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 14 31066667 31066667 + Silent SNP A A G TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr14:31066667A>G c.570A>G c.(568-570)acA>acG p.T190T BLCA 14 31071317 31071317 + Silent SNP C C T TCGA-ZF-AA4N-01A-11D-A38G-08 TCGA-ZF-AA4N-10A-01D-A38J-08 g.chr14:31071317C>T c.990C>T c.(988-990)tcC>tcT p.S330S BLCA 14 31074728 31074728 + Missense_Mutation SNP G G C TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr14:31074728G>C c.1028G>C c.(1027-1029)aGa>aCa p.R343T BLCA 14 31074778 31074778 + Nonsense_Mutation SNP A A T TCGA-ZF-A9R3-01A-11D-A38G-08 TCGA-ZF-A9R3-10A-01D-A38J-08 g.chr14:31074778A>T c.1078A>T c.(1078-1080)Aaa>Taa p.K360* BLCA 14 31077178 31077178 + Missense_Mutation SNP C C G TCGA-DK-A2I2-01A-11D-A17V-08 TCGA-DK-A2I2-10A-01D-A17V-08 g.chr14:31077178C>G c.1403C>G c.(1402-1404)tCt>tGt p.S468C BLCA 14 31081581 31081581 + Missense_Mutation SNP G G A TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr14:31081581G>A c.1669G>A c.(1669-1671)Gaa>Aaa p.E557K BLCA 14 31084653 31084653 + Missense_Mutation SNP C C G TCGA-UY-A78O-01A-12D-A339-08 TCGA-UY-A78O-10A-01D-A339-08 g.chr14:31084653C>G c.1772C>G c.(1771-1773)tCt>tGt p.S591C BLCA 14 31085657 31085657 + Missense_Mutation SNP G G C TCGA-DK-A3IK-01A-32D-A21A-08 TCGA-DK-A3IK-10A-01D-A21A-08 g.chr14:31085657G>C c.2038G>C c.(2038-2040)Gag>Cag p.E680Q BRCA 14 31071093 31071093 + Silent SNP C C T TCGA-E2-A14X-01A-11D-A10Y-09 TCGA-E2-A14X-10A-01D-A110-09 g.chr14:31071093C>T c.870C>T c.(868-870)taC>taT p.Y290Y BRCA 14 31074844 31074844 + Nonsense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr14:31074844C>T c.1144C>T c.(1144-1146)Cga>Tga p.R382* BRCA 14 31077124 31077124 + Missense_Mutation SNP G G T TCGA-AN-A0FL-01A-11W-A050-09 TCGA-AN-A0FL-10A-01W-A055-09 g.chr14:31077124G>T c.1349G>T c.(1348-1350)gGc>gTc p.G450V BRCA 14 31081486 31081486 + Missense_Mutation SNP G G A TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr14:31081486G>A c.1574G>A c.(1573-1575)gGa>gAa p.G525E CESC 14 31061590 31061590 + Missense_Mutation SNP G G A TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr14:31061590G>A c.299G>A c.(298-300)cGa>cAa p.R100Q COAD 14 31056011 31056011 + Missense_Mutation SNP A A G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr14:31056011A>G c.125A>G c.(124-126)tAc>tGc p.Y42C COAD 14 31056013 31056013 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr14:31056013T>C c.127T>C c.(127-129)Tac>Cac p.Y43H COAD 14 31061581 31061581 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr14:31061581G>A c.290G>A c.(289-291)cGa>cAa p.R97Q COAD 14 31061590 31061590 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:31061590G>A c.299G>A c.(298-300)cGa>cAa p.R100Q COAD 14 31061590 31061590 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr14:31061590G>A c.299G>A c.(298-300)cGa>cAa p.R100Q COAD 14 31062799 31062799 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:31062799G>A c.482G>A c.(481-483)cGa>cAa p.R161Q COAD 14 31071043 31071043 + Missense_Mutation SNP C C T TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr14:31071043C>T c.820C>T c.(820-822)Cgg>Tgg p.R274W COAD 14 31071227 31071227 + Missense_Mutation SNP A A C TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr14:31071227A>C c.900A>C c.(898-900)aaA>aaC p.K300N COAD 14 31071311 31071311 + Silent SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr14:31071311T>C c.984T>C c.(982-984)ccT>ccC p.P328P COAD 14 31074845 31074845 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:31074845G>A c.1145G>A c.(1144-1146)cGa>cAa p.R382Q COAD 14 31074996 31074996 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:31074996G>T c.1296G>T c.(1294-1296)aaG>aaT p.K432N COAD 14 31081492 31081492 + Missense_Mutation SNP T T C TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr14:31081492T>C c.1580T>C c.(1579-1581)cTc>cCc p.L527P COAD 14 31081492 31081492 + Missense_Mutation SNP T T C TCGA-CM-6678-01A-11D-1835-10 TCGA-CM-6678-10A-01D-1835-10 g.chr14:31081492T>C c.1580T>C c.(1579-1581)cTc>cCc p.L527P COAD 14 31081492 31081492 + Missense_Mutation SNP T T C TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr14:31081492T>C c.1580T>C c.(1579-1581)cTc>cCc p.L527P COAD 14 31081493 31081493 + Silent SNP C C T TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr14:31081493C>T c.1581C>T c.(1579-1581)ctC>ctT p.L527L COAD 14 31081516 31081516 + Missense_Mutation SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr14:31081516A>G c.1604A>G c.(1603-1605)gAt>gGt p.D535G COADREAD 14 31056011 31056011 + Missense_Mutation SNP A A G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr14:31056011A>G c.125A>G c.(124-126)tAc>tGc p.Y42C COADREAD 14 31056013 31056013 + Missense_Mutation SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr14:31056013T>C c.127T>C c.(127-129)Tac>Cac p.Y43H COADREAD 14 31061581 31061581 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr14:31061581G>A c.290G>A c.(289-291)cGa>cAa p.R97Q COADREAD 14 31061590 31061590 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:31061590G>A c.299G>A c.(298-300)cGa>cAa p.R100Q COADREAD 14 31061590 31061590 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr14:31061590G>A c.299G>A c.(298-300)cGa>cAa p.R100Q COADREAD 14 31062799 31062799 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:31062799G>A c.482G>A c.(481-483)cGa>cAa p.R161Q COADREAD 14 31062822 31062822 + Missense_Mutation SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:31062822T>C c.505T>C c.(505-507)Tgg>Cgg p.W169R COADREAD 14 31071043 31071043 + Missense_Mutation SNP C C T TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr14:31071043C>T c.820C>T c.(820-822)Cgg>Tgg p.R274W COADREAD 14 31071227 31071227 + Missense_Mutation SNP A A C TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr14:31071227A>C c.900A>C c.(898-900)aaA>aaC p.K300N COADREAD 14 31071311 31071311 + Silent SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr14:31071311T>C c.984T>C c.(982-984)ccT>ccC p.P328P COADREAD 14 31074845 31074845 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:31074845G>A c.1145G>A c.(1144-1146)cGa>cAa p.R382Q COADREAD 14 31074996 31074996 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:31074996G>T c.1296G>T c.(1294-1296)aaG>aaT p.K432N COADREAD 14 31081492 31081492 + Missense_Mutation SNP T T C TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr14:31081492T>C c.1580T>C c.(1579-1581)cTc>cCc p.L527P COADREAD 14 31081492 31081492 + Missense_Mutation SNP T T C TCGA-CM-6678-01A-11D-1835-10 TCGA-CM-6678-10A-01D-1835-10 g.chr14:31081492T>C c.1580T>C c.(1579-1581)cTc>cCc p.L527P COADREAD 14 31081492 31081492 + Missense_Mutation SNP T T C TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr14:31081492T>C c.1580T>C c.(1579-1581)cTc>cCc p.L527P COADREAD 14 31081493 31081493 + Silent SNP C C T TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr14:31081493C>T c.1581C>T c.(1579-1581)ctC>ctT p.L527L COADREAD 14 31081500 31081500 + Missense_Mutation SNP A A C TCGA-AG-3598-01A-01W-0833-10 TCGA-AG-3598-10A-01W-0833-10 g.chr14:31081500A>C c.1588A>C c.(1588-1590)Ata>Cta p.I530L COADREAD 14 31081516 31081516 + Missense_Mutation SNP A A G TCGA-AF-6136-01A-11D-1826-10 TCGA-AF-6136-10A-01D-1826-10 g.chr14:31081516A>G c.1604A>G c.(1603-1605)gAt>gGt p.D535G COADREAD 14 31081516 31081516 + Missense_Mutation SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr14:31081516A>G c.1604A>G c.(1603-1605)gAt>gGt p.D535G DLBC 14 31066658 31066658 + Missense_Mutation SNP T T G TCGA-FF-8042-01A-11D-2210-10 TCGA-FF-8042-10A-01D-2210-10 g.chr14:31066658T>G c.561T>G c.(559-561)ttT>ttG p.F187L ESCA 14 31058620 31058622 + In_Frame_Del DEL AAG AAG - TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr14:31058620_31058622delAAG c.167_169delAAG c.(166-171)aaagaa>aaa p.E59del ESCA 14 31058655 31058655 + Missense_Mutation SNP G G T TCGA-L5-A8NJ-01A-11D-A36J-09 TCGA-L5-A8NJ-11A-11D-A36M-09 g.chr14:31058655G>T c.202G>T c.(202-204)Gat>Tat p.D68Y ESCA 14 31066642 31066642 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr14:31066642C>T c.545C>T c.(544-546)gCg>gTg p.A182V ESCA 14 31074770 31074770 + Missense_Mutation SNP T T A TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr14:31074770T>A c.1070T>A c.(1069-1071)aTt>aAt p.I357N ESCA 14 31074771 31074772 + Frame_Shift_Ins INS - - A TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr14:31074771_31074772insA c.1071_1072insA c.(1072-1074)aaafs p.K358fs ESCA 14 31085591 31085591 + Missense_Mutation SNP G G T TCGA-VR-A8EY-01A-11D-A36J-09 TCGA-VR-A8EY-10A-01D-A36M-09 g.chr14:31085591G>T c.1972G>T c.(1972-1974)Gtg>Ttg p.V658L GBM 14 31081472 31081472 + Nonsense_Mutation SNP C C G TCGA-06-0128-01A-01D-1490-08 TCGA-06-0128-10A-01D-1490-08 g.chr14:31081472C>G c.1560C>G c.(1558-1560)taC>taG p.Y520* GBMLGG 14 31074772 31074772 + Nonsense_Mutation SNP A A T TCGA-TQ-A7RK-01A-11D-A33T-08 TCGA-TQ-A7RK-10A-01D-A33W-08 g.chr14:31074772A>T c.1072A>T c.(1072-1074)Aaa>Taa p.K358* GBMLGG 14 31081472 31081472 + Nonsense_Mutation SNP C C G TCGA-06-0128-01A-01D-1490-08 TCGA-06-0128-10A-01D-1490-08 g.chr14:31081472C>G c.1560C>G c.(1558-1560)taC>taG p.Y520* HNSC 14 31071100 31071100 + Splice_Site SNP G G T TCGA-CV-5978-01A-11D-1683-08 TCGA-CV-5978-11A-01D-1683-08 g.chr14:31071100G>T c.877G>T c.(877-879)Gga>Tga p.G293* HNSC 14 31071207 31071207 + Missense_Mutation SNP G G A TCGA-QK-A6VC-01A-23D-A34J-08 TCGA-QK-A6VC-10B-01D-A34M-08 g.chr14:31071207G>A c.880G>A c.(880-882)Gag>Aag p.E294K HNSC 14 31071301 31071301 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr14:31071301G>A c.974G>A c.(973-975)aGa>aAa p.R325K HNSC 14 31081542 31081542 + Missense_Mutation SNP C C G TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr14:31081542C>G c.1630C>G c.(1630-1632)Ctt>Gtt p.L544V KIPAN 14 31061654 31061654 + Splice_Site SNP G G C TCGA-IA-A83T-01A-11D-A34Z-10 TCGA-IA-A83T-11A-11D-A34Z-10 g.chr14:31061654G>C c.e5+1 KIPAN 14 31074726 31074726 + Missense_Mutation SNP T T G TCGA-A3-3358-01A-01D-1534-10 TCGA-A3-3358-11A-01D-1534-10 g.chr14:31074726T>G c.1026T>G c.(1024-1026)ttT>ttG p.F342L KIPAN 14 31081505 31081505 + Silent SNP G G A TCGA-B9-A69E-01A-11D-A31X-10 TCGA-B9-A69E-10A-01D-A31X-10 g.chr14:31081505G>A c.1593G>A c.(1591-1593)acG>acA p.T531T KIPAN 14 31085631 31085631 + Missense_Mutation SNP C C T TCGA-5P-A9K6-01A-11D-A42J-10 TCGA-5P-A9K6-10A-01D-A42M-10 g.chr14:31085631C>T c.2012C>T c.(2011-2013)gCa>gTa p.A671V KIRC 14 31074726 31074726 + Missense_Mutation SNP T T G TCGA-A3-3358-01A-01D-1534-10 TCGA-A3-3358-11A-01D-1534-10 g.chr14:31074726T>G c.1026T>G c.(1024-1026)ttT>ttG p.F342L KIRP 14 31061654 31061654 + Splice_Site SNP G G C TCGA-IA-A83T-01A-11D-A34Z-10 TCGA-IA-A83T-11A-11D-A34Z-10 g.chr14:31061654G>C c.e5+1 KIRP 14 31081505 31081505 + Silent SNP G G A TCGA-B9-A69E-01A-11D-A31X-10 TCGA-B9-A69E-10A-01D-A31X-10 g.chr14:31081505G>A c.1593G>A c.(1591-1593)acG>acA p.T531T KIRP 14 31085631 31085631 + Missense_Mutation SNP C C T TCGA-5P-A9K6-01A-11D-A42J-10 TCGA-5P-A9K6-10A-01D-A42M-10 g.chr14:31085631C>T c.2012C>T c.(2011-2013)gCa>gTa p.A671V LGG 14 31074772 31074772 + Nonsense_Mutation SNP A A T TCGA-TQ-A7RK-01A-11D-A33T-08 TCGA-TQ-A7RK-10A-01D-A33W-08 g.chr14:31074772A>T c.1072A>T c.(1072-1074)Aaa>Taa p.K358* LIHC 14 31058658 31058658 + Missense_Mutation SNP A A G TCGA-DD-AADM-01A-11D-A40R-10 TCGA-DD-AADM-10A-01D-A40U-10 g.chr14:31058658A>G c.205A>G c.(205-207)Atc>Gtc p.I69V LIHC 14 31077159 31077159 + Missense_Mutation SNP C C T TCGA-UB-A7ME-01A-11D-A33K-10 TCGA-UB-A7ME-10A-01D-A33K-10 g.chr14:31077159C>T c.1384C>T c.(1384-1386)Cct>Tct p.P462S LUAD 14 31058632 31058632 + Missense_Mutation SNP G G T TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr14:31058632G>T c.179G>T c.(178-180)gGa>gTa p.G60V LUAD 14 31066643 31066643 + Silent SNP G G T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr14:31066643G>T c.546G>T c.(544-546)gcG>gcT p.A182A LUAD 14 31066645 31066645 + Missense_Mutation SNP G G T TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr14:31066645G>T c.548G>T c.(547-549)gGa>gTa p.G183V LUAD 14 31071081 31071081 + Missense_Mutation SNP G G T TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chr14:31071081G>T c.858G>T c.(856-858)agG>agT p.R286S LUAD 14 31074781 31074782 + Frame_Shift_Ins INS - - T TCGA-73-4670-01A-01D-1265-08 TCGA-73-4670-11A-01D-1265-08 g.chr14:31074781_31074782insT c.1081_1082insT c.(1081-1083)actfs p.T361fs LUAD 14 31077152 31077152 + Silent SNP C C T TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr14:31077152C>T c.1377C>T c.(1375-1377)caC>caT p.H459H LUAD 14 31077153 31077153 + Missense_Mutation SNP G G T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr14:31077153G>T c.1378G>T c.(1378-1380)Ggt>Tgt p.G460C LUAD 14 31077156 31077156 + Frame_Shift_Del DEL G G - TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr14:31077156delG c.1381delG c.(1381-1383)ggtfs p.G461fs LUAD 14 31077238 31077238 + Missense_Mutation SNP A A G TCGA-55-6981-01A-11D-1945-08 TCGA-55-6981-11A-01D-1945-08 g.chr14:31077238A>G c.1463A>G c.(1462-1464)gAt>gGt p.D488G LUAD 14 31081465 31081465 + Missense_Mutation SNP A A G TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr14:31081465A>G c.1553A>G c.(1552-1554)tAt>tGt p.Y518C LUSC 14 31055950 31055950 + Missense_Mutation SNP G G A TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr14:31055950G>A c.64G>A c.(64-66)Gac>Aac p.D22N LUSC 14 31058674 31058674 + Missense_Mutation SNP A A G TCGA-18-3417-01A-01D-1441-08 TCGA-18-3417-11A-01D-1441-08 g.chr14:31058674A>G c.221A>G c.(220-222)aAt>aGt p.N74S LUSC 14 31071217 31071217 + Missense_Mutation SNP A A T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr14:31071217A>T c.890A>T c.(889-891)aAa>aTa p.K297I LUSC 14 31085736 31085736 + Missense_Mutation SNP A A G TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr14:31085736A>G c.2117A>G c.(2116-2118)cAt>cGt p.H706R OV 14 31058619 31058623 + Frame_Shift_Del DEL AAAGA AAAGA - TCGA-13-1509-01A-01W-0549-09 TCGA-13-1509-10A-01W-0550-09 g.chr14:31058619_31058623delAAAGA c.166_170delAAAGA c.(166-171)aaagaafs p.KE56fs OV 14 31081515 31081515 + Missense_Mutation SNP G G A TCGA-25-1313-01A-01W-0492-08 TCGA-25-1313-10A-01W-0492-08 g.chr14:31081515G>A c.1603G>A c.(1603-1605)Gat>Aat p.D535N PAAD 14 31074771 31074772 + Frame_Shift_Ins INS - - A TCGA-2J-AABK-01A-31D-A40W-08 TCGA-2J-AABK-10A-01D-A40W-08 g.chr14:31074771_31074772insA c.1071_1072insA c.(1072-1074)aaafs p.K358fs PAAD 14 31074771 31074772 + Frame_Shift_Ins INS - - A TCGA-FB-A5VM-01A-11D-A32N-08 TCGA-FB-A5VM-10A-01D-A32N-08 g.chr14:31074771_31074772insA c.1071_1072insA c.(1072-1074)aaafs p.K358fs PAAD 14 31074771 31074772 + Frame_Shift_Ins INS - - A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:31074771_31074772insA c.1071_1072insA c.(1072-1074)aaafs p.K358fs PAAD 14 31074771 31074772 + Frame_Shift_Ins INS - - A TCGA-US-A77J-01A-11D-A32N-08 TCGA-US-A77J-11A-11D-A32N-08 g.chr14:31074771_31074772insA c.1071_1072insA c.(1072-1074)aaafs p.K358fs PAAD 14 31077197 31077197 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:31077197C>T c.1422C>T c.(1420-1422)tgC>tgT p.C474C PAAD 14 31085649 31085649 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:31085649C>T c.2030C>T c.(2029-2031)aCa>aTa p.T677I PRAD 14 31066642 31066642 + Missense_Mutation SNP C C T TCGA-CH-5737-01A-11D-1576-08 TCGA-CH-5737-10A-01D-1576-08 g.chr14:31066642C>T c.545C>T c.(544-546)gCg>gTg p.A182V PRAD 14 31066655 31066655 + Silent SNP C C T TCGA-4L-AA1F-01A-11D-A41K-08 TCGA-4L-AA1F-10A-01D-A41N-08 g.chr14:31066655C>T c.558C>T c.(556-558)ttC>ttT p.F186F READ 14 31062822 31062822 + Missense_Mutation SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:31062822T>C c.505T>C c.(505-507)Tgg>Cgg p.W169R READ 14 31081500 31081500 + Missense_Mutation SNP A A C TCGA-AG-3598-01A-01W-0833-10 TCGA-AG-3598-10A-01W-0833-10 g.chr14:31081500A>C c.1588A>C c.(1588-1590)Ata>Cta p.I530L READ 14 31081516 31081516 + Missense_Mutation SNP A A G TCGA-AF-6136-01A-11D-1826-10 TCGA-AF-6136-10A-01D-1826-10 g.chr14:31081516A>G c.1604A>G c.(1603-1605)gAt>gGt p.D535G SKCM 14 31058628 31058628 + Missense_Mutation SNP G G A TCGA-EE-A29A-06A-12D-A196-08 TCGA-EE-A29A-10A-01D-A198-08 g.chr14:31058628G>A c.175G>A c.(175-177)Gaa>Aaa p.E59K SKCM 14 31066625 31066625 + Splice_Site SNP G G T TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr14:31066625G>T c.e7-1 SKCM 14 31071212 31071212 + Missense_Mutation SNP C C A TCGA-GN-A4U7-06A-21D-A32N-08 TCGA-GN-A4U7-10B-01D-A32N-08 g.chr14:31071212C>A c.885C>A c.(883-885)ttC>ttA p.F295L SKCM 14 31074856 31074856 + Missense_Mutation SNP C C T TCGA-D3-A5GR-06A-11D-A27K-08 TCGA-D3-A5GR-10A-01D-A27N-08 g.chr14:31074856C>T c.1156C>T c.(1156-1158)Cct>Tct p.P386S SKCM 14 31084663 31084663 + Silent SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr14:31084663C>T c.1782C>T c.(1780-1782)atC>atT p.I594I SKCM 14 31085542 31085542 + Silent SNP C C T TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr14:31085542C>T c.1923C>T c.