Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 10 75290071 75290071 + Missense_Mutation SNP C C T TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr10:75290071C>T c.1658G>A c.(1657-1659)cGt>cAt p.R553H BLCA 10 75258708 75258708 + Silent SNP G G A TCGA-FD-A3B4-01A-12D-A202-08 TCGA-FD-A3B4-10A-01D-A202-08 g.chr10:75258708G>A c.4734C>T c.(4732-4734)ggC>ggT p.G1578G BLCA 10 75277120 75277120 + Missense_Mutation SNP G G C TCGA-E7-A97P-01A-11D-A38G-08 TCGA-E7-A97P-10A-01D-A38J-08 g.chr10:75277120G>C c.3064C>G c.(3064-3066)Caa>Gaa p.Q1022E BLCA 10 75277138 75277138 + Missense_Mutation SNP C C G TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr10:75277138C>G c.3046G>C c.(3046-3048)Gaa>Caa p.E1016Q BLCA 10 75277409 75277409 + Silent SNP T T C TCGA-UY-A78N-01A-12D-A339-08 TCGA-UY-A78N-10A-01D-A339-08 g.chr10:75277409T>C c.2775A>G c.(2773-2775)tcA>tcG p.S925S BLCA 10 75277427 75277427 + Silent SNP G G A TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr10:75277427G>A c.2757C>T c.(2755-2757)gcC>gcT p.A919A BLCA 10 75279565 75279565 + Nonsense_Mutation SNP G G A TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr10:75279565G>A c.2668C>T c.(2668-2670)Cag>Tag p.Q890* BLCA 10 75279710 75279710 + Silent SNP C C A TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr10:75279710C>A c.2523G>T c.(2521-2523)acG>acT p.T841T BLCA 10 75283447 75283447 + Silent SNP C C T TCGA-FD-A5BZ-01A-11D-A289-08 TCGA-FD-A5BZ-10A-01D-A289-08 g.chr10:75283447C>T c.2256G>A c.(2254-2256)gcG>gcA p.A752A BLCA 10 75283496 75283496 + Missense_Mutation SNP G G A TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr10:75283496G>A c.2207C>T c.(2206-2208)tCt>tTt p.S736F BLCA 10 75289664 75289664 + Nonsense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr10:75289664C>A c.1834G>T c.(1834-1836)Gaa>Taa p.E612* BLCA 10 75289990 75289990 + Missense_Mutation SNP C C T TCGA-KQ-A41Q-01A-11D-A339-08 TCGA-KQ-A41Q-10D-01D-A339-08 g.chr10:75289990C>T c.1739G>A c.(1738-1740)cGa>cAa p.R580Q BLCA 10 75290072 75290072 + Missense_Mutation SNP G G A TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr10:75290072G>A c.1657C>T c.(1657-1659)Cgt>Tgt p.R553C BLCA 10 75290150 75290150 + Missense_Mutation SNP T T C TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr10:75290150T>C c.1579A>G c.(1579-1581)Aat>Gat p.N527D BLCA 10 75290465 75290465 + Missense_Mutation SNP C C T TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr10:75290465C>T c.1444G>A c.(1444-1446)Gaa>Aaa p.E482K BLCA 10 75301468 75301468 + Nonsense_Mutation SNP G G A TCGA-GD-A2C5-01A-12D-A17V-08 TCGA-GD-A2C5-10A-01D-A17V-08 g.chr10:75301468G>A c.601C>T c.(601-603)Cga>Tga p.R201* BLCA 10 75301492 75301492 + Missense_Mutation SNP G G T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr10:75301492G>T c.577C>A c.(577-579)Cag>Aag p.Q193K BLCA 10 75335374 75335374 + Missense_Mutation SNP C C T TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr10:75335374C>T c.43G>A c.(43-45)Gta>Ata p.V15I BRCA 10 75258420 75258420 + Silent SNP G G A TCGA-BH-A1FN-01A-11D-A13L-09 TCGA-BH-A1FN-11A-34D-A13O-09 g.chr10:75258420G>A c.5022C>T c.(5020-5022)atC>atT p.I1674I BRCA 10 75258501 75258501 + Silent SNP A A G TCGA-AN-A0FV-01A-11W-A019-09 TCGA-AN-A0FV-10A-01W-A021-09 g.chr10:75258501A>G c.4941T>C c.(4939-4941)taT>taC p.Y1647Y BRCA 10 75258655 75258655 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:75258655T>G c.4787A>C c.(4786-4788)cAc>cCc p.H1596P BRCA 10 75258663 75258663 + Silent SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:75258663T>G c.4779A>C c.(4777-4779)tcA>tcC p.S1593S BRCA 10 75264684 75264684 + Missense_Mutation SNP A A G TCGA-BH-A0BL-01A-11D-A10Y-09 TCGA-BH-A0BL-10A-01D-A110-09 g.chr10:75264684A>G c.4235T>C c.(4234-4236)tTa>tCa p.L1412S BRCA 10 75276172 75276172 + Missense_Mutation SNP C C G TCGA-B6-A0RN-01A-12D-A099-09 TCGA-B6-A0RN-10A-01D-A099-09 g.chr10:75276172C>G c.4012G>C c.(4012-4014)Ggg>Cgg p.G1338R BRCA 10 75277121 75277121 + Silent SNP A A C TCGA-BH-A0H9-01A-11W-A071-09 TCGA-BH-A0H9-11A-22W-A10F-09 g.chr10:75277121A>C c.3063T>G c.(3061-3063)gcT>gcG p.A1021A BRCA 10 75279643 75279643 + Missense_Mutation SNP G G A TCGA-E9-A249-01A-11D-A167-09 TCGA-E9-A249-10A-01D-A167-09 g.chr10:75279643G>A c.2590C>T c.(2590-2592)Cgc>Tgc p.R864C BRCA 10 75289458 75289458 + Silent SNP A A G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr10:75289458A>G c.2040T>C c.(2038-2040)ccT>ccC p.P680P BRCA 10 75290088 75290088 + Silent SNP G G T TCGA-E9-A1NC-01A-12W-A16L-09 TCGA-E9-A1NC-10A-01D-A159-09 g.chr10:75290088G>T c.1641C>A c.(1639-1641)acC>acA p.T547T BRCA 10 75296096 75296096 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr10:75296096T>G c.1075A>C c.(1075-1077)Acc>Ccc p.T359P CESC 10 75258749 75258749 + Nonsense_Mutation SNP G G A TCGA-C5-A1BM-01A-11D-A13W-08 TCGA-C5-A1BM-10A-01D-A13W-08 g.chr10:75258749G>A c.4693C>T c.(4693-4695)Caa>Taa p.Q1565* CESC 10 75277079 75277079 + Silent SNP G G A TCGA-LP-A4AW-01A-11D-A243-09 TCGA-LP-A4AW-10A-01D-A243-09 g.chr10:75277079G>A c.3105C>T c.(3103-3105)ccC>ccT p.P1035P CESC 10 75277284 75277284 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr10:75277284G>C c.2900C>G c.(2899-2901)tCt>tGt p.S967C CESC 10 75277418 75277418 + Missense_Mutation SNP G G T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr10:75277418G>T c.2766C>A c.(2764-2766)ttC>ttA p.F922L COAD 10 75258739 75258739 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:75258739T>C c.4703A>G c.(4702-4704)tAc>tGc p.Y1568C COAD 10 75276419 75276419 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr10:75276419C>T c.3765G>A c.(3763-3765)ggG>ggA p.G1255G COAD 10 75276479 75276479 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:75276479C>A c.3705G>T c.(3703-3705)gaG>gaT p.E1235D COAD 10 75276602 75276602 + Silent SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr10:75276602A>G c.3582T>C c.(3580-3582)gaT>gaC p.D1194D COAD 10 75276643 75276643 + Missense_Mutation SNP A A G TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr10:75276643A>G c.3541T>C c.(3541-3543)Tgg>Cgg p.W1181R COAD 10 75276685 75276685 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:75276685C>T c.3499G>A c.(3499-3501)Gat>Aat p.D1167N COAD 10 75276916 75276916 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr10:75276916C>T c.3268G>A c.(3268-3270)Gtg>Atg p.V1090M COAD 10 75279710 75279710 + Silent SNP C C T TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr10:75279710C>T c.2523G>A c.(2521-2523)acG>acA p.T841T COAD 10 75280699 75280700 + Frame_Shift_Del DEL CA CA - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr10:75280699_75280700delCA c.2448_2449delTG c.(2446-2451)tgtgctfs p.A819fs COAD 10 75296105 75296105 + Missense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:75296105G>T c.1066C>A c.(1066-1068)Cca>Aca p.P356T COAD 10 75296120 75296120 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:75296120C>A c.1051G>T c.(1051-1053)Gat>Tat p.D351Y COAD 10 75301494 75301494 + Missense_Mutation SNP T T C TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr10:75301494T>C c.575A>G c.(574-576)aAt>aGt p.N192S COAD 10 75302825 75302825 + Missense_Mutation SNP G G A TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr10:75302825G>A c.440C>T c.(439-441)gCc>gTc p.A147V COAD 10 75302825 75302825 + Missense_Mutation SNP G G A TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr10:75302825G>A c.440C>T c.(439-441)gCc>gTc p.A147V COAD 10 75302826 75302826 + Missense_Mutation SNP C C A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr10:75302826C>A c.439G>T c.(439-441)Gcc>Tcc p.A147S COADREAD 10 75258739 75258739 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:75258739T>C c.4703A>G c.(4702-4704)tAc>tGc p.Y1568C COADREAD 10 75276419 75276419 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr10:75276419C>T c.3765G>A c.(3763-3765)ggG>ggA p.G1255G COADREAD 10 75276479 75276479 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:75276479C>A c.3705G>T c.(3703-3705)gaG>gaT p.E1235D COADREAD 10 75276602 75276602 + Silent SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr10:75276602A>G c.3582T>C c.(3580-3582)gaT>gaC p.D1194D COADREAD 10 75276643 75276643 + Missense_Mutation SNP A A G TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr10:75276643A>G c.3541T>C c.(3541-3543)Tgg>Cgg p.W1181R COADREAD 10 75276685 75276685 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:75276685C>T c.3499G>A c.(3499-3501)Gat>Aat p.D1167N COADREAD 10 75276916 75276916 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr10:75276916C>T c.3268G>A c.(3268-3270)Gtg>Atg p.V1090M COADREAD 10 75277235 75277235 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:75277235C>A c.2949G>T c.(2947-2949)aaG>aaT p.K983N COADREAD 10 75279710 75279710 + Silent SNP C C T TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr10:75279710C>T c.2523G>A c.(2521-2523)acG>acA p.T841T COADREAD 10 75280699 75280700 + Frame_Shift_Del DEL CA CA - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr10:75280699_75280700delCA c.2448_2449delTG c.(2446-2451)tgtgctfs p.A819fs COADREAD 10 75289664 75289664 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:75289664C>A c.1834G>T c.(1834-1836)Gaa>Taa p.E612* COADREAD 10 75296105 75296105 + Missense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:75296105G>T c.1066C>A c.(1066-1068)Cca>Aca p.P356T COADREAD 10 75296120 75296120 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:75296120C>A c.1051G>T c.(1051-1053)Gat>Tat p.D351Y COADREAD 10 75301494 75301494 + Missense_Mutation SNP T T C TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr10:75301494T>C c.575A>G c.(574-576)aAt>aGt p.N192S COADREAD 10 75302825 75302825 + Missense_Mutation SNP G G A TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr10:75302825G>A c.440C>T c.(439-441)gCc>gTc p.A147V COADREAD 10 75302825 75302825 + Missense_Mutation SNP G G A TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr10:75302825G>A c.440C>T c.(439-441)gCc>gTc p.A147V COADREAD 10 75302826 75302826 + Missense_Mutation SNP C C A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr10:75302826C>A c.439G>T c.(439-441)Gcc>Tcc p.A147S DLBC 10 75258558 75258558 + Silent SNP G G A TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr10:75258558G>A c.4884C>T c.(4882-4884)acC>acT p.T1628T ESCA 10 75277223 75277225 + In_Frame_Del DEL ATG ATG - TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr10:75277223_75277225delATG c.2959_2961delCAT c.(2959-2961)catdel p.H987del ESCA 10 75286503 75286503 + Missense_Mutation SNP G G C TCGA-Z6-A8JE-01A-11D-A37C-09 TCGA-Z6-A8JE-10A-01D-A37F-09 g.chr10:75286503G>C c.2096C>G c.(2095-2097)cCt>cGt p.P699R ESCA 10 75294426 75294426 + Missense_Mutation SNP G G T TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr10:75294426G>T c.1247C>A c.(1246-1248)tCt>tAt p.S416Y ESCA 10 75305350 75305350 + Silent SNP G G A TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr10:75305350G>A c.321C>T c.(319-321)ttC>ttT p.F107F GBMLGG 10 75260418 75260418 + Missense_Mutation SNP A A G TCGA-S9-A7J3-01A-21D-A34J-08 TCGA-S9-A7J3-10A-01D-A34M-08 g.chr10:75260418A>G c.4490T>C c.(4489-4491)cTc>cCc p.L1497P GBMLGG 10 75294484 75294484 + Missense_Mutation SNP T T C TCGA-S9-A7J0-01A-11D-A34A-08 TCGA-S9-A7J0-10A-01D-A34A-08 g.chr10:75294484T>C c.1189A>G c.(1189-1191)Acg>Gcg p.T397A GBMLGG 10 75331188 75331188 + Silent SNP G G A TCGA-S9-A6U5-01A-12D-A33T-08 TCGA-S9-A6U5-10A-01D-A33W-08 g.chr10:75331188G>A c.231C>T c.(229-231)tgC>tgT p.C77C GBMLGG 10 75331188 75331188 + Silent SNP G G A TCGA-S9-A6UA-01A-12D-A33T-08 TCGA-S9-A6UA-10A-01D-A33W-08 g.chr10:75331188G>A c.231C>T c.(229-231)tgC>tgT p.C77C GBMLGG 10 75335382 75335382 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:75335382C>T c.35G>A c.(34-36)cGt>cAt p.R12H HNSC 10 75276690 75276690 + Missense_Mutation SNP G G A TCGA-CV-7242-01A-11D-2012-08 TCGA-CV-7242-10A-01D-2013-08 g.chr10:75276690G>A c.3494C>T c.(3493-3495)cCt>cTt p.P1165L HNSC 10 75277422 75277422 + Missense_Mutation SNP G G C TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr10:75277422G>C c.2762C>G c.(2761-2763)tCt>tGt p.S921C HNSC 10 75277428 75277428 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr10:75277428G>A c.2756C>T c.(2755-2757)gCc>gTc p.A919V HNSC 10 75279642 75279642 + Missense_Mutation SNP C C T TCGA-BB-4224-01A-01D-1434-08 TCGA-BB-4224-10A-01D-1434-08 g.chr10:75279642C>T c.2591G>A c.(2590-2592)cGc>cAc p.R864H HNSC 10 75286479 75286479 + Missense_Mutation SNP G G A TCGA-HD-A6I0-01A-11D-A31L-08 TCGA-HD-A6I0-10A-01D-A31J-08 g.chr10:75286479G>A c.2120C>T c.(2119-2121)tCg>tTg p.S707L HNSC 10 75289616 75289616 + Missense_Mutation SNP A A G TCGA-CR-7389-01A-11D-2012-08 TCGA-CR-7389-10A-01D-2013-08 g.chr10:75289616A>G c.1882T>C c.(1882-1884)Ttt>Ctt p.F628L HNSC 10 75299343 75299344 + Frame_Shift_Ins INS - - A TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr10:75299343_75299344insA c.833_834insT c.(832-834)ttcfs p.F278fs HNSC 10 75331188 75331188 + Silent SNP G G A TCGA-BA-5558-01A-01D-1512-08 TCGA-BA-5558-10A-01D-1512-08 g.chr10:75331188G>A c.231C>T c.(229-231)tgC>tgT p.C77C HNSC 10 75331243 75331243 + Missense_Mutation SNP C C T TCGA-CQ-A4CE-01A-11D-A25Y-08 TCGA-CQ-A4CE-10A-01D-A25Y-08 g.chr10:75331243C>T c.176G>A c.(175-177)cGt>cAt p.R59H HNSC 10 75335341 75335341 + Missense_Mutation SNP A A T TCGA-CV-5439-01A-01D-1683-08 TCGA-CV-5439-11B-01D-1683-08 g.chr10:75335341A>T c.76T>A c.(76-78)Tcc>Acc p.S26T HNSC 10 75335391 75335391 + Missense_Mutation SNP G G A TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr10:75335391G>A c.26C>T c.(25-27)tCa>tTa p.S9L KICH 10 75331190 75331190 + Missense_Mutation SNP A A C TCGA-KL-8336-01A-11D-2310-10 TCGA-KL-8336-11A-01D-2310-10 g.chr10:75331190A>C c.229T>G c.(229-231)Tgc>Ggc p.C77G KIPAN 10 75258858 75258858 + Missense_Mutation SNP G G T TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr10:75258858G>T c.4584C>A c.(4582-4584)aaC>aaA p.N1528K KIPAN 10 75294429 75294429 + Missense_Mutation SNP G G A TCGA-BQ-5885-01A-11D-1589-08 TCGA-BQ-5885-11A-01D-1589-08 g.chr10:75294429G>A c.1244C>T c.(1243-1245)tCt>tTt p.S415F KIPAN 10 75331190 75331190 + Missense_Mutation SNP A A C TCGA-KL-8336-01A-11D-2310-10 TCGA-KL-8336-11A-01D-2310-10 g.chr10:75331190A>C c.229T>G c.(229-231)Tgc>Ggc p.C77G KIRC 10 75258858 75258858 + Missense_Mutation SNP G G T TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr10:75258858G>T c.4584C>A c.(4582-4584)aaC>aaA p.N1528K KIRP 10 75294429 75294429 + Missense_Mutation SNP G G A TCGA-BQ-5885-01A-11D-1589-08 TCGA-BQ-5885-11A-01D-1589-08 g.chr10:75294429G>A c.1244C>T c.(1243-1245)tCt>tTt p.S415F LGG 10 75260418 75260418 + Missense_Mutation SNP A A G TCGA-S9-A7J3-01A-21D-A34J-08 TCGA-S9-A7J3-10A-01D-A34M-08 g.chr10:75260418A>G c.4490T>C c.(4489-4491)cTc>cCc p.L1497P LGG 10 75294484 75294484 + Missense_Mutation SNP T T C TCGA-S9-A7J0-01A-11D-A34A-08 TCGA-S9-A7J0-10A-01D-A34A-08 g.chr10:75294484T>C c.1189A>G c.(1189-1191)Acg>Gcg p.T397A LGG 10 75331188 75331188 + Silent SNP G G A TCGA-S9-A6U5-01A-12D-A33T-08 TCGA-S9-A6U5-10A-01D-A33W-08 g.chr10:75331188G>A c.231C>T c.(229-231)tgC>tgT p.C77C LGG 10 75331188 75331188 + Silent SNP G G A TCGA-S9-A6UA-01A-12D-A33T-08 TCGA-S9-A6UA-10A-01D-A33W-08 g.chr10:75331188G>A c.231C>T c.(229-231)tgC>tgT p.C77C LGG 10 75335382 75335382 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:75335382C>T c.35G>A c.(34-36)cGt>cAt p.R12H LIHC 10 75264616 75264616 + Frame_Shift_Del DEL G G - TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr10:75264616delG c.4303delC c.(4303-4305)cacfs p.H1435fs LIHC 10 75276369 75276369 + Missense_Mutation SNP G G C TCGA-G3-A6UC-01A-21D-A33K-10 TCGA-G3-A6UC-10A-01D-A33K-10 g.chr10:75276369G>C c.3815C>G c.(3814-3816)tCt>tGt p.S1272C LIHC 10 75276875 75276875 + Missense_Mutation SNP T T G TCGA-DD-AACM-01A-11D-A40R-10 TCGA-DD-AACM-10A-01D-A40U-10 g.chr10:75276875T>G c.3309A>C c.(3307-3309)aaA>aaC p.K1103N LIHC 10 75277370 75277370 + Silent SNP T T C TCGA-CC-A123-01A-11D-A12Z-10 TCGA-CC-A123-10A-01D-A12Z-10 g.chr10:75277370T>C c.2814A>G c.(2812-2814)ccA>ccG p.P938P LIHC 10 75283430 75283448 + Frame_Shift_Del DEL CGAAGTTCCTGTTCCTGCG CGAAGTTCCTGTTCCTGCG - TCGA-DD-AAW1-01A-11D-A40P-10 TCGA-DD-AAW1-10A-01D-A40P-10 g.chr10:75283430_75283448delCGAAGTTCCTGTTCCTGCG c.2255_2273delCGCAGGAACAGGAACTTCG c.(2254-2274)gcgcaggaacaggaacttcgafs p.AQEQELR752fs LIHC 10 75296083 75296083 + Frame_Shift_Del DEL G G - TCGA-DD-AACB-01A-11D-A40R-10 TCGA-DD-AACB-10A-01D-A40U-10 g.chr10:75296083delG c.1088delC c.(1087-1089)cctfs p.P364fs LUAD 10 75258547 75258547 + Missense_Mutation SNP C C T TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr10:75258547C>T c.4895G>A c.(4894-4896)cGa>cAa p.R1632Q LUAD 10 75264652 75264652 + Missense_Mutation SNP C C T TCGA-MP-A4T8-01A-11D-A24P-08 TCGA-MP-A4T8-10A-01D-A24P-08 g.chr10:75264652C>T c.4267G>A c.(4267-4269)Gtt>Att p.V1423I LUAD 10 75276186 75276186 + Missense_Mutation SNP C C A TCGA-93-A4JO-01A-21D-A24P-08 TCGA-93-A4JO-10A-01D-A24P-08 g.chr10:75276186C>A c.3998G>T c.(3997-3999)gGc>gTc p.G1333V LUAD 10 75276381 75276381 + Missense_Mutation SNP C C A TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr10:75276381C>A c.3803G>T c.(3802-3804)aGg>aTg p.R1268M LUAD 10 75276726 75276726 + Missense_Mutation SNP C C G TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr10:75276726C>G c.3458G>C c.(3457-3459)aGa>aCa p.R1153T LUAD 10 75277238 75277238 + Silent SNP C C T TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr10:75277238C>T c.2946G>A c.(2944-2946)gaG>gaA p.E982E LUAD 10 75280781 75280781 + Missense_Mutation SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr10:75280781C>A c.2367G>T c.(2365-2367)agG>agT p.R789S LUAD 10 75283501 75283501 + Missense_Mutation SNP C C G TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr10:75283501C>G c.2202G>C c.(2200-2202)gaG>gaC p.E734D LUAD 10 75286500 75286500 + Missense_Mutation SNP G G A TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr10:75286500G>A c.2099C>T c.(2098-2100)tCc>tTc p.S700F LUAD 10 75289573 75289573 + Missense_Mutation SNP C C G TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chr10:75289573C>G c.1925G>C c.(1924-1926)cGg>cCg p.R642P LUAD 10 75290091 75290091 + Silent SNP C C T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr10:75290091C>T c.1638G>A c.(1636-1638)agG>agA p.R546R LUAD 10 75296160 75296160 + Silent SNP G G A TCGA-97-7938-01A-11D-2167-08 TCGA-97-7938-10A-01D-2167-08 g.chr10:75296160G>A c.1011C>T c.(1009-1011)tgC>tgT p.C337C LUAD 10 75296188 75296188 + Missense_Mutation SNP G G A TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr10:75296188G>A c.983C>T c.(982-984)cCc>cTc p.P328L LUSC 10 75276202 75276202 + Missense_Mutation SNP G G T TCGA-18-5595-01A-01D-1632-08 TCGA-18-5595-11A-01D-1632-08 g.chr10:75276202G>T c.3982C>A c.(3982-3984)Cag>Aag p.Q1328K LUSC 10 75276561 75276561 + Missense_Mutation SNP A A G TCGA-85-6175-01A-11D-1817-08 TCGA-85-6175-10A-01D-1817-08 g.chr10:75276561A>G c.3623T>C c.(3622-3624)cTt>cCt p.L1208P LUSC 10 75276616 75276616 + Silent SNP G G A TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr10:75276616G>A c.3568C>T c.(3568-3570)Ctg>Ttg p.L1190L LUSC 10 75276843 75276843 + Missense_Mutation SNP C C A TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr10:75276843C>A c.3341G>T c.(3340-3342)aGt>aTt p.S1114I LUSC 10 75277120 75277120 + Missense_Mutation SNP G G C TCGA-21-5782-01A-01D-1632-08 TCGA-21-5782-10A-01D-1632-08 g.chr10:75277120G>C c.3064C>G c.(3064-3066)Caa>Gaa p.Q1022E LUSC 10 75279616 75279616 + Nonsense_Mutation SNP G G A TCGA-22-5471-01A-01D-1632-08 TCGA-22-5471-11A-01D-1632-08 g.chr10:75279616G>A c.2617C>T c.(2617-2619)Cag>Tag p.Q873* LUSC 10 75286428 75286428 + Missense_Mutation SNP C C A TCGA-85-6175-01A-11D-1817-08 TCGA-85-6175-10A-01D-1817-08 g.chr10:75286428C>A c.2171G>T c.(2170-2172)tGg>tTg p.W724L LUSC 10 75290488 75290488 + Missense_Mutation SNP G G A TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr10:75290488G>A c.1421C>T c.(1420-1422)cCc>cTc p.P474L LUSC 10 75294514 75294514 + Missense_Mutation SNP T T C TCGA-21-1077-01A-01D-1521-08 TCGA-21-1077-11A-01D-1521-08 g.chr10:75294514T>C c.1159A>G c.(1159-1161)Atc>Gtc p.I387V OV 10 75276724 75276724 + Missense_Mutation SNP T T C TCGA-29-1766-01A-01W-0633-09 TCGA-29-1766-10A-01W-0634-09 g.chr10:75276724T>C c.3460A>G c.(3460-3462)Agt>Ggt p.S1154G OV 10 75276830 75276830 + Silent SNP A A G TCGA-61-1740-01A-01W-0639-09 TCGA-61-1740-11A-01W-0639-09 g.chr10:75276830A>G c.3354T>C c.(3352-3354)taT>taC p.Y1118Y OV 10 75277097 75277097 + Missense_Mutation SNP C C G TCGA-36-2544-01A-01D-1526-09 TCGA-36-2544-10A-01D-1526-09 g.chr10:75277097C>G c.3087G>C c.(3085-3087)aaG>aaC p.K1029N OV 10 75277306 75277306 + Missense_Mutation SNP C C T TCGA-13-0906-01A-01W-0419-10 TCGA-13-0906-10A-01W-0419-10 g.chr10:75277306C>T c.2878G>A c.(2878-2880)Gaa>Aaa p.E960K OV 10 75302825 75302825 + Missense_Mutation SNP G G A TCGA-24-1469-01A-01W-0553-09 TCGA-24-1469-10A-01W-0553-09 g.chr10:75302825G>A c.440C>T c.(439-441)gCc>gTc p.A147V PAAD 10 75277367 75277367 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:75277367C>T c.2817G>A c.(2815-2817)gaG>gaA p.E939E PRAD 10 75258743 75258743 + Missense_Mutation SNP T T C TCGA-CH-5762-01A-11D-1576-08 TCGA-CH-5762-11A-01D-1576-08 g.chr10:75258743T>C c.4699A>G c.(4699-4701)Acc>Gcc p.T1567A PRAD 10 75277322 75277322 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:75277322C>T c.2862G>A c.(2860-2862)aaG>aaA p.K954K READ 10 75277235 75277235 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:75277235C>A c.2949G>T c.(2947-2949)aaG>aaT p.K983N READ 10 75289664 75289664 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:75289664C>A c.1834G>T c.(1834-1836)Gaa>Taa p.E612* SKCM 10 75258467 75258467 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr10:75258467C>T c.4975G>A c.(4975-4977)Gag>Aag p.E1659K SKCM 10 75258871 75258871 + Missense_Mutation SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr10:75258871C>T c.4571G>A c.(4570-4572)gGa>gAa p.G1524E SKCM 10 75276256 75276256 + Nonsense_Mutation SNP G G A TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr10:75276256G>A c.3928C>T c.(3928-3930)Caa>Taa p.Q1310* SKCM 10 75276290 75276290 + Silent SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr10:75276290C>T c.3894G>A c.(3892-3894)gaG>gaA p.E1298E SKCM 10 75276590 75276590 + Silent SNP G G A TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr10:75276590G>A c.3594C>T c.(3592-3594)tcC>tcT p.S1198S SKCM 10 75277230 75277230 + Missense_Mutation SNP G G A TCGA-D3-A1QB-06A-11D-A19A-08 TCGA-D3-A1QB-10A-01D-A19A-08 g.chr10:75277230G>A c.2954C>T c.(2953-2955)tCt>tTt p.S985F SKCM 10 75277247 75277247 + Silent SNP C C A TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chr10:75277247C>A c.2937G>T c.(2935-2937)ggG>ggT p.G979G SKCM 10 75283383 75283383 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:75283383G>A c.2320C>T c.(2320-2322)Cat>Tat p.H774Y SKCM 10 75286500 75286500 + Missense_Mutation SNP G G A TCGA-ER-A2NG-06A-11D-A196-08 TCGA-ER-A2NG-10A-01D-A198-08 g.chr10:75286500G>A c.2099C>T c.(2098-2100)tCc>tTc p.S700F SKCM 10 75289450 75289450 + Missense_Mutation SNP G G A TCGA-ER-A19A-06A-21D-A197-08 TCGA-ER-A19A-10A-01D-A199-08 g.chr10:75289450G>A c.2048C>T c.(2047-2049)tCa>tTa p.S683L SKCM 10 75289504 75289504 + Missense_Mutation SNP C C A TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chr10:75289504C>A c.1994G>T c.(1993-1995)aGt>aTt p.S665I SKCM 10 75289544 75289544 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:75289544G>A c.1954C>T c.(1954-1956)Ccc>Tcc p.P652S SKCM 10 75289602 75289602 + Silent SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr10:75289602G>A c.1896C>T c.(1894-1896)agC>agT p.S632S SKCM 10 75289647 75289647 + Silent SNP T T C TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr10:75289647T>C c.1851A>G c.(1849-1851)gaA>gaG p.E617E SKCM 10 75290181 75290181 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:75290181G>A c.1548C>T c.(1546-1548)atC>atT p.I516I SKCM 10 75290531 75290531 + Missense_Mutation SNP G G A TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr10:75290531G>A c.1378C>T c.(1378-1380)Cgc>Tgc p.R460C SKCM 10 75301396 75301396 + Missense_Mutation SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr10:75301396A>G c.673T>C c.(673-675)Tgt>Cgt p.C225R SKCM 10 75302567 75302567 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr10:75302567G>A c.566C>T c.(565-567)tCc>tTc p.S189F SKCM 10 75302868 75302868 + Missense_Mutation SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr10:75302868G>A c.397C>T c.(397-399)Cac>Tac p.H133Y

