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 4 85594085 85594085 + Missense_Mutation SNP C C T TCGA-OR-A5JT-01A-11D-A29I-10 TCGA-OR-A5JT-10A-01D-A29L-10 g.chr4:85594085C>T c.10517G>A c.(10516-10518)tGt>tAt p.C3506Y ACC 4 85623617 85623617 + Missense_Mutation SNP G G A TCGA-OR-A5K5-01A-11D-A29I-10 TCGA-OR-A5K5-10A-01D-A29L-10 g.chr4:85623617G>A c.8485C>T c.(8485-8487)Cgc>Tgc p.R2829C ACC 4 85626662 85626662 + Missense_Mutation SNP C C A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr4:85626662C>A c.8220G>T c.(8218-8220)gaG>gaT p.E2740D ACC 4 85722990 85722991 + Frame_Shift_Ins INS - - A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr4:85722990_85722991insA c.2634_2635insT c.(2632-2637)gtggcafs p.A879fs BLCA 4 85594022 85594022 + Silent SNP C C T TCGA-GC-A6I1-01A-12D-A31L-08 TCGA-GC-A6I1-10A-01D-A31J-08 g.chr4:85594022C>T c.10580G>A c.(10579-10581)tGa>tAa p.*3527* BLCA 4 85598394 85598394 + Missense_Mutation SNP C C G TCGA-FJ-A3ZE-01A-11D-A23M-08 TCGA-FJ-A3ZE-10A-01D-A23K-08 g.chr4:85598394C>G c.10415G>C c.(10414-10416)aGa>aCa p.R3472T BLCA 4 85598427 85598427 + Missense_Mutation SNP G G A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr4:85598427G>A c.10382C>T c.(10381-10383)tCa>tTa p.S3461L BLCA 4 85598446 85598446 + Missense_Mutation SNP C C T TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr4:85598446C>T c.10363G>A c.(10363-10365)Gaa>Aaa p.E3455K BLCA 4 85600102 85600102 + Nonsense_Mutation SNP C C A TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr4:85600102C>A c.10117G>T c.(10117-10119)Gag>Tag p.E3373* BLCA 4 85600134 85600134 + Missense_Mutation SNP C C A TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chr4:85600134C>A c.10085G>T c.(10084-10086)gGc>gTc p.G3362V BLCA 4 85611688 85611688 + Nonsense_Mutation SNP C C A TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr4:85611688C>A c.9334G>T c.(9334-9336)Gaa>Taa p.E3112* BLCA 4 85611775 85611775 + Missense_Mutation SNP G G C TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr4:85611775G>C c.9247C>G c.(9247-9249)Ctc>Gtc p.L3083V BLCA 4 85611800 85611800 + Silent SNP T T C TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr4:85611800T>C c.9222A>G c.(9220-9222)gaA>gaG p.E3074E BLCA 4 85612877 85612877 + Silent SNP C C T TCGA-ZF-A9R9-01A-11D-A38G-08 TCGA-ZF-A9R9-10A-01D-A38J-08 g.chr4:85612877C>T c.9111G>A c.(9109-9111)caG>caA p.Q3037Q BLCA 4 85612913 85612913 + Missense_Mutation SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr4:85612913G>C c.9075C>G c.(9073-9075)atC>atG p.I3025M BLCA 4 85617303 85617303 + Silent SNP T T C TCGA-DK-A3WY-01A-11D-A22Z-08 TCGA-DK-A3WY-10A-01D-A22Z-08 g.chr4:85617303T>C c.8721A>G c.(8719-8721)ctA>ctG p.L2907L BLCA 4 85617907 85617907 + Missense_Mutation SNP T T A TCGA-UY-A9PF-01A-11D-A38G-08 TCGA-UY-A9PF-10A-01D-A38J-08 g.chr4:85617907T>A c.8666A>T c.(8665-8667)gAa>gTa p.E2889V BLCA 4 85623614 85623614 + Missense_Mutation SNP C C T TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr4:85623614C>T c.8488G>A c.(8488-8490)Gag>Aag p.E2830K BLCA 4 85634326 85634326 + Silent SNP C C A TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr4:85634326C>A c.8028G>T c.(8026-8028)acG>acT p.T2676T BLCA 4 85634393 85634393 + Splice_Site SNP C C T TCGA-GV-A40G-01A-11D-A23M-08 TCGA-GV-A40G-10A-01D-A23K-08 g.chr4:85634393C>T c.e51-1 BLCA 4 85636459 85636459 + Silent SNP G G C TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr4:85636459G>C c.7953C>G c.(7951-7953)gtC>gtG p.V2651V BLCA 4 85636514 85636514 + Missense_Mutation SNP G G C TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr4:85636514G>C c.7898C>G c.(7897-7899)tCt>tGt p.S2633C BLCA 4 85638082 85638082 + Missense_Mutation SNP G G C TCGA-DK-A3IU-01A-11D-A20D-08 TCGA-DK-A3IU-10A-01D-A20D-08 g.chr4:85638082G>C c.7842C>G c.(7840-7842)atC>atG p.I2614M BLCA 4 85642618 85642618 + Missense_Mutation SNP C C T TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr4:85642618C>T c.7549G>A c.(7549-7551)Gag>Aag p.E2517K BLCA 4 85645708 85645708 + Nonsense_Mutation SNP T T A TCGA-UY-A9PA-01A-11D-A38G-08 TCGA-UY-A9PA-10A-01D-A38J-08 g.chr4:85645708T>A c.7312A>T c.(7312-7314)Aaa>Taa p.K2438* BLCA 4 85645714 85645714 + Missense_Mutation SNP C C G TCGA-ZF-AA56-01A-31D-A391-08 TCGA-ZF-AA56-10A-01D-A394-08 g.chr4:85645714C>G c.7306G>C c.(7306-7308)Gac>Cac p.D2436H BLCA 4 85657375 85657375 + Missense_Mutation SNP G G A TCGA-FD-A62O-01A-11D-A30E-08 TCGA-FD-A62O-10A-01D-A30H-08 g.chr4:85657375G>A c.6863C>T c.(6862-6864)tCa>tTa p.S2288L BLCA 4 85662940 85662940 + Missense_Mutation SNP C C G TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr4:85662940C>G c.6208G>C c.(6208-6210)Gat>Cat p.D2070H BLCA 4 85662946 85662946 + Missense_Mutation SNP G G C TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr4:85662946G>C c.6202C>G c.(6202-6204)Ctt>Gtt p.L2068V BLCA 4 85672638 85672638 + Missense_Mutation SNP C C G TCGA-G2-A2EL-01A-12D-A18F-08 TCGA-G2-A2EL-10A-01D-A18F-08 g.chr4:85672638C>G c.5971G>C c.(5971-5973)Gag>Cag p.E1991Q BLCA 4 85672647 85672647 + Missense_Mutation SNP G G C TCGA-BT-A42C-01A-11D-A23M-08 TCGA-BT-A42C-10A-01D-A23K-08 g.chr4:85672647G>C c.5962C>G c.(5962-5964)Ctt>Gtt p.L1988V BLCA 4 85672677 85672677 + Missense_Mutation SNP G G C TCGA-BT-A42C-01A-11D-A23M-08 TCGA-BT-A42C-10A-01D-A23K-08 g.chr4:85672677G>C c.5932C>G c.(5932-5934)Cct>Gct p.P1978A BLCA 4 85672802 85672802 + Missense_Mutation SNP C C G TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr4:85672802C>G c.5807G>C c.(5806-5808)gGg>gCg p.G1936A BLCA 4 85676452 85676453 + Frame_Shift_Ins INS - - A TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr4:85676452_85676453insA c.5525_5526insT c.(5524-5526)ttafs p.L1842fs BLCA 4 85678145 85678145 + Missense_Mutation SNP A A T TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr4:85678145A>T c.5358T>A c.(5356-5358)agT>agA p.S1786R BLCA 4 85687004 85687004 + Missense_Mutation SNP T T A TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr4:85687004T>A c.5147A>T c.(5146-5148)cAg>cTg p.Q1716L BLCA 4 85695995 85695995 + Missense_Mutation SNP G G A TCGA-XF-AAMZ-01A-11D-A42E-08 TCGA-XF-AAMZ-10A-01D-A42H-08 g.chr4:85695995G>A c.4732C>T c.(4732-4734)Cct>Tct p.P1578S BLCA 4 85699717 85699717 + Missense_Mutation SNP C C G TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr4:85699717C>G c.4457G>C c.(4456-4458)gGa>gCa p.G1486A BLCA 4 85701312 85701312 + Silent SNP G G C TCGA-FD-A5C0-01A-11D-A289-08 TCGA-FD-A5C0-10A-01D-A289-08 g.chr4:85701312G>C c.4314C>G c.(4312-4314)gtC>gtG p.V1438V BLCA 4 85707275 85707275 + Missense_Mutation SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr4:85707275C>T c.3919G>A c.(3919-3921)Gaa>Aaa p.E1307K BLCA 4 85722828 85722828 + Nonsense_Mutation SNP G G A TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr4:85722828G>A c.2797C>T c.(2797-2799)Cag>Tag p.Q933* BLCA 4 85724606 85724606 + Missense_Mutation SNP G G A TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr4:85724606G>A c.2444C>T c.(2443-2445)tCt>tTt p.S815F BLCA 4 85731400 85731400 + Missense_Mutation SNP T T C TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr4:85731400T>C c.1985A>G c.(1984-1986)gAa>gGa p.E662G BLCA 4 85741255 85741255 + Missense_Mutation SNP C C A TCGA-GU-A762-01A-11D-A339-08 TCGA-GU-A762-10A-01D-A339-08 g.chr4:85741255C>A c.1676G>T c.(1675-1677)gGa>gTa p.G559V BLCA 4 85741262 85741262 + Missense_Mutation SNP G G A TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr4:85741262G>A c.1669C>T c.(1669-1671)Ctt>Ttt p.L557F BLCA 4 85742534 85742534 + Missense_Mutation SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr4:85742534C>T c.1294G>A c.(1294-1296)Gag>Aag p.E432K BLCA 4 85742700 85742700 + Silent SNP G G A TCGA-FJ-A3Z7-01A-12D-A23M-08 TCGA-FJ-A3Z7-10A-01D-A23K-08 g.chr4:85742700G>A c.1128C>T c.(1126-1128)caC>caT p.H376H BLCA 4 85781566 85781566 + Splice_Site SNP C C T TCGA-CU-A0YN-01A-21D-A10S-08 TCGA-CU-A0YN-11A-11D-A10S-08 g.chr4:85781566C>T c.179G>A c.(178-180)aGg>aAg p.R60K BRCA 4 85603603 85603603 + Missense_Mutation SNP C C A TCGA-E2-A573-01A-11D-A29N-09 TCGA-E2-A573-10A-01D-A29N-09 g.chr4:85603603C>A c.9747G>T c.(9745-9747)ttG>ttT p.L3249F BRCA 4 85617213 85617213 + Silent SNP C C T TCGA-A2-A0YH-01A-11D-A10G-09 TCGA-A2-A0YH-10A-01D-A10G-09 g.chr4:85617213C>T c.8811G>A c.(8809-8811)gaG>gaA p.E2937E BRCA 4 85638146 85638146 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr4:85638146C>G c.7778G>C c.(7777-7779)aGa>aCa p.R2593T BRCA 4 85638146 85638146 + Missense_Mutation SNP C C G TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr4:85638146C>G c.7778G>C c.(7777-7779)aGa>aCa p.R2593T BRCA 4 85642669 85642669 + Missense_Mutation SNP C C T TCGA-E2-A14V-01A-11D-A12B-09 TCGA-E2-A14V-10A-01D-A12B-09 g.chr4:85642669C>T c.7498G>A c.(7498-7500)Gag>Aag p.E2500K BRCA 4 85645723 85645723 + Missense_Mutation SNP C C T TCGA-B6-A40C-01A-11D-A23C-09 TCGA-B6-A40C-10A-01D-A23C-09 g.chr4:85645723C>T c.7297G>A c.(7297-7299)Gta>Ata p.V2433I BRCA 4 85648059 85648059 + Silent SNP C C T TCGA-AO-A0JL-01A-11W-A071-09 TCGA-AO-A0JL-10A-01W-A071-09 g.chr4:85648059C>T c.7227G>A c.(7225-7227)gaG>gaA p.E2409E BRCA 4 85654705 85654705 + Silent SNP G G A TCGA-EW-A1IZ-01A-11D-A188-09 TCGA-EW-A1IZ-10A-01D-A13O-09 g.chr4:85654705G>A c.7051C>T c.(7051-7053)Ctg>Ttg p.L2351L BRCA 4 85657344 85657347 + Frame_Shift_Del DEL ATTA ATTA - TCGA-E2-A10B-01A-11D-A10M-09 TCGA-E2-A10B-10A-01D-A10M-09 g.chr4:85657344_85657347delATTA c.6891_6894delTAAT c.(6889-6894)cttaatfs p.LN2297fs BRCA 4 85663022 85663022 + Silent SNP C C T TCGA-AR-A24H-01A-11D-A167-09 TCGA-AR-A24H-10A-01D-A167-09 g.chr4:85663022C>T c.6126G>A c.(6124-6126)gtG>gtA p.V2042V BRCA 4 85672736 85672736 + Missense_Mutation SNP G G A TCGA-BH-A0BZ-01A-31D-A12Q-09 TCGA-BH-A0BZ-11A-61D-A12Q-09 g.chr4:85672736G>A c.5873C>T c.(5872-5874)gCt>gTt p.A1958V BRCA 4 85674919 85674919 + Missense_Mutation SNP C C T TCGA-AR-A0TX-01A-11D-A099-09 TCGA-AR-A0TX-10A-01D-A099-09 g.chr4:85674919C>T c.5670G>A c.(5668-5670)atG>atA p.M1890I BRCA 4 85678260 85678260 + Missense_Mutation SNP C C T TCGA-BH-A1F8-01A-11D-A13L-09 TCGA-BH-A1F8-11B-21D-A188-09 g.chr4:85678260C>T c.5243G>A c.(5242-5244)cGa>cAa p.R1748Q BRCA 4 85687113 85687114 + Frame_Shift_Ins INS - - T TCGA-A8-A09G-01A-21W-A019-09 TCGA-A8-A09G-10A-01W-A021-09 g.chr4:85687113_85687114insT c.5037_5038insA c.(5035-5040)ttacatfs p.H1680fs BRCA 4 85696135 85696135 + Splice_Site SNP C C G TCGA-AC-A3W5-01A-11D-A228-09 TCGA-AC-A3W5-10A-01D-A22A-09 g.chr4:85696135C>G c.e29-1 BRCA 4 85701312 85701312 + Silent SNP G G C TCGA-AC-A3W6-01A-12D-A228-09 TCGA-AC-A3W6-10A-01D-A22A-09 g.chr4:85701312G>C c.4314C>G c.(4312-4314)gtC>gtG p.V1438V BRCA 4 85708711 85708711 + Missense_Mutation SNP T T G TCGA-BH-A0BA-01A-11W-A071-09 TCGA-BH-A0BA-11A-22W-A100-09 g.chr4:85708711T>G c.3825A>C c.(3823-3825)ttA>ttC p.L1275F BRCA 4 85710959 85710959 + Missense_Mutation SNP C C A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr4:85710959C>A c.3589G>T c.(3589-3591)Gtc>Ttc p.V1197F BRCA 4 85731339 85731339 + Frame_Shift_Del DEL A A - TCGA-AR-A24R-01A-11D-A167-09 TCGA-AR-A24R-10A-01D-A167-09 g.chr4:85731339delA c.2046delT c.(2044-2046)tttfs p.F682fs BRCA 4 85742538 85742538 + Silent SNP A A G TCGA-GM-A2DK-01A-21D-A17W-09 TCGA-GM-A2DK-10C-01D-A17W-09 g.chr4:85742538A>G c.1290T>C c.(1288-1290)ttT>ttC p.F430F BRCA 4 85748077 85748077 + Silent SNP C C G TCGA-BH-A0BW-01A-11D-A10Y-09 TCGA-BH-A0BW-10A-01D-A110-09 g.chr4:85748077C>G c.1014G>C c.(1012-1014)ctG>ctC p.L338L BRCA 4 85758097 85758097 + Silent SNP C C T TCGA-AN-A0XW-01A-11D-A10G-09 TCGA-AN-A0XW-10A-01D-A10G-09 g.chr4:85758097C>T c.561G>A c.(559-561)caG>caA p.Q187Q BRCA 4 85762417 85762417 + Splice_Site SNP C C A TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chr4:85762417C>A c.e6-1 CESC 4 85594031 85594031 + Missense_Mutation SNP C C T TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr4:85594031C>T c.10571G>A c.(10570-10572)cGa>cAa p.R3524Q CESC 4 85605214 85605214 + Missense_Mutation SNP A A G TCGA-C5-A2LX-01A-11D-A18J-09 TCGA-C5-A2LX-10A-01D-A18J-09 g.chr4:85605214A>G c.9608T>C c.(9607-9609)gTg>gCg p.V3203A CESC 4 85614120 85614120 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr4:85614120G>C c.8967C>G c.(8965-8967)atC>atG p.I2989M CESC 4 85623529 85623529 + Missense_Mutation SNP A A G TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr4:85623529A>G c.8573T>C c.(8572-8574)tTc>tCc p.F2858S CESC 4 85664936 85664936 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr4:85664936G>C c.5990C>G c.(5989-5991)tCt>tGt p.S1997C CESC 4 85696122 85696122 + Missense_Mutation SNP C C A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr4:85696122C>A c.4605G>T c.(4603-4605)aaG>aaT p.K1535N CESC 4 85707190 85707190 + Missense_Mutation SNP G G A TCGA-EK-A2PL-01A-11D-A18J-09 TCGA-EK-A2PL-10A-01D-A18J-09 g.chr4:85707190G>A c.4004C>T c.(4003-4005)aCa>aTa p.T1335I CESC 4 85710969 85710969 + Nonsense_Mutation SNP C C T TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr4:85710969C>T c.3579G>A c.(3577-3579)tgG>tgA p.W1193* CESC 4 85731124 85731124 + Nonsense_Mutation SNP G G C TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr4:85731124G>C c.2261C>G c.(2260-2262)tCa>tGa p.S754* CESC 4 85731460 85731460 + Missense_Mutation SNP C C G TCGA-C5-A1BL-01A-11D-A13W-08 TCGA-C5-A1BL-10A-01D-A13W-08 g.chr4:85731460C>G c.1925G>C c.(1924-1926)aGa>aCa p.R642T CHOL 4 85678262 85678262 + Silent SNP G G A TCGA-WD-A7RX-01A-12D-A417-09 TCGA-WD-A7RX-10A-01D-A41A-09 g.chr4:85678262G>A c.5241C>T c.(5239-5241)aaC>aaT p.N1747N CHOL 4 85687060 85687060 + Missense_Mutation SNP A A C TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr4:85687060A>C c.5091T>G c.(5089-5091)aaT>aaG p.N1697K CHOL 4 85716106 85716106 + Missense_Mutation SNP G G T TCGA-W5-AA2U-01A-11D-A417-09 TCGA-W5-AA2U-10A-01D-A41A-09 g.chr4:85716106G>T c.3194C>A c.(3193-3195)cCt>cAt p.P1065H COAD 4 85594125 85594125 + Nonsense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr4:85594125C>A c.10477G>T c.(10477-10479)Gaa>Taa p.E3493* COAD 4 85600239 85600239 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:85600239C>A c.9980G>T c.(9979-9981)gGc>gTc p.G3327V COAD 4 85600317 85600317 + Missense_Mutation SNP G G T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:85600317G>T c.9902C>A c.(9901-9903)cCa>cAa p.P3301Q COAD 4 85600379 85600379 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr4:85600379G>A c.9840C>T c.(9838-9840)gaC>gaT p.D3280D COAD 4 85611693 85611693 + Missense_Mutation SNP G G A TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:85611693G>A c.9329C>T c.(9328-9330)tCc>tTc p.S3110F COAD 4 85611707 85611708 + Frame_Shift_Ins INS - - CA TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr4:85611707_85611708insCA c.9314_9315insTG c.(9313-9315)tggfs p.W3105fs COAD 4 85611756 85611756 + Missense_Mutation SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr4:85611756T>C c.9266A>G c.(9265-9267)aAc>aGc p.N3089S COAD 4 85612867 85612867 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85612867G>T c.9121C>A c.(9121-9123)Ctt>Att p.L3041I COAD 4 85612887 85612887 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:85612887G>A c.9101C>T c.(9100-9102)gCg>gTg p.A3034V COAD 4 85614146 85614146 + Nonsense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:85614146G>A c.8941C>T c.(8941-8943)Cga>Tga p.R2981* COAD 4 85623552 85623552 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85623552G>T c.8550C>A c.(8548-8550)ttC>ttA p.F2850L COAD 4 85626604 85626604 + Missense_Mutation SNP T T G TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr4:85626604T>G c.8278A>C c.(8278-8280)Aca>Cca p.T2760P COAD 4 85626633 85626633 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:85626633C>A c.8249G>T c.(8248-8250)aGa>aTa p.R2750I COAD 4 85634389 85634389 + Missense_Mutation SNP A A T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85634389A>T c.7965T>A c.(7963-7965)ttT>ttA p.F2655L COAD 4 85636510 85636510 + Silent SNP T T C TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr4:85636510T>C c.7902A>G c.(7900-7902)ggA>ggG p.G2634G COAD 4 85639659 85639659 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:85639659A>C c.7670T>G c.(7669-7671)tTt>tGt p.F2557C COAD 4 85642562 85642562 + Splice_Site SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr4:85642562C>A c.7605G>T c.(7603-7605)aaG>aaT p.K2535N COAD 4 85642563 85642563 + Splice_Site DEL T T - TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr4:85642563delT c.7604delA c.(7603-7605)aag>ag p.K2535fs COAD 4 85642695 85642695 + Missense_Mutation SNP C C A TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr4:85642695C>A c.7472G>T c.(7471-7473)cGa>cTa p.R2491L COAD 4 85645590 85645590 + Missense_Mutation SNP G G T TCGA-AA-3530-01A-01W-0995-10 TCGA-AA-3530-10A-01W-0995-10 g.chr4:85645590G>T c.7430C>A c.(7429-7431)gCt>gAt p.A2477D COAD 4 85657414 85657414 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr4:85657414C>T c.6824G>A c.(6823-6825)cGt>cAt p.R2275H COAD 4 85657481 85657481 + Splice_Site SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:85657481C>A c.e42-1 COAD 4 85658517 85658517 + Missense_Mutation SNP G G A TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr4:85658517G>A c.6577C>T c.(6577-6579)Cgt>Tgt p.R2193C COAD 4 85660273 85660273 + Splice_Site SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr4:85660273C>T c.e40-1 COAD 4 85661490 85661490 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr4:85661490C>T c.6314G>A c.(6313-6315)cGg>cAg p.R2105Q COAD 4 85664912 85664912 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:85664912A>C c.6014T>G c.(6013-6015)tTt>tGt p.F2005C COAD 4 85672710 85672710 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:85672710G>A c.5899C>T c.(5899-5901)Cgg>Tgg p.R1967W COAD 4 85672796 85672796 + Missense_Mutation SNP T T A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr4:85672796T>A c.5813A>T c.(5812-5814)aAc>aTc p.N1938I COAD 4 85672858 85672858 + Silent SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr4:85672858A>G c.5751T>C c.(5749-5751)ctT>ctC p.L1917L COAD 4 85676453 85676453 + Frame_Shift_Del DEL A A - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr4:85676453delA c.5525delT c.(5524-5526)ttafs p.L1844fs COAD 4 85676453 85676453 + Frame_Shift_Del DEL A A - TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr4:85676453delA c.5525delT c.(5524-5526)ttafs p.L1844fs COAD 4 85676503 85676503 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr4:85676503G>A c.5475C>T c.(5473-5475)agC>agT p.S1825S COAD 4 85687086 85687086 + Silent SNP T T G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:85687086T>G c.5065A>C c.(5065-5067)Agg>Cgg p.R1689R COAD 4 85687158 85687158 + Missense_Mutation SNP T T C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr4:85687158T>C c.4993A>G c.(4993-4995)Aca>Gca p.T1665A COAD 4 85704149 85704149 + Missense_Mutation SNP G G A TCGA-AA-3842-01A-01W-0995-10 TCGA-AA-3842-10A-01W-0995-10 g.chr4:85704149G>A c.4141C>T c.(4141-4143)Cgg>Tgg p.R1381W COAD 4 85707194 85707194 + Silent SNP G G A TCGA-AA-A01F-01A-01W-A005-10 TCGA-AA-A01F-10A-01W-A005-10 g.chr4:85707194G>A c.4000C>T c.(4000-4002)Cta>Tta p.L1334L COAD 4 85708677 85708677 + Nonsense_Mutation SNP C C A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr4:85708677C>A c.3859G>T c.(3859-3861)Gga>Tga p.G1287* COAD 4 85710928 85710928 + Frame_Shift_Del DEL T T - TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr4:85710928delT c.3620delA c.(3619-3621)aacfs p.N1207fs COAD 4 85710984 85710984 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:85710984G>A c.3564C>T c.(3562-3564)atC>atT p.I1188I COAD 4 85711000 85711000 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:85711000C>T c.3548G>A c.(3547-3549)cGa>cAa p.R1183Q COAD 4 85711007 85711007 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85711007G>A c.3541C>T c.(3541-3543)Cgc>Tgc p.R1181C COAD 4 85715716 85715716 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:85715716C>T c.3443G>A c.(3442-3444)cGa>cAa p.R1148Q COAD 4 85716121 85716121 + Frame_Shift_Del DEL A A - TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr4:85716121delA c.3179delT c.(3178-3180)ttgfs p.L1060fs COAD 4 85717847 85717848 + Missense_Mutation DNP TT TT CC TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr4:85717847_85717848TT>CC c.2993_2994AA>GG c.(2992-2994)gAA>gGG p.E998G COAD 4 85717848 85717848 + Missense_Mutation SNP T T C TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr4:85717848T>C c.2993A>G c.(2992-2994)gAa>gGa p.E998G COAD 4 85729570 85729570 + Splice_Site SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr4:85729570A>G c.2346T>C c.(2344-2346)agT>agC p.S782S COAD 4 85738560 85738560 + Missense_Mutation SNP C C G TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr4:85738560C>G c.1872G>C c.(1870-1872)aaG>aaC p.K624N COAD 4 85738618 85738618 + Missense_Mutation SNP T T A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:85738618T>A c.1814A>T c.(1813-1815)gAc>gTc p.D605V COAD 4 85742700 85742700 + Silent SNP G G A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr4:85742700G>A c.1128C>T c.(1126-1128)caC>caT p.H376H COAD 4 85747966 85747966 + Splice_Site SNP A A G TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr4:85747966A>G c.e10+1 COAD 4 85748006 85748006 + Frame_Shift_Del DEL A A - TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr4:85748006delA c.1085delT c.(1084-1086)ttafs p.L363fs COAD 4 85750172 85750172 + Missense_Mutation SNP C C T TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr4:85750172C>T c.941G>A c.(940-942)tGt>tAt p.C314Y COAD 4 85750200 85750200 + Missense_Mutation SNP G G A TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chr4:85750200G>A c.913C>T c.(913-915)Cgg>Tgg p.R305W COAD 4 85750273 85750273 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85750273G>A c.840C>T c.(838-840)gtC>gtT p.V280V COAD 4 85752605 85752605 + Missense_Mutation SNP G G A TCGA-A6-2683-01A-01W-0831-10 TCGA-A6-2683-10A-01W-0831-10 g.chr4:85752605G>A c.730C>T c.(730-732)Cgt>Tgt p.R244C COAD 4 85758091 85758091 + Silent SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr4:85758091A>G c.567T>C c.(565-567)gtT>gtC p.V189V COAD 4 85771108 85771108 + Missense_Mutation SNP A A T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85771108A>T c.251T>A c.(250-252)gTc>gAc p.V84D COAD 4 85781626 85781626 + Missense_Mutation SNP C C T TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr4:85781626C>T c.119G>A c.(118-120)cGg>cAg p.R40Q COAD 4 85781682 85781682 + Silent SNP G G A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr4:85781682G>A c.63C>T c.(61-63)aaC>aaT p.N21N COAD 4 85781713 85781713 + Missense_Mutation SNP G G A TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr4:85781713G>A c.32C>T c.(31-33)cCg>cTg p.P11L COADREAD 4 85594125 85594125 + Nonsense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr4:85594125C>A c.10477G>T c.(10477-10479)Gaa>Taa p.E3493* COADREAD 4 85600239 85600239 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:85600239C>A c.9980G>T c.(9979-9981)gGc>gTc p.G3327V COADREAD 4 85600317 85600317 + Missense_Mutation SNP G G T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:85600317G>T c.9902C>A c.(9901-9903)cCa>cAa p.P3301Q COADREAD 4 85600379 85600379 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr4:85600379G>A c.9840C>T c.(9838-9840)gaC>gaT p.D3280D COADREAD 4 85611693 85611693 + Missense_Mutation SNP G G A TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:85611693G>A c.9329C>T c.(9328-9330)tCc>tTc p.S3110F COADREAD 4 85611707 85611708 + Frame_Shift_Ins INS - - CA TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr4:85611707_85611708insCA c.9314_9315insTG c.(9313-9315)tggfs p.W3105fs COADREAD 4 85611756 85611756 + Missense_Mutation SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr4:85611756T>C c.9266A>G c.(9265-9267)aAc>aGc p.N3089S COADREAD 4 85612867 85612867 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85612867G>T c.9121C>A c.(9121-9123)Ctt>Att p.L3041I COADREAD 4 85612887 85612887 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:85612887G>A c.9101C>T c.(9100-9102)gCg>gTg p.A3034V COADREAD 4 85614146 85614146 + Nonsense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:85614146G>A c.8941C>T c.(8941-8943)Cga>Tga p.R2981* COADREAD 4 85623552 85623552 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85623552G>T c.8550C>A c.(8548-8550)ttC>ttA p.F2850L COADREAD 4 85626556 85626556 + Missense_Mutation SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr4:85626556C>T c.8326G>A c.(8326-8328)Gat>Aat p.D2776N COADREAD 4 85626604 85626604 + Missense_Mutation SNP T T G TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr4:85626604T>G c.8278A>C c.(8278-8280)Aca>Cca p.T2760P COADREAD 4 85626633 85626633 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:85626633C>A c.8249G>T c.(8248-8250)aGa>aTa p.R2750I COADREAD 4 85634389 85634389 + Missense_Mutation SNP A A T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85634389A>T c.7965T>A c.(7963-7965)ttT>ttA p.F2655L COADREAD 4 85636510 85636510 + Silent SNP T T C TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr4:85636510T>C c.7902A>G c.(7900-7902)ggA>ggG p.G2634G COADREAD 4 85639659 85639659 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:85639659A>C c.7670T>G c.(7669-7671)tTt>tGt p.F2557C COADREAD 4 85642562 85642562 + Splice_Site SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr4:85642562C>A c.7605G>T c.(7603-7605)aaG>aaT p.K2535N COADREAD 4 85642563 85642563 + Splice_Site DEL T T - TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr4:85642563delT c.7604delA c.(7603-7605)aag>ag p.K2535fs COADREAD 4 85642695 85642695 + Missense_Mutation SNP C C A TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr4:85642695C>A c.7472G>T c.(7471-7473)cGa>cTa p.R2491L COADREAD 4 85645590 85645590 + Missense_Mutation SNP G G T TCGA-AA-3530-01A-01W-0995-10 TCGA-AA-3530-10A-01W-0995-10 g.chr4:85645590G>T c.7430C>A c.(7429-7431)gCt>gAt p.A2477D COADREAD 4 85657414 85657414 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr4:85657414C>T c.6824G>A c.(6823-6825)cGt>cAt p.R2275H COADREAD 4 85657481 85657481 + Splice_Site SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:85657481C>A c.e42-1 COADREAD 4 85658388 85658388 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85658388C>T c.6706G>A c.(6706-6708)Gca>Aca p.A2236T COADREAD 4 85658517 85658517 + Missense_Mutation SNP G G A TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr4:85658517G>A c.6577C>T c.(6577-6579)Cgt>Tgt p.R2193C COADREAD 4 85660273 85660273 + Splice_Site SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr4:85660273C>T c.e40-1 COADREAD 4 85661380 85661380 + Missense_Mutation SNP T T A TCGA-AG-A015-01A-01W-A005-10 TCGA-AG-A015-10A-01W-A005-10 g.chr4:85661380T>A c.6424A>T c.(6424-6426)Agc>Tgc p.S2142C COADREAD 4 85661490 85661490 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr4:85661490C>T c.6314G>A c.(6313-6315)cGg>cAg p.R2105Q COADREAD 4 85661548 85661548 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85661548A>C c.6256T>G c.(6256-6258)Ttg>Gtg p.L2086V COADREAD 4 85664912 85664912 + Missense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:85664912A>C c.6014T>G c.(6013-6015)tTt>tGt p.F2005C COADREAD 4 85672710 85672710 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:85672710G>A c.5899C>T c.(5899-5901)Cgg>Tgg p.R1967W COADREAD 4 85672796 85672796 + Missense_Mutation SNP T T A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr4:85672796T>A c.5813A>T c.(5812-5814)aAc>aTc p.N1938I COADREAD 4 85672858 85672858 + Silent SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr4:85672858A>G c.5751T>C c.(5749-5751)ctT>ctC p.L1917L COADREAD 4 85676453 85676453 + Frame_Shift_Del DEL A A - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr4:85676453delA c.5525delT c.(5524-5526)ttafs p.L1844fs COADREAD 4 85676453 85676453 + Frame_Shift_Del DEL A A - TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr4:85676453delA c.5525delT c.(5524-5526)ttafs p.L1844fs COADREAD 4 85676503 85676503 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr4:85676503G>A c.5475C>T c.(5473-5475)agC>agT p.S1825S COADREAD 4 85678299 85678299 + Missense_Mutation SNP C C T TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr4:85678299C>T c.5204G>A c.(5203-5205)aGa>aAa p.R1735K COADREAD 4 85687086 85687086 + Silent SNP T T G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:85687086T>G c.5065A>C c.(5065-5067)Agg>Cgg p.R1689R COADREAD 4 85687158 85687158 + Missense_Mutation SNP T T C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr4:85687158T>C c.4993A>G c.(4993-4995)Aca>Gca p.T1665A COADREAD 4 85696122 85696122 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85696122C>A c.4605G>T c.