Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 16 24582830 24582830 + Missense_Mutation SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr16:24582830G>T c.4443G>T c.(4441-4443)gaG>gaT p.E1481D BLCA 16 24564833 24564833 + Splice_Site SNP G G C TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr16:24564833G>C c.e4-1 BLCA 16 24566966 24566966 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr16:24566966G>A c.379G>A c.(379-381)Gaa>Aaa p.E127K BLCA 16 24567000 24567000 + Missense_Mutation SNP C C G TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr16:24567000C>G c.413C>G c.(412-414)tCt>tGt p.S138C BLCA 16 24567013 24567013 + Nonsense_Mutation SNP C C G TCGA-ZF-A9R2-01A-11D-A391-08 TCGA-ZF-A9R2-10A-01D-A394-08 g.chr16:24567013C>G c.426C>G c.(424-426)taC>taG p.Y142* BLCA 16 24567226 24567226 + Silent SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr16:24567226C>T c.522C>T c.(520-522)tgC>tgT p.C174C BLCA 16 24570899 24570899 + Missense_Mutation SNP G G C TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr16:24570899G>C c.748G>C c.(748-750)Gat>Cat p.D250H BLCA 16 24573026 24573026 + Missense_Mutation SNP T T G TCGA-CF-A3MI-01A-11D-A20D-08 TCGA-CF-A3MI-10A-01D-A20D-08 g.chr16:24573026T>G c.941T>G c.(940-942)tTt>tGt p.F314C BLCA 16 24578570 24578570 + Missense_Mutation SNP C C T TCGA-G2-A2EC-01A-11D-A17V-08 TCGA-G2-A2EC-10A-01D-A17V-08 g.chr16:24578570C>T c.1696C>T c.(1696-1698)Ccg>Tcg p.P566S BLCA 16 24578652 24578652 + Missense_Mutation SNP C C T TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr16:24578652C>T c.1778C>T c.(1777-1779)cCa>cTa p.P593L BLCA 16 24580584 24580584 + Missense_Mutation SNP A A G TCGA-BT-A20V-01A-11D-A14W-08 TCGA-BT-A20V-11A-11D-A14W-08 g.chr16:24580584A>G c.2573A>G c.(2572-2574)gAg>gGg p.E858G BLCA 16 24581389 24581389 + Missense_Mutation SNP G G C TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr16:24581389G>C c.3378G>C c.(3376-3378)aaG>aaC p.K1126N BLCA 16 24582291 24582291 + Missense_Mutation SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr16:24582291G>C c.3904G>C c.(3904-3906)Gac>Cac p.D1302H BLCA 16 24582447 24582447 + Missense_Mutation SNP A A G TCGA-FD-A6TF-01A-52D-A32B-08 TCGA-FD-A6TF-10A-21D-A329-08 g.chr16:24582447A>G c.4060A>G c.(4060-4062)Aca>Gca p.T1354A BLCA 16 24582458 24582458 + Silent SNP A A C TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr16:24582458A>C c.4071A>C c.(4069-4071)tcA>tcC p.S1357S BLCA 16 24582507 24582507 + Missense_Mutation SNP C C G TCGA-E7-A97P-01A-11D-A38G-08 TCGA-E7-A97P-10A-01D-A38J-08 g.chr16:24582507C>G c.4120C>G c.(4120-4122)Cag>Gag p.Q1374E BLCA 16 24582657 24582657 + Nonsense_Mutation SNP C C T TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr16:24582657C>T c.4270C>T c.(4270-4272)Cag>Tag p.Q1424* BLCA 16 24582981 24582981 + Missense_Mutation SNP A A G TCGA-DK-A3IL-01A-11D-A20D-08 TCGA-DK-A3IL-10A-01D-A20D-08 g.chr16:24582981A>G c.4594A>G c.(4594-4596)Agt>Ggt p.S1532G BLCA 16 24582988 24582988 + Missense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr16:24582988C>A c.4601C>A c.(4600-4602)tCt>tAt p.S1534Y BLCA 16 24583000 24583000 + Missense_Mutation SNP G G C TCGA-ZF-A9RD-01A-11D-A42E-08 TCGA-ZF-A9RD-10A-01D-A42H-08 g.chr16:24583000G>C c.4613G>C c.(4612-4614)aGa>aCa p.R1538T BLCA 16 24583041 24583041 + Missense_Mutation SNP A A G TCGA-FD-A3NA-01A-11D-A21A-08 TCGA-FD-A3NA-10A-01D-A21A-08 g.chr16:24583041A>G c.4654A>G c.(4654-4656)Aaa>Gaa p.K1552E BLCA 16 24583382 24583382 + Silent SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr16:24583382G>C c.4995G>C c.(4993-4995)ctG>ctC p.L1665L BLCA 16 24583382 24583382 + Silent SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr16:24583382G>C c.4995G>C c.(4993-4995)ctG>ctC p.L1665L BLCA 16 24583390 24583390 + Missense_Mutation SNP A A G TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr16:24583390A>G c.5003A>G c.(5002-5004)aAa>aGa p.K1668R BRCA 16 24560353 24560353 + Intron SNP A A G TCGA-E9-A1R3-01A-31D-A14K-09 TCGA-E9-A1R3-10A-01D-A14K-09 g.chr16:24560353A>G BRCA 16 24567161 24567161 + Missense_Mutation SNP G G C TCGA-AN-A0FV-01A-11W-A019-09 TCGA-AN-A0FV-10A-01W-A021-09 g.chr16:24567161G>C c.457G>C c.(457-459)Ggt>Cgt p.G153R BRCA 16 24567190 24567190 + Silent SNP C C T TCGA-A2-A0YF-01A-21D-A10G-09 TCGA-A2-A0YF-10A-01D-A10G-09 g.chr16:24567190C>T c.486C>T c.(484-486)ttC>ttT p.F162F BRCA 16 24574557 24574557 + Missense_Mutation SNP G G T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr16:24574557G>T c.1327G>T c.(1327-1329)Gca>Tca p.A443S BRCA 16 24574618 24574618 + Splice_Site SNP T T A TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr16:24574618T>A c.e11+2 BRCA 16 24578496 24578496 + Missense_Mutation SNP G G C TCGA-BH-A209-01A-11D-A17G-09 TCGA-BH-A209-11A-42D-A17G-09 g.chr16:24578496G>C c.1622G>C c.(1621-1623)aGa>aCa p.R541T BRCA 16 24578776 24578776 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr16:24578776A>C c.1902A>C c.(1900-1902)ccA>ccC p.P634P BRCA 16 24578810 24578810 + Nonsense_Mutation SNP C C T TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr16:24578810C>T c.1936C>T c.(1936-1938)Cga>Tga p.R646* BRCA 16 24579150 24579150 + Missense_Mutation SNP G G A TCGA-A7-A26H-01A-11D-A167-09 TCGA-A7-A26H-10A-01D-A167-09 g.chr16:24579150G>A c.1990G>A c.(1990-1992)Gat>Aat p.D664N BRCA 16 24581109 24581109 + Missense_Mutation SNP A A G TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr16:24581109A>G c.3098A>G c.(3097-3099)aAt>aGt p.N1033S BRCA 16 24581246 24581246 + Missense_Mutation SNP C C G TCGA-B6-A0IK-01A-12W-A071-09 TCGA-B6-A0IK-10A-01W-A071-09 g.chr16:24581246C>G c.3235C>G c.(3235-3237)Cag>Gag p.Q1079E BRCA 16 24582488 24582488 + Missense_Mutation SNP T T G TCGA-A8-A075-01A-11D-A099-09 TCGA-A8-A075-10B-01D-A099-09 g.chr16:24582488T>G c.4101T>G c.(4099-4101)agT>agG p.S1367R BRCA 16 24582883 24582883 + Missense_Mutation SNP A A G TCGA-A8-A09W-01A-11W-A019-09 TCGA-A8-A09W-10A-01W-A021-09 g.chr16:24582883A>G c.4496A>G c.(4495-4497)gAc>gGc p.D1499G CESC 16 24557495 24557495 + Missense_Mutation SNP G G A TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chr16:24557495G>A c.178G>A c.(178-180)Gat>Aat p.D60N CESC 16 24578503 24578503 + Silent SNP G G A TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr16:24578503G>A c.1629G>A c.(1627-1629)caG>caA p.Q543Q CHOL 16 24582226 24582226 + Missense_Mutation SNP G G T TCGA-W5-AA2H-01A-31D-A417-09 TCGA-W5-AA2H-10A-01D-A41A-09 g.chr16:24582226G>T c.3839G>T c.(3838-3840)cGg>cTg p.R1280L COAD 16 24560271 24560271 + Missense_Mutation SNP G G T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr16:24560271G>T c.272G>T c.(271-273)cGa>cTa p.R91L COAD 16 24560272 24560272 + Silent SNP A A G TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:24560272A>G c.273A>G c.(271-273)cgA>cgG p.R91R COAD 16 24573231 24573231 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:24573231G>A c.1038G>A c.(1036-1038)ccG>ccA p.P346P COAD 16 24578489 24578489 + Missense_Mutation SNP A A G TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr16:24578489A>G c.1615A>G c.(1615-1617)Agc>Ggc p.S539G COAD 16 24578489 24578489 + Missense_Mutation SNP A A G TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr16:24578489A>G c.1615A>G c.(1615-1617)Agc>Ggc p.S539G COAD 16 24578491 24578491 + Silent SNP C C T TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COAD 16 24578491 24578491 + Silent SNP C C T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COAD 16 24578491 24578491 + Silent SNP C C T TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COAD 16 24578491 24578491 + Silent SNP C C T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COAD 16 24580197 24580197 + Missense_Mutation SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr16:24580197G>A c.2186G>A c.(2185-2187)cGg>cAg p.R729Q COAD 16 24581189 24581189 + Frame_Shift_Del DEL A A - TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr16:24581189delA c.3178delA c.(3178-3180)aaafs p.K1061fs COAD 16 24581212 24581212 + Silent SNP G G C TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chr16:24581212G>C c.3201G>C c.(3199-3201)ccG>ccC p.P1067P COAD 16 24581366 24581366 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:24581366A>G c.3355A>G c.(3355-3357)Aaa>Gaa p.K1119E COAD 16 24581543 24581543 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:24581543C>T c.3532C>T c.(3532-3534)Cca>Tca p.P1178S COAD 16 24582325 24582325 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:24582325T>C c.3938T>C c.(3937-3939)aTg>aCg p.M1313T COAD 16 24582434 24582434 + Frame_Shift_Del DEL A A - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr16:24582434delA c.4047delA c.(4045-4047)atafs p.I1349fs COAD 16 24582525 24582525 + Missense_Mutation SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr16:24582525G>A c.4138G>A c.(4138-4140)Gtg>Atg p.V1380M COAD 16 24582804 24582804 + Frame_Shift_Del DEL A A - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr16:24582804delA c.4417delA c.(4417-4419)aaafs p.K1474fs COAD 16 24583384 24583384 + Missense_Mutation SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr16:24583384A>C c.4997A>C c.(4996-4998)aAa>aCa p.K1666T COAD 16 24583666 24583666 + Missense_Mutation SNP G G A TCGA-AA-3684-01A-02W-0900-09 TCGA-AA-3684-10A-01W-0900-09 g.chr16:24583666G>A c.5279G>A c.(5278-5280)aGc>aAc p.S1760N COAD 16 24583713 24583718 + In_Frame_Del DEL AAAGAG AAAGAG - TCGA-AZ-4323-01A-21D-1835-10 TCGA-AZ-4323-10A-01D-1835-10 g.chr16:24583713_24583718delAAAGAG c.5326_5331delAAAGAG c.(5326-5331)aaagagdel p.KE1780del COADREAD 16 24560271 24560271 + Missense_Mutation SNP G G T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr16:24560271G>T c.272G>T c.(271-273)cGa>cTa p.R91L COADREAD 16 24560272 24560272 + Silent SNP A A G TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:24560272A>G c.273A>G c.(271-273)cgA>cgG p.R91R COADREAD 16 24573231 24573231 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:24573231G>A c.1038G>A c.(1036-1038)ccG>ccA p.P346P COADREAD 16 24578481 24578481 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24578481G>A c.1607G>A c.(1606-1608)cGa>cAa p.R536Q COADREAD 16 24578489 24578489 + Missense_Mutation SNP A A G TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr16:24578489A>G c.1615A>G c.(1615-1617)Agc>Ggc p.S539G COADREAD 16 24578489 24578489 + Missense_Mutation SNP A A G TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr16:24578489A>G c.1615A>G c.(1615-1617)Agc>Ggc p.S539G COADREAD 16 24578491 24578491 + Silent SNP C C T TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COADREAD 16 24578491 24578491 + Silent SNP C C T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COADREAD 16 24578491 24578491 + Silent SNP C C T TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COADREAD 16 24578491 24578491 + Silent SNP C C T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S COADREAD 16 24578770 24578770 + Missense_Mutation SNP A A T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24578770A>T c.1896A>T c.(1894-1896)caA>caT p.Q632H COADREAD 16 24580197 24580197 + Missense_Mutation SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr16:24580197G>A c.2186G>A c.(2185-2187)cGg>cAg p.R729Q COADREAD 16 24581189 24581189 + Frame_Shift_Del DEL A A - TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr16:24581189delA c.3178delA c.(3178-3180)aaafs p.K1061fs COADREAD 16 24581196 24581196 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24581196C>T c.3185C>T c.(3184-3186)gCc>gTc p.A1062V COADREAD 16 24581212 24581212 + Silent SNP G G C TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chr16:24581212G>C c.3201G>C c.(3199-3201)ccG>ccC p.P1067P COADREAD 16 24581366 24581366 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:24581366A>G c.3355A>G c.(3355-3357)Aaa>Gaa p.K1119E COADREAD 16 24581543 24581543 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:24581543C>T c.3532C>T c.(3532-3534)Cca>Tca p.P1178S COADREAD 16 24581622 24581622 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr16:24581622C>T c.3611C>T c.(3610-3612)gCg>gTg p.A1204V COADREAD 16 24582325 24582325 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:24582325T>C c.3938T>C c.(3937-3939)aTg>aCg p.M1313T COADREAD 16 24582434 24582434 + Frame_Shift_Del DEL A A - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr16:24582434delA c.4047delA c.(4045-4047)atafs p.I1349fs COADREAD 16 24582525 24582525 + Missense_Mutation SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr16:24582525G>A c.4138G>A c.(4138-4140)Gtg>Atg p.V1380M COADREAD 16 24582702 24582702 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24582702A>C c.4315A>C c.(4315-4317)Aat>Cat p.N1439H COADREAD 16 24582804 24582804 + Frame_Shift_Del DEL A A - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr16:24582804delA c.4417delA c.(4417-4419)aaafs p.K1474fs COADREAD 16 24582954 24582954 + Frame_Shift_Del DEL A A - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr16:24582954delA c.4567delA c.(4567-4569)aaafs p.K1524fs COADREAD 16 24583384 24583384 + Missense_Mutation SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr16:24583384A>C c.4997A>C c.(4996-4998)aAa>aCa p.K1666T COADREAD 16 24583666 24583666 + Missense_Mutation SNP G G A TCGA-AA-3684-01A-02W-0900-09 TCGA-AA-3684-10A-01W-0900-09 g.chr16:24583666G>A c.5279G>A c.(5278-5280)aGc>aAc p.S1760N COADREAD 16 24583713 24583718 + In_Frame_Del DEL AAAGAG AAAGAG - TCGA-AZ-4323-01A-21D-1835-10 TCGA-AZ-4323-10A-01D-1835-10 g.chr16:24583713_24583718delAAAGAG c.5326_5331delAAAGAG c.(5326-5331)aaagagdel p.KE1780del DLBC 16 24557518 24557518 + Missense_Mutation SNP T T A TCGA-GR-A4D4-01A-11D-A31X-10 TCGA-GR-A4D4-10A-01D-A31X-10 g.chr16:24557518T>A c.201T>A c.(199-201)aaT>aaA p.N67K ESCA 16 24574976 24574976 + Missense_Mutation SNP G G T TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr16:24574976G>T c.1511G>T c.(1510-1512)gGc>gTc p.G504V ESCA 16 24578657 24578657 + Missense_Mutation SNP G G T TCGA-VR-AA4D-01A-11D-A37C-09 TCGA-VR-AA4D-10A-01D-A37F-09 g.chr16:24578657G>T c.1783G>T c.(1783-1785)Gct>Tct p.A595S ESCA 16 24578711 24578711 + Missense_Mutation SNP A A G TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr16:24578711A>G c.1837A>G c.(1837-1839)Aca>Gca p.T613A ESCA 16 24581206 24581206 + Silent SNP G G A TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr16:24581206G>A c.3195G>A c.(3193-3195)gaG>gaA p.E1065E ESCA 16 24581686 24581686 + Missense_Mutation SNP A A G TCGA-V5-A7RC-01B-11D-A403-09 TCGA-V5-A7RC-10A-01D-A403-09 g.chr16:24581686A>G c.3675A>G c.(3673-3675)atA>atG p.I1225M ESCA 16 24582688 24582688 + Missense_Mutation SNP T T A TCGA-IG-A97H-01A-11D-A387-09 TCGA-IG-A97H-10A-01D-A38A-09 g.chr16:24582688T>A c.4301T>A c.(4300-4302)cTg>cAg p.L1434Q ESCA 16 24582975 24582975 + Frame_Shift_Del DEL A A - TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr16:24582975delA c.4588delA c.(4588-4590)aaafs p.K1531fs ESCA 16 24583012 24583012 + Missense_Mutation SNP C C A TCGA-V5-A7RC-01B-11D-A403-09 TCGA-V5-A7RC-10A-01D-A403-09 g.chr16:24583012C>A c.4625C>A c.(4624-4626)cCt>cAt p.P1542H ESCA 16 24583221 24583221 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr16:24583221G>A c.4834G>A c.(4834-4836)Gtc>Atc p.V1612I ESCA 16 24583538 24583538 + Silent SNP T T C TCGA-R6-A6L6-01B-11D-A33E-09 TCGA-R6-A6L6-10A-01D-A33H-09 g.chr16:24583538T>C c.5151T>C c.(5149-5151)agT>agC p.S1717S GBM 16 24552109 24552109 + Silent SNP A A G TCGA-12-5301-01A-01D-1486-08 TCGA-12-5301-10A-01D-1486-08 g.chr16:24552109A>G c.162A>G c.(160-162)aaA>aaG p.K54K GBM 16 24581255 24581256 + Frame_Shift_Ins INS - - A TCGA-19-5947-01A-11D-1696-08 TCGA-19-5947-11A-01D-1696-08 g.chr16:24581255_24581256insA c.3244_3245insA c.(3244-3246)gaafs p.E1082fs GBM 16 24581488 24581489 + Frame_Shift_Del DEL TT TT - TCGA-76-4929-01A-01D-1486-08 TCGA-76-4929-10A-01D-1486-08 g.chr16:24581488_24581489delTT c.3477_3478delTT c.(3475-3480)gattttfs p.F1160fs GBM 16 24582927 24582927 + Missense_Mutation SNP A A C TCGA-06-0686-01A-01W-0348-08 TCGA-06-0686-10A-01W-0348-08 g.chr16:24582927A>C c.4540A>C c.(4540-4542)Aaa>Caa p.K1514Q GBM 16 24583037 24583037 + Silent SNP T T C TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr16:24583037T>C c.4650T>C c.(4648-4650)gaT>gaC p.D1550D GBMLGG 16 24552109 24552109 + Silent SNP A A G TCGA-12-5301-01A-01D-1486-08 TCGA-12-5301-10A-01D-1486-08 g.chr16:24552109A>G c.162A>G c.(160-162)aaA>aaG p.K54K GBMLGG 16 24567681 24567681 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24567681G>T c.587G>T c.(586-588)aGa>aTa p.R196I GBMLGG 16 24567746 24567747 + Frame_Shift_Ins INS - - A TCGA-QH-A65Z-01A-11D-A29Q-08 TCGA-QH-A65Z-10A-01D-A29Q-08 g.chr16:24567746_24567747insA c.652_653insA c.(652-654)tatfs p.Y218fs GBMLGG 16 24578499 24578499 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24578499C>A c.1625C>A c.(1624-1626)tCa>tAa p.S542* GBMLGG 16 24580425 24580425 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24580425C>A c.2414C>A c.(2413-2415)cCa>cAa p.P805Q GBMLGG 16 24581121 24581121 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24581121C>A c.3110C>A c.(3109-3111)cCt>cAt p.P1037H GBMLGG 16 24581255 24581256 + Frame_Shift_Ins INS - - A TCGA-19-5947-01A-11D-1696-08 TCGA-19-5947-11A-01D-1696-08 g.chr16:24581255_24581256insA c.3244_3245insA c.(3244-3246)gaafs p.E1082fs GBMLGG 16 24581321 24581321 + Frame_Shift_Del DEL C C - TCGA-DU-7010-01A-11D-2024-08 TCGA-DU-7010-10A-01D-2024-08 g.chr16:24581321delC c.3310delC c.(3310-3312)ccafs p.P1104fs GBMLGG 16 24581488 24581489 + Frame_Shift_Del DEL TT TT - TCGA-76-4929-01A-01D-1486-08 TCGA-76-4929-10A-01D-1486-08 g.chr16:24581488_24581489delTT c.3477_3478delTT c.(3475-3480)gattttfs p.F1160fs GBMLGG 16 24582708 24582709 + Frame_Shift_Del DEL AA AA - TCGA-R8-A6MK-01A-11D-A32B-08 TCGA-R8-A6MK-10A-01D-A329-08 g.chr16:24582708_24582709delAA c.4321_4322delAA c.(4321-4323)aaafs p.K1441fs GBMLGG 16 24582927 24582927 + Missense_Mutation SNP A A C TCGA-06-0686-01A-01W-0348-08 TCGA-06-0686-10A-01W-0348-08 g.chr16:24582927A>C c.4540A>C c.(4540-4542)Aaa>Caa p.K1514Q GBMLGG 16 24582966 24582966 + Missense_Mutation SNP G G A TCGA-R8-A6MO-01A-11D-A33T-08 TCGA-R8-A6MO-10C-01D-A33W-08 g.chr16:24582966G>A c.4579G>A c.(4579-4581)Gga>Aga p.G1527R GBMLGG 16 24583037 24583037 + Silent SNP T T C TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr16:24583037T>C c.4650T>C c.(4648-4650)gaT>gaC p.D1550D GBMLGG 16 24583552 24583553 + Frame_Shift_Del DEL AA AA - TCGA-S9-A6WP-01A-12D-A34A-08 TCGA-S9-A6WP-10A-01D-A34A-08 g.chr16:24583552_24583553delAA c.5165_5166delAA c.(5164-5166)gaafs p.E1722fs HNSC 16 24551988 24551988 + Missense_Mutation SNP A A G TCGA-CR-7369-01A-11D-2129-08 TCGA-CR-7369-10A-01D-2129-08 g.chr16:24551988A>G c.41A>G c.(40-42)tAt>tGt p.Y14C HNSC 16 24552017 24552017 + Missense_Mutation SNP A A G TCGA-CV-6955-01A-11D-2012-08 TCGA-CV-6955-10A-01D-2013-08 g.chr16:24552017A>G c.70A>G c.(70-72)Atc>Gtc p.I24V HNSC 16 24567192 24567192 + Missense_Mutation SNP G G A TCGA-CN-6995-01A-31D-2012-08 TCGA-CN-6995-10A-01D-2013-08 g.chr16:24567192G>A c.488G>A c.(487-489)cGt>cAt p.R163H HNSC 16 24578538 24578538 + Missense_Mutation SNP T T G TCGA-F7-7848-01A-11D-2129-08 TCGA-F7-7848-10A-01D-2129-08 g.chr16:24578538T>G c.1664T>G c.(1663-1665)gTc>gGc p.V555G HNSC 16 24580072 24580072 + Silent SNP A A G TCGA-CN-6997-01A-11D-2012-08 TCGA-CN-6997-10A-01D-2013-08 g.chr16:24580072A>G c.2061A>G c.(2059-2061)aaA>aaG p.K687K HNSC 16 24580555 24580555 + Silent SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:24580555A>G c.2544A>G c.(2542-2544)ggA>ggG p.G848G HNSC 16 24580864 24580864 + Silent SNP A A T TCGA-CN-4739-01A-02D-1512-08 TCGA-CN-4739-10A-01D-1512-08 g.chr16:24580864A>T c.2853A>T c.(2851-2853)ccA>ccT p.P951P HNSC 16 24581745 24581745 + Missense_Mutation SNP A A C TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chr16:24581745A>C c.3734A>C c.(3733-3735)gAa>gCa p.E1245A KICH 16 24582960 24582960 + Frame_Shift_Del DEL G G - TCGA-KL-8332-01A-11D-2310-10 TCGA-KL-8332-11A-01D-2310-10 g.chr16:24582960delG c.4573delG c.(4573-4575)ggafs p.G1525fs KICH 16 24582961 24582961 + Frame_Shift_Del DEL G G - TCGA-KL-8332-01A-11D-2310-10 TCGA-KL-8332-11A-01D-2310-10 g.chr16:24582961delG c.4574delG c.(4573-4575)ggafs p.G1525fs KICH 16 24583715 24583715 + Silent SNP A A G TCGA-KO-8417-01A-11D-2310-10 TCGA-KO-8417-11A-01D-2311-10 g.chr16:24583715A>G c.5328A>G c.(5326-5328)aaA>aaG p.K1776K KIPAN 16 24551961 24551962 + Frame_Shift_Ins INS - - T TCGA-B0-5116-01A-02D-1421-08 TCGA-B0-5116-11A-01D-1421-08 g.chr16:24551961_24551962insT c.14_15insT c.(13-18)cattatfs p.Y6fs KIPAN 16 24573318 24573318 + Silent SNP T T G TCGA-CJ-4878-01A-01D-1373-10 TCGA-CJ-4878-11A-01D-1373-10 g.chr16:24573318T>G c.1125T>G c.(1123-1125)tcT>tcG p.S375S KIPAN 16 24578519 24578519 + Missense_Mutation SNP T T C TCGA-5P-A9JU-01A-11D-A42J-10 TCGA-5P-A9JU-10A-01D-A42M-10 g.chr16:24578519T>C c.1645T>C c.(1645-1647)Tca>Cca p.S549P KIPAN 16 24580912 24580912 + Silent SNP A A G TCGA-BP-4761-01A-01D-1366-10 TCGA-BP-4761-11A-01D-1366-10 g.chr16:24580912A>G c.2901A>G c.(2899-2901)gaA>gaG p.E967E KIPAN 16 24581079 24581079 + Missense_Mutation SNP A A T TCGA-MH-A55W-01A-11D-A26P-10 TCGA-MH-A55W-10A-01D-A26P-10 g.chr16:24581079A>T c.3068A>T c.(3067-3069)aAt>aTt p.N1023I KIPAN 16 24581248 24581248 + Missense_Mutation SNP G G C TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr16:24581248G>C c.3237G>C c.(3235-3237)caG>caC p.Q1079H KIPAN 16 24582258 24582258 + Missense_Mutation SNP A A C TCGA-G7-7501-01A-11D-2201-08 TCGA-G7-7501-10A-01D-2201-08 g.chr16:24582258A>C c.3871A>C c.(3871-3873)Act>Cct p.T1291P KIPAN 16 24582943 24582943 + Missense_Mutation SNP G G C TCGA-DZ-6132-01A-11D-1961-08 TCGA-DZ-6132-11A-01D-1961-08 g.chr16:24582943G>C c.4556G>C c.(4555-4557)aGa>aCa p.R1519T KIPAN 16 24582960 24582960 + Frame_Shift_Del DEL G G - TCGA-KL-8332-01A-11D-2310-10 TCGA-KL-8332-11A-01D-2310-10 g.chr16:24582960delG c.4573delG c.(4573-4575)ggafs p.G1525fs KIPAN 16 24582961 24582961 + Frame_Shift_Del DEL G G - TCGA-KL-8332-01A-11D-2310-10 TCGA-KL-8332-11A-01D-2310-10 g.chr16:24582961delG c.4574delG c.(4573-4575)ggafs p.G1525fs KIPAN 16 24583192 24583192 + Missense_Mutation SNP A A G TCGA-B2-3924-01A-02D-1386-10 TCGA-B2-3924-11A-01D-1251-10 g.chr16:24583192A>G c.4805A>G c.(4804-4806)cAa>cGa p.Q1602R KIPAN 16 24583715 24583715 + Silent SNP A A G TCGA-KO-8417-01A-11D-2310-10 TCGA-KO-8417-11A-01D-2311-10 g.chr16:24583715A>G c.5328A>G c.(5326-5328)aaA>aaG p.K1776K KIRC 16 24551961 24551962 + Frame_Shift_Ins INS - - T TCGA-B0-5116-01A-02D-1421-08 TCGA-B0-5116-11A-01D-1421-08 g.chr16:24551961_24551962insT c.14_15insT c.(13-18)cattatfs p.Y6fs KIRC 16 24573318 24573318 + Silent SNP T T G TCGA-CJ-4878-01A-01D-1373-10 TCGA-CJ-4878-11A-01D-1373-10 g.chr16:24573318T>G c.1125T>G c.(1123-1125)tcT>tcG p.S375S KIRC 16 24580912 24580912 + Silent SNP A A G TCGA-BP-4761-01A-01D-1366-10 TCGA-BP-4761-11A-01D-1366-10 g.chr16:24580912A>G c.2901A>G c.(2899-2901)gaA>gaG p.E967E KIRC 16 24581248 24581248 + Missense_Mutation SNP G G C TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr16:24581248G>C c.3237G>C c.(3235-3237)caG>caC p.Q1079H KIRC 16 24583192 24583192 + Missense_Mutation SNP A A G TCGA-B2-3924-01A-02D-1386-10 TCGA-B2-3924-11A-01D-1251-10 g.chr16:24583192A>G c.4805A>G c.(4804-4806)cAa>cGa p.Q1602R KIRP 16 24578519 24578519 + Missense_Mutation SNP T T C TCGA-5P-A9JU-01A-11D-A42J-10 TCGA-5P-A9JU-10A-01D-A42M-10 g.chr16:24578519T>C c.1645T>C c.(1645-1647)Tca>Cca p.S549P KIRP 16 24581079 24581079 + Missense_Mutation SNP A A T TCGA-MH-A55W-01A-11D-A26P-10 TCGA-MH-A55W-10A-01D-A26P-10 g.chr16:24581079A>T c.3068A>T c.(3067-3069)aAt>aTt p.N1023I KIRP 16 24582258 24582258 + Missense_Mutation SNP A A C TCGA-G7-7501-01A-11D-2201-08 TCGA-G7-7501-10A-01D-2201-08 g.chr16:24582258A>C c.3871A>C c.(3871-3873)Act>Cct p.T1291P KIRP 16 24582943 24582943 + Missense_Mutation SNP G G C TCGA-DZ-6132-01A-11D-1961-08 TCGA-DZ-6132-11A-01D-1961-08 g.chr16:24582943G>C c.4556G>C c.(4555-4557)aGa>aCa p.R1519T LGG 16 24567681 24567681 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24567681G>T c.587G>T c.(586-588)aGa>aTa p.R196I LGG 16 24567746 24567747 + Frame_Shift_Ins INS - - A TCGA-QH-A65Z-01A-11D-A29Q-08 TCGA-QH-A65Z-10A-01D-A29Q-08 g.chr16:24567746_24567747insA c.652_653insA c.(652-654)tatfs p.Y218fs LGG 16 24578499 24578499 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24578499C>A c.1625C>A c.(1624-1626)tCa>tAa p.S542* LGG 16 24580425 24580425 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24580425C>A c.2414C>A c.(2413-2415)cCa>cAa p.P805Q LGG 16 24581121 24581121 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:24581121C>A c.3110C>A c.(3109-3111)cCt>cAt p.P1037H LGG 16 24581321 24581321 + Frame_Shift_Del DEL C C - TCGA-DU-7010-01A-11D-2024-08 TCGA-DU-7010-10A-01D-2024-08 g.chr16:24581321delC c.3310delC c.(3310-3312)ccafs p.P1104fs LGG 16 24582708 24582709 + Frame_Shift_Del DEL AA AA - TCGA-R8-A6MK-01A-11D-A32B-08 TCGA-R8-A6MK-10A-01D-A329-08 g.chr16:24582708_24582709delAA c.4321_4322delAA c.(4321-4323)aaafs p.K1441fs LGG 16 24582966 24582966 + Missense_Mutation SNP G G A TCGA-R8-A6MO-01A-11D-A33T-08 TCGA-R8-A6MO-10C-01D-A33W-08 g.chr16:24582966G>A c.4579G>A c.(4579-4581)Gga>Aga p.G1527R LGG 16 24583552 24583553 + Frame_Shift_Del DEL AA AA - TCGA-S9-A6WP-01A-12D-A34A-08 TCGA-S9-A6WP-10A-01D-A34A-08 g.chr16:24583552_24583553delAA c.5165_5166delAA c.(5164-5166)gaafs p.E1722fs LIHC 16 24560285 24560285 + Missense_Mutation SNP A A G TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr16:24560285A>G c.286A>G c.(286-288)Atg>Gtg p.M96V LIHC 16 24579152 24579152 + Missense_Mutation SNP T T G TCGA-CC-A7IF-01A-11D-A33K-10 TCGA-CC-A7IF-10A-01D-A33K-10 g.chr16:24579152T>G c.1992T>G c.(1990-1992)gaT>gaG p.D664E LIHC 16 24580479 24580479 + Frame_Shift_Del DEL A A - TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr16:24580479delA c.2468delA c.(2467-2469)gaafs p.E823fs LIHC 16 24583041 24583041 + Missense_Mutation SNP A A G TCGA-5C-A9VG-01A-11D-A36X-10 TCGA-5C-A9VG-10A-01D-A370-10 g.chr16:24583041A>G c.4654A>G c.(4654-4656)Aaa>Gaa p.K1552E LIHC 16 24583179 24583180 + Frame_Shift_Ins INS - - T TCGA-MI-A75G-01A-11D-A32G-10 TCGA-MI-A75G-10A-01D-A32G-10 g.chr16:24583179_24583180insT c.4792_4793insT c.(4792-4794)gttfs p.V1598fs LIHC 16 24583618 24583618 + Missense_Mutation SNP A A G TCGA-DD-AACJ-01A-11D-A40R-10 TCGA-DD-AACJ-10A-01D-A40U-10 g.chr16:24583618A>G c.5231A>G c.(5230-5232)cAt>cGt p.H1744R LUAD 16 24551983 24551983 + Silent SNP C C T TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr16:24551983C>T c.36C>T c.(34-36)ctC>ctT p.L12L LUAD 16 24564863 24564863 + Silent SNP G G T TCGA-44-A479-01A-31D-A24D-08 TCGA-44-A479-10A-01D-A24F-08 g.chr16:24564863G>T c.333G>T c.(331-333)ctG>ctT p.L111L LUAD 16 24564864 24564864 + Missense_Mutation SNP G G T TCGA-44-A479-01A-31D-A24D-08 TCGA-44-A479-10A-01D-A24F-08 g.chr16:24564864G>T c.334G>T c.(334-336)Gcc>Tcc p.A112S LUAD 16 24567011 24567011 + Missense_Mutation SNP T T A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr16:24567011T>A c.424T>A c.(424-426)Tac>Aac p.Y142N LUAD 16 24570953 24570953 + Missense_Mutation SNP G G C TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr16:24570953G>C c.802G>C c.(802-804)Gat>Cat p.D268H LUAD 16 24573246 24573246 + Silent SNP G G A TCGA-55-6982-01A-11D-1945-08 TCGA-55-6982-11A-01D-1945-08 g.chr16:24573246G>A c.1053G>A c.(1051-1053)caG>caA p.Q351Q LUAD 16 24573481 24573481 + Splice_Site SNP C C T TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr16:24573481C>T c.1288C>T c.(1288-1290)Cgg>Tgg p.R430W LUAD 16 24578506 24578506 + Missense_Mutation SNP G G C TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr16:24578506G>C c.1632G>C c.(1630-1632)agG>agC p.R544S LUAD 16 24578601 24578601 + Missense_Mutation SNP C C T TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr16:24578601C>T c.1727C>T c.(1726-1728)cCg>cTg p.P576L LUAD 16 24580271 24580271 + Missense_Mutation SNP C C T TCGA-86-7955-01A-11D-2184-08 TCGA-86-7955-10A-01D-2184-08 g.chr16:24580271C>T c.2260C>T c.(2260-2262)Cat>Tat p.H754Y LUAD 16 24580361 24580362 + Frame_Shift_Del DEL CG CG - TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chr16:24580361_24580362delCG c.2350_2351delCG c.(2350-2352)cgtfs p.R784fs LUAD 16 24580457 24580457 + Missense_Mutation SNP G G A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr16:24580457G>A c.2446G>A c.(2446-2448)Gtt>Att p.V816I LUAD 16 24580583 24580583 + Missense_Mutation SNP G G A TCGA-64-1681-01A-11D-2063-08 TCGA-64-1681-10A-01D-2063-08 g.chr16:24580583G>A c.2572G>A c.