Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 10 103190166 103190166 + Missense_Mutation SNP G G A TCGA-XF-A9SK-01A-11D-A42E-08 TCGA-XF-A9SK-10A-01D-A42H-08 g.chr10:103190166G>A c.113G>A c.(112-114)cGa>cAa p.R38Q BLCA 10 103281473 103281473 + Silent SNP G G A TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr10:103281473G>A c.402G>A c.(400-402)aaG>aaA p.K134K BLCA 10 103294607 103294607 + Silent SNP C C T TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr10:103294607C>T c.1287C>T c.(1285-1287)gtC>gtT p.V429V BLCA 10 103298066 103298066 + Missense_Mutation SNP G G C TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr10:103298066G>C c.1594G>C c.(1594-1596)Gat>Cat p.D532H BLCA 10 103298108 103298109 + Frame_Shift_Del DEL CT CT - TCGA-CF-A9FL-01A-11D-A38G-08 TCGA-CF-A9FL-10A-01D-A38J-08 g.chr10:103298108_103298109delCT c.1636_1637delCT c.(1636-1638)ctcfs p.L546fs BLCA 10 103310522 103310522 + Missense_Mutation SNP G G A TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr10:103310522G>A c.1723G>A c.(1723-1725)Gac>Aac p.D575N BRCA 10 103190166 103190166 + Missense_Mutation SNP G G A TCGA-LL-A5YL-01A-12D-A29N-09 TCGA-LL-A5YL-10A-01D-A29N-09 g.chr10:103190166G>A c.113G>A c.(112-114)cGa>cAa p.R38Q BRCA 10 103285793 103285793 + Missense_Mutation SNP G G C TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr10:103285793G>C c.580G>C c.(580-582)Gag>Cag p.E194Q BRCA 10 103292145 103292145 + Missense_Mutation SNP G G A TCGA-C8-A275-01A-21D-A16D-09 TCGA-C8-A275-10A-01D-A16D-09 g.chr10:103292145G>A c.934G>A c.(934-936)Gat>Aat p.D312N BRCA 10 103295142 103295142 + Missense_Mutation SNP G G C TCGA-GM-A3XL-01A-11D-A22X-09 TCGA-GM-A3XL-10A-01D-A22X-09 g.chr10:103295142G>C c.1379G>C c.(1378-1380)aGg>aCg p.R460T BRCA 10 103295203 103295203 + Silent SNP G G C TCGA-A8-A08P-01A-11W-A019-09 TCGA-A8-A08P-10A-01W-A021-09 g.chr10:103295203G>C c.1440G>C c.(1438-1440)gtG>gtC p.V480V CESC 10 103190136 103190136 + Missense_Mutation SNP C C G TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr10:103190136C>G c.83C>G c.(82-84)tCc>tGc p.S28C CHOL 10 103281468 103281468 + Missense_Mutation SNP G G A TCGA-ZH-A8Y1-01A-11D-A417-09 TCGA-ZH-A8Y1-10A-01D-A41A-09 g.chr10:103281468G>A c.397G>A c.(397-399)Gaa>Aaa p.E133K CHOL 10 103294590 103294590 + Nonsense_Mutation SNP G G T TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr10:103294590G>T c.1270G>T c.(1270-1272)Gga>Tga p.G424* COAD 10 103221777 103221777 + Missense_Mutation SNP C C A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr10:103221777C>A c.196C>A c.(196-198)Cct>Act p.P66T COAD 10 103285923 103285923 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:103285923C>T c.710C>T c.(709-711)tCt>tTt p.S237F COAD 10 103291027 103291027 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr10:103291027C>T c.777C>T c.(775-777)gaC>gaT p.D259D COAD 10 103291060 103291060 + Silent SNP A A C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr10:103291060A>C c.810A>C c.(808-810)gcA>gcC p.A270A COAD 10 103291074 103291074 + Missense_Mutation SNP T T G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:103291074T>G c.824T>G c.(823-825)aTt>aGt p.I275S COAD 10 103292173 103292173 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr10:103292173G>A c.962G>A c.(961-963)cGa>cAa p.R321Q COAD 10 103295137 103295137 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:103295137T>G c.1374T>G c.(1372-1374)ttT>ttG p.F458L COAD 10 103296324 103296324 + Silent SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr10:103296324A>G c.1491A>G c.(1489-1491)gcA>gcG p.A497A COAD 10 103296370 103296370 + Nonsense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:103296370C>T c.1537C>T c.(1537-1539)Cga>Tga p.R513* COAD 10 103296399 103296399 + Silent SNP G G T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr10:103296399G>T c.1566G>T c.(1564-1566)ggG>ggT p.G522G COAD 10 103310573 103310573 + Frame_Shift_Del DEL C C - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr10:103310573delC c.1774delC c.(1774-1776)cccfs p.P593fs COADREAD 10 103221777 103221777 + Missense_Mutation SNP C C A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr10:103221777C>A c.196C>A c.(196-198)Cct>Act p.P66T COADREAD 10 103221777 103221777 + Missense_Mutation SNP C C T TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr10:103221777C>T c.196C>T c.(196-198)Cct>Tct p.P66S COADREAD 10 103285772 103285772 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:103285772C>T c.559C>T c.(559-561)Cgg>Tgg p.R187W COADREAD 10 103285923 103285923 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:103285923C>T c.710C>T c.(709-711)tCt>tTt p.S237F COADREAD 10 103291027 103291027 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr10:103291027C>T c.777C>T c.(775-777)gaC>gaT p.D259D COADREAD 10 103291060 103291060 + Silent SNP A A C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr10:103291060A>C c.810A>C c.(808-810)gcA>gcC p.A270A COADREAD 10 103291074 103291074 + Missense_Mutation SNP T T G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:103291074T>G c.824T>G c.(823-825)aTt>aGt p.I275S COADREAD 10 103292173 103292173 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr10:103292173G>A c.962G>A c.(961-963)cGa>cAa p.R321Q COADREAD 10 103294568 103294568 + Missense_Mutation SNP T T G TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr10:103294568T>G c.1248T>G c.(1246-1248)atT>atG p.I416M COADREAD 10 103295137 103295137 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:103295137T>G c.1374T>G c.(1372-1374)ttT>ttG p.F458L COADREAD 10 103296324 103296324 + Silent SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr10:103296324A>G c.1491A>G c.(1489-1491)gcA>gcG p.A497A COADREAD 10 103296370 103296370 + Nonsense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:103296370C>T c.1537C>T c.(1537-1539)Cga>Tga p.R513* COADREAD 10 103296399 103296399 + Silent SNP G G T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr10:103296399G>T c.1566G>T c.(1564-1566)ggG>ggT p.G522G COADREAD 10 103310477 103310477 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:103310477C>T c.1678C>T c.(1678-1680)Cga>Tga p.R560* COADREAD 10 103310573 103310573 + Frame_Shift_Del DEL C C - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr10:103310573delC c.1774delC c.(1774-1776)cccfs p.P593fs ESCA 10 103285773 103285773 + Missense_Mutation SNP G G A TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr10:103285773G>A c.560G>A c.(559-561)cGg>cAg p.R187Q ESCA 10 103291061 103291061 + Missense_Mutation SNP C C T TCGA-2H-A9GQ-01A-11D-A37C-09 TCGA-2H-A9GQ-11A-11D-A37F-09 g.chr10:103291061C>T c.811C>T c.(811-813)Ctt>Ttt p.L271F ESCA 10 103310478 103310478 + Missense_Mutation SNP G G A TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr10:103310478G>A c.1679G>A c.(1678-1680)cGa>cAa p.R560Q GBM 10 103190197 103190197 + Silent SNP C C T TCGA-28-5209-01A-01D-1486-08 TCGA-28-5209-10A-01D-1486-08 g.chr10:103190197C>T c.144C>T c.(142-144)ctC>ctT p.L48L GBM 10 103281492 103281492 + Missense_Mutation SNP T T G TCGA-16-0861-01A-01W-0424-08 TCGA-16-0861-10A-01W-0424-08 g.chr10:103281492T>G c.421T>G c.(421-423)Ttt>Gtt p.F141V GBMLGG 10 103190197 103190197 + Silent SNP C C T TCGA-28-5209-01A-01D-1486-08 TCGA-28-5209-10A-01D-1486-08 g.chr10:103190197C>T c.144C>T c.(142-144)ctC>ctT p.L48L GBMLGG 10 103281443 103281443 + Silent SNP G G A TCGA-E1-5307-01A-01D-1893-08 TCGA-E1-5307-10A-01D-1893-08 g.chr10:103281443G>A c.372G>A c.(370-372)cgG>cgA p.R124R GBMLGG 10 103281492 103281492 + Missense_Mutation SNP T T G TCGA-16-0861-01A-01W-0424-08 TCGA-16-0861-10A-01W-0424-08 g.chr10:103281492T>G c.421T>G c.(421-423)Ttt>Gtt p.F141V GBMLGG 10 103292718 103292718 + Frame_Shift_Del DEL A A - TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:103292718delA c.988delA c.(988-990)aaafs p.K330fs HNSC 10 103190136 103190136 + Missense_Mutation SNP C C G TCGA-CQ-5334-01A-01D-1683-08 TCGA-CQ-5334-10A-01D-1683-08 g.chr10:103190136C>G c.83C>G c.(82-84)tCc>tGc p.S28C HNSC 10 103291078 103291078 + Silent SNP A A T TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr10:103291078A>T c.828A>T c.(826-828)atA>atT p.I276I KIPAN 10 103190124 103190124 + Nonsense_Mutation SNP G G A TCGA-UZ-A9PL-01A-11D-A382-10 TCGA-UZ-A9PL-10A-01D-A385-10 g.chr10:103190124G>A c.71G>A c.(70-72)tGg>tAg p.W24* KIPAN 10 103294516 103294516 + Missense_Mutation SNP G G C TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr10:103294516G>C c.1196G>C c.(1195-1197)tGc>tCc p.C399S KIPAN 10 103294568 103294568 + Missense_Mutation SNP T T G TCGA-AK-3461-01A-02D-1361-10 TCGA-AK-3461-10A-01D-1361-10 g.chr10:103294568T>G c.1248T>G c.(1246-1248)atT>atG p.I416M KIPAN 10 103294568 103294568 + Missense_Mutation SNP T T G TCGA-B0-4697-01A-01D-1361-10 TCGA-B0-4697-11A-01D-1361-10 g.chr10:103294568T>G c.1248T>G c.(1246-1248)atT>atG p.I416M KIRC 10 103294568 103294568 + Missense_Mutation SNP T T G TCGA-AK-3461-01A-02D-1361-10 TCGA-AK-3461-10A-01D-1361-10 g.chr10:103294568T>G c.1248T>G c.(1246-1248)atT>atG p.I416M KIRC 10 103294568 103294568 + Missense_Mutation SNP T T G TCGA-B0-4697-01A-01D-1361-10 TCGA-B0-4697-11A-01D-1361-10 g.chr10:103294568T>G c.1248T>G c.(1246-1248)atT>atG p.I416M KIRP 10 103190124 103190124 + Nonsense_Mutation SNP G G A TCGA-UZ-A9PL-01A-11D-A382-10 TCGA-UZ-A9PL-10A-01D-A385-10 g.chr10:103190124G>A c.71G>A c.(70-72)tGg>tAg p.W24* KIRP 10 103294516 103294516 + Missense_Mutation SNP G G C TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr10:103294516G>C c.1196G>C c.(1195-1197)tGc>tCc p.C399S LGG 10 103281443 103281443 + Silent SNP G G A TCGA-E1-5307-01A-01D-1893-08 TCGA-E1-5307-10A-01D-1893-08 g.chr10:103281443G>A c.372G>A c.(370-372)cgG>cgA p.R124R LGG 10 103292718 103292718 + Frame_Shift_Del DEL A A - TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:103292718delA c.988delA c.(988-990)aaafs p.K330fs LIHC 10 103190119 103190119 + Silent SNP T T C TCGA-FV-A2QR-01A-11D-A20W-10 TCGA-FV-A2QR-11A-11D-A20W-10 g.chr10:103190119T>C c.66T>C c.(64-66)tcT>tcC p.S22S LIHC 10 103239157 103239157 + Missense_Mutation SNP C C G TCGA-DD-AAE6-01A-11D-A40R-10 TCGA-DD-AAE6-10A-01D-A40U-10 g.chr10:103239157C>G c.267C>G c.(265-267)aaC>aaG p.N89K LIHC 10 103281409 103281409 + Missense_Mutation SNP A A T TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr10:103281409A>T c.338A>T c.(337-339)aAt>aTt p.N113I LIHC 10 103285923 103285923 + Missense_Mutation SNP C C A TCGA-DD-AACY-01A-11D-A40R-10 TCGA-DD-AACY-10A-01D-A40U-10 g.chr10:103285923C>A c.710C>A c.(709-711)tCt>tAt p.S237Y LIHC 10 103292148 103292148 + Missense_Mutation SNP G G A TCGA-DD-AADP-01A-11D-A38X-10 TCGA-DD-AADP-10A-01D-A38X-10 g.chr10:103292148G>A c.937G>A c.(937-939)Gat>Aat p.D313N LIHC 10 103296339 103296339 + Missense_Mutation SNP A A T TCGA-DD-AACL-01A-11D-A40R-10 TCGA-DD-AACL-10A-01D-A40U-10 g.chr10:103296339A>T c.1506A>T c.(1504-1506)ttA>ttT p.L502F LUAD 10 103190180 103190180 + Missense_Mutation SNP C C T TCGA-69-8253-01A-11D-2284-08 TCGA-69-8253-10A-01D-2284-08 g.chr10:103190180C>T c.127C>T c.(127-129)Cca>Tca p.P43S LUAD 10 103190200 103190200 + Silent SNP A A T TCGA-97-7546-01A-11D-2036-08 TCGA-97-7546-10A-01D-2036-08 g.chr10:103190200A>T c.147A>T c.(145-147)acA>acT p.T49T LUAD 10 103221745 103221745 + Nonsense_Mutation SNP C C A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr10:103221745C>A c.164C>A c.(163-165)tCa>tAa p.S55* LUAD 10 103281468 103281468 + Missense_Mutation SNP G G A TCGA-73-4670-01A-01D-1265-08 TCGA-73-4670-11A-01D-1265-08 g.chr10:103281468G>A c.397G>A c.(397-399)Gaa>Aaa p.E133K LUAD 10 103285902 103285902 + Missense_Mutation SNP A A T TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chr10:103285902A>T c.689A>T c.(688-690)gAg>gTg p.E230V LUAD 10 103291028 103291028 + Missense_Mutation SNP G G T TCGA-64-1676-01A-01D-0969-08 TCGA-64-1676-10A-01D-0969-08 g.chr10:103291028G>T c.778G>T c.(778-780)Ggg>Tgg p.G260W LUAD 10 103292112 103292112 + Missense_Mutation SNP G G C TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr10:103292112G>C c.901G>C c.(901-903)Gaa>Caa p.E301Q LUAD 10 103292158 103292158 + Missense_Mutation SNP T T C TCGA-50-5941-01A-11D-1753-08 TCGA-50-5941-10A-01D-1753-08 g.chr10:103292158T>C c.947T>C c.(946-948)aTa>aCa p.I316T LUAD 10 103294514 103294514 + Silent SNP C C T TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr10:103294514C>T c.1194C>T c.(1192-1194)acC>acT p.T398T LUAD 10 103294633 103294633 + Missense_Mutation SNP A A T TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr10:103294633A>T c.1313A>T c.(1312-1314)tAc>tTc p.Y438F LUAD 10 103296383 103296383 + Missense_Mutation SNP A A T TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr10:103296383A>T c.1550A>T c.(1549-1551)aAg>aTg p.K517M LUAD 10 103298106 103298106 + Missense_Mutation SNP C C T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr10:103298106C>T c.1634C>T c.(1633-1635)aCa>aTa p.T545I LUAD 10 103310561 103310561 + Missense_Mutation SNP G G T TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr10:103310561G>T c.1762G>T c.(1762-1764)Gcc>Tcc p.A588S LUAD 10 103310589 103310589 + Missense_Mutation SNP C C T TCGA-50-5051-01A-21D-1855-08 TCGA-50-5051-10A-01D-1855-08 g.chr10:103310589C>T c.1790C>T c.(1789-1791)tCt>tTt p.S597F LUSC 10 103281516 103281516 + Nonsense_Mutation SNP C C T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr10:103281516C>T c.445C>T c.(445-447)Caa>Taa p.Q149* OV 10 103221777 103221777 + Missense_Mutation SNP C C T TCGA-13-0887-01A-01W-0421-09 TCGA-13-0887-10A-01W-0421-09 g.chr10:103221777C>T c.196C>T c.(196-198)Cct>Tct p.P66S PAAD 10 103239151 103239151 + Missense_Mutation SNP C C G TCGA-HZ-A8P1-01A-11D-A377-08 TCGA-HZ-A8P1-10A-01D-A37A-08 g.chr10:103239151C>G c.261C>G c.(259-261)tgC>tgG p.C87W PAAD 10 103285770 103285770 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:103285770C>A c.557C>A c.(556-558)gCt>gAt p.A186D PAAD 10 103292106 103292106 + Silent SNP C C A TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr10:103292106C>A c.895C>A c.(895-897)Cga>Aga p.R299R PRAD 10 103221813 103221813 + Nonsense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:103221813C>T c.232C>T c.(232-234)Cag>Tag p.Q78* PRAD 10 103292116 103292116 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:103292116C>T c.905C>T c.(904-906)aCa>aTa p.T302I PRAD 10 103294575 103294575 + Missense_Mutation SNP C C T TCGA-CH-5769-01A-11D-1576-08 TCGA-CH-5769-11A-01D-1576-08 g.chr10:103294575C>T c.1255C>T c.(1255-1257)Cgg>Tgg p.R419W READ 10 103221777 103221777 + Missense_Mutation SNP C C T TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr10:103221777C>T c.196C>T c.(196-198)Cct>Tct p.P66S READ 10 103285772 103285772 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:103285772C>T c.559C>T c.(559-561)Cgg>Tgg p.R187W READ 10 103294568 103294568 + Missense_Mutation SNP T T G TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr10:103294568T>G c.1248T>G c.(1246-1248)atT>atG p.I416M READ 10 103310477 103310477 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:103310477C>T c.1678C>T c.(1678-1680)Cga>Tga p.R560* SARC 10 103291028 103291028 + Missense_Mutation SNP G G A TCGA-DX-AB32-01A-11D-A417-09 TCGA-DX-AB32-10A-01D-A41A-09 g.chr10:103291028G>A c.778G>A c.(778-780)Ggg>Agg p.G260R SKCM 10 103281544 103281544 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr10:103281544C>T c.473C>T c.(472-474)tCc>tTc p.S158F SKCM 10 103292172 103292172 + Nonsense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr10:103292172C>T c.961C>T c.(961-963)Cga>Tga p.R321* SKCM 10 103292777 103292777 + Silent SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr10:103292777C>T c.1047C>T c.(1045-1047)ctC>ctT p.L349L SKCM 10 103292778 103292778 + Nonsense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr10:103292778C>T c.1048C>T c.(1048-1050)Cag>Tag p.Q350* SKCM 10 103294527 103294527 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:103294527C>T c.1207C>T c.(1207-1209)Cgt>Tgt p.R403C SKCM 10 103298056 103298056 + Silent SNP T T A TCGA-FS-A4F8-06A-11D-A25O-08 TCGA-FS-A4F8-10B-01D-A25O-08 g.chr10:103298056T>A c.1584T>A c.(1582-1584)atT>atA p.I528I SKCM 10 103310563 103310563 + Silent SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr10:103310563C>T c.1764C>T c.(1762-1764)gcC>gcT p.A588A SKCM 10 103310575 103310575 + Silent SNP C C T TCGA-FS-A1YY-06A-11D-A197-08 TCGA-FS-A1YY-10A-01D-A199-08 g.chr10:103310575C>T c.1776C>T c.(1774-1776)ccC>ccT p.P592P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 10 103291073 103291073 insertion of <=200bp - T frameshift_variant I234Y? AML-US 10 103291073 103291073 insertion of <=200bp - T frameshift_variant I239Y? AML-US 10 103291073 103291073 insertion of <=200bp - T frameshift_variant I275Y? AML-US 10 103291073 103291073 insertion of <=200bp - T upstream_gene_variant BOCA-FR 10 103112431 103112431 single base substitution A G upstream_gene_variant BOCA-FR 10 103187671 103187671 single base substitution A G intron_variant BOCA-FR 10 103315434 103315434 single base substitution A G 3_prime_UTR_variant BOCA-FR 10 103315434 103315434 single base substitution A G downstream_gene_variant BRCA-EU 10 103109185 103109185 single base substitution G A upstream_gene_variant BRCA-EU 10 103109653 103109653 single base substitution G A upstream_gene_variant BRCA-EU 10 103109783 103109783 single base substitution G A upstream_gene_variant BRCA-EU 10 103111328 103111328 single base substitution T G upstream_gene_variant BRCA-EU 10 103111513 103111513 single base substitution C G upstream_gene_variant BRCA-EU 10 103112007 103112007 single base substitution C G upstream_gene_variant BRCA-EU 10 103112673 103112673 single base substitution C A upstream_gene_variant BRCA-EU 10 103113770 103113770 single base substitution C G upstream_gene_variant BRCA-EU 10 103113988 103113988 single base substitution G A intron_variant BRCA-EU 10 103113988 103113988 single base substitution G A upstream_gene_variant BRCA-EU 10 103115682 103115682 single base substitution A G intron_variant BRCA-EU 10 103116520 103116520 single base substitution C T intron_variant BRCA-EU 10 103116753 103116753 single base substitution G C intron_variant BRCA-EU 10 103120245 103120245 single base substitution C G intron_variant BRCA-EU 10 103120452 103120452 single base substitution C G intron_variant BRCA-EU 10 103120485 103120485 single base substitution G T intron_variant BRCA-EU 10 103123676 103123676 single base substitution G A intron_variant BRCA-EU 10 103124814 103124814 single base substitution C G intron_variant BRCA-EU 10 103124955 103124955 single base substitution T C intron_variant BRCA-EU 10 103125244 103125244 single base substitution T C intron_variant BRCA-EU 10 103125464 103125464 single base substitution A G intron_variant BRCA-EU 10 103127280 103127280 single base substitution C T intron_variant BRCA-EU 10 103128859 103128859 single base substitution T A intron_variant BRCA-EU 10 103129466 103129466 single base substitution C T intron_variant BRCA-EU 10 103129731 103129731 single base substitution C T intron_variant BRCA-EU 10 103132268 103132268 single base substitution C T intron_variant BRCA-EU 10 103132329 103132329 single base substitution A G intron_variant BRCA-EU 10 103132849 103132849 single base substitution G A intron_variant BRCA-EU 10 103133614 103133614 single base substitution G C intron_variant BRCA-EU 10 103134060 103134060 single base substitution C G intron_variant BRCA-EU 10 103134483 103134483 single base substitution T C intron_variant BRCA-EU 10 103135389 103135389 single base substitution T C intron_variant BRCA-EU 10 103135821 103135821 single base substitution G A intron_variant BRCA-EU 10 103137706 103137706 deletion of <=200bp A - intron_variant BRCA-EU 10 103137758 103137758 single base substitution C A intron_variant BRCA-EU 10 103137820 103137820 single base substitution G A intron_variant BRCA-EU 10 103137936 103137936 single base substitution C G intron_variant BRCA-EU 10 103139749 103139753 multiple base substitution (>=2bp and <=200bp) TGCTG TCA intron_variant BRCA-EU 10 103139753 103139753 single base substitution G A intron_variant BRCA-EU 10 103140346 103140346 single base substitution A G intron_variant BRCA-EU 10 103141472 103141472 single base substitution C G intron_variant BRCA-EU 10 103141797 103141797 single base substitution T C intron_variant BRCA-EU 10 103142499 103142499 single base substitution C G intron_variant BRCA-EU 10 103143338 103143338 single base substitution C G intron_variant BRCA-EU 10 103144397 103144397 single base substitution T C intron_variant BRCA-EU 10 103146718 103146718 single base substitution A G intron_variant BRCA-EU 10 103147068 103147068 insertion of <=200bp - T intron_variant BRCA-EU 10 103148114 103148117 deletion of <=200bp TTTA - intron_variant BRCA-EU 10 103150877 103150877 single base substitution C T intron_variant BRCA-EU 10 103152733 103152733 single base substitution G C intron_variant BRCA-EU 10 103153279 103153279 single base substitution G A intron_variant BRCA-EU 10 103153919 103153919 deletion of <=200bp T - intron_variant BRCA-EU 10 103154200 103154200 single base substitution C T intron_variant BRCA-EU 10 103156642 103156642 single base substitution C G intron_variant BRCA-EU 10 103158714 103158714 single base substitution G T intron_variant BRCA-EU 10 103159993 103159993 single base substitution G A intron_variant BRCA-EU 10 103160251 103160251 single base substitution T A intron_variant BRCA-EU 10 103160379 103160379 single base substitution C A intron_variant BRCA-EU 10 103161394 103161394 single base substitution T A intron_variant BRCA-EU 10 103161431 103161431 single base substitution G T intron_variant BRCA-EU 10 103161482 103161482 single base substitution C T intron_variant BRCA-EU 10 103163347 103163347 deletion of <=200bp T - intron_variant BRCA-EU 10 103164386 103164386 single base substitution G A intron_variant BRCA-EU 10 103164477 103164477 single base substitution C T intron_variant BRCA-EU 10 103165359 103165359 single base substitution G T intron_variant BRCA-EU 10 103165420 103165420 single base substitution C T intron_variant BRCA-EU 10 103168345 103168345 single base substitution G A intron_variant BRCA-EU 10 103173979 103173979 single base substitution C T intron_variant BRCA-EU 10 103174472 103174472 single base substitution C T intron_variant BRCA-EU 10 103177113 103177113 single base substitution C T intron_variant BRCA-EU 10 103177543 103177543 