(4603-4605)aaG>aaT p.K1535N COADREAD 4 85704149 85704149 + Missense_Mutation SNP G G A TCGA-AA-3842-01A-01W-0995-10 TCGA-AA-3842-10A-01W-0995-10 g.chr4:85704149G>A c.4141C>T c.(4141-4143)Cgg>Tgg p.R1381W COADREAD 4 85707194 85707194 + Silent SNP G G A TCGA-AA-A01F-01A-01W-A005-10 TCGA-AA-A01F-10A-01W-A005-10 g.chr4:85707194G>A c.4000C>T c.(4000-4002)Cta>Tta p.L1334L COADREAD 4 85708677 85708677 + Nonsense_Mutation SNP C C A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr4:85708677C>A c.3859G>T c.(3859-3861)Gga>Tga p.G1287* COADREAD 4 85708719 85708719 + Missense_Mutation SNP C C G TCGA-AG-3600-01A-01W-0833-10 TCGA-AG-3600-10A-01W-0833-10 g.chr4:85708719C>G c.3817G>C c.(3817-3819)Gaa>Caa p.E1273Q COADREAD 4 85710928 85710928 + Frame_Shift_Del DEL T T - TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr4:85710928delT c.3620delA c.(3619-3621)aacfs p.N1207fs COADREAD 4 85710984 85710984 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:85710984G>A c.3564C>T c.(3562-3564)atC>atT p.I1188I COADREAD 4 85711000 85711000 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:85711000C>T c.3548G>A c.(3547-3549)cGa>cAa p.R1183Q COADREAD 4 85711007 85711007 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85711007G>A c.3541C>T c.(3541-3543)Cgc>Tgc p.R1181C COADREAD 4 85715716 85715716 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:85715716C>T c.3443G>A c.(3442-3444)cGa>cAa p.R1148Q COADREAD 4 85716121 85716121 + Frame_Shift_Del DEL A A - TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr4:85716121delA c.3179delT c.(3178-3180)ttgfs p.L1060fs COADREAD 4 85717847 85717848 + Missense_Mutation DNP TT TT CC TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr4:85717847_85717848TT>CC c.2993_2994AA>GG c.(2992-2994)gAA>gGG p.E998G COADREAD 4 85717848 85717848 + Missense_Mutation SNP T T C TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr4:85717848T>C c.2993A>G c.(2992-2994)gAa>gGa p.E998G COADREAD 4 85729570 85729570 + Splice_Site SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr4:85729570A>G c.2346T>C c.(2344-2346)agT>agC p.S782S COADREAD 4 85738560 85738560 + Missense_Mutation SNP C C G TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr4:85738560C>G c.1872G>C c.(1870-1872)aaG>aaC p.K624N COADREAD 4 85738618 85738618 + Missense_Mutation SNP T T A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:85738618T>A c.1814A>T c.(1813-1815)gAc>gTc p.D605V COADREAD 4 85741252 85741252 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85741252G>T c.1679C>A c.(1678-1680)tCa>tAa p.S560* COADREAD 4 85742596 85742596 + Missense_Mutation SNP T T A TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr4:85742596T>A c.1232A>T c.(1231-1233)tAc>tTc p.Y411F COADREAD 4 85742700 85742700 + Silent SNP G G A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr4:85742700G>A c.1128C>T c.(1126-1128)caC>caT p.H376H COADREAD 4 85747966 85747966 + Splice_Site SNP A A G TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr4:85747966A>G c.e10+1 COADREAD 4 85748006 85748006 + Frame_Shift_Del DEL A A - TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr4:85748006delA c.1085delT c.(1084-1086)ttafs p.L363fs COADREAD 4 85750172 85750172 + Missense_Mutation SNP C C T TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr4:85750172C>T c.941G>A c.(940-942)tGt>tAt p.C314Y COADREAD 4 85750200 85750200 + Missense_Mutation SNP G G A TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chr4:85750200G>A c.913C>T c.(913-915)Cgg>Tgg p.R305W COADREAD 4 85750273 85750273 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85750273G>A c.840C>T c.(838-840)gtC>gtT p.V280V COADREAD 4 85752605 85752605 + Missense_Mutation SNP G G A TCGA-A6-2683-01A-01W-0831-10 TCGA-A6-2683-10A-01W-0831-10 g.chr4:85752605G>A c.730C>T c.(730-732)Cgt>Tgt p.R244C COADREAD 4 85758091 85758091 + Silent SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr4:85758091A>G c.567T>C c.(565-567)gtT>gtC p.V189V COADREAD 4 85771108 85771108 + Missense_Mutation SNP A A T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:85771108A>T c.251T>A c.(250-252)gTc>gAc p.V84D COADREAD 4 85781626 85781626 + Missense_Mutation SNP C C T TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr4:85781626C>T c.119G>A c.(118-120)cGg>cAg p.R40Q COADREAD 4 85781682 85781682 + Silent SNP G G A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr4:85781682G>A c.63C>T c.(61-63)aaC>aaT p.N21N COADREAD 4 85781713 85781713 + Missense_Mutation SNP G G A TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr4:85781713G>A c.32C>T c.(31-33)cCg>cTg p.P11L DLBC 4 85612823 85612823 + Silent SNP T T C TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr4:85612823T>C c.9165A>G c.(9163-9165)gcA>gcG p.A3055A ESCA 4 85594028 85594028 + Missense_Mutation SNP T T G TCGA-LN-A5U7-01A-11D-A31U-09 TCGA-LN-A5U7-10A-01D-A31U-09 g.chr4:85594028T>G c.10574A>C c.(10573-10575)aAt>aCt p.N3525T ESCA 4 85645675 85645675 + Missense_Mutation SNP G G T TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr4:85645675G>T c.7345C>A c.(7345-7347)Ccc>Acc p.P2449T ESCA 4 85658516 85658516 + Missense_Mutation SNP C C T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr4:85658516C>T c.6578G>A c.(6577-6579)cGt>cAt p.R2193H ESCA 4 85660182 85660183 + Frame_Shift_Ins INS - - T TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr4:85660182_85660183insT c.6554_6555insA c.(6553-6555)tacfs p.Y2185fs ESCA 4 85687071 85687071 + Missense_Mutation SNP G G T TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr4:85687071G>T c.5080C>A c.(5080-5082)Cta>Ata p.L1694I ESCA 4 85696071 85696071 + Silent SNP A A C TCGA-2H-A9GH-01A-11D-A37C-09 TCGA-2H-A9GH-11A-11D-A37F-09 g.chr4:85696071A>C c.4656T>G c.(4654-4656)acT>acG p.T1552T ESCA 4 85711028 85711028 + Nonsense_Mutation SNP C C A TCGA-LN-A49L-01A-11D-A247-09 TCGA-LN-A49L-10A-01D-A247-09 g.chr4:85711028C>A c.3520G>T c.(3520-3522)Gaa>Taa p.E1174* ESCA 4 85715781 85715781 + Silent SNP C C T TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr4:85715781C>T c.3378G>A c.(3376-3378)gtG>gtA p.V1126V ESCA 4 85724488 85724488 + Silent SNP G G A TCGA-LN-A7HX-01A-11D-A33E-09 TCGA-LN-A7HX-10A-01D-A33H-09 g.chr4:85724488G>A c.2562C>T c.(2560-2562)gcC>gcT p.A854A ESCA 4 85729487 85729487 + Splice_Site SNP C C G TCGA-LN-A7HX-01A-11D-A33E-09 TCGA-LN-A7HX-10A-01D-A33H-09 g.chr4:85729487C>G c.2429G>C c.(2428-2430)aGg>aCg p.R810T ESCA 4 85731152 85731152 + Missense_Mutation SNP G G T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr4:85731152G>T c.2233C>A c.(2233-2235)Caa>Aaa p.Q745K ESCA 4 85731437 85731437 + Missense_Mutation SNP C C T TCGA-JY-A6FA-01A-11D-A33E-09 TCGA-JY-A6FA-10A-01D-A33H-09 g.chr4:85731437C>T c.1948G>A c.(1948-1950)Gga>Aga p.G650R ESCA 4 85781626 85781626 + Missense_Mutation SNP C C T TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr4:85781626C>T c.119G>A c.(118-120)cGg>cAg p.R40Q GBM 4 85611704 85611704 + Missense_Mutation SNP C C G TCGA-28-5214-01A-01D-1486-08 TCGA-28-5214-10A-01D-1486-08 g.chr4:85611704C>G c.9318G>C c.(9316-9318)gaG>gaC p.E3106D GBM 4 85634313 85634313 + Splice_Site SNP C C T TCGA-28-5213-01A-01D-1486-08 TCGA-28-5213-10A-01D-1486-08 g.chr4:85634313C>T c.8041G>A c.(8041-8043)Gga>Aga p.G2681R GBM 4 85657415 85657415 + Missense_Mutation SNP G G A TCGA-27-1832-01A-01W-0643-08 TCGA-27-1832-10A-01W-0644-08 g.chr4:85657415G>A c.6823C>T c.(6823-6825)Cgt>Tgt p.R2275C GBM 4 85719250 85719250 + Missense_Mutation SNP C C T TCGA-19-5955-01A-11D-1696-08 TCGA-19-5955-11A-01D-1696-08 g.chr4:85719250C>T c.2834G>A c.(2833-2835)cGt>cAt p.R945H GBMLGG 4 85600267 85600267 + Missense_Mutation SNP C C T TCGA-CS-5393-01A-01D-1468-08 TCGA-CS-5393-10A-01D-1468-08 g.chr4:85600267C>T c.9952G>A c.(9952-9954)Gca>Aca p.A3318T GBMLGG 4 85611704 85611704 + Missense_Mutation SNP C C G TCGA-28-5214-01A-01D-1486-08 TCGA-28-5214-10A-01D-1486-08 g.chr4:85611704C>G c.9318G>C c.(9316-9318)gaG>gaC p.E3106D GBMLGG 4 85612794 85612794 + Missense_Mutation SNP T T A TCGA-CS-5397-01A-01D-1893-08 TCGA-CS-5397-10A-03D-1893-08 g.chr4:85612794T>A c.9194A>T c.(9193-9195)gAg>gTg p.E3065V GBMLGG 4 85612906 85612906 + Missense_Mutation SNP T T C TCGA-HT-7485-01A-11D-2024-08 TCGA-HT-7485-10A-01D-2024-08 g.chr4:85612906T>C c.9082A>G c.(9082-9084)Aca>Gca p.T3028A GBMLGG 4 85612936 85612936 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:85612936G>A c.9052C>T c.(9052-9054)Ctc>Ttc p.L3018F GBMLGG 4 85626601 85626601 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:85626601C>A c.8281G>T c.(8281-8283)Gat>Tat p.D2761Y GBMLGG 4 85634313 85634313 + Splice_Site SNP C C T TCGA-28-5213-01A-01D-1486-08 TCGA-28-5213-10A-01D-1486-08 g.chr4:85634313C>T c.8041G>A c.(8041-8043)Gga>Aga p.G2681R GBMLGG 4 85634366 85634366 + Missense_Mutation SNP G G A TCGA-DH-A7UR-01A-11D-A33T-08 TCGA-DH-A7UR-10A-01D-A33W-08 g.chr4:85634366G>A c.7988C>T c.(7987-7989)aCg>aTg p.T2663M GBMLGG 4 85657415 85657415 + Missense_Mutation SNP G G A TCGA-27-1832-01A-01W-0643-08 TCGA-27-1832-10A-01W-0644-08 g.chr4:85657415G>A c.6823C>T c.(6823-6825)Cgt>Tgt p.R2275C GBMLGG 4 85658466 85658466 + Missense_Mutation SNP T T C TCGA-TM-A84C-01A-11D-A36O-08 TCGA-TM-A84C-12A-01D-A367-08 g.chr4:85658466T>C c.6628A>G c.(6628-6630)Agt>Ggt p.S2210G GBMLGG 4 85715705 85715708 + Frame_Shift_Del DEL CAAT CAAT - TCGA-DU-8168-01A-11D-2253-08 TCGA-DU-8168-10A-01D-2253-08 g.chr4:85715705_85715708delCAAT c.3451_3454delATTG c.(3451-3456)attgttfs p.IV1151fs GBMLGG 4 85719250 85719250 + Missense_Mutation SNP C C T TCGA-19-5955-01A-11D-1696-08 TCGA-19-5955-11A-01D-1696-08 g.chr4:85719250C>T c.2834G>A c.(2833-2835)cGt>cAt p.R945H GBMLGG 4 85719252 85719253 + Frame_Shift_Ins INS - - A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:85719252_85719253insA c.2831_2832insT c.(2830-2832)ttafs p.L944fs GBMLGG 4 85731329 85731331 + In_Frame_Del DEL GAA GAA - TCGA-DU-6394-01A-11D-1705-08 TCGA-DU-6394-10A-01D-1705-08 g.chr4:85731329_85731331delGAA c.2054_2056delTTC c.(2053-2058)cttcac>cac p.L685del HNSC 4 85600085 85600085 + Silent SNP G G A TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chr4:85600085G>A c.10134C>T c.(10132-10134)agC>agT p.S3378S HNSC 4 85617191 85617191 + Missense_Mutation SNP T T C TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr4:85617191T>C c.8833A>G c.(8833-8835)Atc>Gtc p.I2945V HNSC 4 85617224 85617224 + Missense_Mutation SNP G G C TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr4:85617224G>C c.8800C>G c.(8800-8802)Ctt>Gtt p.L2934V HNSC 4 85617288 85617288 + Missense_Mutation SNP G G C TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr4:85617288G>C c.8736C>G c.(8734-8736)gaC>gaG p.D2912E HNSC 4 85617976 85617976 + Splice_Site SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr4:85617976C>T c.8597G>A c.(8596-8598)gGc>gAc p.G2866D HNSC 4 85642584 85642584 + Missense_Mutation SNP C C T TCGA-CV-A6JD-01A-11D-A31L-08 TCGA-CV-A6JD-10A-01D-A31J-08 g.chr4:85642584C>T c.7583G>A c.(7582-7584)cGc>cAc p.R2528H HNSC 4 85645602 85645602 + Missense_Mutation SNP T T C TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr4:85645602T>C c.7418A>G c.(7417-7419)gAa>gGa p.E2473G HNSC 4 85654614 85654614 + Missense_Mutation SNP C C G TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr4:85654614C>G c.7142G>C c.(7141-7143)aGg>aCg p.R2381T HNSC 4 85654725 85654725 + Missense_Mutation SNP C C A TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr4:85654725C>A c.7031G>T c.(7030-7032)tGg>tTg p.W2344L HNSC 4 85657475 85657475 + Nonsense_Mutation SNP C C A TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr4:85657475C>A c.6763G>T c.(6763-6765)Gaa>Taa p.E2255* HNSC 4 85661382 85661382 + Missense_Mutation SNP A A T TCGA-CN-6992-01A-11D-1912-08 TCGA-CN-6992-10A-01D-1912-08 g.chr4:85661382A>T c.6422T>A c.(6421-6423)aTt>aAt p.I2141N HNSC 4 85664916 85664916 + Missense_Mutation SNP C C T TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr4:85664916C>T c.6010G>A c.(6010-6012)Gaa>Aaa p.E2004K HNSC 4 85664939 85664939 + Missense_Mutation SNP C C G TCGA-F7-A623-01A-11D-A28R-08 TCGA-F7-A623-10A-01D-A28U-08 g.chr4:85664939C>G c.5987G>C c.(5986-5988)aGg>aCg p.R1996T HNSC 4 85672736 85672736 + Missense_Mutation SNP G G C TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr4:85672736G>C c.5873C>G c.(5872-5874)gCt>gGt p.A1958G HNSC 4 85696000 85696000 + Missense_Mutation SNP C C T TCGA-CV-A6JU-01A-11D-A31L-08 TCGA-CV-A6JU-10A-01D-A31J-08 g.chr4:85696000C>T c.4727G>A c.(4726-4728)gGt>gAt p.G1576D HNSC 4 85701359 85701359 + Missense_Mutation SNP C C A TCGA-CQ-6219-01A-11D-1912-08 TCGA-CQ-6219-10A-01D-1912-08 g.chr4:85701359C>A c.4267G>T c.(4267-4269)Gat>Tat p.D1423Y HNSC 4 85701392 85701392 + Missense_Mutation SNP C C A TCGA-CV-6942-01A-21D-2012-08 TCGA-CV-6942-10A-01D-2013-08 g.chr4:85701392C>A c.4234G>T c.(4234-4236)Gca>Tca p.A1412S HNSC 4 85707147 85707147 + Silent SNP T T C TCGA-CX-7219-01A-11D-2012-08 TCGA-CX-7219-10A-01D-2013-08 g.chr4:85707147T>C c.4047A>G c.(4045-4047)aaA>aaG p.K1349K HNSC 4 85708805 85708805 + Missense_Mutation SNP G G A TCGA-CV-A45R-01A-11D-A24D-08 TCGA-CV-A45R-10A-01D-A24F-08 g.chr4:85708805G>A c.3731C>T c.(3730-3732)aCg>aTg p.T1244M HNSC 4 85716037 85716037 + Missense_Mutation SNP C C A TCGA-CQ-6225-01A-11D-1912-08 TCGA-CQ-6225-10A-01D-1912-08 g.chr4:85716037C>A c.3263G>T c.(3262-3264)gGt>gTt p.G1088V HNSC 4 85717800 85717800 + Missense_Mutation SNP C C T TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr4:85717800C>T c.3041G>A c.(3040-3042)gGa>gAa p.G1014E HNSC 4 85722859 85722859 + Silent SNP G G A TCGA-BA-A8YP-01A-11D-A391-08 TCGA-BA-A8YP-10A-01D-A394-08 g.chr4:85722859G>A c.2766C>T c.(2764-2766)ccC>ccT p.P922P HNSC 4 85724475 85724475 + Missense_Mutation SNP G G C TCGA-QK-A8Z8-01A-11D-A391-08 TCGA-QK-A8Z8-10A-01D-A394-08 g.chr4:85724475G>C c.2575C>G c.(2575-2577)Ctg>Gtg p.L859V HNSC 4 85729569 85729569 + Splice_Site SNP G G A TCGA-BA-A4IH-01A-11D-A25Y-08 TCGA-BA-A4IH-10A-01D-A25Y-08 g.chr4:85729569G>A c.2347C>T c.(2347-2349)Cgt>Tgt p.R783C HNSC 4 85731060 85731060 + Silent SNP T T A TCGA-CN-5361-01A-01D-1434-08 TCGA-CN-5361-10A-01D-1434-08 g.chr4:85731060T>A c.2325A>T c.(2323-2325)gtA>gtT p.V775V HNSC 4 85741276 85741276 + Missense_Mutation SNP G G C TCGA-HD-8314-01A-11D-2394-08 TCGA-HD-8314-10A-01D-2394-08 g.chr4:85741276G>C c.1655C>G c.(1654-1656)aCc>aGc p.T552S HNSC 4 85742694 85742694 + Silent SNP C C G TCGA-D6-A4ZB-01A-11D-A25D-08 TCGA-D6-A4ZB-10A-01D-A25E-08 g.chr4:85742694C>G c.1134G>C c.(1132-1134)gtG>gtC p.V378V HNSC 4 85748035 85748035 + Silent SNP T T A TCGA-CR-6474-01A-11D-1870-08 TCGA-CR-6474-10A-01D-1870-08 g.chr4:85748035T>A c.1056A>T c.(1054-1056)ccA>ccT p.P352P HNSC 4 85748079 85748079 + Silent SNP G G A TCGA-MZ-A7D7-01A-21D-A34J-08 TCGA-MZ-A7D7-10A-01D-A34M-08 g.chr4:85748079G>A c.1012C>T c.(1012-1014)Ctg>Ttg p.L338L HNSC 4 85752750 85752750 + Silent SNP C C T TCGA-CV-7177-01A-11D-2012-08 TCGA-CV-7177-10A-01D-2013-08 g.chr4:85752750C>T c.585G>A c.(583-585)gtG>gtA p.V195V HNSC 4 85758209 85758209 + Missense_Mutation SNP G G T TCGA-BB-A5HY-01A-11D-A28R-08 TCGA-BB-A5HY-10A-01D-A28U-08 g.chr4:85758209G>T c.449C>A c.(448-450)cCt>cAt p.P150H HNSC 4 85781681 85781681 + Missense_Mutation SNP C C G TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr4:85781681C>G c.64G>C c.(64-66)Gcc>Ccc p.A22P KICH 4 85630103 85630103 + Missense_Mutation SNP A A G TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chr4:85630103A>G c.8176T>C c.(8176-8178)Tat>Cat p.Y2726H KICH 4 85758218 85758218 + Missense_Mutation SNP A A G TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr4:85758218A>G c.440T>C c.(439-441)aTg>aCg p.M147T KIPAN 4 85598373 85598374 + Missense_Mutation DNP CA CA AG TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr4:85598373_85598374CA>AG c.10435_10436TG>CT c.(10435-10437)TGt>CTt p.C3479L KIPAN 4 85611661 85611662 + Frame_Shift_Ins INS - - T TCGA-CJ-5676-01A-11D-1534-10 TCGA-CJ-5676-11A-01D-1534-10 g.chr4:85611661_85611662insT c.9360_9361insA c.(9358-9363)aaacagfs p.Q3121fs KIPAN 4 85630103 85630103 + Missense_Mutation SNP A A G TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chr4:85630103A>G c.8176T>C c.(8176-8178)Tat>Cat p.Y2726H KIPAN 4 85630153 85630153 + Frame_Shift_Del DEL A A - TCGA-B9-4617-01A-01D-1252-08 TCGA-B9-4617-10A-01D-1252-08 g.chr4:85630153delA c.8126delT c.(8125-8127)ttgfs p.L2709fs KIPAN 4 85636511 85636511 + Missense_Mutation SNP C C T TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr4:85636511C>T c.7901G>A c.(7900-7902)gGa>gAa p.G2634E KIPAN 4 85642588 85642588 + Missense_Mutation SNP G G T TCGA-2Z-A9JT-01A-11D-A42J-10 TCGA-2Z-A9JT-10A-01D-A42M-10 g.chr4:85642588G>T c.7579C>A c.(7579-7581)Ctg>Atg p.L2527M KIPAN 4 85642627 85642627 + Missense_Mutation SNP A A T TCGA-B0-5080-01A-01D-1501-10 TCGA-B0-5080-11A-01D-1501-10 g.chr4:85642627A>T c.7540T>A c.(7540-7542)Tcc>Acc p.S2514T KIPAN 4 85654653 85654653 + Missense_Mutation SNP T T A TCGA-CJ-4918-01A-01D-1429-08 TCGA-CJ-4918-11A-01D-1429-08 g.chr4:85654653T>A c.7103A>T c.(7102-7104)aAg>aTg p.K2368M KIPAN 4 85664902 85664902 + Silent SNP G G A TCGA-CJ-4912-01A-01D-1429-08 TCGA-CJ-4912-11A-01D-1429-08 g.chr4:85664902G>A c.6024C>T c.(6022-6024)taC>taT p.Y2008Y KIPAN 4 85674870 85674870 + Missense_Mutation SNP T T C TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr4:85674870T>C c.5719A>G c.(5719-5721)Att>Gtt p.I1907V KIPAN 4 85675021 85675021 + Silent SNP T T C TCGA-P4-A5ED-01A-11D-A28G-10 TCGA-P4-A5ED-11A-11D-A28G-10 g.chr4:85675021T>C c.5568A>G c.(5566-5568)caA>caG p.Q1856Q KIPAN 4 85716095 85716095 + Missense_Mutation SNP G G T TCGA-HE-A5NK-01A-11D-A26P-10 TCGA-HE-A5NK-10A-01D-A26P-10 g.chr4:85716095G>T c.3205C>A c.(3205-3207)Cct>Act p.P1069T KIPAN 4 85716133 85716133 + Splice_Site SNP C C T TCGA-2Z-A9JS-01A-21D-A42J-10 TCGA-2Z-A9JS-10A-01D-A42M-10 g.chr4:85716133C>T c.e20-1 KIPAN 4 85722839 85722839 + Missense_Mutation SNP C C A TCGA-A4-A5Y0-01A-11D-A31X-10 TCGA-A4-A5Y0-11A-11D-A31X-10 g.chr4:85722839C>A c.2786G>T c.(2785-2787)cGa>cTa p.R929L KIPAN 4 85722980 85722980 + Missense_Mutation SNP A A G TCGA-CZ-4866-01A-01D-1501-10 TCGA-CZ-4866-11A-01D-1501-10 g.chr4:85722980A>G c.2645T>C c.(2644-2646)tTa>tCa p.L882S KIPAN 4 85724467 85724467 + Silent SNP A A T TCGA-BP-4326-01A-01D-1366-10 TCGA-BP-4326-11A-01D-1366-10 g.chr4:85724467A>T c.2583T>A c.(2581-2583)tcT>tcA p.S861S KIPAN 4 85724573 85724573 + Missense_Mutation SNP T T C TCGA-BP-4965-01A-01D-1462-08 TCGA-BP-4965-11A-01D-1462-08 g.chr4:85724573T>C c.2477A>G c.(2476-2478)aAt>aGt p.N826S KIPAN 4 85729530 85729531 + Frame_Shift_Ins INS - - AG TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr4:85729530_85729531insAG c.2385_2386insCT c.(2383-2388)tcttctfs p.S796fs KIPAN 4 85731169 85731169 + Nonsense_Mutation SNP G G T TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr4:85731169G>T c.2216C>A c.(2215-2217)tCa>tAa p.S739* KIPAN 4 85738690 85738690 + Frame_Shift_Del DEL T T - TCGA-CZ-5456-01A-01D-1501-10 TCGA-CZ-5456-11A-01D-1501-10 g.chr4:85738690delT c.1742delA c.(1741-1743)aagfs p.K581fs KIPAN 4 85742692 85742692 + Missense_Mutation SNP C C G TCGA-B8-4622-01A-02D-1553-08 TCGA-B8-4622-11A-01D-1553-08 g.chr4:85742692C>G c.1136G>C c.(1135-1137)aGa>aCa p.R379T KIPAN 4 85748064 85748064 + Missense_Mutation SNP T T C TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr4:85748064T>C c.1027A>G c.(1027-1029)Aca>Gca p.T343A KIPAN 4 85758174 85758174 + Missense_Mutation SNP C C G TCGA-SX-A7SN-01A-11D-A34Z-10 TCGA-SX-A7SN-10A-01D-A34Z-10 g.chr4:85758174C>G c.484G>C c.(484-486)Gac>Cac p.D162H KIPAN 4 85758218 85758218 + Missense_Mutation SNP A A G TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr4:85758218A>G c.440T>C c.(439-441)aTg>aCg p.M147T KIPAN 4 85758222 85758222 + Missense_Mutation SNP T T C TCGA-B2-5633-01A-01D-1534-10 TCGA-B2-5633-10A-01D-1535-10 g.chr4:85758222T>C c.436A>G c.(436-438)Aca>Gca p.T146A KIPAN 4 85781624 85781624 + Missense_Mutation SNP G G A TCGA-BQ-7059-01A-11D-1961-08 TCGA-BQ-7059-11A-01D-1961-08 g.chr4:85781624G>A c.121C>T c.(121-123)Cac>Tac p.H41Y KIRC 4 85611661 85611662 + Frame_Shift_Ins INS - - T TCGA-CJ-5676-01A-11D-1534-10 TCGA-CJ-5676-11A-01D-1534-10 g.chr4:85611661_85611662insT c.9360_9361insA c.(9358-9363)aaacagfs p.Q3121fs KIRC 4 85642627 85642627 + Missense_Mutation SNP A A T TCGA-B0-5080-01A-01D-1501-10 TCGA-B0-5080-11A-01D-1501-10 g.chr4:85642627A>T c.7540T>A c.(7540-7542)Tcc>Acc p.S2514T KIRC 4 85654653 85654653 + Missense_Mutation SNP T T A TCGA-CJ-4918-01A-01D-1429-08 TCGA-CJ-4918-11A-01D-1429-08 g.chr4:85654653T>A c.7103A>T c.(7102-7104)aAg>aTg p.K2368M KIRC 4 85664902 85664902 + Silent SNP G G A TCGA-CJ-4912-01A-01D-1429-08 TCGA-CJ-4912-11A-01D-1429-08 g.chr4:85664902G>A c.6024C>T c.(6022-6024)taC>taT p.Y2008Y KIRC 4 85674870 85674870 + Missense_Mutation SNP T T C TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr4:85674870T>C c.5719A>G c.(5719-5721)Att>Gtt p.I1907V KIRC 4 85722980 85722980 + Missense_Mutation SNP A A G TCGA-CZ-4866-01A-01D-1501-10 TCGA-CZ-4866-11A-01D-1501-10 g.chr4:85722980A>G c.2645T>C c.(2644-2646)tTa>tCa p.L882S KIRC 4 85724467 85724467 + Silent SNP A A T TCGA-BP-4326-01A-01D-1366-10 TCGA-BP-4326-11A-01D-1366-10 g.chr4:85724467A>T c.2583T>A c.(2581-2583)tcT>tcA p.S861S KIRC 4 85724573 85724573 + Missense_Mutation SNP T T C TCGA-BP-4965-01A-01D-1462-08 TCGA-BP-4965-11A-01D-1462-08 g.chr4:85724573T>C c.2477A>G c.(2476-2478)aAt>aGt p.N826S KIRC 4 85738690 85738690 + Frame_Shift_Del DEL T T - TCGA-CZ-5456-01A-01D-1501-10 TCGA-CZ-5456-11A-01D-1501-10 g.chr4:85738690delT c.1742delA c.(1741-1743)aagfs p.K581fs KIRC 4 85742692 85742692 + Missense_Mutation SNP C C G TCGA-B8-4622-01A-02D-1553-08 TCGA-B8-4622-11A-01D-1553-08 g.chr4:85742692C>G c.1136G>C c.(1135-1137)aGa>aCa p.R379T KIRC 4 85758222 85758222 + Missense_Mutation SNP T T C TCGA-B2-5633-01A-01D-1534-10 TCGA-B2-5633-10A-01D-1535-10 g.chr4:85758222T>C c.436A>G c.(436-438)Aca>Gca p.T146A KIRP 4 85598373 85598374 + Missense_Mutation DNP CA CA AG TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr4:85598373_85598374CA>AG c.10435_10436TG>CT c.(10435-10437)TGt>CTt p.C3479L KIRP 4 85630153 85630153 + Frame_Shift_Del DEL A A - TCGA-B9-4617-01A-01D-1252-08 TCGA-B9-4617-10A-01D-1252-08 g.chr4:85630153delA c.8126delT c.(8125-8127)ttgfs p.L2709fs KIRP 4 85636511 85636511 + Missense_Mutation SNP C C T TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr4:85636511C>T c.7901G>A c.(7900-7902)gGa>gAa p.G2634E KIRP 4 85642588 85642588 + Missense_Mutation SNP G G T TCGA-2Z-A9JT-01A-11D-A42J-10 TCGA-2Z-A9JT-10A-01D-A42M-10 g.chr4:85642588G>T c.7579C>A c.(7579-7581)Ctg>Atg p.L2527M KIRP 4 85675021 85675021 + Silent SNP T T C TCGA-P4-A5ED-01A-11D-A28G-10 TCGA-P4-A5ED-11A-11D-A28G-10 g.chr4:85675021T>C c.5568A>G c.(5566-5568)caA>caG p.Q1856Q KIRP 4 85716095 85716095 + Missense_Mutation SNP G G T TCGA-HE-A5NK-01A-11D-A26P-10 TCGA-HE-A5NK-10A-01D-A26P-10 g.chr4:85716095G>T c.3205C>A c.(3205-3207)Cct>Act p.P1069T KIRP 4 85716133 85716133 + Splice_Site SNP C C T TCGA-2Z-A9JS-01A-21D-A42J-10 TCGA-2Z-A9JS-10A-01D-A42M-10 g.chr4:85716133C>T c.e20-1 KIRP 4 85722839 85722839 + Missense_Mutation SNP C C A TCGA-A4-A5Y0-01A-11D-A31X-10 TCGA-A4-A5Y0-11A-11D-A31X-10 g.chr4:85722839C>A c.2786G>T c.(2785-2787)cGa>cTa p.R929L KIRP 4 85729530 85729531 + Frame_Shift_Ins INS - - AG TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr4:85729530_85729531insAG c.2385_2386insCT c.(2383-2388)tcttctfs p.S796fs KIRP 4 85731169 85731169 + Nonsense_Mutation SNP G G T TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr4:85731169G>T c.2216C>A c.(2215-2217)tCa>tAa p.S739* KIRP 4 85748064 85748064 + Missense_Mutation SNP T T C TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr4:85748064T>C c.1027A>G c.(1027-1029)Aca>Gca p.T343A KIRP 4 85758174 85758174 + Missense_Mutation SNP C C G TCGA-SX-A7SN-01A-11D-A34Z-10 TCGA-SX-A7SN-10A-01D-A34Z-10 g.chr4:85758174C>G c.484G>C c.(484-486)Gac>Cac p.D162H KIRP 4 85781624 85781624 + Missense_Mutation SNP G G A TCGA-BQ-7059-01A-11D-1961-08 TCGA-BQ-7059-11A-01D-1961-08 g.chr4:85781624G>A c.121C>T c.(121-123)Cac>Tac p.H41Y LGG 4 85600267 85600267 + Missense_Mutation SNP C C T TCGA-CS-5393-01A-01D-1468-08 TCGA-CS-5393-10A-01D-1468-08 g.chr4:85600267C>T c.9952G>A c.(9952-9954)Gca>Aca p.A3318T LGG 4 85612794 85612794 + Missense_Mutation SNP T T A TCGA-CS-5397-01A-01D-1893-08 TCGA-CS-5397-10A-03D-1893-08 g.chr4:85612794T>A c.9194A>T c.(9193-9195)gAg>gTg p.E3065V LGG 4 85612906 85612906 + Missense_Mutation SNP T T C TCGA-HT-7485-01A-11D-2024-08 TCGA-HT-7485-10A-01D-2024-08 g.chr4:85612906T>C c.9082A>G c.(9082-9084)Aca>Gca p.T3028A LGG 4 85612936 85612936 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:85612936G>A c.9052C>T c.(9052-9054)Ctc>Ttc p.L3018F LGG 4 85626601 85626601 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:85626601C>A c.8281G>T c.(8281-8283)Gat>Tat p.D2761Y LGG 4 85634366 85634366 + Missense_Mutation SNP G G A TCGA-DH-A7UR-01A-11D-A33T-08 TCGA-DH-A7UR-10A-01D-A33W-08 g.chr4:85634366G>A c.7988C>T c.(7987-7989)aCg>aTg p.T2663M LGG 4 85658466 85658466 + Missense_Mutation SNP T T C TCGA-TM-A84C-01A-11D-A36O-08 TCGA-TM-A84C-12A-01D-A367-08 g.chr4:85658466T>C c.6628A>G c.(6628-6630)Agt>Ggt p.S2210G LGG 4 85715705 85715708 + Frame_Shift_Del DEL CAAT CAAT - TCGA-DU-8168-01A-11D-2253-08 TCGA-DU-8168-10A-01D-2253-08 g.chr4:85715705_85715708delCAAT c.3451_3454delATTG c.(3451-3456)attgttfs p.IV1151fs LGG 4 85719252 85719253 + Frame_Shift_Ins INS - - A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:85719252_85719253insA c.2831_2832insT c.(2830-2832)ttafs p.L944fs LGG 4 85731329 85731331 + In_Frame_Del DEL GAA GAA - TCGA-DU-6394-01A-11D-1705-08 TCGA-DU-6394-10A-01D-1705-08 g.chr4:85731329_85731331delGAA c.2054_2056delTTC c.(2053-2058)cttcac>cac p.L685del LIHC 4 85614081 85614081 + Frame_Shift_Del DEL A A - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr4:85614081delA c.9006delT c.(9004-9006)tttfs p.F3002fs LIHC 4 85623579 85623579 + Silent SNP T T G TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr4:85623579T>G c.8523A>C c.(8521-8523)gcA>gcC p.A2841A LIHC 4 85626603 85626603 + Missense_Mutation SNP G G A TCGA-2Y-A9GW-01A-11D-A382-10 TCGA-2Y-A9GW-10A-01D-A385-10 g.chr4:85626603G>A c.8279C>T c.(8278-8280)aCa>aTa p.T2760I LIHC 4 85639621 85639621 + Missense_Mutation SNP T T A TCGA-DD-AAE7-01A-11D-A40R-10 TCGA-DD-AAE7-10A-01D-A40U-10 g.chr4:85639621T>A c.7708A>T c.(7708-7710)Atg>Ttg p.M2570L LIHC 4 85663028 85663028 + Silent SNP T T C TCGA-DD-AAVY-01A-11D-A40R-10 TCGA-DD-AAVY-10A-01D-A40U-10 g.chr4:85663028T>C c.6120A>G c.(6118-6120)gtA>gtG p.V2040V LIHC 4 85663040 85663040 + Silent SNP T T C TCGA-FV-A23B-01A-11D-A16V-10 TCGA-FV-A23B-11A-11D-A16V-10 g.chr4:85663040T>C c.6108A>G c.(6106-6108)ggA>ggG p.G2036G LIHC 4 85678264 85678264 + Missense_Mutation SNP T T A TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr4:85678264T>A c.5239A>T c.(5239-5241)Aac>Tac p.N1747Y LIHC 4 85707240 85707240 + Silent SNP T T C TCGA-CC-5262-01A-01D-A12Z-10 TCGA-CC-5262-10B-01D-A12Z-10 g.chr4:85707240T>C c.3954A>G c.(3952-3954)ccA>ccG p.P1318P LIHC 4 85711036 85711036 + Missense_Mutation SNP G G A TCGA-BD-A2L6-01A-11D-A20W-10 TCGA-BD-A2L6-11A-21D-A20W-10 g.chr4:85711036G>A c.3512C>T c.(3511-3513)tCa>tTa p.S1171L LIHC 4 85719181 85719181 + Missense_Mutation SNP G G A TCGA-DD-AAVP-01A-11D-A40R-10 TCGA-DD-AAVP-10A-01D-A40U-10 g.chr4:85719181G>A c.2903C>T c.(2902-2904)cCa>cTa p.P968L LIHC 4 85722810 85722810 + Missense_Mutation SNP C C A TCGA-BC-A3KG-01A-11D-A20W-10 TCGA-BC-A3KG-10A-01D-A20W-10 g.chr4:85722810C>A c.2815G>T c.(2815-2817)Gtg>Ttg p.V939L LIHC 4 85724505 85724505 + Missense_Mutation SNP G G A TCGA-DD-A4NN-01A-11D-A28X-10 TCGA-DD-A4NN-10A-01D-A28X-10 g.chr4:85724505G>A c.2545C>T c.(2545-2547)Cct>Tct p.P849S LIHC 4 85731416 85731416 + Silent SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr4:85731416A>G c.1969T>C c.(1969-1971)Ttg>Ctg p.L657L LIHC 4 85758098 85758098 + Missense_Mutation SNP T T A TCGA-BC-A8YO-01A-11D-A36X-10 TCGA-BC-A8YO-10A-01D-A370-10 g.chr4:85758098T>A c.560A>T c.(559-561)cAg>cTg p.Q187L LIHC 4 85781608 85781608 + Missense_Mutation SNP T T A TCGA-DD-AACK-01A-11D-A40R-10 TCGA-DD-AACK-10A-01D-A40U-10 g.chr4:85781608T>A c.137A>T c.(136-138)gAa>gTa p.E46V LUAD 4 85600130 85600130 + Silent SNP G G A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr4:85600130G>A c.10089C>T c.(10087-10089)ccC>ccT p.P3363P LUAD 4 85605170 85605170 + Missense_Mutation SNP A A C TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr4:85605170A>C c.9652T>G c.(9652-9654)Tgc>Ggc p.C3218G LUAD 4 85605244 85605244 + Missense_Mutation SNP T T C TCGA-38-6178-01A-11D-1753-08 TCGA-38-6178-10A-01D-1753-08 g.chr4:85605244T>C c.9578A>G c.(9577-9579)cAt>cGt p.H3193R LUAD 4 85609394 85609394 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr4:85609394C>A c.9388G>T c.(9388-9390)Gtc>Ttc p.V3130F LUAD 4 85617130 85617130 + Missense_Mutation SNP G G A TCGA-MP-A4SY-01A-21D-A24P-08 TCGA-MP-A4SY-10A-01D-A24P-08 g.chr4:85617130G>A c.8894C>T c.