(2572-2574)Gag>Aag p.E858K LUAD 16 24580932 24580932 + Nonsense_Mutation SNP T T A TCGA-50-5941-01A-11D-1753-08 TCGA-50-5941-10A-01D-1753-08 g.chr16:24580932T>A c.2921T>A c.(2920-2922)tTg>tAg p.L974* LUAD 16 24581297 24581297 + Missense_Mutation SNP G G A TCGA-17-Z011-01A-01W-0746-08 TCGA-17-Z011-11A-01W-0746-08 g.chr16:24581297G>A c.3286G>A c.(3286-3288)Gca>Aca p.A1096T LUAD 16 24581790 24581790 + Missense_Mutation SNP G G T TCGA-49-4486-01A-01D-1265-08 TCGA-49-4486-11A-01D-1265-08 g.chr16:24581790G>T c.3779G>T c.(3778-3780)gGa>gTa p.G1260V LUAD 16 24582303 24582303 + Missense_Mutation SNP C C T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr16:24582303C>T c.3916C>T c.(3916-3918)Cca>Tca p.P1306S LUAD 16 24582309 24582309 + Nonsense_Mutation SNP G G T TCGA-49-6742-01A-11D-1855-08 TCGA-49-6742-11A-01D-1855-08 g.chr16:24582309G>T c.3922G>T c.(3922-3924)Gaa>Taa p.E1308* LUAD 16 24582366 24582366 + Nonsense_Mutation SNP G G T TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr16:24582366G>T c.3979G>T c.(3979-3981)Gaa>Taa p.E1327* LUAD 16 24582457 24582457 + Missense_Mutation SNP C C T TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr16:24582457C>T c.4070C>T c.(4069-4071)tCa>tTa p.S1357L LUAD 16 24582841 24582841 + Missense_Mutation SNP C C A TCGA-49-4505-01A-01D-1931-08 TCGA-49-4505-11A-01D-1265-08 g.chr16:24582841C>A c.4454C>A c.(4453-4455)tCc>tAc p.S1485Y LUAD 16 24583167 24583167 + Missense_Mutation SNP C C T TCGA-50-5066-01A-01D-1625-08 TCGA-50-5066-10A-01D-1625-08 g.chr16:24583167C>T c.4780C>T c.(4780-4782)Cca>Tca p.P1594S LUAD 16 24583299 24583299 + Nonsense_Mutation SNP G G T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr16:24583299G>T c.4912G>T c.(4912-4914)Gaa>Taa p.E1638* LUAD 16 24583448 24583448 + Frame_Shift_Del DEL A A - TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr16:24583448delA c.5061delA c.(5059-5061)atafs p.I1687fs LUSC 16 24567164 24567164 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr16:24567164C>T c.460C>T c.(460-462)Cca>Tca p.P154S LUSC 16 24581518 24581518 + Missense_Mutation SNP A A T TCGA-66-2793-01A-01D-1267-08 TCGA-66-2793-11A-01D-1267-08 g.chr16:24581518A>T c.3507A>T c.(3505-3507)aaA>aaT p.K1169N LUSC 16 24582460 24582460 + Missense_Mutation SNP A A G TCGA-22-5489-01A-01D-1632-08 TCGA-22-5489-11A-01D-1632-08 g.chr16:24582460A>G c.4073A>G c.(4072-4074)aAt>aGt p.N1358S LUSC 16 24582687 24582687 + Missense_Mutation SNP C C G TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr16:24582687C>G c.4300C>G c.(4300-4302)Ctg>Gtg p.L1434V LUSC 16 24583481 24583481 + Silent SNP C C G TCGA-46-3768-01A-01D-0983-08 TCGA-46-3768-10A-01D-0983-08 g.chr16:24583481C>G c.5094C>G c.(5092-5094)gtC>gtG p.V1698V OV 16 24560271 24560271 + Missense_Mutation SNP G G A TCGA-24-1427-01A-01W-0549-09 TCGA-24-1427-10A-01W-0549-09 g.chr16:24560271G>A c.272G>A c.(271-273)cGa>cAa p.R91Q OV 16 24578491 24578491 + Silent SNP C C T TCGA-24-1560-01A-01W-0615-10 TCGA-24-1560-10A-01W-0615-10 g.chr16:24578491C>T c.1617C>T c.(1615-1617)agC>agT p.S539S OV 16 24578678 24578678 + Missense_Mutation SNP C C T TCGA-04-1530-01A-02W-0552-10 TCGA-04-1530-10A-01W-0552-10 g.chr16:24578678C>T c.1804C>T c.(1804-1806)Cca>Tca p.P602S OV 16 24581309 24581309 + Nonsense_Mutation SNP C C T TCGA-36-2533-01A-01D-1526-09 TCGA-36-2533-10A-01D-1526-09 g.chr16:24581309C>T c.3298C>T c.(3298-3300)Caa>Taa p.Q1100* OV 16 24582325 24582325 + Missense_Mutation SNP T T C TCGA-24-1557-01A-01W-0615-10 TCGA-24-1557-10A-01W-0615-10 g.chr16:24582325T>C c.3938T>C c.(3937-3939)aTg>aCg p.M1313T OV 16 24582569 24582569 + Silent SNP C C T TCGA-61-1733-01A-01W-0639-09 TCGA-61-1733-11A-01W-0639-09 g.chr16:24582569C>T c.4182C>T c.(4180-4182)aaC>aaT p.N1394N PAAD 16 24560342 24560342 + Intron SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:24560342C>A PAAD 16 24574565 24574565 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:24574565G>T c.1335G>T c.(1333-1335)gaG>gaT p.E445D PAAD 16 24580170 24580170 + Missense_Mutation SNP G G T TCGA-F2-A8YN-01A-11D-A377-08 TCGA-F2-A8YN-10A-01D-A37A-08 g.chr16:24580170G>T c.2159G>T c.(2158-2160)aGc>aTc p.S720I PAAD 16 24581479 24581479 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:24581479A>G c.3468A>G c.(3466-3468)gtA>gtG p.V1156V PAAD 16 24581622 24581622 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:24581622C>T c.3611C>T c.(3610-3612)gCg>gTg p.A1204V PRAD 16 24567694 24567694 + Missense_Mutation SNP G G C TCGA-J4-A67L-01A-11D-A30E-08 TCGA-J4-A67L-10A-01D-A30H-08 g.chr16:24567694G>C c.600G>C c.(598-600)atG>atC p.M200I PRAD 16 24574974 24574974 + Silent SNP A A G TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr16:24574974A>G c.1509A>G c.(1507-1509)ccA>ccG p.P503P READ 16 24578481 24578481 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24578481G>A c.1607G>A c.(1606-1608)cGa>cAa p.R536Q READ 16 24578770 24578770 + Missense_Mutation SNP A A T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24578770A>T c.1896A>T c.(1894-1896)caA>caT p.Q632H READ 16 24581196 24581196 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24581196C>T c.3185C>T c.(3184-3186)gCc>gTc p.A1062V READ 16 24581622 24581622 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr16:24581622C>T c.3611C>T c.(3610-3612)gCg>gTg p.A1204V READ 16 24582702 24582702 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:24582702A>C c.4315A>C c.(4315-4317)Aat>Cat p.N1439H READ 16 24582954 24582954 + Frame_Shift_Del DEL A A - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr16:24582954delA c.4567delA c.(4567-4569)aaafs p.K1524fs SARC 16 24581514 24581514 + Missense_Mutation SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr16:24581514C>T c.3503C>T c.(3502-3504)tCg>tTg p.S1168L SARC 16 24583338 24583338 + Missense_Mutation SNP T T A TCGA-WK-A8XX-01A-11D-A37C-09 TCGA-WK-A8XX-10A-01D-A37F-09 g.chr16:24583338T>A c.4951T>A c.(4951-4953)Tct>Act p.S1651T SKCM 16 24567190 24567190 + Silent SNP C C T TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chr16:24567190C>T c.486C>T c.(484-486)ttC>ttT p.F162F SKCM 16 24573272 24573272 + Missense_Mutation SNP C C T TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr16:24573272C>T c.1079C>T c.(1078-1080)tCt>tTt p.S360F SKCM 16 24573359 24573359 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:24573359C>T c.1166C>T c.(1165-1167)tCt>tTt p.S389F SKCM 16 24573481 24573481 + Splice_Site SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr16:24573481C>T c.1288C>T c.(1288-1290)Cgg>Tgg p.R430W SKCM 16 24574598 24574598 + Silent SNP C C A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr16:24574598C>A c.1368C>A c.(1366-1368)acC>acA p.T456T SKCM 16 24578591 24578591 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:24578591C>T c.1717C>T c.(1717-1719)Cct>Tct p.P573S SKCM 16 24578597 24578597 + Missense_Mutation SNP C C T TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr16:24578597C>T c.1723C>T c.(1723-1725)Cct>Tct p.P575S SKCM 16 24578597 24578597 + Missense_Mutation SNP C C T TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr16:24578597C>T c.1723C>T c.(1723-1725)Cct>Tct p.P575S SKCM 16 24578598 24578598 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:24578598C>T c.1724C>T c.(1723-1725)cCt>cTt p.P575L SKCM 16 24578672 24578672 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:24578672C>T c.1798C>T c.(1798-1800)Cct>Tct p.P600S SKCM 16 24578678 24578678 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr16:24578678C>T c.1804C>T c.(1804-1806)Cca>Tca p.P602S SKCM 16 24578687 24578687 + Missense_Mutation SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr16:24578687C>T c.1813C>T c.(1813-1815)Cct>Tct p.P605S SKCM 16 24578724 24578724 + Missense_Mutation SNP C C T TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr16:24578724C>T c.1850C>T c.(1849-1851)tCa>tTa p.S617L SKCM 16 24580152 24580152 + Missense_Mutation SNP C C T TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr16:24580152C>T c.2141C>T c.(2140-2142)tCt>tTt p.S714F SKCM 16 24580295 24580295 + Missense_Mutation SNP C C T TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chr16:24580295C>T c.2284C>T c.(2284-2286)Cct>Tct p.P762S SKCM 16 24580302 24580302 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:24580302G>A c.2291G>A c.(2290-2292)aGa>aAa p.R764K SKCM 16 24580361 24580361 + Missense_Mutation SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr16:24580361C>T c.2350C>T c.(2350-2352)Cgt>Tgt p.R784C SKCM 16 24581169 24581169 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr16:24581169C>T c.3158C>T c.(3157-3159)cCt>cTt p.P1053L SKCM 16 24581171 24581171 + Nonsense_Mutation SNP C C T TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr16:24581171C>T c.3160C>T c.(3160-3162)Cga>Tga p.R1054* SKCM 16 24581176 24581176 + Frame_Shift_Del DEL T T - TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr16:24581176delT c.3165delT c.(3163-3165)tctfs p.S1055fs SKCM 16 24581490 24581490 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr16:24581490T>G c.3479T>G c.(3478-3480)tTt>tGt p.F1160C SKCM 16 24581764 24581764 + Silent SNP C C T TCGA-D3-A2JL-06A-11D-A196-08 TCGA-D3-A2JL-10A-01D-A198-08 g.chr16:24581764C>T c.3753C>T c.(3751-3753)gtC>gtT p.V1251V SKCM 16 24582320 24582320 + Silent SNP C C T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr16:24582320C>T c.3933C>T c.(3931-3933)atC>atT p.I1311I SKCM 16 24582700 24582700 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr16:24582700G>A c.4313G>A c.(4312-4314)gGa>gAa p.G1438E SKCM 16 24582793 24582793 + Missense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr16:24582793C>T c.4406C>T c.(4405-4407)cCc>cTc p.P1469L SKCM 16 24582974 24582974 + Silent SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr16:24582974C>T c.4587C>T c.(4585-4587)tcC>tcT p.S1529S SKCM 16 24583080 24583080 + Missense_Mutation SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr16:24583080C>T c.4693C>T c.(4693-4695)Cct>Tct p.P1565S SKCM 16 24583226 24583226 + Silent SNP G G A TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr16:24583226G>A c.4839G>A c.(4837-4839)aaG>aaA p.K1613K SKCM 16 24583244 24583244 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr16:24583244T>G c.4857T>G c.(4855-4857)agT>agG p.S1619R

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 16 24573253 24573253 single base substitution C G downstream_gene_variant AML-US 16 24573253 24573253 single base substitution C G exon_variant AML-US 16 24573253 24573253 single base substitution C G missense_variant L221V 661C>G AML-US 16 24573253 24573253 single base substitution C G missense_variant L354V 1060C>G AML-US 16 24573253 24573253 single base substitution C G upstream_gene_variant BLCA-CN 16 24580420 24580420 single base substitution A G downstream_gene_variant BLCA-CN 16 24580420 24580420 single base substitution A G exon_variant BLCA-CN 16 24580420 24580420 single base substitution A G intron_variant BLCA-CN 16 24580420 24580420 single base substitution A G synonymous_variant P670P 2010A>G BLCA-CN 16 24580420 24580420 single base substitution A G synonymous_variant P769P 2307A>G BLCA-CN 16 24580420 24580420 single base substitution A G synonymous_variant P803P 2409A>G BLCA-CN 16 24582769 24582769 single base substitution C G downstream_gene_variant BLCA-CN 16 24582769 24582769 single base substitution C G exon_variant BLCA-CN 16 24582769 24582769 single base substitution C G missense_variant A1427G 4280C>G BLCA-CN 16 24582769 24582769 single base substitution C G missense_variant A1461G 4382C>G BLCA-CN 16 24582769 24582769 single base substitution C G missense_variant A621G 1862C>G BLCA-US 16 24566966 24566966 single base substitution G A 5_prime_UTR_variant BLCA-US 16 24566966 24566966 single base substitution G A exon_variant BLCA-US 16 24566966 24566966 single base substitution G A missense_variant E127K 379G>A BLCA-US 16 24566966 24566966 single base substitution G A upstream_gene_variant BLCA-US 16 24573026 24573026 single base substitution T G downstream_gene_variant BLCA-US 16 24573026 24573026 single base substitution T G exon_variant BLCA-US 16 24573026 24573026 single base substitution T G missense_variant F181C 542T>G BLCA-US 16 24573026 24573026 single base substitution T G missense_variant F314C 941T>G BLCA-US 16 24573026 24573026 single base substitution T G upstream_gene_variant BLCA-US 16 24578570 24578570 single base substitution C T exon_variant BLCA-US 16 24578570 24578570 single base substitution C T intron_variant BLCA-US 16 24578570 24578570 single base substitution C T missense_variant P433S 1297C>T BLCA-US 16 24578570 24578570 single base substitution C T missense_variant P566S 1696C>T BLCA-US 16 24578652 24578652 single base substitution C T exon_variant BLCA-US 16 24578652 24578652 single base substitution C T intron_variant BLCA-US 16 24578652 24578652 single base substitution C T missense_variant P460L 1379C>T BLCA-US 16 24578652 24578652 single base substitution C T missense_variant P593L 1778C>T BLCA-US 16 24582981 24582981 single base substitution A G downstream_gene_variant BLCA-US 16 24582981 24582981 single base substitution A G exon_variant BLCA-US 16 24582981 24582981 single base substitution A G missense_variant S1498G 4492A>G BLCA-US 16 24582981 24582981 single base substitution A G missense_variant S1532G 4594A>G BLCA-US 16 24582981 24582981 single base substitution A G missense_variant S692G 2074A>G BLCA-US 16 24583041 24583041 single base substitution A G downstream_gene_variant BLCA-US 16 24583041 24583041 single base substitution A G exon_variant BLCA-US 16 24583041 24583041 single base substitution A G missense_variant K1518E 4552A>G BLCA-US 16 24583041 24583041 single base substitution A G missense_variant K1552E 4654A>G BLCA-US 16 24583041 24583041 single base substitution A G missense_variant K712E 2134A>G BOCA-FR 16 24567581 24567581 single base substitution A T downstream_gene_variant BOCA-FR 16 24567581 24567581 single base substitution A T intron_variant BRCA-EU 16 24544068 24544068 single base substitution A C upstream_gene_variant BRCA-EU 16 24546879 24546879 single base substitution C T upstream_gene_variant BRCA-EU 16 24547209 24547209 single base substitution C G upstream_gene_variant BRCA-EU 16 24547466 24547466 single base substitution C A upstream_gene_variant BRCA-EU 16 24547753 24547753 single base substitution C T upstream_gene_variant BRCA-EU 16 24547825 24547825 single base substitution G C upstream_gene_variant BRCA-EU 16 24548131 24548131 single base substitution T G upstream_gene_variant BRCA-EU 16 24548988 24548988 single base substitution G C upstream_gene_variant BRCA-EU 16 24549780 24549780 single base substitution T C intron_variant BRCA-EU 16 24549780 24549780 single base substitution T C upstream_gene_variant BRCA-EU 16 24549810 24549810 single base substitution C T intron_variant BRCA-EU 16 24549810 24549810 single base substitution C T upstream_gene_variant BRCA-EU 16 24550963 24550963 single base substitution G C 5_prime_UTR_variant BRCA-EU 16 24550963 24550963 single base substitution G C exon_variant BRCA-EU 16 24550963 24550963 single base substitution G C intron_variant BRCA-EU 16 24550963 24550963 single base substitution G C upstream_gene_variant BRCA-EU 16 24552359 24552359 single base substitution C A downstream_gene_variant BRCA-EU 16 24552359 24552359 single base substitution C A intron_variant BRCA-EU 16 24553476 24553476 single base substitution G C downstream_gene_variant BRCA-EU 16 24553476 24553476 single base substitution G C intron_variant BRCA-EU 16 24553781 24553781 single base substitution T C downstream_gene_variant BRCA-EU 16 24553781 24553781 single base substitution T C intron_variant BRCA-EU 16 24553819 24553819 single base substitution A G downstream_gene_variant BRCA-EU 16 24553819 24553819 single base substitution A G intron_variant BRCA-EU 16 24554768 24554768 single base substitution T A downstream_gene_variant BRCA-EU 16 24554768 24554768 single base substitution T A intron_variant BRCA-EU 16 24555438 24555438 single base substitution C G downstream_gene_variant BRCA-EU 16 24555438 24555438 single base substitution C G intron_variant BRCA-EU 16 24555848 24555848 deletion of <=200bp G - downstream_gene_variant BRCA-EU 16 24555848 24555848 deletion of <=200bp G - intron_variant BRCA-EU 16 24557576 24557580 deletion of <=200bp TATGT - frameshift_variant YV87 BRCA-EU 16 24557576 24557580 deletion of <=200bp TATGT - intron_variant BRCA-EU 16 24557882 24557882 deletion of <=200bp T - intron_variant BRCA-EU 16 24558385 24558385 single base substitution A G intron_variant BRCA-EU 16 24559949 24559949 single base substitution G C intron_variant BRCA-EU 16 24559949 24559949 single base substitution G C upstream_gene_variant BRCA-EU 16 24560071 24560071 single base substitution C G intron_variant BRCA-EU 16 24560071 24560071 single base substitution C G upstream_gene_variant BRCA-EU 16 24561075 24561075 single base substitution C T downstream_gene_variant BRCA-EU 16 24561075 24561075 single base substitution C T intron_variant BRCA-EU 16 24561075 24561075 single base substitution C T upstream_gene_variant BRCA-EU 16 24561198 24561198 single base substitution G C downstream_gene_variant BRCA-EU 16 24561198 24561198 single base substitution G C intron_variant BRCA-EU 16 24561198 24561198 single base substitution G C upstream_gene_variant BRCA-EU 16 24565131 24565131 single base substitution T C downstream_gene_variant BRCA-EU 16 24565131 24565131 single base substitution T C intron_variant BRCA-EU 16 24565131 24565131 single base substitution T C upstream_gene_variant BRCA-EU 16 24566009 24566009 single base substitution A T exon_variant BRCA-EU 16 24566009 24566009 single base substitution A T intron_variant BRCA-EU 16 24566009 24566009 single base substitution A T upstream_gene_variant BRCA-EU 16 24566261 24566261 single base substitution T C exon_variant BRCA-EU 16 24566261 24566261 single base substitution T C intron_variant BRCA-EU 16 24566261 24566261 single base substitution T C upstream_gene_variant BRCA-EU 16 24566286 24566286 single base substitution A G exon_variant BRCA-EU 16 24566286 24566286 single base substitution A G intron_variant BRCA-EU 16 24566286 24566286 single base substitution A G upstream_gene_variant BRCA-EU 16 24567131 24567131 single base substitution C T intron_variant BRCA-EU 16 24567131 24567131 single base substitution C T upstream_gene_variant BRCA-EU 16 24567798 24567798 single base substitution G T downstream_gene_variant BRCA-EU 16 24567798 24567798 single base substitution G T intron_variant BRCA-EU 16 24569102 24569102 single base substitution T A downstream_gene_variant BRCA-EU 16 24569102 24569102 single base substitution T A intron_variant BRCA-EU 16 24570255 24570255 single base substitution G T downstream_gene_variant BRCA-EU 16 24570255 24570255 single base substitution G T intron_variant BRCA-EU 16 24570255 24570255 single base substitution G T upstream_gene_variant BRCA-EU 16 24570461 24570461 single base substitution A G downstream_gene_variant BRCA-EU 16 24570461 24570461 single base substitution A G intron_variant BRCA-EU 16 24570461 24570461 single base substitution A G upstream_gene_variant BRCA-EU 16 24570496 24570496 single base substitution C G downstream_gene_variant BRCA-EU 16 24570496 24570496 single base substitution C G intron_variant BRCA-EU 16 24570496 24570496 single base substitution C G upstream_gene_variant BRCA-EU 16 24573032 24573032 single base substitution G A downstream_gene_variant BRCA-EU 16 24573032 24573032 single base substitution G A exon_variant BRCA-EU 16 24573032 24573032 single base substitution G A missense_variant R183Q 548G>A BRCA-EU 16 24573032 24573032 single base substitution G A missense_variant R316Q 947G>A BRCA-EU 16 24573032 24573032 single base substitution G A upstream_gene_variant BRCA-EU 16 24574378 24574378 single base substitution T C downstream_gene_variant BRCA-EU 16 24574378 24574378 single base substitution T C intron_variant BRCA-EU 16 24574378 24574378 single base substitution T C upstream_gene_variant BRCA-EU 16 24574380 24574380 single base substitution T C downstream_gene_variant BRCA-EU 16 24574380 24574380 single base substitution T C intron_variant BRCA-EU 16 24574380 24574380 single base substitution T C upstream_gene_variant BRCA-EU 16 24575377 24575377 single base substitution G C downstream_gene_variant BRCA-EU 16 24575377 24575377 single base substitution G C intron_variant BRCA-EU 16 24576352 24576352 single base substitution G A downstream_gene_variant BRCA-EU 16 24576352 24576352 single base substitution G A intron_variant BRCA-EU 16 24577031 24577031 single base substitution G A downstream_gene_variant BRCA-EU 16 24577031 24577031 single base substitution G A intron_variant BRCA-EU 16 24578822 24578822 single base substitution G A downstream_gene_variant BRCA-EU 16 24578822 24578822 single base substitution G A exon_variant BRCA-EU 16 24578822 24578822 single base substitution G A intron_variant BRCA-EU 16 24578822 24578822 single base substitution G A missense_variant E517K 1549G>A BRCA-EU 16 24578822 24578822 single base substitution G A missense_variant E650K 1948G>A BRCA-EU 16 24579934 24579934 single base substitution T C downstream_gene_variant BRCA-EU 16 24579934 24579934 single base substitution T C intron_variant BRCA-EU 16 24581077 24581077 single base substitution G C downstream_gene_variant BRCA-EU 16 24581077 24581077 single base substitution G C exon_variant BRCA-EU 16 24581077 24581077 single base substitution G C intron_variant BRCA-EU 16 24581077 24581077 single base substitution G C missense_variant K1022N 3066G>C BRCA-EU 16 24581077 24581077 single base substitution G C missense_variant K889N 2667G>C BRCA-EU 16 24581077 24581077 single base substitution G C missense_variant K988N 2964G>C BRCA-EU 16 24582158 24582158 single base substitution A C downstream_gene_variant BRCA-EU 16 24582158 24582158 single base substitution A C intron_variant BRCA-EU 16 24582378 24582378 single base substitution G A downstream_gene_variant BRCA-EU 16 24582378 24582378 single base substitution G A exon_variant BRCA-EU 16 24582378 24582378 single base substitution G A missense_variant E1297K 3889G>A BRCA-EU 16 24582378 24582378 single base substitution G A missense_variant E1331K 3991G>A BRCA-EU 16 24582378 24582378 single base substitution G A missense_variant E491K 1471G>A BRCA-EU 16 24582877 24582877 single base substitution G A downstream_gene_variant BRCA-EU 16 24582877 24582877 single base substitution G A exon_variant BRCA-EU 16 24582877 24582877 single base substitution G A missense_variant R1463Q 4388G>A BRCA-EU 16 24582877 24582877 single base substitution G A missense_variant R1497Q 4490G>A BRCA-EU 16 24582877 24582877 single base substitution G A missense_variant R657Q 1970G>A BRCA-EU 16 24583593 24583593 insertion of <=200bp - A downstream_gene_variant BRCA-EU 16 24583593 24583593 insertion of <=200bp - A exon_variant BRCA-EU 16 24583593 24583593 insertion of <=200bp - A frameshift_variant K1702K? BRCA-EU 16 24583593 24583593 insertion of <=200bp - A frameshift_variant K1736K? BRCA-EU 16 24583593 24583593 insertion of <=200bp - A frameshift_variant K896K? BRCA-EU 16 24584107 24584107 single base substitution G C 3_prime_UTR_variant BRCA-EU 16 24584107 24584107 single base substitution G C downstream_gene_variant BRCA-EU 16 24584107 24584107 single base substitution G C exon_variant BRCA-EU 16 24585431 24585431 single base substitution G A downstream_gene_variant BRCA-EU 16 24585457 24585457 single base substitution T C downstream_gene_variant BRCA-EU 16 24585563 24585563 single base substitution C T downstream_gene_variant BRCA-EU 16 24585795 24585795 single base substitution C T downstream_gene_variant BRCA-EU 16 24585965 24585965 single base substitution C T downstream_gene_variant BRCA-EU 16 24586220 24586220 single base substitution C T downstream_gene_variant BRCA-EU 16 24586365 24586365 single base substitution C A downstream_gene_variant BRCA-EU 16 24587535 24587535 single base substitution T G downstream_gene_variant BRCA-EU 16 24587978 24587978 single base substitution C T downstream_gene_variant BRCA-EU 16 24588658 24588658 single base substitution C A downstream_gene_variant BRCA-FR 16 24549780 24549780 single base substitution T C intron_variant BRCA-FR 16 24549780 24549780 single base substitution T C upstream_gene_variant BRCA-FR 16 24560071 24560071 single base substitution C G intron_variant BRCA-FR 16 24560071 24560071 single base substitution C G upstream_gene_variant BRCA-FR 16 24564672 24564672 single base substitution G A downstream_gene_variant BRCA-FR 16 24564672 24564672 single base substitution G A exon_variant BRCA-FR 16 24564672 24564672 single base substitution G A intron_variant BRCA-FR 16 24564672 24564672 single base substitution G A upstream_gene_variant BRCA-FR 16 24575377 24575377 single base substitution G C downstream_gene_variant BRCA-FR 16 24575377 24575377 single base substitution G C intron_variant BRCA-FR 16 24578822 24578822 single base substitution G A downstream_gene_variant BRCA-FR 16 24578822 24578822 single base substitution G A exon_variant BRCA-FR 16 24578822 24578822 single base substitution G A intron_variant BRCA-FR 16 24578822 24578822 single base substitution G A missense_variant E517K 1549G>A BRCA-FR 16 24578822 24578822 single base substitution G A missense_variant E650K 1948G>A BRCA-FR 16 24582877 24582877 single base substitution G A downstream_gene_variant BRCA-FR 16 24582877 24582877 single base substitution G A exon_variant BRCA-FR 16 24582877 24582877 single base substitution G A missense_variant R1463Q 4388G>A BRCA-FR 16 24582877 24582877 single base substitution G A missense_variant R1497Q 4490G>A BRCA-FR 16 24582877 24582877 single base substitution G A missense_variant R657Q 1970G>A BRCA-FR 16 24587978 24587978 single base substitution C T downstream_gene_variant BRCA-UK 16 24563308 24563308 single base substitution G C downstream_gene_variant BRCA-UK 16 24563308 24563308 single base substitution G C intron_variant BRCA-UK 16 24563308 24563308 single base substitution G C upstream_gene_variant BRCA-UK 16 24565131 24565131 single base substitution T C downstream_gene_variant BRCA-UK 16 24565131 24565131 single base substitution T C intron_variant BRCA-UK 16 24565131 24565131 single base substitution T C upstream_gene_variant BRCA-US 16 24560353 24560353 single base substitution A G intron_variant BRCA-US 16 24560353 24560353 single base substitution A G synonymous_variant L118L 354A>G BRCA-US 16 24560353 24560353 single base substitution A G upstream_gene_variant BRCA-US 16 24567161 24567161 single base substitution G C exon_variant BRCA-US 16 24567161 24567161 single base substitution G C missense_variant G153R 457G>C BRCA-US 16 24567161 24567161 single base substitution G C missense_variant G20R 58G>C BRCA-US 16 24567190 24567190 single base substitution C T downstream_gene_variant BRCA-US 16 24567190 24567190 single base substitution C T exon_variant BRCA-US 16 24567190 24567190 single base substitution C T synonymous_variant F162F 486C>T BRCA-US 16 24567190 24567190 single base substitution C T synonymous_variant F29F 87C>T BRCA-US 16 24574557 24574557 single base substitution G T downstream_gene_variant BRCA-US 16 24574557 24574557 single base substitution G T exon_variant BRCA-US 16 24574557 24574557 single base substitution G T intron_variant BRCA-US 16 24574557 24574557 single base substitution G T missense_variant A310S 928G>T BRCA-US 16 24574557 24574557 single base substitution G T missense_variant A443S 1327G>T BRCA-US 16 24574557 24574557 single base substitution G T upstream_gene_variant BRCA-US 16 24574618 24574618 single base substitution T A downstream_gene_variant BRCA-US 16 24574618 24574618 single base substitution T A exon_variant BRCA-US 16 24574618 24574618 single base substitution T A intron_variant BRCA-US 16 24574618 24574618 single base substitution T A splice_donor_variant BRCA-US 16 24578496 24578496 single base substitution G C exon_variant BRCA-US 16 24578496 24578496 single base substitution G C intron_variant BRCA-US 16 24578496 24578496 single base substitution G C missense_variant R408T 1223G>C BRCA-US 16 24578496 24578496 single base substitution G C missense_variant R541T 1622G>C BRCA-US 16 24578776 24578776 single base substitution A C downstream_gene_variant BRCA-US 16 24578776 24578776 single base substitution A C exon_variant