395 80967395 single base substitution C T intron_variant MELA-AU 10 80967633 80967633 single base substitution C T intron_variant MELA-AU 10 80968017 80968017 single base substitution C T intron_variant MELA-AU 10 80968370 80968370 single base substitution C T intron_variant MELA-AU 10 80968419 80968419 single base substitution C T intron_variant MELA-AU 10 80969020 80969020 single base substitution C T intron_variant MELA-AU 10 80969429 80969429 single base substitution C T intron_variant MELA-AU 10 80969834 80969834 single base substitution C T intron_variant MELA-AU 10 80969936 80969936 single base substitution C T intron_variant MELA-AU 10 80969952 80969952 single base substitution C T intron_variant MELA-AU 10 80970916 80970916 single base substitution C T intron_variant MELA-AU 10 80970940 80970940 single base substitution C T intron_variant MELA-AU 10 80971049 80971049 single base substitution C T intron_variant MELA-AU 10 80971450 80971450 single base substitution G A intron_variant MELA-AU 10 80972667 80972667 single base substitution C T intron_variant MELA-AU 10 80972897 80972897 single base substitution G T intron_variant MELA-AU 10 80973593 80973593 single base substitution C T intron_variant MELA-AU 10 80974262 80974262 single base substitution C T intron_variant MELA-AU 10 80974335 80974335 single base substitution C T intron_variant MELA-AU 10 80974466 80974466 single base substitution C T intron_variant MELA-AU 10 80974509 80974509 single base substitution C T intron_variant MELA-AU 10 80975524 80975524 single base substitution C T intron_variant MELA-AU 10 80975617 80975618 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 10 80975641 80975641 single base substitution C T intron_variant MELA-AU 10 80975907 80975907 single base substitution C T intron_variant MELA-AU 10 80976929 80976929 single base substitution C T intron_variant MELA-AU 10 80977625 80977625 single base substitution G A intron_variant MELA-AU 10 80978364 80978364 single base substitution C G intron_variant MELA-AU 10 80979963 80979963 single base substitution C T intron_variant MELA-AU 10 80982146 80982146 single base substitution C T intron_variant MELA-AU 10 80982986 80982986 single base substitution C T intron_variant MELA-AU 10 80983210 80983210 single base substitution T G intron_variant MELA-AU 10 80983548 80983571 deletion of <=200bp TGGCCTGGCCTGGGCCAGGGGCCC - intron_variant MELA-AU 10 80983619 80983619 single base substitution C T intron_variant MELA-AU 10 80984439 80984439 single base substitution C T intron_variant MELA-AU 10 80985411 80985412 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80985619 80985619 single base substitution C T intron_variant MELA-AU 10 80986176 80986176 single base substitution A T intron_variant MELA-AU 10 80986178 80986179 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 10 80986234 80986234 single base substitution C T intron_variant MELA-AU 10 80986829 80986829 single base substitution C T intron_variant MELA-AU 10 80987113 80987113 single base substitution C T intron_variant MELA-AU 10 80987119 80987119 single base substitution C T intron_variant MELA-AU 10 80987822 80987822 single base substitution C G intron_variant MELA-AU 10 80987859 80987860 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 80987860 80987860 single base substitution C T intron_variant MELA-AU 10 80988785 80988785 single base substitution T C intron_variant MELA-AU 10 80989610 80989610 single base substitution A G intron_variant MELA-AU 10 80989629 80989629 single base substitution G A intron_variant MELA-AU 10 80989840 80989840 single base substitution C T intron_variant MELA-AU 10 80989893 80989893 single base substitution C T intron_variant MELA-AU 10 80989894 80989894 single base substitution C T intron_variant MELA-AU 10 80989991 80989991 single base substitution C T intron_variant MELA-AU 10 80990026 80990026 single base substitution C T intron_variant MELA-AU 10 80990271 80990271 single base substitution C T intron_variant MELA-AU 10 80990746 80990746 single base substitution C T intron_variant MELA-AU 10 80990787 80990787 single base substitution C T intron_variant MELA-AU 10 80993308 80993308 single base substitution C T intron_variant MELA-AU 10 80994165 80994165 single base substitution C T intron_variant MELA-AU 10 80995342 80995342 single base substitution C T intron_variant MELA-AU 10 80995543 80995543 single base substitution C T intron_variant MELA-AU 10 80995771 80995771 single base substitution C T intron_variant MELA-AU 10 80996196 80996196 single base substitution C T intron_variant MELA-AU 10 80996309 80996309 single base substitution A G intron_variant MELA-AU 10 80996824 80996824 single base substitution G A intron_variant MELA-AU 10 80996845 80996845 single base substitution G C intron_variant MELA-AU 10 80996897 80996897 single base substitution C T intron_variant MELA-AU 10 80997052 80997052 single base substitution C T intron_variant MELA-AU 10 80997476 80997476 single base substitution C T intron_variant MELA-AU 10 80997822 80997822 single base substitution C T intron_variant MELA-AU 10 80997871 80997871 single base substitution C T intron_variant MELA-AU 10 80997910 80997910 single base substitution C T intron_variant MELA-AU 10 80997911 80997911 single base substitution C T intron_variant MELA-AU 10 80997946 80997946 single base substitution G A intron_variant MELA-AU 10 80998412 80998412 single base substitution C T intron_variant MELA-AU 10 80998792 80998792 single base substitution C T intron_variant MELA-AU 10 80998792 80998792 single base substitution C T upstream_gene_variant MELA-AU 10 80999084 80999084 single base substitution T A intron_variant MELA-AU 10 80999084 80999084 single base substitution T A upstream_gene_variant MELA-AU 10 80999648 80999648 single base substitution C T intron_variant MELA-AU 10 80999648 80999648 single base substitution C T upstream_gene_variant MELA-AU 10 81000225 81000226 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 81000225 81000226 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 81003051 81003051 single base substitution C T intron_variant MELA-AU 10 81003051 81003051 single base substitution C T upstream_gene_variant MELA-AU 10 81004909 81004909 single base substitution C T intron_variant MELA-AU 10 81005356 81005356 single base substitution C T intron_variant MELA-AU 10 81006941 81006941 single base substitution G A intron_variant MELA-AU 10 81007055 81007055 single base substitution C G intron_variant MELA-AU 10 81007104 81007104 single base substitution C T intron_variant MELA-AU 10 81007261 81007261 single base substitution G A intron_variant MELA-AU 10 81008859 81008859 single base substitution C T intron_variant MELA-AU 10 81009644 81009644 single base substitution C T intron_variant MELA-AU 10 81009766 81009766 single base substitution C T intron_variant MELA-AU 10 81010221 81010221 single base substitution C T intron_variant MELA-AU 10 81010497 81010497 single base substitution G A intron_variant MELA-AU 10 81010653 81010653 single base substitution C T intron_variant MELA-AU 10 81010713 81010714 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81010949 81010949 single base substitution C T intron_variant MELA-AU 10 81011129 81011129 single base substitution C T intron_variant MELA-AU 10 81011281 81011281 single base substitution C T intron_variant MELA-AU 10 81011517 81011517 single base substitution G A intron_variant MELA-AU 10 81011856 81011857 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81011877 81011877 single base substitution C T intron_variant MELA-AU 10 81012038 81012038 single base substitution T C intron_variant MELA-AU 10 81012131 81012131 single base substitution C T intron_variant MELA-AU 10 81012303 81012304 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 81012706 81012706 single base substitution T C intron_variant MELA-AU 10 81013200 81013201 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 81013443 81013443 single base substitution C A intron_variant MELA-AU 10 81014036 81014036 single base substitution C A intron_variant MELA-AU 10 81014186 81014187 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81014365 81014366 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81014667 81014667 single base substitution G A intron_variant MELA-AU 10 81014980 81014980 single base substitution C T intron_variant MELA-AU 10 81015155 81015155 single base substitution C T intron_variant MELA-AU 10 81015241 81015241 single base substitution C T intron_variant MELA-AU 10 81015323 81015323 single base substitution C T intron_variant MELA-AU 10 81016173 81016173 single base substitution C T intron_variant MELA-AU 10 81017042 81017042 single base substitution C T intron_variant MELA-AU 10 81017302 81017302 single base substitution C T intron_variant MELA-AU 10 81017431 81017431 single base substitution C T intron_variant MELA-AU 10 81018261 81018261 single base substitution C T intron_variant MELA-AU 10 81018646 81018646 single base substitution G A intron_variant MELA-AU 10 81019300 81019300 single base substitution C T intron_variant MELA-AU 10 81019336 81019336 single base substitution C T intron_variant MELA-AU 10 81019769 81019769 single base substitution C T intron_variant MELA-AU 10 81020574 81020574 single base substitution C T intron_variant MELA-AU 10 81022423 81022423 single base substitution C T intron_variant MELA-AU 10 81022584 81022584 single base substitution G A intron_variant MELA-AU 10 81022837 81022837 single base substitution T C intron_variant MELA-AU 10 81022838 81022838 single base substitution C T intron_variant MELA-AU 10 81023330 81023331 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81024156 81024156 single base substitution C T intron_variant MELA-AU 10 81025426 81025426 single base substitution C T intron_variant MELA-AU 10 81027250 81027250 single base substitution G A intron_variant MELA-AU 10 81028278 81028278 single base substitution T A intron_variant MELA-AU 10 81028460 81028460 single base substitution C T intron_variant MELA-AU 10 81028983 81028983 single base substitution C T intron_variant MELA-AU 10 81029329 81029329 single base substitution C T intron_variant MELA-AU 10 81030050 81030050 single base substitution G A intron_variant MELA-AU 10 81030163 81030163 single base substitution C T intron_variant MELA-AU 10 81030812 81030812 single base substitution C G intron_variant MELA-AU 10 81030949 81030949 single base substitution C T intron_variant MELA-AU 10 81031512 81031512 single base substitution G A intron_variant MELA-AU 10 81032169 81032169 single base substitution C T intron_variant MELA-AU 10 81032169 81032169 single base substitution C T upstream_gene_variant MELA-AU 10 81032196 81032196 single base substitution C T intron_variant MELA-AU 10 81032196 81032196 single base substitution C T upstream_gene_variant MELA-AU 10 81032263 81032263 single base substitution C T intron_variant MELA-AU 10 81032263 81032263 single base substitution C T upstream_gene_variant MELA-AU 10 81032369 81032369 single base substitution C T intron_variant MELA-AU 10 81032369 81032369 single base substitution C T upstream_gene_variant MELA-AU 10 81032618 81032618 single base substitution C T intron_variant MELA-AU 10 81032618 81032618 single base substitution C T upstream_gene_variant MELA-AU 10 81033055 81033055 single base substitution C T intron_variant MELA-AU 10 81033055 81033055 single base substitution C T upstream_gene_variant MELA-AU 10 81033274 81033274 single base substitution C T intron_variant MELA-AU 10 81033274 81033274 single base substitution C T upstream_gene_variant MELA-AU 10 81033830 81033830 single base substitution C T intron_variant MELA-AU 10 81033830 81033830 single base substitution C T upstream_gene_variant MELA-AU 10 81034093 81034093 single base substitution C T intron_variant MELA-AU 10 81034093 81034093 single base substitution C T upstream_gene_variant MELA-AU 10 81036350 81036350 single base substitution G T intron_variant MELA-AU 10 81036350 81036350 single base substitution G T upstream_gene_variant MELA-AU 10 81036454 81036454 single base substitution C T intron_variant MELA-AU 10 81036454 81036454 single base substitution C T upstream_gene_variant MELA-AU 10 81037959 81037959 single base substitution C T intron_variant MELA-AU 10 81038958 81038958 single base substitution C T intron_variant MELA-AU 10 81040257 81040257 single base substitution C T intron_variant MELA-AU 10 81040519 81040520 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 10 81040743 81040743 single base substitution C T intron_variant MELA-AU 10 81041184 81041184 single base substitution G A intron_variant MELA-AU 10 81041450 81041450 single base substitution C T intron_variant MELA-AU 10 81041670 81041670 single base substitution T C intron_variant MELA-AU 10 81041967 81041967 single base substitution G A intron_variant MELA-AU 10 81042509 81042509 single base substitution