(1921-1923)tcC>tcT p.S641S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 14 31074728 31074728 single base substitution G C 3_prime_UTR_variant BLCA-US 14 31074728 31074728 single base substitution G C exon_variant BLCA-US 14 31074728 31074728 single base substitution G C intron_variant BLCA-US 14 31074728 31074728 single base substitution G C missense_variant R108T 323G>C BLCA-US 14 31074728 31074728 single base substitution G C missense_variant R297T 890G>C BLCA-US 14 31074728 31074728 single base substitution G C missense_variant R343T 1028G>C BLCA-US 14 31074728 31074728 single base substitution G C missense_variant R373T 1118G>C BLCA-US 14 31077178 31077178 single base substitution C G downstream_gene_variant BLCA-US 14 31077178 31077178 single base substitution C G exon_variant BLCA-US 14 31077178 31077178 single base substitution C G intron_variant BLCA-US 14 31077178 31077178 single base substitution C G missense_variant S422C 1265C>G BLCA-US 14 31077178 31077178 single base substitution C G missense_variant S468C 1403C>G BLCA-US 14 31077178 31077178 single base substitution C G missense_variant S498C 1493C>G BLCA-US 14 31077178 31077178 single base substitution C G upstream_gene_variant BLCA-US 14 31085657 31085657 single base substitution G C downstream_gene_variant BLCA-US 14 31085657 31085657 single base substitution G C exon_variant BLCA-US 14 31085657 31085657 single base substitution G C missense_variant E634Q 1900G>C BLCA-US 14 31085657 31085657 single base substitution G C missense_variant E680Q 2038G>C BLCA-US 14 31085657 31085657 single base substitution G C missense_variant E710Q 2128G>C BOCA-FR 14 31087561 31087561 single base substitution A T 3_prime_UTR_variant BOCA-FR 14 31087561 31087561 single base substitution A T downstream_gene_variant BRCA-EU 14 31024438 31024438 single base substitution G C upstream_gene_variant BRCA-EU 14 31025225 31025225 single base substitution C G upstream_gene_variant BRCA-EU 14 31025921 31025921 deletion of <=200bp A - upstream_gene_variant BRCA-EU 14 31026332 31026332 single base substitution G T upstream_gene_variant BRCA-EU 14 31027205 31027205 single base substitution G A upstream_gene_variant BRCA-EU 14 31027653 31027653 single base substitution G C upstream_gene_variant BRCA-EU 14 31028336 31028336 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 14 31028336 31028336 single base substitution C G upstream_gene_variant BRCA-EU 14 31028462 31028462 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 14 31028462 31028462 single base substitution C A exon_variant BRCA-EU 14 31028462 31028462 single base substitution C A upstream_gene_variant BRCA-EU 14 31031488 31031488 single base substitution G C intron_variant BRCA-EU 14 31031804 31031804 single base substitution G A intron_variant BRCA-EU 14 31032083 31032083 single base substitution C T intron_variant BRCA-EU 14 31034822 31034822 single base substitution T G intron_variant BRCA-EU 14 31034833 31034833 single base substitution G A intron_variant BRCA-EU 14 31035742 31035742 single base substitution G T intron_variant BRCA-EU 14 31036040 31036040 single base substitution C T intron_variant BRCA-EU 14 31036744 31036744 single base substitution C T intron_variant BRCA-EU 14 31038087 31038087 single base substitution T G intron_variant BRCA-EU 14 31038142 31038142 single base substitution A G intron_variant BRCA-EU 14 31038472 31038472 single base substitution C G intron_variant BRCA-EU 14 31041134 31041134 single base substitution C T intron_variant BRCA-EU 14 31041134 31041134 single base substitution C T upstream_gene_variant BRCA-EU 14 31041238 31041238 single base substitution C T intron_variant BRCA-EU 14 31041238 31041238 single base substitution C T upstream_gene_variant BRCA-EU 14 31041240 31041240 single base substitution C T intron_variant BRCA-EU 14 31041240 31041240 single base substitution C T upstream_gene_variant BRCA-EU 14 31043437 31043437 single base substitution C G intron_variant BRCA-EU 14 31043437 31043437 single base substitution C G upstream_gene_variant BRCA-EU 14 31044352 31044352 single base substitution A G intron_variant BRCA-EU 14 31044352 31044352 single base substitution A G upstream_gene_variant BRCA-EU 14 31044468 31044468 single base substitution T G intron_variant BRCA-EU 14 31044468 31044468 single base substitution T G upstream_gene_variant BRCA-EU 14 31044553 31044553 single base substitution C G intron_variant BRCA-EU 14 31044553 31044553 single base substitution C G upstream_gene_variant BRCA-EU 14 31046536 31046536 deletion of <=200bp T - intron_variant BRCA-EU 14 31046536 31046536 deletion of <=200bp T - upstream_gene_variant BRCA-EU 14 31047908 31047908 single base substitution G A intron_variant BRCA-EU 14 31048298 31048298 single base substitution G C intron_variant BRCA-EU 14 31048338 31048338 single base substitution G C intron_variant BRCA-EU 14 31048340 31048340 single base substitution G C intron_variant BRCA-EU 14 31048436 31048436 single base substitution G A intron_variant BRCA-EU 14 31048715 31048715 single base substitution G A intron_variant BRCA-EU 14 31049449 31049449 single base substitution G A intron_variant BRCA-EU 14 31049568 31049568 single base substitution A G intron_variant BRCA-EU 14 31050991 31050991 single base substitution C T intron_variant BRCA-EU 14 31051218 31051218 single base substitution G T intron_variant BRCA-EU 14 31053145 31053145 single base substitution G A intron_variant BRCA-EU 14 31054787 31054787 insertion of <=200bp - C intron_variant BRCA-EU 14 31054867 31054867 single base substitution A G intron_variant BRCA-EU 14 31056752 31056752 single base substitution G T intron_variant BRCA-EU 14 31056752 31056752 single base substitution G T upstream_gene_variant BRCA-EU 14 31057359 31057359 single base substitution G A intron_variant BRCA-EU 14 31057359 31057359 single base substitution G A upstream_gene_variant BRCA-EU 14 31057711 31057711 single base substitution T A intron_variant BRCA-EU 14 31057711 31057711 single base substitution T A upstream_gene_variant BRCA-EU 14 31057757 31057757 single base substitution G T intron_variant BRCA-EU 14 31057757 31057757 single base substitution G T upstream_gene_variant BRCA-EU 14 31057849 31057849 single base substitution G C intron_variant BRCA-EU 14 31057849 31057849 single base substitution G C upstream_gene_variant BRCA-EU 14 31058035 31058035 single base substitution A T intron_variant BRCA-EU 14 31058035 31058035 single base substitution A T upstream_gene_variant BRCA-EU 14 31058402 31058402 single base substitution C T intron_variant BRCA-EU 14 31058402 31058402 single base substitution C T upstream_gene_variant BRCA-EU 14 31059412 31059412 single base substitution G A downstream_gene_variant BRCA-EU 14 31059412 31059412 single base substitution G A intron_variant BRCA-EU 14 31059412 31059412 single base substitution G A upstream_gene_variant BRCA-EU 14 31059586 31059586 single base substitution G C downstream_gene_variant BRCA-EU 14 31059586 31059586 single base substitution G C intron_variant BRCA-EU 14 31059586 31059586 single base substitution G C upstream_gene_variant BRCA-EU 14 31059996 31059996 single base substitution A C 3_prime_UTR_variant BRCA-EU 14 31059996 31059996 single base substitution A C downstream_gene_variant BRCA-EU 14 31059996 31059996 single base substitution A C exon_variant BRCA-EU 14 31059996 31059996 single base substitution A C intron_variant BRCA-EU 14 31059996 31059996 single base substitution A C upstream_gene_variant BRCA-EU 14 31060607 31060607 single base substitution G A 3_prime_UTR_variant BRCA-EU 14 31060607 31060607 single base substitution G A downstream_gene_variant BRCA-EU 14 31060607 31060607 single base substitution G A intron_variant BRCA-EU 14 31060607 31060607 single base substitution G A upstream_gene_variant BRCA-EU 14 31060706 31060707 deletion of <=200bp AA - 3_prime_UTR_variant BRCA-EU 14 31060706 31060707 deletion of <=200bp AA - downstream_gene_variant BRCA-EU 14 31060706 31060707 deletion of <=200bp AA - intron_variant BRCA-EU 14 31060706 31060707 deletion of <=200bp AA - upstream_gene_variant BRCA-EU 14 31061379 31061379 single base substitution C T 3_prime_UTR_variant BRCA-EU 14 31061379 31061379 single base substitution C T downstream_gene_variant BRCA-EU 14 31061379 31061379 single base substitution C T intron_variant BRCA-EU 14 31061379 31061379 single base substitution C T upstream_gene_variant BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - 3_prime_UTR_variant BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - downstream_gene_variant BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - exon_variant BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - inframe_deletion LV3L BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - inframe_deletion PC117P BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - inframe_deletion PC163P BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - inframe_deletion PC193P BRCA-EU 14 31062806 31062808 deletion of <=200bp TTG - upstream_gene_variant BRCA-EU 14 31064166 31064166 deletion of <=200bp C - downstream_gene_variant BRCA-EU 14 31064166 31064166 deletion of <=200bp C - intron_variant BRCA-EU 14 31064166 31064166 deletion of <=200bp C - upstream_gene_variant BRCA-EU 14 31064166 31064166 single base substitution C T downstream_gene_variant BRCA-EU 14 31064166 31064166 single base substitution C T intron_variant BRCA-EU 14 31064166 31064166 single base substitution C T upstream_gene_variant BRCA-EU 14 31064254 31064254 single base substitution G C downstream_gene_variant BRCA-EU 14 31064254 31064254 single base substitution G C intron_variant BRCA-EU 14 31064254 31064254 single base substitution G C upstream_gene_variant BRCA-EU 14 31067712 31067712 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU 14 31067712 31067712 deletion of <=200bp A - downstream_gene_variant BRCA-EU 14 31067712 31067712 deletion of <=200bp A - frameshift_variant E174 BRCA-EU 14 31067712 31067712 deletion of <=200bp A - frameshift_variant E220 BRCA-EU 14 31067712 31067712 deletion of <=200bp A - frameshift_variant E250 BRCA-EU 14 31067712 31067712 deletion of <=200bp A - intron_variant BRCA-EU 14 31067712 31067712 deletion of <=200bp A - upstream_gene_variant BRCA-EU 14 31068848 31068848 single base substitution A G downstream_gene_variant BRCA-EU 14 31068848 31068848 single base substitution A G intron_variant BRCA-EU 14 31068848 31068848 single base substitution A G upstream_gene_variant BRCA-EU 14 31070067 31070067 single base substitution C G downstream_gene_variant BRCA-EU 14 31070067 31070067 single base substitution C G intron_variant BRCA-EU 14 31070067 31070067 single base substitution C G upstream_gene_variant BRCA-EU 14 31070297 31070297 single base substitution G T downstream_gene_variant BRCA-EU 14 31070297 31070297 single base substitution G T intron_variant BRCA-EU 14 31070297 31070297 single base substitution G T upstream_gene_variant BRCA-EU 14 31074411 31074411 single base substitution G C intron_variant BRCA-EU 14 31074781 31074781 single base substitution A T downstream_gene_variant BRCA-EU 14 31074781 31074781 single base substitution A T exon_variant BRCA-EU 14 31074781 31074781 single base substitution A T intron_variant BRCA-EU 14 31074781 31074781 single base substitution A T missense_variant T315S 943A>T BRCA-EU 14 31074781 31074781 single base substitution A T missense_variant T361S 1081A>T BRCA-EU 14 31074781 31074781 single base substitution A T missense_variant T391S 1171A>T BRCA-EU 14 31076530 31076530 single base substitution G A downstream_gene_variant BRCA-EU 14 31076530 31076530 single base substitution G A intron_variant BRCA-EU 14 31076530 31076530 single base substitution G A upstream_gene_variant BRCA-EU 14 31077178 31077178 single base substitution C G downstream_gene_variant BRCA-EU 14 31077178 31077178 single base substitution C G exon_variant BRCA-EU 14 31077178 31077178 single base substitution C G intron_variant BRCA-EU 14 31077178 31077178 single base substitution C G missense_variant S422C 1265C>G BRCA-EU 14 31077178 31077178 single base substitution C G missense_variant S468C 1403C>G BRCA-EU 14 31077178 31077178 single base substitution C G missense_variant S498C 1493C>G BRCA-EU 14 31077178 31077178 single base substitution C G upstream_gene_variant BRCA-EU 14 31077319 31077319 single base substitution G C downstream_gene_variant BRCA-EU 14 31077319 31077319 single base substitution G C intron_variant BRCA-EU 14 31077319 31077319 single base substitution G C upstream_gene_variant BRCA-EU 14 31077719 31077719 single base substitution G A downstream_gene_variant BRCA-EU 14 31077719 31077719 single base substitution G A intron_variant BRCA-EU 14 31077719 31077719 single base substitution G A upstream_gene_variant BRCA-EU 14 31078137 31078137 single base substitution G A downstream_gene_variant BRCA-EU 14 31078137 31078137 single base substitution G A intron_variant BRCA-EU 14 31078137 31078137 single base substitution G A upstream_gene_variant BRCA-EU 14 31078188 31078188 deletion of <=200bp A - downstream_gene_variant BRCA-EU 14 31078188 31078188 deletion of <=200bp A - intron_variant BRCA-EU 14 31078188 31078188 deletion of <=200bp A - upstream_gene_variant BRCA-EU 14 31078444 31078444 deletion of <=200bp A - downstream_gene_variant BRCA-EU 14 31078444 31078444 deletion of <=200bp A - intron_variant BRCA-EU 14 31078444 31078444 deletion of <=200bp A - upstream_gene_variant BRCA-EU 14 31080666 31080666 single base substitution C G downstream_gene_variant BRCA-EU 14 31080666 31080666 single base substitution C G exon_variant BRCA-EU 14 31080666 31080666 single base substitution C G intron_variant BRCA-EU 14 31080860 31080860 deletion of <=200bp T - downstream_gene_variant BRCA-EU 14 31080860 31080860 deletion of <=200bp T - exon_variant BRCA-EU 14 31080860 31080860 deletion of <=200bp T - intron_variant BRCA-EU 14 31081411 31081411 single base substitution A C downstream_gene_variant BRCA-EU 14 31081411 31081411 single base substitution A C exon_variant BRCA-EU 14 31081411 31081411 single base substitution A C splice_acceptor_variant BRCA-EU 14 31085020 31085020 single base substitution A G downstream_gene_variant BRCA-EU 14 31085020 31085020 single base substitution A G intron_variant BRCA-EU 14 31086075 31086075 single base substitution T C 3_prime_UTR_variant BRCA-EU 14 31086075 31086075 single base substitution T C downstream_gene_variant BRCA-EU 14 31086075 31086075 single base substitution T C exon_variant BRCA-EU 14 31086590 31086590 single base substitution T A 3_prime_UTR_variant BRCA-EU 14 31086590 31086590 single base substitution T A downstream_gene_variant BRCA-EU 14 31086590 31086590 single base substitution T A exon_variant BRCA-EU 14 31088786 31088786 single base substitution T C 3_prime_UTR_variant BRCA-EU 14 31088786 31088786 single base substitution T C downstream_gene_variant BRCA-EU 14 31090496 31090496 single base substitution A G downstream_gene_variant BRCA-EU 14 31091600 31091600 single base substitution A G downstream_gene_variant BRCA-EU 14 31092762 31092762 single base substitution A G downstream_gene_variant BRCA-EU 14 31092849 31092849 single base substitution G C downstream_gene_variant BRCA-EU 14 31093071 31093071 single base substitution G C downstream_gene_variant BRCA-EU 14 31093467 31093467 single base substitution C T downstream_gene_variant BRCA-EU 14 31093956 31093956 single base substitution G C downstream_gene_variant BRCA-FR 14 31031488 31031488 single base substitution G C intron_variant BRCA-FR 14 31032083 31032083 single base substitution C T intron_variant BRCA-FR 14 31048298 31048298 single base substitution G C intron_variant BRCA-FR 14 31048338 31048338 single base substitution G C intron_variant BRCA-FR 14 31060565 31060565 single base substitution A C 3_prime_UTR_variant BRCA-FR 14 31060565 31060565 single base substitution A C downstream_gene_variant BRCA-FR 14 31060565 31060565 single base substitution A C intron_variant BRCA-FR 14 31060565 31060565 single base substitution A C upstream_gene_variant BRCA-FR 14 31077319 31077319 single base substitution G C downstream_gene_variant BRCA-FR 14 31077319 31077319 single base substitution G C intron_variant BRCA-FR 14 31077319 31077319 single base substitution G C upstream_gene_variant BRCA-FR 14 31078137 31078137 single base substitution G A downstream_gene_variant BRCA-FR 14 31078137 31078137 single base substitution G A intron_variant BRCA-FR 14 31078137 31078137 single base substitution G A upstream_gene_variant BRCA-FR 14 31088786 31088786 single base substitution T C 3_prime_UTR_variant BRCA-FR 14 31088786 31088786 single base substitution T C downstream_gene_variant BRCA-FR 14 31092849 31092849 single base substitution G C downstream_gene_variant BRCA-UK 14 31068848 31068848 single base substitution A G downstream_gene_variant BRCA-UK 14 31068848 31068848 single base substitution A G intron_variant BRCA-UK 14 31068848 31068848 single base substitution A G upstream_gene_variant BRCA-UK 14 31093956 31093956 single base substitution G C downstream_gene_variant BRCA-US 14 31071093 31071093 single base substitution C T 3_prime_UTR_variant BRCA-US 14 31071093 31071093 single base substitution C T downstream_gene_variant BRCA-US 14 31071093 31071093 single base substitution C T exon_variant BRCA-US 14 31071093 31071093 single base substitution C T synonymous_variant Y244Y 732C>T BRCA-US 14 31071093 31071093 single base substitution C T synonymous_variant Y290Y 870C>T BRCA-US 14 31071093 31071093 single base substitution C T synonymous_variant Y320Y 960C>T BRCA-US 14 31071093 31071093 single base substitution C T synonymous_variant Y55Y 165C>T BRCA-US 14 31071093 31071093 single base substitution C T upstream_gene_variant BRCA-US 14 31074844 31074844 single base substitution C T downstream_gene_variant BRCA-US 14 31074844 31074844 single base substitution C T exon_variant BRCA-US 14 31074844 31074844 single base substitution C T intron_variant BRCA-US 14 31074844 31074844 single base substitution C T stop_gained R336* 1006C>T BRCA-US 14 31074844 31074844 single base substitution C T stop_gained R382* 1144C>T BRCA-US 14 31074844 31074844 single base substitution C T stop_gained R412* 1234C>T BRCA-US 14 31077124 31077124 single base substitution G T downstream_gene_variant BRCA-US 14 31077124 31077124 single base substitution G T exon_variant BRCA-US 14 31077124 31077124 single base substitution G T intron_variant BRCA-US 14 31077124 31077124 single base substitution G T missense_variant G404V 1211G>T BRCA-US 14 31077124 31077124 single base substitution G T missense_variant G450V 1349G>T BRCA-US 14 31077124 31077124 single base substitution G T missense_variant G480V 1439G>T BRCA-US 14 31077124 31077124 single base substitution G T upstream_gene_variant BRCA-US 14 31081486 31081486 single base substitution G A 3_prime_UTR_variant BRCA-US 14 31081486 31081486 single base substitution G A downstream_gene_variant BRCA-US 14 31081486 31081486 single base substitution G A exon_variant BRCA-US 14 31081486 31081486 single base substitution G A missense_variant G479E 1436G>A BRCA-US 14 31081486 31081486 single base substitution G A missense_variant G525E 1574G>A BRCA-US 14 31081486 31081486 single base substitution G A missense_variant G555E 1664G>A BTCA-JP 14 31066757 31066757 insertion of <=200bp - A downstream_gene_variant BTCA-JP 14 31066757 31066757 insertion of <=200bp - A intron_variant BTCA-JP 14 31066757 31066757 insertion of <=200bp - A upstream_gene_variant CESC-US 14 31061590 31061590 single base substitution G A 3_prime_UTR_variant CESC-US 14 31061590 31061590 single base substitution G A downstream_gene_variant CESC-US 14 31061590 31061590 single base substitution G A exon_variant CESC-US 14 31061590 31061590 single base substitution G A missense_variant R100Q 299G>A CESC-US 14 31061590 31061590 single base substitution G A missense_variant R130Q 389G>A CESC-US 14 31061590 31061590 single base substitution G A missense_variant R54Q 161G>A CESC-US 14 31061590 31061590 single base substitution G A upstream_gene_variant CLLE-ES 14 31057149 31057149 single base substitution T C intron_variant CLLE-ES 14 31057149 31057149 single base substitution T C upstream_gene_variant COAD-US 14 31056013 31056013 single base substitution T C 5_prime_UTR_variant COAD-US 14 31056013 31056013 single base substitution T C exon_variant COAD-US 14 31056013 31056013 single base substitution T C missense_variant Y43H 127T>C COAD-US 14 31056013 31056013 single base substitution T C missense_variant Y73H 217T>C COAD-US 14 31061590 31061590 single base substitution G A 3_prime_UTR_variant COAD-US 14 31061590 31061590 single base substitution G A downstream_gene_variant COAD-US 14 31061590 31061590 single base substitution G A exon_variant COAD-US 14 31061590 31061590 single base substitution G A missense_variant R100Q 299G>A COAD-US 14 31061590 31061590 