BRCA-US 16 24578776 24578776 single base substitution A C intron_variant BRCA-US 16 24578776 24578776 single base substitution A C synonymous_variant P501P 1503A>C BRCA-US 16 24578776 24578776 single base substitution A C synonymous_variant P634P 1902A>C BRCA-US 16 24578810 24578810 single base substitution C T downstream_gene_variant BRCA-US 16 24578810 24578810 single base substitution C T exon_variant BRCA-US 16 24578810 24578810 single base substitution C T intron_variant BRCA-US 16 24578810 24578810 single base substitution C T stop_gained R513* 1537C>T BRCA-US 16 24578810 24578810 single base substitution C T stop_gained R646* 1936C>T BRCA-US 16 24579150 24579150 single base substitution G A downstream_gene_variant BRCA-US 16 24579150 24579150 single base substitution G A intron_variant BRCA-US 16 24579150 24579150 single base substitution G A missense_variant D531N 1591G>A BRCA-US 16 24579150 24579150 single base substitution G A missense_variant D664N 1990G>A BRCA-US 16 24581109 24581109 single base substitution A G downstream_gene_variant BRCA-US 16 24581109 24581109 single base substitution A G exon_variant BRCA-US 16 24581109 24581109 single base substitution A G intron_variant BRCA-US 16 24581109 24581109 single base substitution A G missense_variant N1033S 3098A>G BRCA-US 16 24581109 24581109 single base substitution A G missense_variant N900S 2699A>G BRCA-US 16 24581109 24581109 single base substitution A G missense_variant N999S 2996A>G BRCA-US 16 24581246 24581246 single base substitution C G downstream_gene_variant BRCA-US 16 24581246 24581246 single base substitution C G exon_variant BRCA-US 16 24581246 24581246 single base substitution C G intron_variant BRCA-US 16 24581246 24581246 single base substitution C G missense_variant Q1045E 3133C>G BRCA-US 16 24581246 24581246 single base substitution C G missense_variant Q1079E 3235C>G BRCA-US 16 24581246 24581246 single base substitution C G missense_variant Q946E 2836C>G BRCA-US 16 24582488 24582488 single base substitution T G downstream_gene_variant BRCA-US 16 24582488 24582488 single base substitution T G exon_variant BRCA-US 16 24582488 24582488 single base substitution T G missense_variant S1333R 3999T>G BRCA-US 16 24582488 24582488 single base substitution T G missense_variant S1367R 4101T>G BRCA-US 16 24582488 24582488 single base substitution T G missense_variant S527R 1581T>G BRCA-US 16 24582883 24582883 single base substitution A G downstream_gene_variant BRCA-US 16 24582883 24582883 single base substitution A G exon_variant BRCA-US 16 24582883 24582883 single base substitution A G missense_variant D1465G 4394A>G BRCA-US 16 24582883 24582883 single base substitution A G missense_variant D1499G 4496A>G BRCA-US 16 24582883 24582883 single base substitution A G missense_variant D659G 1976A>G BRCA-US 16 24583718 24583718 single base substitution G T downstream_gene_variant BRCA-US 16 24583718 24583718 single base substitution G T exon_variant BRCA-US 16 24583718 24583718 single base substitution G T missense_variant E1743D 5229G>T BRCA-US 16 24583718 24583718 single base substitution G T missense_variant E1777D 5331G>T BRCA-US 16 24583718 24583718 single base substitution G T missense_variant E937D 2811G>T BTCA-JP 16 24564895 24564895 single base substitution A T downstream_gene_variant BTCA-JP 16 24564895 24564895 single base substitution A T intron_variant BTCA-JP 16 24564895 24564895 single base substitution A T upstream_gene_variant BTCA-JP 16 24570800 24570800 single base substitution T A downstream_gene_variant BTCA-JP 16 24570800 24570800 single base substitution T A intron_variant BTCA-JP 16 24570800 24570800 single base substitution T A upstream_gene_variant BTCA-JP 16 24573376 24573376 single base substitution G A downstream_gene_variant BTCA-JP 16 24573376 24573376 single base substitution G A exon_variant BTCA-JP 16 24573376 24573376 single base substitution G A missense_variant A262T 784G>A BTCA-JP 16 24573376 24573376 single base substitution G A missense_variant A395T 1183G>A BTCA-JP 16 24573376 24573376 single base substitution G A upstream_gene_variant BTCA-JP 16 24574508 24574508 single base substitution T A downstream_gene_variant BTCA-JP 16 24574508 24574508 single base substitution T A intron_variant BTCA-JP 16 24574508 24574508 single base substitution T A upstream_gene_variant BTCA-JP 16 24574510 24574510 single base substitution T G downstream_gene_variant BTCA-JP 16 24574510 24574510 single base substitution T G intron_variant BTCA-JP 16 24574510 24574510 single base substitution T G upstream_gene_variant BTCA-JP 16 24580587 24580587 single base substitution A G downstream_gene_variant BTCA-JP 16 24580587 24580587 single base substitution A G exon_variant BTCA-JP 16 24580587 24580587 single base substitution A G intron_variant BTCA-JP 16 24580587 24580587 single base substitution A G missense_variant N726S 2177A>G BTCA-JP 16 24580587 24580587 single base substitution A G missense_variant N825S 2474A>G BTCA-JP 16 24580587 24580587 single base substitution A G missense_variant N859S 2576A>G BTCA-JP 16 24581106 24581106 single base substitution A G downstream_gene_variant BTCA-JP 16 24581106 24581106 single base substitution A G exon_variant BTCA-JP 16 24581106 24581106 single base substitution A G intron_variant BTCA-JP 16 24581106 24581106 single base substitution A G missense_variant E1032G 3095A>G BTCA-JP 16 24581106 24581106 single base substitution A G missense_variant E899G 2696A>G BTCA-JP 16 24581106 24581106 single base substitution A G missense_variant E998G 2993A>G BTCA-JP 16 24583125 24583128 deletion of <=200bp AAAG - downstream_gene_variant BTCA-JP 16 24583125 24583128 deletion of <=200bp AAAG - exon_variant BTCA-JP 16 24583125 24583128 deletion of <=200bp AAAG - frameshift_variant KE1546 BTCA-JP 16 24583125 24583128 deletion of <=200bp AAAG - frameshift_variant KE1580 BTCA-JP 16 24583125 24583128 deletion of <=200bp AAAG - frameshift_variant KE740 CESC-US 16 24557495 24557495 single base substitution G A intron_variant CESC-US 16 24557495 24557495 single base substitution G A missense_variant D60N 178G>A CESC-US 16 24578503 24578503 single base substitution G A exon_variant CESC-US 16 24578503 24578503 single base substitution G A intron_variant CESC-US 16 24578503 24578503 single base substitution G A synonymous_variant Q410Q 1230G>A CESC-US 16 24578503 24578503 single base substitution G A synonymous_variant Q543Q 1629G>A CLLE-ES 16 24544134 24544134 single base substitution G A upstream_gene_variant CLLE-ES 16 24561684 24561684 single base substitution G T downstream_gene_variant CLLE-ES 16 24561684 24561684 single base substitution G T intron_variant CLLE-ES 16 24561684 24561684 single base substitution G T upstream_gene_variant CLLE-ES 16 24577666 24577666 single base substitution G C downstream_gene_variant CLLE-ES 16 24577666 24577666 single base substitution G C intron_variant COAD-US 16 24580197 24580197 single base substitution G A downstream_gene_variant COAD-US 16 24580197 24580197 single base substitution G A exon_variant COAD-US 16 24580197 24580197 single base substitution G A intron_variant COAD-US 16 24580197 24580197 single base substitution G A missense_variant R596Q 1787G>A COAD-US 16 24580197 24580197 single base substitution G A missense_variant R695Q 2084G>A COAD-US 16 24580197 24580197 single base substitution G A missense_variant R729Q 2186G>A COAD-US 16 24581189 24581189 deletion of <=200bp A - downstream_gene_variant COAD-US 16 24581189 24581189 deletion of <=200bp A - exon_variant COAD-US 16 24581189 24581189 deletion of <=200bp A - frameshift_variant K1026 COAD-US 16 24581189 24581189 deletion of <=200bp A - frameshift_variant K1060 COAD-US 16 24581189 24581189 deletion of <=200bp A - frameshift_variant K927 COAD-US 16 24581189 24581189 deletion of <=200bp A - intron_variant COAD-US 16 24581366 24581366 single base substitution A G downstream_gene_variant COAD-US 16 24581366 24581366 single base substitution A G exon_variant COAD-US 16 24581366 24581366 single base substitution A G intron_variant COAD-US 16 24581366 24581366 single base substitution A G missense_variant K1085E 3253A>G COAD-US 16 24581366 24581366 single base substitution A G missense_variant K1119E 3355A>G COAD-US 16 24581366 24581366 single base substitution A G missense_variant K986E 2956A>G COAD-US 16 24581543 24581543 single base substitution C T downstream_gene_variant COAD-US 16 24581543 24581543 single base substitution C T exon_variant COAD-US 16 24581543 24581543 single base substitution C T intron_variant COAD-US 16 24581543 24581543 single base substitution C T missense_variant P1144S 3430C>T COAD-US 16 24581543 24581543 single base substitution C T missense_variant P1178S 3532C>T COAD-US 16 24582525 24582525 single base substitution G A downstream_gene_variant COAD-US 16 24582525 24582525 single base substitution G A exon_variant COAD-US 16 24582525 24582525 single base substitution G A missense_variant V1346M 4036G>A COAD-US 16 24582525 24582525 single base substitution G A missense_variant V1380M 4138G>A COAD-US 16 24582525 24582525 single base substitution G A missense_variant V540M 1618G>A COAD-US 16 24582804 24582804 deletion of <=200bp A - downstream_gene_variant COAD-US 16 24582804 24582804 deletion of <=200bp A - exon_variant COAD-US 16 24582804 24582804 deletion of <=200bp A - frameshift_variant K1439 COAD-US 16 24582804 24582804 deletion of <=200bp A - frameshift_variant K1473 COAD-US 16 24582804 24582804 deletion of <=200bp A - frameshift_variant K633 COCA-CN 16 24551970 24551970 single base substitution T G downstream_gene_variant COCA-CN 16 24551970 24551970 single base substitution T G intron_variant COCA-CN 16 24551970 24551970 single base substitution T G missense_variant F8C 23T>G COCA-CN 16 24566966 24566968 deletion of <=200bp GAA - 5_prime_UTR_variant COCA-CN 16 24566966 24566968 deletion of <=200bp GAA - exon_variant COCA-CN 16 24566966 24566968 deletion of <=200bp GAA - inframe_deletion E127 COCA-CN 16 24566966 24566968 deletion of <=200bp GAA - upstream_gene_variant COCA-CN 16 24566994 24566994 single base substitution C T exon_variant COCA-CN 16 24566994 24566994 single base substitution C T missense_variant S136L 407C>T COCA-CN 16 24566994 24566994 single base substitution C T missense_variant S3L 8C>T COCA-CN 16 24566994 24566994 single base substitution C T upstream_gene_variant COCA-CN 16 24570764 24570764 single base substitution A G downstream_gene_variant COCA-CN 16 24570764 24570764 single base substitution A G intron_variant COCA-CN 16 24570764 24570764 single base substitution A G upstream_gene_variant COCA-CN 16 24576228 24576228 single base substitution T A downstream_gene_variant COCA-CN 16 24576228 24576228 single base substitution T A intron_variant COCA-CN 16 24578602 24578602 single base substitution G T exon_variant COCA-CN 16 24578602 24578602 single base substitution G T intron_variant COCA-CN 16 24578602 24578602 single base substitution G T synonymous_variant P443P 1329G>T COCA-CN 16 24578602 24578602 single base substitution G T synonymous_variant P576P 1728G>T COCA-CN 16 24580026 24580026 single base substitution T C downstream_gene_variant COCA-CN 16 24580026 24580026 single base substitution T C intron_variant COCA-CN 16 24581638 24581638 single base substitution C A downstream_gene_variant COCA-CN 16 24581638 24581638 single base substitution C A exon_variant COCA-CN 16 24581638 24581638 single base substitution C A intron_variant COCA-CN 16 24581638 24581638 single base substitution C A synonymous_variant I1175I 3525C>A COCA-CN 16 24581638 24581638 single base substitution C A synonymous_variant I1209I 3627C>A COCA-CN 16 24582876 24582876 single base substitution C T downstream_gene_variant COCA-CN 16 24582876 24582876 single base substitution C T exon_variant COCA-CN 16 24582876 24582876 single base substitution C T stop_gained R1463* 4387C>T COCA-CN 16 24582876 24582876 single base substitution C T stop_gained R1497* 4489C>T COCA-CN 16 24582876 24582876 single base substitution C T stop_gained R657* 1969C>T COCA-CN 16 24582882 24582882 single base substitution G T downstream_gene_variant COCA-CN 16 24582882 24582882 single base substitution G T exon_variant COCA-CN 16 24582882 24582882 single base substitution G T missense_variant D1465Y 4393G>T COCA-CN 16 24582882 24582882 single base substitution G T missense_variant D1499Y 4495G>T COCA-CN 16 24582882 24582882 single base substitution G T missense_variant D659Y 1975G>T COCA-CN 16 24582988 24582988 single base substitution C A downstream_gene_variant COCA-CN 16 24582988 24582988 single base substitution C A exon_variant COCA-CN 16 24582988 24582988 single base substitution C A missense_variant S1500Y 4499C>A COCA-CN 16 24582988 24582988 single base substitution C A missense_variant S1534Y 4601C>A COCA-CN 16 24582988 24582988 single base substitution C A missense_variant S694Y 2081C>A COCA-CN 16 24585368 24585368 single base substitution C T downstream_gene_variant COCA-CN 16 24585373 24585373 single base substitution A C downstream_gene_variant EOPC-DE 16 24566071 24566071 single base substitution C A exon_variant EOPC-DE 16 24566071 24566071 single base substitution C A intron_variant EOPC-DE 16 24566071 24566071 single base substitution C A upstream_gene_variant EOPC-DE 16 24584671 24584671 single base substitution G A downstream_gene_variant ESAD-UK 16 24545190 24545190 single base substitution G C upstream_gene_variant ESAD-UK 16 24545622 24545622 single base substitution A G upstream_gene_variant ESAD-UK 16 24546020 24546020 single base substitution C A upstream_gene_variant ESAD-UK 16 24546404 24546404 deletion of <=200bp A - upstream_gene_variant ESAD-UK 16 24548705 24548705 single base substitution T A upstream_gene_variant ESAD-UK 16 24548706 24548706 single base substitution A T upstream_gene_variant ESAD-UK 16 24550889 24550889 single base substitution A C 5_prime_UTR_variant ESAD-UK 16 24550889 24550889 single base substitution A C intron_variant ESAD-UK 16 24550889 24550889 single base substitution A C upstream_gene_variant ESAD-UK 16 24557620 24557620 deletion of <=200bp T - intron_variant ESAD-UK 16 24559564 24559564 single base substitution C T intron_variant ESAD-UK 16 24562922 24562922 single base substitution A G downstream_gene_variant ESAD-UK 16 24562922 24562922 single base substitution A G intron_variant ESAD-UK 16 24562922 24562922 single base substitution A G upstream_gene_variant ESAD-UK 16 24564476 24564476 single base substitution G T downstream_gene_variant ESAD-UK 16 24564476 24564476 single base substitution G T intron_variant ESAD-UK 16 24564476 24564476 single base substitution G T upstream_gene_variant ESAD-UK 16 24566095 24566095 single base substitution T G exon_variant ESAD-UK 16 24566095 24566095 single base substitution T G intron_variant ESAD-UK 16 24566095 24566095 single base substitution T G upstream_gene_variant ESAD-UK 16 24567596 24567596 single base substitution C G downstream_gene_variant ESAD-UK 16 24567596 24567596 single base substitution C G intron_variant ESAD-UK 16 24568476 24568476 single base substitution C T downstream_gene_variant ESAD-UK 16 24568476 24568476 single base substitution C T intron_variant ESAD-UK 16 24570516 24570516 single base substitution A G downstream_gene_variant ESAD-UK 16 24570516 24570516 single base substitution A G intron_variant ESAD-UK 16 24570516 24570516 single base substitution A G upstream_gene_variant ESAD-UK 16 24571716 24571716 single base substitution C T downstream_gene_variant ESAD-UK 16 24571716 24571716 single base substitution C T intron_variant ESAD-UK 16 24571716 24571716 single base substitution C T upstream_gene_variant ESAD-UK 16 24574280 24574280 single base substitution A G downstream_gene_variant ESAD-UK 16 24574280 24574280 single base substitution A G intron_variant ESAD-UK 16 24574280 24574280 single base substitution A G upstream_gene_variant ESAD-UK 16 24575582 24575582 single base substitution A T downstream_gene_variant ESAD-UK 16 24575582 24575582 single base substitution A T intron_variant ESAD-UK 16 24575895 24575895 single base substitution G C downstream_gene_variant ESAD-UK 16 24575895 24575895 single base substitution G C intron_variant ESAD-UK 16 24576866 24576866 single base substitution C T downstream_gene_variant ESAD-UK 16 24576866 24576866 single base substitution C T intron_variant ESAD-UK 16 24577772 24577772 single base substitution T G downstream_gene_variant ESAD-UK 16 24577772 24577772 single base substitution T G intron_variant ESAD-UK 16 24578253 24578253 single base substitution T C intron_variant ESAD-UK 16 24581477 24581477 single base substitution G A downstream_gene_variant ESAD-UK 16 24581477 24581477 single base substitution G A exon_variant ESAD-UK 16 24581477 24581477 single base substitution G A intron_variant ESAD-UK 16 24581477 24581477 single base substitution G A missense_variant V1122I 3364G>A ESAD-UK 16 24581477 24581477 single base substitution G A missense_variant V1156I 3466G>A ESAD-UK 16 24582271 24582271 single base substitution C T downstream_gene_variant ESAD-UK 16 24582271 24582271 single base substitution C T exon_variant ESAD-UK 16 24582271 24582271 single base substitution C T missense_variant T1261M 3782C>T ESAD-UK 16 24582271 24582271 single base substitution C T missense_variant T1295M 3884C>T ESAD-UK 16 24582271 24582271 single base substitution C T missense_variant T455M 1364C>T ESAD-UK 16 24582497 24582497 single base substitution C T downstream_gene_variant ESAD-UK 16 24582497 24582497 single base substitution C T exon_variant ESAD-UK 16 24582497 24582497 single base substitution C T synonymous_variant S1336S 4008C>T ESAD-UK 16 24582497 24582497 single base substitution C T synonymous_variant S1370S 4110C>T ESAD-UK 16 24582497 24582497 single base substitution C T synonymous_variant S530S 1590C>T ESAD-UK 16 24583639 24583639 single base substitution C T downstream_gene_variant ESAD-UK 16 24583639 24583639 single base substitution C T exon_variant ESAD-UK 16 24583639 24583639 single base substitution C T missense_variant A1717V 5150C>T ESAD-UK 16 24583639 24583639 single base substitution C T missense_variant A1751V 5252C>T ESAD-UK 16 24583639 24583639 single base substitution C T missense_variant A911V 2732C>T ESAD-UK 16 24584626 24584626 single base substitution C T downstream_gene_variant ESCA-CN 16 24574718 24574718 single base substitution C T downstream_gene_variant ESCA-CN 16 24574718 24574718 single base substitution C T exon_variant ESCA-CN 16 24574718 24574718 single base substitution C T intron_variant GBM-US 16 24552109 24552109 single base substitution A G downstream_gene_variant GBM-US 16 24552109 24552109 single base substitution A G intron_variant GBM-US 16 24552109 24552109 single base substitution A G synonymous_variant K54K 162A>G GBM-US 16 24581488 24581489 deletion of <=200bp TT - downstream_gene_variant GBM-US 16 24581488 24581489 deletion of <=200bp TT - exon_variant GBM-US 16 24581488 24581489 deletion of <=200bp TT - frameshift_variant DF1125 GBM-US 16 24581488 24581489 deletion of <=200bp TT - frameshift_variant DF1159 GBM-US 16 24581488 24581489 deletion of <=200bp TT - intron_variant GBM-US 16 24582927 24582927 single base substitution A C downstream_gene_variant GBM-US 16 24582927 24582927 single base substitution A C exon_variant GBM-US 16 24582927 24582927 single base substitution A C missense_variant K1480Q 4438A>C GBM-US 16 24582927 24582927 single base substitution A C missense_variant K1514Q 4540A>C GBM-US 16 24582927 24582927 single base substitution A C missense_variant K674Q 2020A>C GBM-US 16 24583037 24583037 single base substitution T C downstream_gene_variant GBM-US 16 24583037 24583037 single base substitution T C exon_variant GBM-US 16 24583037 24583037 single base substitution T C synonymous_variant D1516D 4548T>C GBM-US 16 24583037 24583037 single base substitution T C synonymous_variant D1550D 4650T>C GBM-US 16 24583037 24583037 single base substitution T C synonymous_variant D710D 2130T>C KIRC-US 16 24551961 24551961 insertion of <=200bp - T downstream_gene_variant KIRC-US 16 24551961 24551961 insertion of <=200bp - T frameshift_variant H5L? KIRC-US 16 24551961 24551961 insertion of <=200bp - T intron_variant KIRC-US 16 24573318 24573318 single base substitution T G downstream_gene_variant KIRC-US 16 24573318 24573318 single base substitution T G exon_variant KIRC-US 16 24573318 24573318 single base substitution T G synonymous_variant S242S 726T>G KIRC-US 16 24573318 24573318 single base substitution T G synonymous_variant S375S 1125T>G KIRC-US 16 24573318 24573318 single base substitution T G upstream_gene_variant KIRC-US 16 24580912 24580912 single base substitution A G downstream_gene_variant KIRC-US 16 24580912 24580912 single base substitution A G exon_variant KIRC-US 16 24580912 24580912 single base substitution A G intron_variant KIRC-US 16 24580912 24580912 single base substitution A G synonymous_variant E834E 2502A>G KIRC-US 16 24580912 24580912 single base substitution A G synonymous_variant E933E 2799A>G KIRC-US 16 24580912 24580912 single base substitution A G synonymous_variant E967E 2901A>G KIRC-US 16 24581248 24581248 single base substitution G C downstream_gene_variant KIRC-US 16 24581248 24581248 single base substitution G C exon_variant KIRC-US 16 24581248 24581248 single base substitution G C intron_variant KIRC-US 16 24581248 24581248 single base substitution G C missense_variant Q1045H 3135G>C KIRC-US 16 24581248 24581248 single base substitution G C missense_variant Q1079H 3237G>C KIRC-US 16 24581248 24581248 single base substitution G C missense_variant Q946H 2838G>C KIRC-US 16 24581249 24581249 single base substitution A T downstream_gene_variant KIRC-US 16 24581249 24581249 single base substitution A T exon_variant KIRC-US 16 24581249 24581249 single base substitution A T intron_variant KIRC-US 16 24581249 24581249 single base substitution A T stop_gained K1046* 3136A>T KIRC-US 16 24581249 24581249 single base substitution A T stop_gained K1080* 3238A>T KIRC-US 16 24581249 24581249 single base substitution A T stop_gained K947* 2839A>T KIRC-US 16 24583192 24583192 single base substitution A G downstream_gene_variant KIRC-US 16 24583192 24583192 single base substitution A G exon_variant KIRC-US 16 24583192 24583192 single base substitution A G missense_variant Q1568R 4703A>G KIRC-US 16 24583192 24583192 single base substitution A G missense_variant Q1602R 4805A>G KIRC-US 16 24583192 24583192 single base substitution A G missense_variant Q762R 2285A>G KIRC-US 16 24583718 24583718 single base substitution G T downstream_gene_variant KIRC-US 16 24583718 24583718 single base substitution G T exon_variant KIRC-US 16 24583718 24583718 single base substitution G T missense_variant E1743D 5229G>T KIRC-US 16 24583718 24583718 single base substitution G T missense_variant E1777D 5331G>T KIRC-US 16 24583718 24583718 single base substitution G T missense_variant E937D 2811G>T KIRP-US 16 24581079 24581079 single base substitution A T downstream_gene_variant KIRP-US 16 24581079 24581079 single base substitution A T exon_variant KIRP-US 16 24581079 24581079 single base substitution A T intron_variant KIRP-US 16 24581079 24581079 single base substitution A T missense_variant N1023I 3068A>T KIRP-US 16 24581079 24581079 single base substitution A T missense_variant N890I 2669A>T KIRP-US 16 24581079 24581079 single base substitution A T missense_variant N989I 2966A>T KIRP-US 16 24581493 24581493 single base substitution A T downstream_gene_variant KIRP-US 16 24581493 24581493 single base substitution A T exon_variant KIRP-US 16 24581493 24581493 single base substitution A T intron_variant KIRP-US 16 24581493 24581493 single base substitution A T missense_variant E1127V 3380A>T KIRP-US 16 24581493 24581493 single base substitution A T missense_variant E1161V 3482A>T KIRP-US 16 24582258 24582258 single base substitution A C downstream_gene_variant KIRP-US 16 24582258 24582258 single base substitution A C exon_variant KIRP-US 16 24582258 24582258 single base substitution A C missense_variant T1257P 3769A>C KIRP-US 16 24582258 24582258 single base substitution A C missense_variant T1291P 3871A>C KIRP-US 16 24582258 24582258 single base substitution A C missense_variant T451P 1351A>C KIRP-US 16 24582943 24582943 single base substitution G C downstream_gene_variant KIRP-US 16 24582943 24582943 single base substitution G C exon_variant KIRP-US 16 24582943 24582943 single base substitution G C missense_variant R1485T 4454G>C KIRP-US 16 24582943 24582943 single base substitution G C missense_variant R1519T 4556G>C KIRP-US 16 24582943 24582943 single base substitution G C missense_variant R679T 2036G>C LAML-KR 16 24574714 24574714 single base substitution A T downstream_gene_variant LAML-KR 16 24574714 24574714 single base substitution A T exon_variant LAML-KR 16 24574714 24574714 single base substitution A T intron_variant LAML-KR 16 24585368 24585368 single base substitution C T downstream_gene_variant LAML-KR 16 24586107 24586107 single base substitution G A downstream_gene_variant LAML-KR 16 24586108 24586108 single base substitution C A downstream_gene_variant LAML-KR 16 24587120 24587120 single base substitution A G downstream_gene_variant LGG-US 16 24567746 24567746 insertion of <=200bp - A downstream_gene_variant LGG-US 16 24567746 24567746 insertion of <=200bp - A exon_variant LGG-US 16 24567746 24567746 insertion of <=200bp - A frameshift_variant Y218I? LGG-US 16 24567746 24567746 insertion of <=200bp - A frameshift_variant Y85I? LGG-US 16 24581321 24581321 deletion of <=200bp C - downstream_gene_variant LGG-US 16 24581321 24581321 deletion of <=200bp C - exon_variant LGG-US 16 24581321 24581321 deletion of <=200bp C - frameshift_variant P1070 LGG-US 16 24581321 24581321 deletion of <=200bp C - frameshift_variant P1104 LGG-US 16 24581321 24581321 deletion of <=200bp C - frameshift_variant P971 LGG-US 16 24581321 24581321 deletion of <=200bp C - intron_variant LICA-CN 16 24578568 24578568 single base substitution A T exon_variant LICA-CN 16 24578568 24578568 single base substitution A T intron_variant LICA-CN 16 24578568 24578568 single base substitution A T missense_variant Y432F 1295A>T LICA-CN 16 24578568 24578568 single base substitution A T missense_variant Y565F 1694A>T LICA-FR 16 24551954 24551954 single base substitution T C downstream_gene_variant LICA-FR 16 24551954 24551954 single base substitution T C intron_variant LICA-FR 16 24551954 24551954 single base substitution T C missense_variant C3R 7T>C LICA-FR 16 24564837 24564837 single base substitution G A 5_prime_UTR_variant LICA-FR 16 24564837 24564837 single base substitution G A downstream_gene_variant LICA-FR 16 24564837 24564837 single base substitution G A exon_variant LICA-FR 16 24564837 24564837 single base substitution G A missense_variant D103N 307G>A LICA-FR 16 24564837 24564837 single base substitution G A upstream_gene_variant LICA-FR 16 24568317 24568317 insertion of <=200bp - TT downstream_gene_variant LICA-FR 16 24568317 24568317 insertion of <=200bp - TT intron_variant LICA-FR 16 24574714 24574714 single base substitution A T downstream_gene_variant LICA-FR 16 24574714 24574714 single base substitution A T exon_variant LICA-FR 16 24574714 24574714 single base substitution A T intron_variant LICA-FR 16 24575611 24575611 single base substitution A T downstream_gene_variant LICA-FR 16 24575611 24575611 single base substitution A T intron_variant LICA-FR 16 24575890 24575890 single base substitution A G downstream_gene_variant LICA-FR 16 24575890 24575890 single base substitution A G intron_variant LICA-FR 16 24582445 24582445 single base substitution G T downstream_gene_variant LICA-FR 16 24582445 24582445 single base substitution G T exon_variant LICA-FR 16 24582445 24582445 single base substitution G T missense_variant S1319I 3956G>T LICA-FR 16 24582445 24582445 single base substitution G T missense_variant S1353I 4058G>T LICA-FR 16 24582445 24582445 single base substitution G T missense_variant S513I 1538G>T LICA-FR 16 24582634 24582634 single base substitution C G downstream_gene_variant LICA-FR 16 24582634 24582634 single base substitution C G exon_variant LICA-FR 16 24582634 24582634 single base substitution C G missense_variant P1382R 4145C>G LICA-FR 16 24582634 24582634 single base substitution C G missense_variant P1416R 4247C>G