T C intron_variant MELA-AU 10 81043193 81043193 single base substitution C T intron_variant MELA-AU 10 81043374 81043374 single base substitution T G intron_variant MELA-AU 10 81043625 81043626 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81044078 81044078 single base substitution G A intron_variant MELA-AU 10 81044229 81044229 single base substitution C T intron_variant MELA-AU 10 81045290 81045290 single base substitution A G intron_variant MELA-AU 10 81045956 81045956 single base substitution G A intron_variant MELA-AU 10 81045984 81045984 single base substitution C T intron_variant MELA-AU 10 81047371 81047371 single base substitution G A intron_variant MELA-AU 10 81048265 81048265 single base substitution C T intron_variant MELA-AU 10 81048568 81048568 single base substitution C T intron_variant MELA-AU 10 81048703 81048704 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81048791 81048791 single base substitution C T intron_variant MELA-AU 10 81048799 81048799 single base substitution G T intron_variant MELA-AU 10 81048810 81048810 single base substitution T C intron_variant MELA-AU 10 81048824 81048824 single base substitution T C intron_variant MELA-AU 10 81049406 81049407 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81049540 81049540 single base substitution C T exon_variant MELA-AU 10 81049540 81049540 single base substitution C T missense_variant S145L 434C>T MELA-AU 10 81049560 81049560 single base substitution C T exon_variant MELA-AU 10 81049560 81049560 single base substitution C T missense_variant P152S 454C>T MELA-AU 10 81049601 81049601 single base substitution C T exon_variant MELA-AU 10 81049601 81049601 single base substitution C T synonymous_variant S165S 495C>T MELA-AU 10 81050609 81050609 single base substitution C T intron_variant MELA-AU 10 81051137 81051137 single base substitution C T downstream_gene_variant MELA-AU 10 81051137 81051137 single base substitution C T intron_variant MELA-AU 10 81051192 81051192 single base substitution C T downstream_gene_variant MELA-AU 10 81051192 81051192 single base substitution C T intron_variant MELA-AU 10 81051460 81051460 single base substitution C T downstream_gene_variant MELA-AU 10 81051460 81051460 single base substitution C T intron_variant MELA-AU 10 81051788 81051788 single base substitution C T downstream_gene_variant MELA-AU 10 81051788 81051788 single base substitution C T intron_variant MELA-AU 10 81051866 81051866 single base substitution C T downstream_gene_variant MELA-AU 10 81051866 81051866 single base substitution C T intron_variant MELA-AU 10 81052815 81052815 single base substitution C T downstream_gene_variant MELA-AU 10 81052815 81052815 single base substitution C T intron_variant MELA-AU 10 81052852 81052852 single base substitution C T downstream_gene_variant MELA-AU 10 81052852 81052852 single base substitution C T intron_variant MELA-AU 10 81053254 81053255 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 81053254 81053255 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 10 81053254 81053255 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SG358SR MELA-AU 10 81053298 81053299 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 81053298 81053299 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 10 81053298 81053299 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P373L 1118CC>TT MELA-AU 10 81053357 81053357 single base substitution C T downstream_gene_variant MELA-AU 10 81053357 81053357 single base substitution C T exon_variant MELA-AU 10 81053357 81053357 single base substitution C T missense_variant P393S 1177C>T MELA-AU 10 81053584 81053584 single base substitution C T downstream_gene_variant MELA-AU 10 81053584 81053584 single base substitution C T exon_variant MELA-AU 10 81053584 81053584 single base substitution C T intron_variant MELA-AU 10 81053585 81053585 single base substitution C T downstream_gene_variant MELA-AU 10 81053585 81053585 single base substitution C T exon_variant MELA-AU 10 81053585 81053585 single base substitution C T intron_variant MELA-AU 10 81053706 81053706 single base substitution C T downstream_gene_variant MELA-AU 10 81053706 81053706 single base substitution C T exon_variant MELA-AU 10 81053706 81053706 single base substitution C T intron_variant MELA-AU 10 81054884 81054884 single base substitution C A downstream_gene_variant MELA-AU 10 81054884 81054884 single base substitution C A exon_variant MELA-AU 10 81054884 81054884 single base substitution C A intron_variant MELA-AU 10 81055789 81055789 single base substitution C T downstream_gene_variant MELA-AU 10 81055789 81055789 single base substitution C T exon_variant MELA-AU 10 81055789 81055789 single base substitution C T intron_variant MELA-AU 10 81056076 81056076 single base substitution A C exon_variant MELA-AU 10 81056076 81056076 single base substitution A C intron_variant MELA-AU 10 81056243 81056243 single base substitution C T exon_variant MELA-AU 10 81056243 81056243 single base substitution C T stop_gained Q416* 1246C>T MELA-AU 10 81056269 81056269 single base substitution C T exon_variant MELA-AU 10 81056269 81056269 single base substitution C T synonymous_variant F424F 1272C>T MELA-AU 10 81057436 81057436 single base substitution A G downstream_gene_variant MELA-AU 10 81057436 81057436 single base substitution A G missense_variant N494D 1480A>G MELA-AU 10 81057681 81057681 single base substitution G A downstream_gene_variant MELA-AU 10 81057681 81057681 single base substitution G A intron_variant MELA-AU 10 81058648 81058648 single base substitution C T downstream_gene_variant MELA-AU 10 81058648 81058648 single base substitution C T intron_variant MELA-AU 10 81059014 81059014 single base substitution G A downstream_gene_variant MELA-AU 10 81059014 81059014 single base substitution G A intron_variant MELA-AU 10 81059095 81059095 single base substitution C T downstream_gene_variant MELA-AU 10 81059095 81059095 single base substitution C T intron_variant MELA-AU 10 81059234 81059234 single base substitution C T downstream_gene_variant MELA-AU 10 81059234 81059234 single base substitution C T intron_variant MELA-AU 10 81059732 81059732 single base substitution C T downstream_gene_variant MELA-AU 10 81059732 81059732 single base substitution C T intron_variant MELA-AU 10 81060431 81060432 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 81060431 81060432 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 81061150 81061150 single base substitution C T downstream_gene_variant MELA-AU 10 81061150 81061150 single base substitution C T intron_variant MELA-AU 10 81061150 81061150 single base substitution C T upstream_gene_variant MELA-AU 10 81061232 81061232 single base substitution C T downstream_gene_variant MELA-AU 10 81061232 81061232 single base substitution C T intron_variant MELA-AU 10 81061232 81061232 single base substitution C T upstream_gene_variant MELA-AU 10 81061910 81061910 single base substitution C T missense_variant S689F 2066C>T MELA-AU 10 81061910 81061910 single base substitution C T upstream_gene_variant MELA-AU 10 81063297 81063297 single base substitution C T intron_variant MELA-AU 10 81063297 81063297 single base substitution C T upstream_gene_variant MELA-AU 10 81063571 81063571 single base substitution C T intron_variant MELA-AU 10 81063571 81063571 single base substitution C T upstream_gene_variant MELA-AU 10 81065005 81065005 single base substitution C T intron_variant MELA-AU 10 81065005 81065005 single base substitution C T upstream_gene_variant MELA-AU 10 81065026 81065026 single base substitution C T intron_variant MELA-AU 10 81065026 81065026 single base substitution C T upstream_gene_variant MELA-AU 10 81065244 81065244 single base substitution C T intron_variant MELA-AU 10 81065244 81065244 single base substitution C T upstream_gene_variant MELA-AU 10 81065337 81065337 single base substitution G A missense_variant G801E 2402G>A MELA-AU 10 81065337 81065337 single base substitution G A upstream_gene_variant MELA-AU 10 81065958 81065958 single base substitution C T missense_variant S842F 2525C>T MELA-AU 10 81065958 81065958 single base substitution C T upstream_gene_variant MELA-AU 10 81066052 81066052 single base substitution C T synonymous_variant P26P 78C>T MELA-AU 10 81066052 81066052 single base substitution C T synonymous_variant P873P 2619C>T MELA-AU 10 81066134 81066134 single base substitution G A intron_variant MELA-AU 10 81066400 81066400 single base substitution C T intron_variant MELA-AU 10 81066658 81066658 single base substitution C T intron_variant MELA-AU 10 81067124 81067125 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 81067154 81067154 single base substitution C T splice_region_variant MELA-AU 10 81067264 81067265 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P77L 230CC>TT MELA-AU 10 81067264 81067265 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P924L 2771CC>TT MELA-AU 10 81067311 81067311 single base substitution C T missense_variant H93Y 277C>T MELA-AU 10 81067311 81067311 single base substitution C T missense_variant H940Y 2818C>T MELA-AU 10 81067404 81067404 single base substitution C T intron_variant MELA-AU 10 81067552 81067552 single base substitution G A intron_variant MELA-AU 10 81067746 81067746 single base substitution G A intron_variant MELA-AU 10 81067829 81067829 single base substitution C T intron_variant MELA-AU 10 81068549 81068549 deletion of <=200bp C - intron_variant MELA-AU 10 81068568 81068568 single base substitution C T intron_variant MELA-AU 10 81068869 81068869 single base substitution C T intron_variant MELA-AU 10 81069295 81069295 single base substitution G C intron_variant MELA-AU 10 81069716 81069716 single base substitution C T intron_variant MELA-AU 10 81069949 81069949 single base substitution C T intron_variant MELA-AU 10 81070063 81070063 single base substitution C T intron_variant MELA-AU 10 81070309 81070309 single base substitution G A intron_variant MELA-AU 10 81070488 81070489 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 81070873 81070873 single base substitution C T intron_variant MELA-AU 10 81070873 81070873 single base substitution C T missense_variant P1010S 3028C>T MELA-AU 10 81071355 81071355 single base substitution C T intron_variant MELA-AU 10 81071954 81071954 single base substitution G A intron_variant MELA-AU 10 81072293 81072293 single base substitution T C intron_variant MELA-AU 10 81072547 81072547 single base substitution T C 3_prime_UTR_variant MELA-AU 10 81072547 81072547 single base substitution T C downstream_gene_variant MELA-AU 10 81072933 81072933 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81072933 81072933 single base substitution C T downstream_gene_variant MELA-AU 10 81073327 81073327 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81073327 81073327 single base substitution C T downstream_gene_variant MELA-AU 10 81073532 81073532 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81073532 81073532 single base substitution C T downstream_gene_variant MELA-AU 10 81073681 81073681 single base substitution C A 3_prime_UTR_variant MELA-AU 10 81073681 81073681 single base substitution C A downstream_gene_variant MELA-AU 10 81073790 81073790 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81073790 81073790 single base substitution C T downstream_gene_variant MELA-AU 10 81073795 81073795 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81073795 81073795 single base substitution C T downstream_gene_variant MELA-AU 10 81074069 81074069 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81074069 81074069 single base substitution C T downstream_gene_variant MELA-AU 10 81074239 81074239 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81074239 81074239 single base substitution C T downstream_gene_variant MELA-AU 10 81074612 81074612 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81074612 81074612 single base substitution C T downstream_gene_variant MELA-AU 10 81075128 81075128 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81075128 81075128 single base substitution C T downstream_gene_variant MELA-AU 10 81075659 81075659 single base substitution C T 3_prime_UTR_variant MELA-AU 10 81075659 81075659 single base substitution C T downstream_gene_variant MELA-AU 10 81078215 81078215 single base substitution C T downstream_gene_variant MELA-AU 10 81078369 81078369 single base substitution C T downstream_gene_variant MELA-AU 10 81078470 81078470 single base substitution C T downstream_gene_variant MELA-AU 10 81078613 81078613 single base substitution T C downstream_gene_variant MELA-AU 10 81079125 81079125 single base substitution G A downstream_gene_variant MELA-AU 10 81079257 81079257 single base substitution C T downstream_gene_variant MELA-AU 10 81079386 81079387 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 81079739 81079739 single base substitution G A downstream_gene_variant MELA-AU 10 81079982 81079982 single base substitution