(8893-8895)cCt>cTt p.P2965L LUAD 4 85617181 85617181 + Missense_Mutation SNP G G A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr4:85617181G>A c.8843C>T c.(8842-8844)cCa>cTa p.P2948L LUAD 4 85623505 85623505 + Splice_Site SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr4:85623505C>A c.e56+1 LUAD 4 85623548 85623548 + Frame_Shift_Del DEL A A - TCGA-50-5066-01A-01D-1625-08 TCGA-50-5066-10A-01D-1625-08 g.chr4:85623548delA c.8554delT c.(8554-8556)tatfs p.Y2852fs LUAD 4 85626628 85626628 + Silent SNP G G A TCGA-50-5942-01A-21D-1753-08 TCGA-50-5942-10A-01D-1753-08 g.chr4:85626628G>A c.8254C>T c.(8254-8256)Ctg>Ttg p.L2752L LUAD 4 85630181 85630181 + Splice_Site SNP T T C TCGA-MP-A5C7-01A-11D-A25L-08 TCGA-MP-A5C7-10A-01D-A25L-08 g.chr4:85630181T>C c.8098A>G c.(8098-8100)Aga>Gga p.R2700G LUAD 4 85634326 85634326 + Silent SNP C C G TCGA-NJ-A55O-01A-11D-A25L-08 TCGA-NJ-A55O-10A-01D-A25L-08 g.chr4:85634326C>G c.8028G>C c.(8026-8028)acG>acC p.T2676T LUAD 4 85639593 85639593 + Missense_Mutation SNP A A G TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr4:85639593A>G c.7736T>C c.(7735-7737)aTt>aCt p.I2579T LUAD 4 85639672 85639672 + Missense_Mutation SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr4:85639672C>A c.7657G>T c.(7657-7659)Ggg>Tgg p.G2553W LUAD 4 85642574 85642574 + Missense_Mutation SNP C C A TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr4:85642574C>A c.7593G>T c.(7591-7593)gaG>gaT p.E2531D LUAD 4 85642649 85642649 + Silent SNP T T C TCGA-05-4415-01A-22D-1855-08 TCGA-05-4415-10A-01D-1855-08 g.chr4:85642649T>C c.7518A>G c.(7516-7518)caA>caG p.Q2506Q LUAD 4 85654535 85654535 + Splice_Site SNP C C A TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr4:85654535C>A c.7221G>T c.(7219-7221)gcG>gcT p.A2407A LUAD 4 85654540 85654540 + Missense_Mutation SNP C C T TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr4:85654540C>T c.7216G>A c.(7216-7218)Gtg>Atg p.V2406M LUAD 4 85656259 85656259 + Nonsense_Mutation SNP C C T TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr4:85656259C>T c.6930G>A c.(6928-6930)tgG>tgA p.W2310* LUAD 4 85658404 85658404 + Silent SNP G G A TCGA-71-8520-01A-11D-2393-08 TCGA-71-8520-10A-01D-2393-08 g.chr4:85658404G>A c.6690C>T c.(6688-6690)caC>caT p.H2230H LUAD 4 85660237 85660237 + Missense_Mutation SNP C C A TCGA-50-6593-01A-11D-1753-08 TCGA-50-6593-11A-01D-1753-08 g.chr4:85660237C>A c.6500G>T c.(6499-6501)cGc>cTc p.R2167L LUAD 4 85660262 85660262 + Nonsense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr4:85660262C>A c.6475G>T c.(6475-6477)Gga>Tga p.G2159* LUAD 4 85661360 85661360 + Missense_Mutation SNP C C G TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr4:85661360C>G c.6444G>C c.(6442-6444)ttG>ttC p.L2148F LUAD 4 85661484 85661484 + Missense_Mutation SNP T T A TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr4:85661484T>A c.6320A>T c.(6319-6321)cAc>cTc p.H2107L LUAD 4 85662997 85662997 + Missense_Mutation SNP G G A TCGA-49-4506-01A-01D-1265-08 TCGA-49-4506-11A-01D-1265-08 g.chr4:85662997G>A c.6151C>T c.(6151-6153)Cgt>Tgt p.R2051C LUAD 4 85672768 85672768 + Silent SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr4:85672768C>A c.5841G>T c.(5839-5841)gtG>gtT p.V1947V LUAD 4 85676452 85676453 + Frame_Shift_Ins INS - - A TCGA-69-7973-01A-11D-2184-08 TCGA-69-7973-10A-01D-2184-08 g.chr4:85676452_85676453insA c.5525_5526insT c.(5524-5526)ttafs p.L1842fs LUAD 4 85678286 85678286 + Silent SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr4:85678286C>A c.5217G>T c.(5215-5217)ggG>ggT p.G1739G LUAD 4 85686979 85686979 + Missense_Mutation SNP C C A TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr4:85686979C>A c.5172G>T c.(5170-5172)aaG>aaT p.K1724N LUAD 4 85687018 85687018 + Silent SNP T T G TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr4:85687018T>G c.5133A>C c.(5131-5133)ggA>ggC p.G1711G LUAD 4 85687123 85687123 + Silent SNP C C T TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr4:85687123C>T c.5028G>A c.(5026-5028)gaG>gaA p.E1676E LUAD 4 85687162 85687162 + Silent SNP C C T TCGA-55-6712-01A-11D-1855-08 TCGA-55-6712-10A-01D-1855-08 g.chr4:85687162C>T c.4989G>A c.(4987-4989)gtG>gtA p.V1663V LUAD 4 85694065 85694065 + Missense_Mutation SNP G G C TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr4:85694065G>C c.4772C>G c.(4771-4773)tCt>tGt p.S1591C LUAD 4 85701338 85701338 + Missense_Mutation SNP C C A TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr4:85701338C>A c.4288G>T c.(4288-4290)Gca>Tca p.A1430S LUAD 4 85701425 85701425 + Missense_Mutation SNP C C G TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr4:85701425C>G c.4201G>C c.(4201-4203)Gtt>Ctt p.V1401L LUAD 4 85707201 85707201 + Silent SNP C C A TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr4:85707201C>A c.3993G>T c.(3991-3993)gtG>gtT p.V1331V LUAD 4 85707203 85707203 + Missense_Mutation SNP C C A TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr4:85707203C>A c.3991G>T c.(3991-3993)Gtg>Ttg p.V1331L LUAD 4 85715676 85715677 + Frame_Shift_Ins INS - - T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr4:85715676_85715677insT c.3482_3483insA c.(3481-3483)aatfs p.N1161fs LUAD 4 85716095 85716095 + Missense_Mutation SNP G G A TCGA-55-8621-01A-11D-2393-08 TCGA-55-8621-10A-01D-2393-08 g.chr4:85716095G>A c.3205C>T c.(3205-3207)Cct>Tct p.P1069S LUAD 4 85716110 85716110 + Missense_Mutation SNP C C A TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chr4:85716110C>A c.3190G>T c.(3190-3192)Gcc>Tcc p.A1064S LUAD 4 85716111 85716111 + Missense_Mutation SNP C C G TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chr4:85716111C>G c.3189G>C c.(3187-3189)ttG>ttC p.L1063F LUAD 4 85717736 85717736 + Missense_Mutation SNP T T A TCGA-62-A46P-01A-11D-A24D-08 TCGA-62-A46P-10A-01D-A24F-08 g.chr4:85717736T>A c.3105A>T c.(3103-3105)agA>agT p.R1035S LUAD 4 85722828 85722828 + Missense_Mutation SNP G G C TCGA-55-6982-01A-11D-1945-08 TCGA-55-6982-11A-01D-1945-08 g.chr4:85722828G>C c.2797C>G c.(2797-2799)Cag>Gag p.Q933E LUAD 4 85724565 85724565 + Missense_Mutation SNP C C A TCGA-97-7546-01A-11D-2036-08 TCGA-97-7546-10A-01D-2036-08 g.chr4:85724565C>A c.2485G>T c.(2485-2487)Gac>Tac p.D829Y LUAD 4 85724621 85724621 + Splice_Site SNP C C A TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr4:85724621C>A c.e16-1 LUAD 4 85729562 85729562 + Missense_Mutation SNP T T A TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr4:85729562T>A c.2354A>T c.(2353-2355)gAa>gTa p.E785V LUAD 4 85729569 85729569 + Splice_Site SNP G G A TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr4:85729569G>A c.2347C>T c.(2347-2349)Cgt>Tgt p.R783C LUAD 4 85731115 85731115 + Missense_Mutation SNP G G A TCGA-86-7711-01A-11D-2063-08 TCGA-86-7711-10A-01D-2063-08 g.chr4:85731115G>A c.2270C>T c.(2269-2271)tCa>tTa p.S757L LUAD 4 85731139 85731139 + Missense_Mutation SNP T T A TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr4:85731139T>A c.2246A>T c.(2245-2247)gAg>gTg p.E749V LUAD 4 85731316 85731316 + Missense_Mutation SNP C C A TCGA-55-A48Z-01A-12D-A24P-08 TCGA-55-A48Z-10A-01D-A24P-08 g.chr4:85731316C>A c.2069G>T c.(2068-2070)tGc>tTc p.C690F LUAD 4 85731329 85731329 + Missense_Mutation SNP G G A TCGA-55-7574-01A-11D-2036-08 TCGA-55-7574-10A-01D-2036-08 g.chr4:85731329G>A c.2056C>T c.(2056-2058)Cac>Tac p.H686Y LUAD 4 85731345 85731345 + Silent SNP T T C TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr4:85731345T>C c.2040A>G c.(2038-2040)caA>caG p.Q680Q LUAD 4 85731418 85731418 + Missense_Mutation SNP G G C TCGA-49-4487-01A-21D-1855-08 TCGA-49-4487-11A-01D-1855-08 g.chr4:85731418G>C c.1967C>G c.(1966-1968)tCc>tGc p.S656C LUAD 4 85738544 85738544 + Splice_Site SNP C C A TCGA-49-4514-01A-21D-1855-08 TCGA-49-4514-11A-01D-1855-08 g.chr4:85738544C>A c.e13+1 LUAD 4 85748105 85748105 + Missense_Mutation SNP T T C TCGA-91-6836-01A-21D-1855-08 TCGA-91-6836-11A-01D-1855-08 g.chr4:85748105T>C c.986A>G c.(985-987)aAa>aGa p.K329R LUAD 4 85748131 85748131 + Missense_Mutation SNP C C A TCGA-55-7728-01A-11D-2184-08 TCGA-55-7728-10A-01D-2184-08 g.chr4:85748131C>A c.960G>T c.(958-960)ttG>ttT p.L320F LUAD 4 85750167 85750167 + Missense_Mutation SNP G G C TCGA-17-Z048-01A-01W-0746-08 TCGA-17-Z048-11A-01W-0746-08 g.chr4:85750167G>C c.946C>G c.(946-948)Ctc>Gtc p.L316V LUAD 4 85752722 85752722 + Nonsense_Mutation SNP C C A TCGA-17-Z005-01A-01W-0746-08 TCGA-17-Z005-11A-01W-0746-08 g.chr4:85752722C>A c.613G>T c.(613-615)Gag>Tag p.E205* LUAD 4 85771070 85771070 + Missense_Mutation SNP A A G TCGA-17-Z023-01A-01W-0746-08 TCGA-17-Z023-11A-01W-0746-08 g.chr4:85771070A>G c.289T>C c.(289-291)Tca>Cca p.S97P LUAD 4 85771114 85771114 + Missense_Mutation SNP G G A TCGA-17-Z020-01A-01W-0746-08 TCGA-17-Z020-11A-01W-0746-08 g.chr4:85771114G>A c.245C>T c.(244-246)aCa>aTa p.T82I LUAD 4 85771119 85771119 + Silent SNP G G A TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr4:85771119G>A c.240C>T c.(238-240)ttC>ttT p.F80F LUAD 4 85781564 85781564 + Splice_Site SNP C C A TCGA-55-8301-01A-11D-2284-08 TCGA-55-8301-10A-01D-2284-08 g.chr4:85781564C>A c.e4+1 LUAD 4 85781638 85781638 + Missense_Mutation SNP C C T TCGA-50-5944-01A-11D-1753-08 TCGA-50-5944-10A-01D-1753-08 g.chr4:85781638C>T c.107G>A c.(106-108)tGc>tAc p.C36Y LUSC 4 85594031 85594031 + Missense_Mutation SNP C C T TCGA-66-2768-01A-01D-1522-08 TCGA-66-2768-11A-01D-1522-08 g.chr4:85594031C>T c.10571G>A c.(10570-10572)cGa>cAa p.R3524Q LUSC 4 85598396 85598396 + Missense_Mutation SNP T T G TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr4:85598396T>G c.10413A>C c.(10411-10413)gaA>gaC p.E3471D LUSC 4 85598453 85598453 + Silent SNP C C G TCGA-37-4133-01A-01D-1352-08 TCGA-37-4133-10A-01D-1352-08 g.chr4:85598453C>G c.10356G>C c.(10354-10356)gtG>gtC p.V3452V LUSC 4 85611771 85611771 + Missense_Mutation SNP C C A TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr4:85611771C>A c.9251G>T c.(9250-9252)tGt>tTt p.C3084F LUSC 4 85638087 85638087 + Missense_Mutation SNP C C A TCGA-22-5492-01A-01D-1632-08 TCGA-22-5492-11A-01D-1632-08 g.chr4:85638087C>A c.7837G>T c.(7837-7839)Gat>Tat p.D2613Y LUSC 4 85638146 85638146 + Missense_Mutation SNP C C G TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr4:85638146C>G c.7778G>C c.(7777-7779)aGa>aCa p.R2593T LUSC 4 85664938 85664938 + Silent SNP C C T TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr4:85664938C>T c.5988G>A c.(5986-5988)agG>agA p.R1996R LUSC 4 85687027 85687027 + Silent SNP G G A TCGA-39-5022-01A-21D-1817-08 TCGA-39-5022-11A-01D-1817-08 g.chr4:85687027G>A c.5124C>T c.(5122-5124)ctC>ctT p.L1708L LUSC 4 85717868 85717868 + Missense_Mutation SNP A A C TCGA-22-4591-01A-01D-1267-08 TCGA-22-4591-11A-01D-1267-08 g.chr4:85717868A>C c.2973T>G c.(2971-2973)gaT>gaG p.D991E LUSC 4 85722993 85722993 + Missense_Mutation SNP C C A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr4:85722993C>A c.2632G>T c.(2632-2634)Gtg>Ttg p.V878L LUSC 4 85750243 85750243 + Silent SNP G G A TCGA-21-5782-01A-01D-1632-08 TCGA-21-5782-10A-01D-1632-08 g.chr4:85750243G>A c.870C>T c.(868-870)ctC>ctT p.L290L LUSC 4 85750301 85750301 + Nonsense_Mutation SNP G G C TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr4:85750301G>C c.812C>G c.(811-813)tCa>tGa p.S271* LUSC 4 85771053 85771053 + Splice_Site SNP A A G TCGA-39-5036-01A-01D-1441-08 TCGA-39-5036-11A-01D-1441-08 g.chr4:85771053A>G c.e5+1 OV 4 85598394 85598394 + Missense_Mutation SNP C C A TCGA-29-1707-01A-01W-0633-09 TCGA-29-1707-10A-01W-0633-09 g.chr4:85598394C>A c.10415G>T c.(10414-10416)aGa>aTa p.R3472I OV 4 85696070 85696070 + Missense_Mutation SNP G G C TCGA-36-2547-01A-01D-1526-09 TCGA-36-2547-10A-01D-1526-09 g.chr4:85696070G>C c.4657C>G c.(4657-4659)Ctt>Gtt p.L1553V OV 4 85717847 85717847 + Missense_Mutation SNP T T A TCGA-25-1634-01A-01W-0615-10 TCGA-25-1634-10A-01W-0616-10 g.chr4:85717847T>A c.2994A>T c.(2992-2994)gaA>gaT p.E998D OV 4 85742327 85742327 + Missense_Mutation SNP T T C TCGA-29-1701-01A-01W-0633-09 TCGA-29-1701-10A-01W-0633-09 g.chr4:85742327T>C c.1501A>G c.(1501-1503)Agg>Ggg p.R501G OV 4 85742596 85742596 + Missense_Mutation SNP T T G TCGA-61-2009-01A-01W-0722-08 TCGA-61-2009-10A-01W-0722-08 g.chr4:85742596T>G c.1232A>C c.(1231-1233)tAc>tCc p.Y411S PAAD 4 85600086 85600086 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:85600086C>T c.10133G>A c.(10132-10134)aGc>aAc p.S3378N PAAD 4 85605150 85605150 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:85605150G>A c.9672C>T c.(9670-9672)aaC>aaT p.N3224N PAAD 4 85617954 85617954 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:85617954C>T c.8619G>A c.(8617-8619)aaG>aaA p.K2873K PAAD 4 85678099 85678099 + Frame_Shift_Del DEL G G - TCGA-LB-A8F3-01A-11D-A36O-08 TCGA-LB-A8F3-10A-01D-A367-08 g.chr4:85678099delG c.5404delC c.(5404-5406)cggfs p.R1802fs PAAD 4 85708746 85708746 + Missense_Mutation SNP G G A TCGA-FB-A78T-01A-12D-A32N-08 TCGA-FB-A78T-10A-01D-A32N-08 g.chr4:85708746G>A c.3790C>T c.(3790-3792)Cgc>Tgc p.R1264C PAAD 4 85715716 85715716 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:85715716C>T c.3443G>A c.(3442-3444)cGa>cAa p.R1148Q PAAD 4 85715780 85715780 + Missense_Mutation SNP G G A TCGA-HV-A7OL-01A-11D-A33T-08 TCGA-HV-A7OL-10A-01D-A33W-08 g.chr4:85715780G>A c.3379C>T c.(3379-3381)Cgc>Tgc p.R1127C PAAD 4 85741302 85741302 + Frame_Shift_Del DEL T T - TCGA-2L-AAQE-01A-11D-A397-08 TCGA-2L-AAQE-11A-11D-A39A-08 g.chr4:85741302delT c.1629delA c.(1627-1629)aaafs p.K543fs PAAD 4 85741302 85741302 + Frame_Shift_Del DEL T T - TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-10A-01D-A367-08 g.chr4:85741302delT c.1629delA c.(1627-1629)aaafs p.K543fs PAAD 4 85750255 85750255 + Silent SNP A A C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:85750255A>C c.858T>G c.(856-858)ctT>ctG p.L286L PAAD 4 85750273 85750273 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:85750273G>A c.840C>T c.(838-840)gtC>gtT p.V280V PAAD 4 85758135 85758135 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:85758135T>G c.523A>C c.(523-525)Aat>Cat p.N175H PCPG 4 85636525 85636525 + Silent SNP C C A TCGA-WB-A80M-01A-11D-A35I-08 TCGA-WB-A80M-10A-01D-A35G-08 g.chr4:85636525C>A c.7887G>T c.(7885-7887)gtG>gtT p.V2629V PRAD 4 85603587 85603587 + Missense_Mutation SNP G G A TCGA-EJ-5518-01A-01D-1576-08 TCGA-EJ-5518-10A-01D-1577-08 g.chr4:85603587G>A c.9763C>T c.(9763-9765)Cca>Tca p.P3255S PRAD 4 85609385 85609385 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:85609385C>T c.9397G>A c.(9397-9399)Gcc>Acc p.A3133T PRAD 4 85611673 85611673 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:85611673C>T c.9349G>A c.(9349-9351)Gtc>Atc p.V3117I PRAD 4 85626574 85626574 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:85626574G>A c.8308C>T c.(8308-8310)Cgg>Tgg p.R2770W PRAD 4 85656271 85656271 + Missense_Mutation SNP C C A TCGA-YL-A8SJ-01B-11D-A377-08 TCGA-YL-A8SJ-10A-01D-A37A-08 g.chr4:85656271C>A c.6918G>T c.(6916-6918)gaG>gaT p.E2306D PRAD 4 85699758 85699758 + Silent SNP G G A TCGA-KK-A6E4-01A-11D-A30E-08 TCGA-KK-A6E4-11A-11D-A30H-08 g.chr4:85699758G>A c.4416C>T c.(4414-4416)atC>atT p.I1472I PRAD 4 85719250 85719250 + Missense_Mutation SNP C C T TCGA-EJ-5524-01A-01D-1576-08 TCGA-EJ-5524-10A-01D-1577-08 g.chr4:85719250C>T c.2834G>A c.(2833-2835)cGt>cAt p.R945H PRAD 4 85731295 85731295 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:85731295C>T c.2090G>A c.(2089-2091)cGc>cAc p.R697H PRAD 4 85738568 85738568 + Nonsense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:85738568G>A c.1864C>T c.(1864-1866)Cag>Tag p.Q622* PRAD 4 85758212 85758212 + Missense_Mutation SNP A A G TCGA-EJ-A46D-01A-21D-A257-08 TCGA-EJ-A46D-10A-01D-A25A-08 g.chr4:85758212A>G c.446T>C c.(445-447)gTg>gCg p.V149A READ 4 85626556 85626556 + Missense_Mutation SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr4:85626556C>T c.8326G>A c.(8326-8328)Gat>Aat p.D2776N READ 4 85658388 85658388 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85658388C>T c.6706G>A c.(6706-6708)Gca>Aca p.A2236T READ 4 85661380 85661380 + Missense_Mutation SNP T T A TCGA-AG-A015-01A-01W-A005-10 TCGA-AG-A015-10A-01W-A005-10 g.chr4:85661380T>A c.6424A>T c.(6424-6426)Agc>Tgc p.S2142C READ 4 85661548 85661548 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85661548A>C c.6256T>G c.(6256-6258)Ttg>Gtg p.L2086V READ 4 85678299 85678299 + Missense_Mutation SNP C C T TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr4:85678299C>T c.5204G>A c.(5203-5205)aGa>aAa p.R1735K READ 4 85696122 85696122 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85696122C>A c.4605G>T c.(4603-4605)aaG>aaT p.K1535N READ 4 85708719 85708719 + Missense_Mutation SNP C C G TCGA-AG-3600-01A-01W-0833-10 TCGA-AG-3600-10A-01W-0833-10 g.chr4:85708719C>G c.3817G>C c.(3817-3819)Gaa>Caa p.E1273Q READ 4 85741252 85741252 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:85741252G>T c.1679C>A c.(1678-1680)tCa>tAa p.S560* READ 4 85742596 85742596 + Missense_Mutation SNP T T A TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr4:85742596T>A c.1232A>T c.(1231-1233)tAc>tTc p.Y411F SARC 4 85625498 85625498 + Missense_Mutation SNP C C G TCGA-QQ-A5V9-01A-11D-A32I-09 TCGA-QQ-A5V9-11A-31D-A32I-09 g.chr4:85625498C>G c.8435G>C c.(8434-8436)aGg>aCg p.R2812T SARC 4 85674951 85674951 + Frame_Shift_Del DEL G G - TCGA-DX-AB2L-01A-32D-A417-09 TCGA-DX-AB2L-10A-01D-A41A-09 g.chr4:85674951delG c.5638delC c.(5638-5640)cacfs p.H1880fs SARC 4 85701377 85701377 + Silent SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr4:85701377G>A c.4249C>T c.(4249-4251)Ctg>Ttg p.L1417L SARC 4 85731189 85731189 + Silent SNP G G A TCGA-QQ-A5VB-01A-11D-A36J-09 TCGA-QQ-A5VB-11B-11D-A36M-09 g.chr4:85731189G>A c.2196C>T c.(2194-2196)agC>agT p.S732S SARC 4 85742335 85742335 + Missense_Mutation SNP T T C TCGA-PC-A5DN-01A-12D-A27P-09 TCGA-PC-A5DN-10A-01D-A27P-09 g.chr4:85742335T>C c.1493A>G c.(1492-1494)gAc>gGc p.D498G SARC 4 85758160 85758160 + Silent SNP C C T TCGA-WK-A8XT-01A-11D-A37C-09 TCGA-WK-A8XT-10A-01D-A37F-09 g.chr4:85758160C>T c.498G>A c.(496-498)gtG>gtA p.V166V SKCM 4 85594125 85594125 + Missense_Mutation SNP C C T TCGA-EE-A2GB-06A-11D-A197-08 TCGA-EE-A2GB-10A-01D-A199-08 g.chr4:85594125C>T c.10477G>A c.(10477-10479)Gaa>Aaa p.E3493K SKCM 4 85599427 85599427 + Nonsense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr4:85599427G>A c.10153C>T c.(10153-10155)Cga>Tga p.R3385* SKCM 4 85611810 85611810 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr4:85611810G>A c.9212C>T c.(9211-9213)aCt>aTt p.T3071I SKCM 4 85612913 85612913 + Silent SNP G G A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr4:85612913G>A c.9075C>T c.(9073-9075)atC>atT p.I3025I SKCM 4 85617207 85617207 + Silent SNP T T C TCGA-DA-A1I8-06A-11D-A197-08 TCGA-DA-A1I8-10A-01D-A199-08 g.chr4:85617207T>C c.8817A>G c.(8815-8817)caA>caG p.Q2939Q SKCM 4 85617227 85617227 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr4:85617227G>A c.8797C>T c.(8797-8799)Cat>Tat p.H2933Y SKCM 4 85617242 85617242 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr4:85617242C>T c.8782G>A c.(8782-8784)Gta>Ata p.V2928I SKCM 4 85623601 85623601 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr4:85623601G>A c.8501C>T c.(8500-8502)tCa>tTa p.S2834L SKCM 4 85639647 85639647 + Missense_Mutation SNP T T C TCGA-FW-A3I3-06A-11D-A21A-08 TCGA-FW-A3I3-10A-01D-A21A-08 g.chr4:85639647T>C c.7682A>G c.(7681-7683)cAt>cGt p.H2561R SKCM 4 85642710 85642710 + Missense_Mutation SNP G G A TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr4:85642710G>A c.7457C>T c.(7456-7458)cCt>cTt p.P2486L SKCM 4 85642712 85642712 + Silent SNP A A T TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr4:85642712A>T c.7455T>A c.(7453-7455)ccT>ccA p.P2485P SKCM 4 85645656 85645656 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr4:85645656G>A c.7364C>T c.(7363-7365)gCc>gTc p.A2455V SKCM 4 85654607 85654607 + Silent SNP C C T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr4:85654607C>T c.7149G>A c.(7147-7149)aaG>aaA p.K2383K SKCM 4 85657478 85657478 + Missense_Mutation SNP G G A TCGA-ER-A19E-06A-11D-A197-08 TCGA-ER-A19E-10A-01D-A199-08 g.chr4:85657478G>A c.6760C>T c.(6760-6762)Cat>Tat p.H2254Y SKCM 4 85658343 85658343 + Missense_Mutation SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr4:85658343G>A c.6751C>T c.(6751-6753)Cat>Tat p.H2251Y SKCM 4 85660250 85660250 + Missense_Mutation SNP C C T TCGA-EE-A3JH-06A-11D-A21A-08 TCGA-EE-A3JH-10A-01D-A21A-08 g.chr4:85660250C>T c.6487G>A c.(6487-6489)Gaa>Aaa p.E2163K SKCM 4 85660251 85660251 + Silent SNP C C T TCGA-EE-A3JH-06A-11D-A21A-08 TCGA-EE-A3JH-10A-01D-A21A-08 g.chr4:85660251C>T c.6486G>A c.(6484-6486)ctG>ctA p.L2162L SKCM 4 85663060 85663060 + Silent SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr4:85663060G>A c.6088C>T c.(6088-6090)Ctg>Ttg p.L2030L SKCM 4 85664947 85664947 + Silent SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr4:85664947G>A c.5979C>T c.(5977-5979)tcC>tcT p.S1993S SKCM 4 85672726 85672726 + Silent SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr4:85672726G>A c.5883C>T c.(5881-5883)ttC>ttT p.F1961F SKCM 4 85674877 85674877 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr4:85674877G>A c.5712C>T c.(5710-5712)ccC>ccT p.P1904P SKCM 4 85674967 85674967 + Silent SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr4:85674967G>A c.5622C>T c.(5620-5622)ttC>ttT p.F1874F SKCM 4 85676482 85676482 + Silent SNP G G A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr4:85676482G>A c.5496C>T c.(5494-5496)atC>atT p.I1832I SKCM 4 85676491 85676491 + Silent SNP G G A TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr4:85676491G>A c.5487C>T c.(5485-5487)gtC>gtT p.V1829V SKCM 4 85676507 85676507 + Missense_Mutation SNP G G A TCGA-EE-A29G-06A-12D-A196-08 TCGA-EE-A29G-10A-01D-A198-08 g.chr4:85676507G>A c.5471C>T c.(5470-5472)tCc>tTc p.S1824F SKCM 4 85694006 85694006 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr4:85694006C>T c.4831G>A c.(4831-4833)Gaa>Aaa p.E1611K SKCM 4 85694049 85694049 + Silent SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr4:85694049G>A c.4788C>T c.(4786-4788)acC>acT p.T1596T SKCM 4 85695995 85695995 + Missense_Mutation SNP G G A TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr4:85695995G>A c.4732C>T c.(4732-4734)Cct>Tct p.P1578S SKCM 4 85696067 85696067 + Nonsense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr4:85696067G>A c.4660C>T c.(4660-4662)Cga>Tga p.R1554* SKCM 4 85696089 85696089 + Silent SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr4:85696089G>A c.4638C>T c.(4636-4638)atC>atT p.I1546I SKCM 4 85701308 85701308 + Missense_Mutation SNP T T A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr4:85701308T>A c.4318A>T c.(4318-4320)Agt>Tgt p.S1440C SKCM 4 85707256 85707256 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr4:85707256G>A c.3938C>T c.(3937-3939)cCt>cTt p.P1313L SKCM 4 85707259 85707259 + Missense_Mutation SNP G G A TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr4:85707259G>A c.3935C>T c.(3934-3936)tCc>tTc p.S1312F SKCM 4 85710914 85710914 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr4:85710914G>A c.3634C>T c.(3634-3636)Ctt>Ttt p.L1212F SKCM 4 85711007 85711007 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr4:85711007G>A c.3541C>T c.(3541-3543)Cgc>Tgc p.R1181C SKCM 4 85711043 85711043 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr4:85711043C>T c.3505G>A c.(3505-3507)Gag>Aag p.E1169K SKCM 4 85715819 85715819 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr4:85715819G>A c.3340C>T c.(3340-3342)Cct>Tct p.P1114S SKCM 4 85715845 85715845 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr4:85715845C>G c.3314G>C c.(3313-3315)tGg>tCg p.W1105S SKCM 4 85715876 85715876 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr4:85715876G>A c.3283C>T c.(3283-3285)Cct>Tct p.P1095S SKCM 4 85724537 85724537 + Missense_Mutation SNP G G C TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr4:85724537G>C c.2513C>G c.(2512-2514)tCt>tGt p.S838C SKCM 4 85724567 85724567 + Missense_Mutation SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr4:85724567G>A c.2483C>T c.(2482-2484)gCc>gTc p.A828V SKCM 4 85729554 85729554 + Missense_Mutation SNP G G A TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr4:85729554G>A c.2362C>T c.(2362-2364)Cct>Tct p.P788S SKCM 4 85731300 85731300 + Silent SNP T T G TCGA-EE-A2MG-06A-11D-A197-08 TCGA-EE-A2MG-10A-01D-A199-08 g.chr4:85731300T>G c.2085A>C c.(2083-2085)gcA>gcC p.A695A SKCM 4 85731436 85731436 + Missense_Mutation SNP C C A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr4:85731436C>A c.1949G>T c.(1948-1950)gGa>gTa p.G650V SKCM 4 85731442 85731442 + Missense_Mutation SNP A A G TCGA-EE-A29G-06A-12D-A196-08 TCGA-EE-A29G-10A-01D-A198-08 g.chr4:85731442A>G c.1943T>C c.(1942-1944)gTt>gCt p.V648A SKCM 4 85731467 85731467 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr4:85731467G>A c.1918C>T c.(1918-1920)Cgt>Tgt p.R640C SKCM 4 85731479 85731479 + Nonsense_Mutation SNP G G A TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr4:85731479G>A c.1906C>T c.(1906-1908)Cga>Tga p.R636* SKCM 4 85742315 85742315 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr4:85742315G>A c.1513C>T c.(1513-1515)Ctt>Ttt p.L505F SKCM 4 85742679 85742679 + Silent SNP G G A TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr4:85742679G>A c.1149C>T c.(1147-1149)gcC>gcT p.A383A SKCM 4 85781645 85781645 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr4:85781645C>T c.100G>A c.(100-102)Gag>Aag p.E34K