LICA-FR 16 24582634 24582634 single base substitution C G missense_variant P576R 1727C>G LICA-FR 16 24585813 24585813 single base substitution C A downstream_gene_variant LIHC-US 16 24579152 24579152 single base substitution T G downstream_gene_variant LIHC-US 16 24579152 24579152 single base substitution T G intron_variant LIHC-US 16 24579152 24579152 single base substitution T G missense_variant D531E 1593T>G LIHC-US 16 24579152 24579152 single base substitution T G missense_variant D664E 1992T>G LIHC-US 16 24583179 24583179 insertion of <=200bp - T downstream_gene_variant LIHC-US 16 24583179 24583179 insertion of <=200bp - T exon_variant LIHC-US 16 24583179 24583179 insertion of <=200bp - T frameshift_variant V1564C? LIHC-US 16 24583179 24583179 insertion of <=200bp - T frameshift_variant V1598C? LIHC-US 16 24583179 24583179 insertion of <=200bp - T frameshift_variant V758C? LINC-JP 16 24551697 24551697 single base substitution C T 5_prime_UTR_variant LINC-JP 16 24551697 24551697 single base substitution C T downstream_gene_variant LINC-JP 16 24551697 24551697 single base substitution C T intron_variant LINC-JP 16 24551697 24551697 single base substitution C T upstream_gene_variant LINC-JP 16 24559355 24559355 deletion of <=200bp T - intron_variant LINC-JP 16 24560101 24560101 single base substitution A G intron_variant LINC-JP 16 24560101 24560101 single base substitution A G upstream_gene_variant LINC-JP 16 24573706 24573706 single base substitution G A downstream_gene_variant LINC-JP 16 24573706 24573706 single base substitution G A intron_variant LINC-JP 16 24573706 24573706 single base substitution G A upstream_gene_variant LINC-JP 16 24575979 24575979 single base substitution C T downstream_gene_variant LINC-JP 16 24575979 24575979 single base substitution C T intron_variant LINC-JP 16 24581229 24581229 single base substitution A T downstream_gene_variant LINC-JP 16 24581229 24581229 single base substitution A T exon_variant LINC-JP 16 24581229 24581229 single base substitution A T intron_variant LINC-JP 16 24581229 24581229 single base substitution A T missense_variant K1039I 3116A>T LINC-JP 16 24581229 24581229 single base substitution A T missense_variant K1073I 3218A>T LINC-JP 16 24581229 24581229 single base substitution A T missense_variant K940I 2819A>T LIRI-JP 16 24544473 24544473 single base substitution G T upstream_gene_variant LIRI-JP 16 24544871 24544871 single base substitution A G upstream_gene_variant LIRI-JP 16 24545224 24545224 single base substitution G C upstream_gene_variant LIRI-JP 16 24547034 24547034 single base substitution T C upstream_gene_variant LIRI-JP 16 24547159 24547159 single base substitution T C upstream_gene_variant LIRI-JP 16 24548073 24548073 single base substitution C A upstream_gene_variant LIRI-JP 16 24548287 24548287 single base substitution C T upstream_gene_variant LIRI-JP 16 24548640 24548640 single base substitution A G upstream_gene_variant LIRI-JP 16 24549548 24549548 single base substitution A G intron_variant LIRI-JP 16 24549548 24549548 single base substitution A G upstream_gene_variant LIRI-JP 16 24551107 24551107 single base substitution A T exon_variant LIRI-JP 16 24551107 24551107 single base substitution A T intron_variant LIRI-JP 16 24551107 24551107 single base substitution A T upstream_gene_variant LIRI-JP 16 24554665 24554665 single base substitution C T downstream_gene_variant LIRI-JP 16 24554665 24554665 single base substitution C T intron_variant LIRI-JP 16 24556083 24556083 single base substitution C T downstream_gene_variant LIRI-JP 16 24556083 24556083 single base substitution C T intron_variant LIRI-JP 16 24557288 24557288 single base substitution T G intron_variant LIRI-JP 16 24557392 24557392 insertion of <=200bp - T intron_variant LIRI-JP 16 24557917 24557917 single base substitution A G intron_variant LIRI-JP 16 24559720 24559720 single base substitution T G intron_variant LIRI-JP 16 24559720 24559720 single base substitution T G upstream_gene_variant LIRI-JP 16 24560161 24560161 single base substitution A G intron_variant LIRI-JP 16 24560161 24560161 single base substitution A G upstream_gene_variant LIRI-JP 16 24561390 24561390 single base substitution G C downstream_gene_variant LIRI-JP 16 24561390 24561390 single base substitution G C intron_variant LIRI-JP 16 24561390 24561390 single base substitution G C upstream_gene_variant LIRI-JP 16 24562349 24562349 single base substitution A C downstream_gene_variant LIRI-JP 16 24562349 24562349 single base substitution A C intron_variant LIRI-JP 16 24562349 24562349 single base substitution A C upstream_gene_variant LIRI-JP 16 24563604 24563604 single base substitution A G downstream_gene_variant LIRI-JP 16 24563604 24563604 single base substitution A G intron_variant LIRI-JP 16 24563604 24563604 single base substitution A G upstream_gene_variant LIRI-JP 16 24565437 24565437 single base substitution T G downstream_gene_variant LIRI-JP 16 24565437 24565437 single base substitution T G intron_variant LIRI-JP 16 24565437 24565437 single base substitution T G upstream_gene_variant LIRI-JP 16 24566652 24566652 single base substitution C G exon_variant LIRI-JP 16 24566652 24566652 single base substitution C G intron_variant LIRI-JP 16 24566652 24566652 single base substitution C G upstream_gene_variant LIRI-JP 16 24571282 24571282 single base substitution T A downstream_gene_variant LIRI-JP 16 24571282 24571282 single base substitution T A intron_variant LIRI-JP 16 24571282 24571282 single base substitution T A upstream_gene_variant LIRI-JP 16 24571717 24571717 single base substitution G A downstream_gene_variant LIRI-JP 16 24571717 24571717 single base substitution G A intron_variant LIRI-JP 16 24571717 24571717 single base substitution G A upstream_gene_variant LIRI-JP 16 24575186 24575186 single base substitution A T downstream_gene_variant LIRI-JP 16 24575186 24575186 single base substitution A T intron_variant LIRI-JP 16 24575379 24575379 single base substitution T C downstream_gene_variant LIRI-JP 16 24575379 24575379 single base substitution T C intron_variant LIRI-JP 16 24576336 24576336 single base substitution A C downstream_gene_variant LIRI-JP 16 24576336 24576336 single base substitution A C intron_variant LIRI-JP 16 24576534 24576534 single base substitution T C downstream_gene_variant LIRI-JP 16 24576534 24576534 single base substitution T C intron_variant LIRI-JP 16 24578531 24578531 single base substitution A G exon_variant LIRI-JP 16 24578531 24578531 single base substitution A G intron_variant LIRI-JP 16 24578531 24578531 single base substitution A G missense_variant T420A 1258A>G LIRI-JP 16 24578531 24578531 single base substitution A G missense_variant T553A 1657A>G LIRI-JP 16 24578963 24578963 single base substitution A G downstream_gene_variant LIRI-JP 16 24578963 24578963 single base substitution A G intron_variant LIRI-JP 16 24579693 24579693 single base substitution G A downstream_gene_variant LIRI-JP 16 24579693 24579693 single base substitution G A intron_variant LIRI-JP 16 24581282 24581282 single base substitution G A downstream_gene_variant LIRI-JP 16 24581282 24581282 single base substitution G A exon_variant LIRI-JP 16 24581282 24581282 single base substitution G A intron_variant LIRI-JP 16 24581282 24581282 single base substitution G A missense_variant A1057T 3169G>A LIRI-JP 16 24581282 24581282 single base substitution G A missense_variant A1091T 3271G>A LIRI-JP 16 24581282 24581282 single base substitution G A missense_variant A958T 2872G>A LIRI-JP 16 24581919 24581919 single base substitution A G downstream_gene_variant LIRI-JP 16 24581919 24581919 single base substitution A G intron_variant LIRI-JP 16 24582267 24582267 single base substitution A G downstream_gene_variant LIRI-JP 16 24582267 24582267 single base substitution A G exon_variant LIRI-JP 16 24582267 24582267 single base substitution A G missense_variant K1260E 3778A>G LIRI-JP 16 24582267 24582267 single base substitution A G missense_variant K1294E 3880A>G LIRI-JP 16 24582267 24582267 single base substitution A G missense_variant K454E 1360A>G LIRI-JP 16 24582719 24582719 single base substitution T G downstream_gene_variant LIRI-JP 16 24582719 24582719 single base substitution T G exon_variant LIRI-JP 16 24582719 24582719 single base substitution T G synonymous_variant S1410S 4230T>G LIRI-JP 16 24582719 24582719 single base substitution T G synonymous_variant S1444S 4332T>G LIRI-JP 16 24582719 24582719 single base substitution T G synonymous_variant S604S 1812T>G LIRI-JP 16 24582994 24582994 single base substitution C T downstream_gene_variant LIRI-JP 16 24582994 24582994 single base substitution C T exon_variant LIRI-JP 16 24582994 24582994 single base substitution C T missense_variant P1502L 4505C>T LIRI-JP 16 24582994 24582994 single base substitution C T missense_variant P1536L 4607C>T LIRI-JP 16 24582994 24582994 single base substitution C T missense_variant P696L 2087C>T LIRI-JP 16 24583247 24583247 single base substitution T A downstream_gene_variant LIRI-JP 16 24583247 24583247 single base substitution T A exon_variant LIRI-JP 16 24583247 24583247 single base substitution T A missense_variant H1586Q 4758T>A LIRI-JP 16 24583247 24583247 single base substitution T A missense_variant H1620Q 4860T>A LIRI-JP 16 24583247 24583247 single base substitution T A missense_variant H780Q 2340T>A LIRI-JP 16 24583521 24583521 single base substitution C G downstream_gene_variant LIRI-JP 16 24583521 24583521 single base substitution C G exon_variant LIRI-JP 16 24583521 24583521 single base substitution C G missense_variant R1678G 5032C>G LIRI-JP 16 24583521 24583521 single base substitution C G missense_variant R1712G 5134C>G LIRI-JP 16 24583521 24583521 single base substitution C G missense_variant R872G 2614C>G LIRI-JP 16 24584093 24584093 single base substitution C A 3_prime_UTR_variant LIRI-JP 16 24584093 24584093 single base substitution C A downstream_gene_variant LIRI-JP 16 24584093 24584093 single base substitution C A exon_variant LIRI-JP 16 24584201 24584201 single base substitution T C downstream_gene_variant LIRI-JP 16 24584368 24584368 single base substitution G A downstream_gene_variant LUSC-KR 16 24544097 24544097 single base substitution C A upstream_gene_variant LUSC-KR 16 24544341 24544341 single base substitution G A upstream_gene_variant LUSC-KR 16 24544404 24544404 single base substitution G T upstream_gene_variant LUSC-KR 16 24546241 24546241 single base substitution A G upstream_gene_variant LUSC-KR 16 24548006 24548006 single base substitution C T upstream_gene_variant LUSC-KR 16 24552104 24552104 single base substitution A G downstream_gene_variant LUSC-KR 16 24552104 24552104 single base substitution A G intron_variant LUSC-KR 16 24552104 24552104 single base substitution A G missense_variant T53A 157A>G LUSC-KR 16 24552711 24552711 single base substitution C A downstream_gene_variant LUSC-KR 16 24552711 24552711 single base substitution C A intron_variant LUSC-KR 16 24553792 24553792 single base substitution T C downstream_gene_variant LUSC-KR 16 24553792 24553792 single base substitution T C intron_variant LUSC-KR 16 24563747 24563747 single base substitution G A downstream_gene_variant LUSC-KR 16 24563747 24563747 single base substitution G A intron_variant LUSC-KR 16 24563747 24563747 single base substitution G A upstream_gene_variant LUSC-KR 16 24567320 24567320 single base substitution A G downstream_gene_variant LUSC-KR 16 24567320 24567320 single base substitution A G intron_variant LUSC-KR 16 24567818 24567818 single base substitution G A downstream_gene_variant LUSC-KR 16 24567818 24567818 single base substitution G A intron_variant LUSC-KR 16 24570757 24570757 single base substitution T C downstream_gene_variant LUSC-KR 16 24570757 24570757 single base substitution T C intron_variant LUSC-KR 16 24570757 24570757 single base substitution T C upstream_gene_variant LUSC-KR 16 24581876 24581876 single base substitution G T downstream_gene_variant LUSC-KR 16 24581876 24581876 single base substitution G T intron_variant LUSC-KR 16 24582057 24582057 single base substitution C A downstream_gene_variant LUSC-KR 16 24582057 24582057 single base substitution C A intron_variant LUSC-KR 16 24583211 24583211 single base substitution C A downstream_gene_variant LUSC-KR 16 24583211 24583211 single base substitution C A exon_variant LUSC-KR 16 24583211 24583211 single base substitution C A missense_variant D1574E 4722C>A LUSC-KR 16 24583211 24583211 single base substitution C A missense_variant D1608E 4824C>A LUSC-KR 16 24583211 24583211 single base substitution C A missense_variant D768E 2304C>A LUSC-KR 16 24583765 24583765 single base substitution A G downstream_gene_variant LUSC-KR 16 24583765 24583765 single base substitution A G exon_variant LUSC-KR 16 24583765 24583765 single base substitution A G stop_retained_variant *1759* 5276A>G LUSC-KR 16 24583765 24583765 single base substitution A G stop_retained_variant *1793* 5378A>G LUSC-KR 16 24583765 24583765 single base substitution A G stop_retained_variant *953* 2858A>G LUSC-KR 16 24585368 24585368 single base substitution C T downstream_gene_variant LUSC-KR 16 24585577 24585577 single base substitution C T downstream_gene_variant LUSC-KR 16 24585885 24585885 single base substitution T C downstream_gene_variant LUSC-KR 16 24586002 24586002 single base substitution T C downstream_gene_variant LUSC-KR 16 24586985 24586985 single base substitution G A downstream_gene_variant LUSC-KR 16 24587120 24587120 single base substitution A G downstream_gene_variant LUSC-KR 16 24588005 24588005 single base substitution C G downstream_gene_variant LUSC-KR 16 24588957 24588957 single base substitution C A downstream_gene_variant LUSC-US 16 24567164 24567164 single base substitution C T exon_variant LUSC-US 16 24567164 24567164 single base substitution C T missense_variant P154S 460C>T LUSC-US 16 24567164 24567164 single base substitution C T missense_variant P21S 61C>T LUSC-US 16 24581518 24581518 single base substitution A T downstream_gene_variant LUSC-US 16 24581518 24581518 single base substitution A T exon_variant LUSC-US 16 24581518 24581518 single base substitution A T intron_variant LUSC-US 16 24581518 24581518 single base substitution A T missense_variant K1135N 3405A>T LUSC-US 16 24581518 24581518 single base substitution A T missense_variant K1169N 3507A>T LUSC-US 16 24582460 24582460 single base substitution A G downstream_gene_variant LUSC-US 16 24582460 24582460 single base substitution A G exon_variant LUSC-US 16 24582460 24582460 single base substitution A G missense_variant N1324S 3971A>G LUSC-US 16 24582460 24582460 single base substitution A G missense_variant N1358S 4073A>G LUSC-US 16 24582460 24582460 single base substitution A G missense_variant N518S 1553A>G LUSC-US 16 24582687 24582687 single base substitution C G downstream_gene_variant LUSC-US 16 24582687 24582687 single base substitution C G exon_variant LUSC-US 16 24582687 24582687 single base substitution C G missense_variant L1400V 4198C>G LUSC-US 16 24582687 24582687 single base substitution C G missense_variant L1434V 4300C>G LUSC-US 16 24582687 24582687 single base substitution C G missense_variant L594V 1780C>G LUSC-US 16 24583481 24583481 single base substitution C G downstream_gene_variant LUSC-US 16 24583481 24583481 single base substitution C G exon_variant LUSC-US 16 24583481 24583481 single base substitution C G synonymous_variant V1664V 4992C>G LUSC-US 16 24583481 24583481 single base substitution C G synonymous_variant V1698V 5094C>G LUSC-US 16 24583481 24583481 single base substitution C G synonymous_variant V858V 2574C>G MALY-DE 16 24546412 24546412 single base substitution T A upstream_gene_variant MALY-DE 16 24557573 24557573 single base substitution A T intron_variant MALY-DE 16 24557573 24557573 single base substitution A T missense_variant T86S 256A>T MALY-DE 16 24560937 24560937 single base substitution T G downstream_gene_variant MALY-DE 16 24560937 24560937 single base substitution T G intron_variant MALY-DE 16 24560937 24560937 single base substitution T G upstream_gene_variant MALY-DE 16 24574456 24574456 single base substitution T A downstream_gene_variant MALY-DE 16 24574456 24574456 single base substitution T A intron_variant MALY-DE 16 24574456 24574456 single base substitution T A upstream_gene_variant MALY-DE 16 24574595 24574595 single base substitution T A downstream_gene_variant MALY-DE 16 24574595 24574595 single base substitution T A exon_variant MALY-DE 16 24574595 24574595 single base substitution T A intron_variant MALY-DE 16 24574595 24574595 single base substitution T A synonymous_variant I322I 966T>A MALY-DE 16 24574595 24574595 single base substitution T A synonymous_variant I455I 1365T>A MALY-DE 16 24574595 24574595 single base substitution T A upstream_gene_variant MALY-DE 16 24584763 24584763 single base substitution G A downstream_gene_variant MALY-DE 16 24586800 24586800 deletion of <=200bp C - downstream_gene_variant MALY-DE 16 24588888 24588888 single base substitution T A downstream_gene_variant MELA-AU 16 24544189 24544189 single base substitution C T upstream_gene_variant MELA-AU 16 24544194 24544194 single base substitution G A upstream_gene_variant MELA-AU 16 24544269 24544269 single base substitution G A upstream_gene_variant MELA-AU 16 24544332 24544332 single base substitution G A upstream_gene_variant MELA-AU 16 24544393 24544393 single base substitution C T upstream_gene_variant MELA-AU 16 24544409 24544409 single base substitution C T upstream_gene_variant MELA-AU 16 24544696 24544696 single base substitution G A upstream_gene_variant MELA-AU 16 24545311 24545311 single base substitution T G upstream_gene_variant MELA-AU 16 24546118 24546118 single base substitution G A upstream_gene_variant MELA-AU 16 24546363 24546363 single base substitution C T upstream_gene_variant MELA-AU 16 24546710 24546710 single base substitution C T upstream_gene_variant MELA-AU 16 24546770 24546770 single base substitution G A upstream_gene_variant MELA-AU 16 24546911 24546911 single base substitution G A upstream_gene_variant MELA-AU 16 24547635 24547635 single base substitution C T upstream_gene_variant MELA-AU 16 24547714 24547714 single base substitution C T upstream_gene_variant MELA-AU 16 24547728 24547728 single base substitution C T upstream_gene_variant MELA-AU 16 24547762 24547762 single base substitution G A upstream_gene_variant MELA-AU 16 24547795 24547795 single base substitution G A upstream_gene_variant MELA-AU 16 24547903 24547904 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 24548226 24548226 single base substitution G A upstream_gene_variant MELA-AU 16 24548463 24548463 single base substitution G A upstream_gene_variant MELA-AU 16 24548971 24548971 single base substitution C T upstream_gene_variant MELA-AU 16 24549013 24549013 single base substitution C T upstream_gene_variant MELA-AU 16 24549100 24549100 single base substitution G A 5_prime_UTR_variant MELA-AU 16 24549100 24549100 single base substitution G A upstream_gene_variant MELA-AU 16 24549495 24549495 single base substitution G A intron_variant MELA-AU 16 24549495 24549495 single base substitution G A upstream_gene_variant MELA-AU 16 24549951 24549951 single base substitution G A intron_variant MELA-AU 16 24549951 24549951 single base substitution G A upstream_gene_variant MELA-AU 16 24550741 24550741 single base substitution C T intron_variant MELA-AU 16 24550741 24550741 single base substitution C T upstream_gene_variant MELA-AU 16 24550765 24550766 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 24550765 24550766 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 24551053 24551053 single base substitution C T 5_prime_UTR_variant MELA-AU 16 24551053 24551053 single base substitution C T exon_variant MELA-AU 16 24551053 24551053 single base substitution C T intron_variant MELA-AU 16 24551053 24551053 single base substitution C T upstream_gene_variant MELA-AU 16 24551556 24551556 single base substitution C T 5_prime_UTR_variant MELA-AU 16 24551556 24551556 single base substitution C T exon_variant MELA-AU 16 24551556 24551556 single base substitution C T intron_variant MELA-AU 16 24551556 24551556 single base substitution C T upstream_gene_variant MELA-AU 16 24553437 24553437 single base substitution C T downstream_gene_variant MELA-AU 16 24553437 24553437 single base substitution C T intron_variant MELA-AU 16 24553517 24553517 single base substitution G A downstream_gene_variant MELA-AU 16 24553517 24553517 single base substitution G A intron_variant MELA-AU 16 24554017 24554017 single base substitution C T downstream_gene_variant MELA-AU 16 24554017 24554017 single base substitution C T intron_variant MELA-AU 16 24555756 24555756 single base substitution G A downstream_gene_variant MELA-AU 16 24555756 24555756 single base substitution G A intron_variant MELA-AU 16 24556366 24556366 single base substitution C T downstream_gene_variant MELA-AU 16 24556366 24556366 single base substitution C T intron_variant MELA-AU 16 24556544 24556544 single base substitution C T downstream_gene_variant MELA-AU 16 24556544 24556544 single base substitution C T intron_variant MELA-AU 16 24556845 24556845 single base substitution C T intron_variant MELA-AU 16 24557663 24557663 single base substitution G A intron_variant MELA-AU 16 24557742 24557742 single base substitution T C intron_variant MELA-AU 16 24557893 24557893 single base substitution G A intron_variant MELA-AU 16 24558407 24558407 single base substitution T A intron_variant MELA-AU 16 24559421 24559421 single base substitution C T intron_variant MELA-AU 16 24560039 24560039 single base substitution C T intron_variant MELA-AU 16 24560039 24560039 single base substitution C T upstream_gene_variant MELA-AU 16 24560825 24560825 single base substitution A G downstream_gene_variant MELA-AU 16 24560825 24560825 single base substitution A G intron_variant MELA-AU 16 24560825 24560825 single base substitution A G upstream_gene_variant MELA-AU 16 24560845 24560846 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 24560845 24560846 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 24560845 24560846 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 24561486 24561486 single base substitution C T downstream_gene_variant MELA-AU 16 24561486 24561486 single base substitution C T intron_variant MELA-AU 16 24561486 24561486 single base substitution C T upstream_gene_variant MELA-AU 16 24561654 24561654 single base substitution C T downstream_gene_variant MELA-AU 16 24561654 24561654 single base substitution C T intron_variant MELA-AU 16 24561654 24561654 single base substitution C T upstream_gene_variant MELA-AU 16 24561684 24561684 single base substitution G T downstream_gene_variant MELA-AU 16 24561684 24561684 single base substitution G T intron_variant MELA-AU 16 24561684 24561684 single base substitution G T upstream_gene_variant MELA-AU 16 24561797 24561797 single base substitution G A downstream_gene_variant MELA-AU 16 24561797 24561797 single base substitution G A intron_variant MELA-AU 16 24561797 24561797 single base substitution G A upstream_gene_variant MELA-AU 16 24562399 24562399 single base substitution C T downstream_gene_variant MELA-AU 16 24562399 24562399 single base substitution C T intron_variant MELA-AU 16 24562399 24562399 single base substitution C T upstream_gene_variant MELA-AU 16 24563745 24563745 single base substitution A G downstream_gene_variant MELA-AU 16 24563745 24563745 single base substitution A G intron_variant MELA-AU 16 24563745 24563745 single base substitution A G upstream_gene_variant MELA-AU 16 24563865 24563865 single base substitution A G downstream_gene_variant MELA-AU 16 24563865 24563865 single base substitution A G intron_variant MELA-AU 16 24563865 24563865 single base substitution A G upstream_gene_variant MELA-AU 16 24564365 24564365 single base substitution A T downstream_gene_variant MELA-AU 16 24564365 24564365 single base substitution A T intron_variant MELA-AU 16 24564365 24564365 single base substitution A T upstream_gene_variant MELA-AU 16 24564880 24564881 deletion of <=200bp TA - downstream_gene_variant MELA-AU 16 24564880 24564881 deletion of <=200bp TA - splice_donor_variant MELA-AU 16 24564880 24564881 deletion of <=200bp TA - upstream_gene_variant MELA-AU 16 24567030 24567030 single base substitution T C intron_variant MELA-AU 16 24567030 24567030 single base substitution T C splice_region_variant MELA-AU 16 24567030 24567030 single base substitution T C upstream_gene_variant MELA-AU 16 24567280 24567280 single base substitution C T downstream_gene_variant MELA-AU 16 24567280 24567280 single base substitution C T intron_variant MELA-AU 16 24567414 24567414 single base substitution G A downstream_gene_variant MELA-AU 16 24567414 24567414 single base substitution G A intron_variant MELA-AU 16 24568028 24568028 single base substitution C T downstream_gene_variant MELA-AU 16 24568028 24568028 single base substitution C T intron_variant MELA-AU 16 24568303 24568303 single base substitution A G downstream_gene_variant MELA-AU 16 24568303 24568303 single base substitution A G intron_variant MELA-AU 16 24568612 24568612 single base substitution C T downstream_gene_variant MELA-AU 16 24568612 24568612 single base substitution C T intron_variant MELA-AU 16 24570328 24570328 single base substitution C T downstream_gene_variant MELA-AU 16 24570328 24570328 single base substitution C T intron_variant MELA-AU 16 24570328 24570328 single base substitution C T upstream_gene_variant MELA-AU 16 24571924 24571925 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 24571924 24571925 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 24571924 24571925 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 24573151 24573151 single base substitution A T downstream_gene_variant MELA-AU 16 24573151 24573151 single base substitution A T exon_variant MELA-AU 16 24573151 24573151 single base substitution A T missense_variant N187Y 559A>T MELA-AU 16 24573151 24573151 single base substitution A T missense_variant N320Y 958A>T MELA-AU 16 24573151 24573151 single base substitution A T upstream_gene_variant MELA-AU 16 24573205 24573206 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 24573205 24573206 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 16 24573205 24573206 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P205F 613CC>TT MELA-AU 16 24573205 24573206 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P338F 1012CC>TT MELA-AU 16 24573205 24573206 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 24573397 24573397 single base substitution C A downstream_gene_variant MELA-AU 16 24573397 24573397 single base substitution C A exon_variant MELA-AU 16 24573397 24573397 single base substitution C A missense_variant P269T 805C>A MELA-AU 16 24573397 24573397 single base substitution C A missense_variant P402T 1204C>A MELA-AU 16 24573397 24573397 single base substitution C A upstream_gene_variant MELA-AU 16 24573397 24573397 single base substitution C T downstream_gene_variant MELA-AU 16 24573397 24573397 single base substitution C T exon_variant MELA-AU 16 24573397 24573397 single base substitution C T missense_variant P269S 805C>T MELA-AU 16 24573397 24573397 single base substitution C T missense_variant P402S 1204C>T MELA-AU 16 24573397 24573397 single base substitution C T upstream_gene_variant MELA-AU 16 24573854 24573856 multiple base substitution (>=2bp and <=200bp) GAA CTC downstream_gene_variant MELA-AU 16 24573854 24573856 multiple base substitution (>=2bp and <=200bp) GAA CTC intron_variant MELA-AU 16 24573854 24573856 multiple base substitution (>=2bp and <=200bp) GAA CTC upstream_gene_variant MELA-AU 16 24574124 24574124 single base substitution G T downstream_gene_variant MELA-AU 16 24574124 24574124 single base substitution G T intron_variant MELA-AU 16 24574124 24574124 single base substitution G T upstream_gene_variant MELA-AU 16 24574174 24574174 single base substitution C T downstream_gene_variant MELA-AU 16 24574174 24574174 single base substitution C T intron_variant MELA-AU 16 24574174 24574174 single base substitution C T upstream_gene_variant MELA-AU 16 24574788 24574788 single base substitution G A downstream_gene_variant MELA-AU 16 24574788 24574788 single base substitution G A exon_variant MELA-AU 16 24574788 24574788 single base substitution G