single base substitution G A intron_variant BRCA-EU 10 103178125 103178125 deletion of <=200bp A - intron_variant BRCA-EU 10 103179281 103179281 single base substitution C G intron_variant BRCA-EU 10 103180669 103180669 insertion of <=200bp - A intron_variant BRCA-EU 10 103180735 103180735 single base substitution C A intron_variant BRCA-EU 10 103181573 103181573 single base substitution G A intron_variant BRCA-EU 10 103181753 103181753 single base substitution A G intron_variant BRCA-EU 10 103183167 103183167 single base substitution C A intron_variant BRCA-EU 10 103183480 103183480 single base substitution A G intron_variant BRCA-EU 10 103184658 103184658 single base substitution C G intron_variant BRCA-EU 10 103185579 103185579 single base substitution G A intron_variant BRCA-EU 10 103186297 103186297 single base substitution C G intron_variant BRCA-EU 10 103186746 103186746 single base substitution C G intron_variant BRCA-EU 10 103186997 103186997 single base substitution C T intron_variant BRCA-EU 10 103187744 103187744 insertion of <=200bp - A intron_variant BRCA-EU 10 103187974 103187974 single base substitution A T intron_variant BRCA-EU 10 103192097 103192097 single base substitution C G intron_variant BRCA-EU 10 103192110 103192110 single base substitution C T intron_variant BRCA-EU 10 103192118 103192118 single base substitution C G intron_variant BRCA-EU 10 103194713 103194713 single base substitution C G intron_variant BRCA-EU 10 103197078 103197078 single base substitution C T intron_variant BRCA-EU 10 103199279 103199279 single base substitution G A intron_variant BRCA-EU 10 103200201 103200201 single base substitution G A intron_variant BRCA-EU 10 103201762 103201762 single base substitution T G intron_variant BRCA-EU 10 103202214 103202214 single base substitution C G intron_variant BRCA-EU 10 103202825 103202825 single base substitution G C intron_variant BRCA-EU 10 103203251 103203251 single base substitution C A intron_variant BRCA-EU 10 103203390 103203390 single base substitution A G intron_variant BRCA-EU 10 103204060 103204060 single base substitution C G intron_variant BRCA-EU 10 103209309 103209309 insertion of <=200bp - A intron_variant BRCA-EU 10 103210295 103210295 single base substitution A G intron_variant BRCA-EU 10 103211626 103211626 single base substitution C A intron_variant BRCA-EU 10 103212766 103212766 deletion of <=200bp T - intron_variant BRCA-EU 10 103213707 103213707 single base substitution G T intron_variant BRCA-EU 10 103216114 103216114 single base substitution C G intron_variant BRCA-EU 10 103216600 103216600 single base substitution A G intron_variant BRCA-EU 10 103216916 103216916 single base substitution T G intron_variant BRCA-EU 10 103219381 103219381 single base substitution A T intron_variant BRCA-EU 10 103219866 103219866 single base substitution G A intron_variant BRCA-EU 10 103222528 103222528 single base substitution A T intron_variant BRCA-EU 10 103223509 103223509 single base substitution G C intron_variant BRCA-EU 10 103223604 103223604 single base substitution A T intron_variant BRCA-EU 10 103226730 103226730 single base substitution G C intron_variant BRCA-EU 10 103227863 103227863 single base substitution C T intron_variant BRCA-EU 10 103229464 103229464 single base substitution T C intron_variant BRCA-EU 10 103230702 103230702 single base substitution C A intron_variant BRCA-EU 10 103236644 103236644 single base substitution G A intron_variant BRCA-EU 10 103237010 103237010 single base substitution C T intron_variant BRCA-EU 10 103238597 103238597 single base substitution G A intron_variant BRCA-EU 10 103239498 103239498 single base substitution G A intron_variant BRCA-EU 10 103241785 103241785 deletion of <=200bp T - intron_variant BRCA-EU 10 103241785 103241785 insertion of <=200bp - T intron_variant BRCA-EU 10 103247065 103247065 single base substitution G C intron_variant BRCA-EU 10 103249770 103249770 single base substitution C T intron_variant BRCA-EU 10 103249842 103249842 single base substitution A C intron_variant BRCA-EU 10 103250909 103250909 single base substitution C G intron_variant BRCA-EU 10 103251729 103251729 single base substitution T G intron_variant BRCA-EU 10 103252973 103252973 single base substitution G A intron_variant BRCA-EU 10 103254270 103254270 single base substitution C T intron_variant BRCA-EU 10 103254996 103254996 single base substitution G T intron_variant BRCA-EU 10 103255234 103255235 deletion of <=200bp TG - intron_variant BRCA-EU 10 103258491 103258494 multiple base substitution (>=2bp and <=200bp) TATT TA intron_variant BRCA-EU 10 103258495 103258495 single base substitution C A intron_variant BRCA-EU 10 103260050 103260050 single base substitution T G intron_variant BRCA-EU 10 103260854 103260854 single base substitution G A intron_variant BRCA-EU 10 103260928 103260928 single base substitution G C intron_variant BRCA-EU 10 103261097 103261097 single base substitution G C intron_variant BRCA-EU 10 103264041 103264041 single base substitution C T intron_variant BRCA-EU 10 103265061 103265061 single base substitution G T intron_variant BRCA-EU 10 103265070 103265070 single base substitution T G intron_variant BRCA-EU 10 103265155 103265155 single base substitution T C intron_variant BRCA-EU 10 103265752 103265752 single base substitution A G intron_variant BRCA-EU 10 103266953 103266953 single base substitution A T intron_variant BRCA-EU 10 103267380 103267380 single base substitution T A intron_variant BRCA-EU 10 103269313 103269313 single base substitution T G intron_variant BRCA-EU 10 103271793 103271793 single base substitution C G intron_variant BRCA-EU 10 103272041 103272041 deletion of <=200bp C - intron_variant BRCA-EU 10 103276227 103276227 single base substitution G C intron_variant BRCA-EU 10 103277299 103277299 single base substitution G T intron_variant BRCA-EU 10 103278045 103278045 single base substitution A G intron_variant BRCA-EU 10 103278177 103278177 single base substitution C G intron_variant BRCA-EU 10 103278535 103278535 single base substitution G A intron_variant BRCA-EU 10 103279065 103279065 single base substitution G C intron_variant BRCA-EU 10 103280437 103280437 single base substitution G A intron_variant BRCA-EU 10 103280856 103280856 single base substitution C G intron_variant BRCA-EU 10 103280862 103280862 deletion of <=200bp A - intron_variant BRCA-EU 10 103281537 103281537 single base substitution C G downstream_gene_variant BRCA-EU 10 103281537 103281537 single base substitution C G exon_variant BRCA-EU 10 103281537 103281537 single base substitution C G missense_variant L115V 343C>G BRCA-EU 10 103281537 103281537 single base substitution C G missense_variant L120V 358C>G BRCA-EU 10 103281537 103281537 single base substitution C G missense_variant L138V 412C>G BRCA-EU 10 103281537 103281537 single base substitution C G missense_variant L156V 466C>G BRCA-EU 10 103285793 103285793 single base substitution G C downstream_gene_variant BRCA-EU 10 103285793 103285793 single base substitution G C exon_variant BRCA-EU 10 103285793 103285793 single base substitution G C missense_variant E153Q 457G>C BRCA-EU 10 103285793 103285793 single base substitution G C missense_variant E158Q 472G>C BRCA-EU 10 103285793 103285793 single base substitution G C missense_variant E176Q 526G>C BRCA-EU 10 103285793 103285793 single base substitution G C missense_variant E194Q 580G>C BRCA-EU 10 103288547 103288547 single base substitution A G downstream_gene_variant BRCA-EU 10 103288547 103288547 single base substitution A G intron_variant BRCA-EU 10 103290654 103290654 single base substitution G C downstream_gene_variant BRCA-EU 10 103290654 103290654 single base substitution G C intron_variant BRCA-EU 10 103290654 103290654 single base substitution G C upstream_gene_variant BRCA-EU 10 103290705 103290705 single base substitution G A downstream_gene_variant BRCA-EU 10 103290705 103290705 single base substitution G A intron_variant BRCA-EU 10 103290705 103290705 single base substitution G A upstream_gene_variant BRCA-EU 10 103291326 103291326 single base substitution A G intron_variant BRCA-EU 10 103291326 103291326 single base substitution A G upstream_gene_variant BRCA-EU 10 103291920 103291920 deletion of <=200bp T - intron_variant BRCA-EU 10 103291920 103291920 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 103292565 103292565 single base substitution G T intron_variant BRCA-EU 10 103292565 103292565 single base substitution G T upstream_gene_variant BRCA-EU 10 103292566 103292566 single base substitution C T intron_variant BRCA-EU 10 103292566 103292566 single base substitution C T upstream_gene_variant BRCA-EU 10 103295056 103295056 single base substitution A T intron_variant BRCA-EU 10 103295056 103295056 single base substitution A T upstream_gene_variant BRCA-EU 10 103295130 103295130 single base substitution G C missense_variant C415S 1244G>C BRCA-EU 10 103295130 103295130 single base substitution G C missense_variant C420S 1259G>C BRCA-EU 10 103295130 103295130 single base substitution G C missense_variant C456S 1367G>C BRCA-EU 10 103295130 103295130 single base substitution G C upstream_gene_variant BRCA-EU 10 103297112 103297112 single base substitution C A intron_variant BRCA-EU 10 103300439 103300439 single base substitution G T intron_variant BRCA-EU 10 103300896 103300896 single base substitution A G intron_variant BRCA-EU 10 103301117 103301117 single base substitution C T intron_variant BRCA-EU 10 103301494 103301494 deletion of <=200bp T - intron_variant BRCA-EU 10 103302187 103302187 single base substitution C T intron_variant BRCA-EU 10 103302506 103302506 deletion of <=200bp T - intron_variant BRCA-EU 10 103305460 103305460 single base substitution A G intron_variant BRCA-EU 10 103308347 103308347 single base substitution A G intron_variant BRCA-EU 10 103308549 103308549 single base substitution G C intron_variant BRCA-EU 10 103308743 103308743 single base substitution G C intron_variant BRCA-EU 10 103310775 103310775 single base substitution G C exon_variant BRCA-EU 10 103310775 103310775 single base substitution G C intron_variant BRCA-EU 10 103313803 103313803 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 103313803 103313803 single base substitution G A downstream_gene_variant BRCA-EU 10 103316521 103316521 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 103317663 103317663 single base substitution C T downstream_gene_variant BRCA-EU 10 103318032 103318032 single base substitution A G downstream_gene_variant BRCA-EU 10 103318231 103318231 single base substitution G A downstream_gene_variant BRCA-EU 10 103320497 103320497 single base substitution C G downstream_gene_variant BRCA-EU 10 103320785 103320785 single base substitution G T downstream_gene_variant BRCA-FR 10 103120452 103120452 single base substitution C G intron_variant BRCA-FR 10 103123676 103123676 single base substitution G A intron_variant BRCA-FR 10 103142499 103142499 single base substitution C G intron_variant BRCA-FR 10 103152879 103152879 single base substitution C G intron_variant BRCA-FR 10 103156642 103156642 single base substitution C G intron_variant BRCA-FR 10 103160251 103160251 single base substitution T A intron_variant BRCA-FR 10 103165420 103165420 single base substitution C T intron_variant BRCA-FR 10 103174472 103174472 single base substitution C T intron_variant BRCA-FR 10 103197078 103197078 single base substitution C T intron_variant BRCA-FR 10 103198316 103198316 single base substitution T C intron_variant BRCA-FR 10 103201762 103201762 single base substitution T G intron_variant BRCA-FR 10 103211076 103211076 single base substitution C T intron_variant BRCA-FR 10 103227863 103227863 single base substitution C T intron_variant BRCA-FR 10 103229988 103229988 single base substitution C T intron_variant BRCA-FR 10 103230395 103230395 single base substitution C A intron_variant BRCA-FR 10 103234324 103234324 single base substitution G A intron_variant BRCA-FR 10 103238597 103238597 single base substitution G A intron_variant BRCA-FR 10 103240468 103240468 single base substitution C G intron_variant BRCA-FR 10 103250909 103250909 single base substitution C G intron_variant BRCA-FR 10 103279065 103279065 single base substitution G C intron_variant BRCA-FR 10 103285793 103285793 single base substitution G C downstream_gene_variant BRCA-FR 10 103285793 103285793 single base substitution G C exon_variant BRCA-FR 10 103285793 103285793 single base substitution G C missense_variant E153Q 457G>C BRCA-FR 10 103285793 103285793 single base substitution G C missense_variant E158Q 472G>C BRCA-FR 10 103285793 103285793 single base substitution G C missense_variant E176Q 526G>C BRCA-FR 10 103285793 103285793 single base substitution G C missense_variant E194Q 580G>C BRCA-FR 10 103290654 103290654 single base substitution G C downstream_gene_variant BRCA-FR 10 103290654 103290654 single base substitution G C intron_variant BRCA-FR 10 103290654 103290654 single base substitution G C upstream_gene_variant BRCA-FR 10 103296447 103296447 single base substitution T A intron_variant BRCA-FR 10 103313317 103313317 single base substitution G A 3_prime_UTR_variant BRCA-FR 10 103313317 103313317 single base substitution G A downstream_gene_variant BRCA-FR 10 103316521 103316521 single base substitution C G 3_prime_UTR_variant BRCA-FR 10 103320497 103320497 single base substitution C G downstream_gene_variant BRCA-UK 10 103111513 103111513 single base substitution C G upstream_gene_variant BRCA-UK 10 103148935 103148935 single base substitution C T intron_variant BRCA-UK 10 103173025 103173025 single base substitution T C intron_variant BRCA-UK 10 103192384 103192384 single base substitution G C intron_variant BRCA-US 10 103190166 103190166 single base substitution G A exon_variant BRCA-US 10 103190166 103190166 single base substitution G A intron_variant BRCA-US 10 103190166 103190166 single base substitution G A missense_variant R20Q 59G>A BRCA-US 10 103190166 103190166 single base substitution G A missense_variant R23Q 68G>A BRCA-US 10 103190166 103190166 single base substitution G A missense_variant R38Q 113G>A BRCA-US 10 103285793 103285793 single base substitution G C downstream_gene_variant BRCA-US 10 103285793 103285793 single base substitution G C exon_variant BRCA-US 10 103285793 103285793 single base substitution G C missense_variant E153Q 457G>C BRCA-US 10 103285793 103285793 single base substitution G C missense_variant E158Q 472G>C BRCA-US 10 103285793 103285793 single base substitution G C missense_variant E176Q 526G>C BRCA-US 10 103285793 103285793 single base substitution G C missense_variant E194Q 580G>C BRCA-US 10 103292145 103292145 single base substitution G A missense_variant D271N 811G>A BRCA-US 10 103292145 103292145 single base substitution G A missense_variant D276N 826G>A BRCA-US 10 103292145 103292145 single base substitution G A missense_variant D312N 934G>A BRCA-US 10 103292145 103292145 single base substitution G A upstream_gene_variant BRCA-US 10 103295142 103295142 single base substitution G C exon_variant BRCA-US 10 103295142 103295142 single base substitution G C missense_variant R419T 1256G>C BRCA-US 10 103295142 103295142 single base substitution G C missense_variant R424T 1271G>C BRCA-US 10 103295142 103295142 single base substitution G C missense_variant R460T 1379G>C BRCA-US 10 103295203 103295203 single base substitution G C exon_variant BRCA-US 10 103295203 103295203 single base substitution G C synonymous_variant V439V 1317G>C BRCA-US 10 103295203 103295203 single base substitution G C synonymous_variant V444V 1332G>C BRCA-US 10 103295203 103295203 single base substitution G C synonymous_variant V480V 1440G>C BTCA-JP 10 103310654 103310654 single base substitution G A exon_variant BTCA-JP 10 103310654 103310654 single base substitution G A splice_region_variant CESC-US 10 103190136 103190136 single base substitution C G exon_variant CESC-US 10 103190136 103190136 single base substitution C G intron_variant CESC-US 10 103190136 103190136 single base substitution C G missense_variant S10C 29C>G CESC-US 10 103190136 103190136 single base substitution C G missense_variant S13C 38C>G CESC-US 10 103190136 103190136 single base substitution C G missense_variant S28C 83C>G CLLE-ES 10 103109046 103109046 single base substitution G C upstream_gene_variant CLLE-ES 10 103136305 103136305 single base substitution A C intron_variant CLLE-ES 10 103136448 103136448 single base substitution A G intron_variant CLLE-ES 10 103136523 103136523 single base substitution T C intron_variant CLLE-ES 10 103136561 103136561 single base substitution A G intron_variant CLLE-ES 10 103147248 103147248 single base substitution T C intron_variant CLLE-ES 10 103173498 103173498 single base substitution T C intron_variant CLLE-ES 10 103217384 103217384 single base substitution T A intron_variant CLLE-ES 10 103238949 103238949 single base substitution G T intron_variant CLLE-ES 10 103284392 103284392 single base substitution G A downstream_gene_variant CLLE-ES 10 103284392 103284392 single base substitution G A intron_variant CLLE-ES 10 103320583 103320583 single base substitution C T downstream_gene_variant COAD-US 10 103285923 103285923 single base substitution C T downstream_gene_variant COAD-US 10 103285923 103285923 single base substitution C T exon_variant COAD-US 10 103285923 103285923 single base substitution C T missense_variant S196F 587C>T COAD-US 10 103285923 103285923 single base substitution C T missense_variant S201F 602C>T COAD-US 10 103285923 103285923 single base substitution C T missense_variant S237F 710C>T COAD-US 10 103291027 103291027 single base substitution C T synonymous_variant D218D 654C>T COAD-US 10 103291027 103291027 single base substitution C T synonymous_variant D223D 669C>T COAD-US 10 103291027 103291027 single base substitution C T synonymous_variant D259D 777C>T COAD-US 10 103291027 103291027 single base substitution C T upstream_gene_variant COAD-US 10 103291060 103291060 single base substitution A C synonymous_variant A229A 687A>C COAD-US 10 103291060 103291060 single base substitution A C synonymous_variant A234A 702A>C COAD-US 10 103291060 103291060 single base substitution A C synonymous_variant A270A 810A>C COAD-US 10 103291060 103291060 single base substitution A C upstream_gene_variant COAD-US 10 103295137 103295137 single base substitution T G missense_variant F417L 1251T>G COAD-US 10 103295137 103295137 single base substitution T G missense_variant F422L 1266T>G COAD-US 10 103295137 103295137 single base substitution T G missense_variant F458L 1374T>G COAD-US 10 103295137 103295137 single base substitution T G upstream_gene_variant COAD-US 10 103296370 103296370 single base substitution C T exon_variant COAD-US 10 103296370 103296370 single base substitution C T stop_gained R472* 1414C>T COAD-US 10 103296370 103296370 single base substitution C T stop_gained R477* 1429C>T COAD-US 10 103296370 103296370 single base substitution C T stop_gained R513* 1537C>T COAD-US 10 103296399 103296399 single base substitution G T exon_variant COAD-US 10 103296399 103296399 single base substitution G T synonymous_variant G481G 1443G>T COAD-US 10 103296399 103296399 single base substitution G T synonymous_variant G486G 1458G>T COAD-US 10 103296399 103296399 single base substitution G T synonymous_variant G522G 1566G>T COAD-US 10 103310573 103310573 deletion of <=200bp C - exon_variant COAD-US 10 103310573 103310573 deletion of <=200bp C - frameshift_variant P551 COAD-US 10 103310573 103310573 deletion of <=200bp C - frameshift_variant P556 COAD-US 10 103310573 103310573 deletion of <=200bp C - frameshift_variant P592 COCA-CN 10 103112148 103112148 single base substitution A C upstream_gene_variant COCA-CN 10 103118029 103118029 single base substitution T C intron_variant COCA-CN 10 103127435 103127435 single base substitution G A intron_variant COCA-CN 10 103143155 103143155 single base substitution A T intron_variant COCA-CN 10 103156326 103156326 single base substitution A C intron_variant COCA-CN 10 103187153 103187153 single base substitution G T intron_variant COCA-CN 10 103190024 103190024 single base substitution G A intron_variant COCA-CN 10 103190074 103190074 single base substitution C A intron_variant COCA-CN 10 103190099 103190099 single base substitution C T intron_variant COCA-CN 10 103190099 103190099 single base substitution C T splice_region_variant COCA-CN 10 103201582 103201582 single base substitution C G intron_variant COCA-CN 10 103215740 103215740 single base substitution A C intron_variant COCA-CN 10 103232029 103232029 single base substitution T C intron_variant COCA-CN 10 103232032 103232032 single base substitution C T intron_variant COCA-CN 10 103236946 103236946 single base substitution C T intron_variant COCA-CN 10 103239081 103239081 single base substitution T G intron_variant COCA-CN 10 103239115 103239115 single base substitution C A intron_variant COCA-CN 10 103285923 103285923 single base substitution C A downstream_gene_variant COCA-CN 10 103285923 103285923 single base substitution C A exon_variant COCA-CN 10 103285923 103285923 single base substitution C A missense_variant S196Y 587C>A COCA-CN 10 103285923 103285923 single base substitution C A missense_variant S201Y 602C>A COCA-CN 10 103285923 103285923 single base substitution C A missense_variant S237Y 710C>A COCA-CN 10 103287545 103287545 single base substitution T A downstream_gene_variant COCA-CN 10 103287545 103287545 single base substitution T A intron_variant COCA-CN 10 103287547 103287547 single base substitution T A downstream_gene_variant COCA-CN 10 103287547 103287547 single base substitution T A intron_variant COCA-CN 10 103287548 103287548 single base substitution C T downstream_gene_variant COCA-CN 10 103287548 103287548 single base substitution C T intron_variant COCA-CN 10 103291009 103291009 single base substitution C A missense_variant F212L 636C>A COCA-CN 10 103291009 103291009 single base substitution C A missense_variant F217L 651C>A COCA-CN 10 103291009 103291009 single base substitution C A missense_variant F253L 759C>A COCA-CN 10 103291009 103291009 single base substitution C A upstream_gene_variant COCA-CN 10 103292550 103292550 single base substitution C T intron_variant COCA-CN 10 103292550 103292550 single base substitution C