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 4 85752692 85752692 single base substitution G A exon_variant BLCA-CN 4 85752692 85752692 single base substitution G A missense_variant L215F 643C>T BLCA-US 4 85598394 85598394 single base substitution C G exon_variant BLCA-US 4 85598394 85598394 single base substitution C G missense_variant R3455T 10364G>C BLCA-US 4 85598394 85598394 single base substitution C G missense_variant R3472T 10415G>C BLCA-US 4 85611708 85611709 deletion of <=200bp CA - downstream_gene_variant BLCA-US 4 85611708 85611709 deletion of <=200bp CA - frameshift_variant W3088 BLCA-US 4 85611708 85611709 deletion of <=200bp CA - frameshift_variant W3105 BLCA-US 4 85617303 85617303 single base substitution T C synonymous_variant L2890L 8670A>G BLCA-US 4 85617303 85617303 single base substitution T C synonymous_variant L2907L 8721A>G BLCA-US 4 85617303 85617303 single base substitution T C synonymous_variant L510L 1530A>G BLCA-US 4 85634326 85634326 single base substitution C A synonymous_variant T2659T 7977G>T BLCA-US 4 85634326 85634326 single base substitution C A synonymous_variant T2676T 8028G>T BLCA-US 4 85634326 85634326 single base substitution C A synonymous_variant T279T 837G>T BLCA-US 4 85634393 85634393 single base substitution C T splice_acceptor_variant BLCA-US 4 85638082 85638082 single base substitution G C missense_variant I217M 651C>G BLCA-US 4 85638082 85638082 single base substitution G C missense_variant I2597M 7791C>G BLCA-US 4 85638082 85638082 single base substitution G C missense_variant I2614M 7842C>G BLCA-US 4 85662946 85662946 single base substitution G C missense_variant L2068V 6202C>G BLCA-US 4 85662946 85662946 single base substitution G C upstream_gene_variant BLCA-US 4 85672647 85672647 single base substitution G C exon_variant BLCA-US 4 85672647 85672647 single base substitution G C missense_variant L1988V 5962C>G BLCA-US 4 85672677 85672677 single base substitution G C exon_variant BLCA-US 4 85672677 85672677 single base substitution G C missense_variant P1978A 5932C>G BLCA-US 4 85672802 85672802 single base substitution C G exon_variant BLCA-US 4 85672802 85672802 single base substitution C G missense_variant G1936A 5807G>C BLCA-US 4 85678145 85678145 single base substitution A T missense_variant S1786R 5358T>A BLCA-US 4 85678145 85678145 single base substitution A T upstream_gene_variant BLCA-US 4 85687004 85687004 single base substitution T A missense_variant Q1716L 5147A>T BLCA-US 4 85731400 85731400 single base substitution T C exon_variant BLCA-US 4 85731400 85731400 single base substitution T C missense_variant E662G 1985A>G BLCA-US 4 85731400 85731400 single base substitution T C upstream_gene_variant BLCA-US 4 85741262 85741262 single base substitution G A exon_variant BLCA-US 4 85741262 85741262 single base substitution G A missense_variant L557F 1669C>T BLCA-US 4 85742700 85742700 single base substitution G A exon_variant BLCA-US 4 85742700 85742700 single base substitution G A synonymous_variant H376H 1128C>T BLCA-US 4 85781566 85781566 single base substitution C T downstream_gene_variant BLCA-US 4 85781566 85781566 single base substitution C T missense_variant R60K 179G>A BLCA-US 4 85781566 85781566 single base substitution C T splice_region_variant BOCA-FR 4 85644421 85644421 single base substitution T C intron_variant BOCA-FR 4 85686872 85686872 single base substitution T C intron_variant BOCA-FR 4 85802309 85802309 single base substitution G A intron_variant BOCA-FR 4 85812951 85812951 single base substitution C T intron_variant BRCA-EU 4 85586418 85586418 single base substitution C A downstream_gene_variant BRCA-EU 4 85586468 85586468 single base substitution C T downstream_gene_variant BRCA-EU 4 85586478 85586478 single base substitution T C downstream_gene_variant BRCA-EU 4 85586481 85586481 single base substitution C T downstream_gene_variant BRCA-EU 4 85587581 85587581 single base substitution G C downstream_gene_variant BRCA-EU 4 85588070 85588070 single base substitution C G downstream_gene_variant BRCA-EU 4 85588900 85588900 single base substitution C A downstream_gene_variant BRCA-EU 4 85588921 85588921 single base substitution G A downstream_gene_variant BRCA-EU 4 85589577 85589577 deletion of <=200bp A - downstream_gene_variant BRCA-EU 4 85590139 85590139 single base substitution C G downstream_gene_variant BRCA-EU 4 85590216 85590216 single base substitution G C downstream_gene_variant BRCA-EU 4 85590386 85590386 single base substitution T C downstream_gene_variant BRCA-EU 4 85594940 85594940 single base substitution A T intron_variant BRCA-EU 4 85596580 85596588 deletion of <=200bp CCTGTTTTG - intron_variant BRCA-EU 4 85597373 85597373 deletion of <=200bp A - intron_variant BRCA-EU 4 85598094 85598094 single base substitution G A intron_variant BRCA-EU 4 85599017 85599017 single base substitution G C intron_variant BRCA-EU 4 85601568 85601568 single base substitution G A intron_variant BRCA-EU 4 85605439 85605439 deletion of <=200bp A - intron_variant BRCA-EU 4 85605439 85605439 deletion of <=200bp A - upstream_gene_variant BRCA-EU 4 85605795 85605795 single base substitution C G intron_variant BRCA-EU 4 85605795 85605795 single base substitution C G upstream_gene_variant BRCA-EU 4 85606364 85606364 single base substitution C T intron_variant BRCA-EU 4 85606364 85606364 single base substitution C T upstream_gene_variant BRCA-EU 4 85606535 85606535 single base substitution C G intron_variant BRCA-EU 4 85606535 85606535 single base substitution C G upstream_gene_variant BRCA-EU 4 85607263 85607263 single base substitution C G intron_variant BRCA-EU 4 85607263 85607263 single base substitution C G upstream_gene_variant BRCA-EU 4 85609044 85609044 single base substitution C T downstream_gene_variant BRCA-EU 4 85609044 85609044 single base substitution C T intron_variant BRCA-EU 4 85609044 85609044 single base substitution C T upstream_gene_variant BRCA-EU 4 85609561 85609561 single base substitution C T downstream_gene_variant BRCA-EU 4 85609561 85609561 single base substitution C T intron_variant BRCA-EU 4 85609864 85609864 single base substitution T A downstream_gene_variant BRCA-EU 4 85609864 85609864 single base substitution T A intron_variant BRCA-EU 4 85613093 85613093 deletion of <=200bp T - intron_variant BRCA-EU 4 85614947 85614947 single base substitution G C intron_variant BRCA-EU 4 85615243 85615243 single base substitution G C intron_variant BRCA-EU 4 85615252 85615252 single base substitution A C intron_variant BRCA-EU 4 85615527 85615527 single base substitution C G intron_variant BRCA-EU 4 85617447 85617447 single base substitution A C intron_variant BRCA-EU 4 85618136 85618136 single base substitution C G intron_variant BRCA-EU 4 85618226 85618226 single base substitution G C intron_variant BRCA-EU 4 85619339 85619339 single base substitution G C intron_variant BRCA-EU 4 85620932 85620932 single base substitution G T intron_variant BRCA-EU 4 85620948 85620948 single base substitution C T intron_variant BRCA-EU 4 85622520 85622520 single base substitution G A intron_variant BRCA-EU 4 85624008 85624008 single base substitution C T intron_variant BRCA-EU 4 85625416 85625416 single base substitution G A intron_variant BRCA-EU 4 85626545 85626545 single base substitution A G splice_donor_variant BRCA-EU 4 85626639 85626639 single base substitution G A missense_variant T2731M 8192C>T BRCA-EU 4 85626639 85626639 single base substitution G A missense_variant T2748M 8243C>T BRCA-EU 4 85626639 85626639 single base substitution G A missense_variant T351M 1052C>T BRCA-EU 4 85627360 85627360 single base substitution C T intron_variant BRCA-EU 4 85629684 85629684 single base substitution T A intron_variant BRCA-EU 4 85630576 85630576 single base substitution T G intron_variant BRCA-EU 4 85632536 85632536 single base substitution G C intron_variant BRCA-EU 4 85634199 85634199 single base substitution T A intron_variant BRCA-EU 4 85635424 85635424 single base substitution G A intron_variant BRCA-EU 4 85637795 85637795 single base substitution C G intron_variant BRCA-EU 4 85640103 85640103 single base substitution T C intron_variant BRCA-EU 4 85640486 85640486 single base substitution T A intron_variant BRCA-EU 4 85641265 85641265 single base substitution T C intron_variant BRCA-EU 4 85642877 85642877 single base substitution C A intron_variant BRCA-EU 4 85645011 85645011 single base substitution C T intron_variant BRCA-EU 4 85647835 85647835 single base substitution A G intron_variant BRCA-EU 4 85648303 85648303 single base substitution G C intron_variant BRCA-EU 4 85648609 85648609 single base substitution C G intron_variant BRCA-EU 4 85649297 85649297 single base substitution G A intron_variant BRCA-EU 4 85651102 85651102 single base substitution G A intron_variant BRCA-EU 4 85652122 85652122 single base substitution C G downstream_gene_variant BRCA-EU 4 85652122 85652122 single base substitution C G intron_variant BRCA-EU 4 85653892 85653892 single base substitution T C downstream_gene_variant BRCA-EU 4 85653892 85653892 single base substitution T C intron_variant BRCA-EU 4 85654281 85654281 single base substitution T G downstream_gene_variant BRCA-EU 4 85654281 85654281 single base substitution T G intron_variant BRCA-EU 4 85654667 85654667 single base substitution G T downstream_gene_variant BRCA-EU 4 85654667 85654667 single base substitution G T synonymous_variant G2363G 7089C>A BRCA-EU 4 85654667 85654667 single base substitution G T upstream_gene_variant BRCA-EU 4 85655359 85655359 single base substitution G A downstream_gene_variant BRCA-EU 4 85655359 85655359 single base substitution G A intron_variant BRCA-EU 4 85655359 85655359 single base substitution G A upstream_gene_variant BRCA-EU 4 85657888 85657888 single base substitution C G intron_variant BRCA-EU 4 85657888 85657888 single base substitution C G upstream_gene_variant BRCA-EU 4 85658625 85658625 single base substitution A G intron_variant BRCA-EU 4 85658625 85658625 single base substitution A G upstream_gene_variant BRCA-EU 4 85658816 85658816 single base substitution A C intron_variant BRCA-EU 4 85658816 85658816 single base substitution A C upstream_gene_variant BRCA-EU 4 85658837 85658837 single base substitution A C intron_variant BRCA-EU 4 85658837 85658837 single base substitution A C upstream_gene_variant BRCA-EU 4 85659116 85659116 single base substitution G A intron_variant BRCA-EU 4 85659116 85659116 single base substitution G A upstream_gene_variant BRCA-EU 4 85660312 85660312 single base substitution G A exon_variant BRCA-EU 4 85660312 85660312 single base substitution G A intron_variant BRCA-EU 4 85661783 85661783 deletion of <=200bp A - intron_variant BRCA-EU 4 85661783 85661783 deletion of <=200bp A - upstream_gene_variant BRCA-EU 4 85661956 85661956 deletion of <=200bp T - intron_variant BRCA-EU 4 85661956 85661956 deletion of <=200bp T - upstream_gene_variant BRCA-EU 4 85668547 85668547 single base substitution C T downstream_gene_variant BRCA-EU 4 85668547 85668547 single base substitution C T intron_variant BRCA-EU 4 85669249 85669249 single base substitution C T downstream_gene_variant BRCA-EU 4 85669249 85669249 single base substitution C T intron_variant BRCA-EU 4 85669851 85669851 insertion of <=200bp - T downstream_gene_variant BRCA-EU 4 85669851 85669851 insertion of <=200bp - T intron_variant BRCA-EU 4 85670147 85670147 single base substitution C T downstream_gene_variant BRCA-EU 4 85670147 85670147 single base substitution C T intron_variant BRCA-EU 4 85670341 85670341 single base substitution C A downstream_gene_variant BRCA-EU 4 85670341 85670341 single base substitution C A intron_variant BRCA-EU 4 85670391 85670391 single base substitution T G downstream_gene_variant BRCA-EU 4 85670391 85670391 single base substitution T G intron_variant BRCA-EU 4 85670457 85670457 single base substitution C T downstream_gene_variant BRCA-EU 4 85670457 85670457 single base substitution C T intron_variant BRCA-EU 4 85671004 85671004 deletion of <=200bp C - downstream_gene_variant BRCA-EU 4 85671004 85671004 deletion of <=200bp C - intron_variant BRCA-EU 4 85671735 85671735 single base substitution C T downstream_gene_variant BRCA-EU 4 85671735 85671735 single base substitution C T intron_variant BRCA-EU 4 85671910 85671910 single base substitution G A downstream_gene_variant BRCA-EU 4 85671910 85671910 single base substitution G A intron_variant BRCA-EU 4 85672790 85672790 single base substitution C G exon_variant BRCA-EU 4 85672790 85672790 single base substitution C G missense_variant S1940T 5819G>C BRCA-EU 4 85674025 85674025 single base substitution A T intron_variant BRCA-EU 4 85674040 85674040 single base substitution C T intron_variant BRCA-EU 4 85676167 85676167 single base substitution A G intron_variant BRCA-EU 4 85677559 85677559 single base substitution G A intron_variant BRCA-EU 4 85677559 85677559 single base substitution G A upstream_gene_variant BRCA-EU 4 85678988 85678988 single base substitution G C intron_variant BRCA-EU 4 85678988 85678988 single base substitution G C upstream_gene_variant BRCA-EU 4 85682703 85682703 single base substitution C G intron_variant BRCA-EU 4 85683747 85683747 single base substitution C G intron_variant BRCA-EU 4 85684603 85684603 single base substitution T A intron_variant BRCA-EU 4 85686835 85686835 single base substitution C G intron_variant BRCA-EU 4 85692197 85692197 single base substitution C T intron_variant BRCA-EU 4 85694366 85694366 single base substitution C A intron_variant BRCA-EU 4 85696946 85696946 single base substitution G A intron_variant BRCA-EU 4 85697991 85697991 single base substitution A C intron_variant BRCA-EU 4 85699552 85699552 single base substitution T C intron_variant BRCA-EU 4 85701492 85701492 single base substitution C T intron_variant BRCA-EU 4 85704444 85704444 single base substitution G C intron_variant BRCA-EU 4 85705246 85705246 single base substitution G A intron_variant BRCA-EU 4 85705256 85705256 single base substitution C T intron_variant BRCA-EU 4 85706455 85706455 single base substitution G T intron_variant BRCA-EU 4 85706541 85706541 single base substitution C G intron_variant BRCA-EU 4 85706759 85706759 single base substitution C G intron_variant BRCA-EU 4 85708996 85708996 single base substitution G C intron_variant BRCA-EU 4 85710074 85710074 single base substitution G A intron_variant BRCA-EU 4 85711167 85711167 single base substitution G T intron_variant BRCA-EU 4 85713863 85713863 single base substitution A T intron_variant BRCA-EU 4 85715270 85715270 single base substitution A G intron_variant BRCA-EU 4 85717658 85717658 single base substitution C T intron_variant BRCA-EU 4 85718011 85718011 deletion of <=200bp T - downstream_gene_variant BRCA-EU 4 85718011 85718011 deletion of <=200bp T - intron_variant BRCA-EU 4 85718078 85718078 single base substitution C T downstream_gene_variant BRCA-EU 4 85718078 85718078 single base substitution C T intron_variant BRCA-EU 4 85718757 85718757 single base substitution G A downstream_gene_variant BRCA-EU 4 85718757 85718757 single base substitution G A intron_variant BRCA-EU 4 85719251 85719251 single base substitution G A downstream_gene_variant BRCA-EU 4 85719251 85719251 single base substitution G A missense_variant R945C 2833C>T BRCA-EU 4 85720137 85720137 single base substitution G A downstream_gene_variant BRCA-EU 4 85720137 85720137 single base substitution G A intron_variant BRCA-EU 4 85720204 85720204 single base substitution C T downstream_gene_variant BRCA-EU 4 85720204 85720204 single base substitution C T intron_variant BRCA-EU 4 85720496 85720496 single base substitution T A downstream_gene_variant BRCA-EU 4 85720496 85720496 single base substitution T A intron_variant BRCA-EU 4 85720916 85720916 single base substitution C T downstream_gene_variant BRCA-EU 4 85720916 85720916 single base substitution C T intron_variant BRCA-EU 4 85721146 85721146 single base substitution C G downstream_gene_variant BRCA-EU 4 85721146 85721146 single base substitution C G intron_variant BRCA-EU 4 85722993 85722993 single base substitution C T exon_variant BRCA-EU 4 85722993 85722993 single base substitution C T missense_variant V878M 2632G>A BRCA-EU 4 85723414 85723414 single base substitution T A intron_variant BRCA-EU 4 85724018 85724018 single base substitution A T intron_variant BRCA-EU 4 85724149 85724149 single base substitution C T intron_variant BRCA-EU 4 85724183 85724185 deletion of <=200bp AGG - intron_variant BRCA-EU 4 85724310 85724310 deletion of <=200bp T - intron_variant BRCA-EU 4 85724978 85724978 single base substitution G C intron_variant BRCA-EU 4 85725231 85725231 single base substitution T G downstream_gene_variant BRCA-EU 4 85725231 85725231 single base substitution T G exon_variant BRCA-EU 4 85725231 85725231 single base substitution T G intron_variant BRCA-EU 4 85725457 85725457 single base substitution C T downstream_gene_variant BRCA-EU 4 85725457 85725457 single base substitution C T intron_variant BRCA-EU 4 85725457 85725457 single base substitution C T upstream_gene_variant BRCA-EU 4 85727447 85727447 single base substitution C T downstream_gene_variant BRCA-EU 4 85727447 85727447 single base substitution C T intron_variant BRCA-EU 4 85727447 85727447 single base substitution C T upstream_gene_variant BRCA-EU 4 85729850 85729850 single base substitution C A downstream_gene_variant BRCA-EU 4 85729850 85729850 single base substitution C A intron_variant BRCA-EU 4 85729850 85729850 single base substitution C A upstream_gene_variant BRCA-EU 4 85729982 85729982 single base substitution G A downstream_gene_variant BRCA-EU 4 85729982 85729982 single base substitution G A intron_variant BRCA-EU 4 85729982 85729982 single base substitution G A upstream_gene_variant BRCA-EU 4 85732875 85732875 deletion of <=200bp T - intron_variant BRCA-EU 4 85732875 85732875 deletion of <=200bp T - upstream_gene_variant BRCA-EU 4 85734529 85734529 single base substitution A G intron_variant BRCA-EU 4 85734529 85734529 single base substitution A G upstream_gene_variant BRCA-EU 4 85737009 85737009 single base substitution A G intron_variant BRCA-EU 4 85737556 85737556 single base substitution T C intron_variant BRCA-EU 4 85738847 85738847 single base substitution T G intron_variant BRCA-EU 4 85741520 85741520 single base substitution C T intron_variant BRCA-EU 4 85743306 85743306 deletion of <=200bp A - intron_variant BRCA-EU 4 85743693 85743693 deletion of <=200bp A - intron_variant BRCA-EU 4 85744091 85744091 single base substitution G C intron_variant BRCA-EU 4 85744238 85744238 single base substitution G C intron_variant BRCA-EU 4 85744277 85744277 insertion of <=200bp - GT intron_variant BRCA-EU 4 85744758 85744758 single base substitution A G intron_variant BRCA-EU 4 85747269 85747269 single base substitution G A intron_variant BRCA-EU 4 85747688 85747688 single base substitution G A intron_variant BRCA-EU 4 85747891 85747891 single base substitution G C intron_variant BRCA-EU 4 85748160 85748160 insertion of <=200bp - T intron_variant BRCA-EU 4 85749740 85749740 single base substitution C G intron_variant BRCA-EU 4 85750372 85750389 deletion of <=200bp GCATTATTCCTGACAATC - intron_variant BRCA-EU 4 85750735 85750735 single base substitution G T intron_variant BRCA-EU 4 85751011 85751011 single base substitution A G intron_variant BRCA-EU 4 85751609 85751609 single base substitution G C intron_variant BRCA-EU 4 85751665 85751665 single base substitution C G intron_variant BRCA-EU 4 85751910 85751910 single base substitution G C intron_variant BRCA-EU 4 85753497 85753497 single base substitution C T intron_variant BRCA-EU 4 85755484 85755484 single base substitution G A intron_variant BRCA-EU 4 85755566 85755566 single base substitution G A intron_variant BRCA-EU 4 85755771 85755771 single base substitution T A intron_variant BRCA-EU 4 85757742 85757742 single base substitution G A downstream_gene_variant BRCA-EU 4 85757742 85757742 single base substitution G A intron_variant BRCA-EU 4 85758594 85758594 single base substitution C A downstream_gene_variant BRCA-EU 4 85758594 85758594 single base substitution C A intron_variant BRCA-EU 4 85761744 85761744 deletion of <=200bp T - downstream_gene_variant BRCA-EU 4 85761744 85761744 deletion of <=200bp T - intron_variant BRCA-EU 4 85761804 85761804 single base substitution C T downstream_gene_variant BRCA-EU 4 85761804 85761804 single base substitution C T intron_variant BRCA-EU 4 85761986 85761986 single base substitution G A downstream_gene_variant BRCA-EU 4 85761986 85761986 single base substitution G A intron_variant BRCA-EU 4 85762531 85762531 single base substitution T G intron_variant BRCA-EU 4 85762982 85762982 single base substitution T G intron_variant BRCA-EU 4 85763044 85763044 single base substitution A T intron_variant BRCA-EU 4 85763473 85763473 single base substitution T A intron_variant BRCA-EU 4 85765476 85765476 single base substitution C T intron_variant BRCA-EU 4 85765504 85765504 deletion of <=200bp A - intron_variant BRCA-EU 4 85765669 85765669 deletion of <=200bp A - intron_variant BRCA-EU 4 85765669 85765669 deletion of <=200bp A - splice_region_variant BRCA-EU 4 85766267 85766267 deletion of <=200bp A - downstream_gene_variant BRCA-EU 4 85766267 85766267 deletion of <=200bp A - intron_variant BRCA-EU 4 85766424 85766424 deletion of <=200bp T - downstream_gene_variant BRCA-EU 4 85766424 85766424 deletion of <=200bp T - intron_variant BRCA-EU 4 85767867 85767867 deletion of <=200bp T - downstream_gene_variant BRCA-EU 4 85767867 85767867 deletion of <=200bp T - intron_variant BRCA-EU 4 85770547 85770547 single base substitution G A downstream_gene_variant BRCA-EU 4 85770547 85770547 single base substitution G A intron_variant BRCA-EU 4 85773713 85773713 single base substitution T C intron_variant BRCA-EU 4 85773713 85773713 single base substitution T C upstream_gene_variant BRCA-EU 4 85773972 85773972 single base substitution G A intron_variant BRCA-EU 4 85773972 85773972 single base substitution G A upstream_gene_variant BRCA-EU 4 85776730 85776730 single base substitution T G downstream_gene_variant BRCA-EU 4 85776730 85776730 single base substitution T G intron_variant BRCA-EU 4 85777397 85777397 single base substitution C T downstream_gene_variant BRCA-EU 4 85777397 85777397 single base substitution C T intron_variant BRCA-EU 4 85778186 85778186 single base substitution T G downstream_gene_variant BRCA-EU 4 85778186 85778186 single base substitution T G intron_variant BRCA-EU 4 85779206 85779209 deletion of <=200bp TCTT - downstream_gene_variant BRCA-EU 4 85779206 85779209 deletion of <=200bp TCTT - intron_variant BRCA-EU 4 85785193 85785193 single base substitution A G intron_variant BRCA-EU 4 85785193 85785193 single base substitution A G upstream_gene_variant BRCA-EU 4 85788083 85788083 single base substitution A G intron_variant BRCA-EU 4 85788141 85788141 single base substitution C T intron_variant BRCA-EU 4 85789232 85789232 single base substitution G A intron_variant BRCA-EU 4 85789835 85789835 single base substitution A G intron_variant BRCA-EU 4 85791904 85791904 single base substitution A G intron_variant BRCA-EU 4 85792228 85792228 single base substitution A C intron_variant BRCA-EU 4 85793301 85793301 single base substitution A G intron_variant BRCA-EU 4 85794073 85794073 single base substitution G C intron_variant BRCA-EU 4 85794090 85794090 single base substitution T A intron_variant BRCA-EU 4 85794211 85794211 single base substitution G A intron_variant BRCA-EU 4 85794917 85794917 deletion of <=200bp T - intron_variant BRCA-EU 4 85797540 85797540 single base substitution C T intron_variant BRCA-EU 4 85797593 85797593 single base substitution G T intron_variant BRCA-EU 4 85799077 85799077 single base substitution C G intron_variant BRCA-EU 4 85800693 85800693 single base substitution G C intron_variant BRCA-EU 4 85801799 85801799 single base substitution A G intron_variant BRCA-EU 4 85803737 85803737 single base substitution G C intron_variant BRCA-EU 4 85804681 85804681 single base substitution A C intron_variant BRCA-EU 4 85805226 85805226 deletion of <=200bp T - intron_variant BRCA-EU 4 85805770 85805770 single base substitution C G intron_variant BRCA-EU 4 85806288 85806288 single base substitution G A intron_variant BRCA-EU 4 85806321 85806321 deletion of <=200bp T - intron_variant BRCA-EU 4 85806787 85806787 single base substitution C G intron_variant BRCA-EU 4 85810004 85810004 single base substitution C T intron_variant BRCA-EU 4 85810050 85810050 deletion of <=200bp G - intron_variant BRCA-EU 4 85810817 85810817 single base substitution G A intron_variant BRCA-EU 4 85810885 85810885 single base substitution A G intron_variant BRCA-EU 4 85812524 85812524 deletion of <=200bp A - intron_variant BRCA-EU 4 85812825 85812825 deletion of <=200bp A - intron_variant BRCA-EU 4 85813357 85813357 single base substitution C T intron_variant BRCA-EU 4 85813399 85813399 single base substitution T A intron_variant BRCA-EU 4 85813437 85813437 single base substitution T G intron_variant BRCA-EU 4 85813531 85813531 deletion of <=200bp A - intron_variant BRCA-EU 4 85814398 85814398 single base substitution C G intron_variant BRCA-EU 4 85814458 85814458 single base substitution G A intron_variant BRCA-EU 4 85817688 85817688 single base substitution G C intron_variant BRCA-EU 4 85817704 85817704 single base substitution A G intron_variant BRCA-EU 4 85818178 85818178 deletion of <=200bp A - intron_variant BRCA-EU 4 85818178 85818178 deletion of <=200bp A - upstream_gene_variant BRCA-EU 4 85818976 85818976 single base substitution T C intron_variant BRCA-EU 4 85818976 85818976 single base substitution T C upstream_gene_variant BRCA-EU 4 85821634 85821634 single base substitution G A intron_variant BRCA-EU 4 85821634 85821634 single base substitution G A upstream_gene_variant BRCA-EU 4 85822092 85822092 single base substitution A T intron_variant BRCA-EU 4 85822092 85822092 single base substitution A T upstream_gene_variant BRCA-EU 4 85822567 85822567 single base substitution G A intron_variant BRCA-EU 4 85822567 85822567 single base substitution G A upstream_gene_variant BRCA-EU 4 85823807 85823807 single base substitution G A intron_variant BRCA-EU 4 85824278 85824278 single base substitution C A intron_variant BRCA-EU 4 85826005 85826005 single base substitution T C intron_variant BRCA-EU 4 85826263 85826263 single base substitution C T intron_variant BRCA-EU 4 85828847 85828847 single base substitution G C intron_variant BRCA-EU 4 85830599 85830599 single base substitution T A intron_variant BRCA-EU 4 85832074 85832074 single base substitution C T intron_variant BRCA-EU 4 85833213 85833213 single base substitution A G intron_variant BRCA-EU 4 85835401 85835401 single base substitution C A intron_variant BRCA-EU 4 85836026 85836026 single base substitution A G intron_variant BRCA-EU 4 85836576 85836576 single base substitution A C intron_variant BRCA-EU 4 85836669 85836669 single base substitution G C intron_variant BRCA-EU 4 85837070 85837070 single base substitution C G intron_variant BRCA-EU 4 85837678 85837678 single base substitution C A intron_variant BRCA-EU 4 85838214 85838214 single base substitution G A intron_variant BRCA-EU 4 85838577 85838577 single base substitution C A intron_variant BRCA-EU 4 85839575 85839575 single base substitution C T intron_variant BRCA-EU 4 85842187 85842187 single base substitution A C intron_variant BRCA-EU 4 85845501 85845501 single base substitution G C intron_variant BRCA-EU 4 85846942 85846942 single base substitution G A intron_variant BRCA-EU 4 85848184 85848184 single base substitution G C intron_variant BRCA-EU 4 85849745 85849745 single base substitution C T intron_variant BRCA-EU 4 85849933 85849933 single base substitution G C intron_variant BRCA-EU 4 85851292 85851292 single base substitution A G intron_variant BRCA-EU 4 85854469 85854469 single base substitution C T intron_variant BRCA-EU 4 85858488 85858488 single base substitution C A intron_variant BRCA-EU 4 85859051 85859051 single base substitution T A intron_variant BRCA-EU 4 85859067 85859067 single base substitution T C intron_variant BRCA-EU 4 85860631 85860631 single base substitution T G intron_variant BRCA-EU 4 85862572 85862572 single base substitution G A intron_variant BRCA-EU 4 85862744 85862744 single base substitution G T intron_variant BRCA-EU 4 85863588 85863588 single base substitution C A intron_variant BRCA-EU 4 85864065 85864065 single base substitution T A intron_variant BRCA-EU 4 85864552 85864552 single base substitution G C intron_variant BRCA-EU 4 85864652 85864652 single base substitution G A intron_variant BRCA-EU 4 85867277 85867277 single base substitution T A intron_variant BRCA-EU 4 85868540 85868540 single base substitution C A intron_variant BRCA-EU 4 85869366 85869366 single base substitution G A intron_variant BRCA-EU 4 85871030 85871030 single base substitution G C intron_variant BRCA-EU 4 85871284 85871284 deletion of <=200bp A - intron_variant BRCA-EU 4 85871440 85871440 single base substitution T A intron_variant BRCA-EU 4 85873482 85873482 single base substitution T C intron_variant BRCA-EU 4 85874823 85874823 deletion of <=200bp T - intron_variant BRCA-EU 4 85875109 85875109 single base substitution C T intron_variant BRCA-EU 4 85876594 85876594 single base substitution G C intron_variant BRCA-EU 4 85879155 85879155 single base substitution A G intron_variant BRCA-EU 4 85879627 85879627 single base substitution G C intron_variant BRCA-EU 4 85881212 85881212 insertion of <=200bp - T intron_variant BRCA-EU 4 85881809 85881809 deletion of <=200bp A - intron_variant BRCA-EU 4 85884532 85884532 single base substitution G A intron_variant BRCA-EU 4 85884588 85884588 single base substitution A C intron_variant BRCA-EU 4 85884653 85884653 single base substitution G C intron_variant BRCA-EU 4 85885219 85885219 single base substitution G A intron_variant BRCA-EU 4 85887579 85887579 single base substitution G T upstream_gene_variant BRCA-EU 4 85889291 85889294 deletion of <=200bp TAAC - upstream_gene_variant BRCA-EU 4 85890114 85890114 insertion of <=200bp - A upstream_gene_variant BRCA-EU 4 85890469 85890469 single base substitution G C upstream_gene_variant BRCA-EU 4 85890800 85890800 single base substitution A T upstream_gene_variant BRCA-EU 4 85890942 85890942 deletion of <=200bp G - upstream_gene_variant BRCA-EU 4 85891754 85891754 single base substitution G C upstream_gene_variant BRCA-FR 4 85587979 85587979 single base substitution C T downstream_gene_variant BRCA-FR 4 85590139 85590139 single base substitution C G downstream_gene_variant BRCA-FR 4 85609044 85609044 single base substitution C T downstream_gene_variant BRCA-FR 4 85609044 85609044 single base substitution C T intron_variant BRCA-FR 4 85609044 85609044 single base substitution C T upstream_gene_variant BRCA-FR 4 85611790 85611790 single base substitution C G downstream_gene_variant BRCA-FR 4 85611790 85611790 single base substitution C G missense_variant E3061Q 9181G>C BRCA-FR 4 85611790 85611790 single base substitution C G missense_variant E3078Q 9232G>C BRCA-FR 4 85615243 85615243 single base substitution G C intron_variant BRCA-FR 4 85615252 85615252 single base substitution A C intron_variant BRCA-FR 4 85615527 85615527 single base substitution C G intron_variant BRCA-FR 4 85619447 85619447 single base substitution T A intron_variant BRCA-FR 4 85625416 85625416 single base substitution G A intron_variant BRCA-FR 4 85668547 85668547 single base substitution C T downstream_gene_variant BRCA-FR 4 85668547 85668547 single base substitution C T intron_variant BRCA-FR 4 85672790 85672790 single base substitution C G exon_variant BRCA-FR 4 85672790 85672790 single base substitution C G missense_variant S1940T 5819G>C BRCA-FR 4 85683747 85683747 single base substitution C G intron_variant BRCA-FR 4 85686835 85686835 single base substitution C G intron_variant BRCA-FR 4 85694795 85694795 single base substitution T C intron_variant BRCA-FR 4 85705246 85705246 single base substitution G A intron_variant BRCA-FR 4 85721146 85721146 single base