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 75290505 75290505 single base substitution C T 5_prime_UTR_variant BLCA-CN 10 75290505 75290505 single base substitution C T exon_variant BLCA-CN 10 75290505 75290505 single base substitution C T intron_variant BLCA-CN 10 75290505 75290505 single base substitution C T synonymous_variant R318R 954G>A BLCA-CN 10 75290505 75290505 single base substitution C T synonymous_variant R468R 1404G>A BLCA-CN 10 75290505 75290505 single base substitution C T upstream_gene_variant BLCA-CN 10 75301217 75301217 single base substitution C T 5_prime_UTR_variant BLCA-CN 10 75301217 75301217 single base substitution C T downstream_gene_variant BLCA-CN 10 75301217 75301217 single base substitution C T exon_variant BLCA-CN 10 75301217 75301217 single base substitution C T intron_variant BLCA-CN 10 75301217 75301217 single base substitution C T synonymous_variant T247T 741G>A BLCA-US 10 75279710 75279710 single base substitution C A 5_prime_UTR_variant BLCA-US 10 75279710 75279710 single base substitution C A exon_variant BLCA-US 10 75279710 75279710 single base substitution C A intron_variant BLCA-US 10 75279710 75279710 single base substitution C A synonymous_variant T23T 69G>T BLCA-US 10 75279710 75279710 single base substitution C A synonymous_variant T691T 2073G>T BLCA-US 10 75279710 75279710 single base substitution C A synonymous_variant T841T 2523G>T BLCA-US 10 75301468 75301468 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BLCA-US 10 75301468 75301468 single base substitution G A downstream_gene_variant BLCA-US 10 75301468 75301468 single base substitution G A exon_variant BLCA-US 10 75301468 75301468 single base substitution G A intron_variant BLCA-US 10 75301468 75301468 single base substitution G A stop_gained R201* 601C>T BLCA-US 10 75301468 75301468 single base substitution G A upstream_gene_variant BRCA-EU 10 75253513 75253513 single base substitution T C downstream_gene_variant BRCA-EU 10 75256852 75256852 single base substitution C G downstream_gene_variant BRCA-EU 10 75257215 75257215 single base substitution A G downstream_gene_variant BRCA-EU 10 75260961 75260961 deletion of <=200bp A - intron_variant BRCA-EU 10 75261139 75261139 single base substitution T C intron_variant BRCA-EU 10 75262257 75262257 single base substitution G C intron_variant BRCA-EU 10 75262353 75262353 single base substitution G A intron_variant BRCA-EU 10 75262867 75262867 single base substitution C G intron_variant BRCA-EU 10 75263384 75263384 single base substitution G A intron_variant BRCA-EU 10 75265257 75265257 single base substitution C G intron_variant BRCA-EU 10 75265257 75265257 single base substitution C G upstream_gene_variant BRCA-EU 10 75265654 75265654 single base substitution G C intron_variant BRCA-EU 10 75265654 75265654 single base substitution G C upstream_gene_variant BRCA-EU 10 75265761 75265761 single base substitution T C intron_variant BRCA-EU 10 75265761 75265761 single base substitution T C upstream_gene_variant BRCA-EU 10 75265794 75265794 single base substitution G T intron_variant BRCA-EU 10 75265794 75265794 single base substitution G T upstream_gene_variant BRCA-EU 10 75265937 75265937 single base substitution A G intron_variant BRCA-EU 10 75265937 75265937 single base substitution A G upstream_gene_variant BRCA-EU 10 75266292 75266292 insertion of <=200bp - AT intron_variant BRCA-EU 10 75266292 75266292 insertion of <=200bp - AT upstream_gene_variant BRCA-EU 10 75266292 75266293 deletion of <=200bp AT - intron_variant BRCA-EU 10 75266292 75266293 deletion of <=200bp AT - upstream_gene_variant BRCA-EU 10 75268056 75268056 single base substitution T G intron_variant BRCA-EU 10 75268056 75268056 single base substitution T G upstream_gene_variant BRCA-EU 10 75269199 75269199 single base substitution A T intron_variant BRCA-EU 10 75269199 75269199 single base substitution A T upstream_gene_variant BRCA-EU 10 75270973 75270973 single base substitution C G intron_variant BRCA-EU 10 75271088 75271088 single base substitution C G intron_variant BRCA-EU 10 75271908 75271908 deletion of <=200bp T - intron_variant BRCA-EU 10 75273096 75273096 single base substitution G T intron_variant BRCA-EU 10 75273124 75273124 single base substitution G A intron_variant BRCA-EU 10 75273128 75273128 single base substitution C T intron_variant BRCA-EU 10 75273195 75273195 single base substitution C T intron_variant BRCA-EU 10 75273346 75273346 single base substitution C T intron_variant BRCA-EU 10 75273570 75273570 insertion of <=200bp - T downstream_gene_variant BRCA-EU 10 75273570 75273570 insertion of <=200bp - T intron_variant BRCA-EU 10 75273800 75273800 single base substitution C G downstream_gene_variant BRCA-EU 10 75273800 75273800 single base substitution C G intron_variant BRCA-EU 10 75274237 75274237 single base substitution C A downstream_gene_variant BRCA-EU 10 75274237 75274237 single base substitution C A intron_variant BRCA-EU 10 75275041 75275041 single base substitution T A downstream_gene_variant BRCA-EU 10 75275041 75275041 single base substitution T A intron_variant BRCA-EU 10 75276813 75276813 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 75276813 75276813 single base substitution C T downstream_gene_variant BRCA-EU 10 75276813 75276813 single base substitution C T exon_variant BRCA-EU 10 75276813 75276813 single base substitution C T missense_variant S1124N 3371G>A BRCA-EU 10 75276813 75276813 single base substitution C T missense_variant S212N 635G>A BRCA-EU 10 75276813 75276813 single base substitution C T missense_variant S306N 917G>A BRCA-EU 10 75276813 75276813 single base substitution C T missense_variant S974N 2921G>A BRCA-EU 10 75277234 75277238 deletion of <=200bp TCTTC - 3_prime_UTR_variant BRCA-EU 10 75277234 75277238 deletion of <=200bp TCTTC - downstream_gene_variant BRCA-EU 10 75277234 75277238 deletion of <=200bp TCTTC - exon_variant BRCA-EU 10 75277234 75277238 deletion of <=200bp TCTTC - frameshift_variant EKN164 BRCA-EU 10 75277234 75277238 deletion of <=200bp TCTTC - frameshift_variant EKN70 BRCA-EU 10 75277234 75277238 deletion of <=200bp TCTTC - frameshift_variant EKN832 BRCA-EU 10 75277234 75277238 deletion of <=200bp TCTTC - frameshift_variant EKN982 BRCA-EU 10 75281239 75281239 single base substitution T C intron_variant BRCA-EU 10 75281774 75281774 deletion of <=200bp A - intron_variant BRCA-EU 10 75284195 75284195 single base substitution A G downstream_gene_variant BRCA-EU 10 75284195 75284195 single base substitution A G intron_variant BRCA-EU 10 75284195 75284195 single base substitution A G upstream_gene_variant BRCA-EU 10 75286015 75286015 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 75286015 75286015 deletion of <=200bp T - intron_variant BRCA-EU 10 75286015 75286015 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 75286230 75286230 single base substitution C A downstream_gene_variant BRCA-EU 10 75286230 75286230 single base substitution C A intron_variant BRCA-EU 10 75286230 75286230 single base substitution C A upstream_gene_variant BRCA-EU 10 75288669 75288669 single base substitution T C downstream_gene_variant BRCA-EU 10 75288669 75288669 single base substitution T C intron_variant BRCA-EU 10 75289746 75289746 single base substitution T A intron_variant BRCA-EU 10 75290117 75290119 deletion of <=200bp CTC - 5_prime_UTR_variant BRCA-EU 10 75290117 75290119 deletion of <=200bp CTC - disruptive_inframe_deletion GD387D BRCA-EU 10 75290117 75290119 deletion of <=200bp CTC - disruptive_inframe_deletion GD537D BRCA-EU 10 75290117 75290119 deletion of <=200bp CTC - exon_variant BRCA-EU 10 75290995 75290995 single base substitution G A downstream_gene_variant BRCA-EU 10 75290995 75290995 single base substitution G A intron_variant BRCA-EU 10 75290995 75290995 single base substitution G A upstream_gene_variant BRCA-EU 10 75291787 75291787 single base substitution A C downstream_gene_variant BRCA-EU 10 75291787 75291787 single base substitution A C intron_variant BRCA-EU 10 75291787 75291787 single base substitution A C upstream_gene_variant BRCA-EU 10 75293665 75293665 single base substitution G C downstream_gene_variant BRCA-EU 10 75293665 75293665 single base substitution G C intron_variant BRCA-EU 10 75293665 75293665 single base substitution G C upstream_gene_variant BRCA-EU 10 75295738 75295738 single base substitution G A downstream_gene_variant BRCA-EU 10 75295738 75295738 single base substitution G A intron_variant BRCA-EU 10 75295738 75295738 single base substitution G A upstream_gene_variant BRCA-EU 10 75296918 75296918 single base substitution A C downstream_gene_variant BRCA-EU 10 75296918 75296918 single base substitution A C intron_variant BRCA-EU 10 75296918 75296918 single base substitution A C upstream_gene_variant BRCA-EU 10 75297111 75297111 single base substitution G T downstream_gene_variant BRCA-EU 10 75297111 75297111 single base substitution G T intron_variant BRCA-EU 10 75297111 75297111 single base substitution G T upstream_gene_variant BRCA-EU 10 75297324 75297324 single base substitution C A downstream_gene_variant BRCA-EU 10 75297324 75297324 single base substitution C A intron_variant BRCA-EU 10 75297324 75297324 single base substitution C A upstream_gene_variant BRCA-EU 10 75299152 75299152 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 75299152 75299152 deletion of <=200bp T - intron_variant BRCA-EU 10 75299152 75299152 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 75299239 75299239 single base substitution C A 5_prime_UTR_variant BRCA-EU 10 75299239 75299239 single base substitution C A downstream_gene_variant BRCA-EU 10 75299239 75299239 single base substitution C A exon_variant BRCA-EU 10 75299239 75299239 single base substitution C A missense_variant R163L 488G>T BRCA-EU 10 75299239 75299239 single base substitution C A missense_variant R313L 938G>T BRCA-EU 10 75299239 75299239 single base substitution C A upstream_gene_variant BRCA-EU 10 75300075 75300075 single base substitution T A downstream_gene_variant BRCA-EU 10 75300075 75300075 single base substitution T A intron_variant BRCA-EU 10 75301989 75301989 single base substitution T A downstream_gene_variant BRCA-EU 10 75301989 75301989 single base substitution T A intron_variant BRCA-EU 10 75301989 75301989 single base substitution T A upstream_gene_variant BRCA-EU 10 75302127 75302127 single base substitution G T downstream_gene_variant BRCA-EU 10 75302127 75302127 single base substitution G T intron_variant BRCA-EU 10 75302127 75302127 single base substitution G T upstream_gene_variant BRCA-EU 10 75302408 75302408 single base substitution G C downstream_gene_variant BRCA-EU 10 75302408 75302408 single base substitution G C intron_variant BRCA-EU 10 75302408 75302408 single base substitution G C upstream_gene_variant BRCA-EU 10 75303844 75303844 single base substitution G T intron_variant BRCA-EU 10 75303844 75303844 single base substitution G T upstream_gene_variant BRCA-EU 10 75304629 75304629 insertion of <=200bp - GC intron_variant BRCA-EU 10 75304629 75304629 insertion of <=200bp - GC upstream_gene_variant BRCA-EU 10 75304683 75304683 single base substitution G C intron_variant BRCA-EU 10 75304683 75304683 single base substitution G C upstream_gene_variant BRCA-EU 10 75305153 75305153 single base substitution G A intron_variant BRCA-EU 10 75305153 75305153 single base substitution G A upstream_gene_variant BRCA-EU 10 75306122 75306122 deletion of <=200bp T - intron_variant BRCA-EU 10 75306122 75306122 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 75309206 75309206 single base substitution A T intron_variant BRCA-EU 10 75309206 75309206 single base substitution A T upstream_gene_variant BRCA-EU 10 75309693 75309693 single base substitution T C intron_variant BRCA-EU 10 75309693 75309693 single base substitution T C upstream_gene_variant BRCA-EU 10 75314947 75314947 single base substitution A C intron_variant BRCA-EU 10 75314947 75314947 single base substitution A C upstream_gene_variant BRCA-EU 10 75316456 75316456 single base substitution G C intron_variant BRCA-EU 10 75316456 75316456 single base substitution G C upstream_gene_variant BRCA-EU 10 75316859 75316859 single base substitution G T intron_variant BRCA-EU 10 75316859 75316859 single base substitution G T upstream_gene_variant BRCA-EU 10 75317527 75317527 single base substitution A T intron_variant BRCA-EU 10 75317527 75317527 single base substitution A T upstream_gene_variant BRCA-EU 10 75318998 75318998 single base substitution G T intron_variant BRCA-EU 10 75319083 75319083 single base substitution C A intron_variant BRCA-EU 10 75322706 75322706 single base substitution A G intron_variant BRCA-EU 10 75322901 75322901 single base substitution C T intron_variant BRCA-EU 10 75323135 75323135 single base substitution A G intron_variant BRCA-EU 10 75323676 75323676 deletion of <=200bp T - intron_variant BRCA-EU 10 75323850 75323850 single base substitution C T intron_variant BRCA-EU 10 75325408 75325408 single base substitution G A intron_variant BRCA-EU 10 75326445 75326445 single base substitution T C downstream_gene_variant BRCA-EU 10 75326445 75326445 single base substitution T C intron_variant BRCA-EU 10 75326895 75326895 single base substitution C G downstream_gene_variant BRCA-EU 10 75326895 75326895 single base substitution C G intron_variant BRCA-EU 10 75328355 75328355 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 75328355 75328355 deletion of <=200bp A - intron_variant BRCA-EU 10 75329839 75329839 single base substitution C T downstream_gene_variant BRCA-EU 10 75329839 75329839 single base substitution C T intron_variant BRCA-EU 10 75330446 75330446 single base substitution G C downstream_gene_variant BRCA-EU 10 75330446 75330446 single base substitution G C intron_variant BRCA-EU 10 75331383 75331383 single base substitution A G downstream_gene_variant BRCA-EU 10 75331383 75331383 single base substitution A G intron_variant BRCA-EU 10 75333051 75333051 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 75333051 75333051 deletion of <=200bp A - intron_variant BRCA-EU 10 75336080 75336083 deletion of <=200bp TCTT - 5_prime_UTR_variant BRCA-EU 10 75336080 75336083 deletion of <=200bp TCTT - exon_variant BRCA-EU 10 75336080 75336083 deletion of <=200bp TCTT - intron_variant BRCA-EU 10 75336080 75336083 deletion of <=200bp TCTT - upstream_gene_variant BRCA-EU 10 75336167 75336167 single base substitution C A intron_variant BRCA-EU 10 75336167 75336167 single base substitution C A upstream_gene_variant BRCA-EU 10 75338313 75338313 single base substitution G A intron_variant BRCA-EU 10 75338313 75338313 single base substitution G A upstream_gene_variant BRCA-EU 10 75340826 75340826 single base substitution A C intron_variant BRCA-EU 10 75340826 75340826 single base substitution A C upstream_gene_variant BRCA-EU 10 75342233 75342233 single base substitution T A intron_variant BRCA-EU 10 75342626 75342626 single base substitution T A intron_variant BRCA-EU 10 75344006 75344006 single base substitution C T intron_variant BRCA-EU 10 75344899 75344899 single base substitution C T intron_variant BRCA-EU 10 75345052 75345052 single base substitution T C intron_variant BRCA-EU 10 75345291 75345291 single base substitution G A intron_variant BRCA-EU 10 75345480 75345480 single base substitution G A intron_variant BRCA-EU 10 75347028 75347028 single base substitution G A intron_variant BRCA-EU 10 75350258 75350258 single base substitution T A intron_variant BRCA-EU 10 75351189 75351189 deletion of <=200bp A - 5_prime_UTR_variant BRCA-EU 10 75351189 75351189 deletion of <=200bp A - exon_variant BRCA-EU 10 75351189 75351189 deletion of <=200bp A - intron_variant BRCA-EU 10 75351189 75351189 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 75352775 75352775 single base substitution T C intron_variant BRCA-EU 10 75352775 75352775 single base substitution T C upstream_gene_variant BRCA-EU 10 75352969 75352969 single base substitution A G intron_variant BRCA-EU 10 75352969 75352969 single base substitution A G upstream_gene_variant BRCA-EU 10 75353038 75353038 single base substitution G A intron_variant BRCA-EU 10 75353038 75353038 single base substitution G A upstream_gene_variant BRCA-EU 10 75356304 75356304 single base substitution G C intron_variant BRCA-EU 10 75356694 75356694 single base substitution C A intron_variant BRCA-EU 10 75356821 75356821 single base substitution A G intron_variant BRCA-EU 10 75357843 75357843 deletion of <=200bp A - intron_variant BRCA-EU 10 75361294 75361294 insertion of <=200bp - TGCC intron_variant BRCA-EU 10 75361385 75361385 single base substitution G A intron_variant BRCA-EU 10 75362010 75362010 single base substitution C T intron_variant BRCA-EU 10 75362446 75362446 insertion of <=200bp - T intron_variant BRCA-EU 10 75366592 75366592 single base substitution G A intron_variant BRCA-EU 10 75369724 75369724 single base substitution C T intron_variant BRCA-EU 10 75370145 75370145 single base substitution C A intron_variant BRCA-EU 10 75372248 75372248 single base substitution G C intron_variant BRCA-EU 10 75372855 75372855 single base substitution T C intron_variant BRCA-EU 10 75372983 75372983 single base substitution C A intron_variant BRCA-EU 10 75374577 75374577 single base substitution A C intron_variant BRCA-EU 10 75375039 75375039 single base substitution C T intron_variant BRCA-EU 10 75377492 75377492 single base substitution G T intron_variant BRCA-EU 10 75377870 75377870 single base substitution G C intron_variant BRCA-EU 10 75378736 75378736 single base substitution C T intron_variant BRCA-EU 10 75380847 75380847 single base substitution G C intron_variant BRCA-EU 10 75382372 75382372 single base substitution G A intron_variant BRCA-EU 10 75390105 75390105 single base substitution T A upstream_gene_variant BRCA-EU 10 75390378 75390378 single base substitution G A upstream_gene_variant BRCA-FR 10 75262257 75262257 single base substitution G C intron_variant BRCA-FR 10 75263384 75263384 single base substitution G A intron_variant BRCA-FR 10 75265937 75265937 single base substitution A G intron_variant BRCA-FR 10 75265937 75265937 single base substitution A G upstream_gene_variant BRCA-FR 10 75272333 75272333 single base substitution C G intron_variant BRCA-FR 10 75288669 75288669 single base substitution T C downstream_gene_variant BRCA-FR 10 75288669 75288669 single base substitution T C intron_variant BRCA-FR 10 75291787 75291787 single base substitution A C downstream_gene_variant BRCA-FR 10 75291787 75291787 single base substitution A C intron_variant BRCA-FR 10 75291787 75291787 single base substitution A C upstream_gene_variant BRCA-FR 10 75297324 75297324 single base substitution C A downstream_gene_variant BRCA-FR 10 75297324 75297324 single base substitution C A intron_variant BRCA-FR 10 75297324 75297324 single base substitution C A upstream_gene_variant BRCA-FR 10 75302408 75302408 single base substitution G C downstream_gene_variant BRCA-FR 10 75302408 75302408 single base substitution G C intron_variant BRCA-FR 10 75302408 75302408 single base substitution G C upstream_gene_variant BRCA-FR 10 75303844 75303844 single base substitution G T intron_variant BRCA-FR 10 75303844 75303844 single base substitution G T upstream_gene_variant BRCA-FR 10 75309286 75309286 single base substitution C T intron_variant BRCA-FR 10 75309286 75309286 single base substitution C T upstream_gene_variant BRCA-FR 10 75316456 75316456 single base substitution G C intron_variant BRCA-FR 10 75316456 75316456 single base substitution G C upstream_gene_variant BRCA-FR 10 75347024 75347024 single base substitution G A intron_variant BRCA-FR 10 75347028 75347028 single base substitution G A intron_variant BRCA-FR 10 75363951 75363951 single base substitution G A intron_variant BRCA-FR 10 75368032 75368032 single base substitution C A intron_variant BRCA-FR 10 75370236 75370236 single base substitution C A intron_variant BRCA-FR 10 75370336 75370336 single base substitution C T intron_variant BRCA-FR 10 75382372 75382372 single base substitution G A intron_variant BRCA-KR 10 75276292 75276292 single base substitution C G 3_prime_UTR_variant BRCA-KR 10 75276292 75276292 single base substitution C G downstream_gene_variant BRCA-KR 10 75276292 75276292 single base substitution C G exon_variant BRCA-KR 10 75276292 75276292 single base substitution C G missense_variant E1148Q 3442G>C BRCA-KR 10 75276292 75276292 single base substitution C G missense_variant E1298Q 3892G>C BRCA-KR 10 75276292 75276292 single base substitution C G missense_variant E386Q 1156G>C BRCA-KR 10 75276292 75276292 single base substitution C G missense_variant E480Q 1438G>C BRCA-UK 10 75301989 75301989 single base substitution T A downstream_gene_variant BRCA-UK 10 75301989 75301989 single base substitution T A intron_variant BRCA-UK 10 75301989 75301989 single base substitution T A upstream_gene_variant BRCA-UK 10 75352775 75352775 single base substitution T C intron_variant BRCA-UK 10 75352775 75352775 single base substitution T C upstream_gene_variant BRCA-UK 10 75370145 75370145 single base substitution C A intron_variant BRCA-US 10 75258420 75258420 single base substitution G A 3_prime_UTR_variant BRCA-US 10 75258420 75258420 single base substitution G A downstream_gene_variant BRCA-US 10 75258420 75258420 single base substitution G A exon_variant BRCA-US 10 75258420 75258420 single base substitution G A synonymous_variant I1524I 4572C>T BRCA-US 10 75258420 75258420 single base substitution G A synonymous_variant I1674I 5022C>T BRCA-US 10 75258420 75258420 single base substitution G A synonymous_variant I715I 2145C>T BRCA-US 10 75258420 75258420 single base substitution G A synonymous_variant I809I 2427C>T BRCA-US 10 75258501 75258501 single base substitution A G 3_prime_UTR_variant BRCA-US 10 75258501 75258501 single base substitution A G downstream_gene_variant BRCA-US 10 75258501 75258501 single base substitution A G exon_variant BRCA-US 10 75258501 75258501 single base substitution A G synonymous_variant Y1497Y 4491T>C BRCA-US 10 75258501 75258501 single base substitution A G synonymous_variant Y1647Y 4941T>C BRCA-US 10 75258501 75258501 single base substitution A G synonymous_variant Y688Y 2064T>C BRCA-US 10 75258501 75258501 single base substitution A G synonymous_variant Y782Y 2346T>C BRCA-US 10 75258655 75258655 single base substitution T G 3_prime_UTR_variant BRCA-US 10 75258655 75258655 single base substitution T G downstream_gene_variant BRCA-US 10 75258655 75258655 single base substitution T G exon_variant BRCA-US 10 75258655 75258655 single base substitution T G missense_variant H1446P 4337A>C BRCA-US 10 75258655 75258655 single base substitution T G missense_variant H1596P 4787A>C BRCA-US 10 75258655 75258655 single base substitution T G missense_variant H637P 1910A>C BRCA-US 10 75258655 75258655 single base substitution T G missense_variant H731P 2192A>C BRCA-US 10 75258663 75258663 single base substitution T G 3_prime_UTR_variant BRCA-US 10 75258663 75258663 single base substitution T G downstream_gene_variant BRCA-US 10 75258663 75258663 single base substitution T G exon_variant BRCA-US 10 75258663 75258663 single base substitution T G synonymous_variant S1443S 4329A>C BRCA-US 10 75258663 75258663 single base substitution T G synonymous_variant S1593S 4779A>C BRCA-US 10 75258663 75258663 single base substitution T G synonymous_variant S634S 1902A>C BRCA-US 10 75258663 75258663 single base substitution T G synonymous_variant S728S 2184A>C BRCA-US 10 75264684 75264684 single base substitution A G 3_prime_UTR_variant BRCA-US 10 75264684 75264684 single base substitution A G exon_variant BRCA-US 10 75264684 75264684 single base substitution A G intron_variant BRCA-US 10 75264684 75264684 single base substitution A G missense_variant L1262S 3785T>C BRCA-US 10 75264684 75264684 single base substitution A G missense_variant L1412S 4235T>C BRCA-US 10 75276172 75276172 single base substitution C G 3_prime_UTR_variant BRCA-US 10 75276172 75276172 single base substitution C G downstream_gene_variant BRCA-US 10 75276172 75276172 single base substitution C G exon_variant BRCA-US 10 75276172 75276172 single base substitution C G missense_variant G1188R 3562G>C BRCA-US 10 75276172 75276172 single base substitution C G missense_variant G1338R 4012G>C BRCA-US 10 75276172 75276172 single base substitution C G missense_variant G426R 1276G>C BRCA-US 10 75276172 75276172 single base substitution C G missense_variant G520R 1558G>C BRCA-US 10 75277121 75277121 single base substitution A C 3_prime_UTR_variant BRCA-US 10 75277121 75277121 single base substitution A C downstream_gene_variant BRCA-US 10 75277121 75277121 single base substitution A C exon_variant BRCA-US 10 75277121 75277121 single base substitution A C synonymous_variant A1021A 3063T>G BRCA-US 10 75277121 75277121 single base substitution A C synonymous_variant A109A 327T>G BRCA-US 10 75277121 75277121 single base substitution A C synonymous_variant A203A 609T>G BRCA-US 10 75277121 75277121 single base substitution A C synonymous_variant A871A 2613T>G BRCA-US 10 75279643 75279643 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 10 75279643 75279643 single base substitution G A exon_variant BRCA-US 10 75279643 75279643 single base substitution G A intron_variant BRCA-US 10 75279643 75279643 single base substitution G A missense_variant R46C 136C>T BRCA-US 10 75279643 75279643 single base substitution G A missense_variant R714C 2140C>T BRCA-US 10 75279643 75279643 single base substitution G A missense_variant R864C 2590C>T BRCA-US 10 75289313 75289313 deletion of <=200bp A - exon_variant BRCA-US 10 75289313 75289313 deletion of <=200bp A - frameshift_variant S729 BRCA-US 10 75289313 75289313 deletion of <=200bp A - intron_variant BRCA-US 10 75289458 75289458 single base substitution A G 5_prime_UTR_variant BRCA-US 10 75289458 75289458 single base substitution A G exon_variant BRCA-US 10 75289458 75289458 single base substitution A G synonymous_variant P530P 1590T>C BRCA-US 10 75289458 75289458 single base substitution A G synonymous_variant P680P 2040T>C BRCA-US 10 75296096 75296096 single base substitution T G 5_prime_UTR_variant BRCA-US 10 75296096 75296096 single base substitution T G downstream_gene_variant BRCA-US 10 75296096 75296096 single base substitution T G exon_variant BRCA-US 10 75296096 75296096 single base substitution T G missense_variant T209P 625A>C BRCA-US 10 75296096 75296096 single base substitution T G missense_variant T359P 1075A>C BRCA-US 10 75296096 75296096 single base substitution T G upstream_gene_variant BTCA-JP 10 75255427 75255427 insertion of <=200bp - T downstream_gene_variant BTCA-JP 10 75335161 75335161 single base substitution C G downstream_gene_variant BTCA-JP 10 75335161 75335161 single base substitution C G intron_variant CESC-US 10 75255357 75255357 single base substitution G C downstream_gene_variant CESC-US 10 75258749 75258749 single base substitution G A 3_prime_UTR_variant CESC-US 10 75258749 75258749 single base substitution G A downstream_gene_variant CESC-US 10 75258749 75258749 single base substitution G A exon_variant CESC-US 10 75258749 75258749 single base substitution G A stop_gained Q1415* 4243C>T CESC-US 10 75258749 75258749 single base substitution G A stop_gained Q1565* 4693C>T CESC-US 10 75258749 75258749 single base substitution G A stop_gained Q606* 1816C>T CESC-US 10 75258749 75258749 single base substitution G A stop_gained Q700* 2098C>T CESC-US 10 75277079 75277079 single base substitution G A 3_prime_UTR_variant CESC-US 10 75277079 75277079 single base substitution G A downstream_gene_variant CESC-US 10 75277079 75277079 single base substitution G A exon_variant CESC-US 10 75277079 75277079 single base substitution G A synonymous_variant P1035P 3105C>T CESC-US 10 75277079 75277079 single base substitution G A synonymous_variant P123P 369C>T CESC-US 10 75277079 75277079 single base substitution G A synonymous_variant P217P 651C>T CESC-US 10 75277079 75277079 single base substitution G A synonymous_variant P885P 2655C>T CESC-US 10 75277284 75277284 single base substitution G C 3_prime_UTR_variant CESC-US 10 75277284 75277284 single base substitution G C downstream_gene_variant CESC-US 10 75277284 75277284 single base substitution G C exon_variant CESC-US 10 75277284 75277284 single base substitution G C missense_variant S149C 446C>G CESC-US 10 75277284 75277284 single base substitution G C missense_variant S55C 164C>G CESC-US 10 75277284 75277284 single base substitution G C missense_variant S817C 2450C>G CESC-US 10 75277284 75277284 single base substitution G C missense_variant S967C 2900C>G CESC-US 10 75277418 75277418 single base substitution G T 3_prime_UTR_variant CESC-US 10 75277418 75277418 single base substitution G T downstream_gene_variant CESC-US 10 75277418 75277418 single base substitution G T exon_variant CESC-US 10 75277418 75277418 single base substitution G T missense_variant F104L 312C>A CESC-US 10 75277418 75277418 single base substitution G T missense_variant