A intron_variant MELA-AU 16 24574788 24574788 single base substitution G A synonymous_variant Q344Q 1032G>A MELA-AU 16 24574788 24574788 single base substitution G A synonymous_variant Q477Q 1431G>A MELA-AU 16 24575103 24575103 single base substitution T C downstream_gene_variant MELA-AU 16 24575103 24575103 single base substitution T C intron_variant MELA-AU 16 24575187 24575187 single base substitution G A downstream_gene_variant MELA-AU 16 24575187 24575187 single base substitution G A intron_variant MELA-AU 16 24575350 24575350 single base substitution T C downstream_gene_variant MELA-AU 16 24575350 24575350 single base substitution T C intron_variant MELA-AU 16 24575441 24575441 single base substitution C T downstream_gene_variant MELA-AU 16 24575441 24575441 single base substitution C T intron_variant MELA-AU 16 24576105 24576105 single base substitution T G downstream_gene_variant MELA-AU 16 24576105 24576105 single base substitution T G intron_variant MELA-AU 16 24576428 24576428 single base substitution C T downstream_gene_variant MELA-AU 16 24576428 24576428 single base substitution C T intron_variant MELA-AU 16 24576625 24576625 single base substitution C T downstream_gene_variant MELA-AU 16 24576625 24576625 single base substitution C T intron_variant MELA-AU 16 24576757 24576757 single base substitution C T downstream_gene_variant MELA-AU 16 24576757 24576757 single base substitution C T intron_variant MELA-AU 16 24577588 24577588 single base substitution A G downstream_gene_variant MELA-AU 16 24577588 24577588 single base substitution A G intron_variant MELA-AU 16 24577691 24577691 single base substitution G A downstream_gene_variant MELA-AU 16 24577691 24577691 single base substitution G A intron_variant MELA-AU 16 24578460 24578460 single base substitution C T intron_variant MELA-AU 16 24578460 24578460 single base substitution C T splice_region_variant MELA-AU 16 24578461 24578461 single base substitution C T intron_variant MELA-AU 16 24578461 24578461 single base substitution C T splice_region_variant MELA-AU 16 24578612 24578612 single base substitution C T exon_variant MELA-AU 16 24578612 24578612 single base substitution C T intron_variant MELA-AU 16 24578612 24578612 single base substitution C T missense_variant P447S 1339C>T MELA-AU 16 24578612 24578612 single base substitution C T missense_variant P580S 1738C>T MELA-AU 16 24578842 24578842 single base substitution T G downstream_gene_variant MELA-AU 16 24578842 24578842 single base substitution T G intron_variant MELA-AU 16 24578864 24578864 single base substitution C T downstream_gene_variant MELA-AU 16 24578864 24578864 single base substitution C T intron_variant MELA-AU 16 24579538 24579538 single base substitution C T downstream_gene_variant MELA-AU 16 24579538 24579538 single base substitution C T intron_variant MELA-AU 16 24579640 24579640 single base substitution C T downstream_gene_variant MELA-AU 16 24579640 24579640 single base substitution C T intron_variant MELA-AU 16 24579641 24579641 single base substitution C T downstream_gene_variant MELA-AU 16 24579641 24579641 single base substitution C T intron_variant MELA-AU 16 24579904 24579904 single base substitution A G downstream_gene_variant MELA-AU 16 24579904 24579904 single base substitution A G intron_variant MELA-AU 16 24580646 24580646 single base substitution C T downstream_gene_variant MELA-AU 16 24580646 24580646 single base substitution C T exon_variant MELA-AU 16 24580646 24580646 single base substitution C T intron_variant MELA-AU 16 24580646 24580646 single base substitution C T missense_variant R746C 2236C>T MELA-AU 16 24580646 24580646 single base substitution C T missense_variant R845C 2533C>T MELA-AU 16 24580646 24580646 single base substitution C T missense_variant R879C 2635C>T MELA-AU 16 24580944 24580944 single base substitution C T downstream_gene_variant MELA-AU 16 24580944 24580944 single base substitution C T exon_variant MELA-AU 16 24580944 24580944 single base substitution C T intron_variant MELA-AU 16 24580944 24580944 single base substitution C T missense_variant P845L 2534C>T MELA-AU 16 24580944 24580944 single base substitution C T missense_variant P944L 2831C>T MELA-AU 16 24580944 24580944 single base substitution C T missense_variant P978L 2933C>T MELA-AU 16 24581169 24581169 single base substitution C T downstream_gene_variant MELA-AU 16 24581169 24581169 single base substitution C T exon_variant MELA-AU 16 24581169 24581169 single base substitution C T intron_variant MELA-AU 16 24581169 24581169 single base substitution C T missense_variant P1019L 3056C>T MELA-AU 16 24581169 24581169 single base substitution C T missense_variant P1053L 3158C>T MELA-AU 16 24581169 24581169 single base substitution C T missense_variant P920L 2759C>T MELA-AU 16 24583081 24583081 single base substitution C T downstream_gene_variant MELA-AU 16 24583081 24583081 single base substitution C T exon_variant MELA-AU 16 24583081 24583081 single base substitution C T missense_variant P1531L 4592C>T MELA-AU 16 24583081 24583081 single base substitution C T missense_variant P1565L 4694C>T MELA-AU 16 24583081 24583081 single base substitution C T missense_variant P725L 2174C>T MELA-AU 16 24583864 24583864 single base substitution A C 3_prime_UTR_variant MELA-AU 16 24583864 24583864 single base substitution A C downstream_gene_variant MELA-AU 16 24583864 24583864 single base substitution A C exon_variant MELA-AU 16 24584088 24584088 single base substitution A G 3_prime_UTR_variant MELA-AU 16 24584088 24584088 single base substitution A G downstream_gene_variant MELA-AU 16 24584088 24584088 single base substitution A G exon_variant MELA-AU 16 24584235 24584235 single base substitution A G downstream_gene_variant MELA-AU 16 24584237 24584237 single base substitution C A downstream_gene_variant MELA-AU 16 24584447 24584447 single base substitution C T downstream_gene_variant MELA-AU 16 24584557 24584557 single base substitution C T downstream_gene_variant MELA-AU 16 24584657 24584657 single base substitution T C downstream_gene_variant MELA-AU 16 24584670 24584670 single base substitution C T downstream_gene_variant MELA-AU 16 24585191 24585191 single base substitution C T downstream_gene_variant MELA-AU 16 24585204 24585204 single base substitution C T downstream_gene_variant MELA-AU 16 24585247 24585247 single base substitution C T downstream_gene_variant MELA-AU 16 24585327 24585327 single base substitution C T downstream_gene_variant MELA-AU 16 24586444 24586444 single base substitution C T downstream_gene_variant MELA-AU 16 24586485 24586486 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 24586609 24586609 single base substitution T C downstream_gene_variant MELA-AU 16 24586780 24586780 single base substitution C T downstream_gene_variant MELA-AU 16 24586781 24586781 single base substitution C T downstream_gene_variant MELA-AU 16 24586903 24586903 single base substitution G A downstream_gene_variant MELA-AU 16 24587401 24587401 single base substitution C T downstream_gene_variant MELA-AU 16 24587826 24587826 single base substitution C T downstream_gene_variant MELA-AU 16 24588056 24588056 single base substitution C T downstream_gene_variant MELA-AU 16 24588143 24588143 single base substitution C T downstream_gene_variant MELA-AU 16 24588151 24588151 single base substitution G A downstream_gene_variant MELA-AU 16 24588352 24588352 single base substitution C T downstream_gene_variant MELA-AU 16 24588382 24588382 single base substitution C T downstream_gene_variant MELA-AU 16 24588501 24588501 single base substitution C T downstream_gene_variant MELA-AU 16 24588824 24588824 single base substitution C T downstream_gene_variant MELA-AU 16 24588979 24588979 single base substitution G A downstream_gene_variant MELA-AU 16 24589087 24589087 single base substitution C T downstream_gene_variant ORCA-IN 16 24544665 24544665 deletion of <=200bp C - upstream_gene_variant ORCA-IN 16 24580426 24580426 single base substitution A G downstream_gene_variant ORCA-IN 16 24580426 24580426 single base substitution A G exon_variant ORCA-IN 16 24580426 24580426 single base substitution A G intron_variant ORCA-IN 16 24580426 24580426 single base substitution A G synonymous_variant P672P 2016A>G ORCA-IN 16 24580426 24580426 single base substitution A G synonymous_variant P771P 2313A>G ORCA-IN 16 24580426 24580426 single base substitution A G synonymous_variant P805P 2415A>G ORCA-IN 16 24582256 24582256 single base substitution G A downstream_gene_variant ORCA-IN 16 24582256 24582256 single base substitution G A exon_variant ORCA-IN 16 24582256 24582256 single base substitution G A missense_variant R1256Q 3767G>A ORCA-IN 16 24582256 24582256 single base substitution G A missense_variant R1290Q 3869G>A ORCA-IN 16 24582256 24582256 single base substitution G A missense_variant R450Q 1349G>A OV-AU 16 24550925 24550925 single base substitution A G 5_prime_UTR_variant OV-AU 16 24550925 24550925 single base substitution A G exon_variant OV-AU 16 24550925 24550925 single base substitution A G intron_variant OV-AU 16 24550925 24550925 single base substitution A G upstream_gene_variant OV-AU 16 24556223 24556223 single base substitution C G downstream_gene_variant OV-AU 16 24556223 24556223 single base substitution C G intron_variant OV-AU 16 24560079 24560079 single base substitution A C intron_variant OV-AU 16 24560079 24560079 single base substitution A C upstream_gene_variant OV-AU 16 24571686 24571686 single base substitution C G downstream_gene_variant OV-AU 16 24571686 24571686 single base substitution C G intron_variant OV-AU 16 24571686 24571686 single base substitution C G upstream_gene_variant OV-AU 16 24574379 24574379 single base substitution C G downstream_gene_variant OV-AU 16 24574379 24574379 single base substitution C G intron_variant OV-AU 16 24574379 24574379 single base substitution C G upstream_gene_variant OV-AU 16 24581801 24581801 single base substitution A G downstream_gene_variant OV-AU 16 24581801 24581801 single base substitution A G exon_variant OV-AU 16 24581801 24581801 single base substitution A G intron_variant OV-AU 16 24581801 24581801 single base substitution A G missense_variant T1230A 3688A>G OV-AU 16 24581801 24581801 single base substitution A G missense_variant T1264A 3790A>G OV-AU 16 24582717 24582717 single base substitution T C downstream_gene_variant OV-AU 16 24582717 24582717 single base substitution T C exon_variant OV-AU 16 24582717 24582717 single base substitution T C missense_variant S1410P 4228T>C OV-AU 16 24582717 24582717 single base substitution T C missense_variant S1444P 4330T>C OV-AU 16 24582717 24582717 single base substitution T C missense_variant S604P 1810T>C OV-AU 16 24583211 24583211 single base substitution C G downstream_gene_variant OV-AU 16 24583211 24583211 single base substitution C G exon_variant OV-AU 16 24583211 24583211 single base substitution C G missense_variant D1574E 4722C>G OV-AU 16 24583211 24583211 single base substitution C G missense_variant D1608E 4824C>G OV-AU 16 24583211 24583211 single base substitution C G missense_variant D768E 2304C>G OV-AU 16 24586363 24586363 single base substitution G C downstream_gene_variant OV-US 16 24560271 24560271 single base substitution G A intron_variant OV-US 16 24560271 24560271 single base substitution G A missense_variant R91Q 272G>A OV-US 16 24560271 24560271 single base substitution G A upstream_gene_variant PACA-AU 16 24548438 24548438 single base substitution G A upstream_gene_variant PACA-AU 16 24548705 24548705 single base substitution T A upstream_gene_variant PACA-AU 16 24551264 24551264 single base substitution G A exon_variant PACA-AU 16 24551264 24551264 single base substitution G A intron_variant PACA-AU 16 24551264 24551264 single base substitution G A upstream_gene_variant PACA-AU 16 24553403 24553403 single base substitution C G downstream_gene_variant PACA-AU 16 24553403 24553403 single base substitution C G intron_variant PACA-AU 16 24555049 24555049 single base substitution G A downstream_gene_variant PACA-AU 16 24555049 24555049 single base substitution G A intron_variant PACA-AU 16 24567768 24567768 single base substitution C T downstream_gene_variant PACA-AU 16 24567768 24567768 single base substitution C T missense_variant A225V 674C>T PACA-AU 16 24567768 24567768 single base substitution C T missense_variant A92V 275C>T PACA-AU 16 24567768 24567768 single base substitution C T splice_region_variant PACA-AU 16 24572617 24572617 insertion of <=200bp - C downstream_gene_variant PACA-AU 16 24572617 24572617 insertion of <=200bp - C intron_variant PACA-AU 16 24572617 24572617 insertion of <=200bp - C upstream_gene_variant PACA-AU 16 24573008 24573008 single base substitution C T downstream_gene_variant PACA-AU 16 24573008 24573008 single base substitution C T exon_variant PACA-AU 16 24573008 24573008 single base substitution C T missense_variant A175V 524C>T PACA-AU 16 24573008 24573008 single base substitution C T missense_variant A308V 923C>T PACA-AU 16 24573008 24573008 single base substitution C T upstream_gene_variant PACA-AU 16 24581512 24581512 single base substitution C T downstream_gene_variant PACA-AU 16 24581512 24581512 single base substitution C T exon_variant PACA-AU 16 24581512 24581512 single base substitution C T intron_variant PACA-AU 16 24581512 24581512 single base substitution C T synonymous_variant I1133I 3399C>T PACA-AU 16 24581512 24581512 single base substitution C T synonymous_variant I1167I 3501C>T PACA-AU 16 24582988 24582988 single base substitution C A downstream_gene_variant PACA-AU 16 24582988 24582988 single base substitution C A exon_variant PACA-AU 16 24582988 24582988 single base substitution C A missense_variant S1500Y 4499C>A PACA-AU 16 24582988 24582988 single base substitution C A missense_variant S1534Y 4601C>A PACA-AU 16 24582988 24582988 single base substitution C A missense_variant S694Y 2081C>A PACA-AU 16 24586822 24586822 single base substitution C T downstream_gene_variant PACA-CA 16 24544252 24544252 insertion of <=200bp - T upstream_gene_variant PACA-CA 16 24548706 24548706 single base substitution A T upstream_gene_variant PACA-CA 16 24549115 24549115 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 16 24549115 24549115 single base substitution C T upstream_gene_variant PACA-CA 16 24550794 24550794 single base substitution G T intron_variant PACA-CA 16 24550794 24550794 single base substitution G T upstream_gene_variant PACA-CA 16 24550795 24550795 single base substitution A T intron_variant PACA-CA 16 24550795 24550795 single base substitution A T upstream_gene_variant PACA-CA 16 24552060 24552060 single base substitution A C downstream_gene_variant PACA-CA 16 24552060 24552060 single base substitution A C intron_variant PACA-CA 16 24552060 24552060 single base substitution A C missense_variant K38T 113A>C PACA-CA 16 24553791 24553791 single base substitution T C downstream_gene_variant PACA-CA 16 24553791 24553791 single base substitution T C intron_variant PACA-CA 16 24556029 24556029 single base substitution C T downstream_gene_variant PACA-CA 16 24556029 24556029 single base substitution C T intron_variant PACA-CA 16 24557524 24557524 single base substitution T C intron_variant PACA-CA 16 24557524 24557524 single base substitution T C synonymous_variant S69S 207T>C PACA-CA 16 24562953 24562953 insertion of <=200bp - A downstream_gene_variant PACA-CA 16 24562953 24562953 insertion of <=200bp - A intron_variant PACA-CA 16 24562953 24562953 insertion of <=200bp - A upstream_gene_variant PACA-CA 16 24564851 24564851 single base substitution G A 5_prime_UTR_variant PACA-CA 16 24564851 24564851 single base substitution G A downstream_gene_variant PACA-CA 16 24564851 24564851 single base substitution G A exon_variant PACA-CA 16 24564851 24564851 single base substitution G A synonymous_variant A107A 321G>A PACA-CA 16 24564851 24564851 single base substitution G A upstream_gene_variant PACA-CA 16 24568376 24568376 single base substitution G T downstream_gene_variant PACA-CA 16 24568376 24568376 single base substitution G T intron_variant PACA-CA 16 24568536 24568536 single base substitution C T downstream_gene_variant PACA-CA 16 24568536 24568536 single base substitution C T intron_variant PACA-CA 16 24570987 24570987 single base substitution A G downstream_gene_variant PACA-CA 16 24570987 24570987 single base substitution A G exon_variant PACA-CA 16 24570987 24570987 single base substitution A G missense_variant Y146C 437A>G PACA-CA 16 24570987 24570987 single base substitution A G missense_variant Y279C 836A>G PACA-CA 16 24570987 24570987 single base substitution A G upstream_gene_variant PACA-CA 16 24572979 24572979 single base substitution G A downstream_gene_variant PACA-CA 16 24572979 24572979 single base substitution G A exon_variant PACA-CA 16 24572979 24572979 single base substitution G A synonymous_variant T165T 495G>A PACA-CA 16 24572979 24572979 single base substitution G A synonymous_variant T298T 894G>A PACA-CA 16 24572979 24572979 single base substitution G A upstream_gene_variant PACA-CA 16 24573439 24573439 single base substitution G T downstream_gene_variant PACA-CA 16 24573439 24573439 single base substitution G T exon_variant PACA-CA 16 24573439 24573439 single base substitution G T missense_variant V283L 847G>T PACA-CA 16 24573439 24573439 single base substitution G T missense_variant V416L 1246G>T PACA-CA 16 24573439 24573439 single base substitution G T upstream_gene_variant PACA-CA 16 24573887 24573887 single base substitution G T downstream_gene_variant PACA-CA 16 24573887 24573887 single base substitution G T intron_variant PACA-CA 16 24573887 24573887 single base substitution G T upstream_gene_variant PACA-CA 16 24574593 24574593 single base substitution A G downstream_gene_variant PACA-CA 16 24574593 24574593 single base substitution A G exon_variant PACA-CA 16 24574593 24574593 single base substitution A G intron_variant PACA-CA 16 24574593 24574593 single base substitution A G missense_variant I322V 964A>G PACA-CA 16 24574593 24574593 single base substitution A G missense_variant I455V 1363A>G PACA-CA 16 24574593 24574593 single base substitution A G upstream_gene_variant PACA-CA 16 24574861 24574861 deletion of <=200bp A - downstream_gene_variant PACA-CA 16 24574861 24574861 deletion of <=200bp A - intron_variant PACA-CA 16 24575328 24575328 single base substitution T G downstream_gene_variant PACA-CA 16 24575328 24575328 single base substitution T G intron_variant PACA-CA 16 24579037 24579037 single base substitution G T downstream_gene_variant PACA-CA 16 24579037 24579037 single base substitution G T intron_variant PACA-CA 16 24582629 24582629 single base substitution G A downstream_gene_variant PACA-CA 16 24582629 24582629 single base substitution G A exon_variant PACA-CA 16 24582629 24582629 single base substitution G A synonymous_variant E1380E 4140G>A PACA-CA 16 24582629 24582629 single base substitution G A synonymous_variant E1414E 4242G>A PACA-CA 16 24582629 24582629 single base substitution G A synonymous_variant E574E 1722G>A PACA-CA 16 24584059 24584059 deletion of <=200bp T - 3_prime_UTR_variant PACA-CA 16 24584059 24584059 deletion of <=200bp T - downstream_gene_variant PACA-CA 16 24584059 24584059 deletion of <=200bp T - exon_variant PACA-CA 16 24584230 24584230 single base substitution T C downstream_gene_variant PACA-CA 16 24584561 24584561 single base substitution G C downstream_gene_variant PACA-CA 16 24585462 24585462 single base substitution C T downstream_gene_variant PACA-CA 16 24586444 24586444 single base substitution C T downstream_gene_variant PBCA-DE 16 24545268 24545268 insertion of <=200bp - TTATTTAT upstream_gene_variant PBCA-DE 16 24547886 24547886 single base substitution T A upstream_gene_variant PBCA-DE 16 24548460 24548460 single base substitution T A upstream_gene_variant PBCA-DE 16 24551896 24551896 single base substitution A G 5_prime_UTR_variant PBCA-DE 16 24551896 24551896 single base substitution A G downstream_gene_variant PBCA-DE 16 24551896 24551896 single base substitution A G intron_variant PBCA-DE 16 24551896 24551896 single base substitution A G upstream_gene_variant PBCA-DE 16 24552838 24552838 insertion of <=200bp - T downstream_gene_variant PBCA-DE 16 24552838 24552838 insertion of <=200bp - T intron_variant PBCA-DE 16 24561715 24561715 single base substitution C A downstream_gene_variant PBCA-DE 16 24561715 24561715 single base substitution C A intron_variant PBCA-DE 16 24561715 24561715 single base substitution C A upstream_gene_variant PBCA-DE 16 24563881 24563881 deletion of <=200bp T - downstream_gene_variant PBCA-DE 16 24563881 24563881 deletion of <=200bp T - intron_variant PBCA-DE 16 24563881 24563881 deletion of <=200bp T - upstream_gene_variant PBCA-DE 16 24564880 24564881 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 16 24564880 24564881 deletion of <=200bp TA - splice_donor_variant PBCA-DE 16 24564880 24564881 deletion of <=200bp TA - upstream_gene_variant PBCA-DE 16 24568893 24568893 insertion of <=200bp - A downstream_gene_variant PBCA-DE 16 24568893 24568893 insertion of <=200bp - A intron_variant PBCA-DE 16 24572596 24572596 single base substitution T G downstream_gene_variant PBCA-DE 16 24572596 24572596 single base substitution T G intron_variant PBCA-DE 16 24572596 24572596 single base substitution T G upstream_gene_variant PBCA-DE 16 24579333 24579333 single base substitution T A downstream_gene_variant PBCA-DE 16 24579333 24579333 single base substitution T A intron_variant PBCA-DE 16 24583113 24583113 single base substitution G T downstream_gene_variant PBCA-DE 16 24583113 24583113 single base substitution G T exon_variant PBCA-DE 16 24583113 24583113 single base substitution G T missense_variant A1542S 4624G>T PBCA-DE 16 24583113 24583113 single base substitution G T missense_variant A1576S 4726G>T PBCA-DE 16 24583113 24583113 single base substitution G T missense_variant A736S 2206G>T PRAD-CA 16 24544998 24544998 single base substitution G A upstream_gene_variant PRAD-CA 16 24545000 24545000 single base substitution A G upstream_gene_variant PRAD-CA 16 24569720 24569720 single base substitution C T downstream_gene_variant PRAD-CA 16 24569720 24569720 single base substitution C T intron_variant PRAD-CA 16 24569720 24569720 single base substitution C T upstream_gene_variant PRAD-CA 16 24570977 24570977 single base substitution G T downstream_gene_variant PRAD-CA 16 24570977 24570977 single base substitution G T exon_variant PRAD-CA 16 24570977 24570977 single base substitution G T stop_gained G143* 427G>T PRAD-CA 16 24570977 24570977 single base substitution G T stop_gained G276* 826G>T PRAD-CA 16 24570977 24570977 single base substitution G T upstream_gene_variant PRAD-CA 16 24588718 24588718 single base substitution T C downstream_gene_variant PRAD-UK 16 24563249 24563249 single base substitution A G downstream_gene_variant PRAD-UK 16 24563249 24563249 single base substitution A G intron_variant PRAD-UK 16 24563249 24563249 single base substitution A G upstream_gene_variant PRAD-UK 16 24566593 24566593 single base substitution C T exon_variant PRAD-UK 16 24566593 24566593 single base substitution C T intron_variant PRAD-UK 16 24566593 24566593 single base substitution C T upstream_gene_variant PRAD-UK 16 24585470 24585470 single base substitution G A downstream_gene_variant PRAD-UK 16 24587270 24587279 deletion of <=200bp GAGGGAGAGG - downstream_gene_variant PRAD-US 16 24567694 24567694 single base substitution G C downstream_gene_variant PRAD-US 16 24567694 24567694 single base substitution G C exon_variant PRAD-US 16 24567694 24567694 single base substitution G C missense_variant M200I 600G>C PRAD-US 16 24567694 24567694 single base substitution G C missense_variant M67I 201G>C PRAD-US 16 24574974 24574974 single base substitution A G downstream_gene_variant PRAD-US 16 24574974 24574974 single base substitution A G exon_variant PRAD-US 16 24574974 24574974 single base substitution A G intron_variant PRAD-US 16 24574974 24574974 single base substitution A G synonymous_variant P370P 1110A>G PRAD-US 16 24574974 24574974 single base substitution A G synonymous_variant P503P 1509A>G READ-US 16 24578822 24578822 single base substitution G T downstream_gene_variant READ-US 16 24578822 24578822 single base substitution G T exon_variant READ-US 16 24578822 24578822 single base substitution G T intron_variant READ-US 16 24578822 24578822 single base substitution G T stop_gained E517* 1549G>T READ-US 16 24578822 24578822 single base substitution G T stop_gained E650* 1948G>T READ-US 16 24581613 24581613 single base substitution C A downstream_gene_variant READ-US 16 24581613 24581613 single base substitution C A exon_variant READ-US 16 24581613 24581613 single base substitution C A intron_variant READ-US 16 24581613 24581613 single base substitution C A missense_variant S1167Y 3500C>A READ-US 16 24581613 24581613 single base substitution C A missense_variant S1201Y 3602C>A READ-US 16 24582783 24582783 single base substitution G T downstream_gene_variant READ-US 16 24582783 24582783 single base substitution G T exon_variant READ-US 16 24582783 24582783 single base substitution G T missense_variant D1432Y 4294G>T READ-US 16 24582783 24582783 single base substitution G T missense_variant D1466Y 4396G>T READ-US 16 24582783 24582783 single base substitution G T missense_variant D626Y 1876G>T READ-US 16 24582954 24582954 deletion of <=200bp A - downstream_gene_variant READ-US 16 24582954 24582954 deletion of <=200bp A - exon_variant READ-US 16 24582954 24582954 deletion of <=200bp A - frameshift_variant K1489 READ-US 16 24582954 24582954 deletion of <=200bp A - frameshift_variant K1523 READ-US 16 24582954 24582954 deletion of <=200bp A - frameshift_variant K683 RECA-EU 16 24551550 24551550 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant RECA-EU 16 24551550 24551550 single base substitution A C exon_variant RECA-EU 16 24551550 24551550 single base substitution A C intron_variant RECA-EU 16 24551550 24551550 single base substitution A C upstream_gene_variant RECA-EU 16 24554615 24554615 single base substitution T G downstream_gene_variant RECA-EU 16 24554615 24554615 single base substitution T G intron_variant RECA-EU 16 24560134 24560134 single base substitution G A intron_variant RECA-EU 16 24560134 24560134 single base substitution G A upstream_gene_variant RECA-EU 16 24564629 24564629 single base substitution C A downstream_gene_variant RECA-EU 16 24564629 24564629 single base substitution C A exon_variant RECA-EU 16 24564629 24564629 single base substitution C A intron_variant RECA-EU 16 24564629 24564629 single base substitution C A upstream_gene_variant RECA-EU 16 24567697 24567697 single base substitution A T downstream_gene_variant RECA-EU 16 24567697 24567697 single base substitution A T exon_variant RECA-EU 16 24567697 24567697 single base substitution A T missense_variant E201D 603A>T RECA-EU 16 24567697 24567697 single base substitution A T missense_variant E68D 204A>T RECA-EU 16 24571182 24571182 single base substitution G C downstream_gene_variant RECA-EU 16 24571182 24571182 single base substitution G C intron_variant RECA-EU 16 24571182 24571182 single base substitution G C upstream_gene_variant RECA-EU 16 24574466 24574466 single base substitution T C downstream_gene_variant RECA-EU 16 24574466 24574466 single base substitution T C intron_variant RECA-EU 16 24574466 24574466 single base substitution T C upstream_gene_variant RECA-EU 16 24582883 24582883 single base substitution A G downstream_gene_variant RECA-EU 16 24582883 24582883 single base substitution A G exon_variant RECA-EU 16 24582883 24582883 single base substitution A G missense_variant D1465G 4394A>G RECA-EU 16 24582883 24582883 single base substitution A G missense_variant D1499G 4496A>G RECA-EU 16 24582883 24582883 single base substitution A G missense_variant D659G 1976A>G RECA-EU 16 24583625 24583625 single base substitution G A downstream_gene_variant RECA-EU 16 24583625 24583625 single base substitution G A exon_variant RECA-EU 16 24583625 24583625 single base substitution G A synonymous_variant K1712K 5136G>A RECA-EU 16 24583625 24583625 single base substitution G A synonymous_variant K1746K 5238G>A RECA-EU 16 24583625 24583625 single base substitution G A synonymous_variant K906K 2718G>A RECA-EU 16 24585378 24585378 single base substitution C T