substitution C G downstream_gene_variant BRCA-FR 4 85721146 85721146 single base substitution C G intron_variant BRCA-FR 4 85724978 85724978 single base substitution G C intron_variant BRCA-FR 4 85738847 85738847 single base substitution T G intron_variant BRCA-FR 4 85747269 85747269 single base substitution G A intron_variant BRCA-FR 4 85766821 85766821 single base substitution T G downstream_gene_variant BRCA-FR 4 85766821 85766821 single base substitution T G intron_variant BRCA-FR 4 85769259 85769259 single base substitution G A downstream_gene_variant BRCA-FR 4 85769259 85769259 single base substitution G A intron_variant BRCA-FR 4 85777397 85777397 single base substitution C T downstream_gene_variant BRCA-FR 4 85777397 85777397 single base substitution C T intron_variant BRCA-FR 4 85779225 85779225 single base substitution C A downstream_gene_variant BRCA-FR 4 85779225 85779225 single base substitution C A intron_variant BRCA-FR 4 85794211 85794211 single base substitution G A intron_variant BRCA-FR 4 85801799 85801799 single base substitution A G intron_variant BRCA-FR 4 85805770 85805770 single base substitution C G intron_variant BRCA-FR 4 85817177 85817177 single base substitution G A intron_variant BRCA-FR 4 85825486 85825486 single base substitution T C intron_variant BRCA-FR 4 85826263 85826263 single base substitution C T intron_variant BRCA-FR 4 85826421 85826421 single base substitution G T intron_variant BRCA-FR 4 85831849 85831849 single base substitution C A intron_variant BRCA-FR 4 85859051 85859051 single base substitution T A intron_variant BRCA-FR 4 85859067 85859067 single base substitution T C intron_variant BRCA-FR 4 85862744 85862744 single base substitution G T intron_variant BRCA-FR 4 85863588 85863588 single base substitution C A intron_variant BRCA-FR 4 85869366 85869366 single base substitution G A intron_variant BRCA-FR 4 85885219 85885219 single base substitution G A intron_variant BRCA-FR 4 85891754 85891754 single base substitution G C upstream_gene_variant BRCA-KR 4 85708910 85708910 single base substitution C A intron_variant BRCA-KR 4 85724496 85724496 single base substitution T G exon_variant BRCA-KR 4 85724496 85724496 single base substitution T G missense_variant M852L 2554A>C BRCA-UK 4 85642877 85642877 single base substitution C A intron_variant BRCA-UK 4 85693913 85693913 single base substitution C G intron_variant BRCA-UK 4 85745718 85745718 single base substitution G C intron_variant BRCA-UK 4 85748662 85748662 single base substitution G T intron_variant BRCA-UK 4 85758097 85758097 single base substitution C G downstream_gene_variant BRCA-UK 4 85758097 85758097 single base substitution C G exon_variant BRCA-UK 4 85758097 85758097 single base substitution C G missense_variant Q187H 561G>C BRCA-UK 4 85758979 85758979 single base substitution C T downstream_gene_variant BRCA-UK 4 85758979 85758979 single base substitution C T intron_variant BRCA-UK 4 85777217 85777217 single base substitution C G downstream_gene_variant BRCA-UK 4 85777217 85777217 single base substitution C G intron_variant BRCA-UK 4 85779863 85779863 single base substitution G C downstream_gene_variant BRCA-UK 4 85779863 85779863 single base substitution G C intron_variant BRCA-UK 4 85803234 85803234 single base substitution C G intron_variant BRCA-UK 4 85810004 85810004 single base substitution C T intron_variant BRCA-UK 4 85817688 85817688 single base substitution G C intron_variant BRCA-UK 4 85864552 85864552 single base substitution G C intron_variant BRCA-UK 4 85871440 85871440 single base substitution T A intron_variant BRCA-UK 4 85887601 85887601 single base substitution G T upstream_gene_variant BRCA-US 4 85603603 85603603 single base substitution C A exon_variant BRCA-US 4 85603603 85603603 single base substitution C A missense_variant L3232F 9696G>T BRCA-US 4 85603603 85603603 single base substitution C A missense_variant L3249F 9747G>T BRCA-US 4 85617213 85617213 single base substitution C T synonymous_variant E2920E 8760G>A BRCA-US 4 85617213 85617213 single base substitution C T synonymous_variant E2937E 8811G>A BRCA-US 4 85617213 85617213 single base substitution C T synonymous_variant E540E 1620G>A BRCA-US 4 85638146 85638146 single base substitution C G missense_variant R196T 587G>C BRCA-US 4 85638146 85638146 single base substitution C G missense_variant R2576T 7727G>C BRCA-US 4 85638146 85638146 single base substitution C G missense_variant R2593T 7778G>C BRCA-US 4 85642669 85642669 single base substitution C T missense_variant E103K 307G>A BRCA-US 4 85642669 85642669 single base substitution C T missense_variant E2483K 7447G>A BRCA-US 4 85642669 85642669 single base substitution C T missense_variant E2500K 7498G>A BRCA-US 4 85645723 85645723 single base substitution C T missense_variant V2416I 7246G>A BRCA-US 4 85645723 85645723 single base substitution C T missense_variant V2433I 7297G>A BRCA-US 4 85645723 85645723 single base substitution C T missense_variant V36I 106G>A BRCA-US 4 85648059 85648059 single base substitution C T intron_variant BRCA-US 4 85648059 85648059 single base substitution C T synonymous_variant E2409E 7227G>A BRCA-US 4 85654705 85654705 single base substitution G A downstream_gene_variant BRCA-US 4 85654705 85654705 single base substitution G A synonymous_variant L2351L 7051C>T BRCA-US 4 85654705 85654705 single base substitution G A upstream_gene_variant BRCA-US 4 85657344 85657347 deletion of <=200bp ATTA - exon_variant BRCA-US 4 85657344 85657347 deletion of <=200bp ATTA - frameshift_variant LN2297 BRCA-US 4 85657344 85657347 deletion of <=200bp ATTA - upstream_gene_variant BRCA-US 4 85663022 85663022 single base substitution C T synonymous_variant V2042V 6126G>A BRCA-US 4 85663022 85663022 single base substitution C T upstream_gene_variant BRCA-US 4 85672736 85672736 single base substitution G A exon_variant BRCA-US 4 85672736 85672736 single base substitution G A missense_variant A1958V 5873C>T BRCA-US 4 85674919 85674919 single base substitution C T exon_variant BRCA-US 4 85674919 85674919 single base substitution C T missense_variant M1890I 5670G>A BRCA-US 4 85678260 85678260 single base substitution C T missense_variant R1748Q 5243G>A BRCA-US 4 85678260 85678260 single base substitution C T upstream_gene_variant BRCA-US 4 85687113 85687113 insertion of <=200bp - T frameshift_variant H1680Q? BRCA-US 4 85696135 85696135 single base substitution C G splice_acceptor_variant BRCA-US 4 85701312 85701312 single base substitution G C synonymous_variant V1438V 4314C>G BRCA-US 4 85708711 85708711 single base substitution T G missense_variant L1275F 3825A>C BRCA-US 4 85710959 85710959 single base substitution C A missense_variant V1197F 3589G>T BRCA-US 4 85731339 85731339 deletion of <=200bp A - exon_variant BRCA-US 4 85731339 85731339 deletion of <=200bp A - frameshift_variant F682 BRCA-US 4 85731339 85731339 deletion of <=200bp A - upstream_gene_variant BRCA-US 4 85742538 85742538 single base substitution A G exon_variant BRCA-US 4 85742538 85742538 single base substitution A G synonymous_variant F430F 1290T>C BRCA-US 4 85748077 85748077 single base substitution C G exon_variant BRCA-US 4 85748077 85748077 single base substitution C G synonymous_variant L338L 1014G>C BRCA-US 4 85758097 85758097 single base substitution C T downstream_gene_variant BRCA-US 4 85758097 85758097 single base substitution C T exon_variant BRCA-US 4 85758097 85758097 single base substitution C T synonymous_variant Q187Q 561G>A BRCA-US 4 85762417 85762417 single base substitution C A splice_acceptor_variant BRCA-US 4 85887858 85887858 single base substitution A G upstream_gene_variant BRCA-US 4 85888197 85888197 single base substitution C G upstream_gene_variant BTCA-JP 4 85634395 85634395 single base substitution G A splice_region_variant BTCA-JP 4 85639839 85639839 single base substitution G T intron_variant BTCA-JP 4 85647942 85647942 deletion of <=200bp A - intron_variant BTCA-JP 4 85660163 85660163 single base substitution C G missense_variant G2192R 6574G>C BTCA-JP 4 85660163 85660163 single base substitution C G splice_region_variant BTCA-JP 4 85663139 85663139 deletion of <=200bp A - intron_variant BTCA-JP 4 85663139 85663139 deletion of <=200bp A - upstream_gene_variant BTCA-JP 4 85674763 85674763 deletion of <=200bp A - intron_variant BTCA-JP 4 85676453 85676453 deletion of <=200bp A - exon_variant BTCA-JP 4 85676453 85676453 deletion of <=200bp A - frameshift_variant L1842 BTCA-JP 4 85724310 85724310 deletion of <=200bp T - intron_variant BTCA-JP 4 85729531 85729531 single base substitution A C downstream_gene_variant BTCA-JP 4 85729531 85729531 single base substitution A C intron_variant BTCA-JP 4 85729531 85729531 single base substitution A C synonymous_variant S795S 2385T>G BTCA-JP 4 85729531 85729531 single base substitution A C upstream_gene_variant BTCA-JP 4 85730901 85730901 single base substitution T C exon_variant BTCA-JP 4 85730901 85730901 single base substitution T C intron_variant BTCA-JP 4 85731227 85731227 single base substitution G A exon_variant BTCA-JP 4 85731227 85731227 single base substitution G A stop_gained R720* 2158C>T BTCA-JP 4 85731455 85731455 single base substitution C T exon_variant BTCA-JP 4 85731455 85731455 single base substitution C T missense_variant V644I 1930G>A BTCA-JP 4 85731455 85731455 single base substitution C T upstream_gene_variant BTCA-JP 4 85752646 85752646 single base substitution G A exon_variant BTCA-JP 4 85752646 85752646 single base substitution G A missense_variant P230L 689C>T BTCA-JP 4 85752647 85752647 single base substitution G T exon_variant BTCA-JP 4 85752647 85752647 single base substitution G T missense_variant P230T 688C>A BTCA-JP 4 85762429 85762429 single base substitution A C intron_variant CESC-US 4 85594031 85594031 single base substitution C T exon_variant CESC-US 4 85594031 85594031 single base substitution C T missense_variant R3507Q 10520G>A CESC-US 4 85594031 85594031 single base substitution C T missense_variant R3524Q 10571G>A CESC-US 4 85605214 85605214 single base substitution A G missense_variant V3186A 9557T>C CESC-US 4 85605214 85605214 single base substitution A G missense_variant V3203A 9608T>C CESC-US 4 85605214 85605214 single base substitution A G upstream_gene_variant CESC-US 4 85609036 85609036 single base substitution C T downstream_gene_variant CESC-US 4 85609036 85609036 single base substitution C T intron_variant CESC-US 4 85609036 85609036 single base substitution C T upstream_gene_variant CESC-US 4 85614120 85614120 single base substitution G C missense_variant I2972M 8916C>G CESC-US 4 85614120 85614120 single base substitution G C missense_variant I2989M 8967C>G CESC-US 4 85614120 85614120 single base substitution G C missense_variant I592M 1776C>G CESC-US 4 85623529 85623529 single base substitution A G missense_variant F2841S 8522T>C CESC-US 4 85623529 85623529 single base substitution A G missense_variant F2858S 8573T>C CESC-US 4 85623529 85623529 single base substitution A G missense_variant F461S 1382T>C CESC-US 4 85664936 85664936 single base substitution G C missense_variant S1997C 5990C>G CESC-US 4 85664936 85664936 single base substitution G C upstream_gene_variant CESC-US 4 85696122 85696122 single base substitution C A missense_variant K1535N 4605G>T CESC-US 4 85707190 85707190 single base substitution G A missense_variant T1335I 4004C>T CESC-US 4 85710969 85710969 single base substitution C T stop_gained W1193* 3579G>A CESC-US 4 85731124 85731124 single base substitution G C exon_variant CESC-US 4 85731124 85731124 single base substitution G C stop_gained S754* 2261C>G CESC-US 4 85731460 85731460 single base substitution C G exon_variant CESC-US 4 85731460 85731460 single base substitution C G missense_variant R642T 1925G>C CESC-US 4 85731460 85731460 single base substitution C G upstream_gene_variant CESC-US 4 85888148 85888148 single base substitution C T upstream_gene_variant CLLE-ES 4 85589577 85589577 single base substitution A C downstream_gene_variant CLLE-ES 4 85603786 85603786 single base substitution C T exon_variant CLLE-ES 4 85603786 85603786 single base substitution C T intron_variant CLLE-ES 4 85649356 85649356 single base substitution C T intron_variant CLLE-ES 4 85655683 85655683 single base substitution A C downstream_gene_variant CLLE-ES 4 85655683 85655683 single base substitution A C intron_variant CLLE-ES 4 85655683 85655683 single base substitution A C upstream_gene_variant CLLE-ES 4 85660633 85660633 single base substitution G T intron_variant CLLE-ES 4 85660633 85660633 single base substitution G T upstream_gene_variant CLLE-ES 4 85669746 85669746 single base substitution A C downstream_gene_variant CLLE-ES 4 85669746 85669746 single base substitution A C intron_variant CLLE-ES 4 85673289 85673289 single base substitution A G intron_variant CLLE-ES 4 85677474 85677474 single base substitution G C intron_variant CLLE-ES 4 85677474 85677474 single base substitution G C upstream_gene_variant CLLE-ES 4 85690517 85690517 single base substitution G A intron_variant CLLE-ES 4 85691481 85691481 single base substitution G A intron_variant CLLE-ES 4 85694171 85694171 single base substitution T A intron_variant CLLE-ES 4 85700376 85700376 single base substitution A G intron_variant CLLE-ES 4 85700836 85700836 single base substitution G A intron_variant CLLE-ES 4 85706151 85706151 single base substitution G A intron_variant CLLE-ES 4 85711372 85711372 single base substitution G A intron_variant CLLE-ES 4 85716871 85716871 single base substitution C T intron_variant CLLE-ES 4 85717383 85717383 single base substitution C T intron_variant CLLE-ES 4 85744407 85744407 single base substitution A G intron_variant CLLE-ES 4 85766944 85766944 single base substitution G A downstream_gene_variant CLLE-ES 4 85766944 85766944 single base substitution G A intron_variant CLLE-ES 4 85778864 85778864 single base substitution T C downstream_gene_variant CLLE-ES 4 85778864 85778864 single base substitution T C intron_variant CLLE-ES 4 85791149 85791149 single base substitution C T intron_variant CLLE-ES 4 85793010 85793010 single base substitution A T intron_variant CLLE-ES 4 85810417 85810417 single base substitution T A intron_variant CLLE-ES 4 85818221 85818221 single base substitution A G intron_variant CLLE-ES 4 85818221 85818221 single base substitution A G upstream_gene_variant CLLE-ES 4 85818986 85818986 single base substitution A T intron_variant CLLE-ES 4 85818986 85818986 single base substitution A T upstream_gene_variant CLLE-ES 4 85820419 85820419 single base substitution C G intron_variant CLLE-ES 4 85820419 85820419 single base substitution C G upstream_gene_variant CLLE-ES 4 85825750 85825750 single base substitution A T intron_variant CLLE-ES 4 85840367 85840367 single base substitution G A intron_variant CLLE-ES 4 85841074 85841074 single base substitution C T intron_variant CLLE-ES 4 85846076 85846076 single base substitution C A intron_variant CLLE-ES 4 85852516 85852516 single base substitution C T intron_variant CLLE-ES 4 85877860 85877860 single base substitution A G intron_variant CLLE-ES 4 85883282 85883282 single base substitution G A intron_variant COAD-US 4 85611693 85611693 single base substitution G A downstream_gene_variant COAD-US 4 85611693 85611693 single base substitution G A missense_variant S3093F 9278C>T COAD-US 4 85611693 85611693 single base substitution G A missense_variant S3110F 9329C>T COAD-US 4 85611722 85611722 single base substitution C T downstream_gene_variant COAD-US 4 85611722 85611722 single base substitution C T synonymous_variant T3083T 9249G>A COAD-US 4 85611722 85611722 single base substitution C T synonymous_variant T3100T 9300G>A COAD-US 4 85612894 85612894 single base substitution T C missense_variant I3015V 9043A>G COAD-US 4 85612894 85612894 single base substitution T C missense_variant I3032V 9094A>G COAD-US 4 85612894 85612894 single base substitution T C missense_variant I635V 1903A>G COAD-US 4 85614146 85614146 single base substitution G A stop_gained R2964* 8890C>T COAD-US 4 85614146 85614146 single base substitution G A stop_gained R2981* 8941C>T COAD-US 4 85614146 85614146 single base substitution G A stop_gained R584* 1750C>T COAD-US 4 85639659 85639659 single base substitution A C missense_variant F160C 479T>G COAD-US 4 85639659 85639659 single base substitution A C missense_variant F2540C 7619T>G COAD-US 4 85639659 85639659 single base substitution A C missense_variant F2557C 7670T>G COAD-US 4 85642695 85642695 single base substitution C A missense_variant R2474L 7421G>T COAD-US 4 85642695 85642695 single base substitution C A missense_variant R2491L 7472G>T COAD-US 4 85642695 85642695 single base substitution C A missense_variant R94L 281G>T COAD-US 4 85657414 85657414 single base substitution C T exon_variant COAD-US 4 85657414 85657414 single base substitution C T missense_variant R2275H 6824G>A COAD-US 4 85657414 85657414 single base substitution C T upstream_gene_variant COAD-US 4 85658517 85658517 single base substitution G A missense_variant R2193C 6577C>T COAD-US 4 85658517 85658517 single base substitution G A splice_region_variant COAD-US 4 85658517 85658517 single base substitution G A upstream_gene_variant COAD-US 4 85660273 85660273 single base substitution C T exon_variant COAD-US 4 85660273 85660273 single base substitution C T splice_acceptor_variant COAD-US 4 85661490 85661490 single base substitution C T missense_variant R2105Q 6314G>A COAD-US 4 85661490 85661490 single base substitution C T upstream_gene_variant COAD-US 4 85672710 85672710 single base substitution G A exon_variant COAD-US 4 85672710 85672710 single base substitution G A missense_variant R1967W 5899C>T COAD-US 4 85672858 85672858 single base substitution A G exon_variant COAD-US 4 85672858 85672858 single base substitution A G synonymous_variant L1917L 5751T>C COAD-US 4 85676453 85676453 deletion of <=200bp A - exon_variant COAD-US 4 85676453 85676453 deletion of <=200bp A - frameshift_variant L1842 COAD-US 4 85676503 85676503 single base substitution G A exon_variant COAD-US 4 85676503 85676503 single base substitution G A synonymous_variant S1825S 5475C>T COAD-US 4 85710984 85710984 single base substitution G A synonymous_variant I1188I 3564C>T COAD-US 4 85715716 85715716 single base substitution C T missense_variant R1148Q 3443G>A COAD-US 4 85729570 85729570 single base substitution A G downstream_gene_variant COAD-US 4 85729570 85729570 single base substitution A G intron_variant COAD-US 4 85729570 85729570 single base substitution A G splice_region_variant COAD-US 4 85729570 85729570 single base substitution A G upstream_gene_variant COAD-US 4 85731291 85731291 single base substitution A G exon_variant COAD-US 4 85731291 85731291 single base substitution A G synonymous_variant Y698Y 2094T>C COAD-US 4 85731291 85731291 single base substitution A G upstream_gene_variant COAD-US 4 85738560 85738560 single base substitution C G exon_variant COAD-US 4 85738560 85738560 single base substitution C G missense_variant K624N 1872G>C COAD-US 4 85738618 85738618 single base substitution T A exon_variant COAD-US 4 85738618 85738618 single base substitution T A missense_variant D605V 1814A>T COAD-US 4 85750200 85750200 single base substitution G A exon_variant COAD-US 4 85750200 85750200 single base substitution G A missense_variant R305W 913C>T COAD-US 4 85758091 85758091 single base substitution A G downstream_gene_variant COAD-US 4 85758091 85758091 single base substitution A G exon_variant COAD-US 4 85758091 85758091 single base substitution A G synonymous_variant V189V 567T>C COAD-US 4 85781682 85781682 single base substitution G A downstream_gene_variant COAD-US 4 85781682 85781682 single base substitution G A exon_variant COAD-US 4 85781682 85781682 single base substitution G A synonymous_variant N21N 63C>T COAD-US 4 85781713 85781713 single base substitution G A downstream_gene_variant COAD-US 4 85781713 85781713 single base substitution G A exon_variant COAD-US 4 85781713 85781713 single base substitution G A missense_variant P11L 32C>T COCA-CN 4 85600268 85600268 single base substitution G A exon_variant COCA-CN 4 85600268 85600268 single base substitution G A synonymous_variant R3300R 9900C>T COCA-CN 4 85600268 85600268 single base substitution G A synonymous_variant R3317R 9951C>T COCA-CN 4 85611768 85611768 single base substitution G A downstream_gene_variant COCA-CN 4 85611768 85611768 single base substitution G A missense_variant A3068V 9203C>T COCA-CN 4 85611768 85611768 single base substitution G A missense_variant A3085V 9254C>T COCA-CN 4 85611927 85611927 single base substitution C T downstream_gene_variant COCA-CN 4 85611927 85611927 single base substitution C T intron_variant COCA-CN 4 85612949 85612949 single base substitution G T intron_variant COCA-CN 4 85614222 85614222 single base substitution G T intron_variant COCA-CN 4 85617196 85617196 single base substitution T C missense_variant Y2926C 8777A>G COCA-CN 4 85617196 85617196 single base substitution T C missense_variant Y2943C 8828A>G COCA-CN 4 85617196 85617196 single base substitution T C missense_variant Y546C 1637A>G COCA-CN 4 85617261 85617261 single base substitution G A synonymous_variant G2904G 8712C>T COCA-CN 4 85617261 85617261 single base substitution G A synonymous_variant G2921G 8763C>T COCA-CN 4 85617261 85617261 single base substitution G A synonymous_variant G524G 1572C>T COCA-CN 4 85617910 85617910 single base substitution C T missense_variant R2871Q 8612G>A COCA-CN 4 85617910 85617910 single base substitution C T missense_variant R2888Q 8663G>A COCA-CN 4 85617910 85617910 single base substitution C T missense_variant R491Q 1472G>A COCA-CN 4 85630335 85630335 single base substitution A C intron_variant COCA-CN 4 85636343 85636343 single base substitution G T intron_variant COCA-CN 4 85637362 85637362 single base substitution A G intron_variant COCA-CN 4 85638217 85638217 single base substitution A C intron_variant COCA-CN 4 85645657 85645657 single base substitution C T missense_variant A2438T 7312G>A COCA-CN 4 85645657 85645657 single base substitution C T missense_variant A2455T 7363G>A COCA-CN 4 85645657 85645657 single base substitution C T missense_variant A58T 172G>A COCA-CN 4 85656350 85656350 single base substitution T C intron_variant COCA-CN 4 85656350 85656350 single base substitution T C upstream_gene_variant COCA-CN 4 85657364 85657364 single base substitution G A exon_variant COCA-CN 4 85657364 85657364 single base substitution G A stop_gained R2292* 6874C>T COCA-CN 4 85657364 85657364 single base substitution G A upstream_gene_variant COCA-CN 4 85658452 85658452 single base substitution G T exon_variant COCA-CN 4 85658452 85658452 single base substitution G T synonymous_variant V2214V 6642C>A COCA-CN 4 85658452 85658452 single base substitution G T upstream_gene_variant COCA-CN 4 85660085 85660085 single base substitution G A intron_variant COCA-CN 4 85661513 85661513 single base substitution C A missense_variant R2097S 6291G>T COCA-CN 4 85661513 85661513 single base substitution C A upstream_gene_variant COCA-CN 4 85676401 85676401 single base substitution G A intron_variant COCA-CN 4 85678025 85678025 single base substitution C T intron_variant COCA-CN 4 85678025 85678025 single base substitution C T upstream_gene_variant COCA-CN 4 85687394 85687394 single base substitution G T intron_variant COCA-CN 4 85708627 85708627 single base substitution T G splice_region_variant COCA-CN 4 85709725 85709725 single base substitution C T intron_variant COCA-CN 4 85715721 85715721 single base substitution T G missense_variant K1146N 3438A>C COCA-CN 4 85715917 85715917 single base substitution C A intron_variant COCA-CN 4 85715975 85715975 single base substitution A C intron_variant COCA-CN 4 85729458 85729458 single base substitution G A downstream_gene_variant COCA-CN 4 85729458 85729458 single base substitution G A intron_variant COCA-CN 4 85729458 85729458 single base substitution G A upstream_gene_variant COCA-CN 4 85729509 85729509 single base substitution T C downstream_gene_variant COCA-CN 4 85729509 85729509 single base substitution T C intron_variant COCA-CN 4 85729509 85729509 single base substitution T C missense_variant T803A 2407A>G COCA-CN 4 85729509 85729509 single base substitution T C upstream_gene_variant COCA-CN 4 85729570 85729570 single base substitution A T downstream_gene_variant COCA-CN 4 85729570 85729570 single base substitution A T intron_variant COCA-CN 4 85729570 85729570 single base substitution A T missense_variant S782R 2346T>A COCA-CN 4 85729570 85729570 single base substitution A T upstream_gene_variant COCA-CN 4 85730875 85730875 single base substitution A G exon_variant COCA-CN 4 85730875 85730875 single base substitution A G intron_variant COCA-CN 4 85742532 85742532 single base substitution C A exon_variant COCA-CN 4 85742532 85742532 single base substitution C A missense_variant E432D 1296G>T COCA-CN 4 85748033 85748033 single base substitution G A exon_variant COCA-CN 4 85748033 85748033 single base substitution G A missense_variant A353V 1058C>T COCA-CN 4 85758108 85758108 single base substitution C T downstream_gene_variant COCA-CN 4 85758108 85758108 single base substitution C T exon_variant COCA-CN 4 85758108 85758108 single base substitution C T missense_variant G184R 550G>A COCA-CN 4 85762403 85762403 single base substitution C A exon_variant COCA-CN 4 85762403 85762403 single base substitution C A synonymous_variant R106R 318G>T COCA-CN 4 85762403 85762403 single base substitution C A synonymous_variant R60R 180G>T COCA-CN 4 85762452 85762452 single base substitution A C intron_variant COCA-CN 4 85765541 85765541 single base substitution T C intron_variant COCA-CN 4 85765669 85765669 single base substitution A T intron_variant COCA-CN 4 85765669 85765669 single base substitution A T splice_region_variant COCA-CN 4 85781623 85781623 single base substitution T G downstream_gene_variant COCA-CN 4 85781623 85781623 single base substitution T G exon_variant COCA-CN 4 85781623 85781623 single base substitution T G missense_variant H41P 122A>C COCA-CN 4 85837858 85837858 single base substitution C A intron_variant COCA-CN 4 85843506 85843506 single base substitution C T intron_variant COCA-CN 4 85847091 85847091 single base substitution T C intron_variant EOPC-DE 4 85591650 85591650 single base substitution A T 3_prime_UTR_variant EOPC-DE 4 85591650 85591650 single base substitution A T downstream_gene_variant EOPC-DE 4 85610237 85610237 single base substitution A G downstream_gene_variant EOPC-DE 4 85610237 85610237 single base substitution A G intron_variant EOPC-DE 4 85657280 85657280 single base substitution C T intron_variant EOPC-DE 4 85657280 85657280 single base substitution C T upstream_gene_variant EOPC-DE 4 85675517 85675517 single base substitution T C intron_variant EOPC-DE 4 85697962 85697962 single base substitution C G intron_variant EOPC-DE 4 85702913 85702913 single base substitution T C intron_variant EOPC-DE 4 85756179 85756179 single base substitution A G intron_variant EOPC-DE 4 85768974 85768974 single base substitution C A downstream_gene_variant EOPC-DE 4 85768974 85768974 single base substitution C A intron_variant EOPC-DE 4 85820214 85820214 single base substitution C T intron_variant EOPC-DE 4 85820214 85820214 single base substitution C T upstream_gene_variant EOPC-DE 4 85822222 85822222 single base substitution C T intron_variant EOPC-DE 4 85822222 85822222 single base substitution C T upstream_gene_variant EOPC-DE 4 85826237 85826237 single base substitution T C intron_variant ESAD-UK 4 85586191 85586191 single base substitution G A downstream_gene_variant ESAD-UK 4 85589656 85589656 single base substitution G T downstream_gene_variant ESAD-UK 4 85589813 85589813 single base substitution G A downstream_gene_variant ESAD-UK 4 85590292 85590292 insertion of <=200bp - AT downstream_gene_variant ESAD-UK 4 85590293 85590293 single base substitution C T downstream_gene_variant ESAD-UK 4 85590695 85590695 single base substitution C G downstream_gene_variant ESAD-UK 4 85591473 85591473 single base substitution A T 3_prime_UTR_variant ESAD-UK 4 85591473 85591473 single base substitution A T downstream_gene_variant ESAD-UK 4 85592076 85592076 single base substitution C G 3_prime_UTR_variant ESAD-UK 4 85592076 85592076 single base substitution C G downstream_gene_variant ESAD-UK 4 85592646 85592646 insertion of <=200bp - TA 3_prime_UTR_variant ESAD-UK 4 85592646 85592646 insertion of <=200bp - TA downstream_gene_variant ESAD-UK 4 85592834 85592834 single base substitution A T 3_prime_UTR_variant ESAD-UK 4 85592834 85592834 single base substitution A T downstream_gene_variant ESAD-UK 4 85595027 85595027 single base substitution