F10L 30C>A CESC-US 10 75277418 75277418 single base substitution G T missense_variant F772L 2316C>A CESC-US 10 75277418 75277418 single base substitution G T missense_variant F922L 2766C>A CLLE-ES 10 75254296 75254296 single base substitution G C downstream_gene_variant CLLE-ES 10 75254504 75254504 single base substitution C T downstream_gene_variant CLLE-ES 10 75256612 75256612 single base substitution C T downstream_gene_variant CLLE-ES 10 75264021 75264021 single base substitution T A intron_variant CLLE-ES 10 75270914 75270914 single base substitution C T intron_variant CLLE-ES 10 75283292 75283296 deletion of <=200bp CCTTT - intron_variant CLLE-ES 10 75298983 75298983 single base substitution G A downstream_gene_variant CLLE-ES 10 75298983 75298983 single base substitution G A intron_variant CLLE-ES 10 75298983 75298983 single base substitution G A upstream_gene_variant CLLE-ES 10 75305980 75305980 single base substitution A G intron_variant CLLE-ES 10 75305980 75305980 single base substitution A G upstream_gene_variant CLLE-ES 10 75311734 75311734 single base substitution T C intron_variant CLLE-ES 10 75361307 75361307 single base substitution A G intron_variant COAD-US 10 75258739 75258739 single base substitution T C 3_prime_UTR_variant COAD-US 10 75258739 75258739 single base substitution T C downstream_gene_variant COAD-US 10 75258739 75258739 single base substitution T C exon_variant COAD-US 10 75258739 75258739 single base substitution T C missense_variant Y1418C 4253A>G COAD-US 10 75258739 75258739 single base substitution T C missense_variant Y1568C 4703A>G COAD-US 10 75258739 75258739 single base substitution T C missense_variant Y609C 1826A>G COAD-US 10 75258739 75258739 single base substitution T C missense_variant Y703C 2108A>G COAD-US 10 75276419 75276419 single base substitution C T 3_prime_UTR_variant COAD-US 10 75276419 75276419 single base substitution C T downstream_gene_variant COAD-US 10 75276419 75276419 single base substitution C T exon_variant COAD-US 10 75276419 75276419 single base substitution C T synonymous_variant G1105G 3315G>A COAD-US 10 75276419 75276419 single base substitution C T synonymous_variant G1255G 3765G>A COAD-US 10 75276419 75276419 single base substitution C T synonymous_variant G343G 1029G>A COAD-US 10 75276419 75276419 single base substitution C T synonymous_variant G437G 1311G>A COAD-US 10 75276479 75276479 single base substitution C A 3_prime_UTR_variant COAD-US 10 75276479 75276479 single base substitution C A downstream_gene_variant COAD-US 10 75276479 75276479 single base substitution C A exon_variant COAD-US 10 75276479 75276479 single base substitution C A missense_variant E1085D 3255G>T COAD-US 10 75276479 75276479 single base substitution C A missense_variant E1235D 3705G>T COAD-US 10 75276479 75276479 single base substitution C A missense_variant E323D 969G>T COAD-US 10 75276479 75276479 single base substitution C A missense_variant E417D 1251G>T COAD-US 10 75280699 75280700 deletion of <=200bp CA - 5_prime_UTR_variant COAD-US 10 75280699 75280700 deletion of <=200bp CA - exon_variant COAD-US 10 75280699 75280700 deletion of <=200bp CA - frameshift_variant CA666 COAD-US 10 75280699 75280700 deletion of <=200bp CA - frameshift_variant CA816 COAD-US 10 75280699 75280700 deletion of <=200bp CA - intron_variant COAD-US 10 75290596 75290596 insertion of <=200bp - A intron_variant COAD-US 10 75290596 75290596 insertion of <=200bp - A splice_region_variant COAD-US 10 75290596 75290596 insertion of <=200bp - A upstream_gene_variant COAD-US 10 75296105 75296105 single base substitution G T 5_prime_UTR_variant COAD-US 10 75296105 75296105 single base substitution G T downstream_gene_variant COAD-US 10 75296105 75296105 single base substitution G T exon_variant COAD-US 10 75296105 75296105 single base substitution G T missense_variant P206T 616C>A COAD-US 10 75296105 75296105 single base substitution G T missense_variant P356T 1066C>A COAD-US 10 75296105 75296105 single base substitution G T upstream_gene_variant COCA-CN 10 75258578 75258578 single base substitution G A 3_prime_UTR_variant COCA-CN 10 75258578 75258578 single base substitution G A downstream_gene_variant COCA-CN 10 75258578 75258578 single base substitution G A exon_variant COCA-CN 10 75258578 75258578 single base substitution G A missense_variant P1472S 4414C>T COCA-CN 10 75258578 75258578 single base substitution G A missense_variant P1622S 4864C>T COCA-CN 10 75258578 75258578 single base substitution G A missense_variant P663S 1987C>T COCA-CN 10 75258578 75258578 single base substitution G A missense_variant P757S 2269C>T COCA-CN 10 75265281 75265281 single base substitution T G intron_variant COCA-CN 10 75265281 75265281 single base substitution T G upstream_gene_variant COCA-CN 10 75272066 75272066 single base substitution T C intron_variant COCA-CN 10 75276379 75276379 single base substitution A G 3_prime_UTR_variant COCA-CN 10 75276379 75276379 single base substitution A G downstream_gene_variant COCA-CN 10 75276379 75276379 single base substitution A G exon_variant COCA-CN 10 75276379 75276379 single base substitution A G missense_variant F1119L 3355T>C COCA-CN 10 75276379 75276379 single base substitution A G missense_variant F1269L 3805T>C COCA-CN 10 75276379 75276379 single base substitution A G missense_variant F357L 1069T>C COCA-CN 10 75276379 75276379 single base substitution A G missense_variant F451L 1351T>C COCA-CN 10 75289572 75289572 single base substitution C T 5_prime_UTR_variant COCA-CN 10 75289572 75289572 single base substitution C T exon_variant COCA-CN 10 75289572 75289572 single base substitution C T synonymous_variant R492R 1476G>A COCA-CN 10 75289572 75289572 single base substitution C T synonymous_variant R642R 1926G>A COCA-CN 10 75289625 75289625 single base substitution C T 5_prime_UTR_variant COCA-CN 10 75289625 75289625 single base substitution C T exon_variant COCA-CN 10 75289625 75289625 single base substitution C T missense_variant D475N 1423G>A COCA-CN 10 75289625 75289625 single base substitution C T missense_variant D625N 1873G>A COCA-CN 10 75290062 75290062 single base substitution T C 5_prime_UTR_variant COCA-CN 10 75290062 75290062 single base substitution T C exon_variant COCA-CN 10 75290062 75290062 single base substitution T C missense_variant E406G 1217A>G COCA-CN 10 75290062 75290062 single base substitution T C missense_variant E556G 1667A>G COCA-CN 10 75290071 75290071 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 10 75290071 75290071 single base substitution C T exon_variant COCA-CN 10 75290071 75290071 single base substitution C T missense_variant R403H 1208G>A COCA-CN 10 75290071 75290071 single base substitution C T missense_variant R553H 1658G>A COCA-CN 10 75294508 75294508 single base substitution T C 5_prime_UTR_variant COCA-CN 10 75294508 75294508 single base substitution T C downstream_gene_variant COCA-CN 10 75294508 75294508 single base substitution T C exon_variant COCA-CN 10 75294508 75294508 single base substitution T C intron_variant COCA-CN 10 75294508 75294508 single base substitution T C missense_variant S239G 715A>G COCA-CN 10 75294508 75294508 single base substitution T C missense_variant S389G 1165A>G COCA-CN 10 75294508 75294508 single base substitution T C upstream_gene_variant COCA-CN 10 75295987 75295987 single base substitution G T downstream_gene_variant COCA-CN 10 75295987 75295987 single base substitution G T exon_variant COCA-CN 10 75295987 75295987 single base substitution G T intron_variant COCA-CN 10 75295987 75295987 single base substitution G T upstream_gene_variant COCA-CN 10 75299050 75299050 single base substitution A T downstream_gene_variant COCA-CN 10 75299050 75299050 single base substitution A T intron_variant COCA-CN 10 75299050 75299050 single base substitution A T upstream_gene_variant COCA-CN 10 75301463 75301463 single base substitution C A 5_prime_UTR_variant COCA-CN 10 75301463 75301463 single base substitution C A downstream_gene_variant COCA-CN 10 75301463 75301463 single base substitution C A exon_variant COCA-CN 10 75301463 75301463 single base substitution C A intron_variant COCA-CN 10 75301463 75301463 single base substitution C A missense_variant E202D 606G>T COCA-CN 10 75301463 75301463 single base substitution C A upstream_gene_variant COCA-CN 10 75308714 75308714 single base substitution C A intron_variant COCA-CN 10 75308714 75308714 single base substitution C A upstream_gene_variant COCA-CN 10 75326504 75326504 single base substitution A C downstream_gene_variant COCA-CN 10 75326504 75326504 single base substitution A C intron_variant COCA-CN 10 75331165 75331165 single base substitution T G downstream_gene_variant COCA-CN 10 75331165 75331165 single base substitution T G intron_variant COCA-CN 10 75344109 75344109 single base substitution G A intron_variant COCA-CN 10 75354407 75354407 single base substitution T G intron_variant COCA-CN 10 75354407 75354407 single base substitution T G upstream_gene_variant COCA-CN 10 75368254 75368254 single base substitution A G intron_variant COCA-CN 10 75370419 75370419 single base substitution A G intron_variant COCA-CN 10 75389280 75389280 single base substitution G T upstream_gene_variant EOPC-DE 10 75307317 75307317 single base substitution A C intron_variant EOPC-DE 10 75307317 75307317 single base substitution A C upstream_gene_variant EOPC-DE 10 75315827 75315827 single base substitution A T intron_variant EOPC-DE 10 75315827 75315827 single base substitution A T upstream_gene_variant ESAD-UK 10 75258328 75258328 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 75258328 75258328 single base substitution G A downstream_gene_variant ESAD-UK 10 75258328 75258328 single base substitution G A exon_variant ESAD-UK 10 75259784 75259784 single base substitution C G downstream_gene_variant ESAD-UK 10 75259784 75259784 single base substitution C G intron_variant ESAD-UK 10 75260564 75260564 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 75260564 75260564 single base substitution G A exon_variant ESAD-UK 10 75260564 75260564 single base substitution G A synonymous_variant T1298T 3894C>T ESAD-UK 10 75260564 75260564 single base substitution G A synonymous_variant T1448T 4344C>T ESAD-UK 10 75260564 75260564 single base substitution G A synonymous_variant T489T 1467C>T ESAD-UK 10 75260564 75260564 single base substitution G A synonymous_variant T583T 1749C>T ESAD-UK 10 75262022 75262022 single base substitution G A intron_variant ESAD-UK 10 75262615 75262615 single base substitution A G intron_variant ESAD-UK 10 75262918 75262918 single base substitution G C intron_variant ESAD-UK 10 75266648 75266648 single base substitution G C intron_variant ESAD-UK 10 75266648 75266648 single base substitution G C upstream_gene_variant ESAD-UK 10 75267567 75267567 single base substitution G A intron_variant ESAD-UK 10 75267567 75267567 single base substitution G A upstream_gene_variant ESAD-UK 10 75267573 75267573 single base substitution C T intron_variant ESAD-UK 10 75267573 75267573 single base substitution C T upstream_gene_variant ESAD-UK 10 75268058 75268058 single base substitution G A intron_variant ESAD-UK 10 75268058 75268058 single base substitution G A upstream_gene_variant ESAD-UK 10 75269136 75269136 single base substitution G C intron_variant ESAD-UK 10 75269136 75269136 single base substitution G C upstream_gene_variant ESAD-UK 10 75271344 75271344 single base substitution G T intron_variant ESAD-UK 10 75271908 75271908 deletion of <=200bp T - intron_variant ESAD-UK 10 75275762 75275762 single base substitution G T downstream_gene_variant ESAD-UK 10 75275762 75275762 single base substitution G T intron_variant ESAD-UK 10 75277452 75277452 single base substitution G C 3_prime_UTR_variant ESAD-UK 10 75277452 75277452 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 10 75277452 75277452 single base substitution G C downstream_gene_variant ESAD-UK 10 75277452 75277452 single base substitution G C exon_variant ESAD-UK 10 75277452 75277452 single base substitution G C missense_variant S761C 2282C>G ESAD-UK 10 75277452 75277452 single base substitution G C missense_variant S911C 2732C>G ESAD-UK 10 75277452 75277452 single base substitution G C missense_variant S93C 278C>G ESAD-UK 10 75277506 75277506 single base substitution C A downstream_gene_variant ESAD-UK 10 75277506 75277506 single base substitution C A splice_acceptor_variant ESAD-UK 10 75278045 75278045 single base substitution T A downstream_gene_variant ESAD-UK 10 75278045 75278045 single base substitution T A intron_variant ESAD-UK 10 75281733 75281733 single base substitution T C intron_variant ESAD-UK 10 75281734 75281734 single base substitution A T intron_variant ESAD-UK 10 75288521 75288521 single base substitution C T downstream_gene_variant ESAD-UK 10 75288521 75288521 single base substitution C T intron_variant ESAD-UK 10 75289701 75289701 single base substitution G T intron_variant ESAD-UK 10 75291476 75291476 single base substitution C T downstream_gene_variant ESAD-UK 10 75291476 75291476 single base substitution C T intron_variant ESAD-UK 10 75291476 75291476 single base substitution C T upstream_gene_variant ESAD-UK 10 75294534 75294534 single base substitution A G downstream_gene_variant ESAD-UK 10 75294534 75294534 single base substitution A G intron_variant ESAD-UK 10 75294534 75294534 single base substitution A G splice_region_variant ESAD-UK 10 75294534 75294534 single base substitution A G upstream_gene_variant ESAD-UK 10 75297888 75297888 single base substitution G A downstream_gene_variant ESAD-UK 10 75297888 75297888 single base substitution G A intron_variant ESAD-UK 10 75297888 75297888 single base substitution G A upstream_gene_variant ESAD-UK 10 75299511 75299511 single base substitution A C downstream_gene_variant ESAD-UK 10 75299511 75299511 single base substitution A C intron_variant ESAD-UK 10 75299511 75299511 single base substitution A C upstream_gene_variant ESAD-UK 10 75301407 75301407 single base substitution T A 5_prime_UTR_variant ESAD-UK 10 75301407 75301407 single base substitution T A downstream_gene_variant ESAD-UK 10 75301407 75301407 single base substitution T A exon_variant ESAD-UK 10 75301407 75301407 single base substitution T A intron_variant ESAD-UK 10 75301407 75301407 single base substitution T A missense_variant D221V 662A>T ESAD-UK 10 75307331 75307331 single base substitution A T intron_variant ESAD-UK 10 75307331 75307331 single base substitution A T upstream_gene_variant ESAD-UK 10 75308247 75308247 single base substitution A G intron_variant ESAD-UK 10 75308247 75308247 single base substitution A G upstream_gene_variant ESAD-UK 10 75308310 75308310 deletion of <=200bp A - intron_variant ESAD-UK 10 75308310 75308310 deletion of <=200bp A - upstream_gene_variant ESAD-UK 10 75309653 75309653 single base substitution C T intron_variant ESAD-UK 10 75309653 75309653 single base substitution C T upstream_gene_variant ESAD-UK 10 75311792 75311792 single base substitution G C intron_variant ESAD-UK 10 75312007 75312007 single base substitution C G intron_variant ESAD-UK 10 75312662 75312662 single base substitution C T intron_variant ESAD-UK 10 75315264 75315264 single base substitution G A intron_variant ESAD-UK 10 75315264 75315264 single base substitution G A upstream_gene_variant ESAD-UK 10 75315675 75315675 insertion of <=200bp - A intron_variant ESAD-UK 10 75315675 75315675 insertion of <=200bp - A upstream_gene_variant ESAD-UK 10 75315943 75315943 single base substitution G A intron_variant ESAD-UK 10 75315943 75315943 single base substitution G A upstream_gene_variant ESAD-UK 10 75316796 75316796 single base substitution G A intron_variant ESAD-UK 10 75316796 75316796 single base substitution G A upstream_gene_variant ESAD-UK 10 75318349 75318349 single base substitution G A intron_variant ESAD-UK 10 75318591 75318591 single base substitution C G intron_variant ESAD-UK 10 75321218 75321218 single base substitution A T intron_variant ESAD-UK 10 75321807 75321807 single base substitution C T intron_variant ESAD-UK 10 75322544 75322544 single base substitution G T intron_variant ESAD-UK 10 75323346 75323346 single base substitution C G intron_variant ESAD-UK 10 75325193 75325193 single base substitution G C intron_variant ESAD-UK 10 75325251 75325251 single base substitution G A intron_variant ESAD-UK 10 75326489 75326489 insertion of <=200bp - A downstream_gene_variant ESAD-UK 10 75326489 75326489 insertion of <=200bp - A intron_variant ESAD-UK 10 75327418 75327418 single base substitution G A downstream_gene_variant ESAD-UK 10 75327418 75327418 single base substitution G A intron_variant ESAD-UK 10 75328923 75328923 single base substitution C T downstream_gene_variant ESAD-UK 10 75328923 75328923 single base substitution C T intron_variant ESAD-UK 10 75336698 75336698 single base substitution T C intron_variant ESAD-UK 10 75336698 75336698 single base substitution T C upstream_gene_variant ESAD-UK 10 75337241 75337241 single base substitution C T intron_variant ESAD-UK 10 75337241 75337241 single base substitution C T upstream_gene_variant ESAD-UK 10 75342895 75342895 single base substitution A T intron_variant ESAD-UK 10 75343344 75343344 insertion of <=200bp - A intron_variant ESAD-UK 10 75344982 75344982 single base substitution A C intron_variant ESAD-UK 10 75348338 75348338 single base substitution G A intron_variant ESAD-UK 10 75349586 75349588 deletion of <=200bp AAG - intron_variant ESAD-UK 10 75349598 75349598 single base substitution T C intron_variant ESAD-UK 10 75353050 75353050 single base substitution C T intron_variant ESAD-UK 10 75353050 75353050 single base substitution C T upstream_gene_variant ESAD-UK 10 75353410 75353410 single base substitution T C intron_variant ESAD-UK 10 75353410 75353410 single base substitution T C upstream_gene_variant ESAD-UK 10 75354701 75354701 single base substitution G C intron_variant ESAD-UK 10 75354701 75354701 single base substitution G C upstream_gene_variant ESAD-UK 10 75355938 75355938 single base substitution G T intron_variant ESAD-UK 10 75355938 75355938 single base substitution G T upstream_gene_variant ESAD-UK 10 75355947 75355947 single base substitution A C intron_variant ESAD-UK 10 75355947 75355947 single base substitution A C upstream_gene_variant ESAD-UK 10 75359301 75359301 single base substitution C T intron_variant ESAD-UK 10 75363009 75363009 single base substitution C T intron_variant ESAD-UK 10 75364989 75364989 single base substitution A G intron_variant ESAD-UK 10 75365475 75365475 single base substitution C T intron_variant ESAD-UK 10 75366363 75366363 single base substitution G A intron_variant ESAD-UK 10 75367928 75367928 single base substitution G T intron_variant ESAD-UK 10 75368278 75368278 single base substitution G A intron_variant ESAD-UK 10 75373235 75373235 insertion of <=200bp - A intron_variant ESAD-UK 10 75378096 75378096 single base substitution T C intron_variant ESAD-UK 10 75385258 75385258 single base substitution C G intron_variant ESAD-UK 10 75388020 75388021 deletion of <=200bp AC - upstream_gene_variant ESAD-UK 10 75389845 75389845 single base substitution C T upstream_gene_variant ESCA-CN 10 75258704 75258704 single base substitution G A 3_prime_UTR_variant ESCA-CN 10 75258704 75258704 single base substitution G A downstream_gene_variant ESCA-CN 10 75258704 75258704 single base substitution G A exon_variant ESCA-CN 10 75258704 75258704 single base substitution G A stop_gained Q1430* 4288C>T ESCA-CN 10 75258704 75258704 single base substitution G A stop_gained Q1580* 4738C>T ESCA-CN 10 75258704 75258704 single base substitution G A stop_gained Q621* 1861C>T ESCA-CN 10 75258704 75258704 single base substitution G A stop_gained Q715* 2143C>T ESCA-CN 10 75280667 75280667 single base substitution G C intron_variant ESCA-CN 10 75280667 75280667 single base substitution G C missense_variant I677M 2031C>G ESCA-CN 10 75280667 75280667 single base substitution G C missense_variant I827M 2481C>G ESCA-CN 10 75280667 75280667 single base substitution G C splice_region_variant ESCA-CN 10 75290011 75290011 single base substitution C T 5_prime_UTR_variant ESCA-CN 10 75290011 75290011 single base substitution C T exon_variant ESCA-CN 10 75290011 75290011 single base substitution C T missense_variant R423H 1268G>A ESCA-CN 10 75290011 75290011 single base substitution C T missense_variant R573H 1718G>A KIRC-US 10 75258858 75258858 single base substitution G T 3_prime_UTR_variant KIRC-US 10 75258858 75258858 single base substitution G T downstream_gene_variant KIRC-US 10 75258858 75258858 single base substitution G T exon_variant KIRC-US 10 75258858 75258858 single base substitution G T missense_variant N1378K 4134C>A KIRC-US 10 75258858 75258858 single base substitution G T missense_variant N1528K 4584C>A KIRC-US 10 75258858 75258858 single base substitution G T missense_variant N569K 1707C>A KIRC-US 10 75258858 75258858 single base substitution G T missense_variant N663K 1989C>A KIRC-US 10 75294440 75294440 single base substitution G T 5_prime_UTR_variant KIRC-US 10 75294440 75294440 single base substitution G T downstream_gene_variant KIRC-US 10 75294440 75294440 single base substitution G T exon_variant KIRC-US 10 75294440 75294440 single base substitution G T intron_variant KIRC-US 10 75294440 75294440 single base substitution G T synonymous_variant V261V 783C>A KIRC-US 10 75294440 75294440 single base substitution G T synonymous_variant V411V 1233C>A KIRC-US 10 75294440 75294440 single base substitution G T upstream_gene_variant KIRP-US 10 75294429 75294429 single base substitution G A 5_prime_UTR_variant KIRP-US 10 75294429 75294429 single base substitution G A downstream_gene_variant KIRP-US 10 75294429 75294429 single base substitution G A exon_variant KIRP-US 10 75294429 75294429 single base substitution G A intron_variant KIRP-US 10 75294429 75294429 single base substitution G A missense_variant S265F 794C>T KIRP-US 10 75294429 75294429 single base substitution G A missense_variant S415F 1244C>T KIRP-US 10 75294429 75294429 single base substitution G A upstream_gene_variant LAML-KR 10 75259077 75259077 single base substitution T C downstream_gene_variant LAML-KR 10 75259077 75259077 single base substitution T C intron_variant LAML-KR 10 75371762 75371762 single base substitution G A intron_variant LICA-FR 10 75268162 75268162 deletion of <=200bp A - intron_variant LICA-FR 10 75268162 75268162 deletion of <=200bp A - upstream_gene_variant LICA-FR 10 75280739 75280739 single base substitution C T 5_prime_UTR_variant LICA-FR 10 75280739 75280739 single base substitution C T exon_variant LICA-FR 10 75280739 75280739 single base substitution C T intron_variant LICA-FR 10 75280739 75280739 single base substitution C T synonymous_variant V653V 1959G>A LICA-FR 10 75280739 75280739 single base substitution C T synonymous_variant V803V 2409G>A LICA-FR 10 75297122 75297122 single base substitution T C downstream_gene_variant LICA-FR 10 75297122 75297122 single base substitution T C intron_variant LICA-FR 10 75297122 75297122 single base substitution T C upstream_gene_variant LICA-FR 10 75301177 75301177 single base substitution C T 5_prime_UTR_variant LICA-FR 10 75301177 75301177 single base substitution C T downstream_gene_variant LICA-FR 10 75301177 75301177 single base substitution C T exon_variant LICA-FR 10 75301177 75301177 single base substitution C T intron_variant LICA-FR 10 75301177 75301177 single base substitution C T missense_variant E261K 781G>A LICA-FR 10 75317246 75317246 deletion of <=200bp T - intron_variant LICA-FR 10 75317246 75317246 deletion of <=200bp T - upstream_gene_variant LICA-FR 10 75320887 75320887 single base substitution G A intron_variant LICA-FR 10 75340200 75340200 single base substitution C T intron_variant LICA-FR 10 75340200 75340200 single base substitution C T upstream_gene_variant LICA-FR 10 75382305 75382305 single base substitution C T intron_variant LIHC-US 10 75276369 75276369 single base substitution G C 3_prime_UTR_variant LIHC-US 10 75276369 75276369 single base substitution G C downstream_gene_variant LIHC-US 10 75276369 75276369 single base substitution G C exon_variant LIHC-US 10 75276369 75276369 single base substitution G C missense_variant S1122C 3365C>G LIHC-US 10 75276369 75276369 single base substitution G C missense_variant S1272C 3815C>G LIHC-US 10 75276369 75276369 single base substitution G C missense_variant S360C 1079C>G LIHC-US 10 75276369 75276369 single base substitution G C missense_variant S454C 1361C>G LIHC-US 10 75277370 75277370 single base substitution T C 3_prime_UTR_variant LIHC-US 10 75277370 75277370 single base substitution T C downstream_gene_variant LIHC-US 10 75277370 75277370 single base substitution T C exon_variant LIHC-US 10 75277370 75277370 single base substitution T C synonymous_variant P120P 360A>G LIHC-US 10 75277370 75277370 single base substitution T C synonymous_variant P26P 78A>G LIHC-US 10 75277370 75277370 single base substitution T C synonymous_variant P788P 2364A>G LIHC-US 10 75277370 75277370 single base substitution T C synonymous_variant P938P 2814A>G LINC-JP 10 75253251 75253251 single base substitution T C downstream_gene_variant LINC-JP 10 75253920 75253920 deletion of <=200bp T - downstream_gene_variant LINC-JP 10 75260844 75260844 single base substitution C T intron_variant LINC-JP 10 75265771 75265771 single base substitution T C intron_variant LINC-JP 10 75265771 75265771 single base substitution T C upstream_gene_variant LINC-JP 10 75277396 75277396 single base substitution G A 3_prime_UTR_variant LINC-JP 10 75277396 75277396 single base substitution G A downstream_gene_variant LINC-JP 10 75277396 75277396 single base substitution G A exon_variant LINC-JP 10 75277396 75277396 single base substitution G A missense_variant H112Y 334C>T LINC-JP 10 75277396 75277396 single base substitution G A missense_variant H18Y 52C>T LINC-JP 10 75277396 75277396 single base substitution G A missense_variant H780Y 2338C>T LINC-JP 10 75277396 75277396 single base substitution G A missense_variant H930Y 2788C>T LINC-JP 10 75283683 75283683 single base substitution T A intron_variant LINC-JP 10 75283683 75283683 single base substitution T A upstream_gene_variant LINC-JP 10 75290513 75290513 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 10 75290513 75290513 single base substitution G A exon_variant LINC-JP 10 75290513 75290513 single base substitution G A intron_variant LINC-JP 10 75290513 75290513 single base substitution G A missense_variant R316W 946C>T LINC-JP 10 75290513 75290513 single base substitution G A missense_variant R466W 1396C>T LINC-JP 10 75290513 75290513 single base substitution G A upstream_gene_variant LINC-JP 10 75292343 75292343 single base substitution G A