single base substitution G A missense_variant R130Q 389G>A COAD-US 14 31061590 31061590 single base substitution G A missense_variant R54Q 161G>A COAD-US 14 31061590 31061590 single base substitution G A upstream_gene_variant COAD-US 14 31062799 31062799 single base substitution G A 3_prime_UTR_variant COAD-US 14 31062799 31062799 single base substitution G A downstream_gene_variant COAD-US 14 31062799 31062799 single base substitution G A exon_variant COAD-US 14 31062799 31062799 single base substitution G A missense_variant E1K 1G>A COAD-US 14 31062799 31062799 single base substitution G A missense_variant R115Q 344G>A COAD-US 14 31062799 31062799 single base substitution G A missense_variant R161Q 482G>A COAD-US 14 31062799 31062799 single base substitution G A missense_variant R191Q 572G>A COAD-US 14 31062799 31062799 single base substitution G A upstream_gene_variant COAD-US 14 31071227 31071227 single base substitution A C 3_prime_UTR_variant COAD-US 14 31071227 31071227 single base substitution A C downstream_gene_variant COAD-US 14 31071227 31071227 single base substitution A C exon_variant COAD-US 14 31071227 31071227 single base substitution A C missense_variant K254N 762A>C COAD-US 14 31071227 31071227 single base substitution A C missense_variant K300N 900A>C COAD-US 14 31071227 31071227 single base substitution A C missense_variant K330N 990A>C COAD-US 14 31071227 31071227 single base substitution A C missense_variant K65N 195A>C COAD-US 14 31071227 31071227 single base substitution A C upstream_gene_variant COAD-US 14 31074845 31074845 single base substitution G A downstream_gene_variant COAD-US 14 31074845 31074845 single base substitution G A exon_variant COAD-US 14 31074845 31074845 single base substitution G A intron_variant COAD-US 14 31074845 31074845 single base substitution G A missense_variant R336Q 1007G>A COAD-US 14 31074845 31074845 single base substitution G A missense_variant R382Q 1145G>A COAD-US 14 31074845 31074845 single base substitution G A missense_variant R412Q 1235G>A COAD-US 14 31074996 31074996 single base substitution G T downstream_gene_variant COAD-US 14 31074996 31074996 single base substitution G T exon_variant COAD-US 14 31074996 31074996 single base substitution G T intron_variant COAD-US 14 31074996 31074996 single base substitution G T missense_variant K386N 1158G>T COAD-US 14 31074996 31074996 single base substitution G T missense_variant K432N 1296G>T COAD-US 14 31074996 31074996 single base substitution G T missense_variant K462N 1386G>T COCA-CN 14 31050199 31050199 single base substitution T C intron_variant COCA-CN 14 31050215 31050215 single base substitution A T intron_variant COCA-CN 14 31056077 31056077 single base substitution A C intron_variant COCA-CN 14 31067714 31067714 single base substitution A G 3_prime_UTR_variant COCA-CN 14 31067714 31067714 single base substitution A G downstream_gene_variant COCA-CN 14 31067714 31067714 single base substitution A G intron_variant COCA-CN 14 31067714 31067714 single base substitution A G missense_variant N175D 523A>G COCA-CN 14 31067714 31067714 single base substitution A G missense_variant N221D 661A>G COCA-CN 14 31067714 31067714 single base substitution A G missense_variant N251D 751A>G COCA-CN 14 31067714 31067714 single base substitution A G upstream_gene_variant COCA-CN 14 31067716 31067716 single base substitution C T 3_prime_UTR_variant COCA-CN 14 31067716 31067716 single base substitution C T downstream_gene_variant COCA-CN 14 31067716 31067716 single base substitution C T intron_variant COCA-CN 14 31067716 31067716 single base substitution C T synonymous_variant N175N 525C>T COCA-CN 14 31067716 31067716 single base substitution C T synonymous_variant N221N 663C>T COCA-CN 14 31067716 31067716 single base substitution C T synonymous_variant N251N 753C>T COCA-CN 14 31067716 31067716 single base substitution C T upstream_gene_variant COCA-CN 14 31067783 31067783 single base substitution C T 3_prime_UTR_variant COCA-CN 14 31067783 31067783 single base substitution C T downstream_gene_variant COCA-CN 14 31067783 31067783 single base substitution C T exon_variant COCA-CN 14 31067783 31067783 single base substitution C T intron_variant COCA-CN 14 31067783 31067783 single base substitution C T stop_gained R198* 592C>T COCA-CN 14 31067783 31067783 single base substitution C T stop_gained R244* 730C>T COCA-CN 14 31067783 31067783 single base substitution C T stop_gained R274* 820C>T COCA-CN 14 31067783 31067783 single base substitution C T upstream_gene_variant COCA-CN 14 31074595 31074595 single base substitution A G intron_variant COCA-CN 14 31077142 31077142 single base substitution C A downstream_gene_variant COCA-CN 14 31077142 31077142 single base substitution C A exon_variant COCA-CN 14 31077142 31077142 single base substitution C A intron_variant COCA-CN 14 31077142 31077142 single base substitution C A missense_variant S410Y 1229C>A COCA-CN 14 31077142 31077142 single base substitution C A missense_variant S456Y 1367C>A COCA-CN 14 31077142 31077142 single base substitution C A missense_variant S486Y 1457C>A COCA-CN 14 31077142 31077142 single base substitution C A upstream_gene_variant COCA-CN 14 31085437 31085437 single base substitution G T downstream_gene_variant COCA-CN 14 31085437 31085437 single base substitution G T intron_variant EOPC-DE 14 31088474 31088474 single base substitution T G 3_prime_UTR_variant EOPC-DE 14 31088474 31088474 single base substitution T G downstream_gene_variant ESAD-UK 14 31024067 31024067 deletion of <=200bp C - upstream_gene_variant ESAD-UK 14 31025641 31025641 single base substitution G A upstream_gene_variant ESAD-UK 14 31025771 31025771 single base substitution C T upstream_gene_variant ESAD-UK 14 31026132 31026132 single base substitution T G upstream_gene_variant ESAD-UK 14 31029758 31029759 deletion of <=200bp AG - 5_prime_UTR_variant ESAD-UK 14 31029758 31029759 deletion of <=200bp AG - intron_variant ESAD-UK 14 31029895 31029895 single base substitution G T 5_prime_UTR_variant ESAD-UK 14 31029895 31029895 single base substitution G T intron_variant ESAD-UK 14 31032447 31032447 single base substitution A G intron_variant ESAD-UK 14 31035113 31035113 single base substitution C T intron_variant ESAD-UK 14 31037998 31037998 single base substitution G A intron_variant ESAD-UK 14 31038948 31038948 deletion of <=200bp G - intron_variant ESAD-UK 14 31038948 31038948 deletion of <=200bp G - upstream_gene_variant ESAD-UK 14 31041552 31041552 single base substitution G A intron_variant ESAD-UK 14 31041552 31041552 single base substitution G A upstream_gene_variant ESAD-UK 14 31041975 31041975 single base substitution C T intron_variant ESAD-UK 14 31041975 31041975 single base substitution C T upstream_gene_variant ESAD-UK 14 31044460 31044460 single base substitution C G intron_variant ESAD-UK 14 31044460 31044460 single base substitution C G upstream_gene_variant ESAD-UK 14 31045700 31045700 single base substitution C T intron_variant ESAD-UK 14 31045700 31045700 single base substitution C T upstream_gene_variant ESAD-UK 14 31047829 31047829 single base substitution T C intron_variant ESAD-UK 14 31050140 31050140 single base substitution T A 5_prime_UTR_variant ESAD-UK 14 31050140 31050140 single base substitution T A intron_variant ESAD-UK 14 31057202 31057202 single base substitution T G intron_variant ESAD-UK 14 31057202 31057202 single base substitution T G upstream_gene_variant ESAD-UK 14 31057616 31057616 single base substitution G A intron_variant ESAD-UK 14 31057616 31057616 single base substitution G A upstream_gene_variant ESAD-UK 14 31057930 31057930 single base substitution A C intron_variant ESAD-UK 14 31057930 31057930 single base substitution A C upstream_gene_variant ESAD-UK 14 31057941 31057941 single base substitution A C intron_variant ESAD-UK 14 31057941 31057941 single base substitution A C upstream_gene_variant ESAD-UK 14 31059920 31059920 single base substitution C T downstream_gene_variant ESAD-UK 14 31059920 31059920 single base substitution C T exon_variant ESAD-UK 14 31059920 31059920 single base substitution C T intron_variant ESAD-UK 14 31059920 31059920 single base substitution C T upstream_gene_variant ESAD-UK 14 31060500 31060500 single base substitution C A 3_prime_UTR_variant ESAD-UK 14 31060500 31060500 single base substitution C A downstream_gene_variant ESAD-UK 14 31060500 31060500 single base substitution C A intron_variant ESAD-UK 14 31060500 31060500 single base substitution C A upstream_gene_variant ESAD-UK 14 31060787 31060787 single base substitution C T downstream_gene_variant ESAD-UK 14 31060787 31060787 single base substitution C T intron_variant ESAD-UK 14 31060787 31060787 single base substitution C T upstream_gene_variant ESAD-UK 14 31062307 31062307 deletion of <=200bp T - downstream_gene_variant ESAD-UK 14 31062307 31062307 deletion of <=200bp T - intron_variant ESAD-UK 14 31062307 31062307 deletion of <=200bp T - upstream_gene_variant ESAD-UK 14 31066383 31066383 insertion of <=200bp - A downstream_gene_variant ESAD-UK 14 31066383 31066383 insertion of <=200bp - A intron_variant ESAD-UK 14 31066383 31066383 insertion of <=200bp - A upstream_gene_variant ESAD-UK 14 31068036 31068036 single base substitution G C downstream_gene_variant ESAD-UK 14 31068036 31068036 single base substitution G C intron_variant ESAD-UK 14 31068036 31068036 single base substitution G C upstream_gene_variant ESAD-UK 14 31068431 31068431 deletion of <=200bp T - downstream_gene_variant ESAD-UK 14 31068431 31068431 deletion of <=200bp T - intron_variant ESAD-UK 14 31068431 31068431 deletion of <=200bp T - upstream_gene_variant ESAD-UK 14 31068729 31068729 single base substitution G A downstream_gene_variant ESAD-UK 14 31068729 31068729 single base substitution G A intron_variant ESAD-UK 14 31068729 31068729 single base substitution G A upstream_gene_variant ESAD-UK 14 31070122 31070122 single base substitution A C downstream_gene_variant ESAD-UK 14 31070122 31070122 single base substitution A C intron_variant ESAD-UK 14 31070122 31070122 single base substitution A C upstream_gene_variant ESAD-UK 14 31074027 31074027 single base substitution T C intron_variant ESAD-UK 14 31074326 31074326 single base substitution T A intron_variant ESAD-UK 14 31074987 31074987 single base substitution C T downstream_gene_variant ESAD-UK 14 31074987 31074987 single base substitution C T exon_variant ESAD-UK 14 31074987 31074987 single base substitution C T intron_variant ESAD-UK 14 31074987 31074987 single base substitution C T synonymous_variant S383S 1149C>T ESAD-UK 14 31074987 31074987 single base substitution C T synonymous_variant S429S 1287C>T ESAD-UK 14 31074987 31074987 single base substitution C T synonymous_variant S459S 1377C>T ESAD-UK 14 31075928 31075928 single base substitution G C downstream_gene_variant ESAD-UK 14 31075928 31075928 single base substitution G C intron_variant ESAD-UK 14 31075928 31075928 single base substitution G C upstream_gene_variant ESAD-UK 14 31077576 31077576 single base substitution G C downstream_gene_variant ESAD-UK 14 31077576 31077576 single base substitution G C intron_variant ESAD-UK 14 31077576 31077576 single base substitution G C upstream_gene_variant ESAD-UK 14 31081700 31081700 single base substitution T A downstream_gene_variant ESAD-UK 14 31081700 31081700 single base substitution T A intron_variant ESAD-UK 14 31082307 31082307 single base substitution A T intron_variant ESAD-UK 14 31082916 31082916 single base substitution A T intron_variant ESAD-UK 14 31085239 31085239 single base substitution T C downstream_gene_variant ESAD-UK 14 31085239 31085239 single base substitution T C intron_variant ESAD-UK 14 31085879 31085879 single base substitution G C 3_prime_UTR_variant ESAD-UK 14 31085879 31085879 single base substitution G C downstream_gene_variant ESAD-UK 14 31085879 31085879 single base substitution G C exon_variant ESAD-UK 14 31089583 31089583 single base substitution C T downstream_gene_variant ESAD-UK 14 31089751 31089751 single base substitution T C downstream_gene_variant ESAD-UK 14 31091533 31091533 single base substitution G C downstream_gene_variant ESAD-UK 14 31094053 31094053 single base substitution G A downstream_gene_variant GBM-US 14 31081472 31081472 single base substitution C G 3_prime_UTR_variant GBM-US 14 31081472 31081472 single base substitution C G downstream_gene_variant GBM-US 14 31081472 31081472 single base substitution C G exon_variant GBM-US 14 31081472 31081472 single base substitution C G stop_gained Y474* 1422C>G GBM-US 14 31081472 31081472 single base substitution C G stop_gained Y520* 1560C>G GBM-US 14 31081472 31081472 single base substitution C G stop_gained Y550* 1650C>G KIRC-US 14 31074726 31074726 single base substitution T G 3_prime_UTR_variant KIRC-US 14 31074726 31074726 single base substitution T G exon_variant KIRC-US 14 31074726 31074726 single base substitution T G intron_variant KIRC-US 14 31074726 31074726 single base substitution T G missense_variant F107L 321T>G KIRC-US 14 31074726 31074726 single base substitution T G missense_variant F296L 888T>G KIRC-US 14 31074726 31074726 single base substitution T G missense_variant F342L 1026T>G KIRC-US 14 31074726 31074726 single base substitution T G missense_variant F372L 1116T>G KIRC-US 14 31074772 31074772 deletion of <=200bp A - downstream_gene_variant KIRC-US 14 31074772 31074772 deletion of <=200bp A - exon_variant KIRC-US 14 31074772 31074772 deletion of <=200bp A - frameshift_variant K312 KIRC-US 14 31074772 31074772 deletion of <=200bp A - frameshift_variant K358 KIRC-US 14 31074772 31074772 deletion of <=200bp A - frameshift_variant K388 KIRC-US 14 31074772 31074772 deletion of <=200bp A - intron_variant KIRP-US 14 31081505 31081505 single base substitution G A 3_prime_UTR_variant KIRP-US 14 31081505 31081505 single base substitution G A downstream_gene_variant KIRP-US 14 31081505 31081505 single base substitution G A exon_variant KIRP-US 14 31081505 31081505 single base substitution G A synonymous_variant T485T 1455G>A KIRP-US 14 31081505 31081505 single base substitution G A synonymous_variant T531T 1593G>A KIRP-US 14 31081505 31081505 single base substitution G A synonymous_variant T561T 1683G>A KIRP-US 14 31091558 31091558 single base substitution C T downstream_gene_variant LICA-FR 14 31024330 31024330 single base substitution C T upstream_gene_variant LICA-FR 14 31026207 31026207 insertion of <=200bp - A upstream_gene_variant LICA-FR 14 31032186 31032186 single base substitution C T intron_variant LICA-FR 14 31032229 31032229 single base substitution A G intron_variant LICA-FR 14 31035962 31035962 single base substitution T C intron_variant LICA-FR 14 31049839 31049839 single base substitution G T intron_variant LICA-FR 14 31054033 31054033 deletion of <=200bp T - intron_variant LICA-FR 14 31068619 31068619 single base substitution G C downstream_gene_variant LICA-FR 14 31068619 31068619 single base substitution G C intron_variant LICA-FR 14 31068619 31068619 single base substitution G C upstream_gene_variant LICA-FR 14 31074896 31074896 single base substitution A G downstream_gene_variant LICA-FR 14 31074896 31074896 single base substitution A G exon_variant LICA-FR 14 31074896 31074896 single base substitution A G intron_variant LICA-FR 14 31074896 31074896 single base substitution A G missense_variant D353G 1058A>G LICA-FR 14 31074896 31074896 single base substitution A G missense_variant D399G 1196A>G LICA-FR 14 31074896 31074896 single base substitution A G missense_variant D429G 1286A>G LIHC-US 14 31077159 31077159 single base substitution C T downstream_gene_variant LIHC-US 14 31077159 31077159 single base substitution C T exon_variant LIHC-US 14 31077159 31077159 single base substitution C T intron_variant LIHC-US 14 31077159 31077159 single base substitution C T missense_variant P416S 1246C>T LIHC-US 14 31077159 31077159 single base substitution C T missense_variant P462S 1384C>T LIHC-US 14 31077159 31077159 single base substitution C T missense_variant P492S 1474C>T LIHC-US 14 31077159 31077159 single base substitution C T upstream_gene_variant LIHC-US 14 31084590 31084590 single base substitution A G 3_prime_UTR_variant LIHC-US 14 31084590 31084590 single base substitution A G exon_variant LIHC-US 14 31084590 31084590 single base substitution A G missense_variant E524G 1571A>G LIHC-US 14 31084590 31084590 single base substitution A G missense_variant E570G 1709A>G LIHC-US 14 31084590 31084590 single base substitution A G missense_variant E600G 1799A>G LINC-JP 14 31040251 31040251 single base substitution G C intron_variant LINC-JP 14 31040251 31040251 single base substitution G C upstream_gene_variant LINC-JP 14 31058633 31058633 single base substitution A G exon_variant LINC-JP 14 31058633 31058633 single base substitution A G synonymous_variant G14G 42A>G LINC-JP 14 31058633 31058633 single base substitution A G synonymous_variant G60G 180A>G LINC-JP 14 31058633 31058633 single base substitution A G synonymous_variant G90G 270A>G LINC-JP 14 31058633 31058633 single base substitution A G upstream_gene_variant LINC-JP 14 31058713 31058713 insertion of <=200bp - G downstream_gene_variant LINC-JP 14 31058713 31058713 insertion of <=200bp - G intron_variant LINC-JP 14 31058713 31058713 insertion of <=200bp - G upstream_gene_variant LINC-JP 14 31066769 31066769 deletion of <=200bp T - downstream_gene_variant LINC-JP 14 31066769 31066769 deletion of <=200bp T - intron_variant LINC-JP 14 31066769 31066769 deletion of <=200bp T - upstream_gene_variant LINC-JP 14 31071983 31071983 single base substitution A G downstream_gene_variant LINC-JP 14 31071983 31071983 single base substitution A G exon_variant LINC-JP 14 31071983 31071983 single base substitution A G intron_variant LINC-JP 14 31081606 31081606 single base substitution T C downstream_gene_variant LINC-JP 14 31081606 31081606 single base substitution T C intron_variant LINC-JP 14 31084482 31084482 single base substitution G C intron_variant LINC-JP 14 31084807 31084807 single base substitution G T downstream_gene_variant LINC-JP 14 31084807 31084807 single base substitution G T intron_variant LINC-JP 14 31092667 31092667 single base substitution T C downstream_gene_variant LIRI-JP 14 31023420 31023420 single base substitution T C upstream_gene_variant LIRI-JP 14 31024165 31024165 single base substitution G T upstream_gene_variant LIRI-JP 14 31024600 31024600 single base substitution C T upstream_gene_variant LIRI-JP 14 31027201 31027201 single base substitution C T upstream_gene_variant LIRI-JP 14 31027510 31027510 single base substitution G A upstream_gene_variant LIRI-JP 14 31027854 31027858 deletion of <=200bp CTTGG - upstream_gene_variant LIRI-JP 14 31030727 31030727 single base substitution T C intron_variant LIRI-JP 14 31033108 31033108 single base substitution A G intron_variant LIRI-JP 14 31039793 31039793 single base substitution A G intron_variant LIRI-JP 