T upstream_gene_variant COCA-CN 10 103294405 103294405 single base substitution C A intron_variant COCA-CN 10 103294405 103294405 single base substitution C A upstream_gene_variant COCA-CN 10 103295067 103295067 single base substitution A T intron_variant COCA-CN 10 103295067 103295067 single base substitution A T upstream_gene_variant COCA-CN 10 103298179 103298179 single base substitution T G intron_variant COCA-CN 10 103303221 103303221 single base substitution G T intron_variant COCA-CN 10 103311559 103311559 single base substitution C T downstream_gene_variant COCA-CN 10 103311559 103311559 single base substitution C T intron_variant EOPC-DE 10 103145984 103145984 single base substitution A C intron_variant EOPC-DE 10 103178269 103178269 single base substitution T G intron_variant EOPC-DE 10 103259585 103259585 single base substitution A T intron_variant EOPC-DE 10 103264792 103264792 single base substitution G A intron_variant EOPC-DE 10 103269307 103269307 single base substitution A G intron_variant EOPC-DE 10 103269314 103269314 single base substitution T C intron_variant EOPC-DE 10 103312037 103312037 single base substitution C T downstream_gene_variant EOPC-DE 10 103312037 103312037 single base substitution C T intron_variant EOPC-DE 10 103320050 103320050 single base substitution C T downstream_gene_variant ESAD-UK 10 103108866 103108866 single base substitution G T upstream_gene_variant ESAD-UK 10 103112051 103112051 single base substitution G T upstream_gene_variant ESAD-UK 10 103112392 103112392 single base substitution T A upstream_gene_variant ESAD-UK 10 103112635 103112635 single base substitution G T upstream_gene_variant ESAD-UK 10 103112690 103112690 single base substitution G A upstream_gene_variant ESAD-UK 10 103113329 103113329 single base substitution C T upstream_gene_variant ESAD-UK 10 103116148 103116148 single base substitution C T intron_variant ESAD-UK 10 103118344 103118344 deletion of <=200bp A - intron_variant ESAD-UK 10 103118825 103118825 single base substitution C T intron_variant ESAD-UK 10 103123685 103123685 single base substitution C T intron_variant ESAD-UK 10 103128979 103128979 single base substitution T A intron_variant ESAD-UK 10 103130478 103130478 single base substitution A T intron_variant ESAD-UK 10 103140334 103140334 single base substitution C T intron_variant ESAD-UK 10 103141054 103141054 insertion of <=200bp - T intron_variant ESAD-UK 10 103141900 103141900 single base substitution C T intron_variant ESAD-UK 10 103142294 103142294 single base substitution T C intron_variant ESAD-UK 10 103142756 103142756 single base substitution T A intron_variant ESAD-UK 10 103143369 103143369 single base substitution G A intron_variant ESAD-UK 10 103143999 103143999 single base substitution G A intron_variant ESAD-UK 10 103144981 103144981 single base substitution G A intron_variant ESAD-UK 10 103146719 103146719 single base substitution C T intron_variant ESAD-UK 10 103150807 103150807 single base substitution C G intron_variant ESAD-UK 10 103155252 103155252 single base substitution C T intron_variant ESAD-UK 10 103155922 103155922 deletion of <=200bp A - intron_variant ESAD-UK 10 103157525 103157525 single base substitution T C intron_variant ESAD-UK 10 103160479 103160479 single base substitution T G intron_variant ESAD-UK 10 103160601 103160601 single base substitution C G intron_variant ESAD-UK 10 103161500 103161500 single base substitution C T intron_variant ESAD-UK 10 103163472 103163472 single base substitution C G intron_variant ESAD-UK 10 103165466 103165466 single base substitution C T intron_variant ESAD-UK 10 103169530 103169530 single base substitution A C intron_variant ESAD-UK 10 103169973 103169973 single base substitution C T intron_variant ESAD-UK 10 103173063 103173063 single base substitution G A intron_variant ESAD-UK 10 103173912 103173912 single base substitution C G intron_variant ESAD-UK 10 103174025 103174025 single base substitution G A intron_variant ESAD-UK 10 103174215 103174215 single base substitution G C intron_variant ESAD-UK 10 103179232 103179232 single base substitution G T intron_variant ESAD-UK 10 103179577 103179577 single base substitution T C intron_variant ESAD-UK 10 103180881 103180881 single base substitution A G intron_variant ESAD-UK 10 103184909 103184909 single base substitution A T intron_variant ESAD-UK 10 103189448 103189448 deletion of <=200bp C - intron_variant ESAD-UK 10 103189455 103189455 deletion of <=200bp C - intron_variant ESAD-UK 10 103189903 103189903 single base substitution C A intron_variant ESAD-UK 10 103194781 103194781 single base substitution G A intron_variant ESAD-UK 10 103195126 103195126 single base substitution C T intron_variant ESAD-UK 10 103195367 103195367 single base substitution G A intron_variant ESAD-UK 10 103195476 103195476 single base substitution G C intron_variant ESAD-UK 10 103196177 103196177 single base substitution G A intron_variant ESAD-UK 10 103202415 103202415 single base substitution C T intron_variant ESAD-UK 10 103203306 103203306 single base substitution C T intron_variant ESAD-UK 10 103203919 103203919 single base substitution C T intron_variant ESAD-UK 10 103204171 103204171 single base substitution T A intron_variant ESAD-UK 10 103206759 103206759 deletion of <=200bp G - intron_variant ESAD-UK 10 103207680 103207680 deletion of <=200bp A - intron_variant ESAD-UK 10 103207847 103207847 single base substitution A G intron_variant ESAD-UK 10 103209873 103209873 single base substitution G A intron_variant ESAD-UK 10 103210251 103210251 single base substitution T C intron_variant ESAD-UK 10 103211100 103211100 single base substitution T G intron_variant ESAD-UK 10 103211399 103211399 deletion of <=200bp T - intron_variant ESAD-UK 10 103211481 103211481 single base substitution G C intron_variant ESAD-UK 10 103211808 103211808 single base substitution A T intron_variant ESAD-UK 10 103214762 103214762 single base substitution C T intron_variant ESAD-UK 10 103215840 103215840 single base substitution A T intron_variant ESAD-UK 10 103217240 103217240 single base substitution T G intron_variant ESAD-UK 10 103217795 103217795 deletion of <=200bp C - intron_variant ESAD-UK 10 103218148 103218148 single base substitution G T intron_variant ESAD-UK 10 103223713 103223713 single base substitution A C intron_variant ESAD-UK 10 103224528 103224528 single base substitution T G intron_variant ESAD-UK 10 103224761 103224761 deletion of <=200bp T - intron_variant ESAD-UK 10 103228354 103228354 single base substitution T C intron_variant ESAD-UK 10 103229621 103229621 single base substitution C T intron_variant ESAD-UK 10 103230129 103230129 single base substitution G A intron_variant ESAD-UK 10 103233344 103233344 single base substitution C T intron_variant ESAD-UK 10 103234934 103234934 single base substitution T A intron_variant ESAD-UK 10 103235112 103235112 single base substitution C T intron_variant ESAD-UK 10 103236766 103236766 single base substitution C T intron_variant ESAD-UK 10 103241317 103241317 insertion of <=200bp - GT intron_variant ESAD-UK 10 103241319 103241319 single base substitution T G intron_variant ESAD-UK 10 103250200 103250200 single base substitution G A intron_variant ESAD-UK 10 103251897 103251897 single base substitution G A intron_variant ESAD-UK 10 103252224 103252224 single base substitution G A intron_variant ESAD-UK 10 103252352 103252352 single base substitution T C intron_variant ESAD-UK 10 103256851 103256851 single base substitution G A intron_variant ESAD-UK 10 103257723 103257723 single base substitution G A intron_variant ESAD-UK 10 103260781 103260781 single base substitution G A intron_variant ESAD-UK 10 103261522 103261522 single base substitution A G intron_variant ESAD-UK 10 103263851 103263851 single base substitution C G intron_variant ESAD-UK 10 103264229 103264229 single base substitution C T intron_variant ESAD-UK 10 103264431 103264431 single base substitution C A intron_variant ESAD-UK 10 103267737 103267737 single base substitution T G intron_variant ESAD-UK 10 103269783 103269783 single base substitution C T intron_variant ESAD-UK 10 103269954 103269954 single base substitution G A intron_variant ESAD-UK 10 103272158 103272158 single base substitution G C intron_variant ESAD-UK 10 103276064 103276064 single base substitution G C intron_variant ESAD-UK 10 103276072 103276072 single base substitution G A intron_variant ESAD-UK 10 103276612 103276612 single base substitution C T intron_variant ESAD-UK 10 103277327 103277327 single base substitution C T intron_variant ESAD-UK 10 103279223 103279223 single base substitution G A intron_variant ESAD-UK 10 103280628 103280628 single base substitution C T intron_variant ESAD-UK 10 103280698 103280698 single base substitution C T intron_variant ESAD-UK 10 103282672 103282672 single base substitution C T downstream_gene_variant ESAD-UK 10 103282672 103282672 single base substitution C T intron_variant ESAD-UK 10 103289414 103289414 single base substitution T C downstream_gene_variant ESAD-UK 10 103289414 103289414 single base substitution T C intron_variant ESAD-UK 10 103292601 103292601 single base substitution T C intron_variant ESAD-UK 10 103292601 103292601 single base substitution T C upstream_gene_variant ESAD-UK 10 103296208 103296208 insertion of <=200bp - C intron_variant ESAD-UK 10 103296208 103296208 single base substitution A T intron_variant ESAD-UK 10 103296214 103296214 single base substitution A G intron_variant ESAD-UK 10 103299473 103299473 single base substitution G T intron_variant ESAD-UK 10 103299997 103299997 single base substitution A C intron_variant ESAD-UK 10 103300026 103300026 single base substitution T C intron_variant ESAD-UK 10 103304132 103304132 single base substitution C A intron_variant ESAD-UK 10 103304587 103304587 single base substitution G A intron_variant ESAD-UK 10 103306610 103306610 single base substitution T G intron_variant ESAD-UK 10 103307878 103307878 single base substitution C T intron_variant ESAD-UK 10 103309615 103309615 single base substitution G C intron_variant ESAD-UK 10 103311911 103311911 deletion of <=200bp T - downstream_gene_variant ESAD-UK 10 103311911 103311911 deletion of <=200bp T - intron_variant ESAD-UK 10 103312037 103312037 single base substitution C G downstream_gene_variant ESAD-UK 10 103312037 103312037 single base substitution C G intron_variant ESAD-UK 10 103312442 103312442 single base substitution T C downstream_gene_variant ESAD-UK 10 103312442 103312442 single base substitution T C intron_variant ESAD-UK 10 103315016 103315016 single base substitution A C 3_prime_UTR_variant ESAD-UK 10 103315016 103315016 single base substitution A C downstream_gene_variant ESAD-UK 10 103315530 103315530 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 103315530 103315530 single base substitution G A downstream_gene_variant ESAD-UK 10 103316781 103316781 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 103317064 103317064 single base substitution A G 3_prime_UTR_variant ESAD-UK 10 103317064 103317064 single base substitution A G downstream_gene_variant ESAD-UK 10 103319054 103319054 single base substitution C T downstream_gene_variant ESAD-UK 10 103321001 103321001 single base substitution G A downstream_gene_variant ESCA-CN 10 103296359 103296359 single base substitution T C exon_variant ESCA-CN 10 103296359 103296359 single base substitution T C missense_variant V468A 1403T>C ESCA-CN 10 103296359 103296359 single base substitution T C missense_variant V473A 1418T>C ESCA-CN 10 103296359 103296359 single base substitution T C missense_variant V509A 1526T>C GACA-CN 10 103281496 103281496 single base substitution A G downstream_gene_variant GACA-CN 10 103281496 103281496 single base substitution A G exon_variant GACA-CN 10 103281496 103281496 single base substitution A G missense_variant E101G 302A>G GACA-CN 10 103281496 103281496 single base substitution A G missense_variant E106G 317A>G GACA-CN 10 103281496 103281496 single base substitution A G missense_variant E124G 371A>G GACA-CN 10 103281496 103281496 single base substitution A G missense_variant E142G 425A>G GBM-US 10 103190197 103190197 single base substitution C T exon_variant GBM-US 10 103190197 103190197 single base substitution C T intron_variant GBM-US 10 103190197 103190197 single base substitution C T synonymous_variant L30L 90C>T GBM-US 10 103190197 103190197 single base substitution C T synonymous_variant L33L 99C>T GBM-US 10 103190197 103190197 single base substitution C T synonymous_variant L48L 144C>T GBM-US 10 103281492 103281492 single base substitution T G downstream_gene_variant GBM-US 10 103281492 103281492 single base substitution T G exon_variant GBM-US 10 103281492 103281492 single base substitution T G missense_variant F100V 298T>G GBM-US 10 103281492 103281492 single base substitution T G missense_variant F105V 313T>G GBM-US 10 103281492 103281492 single base substitution T G missense_variant F123V 367T>G GBM-US 10 103281492 103281492 single base substitution T G missense_variant F141V 421T>G KIRC-US 10 103294568 103294568 single base substitution T G missense_variant I375M 1125T>G KIRC-US 10 103294568 103294568 single base substitution T G missense_variant I380M 1140T>G KIRC-US 10 103294568 103294568 single base substitution T G missense_variant I416M 1248T>G KIRC-US 10 103294568 103294568 single base substitution T G upstream_gene_variant LAML-KR 10 103166534 103166534 single base substitution A G intron_variant LAML-KR 10 103166549 103166549 single base substitution G C intron_variant LAML-KR 10 103232027 103232027 single base substitution T C intron_variant LAML-KR 10 103246220 103246220 single base substitution T A intron_variant LAML-KR 10 103281676 103281676 single base substitution G A downstream_gene_variant LAML-KR 10 103281676 103281676 single base substitution G A intron_variant LAML-KR 10 103285904 103285904 single base substitution A G downstream_gene_variant LAML-KR 10 103285904 103285904 single base substitution A G exon_variant LAML-KR 10 103285904 103285904 single base substitution A G missense_variant R190G 568A>G LAML-KR 10 103285904 103285904 single base substitution A G missense_variant R195G 583A>G LAML-KR 10 103285904 103285904 single base substitution A G missense_variant R231G 691A>G LGG-US 10 103281443 103281443 single base substitution G A exon_variant LGG-US 10 103281443 103281443 single base substitution G A synonymous_variant R106R 318G>A LGG-US 10 103281443 103281443 single base substitution G A synonymous_variant R124R 372G>A LGG-US 10 103281443 103281443 single base substitution G A synonymous_variant R83R 249G>A LGG-US 10 103281443 103281443 single base substitution G A synonymous_variant R88R 264G>A LICA-CN 10 103190165 103190165 single base substitution C T exon_variant LICA-CN 10 103190165 103190165 single base substitution C T intron_variant LICA-CN 10 103190165 103190165 single base substitution C T stop_gained R20* 58C>T LICA-CN 10 103190165 103190165 single base substitution C T stop_gained R23* 67C>T LICA-CN 10 103190165 103190165 single base substitution C T stop_gained R38* 112C>T LICA-CN 10 103292734 103292734 single base substitution G C missense_variant C294S 881G>C LICA-CN 10 103292734 103292734 single base substitution G C missense_variant C299S 896G>C LICA-CN 10 103292734 103292734 single base substitution G C missense_variant C335S 1004G>C LICA-CN 10 103292734 103292734 single base substitution G C upstream_gene_variant LICA-FR 10 103163450 103163450 single base substitution A T intron_variant LICA-FR 10 103222437 103222438 deletion of <=200bp AA - intron_variant LICA-FR 10 103249166 103249166 single base substitution A G intron_variant LICA-FR 10 103252436 103252436 single base substitution A G intron_variant LICA-FR 10 103260945 103260945 insertion of <=200bp - A intron_variant LICA-FR 10 103287691 103287691 single base substitution T C downstream_gene_variant LICA-FR 10 103287691 103287691 single base substitution T C intron_variant LICA-FR 10 103288884 103288884 single base substitution A T downstream_gene_variant LICA-FR 10 103288884 103288884 single base substitution A T intron_variant LICA-FR 10 103292173 103292173 single base substitution G T missense_variant R280L 839G>T LICA-FR 10 103292173 103292173 single base substitution G T missense_variant R285L 854G>T LICA-FR 10 103292173 103292173 single base substitution G T missense_variant R321L 962G>T LICA-FR 10 103292173 103292173 single base substitution G T upstream_gene_variant LICA-FR 10 103299138 103299138 single base substitution A C intron_variant LICA-FR 10 103304185 103304185 single base substitution G T intron_variant LICA-FR 10 103313037 103313037 single base substitution G T 3_prime_UTR_variant LICA-FR 10 103313037 103313037 single base substitution G T downstream_gene_variant LIHC-US 10 103281409 103281409 single base substitution A T exon_variant LIHC-US 10 103281409 103281409 single base substitution A T missense_variant N113I 338A>T LIHC-US 10 103281409 103281409 single base substitution A T missense_variant N72I 215A>T LIHC-US 10 103281409 103281409 single base substitution A T missense_variant N77I 230A>T LIHC-US 10 103281409 103281409 single base substitution A T missense_variant N95I 284A>T LIHC-US 10 103310572 103310572 insertion of <=200bp - C exon_variant LIHC-US 10 103310572 103310572 insertion of <=200bp - C frameshift_variant E550D? LIHC-US 10 103310572 103310572 insertion of <=200bp - C frameshift_variant E555D? LIHC-US 10 103310572 103310572 insertion of <=200bp - C frameshift_variant E591D? LINC-JP 10 103113865 103113865 single base substitution G A 5_prime_UTR_variant LINC-JP 10 103113865 103113865 single base substitution G A exon_variant LINC-JP 10 103113865 103113865 single base substitution G A upstream_gene_variant LINC-JP 10 103117879 103117879 single base substitution A G intron_variant LINC-JP 10 103124746 103124746 single base substitution G A intron_variant LINC-JP 10 103134069 103134069 single base substitution A G intron_variant LINC-JP 10 103134862 103134862 single base substitution G A intron_variant LINC-JP 10 103138525 103138525 single base substitution G T intron_variant LINC-JP 10 103140144 103140144 single base substitution T A intron_variant LINC-JP 10 103160738 103160738 single base substitution G A intron_variant LINC-JP 10 103170466 103170466 single base substitution A T intron_variant LINC-JP 10 103170467 103170467 single base substitution T A intron_variant LINC-JP 10 103185653 103185653 single base substitution A G intron_variant LINC-JP 10 103229682 103229682 single base substitution T G intron_variant LINC-JP 10 103232903 103232903 single base substitution C T intron_variant LINC-JP 10 103242154 103242154 single base substitution T C intron_variant LINC-JP 10 103247728 103247728 single base substitution A G intron_variant LINC-JP 10 103252333 103252333 single base substitution A G intron_variant LINC-JP 10 103259944 103259944 single base substitution T G intron_variant LINC-JP 10 103272328 103272328 single base substitution G A intron_variant LINC-JP 10 103285867 103285867 single base substitution G A downstream_gene_variant LINC-JP 10 103285867 103285867 single base substitution G A exon_variant LINC-JP 10 103285867 103285867 single base substitution G A synonymous_variant V177V 531G>A LINC-JP 10 103285867 103285867 single base substitution G A synonymous_variant V182V 546G>A LINC-JP 10 103285867 103285867 single base substitution G A synonymous_variant V218V 654G>A LINC-JP 10 103295277 103295277 single base substitution A G intron_variant LINC-JP 10 103303045 103303045 single base substitution G C intron_variant LINC-JP 10 103305306 103305306 single base substitution C T intron_variant LINC-JP 10 103310670 103310670 single base substitution A G exon_variant LINC-JP 10 103310670 103310670 single base substitution A G intron_variant LINC-JP 10 103313720 103313728 deletion of <=200bp AACAGTGGA - 3_prime_UTR_variant LINC-JP 10 103313720 103313728 deletion of <=200bp AACAGTGGA - downstream_gene_variant LINC-JP 10 103317092 103317092 deletion of <=200bp T - downstream_gene_variant LINC-JP 10 103317960 103317960 single base substitution G A downstream_gene_variant LIRI-JP 10 103109469 103109469 single base substitution A G upstream_gene_variant LIRI-JP 10 103111929 103111929 single base substitution A G upstream_gene_variant LIRI-JP 10 103122131 103122131 single base substitution A G intron_variant LIRI-JP 10 103123895 103123895 single base substitution A G intron_variant LIRI-JP 10 103127330 103127330 single base substitution C T intron_variant LIRI-JP 10 103127415 103127415 single base substitution T G intron_variant LIRI-JP 10 103127774 103127774 single base substitution A C intron_variant LIRI-JP 10 103128480 103128480 single base substitution A G intron_variant LIRI-JP 10 103129311 103129311 single base substitution T C intron_variant LIRI-JP 10 103130141 103130141 single base substitution T G intron_variant LIRI-JP 10 103137014 103137014 single base substitution A T intron_variant LIRI-JP 10 103138136 103138136 single base substitution T C intron_variant LIRI-JP 10 103138386 103138386 single base substitution A T intron_variant LIRI-JP 10 103138792 103138792 single base substitution A T intron_variant LIRI-JP 10 103139201 103139201 single base substitution C G intron_variant LIRI-JP 10 103139721 103139721 single base substitution A G intron_variant LIRI-JP 10 103141357 103141357 single base substitution T C intron_variant LIRI-JP 10 103144922 103144922 single base substitution T G intron_variant LIRI-JP 10 103146793 103146793 single base substitution A G intron_variant LIRI-JP 10 103147646 103147646 single base substitution C A intron_variant LIRI-JP 10 103149218 103149218 single base substitution A G intron_variant LIRI-JP 10 103149316 103149316 single base substitution T G intron_variant LIRI-JP 10 103151616 103151616 single base substitution A T intron_variant LIRI-JP 10 103153999 103153999 single base substitution G T intron_variant LIRI-JP 10 103155577 103155577 single base substitution A G intron_variant LIRI-JP 10 103156003 103156003 single base substitution T G intron_variant LIRI-JP 10 103156928 103156928 single base substitution T G intron_variant LIRI-JP 10 103158130 103158130 single base substitution G T intron_variant LIRI-JP 10 103163417 103163417 