downstream_gene_variant RECA-EU 16 24586536 24586536 single base substitution C G downstream_gene_variant RECA-EU 16 24587637 24587637 single base substitution A C downstream_gene_variant SKCA-BR 16 24544420 24544420 single base substitution G A upstream_gene_variant SKCA-BR 16 24546060 24546060 single base substitution C T upstream_gene_variant SKCA-BR 16 24550891 24550891 single base substitution T G 5_prime_UTR_variant SKCA-BR 16 24550891 24550891 single base substitution T G intron_variant SKCA-BR 16 24550891 24550891 single base substitution T G upstream_gene_variant SKCA-BR 16 24551259 24551259 single base substitution A G exon_variant SKCA-BR 16 24551259 24551259 single base substitution A G intron_variant SKCA-BR 16 24551259 24551259 single base substitution A G upstream_gene_variant SKCA-BR 16 24551503 24551503 single base substitution A C exon_variant SKCA-BR 16 24551503 24551503 single base substitution A C intron_variant SKCA-BR 16 24551503 24551503 single base substitution A C upstream_gene_variant SKCA-BR 16 24552514 24552514 single base substitution C A downstream_gene_variant SKCA-BR 16 24552514 24552514 single base substitution C A intron_variant SKCA-BR 16 24552523 24552526 deletion of <=200bp AACC - downstream_gene_variant SKCA-BR 16 24552523 24552526 deletion of <=200bp AACC - intron_variant SKCA-BR 16 24552526 24552526 single base substitution C A downstream_gene_variant SKCA-BR 16 24552526 24552526 single base substitution C A intron_variant SKCA-BR 16 24553778 24553778 single base substitution T C downstream_gene_variant SKCA-BR 16 24553778 24553778 single base substitution T C intron_variant SKCA-BR 16 24566082 24566082 single base substitution A G exon_variant SKCA-BR 16 24566082 24566082 single base substitution A G intron_variant SKCA-BR 16 24566082 24566082 single base substitution A G upstream_gene_variant SKCA-BR 16 24569031 24569031 single base substitution T A downstream_gene_variant SKCA-BR 16 24569031 24569031 single base substitution T A intron_variant SKCA-BR 16 24571429 24571432 deletion of <=200bp TTTG - downstream_gene_variant SKCA-BR 16 24571429 24571432 deletion of <=200bp TTTG - intron_variant SKCA-BR 16 24571429 24571432 deletion of <=200bp TTTG - upstream_gene_variant SKCA-BR 16 24571430 24571432 deletion of <=200bp TTG - downstream_gene_variant SKCA-BR 16 24571430 24571432 deletion of <=200bp TTG - intron_variant SKCA-BR 16 24571430 24571432 deletion of <=200bp TTG - upstream_gene_variant SKCA-BR 16 24571443 24571443 single base substitution T G downstream_gene_variant SKCA-BR 16 24571443 24571443 single base substitution T G intron_variant SKCA-BR 16 24571443 24571443 single base substitution T G upstream_gene_variant SKCA-BR 16 24576191 24576191 single base substitution G A downstream_gene_variant SKCA-BR 16 24576191 24576191 single base substitution G A intron_variant SKCA-BR 16 24576191 24576191 single base substitution G A splice_region_variant SKCA-BR 16 24579450 24579450 single base substitution T C downstream_gene_variant SKCA-BR 16 24579450 24579450 single base substitution T C intron_variant SKCA-BR 16 24580572 24580572 single base substitution C T downstream_gene_variant SKCA-BR 16 24580572 24580572 single base substitution C T exon_variant SKCA-BR 16 24580572 24580572 single base substitution C T intron_variant SKCA-BR 16 24580572 24580572 single base substitution C T missense_variant S721L 2162C>T SKCA-BR 16 24580572 24580572 single base substitution C T missense_variant S820L 2459C>T SKCA-BR 16 24580572 24580572 single base substitution C T missense_variant S854L 2561C>T SKCA-BR 16 24581074 24581074 single base substitution G T downstream_gene_variant SKCA-BR 16 24581074 24581074 single base substitution G T exon_variant SKCA-BR 16 24581074 24581074 single base substitution G T intron_variant SKCA-BR 16 24581074 24581074 single base substitution G T synonymous_variant R1021R 3063G>T SKCA-BR 16 24581074 24581074 single base substitution G T synonymous_variant R888R 2664G>T SKCA-BR 16 24581074 24581074 single base substitution G T synonymous_variant R987R 2961G>T SKCA-BR 16 24582530 24582530 single base substitution C T downstream_gene_variant SKCA-BR 16 24582530 24582530 single base substitution C T exon_variant SKCA-BR 16 24582530 24582530 single base substitution C T synonymous_variant S1347S 4041C>T SKCA-BR 16 24582530 24582530 single base substitution C T synonymous_variant S1381S 4143C>T SKCA-BR 16 24582530 24582530 single base substitution C T synonymous_variant S541S 1623C>T SKCA-BR 16 24585062 24585062 single base substitution T A downstream_gene_variant SKCA-BR 16 24585246 24585246 single base substitution T C downstream_gene_variant SKCA-BR 16 24586248 24586248 single base substitution C T downstream_gene_variant SKCA-BR 16 24586311 24586311 single base substitution G A downstream_gene_variant SKCA-BR 16 24587571 24587571 insertion of <=200bp - GATTTTAAGTGGTAT downstream_gene_variant SKCA-BR 16 24587572 24587572 single base substitution C A downstream_gene_variant SKCA-BR 16 24587762 24587762 single base substitution C T downstream_gene_variant SKCM-US 16 24566945 24566945 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 16 24566945 24566945 single base substitution C T exon_variant SKCM-US 16 24566945 24566945 single base substitution C T synonymous_variant L120L 358C>T SKCM-US 16 24566945 24566945 single base substitution C T upstream_gene_variant SKCM-US 16 24567190 24567190 single base substitution C T downstream_gene_variant SKCM-US 16 24567190 24567190 single base substitution C T exon_variant SKCM-US 16 24567190 24567190 single base substitution C T synonymous_variant F162F 486C>T SKCM-US 16 24567190 24567190 single base substitution C T synonymous_variant F29F 87C>T SKCM-US 16 24573272 24573272 single base substitution C T downstream_gene_variant SKCM-US 16 24573272 24573272 single base substitution C T exon_variant SKCM-US 16 24573272 24573272 single base substitution C T missense_variant S227F 680C>T SKCM-US 16 24573272 24573272 single base substitution C T missense_variant S360F 1079C>T SKCM-US 16 24573272 24573272 single base substitution C T upstream_gene_variant SKCM-US 16 24573359 24573359 single base substitution C T downstream_gene_variant SKCM-US 16 24573359 24573359 single base substitution C T exon_variant SKCM-US 16 24573359 24573359 single base substitution C T missense_variant S256F 767C>T SKCM-US 16 24573359 24573359 single base substitution C T missense_variant S389F 1166C>T SKCM-US 16 24573359 24573359 single base substitution C T upstream_gene_variant SKCM-US 16 24573481 24573481 single base substitution C T downstream_gene_variant SKCM-US 16 24573481 24573481 single base substitution C T missense_variant R297W 889C>T SKCM-US 16 24573481 24573481 single base substitution C T missense_variant R430C 1288C>T SKCM-US 16 24573481 24573481 single base substitution C T missense_variant R430W 1288C>T SKCM-US 16 24573481 24573481 single base substitution C T splice_region_variant SKCM-US 16 24573481 24573481 single base substitution C T upstream_gene_variant SKCM-US 16 24578591 24578591 single base substitution C T exon_variant SKCM-US 16 24578591 24578591 single base substitution C T intron_variant SKCM-US 16 24578591 24578591 single base substitution C T missense_variant P440S 1318C>T SKCM-US 16 24578591 24578591 single base substitution C T missense_variant P573S 1717C>T SKCM-US 16 24578597 24578597 single base substitution C T exon_variant SKCM-US 16 24578597 24578597 single base substitution C T intron_variant SKCM-US 16 24578597 24578597 single base substitution C T missense_variant P442S 1324C>T SKCM-US 16 24578597 24578597 single base substitution C T missense_variant P575S 1723C>T SKCM-US 16 24578598 24578598 single base substitution C T exon_variant SKCM-US 16 24578598 24578598 single base substitution C T intron_variant SKCM-US 16 24578598 24578598 single base substitution C T missense_variant P442L 1325C>T SKCM-US 16 24578598 24578598 single base substitution C T missense_variant P575L 1724C>T SKCM-US 16 24578672 24578672 single base substitution C T exon_variant SKCM-US 16 24578672 24578672 single base substitution C T intron_variant SKCM-US 16 24578672 24578672 single base substitution C T missense_variant P467S 1399C>T SKCM-US 16 24578672 24578672 single base substitution C T missense_variant P600S 1798C>T SKCM-US 16 24578678 24578678 single base substitution C T exon_variant SKCM-US 16 24578678 24578678 single base substitution C T intron_variant SKCM-US 16 24578678 24578678 single base substitution C T missense_variant P469S 1405C>T SKCM-US 16 24578678 24578678 single base substitution C T missense_variant P602S 1804C>T SKCM-US 16 24578687 24578687 single base substitution C T exon_variant SKCM-US 16 24578687 24578687 single base substitution C T intron_variant SKCM-US 16 24578687 24578687 single base substitution C T missense_variant P472S 1414C>T SKCM-US 16 24578687 24578687 single base substitution C T missense_variant P605S 1813C>T SKCM-US 16 24578724 24578724 single base substitution C T downstream_gene_variant SKCM-US 16 24578724 24578724 single base substitution C T exon_variant SKCM-US 16 24578724 24578724 single base substitution C T intron_variant SKCM-US 16 24578724 24578724 single base substitution C T missense_variant S484L 1451C>T SKCM-US 16 24578724 24578724 single base substitution C T missense_variant S617L 1850C>T SKCM-US 16 24580152 24580152 single base substitution C T downstream_gene_variant SKCM-US 16 24580152 24580152 single base substitution C T exon_variant SKCM-US 16 24580152 24580152 single base substitution C T intron_variant SKCM-US 16 24580152 24580152 single base substitution C T missense_variant S581F 1742C>T SKCM-US 16 24580152 24580152 single base substitution C T missense_variant S680F 2039C>T SKCM-US 16 24580152 24580152 single base substitution C T missense_variant S714F 2141C>T SKCM-US 16 24580206 24580206 single base substitution C T downstream_gene_variant SKCM-US 16 24580206 24580206 single base substitution C T exon_variant SKCM-US 16 24580206 24580206 single base substitution C T intron_variant SKCM-US 16 24580206 24580206 single base substitution C T missense_variant P599L 1796C>T SKCM-US 16 24580206 24580206 single base substitution C T missense_variant P698L 2093C>T SKCM-US 16 24580206 24580206 single base substitution C T missense_variant P732L 2195C>T SKCM-US 16 24580295 24580295 single base substitution C T downstream_gene_variant SKCM-US 16 24580295 24580295 single base substitution C T exon_variant SKCM-US 16 24580295 24580295 single base substitution C T intron_variant SKCM-US 16 24580295 24580295 single base substitution C T missense_variant P629S 1885C>T SKCM-US 16 24580295 24580295 single base substitution C T missense_variant P728S 2182C>T SKCM-US 16 24580295 24580295 single base substitution C T missense_variant P762S 2284C>T SKCM-US 16 24580302 24580302 single base substitution G A downstream_gene_variant SKCM-US 16 24580302 24580302 single base substitution G A exon_variant SKCM-US 16 24580302 24580302 single base substitution G A intron_variant SKCM-US 16 24580302 24580302 single base substitution G A missense_variant R631K 1892G>A SKCM-US 16 24580302 24580302 single base substitution G A missense_variant R730K 2189G>A SKCM-US 16 24580302 24580302 single base substitution G A missense_variant R764K 2291G>A SKCM-US 16 24580361 24580361 single base substitution C T downstream_gene_variant SKCM-US 16 24580361 24580361 single base substitution C T exon_variant SKCM-US 16 24580361 24580361 single base substitution C T intron_variant SKCM-US 16 24580361 24580361 single base substitution C T missense_variant R651C 1951C>T SKCM-US 16 24580361 24580361 single base substitution C T missense_variant R750C 2248C>T SKCM-US 16 24580361 24580361 single base substitution C T missense_variant R784C 2350C>T SKCM-US 16 24581168 24581168 single base substitution C T downstream_gene_variant SKCM-US 16 24581168 24581168 single base substitution C T exon_variant SKCM-US 16 24581168 24581168 single base substitution C T intron_variant SKCM-US 16 24581168 24581168 single base substitution C T missense_variant P1019S 3055C>T SKCM-US 16 24581168 24581168 single base substitution C T missense_variant P1053S 3157C>T SKCM-US 16 24581168 24581168 single base substitution C T missense_variant P920S 2758C>T SKCM-US 16 24581169 24581169 single base substitution C T downstream_gene_variant SKCM-US 16 24581169 24581169 single base substitution C T exon_variant SKCM-US 16 24581169 24581169 single base substitution C T intron_variant SKCM-US 16 24581169 24581169 single base substitution C T missense_variant P1019L 3056C>T SKCM-US 16 24581169 24581169 single base substitution C T missense_variant P1053L 3158C>T SKCM-US 16 24581169 24581169 single base substitution C T missense_variant P920L 2759C>T SKCM-US 16 24581171 24581171 single base substitution C T downstream_gene_variant SKCM-US 16 24581171 24581171 single base substitution C T exon_variant SKCM-US 16 24581171 24581171 single base substitution C T intron_variant SKCM-US 16 24581171 24581171 single base substitution C T stop_gained R1020* 3058C>T SKCM-US 16 24581171 24581171 single base substitution C T stop_gained R1054* 3160C>T SKCM-US 16 24581171 24581171 single base substitution C T stop_gained R921* 2761C>T SKCM-US 16 24581176 24581176 deletion of <=200bp T - downstream_gene_variant SKCM-US 16 24581176 24581176 deletion of <=200bp T - exon_variant SKCM-US 16 24581176 24581176 deletion of <=200bp T - frameshift_variant S1021 SKCM-US 16 24581176 24581176 deletion of <=200bp T - frameshift_variant S1055 SKCM-US 16 24581176 24581176 deletion of <=200bp T - frameshift_variant S922 SKCM-US 16 24581176 24581176 deletion of <=200bp T - intron_variant SKCM-US 16 24581490 24581490 single base substitution T G downstream_gene_variant SKCM-US 16 24581490 24581490 single base substitution T G exon_variant SKCM-US 16 24581490 24581490 single base substitution T G intron_variant SKCM-US 16 24581490 24581490 single base substitution T G missense_variant F1126C 3377T>G SKCM-US 16 24581490 24581490 single base substitution T G missense_variant F1160C 3479T>G SKCM-US 16 24581764 24581764 single base substitution C T downstream_gene_variant SKCM-US 16 24581764 24581764 single base substitution C T exon_variant SKCM-US 16 24581764 24581764 single base substitution C T intron_variant SKCM-US 16 24581764 24581764 single base substitution C T synonymous_variant V1217V 3651C>T SKCM-US 16 24581764 24581764 single base substitution C T synonymous_variant V1251V 3753C>T SKCM-US 16 24582320 24582320 single base substitution C T downstream_gene_variant SKCM-US 16 24582320 24582320 single base substitution C T exon_variant SKCM-US 16 24582320 24582320 single base substitution C T synonymous_variant I1277I 3831C>T SKCM-US 16 24582320 24582320 single base substitution C T synonymous_variant I1311I 3933C>T SKCM-US 16 24582320 24582320 single base substitution C T synonymous_variant I471I 1413C>T SKCM-US 16 24582700 24582700 single base substitution G A downstream_gene_variant SKCM-US 16 24582700 24582700 single base substitution G A exon_variant SKCM-US 16 24582700 24582700 single base substitution G A missense_variant G1404E 4211G>A SKCM-US 16 24582700 24582700 single base substitution G A missense_variant G1438E 4313G>A SKCM-US 16 24582700 24582700 single base substitution G A missense_variant G598E 1793G>A SKCM-US 16 24582793 24582793 single base substitution C T downstream_gene_variant SKCM-US 16 24582793 24582793 single base substitution C T exon_variant SKCM-US 16 24582793 24582793 single base substitution C T missense_variant P1435L 4304C>T SKCM-US 16 24582793 24582793 single base substitution C T missense_variant P1469L 4406C>T SKCM-US 16 24582793 24582793 single base substitution C T missense_variant P629L 1886C>T SKCM-US 16 24582974 24582974 single base substitution C T downstream_gene_variant SKCM-US 16 24582974 24582974 single base substitution C T exon_variant SKCM-US 16 24582974 24582974 single base substitution C T synonymous_variant S1495S 4485C>T SKCM-US 16 24582974 24582974 single base substitution C T synonymous_variant S1529S 4587C>T SKCM-US 16 24582974 24582974 single base substitution C T synonymous_variant S689S 2067C>T SKCM-US 16 24583080 24583080 single base substitution C T downstream_gene_variant SKCM-US 16 24583080 24583080 single base substitution C T exon_variant SKCM-US 16 24583080 24583080 single base substitution C T missense_variant P1531S 4591C>T SKCM-US 16 24583080 24583080 single base substitution C T missense_variant P1565S 4693C>T SKCM-US 16 24583080 24583080 single base substitution C T missense_variant P725S 2173C>T SKCM-US 16 24583226 24583226 single base substitution G A downstream_gene_variant SKCM-US 16 24583226 24583226 single base substitution G A exon_variant SKCM-US 16 24583226 24583226 single base substitution G A synonymous_variant K1579K 4737G>A SKCM-US 16 24583226 24583226 single base substitution G A synonymous_variant K1613K 4839G>A SKCM-US 16 24583226 24583226 single base substitution G A synonymous_variant K773K 2319G>A SKCM-US 16 24583244 24583244 single base substitution T G downstream_gene_variant SKCM-US 16 24583244 24583244 single base substitution T G exon_variant SKCM-US 16 24583244 24583244 single base substitution T G missense_variant S1585R 4755T>G SKCM-US 16 24583244 24583244 single base substitution T G missense_variant S1619R 4857T>G SKCM-US 16 24583244 24583244 single base substitution T G missense_variant S779R 2337T>G STAD-US 16 24552030 24552030 single base substitution A C downstream_gene_variant STAD-US 16 24552030 24552030 single base substitution A C intron_variant STAD-US 16 24552030 24552030 single base substitution A C missense_variant D28A 83A>C STAD-US 16 24567183 24567183 single base substitution C T downstream_gene_variant STAD-US 16 24567183 24567183 single base substitution C T exon_variant STAD-US 16 24567183 24567183 single base substitution C T missense_variant T160M 479C>T STAD-US 16 24567183 24567183 single base substitution C T missense_variant T27M 80C>T STAD-US 16 24567768 24567768 single base substitution C T downstream_gene_variant STAD-US 16 24567768 24567768 single base substitution C T missense_variant A225V 674C>T STAD-US 16 24567768 24567768 single base substitution C T missense_variant A92V 275C>T STAD-US 16 24567768 24567768 single base substitution C T splice_region_variant STAD-US 16 24578545 24578545 single base substitution A T exon_variant STAD-US 16 24578545 24578545 single base substitution A T intron_variant STAD-US 16 24578545 24578545 single base substitution A T synonymous_variant V424V 1272A>T STAD-US 16 24578545 24578545 single base substitution A T synonymous_variant V557V 1671A>T STAD-US 16 24578677 24578677 single base substitution T C exon_variant STAD-US 16 24578677 24578677 single base substitution T C intron_variant STAD-US 16 24578677 24578677 single base substitution T C synonymous_variant P468P 1404T>C STAD-US 16 24578677 24578677 single base substitution T C synonymous_variant P601P 1803T>C STAD-US 16 24579195 24579195 single base substitution C T downstream_gene_variant STAD-US 16 24579195 24579195 single base substitution C T intron_variant STAD-US 16 24579195 24579195 single base substitution C T missense_variant R546C 1636C>T STAD-US 16 24579195 24579195 single base substitution C T missense_variant R679C 2035C>T STAD-US 16 24580095 24580095 single base substitution A G downstream_gene_variant STAD-US 16 24580095 24580095 single base substitution A G exon_variant STAD-US 16 24580095 24580095 single base substitution A G intron_variant STAD-US 16 24580095 24580095 single base substitution A G missense_variant Y562C 1685A>G STAD-US 16 24580095 24580095 single base substitution A G missense_variant Y661C 1982A>G STAD-US 16 24580095 24580095 single base substitution A G missense_variant Y695C 2084A>G STAD-US 16 24580149 24580149 single base substitution G A downstream_gene_variant STAD-US 16 24580149 24580149 single base substitution G A exon_variant STAD-US 16 24580149 24580149 single base substitution G A intron_variant STAD-US 16 24580149 24580149 single base substitution G A missense_variant R580H 1739G>A STAD-US 16 24580149 24580149 single base substitution G A missense_variant R679H 2036G>A STAD-US 16 24580149 24580149 single base substitution G A missense_variant R713H 2138G>A STAD-US 16 24580275 24580275 single base substitution G A downstream_gene_variant STAD-US 16 24580275 24580275 single base substitution G A exon_variant STAD-US 16 24580275 24580275 single base substitution G A intron_variant STAD-US 16 24580275 24580275 single base substitution G A missense_variant R622Q 1865G>A STAD-US 16 24580275 24580275 single base substitution G A missense_variant R721Q 2162G>A STAD-US 16 24580275 24580275 single base substitution G A missense_variant R755Q 2264G>A STAD-US 16 24580751 24580751 single base substitution A G downstream_gene_variant STAD-US 16 24580751 24580751 single base substitution A G exon_variant STAD-US 16 24580751 24580751 single base substitution A G intron_variant STAD-US 16 24580751 24580751 single base substitution A G missense_variant T781A 2341A>G STAD-US 16 24580751 24580751 single base substitution A G missense_variant T880A 2638A>G STAD-US 16 24580751 24580751 single base substitution A G missense_variant T914A 2740A>G STAD-US 16 24581095 24581095 single base substitution G A downstream_gene_variant STAD-US 16 24581095 24581095 single base substitution G A exon_variant STAD-US 16 24581095 24581095 single base substitution G A intron_variant STAD-US 16 24581095 24581095 single base substitution G A synonymous_variant V1028V 3084G>A STAD-US 16 24581095 24581095 single base substitution G A synonymous_variant V895V 2685G>A STAD-US 16 24581095 24581095 single base substitution G A synonymous_variant V994V 2982G>A STAD-US 16 24581291 24581291 single base substitution A G downstream_gene_variant STAD-US 16 24581291 24581291 single base substitution A G exon_variant STAD-US 16 24581291 24581291 single base substitution A G intron_variant STAD-US 16 24581291 24581291 single base substitution A G missense_variant K1060E 3178A>G STAD-US 16 24581291 24581291 single base substitution A G missense_variant K1094E 3280A>G STAD-US 16 24581291 24581291 single base substitution A G missense_variant K961E 2881A>G STAD-US 16 24581590 24581590 single base substitution G A downstream_gene_variant STAD-US 16 24581590 24581590 single base substitution G A exon_variant STAD-US 16 24581590 24581590 single base substitution G A intron_variant STAD-US 16 24581590 24581590 single base substitution G A synonymous_variant R1159R 3477G>A STAD-US 16 24581590 24581590 single base substitution G A synonymous_variant R1193R 3579G>A STAD-US 16 24581665 24581665 single base substitution A C downstream_gene_variant STAD-US 16 24581665 24581665 single base substitution A C exon_variant STAD-US 16 24581665 24581665 single base substitution A C intron_variant STAD-US 16 24581665 24581665 single base substitution A C missense_variant K1184N 3552A>C STAD-US 16 24581665 24581665 single base substitution A C missense_variant K1218N 3654A>C STAD-US 16 24581781 24581781 single base substitution G A downstream_gene_variant STAD-US 16 24581781 24581781 single base substitution G A exon_variant STAD-US 16 24581781 24581781 single base substitution G A intron_variant STAD-US 16 24581781 24581781 single base substitution G A missense_variant G1223E 3668G>A STAD-US 16 24581781 24581781 single base substitution G A missense_variant G1257E 3770G>A STAD-US 16 24582742 24582742 single base substitution C T downstream_gene_variant STAD-US 16 24582742 24582742 single base substitution C T exon_variant STAD-US 16 24582742 24582742 single base substitution C T missense_variant T1418M 4253C>T STAD-US 16 24582742 24582742 single base substitution C T missense_variant T1452M 4355C>T STAD-US 16 24582742 24582742 single base substitution C T missense_variant T612M 1835C>T STAD-US 16 24582802 24582802 single base substitution A T downstream_gene_variant STAD-US 16 24582802 24582802 single base substitution A T exon_variant STAD-US 16 24582802 24582802 single base substitution A T missense_variant D1438V 4313A>T STAD-US 16 24582802 24582802 single base substitution A T missense_variant D1472V 4415A>T STAD-US 16 24582802 24582802 single base substitution A T missense_variant D632V 1895A>T STAD-US 16 24582804 24582804 deletion of <=200bp A - downstream_gene_variant STAD-US 16 24582804 24582804 deletion of <=200bp A - exon_variant STAD-US 16 24582804 24582804 deletion of <=200bp A - frameshift_variant K1439 STAD-US 16 24582804 24582804 deletion of <=200bp A - frameshift_variant K1473 STAD-US 16 24582804 24582804 deletion of <=200bp A - frameshift_variant K633 STAD-US 16 24583099 24583099 single base substitution A C downstream_gene_variant STAD-US 16 24583099 24583099 single base substitution A C exon_variant STAD-US 16 24583099 24583099 single base substitution A C missense_variant K1537T 4610A>C STAD-US 16 24583099 24583099 single base substitution A C missense_variant K1571T 4712A>C STAD-US 16 24583099 24583099 single base substitution A C missense_variant K731T 2192A>C STAD-US 16 24583197 24583197 insertion of <=200bp - A downstream_gene_variant STAD-US 16 24583197 24583197 insertion of <=200bp - A exon_variant STAD-US 16 24583197 24583197 insertion of <=200bp - A frameshift_variant T1570N? STAD-US 16 24583197 24583197 insertion of <=200bp - A frameshift_variant T1604N? STAD-US 16 24583197 24583197 insertion of <=200bp - A frameshift_variant T764N? STAD-US 16 24583525 24583525 single base substitution G A downstream_gene_variant STAD-US 16 24583525 24583525 single base substitution G A exon_variant STAD-US 16 24583525 24583525 single base substitution G A missense_variant S1679N 5036G>A STAD-US 16 24583525 24583525 single base substitution G A missense_variant S1713N 5138G>A STAD-US 16 24583525 24583525 single base substitution G A missense_variant S873N 2618G>A THCA-SA 16 24551046 24551046 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant THCA-SA 16 24551046 24551046 single base substitution C T exon_variant THCA-SA 16 24551046 24551046 single base substitution C T intron_variant THCA-SA 16 24551046 24551046 single base substitution C T upstream_gene_variant THCA-SA 16 24570844 24570844 single base substitution G A downstream_gene_variant THCA-SA 16 24570844 24570844 single base substitution G A exon_variant THCA-SA 16 24570844 24570844 single base substitution G A synonymous_variant G231G 693G>A THCA-SA 16 24570844 24570844 single base substitution G A synonymous_variant G98G 294G>A THCA-SA 16 24570844 24570844 single base substitution G A upstream_gene_variant THCA-SA 16 24583406 24583406 single base substitution A G downstream_gene_variant THCA-SA 16 24583406 24583406 single base substitution A G exon_variant THCA-SA 16 24583406 24583406 single base substitution A G synonymous_variant A1639A 4917A>G THCA-SA 16 24583406 24583406 single base substitution A G synonymous_variant A1673A 5019A>G THCA-SA 16 24583406 24583406 single base substitution A G synonymous_variant A833A 2499A>G THCA-SA 16 24584131 24584131 single base substitution A T 3_prime_UTR_variant THCA-SA 16 24584131 24584131 single base substitution A T downstream_gene_variant THCA-SA 16 24584131 24584131 single base substitution A T exon_variant THCA-US 16 24581020 24581020 insertion of <=200bp - AC downstream_gene_variant THCA-US 16 24581020 24581020 insertion of <=200bp - AC exon_variant THCA-US 16 24581020 24581020 insertion of <=200bp - AC frameshift_variant E1003E? THCA-US 16 24581020 24581020 insertion of <=200bp - AC frameshift_variant E870E? THCA-US 16 24581020 24581020 insertion of <=200bp - AC frameshift_variant E969E? THCA-US 16 24581020 24581020 insertion of <=200bp - AC intron_variant UCEC-US 16 24560282 24560282 single base substitution G T intron_variant UCEC-US 16 24560282 24560282 single base substitution G T missense_variant A95S 283G>T UCEC-US 16 24560282 24560282 single base substitution G T upstream_gene_variant UCEC-US 16 24564851 24564851 single base substitution G A 5_prime_UTR_variant UCEC-US 16 24564851 24564851 single base substitution G A downstream_gene_variant UCEC-US 16 24564851 24564851 single base substitution G A exon_variant UCEC-US 16 24564851 24564851 single base substitution G A synonymous_variant A107A 