14 31039793 31039793 single base substitution A G upstream_gene_variant LIRI-JP 14 31040543 31040543 single base substitution C A intron_variant LIRI-JP 14 31040543 31040543 single base substitution C A upstream_gene_variant LIRI-JP 14 31041128 31041128 single base substitution T C intron_variant LIRI-JP 14 31041128 31041128 single base substitution T C upstream_gene_variant LIRI-JP 14 31043519 31043519 single base substitution A G intron_variant LIRI-JP 14 31043519 31043519 single base substitution A G upstream_gene_variant LIRI-JP 14 31045580 31045580 single base substitution A G intron_variant LIRI-JP 14 31045580 31045580 single base substitution A G upstream_gene_variant LIRI-JP 14 31045595 31045595 single base substitution A G intron_variant LIRI-JP 14 31045595 31045595 single base substitution A G upstream_gene_variant LIRI-JP 14 31047173 31047173 single base substitution G A intron_variant LIRI-JP 14 31047717 31047717 single base substitution C G intron_variant LIRI-JP 14 31050905 31050905 single base substitution A G intron_variant LIRI-JP 14 31054101 31054101 single base substitution C G intron_variant LIRI-JP 14 31054369 31054369 single base substitution A T intron_variant LIRI-JP 14 31055419 31055419 single base substitution T C intron_variant LIRI-JP 14 31055709 31055720 deletion of <=200bp CACAGTGAAATT - intron_variant LIRI-JP 14 31056434 31056434 single base substitution C T intron_variant LIRI-JP 14 31058459 31058459 single base substitution A G intron_variant LIRI-JP 14 31058459 31058459 single base substitution A G upstream_gene_variant LIRI-JP 14 31058801 31058801 single base substitution A G downstream_gene_variant LIRI-JP 14 31058801 31058801 single base substitution A G intron_variant LIRI-JP 14 31058801 31058801 single base substitution A G upstream_gene_variant LIRI-JP 14 31061145 31061145 single base substitution A G downstream_gene_variant LIRI-JP 14 31061145 31061145 single base substitution A G intron_variant LIRI-JP 14 31061145 31061145 single base substitution A G upstream_gene_variant LIRI-JP 14 31061854 31061866 deletion of <=200bp GACCTAATGATTA - downstream_gene_variant LIRI-JP 14 31061854 31061866 deletion of <=200bp GACCTAATGATTA - intron_variant LIRI-JP 14 31061854 31061866 deletion of <=200bp GACCTAATGATTA - upstream_gene_variant LIRI-JP 14 31062157 31062157 single base substitution A C downstream_gene_variant LIRI-JP 14 31062157 31062157 single base substitution A C intron_variant LIRI-JP 14 31062157 31062157 single base substitution A C upstream_gene_variant LIRI-JP 14 31063600 31063600 single base substitution A G downstream_gene_variant LIRI-JP 14 31063600 31063600 single base substitution A G intron_variant LIRI-JP 14 31063600 31063600 single base substitution A G upstream_gene_variant LIRI-JP 14 31063811 31063811 single base substitution A G downstream_gene_variant LIRI-JP 14 31063811 31063811 single base substitution A G intron_variant LIRI-JP 14 31063811 31063811 single base substitution A G upstream_gene_variant LIRI-JP 14 31065726 31065726 single base substitution T C downstream_gene_variant LIRI-JP 14 31065726 31065726 single base substitution T C intron_variant LIRI-JP 14 31065726 31065726 single base substitution T C upstream_gene_variant LIRI-JP 14 31069061 31069061 single base substitution C T downstream_gene_variant LIRI-JP 14 31069061 31069061 single base substitution C T intron_variant LIRI-JP 14 31069061 31069061 single base substitution C T upstream_gene_variant LIRI-JP 14 31069239 31069239 single base substitution A C downstream_gene_variant LIRI-JP 14 31069239 31069239 single base substitution A C intron_variant LIRI-JP 14 31069239 31069239 single base substitution A C upstream_gene_variant LIRI-JP 14 31069566 31069566 single base substitution A G downstream_gene_variant LIRI-JP 14 31069566 31069566 single base substitution A G intron_variant LIRI-JP 14 31069566 31069566 single base substitution A G upstream_gene_variant LIRI-JP 14 31070215 31070215 single base substitution G C downstream_gene_variant LIRI-JP 14 31070215 31070215 single base substitution G C intron_variant LIRI-JP 14 31070215 31070215 single base substitution G C upstream_gene_variant LIRI-JP 14 31070899 31070899 single base substitution A T downstream_gene_variant LIRI-JP 14 31070899 31070899 single base substitution A T intron_variant LIRI-JP 14 31070899 31070899 single base substitution A T upstream_gene_variant LIRI-JP 14 31071262 31071262 single base substitution C G 3_prime_UTR_variant LIRI-JP 14 31071262 31071262 single base substitution C G downstream_gene_variant LIRI-JP 14 31071262 31071262 single base substitution C G exon_variant LIRI-JP 14 31071262 31071262 single base substitution C G missense_variant T266R 797C>G LIRI-JP 14 31071262 31071262 single base substitution C G missense_variant T312R 935C>G LIRI-JP 14 31071262 31071262 single base substitution C G missense_variant T342R 1025C>G LIRI-JP 14 31071262 31071262 single base substitution C G missense_variant T77R 230C>G LIRI-JP 14 31071262 31071262 single base substitution C G upstream_gene_variant LIRI-JP 14 31071446 31071446 single base substitution A G downstream_gene_variant LIRI-JP 14 31071446 31071446 single base substitution A G intron_variant LIRI-JP 14 31071446 31071446 single base substitution A G upstream_gene_variant LIRI-JP 14 31072033 31072033 single base substitution G T downstream_gene_variant LIRI-JP 14 31072033 31072033 single base substitution G T exon_variant LIRI-JP 14 31072033 31072033 single base substitution G T intron_variant LIRI-JP 14 31074772 31074772 deletion of <=200bp A - downstream_gene_variant LIRI-JP 14 31074772 31074772 deletion of <=200bp A - exon_variant LIRI-JP 14 31074772 31074772 deletion of <=200bp A - frameshift_variant K312 LIRI-JP 14 31074772 31074772 deletion of <=200bp A - frameshift_variant K358 LIRI-JP 14 31074772 31074772 deletion of <=200bp A - frameshift_variant K388 LIRI-JP 14 31074772 31074772 deletion of <=200bp A - intron_variant LIRI-JP 14 31075332 31075332 single base substitution A G downstream_gene_variant LIRI-JP 14 31075332 31075332 single base substitution A G intron_variant LIRI-JP 14 31077221 31077221 single base substitution C T downstream_gene_variant LIRI-JP 14 31077221 31077221 single base substitution C T intron_variant LIRI-JP 14 31077221 31077221 single base substitution C T synonymous_variant T436T 1308C>T LIRI-JP 14 31077221 31077221 single base substitution C T synonymous_variant T482T 1446C>T LIRI-JP 14 31077221 31077221 single base substitution C T synonymous_variant T512T 1536C>T LIRI-JP 14 31077221 31077221 single base substitution C T upstream_gene_variant LIRI-JP 14 31078557 31078557 single base substitution A G downstream_gene_variant LIRI-JP 14 31078557 31078557 single base substitution A G intron_variant LIRI-JP 14 31078557 31078557 single base substitution A G upstream_gene_variant LIRI-JP 14 31079824 31079824 single base substitution T C downstream_gene_variant LIRI-JP 14 31079824 31079824 single base substitution T C intron_variant LIRI-JP 14 31079824 31079824 single base substitution T C upstream_gene_variant LIRI-JP 14 31080347 31080347 single base substitution G A downstream_gene_variant LIRI-JP 14 31080347 31080347 single base substitution G A intron_variant LIRI-JP 14 31080347 31080347 single base substitution G A upstream_gene_variant LIRI-JP 14 31082378 31082378 single base substitution A G intron_variant LIRI-JP 14 31083117 31083117 single base substitution A G intron_variant LIRI-JP 14 31086056 31086056 single base substitution A C 3_prime_UTR_variant LIRI-JP 14 31086056 31086056 single base substitution A C downstream_gene_variant LIRI-JP 14 31086056 31086056 single base substitution A C exon_variant LIRI-JP 14 31091352 31091352 single base substitution G A downstream_gene_variant LIRI-JP 14 31092356 31092356 single base substitution A T downstream_gene_variant LIRI-JP 14 31094255 31094255 single base substitution A G downstream_gene_variant LUSC-KR 14 31024903 31024903 single base substitution G T upstream_gene_variant LUSC-KR 14 31025825 31025825 single base substitution A T upstream_gene_variant LUSC-KR 14 31030023 31030023 single base substitution G C intron_variant LUSC-KR 14 31030023 31030023 single base substitution G C missense_variant E21Q 61G>C LUSC-KR 14 31044420 31044420 single base substitution A G intron_variant LUSC-KR 14 31044420 31044420 single base substitution A G upstream_gene_variant LUSC-KR 14 31049595 31049595 single base substitution A T intron_variant LUSC-KR 14 31049596 31049596 single base substitution G C intron_variant LUSC-KR 14 31050979 31050979 single base substitution A T intron_variant LUSC-KR 14 31055988 31055988 single base substitution G T 5_prime_UTR_variant LUSC-KR 14 31055988 31055988 single base substitution G T exon_variant LUSC-KR 14 31055988 31055988 single base substitution G T missense_variant E34D 102G>T LUSC-KR 14 31055988 31055988 single base substitution G T missense_variant E64D 192G>T LUSC-KR 14 31063718 31063718 single base substitution A T downstream_gene_variant LUSC-KR 14 31063718 31063718 single base substitution A T intron_variant LUSC-KR 14 31063718 31063718 single base substitution A T upstream_gene_variant LUSC-KR 14 31064000 31064000 single base substitution A G downstream_gene_variant LUSC-KR 14 31064000 31064000 single base substitution A G intron_variant LUSC-KR 14 31064000 31064000 single base substitution A G upstream_gene_variant LUSC-KR 14 31085910 31085910 single base substitution G T 3_prime_UTR_variant LUSC-KR 14 31085910 31085910 single base substitution G T downstream_gene_variant LUSC-KR 14 31085910 31085910 single base substitution G T exon_variant LUSC-KR 14 31089826 31089826 single base substitution G C downstream_gene_variant LUSC-US 14 31055950 31055950 single base substitution G A 5_prime_UTR_variant LUSC-US 14 31055950 31055950 single base substitution G A exon_variant LUSC-US 14 31055950 31055950 single base substitution G A missense_variant D22N 64G>A LUSC-US 14 31055950 31055950 single base substitution G A missense_variant D52N 154G>A LUSC-US 14 31058674 31058674 single base substitution A G exon_variant LUSC-US 14 31058674 31058674 single base substitution A G intron_variant LUSC-US 14 31058674 31058674 single base substitution A G missense_variant N104S 311A>G LUSC-US 14 31058674 31058674 single base substitution A G missense_variant N28S 83A>G LUSC-US 14 31058674 31058674 single base substitution A G missense_variant N74S 221A>G LUSC-US 14 31058674 31058674 single base substitution A G upstream_gene_variant LUSC-US 14 31071217 31071217 single base substitution A T 3_prime_UTR_variant LUSC-US 14 31071217 31071217 single base substitution A T downstream_gene_variant LUSC-US 14 31071217 31071217 single base substitution A T exon_variant LUSC-US 14 31071217 31071217 single base substitution A T missense_variant K251I 752A>T LUSC-US 14 31071217 31071217 single base substitution A T missense_variant K297I 890A>T LUSC-US 14 31071217 31071217 single base substitution A T missense_variant K327I 980A>T LUSC-US 14 31071217 31071217 single base substitution A T missense_variant K62I 185A>T LUSC-US 14 31071217 31071217 single base substitution A T upstream_gene_variant LUSC-US 14 31085736 31085736 single base substitution A G downstream_gene_variant LUSC-US 14 31085736 31085736 single base substitution A G exon_variant LUSC-US 14 31085736 31085736 single base substitution A G missense_variant H660R 1979A>G LUSC-US 14 31085736 31085736 single base substitution A G missense_variant H706R 2117A>G LUSC-US 14 31085736 31085736 single base substitution A G missense_variant H736R 2207A>G MALY-DE 14 31023569 31023569 single base substitution C T upstream_gene_variant MALY-DE 14 31026261 31026262 deletion of <=200bp AT - upstream_gene_variant MALY-DE 14 31027619 31027619 single base substitution G A upstream_gene_variant MALY-DE 14 31028744 31028744 single base substitution C T 5_prime_UTR_variant MALY-DE 14 31028744 31028744 single base substitution C T intron_variant MALY-DE 14 31028745 31028745 single base substitution C T 5_prime_UTR_variant MALY-DE 14 31028745 31028745 single base substitution C T intron_variant MALY-DE 14 31034669 31034669 single base substitution T C intron_variant MALY-DE 14 31037928 31037928 single base substitution T C intron_variant MALY-DE 14 31037949 31037949 single base substitution T C intron_variant MALY-DE 14 31037961 31037961 single base substitution T G intron_variant MALY-DE 14 31038850 31038850 single base substitution G A intron_variant MALY-DE 14 31038850 31038850 single base substitution G A upstream_gene_variant MALY-DE 14 31039534 31039534 single base substitution G C intron_variant MALY-DE 14 31039534 31039534 single base substitution G C upstream_gene_variant MALY-DE 14 31042145 31042145 single base substitution A G intron_variant MALY-DE 14 31042145 31042145 single base substitution A G upstream_gene_variant MALY-DE 14 31042242 31042242 single base substitution T C intron_variant MALY-DE 14 31042242 31042242 single base substitution T C upstream_gene_variant MALY-DE 14 31049235 31049235 single base substitution A C intron_variant MALY-DE 14 31054003 31054003 single base substitution A G intron_variant MALY-DE 14 31066757 31066757 insertion of <=200bp - A downstream_gene_variant MALY-DE 14 31066757 31066757 insertion of <=200bp - A intron_variant MALY-DE 14 31066757 31066757 insertion of <=200bp - A upstream_gene_variant MALY-DE 14 31066969 31066969 single base substitution T G downstream_gene_variant MALY-DE 14 31066969 31066969 single base substitution T G intron_variant MALY-DE 14 31066969 31066969 single base substitution T G upstream_gene_variant MALY-DE 14 31069996 31069996 single base substitution C T downstream_gene_variant MALY-DE 14 31069996 31069996 single base substitution C T intron_variant MALY-DE 14 31069996 31069996 single base substitution C T upstream_gene_variant MALY-DE 14 31078322 31078322 single base substitution A C downstream_gene_variant MALY-DE 14 31078322 31078322 single base substitution A C intron_variant MALY-DE 14 31078322 31078322 single base substitution A C upstream_gene_variant MALY-DE 14 31082916 31082916 single base substitution A T intron_variant MALY-DE 14 31085420 31085420 single base substitution A G downstream_gene_variant MALY-DE 14 31085420 31085420 single base substitution A G intron_variant MELA-AU 14 31023460 31023460 single base substitution C T upstream_gene_variant MELA-AU 14 31023908 31023908 single base substitution C T upstream_gene_variant MELA-AU 14 31024434 31024434 single base substitution C T upstream_gene_variant MELA-AU 14 31024480 31024480 single base substitution C T upstream_gene_variant MELA-AU 14 31024845 31024845 single base substitution T G upstream_gene_variant MELA-AU 14 31024894 31024894 single base substitution C T upstream_gene_variant MELA-AU 14 31025002 31025002 single base substitution T A upstream_gene_variant MELA-AU 14 31025029 31025029 single base substitution C T upstream_gene_variant MELA-AU 14 31025244 31025244 single base substitution G A upstream_gene_variant MELA-AU 14 31025341 31025341 single base substitution G A upstream_gene_variant MELA-AU 14 31025503 31025503 single base substitution G A upstream_gene_variant MELA-AU 14 31025674 31025674 single base substitution G A upstream_gene_variant MELA-AU 14 31025690 31025690 single base substitution G A upstream_gene_variant MELA-AU 14 31026053 31026053 single base substitution C G upstream_gene_variant MELA-AU 14 31026951 31026951 single base substitution A G upstream_gene_variant MELA-AU 14 31027212 31027212 single base substitution G A upstream_gene_variant MELA-AU 14 31027415 31027415 single base substitution G A upstream_gene_variant MELA-AU 14 31028329 31028329 single base substitution G A 5_prime_UTR_variant MELA-AU 14 31028329 31028329 single base substitution G A upstream_gene_variant MELA-AU 14 31028335 31028336 multiple base substitution (>=2bp and <=200bp) TC GT 5_prime_UTR_variant MELA-AU 14 31028335 31028336 multiple base substitution (>=2bp and <=200bp) TC GT upstream_gene_variant MELA-AU 14 31028336 31028336 single base substitution C T 5_prime_UTR_variant MELA-AU 14 31028336 31028336 single base substitution C T upstream_gene_variant MELA-AU 14 31028336 31028337 multiple base substitution (>=2bp and <=200bp) CT TT 5_prime_UTR_variant MELA-AU 14 31028336 31028337 multiple base substitution (>=2bp and <=200bp) CT TT upstream_gene_variant MELA-AU 14 31028337 31028337 single base substitution T C 5_prime_UTR_variant MELA-AU 14 31028337 31028337 single base substitution T C upstream_gene_variant MELA-AU 14 31028340 31028340 single base substitution C T 5_prime_UTR_variant MELA-AU 14 31028340 31028340 single base substitution C T upstream_gene_variant MELA-AU 14 31028545 31028545 single base substitution G T 5_prime_UTR_variant MELA-AU 14 31028545 31028545 single base substitution G T intron_variant MELA-AU 14 31028596 31028596 single base substitution G A 5_prime_UTR_variant MELA-AU 14 31028596 31028596 single base substitution G A intron_variant MELA-AU 14 31029522 31029522 single base substitution C T 5_prime_UTR_variant MELA-AU 14 31029522 31029522 single base substitution C T intron_variant MELA-AU 14 31031369 31031369 single base substitution C T intron_variant MELA-AU 14 31031402 31031402 single base substitution G A intron_variant MELA-AU 14 31031645 31031645 single base substitution T C intron_variant MELA-AU 14 31031815 31031815 single base substitution C T intron_variant MELA-AU 14 31032126 31032126 single base substitution C T intron_variant MELA-AU 14 31032164 31032164 single base substitution T A intron_variant MELA-AU 14 31032460 31032460 single base substitution T G intron_variant MELA-AU 14 31032616 31032616 single base substitution C T intron_variant MELA-AU 14 31033041 31033041 single base substitution T C intron_variant MELA-AU 14 31033248 31033248 single base substitution C T intron_variant MELA-AU 14 31033532 31033532 single base substitution C T intron_variant MELA-AU 14 31034321 31034321 single base substitution C T intron_variant MELA-AU 14 31034345 31034345 single base substitution T A intron_variant MELA-AU 14 31034664 31034664 single base substitution C T intron_variant MELA-AU 14 31034910 31034910 single base substitution C T intron_variant MELA-AU 14 31035233 31035233 single base substitution C T intron_variant MELA-AU 14 31035730 31035730 single base substitution C T intron_variant MELA-AU 14 31035811 31035811 single base substitution C T intron_variant MELA-AU 14 31035815 31035815 single base substitution T C intron_variant MELA-AU 14 31037166 31037166 single base substitution C T intron_variant MELA-AU 14 31037614 31037614 single base substitution A T intron_variant MELA-AU 14 31038392 31038392 single base substitution C T intron_variant MELA-AU 14 31039034 31039034 single base substitution A G intron_variant MELA-AU 14 31039034 31039034 single base substitution A