G A downstream_gene_variant MELA-AU 10 81080237 81080237 single base substitution G A downstream_gene_variant MELA-AU 10 81080361 81080361 single base substitution C T downstream_gene_variant MELA-AU 10 81080364 81080364 single base substitution C T downstream_gene_variant MELA-AU 10 81081105 81081105 single base substitution C T downstream_gene_variant ORCA-IN 10 80915064 80915064 single base substitution G T intron_variant ORCA-IN 10 80917129 80917129 single base substitution T G intron_variant ORCA-IN 10 80935382 80935382 single base substitution T G intron_variant ORCA-IN 10 80942122 80942122 deletion of <=200bp G - intron_variant ORCA-IN 10 80943121 80943121 single base substitution A G intron_variant ORCA-IN 10 80964882 80964882 single base substitution A G intron_variant ORCA-IN 10 80978153 80978153 single base substitution G A intron_variant ORCA-IN 10 81036957 81036957 single base substitution C A exon_variant ORCA-IN 10 81036957 81036957 single base substitution C A stop_gained C100* 300C>A ORCA-IN 10 81064644 81064644 single base substitution A G intron_variant ORCA-IN 10 81064644 81064644 single base substitution A G upstream_gene_variant ORCA-IN 10 81067467 81067467 single base substitution C G intron_variant ORCA-IN 10 81067820 81067820 single base substitution C T intron_variant ORCA-IN 10 81070760 81070760 single base substitution C A intron_variant ORCA-IN 10 81070760 81070760 single base substitution C A stop_gained S972* 2915C>A ORCA-IN 10 81072408 81072408 single base substitution G A missense_variant E102K 304G>A ORCA-IN 10 81072408 81072408 single base substitution G A missense_variant E1036K 3106G>A ORCA-IN 10 81077597 81077597 single base substitution C G downstream_gene_variant ORCA-IN 10 81079839 81079839 single base substitution G A downstream_gene_variant OV-AU 10 80825796 80825796 single base substitution T C upstream_gene_variant OV-AU 10 80827237 80827237 single base substitution C G upstream_gene_variant OV-AU 10 80829233 80829233 single base substitution C T intron_variant OV-AU 10 80829234 80829234 single base substitution G T intron_variant OV-AU 10 80829259 80829259 single base substitution C T intron_variant OV-AU 10 80833721 80833721 single base substitution C T intron_variant OV-AU 10 80844658 80844658 single base substitution T G intron_variant OV-AU 10 80845910 80845910 single base substitution G C intron_variant OV-AU 10 80860320 80860320 single base substitution C T intron_variant OV-AU 10 80861489 80861489 single base substitution G C intron_variant OV-AU 10 80863250 80863250 single base substitution G T intron_variant OV-AU 10 80867713 80867713 single base substitution C G intron_variant OV-AU 10 80871847 80871847 single base substitution G C intron_variant OV-AU 10 80882841 80882841 single base substitution G C intron_variant OV-AU 10 80888620 80888620 single base substitution G A intron_variant OV-AU 10 80894434 80894434 single base substitution G T intron_variant OV-AU 10 80896482 80896482 single base substitution T A intron_variant OV-AU 10 80898606 80898606 single base substitution G T intron_variant OV-AU 10 80910106 80910106 single base substitution G A intron_variant OV-AU 10 80914483 80914483 single base substitution A T intron_variant OV-AU 10 80917549 80917549 single base substitution T G intron_variant OV-AU 10 80917783 80917783 single base substitution C T intron_variant OV-AU 10 80918285 80918285 single base substitution C T intron_variant OV-AU 10 80921644 80921644 single base substitution A T intron_variant OV-AU 10 80923170 80923170 single base substitution A G intron_variant OV-AU 10 80928003 80928003 single base substitution T G intron_variant OV-AU 10 80930381 80930381 single base substitution G C intron_variant OV-AU 10 80948605 80948605 single base substitution G A intron_variant OV-AU 10 80950573 80950573 single base substitution G C intron_variant OV-AU 10 80951254 80951254 single base substitution A C intron_variant OV-AU 10 80952951 80952951 single base substitution G C intron_variant OV-AU 10 80956546 80956546 single base substitution A C intron_variant OV-AU 10 80957401 80957401 single base substitution C G intron_variant OV-AU 10 80965070 80965070 single base substitution T C intron_variant OV-AU 10 80972624 80972624 single base substitution G T intron_variant OV-AU 10 80979276 80979276 single base substitution T C intron_variant OV-AU 10 80979277 80979277 single base substitution G T intron_variant OV-AU 10 80979487 80979487 single base substitution C T intron_variant OV-AU 10 80980950 80980950 single base substitution C A intron_variant OV-AU 10 80985328 80985328 single base substitution T A intron_variant OV-AU 10 80985578 80985578 single base substitution G T intron_variant OV-AU 10 80999748 80999748 single base substitution C A intron_variant OV-AU 10 80999748 80999748 single base substitution C A upstream_gene_variant OV-AU 10 81001933 81001933 single base substitution G C intron_variant OV-AU 10 81001933 81001933 single base substitution G C upstream_gene_variant OV-AU 10 81003511 81003511 single base substitution G C intron_variant OV-AU 10 81017012 81017012 single base substitution G A intron_variant OV-AU 10 81023884 81023884 single base substitution G T intron_variant OV-AU 10 81032209 81032209 single base substitution A G intron_variant OV-AU 10 81032209 81032209 single base substitution A G upstream_gene_variant OV-AU 10 81034867 81034867 single base substitution T A intron_variant OV-AU 10 81034867 81034867 single base substitution T A upstream_gene_variant OV-AU 10 81040297 81040297 single base substitution G A intron_variant OV-AU 10 81051354 81051354 single base substitution G C downstream_gene_variant OV-AU 10 81051354 81051354 single base substitution G C intron_variant OV-AU 10 81053331 81053331 single base substitution G A downstream_gene_variant OV-AU 10 81053331 81053331 single base substitution G A exon_variant OV-AU 10 81053331 81053331 single base substitution G A missense_variant R384Q 1151G>A OV-AU 10 81057122 81057122 single base substitution G A downstream_gene_variant OV-AU 10 81057122 81057122 single base substitution G A intron_variant OV-AU 10 81057190 81057190 single base substitution G A downstream_gene_variant OV-AU 10 81057190 81057190 single base substitution G A intron_variant OV-AU 10 81059372 81059372 single base substitution G C downstream_gene_variant OV-AU 10 81059372 81059372 single base substitution G C intron_variant OV-AU 10 81068078 81068078 single base substitution G A intron_variant OV-AU 10 81068987 81068987 single base substitution G C intron_variant OV-AU 10 81070927 81070927 single base substitution G C intron_variant OV-AU 10 81070927 81070927 single base substitution G C missense_variant E1028Q 3082G>C OV-AU 10 81077775 81077775 single base substitution A C downstream_gene_variant OV-AU 10 81078032 81078032 single base substitution A C downstream_gene_variant OV-US 10 81064923 81064923 single base substitution C A stop_gained C763* 2289C>A OV-US 10 81064923 81064923 single base substitution C A upstream_gene_variant PACA-AU 10 80825256 80825256 single base substitution C T upstream_gene_variant PACA-AU 10 80825831 80825831 single base substitution C T upstream_gene_variant PACA-AU 10 80826172 80826172 single base substitution C A upstream_gene_variant PACA-AU 10 80827134 80827134 single base substitution C T upstream_gene_variant PACA-AU 10 80827146 80827146 single base substitution T C upstream_gene_variant PACA-AU 10 80849849 80849849 single base substitution A G intron_variant PACA-AU 10 80850387 80850387 single base substitution C G intron_variant PACA-AU 10 80853047 80853047 insertion of <=200bp - TTTA intron_variant PACA-AU 10 80853047 80853050 deletion of <=200bp TTTA - intron_variant PACA-AU 10 80854106 80854106 single base substitution G A intron_variant PACA-AU 10 80856273 80856273 deletion of <=200bp G - intron_variant PACA-AU 10 80865145 80865145 single base substitution C A intron_variant PACA-AU 10 80865295 80865295 single base substitution G T intron_variant PACA-AU 10 80865891 80865891 deletion of <=200bp C - intron_variant PACA-AU 10 80868589 80868589 single base substitution A G intron_variant PACA-AU 10 80880381 80880381 single base substitution C A intron_variant PACA-AU 10 80885376 80885376 single base substitution G T intron_variant PACA-AU 10 80885377 80885377 single base substitution G T intron_variant PACA-AU 10 80885566 80885566 single base substitution G A intron_variant PACA-AU 10 80886553 80886553 single base substitution T C intron_variant PACA-AU 10 80891107 80891107 deletion of <=200bp G - intron_variant PACA-AU 10 80891548 80891548 single base substitution G A intron_variant PACA-AU 10 80891612 80891612 insertion of <=200bp - A intron_variant PACA-AU 10 80899463 80899463 single base substitution C T 5_prime_UTR_variant PACA-AU 10 80904406 80904406 single base substitution G T intron_variant PACA-AU 10 80904766 80904766 single base substitution A C intron_variant PACA-AU 10 80910937 80910937 single base substitution T C intron_variant PACA-AU 10 80911611 80911611 single base substitution G A intron_variant PACA-AU 10 80913698 80913698 single base substitution G A intron_variant PACA-AU 10 80916503 80916503 single base substitution C A intron_variant PACA-AU 10 80919388 80919388 single base substitution C A intron_variant PACA-AU 10 80925269 80925271 deletion of <=200bp CAG - intron_variant PACA-AU 10 80929348 80929348 single base substitution A C intron_variant PACA-AU 10 80934639 80934639 single base substitution A G intron_variant PACA-AU 10 80938266 80938266 single base substitution G A intron_variant PACA-AU 10 80943599 80943599 insertion of <=200bp - CAC intron_variant PACA-AU 10 80952840 80952840 single base substitution C T intron_variant PACA-AU 10 80963741 80963741 deletion of <=200bp C - intron_variant PACA-AU 10 80966490 80966490 single base substitution A G intron_variant PACA-AU 10 80966851 80966851 single base substitution G A intron_variant PACA-AU 10 80978935 80978935 single base substitution T G intron_variant PACA-AU 10 80978998 80978998 single base substitution G T intron_variant PACA-AU 10 80980862 80980862 single base substitution C T intron_variant PACA-AU 10 81005882 81005882 single base substitution C T intron_variant PACA-AU 10 81011495 81011495 single base substitution G A intron_variant PACA-AU 10 81014610 81014610 single base substitution C T intron_variant PACA-AU 10 81017968 81017968 single base substitution A G intron_variant PACA-AU 10 81020060 81020060 single base substitution A G intron_variant PACA-AU 10 81022029 81022029 single base substitution G T intron_variant PACA-AU 10 81022406 81022406 single base substitution G T intron_variant PACA-AU 10 81022728 81022728 single base substitution G A intron_variant PACA-AU 10 81023143 81023143 single base substitution T G intron_variant PACA-AU 10 81024384 81024384 single base substitution G T intron_variant PACA-AU 10 81025541 81025541 single base substitution G T intron_variant PACA-AU 10 81039061 81039061 single base substitution G C intron_variant PACA-AU 10 81041348 81041348 single base substitution A C intron_variant PACA-AU 10 81043943 81043943 single base substitution A T intron_variant PACA-AU 10 81047477 81047477 single base substitution C T intron_variant PACA-AU 10 81049050 81049050 single base substitution G A intron_variant PACA-AU 10 81059438 81059438 single base substitution G T downstream_gene_variant PACA-AU 10 81059438 81059438 single base substitution G T intron_variant PACA-AU 10 81068750 81068750 single base substitution A G intron_variant PACA-AU 10 81070913 81070913 single base substitution C T intron_variant PACA-AU 10 81070913 81070913 single base substitution C T missense_variant A1023V 3068C>T PACA-AU 10 81079642 81079642 single base substitution C T downstream_gene_variant PACA-AU 10 81081215 81081215 single base substitution G A downstream_gene_variant PACA-CA 10 80834893 80834893 single base substitution C A intron_variant PACA-CA 10 80835948 80835948 single base substitution T C intron_variant PACA-CA 10 80841389 80841389 single base substitution C T intron_variant PACA-CA 10 80847782 80847782 single base substitution T C intron_variant PACA-CA 10 80848593 80848593 single base substitution C T intron_variant PACA-CA 10 80853411 80853411 single base substitution C T intron_variant PACA-CA 10 80853578 80853578 single base substitution A T intron_variant PACA-CA 10 80856324 80856324 single base substitution C T intron_variant PACA-CA 10 80859462 80859462 single base substitution T C intron_variant PACA-CA 10 80863308 80863308 single base substitution G T intron_variant PACA-CA 10 80863874 80863874 single base substitution C T intron_variant PACA-CA 10 80865362 80865362 single base substitution G T intron_variant PACA-CA 10 80866087 80866087 single base substitution G T intron_variant PACA-CA 10 80871032 80871032 single base substitution C G intron_variant PACA-CA 10 80872608 