C T intron_variant ESAD-UK 4 85596404 85596404 single base substitution C T intron_variant ESAD-UK 4 85598752 85598752 single base substitution C A intron_variant ESAD-UK 4 85598926 85598926 single base substitution G C intron_variant ESAD-UK 4 85599891 85599891 single base substitution C G intron_variant ESAD-UK 4 85600993 85601000 deletion of <=200bp ATACACAC - intron_variant ESAD-UK 4 85601028 85601028 insertion of <=200bp - TATA intron_variant ESAD-UK 4 85601859 85601859 single base substitution A T intron_variant ESAD-UK 4 85602680 85602680 single base substitution A G intron_variant ESAD-UK 4 85603638 85603638 single base substitution G C exon_variant ESAD-UK 4 85603638 85603638 single base substitution G C intron_variant ESAD-UK 4 85604979 85604979 single base substitution C A intron_variant ESAD-UK 4 85604979 85604979 single base substitution C A upstream_gene_variant ESAD-UK 4 85605534 85605534 single base substitution C T intron_variant ESAD-UK 4 85605534 85605534 single base substitution C T upstream_gene_variant ESAD-UK 4 85608116 85608116 single base substitution T G downstream_gene_variant ESAD-UK 4 85608116 85608116 single base substitution T G intron_variant ESAD-UK 4 85608116 85608116 single base substitution T G upstream_gene_variant ESAD-UK 4 85608150 85608150 single base substitution C T downstream_gene_variant ESAD-UK 4 85608150 85608150 single base substitution C T intron_variant ESAD-UK 4 85608150 85608150 single base substitution C T upstream_gene_variant ESAD-UK 4 85608653 85608653 single base substitution C T downstream_gene_variant ESAD-UK 4 85608653 85608653 single base substitution C T intron_variant ESAD-UK 4 85608653 85608653 single base substitution C T upstream_gene_variant ESAD-UK 4 85610802 85610802 single base substitution A G downstream_gene_variant ESAD-UK 4 85610802 85610802 single base substitution A G intron_variant ESAD-UK 4 85611674 85611674 single base substitution G A downstream_gene_variant ESAD-UK 4 85611674 85611674 single base substitution G A synonymous_variant T3099T 9297C>T ESAD-UK 4 85611674 85611674 single base substitution G A synonymous_variant T3116T 9348C>T ESAD-UK 4 85611952 85611952 single base substitution G A downstream_gene_variant ESAD-UK 4 85611952 85611952 single base substitution G A intron_variant ESAD-UK 4 85612572 85612572 single base substitution C T downstream_gene_variant ESAD-UK 4 85612572 85612572 single base substitution C T intron_variant ESAD-UK 4 85614047 85614047 single base substitution G T missense_variant P2997T 8989C>A ESAD-UK 4 85614047 85614047 single base substitution G T missense_variant P3014T 9040C>A ESAD-UK 4 85614047 85614047 single base substitution G T missense_variant P617T 1849C>A ESAD-UK 4 85614920 85614920 single base substitution C T intron_variant ESAD-UK 4 85615244 85615244 deletion of <=200bp A - intron_variant ESAD-UK 4 85615407 85615407 single base substitution C A intron_variant ESAD-UK 4 85616261 85616261 single base substitution G T intron_variant ESAD-UK 4 85620828 85620828 single base substitution A C intron_variant ESAD-UK 4 85621513 85621513 single base substitution C T intron_variant ESAD-UK 4 85622523 85622523 single base substitution A T intron_variant ESAD-UK 4 85625282 85625282 single base substitution A G intron_variant ESAD-UK 4 85626043 85626043 single base substitution C T intron_variant ESAD-UK 4 85626763 85626763 single base substitution C T intron_variant ESAD-UK 4 85627092 85627092 single base substitution C T intron_variant ESAD-UK 4 85628392 85628392 single base substitution T C intron_variant ESAD-UK 4 85628580 85628580 single base substitution C T intron_variant ESAD-UK 4 85629086 85629086 single base substitution C T intron_variant ESAD-UK 4 85632853 85632853 single base substitution A C intron_variant ESAD-UK 4 85634017 85634017 single base substitution A T intron_variant ESAD-UK 4 85635205 85635205 single base substitution G A intron_variant ESAD-UK 4 85635771 85635771 single base substitution T C intron_variant ESAD-UK 4 85637139 85637139 single base substitution A T intron_variant ESAD-UK 4 85640026 85640026 single base substitution A C intron_variant ESAD-UK 4 85640591 85640591 single base substitution A T intron_variant ESAD-UK 4 85641094 85641094 single base substitution C A intron_variant ESAD-UK 4 85642503 85642503 single base substitution T G intron_variant ESAD-UK 4 85643047 85643047 single base substitution T C intron_variant ESAD-UK 4 85646924 85646924 single base substitution T A intron_variant ESAD-UK 4 85648117 85648117 single base substitution A G intron_variant ESAD-UK 4 85650812 85650812 single base substitution A C intron_variant ESAD-UK 4 85655384 85655384 single base substitution T C downstream_gene_variant ESAD-UK 4 85655384 85655384 single base substitution T C intron_variant ESAD-UK 4 85655384 85655384 single base substitution T C upstream_gene_variant ESAD-UK 4 85655425 85655425 single base substitution C T downstream_gene_variant ESAD-UK 4 85655425 85655425 single base substitution C T intron_variant ESAD-UK 4 85655425 85655425 single base substitution C T upstream_gene_variant ESAD-UK 4 85657738 85657738 single base substitution C T intron_variant ESAD-UK 4 85657738 85657738 single base substitution C T upstream_gene_variant ESAD-UK 4 85661264 85661264 single base substitution C A intron_variant ESAD-UK 4 85661264 85661264 single base substitution C A upstream_gene_variant ESAD-UK 4 85661792 85661792 deletion of <=200bp G - intron_variant ESAD-UK 4 85661792 85661792 deletion of <=200bp G - upstream_gene_variant ESAD-UK 4 85661965 85661965 single base substitution G A intron_variant ESAD-UK 4 85661965 85661965 single base substitution G A upstream_gene_variant ESAD-UK 4 85661965 85661965 single base substitution G T intron_variant ESAD-UK 4 85661965 85661965 single base substitution G T upstream_gene_variant ESAD-UK 4 85662549 85662549 single base substitution C A intron_variant ESAD-UK 4 85662549 85662549 single base substitution C A upstream_gene_variant ESAD-UK 4 85664421 85664421 deletion of <=200bp A - intron_variant ESAD-UK 4 85664421 85664421 deletion of <=200bp A - upstream_gene_variant ESAD-UK 4 85665049 85665049 single base substitution A T intron_variant ESAD-UK 4 85665049 85665049 single base substitution A T upstream_gene_variant ESAD-UK 4 85665107 85665107 single base substitution A T intron_variant ESAD-UK 4 85665107 85665107 single base substitution A T upstream_gene_variant ESAD-UK 4 85665335 85665335 single base substitution T A intron_variant ESAD-UK 4 85665335 85665335 single base substitution T A upstream_gene_variant ESAD-UK 4 85668380 85668380 single base substitution A G downstream_gene_variant ESAD-UK 4 85668380 85668380 single base substitution A G intron_variant ESAD-UK 4 85669152 85669152 single base substitution G A downstream_gene_variant ESAD-UK 4 85669152 85669152 single base substitution G A intron_variant ESAD-UK 4 85669275 85669275 single base substitution T A downstream_gene_variant ESAD-UK 4 85669275 85669275 single base substitution T A intron_variant ESAD-UK 4 85669884 85669884 single base substitution T C downstream_gene_variant ESAD-UK 4 85669884 85669884 single base substitution T C intron_variant ESAD-UK 4 85671079 85671079 insertion of <=200bp - A downstream_gene_variant ESAD-UK 4 85671079 85671079 insertion of <=200bp - A intron_variant ESAD-UK 4 85671228 85671228 single base substitution T A downstream_gene_variant ESAD-UK 4 85671228 85671228 single base substitution T A intron_variant ESAD-UK 4 85672205 85672205 single base substitution G C downstream_gene_variant ESAD-UK 4 85672205 85672205 single base substitution G C intron_variant ESAD-UK 4 85673160 85673160 single base substitution A T intron_variant ESAD-UK 4 85673233 85673233 single base substitution A C intron_variant ESAD-UK 4 85674692 85674692 single base substitution C T intron_variant ESAD-UK 4 85674702 85674702 single base substitution T C intron_variant ESAD-UK 4 85682827 85682827 single base substitution C A intron_variant ESAD-UK 4 85684655 85684655 single base substitution T G intron_variant ESAD-UK 4 85685148 85685148 single base substitution A G intron_variant ESAD-UK 4 85685426 85685426 single base substitution C A intron_variant ESAD-UK 4 85686283 85686283 single base substitution G A intron_variant ESAD-UK 4 85687802 85687802 single base substitution G A intron_variant ESAD-UK 4 85688541 85688541 single base substitution T A intron_variant ESAD-UK 4 85689462 85689462 single base substitution T C intron_variant ESAD-UK 4 85690854 85690854 single base substitution C G intron_variant ESAD-UK 4 85690941 85690941 single base substitution A G intron_variant ESAD-UK 4 85691160 85691160 deletion of <=200bp A - intron_variant ESAD-UK 4 85691786 85691786 single base substitution T C intron_variant ESAD-UK 4 85692284 85692284 single base substitution C G intron_variant ESAD-UK 4 85693184 85693184 single base substitution A C intron_variant ESAD-UK 4 85693436 85693436 single base substitution A G intron_variant ESAD-UK 4 85693856 85693856 single base substitution C T intron_variant ESAD-UK 4 85694054 85694054 single base substitution G C missense_variant P1595A 4783C>G ESAD-UK 4 85694184 85694184 single base substitution A C intron_variant ESAD-UK 4 85697033 85697033 single base substitution A C intron_variant ESAD-UK 4 85698632 85698632 single base substitution T G intron_variant ESAD-UK 4 85698650 85698650 single base substitution A T intron_variant ESAD-UK 4 85700734 85700734 single base substitution T G intron_variant ESAD-UK 4 85701359 85701359 single base substitution C T missense_variant D1423N 4267G>A ESAD-UK 4 85703066 85703066 single base substitution G A intron_variant ESAD-UK 4 85705322 85705322 single base substitution T G intron_variant ESAD-UK 4 85706210 85706210 single base substitution C A intron_variant ESAD-UK 4 85707919 85707919 single base substitution T C intron_variant ESAD-UK 4 85708235 85708235 single base substitution A G intron_variant ESAD-UK 4 85710772 85710772 single base substitution A T intron_variant ESAD-UK 4 85713563 85713563 single base substitution C T intron_variant ESAD-UK 4 85714226 85714226 single base substitution A T intron_variant ESAD-UK 4 85714766 85714766 single base substitution A G intron_variant ESAD-UK 4 85715115 85715115 single base substitution G C intron_variant ESAD-UK 4 85715241 85715241 single base substitution T C intron_variant ESAD-UK 4 85716111 85716111 single base substitution C A missense_variant L1063F 3189G>T ESAD-UK 4 85717452 85717452 single base substitution A G intron_variant ESAD-UK 4 85718966 85718966 single base substitution C T downstream_gene_variant ESAD-UK 4 85718966 85718966 single base substitution C T intron_variant ESAD-UK 4 85719681 85719681 single base substitution G T downstream_gene_variant ESAD-UK 4 85719681 85719681 single base substitution G T intron_variant ESAD-UK 4 85720238 85720238 single base substitution G A downstream_gene_variant ESAD-UK 4 85720238 85720238 single base substitution G A intron_variant ESAD-UK 4 85720308 85720308 single base substitution C T downstream_gene_variant ESAD-UK 4 85720308 85720308 single base substitution C T intron_variant ESAD-UK 4 85720494 85720494 single base substitution T A downstream_gene_variant ESAD-UK 4 85720494 85720494 single base substitution T A intron_variant ESAD-UK 4 85720495 85720495 single base substitution T A downstream_gene_variant ESAD-UK 4 85720495 85720495 single base substitution T A intron_variant ESAD-UK 4 85721085 85721085 single base substitution G T downstream_gene_variant ESAD-UK 4 85721085 85721085 single base substitution G T intron_variant ESAD-UK 4 85723094 85723094 single base substitution A G intron_variant ESAD-UK 4 85723652 85723652 single base substitution A C intron_variant ESAD-UK 4 85725858 85725858 insertion of <=200bp - A downstream_gene_variant ESAD-UK 4 85725858 85725858 insertion of <=200bp - A intron_variant ESAD-UK 4 85725858 85725858 insertion of <=200bp - A upstream_gene_variant ESAD-UK 4 85726427 85726427 single base substitution A C downstream_gene_variant ESAD-UK 4 85726427 85726427 single base substitution A C intron_variant ESAD-UK 4 85726427 85726427 single base substitution A C upstream_gene_variant ESAD-UK 4 85727564 85727564 single base substitution C G downstream_gene_variant ESAD-UK 4 85727564 85727564 single base substitution C G intron_variant ESAD-UK 4 85727564 85727564 single base substitution C G upstream_gene_variant ESAD-UK 4 85727981 85727981 single base substitution T G downstream_gene_variant ESAD-UK 4 85727981 85727981 single base substitution T G intron_variant ESAD-UK 4 85727981 85727981 single base substitution T G upstream_gene_variant ESAD-UK 4 85729349 85729349 single base substitution C G downstream_gene_variant ESAD-UK 4 85729349 85729349 single base substitution C G intron_variant ESAD-UK 4 85729349 85729349 single base substitution C G upstream_gene_variant ESAD-UK 4 85730155 85730155 single base substitution G T exon_variant ESAD-UK 4 85730155 85730155 single base substitution G T intron_variant ESAD-UK 4 85730155 85730155 single base substitution G T upstream_gene_variant ESAD-UK 4 85732105 85732105 deletion of <=200bp A - intron_variant ESAD-UK 4 85732105 85732105 deletion of <=200bp A - upstream_gene_variant ESAD-UK 4 85732572 85732572 single base substitution G A intron_variant ESAD-UK 4 85732572 85732572 single base substitution G A upstream_gene_variant ESAD-UK 4 85732976 85732976 single base substitution G C intron_variant ESAD-UK 4 85732976 85732976 single base substitution G C upstream_gene_variant ESAD-UK 4 85733127 85733127 single base substitution A C intron_variant ESAD-UK 4 85733127 85733127 single base substitution A C upstream_gene_variant ESAD-UK 4 85737215 85737215 single base substitution T G intron_variant ESAD-UK 4 85737615 85737615 single base substitution G A intron_variant ESAD-UK 4 85739210 85739210 single base substitution A T intron_variant ESAD-UK 4 85739223 85739223 single base substitution G A intron_variant ESAD-UK 4 85740620 85740620 single base substitution A C intron_variant ESAD-UK 4 85740633 85740633 single base substitution T G intron_variant ESAD-UK 4 85741520 85741520 single base substitution C A intron_variant ESAD-UK 4 85744518 85744518 single base substitution T C intron_variant ESAD-UK 4 85745872 85745872 single base substitution A G intron_variant ESAD-UK 4 85746065 85746065 single base substitution T C intron_variant ESAD-UK 4 85746206 85746206 single base substitution C A intron_variant ESAD-UK 4 85748286 85748286 single base substitution C G intron_variant ESAD-UK 4 85749201 85749201 single base substitution C T intron_variant ESAD-UK 4 85749631 85749631 single base substitution C T intron_variant ESAD-UK 4 85751323 85751323 single base substitution T A intron_variant ESAD-UK 4 85752028 85752028 single base substitution A T intron_variant ESAD-UK 4 85753427 85753427 single base substitution G A intron_variant ESAD-UK 4 85753551 85753551 single base substitution A G intron_variant ESAD-UK 4 85753590 85753590 insertion of <=200bp - A intron_variant ESAD-UK 4 85754841 85754841 single base substitution A G intron_variant ESAD-UK 4 85754842 85754846 deletion of <=200bp AAGAG - intron_variant ESAD-UK 4 85755803 85755803 deletion of <=200bp A - intron_variant ESAD-UK 4 85758247 85758247 single base substitution G A downstream_gene_variant ESAD-UK 4 85758247 85758247 single base substitution G A splice_region_variant ESAD-UK 4 85758272 85758272 single base substitution T A downstream_gene_variant ESAD-UK 4 85758272 85758272 single base substitution T A intron_variant ESAD-UK 4 85758724 85758724 single base substitution A G downstream_gene_variant ESAD-UK 4 85758724 85758724 single base substitution A G intron_variant ESAD-UK 4 85759849 85759849 single base substitution C T downstream_gene_variant ESAD-UK 4 85759849 85759849 single base substitution C T intron_variant ESAD-UK 4 85761204 85761204 single base substitution A C downstream_gene_variant ESAD-UK 4 85761204 85761204 single base substitution A C intron_variant ESAD-UK 4 85764480 85764480 insertion of <=200bp - A intron_variant ESAD-UK 4 85764579 85764579 single base substitution G C intron_variant ESAD-UK 4 85771798 85771798 single base substitution G T intron_variant ESAD-UK 4 85771798 85771798 single base substitution G T upstream_gene_variant ESAD-UK 4 85774449 85774449 single base substitution G C intron_variant ESAD-UK 4 85774449 85774449 single base substitution G C upstream_gene_variant ESAD-UK 4 85774468 85774468 single base substitution C A intron_variant ESAD-UK 4 85774468 85774468 single base substitution C A upstream_gene_variant ESAD-UK 4 85783643 85783643 single base substitution C T intron_variant ESAD-UK 4 85783643 85783643 single base substitution C T upstream_gene_variant ESAD-UK 4 85783848 85783848 single base substitution T A intron_variant ESAD-UK 4 85783848 85783848 single base substitution T A upstream_gene_variant ESAD-UK 4 85784732 85784732 single base substitution C T intron_variant ESAD-UK 4 85784732 85784732 single base substitution C T upstream_gene_variant ESAD-UK 4 85785629 85785629 single base substitution A G intron_variant ESAD-UK 4 85785629 85785629 single base substitution A G upstream_gene_variant ESAD-UK 4 85786526 85786526 single base substitution C A intron_variant ESAD-UK 4 85786526 85786526 single base substitution C A upstream_gene_variant ESAD-UK 4 85787060 85787060 insertion of <=200bp - A intron_variant ESAD-UK 4 85787317 85787317 single base substitution A G intron_variant ESAD-UK 4 85787318 85787318 single base substitution A G intron_variant ESAD-UK 4 85788499 85788499 single base substitution G A intron_variant ESAD-UK 4 85794016 85794016 single base substitution A T intron_variant ESAD-UK 4 85794818 85794818 insertion of <=200bp - A intron_variant ESAD-UK 4 85795499 85795499 single base substitution G A intron_variant ESAD-UK 4 85796349 85796349 single base substitution A C intron_variant ESAD-UK 4 85799136 85799136 single base substitution T G intron_variant ESAD-UK 4 85800410 85800410 single base substitution G C intron_variant ESAD-UK 4 85806846 85806846 single base substitution C A intron_variant ESAD-UK 4 85807268 85807268 single base substitution C G intron_variant ESAD-UK 4 85807796 85807796 single base substitution A T intron_variant ESAD-UK 4 85812447 85812447 single base substitution C A intron_variant ESAD-UK 4 85812551 85812551 single base substitution C G intron_variant ESAD-UK 4 85818991 85818991 single base substitution C T intron_variant ESAD-UK 4 85818991 85818991 single base substitution C T upstream_gene_variant ESAD-UK 4 85819213 85819213 single base substitution A C intron_variant ESAD-UK 4 85819213 85819213 single base substitution A C upstream_gene_variant ESAD-UK 4 85820152 85820152 single base substitution T C intron_variant ESAD-UK 4 85820152 85820152 single base substitution T C upstream_gene_variant ESAD-UK 4 85820473 85820473 single base substitution G C intron_variant ESAD-UK 4 85820473 85820473 single base substitution G C upstream_gene_variant ESAD-UK 4 85822307 85822307 single base substitution A G intron_variant ESAD-UK 4 85822307 85822307 single base substitution A G upstream_gene_variant ESAD-UK 4 85822567 85822567 single base substitution G A intron_variant ESAD-UK 4 85822567 85822567 single base substitution G A upstream_gene_variant ESAD-UK 4 85825424 85825424 single base substitution G A intron_variant ESAD-UK 4 85826179 85826179 single base substitution G A intron_variant ESAD-UK 4 85827636 85827636 single base substitution A T intron_variant ESAD-UK 4 85831857 85831857 deletion of <=200bp T - intron_variant ESAD-UK 4 85831996 85831996 single base substitution T A intron_variant ESAD-UK 4 85832455 85832455 single base substitution C T intron_variant ESAD-UK 4 85832486 85832486 deletion of <=200bp A - intron_variant ESAD-UK 4 85832531 85832531 single base substitution T G intron_variant ESAD-UK 4 85834277 85834277 single base substitution G T intron_variant ESAD-UK 4 85834616 85834616 single base substitution G A intron_variant ESAD-UK 4 85835753 85835753 single base substitution T C intron_variant ESAD-UK 4 85839988 85839988 single base substitution A G intron_variant ESAD-UK 4 85843043 85843043 single base substitution C T intron_variant ESAD-UK 4 85843563 85843563 single base substitution T A intron_variant ESAD-UK 4 85844313 85844313 deletion of <=200bp A - intron_variant ESAD-UK 4 85846221 85846221 single base substitution T G intron_variant ESAD-UK 4 85846916 85846916 single base substitution A C intron_variant ESAD-UK 4 85847523 85847523 single base substitution C T intron_variant ESAD-UK 4 85847857 85847857 single base substitution C T intron_variant ESAD-UK 4 85848675 85848675 single base substitution G A intron_variant ESAD-UK 4 85849675 85849675 single base substitution T C intron_variant ESAD-UK 4 85850785 85850785 single base substitution G A intron_variant ESAD-UK 4 85851062 85851062 single base substitution T C intron_variant ESAD-UK 4 85852293 85852293 single base substitution G T intron_variant ESAD-UK 4 85852983 85852983 single base substitution A G intron_variant ESAD-UK 4 85854591 85854591 single base substitution A G intron_variant ESAD-UK 4 85857086 85857086 single base substitution G A intron_variant ESAD-UK 4 85859576 85859576 single base substitution C T intron_variant ESAD-UK 4 85859684 85859684 single base substitution G C intron_variant ESAD-UK 4 85860488 85860488 single base substitution G A intron_variant ESAD-UK 4 85862554 85862554 single base substitution C G intron_variant ESAD-UK 4 85864354 85864354 single base substitution C T intron_variant ESAD-UK 4 85866164 85866164 single base substitution T C intron_variant ESAD-UK 4 85868799 85868799 single base substitution A G intron_variant ESAD-UK 4 85870677 85870677 single base substitution T A intron_variant ESAD-UK 4 85876679 85876679 single base substitution C T intron_variant ESAD-UK 4 85879583 85879583 single base substitution T A intron_variant ESAD-UK 4 85881682 85881682 single base substitution C T intron_variant ESAD-UK 4 85884123 85884123 single base substitution G A intron_variant ESAD-UK 4 85884484 85884484 single base substitution C T intron_variant ESAD-UK 4 85885644 85885647 deletion of <=200bp AATT - intron_variant ESAD-UK 4 85885830 85885830 deletion of <=200bp T - intron_variant ESAD-UK 4 85886209 85886209 single base substitution T A intron_variant ESAD-UK 4 85886868 85886868 single base substitution G A intron_variant ESAD-UK 4 85888754 85888754 single base substitution A G upstream_gene_variant ESAD-UK 4 85889356 85889356 single base substitution A G upstream_gene_variant ESAD-UK 4 85891803 85891803 single base substitution C G upstream_gene_variant ESCA-CN 4 85696066 85696066 single base substitution C T missense_variant R1554Q 4661G>A ESCA-CN 4 85742430 85742430 single base substitution G C exon_variant ESCA-CN 4 85742430 85742430 single base substitution G C synonymous_variant V466V 1398C>G GBM-US 4 85611704 85611704 single base substitution C G downstream_gene_variant GBM-US 4 85611704 85611704 single base substitution C G missense_variant E3089D 9267G>C GBM-US 4 85611704 85611704 single base substitution C G missense_variant E3106D 9318G>C GBM-US 4 85634313 85634313 single base substitution C T missense_variant G2664R 7990G>A GBM-US 4 85634313 85634313 single base substitution C T missense_variant G2681R 8041G>A GBM-US 4 85634313 85634313 single base substitution C T missense_variant G284R 850G>A GBM-US 4 85657415 85657415 single base substitution G A exon_variant GBM-US 4 85657415 85657415 single base substitution G A missense_variant R2275C 6823C>T GBM-US 4 85657415 85657415 single base substitution G A upstream_gene_variant KIRC-US 4 85611661 85611661 insertion of <=200bp - T downstream_gene_variant KIRC-US 4 85611661 85611661 insertion of <=200bp - T frameshift_variant Q3104Q? KIRC-US 4 85611661 85611661 insertion of <=200bp - T frameshift_variant Q3121Q? KIRC-US 4 85642627 85642627 single base substitution A T missense_variant S117T 349T>A KIRC-US 4 85642627 85642627 single base substitution A T missense_variant S2497T 7489T>A KIRC-US 4 85642627 85642627 single base substitution A T missense_variant S2514T 7540T>A KIRC-US 4 85654653 85654653 single base substitution T A downstream_gene_variant KIRC-US 4 85654653 85654653 single base substitution T A missense_variant K2368M 7103A>T KIRC-US 4 85654653 85654653 single base substitution T A upstream_gene_variant KIRC-US 4 85664902 85664902 single base substitution G A synonymous_variant Y2008Y 6024C>T KIRC-US 4 85664902 85664902 single base substitution G A upstream_gene_variant KIRC-US 4 85674870 85674870 single base substitution T C exon_variant KIRC-US 4 85674870 85674870 single base substitution T C missense_variant I1907V 5719A>G KIRC-US 4 85722980 85722980 single base substitution A G exon_variant KIRC-US 4 85722980 85722980 single base substitution A G missense_variant L882S 2645T>C KIRC-US 4 85724467 85724467 single base substitution A T exon_variant KIRC-US 4 85724467 85724467 single base substitution A T synonymous_variant S861S 2583T>A KIRC-US 4 85742692 85742692 single base substitution C G exon_variant KIRC-US 4 85742692 85742692 single base substitution C G missense_variant R379T 1136G>C KIRC-US 4 85748120 85748120 single base substitution T C exon_variant KIRC-US 4 85748120 85748120 single base substitution T C missense_variant K324R 971A>G KIRC-US 4 85758222 85758222 single base substitution T C downstream_gene_variant KIRC-US 4 85758222 85758222 single base substitution T C exon_variant KIRC-US 4 85758222 85758222 single base substitution T C missense_variant T146A 436A>G KIRP-US 4 85630153 85630153 deletion of <=200bp A - frameshift_variant L2692 KIRP-US 4 85630153 85630153 deletion of <=200bp A - frameshift_variant L2709 KIRP-US 4 85630153 85630153 deletion of <=200bp A - frameshift_variant L312 KIRP-US 4 85675021 85675021 single base substitution T C exon_variant KIRP-US 4 85675021 85675021 single base substitution T C synonymous_variant Q1856Q 5568A>G KIRP-US 4 85716095 85716095 single base substitution G T missense_variant P1069T 3205C>A KIRP-US 4 85722839 85722839 single base substitution C A downstream_gene_variant KIRP-US 4 85722839 85722839 single base substitution C A missense_variant R929L 2786G>T KIRP-US 4 85781624 85781624 single base substitution G A downstream_gene_variant KIRP-US 4 85781624 85781624 single base substitution G A exon_variant KIRP-US 4 85781624 85781624 single base substitution G A missense_variant H41Y 121C>T LAML-CN 4 85645725 85645725 single base substitution G C missense_variant A2415G 7244C>G LAML-CN 4 85645725 85645725 single base substitution G C missense_variant A2432G 7295C>G LAML-CN 4 85645725 85645725 single base substitution G C missense_variant A35G 104C>G LAML-KR 4 85588887 85588887 single base substitution G T downstream_gene_variant LAML-KR 4 85644972 85644972 single base substitution A G intron_variant LAML-KR 4 85681807 85681807 single base substitution C T intron_variant LAML-KR 4 85723662 85723662 single base substitution A C intron_variant LAML-KR 4 85763624 85763624 single base substitution T C intron_variant LAML-KR 4 85803886 85803886 single base substitution G T intron_variant LGG-US 4 85600267 85600267 single base substitution C T exon_variant LGG-US 4 85600267 85600267 single base substitution C T missense_variant A3301T 9901G>A LGG-US 4 85600267 85600267 single base substitution C T missense_variant A3318T 9952G>A LGG-US 4 85612794 85612794 single base substitution T A downstream_gene_variant LGG-US 4 85612794 85612794 single base substitution T A missense_variant E3048V 9143A>T LGG-US 4 85612794 85612794 single base substitution T A missense_variant E3065V 9194A>T LGG-US 4 85612906 85612906 single base substitution T C missense_variant T3011A 9031A>G LGG-US 4 85612906 85612906 single base substitution T C missense_variant T3028A 9082A>G LGG-US 4 85612906 85612906 single base substitution T C missense_variant T631A 1891A>G LGG-US 4 85715705 85715708 deletion of <=200bp CAAT - frameshift_variant IV1151 LGG-US 4 85731329 85731331 deletion of <=200bp GAA - disruptive_inframe_deletion LH685H LGG-US 4 85731329 85731331 deletion of <=200bp GAA - exon_variant LGG-US 4 85731329 85731331 deletion of <=200bp GAA - upstream_gene_variant LICA-CN 4 85611702 85611702 single base substitution A T downstream_gene_variant LICA-CN 4 85611702 85611702 single base substitution A T missense_variant M3090K 9269T>A LICA-CN 4 85611702 85611702 single base substitution A T missense_variant M3107K 9320T>A LICA-CN 4 85638094 85638094 single base substitution T G synonymous_variant A213A 639A>C LICA-CN 4 