downstream_gene_variant LINC-JP 10 75292343 75292343 single base substitution G A intron_variant LINC-JP 10 75292343 75292343 single base substitution G A upstream_gene_variant LINC-JP 10 75293208 75293208 single base substitution A T downstream_gene_variant LINC-JP 10 75293208 75293208 single base substitution A T intron_variant LINC-JP 10 75293208 75293208 single base substitution A T upstream_gene_variant LINC-JP 10 75296152 75296152 single base substitution C A 5_prime_UTR_variant LINC-JP 10 75296152 75296152 single base substitution C A downstream_gene_variant LINC-JP 10 75296152 75296152 single base substitution C A exon_variant LINC-JP 10 75296152 75296152 single base substitution C A missense_variant G190V 569G>T LINC-JP 10 75296152 75296152 single base substitution C A missense_variant G340V 1019G>T LINC-JP 10 75296152 75296152 single base substitution C A upstream_gene_variant LINC-JP 10 75305077 75305077 single base substitution T C intron_variant LINC-JP 10 75305077 75305077 single base substitution T C upstream_gene_variant LINC-JP 10 75306764 75306764 single base substitution A G intron_variant LINC-JP 10 75306764 75306764 single base substitution A G upstream_gene_variant LINC-JP 10 75331297 75331297 single base substitution T A downstream_gene_variant LINC-JP 10 75331297 75331297 single base substitution T A intron_variant LINC-JP 10 75335382 75335382 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 10 75335382 75335382 single base substitution C T downstream_gene_variant LINC-JP 10 75335382 75335382 single base substitution C T exon_variant LINC-JP 10 75335382 75335382 single base substitution C T missense_variant R12H 35G>A LINC-JP 10 75341059 75341059 single base substitution G A intron_variant LINC-JP 10 75341059 75341059 single base substitution G A upstream_gene_variant LINC-JP 10 75342346 75342346 single base substitution G A intron_variant LINC-JP 10 75348942 75348942 single base substitution T C intron_variant LINC-JP 10 75352508 75352508 single base substitution T G intron_variant LINC-JP 10 75352508 75352508 single base substitution T G upstream_gene_variant LINC-JP 10 75353721 75353721 single base substitution C T intron_variant LINC-JP 10 75353721 75353721 single base substitution C T upstream_gene_variant LINC-JP 10 75355161 75355161 single base substitution T C intron_variant LINC-JP 10 75355161 75355161 single base substitution T C upstream_gene_variant LINC-JP 10 75366636 75366636 single base substitution C A intron_variant LINC-JP 10 75380905 75380905 single base substitution C T intron_variant LINC-JP 10 75381840 75381840 single base substitution C A intron_variant LIRI-JP 10 75256505 75256505 single base substitution G A downstream_gene_variant LIRI-JP 10 75257393 75257393 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 75257393 75257393 single base substitution T C downstream_gene_variant LIRI-JP 10 75259829 75259829 single base substitution C A downstream_gene_variant LIRI-JP 10 75259829 75259829 single base substitution C A intron_variant LIRI-JP 10 75260581 75260581 single base substitution T G 3_prime_UTR_variant LIRI-JP 10 75260581 75260581 single base substitution T G exon_variant LIRI-JP 10 75260581 75260581 single base substitution T G synonymous_variant R1293R 3877A>C LIRI-JP 10 75260581 75260581 single base substitution T G synonymous_variant R1443R 4327A>C LIRI-JP 10 75260581 75260581 single base substitution T G synonymous_variant R484R 1450A>C LIRI-JP 10 75260581 75260581 single base substitution T G synonymous_variant R578R 1732A>C LIRI-JP 10 75264259 75264259 single base substitution T A intron_variant LIRI-JP 10 75264468 75264468 single base substitution C T intron_variant LIRI-JP 10 75264951 75264951 single base substitution T A exon_variant LIRI-JP 10 75264951 75264951 single base substitution T A intron_variant LIRI-JP 10 75272318 75272318 single base substitution G A intron_variant LIRI-JP 10 75275959 75275959 single base substitution C A downstream_gene_variant LIRI-JP 10 75275959 75275959 single base substitution C A intron_variant LIRI-JP 10 75281448 75281448 single base substitution T C intron_variant LIRI-JP 10 75283571 75283571 single base substitution T C intron_variant LIRI-JP 10 75283571 75283571 single base substitution T C upstream_gene_variant LIRI-JP 10 75284051 75284051 single base substitution C T downstream_gene_variant LIRI-JP 10 75284051 75284051 single base substitution C T intron_variant LIRI-JP 10 75284051 75284051 single base substitution C T upstream_gene_variant LIRI-JP 10 75290247 75290247 single base substitution A G 5_prime_UTR_variant LIRI-JP 10 75290247 75290247 single base substitution A G exon_variant LIRI-JP 10 75290247 75290247 single base substitution A G synonymous_variant N344N 1032T>C LIRI-JP 10 75290247 75290247 single base substitution A G synonymous_variant N494N 1482T>C LIRI-JP 10 75290247 75290247 single base substitution A G upstream_gene_variant LIRI-JP 10 75294742 75294742 single base substitution C T downstream_gene_variant LIRI-JP 10 75294742 75294742 single base substitution C T intron_variant LIRI-JP 10 75294742 75294742 single base substitution C T upstream_gene_variant LIRI-JP 10 75295324 75295324 single base substitution T C downstream_gene_variant LIRI-JP 10 75295324 75295324 single base substitution T C intron_variant LIRI-JP 10 75295324 75295324 single base substitution T C upstream_gene_variant LIRI-JP 10 75296363 75296363 insertion of <=200bp - C downstream_gene_variant LIRI-JP 10 75296363 75296363 insertion of <=200bp - C intron_variant LIRI-JP 10 75296363 75296363 insertion of <=200bp - C upstream_gene_variant LIRI-JP 10 75296473 75296473 single base substitution A G downstream_gene_variant LIRI-JP 10 75296473 75296473 single base substitution A G intron_variant LIRI-JP 10 75296473 75296473 single base substitution A G upstream_gene_variant LIRI-JP 10 75297264 75297264 single base substitution G A downstream_gene_variant LIRI-JP 10 75297264 75297264 single base substitution G A intron_variant LIRI-JP 10 75297264 75297264 single base substitution G A upstream_gene_variant LIRI-JP 10 75300950 75300950 single base substitution A G downstream_gene_variant LIRI-JP 10 75300950 75300950 single base substitution A G intron_variant LIRI-JP 10 75308685 75308685 single base substitution A G intron_variant LIRI-JP 10 75308685 75308685 single base substitution A G upstream_gene_variant LIRI-JP 10 75310893 75310893 single base substitution C T intron_variant LIRI-JP 10 75310893 75310893 single base substitution C T upstream_gene_variant LIRI-JP 10 75312836 75312836 single base substitution G C intron_variant LIRI-JP 10 75316394 75316394 single base substitution G C intron_variant LIRI-JP 10 75316394 75316394 single base substitution G C upstream_gene_variant LIRI-JP 10 75321371 75321371 single base substitution C A intron_variant LIRI-JP 10 75334434 75334434 single base substitution C T downstream_gene_variant LIRI-JP 10 75334434 75334434 single base substitution C T intron_variant LIRI-JP 10 75336577 75336577 single base substitution G T intron_variant LIRI-JP 10 75336577 75336577 single base substitution G T upstream_gene_variant LIRI-JP 10 75337379 75337379 single base substitution T C intron_variant LIRI-JP 10 75337379 75337379 single base substitution T C upstream_gene_variant LIRI-JP 10 75337704 75337704 single base substitution G A intron_variant LIRI-JP 10 75337704 75337704 single base substitution G A upstream_gene_variant LIRI-JP 10 75342389 75342389 single base substitution T A intron_variant LIRI-JP 10 75342586 75342586 single base substitution T C intron_variant LIRI-JP 10 75346008 75346008 single base substitution C T intron_variant LIRI-JP 10 75346324 75346324 single base substitution T A intron_variant LIRI-JP 10 75349236 75349236 single base substitution T A intron_variant LIRI-JP 10 75351607 75351607 single base substitution T G intron_variant LIRI-JP 10 75351607 75351607 single base substitution T G upstream_gene_variant LIRI-JP 10 75351947 75351947 single base substitution T A intron_variant LIRI-JP 10 75351947 75351947 single base substitution T A upstream_gene_variant LIRI-JP 10 75354110 75354110 single base substitution T C intron_variant LIRI-JP 10 75354110 75354110 single base substitution T C upstream_gene_variant LIRI-JP 10 75359478 75359478 single base substitution C G intron_variant LIRI-JP 10 75360825 75360825 single base substitution T C intron_variant LIRI-JP 10 75361316 75361316 single base substitution C A intron_variant LIRI-JP 10 75364176 75364176 single base substitution T C intron_variant LIRI-JP 10 75364979 75364979 single base substitution T C intron_variant LIRI-JP 10 75368873 75368873 single base substitution T C intron_variant LIRI-JP 10 75371546 75371546 single base substitution T A intron_variant LIRI-JP 10 75372557 75372557 single base substitution C T intron_variant LIRI-JP 10 75373192 75373192 single base substitution G A intron_variant LIRI-JP 10 75374698 75374698 single base substitution A C intron_variant LIRI-JP 10 75374997 75374997 single base substitution A T intron_variant LIRI-JP 10 75375172 75375172 single base substitution A G intron_variant LIRI-JP 10 75382191 75382191 single base substitution C T intron_variant LIRI-JP 10 75384371 75384371 single base substitution T C intron_variant LIRI-JP 10 75387173 75387173 single base substitution A G upstream_gene_variant LIRI-JP 10 75387186 75387186 single base substitution A G upstream_gene_variant LIRI-JP 10 75387512 75387512 single base substitution T G upstream_gene_variant LIRI-JP 10 75389335 75389335 single base substitution C T upstream_gene_variant LIRI-JP 10 75390568 75390568 single base substitution C T upstream_gene_variant LUSC-KR 10 75261675 75261675 single base substitution C G intron_variant LUSC-KR 10 75271552 75271552 single base substitution G T intron_variant LUSC-KR 10 75275533 75275533 single base substitution A C downstream_gene_variant LUSC-KR 10 75275533 75275533 single base substitution A C intron_variant LUSC-KR 10 75276420 75276420 single base substitution C A 3_prime_UTR_variant LUSC-KR 10 75276420 75276420 single base substitution C A downstream_gene_variant LUSC-KR 10 75276420 75276420 single base substitution C A exon_variant LUSC-KR 10 75276420 75276420 single base substitution C A missense_variant G1105V 3314G>T LUSC-KR 10 75276420 75276420 single base substitution C A missense_variant G1255V 3764G>T LUSC-KR 10 75276420 75276420 single base substitution C A missense_variant G343V 1028G>T LUSC-KR 10 75276420 75276420 single base substitution C A missense_variant G437V 1310G>T LUSC-KR 10 75276434 75276434 single base substitution G A 3_prime_UTR_variant LUSC-KR 10 75276434 75276434 single base substitution G A downstream_gene_variant LUSC-KR 10 75276434 75276434 single base substitution G A exon_variant LUSC-KR 10 75276434 75276434 single base substitution G A synonymous_variant S1100S 3300C>T LUSC-KR 10 75276434 75276434 single base substitution G A synonymous_variant S1250S 3750C>T LUSC-KR 10 75276434 75276434 single base substitution G A synonymous_variant S338S 1014C>T LUSC-KR 10 75276434 75276434 single base substitution G A synonymous_variant S432S 1296C>T LUSC-KR 10 75278715 75278715 single base substitution C G exon_variant LUSC-KR 10 75278715 75278715 single base substitution C G intron_variant LUSC-KR 10 75288266 75288266 single base substitution G A downstream_gene_variant LUSC-KR 10 75288266 75288266 single base substitution G A intron_variant LUSC-KR 10 75288266 75288266 single base substitution G A upstream_gene_variant LUSC-KR 10 75296690 75296690 single base substitution C G downstream_gene_variant LUSC-KR 10 75296690 75296690 single base substitution C G intron_variant LUSC-KR 10 75296690 75296690 single base substitution C G upstream_gene_variant LUSC-KR 10 75300199 75300199 single base substitution G A downstream_gene_variant LUSC-KR 10 75300199 75300199 single base substitution G A intron_variant LUSC-KR 10 75307042 75307042 single base substitution C A intron_variant LUSC-KR 10 75307042 75307042 single base substitution C A upstream_gene_variant LUSC-KR 10 75308272 75308272 single base substitution A G intron_variant LUSC-KR 10 75308272 75308272 single base substitution A G upstream_gene_variant LUSC-KR 10 75308950 75308950 single base substitution G T intron_variant LUSC-KR 10 75308950 75308950 single base substitution G T upstream_gene_variant LUSC-KR 10 75319061 75319061 single base substitution G A intron_variant LUSC-KR 10 75325368 75325368 single base substitution C T intron_variant LUSC-KR 10 75335825 75335825 single base substitution G A 5_prime_UTR_variant LUSC-KR 10 75335825 75335825 single base substitution G A downstream_gene_variant LUSC-KR 10 75335825 75335825 single base substitution G A exon_variant LUSC-KR 10 75335825 75335825 single base substitution G A intron_variant LUSC-KR 10 75335825 75335825 single base substitution G A upstream_gene_variant LUSC-KR 10 75336243 75336243 single base substitution T A intron_variant LUSC-KR 10 75336243 75336243 single base substitution T A upstream_gene_variant LUSC-KR 10 75343819 75343819 single base substitution C A intron_variant LUSC-KR 10 75350256 75350256 single base substitution A C intron_variant LUSC-KR 10 75354662 75354662 single base substitution T G intron_variant LUSC-KR 10 75354662 75354662 single base substitution T G upstream_gene_variant LUSC-KR 10 75380420 75380420 single base substitution G T intron_variant LUSC-US 10 75276202 75276202 single base substitution G T 3_prime_UTR_variant LUSC-US 10 75276202 75276202 single base substitution G T downstream_gene_variant LUSC-US 10 75276202 75276202 single base substitution G T exon_variant LUSC-US 10 75276202 75276202 single base substitution G T missense_variant Q1178K 3532C>A LUSC-US 10 75276202 75276202 single base substitution G T missense_variant Q1328K 3982C>A LUSC-US 10 75276202 75276202 single base substitution G T missense_variant Q416K 1246C>A LUSC-US 10 75276202 75276202 single base substitution G T missense_variant Q510K 1528C>A LUSC-US 10 75276561 75276561 single base substitution A G 3_prime_UTR_variant LUSC-US 10 75276561 75276561 single base substitution A G downstream_gene_variant LUSC-US 10 75276561 75276561 single base substitution A G exon_variant LUSC-US 10 75276561 75276561 single base substitution A G missense_variant L1058P 3173T>C LUSC-US 10 75276561 75276561 single base substitution A G missense_variant L1208P 3623T>C LUSC-US 10 75276561 75276561 single base substitution A G missense_variant L296P 887T>C LUSC-US 10 75276561 75276561 single base substitution A G missense_variant L390P 1169T>C LUSC-US 10 75276616 75276616 single base substitution G A 3_prime_UTR_variant LUSC-US 10 75276616 75276616 single base substitution G A downstream_gene_variant LUSC-US 10 75276616 75276616 single base substitution G A exon_variant LUSC-US 10 75276616 75276616 single base substitution G A synonymous_variant L1040L 3118C>T LUSC-US 10 75276616 75276616 single base substitution G A synonymous_variant L1190L 3568C>T LUSC-US 10 75276616 75276616 single base substitution G A synonymous_variant L278L 832C>T LUSC-US 10 75276616 75276616 single base substitution G A synonymous_variant L372L 1114C>T LUSC-US 10 75276843 75276843 single base substitution C A 3_prime_UTR_variant LUSC-US 10 75276843 75276843 single base substitution C A downstream_gene_variant LUSC-US 10 75276843 75276843 single base substitution C A exon_variant LUSC-US 10 75276843 75276843 single base substitution C A missense_variant S1114I 3341G>T LUSC-US 10 75276843 75276843 single base substitution C A missense_variant S202I 605G>T LUSC-US 10 75276843 75276843 single base substitution C A missense_variant S296I 887G>T LUSC-US 10 75276843 75276843 single base substitution C A missense_variant S964I 2891G>T LUSC-US 10 75277120 75277120 single base substitution G C 3_prime_UTR_variant LUSC-US 10 75277120 75277120 single base substitution G C downstream_gene_variant LUSC-US 10 75277120 75277120 single base substitution G C exon_variant LUSC-US 10 75277120 75277120 single base substitution G C missense_variant Q1022E 3064C>G LUSC-US 10 75277120 75277120 single base substitution G C missense_variant Q110E 328C>G LUSC-US 10 75277120 75277120 single base substitution G C missense_variant Q204E 610C>G LUSC-US 10 75277120 75277120 single base substitution G C missense_variant Q872E 2614C>G LUSC-US 10 75279616 75279616 single base substitution G A 5_prime_UTR_variant LUSC-US 10 75279616 75279616 single base substitution G A exon_variant LUSC-US 10 75279616 75279616 single base substitution G A intron_variant LUSC-US 10 75279616 75279616 single base substitution G A stop_gained Q55* 163C>T LUSC-US 10 75279616 75279616 single base substitution G A stop_gained Q723* 2167C>T LUSC-US 10 75279616 75279616 single base substitution G A stop_gained Q873* 2617C>T LUSC-US 10 75286428 75286428 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 10 75286428 75286428 single base substitution C A downstream_gene_variant LUSC-US 10 75286428 75286428 single base substitution C A exon_variant LUSC-US 10 75286428 75286428 single base substitution C A missense_variant W574L 1721G>T LUSC-US 10 75286428 75286428 single base substitution C A missense_variant W724L 2171G>T LUSC-US 10 75286428 75286428 single base substitution C A upstream_gene_variant LUSC-US 10 75290488 75290488 single base substitution G A 5_prime_UTR_variant LUSC-US 10 75290488 75290488 single base substitution G A exon_variant LUSC-US 10 75290488 75290488 single base substitution G A intron_variant LUSC-US 10 75290488 75290488 single base substitution G A missense_variant P324L 971C>T LUSC-US 10 75290488 75290488 single base substitution G A missense_variant P474L 1421C>T LUSC-US 10 75290488 75290488 single base substitution G A upstream_gene_variant LUSC-US 10 75294514 75294514 single base substitution T C 5_prime_UTR_variant LUSC-US 10 75294514 75294514 single base substitution T C downstream_gene_variant LUSC-US 10 75294514 75294514 single base substitution T C exon_variant LUSC-US 10 75294514 75294514 single base substitution T C intron_variant LUSC-US 10 75294514 75294514 single base substitution T C missense_variant I237V 709A>G LUSC-US 10 75294514 75294514 single base substitution T C missense_variant I387V 1159A>G LUSC-US 10 75294514 75294514 single base substitution T C upstream_gene_variant MALY-DE 10 75254742 75254742 single base substitution A C downstream_gene_variant MALY-DE 10 75255733 75255733 single base substitution C T downstream_gene_variant MALY-DE 10 75261067 75261067 single base substitution T C intron_variant MALY-DE 10 75276658 75276658 single base substitution G T 3_prime_UTR_variant MALY-DE 10 75276658 75276658 single base substitution G T downstream_gene_variant MALY-DE 10 75276658 75276658 single base substitution G T exon_variant MALY-DE 10 75276658 75276658 single base substitution G T missense_variant Q1026K 3076C>A MALY-DE 10 75276658 75276658 single base substitution G T missense_variant Q1176K 3526C>A MALY-DE 10 75276658 75276658 single base substitution G T missense_variant Q264K 790C>A MALY-DE 10 75276658 75276658 single base substitution G T missense_variant Q358K 1072C>A MALY-DE 10 75277701 75277701 single base substitution T A downstream_gene_variant MALY-DE 10 75277701 75277701 single base substitution T A intron_variant MALY-DE 10 75283247 75283247 single base substitution T A intron_variant MALY-DE 10 75289279 75289279 single base substitution T C downstream_gene_variant MALY-DE 10 75289279 75289279 single base substitution T C intron_variant MALY-DE 10 75289279 75289279 single base substitution T C missense_variant K740R 2219A>G MALY-DE 10 75302751 75302751 insertion of <=200bp - A downstream_gene_variant MALY-DE 10 75302751 75302751 insertion of <=200bp - A intron_variant MALY-DE 10 75302751 75302751 insertion of <=200bp - A upstream_gene_variant MALY-DE 10 75304840 75304840 single base substitution C T intron_variant MALY-DE 10 75304840 75304840 single base substitution C T upstream_gene_variant MALY-DE 10 75306867 75306867 single base substitution A G intron_variant MALY-DE 10 75306867 75306867 single base substitution A G upstream_gene_variant MALY-DE 10 75308310 75308310 insertion of <=200bp - A intron_variant MALY-DE 10 75308310 75308310 insertion of <=200bp - A upstream_gene_variant MALY-DE 10 75328849 75328849 single base substitution C T downstream_gene_variant MALY-DE 10 75328849 75328849 single base substitution C T intron_variant MALY-DE 10 75329451 75329451 single base substitution G A downstream_gene_variant MALY-DE 10 75329451 75329451 single base substitution G A intron_variant MALY-DE 10 75339061 75339061 single base substitution G T intron_variant MALY-DE 10 75339061 75339061 single base substitution G T upstream_gene_variant MALY-DE 10 75339537 75339537 single base substitution C A intron_variant MALY-DE 10 75339537 75339537 single base substitution C A upstream_gene_variant MALY-DE 10 75342644 75342644 single base substitution A G intron_variant MALY-DE 10 75354674 75354674 deletion of <=200bp T - intron_variant MALY-DE 10 75354674 75354674 deletion of <=200bp T - upstream_gene_variant MALY-DE 10 75362645 75362645 single base substitution A G intron_variant MALY-DE 10 75368024 75368024 insertion of <=200bp - A intron_variant MALY-DE 10 75377106 75377131 deletion of <=200bp TGGGAGGCTGAGGTGGGAGAATCACT - intron_variant MALY-DE 10 75378677 75378677 single base substitution T A intron_variant MALY-DE 10 75382059 75382066 deletion of <=200bp TATTTATT - intron_variant MELA-AU 10 75253837 75253837 single base substitution G A downstream_gene_variant MELA-AU 10 75256355 75256355 single base substitution T A downstream_gene_variant MELA-AU 10 75256392 75256393 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 75256589 75256589 single base substitution G A downstream_gene_variant MELA-AU 10 75256856 75256856 single base substitution C T downstream_gene_variant MELA-AU 10 75257041 75257041 single base substitution G A downstream_gene_variant MELA-AU 10 75257266 75257266 single base substitution A G downstream_gene_variant MELA-AU 10 75257678 75257678 single base substitution G A 3_prime_UTR_variant MELA-AU 10 75257678 75257678 single base substitution G A downstream_gene_variant MELA-AU 10 75257784 75257784 single base substitution G A 3_prime_UTR_variant MELA-AU 10 75257784 75257784 single base substitution G A downstream_gene_variant MELA-AU 10 75257907 75257907 single base substitution G A 3_prime_UTR_variant MELA-AU 10 75257907 75257907 single base substitution G A downstream_gene_variant MELA-AU 10 75258309 75258309 single base substitution G A 3_prime_UTR_variant MELA-AU 10 75258309 75258309 single base substitution G A downstream_gene_variant MELA-AU 10 75258309 75258309 single base substitution G A exon_variant MELA-AU 10 75258418 75258418 single base substitution C T 3_prime_UTR_variant MELA-AU 10 75258418 75258418 single base substitution C T downstream_gene_variant MELA-AU 10 75258418 75258418 single base substitution C T exon_variant MELA-AU 10 75258418 75258418 single base substitution C T missense_variant R1525K 4574G>A MELA-AU 10 75258418 75258418 single base substitution C T missense_variant R1675K 5024G>A MELA-AU 10 75258418 75258418 single base substitution C T missense_variant R716K 2147G>A MELA-AU 10 75258418 75258418 single base substitution C T missense_variant R810K 2429G>A MELA-AU 10 75258516 75258516 single base substitution C T 3_prime_UTR_variant MELA-AU 10 75258516 75258516 single base substitution C T downstream_gene_variant MELA-AU 10 75258516 75258516 single base substitution C T exon_variant MELA-AU 10 75258516 75258516 single base substitution C T stop_gained W1492* 4476G>A MELA-AU 10 75258516 75258516 single base substitution C T stop_gained W1642* 4926G>A MELA-AU 10 75258516 75258516 single base substitution C T stop_gained W683* 2049G>A MELA-AU 10 75258516 75258516 single base substitution C T stop_gained W777* 2331G>A MELA-AU 10 75258751 75258751 single base substitution G A 3_prime_UTR_variant MELA-AU 10 75258751 75258751 single base substitution G A downstream_gene_variant MELA-AU 10 75258751 75258751 single base substitution G A exon_variant MELA-AU 10 75258751 75258751 single base substitution G A missense_variant P1414L 4241C>T MELA-AU 10 75258751 75258751 single base substitution G A missense_variant P1564L 4691C>T MELA-AU 10 75258751 75258751 single base substitution G A missense_variant P605L 1814C>T MELA-AU 10 75258751 75258751 single base substitution G A missense_variant P699L 2096C>T MELA-AU 10 75259332 75259332 single base substitution T A downstream_gene_variant MELA-AU 10 75259332 75259332 single base substitution T A intron_variant MELA-AU 10 75260596 75260596 single base substitution C T missense_variant D1288N 3862G>A MELA-AU 10 75260596 75260596 single base substitution C T missense_variant D1438N 4312G>A MELA-AU 10 75260596 75260596 single base substitution C T missense_variant D479N 1435G>A MELA-AU 10 75260596 75260596 single base substitution C T missense_variant D573N 1717G>A MELA-AU 10 75260596 75260596 single base substitution C T splice_region_variant MELA-AU 10 75260674 75260674 single base substitution G A intron_variant MELA-AU 10 75260925 75260925 single base substitution G A intron_variant MELA-AU 10 75261266 75261266 single base substitution A G intron_variant MELA-AU 10 75262059 75262059 single base substitution A G intron_variant MELA-AU 10 75263445 75263445 single base substitution G A intron_variant MELA-AU 10 75263457 75263457 single base substitution G A intron_variant MELA-AU 10 75263814 75263814 single base substitution G A intron_variant MELA-AU 10 75264048 75264049 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 75265411 75265411 single base substitution G A intron_variant MELA-AU 10 75265411 75265411 single base substitution G A upstream_gene_variant MELA-AU 10 75266292 75266292 insertion of <=200bp - AT intron_variant MELA-AU 10 75266292 75266292 insertion of <=200bp - AT upstream_gene_variant MELA-AU 10 75267092 75267092 single base substitution G A intron_variant MELA-AU 10 75267092 75267092 single base substitution G A upstream_gene_variant MELA-AU 10 75267717 75267717 single base substitution C T intron_variant MELA-AU 10 75267717 75267717 single base substitution C T upstream_gene_variant MELA-AU 10 75267725 75267725 single base substitution G A intron_variant MELA-AU 10 75267725 75267725 single base substitution G A upstream_gene_variant MELA-AU 10 75268991 75268991 single base substitution G A intron_variant MELA-AU 10 75268991 75268991 single base substitution G A upstream_gene_variant MELA-AU 10 75269052 75269052 single base substitution T A intron_variant MELA-AU 10 75269052 75269052 single base substitution T A