single base substitution G C intron_variant LIRI-JP 10 103163615 103163615 single base substitution G T intron_variant LIRI-JP 10 103166939 103166939 single base substitution A T intron_variant LIRI-JP 10 103167439 103167439 single base substitution G A intron_variant LIRI-JP 10 103171750 103171750 single base substitution A G intron_variant LIRI-JP 10 103172287 103172287 single base substitution G A intron_variant LIRI-JP 10 103172358 103172358 single base substitution C G intron_variant LIRI-JP 10 103172580 103172580 single base substitution T C intron_variant LIRI-JP 10 103173490 103173490 single base substitution G T intron_variant LIRI-JP 10 103174216 103174216 single base substitution A T intron_variant LIRI-JP 10 103174606 103174606 single base substitution G A intron_variant LIRI-JP 10 103176233 103176233 single base substitution C T intron_variant LIRI-JP 10 103177003 103177003 single base substitution C G intron_variant LIRI-JP 10 103178057 103178057 single base substitution G A intron_variant LIRI-JP 10 103178204 103178204 single base substitution C T intron_variant LIRI-JP 10 103178225 103178225 single base substitution A G intron_variant LIRI-JP 10 103178595 103178595 single base substitution C T intron_variant LIRI-JP 10 103179434 103179434 single base substitution A G intron_variant LIRI-JP 10 103180819 103180819 single base substitution C A intron_variant LIRI-JP 10 103181836 103181836 single base substitution G A intron_variant LIRI-JP 10 103182406 103182406 single base substitution G A intron_variant LIRI-JP 10 103183243 103183243 single base substitution A T intron_variant LIRI-JP 10 103185746 103185746 single base substitution A G intron_variant LIRI-JP 10 103187585 103187585 single base substitution C G intron_variant LIRI-JP 10 103191992 103191992 single base substitution C T intron_variant LIRI-JP 10 103192578 103192578 single base substitution G T intron_variant LIRI-JP 10 103192580 103192580 single base substitution A G intron_variant LIRI-JP 10 103193964 103193964 single base substitution G A intron_variant LIRI-JP 10 103195778 103195778 single base substitution G A intron_variant LIRI-JP 10 103196165 103196165 single base substitution G T intron_variant LIRI-JP 10 103197040 103197040 single base substitution A G intron_variant LIRI-JP 10 103200730 103200730 single base substitution A G intron_variant LIRI-JP 10 103201051 103201051 single base substitution T C intron_variant LIRI-JP 10 103207748 103207748 single base substitution G A intron_variant LIRI-JP 10 103209648 103209648 single base substitution G A intron_variant LIRI-JP 10 103211423 103211423 single base substitution A C intron_variant LIRI-JP 10 103211773 103211773 single base substitution A C intron_variant LIRI-JP 10 103212810 103212810 single base substitution G T intron_variant LIRI-JP 10 103215913 103215913 single base substitution G A intron_variant LIRI-JP 10 103222613 103222613 single base substitution T C intron_variant LIRI-JP 10 103224055 103224055 single base substitution T C intron_variant LIRI-JP 10 103224395 103224395 single base substitution C T intron_variant LIRI-JP 10 103225617 103225617 single base substitution G T intron_variant LIRI-JP 10 103226355 103226355 single base substitution T C intron_variant LIRI-JP 10 103229228 103229228 single base substitution A G intron_variant LIRI-JP 10 103229293 103229293 single base substitution A G intron_variant LIRI-JP 10 103234287 103234287 single base substitution A T intron_variant LIRI-JP 10 103234360 103234360 single base substitution C A intron_variant LIRI-JP 10 103237267 103237267 single base substitution C T intron_variant LIRI-JP 10 103240458 103240458 single base substitution G T intron_variant LIRI-JP 10 103240530 103240530 single base substitution A C intron_variant LIRI-JP 10 103240740 103240740 single base substitution A C intron_variant LIRI-JP 10 103241259 103241259 single base substitution A G intron_variant LIRI-JP 10 103241875 103241875 single base substitution C A intron_variant LIRI-JP 10 103242212 103242212 single base substitution G A intron_variant LIRI-JP 10 103242965 103242965 single base substitution A G intron_variant LIRI-JP 10 103244296 103244296 single base substitution T C intron_variant LIRI-JP 10 103244679 103244679 single base substitution G A intron_variant LIRI-JP 10 103244848 103244848 single base substitution A T intron_variant LIRI-JP 10 103245163 103245176 deletion of <=200bp TTGATTAGGCACGT - intron_variant LIRI-JP 10 103247767 103247767 single base substitution C A intron_variant LIRI-JP 10 103249536 103249536 single base substitution C A intron_variant LIRI-JP 10 103249679 103249679 single base substitution A T intron_variant LIRI-JP 10 103249818 103249818 single base substitution A G intron_variant LIRI-JP 10 103252795 103252795 single base substitution T A intron_variant LIRI-JP 10 103253294 103253294 single base substitution G T intron_variant LIRI-JP 10 103253681 103253681 single base substitution A G intron_variant LIRI-JP 10 103253790 103253790 single base substitution A G intron_variant LIRI-JP 10 103254739 103254739 single base substitution G T intron_variant LIRI-JP 10 103255782 103255782 single base substitution G A intron_variant LIRI-JP 10 103256167 103256167 single base substitution A G intron_variant LIRI-JP 10 103258472 103258472 single base substitution C T intron_variant LIRI-JP 10 103259270 103259270 single base substitution C T intron_variant LIRI-JP 10 103259317 103259317 single base substitution A G intron_variant LIRI-JP 10 103261563 103261563 single base substitution A T intron_variant LIRI-JP 10 103262041 103262041 single base substitution G T intron_variant LIRI-JP 10 103264653 103264653 single base substitution C A intron_variant LIRI-JP 10 103268095 103268095 single base substitution T C intron_variant LIRI-JP 10 103271228 103271228 single base substitution C A intron_variant LIRI-JP 10 103271538 103271538 single base substitution C T intron_variant LIRI-JP 10 103273565 103273565 single base substitution G T intron_variant LIRI-JP 10 103273990 103273990 single base substitution A G intron_variant LIRI-JP 10 103280075 103280075 single base substitution G T intron_variant LIRI-JP 10 103280295 103280295 single base substitution A G intron_variant LIRI-JP 10 103283810 103283810 single base substitution A G downstream_gene_variant LIRI-JP 10 103283810 103283810 single base substitution A G intron_variant LIRI-JP 10 103285035 103285035 single base substitution A G downstream_gene_variant LIRI-JP 10 103285035 103285035 single base substitution A G intron_variant LIRI-JP 10 103285854 103285854 single base substitution A G downstream_gene_variant LIRI-JP 10 103285854 103285854 single base substitution A G exon_variant LIRI-JP 10 103285854 103285854 single base substitution A G missense_variant E173G 518A>G LIRI-JP 10 103285854 103285854 single base substitution A G missense_variant E178G 533A>G LIRI-JP 10 103285854 103285854 single base substitution A G missense_variant E214G 641A>G LIRI-JP 10 103286033 103286033 single base substitution G A downstream_gene_variant LIRI-JP 10 103286033 103286033 single base substitution G A intron_variant LIRI-JP 10 103286597 103286597 single base substitution A G downstream_gene_variant LIRI-JP 10 103286597 103286597 single base substitution A G intron_variant LIRI-JP 10 103289345 103289345 single base substitution A C downstream_gene_variant LIRI-JP 10 103289345 103289345 single base substitution A C intron_variant LIRI-JP 10 103290281 103290281 single base substitution G A downstream_gene_variant LIRI-JP 10 103290281 103290281 single base substitution G A intron_variant LIRI-JP 10 103290281 103290281 single base substitution G A upstream_gene_variant LIRI-JP 10 103291265 103291265 single base substitution T C intron_variant LIRI-JP 10 103291265 103291265 single base substitution T C upstream_gene_variant LIRI-JP 10 103292074 103292074 single base substitution G T missense_variant C247F 740G>T LIRI-JP 10 103292074 103292074 single base substitution G T missense_variant C252F 755G>T LIRI-JP 10 103292074 103292074 single base substitution G T missense_variant C288F 863G>T LIRI-JP 10 103292074 103292074 single base substitution G T upstream_gene_variant LIRI-JP 10 103292910 103292910 single base substitution T A intron_variant LIRI-JP 10 103292910 103292910 single base substitution T A upstream_gene_variant LIRI-JP 10 103297195 103297195 single base substitution G A intron_variant LIRI-JP 10 103297196 103297196 single base substitution A T intron_variant LIRI-JP 10 103300407 103300407 single base substitution G A intron_variant LIRI-JP 10 103300568 103300568 single base substitution C A intron_variant LIRI-JP 10 103301980 103301980 single base substitution A T intron_variant LIRI-JP 10 103302600 103302600 single base substitution C T intron_variant LIRI-JP 10 103303293 103303293 single base substitution T C intron_variant LIRI-JP 10 103305859 103305859 single base substitution A G intron_variant LIRI-JP 10 103306870 103306870 single base substitution A G intron_variant LIRI-JP 10 103308379 103308379 single base substitution G A intron_variant LIRI-JP 10 103308384 103308384 single base substitution C G intron_variant LIRI-JP 10 103309149 103309149 single base substitution C T intron_variant LIRI-JP 10 103309757 103309757 single base substitution A G intron_variant LIRI-JP 10 103310331 103310331 single base substitution G A intron_variant LIRI-JP 10 103310415 103310415 single base substitution A G intron_variant LIRI-JP 10 103313703 103313703 single base substitution G T 3_prime_UTR_variant LIRI-JP 10 103313703 103313703 single base substitution G T downstream_gene_variant LIRI-JP 10 103314121 103314121 single base substitution G A 3_prime_UTR_variant LIRI-JP 10 103314121 103314121 single base substitution G A downstream_gene_variant LIRI-JP 10 103315868 103315868 single base substitution A T 3_prime_UTR_variant LIRI-JP 10 103315868 103315868 single base substitution A T downstream_gene_variant LIRI-JP 10 103319055 103319055 single base substitution G A downstream_gene_variant LUSC-KR 10 103109387 103109387 single base substitution A G upstream_gene_variant LUSC-KR 10 103117197 103117197 single base substitution C A intron_variant LUSC-KR 10 103120149 103120149 single base substitution G T intron_variant LUSC-KR 10 103121011 103121011 single base substitution G C intron_variant LUSC-KR 10 103132388 103132388 single base substitution G T intron_variant LUSC-KR 10 103132782 103132782 single base substitution G A intron_variant LUSC-KR 10 103140230 103140230 single base substitution G A intron_variant LUSC-KR 10 103141837 103141837 single base substitution T A intron_variant LUSC-KR 10 103144532 103144532 single base substitution A G intron_variant LUSC-KR 10 103145297 103145297 single base substitution C G intron_variant LUSC-KR 10 103145805 103145805 single base substitution C G intron_variant LUSC-KR 10 103167147 103167147 single base substitution T A intron_variant LUSC-KR 10 103167808 103167808 single base substitution A G intron_variant LUSC-KR 10 103169947 103169947 single base substitution T A intron_variant LUSC-KR 10 103170205 103170205 single base substitution C G intron_variant LUSC-KR 10 103170773 103170773 single base substitution G T intron_variant LUSC-KR 10 103172139 103172139 single base substitution A T intron_variant LUSC-KR 10 103174954 103174954 single base substitution G T intron_variant LUSC-KR 10 103179755 103179755 single base substitution G A intron_variant LUSC-KR 10 103187443 103187443 single base substitution G A intron_variant LUSC-KR 10 103195362 103195362 single base substitution A G intron_variant LUSC-KR 10 103198871 103198871 single base substitution G T intron_variant LUSC-KR 10 103201240 103201240 single base substitution A G intron_variant LUSC-KR 10 103202667 103202667 single base substitution G T intron_variant LUSC-KR 10 103221297 103221297 single base substitution G T intron_variant LUSC-KR 10 103227978 103227978 single base substitution G A intron_variant LUSC-KR 10 103237050 103237050 single base substitution G T intron_variant LUSC-KR 10 103257415 103257415 single base substitution A T intron_variant LUSC-KR 10 103260430 103260430 single base substitution G T intron_variant LUSC-KR 10 103263516 103263516 single base substitution T A intron_variant LUSC-KR 10 103269905 103269905 single base substitution G T intron_variant LUSC-KR 10 103270448 103270448 single base substitution A T intron_variant LUSC-KR 10 103270459 103270459 single base substitution A G intron_variant LUSC-KR 10 103270978 103270978 single base substitution C G intron_variant LUSC-KR 10 103275287 103275287 single base substitution G T intron_variant LUSC-KR 10 103285943 103285943 single base substitution G A downstream_gene_variant LUSC-KR 10 103285943 103285943 single base substitution G A exon_variant LUSC-KR 10 103285943 103285943 single base substitution G A missense_variant E203K 607G>A LUSC-KR 10 103285943 103285943 single base substitution G A missense_variant E208K 622G>A LUSC-KR 10 103285943 103285943 single base substitution G A missense_variant E244K 730G>A LUSC-KR 10 103291037 103291037 single base substitution C T missense_variant P222S 664C>T LUSC-KR 10 103291037 103291037 single base substitution C T missense_variant P227S 679C>T LUSC-KR 10 103291037 103291037 single base substitution C T missense_variant P263S 787C>T LUSC-KR 10 103291037 103291037 single base substitution C T upstream_gene_variant LUSC-KR 10 103295872 103295872 single base substitution G C intron_variant LUSC-KR 10 103296080 103296080 single base substitution T C intron_variant LUSC-KR 10 103297320 103297320 single base substitution G C intron_variant LUSC-KR 10 103300190 103300190 single base substitution G A intron_variant LUSC-KR 10 103301769 103301769 single base substitution G T intron_variant LUSC-KR 10 103305099 103305099 single base substitution G C intron_variant LUSC-US 10 103281516 103281516 single base substitution C T downstream_gene_variant LUSC-US 10 103281516 103281516 single base substitution C T exon_variant LUSC-US 10 103281516 103281516 single base substitution C T stop_gained Q108* 322C>T LUSC-US 10 103281516 103281516 single base substitution C T stop_gained Q113* 337C>T LUSC-US 10 103281516 103281516 single base substitution C T stop_gained Q131* 391C>T LUSC-US 10 103281516 103281516 single base substitution C T stop_gained Q149* 445C>T MALY-DE 10 103113890 103113890 single base substitution C A 5_prime_UTR_variant MALY-DE 10 103113890 103113890 single base substitution C A exon_variant MALY-DE 10 103113890 103113890 single base substitution C A upstream_gene_variant MALY-DE 10 103125301 103125301 single base substitution C T intron_variant MALY-DE 10 103128979 103128979 single base substitution T A intron_variant MALY-DE 10 103140067 103140067 single base substitution A G intron_variant MALY-DE 10 103144438 103144438 single base substitution A G intron_variant MALY-DE 10 103147206 103147206 single base substitution T G intron_variant MALY-DE 10 103156235 103156235 single base substitution G T intron_variant MALY-DE 10 103158180 103158180 single base substitution C T intron_variant MALY-DE 10 103168062 103168062 single base substitution T A intron_variant MALY-DE 10 103169275 103169275 single base substitution T C intron_variant MALY-DE 10 103170702 103170702 single base substitution A C intron_variant MALY-DE 10 103172001 103172001 single base substitution A T intron_variant MALY-DE 10 103184851 103184851 single base substitution T G intron_variant MALY-DE 10 103190019 103190019 single base substitution G A intron_variant MALY-DE 10 103205606 103205606 single base substitution T C intron_variant MALY-DE 10 103207688 103207688 single base substitution C T intron_variant MALY-DE 10 103213934 103213934 single base substitution T G intron_variant MALY-DE 10 103228301 103228301 single base substitution A C intron_variant MALY-DE 10 103230382 103230382 single base substitution T C intron_variant MALY-DE 10 103232082 103232082 insertion of <=200bp - T intron_variant MALY-DE 10 103238206 103238206 deletion of <=200bp T - intron_variant MALY-DE 10 103253546 103253546 single base substitution T A intron_variant MALY-DE 10 103262368 103262368 single base substitution G A intron_variant MALY-DE 10 103288011 103288011 single base substitution G C downstream_gene_variant MALY-DE 10 103288011 103288011 single base substitution G C intron_variant MALY-DE 10 103290439 103290439 single base substitution G A downstream_gene_variant MALY-DE 10 103290439 103290439 single base substitution G A intron_variant MALY-DE 10 103290439 103290439 single base substitution G A upstream_gene_variant MALY-DE 10 103305918 103305918 single base substitution A G intron_variant MALY-DE 10 103313522 103313522 single base substitution C G 3_prime_UTR_variant MALY-DE 10 103313522 103313522 single base substitution C G downstream_gene_variant MALY-DE 10 103315652 103315652 single base substitution G A 3_prime_UTR_variant MALY-DE 10 103315652 103315652 single base substitution G A downstream_gene_variant MALY-DE 10 103315984 103315984 single base substitution G T 3_prime_UTR_variant MALY-DE 10 103320478 103320478 single base substitution G A downstream_gene_variant MELA-AU 10 103108930 103108930 single base substitution C T upstream_gene_variant MELA-AU 10 103109219 103109219 single base substitution G A upstream_gene_variant MELA-AU 10 103109388 103109388 single base substitution T A upstream_gene_variant MELA-AU 10 103109621 103109621 single base substitution T A upstream_gene_variant MELA-AU 10 103110115 103110115 single base substitution G A upstream_gene_variant MELA-AU 10 103110116 103110116 single base substitution A C upstream_gene_variant MELA-AU 10 103110431 103110431 single base substitution C T upstream_gene_variant MELA-AU 10 103110740 103110740 single base substitution C T upstream_gene_variant MELA-AU 10 103110750 103110750 single base substitution C T upstream_gene_variant MELA-AU 10 103110863 103110863 single base substitution C T upstream_gene_variant MELA-AU 10 103110981 103110981 single base substitution C T upstream_gene_variant MELA-AU 10 103111037 103111037 single base substitution C T upstream_gene_variant MELA-AU 10 103111278 103111278 single base substitution C T upstream_gene_variant MELA-AU 10 103111320 103111320 single base substitution C T upstream_gene_variant MELA-AU 10 103111437 103111437 single base substitution C T upstream_gene_variant MELA-AU 10 103111830 103111830 single base substitution C G upstream_gene_variant MELA-AU 10 103112124 103112124 single base substitution G A upstream_gene_variant MELA-AU 10 103112257 103112257 single base substitution G A upstream_gene_variant MELA-AU 10 103112674 103112674 single base substitution C T upstream_gene_variant MELA-AU 10 103113408 103113408 single base substitution C T upstream_gene_variant MELA-AU 10 103113569 103113569 single base substitution C T upstream_gene_variant MELA-AU 10 103113580 103113580 single base substitution C T upstream_gene_variant MELA-AU 10 103113695 103113695 single base substitution C T upstream_gene_variant MELA-AU 10 103113723 103113723 single base substitution C T upstream_gene_variant MELA-AU 10 103113730 103113730 single base substitution G A upstream_gene_variant MELA-AU 10 103113770 103113770 single base substitution C T upstream_gene_variant MELA-AU 10 103113794 103113795 multiple base substitution (>=2bp and <=200bp) CT AA upstream_gene_variant MELA-AU 10 103114284 103114284 insertion of <=200bp - C intron_variant MELA-AU 10 103114284 103114284 insertion of <=200bp - C upstream_gene_variant MELA-AU 10 103114286 103114286 single base substitution C T intron_variant MELA-AU 10 103114286 103114286 single base substitution C T upstream_gene_variant MELA-AU 10 103114615 103114615 single base substitution C T intron_variant MELA-AU 10 103115567 103115567 single base substitution C T intron_variant MELA-AU 10 103115838 103115838 single base substitution C T intron_variant MELA-AU 10 103117499 103117499 single base substitution C T intron_variant MELA-AU 10 103118304 103118304 single base substitution A G intron_variant MELA-AU 10 103118364 103118364 single base substitution C T intron_variant MELA-AU 10 103120265 103120265 single base substitution G A intron_variant MELA-AU 10 103121084 103121084 single base substitution C T intron_variant MELA-AU 10 103123127 103123127 single base substitution C G intron_variant MELA-AU 10 103123309 103123310 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 103123960 103123960 single base substitution C T intron_variant MELA-AU 10 103124446 103124446 single base substitution C G intron_variant MELA-AU 10 103124526 103124526 single base substitution A T intron_variant MELA-AU 10 103124806 103124806 single base substitution C T intron_variant MELA-AU 10 103124858 103124858 single base substitution T G intron_variant MELA-AU 10 103125798 103125798 single base substitution T G intron_variant MELA-AU 10 103126077 103126077 single base substitution T A intron_variant MELA-AU 10 103126571 103126571 single base substitution A G intron_variant MELA-AU 10 103127131 103127131 single base substitution G A intron_variant MELA-AU 10 103127375 103127376 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 103128283 103128283 single base substitution C T intron_variant MELA-AU 10 103129527 103129527 single base substitution C T intron_variant MELA-AU 10 103129673 103129673 single base substitution C T intron_variant MELA-AU 10 103129754 103129754 single base substitution C T intron_variant MELA-AU 10 103130177 103130177 single base substitution C T intron_variant MELA-AU 10 103131191 103131191 single base substitution C T intron_variant MELA-AU 10 103131247 103131247 single base substitution C T intron_variant MELA-AU 10 103131725 103131725 single base substitution C T intron_variant MELA-AU 10 103132334 103132334 single base substitution C T intron_variant MELA-AU 10 103132505 103132505 single base substitution C T intron_variant MELA-AU 10 103133470 103133470 single base substitution C T intron_variant MELA-AU 10 103133773 103133773 single base substitution G A intron_variant MELA-AU 10 103135724 103135724 single base substitution A G intron_variant MELA-AU 10 103135747 103135747 single base substitution C T intron_variant MELA-AU 10 103136829 103136829 