G upstream_gene_variant MELA-AU 14 31039145 31039145 single base substitution A T intron_variant MELA-AU 14 31039145 31039145 single base substitution A T upstream_gene_variant MELA-AU 14 31040211 31040211 single base substitution G A intron_variant MELA-AU 14 31040211 31040211 single base substitution G A upstream_gene_variant MELA-AU 14 31040346 31040346 single base substitution G A intron_variant MELA-AU 14 31040346 31040346 single base substitution G A upstream_gene_variant MELA-AU 14 31040823 31040823 single base substitution C T intron_variant MELA-AU 14 31040823 31040823 single base substitution C T upstream_gene_variant MELA-AU 14 31041025 31041025 single base substitution A C intron_variant MELA-AU 14 31041025 31041025 single base substitution A C upstream_gene_variant MELA-AU 14 31042346 31042346 single base substitution A C intron_variant MELA-AU 14 31042346 31042346 single base substitution A C upstream_gene_variant MELA-AU 14 31042568 31042568 single base substitution A G intron_variant MELA-AU 14 31042568 31042568 single base substitution A G upstream_gene_variant MELA-AU 14 31043346 31043346 single base substitution C A intron_variant MELA-AU 14 31043346 31043346 single base substitution C A upstream_gene_variant MELA-AU 14 31043400 31043400 single base substitution C T intron_variant MELA-AU 14 31043400 31043400 single base substitution C T upstream_gene_variant MELA-AU 14 31043727 31043727 single base substitution C T intron_variant MELA-AU 14 31043727 31043727 single base substitution C T upstream_gene_variant MELA-AU 14 31043820 31043820 single base substitution C T intron_variant MELA-AU 14 31043820 31043820 single base substitution C T upstream_gene_variant MELA-AU 14 31044005 31044005 single base substitution C T intron_variant MELA-AU 14 31044005 31044005 single base substitution C T upstream_gene_variant MELA-AU 14 31044053 31044054 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 14 31044053 31044054 multiple base substitution (>=2bp and <=200bp) CC AT upstream_gene_variant MELA-AU 14 31044270 31044270 single base substitution C T intron_variant MELA-AU 14 31044270 31044270 single base substitution C T upstream_gene_variant MELA-AU 14 31044400 31044400 single base substitution C T intron_variant MELA-AU 14 31044400 31044400 single base substitution C T upstream_gene_variant MELA-AU 14 31044502 31044502 single base substitution C T intron_variant MELA-AU 14 31044502 31044502 single base substitution C T upstream_gene_variant MELA-AU 14 31045234 31045234 single base substitution C T intron_variant MELA-AU 14 31045234 31045234 single base substitution C T upstream_gene_variant MELA-AU 14 31045274 31045274 single base substitution C T intron_variant MELA-AU 14 31045274 31045274 single base substitution C T upstream_gene_variant MELA-AU 14 31045638 31045639 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 31045638 31045639 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 14 31046026 31046026 single base substitution C T intron_variant MELA-AU 14 31046026 31046026 single base substitution C T upstream_gene_variant MELA-AU 14 31046088 31046088 single base substitution T A intron_variant MELA-AU 14 31046088 31046088 single base substitution T A upstream_gene_variant MELA-AU 14 31046519 31046519 single base substitution G C intron_variant MELA-AU 14 31046519 31046519 single base substitution G C upstream_gene_variant MELA-AU 14 31046867 31046867 single base substitution T C intron_variant MELA-AU 14 31046867 31046867 single base substitution T C upstream_gene_variant MELA-AU 14 31047601 31047601 single base substitution C T intron_variant MELA-AU 14 31047922 31047922 single base substitution A G intron_variant MELA-AU 14 31047991 31047991 single base substitution C T intron_variant MELA-AU 14 31048377 31048377 single base substitution A G intron_variant MELA-AU 14 31048896 31048896 single base substitution C T intron_variant MELA-AU 14 31049160 31049160 single base substitution T G intron_variant MELA-AU 14 31049742 31049742 single base substitution G A intron_variant MELA-AU 14 31049849 31049849 single base substitution G A intron_variant MELA-AU 14 31050054 31050054 single base substitution T C intron_variant MELA-AU 14 31050277 31050277 single base substitution C T intron_variant MELA-AU 14 31050277 31050277 single base substitution C T splice_region_variant MELA-AU 14 31051935 31051935 single base substitution C T intron_variant MELA-AU 14 31054303 31054303 single base substitution G A intron_variant MELA-AU 14 31054410 31054410 single base substitution C T intron_variant MELA-AU 14 31054885 31054885 single base substitution C T intron_variant MELA-AU 14 31055149 31055149 single base substitution G C intron_variant MELA-AU 14 31055367 31055367 single base substitution C T intron_variant MELA-AU 14 31058975 31058975 single base substitution A G downstream_gene_variant MELA-AU 14 31058975 31058975 single base substitution A G intron_variant MELA-AU 14 31058975 31058975 single base substitution A G upstream_gene_variant MELA-AU 14 31059350 31059350 single base substitution T C downstream_gene_variant MELA-AU 14 31059350 31059350 single base substitution T C intron_variant MELA-AU 14 31059350 31059350 single base substitution T C upstream_gene_variant MELA-AU 14 31059554 31059554 single base substitution C T downstream_gene_variant MELA-AU 14 31059554 31059554 single base substitution C T intron_variant MELA-AU 14 31059554 31059554 single base substitution C T upstream_gene_variant MELA-AU 14 31059819 31059819 single base substitution T C downstream_gene_variant MELA-AU 14 31059819 31059819 single base substitution T C exon_variant MELA-AU 14 31059819 31059819 single base substitution T C intron_variant MELA-AU 14 31059819 31059819 single base substitution T C upstream_gene_variant MELA-AU 14 31060312 31060312 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31060312 31060312 single base substitution C T downstream_gene_variant MELA-AU 14 31060312 31060312 single base substitution C T intron_variant MELA-AU 14 31060312 31060312 single base substitution C T upstream_gene_variant MELA-AU 14 31060456 31060456 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31060456 31060456 single base substitution C T downstream_gene_variant MELA-AU 14 31060456 31060456 single base substitution C T intron_variant MELA-AU 14 31060456 31060456 single base substitution C T upstream_gene_variant MELA-AU 14 31060629 31060629 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31060629 31060629 single base substitution C T downstream_gene_variant MELA-AU 14 31060629 31060629 single base substitution C T intron_variant MELA-AU 14 31060629 31060629 single base substitution C T upstream_gene_variant MELA-AU 14 31060981 31060981 single base substitution C T downstream_gene_variant MELA-AU 14 31060981 31060981 single base substitution C T intron_variant MELA-AU 14 31060981 31060981 single base substitution C T upstream_gene_variant MELA-AU 14 31061318 31061318 single base substitution G A 3_prime_UTR_variant MELA-AU 14 31061318 31061318 single base substitution G A downstream_gene_variant MELA-AU 14 31061318 31061318 single base substitution G A intron_variant MELA-AU 14 31061318 31061318 single base substitution G A upstream_gene_variant MELA-AU 14 31061920 31061920 single base substitution C T downstream_gene_variant MELA-AU 14 31061920 31061920 single base substitution C T intron_variant MELA-AU 14 31061920 31061920 single base substitution C T upstream_gene_variant MELA-AU 14 31062324 31062324 single base substitution C T downstream_gene_variant MELA-AU 14 31062324 31062324 single base substitution C T intron_variant MELA-AU 14 31062324 31062324 single base substitution C T upstream_gene_variant MELA-AU 14 31063151 31063151 single base substitution C T downstream_gene_variant MELA-AU 14 31063151 31063151 single base substitution C T intron_variant MELA-AU 14 31063151 31063151 single base substitution C T upstream_gene_variant MELA-AU 14 31063354 31063354 single base substitution T C downstream_gene_variant MELA-AU 14 31063354 31063354 single base substitution T C intron_variant MELA-AU 14 31063354 31063354 single base substitution T C upstream_gene_variant MELA-AU 14 31063714 31063714 single base substitution T C downstream_gene_variant MELA-AU 14 31063714 31063714 single base substitution T C intron_variant MELA-AU 14 31063714 31063714 single base substitution T C upstream_gene_variant MELA-AU 14 31064114 31064114 single base substitution C T downstream_gene_variant MELA-AU 14 31064114 31064114 single base substitution C T intron_variant MELA-AU 14 31064114 31064114 single base substitution C T upstream_gene_variant MELA-AU 14 31064575 31064575 single base substitution A G downstream_gene_variant MELA-AU 14 31064575 31064575 single base substitution A G intron_variant MELA-AU 14 31064575 31064575 single base substitution A G upstream_gene_variant MELA-AU 14 31064802 31064802 single base substitution C T downstream_gene_variant MELA-AU 14 31064802 31064802 single base substitution C T intron_variant MELA-AU 14 31064802 31064802 single base substitution C T upstream_gene_variant MELA-AU 14 31064818 31064818 single base substitution G A downstream_gene_variant MELA-AU 14 31064818 31064818 single base substitution G A intron_variant MELA-AU 14 31064818 31064818 single base substitution G A upstream_gene_variant MELA-AU 14 31065103 31065104 multiple base substitution (>=2bp and <=200bp) AT TA downstream_gene_variant MELA-AU 14 31065103 31065104 multiple base substitution (>=2bp and <=200bp) AT TA intron_variant MELA-AU 14 31065103 31065104 multiple base substitution (>=2bp and <=200bp) AT TA upstream_gene_variant MELA-AU 14 31065223 31065223 single base substitution C T downstream_gene_variant MELA-AU 14 31065223 31065223 single base substitution C T intron_variant MELA-AU 14 31065223 31065223 single base substitution C T upstream_gene_variant MELA-AU 14 31065270 31065270 single base substitution C T downstream_gene_variant MELA-AU 14 31065270 31065270 single base substitution C T intron_variant MELA-AU 14 31065270 31065270 single base substitution C T upstream_gene_variant MELA-AU 14 31067158 31067158 single base substitution C T downstream_gene_variant MELA-AU 14 31067158 31067158 single base substitution C T intron_variant MELA-AU 14 31067158 31067158 single base substitution C T upstream_gene_variant MELA-AU 14 31067205 31067205 single base substitution A C downstream_gene_variant MELA-AU 14 31067205 31067205 single base substitution A C intron_variant MELA-AU 14 31067205 31067205 single base substitution A C upstream_gene_variant MELA-AU 14 31067634 31067634 single base substitution C T downstream_gene_variant MELA-AU 14 31067634 31067634 single base substitution C T intron_variant MELA-AU 14 31067634 31067634 single base substitution C T upstream_gene_variant MELA-AU 14 31068004 31068004 single base substitution T C downstream_gene_variant MELA-AU 14 31068004 31068004 single base substitution T C intron_variant MELA-AU 14 31068004 31068004 single base substitution T C upstream_gene_variant MELA-AU 14 31068191 31068191 single base substitution A G downstream_gene_variant MELA-AU 14 31068191 31068191 single base substitution A G intron_variant MELA-AU 14 31068191 31068191 single base substitution A G upstream_gene_variant MELA-AU 14 31068354 31068354 single base substitution C T downstream_gene_variant MELA-AU 14 31068354 31068354 single base substitution C T intron_variant MELA-AU 14 31068354 31068354 single base substitution C T upstream_gene_variant MELA-AU 14 31068585 31068585 single base substitution C T downstream_gene_variant MELA-AU 14 31068585 31068585 single base substitution C T intron_variant MELA-AU 14 31068585 31068585 single base substitution C T upstream_gene_variant MELA-AU 14 31068760 31068760 single base substitution C T downstream_gene_variant MELA-AU 14 31068760 31068760 single base substitution C T intron_variant MELA-AU 14 31068760 31068760 single base substitution C T upstream_gene_variant MELA-AU 14 31069672 31069672 single base substitution A G downstream_gene_variant MELA-AU 14 31069672 31069672 single base substitution A G intron_variant MELA-AU 14 31069672 31069672 single base substitution A G upstream_gene_variant MELA-AU 14 31069829 31069829 single base substitution A G downstream_gene_variant MELA-AU 14 31069829 31069829 single base substitution A G intron_variant MELA-AU 14 31069829 31069829 single base substitution A G upstream_gene_variant MELA-AU 14 31070990 31070990 single base substitution A G 3_prime_UTR_variant MELA-AU 14 31070990 31070990 single base substitution A G downstream_gene_variant MELA-AU 14 31070990 31070990 single base substitution A G exon_variant MELA-AU 14 31070990 31070990 single base substitution A G missense_variant K210R 629A>G MELA-AU 14 31070990 31070990 single base substitution A G missense_variant K21R 62A>G MELA-AU 14 31070990 31070990 single base substitution A G missense_variant K256R 767A>G MELA-AU 14 31070990 31070990 single base substitution A G missense_variant K286R 857A>G MELA-AU 14 31070990 31070990 single base substitution A G upstream_gene_variant MELA-AU 14 31072630 31072630 single base substitution T C intron_variant MELA-AU 14 31072843 31072843 single base substitution T C intron_variant MELA-AU 14 31073197 31073197 single base substitution C T intron_variant MELA-AU 14 31073259 31073259 single base substitution T A intron_variant MELA-AU 14 31073290 31073290 single base substitution C T intron_variant MELA-AU 14 31073406 31073406 single base substitution C T intron_variant MELA-AU 14 31073584 31073584 single base substitution C T intron_variant MELA-AU 14 31074360 31074360 single base substitution C T intron_variant MELA-AU 14 31074621 31074621 single base substitution C T intron_variant MELA-AU 14 31075018 31075018 single base substitution G T downstream_gene_variant MELA-AU 14 31075018 31075018 single base substitution G T intron_variant MELA-AU 14 31075018 31075018 single base substitution G T missense_variant A394S 1180G>T MELA-AU 14 31075018 31075018 single base substitution G T missense_variant A440S 1318G>T MELA-AU 14 31075018 31075018 single base substitution G T missense_variant A470S 1408G>T MELA-AU 14 31075018 31075018 single base substitution G T splice_region_variant MELA-AU 14 31075324 31075324 single base substitution G A downstream_gene_variant MELA-AU 14 31075324 31075324 single base substitution G A intron_variant MELA-AU 14 31075819 31075819 single base substitution C T downstream_gene_variant MELA-AU 14 31075819 31075819 single base substitution C T intron_variant MELA-AU 14 31075819 31075819 single base substitution C T upstream_gene_variant MELA-AU 14 31076742 31076742 single base substitution T C downstream_gene_variant MELA-AU 14 31076742 31076742 single base substitution T C intron_variant MELA-AU 14 31076742 31076742 single base substitution T C upstream_gene_variant MELA-AU 14 31076791 31076791 single base substitution T C downstream_gene_variant MELA-AU 14 31076791 31076791 single base substitution T C intron_variant MELA-AU 14 31076791 31076791 single base substitution T C upstream_gene_variant MELA-AU 14 31077984 31077984 single base substitution C T downstream_gene_variant MELA-AU 14 31077984 31077984 single base substitution C T intron_variant MELA-AU 14 31077984 31077984 single base substitution C T upstream_gene_variant MELA-AU 14 31078269 31078269 single base substitution C T downstream_gene_variant MELA-AU 14 31078269 31078269 single base substitution C T intron_variant MELA-AU 14 31078269 31078269 single base substitution C T upstream_gene_variant MELA-AU 14 31078278 31078278 single base substitution C T downstream_gene_variant MELA-AU 14 31078278 31078278 single base substitution C T intron_variant MELA-AU 14 31078278 31078278 single base substitution C T upstream_gene_variant MELA-AU 14 31078511 31078511 single base substitution C T downstream_gene_variant MELA-AU 14 31078511 31078511 single base substitution C T intron_variant MELA-AU 14 31078511 31078511 single base substitution C T upstream_gene_variant MELA-AU 14 31078594 31078594 single base substitution C T downstream_gene_variant MELA-AU 14 31078594 31078594 single base substitution C T intron_variant MELA-AU 14 31078594 31078594 single base substitution C T upstream_gene_variant MELA-AU 14 31079441 31079441 single base substitution C T downstream_gene_variant MELA-AU 14 31079441 31079441 single base substitution C T intron_variant MELA-AU 14 31079441 31079441 single base substitution C T upstream_gene_variant MELA-AU 14 31080838 31080838 single base substitution C T downstream_gene_variant MELA-AU 14 31080838 31080838 single base substitution C T exon_variant MELA-AU 14 31080838 31080838 single base substitution C T intron_variant MELA-AU 14 31080843 31080843 single base substitution A T downstream_gene_variant MELA-AU 14 31080843 31080843 single base substitution A T exon_variant MELA-AU 14 31080843 31080843 single base substitution A T intron_variant MELA-AU 14 31081115 31081115 single base substitution C T downstream_gene_variant MELA-AU 14 31081115 31081115 single base substitution C T exon_variant MELA-AU 14 31081115 31081115 single base substitution C T intron_variant MELA-AU 14 31081505 31081505 single base substitution G A 3_prime_UTR_variant MELA-AU 14 31081505 31081505 single base substitution G A downstream_gene_variant MELA-AU 14 31081505 31081505 single base substitution G A exon_variant MELA-AU 14 31081505 31081505 single base substitution G A synonymous_variant T485T 1455G>A MELA-AU 14 31081505 31081505 single base substitution G A synonymous_variant T531T 1593G>A MELA-AU 14 31081505 31081505 single base substitution G A synonymous_variant T561T 1683G>A MELA-AU 14 31083028 31083028 single base substitution C T intron_variant MELA-AU 14 31083446 31083446 single base substitution A G intron_variant MELA-AU 14 31083704 31083704 single base substitution T G intron_variant MELA-AU 14 31084218 31084218 single base substitution G C intron_variant MELA-AU 14 31084494 31084494 single base substitution C T intron_variant MELA-AU 14 31084963 31084963 single base substitution C T downstream_gene_variant MELA-AU 14 31084963 31084963 single base substitution C T intron_variant MELA-AU 14 31085373 31085373 single base substitution C A downstream_gene_variant MELA-AU 14 31085373 31085373 single base substitution C A intron_variant MELA-AU 14 31086718 31086718 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31086718 31086718 single base substitution C T downstream_gene_variant MELA-AU 14 31086718 31086718 single base substitution C T exon_variant MELA-AU 14 31087035 31087035 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31087035 31087035 single base substitution C T downstream_gene_variant MELA-AU 14 31087035 31087035 single base substitution C T exon_variant MELA-AU 14 31087667 31087667 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31087667 