upstream_gene_variant MELA-AU 10 75269349 75269349 single base substitution G T intron_variant MELA-AU 10 75269349 75269349 single base substitution G T upstream_gene_variant MELA-AU 10 75272189 75272189 single base substitution A G intron_variant MELA-AU 10 75274933 75274933 single base substitution G A downstream_gene_variant MELA-AU 10 75274933 75274933 single base substitution G A intron_variant MELA-AU 10 75275407 75275407 single base substitution G A downstream_gene_variant MELA-AU 10 75275407 75275407 single base substitution G A intron_variant MELA-AU 10 75275651 75275651 single base substitution C T downstream_gene_variant MELA-AU 10 75275651 75275651 single base substitution C T intron_variant MELA-AU 10 75276290 75276290 single base substitution C T 3_prime_UTR_variant MELA-AU 10 75276290 75276290 single base substitution C T downstream_gene_variant MELA-AU 10 75276290 75276290 single base substitution C T exon_variant MELA-AU 10 75276290 75276290 single base substitution C T synonymous_variant E1148E 3444G>A MELA-AU 10 75276290 75276290 single base substitution C T synonymous_variant E1298E 3894G>A MELA-AU 10 75276290 75276290 single base substitution C T synonymous_variant E386E 1158G>A MELA-AU 10 75276290 75276290 single base substitution C T synonymous_variant E480E 1440G>A MELA-AU 10 75276413 75276414 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 10 75276413 75276414 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 75276413 75276414 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 10 75276413 75276414 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S1107F 3320CC>TT MELA-AU 10 75276413 75276414 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S1257F 3770CC>TT MELA-AU 10 75276413 75276414 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S345F 1034CC>TT MELA-AU 10 75276413 75276414 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S439F 1316CC>TT MELA-AU 10 75277492 75277492 single base substitution G A 5_prime_UTR_variant MELA-AU 10 75277492 75277492 single base substitution G A downstream_gene_variant MELA-AU 10 75277492 75277492 single base substitution G A exon_variant MELA-AU 10 75277492 75277492 single base substitution G A missense_variant P748S 2242C>T MELA-AU 10 75277492 75277492 single base substitution G A missense_variant P80S 238C>T MELA-AU 10 75277492 75277492 single base substitution G A missense_variant P898S 2692C>T MELA-AU 10 75277770 75277770 single base substitution C A downstream_gene_variant MELA-AU 10 75277770 75277770 single base substitution C A intron_variant MELA-AU 10 75277919 75277919 single base substitution G A downstream_gene_variant MELA-AU 10 75277919 75277919 single base substitution G A intron_variant MELA-AU 10 75277977 75277977 single base substitution G A downstream_gene_variant MELA-AU 10 75277977 75277977 single base substitution G A intron_variant MELA-AU 10 75278404 75278404 single base substitution G A downstream_gene_variant MELA-AU 10 75278404 75278404 single base substitution G A intron_variant MELA-AU 10 75279104 75279104 single base substitution G A exon_variant MELA-AU 10 75279104 75279104 single base substitution G A intron_variant MELA-AU 10 75280038 75280038 single base substitution C T intron_variant MELA-AU 10 75280550 75280550 single base substitution G A intron_variant MELA-AU 10 75281540 75281540 single base substitution G C intron_variant MELA-AU 10 75281759 75281759 single base substitution C T intron_variant MELA-AU 10 75281868 75281868 single base substitution A G intron_variant MELA-AU 10 75282400 75282400 single base substitution G T intron_variant MELA-AU 10 75282418 75282418 single base substitution G A intron_variant MELA-AU 10 75282733 75282733 single base substitution A G intron_variant MELA-AU 10 75282768 75282768 single base substitution G A intron_variant MELA-AU 10 75283707 75283707 single base substitution C T intron_variant MELA-AU 10 75283707 75283707 single base substitution C T upstream_gene_variant MELA-AU 10 75283945 75283945 single base substitution G A intron_variant MELA-AU 10 75283945 75283945 single base substitution G A upstream_gene_variant MELA-AU 10 75284647 75284647 single base substitution A G downstream_gene_variant MELA-AU 10 75284647 75284647 single base substitution A G intron_variant MELA-AU 10 75284647 75284647 single base substitution A G upstream_gene_variant MELA-AU 10 75285796 75285796 single base substitution G A downstream_gene_variant MELA-AU 10 75285796 75285796 single base substitution G A intron_variant MELA-AU 10 75285796 75285796 single base substitution G A upstream_gene_variant MELA-AU 10 75285924 75285924 single base substitution G A downstream_gene_variant MELA-AU 10 75285924 75285924 single base substitution G A intron_variant MELA-AU 10 75285924 75285924 single base substitution G A upstream_gene_variant MELA-AU 10 75286029 75286029 single base substitution G A downstream_gene_variant MELA-AU 10 75286029 75286029 single base substitution G A intron_variant MELA-AU 10 75286029 75286029 single base substitution G A upstream_gene_variant MELA-AU 10 75286801 75286801 single base substitution C T downstream_gene_variant MELA-AU 10 75286801 75286801 single base substitution C T intron_variant MELA-AU 10 75286801 75286801 single base substitution C T upstream_gene_variant MELA-AU 10 75287034 75287034 single base substitution G A downstream_gene_variant MELA-AU 10 75287034 75287034 single base substitution G A intron_variant MELA-AU 10 75287034 75287034 single base substitution G A upstream_gene_variant MELA-AU 10 75287166 75287166 single base substitution G A downstream_gene_variant MELA-AU 10 75287166 75287166 single base substitution G A intron_variant MELA-AU 10 75287166 75287166 single base substitution G A upstream_gene_variant MELA-AU 10 75287955 75287955 single base substitution G A downstream_gene_variant MELA-AU 10 75287955 75287955 single base substitution G A intron_variant MELA-AU 10 75287955 75287955 single base substitution G A upstream_gene_variant MELA-AU 10 75289120 75289120 single base substitution G A 3_prime_UTR_variant MELA-AU 10 75289120 75289120 single base substitution G A downstream_gene_variant MELA-AU 10 75289120 75289120 single base substitution G A intron_variant MELA-AU 10 75289291 75289291 single base substitution G A downstream_gene_variant MELA-AU 10 75289291 75289291 single base substitution G A intron_variant MELA-AU 10 75289291 75289291 single base substitution G A missense_variant T736I 2207C>T MELA-AU 10 75290382 75290382 single base substitution G A intron_variant MELA-AU 10 75290382 75290382 single base substitution G A upstream_gene_variant MELA-AU 10 75290420 75290420 single base substitution G A intron_variant MELA-AU 10 75290420 75290420 single base substitution G A upstream_gene_variant MELA-AU 10 75293757 75293757 single base substitution G A downstream_gene_variant MELA-AU 10 75293757 75293757 single base substitution G A intron_variant MELA-AU 10 75293757 75293757 single base substitution G A upstream_gene_variant MELA-AU 10 75294028 75294028 single base substitution G A downstream_gene_variant MELA-AU 10 75294028 75294028 single base substitution G A intron_variant MELA-AU 10 75294028 75294028 single base substitution G A upstream_gene_variant MELA-AU 10 75294265 75294265 single base substitution G A downstream_gene_variant MELA-AU 10 75294265 75294265 single base substitution G A intron_variant MELA-AU 10 75294265 75294265 single base substitution G A upstream_gene_variant MELA-AU 10 75294806 75294806 single base substitution G A downstream_gene_variant MELA-AU 10 75294806 75294806 single base substitution G A intron_variant MELA-AU 10 75294806 75294806 single base substitution G A upstream_gene_variant MELA-AU 10 75295934 75295934 single base substitution G A downstream_gene_variant MELA-AU 10 75295934 75295934 single base substitution G A intron_variant MELA-AU 10 75295934 75295934 single base substitution G A upstream_gene_variant MELA-AU 10 75296029 75296029 single base substitution G A downstream_gene_variant MELA-AU 10 75296029 75296029 single base substitution G A exon_variant MELA-AU 10 75296029 75296029 single base substitution G A missense_variant S231L 692C>T MELA-AU 10 75296029 75296029 single base substitution G A missense_variant S381L 1142C>T MELA-AU 10 75296029 75296029 single base substitution G A splice_region_variant MELA-AU 10 75296029 75296029 single base substitution G A upstream_gene_variant MELA-AU 10 75296047 75296047 single base substitution C T 5_prime_UTR_variant MELA-AU 10 75296047 75296047 single base substitution C T downstream_gene_variant MELA-AU 10 75296047 75296047 single base substitution C T exon_variant MELA-AU 10 75296047 75296047 single base substitution C T missense_variant C225Y 674G>A MELA-AU 10 75296047 75296047 single base substitution C T missense_variant C375Y 1124G>A MELA-AU 10 75296047 75296047 single base substitution C T upstream_gene_variant MELA-AU 10 75296139 75296139 single base substitution G A 5_prime_UTR_variant MELA-AU 10 75296139 75296139 single base substitution G A downstream_gene_variant MELA-AU 10 75296139 75296139 single base substitution G A exon_variant MELA-AU 10 75296139 75296139 single base substitution G A synonymous_variant P194P 582C>T MELA-AU 10 75296139 75296139 single base substitution G A synonymous_variant P344P 1032C>T MELA-AU 10 75296139 75296139 single base substitution G A upstream_gene_variant MELA-AU 10 75297424 75297424 single base substitution G A downstream_gene_variant MELA-AU 10 75297424 75297424 single base substitution G A intron_variant MELA-AU 10 75297424 75297424 single base substitution G A upstream_gene_variant MELA-AU 10 75297934 75297934 single base substitution A G downstream_gene_variant MELA-AU 10 75297934 75297934 single base substitution A G intron_variant MELA-AU 10 75297934 75297934 single base substitution A G upstream_gene_variant MELA-AU 10 75299833 75299833 single base substitution C T downstream_gene_variant MELA-AU 10 75299833 75299833 single base substitution C T intron_variant MELA-AU 10 75300222 75300222 single base substitution G A downstream_gene_variant MELA-AU 10 75300222 75300222 single base substitution G A intron_variant MELA-AU 10 75300342 75300342 single base substitution G A downstream_gene_variant MELA-AU 10 75300342 75300342 single base substitution G A intron_variant MELA-AU 10 75300558 75300558 single base substitution G A downstream_gene_variant MELA-AU 10 75300558 75300558 single base substitution G A intron_variant MELA-AU 10 75301506 75301506 single base substitution G A downstream_gene_variant MELA-AU 10 75301506 75301506 single base substitution G A exon_variant MELA-AU 10 75301506 75301506 single base substitution G A intron_variant MELA-AU 10 75301506 75301506 single base substitution G A upstream_gene_variant MELA-AU 10 75301521 75301521 single base substitution G A downstream_gene_variant MELA-AU 10 75301521 75301521 single base substitution G A exon_variant MELA-AU 10 75301521 75301521 single base substitution G A intron_variant MELA-AU 10 75301521 75301521 single base substitution G A upstream_gene_variant MELA-AU 10 75302366 75302366 single base substitution G A downstream_gene_variant MELA-AU 10 75302366 75302366 single base substitution G A intron_variant MELA-AU 10 75302366 75302366 single base substitution G A upstream_gene_variant MELA-AU 10 75302576 75302576 single base substitution G A 5_prime_UTR_variant MELA-AU 10 75302576 75302576 single base substitution G A downstream_gene_variant MELA-AU 10 75302576 75302576 single base substitution G A exon_variant MELA-AU 10 75302576 75302576 single base substitution G A intron_variant MELA-AU 10 75302576 75302576 single base substitution G A missense_variant S186F 557C>T MELA-AU 10 75302576 75302576 single base substitution G A upstream_gene_variant MELA-AU 10 75304164 75304164 single base substitution G A intron_variant MELA-AU 10 75304164 75304164 single base substitution G A upstream_gene_variant MELA-AU 10 75305115 75305115 single base substitution G A intron_variant MELA-AU 10 75305115 75305115 single base substitution G A upstream_gene_variant MELA-AU 10 75305605 75305605 single base substitution G A intron_variant MELA-AU 10 75305605 75305605 single base substitution G A upstream_gene_variant MELA-AU 10 75305751 75305751 single base substitution G C intron_variant MELA-AU 10 75305751 75305751 single base substitution G C upstream_gene_variant MELA-AU 10 75305839 75305839 single base substitution A G intron_variant MELA-AU 10 75305839 75305839 single base substitution A G upstream_gene_variant MELA-AU 10 75306391 75306391 single base substitution C T exon_variant MELA-AU 10 75306391 75306391 single base substitution C T intron_variant MELA-AU 10 75306391 75306391 single base substitution C T upstream_gene_variant MELA-AU 10 75306601 75306601 insertion of <=200bp - T intron_variant MELA-AU 10 75306601 75306601 insertion of <=200bp - T upstream_gene_variant MELA-AU 10 75307065 75307065 single base substitution A C intron_variant MELA-AU 10 75307065 75307065 single base substitution A C upstream_gene_variant MELA-AU 10 75307221 75307221 single base substitution C A intron_variant MELA-AU 10 75307221 75307221 single base substitution C A upstream_gene_variant MELA-AU 10 75307278 75307278 single base substitution G A intron_variant MELA-AU 10 75307278 75307278 single base substitution G A upstream_gene_variant MELA-AU 10 75308268 75308268 single base substitution G A intron_variant MELA-AU 10 75308268 75308268 single base substitution G A upstream_gene_variant MELA-AU 10 75308477 75308477 single base substitution G A intron_variant MELA-AU 10 75308477 75308477 single base substitution G A upstream_gene_variant MELA-AU 10 75308509 75308509 single base substitution G A intron_variant MELA-AU 10 75308509 75308509 single base substitution G A upstream_gene_variant MELA-AU 10 75308520 75308520 single base substitution G A intron_variant MELA-AU 10 75308520 75308520 single base substitution G A upstream_gene_variant MELA-AU 10 75309287 75309287 single base substitution G A intron_variant MELA-AU 10 75309287 75309287 single base substitution G A upstream_gene_variant MELA-AU 10 75309785 75309785 single base substitution G A intron_variant MELA-AU 10 75309785 75309785 single base substitution G A upstream_gene_variant MELA-AU 10 75309913 75309913 single base substitution C T intron_variant MELA-AU 10 75309913 75309913 single base substitution C T upstream_gene_variant MELA-AU 10 75309918 75309918 single base substitution A T intron_variant MELA-AU 10 75309918 75309918 single base substitution A T upstream_gene_variant MELA-AU 10 75310102 75310102 single base substitution G A intron_variant MELA-AU 10 75310102 75310102 single base substitution G A upstream_gene_variant MELA-AU 10 75310358 75310358 single base substitution G A intron_variant MELA-AU 10 75310358 75310358 single base substitution G A upstream_gene_variant MELA-AU 10 75310437 75310437 single base substitution G A intron_variant MELA-AU 10 75310437 75310437 single base substitution G A upstream_gene_variant MELA-AU 10 75311868 75311868 single base substitution A T intron_variant MELA-AU 10 75311905 75311905 single base substitution G A intron_variant MELA-AU 10 75312706 75312706 single base substitution G A intron_variant MELA-AU 10 75313168 75313168 single base substitution G A intron_variant MELA-AU 10 75313168 75313168 single base substitution G A upstream_gene_variant MELA-AU 10 75313289 75313289 single base substitution T C intron_variant MELA-AU 10 75313289 75313289 single base substitution T C upstream_gene_variant MELA-AU 10 75313848 75313848 single base substitution G A intron_variant MELA-AU 10 75313848 75313848 single base substitution G A upstream_gene_variant MELA-AU 10 75313932 75313932 single base substitution G A intron_variant MELA-AU 10 75313932 75313932 single base substitution G A upstream_gene_variant MELA-AU 10 75315304 75315304 single base substitution G A intron_variant MELA-AU 10 75315304 75315304 single base substitution G A upstream_gene_variant MELA-AU 10 75318898 75318898 single base substitution A G intron_variant MELA-AU 10 75319849 75319849 single base substitution G A intron_variant MELA-AU 10 75320341 75320341 single base substitution G A intron_variant MELA-AU 10 75320867 75320867 single base substitution A G intron_variant MELA-AU 10 75321694 75321694 single base substitution A C intron_variant MELA-AU 10 75321897 75321897 single base substitution C G intron_variant MELA-AU 10 75322045 75322045 single base substitution G A intron_variant MELA-AU 10 75322598 75322598 single base substitution C T intron_variant MELA-AU 10 75322730 75322730 single base substitution G A intron_variant MELA-AU 10 75323070 75323070 single base substitution A G intron_variant MELA-AU 10 75323094 75323094 single base substitution G A intron_variant MELA-AU 10 75323259 75323259 single base substitution G A intron_variant MELA-AU 10 75323620 75323620 single base substitution C T intron_variant MELA-AU 10 75324594 75324594 single base substitution G A intron_variant MELA-AU 10 75324733 75324733 single base substitution G A intron_variant MELA-AU 10 75325243 75325243 single base substitution C A intron_variant MELA-AU 10 75325326 75325326 single base substitution C T intron_variant MELA-AU 10 75325345 75325345 single base substitution G A intron_variant MELA-AU 10 75325499 75325499 single base substitution A T intron_variant MELA-AU 10 75325712 75325712 single base substitution G A intron_variant MELA-AU 10 75328352 75328352 single base substitution G A downstream_gene_variant MELA-AU 10 75328352 75328352 single base substitution G A intron_variant MELA-AU 10 75329516 75329516 single base substitution A T downstream_gene_variant MELA-AU 10 75329516 75329516 single base substitution A T intron_variant MELA-AU 10 75330171 75330171 single base substitution A C downstream_gene_variant MELA-AU 10 75330171 75330171 single base substitution A C intron_variant MELA-AU 10 75330248 75330248 single base substitution G C downstream_gene_variant MELA-AU 10 75330248 75330248 single base substitution G C intron_variant MELA-AU 10 75330488 75330488 single base substitution G A downstream_gene_variant MELA-AU 10 75330488 75330488 single base substitution G A intron_variant MELA-AU 10 75331728 75331728 single base substitution C T downstream_gene_variant MELA-AU 10 75331728 75331728 single base substitution C T intron_variant MELA-AU 10 75331730 75331730 single base substitution T C downstream_gene_variant MELA-AU 10 75331730 75331730 single base substitution T C intron_variant MELA-AU 10 75331741 75331741 single base substitution G A downstream_gene_variant MELA-AU 10 75331741 75331741 single base substitution G A intron_variant MELA-AU 10 75332118 75332118 single base substitution G A downstream_gene_variant MELA-AU 10 75332118 75332118 single base substitution G A intron_variant MELA-AU 10 75332159 75332159 single base substitution G A downstream_gene_variant MELA-AU 10 75332159 75332159 single base substitution G A intron_variant MELA-AU 10 75332375 75332375 single base substitution G A downstream_gene_variant MELA-AU 10 75332375 75332375 single base substitution G A intron_variant MELA-AU 10 75332730 75332730 single base substitution G A downstream_gene_variant MELA-AU 10 75332730 75332730 single base substitution G A intron_variant MELA-AU 10 75333065 75333065 single base substitution G A downstream_gene_variant MELA-AU 10 75333065 75333065 single base substitution G A intron_variant MELA-AU 10 75334187 75334187 single base substitution G A downstream_gene_variant MELA-AU 10 75334187 75334187 single base substitution G A intron_variant MELA-AU 10 75334249 75334249 single base substitution G A downstream_gene_variant MELA-AU 10 75334249 75334249 single base substitution G A intron_variant MELA-AU 10 75334250 75334250 single base substitution G A downstream_gene_variant MELA-AU 10 75334250 75334250 single base substitution G A intron_variant MELA-AU 10 75335391 75335391 single base substitution G A 5_prime_UTR_variant MELA-AU 10 75335391 75335391 single base substitution G A downstream_gene_variant MELA-AU 10 75335391 75335391 single base substitution G A exon_variant MELA-AU 10 75335391 75335391 single base substitution G A missense_variant S9L 26C>T MELA-AU 10 75335654 75335654 single base substitution A G 5_prime_UTR_variant MELA-AU 10 75335654 75335654 single base substitution A G downstream_gene_variant MELA-AU 10 75335654 75335654 single base substitution A G exon_variant MELA-AU 10 75335654 75335654 single base substitution A G intron_variant MELA-AU 10 75335654 75335654 single base substitution A G upstream_gene_variant MELA-AU 10 75335882 75335882 single base substitution G A 5_prime_UTR_variant MELA-AU 10 75335882 75335882 single base substitution G A downstream_gene_variant MELA-AU 10 75335882 75335882 single base substitution G A exon_variant MELA-AU 10 75335882 75335882 single base substitution G A intron_variant MELA-AU 10 75335882 75335882 single base substitution G A upstream_gene_variant MELA-AU 10 75336276 75336276 single base substitution A T intron_variant MELA-AU 10 75336276 75336276 single base substitution A T upstream_gene_variant MELA-AU 10 75336921 75336921 single base substitution C T intron_variant MELA-AU 10 75336921 75336921 single base substitution C T upstream_gene_variant MELA-AU 10 75337685 75337685 single base substitution G T intron_variant MELA-AU 10 75337685 75337685 single base substitution G T upstream_gene_variant MELA-AU 10 75338094 75338094 single base substitution G A intron_variant MELA-AU 10 75338094 75338094 single base substitution G A upstream_gene_variant MELA-AU 10 75339874 75339874 single base substitution G A intron_variant MELA-AU 10 75339874 75339874 single base substitution G A upstream_gene_variant MELA-AU 10 75340417 75340417 single base substitution G C intron_variant MELA-AU 10 75340417 75340417 single base substitution G C upstream_gene_variant MELA-AU 10 75340975 75340975 single base substitution G A intron_variant MELA-AU 10 75340975 75340975 single base substitution G A upstream_gene_variant MELA-AU 10 75341184 75341184 single base substitution A G intron_variant MELA-AU 10 75342427 75342427 single base substitution G A intron_variant MELA-AU 10 75342688 75342689 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 75342714 75342714 single base substitution G A intron_variant MELA-AU 10 75343871 75343871 single base substitution G T intron_variant MELA-AU 10 75344510 75344510 single base substitution T A intron_variant MELA-AU 10 75344858 75344858 single base substitution G A intron_variant MELA-AU 10 75345324 75345324 single base substitution G A intron_variant MELA-AU 10 75345571 75345571 single base substitution G A intron_variant MELA-AU 10 75346028 75346029 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 75346223 75346223 single base substitution C G intron_variant MELA-AU 10 75347261 75347261 single base substitution G A intron_variant MELA-AU 10 75349020 75349020 single base substitution C T intron_variant MELA-AU 10 75350559 75350560 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 75350694 75350694 single base substitution G A intron_variant MELA-AU 10 75351534 75351534 single base substitution G A intron_variant MELA-AU 10 75351534 75351534 single base substitution G A upstream_gene_variant MELA-AU 10 75352254 75352254 single base substitution A G intron_variant MELA-AU 10 75352254 75352254 single base substitution A G upstream_gene_variant MELA-AU 10 75352675 75352675 single base substitution C T intron_variant MELA-AU 10 75352675 75352675 single base substitution C T upstream_gene_variant MELA-AU 10 75353499 75353499 single base substitution G A intron_variant MELA-AU 10 75353499 75353499 single base substitution G A upstream_gene_variant MELA-AU 10 75353821 75353821 single base substitution G A intron_variant MELA-AU 10 75353821 75353821 single base substitution G A upstream_gene_variant MELA-AU 10 75354395 75354395 single base substitution G A intron_variant MELA-AU 10 75354395 75354395 single base substitution G A upstream_gene_variant MELA-AU 10 75354413 75354414 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 75354413 75354414 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 75354420 75354420 single base substitution G A intron_variant MELA-AU 10 75354420 75354420 single base substitution G A upstream_gene_variant MELA-AU 10 75354597 75354597 single base substitution G A intron_variant MELA-AU 10 75354597 75354597 single base substitution G A upstream_gene_variant MELA-AU 10 75354630 75354630 single base substitution G A intron_variant MELA-AU 10 75354630 75354630 single base substitution G A upstream_gene_variant MELA-AU 10 75354732 75354732 single base substitution G A intron_variant MELA-AU 10 75354732 75354732 single base substitution G A upstream_gene_variant MELA-AU 10 75355823 75355823 single base substitution G A intron_variant MELA-AU 10 75355823 75355823 single base substitution G A upstream_gene_variant MELA-AU 10 75356240 75356240 single base substitution C T intron_variant MELA-AU 10 75356240 75356240 single base substitution C T upstream_gene_variant MELA-AU 10 75356369 75356369 single base substitution C T intron_variant MELA-AU 10 75357199 75357199 single base substitution C T intron_variant MELA-AU 10 75357819 75357819 single base substitution G A intron_variant MELA-AU 10 75358036 75358036 single base substitution C A intron_variant MELA-AU 10 75358301 75358301 single base substitution G A intron_variant MELA-AU 10 75358769 75358769 single base substitution G A intron_variant MELA-AU 10 75358802 75358802 single base substitution A T intron_variant MELA-AU 10 75358923 75358923 single base substitution G A intron_variant MELA-AU 10 75359472 75359472 single base substitution C T intron_variant MELA-AU 10 75359978 75359978 single base substitution C T intron_variant MELA-AU 10 75360297 75360297 single base substitution G A intron_variant MELA-AU 10 75360319 75360319 single base substitution A G intron_variant MELA-AU 10 75360599 75360599 single base substitution G A intron_variant MELA-AU 10 75360651 75360651 single base substitution G A intron_variant MELA-AU 10 75361891 75361891 single base substitution C T intron_variant MELA-AU 10 75362093 75362093 single base substitution G A intron_variant MELA-AU 10 75362435 75362435 single base substitution G A intron_variant MELA-AU 10 75363105 75363105 single base substitution G A intron_variant MELA-AU 10 75363349 75363349 single base substitution C A intron_variant MELA-AU 10 75363591 75363591 single base substitution C T intron_variant MELA-AU 10 75363845 75363845 single base substitution A G intron_variant MELA-AU 10 75364641 75364641 single base substitution