single base substitution C T intron_variant MELA-AU 10 103137319 103137319 single base substitution T G intron_variant MELA-AU 10 103137999 103137999 single base substitution T C intron_variant MELA-AU 10 103138006 103138006 single base substitution T G intron_variant MELA-AU 10 103138507 103138507 single base substitution C T intron_variant MELA-AU 10 103139670 103139670 single base substitution A C intron_variant MELA-AU 10 103140112 103140112 single base substitution T G intron_variant MELA-AU 10 103141418 103141418 single base substitution C T intron_variant MELA-AU 10 103141515 103141515 single base substitution C T intron_variant MELA-AU 10 103141774 103141774 single base substitution C T intron_variant MELA-AU 10 103141945 103141945 single base substitution G C intron_variant MELA-AU 10 103142724 103142724 single base substitution G T intron_variant MELA-AU 10 103143580 103143580 single base substitution G A intron_variant MELA-AU 10 103143659 103143659 single base substitution G A intron_variant MELA-AU 10 103143717 103143718 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 103143898 103143898 single base substitution C T intron_variant MELA-AU 10 103144378 103144378 single base substitution C T intron_variant MELA-AU 10 103145245 103145245 single base substitution T A intron_variant MELA-AU 10 103145630 103145630 single base substitution T C intron_variant MELA-AU 10 103145873 103145873 single base substitution C T intron_variant MELA-AU 10 103146013 103146013 single base substitution C T intron_variant MELA-AU 10 103147028 103147028 single base substitution T G intron_variant MELA-AU 10 103147558 103147558 single base substitution T G intron_variant MELA-AU 10 103147940 103147941 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 103148582 103148582 single base substitution G A intron_variant MELA-AU 10 103148915 103148915 single base substitution C T intron_variant MELA-AU 10 103151509 103151509 single base substitution T C intron_variant MELA-AU 10 103152380 103152380 single base substitution C T intron_variant MELA-AU 10 103152789 103152789 single base substitution C T intron_variant MELA-AU 10 103152844 103152844 single base substitution C T intron_variant MELA-AU 10 103154293 103154293 single base substitution C T intron_variant MELA-AU 10 103154926 103154926 single base substitution C T intron_variant MELA-AU 10 103155525 103155525 single base substitution C T intron_variant MELA-AU 10 103155944 103155944 single base substitution C T intron_variant MELA-AU 10 103155951 103155951 single base substitution C T intron_variant MELA-AU 10 103156087 103156087 single base substitution T C intron_variant MELA-AU 10 103157441 103157441 single base substitution C T intron_variant MELA-AU 10 103158009 103158009 single base substitution C T intron_variant MELA-AU 10 103158183 103158183 single base substitution C T intron_variant MELA-AU 10 103158802 103158802 single base substitution T A intron_variant MELA-AU 10 103158950 103158950 single base substitution G A intron_variant MELA-AU 10 103159296 103159296 single base substitution C T intron_variant MELA-AU 10 103160235 103160235 single base substitution C T intron_variant MELA-AU 10 103160645 103160645 single base substitution C T intron_variant MELA-AU 10 103160984 103160984 single base substitution T A intron_variant MELA-AU 10 103161136 103161136 single base substitution G A intron_variant MELA-AU 10 103162302 103162302 single base substitution C T intron_variant MELA-AU 10 103162913 103162913 single base substitution C T intron_variant MELA-AU 10 103163823 103163823 single base substitution C T intron_variant MELA-AU 10 103163886 103163886 single base substitution C T intron_variant MELA-AU 10 103163988 103163988 single base substitution C G intron_variant MELA-AU 10 103164081 103164081 single base substitution C T intron_variant MELA-AU 10 103164581 103164581 single base substitution C T intron_variant MELA-AU 10 103164928 103164928 single base substitution C T intron_variant MELA-AU 10 103165221 103165221 single base substitution C T intron_variant MELA-AU 10 103165537 103165537 single base substitution C T intron_variant MELA-AU 10 103167158 103167158 single base substitution C T intron_variant MELA-AU 10 103168429 103168429 single base substitution C T intron_variant MELA-AU 10 103169804 103169804 single base substitution C T intron_variant MELA-AU 10 103170010 103170010 single base substitution A G intron_variant MELA-AU 10 103170513 103170513 single base substitution G A intron_variant MELA-AU 10 103171215 103171215 single base substitution C T intron_variant MELA-AU 10 103171422 103171422 single base substitution C T intron_variant MELA-AU 10 103171529 103171529 single base substitution T G intron_variant MELA-AU 10 103172004 103172004 single base substitution C T intron_variant MELA-AU 10 103172358 103172358 single base substitution C T intron_variant MELA-AU 10 103172606 103172607 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 10 103173178 103173178 single base substitution C T intron_variant MELA-AU 10 103173595 103173595 single base substitution C T intron_variant MELA-AU 10 103173744 103173744 single base substitution C T intron_variant MELA-AU 10 103174064 103174064 single base substitution C T intron_variant MELA-AU 10 103174120 103174120 single base substitution C T intron_variant MELA-AU 10 103174891 103174891 single base substitution C T intron_variant MELA-AU 10 103174925 103174925 single base substitution C T intron_variant MELA-AU 10 103175031 103175031 single base substitution G A intron_variant MELA-AU 10 103175166 103175166 single base substitution C T intron_variant MELA-AU 10 103176097 103176097 single base substitution C T intron_variant MELA-AU 10 103176184 103176184 single base substitution G A intron_variant MELA-AU 10 103176505 103176505 single base substitution A T intron_variant MELA-AU 10 103176693 103176693 single base substitution T G intron_variant MELA-AU 10 103177552 103177552 single base substitution C T intron_variant MELA-AU 10 103178609 103178609 single base substitution C T intron_variant MELA-AU 10 103178875 103178875 single base substitution C T intron_variant MELA-AU 10 103178988 103178988 single base substitution G A intron_variant MELA-AU 10 103179059 103179059 single base substitution C T intron_variant MELA-AU 10 103179402 103179402 single base substitution A G intron_variant MELA-AU 10 103179412 103179412 single base substitution T C intron_variant MELA-AU 10 103179824 103179824 single base substitution T G intron_variant MELA-AU 10 103180131 103180131 single base substitution C T intron_variant MELA-AU 10 103180776 103180776 single base substitution C T intron_variant MELA-AU 10 103180911 103180911 single base substitution C T intron_variant MELA-AU 10 103181562 103181562 single base substitution C T intron_variant MELA-AU 10 103182381 103182381 single base substitution C T intron_variant MELA-AU 10 103182723 103182723 single base substitution C T intron_variant MELA-AU 10 103182736 103182736 single base substitution A C intron_variant MELA-AU 10 103182830 103182830 single base substitution T C intron_variant MELA-AU 10 103183597 103183597 single base substitution C T intron_variant MELA-AU 10 103183736 103183736 single base substitution C T intron_variant MELA-AU 10 103184707 103184707 single base substitution C T intron_variant MELA-AU 10 103184818 103184818 single base substitution C T intron_variant MELA-AU 10 103185191 103185191 single base substitution G A intron_variant MELA-AU 10 103185394 103185394 single base substitution T C intron_variant MELA-AU 10 103186044 103186044 single base substitution G C intron_variant MELA-AU 10 103186806 103186806 single base substitution T C intron_variant MELA-AU 10 103186967 103186967 single base substitution C T intron_variant MELA-AU 10 103188313 103188313 single base substitution G A intron_variant MELA-AU 10 103188380 103188380 single base substitution C T intron_variant MELA-AU 10 103188558 103188558 single base substitution C T intron_variant MELA-AU 10 103188656 103188656 single base substitution C A intron_variant MELA-AU 10 103188924 103188924 single base substitution T A intron_variant MELA-AU 10 103189464 103189464 single base substitution G A intron_variant MELA-AU 10 103189677 103189677 single base substitution C T intron_variant MELA-AU 10 103189925 103189925 single base substitution C T intron_variant MELA-AU 10 103192110 103192110 single base substitution C T intron_variant MELA-AU 10 103192376 103192376 single base substitution C T intron_variant MELA-AU 10 103192473 103192473 single base substitution G A intron_variant MELA-AU 10 103192885 103192885 single base substitution C T intron_variant MELA-AU 10 103193853 103193853 single base substitution A G intron_variant MELA-AU 10 103194272 103194272 single base substitution C T intron_variant MELA-AU 10 103195454 103195454 single base substitution C T intron_variant MELA-AU 10 103196850 103196850 single base substitution C T intron_variant MELA-AU 10 103196934 103196934 single base substitution C T intron_variant MELA-AU 10 103197154 103197154 single base substitution C T intron_variant MELA-AU 10 103197403 103197403 single base substitution A G intron_variant MELA-AU 10 103197498 103197498 single base substitution C T intron_variant MELA-AU 10 103197630 103197630 single base substitution C T intron_variant MELA-AU 10 103197923 103197923 single base substitution T C intron_variant MELA-AU 10 103198401 103198401 single base substitution C T intron_variant MELA-AU 10 103199092 103199092 single base substitution G A intron_variant MELA-AU 10 103199526 103199526 single base substitution T A intron_variant MELA-AU 10 103199722 103199722 single base substitution C T intron_variant MELA-AU 10 103200789 103200789 single base substitution A G intron_variant MELA-AU 10 103202650 103202650 single base substitution T C intron_variant MELA-AU 10 103203094 103203094 single base substitution C T intron_variant MELA-AU 10 103204204 103204204 single base substitution G A intron_variant MELA-AU 10 103204229 103204229 single base substitution C T intron_variant MELA-AU 10 103209176 103209176 single base substitution C T intron_variant MELA-AU 10 103209606 103209606 single base substitution C T intron_variant MELA-AU 10 103210967 103210967 single base substitution C T intron_variant MELA-AU 10 103212649 103212649 single base substitution C T intron_variant MELA-AU 10 103213135 103213135 single base substitution C T intron_variant MELA-AU 10 103213203 103213203 single base substitution C T intron_variant MELA-AU 10 103213223 103213223 single base substitution G A intron_variant MELA-AU 10 103214249 103214249 single base substitution C T intron_variant MELA-AU 10 103215582 103215582 single base substitution C T intron_variant MELA-AU 10 103217252 103217252 single base substitution C T intron_variant MELA-AU 10 103217546 103217546 single base substitution C T intron_variant MELA-AU 10 103217605 103217605 single base substitution C T intron_variant MELA-AU 10 103217798 103217798 single base substitution C T intron_variant MELA-AU 10 103219252 103219252 single base substitution G A intron_variant MELA-AU 10 103221000 103221000 single base substitution A G intron_variant MELA-AU 10 103221119 103221119 single base substitution C T intron_variant MELA-AU 10 103221131 103221131 single base substitution T A intron_variant MELA-AU 10 103221504 103221504 single base substitution T A intron_variant MELA-AU 10 103222655 103222655 single base substitution C T intron_variant MELA-AU 10 103223880 103223880 single base substitution C T intron_variant MELA-AU 10 103224236 103224236 single base substitution C T intron_variant MELA-AU 10 103224500 103224500 single base substitution C T intron_variant MELA-AU 10 103224752 103224752 single base substitution C T intron_variant MELA-AU 10 103226238 103226238 single base substitution G A intron_variant MELA-AU 10 103227085 103227085 single base substitution G A intron_variant MELA-AU 10 103227241 103227241 single base substitution C T intron_variant MELA-AU 10 103227769 103227769 single base substitution C T intron_variant MELA-AU 10 103228045 103228045 single base substitution G A intron_variant MELA-AU 10 103228920 103228920 single base substitution C T intron_variant MELA-AU 10 103229833 103229833 single base substitution C T intron_variant MELA-AU 10 103230000 103230000 single base substitution C T intron_variant MELA-AU 10 103230213 103230213 single base substitution C T intron_variant MELA-AU 10 103230312 103230312 single base substitution C T intron_variant MELA-AU 10 103230634 103230634 single base substitution C T intron_variant MELA-AU 10 103230635 103230635 single base substitution C T intron_variant MELA-AU 10 103230923 103230923 single base substitution A C intron_variant MELA-AU 10 103231471 103231471 single base substitution C T intron_variant MELA-AU 10 103232027 103232027 single base substitution T C intron_variant MELA-AU 10 103232064 103232064 single base substitution C T intron_variant MELA-AU 10 103232079 103232080 multiple base substitution (>=2bp and <=200bp) CT TA intron_variant MELA-AU 10 103232548 103232548 single base substitution C T intron_variant MELA-AU 10 103233318 103233318 single base substitution C T intron_variant MELA-AU 10 103233743 103233743 single base substitution C T intron_variant MELA-AU 10 103233943 103233943 single base substitution C T intron_variant MELA-AU 10 103234345 103234345 single base substitution G A intron_variant MELA-AU 10 103235100 103235100 single base substitution C T intron_variant MELA-AU 10 103236437 103236437 single base substitution G A intron_variant MELA-AU 10 103238978 103238978 single base substitution C A intron_variant MELA-AU 10 103238996 103238996 single base substitution C T intron_variant MELA-AU 10 103239671 103239671 single base substitution C T intron_variant MELA-AU 10 103240942 103240942 single base substitution C T intron_variant MELA-AU 10 103241319 103241319 single base substitution T G intron_variant MELA-AU 10 103241380 103241380 single base substitution T C intron_variant MELA-AU 10 103242262 103242262 single base substitution C T intron_variant MELA-AU 10 103242361 103242361 single base substitution C T intron_variant MELA-AU 10 103242557 103242558 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 103242670 103242670 single base substitution C T intron_variant MELA-AU 10 103242839 103242839 single base substitution C T intron_variant MELA-AU 10 103243182 103243182 single base substitution T A intron_variant MELA-AU 10 103243641 103243641 single base substitution G C intron_variant MELA-AU 10 103246229 103246229 single base substitution G A intron_variant MELA-AU 10 103246325 103246325 single base substitution G A intron_variant MELA-AU 10 103246861 103246881 deletion of <=200bp ATTTGTTGTTATATGGGACAA - intron_variant MELA-AU 10 103247467 103247467 single base substitution C T intron_variant MELA-AU 10 103249481 103249481 single base substitution C T intron_variant MELA-AU 10 103249583 103249583 single base substitution C A intron_variant MELA-AU 10 103249730 103249730 single base substitution C T intron_variant MELA-AU 10 103250250 103250250 single base substitution T G intron_variant MELA-AU 10 103250643 103250643 single base substitution T C intron_variant MELA-AU 10 103250761 103250761 single base substitution G T intron_variant MELA-AU 10 103251391 103251391 single base substitution T C intron_variant MELA-AU 10 103251448 103251448 single base substitution C T intron_variant MELA-AU 10 103251606 103251606 single base substitution C T intron_variant MELA-AU 10 103251715 103251715 single base substitution T C intron_variant MELA-AU 10 103252560 103252560 single base substitution G A intron_variant MELA-AU 10 103253112 103253112 single base substitution G A intron_variant MELA-AU 10 103253571 103253571 single base substitution T C intron_variant MELA-AU 10 103253706 103253706 single base substitution T G intron_variant MELA-AU 10 103254406 103254406 single base substitution G A intron_variant MELA-AU 10 103256586 103256586 single base substitution C T intron_variant MELA-AU 10 103257062 103257062 single base substitution C T intron_variant MELA-AU 10 103257079 103257079 single base substitution C T intron_variant MELA-AU 10 103257286 103257286 single base substitution C T intron_variant MELA-AU 10 103257527 103257527 single base substitution C T intron_variant MELA-AU 10 103257861 103257861 single base substitution C T intron_variant MELA-AU 10 103257923 103257923 single base substitution T C intron_variant MELA-AU 10 103257949 103257949 single base substitution C T intron_variant MELA-AU 10 103257995 103257995 single base substitution C T intron_variant MELA-AU 10 103258033 103258034 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 103258270 103258270 single base substitution T C intron_variant MELA-AU 10 103258284 103258284 single base substitution C T intron_variant MELA-AU 10 103258748 103258748 single base substitution C T intron_variant MELA-AU 10 103258899 103258899 single base substitution A G intron_variant MELA-AU 10 103260106 103260106 single base substitution G A intron_variant MELA-AU 10 103261165 103261165 single base substitution C T intron_variant MELA-AU 10 103261654 103261654 single base substitution C T intron_variant MELA-AU 10 103262088 103262088 single base substitution C T intron_variant MELA-AU 10 103262941 103262941 single base substitution C T intron_variant MELA-AU 10 103264091 103264091 single base substitution C T intron_variant MELA-AU 10 103264126 103264126 single base substitution C T intron_variant MELA-AU 10 103264314 103264314 single base substitution C T intron_variant MELA-AU 10 103264333 103264333 single base substitution C T intron_variant MELA-AU 10 103264371 103264371 single base substitution C T intron_variant MELA-AU 10 103264889 103264889 single base substitution T C intron_variant MELA-AU 10 103264891 103264891 single base substitution T C intron_variant MELA-AU 10 103265271 103265271 single base substitution G A intron_variant MELA-AU 10 103265626 103265626 single base substitution C T intron_variant MELA-AU 10 103265710 103265710 single base substitution C T intron_variant MELA-AU 10 103265717 103265717 single base substitution G T intron_variant MELA-AU 10 103265897 103265897 single base substitution C T intron_variant MELA-AU 10 103265916 103265916 single base substitution C T intron_variant MELA-AU 10 103267086 103267086 single base substitution G A intron_variant MELA-AU 10 103268015 103268015 single base substitution C T intron_variant MELA-AU 10 103268139 103268139 single base substitution C T intron_variant MELA-AU 10 103268454 103268454 single base substitution G A intron_variant MELA-AU 10 103268467 103268467 single base substitution C T intron_variant MELA-AU 10 103268568 103268568 single base substitution G A intron_variant MELA-AU 10 103268853 103268853 single base substitution T C intron_variant MELA-AU 10 103268924 103268924 single base substitution C T intron_variant MELA-AU 10 103268935 103268935 single base substitution C T intron_variant MELA-AU 10 103269735 103269735 single base substitution C T intron_variant MELA-AU 10 103270150 103270150 single base substitution C T intron_variant MELA-AU 10 103270383 103270383 single base substitution C T intron_variant MELA-AU 10 103270684 103270684 single base substitution C T intron_variant MELA-AU 10 103271034 103271034 single base substitution C T intron_variant MELA-AU 10 103272103 103272103 single base substitution C T intron_variant MELA-AU 10 103272406 103272406 single base substitution C T intron_variant MELA-AU 10 103274150 103274150 single base substitution T G intron_variant MELA-AU 10 103274333 103274333 single base substitution C T intron_variant MELA-AU 10 103274413 103274413 single base substitution T C intron_variant MELA-AU 10 103274618 103274618 single base substitution C T intron_variant MELA-AU 10 103275190 103275190 single base substitution T A intron_variant MELA-AU 10 103275237 103275237 single base substitution G C intron_variant MELA-AU 10 103275423 103275423 single base substitution C T intron_variant MELA-AU 10 103275649 103275649 single base substitution G C intron_variant MELA-AU 10 103277600 103277600 single base substitution C T intron_variant MELA-AU 10 103278089 103278089 single base substitution C T intron_variant MELA-AU 10 103278113 103278113 single base substitution C T intron_variant MELA-AU 10 103278420 103278420 single base substitution C T intron_variant MELA-AU 10 103279662 103279662 single base substitution G A intron_variant MELA-AU 10 103283312 103283312 single base substitution C T downstream_gene_variant MELA-AU 10 103283312 103283312 single base substitution C T intron_variant MELA-AU 10 103284569 103284569 single base substitution C T downstream_gene_variant MELA-AU 10 103284569 103284569 single base substitution C T intron_variant MELA-AU 10 103284667 103284667 single base substitution A G downstream_gene_variant MELA-AU 10 103284667 103284667 single base substitution A G intron_variant MELA-AU 10 103286308 103286308 single base substitution G A downstream_gene_variant MELA-AU 10 103286308 103286308 single base substitution G A intron_variant MELA-AU 10 103286370 103286371 multiple base substitution (>=2bp and <=200bp) CT TC downstream_gene_variant MELA-AU 10 103286370 103286371 multiple base substitution (>=2bp and <=200bp) CT TC intron_variant MELA-AU 10 103286483 103286483 single base substitution C T downstream_gene_variant MELA-AU 10 103286483 103286483 single base substitution C T intron_variant MELA-AU 10 103287157 103287157 single base substitution T A downstream_gene_variant MELA-AU 10 103287157 103287157 single base substitution T A intron_variant MELA-AU 10 103287257 103287257 single base substitution C T downstream_gene_variant MELA-AU 10 103287257 103287257 single base substitution C T intron_variant MELA-AU 10 103287550 103287550 single base substitution C T downstream_gene_variant MELA-AU 10 103287550 103287550 single base substitution C T intron_variant MELA-AU 10 103287625 103287625 single base substitution C T downstream_gene_variant MELA-AU 10 103287625 103287625 single base substitution C T intron_variant MELA-AU 10 103287667 103287667 single base substitution C T downstream_gene_variant