80872608 single base substitution C A intron_variant PACA-CA 10 80876393 80876393 single base substitution T C intron_variant PACA-CA 10 80885835 80885835 single base substitution C T intron_variant PACA-CA 10 80886834 80886836 deletion of <=200bp CTT - intron_variant PACA-CA 10 80890422 80890422 single base substitution C G intron_variant PACA-CA 10 80890987 80890987 single base substitution C A intron_variant PACA-CA 10 80893069 80893069 single base substitution C G intron_variant PACA-CA 10 80894271 80894271 single base substitution C T intron_variant PACA-CA 10 80898465 80898465 single base substitution G A intron_variant PACA-CA 10 80899182 80899182 single base substitution G A intron_variant PACA-CA 10 80900609 80900609 single base substitution G A intron_variant PACA-CA 10 80903152 80903152 single base substitution C T intron_variant PACA-CA 10 80910779 80910779 insertion of <=200bp - G intron_variant PACA-CA 10 80915707 80915707 single base substitution C G intron_variant PACA-CA 10 80916261 80916261 single base substitution C G intron_variant PACA-CA 10 80920097 80920097 single base substitution G A intron_variant PACA-CA 10 80920234 80920234 single base substitution A G intron_variant PACA-CA 10 80923510 80923510 single base substitution G T intron_variant PACA-CA 10 80925446 80925446 single base substitution G A intron_variant PACA-CA 10 80925522 80925522 single base substitution G A intron_variant PACA-CA 10 80927966 80927966 single base substitution G C intron_variant PACA-CA 10 80930607 80930607 single base substitution G A intron_variant PACA-CA 10 80930724 80930724 single base substitution C T intron_variant PACA-CA 10 80932787 80932787 single base substitution C T intron_variant PACA-CA 10 80938673 80938673 single base substitution G A intron_variant PACA-CA 10 80942365 80942365 single base substitution A G intron_variant PACA-CA 10 80943187 80943187 single base substitution T G intron_variant PACA-CA 10 80943310 80943310 single base substitution C A intron_variant PACA-CA 10 80945941 80945941 single base substitution C T intron_variant PACA-CA 10 80947065 80947065 single base substitution C A intron_variant PACA-CA 10 80947630 80947630 single base substitution C A intron_variant PACA-CA 10 80949043 80949043 single base substitution C T intron_variant PACA-CA 10 80949452 80949452 single base substitution A G intron_variant PACA-CA 10 80950740 80950740 single base substitution A G intron_variant PACA-CA 10 80951131 80951131 deletion of <=200bp G - intron_variant PACA-CA 10 80959014 80959014 single base substitution C T intron_variant PACA-CA 10 80961624 80961624 single base substitution G A intron_variant PACA-CA 10 80968529 80968529 insertion of <=200bp - T intron_variant PACA-CA 10 80968752 80968752 single base substitution G A intron_variant PACA-CA 10 80969868 80969868 single base substitution G C intron_variant PACA-CA 10 80977924 80977924 single base substitution C T intron_variant PACA-CA 10 80979159 80979159 single base substitution G A intron_variant PACA-CA 10 80986433 80986433 single base substitution G A intron_variant PACA-CA 10 80990436 80990436 single base substitution G A intron_variant PACA-CA 10 80993382 80993382 single base substitution G A intron_variant PACA-CA 10 80993602 80993602 single base substitution C T intron_variant PACA-CA 10 80999542 80999542 single base substitution G A intron_variant PACA-CA 10 80999542 80999542 single base substitution G A upstream_gene_variant PACA-CA 10 81005700 81005700 single base substitution A G intron_variant PACA-CA 10 81006453 81006453 single base substitution T G intron_variant PACA-CA 10 81007541 81007541 single base substitution G A intron_variant PACA-CA 10 81010396 81010396 single base substitution C T intron_variant PACA-CA 10 81016215 81016215 single base substitution G A intron_variant PACA-CA 10 81018929 81018929 single base substitution C T intron_variant PACA-CA 10 81022537 81022537 single base substitution A G intron_variant PACA-CA 10 81022897 81022897 single base substitution C T intron_variant PACA-CA 10 81030245 81030245 single base substitution G T intron_variant PACA-CA 10 81030488 81030488 single base substitution C G intron_variant PACA-CA 10 81032149 81032149 single base substitution G C intron_variant PACA-CA 10 81032149 81032149 single base substitution G C upstream_gene_variant PACA-CA 10 81040109 81040109 single base substitution G A intron_variant PACA-CA 10 81044508 81044508 single base substitution G A intron_variant PACA-CA 10 81044805 81044805 single base substitution G A intron_variant PACA-CA 10 81050392 81050392 single base substitution C T intron_variant PACA-CA 10 81057546 81057546 single base substitution G A downstream_gene_variant PACA-CA 10 81057546 81057546 single base substitution G A intron_variant PACA-CA 10 81067462 81067462 single base substitution G A intron_variant PACA-CA 10 81072434 81072434 single base substitution G A synonymous_variant L1044L 3132G>A PACA-CA 10 81072434 81072434 single base substitution G A synonymous_variant L110L 330G>A PACA-CA 10 81074273 81074273 single base substitution G A 3_prime_UTR_variant PACA-CA 10 81074273 81074273 single base substitution G A downstream_gene_variant PACA-CA 10 81074417 81074417 single base substitution A G 3_prime_UTR_variant PACA-CA 10 81074417 81074417 single base substitution A G downstream_gene_variant PAEN-AU 10 80914712 80914712 single base substitution C T intron_variant PAEN-AU 10 80915218 80915218 single base substitution C T intron_variant PAEN-AU 10 80966674 80966674 single base substitution A G intron_variant PAEN-AU 10 80979377 80979377 single base substitution A G intron_variant PAEN-AU 10 81071012 81071012 single base substitution T G intron_variant PAEN-IT 10 80891243 80891243 single base substitution A G intron_variant PAEN-IT 10 80906725 80906725 single base substitution G A intron_variant PAEN-IT 10 80916273 80916273 single base substitution C A intron_variant PAEN-IT 10 80918647 80918647 single base substitution A G intron_variant PAEN-IT 10 81018248 81018248 single base substitution C A intron_variant PAEN-IT 10 81034104 81034104 single base substitution G C intron_variant PAEN-IT 10 81034104 81034104 single base substitution G C upstream_gene_variant PAEN-IT 10 81080454 81080454 single base substitution G A downstream_gene_variant PBCA-DE 10 80835872 80835872 single base substitution C T intron_variant PBCA-DE 10 80844244 80844244 single base substitution A G intron_variant PBCA-DE 10 80844797 80844797 single base substitution G A intron_variant PBCA-DE 10 80852794 80852794 single base substitution G C intron_variant PBCA-DE 10 80853411 80853411 single base substitution C G intron_variant PBCA-DE 10 80859123 80859123 single base substitution A C intron_variant PBCA-DE 10 80882751 80882751 single base substitution G A intron_variant PBCA-DE 10 80896059 80896059 deletion of <=200bp C - intron_variant PBCA-DE 10 80901074 80901074 single base substitution C G intron_variant PBCA-DE 10 80905234 80905234 single base substitution C A intron_variant PBCA-DE 10 80925642 80925642 single base substitution G A intron_variant PBCA-DE 10 80927123 80927123 single base substitution G A intron_variant PBCA-DE 10 80930724 80930724 single base substitution C G intron_variant PBCA-DE 10 80932823 80932823 single base substitution C T intron_variant PBCA-DE 10 80945386 80945388 deletion of <=200bp CTC - intron_variant PBCA-DE 10 80949874 80949874 single base substitution G C intron_variant PBCA-DE 10 80960018 80960018 single base substitution A G intron_variant PBCA-DE 10 80978342 80978343 deletion of <=200bp GT - intron_variant PBCA-DE 10 80981027 80981028 deletion of <=200bp GT - intron_variant PBCA-DE 10 80983650 80983650 single base substitution G T intron_variant PBCA-DE 10 80984040 80984040 single base substitution C T intron_variant PBCA-DE 10 80986809 80986809 single base substitution A G intron_variant PBCA-DE 10 81009174 81009174 single base substitution G A intron_variant PBCA-DE 10 81010587 81010587 single base substitution C T intron_variant PBCA-DE 10 81016280 81016280 single base substitution C T intron_variant PBCA-DE 10 81022625 81022625 single base substitution A C intron_variant PBCA-DE 10 81034670 81034670 single base substitution G A intron_variant PBCA-DE 10 81034670 81034670 single base substitution G A upstream_gene_variant PBCA-DE 10 81047952 81047952 single base substitution C T intron_variant PBCA-DE 10 81052048 81052048 single base substitution A C downstream_gene_variant PBCA-DE 10 81052048 81052048 single base substitution A C exon_variant PBCA-DE 10 81052048 81052048 single base substitution A C missense_variant T298P 892A>C PRAD-CA 10 80858411 80858411 single base substitution G A intron_variant PRAD-CA 10 80874265 80874265 single base substitution T C intron_variant PRAD-CA 10 80874271 80874271 single base substitution T C intron_variant PRAD-CA 10 80882549 80882549 single base substitution G A intron_variant PRAD-CA 10 80901981 80901981 single base substitution G A intron_variant PRAD-CA 10 80906731 80906731 single base substitution A G intron_variant PRAD-CA 10 80974262 80974262 single base substitution C T intron_variant PRAD-CA 10 80978987 80978987 single base substitution G C intron_variant PRAD-CA 10 81036067 81036067 single base substitution C T intron_variant PRAD-CA 10 81036067 81036067 single base substitution C T upstream_gene_variant PRAD-CA 10 81041885 81041885 single base substitution G A intron_variant PRAD-CA 10 81049181 81049181 single base substitution A T intron_variant PRAD-UK 10 80834126 80834126 single base substitution G T intron_variant PRAD-UK 10 80835242 80835242 single base substitution A G intron_variant PRAD-UK 10 80842135 80842135 single base substitution G A intron_variant PRAD-UK 10 80863997 80863997 single base substitution G A intron_variant PRAD-UK 10 80867193 80867193 single base substitution G A intron_variant PRAD-UK 10 80909898 80909898 single base substitution A T intron_variant PRAD-UK 10 80930815 80930815 single base substitution C T intron_variant PRAD-UK 10 80972308 80972308 single base substitution A C intron_variant PRAD-UK 10 80973462 80973462 single base substitution G A intron_variant PRAD-UK 10 80978068 80978068 insertion of <=200bp - A intron_variant PRAD-UK 10 80986711 80986711 single base substitution A G intron_variant PRAD-UK 10 80991575 80991575 single base substitution T G intron_variant PRAD-UK 10 80996804 80996804 single base substitution C G intron_variant PRAD-UK 10 81030602 81030602 single base substitution C T intron_variant PRAD-UK 10 81031792 81031792 single base substitution G A intron_variant PRAD-UK 10 81032351 81032351 single base substitution C T intron_variant PRAD-UK 10 81032351 81032351 single base substitution C T upstream_gene_variant PRAD-UK 10 81038818 81038818 single base substitution G C intron_variant PRAD-UK 10 81064123 81064123 single base substitution C G intron_variant PRAD-UK 10 81064123 81064123 single base substitution C G upstream_gene_variant PRAD-US 10 81058166 81058166 single base substitution C T downstream_gene_variant PRAD-US 10 81058166 81058166 single base substitution C T missense_variant P499S 1495C>T PRAD-US 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D1048 PRAD-US 10 81072446 81072446 deletion of <=200bp C - frameshift_variant D114 READ-US 10 81050890 81050890 single base substitution T C downstream_gene_variant READ-US 10 81050890 81050890 single base substitution T C exon_variant READ-US 10 81050890 81050890 single base substitution T C missense_variant Y239H 715T>C RECA-EU 10 80826510 80826510 single base substitution C G upstream_gene_variant RECA-EU 10 80832636 80832636 single base substitution G C intron_variant RECA-EU 10 80835313 80835313 single base substitution G C intron_variant RECA-EU 10 80835314 80835314 single base substitution C A intron_variant RECA-EU 10 80835350 80835350 single base substitution C A intron_variant RECA-EU 10 80835363 80835363 single base substitution A C intron_variant RECA-EU 10 80839285 80839285 single base substitution T A intron_variant RECA-EU 10 80847750 80847750 single base substitution T A intron_variant RECA-EU 10 80854211 80854211 single base substitution G C intron_variant RECA-EU 10 80854725 80854725 single base substitution A G intron_variant RECA-EU 10 80877630 80877630 single base substitution G A intron_variant RECA-EU 10 80884345 80884345 single base substitution C T intron_variant RECA-EU 10 80888882 80888882 single base substitution T A intron_variant RECA-EU 10 80894640 80894640 single base substitution A G intron_variant RECA-EU 10 80900700 80900700 single base substitution C T intron_variant RECA-EU 10 80905801 80905801 single base substitution C G intron_variant RECA-EU 10 80908362 80908362 single base substitution G T intron_variant RECA-EU 10 80908987 80908987 single base substitution T G intron_variant RECA-EU 10 80916716 80916716 single base substitution A T intron_variant