85638094 85638094 single base substitution T G synonymous_variant A2593A 7779A>C LICA-CN 4 85638094 85638094 single base substitution T G synonymous_variant A2610A 7830A>C LICA-CN 4 85642679 85642679 single base substitution T A synonymous_variant G2479G 7437A>T LICA-CN 4 85642679 85642679 single base substitution T A synonymous_variant G2496G 7488A>T LICA-CN 4 85642679 85642679 single base substitution T A synonymous_variant G99G 297A>T LICA-CN 4 85672726 85672726 single base substitution G A exon_variant LICA-CN 4 85672726 85672726 single base substitution G A synonymous_variant F1961F 5883C>T LICA-CN 4 85672776 85672776 single base substitution A T exon_variant LICA-CN 4 85672776 85672776 single base substitution A T missense_variant C1945S 5833T>A LICA-CN 4 85738623 85738623 single base substitution G A exon_variant LICA-CN 4 85738623 85738623 single base substitution G A synonymous_variant D603D 1809C>T LICA-FR 4 85604858 85604858 single base substitution G A intron_variant LICA-FR 4 85604858 85604858 single base substitution G A upstream_gene_variant LICA-FR 4 85607375 85607375 single base substitution C T intron_variant LICA-FR 4 85607375 85607375 single base substitution C T upstream_gene_variant LICA-FR 4 85629437 85629437 single base substitution T C intron_variant LICA-FR 4 85634369 85634369 single base substitution A G missense_variant L2645P 7934T>C LICA-FR 4 85634369 85634369 single base substitution A G missense_variant L265P 794T>C LICA-FR 4 85634369 85634369 single base substitution A G missense_variant L2662P 7985T>C LICA-FR 4 85641076 85641076 single base substitution T G intron_variant LICA-FR 4 85661343 85661343 single base substitution C T missense_variant G2154E 6461G>A LICA-FR 4 85661343 85661343 single base substitution C T upstream_gene_variant LICA-FR 4 85663030 85663030 single base substitution C T missense_variant V2040I 6118G>A LICA-FR 4 85663030 85663030 single base substitution C T upstream_gene_variant LICA-FR 4 85678650 85678650 single base substitution C T intron_variant LICA-FR 4 85678650 85678650 single base substitution C T upstream_gene_variant LICA-FR 4 85681644 85681644 single base substitution T A intron_variant LICA-FR 4 85704172 85704172 single base substitution G A missense_variant A1373V 4118C>T LICA-FR 4 85715718 85715718 single base substitution G T missense_variant D1147E 3441C>A LICA-FR 4 85726478 85726478 single base substitution A G downstream_gene_variant LICA-FR 4 85726478 85726478 single base substitution A G intron_variant LICA-FR 4 85726478 85726478 single base substitution A G upstream_gene_variant LICA-FR 4 85727220 85727220 single base substitution C A downstream_gene_variant LICA-FR 4 85727220 85727220 single base substitution C A intron_variant LICA-FR 4 85727220 85727220 single base substitution C A upstream_gene_variant LICA-FR 4 85742326 85742326 single base substitution C T exon_variant LICA-FR 4 85742326 85742326 single base substitution C T missense_variant R501K 1502G>A LICA-FR 4 85746511 85746511 deletion of <=200bp T - intron_variant LICA-FR 4 85748252 85748252 single base substitution T C intron_variant LICA-FR 4 85753133 85753133 single base substitution C A intron_variant LICA-FR 4 85760176 85760176 single base substitution G A downstream_gene_variant LICA-FR 4 85760176 85760176 single base substitution G A intron_variant LICA-FR 4 85767833 85767833 single base substitution G T downstream_gene_variant LICA-FR 4 85767833 85767833 single base substitution G T intron_variant LICA-FR 4 85774795 85774795 single base substitution T C intron_variant LICA-FR 4 85774795 85774795 single base substitution T C upstream_gene_variant LICA-FR 4 85790395 85790395 single base substitution T C intron_variant LICA-FR 4 85802007 85802007 single base substitution A G intron_variant LICA-FR 4 85804448 85804448 single base substitution T C intron_variant LICA-FR 4 85824195 85824195 single base substitution C T intron_variant LICA-FR 4 85830557 85830557 single base substitution A C intron_variant LICA-FR 4 85842079 85842079 single base substitution C A intron_variant LICA-FR 4 85851018 85851018 single base substitution C T intron_variant LICA-FR 4 85868668 85868668 insertion of <=200bp - AATAAT intron_variant LICA-FR 4 85878412 85878412 deletion of <=200bp A - intron_variant LIHC-US 4 85623579 85623579 single base substitution T G synonymous_variant A2824A 8472A>C LIHC-US 4 85623579 85623579 single base substitution T G synonymous_variant A2841A 8523A>C LIHC-US 4 85623579 85623579 single base substitution T G synonymous_variant A444A 1332A>C LIHC-US 4 85663040 85663040 single base substitution T C synonymous_variant G2036G 6108A>G LIHC-US 4 85663040 85663040 single base substitution T C upstream_gene_variant LIHC-US 4 85687056 85687056 single base substitution A G missense_variant S1699P 5095T>C LIHC-US 4 85707240 85707240 single base substitution T C synonymous_variant P1318P 3954A>G LIHC-US 4 85724505 85724505 single base substitution G A exon_variant LIHC-US 4 85724505 85724505 single base substitution G A missense_variant P849S 2545C>T LIHC-US 4 85731416 85731416 single base substitution A G exon_variant LIHC-US 4 85731416 85731416 single base substitution A G synonymous_variant L657L 1969T>C LIHC-US 4 85731416 85731416 single base substitution A G upstream_gene_variant LINC-JP 4 85599297 85599297 single base substitution A T intron_variant LINC-JP 4 85614950 85614950 single base substitution A C intron_variant LINC-JP 4 85619821 85619821 deletion of <=200bp A - intron_variant LINC-JP 4 85626612 85626612 single base substitution C A missense_variant G2740V 8219G>T LINC-JP 4 85626612 85626612 single base substitution C A missense_variant G2757V 8270G>T LINC-JP 4 85626612 85626612 single base substitution C A missense_variant G360V 1079G>T LINC-JP 4 85630484 85630484 single base substitution T C missense_variant T2670A 8008A>G LINC-JP 4 85630484 85630484 single base substitution T C missense_variant T2687A 8059A>G LINC-JP 4 85630484 85630484 single base substitution T C missense_variant T290A 868A>G LINC-JP 4 85638061 85638061 single base substitution T C synonymous_variant R224R 672A>G LINC-JP 4 85638061 85638061 single base substitution T C synonymous_variant R2604R 7812A>G LINC-JP 4 85638061 85638061 single base substitution T C synonymous_variant R2621R 7863A>G LINC-JP 4 85644158 85644158 single base substitution C A intron_variant LINC-JP 4 85649028 85649028 single base substitution T C intron_variant LINC-JP 4 85649722 85649722 single base substitution T C intron_variant LINC-JP 4 85662613 85662613 single base substitution G A intron_variant LINC-JP 4 85662613 85662613 single base substitution G A upstream_gene_variant LINC-JP 4 85666034 85666035 deletion of <=200bp GT - intron_variant LINC-JP 4 85673305 85673305 deletion of <=200bp A - intron_variant LINC-JP 4 85673569 85673569 single base substitution T G intron_variant LINC-JP 4 85678342 85678342 single base substitution T C intron_variant LINC-JP 4 85678342 85678342 single base substitution T C upstream_gene_variant LINC-JP 4 85687007 85687007 single base substitution T G missense_variant E1715A 5144A>C LINC-JP 4 85687048 85687048 single base substitution G C synonymous_variant L1701L 5103C>G LINC-JP 4 85687830 85687830 single base substitution T A intron_variant LINC-JP 4 85693982 85693982 single base substitution A G splice_region_variant LINC-JP 4 85703935 85703935 single base substitution G T intron_variant LINC-JP 4 85704183 85704183 single base substitution T C missense_variant I1369M 4107A>G LINC-JP 4 85708824 85708824 single base substitution T A missense_variant N1238Y 3712A>T LINC-JP 4 85711024 85711024 single base substitution A T missense_variant I1175N 3524T>A LINC-JP 4 85714928 85714928 single base substitution C A intron_variant LINC-JP 4 85715105 85715105 single base substitution A G intron_variant LINC-JP 4 85717709 85717709 single base substitution A G synonymous_variant A1044A 3132T>C LINC-JP 4 85721498 85721498 single base substitution G A downstream_gene_variant LINC-JP 4 85721498 85721498 single base substitution G A intron_variant LINC-JP 4 85724666 85724666 single base substitution T C intron_variant LINC-JP 4 85726702 85726702 single base substitution A G downstream_gene_variant LINC-JP 4 85726702 85726702 single base substitution A G intron_variant LINC-JP 4 85726702 85726702 single base substitution A G upstream_gene_variant LINC-JP 4 85733363 85733363 single base substitution G A intron_variant LINC-JP 4 85733363 85733363 single base substitution G A upstream_gene_variant LINC-JP 4 85748073 85748073 single base substitution T C exon_variant LINC-JP 4 85748073 85748073 single base substitution T C missense_variant T340A 1018A>G LINC-JP 4 85751745 85751745 single base substitution T A intron_variant LINC-JP 4 85759033 85759033 single base substitution G A downstream_gene_variant LINC-JP 4 85759033 85759033 single base substitution G A intron_variant LINC-JP 4 85762537 85762537 single base substitution A G intron_variant LINC-JP 4 85768636 85768636 single base substitution A G downstream_gene_variant LINC-JP 4 85768636 85768636 single base substitution A G intron_variant LINC-JP 4 85772531 85772531 single base substitution T A intron_variant LINC-JP 4 85772531 85772531 single base substitution T A upstream_gene_variant LINC-JP 4 85782417 85782417 single base substitution A T intron_variant LINC-JP 4 85782417 85782417 single base substitution A T upstream_gene_variant LINC-JP 4 85788603 85788603 single base substitution T C intron_variant LINC-JP 4 85796113 85796113 single base substitution T C intron_variant LINC-JP 4 85802738 85802738 insertion of <=200bp - A intron_variant LINC-JP 4 85818863 85818863 single base substitution G A intron_variant LINC-JP 4 85818863 85818863 single base substitution G A upstream_gene_variant LINC-JP 4 85822510 85822510 single base substitution C T intron_variant LINC-JP 4 85822510 85822510 single base substitution C T upstream_gene_variant LINC-JP 4 85836609 85836609 single base substitution T C intron_variant LINC-JP 4 85847307 85847307 single base substitution A G intron_variant LINC-JP 4 85862480 85862480 single base substitution T C intron_variant LINC-JP 4 85868077 85868077 single base substitution A G intron_variant LINC-JP 4 85882521 85882521 single base substitution A C intron_variant LIRI-JP 4 85585717 85585717 single base substitution C G downstream_gene_variant LIRI-JP 4 85586939 85586939 single base substitution T C downstream_gene_variant LIRI-JP 4 85588617 85588617 single base substitution C G downstream_gene_variant LIRI-JP 4 85592910 85592910 single base substitution A C 3_prime_UTR_variant LIRI-JP 4 85592910 85592910 single base substitution A C downstream_gene_variant LIRI-JP 4 85593142 85593142 single base substitution C T 3_prime_UTR_variant LIRI-JP 4 85593142 85593142 single base substitution C T downstream_gene_variant LIRI-JP 4 85594590 85594590 single base substitution A C intron_variant LIRI-JP 4 85596930 85596930 single base substitution T C intron_variant LIRI-JP 4 85597404 85597404 single base substitution C T intron_variant LIRI-JP 4 85599279 85599279 single base substitution G A intron_variant LIRI-JP 4 85602390 85602390 single base substitution C G intron_variant LIRI-JP 4 85605637 85605637 single base substitution T C intron_variant LIRI-JP 4 85605637 85605637 single base substitution T C upstream_gene_variant LIRI-JP 4 85606374 85606374 deletion of <=200bp C - intron_variant LIRI-JP 4 85606374 85606374 deletion of <=200bp C - upstream_gene_variant LIRI-JP 4 85606424 85606424 single base substitution C T intron_variant LIRI-JP 4 85606424 85606424 single base substitution C T upstream_gene_variant LIRI-JP 4 85611085 85611085 single base substitution T C downstream_gene_variant LIRI-JP 4 85611085 85611085 single base substitution T C intron_variant LIRI-JP 4 85611498 85611498 insertion of <=200bp - A downstream_gene_variant LIRI-JP 4 85611498 85611498 insertion of <=200bp - A intron_variant LIRI-JP 4 85612255 85612255 single base substitution C T downstream_gene_variant LIRI-JP 4 85612255 85612255 single base substitution C T intron_variant LIRI-JP 4 85613216 85613216 single base substitution G C intron_variant LIRI-JP 4 85616724 85616724 single base substitution T C intron_variant LIRI-JP 4 85621628 85621628 single base substitution A G intron_variant LIRI-JP 4 85625569 85625569 single base substitution G A synonymous_variant T2771T 8313C>T LIRI-JP 4 85625569 85625569 single base substitution G A synonymous_variant T2788T 8364C>T LIRI-JP 4 85625569 85625569 single base substitution G A synonymous_variant T391T 1173C>T LIRI-JP 4 85625637 85625637 single base substitution G T intron_variant LIRI-JP 4 85625665 85625665 single base substitution T C intron_variant LIRI-JP 4 85625782 85625782 single base substitution A G intron_variant LIRI-JP 4 85632292 85632292 single base substitution T C intron_variant LIRI-JP 4 85635620 85635620 single base substitution G A intron_variant LIRI-JP 4 85637120 85637120 single base substitution G A intron_variant LIRI-JP 4 85638009 85638009 single base substitution T C intron_variant LIRI-JP 4 85638823 85638823 single base substitution G T intron_variant LIRI-JP 4 85639113 85639113 single base substitution A T intron_variant LIRI-JP 4 85639313 85639313 single base substitution T C intron_variant LIRI-JP 4 85640631 85640631 single base substitution C A intron_variant LIRI-JP 4 85641129 85641129 single base substitution G C intron_variant LIRI-JP 4 85646183 85646183 single base substitution C A intron_variant LIRI-JP 4 85646624 85646624 single base substitution C T intron_variant LIRI-JP 4 85647472 85647472 single base substitution G A intron_variant LIRI-JP 4 85649000 85649000 single base substitution T C intron_variant LIRI-JP 4 85655401 85655401 single base substitution A C downstream_gene_variant LIRI-JP 4 85655401 85655401 single base substitution A C intron_variant LIRI-JP 4 85655401 85655401 single base substitution A C upstream_gene_variant LIRI-JP 4 85657070 85657070 single base substitution T C intron_variant LIRI-JP 4 85657070 85657070 single base substitution T C upstream_gene_variant LIRI-JP 4 85657901 85657901 single base substitution C A intron_variant LIRI-JP 4 85657901 85657901 single base substitution C A upstream_gene_variant LIRI-JP 4 85658761 85658761 single base substitution T C intron_variant LIRI-JP 4 85658761 85658761 single base substitution T C upstream_gene_variant LIRI-JP 4 85661515 85661515 single base substitution T C missense_variant R2097G 6289A>G LIRI-JP 4 85661515 85661515 single base substitution T C upstream_gene_variant LIRI-JP 4 85663260 85663260 single base substitution T A intron_variant LIRI-JP 4 85663260 85663260 single base substitution T A upstream_gene_variant LIRI-JP 4 85663659 85663659 single base substitution C A intron_variant LIRI-JP 4 85663659 85663659 single base substitution C A upstream_gene_variant LIRI-JP 4 85665555 85665555 single base substitution T C intron_variant LIRI-JP 4 85666365 85666365 single base substitution T C intron_variant LIRI-JP 4 85667914 85667914 single base substitution G C downstream_gene_variant LIRI-JP 4 85667914 85667914 single base substitution G C intron_variant LIRI-JP 4 85667955 85667955 single base substitution A C downstream_gene_variant LIRI-JP 4 85667955 85667955 single base substitution A C intron_variant LIRI-JP 4 85669182 85669182 single base substitution T C downstream_gene_variant LIRI-JP 4 85669182 85669182 single base substitution T C intron_variant LIRI-JP 4 85670994 85670994 single base substitution T C downstream_gene_variant LIRI-JP 4 85670994 85670994 single base substitution T C intron_variant LIRI-JP 4 85675537 85675537 single base substitution T A intron_variant LIRI-JP 4 85680320 85680320 single base substitution C T intron_variant LIRI-JP 4 85680320 85680320 single base substitution C T upstream_gene_variant LIRI-JP 4 85685836 85685836 single base substitution A C intron_variant LIRI-JP 4 85688184 85688184 single base substitution T G intron_variant LIRI-JP 4 85689307 85689307 single base substitution G T intron_variant LIRI-JP 4 85691278 85691278 single base substitution T C intron_variant LIRI-JP 4 85691424 85691424 single base substitution G A intron_variant LIRI-JP 4 85691532 85691532 single base substitution T C intron_variant LIRI-JP 4 85692504 85692504 single base substitution T A intron_variant LIRI-JP 4 85692594 85692594 single base substitution A T intron_variant LIRI-JP 4 85692906 85692906 single base substitution T G intron_variant LIRI-JP 4 85695044 85695044 single base substitution T C intron_variant LIRI-JP 4 85695074 85695074 single base substitution C T intron_variant LIRI-JP 4 85695173 85695173 single base substitution C A intron_variant LIRI-JP 4 85695900 85695900 single base substitution T C intron_variant LIRI-JP 4 85698832 85698832 single base substitution A C intron_variant LIRI-JP 4 85701546 85701546 single base substitution T C intron_variant LIRI-JP 4 85703443 85703443 single base substitution T C intron_variant LIRI-JP 4 85703833 85703833 single base substitution T C intron_variant LIRI-JP 4 85705354 85705354 single base substitution C A intron_variant LIRI-JP 4 85706734 85706734 single base substitution T C intron_variant LIRI-JP 4 85709448 85709448 single base substitution T C intron_variant LIRI-JP 4 85710142 85710142 single base substitution C T intron_variant LIRI-JP 4 85710582 85710582 single base substitution G A intron_variant LIRI-JP 4 85711044 85711044 single base substitution T C synonymous_variant E1168E 3504A>G LIRI-JP 4 85711405 85711405 single base substitution A C intron_variant LIRI-JP 4 85711514 85711514 single base substitution T C intron_variant LIRI-JP 4 85711922 85711922 single base substitution C G intron_variant LIRI-JP 4 85712909 85712909 single base substitution C A intron_variant LIRI-JP 4 85715620 85715620 single base substitution G A intron_variant LIRI-JP 4 85718643 85718643 insertion of <=200bp - A downstream_gene_variant LIRI-JP 4 85718643 85718643 insertion of <=200bp - A intron_variant LIRI-JP 4 85719149 85719149 single base substitution T C downstream_gene_variant LIRI-JP 4 85719149 85719149 single base substitution T C missense_variant S979G 2935A>G LIRI-JP 4 85720291 85720291 single base substitution T C downstream_gene_variant LIRI-JP 4 85720291 85720291 single base substitution T C intron_variant LIRI-JP 4 85724801 85724801 single base substitution G A intron_variant LIRI-JP 4 85725901 85725901 single base substitution C T downstream_gene_variant LIRI-JP 4 85725901 85725901 single base substitution C T intron_variant LIRI-JP 4 85725901 85725901 single base substitution C T upstream_gene_variant LIRI-JP 4 85725927 85725927 single base substitution G A downstream_gene_variant LIRI-JP 4 85725927 85725927 single base substitution G A intron_variant LIRI-JP 4 85725927 85725927 single base substitution G A upstream_gene_variant LIRI-JP 4 85726735 85726735 single base substitution T C downstream_gene_variant LIRI-JP 4 85726735 85726735 single base substitution T C intron_variant LIRI-JP 4 85726735 85726735 single base substitution T C upstream_gene_variant LIRI-JP 4 85727442 85727442 single base substitution G A downstream_gene_variant LIRI-JP 4 85727442 85727442 single base substitution G A intron_variant LIRI-JP 4 85727442 85727442 single base substitution G A upstream_gene_variant LIRI-JP 4 85732441 85732441 single base substitution C T intron_variant LIRI-JP 4 85732441 85732441 single base substitution C T upstream_gene_variant LIRI-JP 4 85734121 85734121 single base substitution T C intron_variant LIRI-JP 4 85734121 85734121 single base substitution T C upstream_gene_variant LIRI-JP 4 85735446 85735446 single base substitution T C intron_variant LIRI-JP 4 85735446 85735446 single base substitution T C upstream_gene_variant LIRI-JP 4 85735466 85735466 single base substitution T C intron_variant LIRI-JP 4 85735466 85735466 single base substitution T C upstream_gene_variant LIRI-JP 4 85737587 85737587 single base substitution T C intron_variant LIRI-JP 4 85738864 85738864 single base substitution C G intron_variant LIRI-JP 4 85740086 85740086 single base substitution T A intron_variant LIRI-JP 4 85740913 85740913 insertion of <=200bp - A intron_variant LIRI-JP 4 85741399 85741399 single base substitution C T intron_variant LIRI-JP 4 85743454 85743454 single base substitution T C intron_variant LIRI-JP 4 85743519 85743519 single base substitution G A intron_variant LIRI-JP 4 85744713 85744713 single base substitution T C intron_variant LIRI-JP 4 85746245 85746245 single base substitution T C intron_variant LIRI-JP 4 85750120 85750120 single base substitution G T intron_variant LIRI-JP 4 85750371 85750371 single base substitution T C intron_variant LIRI-JP 4 85751380 85751380 single base substitution T C intron_variant LIRI-JP 4 85754130 85754130 single base substitution T C intron_variant LIRI-JP 4 85754725 85754725 single base substitution T A intron_variant LIRI-JP 4 85756798 85756799 deletion of <=200bp CT - intron_variant LIRI-JP 4 85757917 85757917 single base substitution A G downstream_gene_variant LIRI-JP 4 85757917 85757917 single base substitution A G intron_variant LIRI-JP 4 85758892 85758892 single base substitution T C downstream_gene_variant LIRI-JP 4 85758892 85758892 single base substitution T C intron_variant LIRI-JP 4 85761716 85761716 single base substitution T C downstream_gene_variant LIRI-JP 4 85761716 85761716 single base substitution T C intron_variant LIRI-JP 4 85764451 85764451 single base substitution T A intron_variant LIRI-JP 4 85771942 85771942 single base substitution A T intron_variant LIRI-JP 4 85771942 85771942 single base substitution A T upstream_gene_variant LIRI-JP 4 85773764 85773764 single base substitution T A intron_variant LIRI-JP 4 85773764 85773764 single base substitution T A upstream_gene_variant LIRI-JP 4 85774671 85774671 single base substitution C T intron_variant LIRI-JP 4 85774671 85774671 single base substitution C T upstream_gene_variant LIRI-JP 4 85776980 85776980 single base substitution T C downstream_gene_variant LIRI-JP 4 85776980 85776980 single base substitution T C intron_variant LIRI-JP 4 85778157 85778157 single base substitution C T downstream_gene_variant LIRI-JP 4 85778157 85778157 single base substitution C T intron_variant LIRI-JP 4 85778267 85778267 single base substitution T C downstream_gene_variant LIRI-JP 4 85778267 85778267 single base substitution T C intron_variant LIRI-JP 4 85778794 85778794 single base substitution A G downstream_gene_variant LIRI-JP 4 85778794 85778794 single base substitution A G intron_variant LIRI-JP 4 85778811 85778811 single base substitution A G downstream_gene_variant LIRI-JP 4 85778811 85778811 single base substitution A G intron_variant LIRI-JP 4 85779012 85779030 deletion of <=200bp TGTGAACTAACCTTCCTGG - downstream_gene_variant LIRI-JP 4 85779012 85779030 deletion of <=200bp TGTGAACTAACCTTCCTGG - intron_variant LIRI-JP 4 85779143 85779143 single base substitution T C downstream_gene_variant LIRI-JP 4 85779143 85779143 single base substitution T C intron_variant LIRI-JP 4 85782284 85782284 single base substitution A T intron_variant LIRI-JP 4 85782284 85782284 single base substitution A T upstream_gene_variant LIRI-JP 4 85783695 85783695 single base substitution T C intron_variant LIRI-JP 4 85783695 85783695 single base substitution T C upstream_gene_variant LIRI-JP 4 85785123 85785123 single base substitution A T intron_variant LIRI-JP 4 85785123 85785123 single base substitution A T upstream_gene_variant LIRI-JP 4 85787203 85787203 single base substitution T A intron_variant LIRI-JP 4 85787868 85787868 single base substitution C T intron_variant LIRI-JP 4 85787946 85787946 single base substitution C T intron_variant LIRI-JP 4 85789032 85789032 single base substitution A G intron_variant LIRI-JP 4 85789431 85789431 single base substitution T C intron_variant LIRI-JP 4 85794352 85794352 single base substitution T C intron_variant LIRI-JP 4 85795674 85795674 single base substitution T C intron_variant LIRI-JP 4 85795692 85795692 single base substitution C A intron_variant LIRI-JP 4 85797111 85797111 single base substitution T C intron_variant LIRI-JP 4 85799706 85799706 single base substitution A C intron_variant LIRI-JP 4 85800041 85800041 single base substitution G A intron_variant LIRI-JP 4 85800805 85800805 single base substitution T C intron_variant LIRI-JP 4 85802840 85802840 single base substitution G A intron_variant LIRI-JP 4 85802969 85802969 single base substitution G A intron_variant LIRI-JP 4 85803164 85803164 single base substitution T C intron_variant LIRI-JP 4 85804102 85804102 single base substitution C T intron_variant LIRI-JP 4 85806679 85806679 single base substitution T C intron_variant LIRI-JP 4 85807323 85807323 single base substitution T C intron_variant LIRI-JP 4 85809213 85809213 single base substitution C A intron_variant LIRI-JP 4 85809549 85809549 single base substitution T A intron_variant LIRI-JP 4 85809938 85809938 single base substitution G A intron_variant LIRI-JP 4 85812226 85812226 single base substitution A C intron_variant LIRI-JP 4 85813013 85813013 single base substitution T G intron_variant LIRI-JP 4 85816206 85816206 single base substitution A G intron_variant LIRI-JP 4 85817781 85817781 single base substitution T C intron_variant LIRI-JP 4 85820630 85820630 single base substitution T C intron_variant LIRI-JP 4 85820630 85820630 single base substitution T C upstream_gene_variant LIRI-JP 4 85821062 85821062 single base substitution G T intron_variant LIRI-JP 4 85821062 85821062 single base substitution G T upstream_gene_variant LIRI-JP 4 85821161 85821161 single base substitution A G intron_variant LIRI-JP 4 85821161 85821161 single base substitution A G upstream_gene_variant LIRI-JP 4 85821193 85821193 single base substitution C T intron_variant LIRI-JP 4 85821193 85821193 single base substitution C T upstream_gene_variant LIRI-JP 4 85821722 85821722 single base substitution T C intron_variant LIRI-JP 4 85821722 85821722 single base substitution T C upstream_gene_variant LIRI-JP 4 85824138 85824138 single base substitution A T intron_variant LIRI-JP 4 85824349 85824349 single base substitution T C intron_variant LIRI-JP 4 85825222 85825222 single base substitution A G intron_variant LIRI-JP 4 85825915 85825915 single base substitution T C intron_variant LIRI-JP 4 85825937 85825937 single base substitution A C intron_variant LIRI-JP 4 85826465 85826465 single base substitution G T intron_variant LIRI-JP 4 85827571 85827571 single base substitution A C intron_variant LIRI-JP 4 85830228 85830228 single base substitution C T intron_variant LIRI-JP 4 85831201 85831201 single base substitution C T intron_variant LIRI-JP 4 85834327 85834327 single base substitution A C intron_variant LIRI-JP 4 85835435 85835435 single base substitution G A intron_variant LIRI-JP 4 85840326 85840326 single base substitution T C intron_variant LIRI-JP 4 85840546 85840546 single base substitution G A intron_variant LIRI-JP 4 85840998 85840998 single base substitution A C intron_variant LIRI-JP 4 85841853 85841853 single base substitution G T intron_variant LIRI-JP 4 85841976 85841976 single base substitution A G intron_variant LIRI-JP 4 85842572 85842572 single base substitution T C intron_variant LIRI-JP 4 85844980 85844980 single base substitution C A intron_variant LIRI-JP 4 85845852 85845852 single base substitution C T intron_variant LIRI-JP 4 85851302 85851302 single base substitution T G intron_variant LIRI-JP 4 85851696 85851696 single base substitution T A intron_variant LIRI-JP 4 85852556 85852556 single base substitution G A intron_variant LIRI-JP 4 85855250 85855250 single base substitution T C intron_variant LIRI-JP 4 85857359 85857359 single base substitution T C intron_variant LIRI-JP 4 85858432 85858432 single base substitution T C intron_variant LIRI-JP 4 85858796 85858796 single base substitution T C intron_variant LIRI-JP 4 85859447 85859449 deletion of <=200bp ACA - intron_variant LIRI-JP 4 85861914 85861914 single base substitution T C intron_variant LIRI-JP 4 85863536 85863536 single base substitution C T intron_variant LIRI-JP 4 85867725 85867725 single base substitution C T intron_variant LIRI-JP 4 85868791 85868791 single base substitution G A intron_variant LIRI-JP 4 85869222 85869222 single base substitution A G intron_variant LIRI-JP 4 85872630 85872630 single base substitution A G intron_variant LIRI-JP 4 85873340 85873340 single base substitution T A intron_variant LIRI-JP 4 85874149 85874149 single base substitution T A intron_variant LIRI-JP 4 85875051 85875051 single base substitution C A intron_variant LIRI-JP 4 85875057 