MELA-AU 10 103287667 103287667 single base substitution C T intron_variant MELA-AU 10 103287790 103287790 single base substitution T C downstream_gene_variant MELA-AU 10 103287790 103287790 single base substitution T C intron_variant MELA-AU 10 103287832 103287832 single base substitution C T downstream_gene_variant MELA-AU 10 103287832 103287832 single base substitution C T intron_variant MELA-AU 10 103288509 103288509 single base substitution T C downstream_gene_variant MELA-AU 10 103288509 103288509 single base substitution T C intron_variant MELA-AU 10 103288864 103288864 single base substitution A T downstream_gene_variant MELA-AU 10 103288864 103288864 single base substitution A T intron_variant MELA-AU 10 103289925 103289925 single base substitution G A downstream_gene_variant MELA-AU 10 103289925 103289925 single base substitution G A intron_variant MELA-AU 10 103290393 103290393 single base substitution C T downstream_gene_variant MELA-AU 10 103290393 103290393 single base substitution C T intron_variant MELA-AU 10 103290393 103290393 single base substitution C T upstream_gene_variant MELA-AU 10 103290659 103290659 single base substitution G A downstream_gene_variant MELA-AU 10 103290659 103290659 single base substitution G A intron_variant MELA-AU 10 103290659 103290659 single base substitution G A upstream_gene_variant MELA-AU 10 103290967 103290967 single base substitution C T intron_variant MELA-AU 10 103290967 103290967 single base substitution C T upstream_gene_variant MELA-AU 10 103291932 103291932 single base substitution C T intron_variant MELA-AU 10 103291932 103291932 single base substitution C T upstream_gene_variant MELA-AU 10 103291935 103291935 single base substitution T C intron_variant MELA-AU 10 103291935 103291935 single base substitution T C upstream_gene_variant MELA-AU 10 103292235 103292235 single base substitution G A intron_variant MELA-AU 10 103292235 103292235 single base substitution G A upstream_gene_variant MELA-AU 10 103292541 103292541 single base substitution G A intron_variant MELA-AU 10 103292541 103292541 single base substitution G A upstream_gene_variant MELA-AU 10 103292657 103292657 single base substitution C T intron_variant MELA-AU 10 103292657 103292657 single base substitution C T upstream_gene_variant MELA-AU 10 103292942 103292942 single base substitution C T intron_variant MELA-AU 10 103292942 103292942 single base substitution C T upstream_gene_variant MELA-AU 10 103293530 103293530 single base substitution C T intron_variant MELA-AU 10 103293530 103293530 single base substitution C T upstream_gene_variant MELA-AU 10 103293544 103293544 single base substitution C T intron_variant MELA-AU 10 103293544 103293544 single base substitution C T upstream_gene_variant MELA-AU 10 103294182 103294182 single base substitution C T intron_variant MELA-AU 10 103294182 103294182 single base substitution C T upstream_gene_variant MELA-AU 10 103294222 103294222 single base substitution C T intron_variant MELA-AU 10 103294222 103294222 single base substitution C T upstream_gene_variant MELA-AU 10 103294715 103294715 single base substitution C T intron_variant MELA-AU 10 103294715 103294715 single base substitution C T upstream_gene_variant MELA-AU 10 103295628 103295628 single base substitution C T intron_variant MELA-AU 10 103295858 103295858 single base substitution G A intron_variant MELA-AU 10 103296321 103296321 single base substitution T G exon_variant MELA-AU 10 103296321 103296321 single base substitution T G synonymous_variant G455G 1365T>G MELA-AU 10 103296321 103296321 single base substitution T G synonymous_variant G460G 1380T>G MELA-AU 10 103296321 103296321 single base substitution T G synonymous_variant G496G 1488T>G MELA-AU 10 103296872 103296872 single base substitution C T intron_variant MELA-AU 10 103297454 103297454 single base substitution G A intron_variant MELA-AU 10 103297761 103297761 single base substitution G A intron_variant MELA-AU 10 103298133 103298133 single base substitution G A splice_region_variant MELA-AU 10 103299733 103299733 single base substitution A T intron_variant MELA-AU 10 103300498 103300498 single base substitution C T intron_variant MELA-AU 10 103300947 103300947 single base substitution A T intron_variant MELA-AU 10 103301286 103301286 single base substitution G A intron_variant MELA-AU 10 103301360 103301360 single base substitution C T intron_variant MELA-AU 10 103302646 103302646 deletion of <=200bp T - intron_variant MELA-AU 10 103302757 103302757 single base substitution C T intron_variant MELA-AU 10 103304042 103304042 single base substitution C T intron_variant MELA-AU 10 103306593 103306593 single base substitution G A intron_variant MELA-AU 10 103306603 103306603 single base substitution C T intron_variant MELA-AU 10 103307118 103307118 single base substitution G A intron_variant MELA-AU 10 103307787 103307797 deletion of <=200bp TAAAATTATAG - intron_variant MELA-AU 10 103308340 103308340 single base substitution C A intron_variant MELA-AU 10 103310133 103310133 single base substitution C T intron_variant MELA-AU 10 103310563 103310563 single base substitution C T exon_variant MELA-AU 10 103310563 103310563 single base substitution C T synonymous_variant A547A 1641C>T MELA-AU 10 103310563 103310563 single base substitution C T synonymous_variant A552A 1656C>T MELA-AU 10 103310563 103310563 single base substitution C T synonymous_variant A588A 1764C>T MELA-AU 10 103311181 103311181 single base substitution G A downstream_gene_variant MELA-AU 10 103311181 103311181 single base substitution G A intron_variant MELA-AU 10 103311346 103311346 single base substitution C T downstream_gene_variant MELA-AU 10 103311346 103311346 single base substitution C T intron_variant MELA-AU 10 103311398 103311398 single base substitution C T downstream_gene_variant MELA-AU 10 103311398 103311398 single base substitution C T intron_variant MELA-AU 10 103312153 103312153 single base substitution T A downstream_gene_variant MELA-AU 10 103312153 103312153 single base substitution T A intron_variant MELA-AU 10 103312195 103312195 single base substitution C T downstream_gene_variant MELA-AU 10 103312195 103312195 single base substitution C T intron_variant MELA-AU 10 103312298 103312298 single base substitution C T downstream_gene_variant MELA-AU 10 103312298 103312298 single base substitution C T intron_variant MELA-AU 10 103312392 103312392 single base substitution C T downstream_gene_variant MELA-AU 10 103312392 103312392 single base substitution C T intron_variant MELA-AU 10 103312467 103312467 single base substitution C T downstream_gene_variant MELA-AU 10 103312467 103312467 single base substitution C T intron_variant MELA-AU 10 103312472 103312472 single base substitution C T downstream_gene_variant MELA-AU 10 103312472 103312472 single base substitution C T intron_variant MELA-AU 10 103313192 103313192 single base substitution C T 3_prime_UTR_variant MELA-AU 10 103313192 103313192 single base substitution C T downstream_gene_variant MELA-AU 10 103313886 103313886 single base substitution C T 3_prime_UTR_variant MELA-AU 10 103313886 103313886 single base substitution C T downstream_gene_variant MELA-AU 10 103314032 103314032 single base substitution C T 3_prime_UTR_variant MELA-AU 10 103314032 103314032 single base substitution C T downstream_gene_variant MELA-AU 10 103315430 103315430 single base substitution C T 3_prime_UTR_variant MELA-AU 10 103315430 103315430 single base substitution C T downstream_gene_variant MELA-AU 10 103315957 103315957 single base substitution A G 3_prime_UTR_variant MELA-AU 10 103316435 103316435 single base substitution C T 3_prime_UTR_variant MELA-AU 10 103317495 103317495 single base substitution G A downstream_gene_variant MELA-AU 10 103317584 103317584 single base substitution G A downstream_gene_variant MELA-AU 10 103317596 103317596 single base substitution C T downstream_gene_variant MELA-AU 10 103317642 103317642 single base substitution C T downstream_gene_variant MELA-AU 10 103317862 103317862 single base substitution C T downstream_gene_variant MELA-AU 10 103318399 103318399 single base substitution C T downstream_gene_variant MELA-AU 10 103318890 103318890 single base substitution C T downstream_gene_variant MELA-AU 10 103319515 103319515 single base substitution C T downstream_gene_variant MELA-AU 10 103319663 103319663 single base substitution C T downstream_gene_variant MELA-AU 10 103319717 103319717 single base substitution A T downstream_gene_variant MELA-AU 10 103320168 103320168 single base substitution G A downstream_gene_variant MELA-AU 10 103320308 103320308 single base substitution C T downstream_gene_variant MELA-AU 10 103320543 103320543 single base substitution C T downstream_gene_variant MELA-AU 10 103320603 103320603 single base substitution C T downstream_gene_variant MELA-AU 10 103320896 103320896 single base substitution C T downstream_gene_variant MELA-AU 10 103321243 103321243 single base substitution C T downstream_gene_variant MELA-AU 10 103321319 103321319 single base substitution G A downstream_gene_variant MELA-AU 10 103321917 103321917 single base substitution C T downstream_gene_variant MELA-AU 10 103321980 103321980 single base substitution C T downstream_gene_variant ORCA-IN 10 103132096 103132096 single base substitution A G intron_variant ORCA-IN 10 103171481 103171481 single base substitution G T intron_variant ORCA-IN 10 103196429 103196429 single base substitution T A intron_variant ORCA-IN 10 103211602 103211602 single base substitution G T intron_variant ORCA-IN 10 103261525 103261525 insertion of <=200bp - A intron_variant ORCA-IN 10 103287236 103287236 single base substitution G T downstream_gene_variant ORCA-IN 10 103287236 103287236 single base substitution G T intron_variant ORCA-IN 10 103293670 103293670 single base substitution C T intron_variant ORCA-IN 10 103293670 103293670 single base substitution C T upstream_gene_variant OV-AU 10 103109970 103109970 single base substitution A C upstream_gene_variant OV-AU 10 103114271 103114271 single base substitution A G intron_variant OV-AU 10 103114271 103114271 single base substitution A G upstream_gene_variant OV-AU 10 103114873 103114873 single base substitution G T intron_variant OV-AU 10 103118268 103118268 single base substitution A G intron_variant OV-AU 10 103120390 103120390 single base substitution A C intron_variant OV-AU 10 103120638 103120638 single base substitution C T intron_variant OV-AU 10 103120833 103120833 single base substitution G T intron_variant OV-AU 10 103121714 103121714 single base substitution G A intron_variant OV-AU 10 103122742 103122742 single base substitution A G intron_variant OV-AU 10 103123244 103123244 single base substitution C G intron_variant OV-AU 10 103123622 103123622 single base substitution G A intron_variant OV-AU 10 103123673 103123673 single base substitution G C intron_variant OV-AU 10 103123955 103123955 single base substitution T C intron_variant OV-AU 10 103151586 103151586 single base substitution G T intron_variant OV-AU 10 103175749 103175749 single base substitution G T intron_variant OV-AU 10 103175919 103175919 single base substitution T C intron_variant OV-AU 10 103178200 103178200 single base substitution A G intron_variant OV-AU 10 103179091 103179091 single base substitution C G intron_variant OV-AU 10 103180511 103180511 single base substitution A G intron_variant OV-AU 10 103183038 103183038 single base substitution G C intron_variant OV-AU 10 103197258 103197258 single base substitution A C intron_variant OV-AU 10 103205875 103205875 single base substitution A C intron_variant OV-AU 10 103216273 103216273 single base substitution T G intron_variant OV-AU 10 103225574 103225574 single base substitution G C intron_variant OV-AU 10 103230343 103230343 single base substitution T G intron_variant OV-AU 10 103235499 103235499 single base substitution C T intron_variant OV-AU 10 103239232 103239232 single base substitution T C intron_variant OV-AU 10 103239741 103239741 single base substitution C T intron_variant OV-AU 10 103249386 103249386 single base substitution C T intron_variant OV-AU 10 103249634 103249634 single base substitution C A intron_variant OV-AU 10 103265386 103265386 single base substitution A T intron_variant OV-AU 10 103270679 103270679 single base substitution T C intron_variant OV-AU 10 103271236 103271236 single base substitution A C intron_variant OV-AU 10 103273738 103273738 single base substitution T C intron_variant OV-AU 10 103275821 103275821 single base substitution C A intron_variant OV-AU 10 103279485 103279485 single base substitution G A intron_variant OV-AU 10 103292533 103292533 single base substitution G A intron_variant OV-AU 10 103292533 103292533 single base substitution G A upstream_gene_variant OV-AU 10 103303222 103303222 single base substitution T G intron_variant OV-AU 10 103307375 103307375 single base substitution C T intron_variant OV-US 10 103221777 103221777 single base substitution C T exon_variant OV-US 10 103221777 103221777 single base substitution C T intron_variant OV-US 10 103221777 103221777 single base substitution C T missense_variant P30S 88C>T OV-US 10 103221777 103221777 single base substitution C T missense_variant P48S 142C>T OV-US 10 103221777 103221777 single base substitution C T missense_variant P66S 196C>T PACA-AU 10 103121574 103121577 deletion of <=200bp TTGT - intron_variant PACA-AU 10 103123219 103123219 deletion of <=200bp T - intron_variant PACA-AU 10 103124893 103124893 single base substitution C T intron_variant PACA-AU 10 103127073 103127073 single base substitution C T intron_variant PACA-AU 10 103127110 103127110 single base substitution C G intron_variant PACA-AU 10 103127804 103127804 single base substitution A G intron_variant PACA-AU 10 103137253 103137253 single base substitution C T intron_variant PACA-AU 10 103144969 103144969 single base substitution A G intron_variant PACA-AU 10 103145290 103145290 single base substitution T C intron_variant PACA-AU 10 103149607 103149607 single base substitution C T intron_variant PACA-AU 10 103162570 103162570 single base substitution C G intron_variant PACA-AU 10 103167354 103167354 single base substitution C T intron_variant PACA-AU 10 103169579 103169579 single base substitution T A intron_variant PACA-AU 10 103178355 103178355 single base substitution C T intron_variant PACA-AU 10 103187640 103187640 single base substitution A T intron_variant PACA-AU 10 103188028 103188028 single base substitution T A intron_variant PACA-AU 10 103198085 103198085 single base substitution G A intron_variant PACA-AU 10 103206490 103206490 single base substitution C A intron_variant PACA-AU 10 103208194 103208194 single base substitution A G intron_variant PACA-AU 10 103212029 103212029 single base substitution T C intron_variant PACA-AU 10 103221133 103221133 deletion of <=200bp T - intron_variant PACA-AU 10 103226614 103226614 insertion of <=200bp - A intron_variant PACA-AU 10 103226806 103226806 single base substitution A C intron_variant PACA-AU 10 103234566 103234566 single base substitution A C intron_variant PACA-AU 10 103237509 103237509 single base substitution C T intron_variant PACA-AU 10 103243465 103243465 single base substitution A T intron_variant PACA-AU 10 103243742 103243742 single base substitution A T intron_variant PACA-AU 10 103246389 103246389 single base substitution C G intron_variant PACA-AU 10 103252754 103252754 single base substitution G A intron_variant PACA-AU 10 103264934 103264934 single base substitution A T intron_variant PACA-AU 10 103268513 103268513 single base substitution T C intron_variant PACA-AU 10 103269316 103269316 single base substitution T C intron_variant PACA-AU 10 103269317 103269317 single base substitution T C intron_variant PACA-AU 10 103275108 103275108 single base substitution T G intron_variant PACA-AU 10 103284589 103284589 single base substitution C T downstream_gene_variant PACA-AU 10 103284589 103284589 single base substitution C T intron_variant PACA-AU 10 103285396 103285396 deletion of <=200bp G - downstream_gene_variant PACA-AU 10 103285396 103285396 deletion of <=200bp G - intron_variant PACA-AU 10 103288459 103288459 single base substitution T A downstream_gene_variant PACA-AU 10 103288459 103288459 single base substitution T A intron_variant PACA-AU 10 103294953 103294953 single base substitution C T intron_variant PACA-AU 10 103294953 103294953 single base substitution C T upstream_gene_variant PACA-AU 10 103297466 103297468 deletion of <=200bp CTT - intron_variant PACA-AU 10 103298242 103298242 single base substitution C T intron_variant PACA-AU 10 103302236 103302236 single base substitution A G intron_variant PACA-AU 10 103302642 103302642 single base substitution G A intron_variant PACA-AU 10 103306665 103306670 deletion of <=200bp CAGATC - intron_variant PACA-CA 10 103111148 103111148 deletion of <=200bp A - upstream_gene_variant PACA-CA 10 103111886 103111886 single base substitution A C upstream_gene_variant PACA-CA 10 103111889 103111889 insertion of <=200bp - A upstream_gene_variant PACA-CA 10 103113046 103113046 single base substitution C G upstream_gene_variant PACA-CA 10 103115114 103115114 single base substitution T C intron_variant PACA-CA 10 103116216 103116216 single base substitution G T intron_variant PACA-CA 10 103116529 103116529 single base substitution T C intron_variant PACA-CA 10 103116985 103116985 single base substitution G T intron_variant PACA-CA 10 103117801 103117802 deletion of <=200bp AC - intron_variant PACA-CA 10 103119815 103119815 insertion of <=200bp - A intron_variant PACA-CA 10 103123694 103123694 single base substitution C T intron_variant PACA-CA 10 103125525 103125525 single base substitution T C intron_variant PACA-CA 10 103127440 103127440 single base substitution T C intron_variant PACA-CA 10 103128990 103128990 single base substitution A T intron_variant PACA-CA 10 103129831 103129831 single base substitution G A intron_variant PACA-CA 10 103130451 103130451 single base substitution C T intron_variant PACA-CA 10 103130964 103130964 single base substitution C T intron_variant PACA-CA 10 103130998 103130998 single base substitution A G intron_variant PACA-CA 10 103132033 103132033 single base substitution A T intron_variant PACA-CA 10 103132305 103132305 single base substitution C G intron_variant PACA-CA 10 103133450 103133450 single base substitution G A intron_variant PACA-CA 10 103133471 103133471 single base substitution G A intron_variant PACA-CA 10 103135012 103135012 single base substitution G A intron_variant PACA-CA 10 103136018 103136018 single base substitution G A intron_variant PACA-CA 10 103137330 103137330 single base substitution A G intron_variant PACA-CA 10 103142031 103142031 single base substitution C T intron_variant PACA-CA 10 103147025 103147025 single base substitution T C intron_variant PACA-CA 10 103150167 103150167 single base substitution T C intron_variant PACA-CA 10 103151870 103151870 single base substitution G A intron_variant PACA-CA 10 103158859 103158859 single base substitution G A intron_variant PACA-CA 10 103165206 103165206 single base substitution A G intron_variant PACA-CA 10 103168825 103168825 deletion of <=200bp A - intron_variant PACA-CA 10 103170390 103170390 single base substitution T C intron_variant PACA-CA 10 103177114 103177114 single base substitution G A intron_variant PACA-CA 10 103178471 103178471 single base substitution T A intron_variant PACA-CA 10 103182152 103182152 single base substitution C T intron_variant PACA-CA 10 103185011 103185011 insertion of <=200bp - T intron_variant PACA-CA 10 103185447 103185447 single base substitution G T intron_variant PACA-CA 10 103188582 103188582 single base substitution T C intron_variant PACA-CA 10 103190196 103190196 single base substitution T G exon_variant PACA-CA 10 103190196 103190196 single base substitution T G intron_variant PACA-CA 10 103190196 103190196 single base substitution T G missense_variant L30R 89T>G PACA-CA 10 103190196 103190196 single base substitution T G missense_variant L33R 98T>G PACA-CA 10 103190196 103190196 single base substitution T G missense_variant L48R 143T>G PACA-CA 10 103194580 103194580 single base substitution G A intron_variant PACA-CA 10 103196585 103196585 single base substitution A C intron_variant PACA-CA 10 103197381 103197381 single base substitution A T intron_variant PACA-CA 10 103198138 103198138 single base substitution C T intron_variant PACA-CA 10 103199093 103199093 deletion of <=200bp A - intron_variant PACA-CA 10 103199744 103199744 single base substitution A G intron_variant PACA-CA 10 103200427 103200427 single base substitution C T intron_variant PACA-CA 10 103201083 103201083 single base substitution A G intron_variant PACA-CA 10 103208929 103208929 single base substitution C T intron_variant PACA-CA 10 103209803 103209803 single base substitution G T intron_variant PACA-CA 10 103211596 103211596 single base substitution C A intron_variant PACA-CA 10 103214252 103214252 single base substitution C T intron_variant PACA-CA 10 103214659 103214659 single base substitution A G intron_variant PACA-CA 10 103215739 103215739 insertion of <=200bp - C intron_variant PACA-CA 10 103218029 103218029 single base substitution C T intron_variant PACA-CA 10 103220964 103220964 single base substitution G A intron_variant PACA-CA 10 103227341 103227341 single base substitution T C intron_variant PACA-CA 10 103230583 103230583 single base substitution C T intron_variant PACA-CA 10 103231327 103231327 single base substitution C A intron_variant PACA-CA 10 103232089 103232089 insertion of <=200bp - C intron_variant PACA-CA 10 103232535 103232547 deletion of <=200bp CTTGTCTCCTAGC - intron_variant PACA-CA 10 103244970 103244970 single base substitution C T intron_variant PACA-CA 10 103246485 103246485 single base substitution G C intron_variant PACA-CA 10 103252668 103252668 single base substitution T G intron_variant PACA-CA 10 103255526 103255526 single base substitution C T intron_variant PACA-CA 10 103261371 103261371 single base substitution T C intron_variant PACA-CA 10 103262671 103262671 single base substitution G C intron_variant PACA-CA 10 103265395 103265395 single base substitution A T intron_variant PACA-CA 10 103276849 103276849 insertion of <=200bp - A