31087667 single base substitution C T downstream_gene_variant MELA-AU 14 31087740 31087740 single base substitution G A 3_prime_UTR_variant MELA-AU 14 31087740 31087740 single base substitution G A downstream_gene_variant MELA-AU 14 31087899 31087899 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31087899 31087899 single base substitution C T downstream_gene_variant MELA-AU 14 31088461 31088461 single base substitution C T 3_prime_UTR_variant MELA-AU 14 31088461 31088461 single base substitution C T downstream_gene_variant MELA-AU 14 31090185 31090185 single base substitution T C downstream_gene_variant MELA-AU 14 31090788 31090788 single base substitution C T downstream_gene_variant MELA-AU 14 31090918 31090918 single base substitution G A downstream_gene_variant MELA-AU 14 31091033 31091033 single base substitution C T downstream_gene_variant MELA-AU 14 31091411 31091411 single base substitution G A downstream_gene_variant MELA-AU 14 31091428 31091428 single base substitution G A downstream_gene_variant MELA-AU 14 31091456 31091456 single base substitution C T downstream_gene_variant MELA-AU 14 31091458 31091458 single base substitution T C downstream_gene_variant MELA-AU 14 31091464 31091464 single base substitution C T downstream_gene_variant MELA-AU 14 31091472 31091472 single base substitution C T downstream_gene_variant MELA-AU 14 31091514 31091514 single base substitution C T downstream_gene_variant MELA-AU 14 31092475 31092475 single base substitution C T downstream_gene_variant MELA-AU 14 31093319 31093319 single base substitution C T downstream_gene_variant MELA-AU 14 31093470 31093470 single base substitution C T downstream_gene_variant MELA-AU 14 31093688 31093688 single base substitution C T downstream_gene_variant MELA-AU 14 31094260 31094260 single base substitution C T downstream_gene_variant ORCA-IN 14 31031767 31031768 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant ORCA-IN 14 31054172 31054172 single base substitution G A intron_variant ORCA-IN 14 31065466 31065466 single base substitution A G downstream_gene_variant ORCA-IN 14 31065466 31065466 single base substitution A G intron_variant ORCA-IN 14 31065466 31065466 single base substitution A G upstream_gene_variant ORCA-IN 14 31070909 31070909 single base substitution G A downstream_gene_variant ORCA-IN 14 31070909 31070909 single base substitution G A intron_variant ORCA-IN 14 31070909 31070909 single base substitution G A upstream_gene_variant ORCA-IN 14 31085655 31085655 single base substitution A G downstream_gene_variant ORCA-IN 14 31085655 31085655 single base substitution A G exon_variant ORCA-IN 14 31085655 31085655 single base substitution A G missense_variant K633R 1898A>G ORCA-IN 14 31085655 31085655 single base substitution A G missense_variant K679R 2036A>G ORCA-IN 14 31085655 31085655 single base substitution A G missense_variant K709R 2126A>G ORCA-IN 14 31090548 31090548 single base substitution C T downstream_gene_variant ORCA-IN 14 31090627 31090627 single base substitution G C downstream_gene_variant OV-AU 14 31023399 31023399 single base substitution G T upstream_gene_variant OV-AU 14 31028625 31028625 single base substitution G T 5_prime_UTR_variant OV-AU 14 31028625 31028625 single base substitution G T intron_variant OV-AU 14 31033241 31033241 single base substitution A C intron_variant OV-AU 14 31039550 31039550 single base substitution T G intron_variant OV-AU 14 31039550 31039550 single base substitution T G upstream_gene_variant OV-AU 14 31046172 31046172 single base substitution C A intron_variant OV-AU 14 31046172 31046172 single base substitution C A upstream_gene_variant OV-AU 14 31047679 31047679 single base substitution G C intron_variant OV-AU 14 31048799 31048799 single base substitution G T intron_variant OV-AU 14 31062414 31062414 single base substitution T C downstream_gene_variant OV-AU 14 31062414 31062414 single base substitution T C intron_variant OV-AU 14 31062414 31062414 single base substitution T C upstream_gene_variant OV-AU 14 31070368 31070368 single base substitution G C downstream_gene_variant OV-AU 14 31070368 31070368 single base substitution G C intron_variant OV-AU 14 31070368 31070368 single base substitution G C upstream_gene_variant OV-AU 14 31077228 31077228 single base substitution A G downstream_gene_variant OV-AU 14 31077228 31077228 single base substitution A G intron_variant OV-AU 14 31077228 31077228 single base substitution A G missense_variant I439V 1315A>G OV-AU 14 31077228 31077228 single base substitution A G missense_variant I485V 1453A>G OV-AU 14 31077228 31077228 single base substitution A G missense_variant I515V 1543A>G OV-AU 14 31077228 31077228 single base substitution A G upstream_gene_variant OV-AU 14 31079088 31079088 single base substitution G T downstream_gene_variant OV-AU 14 31079088 31079088 single base substitution G T intron_variant OV-AU 14 31079088 31079088 single base substitution G T upstream_gene_variant OV-AU 14 31085705 31085705 single base substitution G C downstream_gene_variant OV-AU 14 31085705 31085705 single base substitution G C exon_variant OV-AU 14 31085705 31085705 single base substitution G C missense_variant E650Q 1948G>C OV-AU 14 31085705 31085705 single base substitution G C missense_variant E696Q 2086G>C OV-AU 14 31085705 31085705 single base substitution G C missense_variant E726Q 2176G>C OV-AU 14 31087711 31087711 single base substitution T C 3_prime_UTR_variant OV-AU 14 31087711 31087711 single base substitution T C downstream_gene_variant OV-AU 14 31089979 31089979 single base substitution G T downstream_gene_variant OV-US 14 31058619 31058623 deletion of <=200bp AAAGA - exon_variant OV-US 14 31058619 31058623 deletion of <=200bp AAAGA - frameshift_variant KE10 OV-US 14 31058619 31058623 deletion of <=200bp AAAGA - frameshift_variant KE56 OV-US 14 31058619 31058623 deletion of <=200bp AAAGA - frameshift_variant KE86 OV-US 14 31058619 31058623 deletion of <=200bp AAAGA - upstream_gene_variant PACA-AU 14 31027563 31027563 single base substitution G A upstream_gene_variant PACA-AU 14 31031886 31031886 single base substitution G A intron_variant PACA-AU 14 31033217 31033217 single base substitution G T intron_variant PACA-AU 14 31037780 31037780 single base substitution C G intron_variant PACA-AU 14 31040197 31040197 deletion of <=200bp T - intron_variant PACA-AU 14 31040197 31040197 deletion of <=200bp T - upstream_gene_variant PACA-AU 14 31043719 31043719 single base substitution T C intron_variant PACA-AU 14 31043719 31043719 single base substitution T C upstream_gene_variant PACA-AU 14 31047874 31047874 single base substitution G A intron_variant PACA-AU 14 31054896 31054896 single base substitution T C intron_variant PACA-AU 14 31055899 31055899 single base substitution T A intron_variant PACA-AU 14 31055938 31055938 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant PACA-AU 14 31055938 31055938 single base substitution C T exon_variant PACA-AU 14 31055938 31055938 single base substitution C T stop_gained R18* 52C>T PACA-AU 14 31055938 31055938 single base substitution C T stop_gained R48* 142C>T PACA-AU 14 31069227 31069227 single base substitution T C downstream_gene_variant PACA-AU 14 31069227 31069227 single base substitution T C intron_variant PACA-AU 14 31069227 31069227 single base substitution T C upstream_gene_variant PACA-AU 14 31070603 31070603 single base substitution C T downstream_gene_variant PACA-AU 14 31070603 31070603 single base substitution C T intron_variant PACA-AU 14 31070603 31070603 single base substitution C T upstream_gene_variant PACA-AU 14 31070867 31070867 single base substitution G T downstream_gene_variant PACA-AU 14 31070867 31070867 single base substitution G T intron_variant PACA-AU 14 31070867 31070867 single base substitution G T upstream_gene_variant PACA-AU 14 31072578 31072578 single base substitution C G intron_variant PACA-AU 14 31084733 31084733 single base substitution C G downstream_gene_variant PACA-AU 14 31084733 31084733 single base substitution C G exon_variant PACA-AU 14 31084733 31084733 single base substitution C G missense_variant Q572E 1714C>G PACA-AU 14 31084733 31084733 single base substitution C G missense_variant Q618E 1852C>G PACA-AU 14 31084733 31084733 single base substitution C G missense_variant Q648E 1942C>G PACA-AU 14 31086264 31086275 deletion of <=200bp GTTGTTTAAAAT - 3_prime_UTR_variant PACA-AU 14 31086264 31086275 deletion of <=200bp GTTGTTTAAAAT - downstream_gene_variant PACA-AU 14 31086264 31086275 deletion of <=200bp GTTGTTTAAAAT - exon_variant PACA-AU 14 31091637 31091637 single base substitution C T downstream_gene_variant PACA-CA 14 31024426 31024426 single base substitution T A upstream_gene_variant PACA-CA 14 31029237 31029237 single base substitution A G 5_prime_UTR_variant PACA-CA 14 31029237 31029237 single base substitution A G intron_variant PACA-CA 14 31029564 31029564 single base substitution T C 5_prime_UTR_variant PACA-CA 14 31029564 31029564 single base substitution T C intron_variant PACA-CA 14 31032051 31032051 single base substitution A G intron_variant PACA-CA 14 31032945 31032945 single base substitution G A intron_variant PACA-CA 14 31035482 31035482 insertion of <=200bp - A intron_variant PACA-CA 14 31036371 31036371 single base substitution G T intron_variant PACA-CA 14 31038574 31038574 insertion of <=200bp - AC intron_variant PACA-CA 14 31040765 31040765 insertion of <=200bp - T intron_variant PACA-CA 14 31040765 31040765 insertion of <=200bp - T upstream_gene_variant PACA-CA 14 31043792 31043792 single base substitution G A 5_prime_UTR_variant PACA-CA 14 31043792 31043792 single base substitution G A intron_variant PACA-CA 14 31043792 31043792 single base substitution G A upstream_gene_variant PACA-CA 14 31044116 31044116 single base substitution G A intron_variant PACA-CA 14 31044116 31044116 single base substitution G A upstream_gene_variant PACA-CA 14 31045821 31045822 deletion of <=200bp TA - intron_variant PACA-CA 14 31045821 31045822 deletion of <=200bp TA - upstream_gene_variant PACA-CA 14 31048535 31048535 single base substitution T G intron_variant PACA-CA 14 31049027 31049027 single base substitution T G intron_variant PACA-CA 14 31050288 31050288 single base substitution G T exon_variant PACA-CA 14 31050288 31050288 single base substitution G T intron_variant PACA-CA 14 31050288 31050288 single base substitution G T missense_variant M31I 93G>T PACA-CA 14 31050288 31050288 single base substitution G T start_lost M1I 3G>T PACA-CA 14 31051788 31051788 single base substitution A C intron_variant PACA-CA 14 31062607 31062607 single base substitution A G downstream_gene_variant PACA-CA 14 31062607 31062607 single base substitution A G intron_variant PACA-CA 14 31062607 31062607 single base substitution A G upstream_gene_variant PACA-CA 14 31063477 31063477 single base substitution G A downstream_gene_variant PACA-CA 14 31063477 31063477 single base substitution G A intron_variant PACA-CA 14 31063477 31063477 single base substitution G A upstream_gene_variant PACA-CA 14 31064564 31064564 single base substitution T A downstream_gene_variant PACA-CA 14 31064564 31064564 single base substitution T A intron_variant PACA-CA 14 31064564 31064564 single base substitution T A upstream_gene_variant PACA-CA 14 31067477 31067477 single base substitution A G downstream_gene_variant PACA-CA 14 31067477 31067477 single base substitution A G exon_variant PACA-CA 14 31067477 31067477 single base substitution A G intron_variant PACA-CA 14 31067477 31067477 single base substitution A G upstream_gene_variant PACA-CA 14 31067587 31067587 single base substitution C T downstream_gene_variant PACA-CA 14 31067587 31067587 single base substitution C T intron_variant PACA-CA 14 31067587 31067587 single base substitution C T upstream_gene_variant PACA-CA 14 31072803 31072803 single base substitution T G intron_variant PACA-CA 14 31073133 31073133 single base substitution A G intron_variant PACA-CA 14 31073515 31073515 single base substitution C A intron_variant PACA-CA 14 31075827 31075827 single base substitution C A downstream_gene_variant PACA-CA 14 31075827 31075827 single base substitution C A intron_variant PACA-CA 14 31075827 31075827 single base substitution C A upstream_gene_variant PACA-CA 14 31079534 31079534 single base substitution G T downstream_gene_variant PACA-CA 14 31079534 31079534 single base substitution G T intron_variant PACA-CA 14 31079534 31079534 single base substitution G T upstream_gene_variant PACA-CA 14 31079548 31079548 single base substitution G A downstream_gene_variant PACA-CA 14 31079548 31079548 single base substitution G A intron_variant PACA-CA 14 31079548 31079548 single base substitution G A upstream_gene_variant PACA-CA 14 31079760 31079760 single base substitution G A downstream_gene_variant PACA-CA 14 31079760 31079760 single base substitution G A intron_variant PACA-CA 14 31079760 31079760 single base substitution G A upstream_gene_variant PACA-CA 14 31079850 31079850 single base substitution C T downstream_gene_variant PACA-CA 14 31079850 31079850 single base substitution C T intron_variant PACA-CA 14 31079850 31079850 single base substitution C T upstream_gene_variant PACA-CA 14 31080095 31080095 single base substitution G A downstream_gene_variant PACA-CA 14 31080095 31080095 single base substitution G A intron_variant PACA-CA 14 31080095 31080095 single base substitution G A upstream_gene_variant PACA-CA 14 31080383 31080383 single base substitution G A downstream_gene_variant PACA-CA 14 31080383 31080383 single base substitution G A intron_variant PACA-CA 14 31080383 31080383 single base substitution G A upstream_gene_variant PACA-CA 14 31080490 31080497 deletion of <=200bp ACTCCGAC - downstream_gene_variant PACA-CA 14 31080490 31080497 deletion of <=200bp ACTCCGAC - intron_variant PACA-CA 14 31080490 31080497 deletion of <=200bp ACTCCGAC - upstream_gene_variant PACA-CA 14 31081674 31081674 single base substitution A C downstream_gene_variant PACA-CA 14 31081674 31081674 single base substitution A C intron_variant PACA-CA 14 31081700 31081700 single base substitution T A downstream_gene_variant PACA-CA 14 31081700 31081700 single base substitution T A intron_variant PACA-CA 14 31082872 31082872 single base substitution C G intron_variant PACA-CA 14 31082915 31082915 single base substitution T A intron_variant PACA-CA 14 31082926 31082926 deletion of <=200bp T - intron_variant PACA-CA 14 31083360 31083360 single base substitution C A intron_variant PACA-CA 14 31083685 31083685 single base substitution C G intron_variant PACA-CA 14 31083771 31083771 single base substitution C G intron_variant PACA-CA 14 31084026 31084026 single base substitution C T intron_variant PACA-CA 14 31085012 31085012 single base substitution C G downstream_gene_variant PACA-CA 14 31085012 31085012 single base substitution C G intron_variant PACA-CA 14 31085043 31085043 single base substitution C T downstream_gene_variant PACA-CA 14 31085043 31085043 single base substitution C T intron_variant PACA-CA 14 31085547 31085547 single base substitution C T downstream_gene_variant PACA-CA 14 31085547 31085547 single base substitution C T exon_variant PACA-CA 14 31085547 31085547 single base substitution C T missense_variant P597L 1790C>T PACA-CA 14 31085547 31085547 single base substitution C T missense_variant P643L 1928C>T PACA-CA 14 31085547 31085547 single base substitution C T missense_variant P673L 2018C>T PACA-CA 14 31088810 31088810 single base substitution T C 3_prime_UTR_variant PACA-CA 14 31088810 31088810 single base substitution T C downstream_gene_variant PACA-CA 14 31089899 31089899 single base substitution G A downstream_gene_variant PACA-CA 14 31091435 31091435 single base substitution G A downstream_gene_variant PACA-CA 14 31091533 31091533 single base substitution G T downstream_gene_variant PAEN-AU 14 31035076 31035076 single base substitution T C intron_variant PAEN-AU 14 31065989 31065989 single base substitution T C downstream_gene_variant PAEN-AU 14 31065989 31065989 single base substitution T C intron_variant PAEN-AU 14 31065989 31065989 single base substitution T C upstream_gene_variant PAEN-IT 14 31030278 31030278 single base substitution G A intron_variant PAEN-IT 14 31035745 31035745 single base substitution C A intron_variant PAEN-IT 14 31047560 31047560 single base substitution A G intron_variant PBCA-DE 14 31025921 31025921 insertion of <=200bp - A upstream_gene_variant PBCA-DE 14 31042616 31042617 deletion of <=200bp TG - intron_variant PBCA-DE 14 31042616 31042617 deletion of <=200bp TG - upstream_gene_variant PBCA-DE 14 31056681 31056681 insertion of <=200bp - A intron_variant PBCA-DE 14 31056681 31056681 insertion of <=200bp - A upstream_gene_variant PBCA-DE 14 31060495 31060495 deletion of <=200bp A - 3_prime_UTR_variant PBCA-DE 14 31060495 31060495 deletion of <=200bp A - downstream_gene_variant PBCA-DE 14 31060495 31060495 deletion of <=200bp A - intron_variant PBCA-DE 14 31060495 31060495 deletion of <=200bp A - upstream_gene_variant PBCA-DE 14 31062897 31062897 single base substitution G T downstream_gene_variant PBCA-DE 14 31062897 31062897 single base substitution G T intron_variant PBCA-DE 14 31062897 31062897 single base substitution G T upstream_gene_variant PBCA-DE 14 31071789 31071789 single base substitution G A downstream_gene_variant PBCA-DE 14 31071789 31071789 single base substitution G A intron_variant PBCA-DE 14 31071789 31071789 single base substitution G A upstream_gene_variant PBCA-DE 14 31072680 31072680 single base substitution T C intron_variant PBCA-DE 14 31074772 31074772 insertion of <=200bp - A downstream_gene_variant PBCA-DE 14 31074772 31074772 insertion of <=200bp - A exon_variant PBCA-DE 14 31074772 31074772 insertion of <=200bp - A frameshift_variant K312K? PBCA-DE 14 31074772 31074772 insertion of <=200bp - A frameshift_variant K358K? PBCA-DE 14 31074772 31074772 insertion of <=200bp - A frameshift_variant K388K? PBCA-DE 14 31074772 31074772 insertion of <=200bp - A intron_variant PBCA-DE 14 31077984 31077984 single base substitution C T downstream_gene_variant PBCA-DE 14 31077984 31077984 single base substitution C T intron_variant PBCA-DE 14 31077984 31077984 single base substitution C T upstream_gene_variant PBCA-DE 14 31082524 31082524 insertion of <=200bp - A intron_variant PBCA-DE 14 31089838 31089838 insertion of <=200bp - T downstream_gene_variant PRAD-CA 14 31028221 31028221 single base substitution G A upstream_gene_variant PRAD-CA 14 31037985 31037985 single base substitution A G intron_variant PRAD-CA 14 31053934 31053934 single base substitution G C intron_variant PRAD-CA 14 31077896 31077896 single base substitution C T downstream_gene_variant PRAD-CA 14 31077896 31077896 single base substitution C T intron_variant PRAD-CA 14 31077896 31077896 single base substitution C T upstream_gene_variant PRAD-UK 14 31040496 31040496 single base substitution