RECA-EU 10 80922535 80922535 single base substitution T C intron_variant RECA-EU 10 80927127 80927127 single base substitution G A intron_variant RECA-EU 10 80939380 80939380 single base substitution C T intron_variant RECA-EU 10 80946466 80946466 single base substitution G T intron_variant RECA-EU 10 80950435 80950435 single base substitution G T intron_variant RECA-EU 10 80981328 80981328 single base substitution A G intron_variant RECA-EU 10 80999234 80999234 single base substitution A T intron_variant RECA-EU 10 80999234 80999234 single base substitution A T upstream_gene_variant RECA-EU 10 81010406 81010406 single base substitution G T intron_variant RECA-EU 10 81017556 81017556 single base substitution T C intron_variant RECA-EU 10 81030225 81030225 single base substitution A G intron_variant RECA-EU 10 81033551 81033551 single base substitution A G intron_variant RECA-EU 10 81033551 81033551 single base substitution A G upstream_gene_variant RECA-EU 10 81047148 81047148 single base substitution T A intron_variant RECA-EU 10 81066489 81066489 single base substitution G T intron_variant SKCA-BR 10 80824991 80824991 single base substitution A C upstream_gene_variant SKCA-BR 10 80825186 80825186 single base substitution A G upstream_gene_variant SKCA-BR 10 80827477 80827477 single base substitution C A upstream_gene_variant SKCA-BR 10 80829427 80829430 deletion of <=200bp TCGC - intron_variant SKCA-BR 10 80830304 80830304 single base substitution A C intron_variant SKCA-BR 10 80830314 80830314 single base substitution G C intron_variant SKCA-BR 10 80835333 80835333 insertion of <=200bp - CATGCACACCTGCACACAT intron_variant SKCA-BR 10 80835761 80835761 single base substitution T A intron_variant SKCA-BR 10 80839396 80839396 insertion of <=200bp - CG intron_variant SKCA-BR 10 80844634 80844634 single base substitution T G intron_variant SKCA-BR 10 80846031 80846031 single base substitution C T intron_variant SKCA-BR 10 80850233 80850233 single base substitution G C intron_variant SKCA-BR 10 80853078 80853078 single base substitution A G intron_variant SKCA-BR 10 80853575 80853575 single base substitution A G intron_variant SKCA-BR 10 80854723 80854723 insertion of <=200bp - AAG intron_variant SKCA-BR 10 80860078 80860078 single base substitution T G intron_variant SKCA-BR 10 80863775 80863775 single base substitution T C intron_variant SKCA-BR 10 80867217 80867217 single base substitution T G intron_variant SKCA-BR 10 80868198 80868198 single base substitution T A intron_variant SKCA-BR 10 80874239 80874251 deletion of <=200bp TGTGTGTGTGTGC - intron_variant SKCA-BR 10 80877062 80877062 single base substitution A C intron_variant SKCA-BR 10 80877430 80877430 single base substitution A C intron_variant SKCA-BR 10 80880239 80880239 single base substitution C A intron_variant SKCA-BR 10 80881987 80881987 single base substitution G C intron_variant SKCA-BR 10 80889270 80889271 deletion of <=200bp TG - intron_variant SKCA-BR 10 80895649 80895649 single base substitution A C intron_variant SKCA-BR 10 80902340 80902340 single base substitution A C intron_variant SKCA-BR 10 80902985 80902985 single base substitution G A intron_variant SKCA-BR 10 80903455 80903455 single base substitution C T intron_variant SKCA-BR 10 80903955 80903955 single base substitution A G intron_variant SKCA-BR 10 80905461 80905461 single base substitution C T intron_variant SKCA-BR 10 80906702 80906704 deletion of <=200bp CGT - intron_variant SKCA-BR 10 80906727 80906731 deletion of <=200bp GTGTA - intron_variant SKCA-BR 10 80906729 80906731 deletion of <=200bp GTA - intron_variant SKCA-BR 10 80909804 80909804 single base substitution C T intron_variant SKCA-BR 10 80915827 80915827 single base substitution T C intron_variant SKCA-BR 10 80923995 80923995 single base substitution C T intron_variant SKCA-BR 10 80927789 80927789 single base substitution T G intron_variant SKCA-BR 10 80928625 80928625 single base substitution G T intron_variant SKCA-BR 10 80929521 80929521 single base substitution C T intron_variant SKCA-BR 10 80933137 80933137 single base substitution C T intron_variant SKCA-BR 10 80933880 80933880 single base substitution C T intron_variant SKCA-BR 10 80934569 80934569 single base substitution G C intron_variant SKCA-BR 10 80935363 80935363 single base substitution G A intron_variant SKCA-BR 10 80935369 80935395 deletion of <=200bp GTGTGTGTGTGTGTGTGTGGAGGTTTT - intron_variant SKCA-BR 10 80936752 80936752 single base substitution C T intron_variant SKCA-BR 10 80939604 80939604 single base substitution T G intron_variant SKCA-BR 10 80939622 80939622 single base substitution T G intron_variant SKCA-BR 10 80940611 80940611 single base substitution C G intron_variant SKCA-BR 10 80941186 80941186 single base substitution A G intron_variant SKCA-BR 10 80943115 80943115 insertion of <=200bp - GCACACA intron_variant SKCA-BR 10 80944338 80944338 single base substitution C T intron_variant SKCA-BR 10 80945980 80945980 single base substitution C T intron_variant SKCA-BR 10 80947102 80947102 single base substitution C T intron_variant SKCA-BR 10 80947256 80947256 single base substitution C T intron_variant SKCA-BR 10 80948123 80948123 single base substitution G A intron_variant SKCA-BR 10 80949798 80949798 single base substitution C T intron_variant SKCA-BR 10 80951528 80951528 single base substitution G C intron_variant SKCA-BR 10 80952013 80952013 single base substitution C T intron_variant SKCA-BR 10 80953219 80953219 single base substitution T G intron_variant SKCA-BR 10 80953783 80953783 single base substitution A C intron_variant SKCA-BR 10 80957394 80957394 insertion of <=200bp - CCCCT intron_variant SKCA-BR 10 80961813 80961813 insertion of <=200bp - CA intron_variant SKCA-BR 10 80962927 80962927 single base substitution C T intron_variant SKCA-BR 10 80962928 80962928 single base substitution C T intron_variant SKCA-BR 10 80964941 80964941 single base substitution T G intron_variant SKCA-BR 10 80964975 80964975 single base substitution T C intron_variant SKCA-BR 10 80966255 80966255 single base substitution A G intron_variant SKCA-BR 10 80966860 80966860 single base substitution T C intron_variant SKCA-BR 10 80974032 80974032 single base substitution T A intron_variant SKCA-BR 10 80981942 80981943 deletion of <=200bp GT - intron_variant SKCA-BR 10 80989167 80989167 single base substitution C T intron_variant SKCA-BR 10 80989557 80989557 single base substitution T G intron_variant SKCA-BR 10 80990177 80990177 single base substitution C T intron_variant SKCA-BR 10 80991138 80991138 single base substitution G T intron_variant SKCA-BR 10 80993967 80993967 single base substitution T G intron_variant SKCA-BR 10 80998163 80998163 single base substitution A G intron_variant SKCA-BR 10 80998182 80998182 single base substitution T G intron_variant SKCA-BR 10 80998652 80998652 single base substitution G T intron_variant SKCA-BR 10 80998652 80998652 single base substitution G T upstream_gene_variant SKCA-BR 10 80999833 80999833 single base substitution C T intron_variant SKCA-BR 10 80999833 80999833 single base substitution C T upstream_gene_variant SKCA-BR 10 81002786 81002786 single base substitution A G intron_variant SKCA-BR 10 81002786 81002786 single base substitution A G upstream_gene_variant SKCA-BR 10 81007054 81007054 single base substitution C T intron_variant SKCA-BR 10 81007055 81007055 single base substitution C T intron_variant SKCA-BR 10 81008802 81008802 single base substitution C G intron_variant SKCA-BR 10 81009953 81009953 single base substitution C T intron_variant SKCA-BR 10 81011245 81011245 single base substitution C T intron_variant SKCA-BR 10 81012246 81012246 single base substitution A C intron_variant SKCA-BR 10 81016193 81016193 single base substitution C T intron_variant SKCA-BR 10 81017539 81017539 single base substitution T C intron_variant SKCA-BR 10 81018948 81018948 single base substitution G C intron_variant SKCA-BR 10 81019374 81019374 insertion of <=200bp - CT intron_variant SKCA-BR 10 81021032 81021032 single base substitution C T intron_variant SKCA-BR 10 81021561 81021561 single base substitution C T intron_variant SKCA-BR 10 81024738 81024738 single base substitution C T intron_variant SKCA-BR 10 81025223 81025225 deletion of <=200bp TTC - intron_variant SKCA-BR 10 81030365 81030365 single base substitution T G intron_variant SKCA-BR 10 81032005 81032005 single base substitution T G intron_variant SKCA-BR 10 81032005 81032005 single base substitution T G upstream_gene_variant SKCA-BR 10 81035307 81035307 single base substitution G C intron_variant SKCA-BR 10 81035307 81035307 single base substitution G C upstream_gene_variant SKCA-BR 10 81039153 81039153 single base substitution C T intron_variant SKCA-BR 10 81039749 81039749 insertion of <=200bp - CT intron_variant SKCA-BR 10 81040336 81040338 deletion of <=200bp CAG - intron_variant SKCA-BR 10 81040338 81040338 single base substitution G T intron_variant SKCA-BR 10 81041456 81041456 single base substitution G C intron_variant SKCA-BR 10 81042981 81042981 single base substitution G A intron_variant SKCA-BR 10 81043276 81043276 single base substitution A G intron_variant SKCA-BR 10 81043290 81043290 single base substitution A C intron_variant SKCA-BR 10 81044200 81044200 single base substitution C T intron_variant SKCA-BR 10 81046293 81046293 single base substitution C T intron_variant SKCA-BR 10 81046356 81046356 single base substitution C T intron_variant SKCA-BR 10 81049445 81049445 single base substitution G A intron_variant SKCA-BR 10 81050597 81050597 single base substitution C T intron_variant SKCA-BR 10 81055442 81055442 single base substitution C T downstream_gene_variant SKCA-BR 10 81055442 81055442 single base substitution C T exon_variant SKCA-BR 10 81055442 81055442 single base substitution C T intron_variant SKCA-BR 10 81058493 81058493 single base substitution T G downstream_gene_variant SKCA-BR 10 81058493 81058493 single base substitution T G intron_variant SKCA-BR 10 81062552 81062552 single base substitution G A intron_variant SKCA-BR 10 81062552 81062552 single base substitution G A upstream_gene_variant SKCA-BR 10 81062608 81062608 single base substitution G A intron_variant SKCA-BR 10 81062608 81062608 single base substitution G A upstream_gene_variant SKCA-BR 10 81062618 81062618 insertion of <=200bp - GT intron_variant SKCA-BR 10 81062618 81062618 insertion of <=200bp - GT upstream_gene_variant SKCA-BR 10 81063369 81063369 single base substitution C T intron_variant SKCA-BR 10 81063369 81063369 single base substitution C T upstream_gene_variant SKCA-BR 10 81065524 81065524 single base substitution T G intron_variant SKCA-BR 10 81065524 81065524 single base substitution T G upstream_gene_variant SKCA-BR 10 81067100 81067100 single base substitution C T intron_variant SKCA-BR 10 81067945 81067945 single base substitution T C intron_variant SKCA-BR 10 81068933 81068933 single base substitution C T intron_variant SKCA-BR 10 81072947 81072947 single base substitution G A 3_prime_UTR_variant SKCA-BR 10 81072947 81072947 single base substitution G A downstream_gene_variant SKCA-BR 10 81073770 81073770 single base substitution A G 3_prime_UTR_variant SKCA-BR 10 81073770 81073770 single base substitution A G downstream_gene_variant SKCM-US 10 80968157 80968157 single base substitution C T missense_variant P42L 125C>T SKCM-US 10 81050844 81050844 single base substitution C T downstream_gene_variant SKCM-US 10 81050844 81050844 single base substitution C T exon_variant SKCM-US 10 81050844 81050844 single base substitution C T synonymous_variant F223F 669C>T SKCM-US 10 81051954 81051954 single base substitution C T downstream_gene_variant SKCM-US 10 81051954 81051954 single base substitution C T exon_variant SKCM-US 10 81051954 81051954 single base substitution C T synonymous_variant I266I 798C>T SKCM-US 10 81053203 81053203 single base substitution C T downstream_gene_variant SKCM-US 10 81053203 81053203 single base substitution C T exon_variant SKCM-US 10 81053203 81053203 single base substitution C T synonymous_variant S341S 1023C>T SKCM-US 10 81053372 81053372 single base substitution C T downstream_gene_variant SKCM-US 10 81053372 81053372 single base substitution C T exon_variant SKCM-US 10 81053372 81053372 single base substitution C T missense_variant L398F 1192C>T SKCM-US 10 81056306 81056306 single base substitution C T exon_variant SKCM-US 10 81056306 81056306 single base substitution C T missense_variant P437S 1309C>T SKCM-US 10 81058166 81058166 single base substitution C T downstream_gene_variant SKCM-US 10 81058166 81058166 single base substitution C T missense_variant P499S 1495C>T SKCM-US 10 81058188 81058188 single base substitution A C downstream_gene_variant SKCM-US 10 81058188 81058188 single base substitution A C missense_variant N506T 1517A>C SKCM-US 10 81058192 81058192 single base substitution C T downstream_gene_variant SKCM-US 10 81058192 81058192 single