C T intron_variant MELA-AU 10 75365566 75365566 single base substitution G A intron_variant MELA-AU 10 75365644 75365644 single base substitution G A intron_variant MELA-AU 10 75366208 75366208 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 10 75366208 75366208 single base substitution G A intron_variant MELA-AU 10 75367710 75367710 single base substitution G A intron_variant MELA-AU 10 75367836 75367836 single base substitution G A intron_variant MELA-AU 10 75368219 75368219 single base substitution G A intron_variant MELA-AU 10 75368802 75368802 single base substitution A G intron_variant MELA-AU 10 75368840 75368840 single base substitution G A intron_variant MELA-AU 10 75368895 75368895 single base substitution G A intron_variant MELA-AU 10 75369277 75369277 single base substitution C T intron_variant MELA-AU 10 75369289 75369289 single base substitution G A intron_variant MELA-AU 10 75369588 75369588 single base substitution G A intron_variant MELA-AU 10 75370200 75370200 single base substitution T C intron_variant MELA-AU 10 75370797 75370797 single base substitution G A intron_variant MELA-AU 10 75373350 75373350 single base substitution G A intron_variant MELA-AU 10 75373556 75373556 single base substitution G A intron_variant MELA-AU 10 75374554 75374554 single base substitution G A intron_variant MELA-AU 10 75374747 75374747 single base substitution C T intron_variant MELA-AU 10 75375757 75375757 single base substitution G A intron_variant MELA-AU 10 75375811 75375811 single base substitution G A intron_variant MELA-AU 10 75376116 75376116 single base substitution A T intron_variant MELA-AU 10 75376394 75376394 single base substitution G A intron_variant MELA-AU 10 75376757 75376757 single base substitution G A intron_variant MELA-AU 10 75377360 75377360 single base substitution G A intron_variant MELA-AU 10 75380054 75380054 single base substitution G A intron_variant MELA-AU 10 75380520 75380520 single base substitution A G intron_variant MELA-AU 10 75380889 75380890 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 75381468 75381468 single base substitution A T intron_variant MELA-AU 10 75381815 75381815 single base substitution G A intron_variant MELA-AU 10 75382066 75382066 single base substitution T C intron_variant MELA-AU 10 75382083 75382083 single base substitution T A intron_variant MELA-AU 10 75382361 75382361 single base substitution C T intron_variant MELA-AU 10 75382859 75382859 single base substitution G A intron_variant MELA-AU 10 75382969 75382969 single base substitution C T intron_variant MELA-AU 10 75383213 75383213 single base substitution G A intron_variant MELA-AU 10 75383464 75383464 single base substitution G A intron_variant MELA-AU 10 75384976 75384976 single base substitution C G intron_variant MELA-AU 10 75385363 75385363 single base substitution C A 5_prime_UTR_variant MELA-AU 10 75385363 75385363 single base substitution C A intron_variant MELA-AU 10 75387850 75387850 single base substitution C T upstream_gene_variant MELA-AU 10 75388019 75388019 single base substitution T C upstream_gene_variant MELA-AU 10 75388618 75388618 single base substitution C G upstream_gene_variant MELA-AU 10 75388723 75388724 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 75388865 75388865 single base substitution C T upstream_gene_variant MELA-AU 10 75388990 75388990 single base substitution C T upstream_gene_variant MELA-AU 10 75389044 75389044 single base substitution G C upstream_gene_variant MELA-AU 10 75389264 75389264 single base substitution C T upstream_gene_variant MELA-AU 10 75389288 75389288 single base substitution T G upstream_gene_variant MELA-AU 10 75389416 75389416 single base substitution C T upstream_gene_variant MELA-AU 10 75389482 75389482 single base substitution G A upstream_gene_variant MELA-AU 10 75389592 75389592 single base substitution C T upstream_gene_variant MELA-AU 10 75389641 75389641 single base substitution G A upstream_gene_variant MELA-AU 10 75389702 75389702 single base substitution G A upstream_gene_variant MELA-AU 10 75389806 75389806 single base substitution C T upstream_gene_variant MELA-AU 10 75390549 75390549 single base substitution G A upstream_gene_variant ORCA-IN 10 75274534 75274534 single base substitution A T downstream_gene_variant ORCA-IN 10 75274534 75274534 single base substitution A T intron_variant ORCA-IN 10 75275559 75275559 deletion of <=200bp G - downstream_gene_variant ORCA-IN 10 75275559 75275559 deletion of <=200bp G - intron_variant ORCA-IN 10 75277062 75277062 single base substitution C G 3_prime_UTR_variant ORCA-IN 10 75277062 75277062 single base substitution C G downstream_gene_variant ORCA-IN 10 75277062 75277062 single base substitution C G exon_variant ORCA-IN 10 75277062 75277062 single base substitution C G missense_variant G1041A 3122G>C ORCA-IN 10 75277062 75277062 single base substitution C G missense_variant G129A 386G>C ORCA-IN 10 75277062 75277062 single base substitution C G missense_variant G223A 668G>C ORCA-IN 10 75277062 75277062 single base substitution C G missense_variant G891A 2672G>C ORCA-IN 10 75302183 75302183 single base substitution C A downstream_gene_variant ORCA-IN 10 75302183 75302183 single base substitution C A intron_variant ORCA-IN 10 75302183 75302183 single base substitution C A upstream_gene_variant ORCA-IN 10 75342723 75342723 single base substitution G C intron_variant ORCA-IN 10 75359495 75359495 single base substitution A T intron_variant ORCA-IN 10 75365149 75365149 single base substitution G C intron_variant ORCA-IN 10 75370774 75370774 single base substitution T C intron_variant ORCA-IN 10 75378872 75378872 single base substitution G A intron_variant ORCA-IN 10 75388021 75388021 single base substitution C T upstream_gene_variant OV-AU 10 75256640 75256640 single base substitution C G downstream_gene_variant OV-AU 10 75261441 75261441 single base substitution G A intron_variant OV-AU 10 75262940 75262940 single base substitution T C intron_variant OV-AU 10 75264497 75264497 single base substitution G A intron_variant OV-AU 10 75265839 75265839 single base substitution T C intron_variant OV-AU 10 75265839 75265839 single base substitution T C upstream_gene_variant OV-AU 10 75276115 75276115 single base substitution C A downstream_gene_variant OV-AU 10 75276115 75276115 single base substitution C A intron_variant OV-AU 10 75285263 75285263 single base substitution T G downstream_gene_variant OV-AU 10 75285263 75285263 single base substitution T G intron_variant OV-AU 10 75285263 75285263 single base substitution T G upstream_gene_variant OV-AU 10 75288583 75288583 single base substitution G A downstream_gene_variant OV-AU 10 75288583 75288583 single base substitution G A intron_variant OV-AU 10 75291394 75291394 single base substitution C G downstream_gene_variant OV-AU 10 75291394 75291394 single base substitution C G intron_variant OV-AU 10 75291394 75291394 single base substitution C G upstream_gene_variant OV-AU 10 75299284 75299284 single base substitution T G 5_prime_UTR_variant OV-AU 10 75299284 75299284 single base substitution T G downstream_gene_variant OV-AU 10 75299284 75299284 single base substitution T G exon_variant OV-AU 10 75299284 75299284 single base substitution T G missense_variant Y148S 443A>C OV-AU 10 75299284 75299284 single base substitution T G missense_variant Y298S 893A>C OV-AU 10 75299284 75299284 single base substitution T G upstream_gene_variant OV-AU 10 75304544 75304544 single base substitution T A intron_variant OV-AU 10 75304544 75304544 single base substitution T A upstream_gene_variant OV-AU 10 75310239 75310239 single base substitution C T intron_variant OV-AU 10 75310239 75310239 single base substitution C T upstream_gene_variant OV-AU 10 75329023 75329023 single base substitution C A downstream_gene_variant OV-AU 10 75329023 75329023 single base substitution C A intron_variant OV-AU 10 75329603 75329603 single base substitution T A downstream_gene_variant OV-AU 10 75329603 75329603 single base substitution T A intron_variant OV-AU 10 75339423 75339423 single base substitution G A intron_variant OV-AU 10 75339423 75339423 single base substitution G A upstream_gene_variant OV-AU 10 75352550 75352550 single base substitution T C intron_variant OV-AU 10 75352550 75352550 single base substitution T C upstream_gene_variant OV-AU 10 75364767 75364767 single base substitution C A intron_variant OV-AU 10 75367086 75367086 single base substitution A G intron_variant OV-AU 10 75367331 75367331 single base substitution G C intron_variant OV-AU 10 75370466 75370466 single base substitution T A intron_variant OV-AU 10 75378193 75378193 single base substitution A T intron_variant OV-AU 10 75380735 75380735 single base substitution G A intron_variant OV-AU 10 75381385 75381385 single base substitution A T intron_variant OV-US 10 75302825 75302825 single base substitution G A 5_prime_UTR_variant OV-US 10 75302825 75302825 single base substitution G A exon_variant OV-US 10 75302825 75302825 single base substitution G A intron_variant OV-US 10 75302825 75302825 single base substitution G A missense_variant A147V 440C>T OV-US 10 75302825 75302825 single base substitution G A upstream_gene_variant PACA-AU 10 75255182 75255182 single base substitution T G downstream_gene_variant PACA-AU 10 75263694 75263694 single base substitution G A intron_variant PACA-AU 10 75266839 75266852 deletion of <=200bp AAATTTTAATGAAA - intron_variant PACA-AU 10 75266839 75266852 deletion of <=200bp AAATTTTAATGAAA - upstream_gene_variant PACA-AU 10 75269922 75269922 single base substitution G A intron_variant PACA-AU 10 75269922 75269922 single base substitution G A upstream_gene_variant PACA-AU 10 75270095 75270098 deletion of <=200bp AAAT - intron_variant PACA-AU 10 75277220 75277220 single base substitution A C 3_prime_UTR_variant PACA-AU 10 75277220 75277220 single base substitution A C downstream_gene_variant PACA-AU 10 75277220 75277220 single base substitution A C exon_variant PACA-AU 10 75277220 75277220 single base substitution A C missense_variant S170R 510T>G PACA-AU 10 75277220 75277220 single base substitution A C missense_variant S76R 228T>G PACA-AU 10 75277220 75277220 single base substitution A C missense_variant S838R 2514T>G PACA-AU 10 75277220 75277220 single base substitution A C missense_variant S988R 2964T>G PACA-AU 10 75280252 75280252 single base substitution G A intron_variant PACA-AU 10 75284551 75284551 single base substitution A C downstream_gene_variant PACA-AU 10 75284551 75284551 single base substitution A C intron_variant PACA-AU 10 75284551 75284551 single base substitution A C upstream_gene_variant PACA-AU 10 75289221 75289228 deletion of <=200bp ACATGATA - 3_prime_UTR_variant PACA-AU 10 75289221 75289228 deletion of <=200bp ACATGATA - downstream_gene_variant PACA-AU 10 75289221 75289228 deletion of <=200bp ACATGATA - intron_variant PACA-AU 10 75293042 75293042 single base substitution C A downstream_gene_variant PACA-AU 10 75293042 75293042 single base substitution C A intron_variant PACA-AU 10 75293042 75293042 single base substitution C A upstream_gene_variant PACA-AU 10 75293043 75293043 single base substitution G A downstream_gene_variant PACA-AU 10 75293043 75293043 single base substitution G A intron_variant PACA-AU 10 75293043 75293043 single base substitution G A upstream_gene_variant PACA-AU 10 75298653 75298653 single base substitution G T downstream_gene_variant PACA-AU 10 75298653 75298653 single base substitution G T intron_variant PACA-AU 10 75298653 75298653 single base substitution G T upstream_gene_variant PACA-AU 10 75316000 75316000 single base substitution G C intron_variant PACA-AU 10 75316000 75316000 single base substitution G C upstream_gene_variant PACA-AU 10 75323752 75323752 single base substitution C T intron_variant PACA-AU 10 75323767 75323767 single base substitution A G intron_variant PACA-AU 10 75330850 75330850 single base substitution C T downstream_gene_variant PACA-AU 10 75330850 75330850 single base substitution C T intron_variant PACA-AU 10 75332133 75332133 single base substitution T C downstream_gene_variant PACA-AU 10 75332133 75332133 single base substitution T C intron_variant PACA-AU 10 75343039 75343039 single base substitution A G intron_variant PACA-AU 10 75355168 75355168 single base substitution G T intron_variant PACA-AU 10 75355168 75355168 single base substitution G T upstream_gene_variant PACA-AU 10 75356701 75356701 single base substitution A G intron_variant PACA-AU 10 75358185 75358185 single base substitution C T intron_variant PACA-AU 10 75361299 75361299 single base substitution G C intron_variant PACA-AU 10 75364353 75364353 single base substitution T A intron_variant PACA-AU 10 75367710 75367710 single base substitution G A intron_variant PACA-AU 10 75381451 75381451 single base substitution A G intron_variant PACA-AU 10 75382059 75382059 insertion of <=200bp - TATT intron_variant PACA-AU 10 75383002 75383002 single base substitution C T intron_variant PACA-AU 10 75388205 75388205 single base substitution C A upstream_gene_variant PACA-AU 10 75388985 75388985 single base substitution G T upstream_gene_variant PACA-CA 10 75252497 75252497 insertion of <=200bp - A downstream_gene_variant PACA-CA 10 75265552 75265552 single base substitution C T intron_variant PACA-CA 10 75265552 75265552 single base substitution C T upstream_gene_variant PACA-CA 10 75271395 75271395 single base substitution G C intron_variant PACA-CA 10 75278334 75278334 single base substitution T C downstream_gene_variant PACA-CA 10 75278334 75278334 single base substitution T C intron_variant PACA-CA 10 75292107 75292107 deletion of <=200bp T - downstream_gene_variant PACA-CA 10 75292107 75292107 deletion of <=200bp T - intron_variant PACA-CA 10 75292107 75292107 deletion of <=200bp T - upstream_gene_variant PACA-CA 10 75292925 75292925 single base substitution G A downstream_gene_variant PACA-CA 10 75292925 75292925 single base substitution G A intron_variant PACA-CA 10 75292925 75292925 single base substitution G A upstream_gene_variant PACA-CA 10 75299538 75299539 deletion of <=200bp AG - downstream_gene_variant PACA-CA 10 75299538 75299539 deletion of <=200bp AG - intron_variant PACA-CA 10 75303652 75303652 single base substitution C T intron_variant PACA-CA 10 75303652 75303652 single base substitution C T upstream_gene_variant PACA-CA 10 75314888 75314888 single base substitution C A intron_variant PACA-CA 10 75314888 75314888 single base substitution C A upstream_gene_variant PACA-CA 10 75315483 75315483 single base substitution T C intron_variant PACA-CA 10 75315483 75315483 single base substitution T C upstream_gene_variant PACA-CA 10 75315627 75315627 single base substitution G A intron_variant PACA-CA 10 75315627 75315627 single base substitution G A upstream_gene_variant PACA-CA 10 75321882 75321882 single base substitution G A intron_variant PACA-CA 10 75322119 75322119 single base substitution C A intron_variant PACA-CA 10 75323860 75323860 single base substitution A G intron_variant PACA-CA 10 75327323 75327323 single base substitution G A downstream_gene_variant PACA-CA 10 75327323 75327323 single base substitution G A intron_variant PACA-CA 10 75333389 75333389 single base substitution G C downstream_gene_variant PACA-CA 10 75333389 75333389 single base substitution G C intron_variant PACA-CA 10 75333502 75333502 single base substitution G A downstream_gene_variant PACA-CA 10 75333502 75333502 single base substitution G A intron_variant PACA-CA 10 75338255 75338255 single base substitution C T intron_variant PACA-CA 10 75338255 75338255 single base substitution C T upstream_gene_variant PACA-CA 10 75339942 75339942 single base substitution G A intron_variant PACA-CA 10 75339942 75339942 single base substitution G A upstream_gene_variant PACA-CA 10 75340091 75340091 single base substitution A G intron_variant PACA-CA 10 75340091 75340091 single base substitution A G upstream_gene_variant PACA-CA 10 75340300 75340300 single base substitution A G intron_variant PACA-CA 10 75340300 75340300 single base substitution A G upstream_gene_variant PACA-CA 10 75343537 75343537 single base substitution A T intron_variant PACA-CA 10 75346534 75346534 single base substitution G T intron_variant PACA-CA 10 75350257 75350257 single base substitution A T intron_variant PACA-CA 10 75357843 75357843 deletion of <=200bp A - intron_variant PACA-CA 10 75360228 75360228 single base substitution G T intron_variant PACA-CA 10 75360855 75360855 single base substitution A G intron_variant PACA-CA 10 75364036 75364036 deletion of <=200bp A - intron_variant PACA-CA 10 75369232 75369232 single base substitution G A intron_variant PACA-CA 10 75371703 75371703 single base substitution C T intron_variant PACA-CA 10 75371704 75371704 single base substitution G A intron_variant PACA-CA 10 75374819 75374819 single base substitution G A intron_variant PACA-CA 10 75375903 75375903 single base substitution C T intron_variant PACA-CA 10 75378995 75378995 insertion of <=200bp - T intron_variant PACA-CA 10 75381773 75381773 single base substitution A G intron_variant PACA-CA 10 75381924 75381924 single base substitution G C intron_variant PACA-CA 10 75384309 75384309 single base substitution A T intron_variant PACA-CA 10 75385420 75385420 insertion of <=200bp - AC intron_variant PACA-CA 10 75385420 75385420 insertion of <=200bp - AC upstream_gene_variant PACA-CA 10 75388019 75388019 single base substitution T C upstream_gene_variant PACA-CA 10 75388021 75388021 single base substitution C T upstream_gene_variant PACA-CA 10 75388035 75388035 single base substitution C T upstream_gene_variant PACA-CA 10 75388538 75388538 single base substitution T C upstream_gene_variant PACA-CA 10 75389018 75389018 insertion of <=200bp - T upstream_gene_variant PAEN-AU 10 75272127 75272127 single base substitution G C intron_variant PAEN-AU 10 75277050 75277050 single base substitution G C 3_prime_UTR_variant PAEN-AU 10 75277050 75277050 single base substitution G C downstream_gene_variant PAEN-AU 10 75277050 75277050 single base substitution G C exon_variant PAEN-AU 10 75277050 75277050 single base substitution G C missense_variant S1045C 3134C>G PAEN-AU 10 75277050 75277050 single base substitution G C missense_variant S133C 398C>G PAEN-AU 10 75277050 75277050 single base substitution G C missense_variant S227C 680C>G PAEN-AU 10 75277050 75277050 single base substitution G C missense_variant S895C 2684C>G PAEN-AU 10 75388037 75388037 single base substitution T C upstream_gene_variant PAEN-IT 10 75319790 75319790 single base substitution G A intron_variant PAEN-IT 10 75368032 75368032 single base substitution C A intron_variant PBCA-DE 10 75254681 75254681 insertion of <=200bp - CT downstream_gene_variant PBCA-DE 10 75266292 75266292 insertion of <=200bp - AT intron_variant PBCA-DE 10 75266292 75266292 insertion of <=200bp - AT upstream_gene_variant PBCA-DE 10 75266292 75266293 deletion of <=200bp AT - intron_variant PBCA-DE 10 75266292 75266293 deletion of <=200bp AT - upstream_gene_variant PBCA-DE 10 75267790 75267790 single base substitution G T intron_variant PBCA-DE 10 75267790 75267790 single base substitution G T upstream_gene_variant PBCA-DE 10 75269356 75269356 single base substitution G A intron_variant PBCA-DE 10 75269356 75269356 single base substitution G A upstream_gene_variant PBCA-DE 10 75270050 75270050 deletion of <=200bp A - intron_variant PBCA-DE 10 75275042 75275042 single base substitution A T downstream_gene_variant PBCA-DE 10 75275042 75275042 single base substitution A T intron_variant PBCA-DE 10 75284212 75284212 single base substitution C G downstream_gene_variant PBCA-DE 10 75284212 75284212 single base substitution C G intron_variant PBCA-DE 10 75284212 75284212 single base substitution C G upstream_gene_variant PBCA-DE 10 75286387 75286387 single base substitution C T downstream_gene_variant PBCA-DE 10 75286387 75286387 single base substitution C T intron_variant PBCA-DE 10 75286387 75286387 single base substitution C T upstream_gene_variant PBCA-DE 10 75286809 75286809 insertion of <=200bp - TTTCCTTC downstream_gene_variant PBCA-DE 10 75286809 75286809 insertion of <=200bp - TTTCCTTC intron_variant PBCA-DE 10 75286809 75286809 insertion of <=200bp - TTTCCTTC upstream_gene_variant PBCA-DE 10 75286820 75286820 insertion of <=200bp - C downstream_gene_variant PBCA-DE 10 75286820 75286820 insertion of <=200bp - C intron_variant PBCA-DE 10 75286820 75286820 insertion of <=200bp - C upstream_gene_variant PBCA-DE 10 75286823 75286823 insertion of <=200bp - CTTTCTG downstream_gene_variant PBCA-DE 10 75286823 75286823 insertion of <=200bp - CTTTCTG intron_variant PBCA-DE 10 75286823 75286823 insertion of <=200bp - CTTTCTG upstream_gene_variant PBCA-DE 10 75303080 75303080 single base substitution C T intron_variant PBCA-DE 10 75303080 75303080 single base substitution C T upstream_gene_variant PBCA-DE 10 75311768 75311768 deletion of <=200bp T - intron_variant PBCA-DE 10 75312225 75312226 deletion of <=200bp AC - intron_variant PBCA-DE 10 75315079 75315079 single base substitution T A intron_variant PBCA-DE 10 75315079 75315079 single base substitution T A upstream_gene_variant PBCA-DE 10 75321696 75321696 single base substitution G T intron_variant PBCA-DE 10 75322634 75322634 deletion of <=200bp C - intron_variant PBCA-DE 10 75327584 75327584 single base substitution C A downstream_gene_variant PBCA-DE 10 75327584 75327584 single base substitution C A intron_variant PBCA-DE 10 75330066 75330066 deletion of <=200bp A - downstream_gene_variant PBCA-DE 10 75330066 75330066 deletion of <=200bp A - intron_variant PBCA-DE 10 75336019 75336019 single base substitution G T 5_prime_UTR_variant PBCA-DE 10 75336019 75336019 single base substitution G T exon_variant PBCA-DE 10 75336019 75336019 single base substitution G T intron_variant PBCA-DE 10 75336019 75336019 single base substitution G T upstream_gene_variant PBCA-DE 10 75345685 75345685 insertion of <=200bp - CA intron_variant PBCA-DE 10 75347587 75347587 single base substitution G T intron_variant PBCA-DE 10 75352954 75352954 insertion of <=200bp - A intron_variant PBCA-DE 10 75352954 75352954 insertion of <=200bp - A upstream_gene_variant PBCA-DE 10 75354930 75354930 single base substitution C G intron_variant PBCA-DE 10 75354930 75354930 single base substitution C G upstream_gene_variant PBCA-DE 10 75362311 75362311 insertion of <=200bp - A intron_variant PBCA-DE 10 75368024 75368024 insertion of <=200bp - A intron_variant PBCA-DE 10 75374690 75374690 insertion of <=200bp - ATTCC intron_variant PBCA-DE 10 75386688 75386688 single base substitution C T upstream_gene_variant PRAD-CA 10 75291992 75291992 single base substitution G A downstream_gene_variant PRAD-CA 10 75291992 75291992 single base substitution G A intron_variant PRAD-CA 10 75291992 75291992 single base substitution G A upstream_gene_variant PRAD-CA 10 75299065 75299065 single base substitution A T downstream_gene_variant PRAD-CA 10 75299065 75299065 single base substitution A T intron_variant PRAD-CA 10 75299065 75299065 single base substitution A T upstream_gene_variant PRAD-CA 10 75336264 75336264 single base substitution G A intron_variant PRAD-CA 10 75336264 75336264 single base substitution G A upstream_gene_variant PRAD-CA 10 75344692 75344692 single base substitution C A intron_variant PRAD-CA 10 75353211 75353211 single base substitution G A intron_variant PRAD-CA 10 75353211 75353211 single base substitution G A upstream_gene_variant PRAD-CA 10 75356177 75356177 single base substitution C T intron_variant PRAD-CA 10 75356177 75356177 single base substitution C T upstream_gene_variant PRAD-CA 10 75364816 75364816 single base substitution C A intron_variant PRAD-CA 10 75367095 75367095 single base substitution G A intron_variant PRAD-CA 10 75388021 75388021 single base substitution C T upstream_gene_variant PRAD-UK 10 75262680 75262680 insertion of <=200bp - AA intron_variant PRAD-UK 10 75266808 75266808 single base substitution A C intron_variant PRAD-UK 10 75266808 75266808 single base substitution A C upstream_gene_variant PRAD-UK 10 75290820 75290820 single base substitution C A intron_variant PRAD-UK 10 75290820 75290820 single base substitution C A upstream_gene_variant PRAD-UK 10 75318008 75318008 single base substitution A G intron_variant PRAD-UK 10 75318008 75318008 single base substitution A G upstream_gene_variant PRAD-UK 10 75346867 75346867 single base substitution C G intron_variant PRAD-UK 10 75350714 75350714 single base substitution C A intron_variant PRAD-UK 10 75384813 75384813 single base substitution G C intron_variant PRAD-US 10 75258743 75258743 single base substitution T C 3_prime_UTR_variant PRAD-US 10 75258743 75258743 single base substitution T C downstream_gene_variant PRAD-US 10 75258743 75258743 single base substitution T C exon_variant PRAD-US 10 75258743 75258743 single base substitution T C missense_variant T1417A 4249A>G PRAD-US 10 75258743 75258743 single base substitution T C missense_variant T1567A 4699A>G PRAD-US 10 75258743 75258743 single base substitution T C missense_variant T608A 1822A>G PRAD-US 10 75258743 75258743 single base substitution T C missense_variant T702A 2104A>G READ-US 10 75289528 75289528 single base substitution C T 5_prime_UTR_variant READ-US 10 75289528 75289528 single base substitution C T exon_variant READ-US 10 75289528 75289528 single base substitution C T missense_variant R507Q 1520G>A READ-US 10 75289528 75289528 single base substitution C T missense_variant R657Q 1970G>A READ-US 10 75301468 75301468 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant READ-US 10 75301468 75301468 single base substitution G A downstream_gene_variant READ-US 10 75301468 75301468 single base substitution G A exon_variant READ-US 10 75301468 75301468 single base substitution G A intron_variant READ-US 10 75301468 75301468 single base substitution G A stop_gained R201* 601C>T READ-US 10 75301468 75301468 single base substitution G A upstream_gene_variant READ-US 10 75302791 75302791 single base substitution C A 5_prime_UTR_variant READ-US 10 75302791 75302791 single base substitution C A downstream_gene_variant READ-US 10 75302791 75302791 single base substitution C A exon_variant READ-US 10 75302791 75302791 single base substitution C A intron_variant READ-US 10 75302791 75302791 single base substitution C A missense_variant M158I 474G>T READ-US 10 75302791 75302791 single base substitution C A upstream_gene_variant RECA-EU 10 75253088 75253088 single base substitution A T downstream_gene_variant RECA-EU 10 75258031 75258031 single base substitution T G 3_prime_UTR_variant RECA-EU 10 75258031 75258031 single base substitution T G downstream_gene_variant RECA-EU 10 75260371 75260371 single base