321G>A UCEC-US 16 24564851 24564851 single base substitution G A upstream_gene_variant UCEC-US 16 24566995 24566995 single base substitution G A exon_variant UCEC-US 16 24566995 24566995 single base substitution G A synonymous_variant S136S 408G>A UCEC-US 16 24566995 24566995 single base substitution G A synonymous_variant S3S 9G>A UCEC-US 16 24566995 24566995 single base substitution G A upstream_gene_variant UCEC-US 16 24567141 24567141 single base substitution G A splice_acceptor_variant UCEC-US 16 24567141 24567141 single base substitution G A upstream_gene_variant UCEC-US 16 24567184 24567184 single base substitution G A downstream_gene_variant UCEC-US 16 24567184 24567184 single base substitution G A exon_variant UCEC-US 16 24567184 24567184 single base substitution G A synonymous_variant T160T 480G>A UCEC-US 16 24567184 24567184 single base substitution G A synonymous_variant T27T 81G>A UCEC-US 16 24567634 24567634 single base substitution A C downstream_gene_variant UCEC-US 16 24567634 24567634 single base substitution A C exon_variant UCEC-US 16 24567634 24567634 single base substitution A C missense_variant K180N 540A>C UCEC-US 16 24567634 24567634 single base substitution A C missense_variant K47N 141A>C UCEC-US 16 24567735 24567735 single base substitution A G downstream_gene_variant UCEC-US 16 24567735 24567735 single base substitution A G exon_variant UCEC-US 16 24567735 24567735 single base substitution A G missense_variant N214S 641A>G UCEC-US 16 24567735 24567735 single base substitution A G missense_variant N81S 242A>G UCEC-US 16 24567769 24567769 single base substitution G A downstream_gene_variant UCEC-US 16 24567769 24567769 single base substitution G A splice_donor_variant UCEC-US 16 24573144 24573144 single base substitution G T downstream_gene_variant UCEC-US 16 24573144 24573144 single base substitution G T splice_acceptor_variant UCEC-US 16 24573144 24573144 single base substitution G T upstream_gene_variant UCEC-US 16 24573169 24573169 single base substitution A G downstream_gene_variant UCEC-US 16 24573169 24573169 single base substitution A G exon_variant UCEC-US 16 24573169 24573169 single base substitution A G missense_variant T193A 577A>G UCEC-US 16 24573169 24573169 single base substitution A G missense_variant T326A 976A>G UCEC-US 16 24573169 24573169 single base substitution A G upstream_gene_variant UCEC-US 16 24573186 24573188 deletion of <=200bp ACT - downstream_gene_variant UCEC-US 16 24573186 24573188 deletion of <=200bp ACT - exon_variant UCEC-US 16 24573186 24573188 deletion of <=200bp ACT - inframe_deletion RL198R UCEC-US 16 24573186 24573188 deletion of <=200bp ACT - inframe_deletion RL331R UCEC-US 16 24573186 24573188 deletion of <=200bp ACT - upstream_gene_variant UCEC-US 16 24573206 24573206 single base substitution C A downstream_gene_variant UCEC-US 16 24573206 24573206 single base substitution C A exon_variant UCEC-US 16 24573206 24573206 single base substitution C A missense_variant P205H 614C>A UCEC-US 16 24573206 24573206 single base substitution C A missense_variant P338H 1013C>A UCEC-US 16 24573206 24573206 single base substitution C A upstream_gene_variant UCEC-US 16 24573299 24573299 single base substitution T C downstream_gene_variant UCEC-US 16 24573299 24573299 single base substitution T C exon_variant UCEC-US 16 24573299 24573299 single base substitution T C missense_variant L236P 707T>C UCEC-US 16 24573299 24573299 single base substitution T C missense_variant L369P 1106T>C UCEC-US 16 24573299 24573299 single base substitution T C upstream_gene_variant UCEC-US 16 24573339 24573339 single base substitution G A downstream_gene_variant UCEC-US 16 24573339 24573339 single base substitution G A exon_variant UCEC-US 16 24573339 24573339 single base substitution G A synonymous_variant P249P 747G>A UCEC-US 16 24573339 24573339 single base substitution G A synonymous_variant P382P 1146G>A UCEC-US 16 24573339 24573339 single base substitution G A upstream_gene_variant UCEC-US 16 24574599 24574599 single base substitution G A downstream_gene_variant UCEC-US 16 24574599 24574599 single base substitution G A exon_variant UCEC-US 16 24574599 24574599 single base substitution G A intron_variant UCEC-US 16 24574599 24574599 single base substitution G A missense_variant A324T 970G>A UCEC-US 16 24574599 24574599 single base substitution G A missense_variant A457T 1369G>A UCEC-US 16 24574599 24574599 single base substitution G A upstream_gene_variant UCEC-US 16 24574804 24574804 single base substitution C T downstream_gene_variant UCEC-US 16 24574804 24574804 single base substitution C T exon_variant UCEC-US 16 24574804 24574804 single base substitution C T intron_variant UCEC-US 16 24574804 24574804 single base substitution C T stop_gained Q350* 1048C>T UCEC-US 16 24574804 24574804 single base substitution C T stop_gained Q483* 1447C>T UCEC-US 16 24574952 24574952 single base substitution C T downstream_gene_variant UCEC-US 16 24574952 24574952 single base substitution C T exon_variant UCEC-US 16 24574952 24574952 single base substitution C T intron_variant UCEC-US 16 24574952 24574952 single base substitution C T missense_variant A363V 1088C>T UCEC-US 16 24574952 24574952 single base substitution C T missense_variant A496V 1487C>T UCEC-US 16 24578822 24578822 single base substitution G T downstream_gene_variant UCEC-US 16 24578822 24578822 single base substitution G T exon_variant UCEC-US 16 24578822 24578822 single base substitution G T intron_variant UCEC-US 16 24578822 24578822 single base substitution G T stop_gained E517* 1549G>T UCEC-US 16 24578822 24578822 single base substitution G T stop_gained E650* 1948G>T UCEC-US 16 24580274 24580274 single base substitution C T downstream_gene_variant UCEC-US 16 24580274 24580274 single base substitution C T exon_variant UCEC-US 16 24580274 24580274 single base substitution C T intron_variant UCEC-US 16 24580274 24580274 single base substitution C T stop_gained R622* 1864C>T UCEC-US 16 24580274 24580274 single base substitution C T stop_gained R721* 2161C>T UCEC-US 16 24580274 24580274 single base substitution C T stop_gained R755* 2263C>T UCEC-US 16 24580275 24580275 single base substitution G A downstream_gene_variant UCEC-US 16 24580275 24580275 single base substitution G A exon_variant UCEC-US 16 24580275 24580275 single base substitution G A intron_variant UCEC-US 16 24580275 24580275 single base substitution G A missense_variant R622Q 1865G>A UCEC-US 16 24580275 24580275 single base substitution G A missense_variant R721Q 2162G>A UCEC-US 16 24580275 24580275 single base substitution G A missense_variant R755Q 2264G>A UCEC-US 16 24580461 24580461 single base substitution A C downstream_gene_variant UCEC-US 16 24580461 24580461 single base substitution A C exon_variant UCEC-US 16 24580461 24580461 single base substitution A C intron_variant UCEC-US 16 24580461 24580461 single base substitution A C missense_variant D684A 2051A>C UCEC-US 16 24580461 24580461 single base substitution A C missense_variant D783A 2348A>C UCEC-US 16 24580461 24580461 single base substitution A C missense_variant D817A 2450A>C UCEC-US 16 24580488 24580488 single base substitution G A downstream_gene_variant UCEC-US 16 24580488 24580488 single base substitution G A exon_variant UCEC-US 16 24580488 24580488 single base substitution G A intron_variant UCEC-US 16 24580488 24580488 single base substitution G A missense_variant R693H 2078G>A UCEC-US 16 24580488 24580488 single base substitution G A missense_variant R792H 2375G>A UCEC-US 16 24580488 24580488 single base substitution G A missense_variant R826H 2477G>A UCEC-US 16 24580685 24580685 single base substitution C T downstream_gene_variant UCEC-US 16 24580685 24580685 single base substitution C T exon_variant UCEC-US 16 24580685 24580685 single base substitution C T intron_variant UCEC-US 16 24580685 24580685 single base substitution C T stop_gained R759* 2275C>T UCEC-US 16 24580685 24580685 single base substitution C T stop_gained R858* 2572C>T UCEC-US 16 24580685 24580685 single base substitution C T stop_gained R892* 2674C>T UCEC-US 16 24581211 24581211 single base substitution C T downstream_gene_variant UCEC-US 16 24581211 24581211 single base substitution C T exon_variant UCEC-US 16 24581211 24581211 single base substitution C T intron_variant UCEC-US 16 24581211 24581211 single base substitution C T missense_variant P1033L 3098C>T UCEC-US 16 24581211 24581211 single base substitution C T missense_variant P1067L 3200C>T UCEC-US 16 24581211 24581211 single base substitution C T missense_variant P934L 2801C>T UCEC-US 16 24581341 24581343 deletion of <=200bp GAA - downstream_gene_variant UCEC-US 16 24581341 24581343 deletion of <=200bp GAA - exon_variant UCEC-US 16 24581341 24581343 deletion of <=200bp GAA - inframe_deletion VK1076V UCEC-US 16 24581341 24581343 deletion of <=200bp GAA - inframe_deletion VK1110V UCEC-US 16 24581341 24581343 deletion of <=200bp GAA - inframe_deletion VK977V UCEC-US 16 24581341 24581343 deletion of <=200bp GAA - intron_variant UCEC-US 16 24581419 24581422 deletion of <=200bp AAAC - downstream_gene_variant UCEC-US 16 24581419 24581422 deletion of <=200bp AAAC - exon_variant UCEC-US 16 24581419 24581422 deletion of <=200bp AAAC - frameshift_variant KN1003 UCEC-US 16 24581419 24581422 deletion of <=200bp AAAC - frameshift_variant KN1102 UCEC-US 16 24581419 24581422 deletion of <=200bp AAAC - frameshift_variant KN1136 UCEC-US 16 24581419 24581422 deletion of <=200bp AAAC - intron_variant UCEC-US 16 24581699 24581699 single base substitution G T downstream_gene_variant UCEC-US 16 24581699 24581699 single base substitution G T exon_variant UCEC-US 16 24581699 24581699 single base substitution G T intron_variant UCEC-US 16 24581699 24581699 single base substitution G T stop_gained E1196* 3586G>T UCEC-US 16 24581699 24581699 single base substitution G T stop_gained E1230* 3688G>T UCEC-US 16 24581796 24581796 single base substitution G T downstream_gene_variant UCEC-US 16 24581796 24581796 single base substitution G T exon_variant UCEC-US 16 24581796 24581796 single base substitution G T intron_variant UCEC-US 16 24581796 24581796 single base substitution G T missense_variant S1228I 3683G>T UCEC-US 16 24581796 24581796 single base substitution G T missense_variant S1262I 3785G>T UCEC-US 16 24582237 24582237 single base substitution G T downstream_gene_variant UCEC-US 16 24582237 24582237 single base substitution G T exon_variant UCEC-US 16 24582237 24582237 single base substitution G T stop_gained E1250* 3748G>T UCEC-US 16 24582237 24582237 single base substitution G T stop_gained E1284* 3850G>T UCEC-US 16 24582237 24582237 single base substitution G T stop_gained E444* 1330G>T UCEC-US 16 24582255 24582255 single base substitution C T downstream_gene_variant UCEC-US 16 24582255 24582255 single base substitution C T exon_variant UCEC-US 16 24582255 24582255 single base substitution C T stop_gained R1256* 3766C>T UCEC-US 16 24582255 24582255 single base substitution C T stop_gained R1290* 3868C>T UCEC-US 16 24582255 24582255 single base substitution C T stop_gained R450* 1348C>T UCEC-US 16 24582256 24582256 single base substitution G A downstream_gene_variant UCEC-US 16 24582256 24582256 single base substitution G A exon_variant UCEC-US 16 24582256 24582256 single base substitution G A missense_variant R1256Q 3767G>A UCEC-US 16 24582256 24582256 single base substitution G A missense_variant R1290Q 3869G>A UCEC-US 16 24582256 24582256 single base substitution G A missense_variant R450Q 1349G>A UCEC-US 16 24582375 24582375 single base substitution G A downstream_gene_variant UCEC-US 16 24582375 24582375 single base substitution G A exon_variant UCEC-US 16 24582375 24582375 single base substitution G A missense_variant E1296K 3886G>A UCEC-US 16 24582375 24582375 single base substitution G A missense_variant E1330K 3988G>A UCEC-US 16 24582375 24582375 single base substitution G A missense_variant E490K 1468G>A UCEC-US 16 24582684 24582684 single base substitution C T downstream_gene_variant UCEC-US 16 24582684 24582684 single base substitution C T exon_variant UCEC-US 16 24582684 24582684 single base substitution C T missense_variant R1399C 4195C>T UCEC-US 16 24582684 24582684 single base substitution C T missense_variant R1433C 4297C>T UCEC-US 16 24582684 24582684 single base substitution C T missense_variant R593C 1777C>T UCEC-US 16 24582742 24582742 single base substitution C T downstream_gene_variant UCEC-US 16 24582742 24582742 single base substitution C T exon_variant UCEC-US 16 24582742 24582742 single base substitution C T missense_variant T1418M 4253C>T UCEC-US 16 24582742 24582742 single base substitution C T missense_variant T1452M 4355C>T UCEC-US 16 24582742 24582742 single base substitution C T missense_variant T612M 1835C>T UCEC-US 16 24582752 24582752 single base substitution A G downstream_gene_variant UCEC-US 16 24582752 24582752 single base substitution A G exon_variant UCEC-US 16 24582752 24582752 single base substitution A G synonymous_variant K1421K 4263A>G UCEC-US 16 24582752 24582752 single base substitution A G synonymous_variant K1455K 4365A>G UCEC-US 16 24582752 24582752 single base substitution A G synonymous_variant K615K 1845A>G UCEC-US 16 24582876 24582876 single base substitution C T downstream_gene_variant UCEC-US 16 24582876 24582876 single base substitution C T exon_variant UCEC-US 16 24582876 24582876 single base substitution C T stop_gained R1463* 4387C>T UCEC-US 16 24582876 24582876 single base substitution C T stop_gained R1497* 4489C>T UCEC-US 16 24582876 24582876 single base substitution C T stop_gained R657* 1969C>T UCEC-US 16 24582884 24582885 deletion of <=200bp CT - downstream_gene_variant UCEC-US 16 24582884 24582885 deletion of <=200bp CT - exon_variant UCEC-US 16 24582884 24582885 deletion of <=200bp CT - frameshift_variant DS1465 UCEC-US 16 24582884 24582885 deletion of <=200bp CT - frameshift_variant DS1499 UCEC-US 16 24582884 24582885 deletion of <=200bp CT - frameshift_variant DS659 UCEC-US 16 24582941 24582941 single base substitution G T downstream_gene_variant UCEC-US 16 24582941 24582941 single base substitution G T exon_variant UCEC-US 16 24582941 24582941 single base substitution G T missense_variant E1484D 4452G>T UCEC-US 16 24582941 24582941 single base substitution G T missense_variant E1518D 4554G>T UCEC-US 16 24582941 24582941 single base substitution G T missense_variant E678D 2034G>T UCEC-US 16 24583226 24583226 single base substitution G A downstream_gene_variant UCEC-US 16 24583226 24583226 single base substitution G A exon_variant UCEC-US 16 24583226 24583226 single base substitution G A synonymous_variant K1579K 4737G>A UCEC-US 16 24583226 24583226 single base substitution G A synonymous_variant K1613K 4839G>A UCEC-US 16 24583226 24583226 single base substitution G A synonymous_variant K773K 2319G>A UCEC-US 16 24583347 24583347 single base substitution G T downstream_gene_variant UCEC-US 16 24583347 24583347 single base substitution G T exon_variant UCEC-US 16 24583347 24583347 single base substitution G T stop_gained E1620* 4858G>T UCEC-US 16 24583347 24583347 single base substitution G T stop_gained E1654* 4960G>T UCEC-US 16 24583347 24583347 single base substitution G T stop_gained E814* 2440G>T UCEC-US 16 24583372 24583372 single base substitution C A downstream_gene_variant UCEC-US 16 24583372 24583372 single base substitution C A exon_variant UCEC-US 16 24583372 24583372 single base substitution C A missense_variant S1628Y 4883C>A UCEC-US 16 24583372 24583372 single base substitution C A missense_variant S1662Y 4985C>A UCEC-US 16 24583372 24583372 single base substitution C A missense_variant S822Y 2465C>A UCEC-US 16 24583592 24583592 single base substitution G T downstream_gene_variant UCEC-US 16 24583592 24583592 single base substitution G T exon_variant UCEC-US 16 24583592 24583592 single base substitution G T missense_variant K1701N 5103G>T UCEC-US 16 24583592 24583592 single base substitution G T missense_variant K1735N 5205G>T UCEC-US 16 24583592 24583592 single base substitution G T missense_variant K895N 2685G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand Pat_76_A COSM5850524 c.427G>A p.D143N Substitution - Missense 16:24555693-24555693 + ccRCC-11 COSM1663846 c.368C>G p.A123G Substitution - Missense 16:24555634-24555634 + TCGA-04-1530-01 COSM116145 c.1804C>T p.P602S Substitution - Missense 16:24567357-24567357 + TCGA-DK-A3X1-01 COSM3794707 c.379G>A p.E127K Substitution - Missense 16:24555645-24555645 + J74_T COSM3957361 c.157A>G p.T53A Substitution - Missense 16:24540783-24540783 + TCGA-FD-A3NA-01 COSM1301757 c.4654A>G p.K1552E Substitution - Missense 16:24571720-24571720 + TCGA-BR-6452-01 COSM4059484 c.3084G>A p.V1028V Substitution - coding silent 16:24569774-24569774 + TCGA-EK-A2PM-01 COSM4831393 c.178G>A p.D60N Substitution - Missense 16:24546174-24546174 + TCGA-A8-A09W-01 COSM434957 c.4496A>G p.D1499G Substitution - Missense 16:24571562-24571562 + YUKAT COSM5384567 c.1315G>A p.A439T Substitution - Missense 16:24563224-24563224 + TCGA-AP-A056-01 COSM968961 c.2450A>C p.D817A Substitution - Missense 16:24569140-24569140 + T3094 COSM1376904 c.4047delA p.N1351fs*9 Deletion - Frameshift 16:24571113-24571113 + 587222 COSM1223283 c.329C>A p.S110Y Substitution - Missense 16:24553538-24553538 + TCGA-D5-6927-01 COSM1376900 c.2186G>A p.R729Q Substitution - Missense 16:24568876-24568876 + Gp2D COSM4627387 c.4625C>A p.P1542H Substitution - Missense 16:24571691-24571691 + TCGA-CC-A7IF-01 COSM4915511 c.1992T>G p.D664E Substitution - Missense 16:24567831-24567831 + TCGA-MH-A561-01 COSM3988358 c.3482A>T p.E1161V Substitution - Missense 16:24570172-24570172 + S00050 COSM317964 c.3554A>C p.E1185A Substitution - Missense 16:24570244-24570244 + TCGA-D1-A17C-01 COSM968962 c.2477G>A p.R826H Substitution - Missense 16:24569167-24569167 + Pat_76_B COSM3507995 c.1723C>T p.P575S Substitution - Missense 16:24567276-24567276 + OSCC-GB_00560111 COSM4883698 c.2415A>G p.P805P Substitution - coding silent 16:24569105-24569105 + TCGA-AA-3941-01 COSM296784 c.3201G>C p.P1067P Substitution - coding silent 16:24569891-24569891 + PCSI0048 COSM216369 c.894G>A p.T298T Substitution - coding silent 16:24561658-24561658 + TCGA-B5-A11N-01 COSM968958 c.1948G>T p.E650* Substitution - Nonsense 16:24567501-24567501 + TCGA-D9-A6EC-06 COSM4405593 c.3479T>G p.F1160C Substitution - Missense 16:24570169-24570169 + TCGA-F5-6814-01 COSM3420887 c.3602C>A p.S1201Y Substitution - Missense 16:24570292-24570292 + 8058184 COSM3387317 c.674C>T p.A225V Substitution - Missense 16:24556447-24556447 + OSCC-GB_00850111 COSM968972 c.3869G>A p.R1290Q Substitution - Missense 16:24570935-24570935 + pfg008T COSM1640432 c.3910A>G p.T1304A Substitution - Missense 16:24570976-24570976 + TCGA-J4-A67L-01 COSM4391899 c.600G>C p.M200I Substitution - Missense 16:24556373-24556373 + LS174T COSM3280315 c.1021delC p.P342fs*8 Deletion - Frameshift 16:24561893-24561893 + TCGA-B0-4707-01 COSM3773744 c.5331G>T p.E1777D Substitution - Missense 16:24572397-24572397 + RK104_C01 COSM3701067 c.1657A>G p.T553A Substitution - Missense 16:24567210-24567210 + TCGA-A5-A0VP-01 COSM968947 c.674+1G>A p.? Unknown 16:24556448-24556448 + TCGA-FS-A4F9-06 COSM968980 c.4839G>A p.K1613K Substitution - coding silent 16:24571905-24571905 + T3724 COSM4720580 c.1671A>G p.V557V Substitution - coding silent 16:24567224-24567224 + TCGA-24-1557-01 COSM78399 c.3938T>C p.M1313T Substitution - Missense 16:24571004-24571004 + BD173T COSM5500151 c.2576A>G p.N859S Substitution - Missense 16:24569266-24569266 + TCGA-BR-8077-01 COSM4059486 c.3579G>A p.R1193R Substitution - coding silent 16:24570269-24570269 + TCGA-B5-A11O-01 COSM968957 c.1511G>T p.G504V Substitution - Missense 16:24563655-24563655 + OLID09 COSM132840 c.348+2_348+3delTA p.? Unknown 16:24553559-24553560 + WA46 COSM241374 c.4426_4429delGACT p.D1476fs*18 Deletion - Frameshift 16:24571492-24571495 + 587238 COSM1223280 c.5135G>A p.R1712Q Substitution - Missense 16:24572201-24572201 + 585258 COSM326331 c.3545G>A p.R1182H Substitution - Missense 16:24570235-24570235 + T3 COSM5342730 c.2482C>T p.R828* Substitution - Nonsense 16:24569172-24569172 + LS411 COSM3280361 c.2644G>T p.D882Y Substitution - Missense 16:24569334-24569334 + CSCC-20-T COSM4572637 c.816T>G p.I272M Substitution - Missense 16:24559646-24559646 + TCGA-D8-A1XK-01 COSM3817591 c.1386+2T>A p.? Unknown 16:24563297-24563297 + TCGA-66-2793-01 COSM702931 c.3507A>T p.K1169N Substitution - Missense 16:24570197-24570197 + U2940 COSM5621674 c.1910C>T p.S637F Substitution - Missense 16:24567463-24567463 + TCGA-EE-A29V-06 COSM3280351 c.2350C>T p.R784C Substitution - Missense 16:24569040-24569040 + Pat_41_B COSM5850526 c.1915G>A p.E639K Substitution - Missense 16:24567468-24567468 + TCGA-37-3783-01 COSM702929 c.4300C>G p.L1434V Substitution - Missense 16:24571366-24571366 + YUSCA COSM5384566 c.1204C>T p.P402S Substitution - Missense 16:24562076-24562076 + TCGA-EI-6507-01 COSM1563171 c.4567delA p.G1525fs*37 Deletion - Frameshift 16:24571633-24571633 + pfg057T COSM4751341 c.1618G>A p.E540K Substitution - Missense 16:24567171-24567171 + SJACT004_D COSM4967959 c.1322C>T p.A441V Substitution - Missense 16:24563231-24563231 + 587220 COSM1223281 c.3766A>G p.T1256A Substitution - Missense 16:24570456-24570456 + TCGA-EE-A3JE-06 COSM3507995 c.1723C>T p.P575S Substitution - Missense 16:24567276-24567276 + T3091 COSM4720582 c.2137C>T p.R713C Substitution - Missense 16:24568827-24568827 + CSCC-15-T COSM3280339 c.1870C>T p.H624Y Substitution - Missense 16:24567423-24567423 + 2492721 COSM5724235 c.2559C>T p.P853P Substitution - coding silent 16:24569249-24569249 + ODG3 COSM5731456 c.2647_2648delTA p.Y883fs*7 Deletion - Frameshift 16:24569337-24569338 + PCSI_0048_Pa_P_526 COSM216369 c.894G>A p.T298T Substitution - coding silent 16:24561658-24561658 + T263 COSM4720578 c.1014T>G p.P338P Substitution - coding silent 16:24561886-24561886 + S02296 COSM5689417 c.3464G>C p.G1155A Substitution - Missense 16:24570154-24570154 + CLL063 COSM1290494 c.999delA p.K334fs*16 Deletion - Frameshift 16:24561871-24561871 + C0030T COSM4151282 c.603A>T p.E201D Substitution - Missense 16:24556376-24556376 + ASHPC_0022_Pa_P COSM4962756 c.836A>G p.Y279C Substitution - Missense 16:24559666-24559666 + tumor_4124542 COSM5947217 c.256A>T p.T86S Substitution - Missense 16:24546252-24546252 + Au3 COSM5602191 c.1268delA p.K424fs*61 Deletion - Frameshift 16:24562140-24562140 + TCGA-D1-A177-01 COSM968966 c.3408_3411delAAAC p.K1138fs*18 Deletion - Frameshift 16:24570098-24570101 + ESO-837 COSM1240022 c.2983T>A p.S995T Substitution - Missense 16:24569673-24569673 + 587376 COSM1223285 c.1418C>A p.S473Y Substitution - Missense 16:24563454-24563454 + TCGA-AC-A23H-01 COSM3817590 c.1327G>T p.A443S Substitution - Missense 16:24563236-24563236 + TCGA-B5-A11E-01 COSM968971 c.3868C>T p.R1290* Substitution - Nonsense 16:24570934-24570934 + pfg122T COSM4751343 c.4298G>A p.R1433H Substitution - Missense 16:24571364-24571364 + TCGA-B5-A11E-01 COSM968953 c.1146G>A p.P382P Substitution - coding silent 16:24562018-24562018 + LUAD-RT-S01711 COSM380119 c.4848C>G p.P1616P Substitution - coding silent 16:24571914-24571914 + CSCC-20-T COSM1376901 c.3178delA p.A1062fs*49 Deletion - Frameshift 16:24569868-24569868 + TCGA-G2-A2EC-01 COSM1301755 c.1696C>T p.P566S Substitution - Missense 16:24567249-24567249 + TCGA-IR-A3LA-01 COSM4845011 c.1629G>A p.Q543Q Substitution - coding silent 16:24567182-24567182 + 234 COSM216369 c.894G>A p.T298T Substitution - coding silent 16:24561658-24561658 + TCGA-24-1427-01 COSM76184 c.272G>A p.R91Q Substitution - Missense 16:24548950-24548950 + TCGA-CG-5721-01 COSM4059485 c.3280A>G p.K1094E Substitution - Missense 16:24569970-24569970 + TCGA-BR-A4QL-01 COSM968975 c.4355C>T p.T1452M Substitution - Missense 16:24571421-24571421 + tumor_4128852 COSM5948355 c.1365T>A p.I455I Substitution - coding silent 16:24563274-24563274 + 71 COSM4777656 c.3720_3721insC p.K1241fs*3 Insertion - Frameshift 16:24570410-24570411 + HCT8 COSM3280386 c.4356G>A p.T1452T Substitution - coding silent 16:24571422-24571422 + 587234 COSM1223284 c.2959A>G p.R987G Substitution - Missense 16:24569649-24569649 + TCGA-FS-A1ZW-06 COSM3508007 c.4693C>T p.P1565S Substitution - Missense 16:24571759-24571759 + TCGA-EE-A20C-06 COSM3508001 c.3158C>T p.P1053L Substitution - Missense 16:24569848-24569848 + SNUH_G16_S1 COSM3999806 c.3393G>A p.K1131K Substitution - coding silent 16:24570083-24570083 + TCGA-AP-A0LM-01 COSM968942 c.408G>A p.S136S Substitution - coding silent 16:24555674-24555674 + 5 COSM1237108 c.3061C>T p.R1021W Substitution - Missense 16:24569751-24569751 + 2521262 COSM5892300 c.4001A>G p.K1334R Substitution - Missense 16:24571067-24571067 + HCT8 COSM4634060 c.4458A>G p.K1486K Substitution - coding silent 16:24571524-24571524 + PCSI_0083_Pa_P COSM968941 c.321G>A p.A107A Substitution - coding silent 16:24553530-24553530 + RK051_C01 COSM1629841 c.4607C>T p.P1536L Substitution - Missense 16:24571673-24571673 + PT55 COSM5942672 c.1706C>T p.P569L Substitution - Missense 16:24567259-24567259 + C0004T COSM4151283 c.5238G>A p.K1746K Substitution - coding silent 16:24572304-24572304 + ESCC_158 COSM5646670 c.3970G>C p.D1324H Substitution - Missense 16:24571036-24571036 + TCGA-BS-A0UV-01 COSM968951 c.1013C>A p.P338H Substitution - Missense 16:24561885-24561885 + TCGA-D3-A2JF-06 COSM116145 c.1804C>T p.P602S Substitution - Missense 16:24567357-24567357 + LXFL529 COSM1197133 c.5302A>G p.K1768E Substitution - Missense 16:24572368-24572368 + TCGA-EE-A3JD-06 COSM4397113 c.1798C>T p.P600S Substitution - Missense 16:24567351-24567351 + TCGA-D9-A6EC-06 COSM4400166 c.4857T>G p.S1619R Substitution - Missense 16:24571923-24571923 + CSCC-10-T COSM4459891 c.1145C>T p.P382L Substitution - Missense 16:24562017-24562017 + TCGA-BP-4761-01 COSM3361699 c.2901A>G p.E967E Substitution - coding silent 16:24569591-24569591 + TCGA-D1-A103-01 COSM968975 c.4355C>T p.T1452M Substitution - Missense 16:24571421-24571421 + TCGA-HU-8602-01 COSM968960 c.2264G>A p.R755Q Substitution - Missense 16:24568954-24568954 + TCGA-CG-5726-01 COSM4059489 c.4415A>T p.D1472V Substitution - Missense 16:24571481-24571481 + EWS502 COSM4578841 c.2537C>T p.A846V Substitution - Missense 16:24569227-24569227 + S02279 COSM5683617 c.2647T>G p.Y883D Substitution - Missense 16:24569337-24569337 + TCGA-D1-A17M-01 COSM968968 c.3757C>T p.R1253* Substitution - Nonsense 16:24570447-24570447 + TCGA-BR-8360-01 COSM4059488 c.3770G>A p.G1257E Substitution - Missense 16:24570460-24570460 + ESCC_108 COSM5638644 c.4935C>T p.D1645D Substitution - coding silent 16:24572001-24572001 + AOCS-004-1-5 COSM3948400 c.3790A>G p.T1264A Substitution - Missense 16:24570480-24570480 + Pat_08_A COSM5850528 c.2584C>T p.P862S Substitution - Missense 16:24569274-24569274 + TCGA-D3-A2JL-06 COSM3508003 c.3753C>T p.V1251V Substitution - coding silent 16:24570443-24570443 + T1240 COSM4720584 c.3508C>T p.L1170L Substitution - coding silent 16:24570198-24570198 + TCGA-BS-A0UV-01 COSM968983 c.5205G>T p.K1735N Substitution - Missense 16:24572271-24572271 + GC_299T1-GC_299N COSM4772555 c.3006T>C p.S1002S Substitution - coding silent 16:24569696-24569696 + TCGA-AZ-6598-01 COSM1376906 c.4417delA p.T1475fs*20 Deletion - Frameshift 16:24571483-24571483 + TCGA-06-0686-01 COSM2151550 c.4540A>C p.K1514Q Substitution - Missense 16:24571606-24571606 + TCGA-CG-5728-01 COSM4059487 c.3654A>C p.K1218N Substitution - Missense 16:24570344-24570344 + P04-1243 COSM246964 c.2658G>A p.G886G Substitution - coding silent 16:24569348-24569348 + TCGA-EE-A3JD-06 COSM4397278 c.2291G>A p.R764K Substitution - Missense 16:24568981-24568981 + ESO-114 COSM1263881 c.5205G>A p.K1735K Substitution - coding silent 16:24572271-24572271 + TCGA-AX-A0J1-01 COSM968971 c.3868C>T p.R1290* Substitution - Nonsense 16:24570934-24570934 + 2293782 COSM4608585 c.2827G>T p.E943* Substitution - Nonsense 16:24569517-24569517 + TCGA-BR-4370-01 COSM4059482 c.2138G>A p.R713H Substitution - Missense 16:24568828-24568828 + TCGA-BR-8680-01 COSM4059479 c.1803T>C p.P601P Substitution - coding silent 16:24567356-24567356 + C91 COSM4444528 c.869A>T p.E290V Substitution - Missense 16:24561633-24561633 + 6115237 COSM5573546 c.304-1G>C p.? Unknown 16:24553512-24553512 + TCGA-06-0686 COSM2151550 c.4540A>C p.K1514Q Substitution - Missense 16:24571606-24571606 + TCGA-BR-8680-01 COSM4059476 c.83A>C p.D28A Substitution - Missense 16:24540709-24540709 + PCSI_0074_Pa_X