intron_variant PACA-CA 10 103281184 103281184 single base substitution A C intron_variant PACA-CA 10 103284344 103284344 single base substitution G T downstream_gene_variant PACA-CA 10 103284344 103284344 single base substitution G T intron_variant PACA-CA 10 103285082 103285082 deletion of <=200bp T - downstream_gene_variant PACA-CA 10 103285082 103285082 deletion of <=200bp T - intron_variant PACA-CA 10 103285607 103285607 single base substitution C A downstream_gene_variant PACA-CA 10 103285607 103285607 single base substitution C A intron_variant PACA-CA 10 103292083 103292084 deletion of <=200bp AT - frameshift_variant H250 PACA-CA 10 103292083 103292084 deletion of <=200bp AT - frameshift_variant H255 PACA-CA 10 103292083 103292084 deletion of <=200bp AT - frameshift_variant H291 PACA-CA 10 103292083 103292084 deletion of <=200bp AT - upstream_gene_variant PACA-CA 10 103294662 103294662 single base substitution A G missense_variant I407V 1219A>G PACA-CA 10 103294662 103294662 single base substitution A G missense_variant I412V 1234A>G PACA-CA 10 103294662 103294662 single base substitution A G missense_variant I448V 1342A>G PACA-CA 10 103294662 103294662 single base substitution A G upstream_gene_variant PACA-CA 10 103295592 103295592 single base substitution G A intron_variant PACA-CA 10 103300595 103300595 single base substitution G A intron_variant PACA-CA 10 103303058 103303058 single base substitution T G intron_variant PACA-CA 10 103311664 103311664 single base substitution T C downstream_gene_variant PACA-CA 10 103311664 103311664 single base substitution T C intron_variant PACA-CA 10 103313467 103313467 single base substitution C T 3_prime_UTR_variant PACA-CA 10 103313467 103313467 single base substitution C T downstream_gene_variant PACA-CA 10 103314669 103314669 single base substitution A G 3_prime_UTR_variant PACA-CA 10 103314669 103314669 single base substitution A G downstream_gene_variant PACA-CA 10 103317458 103317459 deletion of <=200bp AC - downstream_gene_variant PACA-CA 10 103318399 103318399 single base substitution C T downstream_gene_variant PACA-CA 10 103318568 103318568 single base substitution G A downstream_gene_variant PAEN-AU 10 103164557 103164557 single base substitution C T intron_variant PAEN-AU 10 103164996 103164996 single base substitution A G intron_variant PAEN-AU 10 103174310 103174315 deletion of <=200bp TAACTG - intron_variant PAEN-AU 10 103179383 103179383 single base substitution A T intron_variant PAEN-AU 10 103195238 103195238 single base substitution C G intron_variant PAEN-AU 10 103197784 103197784 single base substitution T C intron_variant PAEN-IT 10 103157430 103157430 single base substitution C T intron_variant PAEN-IT 10 103245841 103245841 single base substitution G T intron_variant PAEN-IT 10 103305179 103305179 single base substitution A T intron_variant PBCA-DE 10 103113249 103113249 single base substitution A G upstream_gene_variant PBCA-DE 10 103126177 103126177 single base substitution C T intron_variant PBCA-DE 10 103127166 103127166 single base substitution A T intron_variant PBCA-DE 10 103131052 103131052 single base substitution C T intron_variant PBCA-DE 10 103132323 103132327 deletion of <=200bp TGTAT - intron_variant PBCA-DE 10 103132337 103132338 deletion of <=200bp CT - intron_variant PBCA-DE 10 103132340 103132340 insertion of <=200bp - G intron_variant PBCA-DE 10 103145921 103145921 single base substitution A G intron_variant PBCA-DE 10 103150841 103150841 single base substitution G C intron_variant PBCA-DE 10 103161683 103161688 deletion of <=200bp ATGTTG - intron_variant PBCA-DE 10 103163700 103163700 single base substitution T A intron_variant PBCA-DE 10 103165938 103165938 deletion of <=200bp T - intron_variant PBCA-DE 10 103175283 103175283 single base substitution G T intron_variant PBCA-DE 10 103185354 103185354 single base substitution T A intron_variant PBCA-DE 10 103185586 103185586 insertion of <=200bp - A intron_variant PBCA-DE 10 103190765 103190765 insertion of <=200bp - CA intron_variant PBCA-DE 10 103197248 103197248 single base substitution T A intron_variant PBCA-DE 10 103202020 103202020 insertion of <=200bp - TC intron_variant PBCA-DE 10 103209587 103209587 single base substitution C T intron_variant PBCA-DE 10 103209731 103209731 single base substitution G A intron_variant PBCA-DE 10 103220228 103220228 single base substitution T C intron_variant PBCA-DE 10 103222989 103222989 insertion of <=200bp - G intron_variant PBCA-DE 10 103227679 103227679 single base substitution A T intron_variant PBCA-DE 10 103232029 103232029 single base substitution T C intron_variant PBCA-DE 10 103240312 103240312 deletion of <=200bp T - intron_variant PBCA-DE 10 103241194 103241194 single base substitution G A intron_variant PBCA-DE 10 103241319 103241319 single base substitution T G intron_variant PBCA-DE 10 103258751 103258751 insertion of <=200bp - A intron_variant PBCA-DE 10 103264874 103264874 single base substitution A G intron_variant PBCA-DE 10 103270585 103270585 single base substitution A G intron_variant PBCA-DE 10 103270634 103270634 single base substitution C T intron_variant PBCA-DE 10 103299502 103299502 single base substitution T C intron_variant PBCA-DE 10 103307353 103307353 single base substitution C T intron_variant PBCA-DE 10 103310867 103310867 single base substitution C T exon_variant PBCA-DE 10 103310867 103310867 single base substitution C T intron_variant PBCA-DE 10 103311824 103311824 single base substitution C G downstream_gene_variant PBCA-DE 10 103311824 103311824 single base substitution C G intron_variant PBCA-DE 10 103319003 103319003 single base substitution C T downstream_gene_variant PRAD-CA 10 103124605 103124605 single base substitution G A intron_variant PRAD-CA 10 103139908 103139908 single base substitution G A intron_variant PRAD-CA 10 103145087 103145087 single base substitution G A intron_variant PRAD-CA 10 103153895 103153895 single base substitution A G intron_variant PRAD-CA 10 103213960 103213960 single base substitution C T intron_variant PRAD-CA 10 103226378 103226378 single base substitution C T intron_variant PRAD-CA 10 103243421 103243421 single base substitution T G intron_variant PRAD-CA 10 103243739 103243739 single base substitution C T intron_variant PRAD-CA 10 103256351 103256351 single base substitution A C intron_variant PRAD-CA 10 103283276 103283276 single base substitution T A downstream_gene_variant PRAD-CA 10 103283276 103283276 single base substitution T A intron_variant PRAD-CA 10 103286630 103286630 single base substitution T C downstream_gene_variant PRAD-CA 10 103286630 103286630 single base substitution T C intron_variant PRAD-CA 10 103319725 103319725 single base substitution C T downstream_gene_variant PRAD-UK 10 103116810 103116810 single base substitution C T intron_variant PRAD-UK 10 103125082 103125082 single base substitution A T intron_variant PRAD-UK 10 103139693 103139693 single base substitution C A intron_variant PRAD-UK 10 103146626 103146626 single base substitution T G intron_variant PRAD-UK 10 103149974 103149974 single base substitution A G intron_variant PRAD-UK 10 103152544 103152544 single base substitution G C intron_variant PRAD-UK 10 103162856 103162856 single base substitution A C intron_variant PRAD-UK 10 103176972 103176972 single base substitution G A intron_variant PRAD-UK 10 103210225 103210225 single base substitution C G intron_variant PRAD-UK 10 103224307 103224307 insertion of <=200bp - C intron_variant PRAD-UK 10 103240743 103240743 single base substitution C G intron_variant PRAD-UK 10 103249921 103249921 single base substitution A G intron_variant PRAD-UK 10 103263570 103263570 single base substitution C T intron_variant PRAD-UK 10 103278177 103278177 single base substitution C T intron_variant PRAD-UK 10 103283856 103283856 single base substitution T A downstream_gene_variant PRAD-UK 10 103283856 103283856 single base substitution T A intron_variant PRAD-UK 10 103304335 103304335 deletion of <=200bp T - intron_variant PRAD-UK 10 103304339 103304339 single base substitution T A intron_variant PRAD-UK 10 103309782 103309782 single base substitution A G intron_variant PRAD-UK 10 103320333 103320333 single base substitution C G downstream_gene_variant READ-US 10 103285923 103285923 single base substitution C A downstream_gene_variant READ-US 10 103285923 103285923 single base substitution C A exon_variant READ-US 10 103285923 103285923 single base substitution C A missense_variant S196Y 587C>A READ-US 10 103285923 103285923 single base substitution C A missense_variant S201Y 602C>A READ-US 10 103285923 103285923 single base substitution C A missense_variant S237Y 710C>A RECA-EU 10 103111715 103111715 single base substitution C G upstream_gene_variant RECA-EU 10 103132887 103132887 single base substitution A T intron_variant RECA-EU 10 103149925 103149925 single base substitution C T intron_variant RECA-EU 10 103152841 103152841 single base substitution A T intron_variant RECA-EU 10 103181642 103181642 single base substitution G T intron_variant RECA-EU 10 103183729 103183729 single base substitution G T intron_variant RECA-EU 10 103186300 103186300 single base substitution A G intron_variant RECA-EU 10 103192813 103192813 single base substitution A G intron_variant RECA-EU 10 103200250 103200250 single base substitution G C intron_variant RECA-EU 10 103200806 103200806 single base substitution A G intron_variant RECA-EU 10 103212724 103212724 single base substitution C T intron_variant RECA-EU 10 103238731 103238731 single base substitution A G intron_variant RECA-EU 10 103238732 103238732 single base substitution A T intron_variant RECA-EU 10 103241379 103241379 single base substitution C A intron_variant RECA-EU 10 103242765 103242765 single base substitution A C intron_variant RECA-EU 10 103243901 103243901 single base substitution A T intron_variant RECA-EU 10 103270822 103270822 single base substitution A T intron_variant RECA-EU 10 103273342 103273342 single base substitution C G intron_variant RECA-EU 10 103278363 103278363 single base substitution C T intron_variant RECA-EU 10 103293020 103293020 single base substitution C T intron_variant RECA-EU 10 103293020 103293020 single base substitution C T upstream_gene_variant RECA-EU 10 103297708 103297708 single base substitution T C intron_variant RECA-EU 10 103306809 103306809 single base substitution A G intron_variant RECA-EU 10 103307091 103307091 single base substitution T C intron_variant SKCA-BR 10 103109828 103109828 single base substitution A G upstream_gene_variant SKCA-BR 10 103112504 103112504 single base substitution C T upstream_gene_variant SKCA-BR 10 103113580 103113580 single base substitution C T upstream_gene_variant SKCA-BR 10 103113723 103113723 single base substitution C T upstream_gene_variant SKCA-BR 10 103122182 103122182 single base substitution C T intron_variant SKCA-BR 10 103124575 103124576 deletion of <=200bp CT - intron_variant SKCA-BR 10 103126666 103126676 deletion of <=200bp AATATATATTT - intron_variant SKCA-BR 10 103126695 103126695 single base substitution T A intron_variant SKCA-BR 10 103126695 103126707 deletion of <=200bp TTATATATATTTA - intron_variant SKCA-BR 10 103126761 103126761 single base substitution A T intron_variant SKCA-BR 10 103127623 103127623 single base substitution C T intron_variant SKCA-BR 10 103130379 103130379 single base substitution T C intron_variant SKCA-BR 10 103135447 103135447 single base substitution C T intron_variant SKCA-BR 10 103138277 103138278 deletion of <=200bp AT - intron_variant SKCA-BR 10 103138991 103138991 single base substitution A T intron_variant SKCA-BR 10 103140783 103140783 single base substitution T G intron_variant SKCA-BR 10 103140968 103140968 single base substitution T C intron_variant SKCA-BR 10 103143155 103143155 single base substitution A T intron_variant SKCA-BR 10 103145372 103145372 insertion of <=200bp - CTT intron_variant SKCA-BR 10 103145586 103145586 insertion of <=200bp - GT intron_variant SKCA-BR 10 103148087 103148092 deletion of <=200bp TTTTTA - intron_variant SKCA-BR 10 103148868 103148872 deletion of <=200bp TTGTG - intron_variant SKCA-BR 10 103149367 103149370 deletion of <=200bp CTTT - intron_variant SKCA-BR 10 103150110 103150111 deletion of <=200bp TC - intron_variant SKCA-BR 10 103150111 103150111 single base substitution C T intron_variant SKCA-BR 10 103150253 103150253 insertion of <=200bp - CCCGG intron_variant SKCA-BR 10 103152265 103152265 single base substitution C T intron_variant SKCA-BR 10 103152750 103152750 single base substitution C T intron_variant SKCA-BR 10 103162963 103162963 single base substitution T A intron_variant SKCA-BR 10 103163523 103163523 single base substitution G A intron_variant SKCA-BR 10 103163747 103163747 single base substitution A G intron_variant SKCA-BR 10 103163761 103163761 single base substitution A G intron_variant SKCA-BR 10 103163763 103163763 single base substitution A G intron_variant SKCA-BR 10 103163765 103163765 single base substitution A G intron_variant SKCA-BR 10 103163767 103163767 single base substitution A G intron_variant SKCA-BR 10 103163932 103163932 single base substitution T C intron_variant SKCA-BR 10 103164627 103164627 single base substitution T G intron_variant SKCA-BR 10 103164754 103164756 deletion of <=200bp TAA - intron_variant SKCA-BR 10 103168553 103168553 single base substitution C T intron_variant SKCA-BR 10 103173796 103173796 single base substitution G A intron_variant SKCA-BR 10 103175243 103175298 deletion of <=200bp TTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATG - intron_variant SKCA-BR 10 103176641 103176641 single base substitution T A intron_variant SKCA-BR 10 103179836 103179836 single base substitution G A intron_variant SKCA-BR 10 103189623 103189623 insertion of <=200bp - TA intron_variant SKCA-BR 10 103189659 103189659 single base substitution G T intron_variant SKCA-BR 10 103190567 103190567 single base substitution C A intron_variant SKCA-BR 10 103192636 103192636 single base substitution C T intron_variant SKCA-BR 10 103196382 103196398 deletion of <=200bp AATAGATAGATAGATAG - intron_variant SKCA-BR 10 103199589 103199589 single base substitution T A intron_variant SKCA-BR 10 103200655 103200655 single base substitution C T intron_variant SKCA-BR 10 103200656 103200656 single base substitution C T intron_variant SKCA-BR 10 103201440 103201440 single base substitution C T intron_variant SKCA-BR 10 103202041 103202041 single base substitution G C intron_variant SKCA-BR 10 103202047 103202047 single base substitution G C intron_variant SKCA-BR 10 103202053 103202053 single base substitution A C intron_variant SKCA-BR 10 103202061 103202061 single base substitution G A intron_variant SKCA-BR 10 103203537 103203537 single base substitution A C intron_variant SKCA-BR 10 103203552 103203552 single base substitution C T intron_variant SKCA-BR 10 103204179 103204179 single base substitution C T intron_variant SKCA-BR 10 103205858 103205858 insertion of <=200bp - TC intron_variant SKCA-BR 10 103208004 103208004 single base substitution C T intron_variant SKCA-BR 10 103213675 103213675 single base substitution C A intron_variant SKCA-BR 10 103214817 103214817 insertion of <=200bp - CT intron_variant SKCA-BR 10 103214974 103214975 deletion of <=200bp AT - intron_variant SKCA-BR 10 103216168 103216168 single base substitution G A intron_variant SKCA-BR 10 103235296 103235296 insertion of <=200bp - CAAAACA intron_variant SKCA-BR 10 103235758 103235758 single base substitution G A intron_variant SKCA-BR 10 103236425 103236425 single base substitution T C intron_variant SKCA-BR 10 103244229 103244229 single base substitution A C intron_variant SKCA-BR 10 103246742 103246742 single base substitution A G intron_variant SKCA-BR 10 103251471 103251471 single base substitution C T intron_variant SKCA-BR 10 103255765 103255766 deletion of <=200bp AT - intron_variant SKCA-BR 10 103257206 103257206 single base substitution C T intron_variant SKCA-BR 10 103260776 103260776 single base substitution A C intron_variant SKCA-BR 10 103264535 103264535 single base substitution A G intron_variant SKCA-BR 10 103264894 103264894 insertion of <=200bp - ATGTATATG intron_variant SKCA-BR 10 103264914 103264914 insertion of <=200bp - GTATATA intron_variant SKCA-BR 10 103266560 103266560 single base substitution C T intron_variant SKCA-BR 10 103267868 103267868 single base substitution G A intron_variant SKCA-BR 10 103278603 103278603 insertion of <=200bp - CACTTAG intron_variant SKCA-BR 10 103279277 103279277 single base substitution C T intron_variant SKCA-BR 10 103281259 103281259 single base substitution C T intron_variant SKCA-BR 10 103286544 103286544 single base substitution C T downstream_gene_variant SKCA-BR 10 103286544 103286544 single base substitution C T intron_variant SKCA-BR 10 103287547 103287547 single base substitution T A downstream_gene_variant SKCA-BR 10 103287547 103287547 single base substitution T A intron_variant SKCA-BR 10 103287552 103287552 single base substitution T C downstream_gene_variant SKCA-BR 10 103287552 103287552 single base substitution T C intron_variant SKCA-BR 10 103288064 103288064 single base substitution A C downstream_gene_variant SKCA-BR 10 103288064 103288064 single base substitution A C intron_variant SKCA-BR 10 103292541 103292541 insertion of <=200bp - GTA intron_variant SKCA-BR 10 103292541 103292541 insertion of <=200bp - GTA upstream_gene_variant SKCA-BR 10 103301361 103301361 single base substitution C T intron_variant SKCA-BR 10 103307090 103307090 insertion of <=200bp - TC intron_variant SKCA-BR 10 103311230 103311230 single base substitution C T downstream_gene_variant SKCA-BR 10 103311230 103311230 single base substitution C T intron_variant SKCA-BR 10 103312639 103312639 single base substitution C T downstream_gene_variant SKCA-BR 10 103312639 103312639 single base substitution C T intron_variant SKCA-BR 10 103314626 103314626 single base substitution C T 3_prime_UTR_variant SKCA-BR 10 103314626 103314626 single base substitution C T downstream_gene_variant SKCA-BR 10 103314658 103314658 single base substitution T C 3_prime_UTR_variant SKCA-BR 10 103314658 103314658 single base substitution T C downstream_gene_variant SKCA-BR 10 103317821 103317821 single base substitution C A downstream_gene_variant SKCA-BR 10 103320215 103320215 single base substitution C T downstream_gene_variant SKCM-US 10 103281544 103281544 single base substitution C T downstream_gene_variant SKCM-US 10 103281544 103281544 single base substitution C T exon_variant SKCM-US 10 103281544 103281544 single base substitution C T missense_variant S117F 350C>T SKCM-US 10 103281544 103281544 single base substitution C T missense_variant S122F 365C>T SKCM-US 10 103281544 103281544 single base substitution C T missense_variant S140F 419C>T SKCM-US 10 103281544 103281544 single base substitution C T missense_variant S158F 473C>T SKCM-US 10 103292172 103292172 single base substitution C T stop_gained R280* 838C>T SKCM-US 10 103292172 103292172 single base substitution C T stop_gained R285* 853C>T SKCM-US 10 103292172 103292172 single base substitution C T stop_gained R321* 961C>T SKCM-US 10 103292172 103292172 single base substitution C T upstream_gene_variant SKCM-US 10 103294527 103294527 single base substitution C T missense_variant R362C 1084C>T SKCM-US 10 103294527 103294527 single base substitution C T missense_variant R367C 1099C>T SKCM-US 10 103294527 103294527 single base substitution C T missense_variant R403C 1207C>T SKCM-US 10 103294527 103294527 single base substitution C T upstream_gene_variant SKCM-US 10 103298056 103298056 single base substitution T A exon_variant SKCM-US 10 103298056 103298056 single base substitution T A synonymous_variant I487I 1461T>A SKCM-US 10 103298056 103298056 single base substitution T A synonymous_variant I492I 1476T>A SKCM-US 10 103298056 103298056 single base substitution T A synonymous_variant I528I 1584T>A SKCM-US 10 103310477 103310477 single base substitution C T exon_variant SKCM-US 10 103310477 103310477 single base substitution C T stop_gained R519* 1555C>T SKCM-US 10 103310477 103310477 single base substitution C T stop_gained R524* 1570C>T SKCM-US 10 103310477 103310477 single base substitution C T stop_gained R560* 1678C>T SKCM-US 10 103310563 103310563 single base substitution C T exon_variant SKCM-US 10 103310563 103310563 single base substitution C T synonymous_variant A547A 1641C>T SKCM-US 10 103310563 103310563 single base substitution C T synonymous_variant A552A 1656C>T SKCM-US 10 103310563 103310563 single base substitution C T synonymous_variant A588A 1764C>T SKCM-US 10 103310575 103310575 single base substitution C T exon_variant SKCM-US 10 103310575 103310575 single base substitution C T synonymous_variant P551P 1653C>T SKCM-US 10 103310575 103310575 single base substitution C T synonymous_variant P556P 1668C>T SKCM-US 10 103310575 103310575 single base substitution C T synonymous_variant P592P 1776C>T STAD-US 10 103190192 103190192 single base substitution G A exon_variant STAD-US 10 103190192 103190192 single base substitution G A intron_variant STAD-US 10 103190192 103190192 single base substitution G A missense_variant A29T 85G>A STAD-US 10 103190192 103190192 single base substitution G A missense_variant A32T 94G>A STAD-US 10 103190192 103190192 single base substitution G A missense_variant A47T 139G>A STAD-US 10 103221770 103221770 single base substitution C T exon_variant STAD-US 10 103221770 103221770 single base substitution C T intron_variant STAD-US 10 103221770 103221770 single base substitution C T synonymous_variant G27G 81C>T STAD-US 10 103221770 103221770 single base substitution C T synonymous_variant G45G 135C>T STAD-US 10 103221770 103221770 single base substitution C T synonymous_variant G63G 189C>T STAD-US 10 103292822 103292822 single base substitution G T synonymous_variant T323T 969G>T STAD-US 10 103292822 103292822 single base substitution G T synonymous_variant T328T 984G>T STAD-US 10 103292822 103292822 single base substitution G T synonymous_variant T364T 1092G>T STAD-US 10 103292822 103292822 single base substitution G T upstream_gene_variant STAD-US 10 103294454 103294454 single base substitution G A synonymous_variant T337T 1011G>A STAD-US 10 103294454 103294454 single base substitution