T C intron_variant PRAD-UK 14 31040496 31040496 single base substitution T C upstream_gene_variant PRAD-UK 14 31053748 31053748 single base substitution A T intron_variant PRAD-UK 14 31058470 31058470 single base substitution C T intron_variant PRAD-UK 14 31058470 31058470 single base substitution C T upstream_gene_variant PRAD-UK 14 31074881 31074881 single base substitution A T downstream_gene_variant PRAD-UK 14 31074881 31074881 single base substitution A T exon_variant PRAD-UK 14 31074881 31074881 single base substitution A T intron_variant PRAD-UK 14 31074881 31074881 single base substitution A T missense_variant Y348F 1043A>T PRAD-UK 14 31074881 31074881 single base substitution A T missense_variant Y394F 1181A>T PRAD-UK 14 31074881 31074881 single base substitution A T missense_variant Y424F 1271A>T PRAD-UK 14 31080049 31080049 single base substitution T A downstream_gene_variant PRAD-UK 14 31080049 31080049 single base substitution T A intron_variant PRAD-UK 14 31080049 31080049 single base substitution T A upstream_gene_variant PRAD-UK 14 31080051 31080051 single base substitution T A downstream_gene_variant PRAD-UK 14 31080051 31080051 single base substitution T A intron_variant PRAD-UK 14 31080051 31080051 single base substitution T A upstream_gene_variant PRAD-UK 14 31081393 31081415 deletion of <=200bp TATTTTCTCCTTCATTACAGATA - downstream_gene_variant PRAD-UK 14 31081393 31081415 deletion of <=200bp TATTTTCTCCTTCATTACAGATA - exon_variant PRAD-UK 14 31081393 31081415 deletion of <=200bp TATTTTCTCCTTCATTACAGATA - splice_acceptor_variant PRAD-UK 14 31082933 31082933 single base substitution T A intron_variant PRAD-US 14 31066642 31066642 single base substitution C T 3_prime_UTR_variant PRAD-US 14 31066642 31066642 single base substitution C T downstream_gene_variant PRAD-US 14 31066642 31066642 single base substitution C T exon_variant PRAD-US 14 31066642 31066642 single base substitution C T intron_variant PRAD-US 14 31066642 31066642 single base substitution C T missense_variant A136V 407C>T PRAD-US 14 31066642 31066642 single base substitution C T missense_variant A182V 545C>T PRAD-US 14 31066642 31066642 single base substitution C T missense_variant A212V 635C>T PRAD-US 14 31066642 31066642 single base substitution C T upstream_gene_variant RECA-EU 14 31030886 31030886 single base substitution A T intron_variant RECA-EU 14 31042591 31042591 single base substitution C A intron_variant RECA-EU 14 31042591 31042591 single base substitution C A upstream_gene_variant RECA-EU 14 31051316 31051316 single base substitution T C intron_variant RECA-EU 14 31056231 31056231 single base substitution G C intron_variant RECA-EU 14 31056973 31056973 single base substitution C T intron_variant RECA-EU 14 31056973 31056973 single base substitution C T upstream_gene_variant RECA-EU 14 31066134 31066134 single base substitution T A downstream_gene_variant RECA-EU 14 31066134 31066134 single base substitution T A intron_variant RECA-EU 14 31066134 31066134 single base substitution T A upstream_gene_variant RECA-EU 14 31091920 31091920 single base substitution T A downstream_gene_variant RECA-EU 14 31093080 31093080 single base substitution A G downstream_gene_variant SKCA-BR 14 31023672 31023672 single base substitution C T upstream_gene_variant SKCA-BR 14 31025226 31025226 single base substitution C T upstream_gene_variant SKCA-BR 14 31026086 31026086 single base substitution C T upstream_gene_variant SKCA-BR 14 31026185 31026185 single base substitution G A upstream_gene_variant SKCA-BR 14 31026792 31026792 single base substitution C T upstream_gene_variant SKCA-BR 14 31027387 31027387 single base substitution G A upstream_gene_variant SKCA-BR 14 31028336 31028336 single base substitution C T 5_prime_UTR_variant SKCA-BR 14 31028336 31028336 single base substitution C T upstream_gene_variant SKCA-BR 14 31028337 31028337 single base substitution T A 5_prime_UTR_variant SKCA-BR 14 31028337 31028337 single base substitution T A upstream_gene_variant SKCA-BR 14 31028341 31028341 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 14 31028341 31028341 single base substitution C T upstream_gene_variant SKCA-BR 14 31029314 31029314 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 14 31029314 31029314 single base substitution G T intron_variant SKCA-BR 14 31029883 31029883 single base substitution C T 5_prime_UTR_variant SKCA-BR 14 31029883 31029883 single base substitution C T intron_variant SKCA-BR 14 31032901 31032905 deletion of <=200bp TTGTG - intron_variant SKCA-BR 14 31034545 31034545 single base substitution G T intron_variant SKCA-BR 14 31040382 31040382 insertion of <=200bp - CT intron_variant SKCA-BR 14 31040382 31040382 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 14 31041150 31041150 insertion of <=200bp - TA intron_variant SKCA-BR 14 31041150 31041150 insertion of <=200bp - TA upstream_gene_variant SKCA-BR 14 31043630 31043630 insertion of <=200bp - CT intron_variant SKCA-BR 14 31043630 31043630 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 14 31048051 31048051 single base substitution C T intron_variant SKCA-BR 14 31048353 31048353 single base substitution C T intron_variant SKCA-BR 14 31049367 31049367 single base substitution A C intron_variant SKCA-BR 14 31049422 31049422 single base substitution T G intron_variant SKCA-BR 14 31049511 31049511 single base substitution C T intron_variant SKCA-BR 14 31051263 31051263 single base substitution C T intron_variant SKCA-BR 14 31060798 31060798 single base substitution G A downstream_gene_variant SKCA-BR 14 31060798 31060798 single base substitution G A intron_variant SKCA-BR 14 31060798 31060798 single base substitution G A upstream_gene_variant SKCA-BR 14 31061810 31061810 single base substitution T G downstream_gene_variant SKCA-BR 14 31061810 31061810 single base substitution T G intron_variant SKCA-BR 14 31061810 31061810 single base substitution T G upstream_gene_variant SKCA-BR 14 31064132 31064132 single base substitution C T downstream_gene_variant SKCA-BR 14 31064132 31064132 single base substitution C T intron_variant SKCA-BR 14 31064132 31064132 single base substitution C T upstream_gene_variant SKCA-BR 14 31067530 31067530 single base substitution T G downstream_gene_variant SKCA-BR 14 31067530 31067530 single base substitution T G intron_variant SKCA-BR 14 31067530 31067530 single base substitution T G upstream_gene_variant SKCA-BR 14 31068345 31068345 single base substitution C T downstream_gene_variant SKCA-BR 14 31068345 31068345 single base substitution C T intron_variant SKCA-BR 14 31068345 31068345 single base substitution C T upstream_gene_variant SKCA-BR 14 31070964 31070964 single base substitution T C downstream_gene_variant SKCA-BR 14 31070964 31070964 single base substitution T C intron_variant SKCA-BR 14 31070964 31070964 single base substitution T C upstream_gene_variant SKCA-BR 14 31077395 31077395 single base substitution A G downstream_gene_variant SKCA-BR 14 31077395 31077395 single base substitution A G intron_variant SKCA-BR 14 31077395 31077395 single base substitution A G upstream_gene_variant SKCA-BR 14 31077955 31077955 single base substitution C G downstream_gene_variant SKCA-BR 14 31077955 31077955 single base substitution C G intron_variant SKCA-BR 14 31077955 31077955 single base substitution C G upstream_gene_variant SKCA-BR 14 31078559 31078559 single base substitution C A downstream_gene_variant SKCA-BR 14 31078559 31078559 single base substitution C A intron_variant SKCA-BR 14 31078559 31078559 single base substitution C A upstream_gene_variant SKCA-BR 14 31078560 31078560 single base substitution C T downstream_gene_variant SKCA-BR 14 31078560 31078560 single base substitution C T intron_variant SKCA-BR 14 31078560 31078560 single base substitution C T upstream_gene_variant SKCA-BR 14 31081758 31081758 single base substitution C T downstream_gene_variant SKCA-BR 14 31081758 31081758 single base substitution C T intron_variant SKCA-BR 14 31091459 31091459 single base substitution C T downstream_gene_variant SKCM-US 14 31058628 31058628 single base substitution G A exon_variant SKCM-US 14 31058628 31058628 single base substitution G A missense_variant E13K 37G>A SKCM-US 14 31058628 31058628 single base substitution G A missense_variant E59K 175G>A SKCM-US 14 31058628 31058628 single base substitution G A missense_variant E89K 265G>A SKCM-US 14 31058628 31058628 single base substitution G A upstream_gene_variant SKCM-US 14 31066625 31066625 single base substitution G T downstream_gene_variant SKCM-US 14 31066625 31066625 single base substitution G T intron_variant SKCM-US 14 31066625 31066625 single base substitution G T splice_acceptor_variant SKCM-US 14 31066625 31066625 single base substitution G T upstream_gene_variant SKCM-US 14 31074856 31074856 single base substitution C T downstream_gene_variant SKCM-US 14 31074856 31074856 single base substitution C T exon_variant SKCM-US 14 31074856 31074856 single base substitution C T intron_variant SKCM-US 14 31074856 31074856 single base substitution C T missense_variant P340S 1018C>T SKCM-US 14 31074856 31074856 single base substitution C T missense_variant P386S 1156C>T SKCM-US 14 31074856 31074856 single base substitution C T missense_variant P416S 1246C>T SKCM-US 14 31084663 31084663 single base substitution C T 3_prime_UTR_variant SKCM-US 14 31084663 31084663 single base substitution C T exon_variant SKCM-US 14 31084663 31084663 single base substitution C T synonymous_variant I548I 1644C>T SKCM-US 14 31084663 31084663 single base substitution C T synonymous_variant I594I 1782C>T SKCM-US 14 31084663 31084663 single base substitution C T synonymous_variant I624I 1872C>T SKCM-US 14 31084664 31084664 single base substitution C T 3_prime_UTR_variant SKCM-US 14 31084664 31084664 single base substitution C T exon_variant SKCM-US 14 31084664 31084664 single base substitution C T missense_variant L549F 1645C>T SKCM-US 14 31084664 31084664 single base substitution C T missense_variant L595F 1783C>T SKCM-US 14 31084664 31084664 single base substitution C T missense_variant L625F 1873C>T SKCM-US 14 31085542 31085542 single base substitution C T downstream_gene_variant SKCM-US 14 31085542 31085542 single base substitution C T exon_variant SKCM-US 14 31085542 31085542 single base substitution C T synonymous_variant S595S 1785C>T SKCM-US 14 31085542 31085542 single base substitution C T synonymous_variant S641S 1923C>T SKCM-US 14 31085542 31085542 single base substitution C T synonymous_variant S671S 2013C>T STAD-US 14 31050312 31050312 single base substitution A G exon_variant STAD-US 14 31050312 31050312 single base substitution A G intron_variant STAD-US 14 31050312 31050312 single base substitution A G synonymous_variant S39S 117A>G STAD-US 14 31050312 31050312 single base substitution A G synonymous_variant S9S 27A>G STAD-US 14 31067763 31067763 single base substitution G T 3_prime_UTR_variant STAD-US 14 31067763 31067763 single base substitution G T downstream_gene_variant STAD-US 14 31067763 31067763 single base substitution G T intron_variant STAD-US 14 31067763 31067763 single base substitution G T missense_variant R191I 572G>T STAD-US 14 31067763 31067763 single base substitution G T missense_variant R237I 710G>T STAD-US 14 31067763 31067763 single base substitution G T missense_variant R267I 800G>T STAD-US 14 31067763 31067763 single base substitution G T upstream_gene_variant STAD-US 14 31071214 31071214 deletion of <=200bp A - 3_prime_UTR_variant STAD-US 14 31071214 31071214 deletion of <=200bp A - downstream_gene_variant STAD-US 14 31071214 31071214 deletion of <=200bp A - exon_variant STAD-US 14 31071214 31071214 deletion of <=200bp A - frameshift_variant Q250 STAD-US 14 31071214 31071214 deletion of <=200bp A - frameshift_variant Q296 STAD-US 14 31071214 31071214 deletion of <=200bp A - frameshift_variant Q326 STAD-US 14 31071214 31071214 deletion of <=200bp A - frameshift_variant Q61 STAD-US 14 31071214 31071214 deletion of <=200bp A - upstream_gene_variant STAD-US 14 31071242 31071242 single base substitution T A 3_prime_UTR_variant STAD-US 14 31071242 31071242 single base substitution T A downstream_gene_variant STAD-US 14 31071242 31071242 single base substitution T A exon_variant STAD-US 14 31071242 31071242 single base substitution T A missense_variant N259K 777T>A STAD-US 14 31071242 31071242 single base substitution T A missense_variant N305K 915T>A STAD-US 14 31071242 31071242 single base substitution T A missense_variant N335K 1005T>A STAD-US 14 31071242 31071242 single base substitution T A missense_variant N70K 210T>A STAD-US 14 31071242 31071242 single base substitution T A upstream_gene_variant STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - 3_prime_UTR_variant STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - downstream_gene_variant STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - exon_variant STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - frameshift_variant PR278 STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - frameshift_variant PR324 STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - frameshift_variant PR354 STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - frameshift_variant PR89 STAD-US 14 31071299 31071302 deletion of <=200bp CAGA - upstream_gene_variant STAD-US 14 31071327 31071327 single base substitution G C 3_prime_UTR_variant STAD-US 14 31071327 31071327 single base substitution G C downstream_gene_variant STAD-US 14 31071327 31071327 single base substitution G C exon_variant STAD-US 14 31071327 31071327 single base substitution G C missense_variant D288H 862G>C STAD-US 14 31071327 31071327 single base substitution G C missense_variant D334H 1000G>C STAD-US 14 31071327 31071327 single base substitution G C missense_variant D364H 1090G>C STAD-US 14 31071327 31071327 single base substitution G C missense_variant D99H 295G>C STAD-US 14 31071327 31071327 single base substitution G C upstream_gene_variant STAD-US 14 31084704 31084704 single base substitution A G 3_prime_UTR_variant STAD-US 14 31084704 31084704 single base substitution A G exon_variant STAD-US 14 31084704 31084704 single base substitution A G missense_variant K562R 1685A>G STAD-US 14 31084704 31084704 single base substitution A G missense_variant K608R 1823A>G STAD-US 14 31084704 31084704 single base substitution A G missense_variant K638R 1913A>G STAD-US 14 31085623 31085623 single base substitution C G downstream_gene_variant STAD-US 14 31085623 31085623 single base substitution C G exon_variant STAD-US 14 31085623 31085623 single base substitution C G missense_variant N622K 1866C>G STAD-US 14 31085623 31085623 single base substitution C G missense_variant N668K 2004C>G STAD-US 14 31085623 31085623 single base substitution C G missense_variant N698K 2094C>G STAD-US 14 31085717 31085717 single base substitution A C downstream_gene_variant STAD-US 14 31085717 31085717 single base substitution A C exon_variant STAD-US 14 31085717 31085717 single base substitution A C missense_variant S654R 1960A>C STAD-US 14 31085717 31085717 single base substitution A C missense_variant S700R 2098A>C STAD-US 14 31085717 31085717 single base substitution A C missense_variant S730R 2188A>C THCA-US 14 31061616 31061616 single base substitution C G 3_prime_UTR_variant THCA-US 14 31061616 31061616 single base substitution C G downstream_gene_variant THCA-US 14 31061616 31061616 single base substitution C G exon_variant THCA-US 14 31061616 31061616 single base substitution C G missense_variant Q109E 325C>G THCA-US 14 31061616 31061616 single base substitution C G missense_variant Q139E 415C>G THCA-US 14 31061616 31061616 single base substitution C G missense_variant Q63E 187C>G THCA-US 14 31061616 31061616 single base substitution C G upstream_gene_variant UCEC-US 14 31050315 31050315 single base substitution G T exon_variant UCEC-US 14 31050315 31050315 single base substitution G T intron_variant UCEC-US 14 31050315 31050315 single base substitution G T missense_variant Q10H 30G>T UCEC-US 14 31050315 31050315 single base substitution G T missense_variant Q40H 120G>T UCEC-US 14 31055950 31055950 single base substitution G A 5_prime_UTR_variant UCEC-US 14 31055950 31055950 single base substitution G A exon_variant UCEC-US 14 31055950 31055950 single base substitution G A missense_variant D22N 64G>A UCEC-US 14 31055950 31055950 single base substitution G A missense_variant D52N 154G>A UCEC-US 14 31055967 31055967 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 14 31055967 31055967 single base substitution C T exon_variant UCEC-US 14 31055967 31055967 single base substitution C T synonymous_variant Y27Y 81C>T UCEC-US 14 31055967 31055967 single base substitution C T synonymous_variant Y57Y 171C>T UCEC-US 14 31058655 31058655 single base substitution G A exon_variant UCEC-US 14 31058655 31058655 single base substitution G A missense_variant D22N 64G>A UCEC-US 14 31058655 31058655 single base substitution G A missense_variant D68N 202G>A UCEC-US 14 31058655 31058655 single base substitution G A missense_variant D98N 292G>A UCEC-US 14 31058655 31058655 single base substitution G A splice_region_variant UCEC-US 14 31058655 31058655 single base substitution G A upstream_gene_variant UCEC-US 14 31061585 31061585 single base substitution T C 3_prime_UTR_variant UCEC-US 14 31061585 31061585 single base substitution T C downstream_gene_variant UCEC-US 14 31061585 31061585 single base substitution T C exon_variant UCEC-US 14 31061585 31061585 single base substitution T C synonymous_variant C128C 384T>C UCEC-US 14 31061585 31061585 single base substitution T C synonymous_variant C52C 156T>C UCEC-US 14 31061585 31061585 single base substitution T C synonymous_variant C98C 294T>C UCEC-US 14 31061585 31061585 single base substitution T C upstream_gene_variant UCEC-US 14 31061590 31061590 single base substitution G A 3_prime_UTR_variant UCEC-US 14 31061590 31061590 single base substitution G A downstream_gene_variant UCEC-US 14 31061590 31061590 single base substitution G A exon_variant UCEC-US 14 31061590 31061590 single base substitution G A missense_variant R100Q 299G>A UCEC-US 14 31061590 31061590 single base substitution G A missense_variant R130Q 389G>A UCEC-US 14 31061590 31061590 single base substitution G A missense_variant R54Q 161G>A UCEC-US 14 31061590 31061590 single base substitution G A upstream_gene_variant UCEC-US 14 31061644 31061644 single base substitution G A 3_prime_UTR_variant UCEC-US 14 31061644 31061644 single base substitution G A downstream_gene_variant UCEC-US 14 31061644 31061644 single base substitution G A exon_variant UCEC-US 14 31061644 31061644 single base substitution G A missense_variant G118D 353G>A UCEC-US 14 31061644 31061644 single base substitution G A missense_variant G148D 443G>A UCEC-US 14 31061644 31061644 single base substitution G A missense_variant G72D 215G>A UCEC-US 14 31061644 31061644 single base substitution G