substitution G A downstream_gene_variant RECA-EU 10 75260371 75260371 single base substitution G A intron_variant RECA-EU 10 75263998 75263998 single base substitution T A intron_variant RECA-EU 10 75266894 75266894 single base substitution C G intron_variant RECA-EU 10 75266894 75266894 single base substitution C G upstream_gene_variant RECA-EU 10 75268521 75268521 single base substitution G A intron_variant RECA-EU 10 75268521 75268521 single base substitution G A upstream_gene_variant RECA-EU 10 75282886 75282886 single base substitution T C intron_variant RECA-EU 10 75286586 75286586 single base substitution A G downstream_gene_variant RECA-EU 10 75286586 75286586 single base substitution A G intron_variant RECA-EU 10 75286586 75286586 single base substitution A G upstream_gene_variant RECA-EU 10 75289282 75289282 single base substitution C T downstream_gene_variant RECA-EU 10 75289282 75289282 single base substitution C T intron_variant RECA-EU 10 75289282 75289282 single base substitution C T stop_gained W739* 2216G>A RECA-EU 10 75298174 75298174 single base substitution C T downstream_gene_variant RECA-EU 10 75298174 75298174 single base substitution C T intron_variant RECA-EU 10 75298174 75298174 single base substitution C T upstream_gene_variant RECA-EU 10 75298868 75298868 single base substitution C A downstream_gene_variant RECA-EU 10 75298868 75298868 single base substitution C A intron_variant RECA-EU 10 75298868 75298868 single base substitution C A upstream_gene_variant RECA-EU 10 75299738 75299738 single base substitution G T downstream_gene_variant RECA-EU 10 75299738 75299738 single base substitution G T intron_variant RECA-EU 10 75315610 75315610 single base substitution C T intron_variant RECA-EU 10 75315610 75315610 single base substitution C T upstream_gene_variant RECA-EU 10 75317695 75317695 single base substitution C T intron_variant RECA-EU 10 75317695 75317695 single base substitution C T upstream_gene_variant RECA-EU 10 75337659 75337659 single base substitution C A intron_variant RECA-EU 10 75337659 75337659 single base substitution C A upstream_gene_variant RECA-EU 10 75337734 75337734 single base substitution C A intron_variant RECA-EU 10 75337734 75337734 single base substitution C A upstream_gene_variant RECA-EU 10 75354963 75354963 single base substitution C A intron_variant RECA-EU 10 75354963 75354963 single base substitution C A upstream_gene_variant RECA-EU 10 75356329 75356329 single base substitution A T intron_variant RECA-EU 10 75366286 75366286 single base substitution T A intron_variant RECA-EU 10 75374726 75374726 single base substitution A T intron_variant RECA-EU 10 75382460 75382460 single base substitution C A intron_variant RECA-EU 10 75387224 75387224 single base substitution G A upstream_gene_variant SKCA-BR 10 75252959 75252959 single base substitution A G downstream_gene_variant SKCA-BR 10 75255801 75255801 single base substitution T G downstream_gene_variant SKCA-BR 10 75258736 75258736 single base substitution G A 3_prime_UTR_variant SKCA-BR 10 75258736 75258736 single base substitution G A downstream_gene_variant SKCA-BR 10 75258736 75258736 single base substitution G A exon_variant SKCA-BR 10 75258736 75258736 single base substitution G A missense_variant T1419I 4256C>T SKCA-BR 10 75258736 75258736 single base substitution G A missense_variant T1569I 4706C>T SKCA-BR 10 75258736 75258736 single base substitution G A missense_variant T610I 1829C>T SKCA-BR 10 75258736 75258736 single base substitution G A missense_variant T704I 2111C>T SKCA-BR 10 75258843 75258843 single base substitution G A 3_prime_UTR_variant SKCA-BR 10 75258843 75258843 single base substitution G A downstream_gene_variant SKCA-BR 10 75258843 75258843 single base substitution G A exon_variant SKCA-BR 10 75258843 75258843 single base substitution G A synonymous_variant P1383P 4149C>T SKCA-BR 10 75258843 75258843 single base substitution G A synonymous_variant P1533P 4599C>T SKCA-BR 10 75258843 75258843 single base substitution G A synonymous_variant P574P 1722C>T SKCA-BR 10 75258843 75258843 single base substitution G A synonymous_variant P668P 2004C>T SKCA-BR 10 75269198 75269198 single base substitution A T intron_variant SKCA-BR 10 75269198 75269198 single base substitution A T upstream_gene_variant SKCA-BR 10 75274799 75274799 insertion of <=200bp - GA downstream_gene_variant SKCA-BR 10 75274799 75274799 insertion of <=200bp - GA intron_variant SKCA-BR 10 75283631 75283631 insertion of <=200bp - TTTA intron_variant SKCA-BR 10 75283631 75283631 insertion of <=200bp - TTTA upstream_gene_variant SKCA-BR 10 75283651 75283653 deletion of <=200bp TTA - intron_variant SKCA-BR 10 75283651 75283653 deletion of <=200bp TTA - upstream_gene_variant SKCA-BR 10 75289131 75289131 single base substitution T A 3_prime_UTR_variant SKCA-BR 10 75289131 75289131 single base substitution T A downstream_gene_variant SKCA-BR 10 75289131 75289131 single base substitution T A intron_variant SKCA-BR 10 75290920 75290920 single base substitution G A intron_variant SKCA-BR 10 75290920 75290920 single base substitution G A upstream_gene_variant SKCA-BR 10 75292590 75292590 single base substitution G A downstream_gene_variant SKCA-BR 10 75292590 75292590 single base substitution G A intron_variant SKCA-BR 10 75292590 75292590 single base substitution G A upstream_gene_variant SKCA-BR 10 75293546 75293546 single base substitution G A downstream_gene_variant SKCA-BR 10 75293546 75293546 single base substitution G A intron_variant SKCA-BR 10 75293546 75293546 single base substitution G A upstream_gene_variant SKCA-BR 10 75294740 75294740 single base substitution A C downstream_gene_variant SKCA-BR 10 75294740 75294740 single base substitution A C intron_variant SKCA-BR 10 75294740 75294740 single base substitution A C upstream_gene_variant SKCA-BR 10 75296335 75296335 single base substitution C A downstream_gene_variant SKCA-BR 10 75296335 75296335 single base substitution C A intron_variant SKCA-BR 10 75296335 75296335 single base substitution C A upstream_gene_variant SKCA-BR 10 75299065 75299065 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 10 75299065 75299065 insertion of <=200bp - AT intron_variant SKCA-BR 10 75299065 75299065 insertion of <=200bp - AT upstream_gene_variant SKCA-BR 10 75309792 75309792 single base substitution C T intron_variant SKCA-BR 10 75309792 75309792 single base substitution C T upstream_gene_variant SKCA-BR 10 75317704 75317704 single base substitution G A intron_variant SKCA-BR 10 75317704 75317704 single base substitution G A upstream_gene_variant SKCA-BR 10 75329524 75329524 insertion of <=200bp - AG downstream_gene_variant SKCA-BR 10 75329524 75329524 insertion of <=200bp - AG intron_variant SKCA-BR 10 75332119 75332119 single base substitution G A downstream_gene_variant SKCA-BR 10 75332119 75332119 single base substitution G A intron_variant SKCA-BR 10 75333213 75333213 single base substitution G A downstream_gene_variant SKCA-BR 10 75333213 75333213 single base substitution G A intron_variant SKCA-BR 10 75334571 75334571 single base substitution G T downstream_gene_variant SKCA-BR 10 75334571 75334571 single base substitution G T intron_variant SKCA-BR 10 75338406 75338406 single base substitution A C intron_variant SKCA-BR 10 75338406 75338406 single base substitution A C upstream_gene_variant SKCA-BR 10 75340348 75340348 single base substitution G A intron_variant SKCA-BR 10 75340348 75340348 single base substitution G A upstream_gene_variant SKCA-BR 10 75340379 75340379 single base substitution G A intron_variant SKCA-BR 10 75340379 75340379 single base substitution G A upstream_gene_variant SKCA-BR 10 75342019 75342019 single base substitution G A intron_variant SKCA-BR 10 75344287 75344287 single base substitution G A intron_variant SKCA-BR 10 75347048 75347048 single base substitution G A intron_variant SKCA-BR 10 75348365 75348365 single base substitution C T intron_variant SKCA-BR 10 75349068 75349068 single base substitution G A intron_variant SKCA-BR 10 75353318 75353318 single base substitution A G intron_variant SKCA-BR 10 75353318 75353318 single base substitution A G upstream_gene_variant SKCA-BR 10 75359321 75359321 single base substitution G A intron_variant SKCA-BR 10 75363523 75363523 single base substitution A C intron_variant SKCA-BR 10 75365999 75365999 single base substitution G A intron_variant SKCA-BR 10 75367133 75367133 single base substitution G A intron_variant SKCA-BR 10 75367588 75367588 insertion of <=200bp - CAA intron_variant SKCA-BR 10 75377284 75377284 single base substitution G A intron_variant SKCA-BR 10 75378488 75378499 deletion of <=200bp AGACTCCATCTC - intron_variant SKCA-BR 10 75378499 75378501 deletion of <=200bp CAA - intron_variant SKCA-BR 10 75379209 75379209 single base substitution G A intron_variant SKCA-BR 10 75380722 75380722 single base substitution T C intron_variant SKCA-BR 10 75382058 75382066 deletion of <=200bp ATATTTATT - intron_variant SKCA-BR 10 75383917 75383917 insertion of <=200bp - CATATATAT intron_variant SKCA-BR 10 75384257 75384257 single base substitution C T exon_variant SKCA-BR 10 75384257 75384257 single base substitution C T intron_variant SKCA-BR 10 75384975 75384975 single base substitution G C intron_variant SKCA-BR 10 75389280 75389280 insertion of <=200bp - GTT upstream_gene_variant SKCM-US 10 75258467 75258467 single base substitution C T 3_prime_UTR_variant SKCM-US 10 75258467 75258467 single base substitution C T downstream_gene_variant SKCM-US 10 75258467 75258467 single base substitution C T exon_variant SKCM-US 10 75258467 75258467 single base substitution C T missense_variant E1509K 4525G>A SKCM-US 10 75258467 75258467 single base substitution C T missense_variant E1659K 4975G>A SKCM-US 10 75258467 75258467 single base substitution C T missense_variant E700K 2098G>A SKCM-US 10 75258467 75258467 single base substitution C T missense_variant E794K 2380G>A SKCM-US 10 75258871 75258871 single base substitution C T 3_prime_UTR_variant SKCM-US 10 75258871 75258871 single base substitution C T downstream_gene_variant SKCM-US 10 75258871 75258871 single base substitution C T exon_variant SKCM-US 10 75258871 75258871 single base substitution C T missense_variant G1374E 4121G>A SKCM-US 10 75258871 75258871 single base substitution C T missense_variant G1524E 4571G>A SKCM-US 10 75258871 75258871 single base substitution C T missense_variant G565E 1694G>A SKCM-US 10 75258871 75258871 single base substitution C T missense_variant G659E 1976G>A SKCM-US 10 75276256 75276256 single base substitution G A 3_prime_UTR_variant SKCM-US 10 75276256 75276256 single base substitution G A downstream_gene_variant SKCM-US 10 75276256 75276256 single base substitution G A exon_variant SKCM-US 10 75276256 75276256 single base substitution G A stop_gained Q1160* 3478C>T SKCM-US 10 75276256 75276256 single base substitution G A stop_gained Q1310* 3928C>T SKCM-US 10 75276256 75276256 single base substitution G A stop_gained Q398* 1192C>T SKCM-US 10 75276256 75276256 single base substitution G A stop_gained Q492* 1474C>T SKCM-US 10 75276290 75276290 single base substitution C T 3_prime_UTR_variant SKCM-US 10 75276290 75276290 single base substitution C T downstream_gene_variant SKCM-US 10 75276290 75276290 single base substitution C T exon_variant SKCM-US 10 75276290 75276290 single base substitution C T synonymous_variant E1148E 3444G>A SKCM-US 10 75276290 75276290 single base substitution C T synonymous_variant E1298E 3894G>A SKCM-US 10 75276290 75276290 single base substitution C T synonymous_variant E386E 1158G>A SKCM-US 10 75276290 75276290 single base substitution C T synonymous_variant E480E 1440G>A SKCM-US 10 75276590 75276590 single base substitution G A 3_prime_UTR_variant SKCM-US 10 75276590 75276590 single base substitution G A downstream_gene_variant SKCM-US 10 75276590 75276590 single base substitution G A exon_variant SKCM-US 10 75276590 75276590 single base substitution G A synonymous_variant S1048S 3144C>T SKCM-US 10 75276590 75276590 single base substitution G A synonymous_variant S1198S 3594C>T SKCM-US 10 75276590 75276590 single base substitution G A synonymous_variant S286S 858C>T SKCM-US 10 75276590 75276590 single base substitution G A synonymous_variant S380S 1140C>T SKCM-US 10 75277230 75277230 single base substitution G A 3_prime_UTR_variant SKCM-US 10 75277230 75277230 single base substitution G A downstream_gene_variant SKCM-US 10 75277230 75277230 single base substitution G A exon_variant SKCM-US 10 75277230 75277230 single base substitution G A missense_variant S167F 500C>T SKCM-US 10 75277230 75277230 single base substitution G A missense_variant S73F 218C>T SKCM-US 10 75277230 75277230 single base substitution G A missense_variant S835F 2504C>T SKCM-US 10 75277230 75277230 single base substitution G A missense_variant S985F 2954C>T SKCM-US 10 75277247 75277247 single base substitution C A 3_prime_UTR_variant SKCM-US 10 75277247 75277247 single base substitution C A downstream_gene_variant SKCM-US 10 75277247 75277247 single base substitution C A exon_variant SKCM-US 10 75277247 75277247 single base substitution C A synonymous_variant G161G 483G>T SKCM-US 10 75277247 75277247 single base substitution C A synonymous_variant G67G 201G>T SKCM-US 10 75277247 75277247 single base substitution C A synonymous_variant G829G 2487G>T SKCM-US 10 75277247 75277247 single base substitution C A synonymous_variant G979G 2937G>T SKCM-US 10 75283383 75283383 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75283383 75283383 single base substitution G A exon_variant SKCM-US 10 75283383 75283383 single base substitution G A missense_variant H624Y 1870C>T SKCM-US 10 75283383 75283383 single base substitution G A missense_variant H774Y 2320C>T SKCM-US 10 75286499 75286499 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 75286499 75286499 single base substitution G A downstream_gene_variant SKCM-US 10 75286499 75286499 single base substitution G A exon_variant SKCM-US 10 75286499 75286499 single base substitution G A synonymous_variant S550S 1650C>T SKCM-US 10 75286499 75286499 single base substitution G A synonymous_variant S700S 2100C>T SKCM-US 10 75286499 75286499 single base substitution G A upstream_gene_variant SKCM-US 10 75286500 75286500 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75286500 75286500 single base substitution G A downstream_gene_variant SKCM-US 10 75286500 75286500 single base substitution G A exon_variant SKCM-US 10 75286500 75286500 single base substitution G A missense_variant S550F 1649C>T SKCM-US 10 75286500 75286500 single base substitution G A missense_variant S700F 2099C>T SKCM-US 10 75286500 75286500 single base substitution G A upstream_gene_variant SKCM-US 10 75289450 75289450 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75289450 75289450 single base substitution G A exon_variant SKCM-US 10 75289450 75289450 single base substitution G A missense_variant S533L 1598C>T SKCM-US 10 75289450 75289450 single base substitution G A missense_variant S683L 2048C>T SKCM-US 10 75289504 75289504 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 75289504 75289504 single base substitution C A exon_variant SKCM-US 10 75289504 75289504 single base substitution C A missense_variant S515I 1544G>T SKCM-US 10 75289504 75289504 single base substitution C A missense_variant S665I 1994G>T SKCM-US 10 75289544 75289544 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75289544 75289544 single base substitution G A exon_variant SKCM-US 10 75289544 75289544 single base substitution G A missense_variant P502S 1504C>T SKCM-US 10 75289544 75289544 single base substitution G A missense_variant P652S 1954C>T SKCM-US 10 75289602 75289602 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75289602 75289602 single base substitution G A exon_variant SKCM-US 10 75289602 75289602 single base substitution G A synonymous_variant S482S 1446C>T SKCM-US 10 75289602 75289602 single base substitution G A synonymous_variant S632S 1896C>T SKCM-US 10 75289647 75289647 single base substitution T C 5_prime_UTR_variant SKCM-US 10 75289647 75289647 single base substitution T C exon_variant SKCM-US 10 75289647 75289647 single base substitution T C synonymous_variant E467E 1401A>G SKCM-US 10 75289647 75289647 single base substitution T C synonymous_variant E617E 1851A>G SKCM-US 10 75290181 75290181 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75290181 75290181 single base substitution G A exon_variant SKCM-US 10 75290181 75290181 single base substitution G A synonymous_variant I366I 1098C>T SKCM-US 10 75290181 75290181 single base substitution G A synonymous_variant I516I 1548C>T SKCM-US 10 75290181 75290181 single base substitution G A upstream_gene_variant SKCM-US 10 75290531 75290531 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75290531 75290531 single base substitution G A exon_variant SKCM-US 10 75290531 75290531 single base substitution G A intron_variant SKCM-US 10 75290531 75290531 single base substitution G A missense_variant R310C 928C>T SKCM-US 10 75290531 75290531 single base substitution G A missense_variant R460C 1378C>T SKCM-US 10 75290531 75290531 single base substitution G A upstream_gene_variant SKCM-US 10 75301396 75301396 single base substitution A G 5_prime_UTR_variant SKCM-US 10 75301396 75301396 single base substitution A G downstream_gene_variant SKCM-US 10 75301396 75301396 single base substitution A G exon_variant SKCM-US 10 75301396 75301396 single base substitution A G intron_variant SKCM-US 10 75301396 75301396 single base substitution A G missense_variant C225R 673T>C SKCM-US 10 75302567 75302567 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75302567 75302567 single base substitution G A downstream_gene_variant SKCM-US 10 75302567 75302567 single base substitution G A exon_variant SKCM-US 10 75302567 75302567 single base substitution G A intron_variant SKCM-US 10 75302567 75302567 single base substitution G A missense_variant S189F 566C>T SKCM-US 10 75302567 75302567 single base substitution G A upstream_gene_variant SKCM-US 10 75302825 75302825 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75302825 75302825 single base substitution G A exon_variant SKCM-US 10 75302825 75302825 single base substitution G A intron_variant SKCM-US 10 75302825 75302825 single base substitution G A missense_variant A147V 440C>T SKCM-US 10 75302825 75302825 single base substitution G A upstream_gene_variant SKCM-US 10 75302868 75302868 single base substitution G A 5_prime_UTR_variant SKCM-US 10 75302868 75302868 single base substitution G A exon_variant SKCM-US 10 75302868 75302868 single base substitution G A intron_variant SKCM-US 10 75302868 75302868 single base substitution G A missense_variant H133Y 397C>T SKCM-US 10 75302868 75302868 single base substitution G A upstream_gene_variant STAD-US 10 75255610 75255615 deletion of <=200bp GGGGGC - downstream_gene_variant STAD-US 10 75258563 75258563 single base substitution G A 3_prime_UTR_variant STAD-US 10 75258563 75258563 single base substitution G A downstream_gene_variant STAD-US 10 75258563 75258563 single base substitution G A exon_variant STAD-US 10 75258563 75258563 single base substitution G A stop_gained R1477* 4429C>T STAD-US 10 75258563 75258563 single base substitution G A stop_gained R1627* 4879C>T STAD-US 10 75258563 75258563 single base substitution G A stop_gained R668* 2002C>T STAD-US 10 75258563 75258563 single base substitution G A stop_gained R762* 2284C>T STAD-US 10 75260443 75260443 single base substitution T C 3_prime_UTR_variant STAD-US 10 75260443 75260443 single base substitution T C exon_variant STAD-US 10 75260443 75260443 single base substitution T C missense_variant T1339A 4015A>G STAD-US 10 75260443 75260443 single base substitution T C missense_variant T1489A 4465A>G STAD-US 10 75260443 75260443 single base substitution T C missense_variant T530A 1588A>G STAD-US 10 75260443 75260443 single base substitution T C missense_variant T624A 1870A>G STAD-US 10 75265090 75265090 single base substitution T G 3_prime_UTR_variant STAD-US 10 75265090 75265090 single base substitution T G exon_variant STAD-US 10 75265090 75265090 single base substitution T G missense_variant E1232D 3696A>C STAD-US 10 75265090 75265090 single base substitution T G missense_variant E1382D 4146A>C STAD-US 10 75265090 75265090 single base substitution T G missense_variant E470D 1410A>C STAD-US 10 75265090 75265090 single base substitution T G missense_variant E564D 1692A>C STAD-US 10 75265090 75265090 single base substitution T G upstream_gene_variant STAD-US 10 75276308 75276308 single base substitution C T 3_prime_UTR_variant STAD-US 10 75276308 75276308 single base substitution C T downstream_gene_variant STAD-US 10 75276308 75276308 single base substitution C T exon_variant STAD-US 10 75276308 75276308 single base substitution C T synonymous_variant T1142T 3426G>A STAD-US 10 75276308 75276308 single base substitution C T synonymous_variant T1292T 3876G>A STAD-US 10 75276308 75276308 single base substitution C T synonymous_variant T380T 1140G>A STAD-US 10 75276308 75276308 single base substitution C T synonymous_variant T474T 1422G>A STAD-US 10 75276635 75276635 single base substitution C G 3_prime_UTR_variant STAD-US 10 75276635 75276635 single base substitution C G downstream_gene_variant STAD-US 10 75276635 75276635 single base substitution C G exon_variant STAD-US 10 75276635 75276635 single base substitution C G missense_variant W1033C 3099G>C STAD-US 10 75276635 75276635 single base substitution C G missense_variant W1183C 3549G>C STAD-US 10 75276635 75276635 single base substitution C G missense_variant W271C 813G>C STAD-US 10 75276635 75276635 single base substitution C G missense_variant W365C 1095G>C STAD-US 10 75277357 75277357 single base substitution G T 3_prime_UTR_variant STAD-US 10 75277357 75277357 single base substitution G T downstream_gene_variant STAD-US 10 75277357 75277357 single base substitution G T exon_variant STAD-US 10 75277357 75277357 single base substitution G T missense_variant P125T 373C>A STAD-US 10 75277357 75277357 single base substitution G T missense_variant P31T 91C>A STAD-US 10 75277357 75277357 single base substitution G T missense_variant P793T 2377C>A STAD-US 10 75277357 75277357 single base substitution G T missense_variant P943T 2827C>A STAD-US 10 75279629 75279629 single base substitution C T 5_prime_UTR_variant STAD-US 10 75279629 75279629 single base substitution C T exon_variant STAD-US 10 75279629 75279629 single base substitution C T intron_variant STAD-US 10 75279629 75279629 single base substitution C T synonymous_variant Q50Q 150G>A STAD-US 10 75279629 75279629 single base substitution C T synonymous_variant Q718Q 2154G>A STAD-US 10 75279629 75279629 single base substitution C T synonymous_variant Q868Q 2604G>A STAD-US 10 75280778 75280778 single base substitution A G 5_prime_UTR_variant STAD-US 10 75280778 75280778 single base substitution A G exon_variant STAD-US 10 75280778 75280778 single base substitution A G intron_variant STAD-US 10 75280778 75280778 single base substitution A G synonymous_variant S640S 1920T>C STAD-US 10 75280778 75280778 single base substitution A G synonymous_variant S790S 2370T>C STAD-US 10 75289520 75289520 single base substitution A G 5_prime_UTR_variant STAD-US 10 75289520 75289520 single base substitution A G exon_variant STAD-US 10 75289520 75289520 single base substitution A G missense_variant S510P 1528T>C STAD-US 10 75289520 75289520 single base substitution A G missense_variant S660P 1978T>C STAD-US 10 75289589 75289589 single base substitution G A 5_prime_UTR_variant STAD-US 10 75289589 75289589 single base substitution G A exon_variant STAD-US 10 75289589 75289589 single base substitution G A missense_variant R487C 1459C>T STAD-US 10 75289589 75289589 single base substitution G A missense_variant R637C 1909C>T STAD-US 10 75289641 75289641 single base substitution G C 5_prime_UTR_variant STAD-US 10 75289641 75289641 single base substitution G C exon_variant STAD-US 10 75289641 75289641 single base substitution G C missense_variant S469R 1407C>G STAD-US 10 75289641 75289641 single base substitution G C missense_variant S619R 1857C>G STAD-US 10 75290072 75290072 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 10 75290072 75290072 single base substitution G A exon_variant STAD-US 10 75290072 75290072 single base substitution G A missense_variant R403C 1207C>T STAD-US 10 75290072 75290072 single base substitution G A missense_variant R553C 1657C>T STAD-US 10 75290191 75290194 deletion of <=200bp CTGA - 5_prime_UTR_variant STAD-US 10 75290191 75290194 deletion of <=200bp CTGA - exon_variant STAD-US 10 75290191 75290194 deletion of <=200bp CTGA - frameshift_variant VS362 STAD-US 10 75290191 75290194 deletion of <=200bp CTGA - frameshift_variant VS512 STAD-US 10 75290191 75290194 deletion of <=200bp CTGA - upstream_gene_variant STAD-US 10 75290284 75290284 deletion of <=200bp A - splice_region_variant STAD-US 10 75290284 75290284 deletion of <=200bp A - upstream_gene_variant STAD-US 10 75290490 75290490 single base substitution C T 5_prime_UTR_variant STAD-US 10 75290490 75290490 single base substitution C T exon_variant STAD-US 10 75290490 75290490 single base substitution C T intron_variant STAD-US 10 75290490 75290490 single base substitution C T synonymous_variant E323E 969G>A STAD-US 10 75290490 75290490 single base substitution C T synonymous_variant E473E 1419G>A STAD-US 10 75290490 75290490 single base substitution C T upstream_gene_variant STAD-US 10 75296060 75296060 single base substitution A G 5_prime_UTR_variant STAD-US 10 75296060 75296060 single base substitution A G downstream_gene_variant STAD-US 10 75296060 75296060 single base substitution A G exon_variant STAD-US 10 75296060 75296060 single base substitution A G missense_variant Y221H 661T>C STAD-US 10 75296060 75296060 single base substitution A G missense_variant Y371H 1111T>C STAD-US 10 75296060 75296060 single base substitution A G upstream_gene_variant STAD-US 10 75331193 75331193 single base substitution A G 5_prime_UTR_variant STAD-US 10 75331193 75331193 single base substitution A G downstream_gene_variant STAD-US 10 75331193 75331193 single base substitution A G exon_variant STAD-US 10 75331193 75331193 single base substitution A G missense_variant F76L 226T>C STAD-US 10 75331241 75331241 single base substitution T C 5_prime_UTR_variant STAD-US 10 75331241 75331241 single base substitution T C downstream_gene_variant STAD-US 10 75331241 75331241 single base substitution T C exon_variant STAD-US 10 75331241 75331241 single base substitution T C missense_variant S60G 178A>G STAD-US 10 75335385 75335385 deletion of <=200bp C - 5_prime_UTR_variant STAD-US 10 75335385 75335385 deletion of <=200bp C - downstream_gene_variant STAD-US 10 75335385 75335385 deletion of <=200bp C - exon_variant STAD-US 10 75335385 75335385 deletion of <=200bp C - frameshift_variant G11 UCEC-US 10 75258467 75258467 single base substitution C T 3_prime_UTR_variant UCEC-US 10 75258467 75258467 single base substitution C T downstream_gene_variant UCEC-US 10 75258467 75258467 single base substitution C T exon_variant UCEC-US 10 75258467 75258467 single base substitution C T missense_variant E1509K 4525G>A UCEC-US 10 75258467 75258467 single base substitution C T missense_variant E1659K 4975G>A UCEC-US 10 75258467 75258467 single base substitution C T missense_variant E700K 2098G>A UCEC-US 10 75258467 75258467 single base substitution C T missense_variant E794K 2380G>A UCEC-US 10 75258785 75258785 single base substitution C A 3_prime_UTR_variant UCEC-US 10 75258785 75258785 single base substitution C A downstream_gene_variant UCEC-US 10 75258785 75258785 single base substitution C A exon_variant UCEC-US 10 75258785 75258785 single base substitution C A missense_variant G1403W 4207G>T UCEC-US 10 75258785 75258785 single base substitution C A missense_variant G1553W 4657G>T UCEC-US 10 75258785 75258785 single base substitution C A missense_variant G594W 1780G>T UCEC-US 10 75258785 75258785 single base substitution C A missense_variant G688W 2062G>T UCEC-US 10 75260421 75260421 single base substitution C A 3_prime_UTR_variant UCEC-US 10 75260421 75260421 single base substitution C A exon_variant UCEC-US 10 75260421 75260421 single base substitution C A missense_variant R1346I 4037G>T UCEC-US 10 75260421 75260421 single base substitution C A missense_variant R1496I 4487G>T UCEC-US 10 75260421 75260421 single base substitution C A missense_variant R537I 1610G>T UCEC-US 10 75260421 75260421 single base substitution C A missense_variant R631I 1892G>T UCEC-US 10 75264669 75264669 single base substitution C T 3_prime_UTR_variant UCEC-US 10 75264669 75264669 single base substitution C T exon_variant UCEC-US 10 75264669 75264669 single base substitution C T intron_variant UCEC-US 10 75264669 75264669 single base substitution C T missense_variant R1267H 3800G>A UCEC-US 10 75264669 75264669 single base substitution C T missense_variant R1417H 4250G>A UCEC-US 10 75264678 75264678 single base substitution C T 3_prime_UTR_variant UCEC-US 10 75264678 75264678 single base substitution C T exon_variant UCEC-US 10 75264678 75264678 single base substitution C T intron_variant UCEC-US 10 75264678 75264678 single base substitution C T missense_variant R1264H 3791G>A UCEC-US 10 75264678 75264678 single base substitution C T missense_variant R1414H 4241G>A UCEC-US 10 75265139 75265139 single base substitution G T 3_prime_UTR_variant UCEC-US 10 75265139 75265139 single base substitution G T exon_variant UCEC-US 10 75265139 75265139 single base substitution G T missense_variant P1216H 3647C>A UCEC-US 10 75265139 75265139 single base substitution G T missense_variant P1366H 4097C>A UCEC-US 10 75265139 75265139 single base substitution G T missense_variant P454H 1361C>A UCEC-US 10 75265139 75265139 single base substitution G T missense_variant P548H 1643C>A UCEC-US 10 75265139 75265139 single base substitution G T upstream_gene_variant UCEC-US 10 75276158 75276158 single base substitution G A 3_prime_UTR_variant UCEC-US 10 75276158 75276158 single base substitution G A downstream_gene_variant UCEC-US 10 75276158 75276158 single base substitution G A exon_variant UCEC-US 10 75276158 75276158 single base substitution G A synonymous_variant T1192T 3576C>T UCEC-US 10 75276158 75276158 single base substitution G A synonymous_variant T1342T 4026C>T UCEC-US 10 75276158 75276158 single base substitution G A synonymous_variant T430T 1290C>T UCEC-US 10 75276158 75276158 single base substitution G A synonymous_variant T524T 1572C>T UCEC-US 10 75276232 75276232 single base substitution C T 3_prime_UTR_variant UCEC-US 10 75276232 75276232 single base substitution C T downstream_gene_variant UCEC-US 10 75276232 75276232 single base substitution C T exon_variant UCEC-US 10 75276232 75276232 single base substitution C T missense_variant E1168K 3502G>A UCEC-US 10 75276232 75276232 single base substitution C T missense_variant E1318K 3952G>A UCEC-US 10 75276232 75276232 single base substitution C T missense_variant E406K 1216G>A UCEC-US 10 75276232 75276232 single base substitution C T missense_variant E500K 1498G>A UCEC-US 10 75276311 75276311 single base substitution A G 3_prime_UTR_variant UCEC-US 10 75276311 75276311 single base substitution A G downstream_gene_variant UCEC-US 10 75276311 75276311 single base substitution A G exon_variant UCEC-US 10 75276311 75276311 single base substitution A G synonymous_variant H1141H 3423T>C UCEC-US 10 75276311 75276311 single base substitution A G synonymous_variant H1291H 3873T>C UCEC-US 10 75276311 75276311 single base substitution A G synonymous_variant H379H 1137T>C UCEC-US 10 75276311 75276311 single base substitution A G synonymous_variant H473H 1419T>C UCEC-US 10 75276512 75276512 single base substitution C T 3_prime_UTR_variant UCEC-US 10 75276512 75276512 single base substitution C T downstream_gene_variant UCEC-US 10 75276512 75276512 single base substitution C T exon_variant UCEC-US 10 75276512 75276512 single base substitution C T synonymous_variant Q1074Q 3222G>A UCEC-US 10 75276512 75276512 single base substitution C T synonymous_variant Q1224Q 3672G>A UCEC-US 10 75276512 75276512 single base substitution C T synonymous_variant Q312Q 936G>A UCEC-US 10 75276512 75276512 single base substitution C T synonymous_variant Q406Q 1218G>A UCEC-US 10 75279711 75279711 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 75279711 75279711 single base substitution G A exon_variant UCEC-US 10 75279711 75279711 single base substitution G A intron_variant UCEC-US 10 75279711 75279711 single base substitution G A missense_variant T23M 68C>T UCEC-US 10 75279711 75279711 single base substitution G A missense_variant T691M 2072C>T UCEC-US 10 75279711 75279711 single base substitution G A missense_variant T841M 2522C>T UCEC-US 10 75289572 75289572 single base substitution C T 5_prime_UTR_variant UCEC-US 10 75289572 75289572 single base substitution C T exon_variant UCEC-US 10 75289572 75289572 single base substitution C T synonymous_variant R492R 1476G>A UCEC-US 10 75289572 75289572 single base substitution C T synonymous_variant R642R 1926G>A UCEC-US 10 75290129 75290129 single base substitution C T 5_prime_UTR_variant UCEC-US 10 75290129 75290129 single base substitution C T exon_variant UCEC-US 10 75290129 75290129 single base substitution C T missense_variant G384S 1150G>A UCEC-US 10 75290129 75290129 single base substitution C T missense_variant G534S 1600G>A UCEC-US 10 75294366 75294366 single base substitution C T 5_prime_UTR_variant UCEC-US 10 75294366 75294366 single base substitution C T downstream_gene_variant UCEC-US 10 75294366 75294366 single base substitution C T exon_variant UCEC-US 10 75294366 75294366 single base substitution C T intron_variant UCEC-US 10 75294366 75294366 single base substitution C T missense_variant R286Q 857G>A UCEC-US 10 75294366 75294366 single base substitution C T missense_variant R436Q 1307G>A UCEC-US 10 75294366 75294366 single base substitution C T upstream_gene_variant UCEC-US 10 75294498 75294498 single base substitution C T 5_prime_UTR_variant UCEC-US 10 75294498 75294498 single base substitution C T downstream_gene_variant UCEC-US 10 75294498 75294498 single base substitution C T exon_variant UCEC-US 10 75294498 75294498 single base substitution C T intron_variant UCEC-US 10 75294498 75294498 single base substitution C T missense_variant R242Q 725G>A UCEC-US 10 75294498 75294498 single base substitution C T missense_variant R392Q 1175G>A UCEC-US 10 75294498 75294498 single base substitution C T upstream_gene_variant UCEC-US 10 75296056 75296056 single base substitution C A 5_prime_UTR_variant UCEC-US 10 75296056 75296056 single base substitution C A downstream_gene_variant UCEC-US 10 75296056 75296056 single base substitution C A exon_variant UCEC-US 10 75296056 75296056 single base substitution C A missense_variant S222I 665G>T UCEC-US 10 75296056 75296056 single base substitution C A missense_variant S372I 1115G>T UCEC-US 10 75296056 75296056 single base substitution C A upstream_gene_variant UCEC-US 10 75299314 75299314 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 75299314 75299314 single base substitution G C downstream_gene_variant UCEC-US 10 75299314 75299314 single base substitution G C exon_variant UCEC-US 10 75299314 75299314 single base substitution G C missense_variant S138C 413C>G UCEC-US 10 75299314 75299314 single base substitution G C missense_variant S288C 863C>G UCEC-US 10 75299314 75299314 single base substitution G C upstream_gene_variant UCEC-US 10 75301249 75301249 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 75301249 75301249 single base substitution G A downstream_gene_variant UCEC-US 10 75301249 75301249 single base substitution G A exon_variant UCEC-US 10 75301249 75301249 single base substitution G A intron_variant UCEC-US 10 75301249 75301249 single base substitution G A missense_variant R237C 709C>T UCEC-US 10 75302841 75302841 single base substitution C A 5_prime_UTR_variant UCEC-US 10 75302841 75302841 single base substitution C A exon_variant UCEC-US 10 75302841 75302841 single base substitution C A intron_variant UCEC-US 10 75302841 75302841 single base substitution C A stop_gained E142* 424G>T UCEC-US 10 75302841 75302841 single base substitution C A upstream_gene_variant UCEC-US 10 75305336 75305336 single base substitution C T 5_prime_UTR_variant UCEC-US 10 75305336 75305336 single base substitution C T exon_variant UCEC-US 10 75305336 75305336 single base substitution C T missense_variant R112H 335G>A UCEC-US 10 75305336 75305336 single base substitution C T upstream_gene_variant UCEC-US 10 75335312 75335312 single base substitution A G 5_prime_UTR_variant UCEC-US 10 75335312 75335312 single base substitution A G downstream_gene_variant UCEC-US 10 75335312 75335312 single base substitution A G exon_variant UCEC-US 10 75335312 75335312 single base substitution A G synonymous_variant N35N 105T>C UCEC-US 10 75335366 75335366 single base substitution C A 5_prime_UTR_variant UCEC-US 10 75335366 75335366 single base substitution C A downstream_gene_variant UCEC-US 10 75335366 75335366 single base substitution C A exon_variant UCEC-US 10 75335366 75335366 single base substitution C A synonymous_variant G17G 51G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand pfg212T COSM4757633 c.106C>A p.P36T Substitution - Missense 10:73517584-73517584 - Pat_41_B COSM5837291 c.1800_1801delCC p.Q601fs*71 Deletion - Frameshift 10:73499132-73499133 - SC_9071 COSM5563177 c.549A>G p.Q183Q Substitution - coding silent 10:73517141-73517141 - 8031121 COSM3383003 c.228T>G p.S76R Substitution - Missense 10:73517462-73517462 - Mel18 COSM1675350 c.2141C>T p.P714L Substitution - Missense 10:73498792-73498792 - RK229_C01 COSM4780354 c.1576A>C p.R526R Substitution - coding silent 10:73500823-73500823 - YUKLAB COSM1702633 c.1547C>T p.S516F Substitution - Missense 10:73504863-73504863 - Patient_2 COSM5044535 c.1322C>A p.A441E Substitution - Missense 10:73505420-73505420 - TCGA-13-0906-01 COSM120020 c.142G>A p.E48K Substitution - Missense 10:73517548-73517548 - 587376 COSM1232106 c.572A>C p.K191T Substitution - Missense 10:73517118-73517118 - TCGA-AP-A059-01 COSM920331 c.1137T>C p.H379H Substitution - coding silent 10:73516553-73516553 - Pat_45_B COSM5837297 c.914G>A p.G305D Substitution - Missense 10:73516776-73516776 - TCGA-G3-A6UC-01 COSM4929748 c.1079C>G p.S360C Substitution - Missense 10:73516611-73516611 - 86506 COSM95491 c.1658G>A p.G553D Substitution - Missense 10:73500741-73500741 - ESCC_84 COSM5636368 c.704G>C p.S235T Substitution - Missense 10:73516986-73516986 - TCGA-Q1-A73O-01 COSM4834181 c.30C>A p.F10L Substitution - Missense 10:73517660-73517660 - TCGA-D1-A17H-01 COSM920317 c.1757G>A p.S586N Substitution - Missense 10:73499176-73499176 - HCC29T COSM1603713 c.52C>T p.H18Y Substitution - Missense 10:73517638-73517638 - SW48 COSM1963856 c.1123C>T p.P375S Substitution - Missense 10:73516567-73516567 - YUKAT COSM5371106 c.1908G>A p.G636G Substitution - coding silent 10:73499025-73499025 - 255 COSM3732173 c.1419+4C>T p.? Unknown 10:73505319-73505319 - ATL088 COSM5703700 c.506C>T p.S169L Substitution - Missense 10:73517184-73517184 - TCGA-BR-8078-01 COSM4015748 c.91C>A p.P31T Substitution - Missense 10:73517599-73517599 - TCGA-BH-A0H9-01 COSM427893 c.327T>G p.A109A Substitution - coding silent 10:73517363-73517363 - TCGA-CH-5762-01 COSM1470400 c.1948A>G p.T650A Substitution - Missense 10:73498985-73498985 - HX36T COSM1603713 c.52C>T p.H18Y Substitution - Missense 10:73517638-73517638 - TCGA-DA-A1I0-06 COSM1702635 c.1192C>T p.Q398* Substitution - Nonsense 10:73516498-73516498 - TCGA-A8-A0A6-01 COSM3807686 c.2028A>C p.S676S Substitution - coding silent 10:73498905-73498905 - sysucc-1072T COSM5482842 c.2113C>T p.P705S Substitution - Missense 10:73498820-73498820 - TCGA-AZ-4315-01 COSM1349018 c.969G>T p.E323D Substitution - Missense 10:73516721-73516721 - NYU929 COSM4770946 c.459C>T p.S153S Substitution - coding silent 10:73517231-73517231 - tumor_4119279 COSM5947039 c.790C>A p.Q264K Substitution - Missense 10:73516900-73516900 - 86794 COSM95493 c.1490G>T p.R497L Substitution - Missense 10:73504920-73504920 - ESCC_BICR_055T COSM5436591 c.1987C>T p.Q663* Substitution - Nonsense 10:73498946-73498946 - TCGA-33-6737-01 COSM685368 c.832C>T p.L278L Substitution - coding silent 10:73516858-73516858 - TCGA-D1-A17U-01 COSM920321 c.1499G>A p.R500H Substitution - Missense 10:73504911-73504911 - J87_T COSM3978766 c.1014C>T p.S338S Substitution - coding silent 10:73516676-73516676 - KPOPBR-57-T COSM458794 c.1156G>C p.E386Q Substitution - Missense 10:73516534-73516534 - TCGA-EK-A3GK-01 COSM4853600 c.164C>G p.S55C Substitution - Missense 10:73517526-73517526 - Pat_76_A COSM5837295 c.1133C>T p.S378F Substitution - Missense 10:73516557-73516557 - 66 COSM5743411 c.1006C>A p.L336M Substitution - Missense 10:73516684-73516684 - TCGA-LP-A4AW-01 COSM4829681 c.369C>T p.P123P Substitution - coding silent 10:73517321-73517321 - YUCLAT COSM1702635 c.1192C>T p.Q398* Substitution - Nonsense 10:73516498-73516498 - SA065 COSM213128 c.1751C>G p.S584* Substitution - Nonsense 10:73499182-73499182 - OSCC-GB_00480111 COSM3709951 c.386G>C p.G129A Substitution - Missense 10:73517304-73517304 - HCC1008 COSM32513 c.886C>G p.L296V Substitution - Missense 10:73516804-73516804 - HCC29 COSM1603713 c.52C>T p.H18Y Substitution - Missense 10:73517638-73517638 - Pat_41_B COSM5837293 c.1160G>A p.R387K Substitution - Missense 10:73516530-73516530 - EWS502 COSM4573813 c.1122C>G p.S374S Substitution - coding silent 10:73516568-73516568 - LS411 COSM1963842 c.1419+1G>A p.? Unknown 10:73505322-73505322 - TCGA-CJ-4895-01 COSM3358861 c.1833C>A p.N611K Substitution - Missense 10:73499100-73499100 - TCGA-C5-A1BM-01 COSM4826506 c.1942C>T p.Q648* Substitution - Nonsense 10:73498991-73498991 - 587376 COSM1232102 c.1699G>T p.D567Y Substitution - Missense 10:73500700-73500700 - 587376 COSM1232104 c.724A>C p.S242R Substitution - Missense 10:73516966-73516966 - TCGA-66-2795-01 COSM685366 c.605G>T p.S202I Substitution - Missense 10:73517085-73517085 - TCGA-AX-A0J1-01 COSM920325 c.1361C>A p.P454H Substitution - Missense 10:73505381-73505381 - Pat_06_A COSM5837289 c.1955C>T p.T652I Substitution - Missense 10:73498978-73498978 - TCGA-CC-A123-01 COSM4915314 c.78A>G p.P26P Substitution - coding silent 10:73517612-73517612 - TCGA-EE-A3AA-06 COSM3440436 c.1158G>A p.E386E Substitution - coding silent 10:73516532-73516532 - TCGA-18-5595-01 COSM685372 c.1246C>A p.Q416K Substitution - Missense 10:73516444-73516444 - T3658 COSM4739927 c.1554_1555delCA p.H518fs*3 Deletion - Frameshift 10:73504855-73504856 - CSCC-55-T COSM4484793 c.116C>T p.S39F Substitution - Missense 10:73517574-73517574 - TARGET-30-PASNZU COSM1288864 c.321C>A p.G107G Substitution - coding silent 10:73517369-73517369 - TCGA-A8-A0A6-01 COSM3807684 c.2036A>C p.H679P Substitution - Missense 10:73498897-73498897 - TCGA-FD-A3B4-01 COSM1297420 c.1983C>T p.G661G Substitution - coding silent 10:73498950-73498950 - TCGA-BS-A0UA-01 COSM920321 c.1499G>A p.R500H Substitution - Missense 10:73504911-73504911 - ESO-007 COSM1270111 c.2027C>T p.S676L Substitution - Missense 10:73498906-73498906 - TCGA-BR-8360-01 COSM4015744 c.1140G>A p.T380T Substitution - coding silent 10:73516550-73516550 - DU-145 COSM1675352 c.1504C>A p.L502I Substitution - Missense 10:73504906-73504906 - Pat_76_B COSM5837295 c.1133C>T p.S378F Substitution - Missense 10:73516557-73516557 - 11M COSM5577190 c.588A>T p.L196F Substitution - Missense 10:73517102-73517102 - 587234 COSM1232099 c.1141T>C p.C381R Substitution - Missense 10:73516549-73516549 - PD2203a COSM25717 c.1531delG p.E511fs*15 Deletion - Frameshift 10:73504879-73504879 - TCGA-BH-A0BL-01 COSM427889 c.1484T>C p.L495S Substitution - Missense 10:73504926-73504926 - TCGA-36-2544-01 COSM1321226 c.351G>C p.K117N Substitution - Missense 10:73517339-73517339 - B81 COSM1745319 c.1593_1595delCGG p.G532delG Deletion - In frame 10:73500804-73500806 - TCGA-AP-A056-01 COSM920313 c.2224G>A p.E742K Substitution - Missense 10:73498709-73498709 - TCGA-29-1766-01 COSM1321230 c.724A>G p.S242G Substitution - Missense 10:73516966-73516966 - TCGA-DR-A0ZM-01 COSM458794 c.1156G>C p.E386Q Substitution - Missense 10:73516534-73516534 - TCGA-CG-4305-01 COSM4015742 c.1410A>C p.E470D Substitution - Missense 10:73505332-73505332 - TCGA-AP-A059-01 COSM920323 c.1490G>A p.R497H Substitution - Missense 10:73504920-73504920 - TCGA-21-5782-01 COSM685364 c.328C>G p.Q110E Substitution - Missense 10:73517362-73517362 - 585258 COSM324225 c.1196A>C p.D399A Substitution - Missense 10:73516494-73516494 - PR-01-2382 COSM248259 c.1937A>G p.N646S Substitution - Missense 10:73498996-73498996 - 111664 COSM95495 c.714C>G p.F238L Substitution - Missense 10:73516976-73516976 - 1743_PT COSM5753537 c.347A>T p.E116V Substitution - Missense 10:73517343-73517343 - HRA19 COSM4637589 c.929G>A p.G310E Substitution - Missense 10:73516761-73516761 - CSCC-27-T COSM4497496 c.2233C>T p.L745L Substitution - coding silent 10:73498700-73498700 - TCGA-AP-A051-01 COSM920315 c.1906G>T p.G636W Substitution - Missense 10:73499027-73499027 - 48T COSM3709951 c.386G>C p.G129A Substitution - Missense 10:73517304-73517304 - 219 COSM4424973 c.761C>G p.S254C Substitution - Missense 10:73516929-73516929 - TCGA-EB-A5UL-06 COSM3867802 c.201G>T p.G67G Substitution - coding silent 10:73517489-73517489 - TCGA-61-1740-01 COSM1321228 c.618T>C p.Y206Y Substitution - coding silent 10:73517072-73517072 - J87_T COSM3978764 c.1028G>T p.G343V Substitution - Missense 10:73516662-73516662 - TCGA-CW-5584-01 COSM465948 c.612G>T p.E204D Substitution - Missense 10:73517078-73517078 - SK-MEL-28 COSM1675350 c.2141C>T p.P714L Substitution - Missense 10:73498792-73498792 - TCGA-HU-A4H4-01 COSM4015746 c.813G>C p.W271C Substitution - Missense 10:73516877-73516877 - PD23559a COSM5801748 c.210_214delGAAGA p.K71fs*4 Deletion - Frameshift 10:73517476-73517480 - TCGA-85-6175-01 COSM685370 c.887T>C p.L296P Substitution - Missense 10:73516803-73516803 - pfg043T COSM4757627 c.1481A>C p.N494T Substitution - Missense 10:73504929-73504929 - TCGA-CD-5802-01 COSM4015738 c.2128C>T p.R710* Substitution - Nonsense 10:73498805-73498805 - TCGA-BH-A1FN-01 COSM1474757 c.2271C>T p.I757I Substitution - coding silent 10:73498662-73498662 - TCGA-D3-A1QB-06 COSM3440440 c.218C>T p.S73F Substitution - Missense 10:73517472-73517472 - TCGA-AP-A051-01 COSM920319 c.1736G>T p.R579I Substitution - Missense 10:73500663-73500663 - TCGA-BR-6452-01 COSM4015740 c.1714A>G p.T572A Substitution - Missense 10:73500685-73500685 - TCGA-D1-A103-01 COSM920321 c.1499G>A p.R500H Substitution - Missense 10:73504911-73504911 - TCGA-D9-A3Z1-06 COSM3440438 c.858C>T p.S286S Substitution - coding silent 10:73516832-73516832 - TCGA-AA-3510-01 COSM1349016 c.1029G>A p.G343G Substitution - coding silent 10:73516661-73516661 - TCGA-AN-A0FV-01 COSM427887 c.2190T>C p.Y730Y Substitution - coding silent 10:73498743-73498743 - CSCC-27-T COSM4547350 c.1456G>A p.E486K Substitution - Missense 10:73504954-73504954 - TCGA-AA-3672-01 COSM267738 c.763G>A p.D255N Substitution - Missense 10:73516927-73516927 - TCGA-AP-A056-01 COSM920333 c.936G>A p.Q312Q Substitution - coding silent 10:73516754-73516754 - STC246 COSM5050326 c.1419+3G>A p.? Unknown 10:73505320-73505320 - CHEWS010 COSM4573815 c.428G>A p.C143Y Substitution - Missense 10:73517262-73517262 - TCGA-EE-A181-06 COSM920313 c.2224G>A p.E742K Substitution - Missense 10:73498709-73498709 - 107544 COSM95497 c.661G>A p.A221T Substitution - Missense 10:73517029-73517029 - T578 COSM4739929 c.1079C>A p.S360Y Substitution - Missense 10:73516611-73516611 - TCGA-CA-6717-01 COSM1349014 c.1952A>G p.Y651C Substitution - Missense 10:73498981-73498981 - ACINAR28 COSM1735378 c.2053C>A p.P685T Substitution - Missense 10:73498880-73498880 - I2L-P7-Tumor-Organoid COSM5360291 c.687T>C p.G229G Substitution - coding silent 10:73517003-73517003 - 2521262 COSM5892111 c.1156G>A p.E386K Substitution - Missense 10:73516534-73516534 - CSCC-42-T COSM4545681 c.1103G>A p.R368K Substitution - Missense 10:73516587-73516587 - TCGA-B6-A0RN-01 COSM427891 c.1276G>C p.G426R Substitution - Missense 10:73516414-73516414 - 8065669 COSM4135662 c.398C>G p.S133C Substitution - Missense 10:73517292-73517292 - TCGA-EE-A29V-06 COSM3440434 c.1820G>A p.G607E Substitution - Missense 10:73499113-73499113 - TCGA-AX-A05Z-01 COSM920329 c.1216G>A p.E406K Substitution - Missense 10:73516474-73516474 - CSCC-40-T COSM4491778 c.1126C>T p.H376Y Substitution - Missense 10:73516564-73516564 - TCGA-AX-A06H-01 COSM920327 c.1290C>T p.T430T Substitution - coding silent 10:73516400-73516400 - Au4 COSM5605312 c.2273G>A p.R758K Substitution - Missense 10:73498660-73498660 - TCGA-AA-3833-01 COSM271595 c.805T>C p.W269R Substitution - Missense 10:73516885-73516885 - CR108 COSM4994800 c.877C>A p.H293N Substitution - Missense 10:73516813-73516813 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.657352;Hs.657354;Hs.657355 10q22.2

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Synonymous p.A1021A c.3063T>G 10 75277121 BRCA A G Missense p.F628L c.1882T>C 10 75289616 HNSC A G Missense p.L1208P c.3623T>C 10 75276561 LUSC A G Missense p.L1412S c.4235T>C 10 75264684 BRCA A G Missense p.Y371H c.1111T>C 10 75296060 STAD A G Synonymous p.D1194D c.3582T>C 10 75276602 COREAD A G Synonymous p.N35N c.105T>C 10 75335312 UCEC A G Synonymous p.S790S c.2370T>C 10 75280778 STAD A G Synonymous p.Y1647Y c.4941T>C 10 75258501 BRCA A T Missense p.S26T c.76T>A 10 75335341 HNSC C A Missense p.R1268M c.3803G>T 10 75276381 LUAD C A Missense p.R789S c.2367G>T 10 75280781 LUAD C A Missense p.S1114I c.3341G>T 10 75276843 LUSC C A Missense p.S372I c.1115G>T 10 75296056 UCEC C A Missense p.S665I c.1994G>T 10 75289504 CM C A Missense p.W724L c.2171G>T 10 75286428 LUSC C A Synonymous p.T841T c.2523G>T 10 75279710 BLCA CC TT Missense p.G1660R c.4977_4978delinsAA 10 75258464 CM C G Missense p.E734D c.2202G>C 10 75283501 LUAD C G Missense p.G1338R c.4012G>C 10 75276172 BRCA C G Missense p.L1208V c.3622C>G 10 75276562 BRCA C G Missense p.R642P c.1925G>C 10 75289573 LUAD C T 3-UTRSNV . c.5052+100G>A 10 75258290 CM CTGA - Frameshift p.V512Afs*3 c.1535_1538delTCAG 10 75290191 STAD C T Missense p.E1659K c.4975G>A 10 75258467 CM C T Missense p.E960K c.2878G>A 10 75277306 OV C T Missense p.G1157S c.3469G>A 10 75276715 CM C T Missense p.G1524E c.4571G>A 10 75258871 CM C T Missense p.G973D c.2918G>A 10 75277266 CM C T Missense p.R112H c.335G>A 10 75305336 UCEC C T Missense p.R1417H c.4250G>A 10 75264669 UCEC C T Missense p.R1632Q c.4895G>A 10 75258547 LUAD C T Missense p.R864H c.2591G>A 10 75279642 HNSC C T Synonymous p.E1298E c.3894G>A 10 75276290 CM C T Synonymous p.R546R c.1638G>A 10 75290091 LUAD C T Synonymous p.R642R c.1926G>A 10 75289572 UCEC G A Missense p.A147V c.440C>T 10 75302825 CM G A Missense p.A147V c.440C>T 10 75302825 OV G A Missense p.H133Y c.397C>T 10 75302868 CM G A Missense p.P1037L c.3110C>T 10 75277074 LUAD G A Missense p.P1123S c.3367C>T 10 75276817 CM G A Missense p.P1165L c.3494C>T 10 75276690 HNSC G A Missense p.P474L c.1421C>T 10 75290488 LUSC G A Missense p.P574L c.1721C>T 10 75290008 ALL G A Missense p.P689S c.2065C>T 10 75286534 CM G A Missense p.R237C c.709C>T 10 75301249 UCEC G A Missense p.R460C c.1378C>T 10 75290531 CM G A Missense p.R637C c.1909C>T 10 75289589 STAD G A Missense p.R864C c.2590C>T 10 75279643 BRCA G A Missense p.S1198F c.3593C>T 10 75276591 STAD G A Missense p.S1593L c.4778C>T 10 75258664 ESCA G A Missense p.S189F c.566C>T 10 75302567 CM G A Missense p.S683L c.2048C>T 10 75289450 CM G A Missense p.S700F c.2099C>T 10 75286500 CM G A Missense p.S985F c.2954C>T 10 75277230 CM G A Missense p.S9L c.26C>T 10 75335391 CM G A Missense p.S9L c.26C>T 10 75335391 HNSC G A Nonsense p.Q1310* c.3928C>T 10 75276256 CM G A Nonsense p.Q873* c.2617C>T 10 75279616 LUSC G A Nonsense p.R1627* c.4879C>T 10 75258563 STAD G A Nonsense p.R201* c.601C>T 10 75301468 BLCA G A Synonymous p.C77C c.231C>T 10 75331188 HNSC G A Synonymous p.F57F c.171C>T 10 75331248 CM G A Synonymous p.G1578G c.4734C>T 10 75258708 BLCA G A Synonymous p.I1674I c.5022C>T 10 75258420 BRCA G A Synonymous p.I233I c.699C>T 10 75301259 BRCA G A Synonymous p.L1190L c.3568C>T 10 75276616 LUSC G A Synonymous p.S632S c.1896C>T 10 75289602 CM G A Synonymous p.T1342T c.4026C>T 10 75276158 UCEC G A Synonymous p.T547T c.1641C>T 10 75290088 SCLC G C Missense p.Q1022E c.3064C>G 10 75277120 LUSC G C Missense p.S288C c.863C>G 10 75299314 UCEC G C Missense p.S619R c.1857C>G 10 75289641 STAD G C Missense p.S921C c.2762C>G 10 75277422 HNSC G C Nonsense p.S1501* c.4502C>G 10 75258940 BRCA G T Missense p.L128I c.382C>A 10 75302883 SCLC G T Missense p.N1528K c.4584C>A 10 75258858 RCCC G T Missense p.Q1328K c.3982C>A 10 75276202 LUSC G T Synonymous p.G1019G c.3057C>A 10 75277127 NB G T Synonymous p.T547T c.1641C>A 10 75290088 BRCA G T Synonymous p.V411V c.1233C>A 10 75294440 RCCC T C 3-UTRSNV . c.5052+997A>G 10 75257393 HC T C IntronicSNV . c.4171-110A>G 10 75264858 CM T C Missense p.H596R c.1787A>G 10 75289942 STAD T C Missense p.I387V c.1159A>G 10 75294514 LUSC T C Missense p.K509E c.1525A>G 10 75290204 SCLC T C Missense p.N192S c.575A>G 10 75301494 COREAD T C Missense p.N447D c.1339A>G 10 75290570 STAD T C Missense p.T1567A c.4699A>G 10 75258743 PRAD T C Missense p.Y662C c.1985A>G 10 75289513 ESCA T C Synonymous p.E617E c.1851A>G 10 75289647 CM T G Missense p.D1311A c.3932A>C 10 75276252 SCLC T G Missense p.E1382D c.4146A>C 10 75265090 STAD