COSM3377839 c.4242G>A p.E1414E Substitution - coding silent 16:24571308-24571308 + TCGA-BS-A0UF-01 COSM968970 c.3850G>T p.E1284* Substitution - Nonsense 16:24570916-24570916 + TCGA-AN-A0FV-01 COSM434952 c.457G>C p.G153R Substitution - Missense 16:24555840-24555840 + 002 COSM1162132 c.2296_2297insT p.Y766fs*12 Insertion - Frameshift 16:24568986-24568987 + TCGA-GN-A266-06 COSM1518646 c.1288C>T p.R430W Substitution - Missense 16:24562160-24562160 + TCGA-AP-A0LM-01 COSM968973 c.3988G>A p.E1330K Substitution - Missense 16:24571054-24571054 + 3206A7_009_T COSM5043048 c.5041G>T p.A1681S Substitution - Missense 16:24572107-24572107 + SNU-175 COSM3280359 c.2511G>A p.W837* Substitution - Nonsense 16:24569201-24569201 + CRC-4 COSM304425 c.3914C>T p.A1305V Substitution - Missense 16:24570980-24570980 + sysucc-1370T COSM968977 c.4489C>T p.R1497* Substitution - Nonsense 16:24571555-24571555 + RMS10_ COSM3773744 c.5331G>T p.E1777D Substitution - Missense 16:24572397-24572397 + 4095_T COSM3957363 c.1786G>T p.G596W Substitution - Missense 16:24567339-24567339 + PACA-59-T COSM1158281 c.4601C>A p.S1534Y Substitution - Missense 16:24571667-24571667 + Pat_76_A COSM3507995 c.1723C>T p.P575S Substitution - Missense 16:24567276-24567276 + PCSI_0022_Pa_P COSM3787121 c.1246G>T p.V416L Substitution - Missense 16:24562118-24562118 + RKO COSM3280346 c.2041C>T p.R681C Substitution - Missense 16:24567880-24567880 + TCGA-BS-A0UF-01 COSM968941 c.321G>A p.A107A Substitution - coding silent 16:24553530-24553530 + TCGA-B6-A0IK-01 COSM434955 c.3235C>G p.Q1079E Substitution - Missense 16:24569925-24569925 + ccRCC-100 COSM1660166 c.71T>C p.I24T Substitution - Missense 16:24540697-24540697 + TCGA-AP-A054-01 COSM968949 c.976A>G p.T326A Substitution - Missense 16:24561848-24561848 + TCGA-BS-A0UF-01 COSM968981 c.4960G>T p.E1654* Substitution - Nonsense 16:24572026-24572026 + PACA59 COSM1158281 c.4601C>A p.S1534Y Substitution - Missense 16:24571667-24571667 + T207 COSM4720577 c.988A>G p.K330E Substitution - Missense 16:24561860-24561860 + TCGA-KK-A59V-01 COSM4878818 c.1509A>G p.P503P Substitution - coding silent 16:24563653-24563653 + TCGA-BT-A20V-01 COSM417093 c.2573A>G p.E858G Substitution - Missense 16:24569263-24569263 + Pat_41_B COSM5850527 c.2573A>T p.E858V Substitution - Missense 16:24569263-24569263 + Pa11X COSM84339 c.1918G>T p.E640* Substitution - Nonsense 16:24567471-24567471 + CHC1704T COSM4803995 c.4058G>T p.S1353I Substitution - Missense 16:24571124-24571124 + 2492723 COSM5724235 c.2559C>T p.P853P Substitution - coding silent 16:24569249-24569249 + TCGA-CJ-4892-01 COSM3361701 c.3238A>T p.K1080* Substitution - Nonsense 16:24569928-24569928 + 1N26-VS-1T26 COSM4973490 c.3242A>T p.D1081V Substitution - Missense 16:24569932-24569932 + 428 COSM4433180 c.2120C>G p.S707C Substitution - Missense 16:24568810-24568810 + TCGA-AA-3684-01 COSM268149 c.5279G>A p.S1760N Substitution - Missense 16:24572345-24572345 + TCGA-EI-6917-01 COSM3420888 c.4396G>T p.D1466Y Substitution - Missense 16:24571462-24571462 + LUAD-CHTN-Z4716A COSM361839 c.2587_2588GA>TT p.E863>? Complex 16:24569277-24569278 + T3454 COSM4720579 c.1650A>G p.L550L Substitution - coding silent 16:24567203-24567203 + TCGA-D1-A16X-01 COSM968974 c.4297C>T p.R1433C Substitution - Missense 16:24571363-24571363 + TCGA-24-1560-01 COSM82327 c.1617C>T p.S539S Substitution - coding silent 16:24567170-24567170 + TCGA-FW-A3R5-06 COSM3888253 c.1724C>T p.P575L Substitution - Missense 16:24567277-24567277 + DLD1 COSM3280386 c.4356G>A p.T1452T Substitution - coding silent 16:24571422-24571422 + TCGA-CJ-4881-01 COSM3361700 c.3237G>C p.Q1079H Substitution - Missense 16:24569927-24569927 + RK193_C01 COSM3741858 c.4332T>G p.S1444S Substitution - coding silent 16:24571398-24571398 + PD6732b COSM5768968 c.947G>A p.R316Q Substitution - Missense 16:24561711-24561711 + CSCC-18-T COSM4450054 c.4290delT p.L1431fs*4 Deletion - Frameshift 16:24571356-24571356 + PCSI_0090_Pa_X COSM3377838 c.1363A>G p.I455V Substitution - Missense 16:24563272-24563272 + Au3 COSM5602192 c.1269A>T p.E423D Substitution - Missense 16:24562141-24562141 + TCGA-DK-A3IL-01 COSM1301756 c.4594A>G p.S1532G Substitution - Missense 16:24571660-24571660 + TCGA-EE-A2MJ-06 COSM3508005 c.4313G>A p.G1438E Substitution - Missense 16:24571379-24571379 + ESO-859 COSM1240022 c.2983T>A p.S995T Substitution - Missense 16:24569673-24569673 + CHC2098T COSM4788244 c.7T>C p.C3R Substitution - Missense 16:24540633-24540633 + CHC2098T COSM4788244 c.7T>C p.C3R Substitution - Missense 16:24540633-24540633 + TCGA-CF-A3MI-01 COSM1301754 c.941T>G p.F314C Substitution - Missense 16:24561705-24561705 + CSCC-44-T COSM4540697 c.2884G>C p.E962Q Substitution - Missense 16:24569574-24569574 + T578 COSM4720585 c.3899A>C p.N1300T Substitution - Missense 16:24570965-24570965 + PT38 COSM5923171 c.2066C>T p.P689L Substitution - Missense 16:24568756-24568756 + YUMOOK COSM1708986 c.3503C>T p.S1168L Substitution - Missense 16:24570193-24570193 + AOCS-106-1-1 COSM3948402 c.4824C>G p.D1608E Substitution - Missense 16:24571890-24571890 + BK0076 COSM4188699 c.4260G>C p.K1420N Substitution - Missense 16:24571326-24571326 + TCGA-FS-A1ZP-06 COSM3507995 c.1723C>T p.P575S Substitution - Missense 16:24567276-24567276 + PTC-14C COSM4128834 c.3371C>G p.T1124R Substitution - Missense 16:24570061-24570061 + TCGA-DZ-6132-01 COSM3988360 c.4556G>C p.R1519T Substitution - Missense 16:24571622-24571622 + T3090 COSM1376906 c.4417delA p.T1475fs*20 Deletion - Frameshift 16:24571483-24571483 + C008 COSM5523644 c.991A>C p.R331R Substitution - coding silent 16:24561863-24561863 + Pat_41_A COSM5850527 c.2573A>T p.E858V Substitution - Missense 16:24569263-24569263 + RMS106_ COSM3773744 c.5331G>T p.E1777D Substitution - Missense 16:24572397-24572397 + TCGA-AP-A056-01 COSM968954 c.1369G>A p.A457T Substitution - Missense 16:24563278-24563278 + C058 COSM5525499 c.4436C>T p.T1479I Substitution - Missense 16:24571502-24571502 + TCGA-MH-A55W-01 COSM3988357 c.3068A>T p.N1023I Substitution - Missense 16:24569758-24569758 + PCSI_0074_Pa_P_526 COSM3377839 c.4242G>A p.E1414E Substitution - coding silent 16:24571308-24571308 + TCGA-A8-A075-01 COSM434956 c.4101T>G p.S1367R Substitution - Missense 16:24571167-24571167 + TCGA-18-3409-01 COSM702932 c.460C>T p.P154S Substitution - Missense 16:24555843-24555843 + S00837 COSM314704 c.3651G>C p.K1217N Substitution - Missense 16:24570341-24570341 + YUFIT COSM5384568 c.2362C>T p.Q788* Substitution - Nonsense 16:24569052-24569052 + TCGA-D1-A103-01 COSM968956 c.1487C>T p.A496V Substitution - Missense 16:24563631-24563631 + HCC063T COSM5812816 c.1694A>T p.Y565F Substitution - Missense 16:24567247-24567247 + TCGA-36-2533-01 COSM1323633 c.3298C>T p.Q1100* Substitution - Nonsense 16:24569988-24569988 + B81-1-Tumor COSM1749505 c.2409A>G p.P803P Substitution - coding silent 16:24569099-24569099 + TCGA-QB-A6FS-06 COSM3888254 c.1813C>T p.P605S Substitution - Missense 16:24567366-24567366 + TARGET-20-PASFLM-09A-01D COSM5487330 c.1060C>G p.L354V Substitution - Missense 16:24561932-24561932 + TCGA-D1-A165-01 COSM968950 c.993_995delACT p.L332delL Deletion - In frame 16:24561865-24561867 + 1946219 COSM1578209 c.3511G>T p.E1171* Substitution - Nonsense 16:24570201-24570201 + CSCC-5-T COSM4543593 c.3405G>C p.E1135D Substitution - Missense 16:24570095-24570095 + TCGA-BS-A0UV-01 COSM968972 c.3869G>A p.R1290Q Substitution - Missense 16:24570935-24570935 + CHOL48 COSM1744241 c.3431G>A p.G1144E Substitution - Missense 16:24570121-24570121 + Gp2D COSM4627386 c.4438A>G p.R1480G Substitution - Missense 16:24571504-24571504 + CSCC-37-T COSM4542255 c.3150G>A p.E1050E Substitution - coding silent 16:24569840-24569840 + TCGA-AG-A002-01 COSM263270 c.3185C>T p.A1062V Substitution - Missense 16:24569875-24569875 + TCGA-A7-A26H-01 COSM1478694 c.1990G>A p.D664N Substitution - Missense 16:24567829-24567829 + TCGA-F4-6570-01 COSM1376901 c.3178delA p.A1062fs*49 Deletion - Frameshift 16:24569868-24569868 + TCGA-AX-A0J0-01 COSM968976 c.4365A>G p.K1455K Substitution - coding silent 16:24571431-24571431 + pfg068T COSM4751342 c.3429G>T p.K1143N Substitution - Missense 16:24570119-24570119 + B109 COSM1749506 c.4382C>G p.A1461G Substitution - Missense 16:24571448-24571448 + TCGA-GC-A3RC-01 COSM3280333 c.1778C>T p.P593L Substitution - Missense 16:24567331-24567331 + C0061T COSM434957 c.4496A>G p.D1499G Substitution - Missense 16:24571562-24571562 + ATL021 COSM5706089 c.2275A>T p.R759W Substitution - Missense 16:24568965-24568965 + Pat_08_B COSM5850528 c.2584C>T p.P862S Substitution - Missense 16:24569274-24569274 + TCGA-AP-A056-01 COSM968979 c.4554G>T p.E1518D Substitution - Missense 16:24571620-24571620 + PD18754a COSM5783942 c.3991G>A p.E1331K Substitution - Missense 16:24571057-24571057 + CCK81 COSM3280356 c.2396A>G p.Y799C Substitution - Missense 16:24569086-24569086 + YUDEXA COSM1708987 c.5119T>A p.S1707T Substitution - Missense 16:24572185-24572185 + TCGA-AZ-4315-01 COSM1376903 c.3532C>T p.P1178S Substitution - Missense 16:24570222-24570222 + TCGA-BR-4256-01 COSM4059483 c.2740A>G p.T914A Substitution - Missense 16:24569430-24569430 + 16461 COSM5616853 c.3459A>G p.E1153E Substitution - coding silent 16:24570149-24570149 + TCGA-06-0214-01 COSM3402203 c.4650T>C p.D1550D Substitution - coding silent 16:24571716-24571716 + TCGA-A5-A0GM-01 COSM968955 c.1447C>T p.Q483* Substitution - Nonsense 16:24563483-24563483 + T3498 COSM4720583 c.3236A>G p.Q1079R Substitution - Missense 16:24569926-24569926 + 104 COSM5012991 c.790G>A p.D264N Substitution - Missense 16:24559620-24559620 + LS180 COSM3280315 c.1021delC p.P342fs*8 Deletion - Frameshift 16:24561893-24561893 + LC_S15 COSM1189219 c.361G>T p.A121S Substitution - Missense 16:24555627-24555627 + TCGA-BR-4184-01 COSM4059491 c.5138G>A p.S1713N Substitution - Missense 16:24572204-24572204 + TCGA-F5-6814-01 COSM968958 c.1948G>T p.E650* Substitution - Nonsense 16:24567501-24567501 + MedB-1 COSM5621675 c.4052A>G p.N1351S Substitution - Missense 16:24571118-24571118 + PTC-7C COSM4128833 c.1280G>T p.G427V Substitution - Missense 16:24562152-24562152 + B109-Tumor COSM1749506 c.4382C>G p.A1461G Substitution - Missense 16:24571448-24571448 + S00837 COSM314704 c.3651G>C p.K1217N Substitution - Missense 16:24570341-24570341 + TCGA-AP-A051-01 COSM968943 c.438-1G>A p.? Unknown 16:24555820-24555820 + TCGA-C8-A3M7-01 COSM3817594 c.3098A>G p.N1033S Substitution - Missense 16:24569788-24569788 + TCGA-D9-A4Z3-01 COSM3508000 c.3157C>T p.P1053S Substitution - Missense 16:24569847-24569847 + HCC58T COSM3706954 c.3218A>T p.K1073I Substitution - Missense 16:24569908-24569908 + TCGA-EE-A2GJ-06 COSM3507994 c.1079C>T p.S360F Substitution - Missense 16:24561951-24561951 + PCSI_0083_Pa_P_526 COSM968941 c.321G>A p.A107A Substitution - coding silent 16:24553530-24553530 + T3064 COSM4720581 c.1900delC p.P634fs*15 Deletion - Frameshift 16:24567453-24567453 + CHC1137T COSM4803222 c.307G>A p.D103N Substitution - Missense 16:24553516-24553516 + TCGA-AP-A051-01 COSM968940 c.283G>T p.A95S Substitution - Missense 16:24548961-24548961 + TCGA-EE-A2GD-06 COSM3507999 c.2284C>T p.P762S Substitution - Missense 16:24568974-24568974 + SJDES007-R2 COSM4578843 c.4416_4417insA p.T1475fs*2 Insertion - Frameshift 16:24571482-24571483 + TCGA-AP-A0LM-01 COSM968946 c.641A>G p.N214S Substitution - Missense 16:24556414-24556414 + TCGA-AP-A059-01 COSM968963 c.2674C>T p.R892* Substitution - Nonsense 16:24569364-24569364 + TCGA-AA-3713-01 COSM1376902 c.3355A>G p.K1119E Substitution - Missense 16:24570045-24570045 + YUPLA COSM5384569 c.4004C>T p.S1335F Substitution - Missense 16:24571070-24571070 + RK165_C01 COSM1629840 c.3880A>G p.K1294E Substitution - Missense 16:24570946-24570946 + PCSI_0018_Pa_X COSM3377837 c.207T>C p.S69S Substitution - coding silent 16:24546203-24546203 + ESO-007 COSM1263879 c.3391A>G p.K1131E Substitution - Missense 16:24570081-24570081 + 2318503 COSM4777416 c.1783G>A p.A595T Substitution - Missense 16:24567336-24567336 + CRC-19T COSM5482365 c.379_381delGAA p.E128delE Deletion - In frame 16:24555645-24555647 + TCGA-GN-A26C-01 COSM3507998 c.2195C>T p.P732L Substitution - Missense 16:24568885-24568885 + TCGA-FS-A1ZA-06 COSM3507997 c.2141C>T p.S714F Substitution - Missense 16:24568831-24568831 + EV002-R9 COSM4410625 c.2295_2296insT p.Y766fs*12 Insertion - Frameshift 16:24568985-24568986 + TCGA-D1-A17Q-01 COSM968967 c.3688G>T p.E1230* Substitution - Nonsense 16:24570378-24570378 + 2492720 COSM5724235 c.2559C>T p.P853P Substitution - coding silent 16:24569249-24569249 + 2492722 COSM5724235 c.2559C>T p.P853P Substitution - coding silent 16:24569249-24569249 + BCM703T COSM4802959 c.4247C>G p.P1416R Substitution - Missense 16:24571313-24571313 + TCGA-EB-A24D-01 COSM3507993 c.358C>T p.L120L Substitution - coding silent 16:24555624-24555624 + S00050 COSM317964 c.3554A>C p.E1185A Substitution - Missense 16:24570244-24570244 + TCGA-D1-A0ZS-01 COSM968964 c.3200C>T p.P1067L Substitution - Missense 16:24569890-24569890 + 4132_T COSM3957362 c.1206G>C p.P402P Substitution - coding silent 16:24562078-24562078 + Pat_41_B COSM5850525 c.1465+1G>A p.? Unknown 16:24563502-24563502 + EGC3 COSM3280346 c.2041C>T p.R681C Substitution - Missense 16:24567880-24567880 + CSCC-32-T COSM4539920 c.2757G>A p.K919K Substitution - coding silent 16:24569447-24569447 + 01-P034 COSM4578844 c.4945A>G p.N1649D Substitution - Missense 16:24572011-24572011 + TCGA-D1-A103-01 COSM968977 c.4489C>T p.R1497* Substitution - Nonsense 16:24571555-24571555 + TCGA-EE-A2A2-06 COSM3508004 c.3933C>T p.I1311I Substitution - coding silent 16:24570999-24570999 + TCGA-BR-8284-01 COSM4059480 c.2035C>T p.R679C Substitution - Missense 16:24567874-24567874 + RK243_C01 COSM4779818 c.3271G>A p.A1091T Substitution - Missense 16:24569961-24569961 + CHC1704T COSM4803995 c.4058G>T p.S1353I Substitution - Missense 16:24571124-24571124 + TCGA-AP-A051-01 COSM968948 c.952-1G>T p.? Unknown 16:24561823-24561823 + TCGA-EE-A181-06 COSM3280393 c.4587C>T p.S1529S Substitution - coding silent 16:24571653-24571653 + TCGA-BS-A0UV-01 COSM968982 c.4985C>A p.S1662Y Substitution - Missense 16:24572051-24572051 + TCGA-AG-3892-01 COSM257864 c.3611C>T p.A1204V Substitution - Missense 16:24570301-24570301 + ESO-1133 COSM1263880 c.1752T>C p.S584S Substitution - coding silent 16:24567305-24567305 + LN18 COSM1376907 c.5326_5331delAAAGAG p.E1781_K1782delEK Deletion - In frame 16:24572392-24572397 + TCGA-FW-A3R5-06 COSM3888252 c.1717C>T p.P573S Substitution - Missense 16:24567270-24567270 + LUAD-S01357 COSM386722 c.3803A>T p.Y1268F Substitution - Missense 16:24570493-24570493 + B65 COSM1745216 c.3985_3987delGAA p.E1331delE Deletion - In frame 16:24571051-24571053 + TCGA-61-1733-01 COSM1323632 c.4182C>T p.N1394N Substitution - coding silent 16:24571248-24571248 + TCGA-46-3768-01 COSM702928 c.5094C>G p.V1698V Substitution - coding silent 16:24572160-24572160 + TCGA-F1-A448-01 COSM4059477 c.479C>T p.T160M Substitution - Missense 16:24555862-24555862 + 8034048 COSM3387319 c.3501C>T p.I1167I Substitution - coding silent 16:24570191-24570191 + LUAD-CHTN-3090346 COSM356812 c.4891G>A p.E1631K Substitution - Missense 16:24571957-24571957 + 35M COSM3507995 c.1723C>T p.P575S Substitution - Missense 16:24567276-24567276 + LP6005935-DNA_D01 COSM5034764 c.4110C>T p.S1370S Substitution - coding silent 16:24571176-24571176 + TCGA-BR-4184-01 COSM3387317 c.674C>T p.A225V Substitution - Missense 16:24556447-24556447 + 3101B7_032_T COSM5039626 c.58G>A p.D20N Substitution - Missense 16:24540684-24540684 + pfg016T COSM1640433 c.3931_3933delATC p.I1312delI Deletion - In frame 16:24570997-24570999 + PT55 COSM5942673 c.2851C>G p.P951A Substitution - Missense 16:24569541-24569541 + TCGA-AN-A0AK-01 COSM3817593 c.1936C>T p.R646* Substitution - Nonsense 16:24567489-24567489 + AOCS-148-1-4 COSM3948401 c.4330T>C p.S1444P Substitution - Missense 16:24571396-24571396 + TC32 COSM4578842 c.2792A>G p.N931S Substitution - Missense 16:24569482-24569482 + I2L-P7-Tumor-Organoid COSM5363619 c.1118T>C p.V373A Substitution - Missense 16:24561990-24561990 + PCSI_0075_Pa_P COSM3377836 c.113A>C p.K38T Substitution - Missense 16:24540739-24540739 + TCGA-A7-A3RF-01 COSM3773744 c.5331G>T p.E1777D Substitution - Missense 16:24572397-24572397 + SNUH_G10_S1 COSM3999805 c.1590-6T>C p.? Unknown 16:24567137-24567137 + PT37 COSM5921036 c.3979G>A p.E1327K Substitution - Missense 16:24571045-24571045 + sysucc-1163T COSM557394 c.1728G>T p.P576P Substitution - coding silent 16:24567281-24567281 + HCC58 COSM3706954 c.3218A>T p.K1073I Substitution - Missense 16:24569908-24569908 + CHC1137T COSM4803222 c.307G>A p.D103N Substitution - Missense 16:24553516-24553516 + TCGA-BS-A0UV-01 COSM968981 c.4960G>T p.E1654* Substitution - Nonsense 16:24572026-24572026 + TCGA-BS-A0TJ-01 COSM968965 c.3330_3332delGAA p.K1112delK Deletion - In frame 16:24570020-24570022 + RK035_C01 COSM1629842 c.5134C>G p.R1712G Substitution - Missense 16:24572200-24572200 + B81-1 COSM1749505 c.2409A>G p.P803P Substitution - coding silent 16:24569099-24569099 + TCGA-CJ-4878-01 COSM3361698 c.1125T>G p.S375S Substitution - coding silent 16:24561997-24561997 + TCGA-BH-A209-01 COSM1478693 c.1622G>C p.R541T Substitution - Missense 16:24567175-24567175 + TCGA-BS-A0UJ-01 COSM968952 c.1106T>C p.L369P Substitution - Missense 16:24561978-24561978 + PCSI_0048_Pa_P COSM216369 c.894G>A p.T298T Substitution - coding silent 16:24561658-24561658 + TCGA-A8-A0A6-01 COSM3817592 c.1902A>C p.P634P Substitution - coding silent 16:24567455-24567455 + pfg008T COSM1640432 c.3910A>G p.T1304A Substitution - Missense 16:24570976-24570976 + 16461 COSM5614337 c.2264G>T p.R755L Substitution - Missense 16:24568954-24568954 + Esp66 COSM1742605 c.1267G>A p.E423K Substitution - Missense 16:24562139-24562139 + TCGA-BR-6452-01 COSM4059478 c.1671A>T p.V557V Substitution - coding silent 16:24567224-24567224 + 587316 COSM1223282 c.2694T>A p.Y898* Substitution - Nonsense 16:24569384-24569384 + TCGA-B5-A11E-01 COSM968969 c.3785G>T p.S1262I Substitution - Missense 16:24570475-24570475 + TCGA-D1-A177-01 COSM968978 c.4497_4498delCT p.P1501fs*4 Deletion - Frameshift 16:24571563-24571564 + TCGA-AP-A0LM-01 COSM968960 c.2264G>A p.R755Q Substitution - Missense 16:24568954-24568954 + BD35T COSM5520234 c.1183G>A p.A395T Substitution - Missense 16:24562055-24562055 + TCGA-G7-7501-01 COSM3988359 c.3871A>C p.T1291P Substitution - Missense 16:24570937-24570937 + TCGA-B2-3924-01 COSM471515 c.4805A>G p.Q1602R Substitution - Missense 16:24571871-24571871 + C467 COSM4442006 c.953C>T p.A318V Substitution - Missense 16:24561825-24561825 + TCGA-12-5301-01 COSM3402202 c.162A>G p.K54K Substitution - coding silent 16:24540788-24540788 + TCGA-AP-A056-01 COSM968959 c.2263C>T p.R755* Substitution - Nonsense 16:24568953-24568953 + ESO-152 COSM1263882 c.2233C>T p.R745C Substitution - Missense 16:24568923-24568923 + RK119_C01 COSM3741859 c.4860T>A p.H1620Q Substitution - Missense 16:24571926-24571926 + BD72T COSM5513177 c.4738_4741delAAAG p.K1580fs*38 Deletion - Frameshift 16:24571804-24571807 + TCGA-FW-A3R5-06 COSM3888251 c.1166C>T p.S389F Substitution - Missense 16:24562038-24562038 + TCGA-A2-A0YF-01 COSM434953 c.486C>T p.F162F Substitution - coding silent 16:24555869-24555869 + PD24190a COSM5801604 c.259_263delTATGT p.V88fs*4 Deletion - Frameshift 16:24546255-24546259 + 8016470 COSM3387318 c.923C>T p.A308V Substitution - Missense 16:24561687-24561687 + TCGA-EE-A2GP-06 COSM3508002 c.3160C>T p.R1054* Substitution - Nonsense 16:24569850-24569850 + TCGA-B5-A0JY-01 COSM968945 c.540A>C p.K180N Substitution - Missense 16:24556313-24556313 + pfg008T COSM1640434 c.4623A>G p.K1541K Substitution - coding silent 16:24571689-24571689 + CSCC-27-T COSM4470539 c.1665C>T p.V555V Substitution - coding silent 16:24567218-24567218 + Gp5D COSM3280348 c.2099A>G p.Y700C Substitution - Missense 16:24568789-24568789 + RKO COSM3280371 c.3619delA p.I1209fs*47 Deletion - Frameshift 16:24570309-24570309 + T98G COSM1376907 c.5326_5331delAAAGAG p.E1781_K1782delEK Deletion - In frame 16:24572392-24572397 + YULAPE COSM1708985 c.2081C>T p.S694L Substitution - Missense 16:24568771-24568771 + TCGA-AP-A059-01 COSM968980 c.4839G>A p.K1613K Substitution - coding silent 16:24571905-24571905 + J90_T COSM3957364 c.5378A>T p.*1793L Nonstop extension 16:24572444-24572444 + TCGA-AD-5900-01 COSM1376905 c.4138G>A p.V1380M Substitution - Missense 16:24571204-24571204 + CPCG0369-F1 COSM4881084 c.826G>T p.G276* Substitution - Nonsense 16:24559656-24559656 + TCGA-BR-4361-01 COSM4059481 c.2084A>G p.Y695C Substitution - Missense 16:24568774-24568774 + TCGA-BS-A0UV-01 COSM968944 c.480G>A p.T160T Substitution - coding silent 16:24555863-24555863 + TCGA-22-5489-01 COSM702930 c.4073A>G p.N1358S Substitution - Missense 16:24571139-24571139 + TCGA-BR-4370-01 COSM4059490 c.4712A>C p.K1571T Substitution - Missense 16:24571778-24571778 + Pat_41_B COSM5850529 c.3706G>A p.E1236K Substitution - Missense 16:24570396-24570396 + QC2-39-T2 COSM5655791 c.4552G>A p.E1518K Substitution - Missense 16:24571618-24571618 + CSCC-7-T COSM4571151 c.3900T>G p.N1300K Substitution - Missense 16:24570966-24570966 + PD9573a COSM5801810 c.5206_5207insA p.H1738fs*5 Insertion - Frameshift 16:24572272-24572273 + ESCC_10 COSM5623832 c.3935T>A p.I1312N Substitution - Missense 16:24571001-24571001 + S01022 COSM5665777 c.52A>G p.T18A Substitution - Missense 16:24540678-24540678 + XHDG22 COSM4769029 c.4960G>C p.E1654Q Substitution - Missense 16:24572026-24572026 + BCM703T COSM4802959 c.4247C>G p.P1416R Substitution - Missense 16:24571313-24571313 + LUAD-S01315 COSM344417 c.4333C>T p.Q1445* Substitution - Nonsense 16:24571399-24571399 + DLD1 COSM4623277 c.580A>C p.I194L Substitution - Missense 16:24556353-24556353 + CSCC-18-T COSM968959 c.2263C>T p.R755* Substitution - Nonsense 16:24568953-24568953 + HCT15 COSM3280386 c.4356G>A p.T1452T Substitution - coding silent 16:24571422-24571422 + Gp2D COSM3280348 c.2099A>G p.Y700C Substitution - Missense 16:24568789-24568789 + 587238 COSM1223279 c.5057G>A p.G1686D Substitution - Missense 16:24572123-24572123 + TCGA-GF-A3OT-06 COSM3507996 c.1850C>T p.S617L Substitution - Missense 16:24567403-24567403 + TCGA-ER-A19N-06 COSM434953 c.486C>T p.F162F Substitution - coding silent 16:24555869-24555869 + TCGA-EE-A2MJ-06 COSM3508006 c.4406C>T p.P1469L Substitution - Missense 16:24571472-24571472 + T3152 COSM4720576 c.644C>T p.T215I Substitution - Missense 16:24556417-24556417 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.188553 16p12.2 600938

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAAC - Frameshift p.K1138Hfs*18 c.3412_3415delAAAC 16 24581419 UCEC AAGATC - InFrameDeletion p.R541_S542delRS c.1621_1626delAGATCA 16 24578494 BRCA - AC Frameshift p.K1004Nfs*33 c.3011_3012insCA 16 24581021 THCA A C Missense p.D1117A c.3350A>C 16 24581361 CM A C Missense p.E1185A c.3554A>C 16 24581565 SCLC A C Missense p.E1245A c.3734A>C 16 24581745 HNSC A C Missense p.K1218N c.3654A>C 16 24581665 STAD A C Missense p.K1514Q c.4540A>C 16 24582927 GBM A C Missense p.K1571T c.4712A>C 16 24583099 STAD ACT - InFrameDeletion p.L332delL c.995_997delTAC 16 24573186 UCEC - A Frameshift p.I1084Nfs*11 c.3250dupA 16 24581256 GBM A - Frameshift p.R333Qfs*17 c.998delG 16 24573191 CLL A - Frameshift p.S1688Afs*100 c.5062delA 16 24583448 LUAD A G IntronicSNV . c.303+51A>G 16 24560353 BRCA A G Missense p.D1499G c.4496A>G 16 24582883 BRCA A G Missense p.E858G c.2573A>G 16 24580584 BLCA A G Missense p.I24V c.70A>G 16 24552017 HNSC A G Missense p.K1131E c.3391A>G 16 24581402 ESCA A G Missense p.K1552E c.4654A>G 16 24583041 BLCA A G Missense p.N1358S c.4073A>G 16 24582460 LUSC A G Missense p.Q1602R c.4805A>G 16 24583192 RCCC A G Missense p.S1532G c.4594A>G 16 24582981 BLCA A G Missense p.T1304A c.3910A>G 16 24582297 STAD A G Missense p.T326A c.976A>G 16 24573169 UCEC A G Missense p.T914A c.2740A>G 16 24580751 STAD A G Missense p.Y14C c.41A>G 16 24551988 HNSC A G Synonymous p.E1153E c.3459A>G 16 24581470 NSCLC A G Synonymous p.E967E c.2901A>G 16 24580912 RCCC A G Synonymous p.K1541K c.4623A>G 16 24583010 STAD A G Synonymous p.K54K c.162A>G 16 24552109 GBM A G Synonymous p.K687K c.2061A>G 16 24580072 HNSC ATC - InFrameDeletion p.I1312delI c.3933_3935delCAT 16 24582318 STAD A T Missense p.D1472V c.4415A>T 16 24582802 STAD A T Missense p.K1169N c.3507A>T 16 24581518 LUSC A T Nonsense p.K1080* c.3238A>T 16 24581249 RCCC A T Synonymous p.P951P c.2853A>T 16 24580864 HNSC C A Missense p.S1485Y c.4454C>A 16 24582841 LUAD C A Missense p.S1502Y c.4505C>A 16 24582892 CM C A Missense p.T115K c.344C>A 16 24564874 RCCC CG - Frameshift p.R784*fs*1 c.2350_2351delCG 16 24580361 LUAD C G IntronicSNV . c.349-284C>G 16 24566652 HC C G Missense p.L1434V c.4300C>G 16 24582687 LUSC C G Missense p.Q1079E c.3235C>G 16 24581246 BRCA C G Missense p.R1712G c.5134C>G 16 24583521 HC C G Synonymous p.V1698V c.5094C>G 16 24583481 LUSC CT - Frameshift p.P1501Ffs*4 c.4500_4501delTC 16 24582884 UCEC C T IntronicSNV . c.847+17C>T 16 24571015 CM C T Missense p.P1067L c.3200C>T 16 24581211 UCEC C T Missense p.P1469L c.4406C>T 16 24582793 CM C T Missense p.P1515L c.4544C>T 16 24582931 CM C T Missense p.P1536L c.4607C>T 16 24582994 HC C T Missense p.P1565S c.4693C>T 16 24583080 CM C T Missense p.P1594S c.4780C>T 16 24583167 LUAD C T Missense p.P566S c.1696C>T 16 24578570 BLCA C T Missense p.P575S c.1723C>T 16 24578597 CM C T Missense p.P576L c.1727C>T 16 24578601 LUAD C T Missense p.P600S c.1798C>T 16 24578672 CM C T Missense p.P602S c.1804C>T 16 24578678 CM C T Missense p.P602S c.1804C>T 16 24578678 OV C T Missense p.P732L c.2195C>T 16 24580206 CM C T Missense p.P762S c.2284C>T 16 24580295 CM C T Missense p.R745C c.2233C>T 16 24580244 ESCA C T Missense p.R784C c.2350C>T 16 24580361 CM C T Missense p.S360F c.1079C>T 16 24573272 CM C T Missense p.S694L c.2081C>T 16 24580092 CM C T Missense p.S714F c.2141C>T 16 24580152 CM C T Nonsense p.Q483* c.1447C>T 16 24574804 UCEC C T Nonsense p.R1054* c.3160C>T 16 24581171 CM C T Synonymous p.F162F c.486C>T 16 24567190 BRCA C T Synonymous p.F162F c.486C>T 16 24567190 CM C T Synonymous p.I1311I c.3933C>T 16 24582320 CM C T Synonymous p.L120L c.358C>T 16 24566945 CM C T Synonymous p.L1211L c.3633C>T 16 24581644 CM C T Synonymous p.N277N c.831C>T 16 24570982 CM C T Synonymous p.S1529S c.4587C>T 16 24582974 CM C T Synonymous p.S451S c.1353C>T 16 24574583 CM C T Synonymous p.S539S c.1617C>T 16 24578491 OV C T Synonymous p.V1251V c.3753C>T 16 24581764 CM C T Synonymous p.V599V c.1797C>T 16 24578671 CM GAA - InFrameDeletion p.K1112delK c.3334_3336delAAG 16 24581341 UCEC G A Missense p.A1096T c.3286G>A 16 24581297 LUAD G A Missense p.D664N c.1990G>A 16 24579150 BRCA G A Missense p.G1438E c.4313G>A 16 24582700 CM G A Missense p.R1182H c.3545G>A 16 24581556 SCLC G A Missense p.R163H c.488G>A 16 24567192 HNSC G A Missense p.R713H c.2138G>A 16 24580149 STAD G A Missense p.R764K c.2291G>A 16 24580302 CM G A Missense p.R826H c.2477G>A 16 24580488 UCEC G A Missense p.R91Q c.272G>A 16 24560271 OV G A Missense p.S1760N c.5279G>A 16 24583666 COREAD G A Missense p.V816I c.2446G>A 16 24580457 LUAD G A SpliceDonorSNV . c.674+1G>A 16 24567769 UCEC G A Synonymous p.K1735K c.5205G>A 16 24583592 ESCA G A Synonymous p.T298T c.894G>A 16 24572979 PAAD G C Missense p.G153R c.457G>C 16 24567161 BRCA G C Missense p.K1217N c.3651G>C 16 24581662 SCLC G C Missense p.M200I c.600G>C 16 24567694 PRAD G C Missense p.Q1079H c.3237G>C 16 24581248 RCCC G C Missense p.R541T c.1622G>C 16 24578496 BRCA G C Missense p.R544S c.1632G>C 16 24578506 LUAD G C Synonymous p.P1067P c.3201G>C 16 24581212 COREAD G C Synonymous p.P576P c.1728G>C 16 24578602 CM G T Missense p.G1260V c.3779G>T 16 24581790 LUAD G T Missense p.R755L c.2264G>T 16 24580275 NSCLC G T Nonsense p.E1308* c.3922G>T 16 24582309 LUAD G T Nonsense p.E640* c.1918G>T 16 24578792 PAAD G T Synonymous p.P576P c.1728G>T 16 24578602 LUAD T A Missense p.S995T c.2983T>A 16 24580994 ESCA T A Nonsense p.L974* c.2921T>A 16 24580932 LUAD T C Missense p.M1313T c.3938T>C 16 24582325 OV T C Synonymous p.D1550D c.4650T>C 16 24583037 GBM T C Synonymous p.S584S c.1752T>C 16 24578626 ESCA T - Frameshift p.E1056Nfs*55 c.3165delT 16 24581176 CM - T Frameshift p.Y6Lfs*2 c.16dupT 16 24551962 RCCC T G Missense p.F314C c.941T>G 16 24573026 BLCA T G Missense p.S1367R c.4101T>G 16 24582488 BRCA T G Missense p.V555G c.1664T>G 16 24578538 HNSC T G Synonymous p.S375S c.1125T>G 16 24573318 RCCC TT - Frameshift p.F1160*fs*1 c.3479_3480delTT 16 24581488 GBM TTTC - IntronicDeletion . c.535-181_535-178delTCTT 16 24567446 ESCA