G A synonymous_variant T342T 1026G>A STAD-US 10 103294454 103294454 single base substitution G A synonymous_variant T378T 1134G>A STAD-US 10 103294454 103294454 single base substitution G A upstream_gene_variant STAD-US 10 103294488 103294488 single base substitution C T missense_variant R349C 1045C>T STAD-US 10 103294488 103294488 single base substitution C T missense_variant R354C 1060C>T STAD-US 10 103294488 103294488 single base substitution C T missense_variant R390C 1168C>T STAD-US 10 103294488 103294488 single base substitution C T upstream_gene_variant STAD-US 10 103294576 103294576 single base substitution G A missense_variant R378Q 1133G>A STAD-US 10 103294576 103294576 single base substitution G A missense_variant R383Q 1148G>A STAD-US 10 103294576 103294576 single base substitution G A missense_variant R419Q 1256G>A STAD-US 10 103294576 103294576 single base substitution G A upstream_gene_variant STAD-US 10 103295124 103295124 single base substitution G A missense_variant S413N 1238G>A STAD-US 10 103295124 103295124 single base substitution G A missense_variant S418N 1253G>A STAD-US 10 103295124 103295124 single base substitution G A missense_variant S454N 1361G>A STAD-US 10 103295124 103295124 single base substitution G A upstream_gene_variant STAD-US 10 103298091 103298091 single base substitution G A exon_variant STAD-US 10 103298091 103298091 single base substitution G A missense_variant R499H 1496G>A STAD-US 10 103298091 103298091 single base substitution G A missense_variant R504H 1511G>A STAD-US 10 103298091 103298091 single base substitution G A missense_variant R540H 1619G>A STAD-US 10 103310573 103310573 deletion of <=200bp C - exon_variant STAD-US 10 103310573 103310573 deletion of <=200bp C - frameshift_variant P551 STAD-US 10 103310573 103310573 deletion of <=200bp C - frameshift_variant P556 STAD-US 10 103310573 103310573 deletion of <=200bp C - frameshift_variant P592 STAD-US 10 103310573 103310573 insertion of <=200bp - C exon_variant STAD-US 10 103310573 103310573 insertion of <=200bp - C frameshift_variant P551P? STAD-US 10 103310573 103310573 insertion of <=200bp - C frameshift_variant P556P? STAD-US 10 103310573 103310573 insertion of <=200bp - C frameshift_variant P592P? THCA-US 10 103292735 103292735 single base substitution C T synonymous_variant C294C 882C>T THCA-US 10 103292735 103292735 single base substitution C T synonymous_variant C299C 897C>T THCA-US 10 103292735 103292735 single base substitution C T synonymous_variant C335C 1005C>T THCA-US 10 103292735 103292735 single base substitution C T upstream_gene_variant UCEC-US 10 103239193 103239193 single base substitution G T exon_variant UCEC-US 10 103239193 103239193 single base substitution G T missense_variant K101N 303G>T UCEC-US 10 103239193 103239193 single base substitution G T missense_variant K60N 180G>T UCEC-US 10 103239193 103239193 single base substitution G T missense_variant K65N 195G>T UCEC-US 10 103239193 103239193 single base substitution G T missense_variant K83N 249G>T UCEC-US 10 103281473 103281473 single base substitution G T downstream_gene_variant UCEC-US 10 103281473 103281473 single base substitution G T exon_variant UCEC-US 10 103281473 103281473 single base substitution G T missense_variant K116N 348G>T UCEC-US 10 103281473 103281473 single base substitution G T missense_variant K134N 402G>T UCEC-US 10 103281473 103281473 single base substitution G T missense_variant K93N 279G>T UCEC-US 10 103281473 103281473 single base substitution G T missense_variant K98N 294G>T UCEC-US 10 103285901 103285901 single base substitution G A downstream_gene_variant UCEC-US 10 103285901 103285901 single base substitution G A exon_variant UCEC-US 10 103285901 103285901 single base substitution G A missense_variant E189K 565G>A UCEC-US 10 103285901 103285901 single base substitution G A missense_variant E194K 580G>A UCEC-US 10 103285901 103285901 single base substitution G A missense_variant E230K 688G>A UCEC-US 10 103285923 103285923 single base substitution C A downstream_gene_variant UCEC-US 10 103285923 103285923 single base substitution C A exon_variant UCEC-US 10 103285923 103285923 single base substitution C A missense_variant S196Y 587C>A UCEC-US 10 103285923 103285923 single base substitution C A missense_variant S201Y 602C>A UCEC-US 10 103285923 103285923 single base substitution C A missense_variant S237Y 710C>A UCEC-US 10 103285953 103285953 single base substitution G T downstream_gene_variant UCEC-US 10 103285953 103285953 single base substitution G T missense_variant G206V 617G>T UCEC-US 10 103285953 103285953 single base substitution G T missense_variant G211V 632G>T UCEC-US 10 103285953 103285953 single base substitution G T missense_variant G247V 740G>T UCEC-US 10 103291047 103291047 single base substitution C A missense_variant S225Y 674C>A UCEC-US 10 103291047 103291047 single base substitution C A missense_variant S230Y 689C>A UCEC-US 10 103291047 103291047 single base substitution C A missense_variant S266Y 797C>A UCEC-US 10 103291047 103291047 single base substitution C A upstream_gene_variant UCEC-US 10 103292062 103292062 single base substitution C A missense_variant S243Y 728C>A UCEC-US 10 103292062 103292062 single base substitution C A missense_variant S248Y 743C>A UCEC-US 10 103292062 103292062 single base substitution C A missense_variant S284Y 851C>A UCEC-US 10 103292062 103292062 single base substitution C A upstream_gene_variant UCEC-US 10 103292745 103292745 single base substitution C T missense_variant L298F 892C>T UCEC-US 10 103292745 103292745 single base substitution C T missense_variant L303F 907C>T UCEC-US 10 103292745 103292745 single base substitution C T missense_variant L339F 1015C>T UCEC-US 10 103292745 103292745 single base substitution C T upstream_gene_variant UCEC-US 10 103294576 103294576 single base substitution G A missense_variant R378Q 1133G>A UCEC-US 10 103294576 103294576 single base substitution G A missense_variant R383Q 1148G>A UCEC-US 10 103294576 103294576 single base substitution G A missense_variant R419Q 1256G>A UCEC-US 10 103294576 103294576 single base substitution G A upstream_gene_variant UCEC-US 10 103294633 103294633 single base substitution A G missense_variant Y397C 1190A>G UCEC-US 10 103294633 103294633 single base substitution A G missense_variant Y402C 1205A>G UCEC-US 10 103294633 103294633 single base substitution A G missense_variant Y438C 1313A>G UCEC-US 10 103294633 103294633 single base substitution A G upstream_gene_variant UCEC-US 10 103295126 103295126 single base substitution A G missense_variant T414A 1240A>G UCEC-US 10 103295126 103295126 single base substitution A G missense_variant T419A 1255A>G UCEC-US 10 103295126 103295126 single base substitution A G missense_variant T455A 1363A>G UCEC-US 10 103295126 103295126 single base substitution A G upstream_gene_variant UCEC-US 10 103296370 103296370 single base substitution C T exon_variant UCEC-US 10 103296370 103296370 single base substitution C T stop_gained R472* 1414C>T UCEC-US 10 103296370 103296370 single base substitution C T stop_gained R477* 1429C>T UCEC-US 10 103296370 103296370 single base substitution C T stop_gained R513* 1537C>T UCEC-US 10 103310493 103310493 single base substitution A G exon_variant UCEC-US 10 103310493 103310493 single base substitution A G missense_variant E524G 1571A>G UCEC-US 10 103310493 103310493 single base substitution A G missense_variant E529G 1586A>G UCEC-US 10 103310493 103310493 single base substitution A G missense_variant E565G 1694A>G UCEC-US 10 103310583 103310583 single base substitution C T exon_variant UCEC-US 10 103310583 103310583 single base substitution C T missense_variant S554F 1661C>T UCEC-US 10 103310583 103310583 single base substitution C T missense_variant S559F 1676C>T UCEC-US 10 103310583 103310583 single base substitution C T missense_variant S595F 1784C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-HU-A4GT-01 COSM914033 c.1256G>A p.R419Q Substitution - Missense 10:101534819-101534819 + TCGA-BS-A0UF-01 COSM914031 c.851C>A p.S284Y Substitution - Missense 10:101532305-101532305 + 2334191 COSM318965 c.349A>G p.S117G Substitution - Missense 10:101521663-101521663 + TCGA-16-0861-01 COSM3396880 c.421T>G p.F141V Substitution - Missense 10:101521735-101521735 + Au2 COSM5599147 c.1003T>C p.C335R Substitution - Missense 10:101532976-101532976 + TCGA-GM-A3XL-01 COSM3806312 c.1379G>C p.R460T Substitution - Missense 10:101535385-101535385 + 2492701 COSM5599147 c.1003T>C p.C335R Substitution - Missense 10:101532976-101532976 + H23 COSM1196427 c.1814G>A p.R605K Substitution - Missense 10:101550856-101550856 + 2492703 COSM5599147 c.1003T>C p.C335R Substitution - Missense 10:101532976-101532976 + TCGA-BR-4184-01 COSM4011124 c.1168C>T p.R390C Substitution - Missense 10:101534731-101534731 + pfg068T COSM4759611 c.366G>T p.K122N Substitution - Missense 10:101521680-101521680 + SW620 COSM1675503 c.1146T>G p.H382Q Substitution - Missense 10:101534709-101534709 + TCGA-CA-6717-01 COSM1345391 c.1374T>G p.F458L Substitution - Missense 10:101535380-101535380 + PT19_1 COSM5899591 c.540C>A p.F180L Substitution - Missense 10:101521854-101521854 + T263 COSM4666418 c.1773_1774insC p.R594fs*>13 Insertion - Frameshift 10:101550815-101550816 + TCGA-AZ-4315-01 COSM914036 c.1537C>T p.R513* Substitution - Nonsense 10:101536613-101536613 + 2492700 COSM5599147 c.1003T>C p.C335R Substitution - Missense 10:101532976-101532976 + TCGA-BS-A0U7-01 COSM914029 c.740G>T p.G247V Substitution - Missense 10:101526196-101526196 + S00472 COSM5657629 c.83C>T p.S28F Substitution - Missense 10:101430379-101430379 + TCGA-A6-5661-01 COSM1345392 c.1566G>T p.G522G Substitution - coding silent 10:101536642-101536642 + TCGA-13-0887-01 COSM73873 c.196C>T p.P66S Substitution - Missense 10:101462020-101462020 + TCGA-BS-A0UL-01 COSM914038 c.1784C>T p.S595F Substitution - Missense 10:101550826-101550826 + TCGA-AX-A05Z-01 COSM914030 c.797C>A p.S266Y Substitution - Missense 10:101531290-101531290 + TCGA-EP-A2KB-01 COSM4921592 c.338A>T p.N113I Substitution - Missense 10:101521652-101521652 + TCGA-EE-A181-06 COSM3433646 c.961C>T p.R321* Substitution - Nonsense 10:101532415-101532415 + HCC026T COSM5817910 c.1004G>C p.C335S Substitution - Missense 10:101532977-101532977 + PCSI_0358_Pa_P_526 COSM5761171 c.143T>G p.L48R Substitution - Missense 10:101430439-101430439 + TCGA-AX-A063-01 COSM914034 c.1313A>G p.Y438C Substitution - Missense 10:101534876-101534876 + S02290 COSM5686390 c.344C>T p.T115I Substitution - Missense 10:101521658-101521658 + CSCC-55-T COSM4563526 c.978G>A p.K326K Substitution - coding silent 10:101532432-101532432 + ESCC_37 COSM2058532 c.1528C>T p.R510C Substitution - Missense 10:101536604-101536604 + 2521249 COSM5888073 c.53C>T p.S18F Substitution - Missense 10:101430349-101430349 + T3436 COSM4666417 c.1277G>A p.R426Q Substitution - Missense 10:101534840-101534840 + ESCC-D19 COSM5045750 c.878T>C p.L293S Substitution - Missense 10:101532332-101532332 + ESCC_BICR_016T COSM5439454 c.1526T>C p.V509A Substitution - Missense 10:101536602-101536602 + TCGA-EI-6917-01 COSM914028 c.710C>A p.S237Y Substitution - Missense 10:101526166-101526166 + S02404 COSM5700644 c.1388A>G p.N463S Substitution - Missense 10:101535394-101535394 + TCGA-AY-5543-01 COSM1345390 c.810A>C p.A270A Substitution - coding silent 10:101531303-101531303 + EGC15 COSM5049842 c.1009C>T p.R337* Substitution - Nonsense 10:101532982-101532982 + TCGA-D8-A27G-01 COSM3806311 c.580G>C p.E194Q Substitution - Missense 10:101526036-101526036 + HSJD_DIPG001 COSM4746028 c.710C>G p.S237C Substitution - Missense 10:101526166-101526166 + CN-AML-25-T COSM4908623 c.691A>G p.R231G Substitution - Missense 10:101526147-101526147 + TCGA-CD-A4MJ-01 COSM1185067 c.139G>A p.A47T Substitution - Missense 10:101430435-101430435 + CN-AML-CR-59-Dx COSM4908623 c.691A>G p.R231G Substitution - Missense 10:101526147-101526147 + T2389 COSM4666415 c.108G>A p.S36S Substitution - coding silent 10:101430404-101430404 + TCGA-A8-A08P-01 COSM426956 c.1440G>C p.V480V Substitution - coding silent 10:101535446-101535446 + TCGA-B0-4697-01 COSM287879 c.1248T>G p.I416M Substitution - Missense 10:101534811-101534811 + TCGA-EE-A20C-06 COSM3433649 c.1764C>T p.A588A Substitution - coding silent 10:101550806-101550806 + YUSCO COSM1702935 c.896G>A p.R299Q Substitution - Missense 10:101532350-101532350 + T1194 COSM1185067 c.139G>A p.A47T Substitution - Missense 10:101430435-101430435 + 2492702 COSM5599147 c.1003T>C p.C335R Substitution - Missense 10:101532976-101532976 + TCGA-AP-A0LM-01 COSM914037 c.1694A>G p.E565G Substitution - Missense 10:101550736-101550736 + HCC96T COSM3665445 c.654G>A p.V218V Substitution - coding silent 10:101526110-101526110 + TCGA-BS-A0UF-01 COSM914032 c.1015C>T p.L339F Substitution - Missense 10:101532988-101532988 + TCGA-AX-A06H-01 COSM914026 c.402G>T p.K134N Substitution - Missense 10:101521716-101521716 + K347 COSM249306 c.1793G>A p.R598Q Substitution - Missense 10:101550835-101550835 + CN-AML-NR-25-Dx COSM4908623 c.691A>G p.R231G Substitution - Missense 10:101526147-101526147 + LUAD-NYU284 COSM372625 c.144C>T p.L48L Substitution - coding silent 10:101430440-101430440 + TCGA-AG-3583-01 COSM287879 c.1248T>G p.I416M Substitution - Missense 10:101534811-101534811 + TCGA-60-2698-01 COSM682465 c.445C>T p.Q149* Substitution - Nonsense 10:101521759-101521759 + TCGA-EE-A2MR-06 COSM3433647 c.1207C>T p.R403C Substitution - Missense 10:101534770-101534770 + TCGA-E1-5307-01 COSM3966837 c.372G>A p.R124R Substitution - coding silent 10:101521686-101521686 + C086 COSM5527463 c.540C>T p.F180F Substitution - coding silent 10:101521854-101521854 + GC1_T COSM147032 c.425A>G p.E142G Substitution - Missense 10:101521739-101521739 + CHC1531T COSM4804813 c.962G>T p.R321L Substitution - Missense 10:101532416-101532416 + PCSI_0078_Pa_P_526 COSM3375369 c.1342A>G p.I448V Substitution - Missense 10:101534905-101534905 + T204 COSM3806310 c.113G>A p.R38Q Substitution - Missense 10:101430409-101430409 + TARGET-20-PASVVS-09A-01D COSM5487334 c.823_824insT p.I276fs*5 Insertion - Frameshift 10:101531316-101531317 + PD18247a COSM5770941 c.466C>G p.L156V Substitution - Missense 10:101521780-101521780 + RK207_C01 COSM3741468 c.863G>T p.C288F Substitution - Missense 10:101532317-101532317 + TCGA-24-2289-01 COSM117781 c.1541T>A p.F514Y Substitution - Missense 10:101536617-101536617 + 8012854 COSM1158896 c.694A>G p.M232V Substitution - Missense 10:101526150-101526150 + TCGA-BR-8680-01 COSM4011123 c.1134G>A p.T378T Substitution - coding silent 10:101534697-101534697 + 6115114 COSM5555110 c.76G>C p.G26R Substitution - Missense 10:101430372-101430372 + SW620 COSM1675503 c.1146T>G p.H382Q Substitution - Missense 10:101534709-101534709 + Gp2D COSM2058523 c.815A>G p.Y272C Substitution - Missense 10:101531308-101531308 + SNUH_G26_S1 COSM3997739 c.556+7C>G p.? Unknown 10:101521877-101521877 + TCGA-BF-A3DJ-01 COSM169535 c.1678C>T p.R560* Substitution - Nonsense 10:101550720-101550720 + NCI-H23 COSM1196427 c.1814G>A p.R605K Substitution - Missense 10:101550856-101550856 + TCGA-FS-A1YY-06 COSM3433650 c.1776C>T p.P592P Substitution - coding silent 10:101550818-101550818 + CSCC-45-T COSM4510852 c.84C>T p.S28S Substitution - coding silent 10:101430380-101430380 + TCGA-BR-4257-01 COSM4011122 c.1092G>T p.T364T Substitution - coding silent 10:101533065-101533065 + SC_9047 COSM1185067 c.139G>A p.A47T Substitution - Missense 10:101430435-101430435 + T3094 COSM1345393 c.1774delC p.R594fs*>12 Deletion - Frameshift 10:101550816-101550816 + pfg181T COSM1345393 c.1774delC p.R594fs*>12 Deletion - Frameshift 10:101550816-101550816 + TCGA-FS-A4F8-06 COSM3433648 c.1584T>A p.I528I Substitution - coding silent 10:101538299-101538299 + CSCC-44-T COSM4548252 c.442G>A p.D148N Substitution - Missense 10:101521756-101521756 + PT37 COSM5919801 c.1322C>T p.S441F Substitution - Missense 10:101534885-101534885 + TCGA-AK-3461-01 COSM287879 c.1248T>G p.I416M Substitution - Missense 10:101534811-101534811 + LUAD-RT-S01866 COSM385095 c.555A>T p.P185P Substitution - coding silent 10:101521869-101521869 + ICGC_0029 COSM1158896 c.694A>G p.M232V Substitution - Missense 10:101526150-101526150 + EGC15 COSM200156 c.962G>A p.R321Q Substitution - Missense 10:101532416-101532416 + TCGA-LL-A5YL-01 COSM3806310 c.113G>A p.R38Q Substitution - Missense 10:101430409-101430409 + T2269 COSM4666416 c.833A>G p.D278G Substitution - Missense 10:101531326-101531326 + TCGA-B5-A0JY-01 COSM914036 c.1537C>T p.R513* Substitution - Nonsense 10:101536613-101536613 + TCGA-BR-6457-01 COSM4011126 c.1619G>A p.R540H Substitution - Missense 10:101538334-101538334 + CSCC-40-T COSM914033 c.1256G>A p.R419Q Substitution - Missense 10:101534819-101534819 + TCGA-A6-5665-01 COSM1345389 c.777C>T p.D259D Substitution - coding silent 10:101531270-101531270 + D28 COSM1504226 c.1194C>T p.T398T Substitution - coding silent 10:101534757-101534757 + UM-SCC-17B COSM4598775 c.1493G>A p.C498Y Substitution - Missense 10:101536569-101536569 + YUKIL COSM1702934 c.869G>A p.R290K Substitution - Missense 10:101532323-101532323 + RK046_C01 COSM1627284 c.641A>G p.E214G Substitution - Missense 10:101526097-101526097 + TCGA-D1-A16X-01 COSM914035 c.1363A>G p.T455A Substitution - Missense 10:101535369-101535369 + 587376 COSM169535 c.1678C>T p.R560* Substitution - Nonsense 10:101550720-101550720 + HSJD_DIPG001 COSM4746029 c.709T>A p.S237T Substitution - Missense 10:101526165-101526165 + 587228 COSM1185067 c.139G>A p.A47T Substitution - Missense 10:101430435-101430435 + 30996 COSM5043985 c.765C>G p.N255K Substitution - Missense 10:101531258-101531258 + TCGA-DI-A0WH-01 COSM914033 c.1256G>A p.R419Q Substitution - Missense 10:101534819-101534819 + PD4954a COSM5778253 c.48+3G>A p.? Unknown 10:101354231-101354231 + TCGA-CG-5726-01 COSM4011121 c.189C>T p.G63G Substitution - coding silent 10:101462013-101462013 + TCGA-AP-A051-01 COSM914025 c.303G>T p.K101N Substitution - Missense 10:101479436-101479436 + TCGA-A6-6780-01 COSM1345393 c.1774delC p.R594fs*>12 Deletion - Frameshift 10:101550816-101550816 + HCC96 COSM3665445 c.654G>A p.V218V Substitution - coding silent 10:101526110-101526110 + ATL041 COSM5703425 c.964G>A p.D322N Substitution - Missense 10:101532418-101532418 + LC_C9 COSM1188028 c.102G>T p.M34I Substitution - Missense 10:101430398-101430398 + TCGA-EL-A3CZ-01 COSM3367857 c.1005C>T p.C335C Substitution - coding silent 10:101532978-101532978 + TCGA-BS-A0UV-01 COSM914028 c.710C>A p.S237Y Substitution - Missense 10:101526166-101526166 + Gp5D COSM2058523 c.815A>G p.Y272C Substitution - Missense 10:101531308-101531308 + TCGA-C8-A275-01 COSM1474310 c.934G>A p.D312N Substitution - Missense 10:101532388-101532388 + sysucc-1397T COSM5472959 c.49-3C>T p.? Unknown 10:101430342-101430342 + PCSI_0078_Pa_X COSM3375369 c.1342A>G p.I448V Substitution - Missense 10:101534905-101534905 + K126 COSM249416 c.920A>T p.Y307F Substitution - Missense 10:101532374-101532374 + KM12 COSM1345393 c.1774delC p.R594fs*>12 Deletion - Frameshift 10:101550816-101550816 + LIM2405 COSM1345393 c.1774delC p.R594fs*>12 Deletion - Frameshift 10:101550816-101550816 + TCGA-AP-A0LM-01 COSM914027 c.688G>A p.E230K Substitution - Missense 10:101526144-101526144 + HCC078T COSM426955 c.112C>T p.R38* Substitution - Nonsense 10:101430408-101430408 + TCGA-DG-A2KK-01 COSM4828330 c.83C>G p.S28C Substitution - Missense 10:101430379-101430379 + TCGA-EE-A181-06 COSM3433645 c.473C>T p.S158F Substitution - Missense 10:101521787-101521787 + T3262 COSM4666419 c.1780C>T p.R594C Substitution - Missense 10:101550822-101550822 + TCGA-CA-6717-01 COSM1345388 c.710C>T p.S237F Substitution - Missense 10:101526166-101526166 + CHC1531T COSM4804813 c.962G>T p.R321L Substitution - Missense 10:101532416-101532416 + LUAD-NYU284 COSM372626 c.779G>T p.G260V Substitution - Missense 10:101531272-101531272 + LUAD-B02594 COSM336315 c.1691A>T p.D564V Substitution - Missense 10:101550733-101550733 + TCGA-BR-8372-01 COSM4011125 c.1361G>A p.S454N Substitution - Missense 10:101535367-101535367 + Gp5D COSM2058530 c.1315A>C p.I439L Substitution - Missense 10:101534878-101534878 + TCGA-28-5209-01 COSM372625 c.144C>T p.L48L Substitution - coding silent 10:101430440-101430440 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.643802 10q24.32 603482

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.E133G c.398A>G 10 103281469 CM A G Missense p.E214G c.641A>G 10 103285854 HC A G Missense p.M232V c.694A>G 10 103285907 PAAD A G Missense p.S117G c.349A>G 10 103281420 SCLC A G Missense p.Y438C c.1313A>G 10 103294633 UCEC A G Synonymous p.A497A c.1491A>G 10 103296324 COREAD A T Synonymous p.I276I c.828A>T 10 103291078 HNSC CC TT Missense p.Q350* c.1047_1048delinsTT 10 103292777 CM C G Missense p.S28C c.83C>G 10 103190136 HNSC C T IntronicSNV . c.1815+39C>T 10 103310653 CM C T Missense p.P66S c.196C>T 10 103221777 OV C T Missense p.S158F c.473C>T 10 103281544 CM C T Missense p.S595F c.1784C>T 10 103310583 UCEC C T Missense p.S597F c.1790C>T 10 103310589 LUAD C T Missense p.T545I c.1634C>T 10 103298106 LUAD C T Nonsense p.R321* c.961C>T 10 103292172 CM C T Nonsense p.R38* c.112C>T 10 103190165 BRCA C T Nonsense p.R560* c.1678C>T 10 103310477 CM C T Synonymous p.A588A c.1764C>T 10 103310563 CM C T Synonymous p.C335C c.1005C>T 10 103292735 THCA C T Synonymous p.G63G c.189C>T 10 103221770 STAD C T Synonymous p.L48L c.144C>T 10 103190197 GBM C T Synonymous p.P592P c.1776C>T 10 103310575 CM G A Missense p.D312N c.934G>A 10 103292145 BRCA G A Missense p.E133K c.397G>A 10 103281468 LUAD G A Missense p.R419Q c.1256G>A 10 103294576 UCEC G A Missense p.R467Q c.1400G>A 10 103295163 STAD G A Synonymous p.R124R c.372G>A 10 103281443 LGG G C Synonymous p.V480V c.1440G>C 10 103295203 BRCA G T 3-UTRSNV . c.1815+5370G>T 10 103315984 DLBCL G T Missense p.G247V c.740G>T 10 103285953 UCEC G T Missense p.G260W c.778G>T 10 103291028 LUAD G T Missense p.G544W c.1630G>T 10 103298102 LUAD G T Missense p.K134N c.402G>T 10 103281473 UCEC G T SpliceAcceptorSNV . c.744-1G>T 10 103290993 STAD G T Synonymous p.T364T c.1092G>T 10 103292822 STAD T A IntronicSNV . c.157-4354T>A 10 103217384 CLL T A Missense p.F514Y c.1541T>A 10 103296374 OV T C IntronicSNV . c.48+10694T>C 10 103124679 CM T C Missense p.I316T c.947T>C 10 103292158 LUAD T G Missense p.F141V c.421T>G 10 103281492 GBM T G Missense p.I416M c.1248T>G 10 103294568 COREAD T G Missense p.I416M c.1248T>G 10 103294568 RCCC