base substitution C T synonymous_variant Y507Y 1521C>T SKCM-US 10 81060673 81060673 single base substitution C T downstream_gene_variant SKCM-US 10 81060673 81060673 single base substitution C T stop_gained Q665* 1993C>T SKCM-US 10 81061875 81061875 single base substitution C T synonymous_variant F677F 2031C>T SKCM-US 10 81061875 81061875 single base substitution C T upstream_gene_variant SKCM-US 10 81061902 81061902 single base substitution C T synonymous_variant S686S 2058C>T SKCM-US 10 81061902 81061902 single base substitution C T upstream_gene_variant SKCM-US 10 81063817 81063817 single base substitution C T missense_variant T724I 2171C>T SKCM-US 10 81063817 81063817 single base substitution C T upstream_gene_variant SKCM-US 10 81065942 81065942 single base substitution C T missense_variant P837S 2509C>T SKCM-US 10 81065942 81065942 single base substitution C T upstream_gene_variant SKCM-US 10 81065958 81065958 single base substitution C T missense_variant S842F 2525C>T SKCM-US 10 81065958 81065958 single base substitution C T upstream_gene_variant SKCM-US 10 81066066 81066066 single base substitution C T missense_variant P31L 92C>T SKCM-US 10 81066066 81066066 single base substitution C T missense_variant P878L 2633C>T SKCM-US 10 81070787 81070789 deletion of <=200bp CTC - inframe_deletion AP981A SKCM-US 10 81070787 81070789 deletion of <=200bp CTC - intron_variant SKCM-US 10 81070838 81070838 single base substitution C T intron_variant SKCM-US 10 81070838 81070838 single base substitution C T missense_variant P998L 2993C>T SKCM-US 10 81070875 81070875 single base substitution C A intron_variant SKCM-US 10 81070875 81070875 single base substitution C A synonymous_variant P1010P 3030C>A STAD-US 10 80968104 80968104 single base substitution T A missense_variant N24K 72T>A STAD-US 10 80968205 80968205 single base substitution C T missense_variant T58M 173C>T STAD-US 10 81037036 81037036 deletion of <=200bp C - exon_variant STAD-US 10 81037036 81037036 deletion of <=200bp C - frameshift_variant P127 STAD-US 10 81050715 81050715 single base substitution G T splice_acceptor_variant STAD-US 10 81050777 81050777 single base substitution C T exon_variant STAD-US 10 81050777 81050777 single base substitution C T missense_variant A201V 602C>T STAD-US 10 81051995 81051995 single base substitution C T downstream_gene_variant STAD-US 10 81051995 81051995 single base substitution C T exon_variant STAD-US 10 81051995 81051995 single base substitution C T missense_variant A280V 839C>T STAD-US 10 81052014 81052014 single base substitution G A downstream_gene_variant STAD-US 10 81052014 81052014 single base substitution G A exon_variant STAD-US 10 81052014 81052014 single base substitution G A synonymous_variant A286A 858G>A STAD-US 10 81052021 81052021 single base substitution G A downstream_gene_variant STAD-US 10 81052021 81052021 single base substitution G A exon_variant STAD-US 10 81052021 81052021 single base substitution G A missense_variant A289T 865G>A STAD-US 10 81052026 81052026 single base substitution A G downstream_gene_variant STAD-US 10 81052026 81052026 single base substitution A G exon_variant STAD-US 10 81052026 81052026 single base substitution A G synonymous_variant A290A 870A>G STAD-US 10 81053157 81053157 single base substitution A C downstream_gene_variant STAD-US 10 81053157 81053157 single base substitution A C exon_variant STAD-US 10 81053157 81053157 single base substitution A C missense_variant Y326S 977A>C STAD-US 10 81053206 81053206 deletion of <=200bp G - downstream_gene_variant STAD-US 10 81053206 81053206 deletion of <=200bp G - exon_variant STAD-US 10 81053206 81053206 deletion of <=200bp G - frameshift_variant M342 STAD-US 10 81053363 81053363 single base substitution C G downstream_gene_variant STAD-US 10 81053363 81053363 single base substitution C G exon_variant STAD-US 10 81053363 81053363 single base substitution C G missense_variant P395A 1183C>G STAD-US 10 81056311 81056311 single base substitution G A exon_variant STAD-US 10 81056311 81056311 single base substitution G A synonymous_variant R438R 1314G>A STAD-US 10 81056357 81056357 single base substitution C T exon_variant STAD-US 10 81056357 81056357 single base substitution C T missense_variant P454S 1360C>T STAD-US 10 81058191 81058191 single base substitution A G downstream_gene_variant STAD-US 10 81058191 81058191 single base substitution A G missense_variant Y507C 1520A>G STAD-US 10 81058854 81058854 single base substitution G A downstream_gene_variant STAD-US 10 81058854 81058854 single base substitution G A missense_variant V572M 1714G>A STAD-US 10 81060696 81060696 single base substitution C T downstream_gene_variant STAD-US 10 81060696 81060696 single base substitution C T synonymous_variant C672C 2016C>T STAD-US 10 81061949 81061949 single base substitution C T missense_variant A702V 2105C>T STAD-US 10 81061949 81061949 single base substitution C T upstream_gene_variant STAD-US 10 81064968 81064968 single base substitution C A synonymous_variant T778T 2334C>A STAD-US 10 81064968 81064968 single base substitution C A upstream_gene_variant STAD-US 10 81067236 81067236 single base substitution A G missense_variant M68V 202A>G STAD-US 10 81067236 81067236 single base substitution A G missense_variant M915V 2743A>G STAD-US 10 81067262 81067262 deletion of <=200bp C - frameshift_variant H76 STAD-US 10 81067262 81067262 deletion of <=200bp C - frameshift_variant H923 STAD-US 10 81067262 81067262 insertion of <=200bp - C frameshift_variant H76H? STAD-US 10 81067262 81067262 insertion of <=200bp - C frameshift_variant H923H? STAD-US 10 81072446 81072446 insertion of <=200bp - C frameshift_variant D1048D? STAD-US 10 81072446 81072446 insertion of <=200bp - C frameshift_variant D114D? THCA-SA 10 81073515 81073515 single base substitution C G 3_prime_UTR_variant THCA-SA 10 81073515 81073515 single base substitution C G downstream_gene_variant THCA-SA 10 81075168 81075168 single base substitution C T 3_prime_UTR_variant THCA-SA 10 81075168 81075168 single base substitution C T downstream_gene_variant THCA-US 10 81058872 81058872 single base substitution C T downstream_gene_variant THCA-US 10 81058872 81058872 single base substitution C T missense_variant R578C 1732C>T THCA-US 10 81060655 81060655 single base substitution C G downstream_gene_variant THCA-US 10 81060655 81060655 single base substitution C G missense_variant P659A 1975C>G UCEC-US 10 80961430 80961430 single base substitution G A missense_variant R14Q 41G>A UCEC-US 10 80968135 80968135 single base substitution C T synonymous_variant L35L 103C>T UCEC-US 10 81036951 81036951 single base substitution C T exon_variant UCEC-US 10 81036951 81036951 single base substitution C T synonymous_variant S98S 294C>T UCEC-US 10 81049540 81049540 single base substitution C T exon_variant UCEC-US 10 81049540 81049540 single base substitution C T missense_variant S145L 434C>T UCEC-US 10 81049608 81049608 single base substitution A T exon_variant UCEC-US 10 81049608 81049608 single base substitution A T missense_variant T168S 502A>T UCEC-US 10 81050780 81050780 single base substitution C T exon_variant UCEC-US 10 81050780 81050780 single base substitution C T missense_variant S202L 605C>T UCEC-US 10 81053330 81053330 single base substitution C T downstream_gene_variant UCEC-US 10 81053330 81053330 single base substitution C T exon_variant UCEC-US 10 81053330 81053330 single base substitution C T missense_variant R384W 1150C>T UCEC-US 10 81053452 81053452 single base substitution A G downstream_gene_variant UCEC-US 10 81053452 81053452 single base substitution A G exon_variant UCEC-US 10 81053452 81053452 single base substitution A G intron_variant UCEC-US 10 81058873 81058873 single base substitution G A downstream_gene_variant UCEC-US 10 81058873 81058873 single base substitution G A missense_variant R578H 1733G>A UCEC-US 10 81061875 81061875 single base substitution C T synonymous_variant F677F 2031C>T UCEC-US 10 81061875 81061875 single base substitution C T upstream_gene_variant UCEC-US 10 81063777 81063777 single base substitution C T missense_variant R711W 2131C>T UCEC-US 10 81063777 81063777 single base substitution C T upstream_gene_variant UCEC-US 10 81063871 81063871 single base substitution G T missense_variant C742F 2225G>T UCEC-US 10 81063871 81063871 single base substitution G T upstream_gene_variant UCEC-US 10 81065963 81065963 single base substitution C T missense_variant R844W 2530C>T UCEC-US 10 81065963 81065963 single base substitution C T upstream_gene_variant UCEC-US 10 81070924 81070924 single base substitution C T intron_variant UCEC-US 10 81070924 81070924 single base substitution C T missense_variant P1027S 3079C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand SNUH_G15_S1 COSM3675882 c.861A>G p.A287A Substitution - coding silent 10:79292260-79292260 + LUAD-S01356 COSM397929 c.137A>T p.Q46L Substitution - Missense 10:79208412-79208412 + U251 COSM1675386 c.118G>T p.G40* Substitution - Nonsense 10:79208393-79208393 + BD134T COSM5494452 c.280+10C>T p.? Unknown 10:79216284-79216284 + TCGA-AA-3663-01 COSM1349260 c.2634A>C p.P878P Substitution - coding silent 10:79306310-79306310 + sysucc-882T COSM5446866 c.1905G>A p.T635T Substitution - coding silent 10:79300828-79300828 + OSCC-GB_00850111 COSM4891460 c.300C>A p.C100* Substitution - Nonsense 10:79277200-79277200 + B86-Tumor COSM1745923 c.1008G>A p.P336P Substitution - coding silent 10:79293431-79293431 + ccRCC-97 COSM1665107 c.3091C>A p.L1031M Substitution - Missense 10:79311179-79311179 + TCGA-CM-4746-01 COSM1349263 c.3144delC p.D1051fs*>17 Deletion - Frameshift 10:79312689-79312689 + Gp2D COSM1966356 c.1468T>C p.Y490H Substitution - Missense 10:79297667-79297667 + HCC82 COSM1603779 c.2153C>T p.A718V Substitution - Missense 10:79304042-79304042 + T3301 COSM1603779 c.2153C>T p.A718V Substitution - Missense 10:79304042-79304042 + Pat_40_A COSM1349263 c.3144delC p.D1051fs*>17 Deletion - Frameshift 10:79312689-79312689 + TCGA-AP-A059-01 COSM920724 c.3079C>T p.P1027S Substitution - Missense 10:79311167-79311167 + TCGA-FK-A3SH-01 COSM3368134 c.1732C>T p.R578C Substitution - Missense 10:79299115-79299115 + 2492713 COSM5718681 c.1727C>T p.P576L Substitution - Missense 10:79299110-79299110 + TCGA-B1-A656-01 COSM4413898 c.70A>T p.N24Y Substitution - Missense 10:79208345-79208345 + T2940 COSM4742869 c.22A>G p.I8V Substitution - Missense 10:79201654-79201654 + P128 COSM1736872 c.901G>A p.A301T Substitution - Missense 10:79292300-79292300 + AOCS-088-3-8 COSM3981153 c.3082G>C p.E1028Q Substitution - Missense 10:79311170-79311170 + BN33T COSM1603780 c.2296C>G p.L766V Substitution - Missense 10:79305173-79305173 + BN24 COSM1603781 c.2709C>T p.H903H Substitution - coding silent 10:79307445-79307445 + T2969 COSM4742873 c.871G>A p.A291T Substitution - Missense 10:79292270-79292270 + TCGA-G4-6320-01 COSM3383050 c.3068C>T p.A1023V Substitution - Missense 10:79311156-79311156 + TCGA-A6-5665-01 COSM1349257 c.351C>T p.S117S Substitution - coding silent 10:79277251-79277251 + TCGA-CU-A3YL-01 COSM3790981 c.387C>G p.L129L Substitution - coding silent 10:79277287-79277287 + 2492701 COSM5716611 c.1989C>T p.T663T Substitution - coding silent 10:79300912-79300912 + TCGA-22-5471-01 COSM685249 c.1630A>G p.I544V Substitution - Missense 10:79298544-79298544 + HCC106T COSM1603778 c.1692C>T p.L564L Substitution - coding silent 10:79299075-79299075 + ESCC_25 COSM5050359 c.2132G>A p.R711Q Substitution - Missense 10:79304021-79304021 + LS411 COSM1966383 c.2470C>T p.P824S Substitution - Missense 10:79306146-79306146 + ESCC_13 COSM5625054 c.1479G>A p.G493G Substitution - coding silent 10:79297678-79297678 + TCGA-13-1481-01 COSM79323 c.2289C>A p.C763* Substitution - Nonsense 10:79305166-79305166 + LUAD-NYU608 COSM392028 c.2942_2944delCTC p.P986delP Deletion - In frame 10:79311030-79311032 + LUAD-B00416 COSM330771 c.2471C>T p.P824L Substitution - Missense 10:79306147-79306147 + Pat_65_A COSM1349263 c.3144delC p.D1051fs*>17 Deletion - Frameshift 10:79312689-79312689 + T2197 COSM4742870 c.352G>A p.D118N Substitution - Missense 10:79277252-79277252 + I2L-P9-Tumor-Biopsy COSM5360362 c.2835T>G p.T945T Substitution - coding silent 10:79307571-79307571 + T3262 COSM4742876 c.1824G>A p.L608L Substitution - coding silent 10:79300747-79300747 + TCGA-GC-A3RC-01 COSM3790982 c.465G>A p.Q155Q Substitution - coding silent 10:79289814-79289814 + T3610 COSM392028 c.2942_2944delCTC p.P986delP Deletion - In frame 10:79311030-79311032 + LUAD-NYU608 COSM375293 c.1180C>T p.R394W Substitution - Missense 10:79293603-79293603 + 1517_CLM COSM5753546 c.2543T>C p.M848T Substitution - Missense 10:79306219-79306219 + TCGA-G4-6586-01 COSM1349261 c.2956C>T p.P986S Substitution - Missense 10:79311044-79311044 + HOP-92 COSM1675386 c.118G>T p.G40* Substitution - Nonsense 10:79208393-79208393 + CSCC-44-T COSM4484144 c.2772C>T p.P924P Substitution - coding silent 10:79307508-79307508 + TCGA-BR-4361-01 COSM4016213 c.541-1G>T