A upstream_gene_variant UCEC-US 14 31074733 31074733 single base substitution A C 3_prime_UTR_variant UCEC-US 14 31074733 31074733 single base substitution A C exon_variant UCEC-US 14 31074733 31074733 single base substitution A C intron_variant UCEC-US 14 31074733 31074733 single base substitution A C missense_variant N110H 328A>C UCEC-US 14 31074733 31074733 single base substitution A C missense_variant N299H 895A>C UCEC-US 14 31074733 31074733 single base substitution A C missense_variant N345H 1033A>C UCEC-US 14 31074733 31074733 single base substitution A C missense_variant N375H 1123A>C UCEC-US 14 31074788 31074788 single base substitution G T downstream_gene_variant UCEC-US 14 31074788 31074788 single base substitution G T exon_variant UCEC-US 14 31074788 31074788 single base substitution G T intron_variant UCEC-US 14 31074788 31074788 single base substitution G T missense_variant R317I 950G>T UCEC-US 14 31074788 31074788 single base substitution G T missense_variant R363I 1088G>T UCEC-US 14 31074788 31074788 single base substitution G T missense_variant R393I 1178G>T UCEC-US 14 31074877 31074877 single base substitution G C downstream_gene_variant UCEC-US 14 31074877 31074877 single base substitution G C exon_variant UCEC-US 14 31074877 31074877 single base substitution G C intron_variant UCEC-US 14 31074877 31074877 single base substitution G C missense_variant A347P 1039G>C UCEC-US 14 31074877 31074877 single base substitution G C missense_variant A393P 1177G>C UCEC-US 14 31074877 31074877 single base substitution G C missense_variant A423P 1267G>C UCEC-US 14 31074967 31074969 deletion of <=200bp TCA - downstream_gene_variant UCEC-US 14 31074967 31074969 deletion of <=200bp TCA - exon_variant UCEC-US 14 31074967 31074969 deletion of <=200bp TCA - inframe_deletion S377 UCEC-US 14 31074967 31074969 deletion of <=200bp TCA - inframe_deletion S423 UCEC-US 14 31074967 31074969 deletion of <=200bp TCA - inframe_deletion S453 UCEC-US 14 31074967 31074969 deletion of <=200bp TCA - intron_variant UCEC-US 14 31074996 31074996 single base substitution G T downstream_gene_variant UCEC-US 14 31074996 31074996 single base substitution G T exon_variant UCEC-US 14 31074996 31074996 single base substitution G T intron_variant UCEC-US 14 31074996 31074996 single base substitution G T missense_variant K386N 1158G>T UCEC-US 14 31074996 31074996 single base substitution G T missense_variant K432N 1296G>T UCEC-US 14 31074996 31074996 single base substitution G T missense_variant K462N 1386G>T UCEC-US 14 31081550 31081550 single base substitution C T 3_prime_UTR_variant UCEC-US 14 31081550 31081550 single base substitution C T downstream_gene_variant UCEC-US 14 31081550 31081550 single base substitution C T exon_variant UCEC-US 14 31081550 31081550 single base substitution C T synonymous_variant Y500Y 1500C>T UCEC-US 14 31081550 31081550 single base substitution C T synonymous_variant Y546Y 1638C>T UCEC-US 14 31081550 31081550 single base substitution C T synonymous_variant Y576Y 1728C>T UCEC-US 14 31085723 31085723 single base substitution C A downstream_gene_variant UCEC-US 14 31085723 31085723 single base substitution C A exon_variant UCEC-US 14 31085723 31085723 single base substitution C A missense_variant H656N 1966C>A UCEC-US 14 31085723 31085723 single base substitution C A missense_variant H702N 2104C>A UCEC-US 14 31085723 31085723 single base substitution C A missense_variant H732N 2194C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand HCT15 COSM2034137 c.810C>T p.C270C Substitution - coding silent 14:30601827-30601827 + 8047896 COSM2034117 c.52C>T p.R18* Substitution - Nonsense 14:30586732-30586732 + TCGA-B5-A0JY-01 COSM955200 c.2104C>A p.H702N Substitution - Missense 14:30616517-30616517 + Pat_59_B COSM5848001 c.293G>A p.C98Y Substitution - Missense 14:30592378-30592378 + TCGA-ER-A19P-06 COSM3495622 c.529-1G>T p.? Unknown 14:30597419-30597419 + YUWAND COSM1707241 c.310T>A p.F104I Substitution - Missense 14:30592395-30592395 + LUAD-S01381 COSM398457 c.290G>T p.R97L Substitution - Missense 14:30592375-30592375 + HCC2998 COSM2034149 c.1367C>A p.S456Y Substitution - Missense 14:30607936-30607936 + CCK81 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-B5-A11E-01 COSM955191 c.299G>A p.R100Q Substitution - Missense 14:30592384-30592384 + ESO-859 COSM1238950 c.237+1G>A p.? Unknown 14:30589485-30589485 + ME030T COSM227106 c.1385C>T p.P462L Substitution - Missense 14:30607954-30607954 + TCGA-UB-A7ME-01 COSM4910167 c.1384C>T p.P462S Substitution - Missense 14:30607953-30607953 + CAL33 COSM2034155 c.1685G>T p.G562V Substitution - Missense 14:30615360-30615360 + T3225 COSM4686016 c.456G>A p.E152E Substitution - coding silent 14:30593567-30593567 + WSU-HN6 COSM4602160 c.325C>T p.Q109* Substitution - Nonsense 14:30592410-30592410 + TCGA-06-0128-01 COSM3401282 c.1560C>G p.Y520* Substitution - Nonsense 14:30612266-30612266 + 587222 COSM1207724 c.2102C>T p.S701F Substitution - Missense 14:30616515-30616515 + BCM769T COSM4799380 c.1196A>G p.D399G Substitution - Missense 14:30605690-30605690 + TCGA-E3-A3DY-01 COSM3369961 c.325C>G p.Q109E Substitution - Missense 14:30592410-30592410 + BN05 COSM3706232 c.180A>G p.G60G Substitution - coding silent 14:30589427-30589427 + T2269 COSM4686017 c.1398C>A p.F466L Substitution - Missense 14:30607967-30607967 + pfg068T COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-AP-A056-01 COSM955196 c.1177G>C p.A393P Substitution - Missense 14:30605671-30605671 + TCGA-EE-A2GJ-06 COSM3495626 c.1923C>T p.S641S Substitution - coding silent 14:30616336-30616336 + TCGA-D1-A17Q-01 COSM955187 c.30G>T p.Q10H Substitution - Missense 14:30581109-30581109 + CSCC-46-T COSM4550690 c.506G>A p.W169* Substitution - Nonsense 14:30593617-30593617 + T3479 COSM4686015 c.382C>T p.R128* Substitution - Nonsense 14:30593493-30593493 + TCGA-BP-5182-01 COSM469887 c.977A>T p.Q326L Substitution - Missense 14:30602098-30602098 + TCGA-BR-4366-01 COSM4050434 c.2004C>G p.N668K Substitution - Missense 14:30616417-30616417 + TCGA-BK-A0C9-01 COSM955193 c.974G>A p.R325K Substitution - Missense 14:30602095-30602095 + 2521244 COSM5887420 c.135-4C>T p.? Unknown 14:30589378-30589378 + 587376 COSM1207728 c.1795T>G p.F599V Substitution - Missense 14:30615470-30615470 + TCGA-18-3417-01 COSM698000 c.221A>G p.N74S Substitution - Missense 14:30589468-30589468 + TCGA-BS-A0TC-01 COSM955194 c.1033A>C p.N345H Substitution - Missense 14:30605527-30605527 + 587352 COSM1207725 c.482G>A p.R161Q Substitution - Missense 14:30593593-30593593 + TCGA-D5-6928-01 COSM1369491 c.900A>C p.K300N Substitution - Missense 14:30602021-30602021 + CSCC-32-T COSM4517794 c.422_423CC>GT p.S141C Substitution - Missense 14:30593533-30593534 + TCGA-DK-A2I2-01 COSM1300557 c.1403C>G p.S468C Substitution - Missense 14:30607972-30607972 + AOCS-134-3-9 COSM3983230 c.2086G>C p.E696Q Substitution - Missense 14:30616499-30616499 + TCGA-FD-A3SS-01 COSM3793641 c.1028G>C p.R343T Substitution - Missense 14:30605522-30605522 + TCGA-EB-A41A-01 COSM3495625 c.1783C>T p.L595F Substitution - Missense 14:30615458-30615458 + TCGA-LG-A6GG-01 COSM4939625 c.1709A>G p.E570G Substitution - Missense 14:30615384-30615384 + TCGA-B5-A11E-01 COSM698001 c.64G>A p.D22N Substitution - Missense 14:30586744-30586744 + RK042_C01 COSM1629267 c.935C>G p.T312R Substitution - Missense 14:30602056-30602056 + TCGA-25-1313-01 COSM70844 c.1603G>A p.D535N Substitution - Missense 14:30612309-30612309 + PCSI_0528_Pa_P_526 COSM5031769 c.1928C>T p.P643L Substitution - Missense 14:30616341-30616341 + 41T COSM3711446 c.2036A>G p.K679R Substitution - Missense 14:30616449-30616449 + 587376 COSM1207726 c.1144C>T p.R382* Substitution - Nonsense 14:30605638-30605638 + 0070_CRUK_PC_0070_T1_DNA COSM4417864 c.1181A>T p.Y394F Substitution - Missense 14:30605675-30605675 + LP6005409-DNA_A02 COSM4409559 c.1287C>T p.S429S Substitution - coding silent 14:30605781-30605781 + CP66-MEL COSM25418 c.1579C>T p.L527F Substitution - Missense 14:30612285-30612285 + BN05T COSM3706232 c.180A>G p.G60G Substitution - coding silent 14:30589427-30589427 + sysucc-1370T COSM5470231 c.730C>T p.R244* Substitution - Nonsense 14:30598577-30598577 + TCGA-AA-A00N-01 COSM275239 c.290G>A p.R97Q Substitution - Missense 14:30592375-30592375 + YUSPO COSM2034143 c.1072A>T p.K358* Substitution - Nonsense 14:30605566-30605566 + ESCC_143 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-85-6561-01 COSM697998 c.2117A>G p.H706R Substitution - Missense 14:30616530-30616530 + SW48 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-66-2787-01 COSM698001 c.64G>A p.D22N Substitution - Missense 14:30586744-30586744 + TCGA-BR-6452-01 COSM4050429 c.27A>G p.S9S Substitution - coding silent 14:30581106-30581106 + TCGA-HU-A4GX-01 COSM4050430 c.710G>T p.R237I Substitution - Missense 14:30598557-30598557 + TCGA-13-1509-01 COSM69058 c.166_170delAAAGA p.K56fs*18 Deletion - Frameshift 14:30589413-30589417 + 1N32-VS-1T32 COSM4974531 c.395T>C p.I132T Substitution - Missense 14:30593506-30593506 + 587376 COSM1207729 c.1897C>T p.L633F Substitution - Missense 14:30616310-30616310 + HOP-62 COSM1684379 c.517_518delGA p.D173fs*15 Deletion - Frameshift 14:30593628-30593629 + TCGA-AN-A046-01 COSM1207726 c.1144C>T p.R382* Substitution - Nonsense 14:30605638-30605638 + OSCC-GB_00410111 COSM3711446 c.2036A>G p.K679R Substitution - Missense 14:30616449-30616449 + RK212_C01 COSM3744298 c.1446C>T p.T482T Substitution - coding silent 14:30608015-30608015 + pfg103T COSM4752086 c.1592C>T p.T531M Substitution - Missense 14:30612298-30612298 + A6 COSM5350186 c.1847A>T p.Y616F Substitution - Missense 14:30615522-30615522 + TCGA-CH-5737-01 COSM1128270 c.545C>T p.A182V Substitution - Missense 14:30597436-30597436 + ESO-582 COSM1252913 c.370T>C p.C124R Substitution - Missense 14:30593481-30593481 + TCGA-BS-A0UV-01 COSM955192 c.353G>A p.G118D Substitution - Missense 14:30592438-30592438 + PT37 COSM1207725 c.482G>A p.R161Q Substitution - Missense 14:30593593-30593593 + YURUS COSM1707243 c.1898T>C p.L633P Substitution - Missense 14:30616311-30616311 + PT24_2 COSM5904623 c.1717C>T p.Q573* Substitution - Nonsense 14:30615392-30615392 + CSCC-49-T COSM4534484 c.2092G>A p.E698K Substitution - Missense 14:30616505-30616505 + sysucc-311T COSM5478673 c.663C>T p.N221N Substitution - coding silent 14:30598510-30598510 + TCGA-AX-A0J1-01 COSM955199 c.1638C>T p.Y546Y Substitution - coding silent 14:30612344-30612344 + HN_62854 COSM123294 c.637G>A p.D213N Substitution - Missense 14:30598484-30598484 + TCGA-CZ-5458-01 COSM469889 c.1254A>G p.Q418Q Substitution - coding silent 14:30605748-30605748 + C086 COSM5531544 c.313C>T p.P105S Substitution - Missense 14:30592398-30592398 + TCGA-AZ-4315-01 COSM955191 c.299G>A p.R100Q Substitution - Missense 14:30592384-30592384 + S00501 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-BR-8078-01 COSM4050433 c.1823A>G p.K608R Substitution - Missense 14:30615498-30615498 + TCGA-DG-A2KK-01 COSM955191 c.299G>A p.R100Q Substitution - Missense 14:30592384-30592384 + SNU-175 COSM2034144 c.1133C>T p.A378V Substitution - Missense 14:30605627-30605627 + LS411 COSM2034135 c.569C>T p.T190I Substitution - Missense 14:30597460-30597460 + 386 COSM4427111 c.287C>G p.P96R Substitution - Missense 14:30592372-30592372 + TCGA-D1-A16F-01 COSM955197 c.1267_1269delTCA p.S424delS Deletion - In frame 14:30605761-30605763 + I2L-P7-Tumor-Organoid COSM5159794 c.877+5delT p.? Unknown 14:30601899-30601899 + C008 COSM5522735 c.706C>T p.R236* Substitution - Nonsense 14:30598553-30598553 + PD11343a COSM5767082 c.1081A>T p.T361S Substitution - Missense 14:30605575-30605575 + YUKLAB COSM1707242 c.1897C>G p.L633V Substitution - Missense 14:30616310-30616310 + TCGA-EE-A29A-06 COSM3495621 c.175G>A p.E59K Substitution - Missense 14:30589422-30589422 + WSU-HN13 COSM4601536 c.1390C>A p.P464T Substitution - Missense 14:30607959-30607959 + LOVO COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + LOVO COSM2034120 c.116C>T p.T39I Substitution - Missense 14:30586796-30586796 + 587376 COSM1207727 c.1313C>A p.S438Y Substitution - Missense 14:30605807-30605807 + ESCC_142 COSM5643689 c.1488G>C p.Q496H Substitution - Missense 14:30608057-30608057 + J65_T COSM3955977 c.102G>T p.E34D Substitution - Missense 14:30586782-30586782 + A3 COSM5350185 c.96T>G p.T32T Substitution - coding silent 14:30586776-30586776 + TCGA-BR-6452-01 COSM4050431 c.915T>A p.N305K Substitution - Missense 14:30602036-30602036 + PCSI_0473_Pa_P_526 COSM4961553 c.3G>T p.M1I Substitution - Missense 14:30581082-30581082 + HCA7 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-AA-3510-01 COSM955198 c.1296G>T p.K432N Substitution - Missense 14:30605790-30605790 + BCM769T COSM4799380 c.1196A>G p.D399G Substitution - Missense 14:30605690-30605690 + TCGA-B9-A69E-01 COSM3987610 c.1593G>A p.T531T Substitution - coding silent 14:30612299-30612299 + TCGA-60-2698-01 COSM697999 c.890A>T p.K297I Substitution - Missense 14:30602011-30602011 + pfg008T COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-A5-A0GP-01 COSM955198 c.1296G>T p.K432N Substitution - Missense 14:30605790-30605790 + MEL-JWCI-WGS-6 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + ACINAR28 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + STC232 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + CSCC-40-T COSM4498069 c.511C>T p.H171Y Substitution - Missense 14:30593622-30593622 + ESO-D76 COSM1252914 c.1423C>T p.L475F Substitution - Missense 14:30607992-30607992 + 388 COSM4427395 c.1430A>G p.Y477C Substitution - Missense 14:30607999-30607999 + LUAD-B01811 COSM333942 c.821G>C p.R274P Substitution - Missense 14:30601838-30601838 + YUWAND COSM1707244 c.2069G>A p.R690K Substitution - Missense 14:30616482-30616482 + RKO COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-AN-A0FL-01 COSM3814663 c.1349G>T p.G450V Substitution - Missense 14:30607918-30607918 + TCGA-E2-A14X-01 COSM432986 c.870C>T p.Y290Y Substitution - coding silent 14:30601887-30601887 + Gp5D COSM4629112 c.672A>T p.Q224H Substitution - Missense 14:30598519-30598519 + TCGA-B5-A11E-01 COSM955190 c.294T>C p.C98C Substitution - coding silent 14:30592379-30592379 + ESCC_62 COSM5633037 c.1302G>T p.L434F Substitution - Missense 14:30605796-30605796 + AOCS-107-1-4 COSM3983229 c.1453A>G p.I485V Substitution - Missense 14:30608022-30608022 + Pat_70_B COSM5129990 c.1071_1072insA p.T361fs*2 Insertion - Frameshift 14:30605565-30605566 + TCGA-D7-8570-01 COSM4050432 c.1000G>C p.D334H Substitution - Missense 14:30602121-30602121 + 8030032 COSM1159451 c.1852C>G p.Q618E Substitution - Missense 14:30615527-30615527 + PT36 COSM5916355 c.1060G>A p.G354R Substitution - Missense 14:30605554-30605554 + ccRCC-94 COSM1661932 c.406A>C p.N136H Substitution - Missense 14:30593517-30593517 + ESCC_122 COSM5640645 c.1038A>G p.V346V Substitution - coding silent 14:30605532-30605532 + ESO-717 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-BR-8680-01 COSM4050435 c.2098A>C p.S700R Substitution - Missense 14:30616511-30616511 + sysucc-1370T COSM5470230 c.661A>G p.N221D Substitution - Missense 14:30598508-30598508 + 0061_CRUK_PC_0061_T1_DNA COSM5423940 c.1501-20_1503del23 p.? Unknown 14:30612187-30612209 + PT24_2 COSM5904622 c.622C>T p.H208Y Substitution - Missense 14:30597513-30597513 + TCGA-AZ-4315-01 COSM1369493 c.1145G>A p.R382Q Substitution - Missense 14:30605639-30605639 + SNU-C2B COSM2034138 c.862A>G p.I288V Substitution - Missense 14:30601879-30601879 + ICGC_0061 COSM1159451 c.1852C>G p.Q618E Substitution - Missense 14:30615527-30615527 + 3N02-VS-3T02 COSM4978435 c.748G>C p.D250H Substitution - Missense 14:30598595-30598595 + TCGA-EE-A2MS-06 COSM3495624 c.1782C>T p.I594I Substitution - coding silent 14:30615457-30615457 + TCGA-BS-A0UF-01 COSM955195 c.1088G>T p.R363I Substitution - Missense 14:30605582-30605582 + TCGA-AA-3510-01 COSM1207725 c.482G>A p.R161Q Substitution - Missense 14:30593593-30593593 + KM12 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + RK042_C COSM1629267 c.935C>G p.T312R Substitution - Missense 14:30602056-30602056 + TCGA-D3-A5GR-06 COSM3495623 c.1156C>T p.P386S Substitution - Missense 14:30605650-30605650 + TCGA-AA-3663-01 COSM1369489 c.127T>C p.Y43H Substitution - Missense 14:30586807-30586807 + TCGA-A3-3358-01 COSM469888 c.1026T>G p.F342L Substitution - Missense 14:30605520-30605520 + TCGA-DK-A3IK-01 COSM1300558 c.2038G>C p.E680Q Substitution - Missense 14:30616451-30616451 + TCGA-A8-A09Z-01 COSM3814664 c.1574G>A p.G525E Substitution - Missense 14:30612280-30612280 + LUAD-D01382 COSM337003 c.1011G>A p.R337R Substitution - coding silent 14:30605505-30605505 + LIM2405 COSM1167627 c.1072delA p.T361fs*16 Deletion - Frameshift 14:30605566-30605566 + TCGA-A5-A0GB-01 COSM955188 c.81C>T p.Y27Y Substitution - coding silent 14:30586761-30586761 + TCGA-AX-A0J0-01 COSM955189 c.202G>A p.D68N Substitution - Missense 14:30589449-30589449 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.509005;Hs.509008 14q12 611299

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAAGA - Frameshift p.K56Rfs*18 c.167_171delAAGAA 14 31058619 OV A C 3-UTRSNV . c.2118+319A>C 14 31086056 HC A C Missense p.I530L c.1588A>C 14 31081500 COREAD A C Missense p.N345H c.1033A>C 14 31074733 UCEC A - Frameshift p.A298Pfs*39 c.891delA 14 31071214 STAD A - Frameshift p.T361Lfs*16 c.1081delA 14 31074772 RCCC A - Frameshift p.T361Lfs*16 c.1081delA 14 31074772 STAD A G Missense p.H706R c.2117A>G 14 31085736 LUSC A G Missense p.N74S c.221A>G 14 31058674 LUSC C A Missense p.P105Q c.314C>A 14 31061605 STAD C A Missense p.P210T c.628C>A 14 31066725 CM C G Missense p.L544V c.1630C>G 14 31081542 HNSC C G Missense p.N668K c.2004C>G 14 31085623 STAD C G Missense p.Q109E c.325C>G 14 31061616 THCA C G Missense p.Q618E c.1852C>G 14 31084733 PAAD C G Missense p.S468C c.1403C>G 14 31077178 BLCA C G Missense p.T312R c.935C>G 14 31071262 HC C G Nonsense p.Y520* c.1560C>G 14 31081472 GBM C T Missense p.A182V c.545C>T 14 31066642 PRAD C T Missense p.L475F c.1423C>T 14 31077198 ESCA C T Missense p.P462L c.1385C>T 14 31077160 CM C T Missense p.R274W c.820C>T 14 31071043 MM C T Synonymous p.I594I c.1782C>T 14 31084663 CM C T Synonymous p.S641S c.1923C>T 14 31085542 CM C T Synonymous p.Y27Y c.81C>T 14 31055967 UCEC C T Synonymous p.Y290Y c.870C>T 14 31071093 BRCA G A Missense p.D213N c.637G>A 14 31067690 HNSC G A Missense p.D22N c.64G>A 14 31055950 LUSC G A Missense p.D535N c.1603G>A 14 31081515 OV G A Missense p.E59K c.175G>A 14 31058628 CM G A SpliceDonorSNV . c.237+1G>A 14 31058691 ESCA G A Synonymous p.E421E c.1263G>A 14 31074963 STAD G C Missense p.E680Q c.2038G>C 14 31085657 BLCA G T Missense p.G460C c.1378G>T 14 31077153 LUAD G T Missense p.K432N c.1296G>T 14 31074996 UCEC G T Nonsense p.G293* c.877G>T 14 31071100 HNSC G T SpliceAcceptorSNV . c.529-1G>T 14 31066625 CM TCA - InFrameDeletion p.S424delS c.1271_1273delCAT 14 31074967 UCEC T C Missense p.C124R c.370T>C 14 31062687 ESCA T G Missense p.F342L c.1026T>G 14 31074726 RCCC - T Nonsense p.K362*fs*1 c.1083dupT 14 31074782 LUAD