p.? Unknown 10:79290958-79290958 + RK233_C01 COSM4778431 c.280G>T p.A94S Substitution - Missense 10:79216274-79216274 + Pat_44_B COSM1966394 c.2752delC p.Q920fs*87 Deletion - Frameshift 10:79307488-79307488 + TCGA-BR-4292-01 COSM4016206 c.173C>T p.T58M Substitution - Missense 10:79208448-79208448 + 1N03-VS-1T03 COSM4972576 c.1362G>A p.P454P Substitution - coding silent 10:79296602-79296602 + SNUH_G15_S1 COSM3675881 c.813G>C p.R271S Substitution - Missense 10:79292212-79292212 + 587350 COSM1233512 c.2816G>T p.S939I Substitution - Missense 10:79307552-79307552 + 2020 COSM1645138 c.1502C>T p.P501L Substitution - Missense 10:79298416-79298416 + 6P2-1 COSM3734276 c.905C>T p.T302I Substitution - Missense 10:79292304-79292304 + TCGA-EA-A3HT-01 COSM1966410 c.3084G>A p.E1028E Substitution - coding silent 10:79311172-79311172 + DLD1 COSM1966392 c.2683G>T p.G895C Substitution - Missense 10:79307419-79307419 + TCGA-BR-6452-01 COSM4016205 c.72T>A p.N24K Substitution - Missense 10:79208347-79208347 + SW48 COSM392028 c.2942_2944delCTC p.P986delP Deletion - In frame 10:79311030-79311032 + TCGA-EE-A29A-06 COSM3440915 c.125C>T p.P42L Substitution - Missense 10:79208400-79208400 + TCGA-AN-A0AK-01 COSM3807806 c.1882G>A p.V628M Substitution - Missense 10:79300805-79300805 + TCGA-BR-4257-01 COSM4016218 c.977A>C p.Y326S Substitution - Missense 10:79293400-79293400 + TCGA-JW-A5VK-01 COSM4855170 c.2845G>A p.A949T Substitution - Missense 10:79310933-79310933 + CSCC-5-T COSM1966344 c.1149G>A p.Q383Q Substitution - coding silent 10:79293572-79293572 + HCC106 COSM1603778 c.1692C>T p.L564L Substitution - coding silent 10:79299075-79299075 + ESO-859 COSM1240712 c.694C>T p.P232S Substitution - Missense 10:79291112-79291112 + B86 COSM1745923 c.1008G>A p.P336P Substitution - coding silent 10:79293431-79293431 + OSCC-GB_01360111 COSM5955532 c.3106G>A p.E1036K Substitution - Missense 10:79312651-79312651 + CHC1040T COSM4799601 c.2179G>A p.G727R Substitution - Missense 10:79304068-79304068 + TCGA-EE-A2GO-06 COSM3440918 c.798C>T p.I266I Substitution - coding silent 10:79292197-79292197 + BN24T COSM1603781 c.2709C>T p.H903H Substitution - coding silent 10:79307445-79307445 + Pat_40_A COSM5837371 c.3055G>A p.G1019R Substitution - Missense 10:79311143-79311143 + TCGA-DU-7009-01 COSM3967177 c.859G>A p.A287T Substitution - Missense 10:79292258-79292258 + TCGA-BR-4361-01 COSM4016222 c.1520A>G p.Y507C Substitution - Missense 10:79298434-79298434 + QC2-15-T2 COSM5652494 c.2145C>T p.S715S Substitution - coding silent 10:79304034-79304034 + TCGA-EE-A20C-06 COSM3440923 c.2525C>T p.S842F Substitution - Missense 10:79306201-79306201 + ESO-122 COSM1270982 c.3090G>A p.S1030S Substitution - coding silent 10:79311178-79311178 + T475 COSM1966373 c.2032G>A p.V678M Substitution - Missense 10:79302119-79302119 + ACC-3 COSM4967698 c.1295_1392>15 p.P436fs*13 Unknown 10:79296535-79296632 + 2_PRE-TREATMENT COSM1722976 c.1305delC p.P437fs*84 Deletion - Frameshift 10:79296545-79296545 + I2L-P19Ta-Tumor-Biopsy COSM5359949 c.2751G>C p.G917G Substitution - coding silent 10:79307487-79307487 + B60-Tumor COSM1745925 c.2601C>T p.P867P Substitution - coding silent 10:79306277-79306277 + TCGA-GF-A6C9-06 COSM4901488 c.1192C>T p.L398F Substitution - Missense 10:79293615-79293615 + SNUH_G15_S1 COSM3675883 c.987A>C p.Q329H Substitution - Missense 10:79293410-79293410 + TCGA-BR-8361-01 COSM4016217 c.870A>G p.A290A Substitution - coding silent 10:79292269-79292269 + PD6350a COSM1636934 c.770G>C p.G257A Substitution - Missense 10:79292169-79292169 + pfg125T COSM4758111 c.1876G>A p.A626T Substitution - Missense 10:79300799-79300799 + TCGA-BR-7707-01 COSM4016214 c.839C>T p.A280V Substitution - Missense 10:79292238-79292238 + ESCC_25 COSM5626570 c.27G>A p.Q9Q Substitution - coding silent 10:79201659-79201659 + TCGA-EB-A431-01 COSM3440921 c.2058C>T p.S686S Substitution - coding silent 10:79302145-79302145 + TCGA-A2-A0T5-01 COSM3807807 c.2768A>C p.H923P Substitution - Missense 10:79307504-79307504 + S00947 COSM316697 c.2066C>G p.S689C Substitution - Missense 10:79302153-79302153 + 07-P1079 COSM4573850 c.2037G>A p.L679L Substitution - coding silent 10:79302124-79302124 + TCGA-BS-A0UV-01 COSM920714 c.294C>T p.S98S Substitution - coding silent 10:79277194-79277194 + TCGA-D3-A3C8-06 COSM3440925 c.2993C>T p.P998L Substitution - Missense 10:79311081-79311081 + Pat_14_A COSM1349263 c.3144delC p.D1051fs*>17 Deletion - Frameshift 10:79312689-79312689 + CSCC-44-T COSM4506508 c.721C>T p.R241W Substitution - Missense 10:79291139-79291139 + EGC3 COSM5050358 c.1622C>T p.P541L Substitution - Missense 10:79298536-79298536 + TCGA-G4-6586-01 COSM1349263 c.3144delC p.D1051fs*>17 Deletion - Frameshift 10:79312689-79312689 + TCGA-AP-A059-01 COSM920717 c.1150C>T p.R384W Substitution - Missense 10:79293573-79293573 + MBRep_T29 COSM215440 c.892A>C p.T298P Substitution - Missense 10:79292291-79292291 + TCGA-BR-A4QL-01 COSM4016219 c.1183C>G p.P395A Substitution - Missense 10:79293606-79293606 + Gp5D COSM1966298 c.221G>C p.G74A Substitution - Missense 10:79216215-79216215 + CSCC-47-T COSM4459582 c.1130C>T p.P377L Substitution - Missense 10:79293553-79293553 + T2197 COSM4742875 c.1144G>A p.G382R Substitution - Missense 10:79293567-79293567 + TCGA-A8-A097-01 COSM1966414 c.3143_3144insC p.D1051fs*6 Insertion - Frameshift 10:79312688-79312689 + TCGA-B5-A0JY-01 COSM920718 c.1733G>A p.R578H Substitution - Missense 10:79299116-79299116 + SNUH_G10_S1 COSM3675884 c.2772C>A p.P924P Substitution - coding silent 10:79307508-79307508 + CHC1040T COSM4799601 c.2179G>A p.G727R Substitution - Missense 10:79304068-79304068 + CSCC-38-T COSM4527802 c.1490G>A p.R497K Substitution - Missense 10:79297689-79297689 + TCGA-D1-A15X-01 COSM920716 c.502A>T p.T168S Substitution - Missense 10:79289851-79289851 + S40_pre COSM5575095 c.2751_2752insC p.Q920fs*34 Insertion - Frameshift 10:79307487-79307488 + TCGA-41-4097-01 COSM3397265 c.2579A>C p.E860A Substitution - Missense 10:79306255-79306255 + TCGA-C8-A134-01 COSM427978 c.2732T>G p.M911R Substitution - Missense 10:79307468-79307468 + LUAD_E01086 COSM354697 c.1462A>T p.S488C Substitution - Missense 10:79297661-79297661 + 2492711 COSM5718681 c.1727C>T p.P576L Substitution - Missense 10:79299110-79299110 + TCGA-EE-A29D-06 COSM3440920 c.1993C>T p.Q665* Substitution - Nonsense 10:79300916-79300916 + 2492702 COSM5716611 c.1989C>T p.T663T Substitution - coding silent 10:79300912-79300912 + BD95T COSM5505608 c.1517A>G p.N506S Substitution - Missense 10:79298431-79298431 + CSCC-37-T COSM4480511 c.2426C>T p.S809F Substitution - Missense 10:79306102-79306102 + T3064 COSM4742878 c.2988C>T p.A996A Substitution - coding silent 10:79311076-79311076 + Pat_53_B COSM5837368 c.2051G>A p.R684Q Substitution - Missense 10:79302138-79302138 + Pat_54_A COSM1349263 c.3144delC p.D1051fs*>17 Deletion - Frameshift 10:79312689-79312689 + YUKAT COSM5371173 c.540+1G>A p.? Unknown 10:79289890-79289890 + TCGA-EB-A551-01 COSM3440919 c.1521C>T p.Y507Y Substitution - coding silent 10:79298435-79298435 + TCGA-B5-A0K9-01 COSM920711 c.103C>T p.L35L Substitution - coding silent 10:79208378-79208378 + YUDAB COSM1702677 c.2767C>T p.H923Y Substitution - Missense 10:79307503-79307503 + T3724 COSM4742877 c.2584A>C p.I862L Substitution - Missense 10:79306260-79306260 + PTC-54C COSM4144895 c.2793G>T p.M931I Substitution - Missense 10:79307529-79307529 + T2940 COSM1966333 c.1032C>T p.G344G Substitution - coding silent 10:79293455-79293455 + TCGA-D1-A17Q-01 COSM920719 c.2031C>T p.F677F Substitution - coding silent 10:79302118-79302118 + TCGA-EE-A29S-06 COSM920719 c.2031C>T p.F677F Substitution - coding silent 10:79302118-79302118 + STC252 COSM5050359 c.2132G>A p.R711Q Substitution - Missense 10:79304021-79304021 + 399 COSM4429070 c.1230+3G>C p.? Unknown 10:79293656-79293656 + J36_T COSM3978816 c.606G>A p.S202S Substitution - coding silent 10:79291024-79291024 + Gp5D COSM330771 c.2471C>T p.P824L Substitution - Missense 10:79306147-79306147 + TCGA-DK-A3IS-01 COSM1297461 c.3172G>A p.D1058N Substitution - Missense 10:79312717-79312717 + YUJUBE COSM5371174 c.779C>T p.A260V Substitution - Missense 10:79292178-79292178 + PT40 COSM5923896 c.2669-4C>T p.? Unknown 10:79307401-79307401 + D28 COSM5546141 c.1788C>T p.V596V Substitution - coding silent 10:79299171-79299171 + TCGA-ER-A194-01 COSM3867915 c.1517A>C p.N506T Substitution - Missense 10:79298431-79298431 + B60 COSM1745925 c.2601C>T p.P867P Substitution - coding silent 10:79306277-79306277 + 46 COSM5734317 c.1874C>A p.P625H Substitution - Missense 10:79300797-79300797 + B89-12 COSM1745343 c.1911_1928del18 p.T638_D643delTIERGD Deletion - In frame 10:79300834-79300851 + TCGA-G4-6628-01 COSM1349262 c.3054C>T p.A1018A Substitution - coding silent 10:79311142-79311142 + TCGA-EM-A3O3-01 COSM3368135 c.1975C>G p.P659A Substitution - Missense 10:79300898-79300898 + TCGA-FW-A3R5-06 COSM3867913 c.1023C>T p.S341S Substitution - coding silent 10:79293446-79293446 + ESCC_143 COSM5643956 c.867A>G p.A289A Substitution - coding silent 10:79292266-79292266 + Gp2D COSM330771 c.2471C>T p.P824L Substitution - Missense 10:79306147-79306147 + CN-AML-CR-50-Dx COSM5428480 c.883G>A p.A295T Substitution - Missense 10:79292282-79292282 + RK277_C01 COSM4780796 c.1298C>T p.A433V Substitution - Missense 10:79296538-79296538 + tumor_4107137 COSM3356132 c.1881G>A p.S627S Substitution - coding silent 10:79300804-79300804 + TCGA-D5-6928-01 COSM1349256 c.344G>A p.R115H Substitution - Missense 10:79277244-79277244 + TCGA-EE-A2MS-06 COSM3440922 c.2171C>T p.T724I Substitution - Missense 10:79304060-79304060 + 545 COSM5612878 c.270G>A p.P90P Substitution - coding silent 10:79216264-79216264 + Pat_06_A COSM5837370 c.2629delC p.P878fs*34 Deletion - Frameshift 10:79306305-79306305 + HT55 COSM1966370 c.2005A>T p.T669S Substitution - Missense 10:79300928-79300928 + TCGA-AP-A0LM-01 COSM920715 c.434C>T p.S145L Substitution - Missense 10:79289783-79289783 + TCGA-FW-A3R5-06 COSM3867912 c.669C>T p.F223F Substitution - coding silent 10:79291087-79291087 + TCGA-EW-A1J2-01 COSM1474802 c.2191G>T p.V731L Substitution - Missense 10:79304080-79304080 + LUAD-FH5PJ COSM394386 c.254G>A p.R85Q Substitution - Missense 10:79216248-79216248 + TCGA-EU-5907-01 COSM466006 c.2486C>T p.S829L Substitution - Missense 10:79306162-79306162 + Pat_01_B COSM5837369 c.2561T>C p.I854T Substitution - Missense 10:79306237-79306237 + Gp2D COSM1966314 c.319C>T p.L107L Substitution - coding silent 10:79277219-79277219 + ESO-0459 COSM1270981 c.1389G>A p.T463T Substitution - coding silent 10:79296629-79296629 + TCGA-EE-A2ML-06 COSM3440926 c.3030C>A p.P1010P Substitution - coding silent 10:79311118-79311118 + 2492703 COSM5715888 c.639C>T p.S213S Substitution - coding silent 10:79291057-79291057 + Pat_30_A COSM5837367 c.1972C>T p.Q658* Substitution - Nonsense 10:79300895-79300895 + TCGA-HU-A4GU-01 COSM4016226 c.2105C>T p.A702V Substitution - Missense 10:79302192-79302192 + HCC084T COSM920723 c.2530C>T p.R844W Substitution - Missense 10:79306206-79306206 + 08-P462 COSM4573847 c.314G>A p.R105H Substitution - Missense 10:79277214-79277214 + SNU-283 COSM1966341 c.1091C>T p.P364L Substitution - Missense 10:79293514-79293514 + Gp5D COSM1966396 c.2797G>A p.A933T Substitution - Missense 10:79307533-79307533 + HCC2218 COSM32244 c.1651C>G p.L551V Substitution - Missense 10:79298565-79298565 + CSCC-31-T COSM4517998 c.489_490CC>TT p.L164F Substitution - Missense 10:79289838-79289839 + TCGA-B5-A0JT-01 COSM920722 c.2225G>T p.C742F Substitution - Missense 10:79304114-79304114 + TCGA-FD-A3SJ-01 COSM3790984 c.2186A>C p.D729A Substitution - Missense 10:79304075-79304075 + I2L-P19Ta-Tumor-Organoid COSM5359949 c.2751G>C p.G917G Substitution - coding silent 10:79307487-79307487 + LOVO COSM920723 c.2530C>T p.R844W Substitution - Missense 10:79306206-79306206 + YUNEKI COSM5371175 c.2507_2508AC>GT p.D836G Substitution - Missense 10:79306183-79306184 + HCC120T COSM3665905 c.2668+10G>A p.? Unknown 10:79306354-79306354 + C086 COSM5542059 c.1545C>T p.N515N Substitution - coding silent 10:79298459-79298459 + TCGA-AP-A0LM-01 COSM920721 c.2131C>T p.R711W Substitution - Missense 10:79304020-79304020 + CSCC-29-T COSM4463596 c.1299C>T p.A433A Substitution - coding silent 10:79296539-79296539 + 2_RESISTANT COSM1722976 c.1305delC p.P437fs*84 Deletion - Frameshift 10:79296545-79296545 + TCGA-IN-8663-01 COSM4016215 c.858G>A p.A286A Substitution - coding silent 10:79292257-79292257 + 587342 COSM1233513 c.710G>A p.S237N Substitution - Missense 10:79291128-79291128 + TCGA-G9-6342-01 COSM3670611 c.687C>A p.P229P Substitution - coding silent 10:79291105-79291105 + 2492702 COSM5715888 c.639C>T p.S213S Substitution - coding silent 10:79291057-79291057 + 587338 COSM1233511 c.2653G>A p.D885N Substitution - Missense 10:79306329-79306329 + CSCC-56-T COSM4517001 c.2629_2630CC>TT p.P877F Substitution - Missense 10:79306305-79306306 + Pat_06_A COSM5837366 c.654_656delGCA p.Q222delQ Deletion - In frame 10:79291072-79291074 + S00947 COSM316697 c.2066C>G p.S689C Substitution - Missense 10:79302153-79302153 + TCGA-F5-6814-01 COSM3415275 c.715T>C p.Y239H Substitution - Missense 10:79291133-79291133 + PT40 COSM5923895 c.2669-5C>T p.? Unknown 10:79307400-79307400 + TCGA-EE-A2GS-06 COSM3440924 c.2633C>T p.P878L Substitution - Missense 10:79306309-79306309 + PD13753a COSM5770509 c.1320C>T p.L440L Substitution - coding silent 10:79296560-79296560 + TCGA-19-1790-01 COSM3397264 c.2095C>T p.L699F Substitution - Missense 10:79302182-79302182 + TCGA-76-4925 COSM1736872 c.901G>A p.A301T Substitution - Missense 10:79292300-79292300 + TCGA-AB-2854-03 COSM1317429 c.1572C>A p.S524R Substitution - Missense 10:79298486-79298486 + 631056 COSM324424 c.598A>G p.M200V Substitution - Missense 10:79291016-79291016 + Gp2D COSM1966316 c.380C>T p.P127L Substitution - Missense 10:79277280-79277280 + TCGA-CG-4305-01 COSM4016223 c.1714G>A p.V572M Substitution - Missense 10:79299097-79299097 + LUAD-S01306 COSM343409 c.2844C>A p.H948Q Substitution - Missense 10:79310932-79310932 + YUWAPO COSM5371171 c.93C>T p.A31A Substitution - coding silent 10:79208368-79208368 + TCGA-G9-6351-01 COSM3670612 c.1310C>A p.P437Q Substitution - Missense 10:79296550-79296550 + LUAD-5V8LT COSM401070 c.2417T>A p.I806N Substitution - Missense 10:79305595-79305595 + AOCS-091-3-0 COSM3981152 c.1151G>A p.R384Q Substitution - Missense 10:79293574-79293574 + RK220_C01 COSM3738747 c.2781G>A p.M927I Substitution - Missense 10:79307517-79307517 + TCGA-B5-A0JY-01 COSM920710 c.41G>A p.R14Q Substitution - Missense 10:79201673-79201673 + 2492712 COSM5718681 c.1727C>T p.P576L Substitution - Missense 10:79299110-79299110 + LP6007597 COSM1745924 c.1302C>A p.P434P Substitution - coding silent 10:79296542-79296542 + TCGA-66-2757-01 COSM685248 c.2116A>G p.I706V Substitution - Missense 10:79302203-79302203 + TCGA-FW-A3R5-06 COSM3867914 c.1309C>T p.P437S Substitution - Missense 10:79296549-79296549 + S01542 COSM4181388 c.840G>A p.A280A Substitution - coding silent 10:79292239-79292239 + T1154 COSM4742874 c.1026delG p.G344fs*3 Deletion - Frameshift 10:79293449-79293449 + OSCC-GB_00640111 COSM4885144 c.2915C>A p.S972* Substitution - Nonsense 10:79311003-79311003 + I2L-P9-Tumor-Organoid COSM5360362 c.2835T>G p.T945T Substitution - coding silent 10:79307571-79307571 + T36 COSM4742872 c.778G>A p.A260T Substitution - Missense 10:79292177-79292177 + RKO COSM1966388 c.2641A>G p.T881A Substitution - Missense 10:79306317-79306317 + TCGA-HU-A4GY-01 COSM4016227 c.2334C>A p.T778T Substitution - coding silent 10:79305211-79305211 + TCGA-AA-3663-01 COSM1349255 c.260A>G p.K87R Substitution - Missense 10:79216254-79216254 + 2492701 COSM5715888 c.639C>T p.S213S Substitution - coding silent 10:79291057-79291057 + 2521259 COSM5890554 c.2549C>T p.P850L Substitution - Missense 10:79306225-79306225 + TCGA-AN-A0XU-01 COSM427977 c.1606G>A p.V536I Substitution - Missense 10:79298520-79298520 + C086 COSM5542060 c.2811C>T p.P937P Substitution - coding silent 10:79307547-79307547 + TCGA-36-2551-01 COSM1321186 c.2964G>A p.Q988Q Substitution - coding silent 10:79311052-79311052 + TCGA-B5-A0JY-01 COSM920717 c.1150C>T p.R384W Substitution - Missense 10:79293573-79293573 + Region-3 COSM5749102 c.2759A>C p.Q920P Substitution - Missense 10:79307495-79307495 + 2492730 COSM5728862 c.95C>T p.A32V Substitution - Missense 10:79208370-79208370 + HCT15 COSM1966392 c.2683G>T p.G895C Substitution - Missense 10:79307419-79307419 + PD9578a COSM5800227 c.3096+9G>A p.? Unknown 10:79311193-79311193 + ODG6 COSM3967177 c.859G>A p.A287T Substitution - Missense 10:79292258-79292258 + TCGA-BR-A4QM-01 COSM4016216 c.865G>A p.A289T Substitution - Missense 10:79292264-79292264 + ESO-0009 COSM1270979 c.1957C>T p.L653L Substitution - coding silent 10:79300880-79300880 + Pat_70_B COSM1349263 c.3144delC p.D1051fs*>17 Deletion - Frameshift 10:79312689-79312689 + CSCC-6-T COSM4514911 c.990C>T p.F330F Substitution - coding silent 10:79293413-79293413 + TCGA-29-1695-01 COSM1321187 c.1067C>T p.T356M Substitution - Missense 10:79293490-79293490 + Au1 COSM920719 c.2031C>T p.F677F Substitution - coding silent 10:79302118-79302118 + 2492714 COSM5718681 c.1727C>T p.P576L Substitution - Missense 10:79299110-79299110 + BN33 COSM1603780 c.2296C>G p.L766V Substitution - Missense 10:79305173-79305173 + HCC120 COSM3665905 c.2668+10G>A p.? Unknown 10:79306354-79306354 + TCGA-FJ-A3Z7-01 COSM3790983 c.549G>A p.G183G Substitution - coding silent 10:79290967-79290967 + 2492700 COSM5716611 c.1989C>T p.T663T Substitution - coding silent 10:79300912-79300912 + RK150_C01 COSM3738745 c.140G>A p.R47Q Substitution - Missense 10:79208415-79208415 + TCGA-HU-8602-01 COSM4016228 c.2743A>G p.M915V Substitution - Missense 10:79307479-79307479 + TCGA-BR-8363-01 COSM4016221 c.1360C>T p.P454S Substitution - Missense 10:79296600-79296600 + YUKAT COSM5371172 c.369C>T p.L123L Substitution - coding silent 10:79277269-79277269 + ESCC_24 COSM5626405 c.2385G>A p.V795V Substitution - coding silent 10:79305563-79305563 + 61 COSM5738960 c.313C>A p.R105S Substitution - Missense 10:79277213-79277213 + PR-00-1165 COSM248479 c.496G>A p.V166M Substitution - Missense 10:79289845-79289845 + CSCC-11-T COSM4465464 c.1385C>T p.P462L Substitution - Missense 10:79296625-79296625 + T2932 COSM4742871 c.711C>T p.S237S Substitution - coding silent 10:79291129-79291129 + 2492700 COSM5715888 c.639C>T p.S213S Substitution - coding silent 10:79291057-79291057 + KM12 COSM1745923 c.1008G>A p.P336P Substitution - coding silent 10:79293431-79293431 + TCGA-BR-7707-01 COSM4016224 c.2016C>T p.C672C Substitution - coding silent 10:79300939-79300939 + Gp5D COSM1966314 c.319C>T p.L107L Substitution - coding silent 10:79277219-79277219 + Gp5D COSM1966316 c.380C>T p.P127L Substitution - Missense 10:79277280-79277280 + B22 COSM1745924 c.1302C>A p.P434P Substitution - coding silent 10:79296542-79296542 + Gp2D COSM1966298 c.221G>C p.G74A Substitution - Missense 10:79216215-79216215 + 6P2-2 COSM3734276 c.905C>T p.T302I Substitution - Missense 10:79292304-79292304 + 2_RESISTANT COSM1723363 c.1298delC p.N435fs*86 Deletion - Frameshift 10:79296538-79296538 + TCGA-FW-A3R5-06 COSM3867916 c.2509C>T p.P837S Substitution - Missense 10:79306185-79306185 + CSCC-44-T COSM4516943 c.2549_2550CC>TT p.P850L Substitution - Missense 10:79306225-79306226 + YUCHIME COSM1702676 c.262T>C p.F88L Substitution - Missense 10:79216256-79216256 + SC_9081 COSM5567168 c.3000C>A p.S1000R Substitution - Missense 10:79311088-79311088 + EGC3 COSM5050357 c.1019C>T p.A340V Substitution - Missense 10:79293442-79293442 + TCGA-39-5019-01 COSM685247 c.2892C>A p.H964Q Substitution - Missense 10:79310980-79310980 + TCGA-EJ-7330-01 COSM1470394 c.1495C>T p.P499S Substitution - Missense 10:79298409-79298409 + HCC82T COSM1603779 c.2153C>T p.A718V Substitution - Missense 10:79304042-79304042 + TCGA-AZ-6598-01 COSM1349259 c.1899C>T p.N633N Substitution - coding silent 10:79300822-79300822 + 01-P1216 COSM4573849 c.2001C>T p.T667T Substitution - coding silent 10:79300924-79300924 + CSCC-31-T COSM3867913 c.1023C>T p.S341S Substitution - coding silent 10:79293446-79293446 + PT37 COSM5920034 c.1594C>T p.P532S Substitution - Missense 10:79298508-79298508 + LUAD-D02185 COSM338416 c.1339G>C p.G447R Substitution - Missense 10:79296579-79296579 + TCGA-P4-A5E6-01 COSM3985776 c.381C>G p.P127P Substitution - coding silent 10:79277281-79277281 + TCGA-B5-A11E-01 COSM920723 c.2530C>T p.R844W Substitution - Missense 10:79306206-79306206 + TCGA-HU-A4H8-01 COSM242340 c.602C>T p.A201V Substitution - Missense 10:79291020-79291020 + 7 COSM5732429 c.2381A>C p.E794A Substitution - Missense 10:79305559-79305559 + TCGA-CG-5721-01 COSM4016220 c.1314G>A p.R438R Substitution - coding silent 10:79296554-79296554 + TCGA-D1-A103-01 COSM176953 c.605C>T p.S202L Substitution - Missense 10:79291023-79291023 + 587228 COSM1233510 c.2713A>G p.N905D Substitution - Missense 10:79307449-79307449 + TCGA-EE-A2MR-06 COSM1470394 c.1495C>T p.P499S Substitution - Missense 10:79298409-79298409 + 2492703 COSM5716611 c.1989C>T p.T663T Substitution - coding silent 10:79300912-79300912 + TCGA-24-2261-01 COSM73382 c.889G>A p.A297T Substitution - Missense 10:79292288-79292288 + WA16 COSM242340 c.602C>T p.A201V Substitution - Missense 10:79291020-79291020 + ZZUFHECRKL-G020T COSM5445277 c.804G>A p.P268P Substitution - coding silent 10:79292203-79292203 + 2293782 COSM4608325 c.1825C>A p.Q609K Substitution - Missense 10:79300748-79300748 + SW1417 COSM1966409 c.3076A>G p.M1026V Substitution - Missense 10:79311164-79311164 + TCGA-D1-A176-01 COSM920720 c.2035C>T p.L679L Substitution - coding silent 10:79302122-79302122 + WA56 COSM242341 c.890C>G p.A297G Substitution - Missense 10:79292289-79292289 + Gp5D COSM1966356 c.1468T>C p.Y490H Substitution - Missense 10:79297667-79297667 + H1672 COSM316696 c.810C>A p.T270T Substitution - coding silent 10:79292209-79292209 + 12-P4072 COSM4573848 c.1784C>T p.T595M Substitution - Missense 10:79299167-79299167 + 49M COSM5594040 c.2247C>T p.I749I Substitution - coding silent 10:79304136-79304136 + TCGA-27-2521-01 COSM3397263 c.1691T>G p.L564R Substitution - Missense 10:79299074-79299074 + 8036161 COSM3383050 c.3068C>T p.A1023V Substitution - Missense 10:79311156-79311156 + ESO-0053 COSM1270980 c.1875C>T p.P625P Substitution - coding silent 10:79300798-79300798 + 1T COSM107294 c.3039C>T p.A1013A Substitution - coding silent 10:79311127-79311127 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.193118 10q22.3 607159

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E860A c.2579A>C 10 81066012 GBM A C Missense p.N506T c.1517A>C 10 81058188 CM A C Missense p.T298P c.892A>C 10 81052048 MB A C Missense p.T323P c.967A>C 10 81053147 BRCA A C Missense p.Y326S c.977A>C 10 81053157 STAD A G IntronicSNV . c.1230+42A>G 10 81053452 UCEC A G Missense p.I544V c.1630A>G 10 81058301 LUSC A G Missense p.I706V c.2116A>G 10 81061960 LUSC A G Missense p.M200V c.598A>G 10 81050773 SCLC C A Missense p.H964Q c.2892C>A 10 81070737 LUSC C A Missense p.P147H c.440C>A 10 81049546 CM C A Nonsense p.C763* c.2289C>A 10 81064923 OV C A Synonymous p.P1010P c.3030C>A 10 81070875 CM C A Synonymous p.P199P c.597C>A 10 81050772 STAD C - Frameshift p.D1051Tfs*73 c.3150delC 10 81072446 LGG C - Frameshift p.D1051Tfs*73 c.3150delC 10 81072446 PRAD C - Frameshift p.D1051Tfs*73 c.3150delC 10 81072446 THCA - C Frameshift p.P994Afs*16 c.2978dupC 10 81070822 RCCC C G Missense p.P659A c.1975C>G 10 81060655 THCA C G Missense p.S689C c.2066C>G 10 81061910 SCLC CTC - InFrameDeletion p.P986delP c.2956_2958delCCT 10 81070787 CM C T IntronicSNV . c.1-70333C>T 10 80891057 PIA C T Missense p.A301V c.902C>T 10 81052058 LUAD C T Missense p.A933V c.2798C>T 10 81067291 CM C T Missense p.L699F c.2095C>T 10 81061939 GBM C T Missense p.P232S c.694C>T 10 81050869 ESCA C T Missense p.P258S c.772C>T 10 81051928 CM C T Missense p.P42L c.125C>T 10 80968157 CM C T Missense p.P499S c.1495C>T 10 81058166 PRAD C T Missense p.P878L c.2633C>T 10 81066066 CM C T Missense p.R578C c.1732C>T 10 81058872 THCA C T Missense p.S686F c.2057C>T 10 81061901 CM C T Missense p.S829L c.2486C>T 10 81065919 RCCC C T Missense p.S842F c.2525C>T 10 81065958 CM C T Missense p.T58M c.173C>T 10 80968205 STAD C T Missense p.T724I c.2171C>T 10 81063817 CM C T Synonymous p.A805A c.2415C>T 10 81065350 LUAD C T Synonymous p.F677F c.2031C>T 10 81061875 CM C T Synonymous p.G571G c.1713C>T 10 81058853 HNSC C T Synonymous p.H675H c.2025C>T 10 81061869 CM C T Synonymous p.I266I c.798C>T 10 81051954 CM C T Synonymous p.I744I c.2232C>T 10 81063878 HNSC C T Synonymous p.L1061L c.3181C>T 10 81072483 CM C T Synonymous p.L35L c.103C>T 10 80968135 UCEC C T Synonymous p.L653L c.1957C>T 10 81060637 ESCA C T Synonymous p.P625P c.1875C>T 10 81060555 ESCA C T Synonymous p.P877P c.2631C>T 10 81066064 CM GAGGTTTT - IntronicDeletion . c.1-26002_1-25995delGAGGTTTT 10 80935388 CM G A IntronicSNV . c.281-29701G>A 10 81007237 CLL G A Missense p.A287T c.859G>A 10 81052015 LGG G A Missense p.A297T c.889G>A 10 81052045 OV G A Missense p.D1058N c.3172G>A 10 81072474 BLCA G A Missense p.S130N c.389G>A 10 81037046 LUAD G A Missense p.V166M c.496G>A 10 81049602 LUAD G A Missense p.V536I c.1606G>A 10 81058277 BRCA G A Missense p.V572M c.1714G>A 10 81058854 STAD G A Synonymous p.S1030S c.3090G>A 10 81070935 ESCA G A Synonymous p.T463T c.1389G>A 10 81056386 ESCA GCAGCAGCGGCAGTGGCAGCA - InFrameDeletion p.A287_A293delAVAAAAA c.858_878delGGCAGTGGCAGCAGCAGCAGC 10 81052006 BLCA G C IntronicSNV . c.281-10511G>C 10 81026427 PIA G C Synonymous p.A201A c.603G>C 10 81050778 HNSC GG AA MultiAAMissense p.W171_G172delins* c.513_514delinsAA 10 81049619 CM GG - Frameshift p.D570Wfs*35 c.1707_1708delGG 10 81058846 LUSC G T Missense p.C742F c.2225G>T 10 81063871 UCEC G T Missense p.C820F c.2459G>T 10 81065892 GBM G T Missense p.G362C c.1084G>T 10 81053264 LUAD G T Missense p.V731L c.2191G>T 10 81063837 BRCA G T Nonsense p.G801* c.2401G>T 10 81065336 LUAD T G Missense p.L564R c.1691T>G 10 81058831 GBM T G Missense p.M911R c.2732T>G 10 81067225 BRCA