85875057 single base substitution C A intron_variant LIRI-JP 4 85875234 85875234 single base substitution C T intron_variant LIRI-JP 4 85875847 85875847 single base substitution G T intron_variant LIRI-JP 4 85876722 85876722 single base substitution T C intron_variant LIRI-JP 4 85876956 85876956 single base substitution C T intron_variant LIRI-JP 4 85877526 85877526 single base substitution C T intron_variant LIRI-JP 4 85877996 85877996 single base substitution C T intron_variant LIRI-JP 4 85878735 85878735 single base substitution A G intron_variant LIRI-JP 4 85879633 85879633 single base substitution C A intron_variant LIRI-JP 4 85880650 85880650 single base substitution T C intron_variant LIRI-JP 4 85884361 85884361 single base substitution G T intron_variant LIRI-JP 4 85884988 85884988 single base substitution T A intron_variant LIRI-JP 4 85885037 85885038 deletion of <=200bp TG - intron_variant LIRI-JP 4 85886023 85886023 single base substitution A G intron_variant LIRI-JP 4 85889622 85889622 single base substitution A G upstream_gene_variant LIRI-JP 4 85889667 85889667 single base substitution A G upstream_gene_variant LIRI-JP 4 85890133 85890133 single base substitution A T upstream_gene_variant LUSC-KR 4 85596413 85596413 single base substitution T A intron_variant LUSC-KR 4 85596990 85596990 single base substitution G T intron_variant LUSC-KR 4 85597691 85597691 single base substitution T C intron_variant LUSC-KR 4 85600258 85600258 single base substitution C A exon_variant LUSC-KR 4 85600258 85600258 single base substitution C A missense_variant A3304S 9910G>T LUSC-KR 4 85600258 85600258 single base substitution C A missense_variant A3321S 9961G>T LUSC-KR 4 85608032 85608032 single base substitution C T downstream_gene_variant LUSC-KR 4 85608032 85608032 single base substitution C T intron_variant LUSC-KR 4 85608032 85608032 single base substitution C T upstream_gene_variant LUSC-KR 4 85610175 85610175 single base substitution C A downstream_gene_variant LUSC-KR 4 85610175 85610175 single base substitution C A intron_variant LUSC-KR 4 85610274 85610274 single base substitution A G downstream_gene_variant LUSC-KR 4 85610274 85610274 single base substitution A G intron_variant LUSC-KR 4 85614803 85614803 single base substitution C A intron_variant LUSC-KR 4 85614870 85614870 single base substitution G A intron_variant LUSC-KR 4 85615907 85615907 single base substitution G C intron_variant LUSC-KR 4 85618301 85618301 single base substitution T C intron_variant LUSC-KR 4 85621940 85621940 single base substitution T G intron_variant LUSC-KR 4 85630203 85630203 single base substitution T A intron_variant LUSC-KR 4 85630616 85630616 single base substitution C G intron_variant LUSC-KR 4 85631416 85631416 single base substitution T C intron_variant LUSC-KR 4 85631536 85631536 single base substitution C A intron_variant LUSC-KR 4 85633325 85633325 single base substitution C A intron_variant LUSC-KR 4 85635661 85635661 single base substitution T A intron_variant LUSC-KR 4 85638416 85638416 single base substitution G C intron_variant LUSC-KR 4 85643626 85643626 single base substitution T G intron_variant LUSC-KR 4 85645928 85645928 single base substitution G A intron_variant LUSC-KR 4 85649882 85649882 single base substitution T C intron_variant LUSC-KR 4 85652339 85652339 single base substitution G C downstream_gene_variant LUSC-KR 4 85652339 85652339 single base substitution G C intron_variant LUSC-KR 4 85653111 85653111 single base substitution A C downstream_gene_variant LUSC-KR 4 85653111 85653111 single base substitution A C intron_variant LUSC-KR 4 85654532 85654532 single base substitution C T downstream_gene_variant LUSC-KR 4 85654532 85654532 single base substitution C T intron_variant LUSC-KR 4 85654532 85654532 single base substitution C T splice_region_variant LUSC-KR 4 85656350 85656350 single base substitution T C intron_variant LUSC-KR 4 85656350 85656350 single base substitution T C upstream_gene_variant LUSC-KR 4 85658360 85658360 single base substitution A C exon_variant LUSC-KR 4 85658360 85658360 single base substitution A C missense_variant L2245R 6734T>G LUSC-KR 4 85658360 85658360 single base substitution A C upstream_gene_variant LUSC-KR 4 85678845 85678845 single base substitution C A intron_variant LUSC-KR 4 85678845 85678845 single base substitution C A upstream_gene_variant LUSC-KR 4 85681807 85681807 single base substitution C T intron_variant LUSC-KR 4 85682000 85682000 single base substitution G A intron_variant LUSC-KR 4 85698443 85698443 single base substitution G C intron_variant LUSC-KR 4 85701746 85701746 single base substitution G A intron_variant LUSC-KR 4 85704064 85704064 single base substitution A G intron_variant LUSC-KR 4 85706356 85706356 single base substitution C T intron_variant LUSC-KR 4 85707076 85707076 single base substitution G A intron_variant LUSC-KR 4 85714047 85714047 single base substitution C A intron_variant LUSC-KR 4 85715013 85715013 single base substitution G C intron_variant LUSC-KR 4 85719407 85719407 single base substitution G A downstream_gene_variant LUSC-KR 4 85719407 85719407 single base substitution G A intron_variant LUSC-KR 4 85723017 85723017 single base substitution G A missense_variant H870Y 2608C>T LUSC-KR 4 85723017 85723017 single base substitution G A splice_region_variant LUSC-KR 4 85725555 85725555 single base substitution T C downstream_gene_variant LUSC-KR 4 85725555 85725555 single base substitution T C intron_variant LUSC-KR 4 85725555 85725555 single base substitution T C upstream_gene_variant LUSC-KR 4 85736061 85736061 single base substitution G C intron_variant LUSC-KR 4 85736061 85736061 single base substitution G C upstream_gene_variant LUSC-KR 4 85739999 85739999 single base substitution G A intron_variant LUSC-KR 4 85753039 85753039 single base substitution G A intron_variant LUSC-KR 4 85753992 85753992 single base substitution C G intron_variant LUSC-KR 4 85756631 85756631 single base substitution C G intron_variant LUSC-KR 4 85757926 85757926 single base substitution G C downstream_gene_variant LUSC-KR 4 85757926 85757926 single base substitution G C intron_variant LUSC-KR 4 85758247 85758247 single base substitution G A downstream_gene_variant LUSC-KR 4 85758247 85758247 single base substitution G A splice_region_variant LUSC-KR 4 85762338 85762338 single base substitution G A downstream_gene_variant LUSC-KR 4 85762338 85762338 single base substitution G A exon_variant LUSC-KR 4 85762338 85762338 single base substitution G A missense_variant T128M 383C>T LUSC-KR 4 85762811 85762811 single base substitution C A intron_variant LUSC-KR 4 85762919 85762919 single base substitution C T intron_variant LUSC-KR 4 85763437 85763437 single base substitution C A intron_variant LUSC-KR 4 85765381 85765381 single base substitution T C intron_variant LUSC-KR 4 85768586 85768586 single base substitution G A downstream_gene_variant LUSC-KR 4 85768586 85768586 single base substitution G A intron_variant LUSC-KR 4 85772478 85772478 single base substitution T C intron_variant LUSC-KR 4 85772478 85772478 single base substitution T C upstream_gene_variant LUSC-KR 4 85773123 85773123 single base substitution T C intron_variant LUSC-KR 4 85773123 85773123 single base substitution T C upstream_gene_variant LUSC-KR 4 85776632 85776632 single base substitution C G downstream_gene_variant LUSC-KR 4 85776632 85776632 single base substitution C G intron_variant LUSC-KR 4 85778589 85778589 single base substitution C T downstream_gene_variant LUSC-KR 4 85778589 85778589 single base substitution C T intron_variant LUSC-KR 4 85780298 85780298 single base substitution G C downstream_gene_variant LUSC-KR 4 85780298 85780298 single base substitution G C intron_variant LUSC-KR 4 85788896 85788896 single base substitution C A intron_variant LUSC-KR 4 85790615 85790615 single base substitution G T intron_variant LUSC-KR 4 85797090 85797090 single base substitution T G intron_variant LUSC-KR 4 85802506 85802506 single base substitution C A intron_variant LUSC-KR 4 85806039 85806039 single base substitution C A intron_variant LUSC-KR 4 85816725 85816725 single base substitution C A intron_variant LUSC-KR 4 85835345 85835345 single base substitution C T intron_variant LUSC-KR 4 85835523 85835523 single base substitution C A intron_variant LUSC-KR 4 85838261 85838261 single base substitution T C intron_variant LUSC-KR 4 85841082 85841082 single base substitution C G intron_variant LUSC-KR 4 85841768 85841768 single base substitution A C intron_variant LUSC-KR 4 85844435 85844435 single base substitution G A intron_variant LUSC-KR 4 85856806 85856806 single base substitution G A intron_variant LUSC-KR 4 85876966 85876966 single base substitution G C intron_variant LUSC-KR 4 85886371 85886371 single base substitution T C intron_variant LUSC-KR 4 85887093 85887093 single base substitution C G intron_variant LUSC-US 4 85594031 85594031 single base substitution C T exon_variant LUSC-US 4 85594031 85594031 single base substitution C T missense_variant R3507Q 10520G>A LUSC-US 4 85594031 85594031 single base substitution C T missense_variant R3524Q 10571G>A LUSC-US 4 85598396 85598396 single base substitution T G exon_variant LUSC-US 4 85598396 85598396 single base substitution T G missense_variant E3454D 10362A>C LUSC-US 4 85598396 85598396 single base substitution T G missense_variant E3471D 10413A>C LUSC-US 4 85598453 85598453 single base substitution C G exon_variant LUSC-US 4 85598453 85598453 single base substitution C G synonymous_variant V3435V 10305G>C LUSC-US 4 85598453 85598453 single base substitution C G synonymous_variant V3452V 10356G>C LUSC-US 4 85611771 85611771 single base substitution C A downstream_gene_variant LUSC-US 4 85611771 85611771 single base substitution C A missense_variant C3067F 9200G>T LUSC-US 4 85611771 85611771 single base substitution C A missense_variant C3084F 9251G>T LUSC-US 4 85638087 85638087 single base substitution C A missense_variant D216Y 646G>T LUSC-US 4 85638087 85638087 single base substitution C A missense_variant D2596Y 7786G>T LUSC-US 4 85638087 85638087 single base substitution C A missense_variant D2613Y 7837G>T LUSC-US 4 85638146 85638146 single base substitution C G missense_variant R196T 587G>C LUSC-US 4 85638146 85638146 single base substitution C G missense_variant R2576T 7727G>C LUSC-US 4 85638146 85638146 single base substitution C G missense_variant R2593T 7778G>C LUSC-US 4 85664938 85664938 single base substitution C T synonymous_variant R1996R 5988G>A LUSC-US 4 85664938 85664938 single base substitution C T upstream_gene_variant LUSC-US 4 85687027 85687027 single base substitution G A synonymous_variant L1708L 5124C>T LUSC-US 4 85717868 85717868 single base substitution A C missense_variant D991E 2973T>G LUSC-US 4 85722993 85722993 single base substitution C A exon_variant LUSC-US 4 85722993 85722993 single base substitution C A missense_variant V878L 2632G>T LUSC-US 4 85750243 85750243 single base substitution G A exon_variant LUSC-US 4 85750243 85750243 single base substitution G A synonymous_variant L290L 870C>T LUSC-US 4 85750301 85750301 single base substitution G C exon_variant LUSC-US 4 85750301 85750301 single base substitution G C stop_gained S271* 812C>G LUSC-US 4 85771053 85771053 single base substitution A G exon_variant LUSC-US 4 85771053 85771053 single base substitution A G splice_donor_variant MALY-DE 4 85589015 85589015 single base substitution G A downstream_gene_variant MALY-DE 4 85591608 85591608 single base substitution C T 3_prime_UTR_variant MALY-DE 4 85591608 85591608 single base substitution C T downstream_gene_variant MALY-DE 4 85593316 85593316 single base substitution C T 3_prime_UTR_variant MALY-DE 4 85593316 85593316 single base substitution C T downstream_gene_variant MALY-DE 4 85594307 85594307 single base substitution T A intron_variant MALY-DE 4 85597750 85597750 deletion of <=200bp A - intron_variant MALY-DE 4 85598261 85598261 single base substitution G A intron_variant MALY-DE 4 85600577 85600577 single base substitution T C intron_variant MALY-DE 4 85601648 85601648 single base substitution T G intron_variant MALY-DE 4 85603275 85603275 single base substitution G A intron_variant MALY-DE 4 85603823 85603823 single base substitution G T exon_variant MALY-DE 4 85603823 85603823 single base substitution G T intron_variant MALY-DE 4 85605616 85605616 single base substitution T G intron_variant MALY-DE 4 85605616 85605616 single base substitution T G upstream_gene_variant MALY-DE 4 85606127 85606127 single base substitution G T intron_variant MALY-DE 4 85606127 85606127 single base substitution G T upstream_gene_variant MALY-DE 4 85608303 85608303 single base substitution C G downstream_gene_variant MALY-DE 4 85608303 85608303 single base substitution C G intron_variant MALY-DE 4 85608303 85608303 single base substitution C G upstream_gene_variant MALY-DE 4 85608307 85608307 deletion of <=200bp T - downstream_gene_variant MALY-DE 4 85608307 85608307 deletion of <=200bp T - intron_variant MALY-DE 4 85608307 85608307 deletion of <=200bp T - upstream_gene_variant MALY-DE 4 85613200 85613200 single base substitution C T intron_variant MALY-DE 4 85614905 85614905 single base substitution G T intron_variant MALY-DE 4 85615277 85615277 single base substitution G A intron_variant MALY-DE 4 85617633 85617633 single base substitution T G intron_variant MALY-DE 4 85617780 85617780 single base substitution G C intron_variant MALY-DE 4 85619053 85619053 single base substitution T C intron_variant MALY-DE 4 85619421 85619421 single base substitution T G intron_variant MALY-DE 4 85619445 85619445 insertion of <=200bp - A intron_variant MALY-DE 4 85619821 85619821 deletion of <=200bp A - intron_variant MALY-DE 4 85624694 85624694 single base substitution T C intron_variant MALY-DE 4 85629363 85629365 deletion of <=200bp TCT - intron_variant MALY-DE 4 85632236 85632236 single base substitution T G intron_variant MALY-DE 4 85632857 85632857 single base substitution A T intron_variant MALY-DE 4 85635118 85635118 single base substitution A C intron_variant MALY-DE 4 85644342 85644342 single base substitution T G intron_variant MALY-DE 4 85651140 85651140 single base substitution C A intron_variant MALY-DE 4 85655688 85655688 single base substitution A C downstream_gene_variant MALY-DE 4 85655688 85655688 single base substitution A C intron_variant MALY-DE 4 85655688 85655688 single base substitution A C upstream_gene_variant MALY-DE 4 85656131 85656131 single base substitution C T downstream_gene_variant MALY-DE 4 85656131 85656131 single base substitution C T intron_variant MALY-DE 4 85656131 85656131 single base substitution C T upstream_gene_variant MALY-DE 4 85656847 85656847 single base substitution T G intron_variant MALY-DE 4 85656847 85656847 single base substitution T G upstream_gene_variant MALY-DE 4 85658778 85658778 insertion of <=200bp - TA intron_variant MALY-DE 4 85658778 85658778 insertion of <=200bp - TA upstream_gene_variant MALY-DE 4 85659281 85659281 single base substitution C T intron_variant MALY-DE 4 85659281 85659281 single base substitution C T upstream_gene_variant MALY-DE 4 85661956 85661956 insertion of <=200bp - T intron_variant MALY-DE 4 85661956 85661956 insertion of <=200bp - T upstream_gene_variant MALY-DE 4 85663139 85663139 insertion of <=200bp - A intron_variant MALY-DE 4 85663139 85663139 insertion of <=200bp - A upstream_gene_variant MALY-DE 4 85668505 85668505 single base substitution C G downstream_gene_variant MALY-DE 4 85668505 85668505 single base substitution C G intron_variant MALY-DE 4 85670468 85670468 insertion of <=200bp - T downstream_gene_variant MALY-DE 4 85670468 85670468 insertion of <=200bp - T intron_variant MALY-DE 4 85671188 85671188 single base substitution G T downstream_gene_variant MALY-DE 4 85671188 85671188 single base substitution G T intron_variant MALY-DE 4 85672593 85672593 single base substitution A C exon_variant MALY-DE 4 85672593 85672593 single base substitution A C intron_variant MALY-DE 4 85673306 85673306 single base substitution A T intron_variant MALY-DE 4 85677194 85677194 single base substitution T C intron_variant MALY-DE 4 85677194 85677194 single base substitution T C upstream_gene_variant MALY-DE 4 85677557 85677557 single base substitution G T intron_variant MALY-DE 4 85677557 85677557 single base substitution G T upstream_gene_variant MALY-DE 4 85685704 85685704 single base substitution G C intron_variant MALY-DE 4 85685946 85685946 single base substitution A C intron_variant MALY-DE 4 85686926 85686926 single base substitution G T intron_variant MALY-DE 4 85687303 85687303 insertion of <=200bp - A intron_variant MALY-DE 4 85692080 85692080 single base substitution C T intron_variant MALY-DE 4 85697027 85697027 single base substitution T A intron_variant MALY-DE 4 85699913 85699913 single base substitution A T intron_variant MALY-DE 4 85700605 85700605 single base substitution G A intron_variant MALY-DE 4 85701920 85701920 insertion of <=200bp - AAAT intron_variant MALY-DE 4 85702472 85702472 single base substitution A T intron_variant MALY-DE 4 85702474 85702474 single base substitution A C intron_variant MALY-DE 4 85703731 85703731 single base substitution G A intron_variant MALY-DE 4 85704351 85704351 single base substitution A C intron_variant MALY-DE 4 85705016 85705016 insertion of <=200bp - ACAC intron_variant MALY-DE 4 85707759 85707759 single base substitution C A intron_variant MALY-DE 4 85707942 85707943 deletion of <=200bp CA - intron_variant MALY-DE 4 85710915 85710915 single base substitution G T synonymous_variant A1211A 3633C>A MALY-DE 4 85712310 85712310 single base substitution T A intron_variant MALY-DE 4 85714439 85714439 single base substitution C T intron_variant MALY-DE 4 85714466 85714466 single base substitution G A intron_variant MALY-DE 4 85715378 85715378 single base substitution A C intron_variant MALY-DE 4 85715953 85715953 single base substitution C A intron_variant MALY-DE 4 85716301 85716301 single base substitution G A intron_variant MALY-DE 4 85717407 85717407 single base substitution T A intron_variant MALY-DE 4 85718264 85718264 single base substitution T C downstream_gene_variant MALY-DE 4 85718264 85718264 single base substitution T C intron_variant MALY-DE 4 85719336 85719336 single base substitution A G downstream_gene_variant MALY-DE 4 85719336 85719336 single base substitution A G intron_variant MALY-DE 4 85720528 85720528 single base substitution T G downstream_gene_variant MALY-DE 4 85720528 85720528 single base substitution T G intron_variant MALY-DE 4 85726339 85726339 single base substitution T A downstream_gene_variant MALY-DE 4 85726339 85726339 single base substitution T A intron_variant MALY-DE 4 85726339 85726339 single base substitution T A upstream_gene_variant MALY-DE 4 85727056 85727056 single base substitution A C downstream_gene_variant MALY-DE 4 85727056 85727056 single base substitution A C intron_variant MALY-DE 4 85727056 85727056 single base substitution A C upstream_gene_variant MALY-DE 4 85729217 85729217 single base substitution A G downstream_gene_variant MALY-DE 4 85729217 85729217 single base substitution A G intron_variant MALY-DE 4 85729217 85729217 single base substitution A G upstream_gene_variant MALY-DE 4 85729379 85729379 deletion of <=200bp A - downstream_gene_variant MALY-DE 4 85729379 85729379 deletion of <=200bp A - intron_variant MALY-DE 4 85729379 85729379 deletion of <=200bp A - upstream_gene_variant MALY-DE 4 85730155 85730155 single base substitution G A exon_variant MALY-DE 4 85730155 85730155 single base substitution G A intron_variant MALY-DE 4 85730155 85730155 single base substitution G A upstream_gene_variant MALY-DE 4 85730447 85730447 single base substitution C A exon_variant MALY-DE 4 85730447 85730447 single base substitution C A intron_variant MALY-DE 4 85732883 85732883 single base substitution T A intron_variant MALY-DE 4 85732883 85732883 single base substitution T A upstream_gene_variant MALY-DE 4 85733507 85733508 deletion of <=200bp CA - intron_variant MALY-DE 4 85733507 85733508 deletion of <=200bp CA - upstream_gene_variant MALY-DE 4 85735975 85735975 single base substitution C T intron_variant MALY-DE 4 85735975 85735975 single base substitution C T upstream_gene_variant MALY-DE 4 85737046 85737046 single base substitution A G intron_variant MALY-DE 4 85743100 85743100 single base substitution C T intron_variant MALY-DE 4 85745919 85745919 single base substitution A C intron_variant MALY-DE 4 85748667 85748667 single base substitution T A intron_variant MALY-DE 4 85749528 85749528 single base substitution A C intron_variant MALY-DE 4 85753419 85753419 single base substitution C G intron_variant MALY-DE 4 85755835 85755835 single base substitution C A intron_variant MALY-DE 4 85759315 85759315 single base substitution C T downstream_gene_variant MALY-DE 4 85759315 85759315 single base substitution C T intron_variant MALY-DE 4 85766121 85766121 single base substitution C T downstream_gene_variant MALY-DE 4 85766121 85766121 single base substitution C T intron_variant MALY-DE 4 85766953 85766953 single base substitution A C downstream_gene_variant MALY-DE 4 85766953 85766953 single base substitution A C intron_variant MALY-DE 4 85768140 85768140 single base substitution A T downstream_gene_variant MALY-DE 4 85768140 85768140 single base substitution A T intron_variant MALY-DE 4 85768222 85768222 single base substitution G A downstream_gene_variant MALY-DE 4 85768222 85768222 single base substitution G A intron_variant MALY-DE 4 85769588 85769588 single base substitution C A downstream_gene_variant MALY-DE 4 85769588 85769588 single base substitution C A intron_variant MALY-DE 4 85771485 85771485 single base substitution T G intron_variant MALY-DE 4 85771485 85771485 single base substitution T G upstream_gene_variant MALY-DE 4 85785306 85785306 single base substitution C T intron_variant MALY-DE 4 85785306 85785306 single base substitution C T upstream_gene_variant MALY-DE 4 85788150 85788150 single base substitution C A intron_variant MALY-DE 4 85790313 85790313 single base substitution T G intron_variant MALY-DE 4 85790850 85790850 single base substitution G C intron_variant MALY-DE 4 85792220 85792220 deletion of <=200bp C - intron_variant MALY-DE 4 85794826 85794826 single base substitution A G intron_variant MALY-DE 4 85796199 85796199 single base substitution G A intron_variant MALY-DE 4 85797823 85797823 single base substitution G A intron_variant MALY-DE 4 85800192 85800192 single base substitution T C intron_variant MALY-DE 4 85801194 85801194 single base substitution A C intron_variant MALY-DE 4 85809880 85809880 single base substitution T G intron_variant MALY-DE 4 85809988 85809988 single base substitution T G intron_variant MALY-DE 4 85810121 85810121 single base substitution T C intron_variant MALY-DE 4 85811032 85811032 single base substitution T A intron_variant MALY-DE 4 85813515 85813515 deletion of <=200bp A - intron_variant MALY-DE 4 85814377 85814377 deletion of <=200bp A - intron_variant MALY-DE 4 85814377 85814377 insertion of <=200bp - A intron_variant MALY-DE 4 85814967 85814967 single base substitution G A intron_variant MALY-DE 4 85821072 85821072 single base substitution C T intron_variant MALY-DE 4 85821072 85821072 single base substitution C T upstream_gene_variant MALY-DE 4 85822015 85822015 single base substitution A C intron_variant MALY-DE 4 85822015 85822015 single base substitution A C upstream_gene_variant MALY-DE 4 85822824 85822824 single base substitution A C intron_variant MALY-DE 4 85822824 85822824 single base substitution A C upstream_gene_variant MALY-DE 4 85826091 85826091 single base substitution C T intron_variant MALY-DE 4 85827313 85827313 single base substitution G A intron_variant MALY-DE 4 85830183 85830183 insertion of <=200bp - AC intron_variant MALY-DE 4 85830324 85830324 single base substitution T A intron_variant MALY-DE 4 85831471 85831471 single base substitution G C intron_variant MALY-DE 4 85834856 85834856 single base substitution A C intron_variant MALY-DE 4 85834908 85834908 deletion of <=200bp A - intron_variant MALY-DE 4 85836507 85836507 single base substitution A C intron_variant MALY-DE 4 85840712 85840712 single base substitution A G intron_variant MALY-DE 4 85842601 85842601 single base substitution G C intron_variant MALY-DE 4 85842616 85842616 single base substitution A G intron_variant MALY-DE 4 85845770 85845770 single base substitution C T intron_variant MALY-DE 4 85846482 85846482 insertion of <=200bp - A intron_variant MALY-DE 4 85851092 85851092 single base substitution A G intron_variant MALY-DE 4 85851383 85851383 single base substitution C T intron_variant MALY-DE 4 85854846 85854846 single base substitution T G intron_variant MALY-DE 4 85856405 85856405 single base substitution T C intron_variant MALY-DE 4 85859112 85859112 single base substitution A G intron_variant MALY-DE 4 85864606 85864606 single base substitution G A intron_variant MALY-DE 4 85865055 85865055 single base substitution A G intron_variant MALY-DE 4 85865398 85865398 single base substitution C T intron_variant MALY-DE 4 85867311 85867311 single base substitution T C intron_variant MALY-DE 4 85867464 85867464 single base substitution A C intron_variant MALY-DE 4 85868668 85868668 insertion of <=200bp - AAT intron_variant MALY-DE 4 85868952 85868952 single base substitution T G intron_variant MALY-DE 4 85871382 85871382 single base substitution C A intron_variant MALY-DE 4 85873303 85873303 single base substitution C T intron_variant MALY-DE 4 85874725 85874725 single base substitution A C intron_variant MALY-DE 4 85878293 85878293 single base substitution A C intron_variant MALY-DE 4 85879583 85879583 single base substitution T A intron_variant MALY-DE 4 85880096 85880096 single base substitution T G intron_variant MALY-DE 4 85880438 85880438 single base substitution A G intron_variant MALY-DE 4 85885842 85885842 deletion of <=200bp T - intron_variant MALY-DE 4 85886210 85886210 single base substitution A T intron_variant MELA-AU 4 85585887 85585887 single base substitution G A downstream_gene_variant MELA-AU 4 85586130 85586131 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 4 85586449 85586449 single base substitution G A downstream_gene_variant MELA-AU 4 85586706 85586706 single base substitution G A downstream_gene_variant MELA-AU 4 85587139 85587139 single base substitution G A downstream_gene_variant MELA-AU 4 85587191 85587191 single base substitution A G downstream_gene_variant MELA-AU 4 85587304 85587304 single base substitution C T downstream_gene_variant MELA-AU 4 85588060 85588060 single base substitution G A downstream_gene_variant MELA-AU 4 85588641 85588641 single base substitution G C downstream_gene_variant MELA-AU 4 85588870 85588870 single base substitution G C downstream_gene_variant MELA-AU 4 85589296 85589296 single base substitution A G downstream_gene_variant MELA-AU 4 85589607 85589607 single base substitution G A downstream_gene_variant MELA-AU 4 85589689 85589689 single base substitution G A downstream_gene_variant MELA-AU 4 85589729 85589729 single base substitution G A downstream_gene_variant MELA-AU 4 85589942 85589942 single base substitution A G downstream_gene_variant MELA-AU 4 85590351 85590351 single base substitution G A downstream_gene_variant MELA-AU 4 85590753 85590753 single base substitution C T 3_prime_UTR_variant MELA-AU 4 85590753 85590753 single base substitution C T downstream_gene_variant MELA-AU 4 85591974 85591974 single base substitution C T 3_prime_UTR_variant MELA-AU 4 85591974 85591974 single base substitution C T downstream_gene_variant MELA-AU 4 85592104 85592104 single base substitution G A 3_prime_UTR_variant MELA-AU 4 85592104 85592104 single base substitution G A downstream_gene_variant MELA-AU 4 85592120 85592120 single base substitution A T 3_prime_UTR_variant MELA-AU 4 85592120 85592120 single base substitution A T downstream_gene_variant MELA-AU 4 85592229 85592229 single base substitution A G 3_prime_UTR_variant MELA-AU 4 85592229 85592229 single base substitution A G downstream_gene_variant MELA-AU 4 85592476 85592476 single base substitution G A 3_prime_UTR_variant MELA-AU 4 85592476 85592476 single base substitution G A downstream_gene_variant MELA-AU 4 85592751 85592751 single base substitution G A 3_prime_UTR_variant MELA-AU 4 85592751 85592751 single base substitution G A downstream_gene_variant MELA-AU 4 85593420 85593420 single base substitution G A 3_prime_UTR_variant MELA-AU 4 85593420 85593420 single base substitution G A downstream_gene_variant MELA-AU 4 85593666 85593666 single base substitution G C 3_prime_UTR_variant MELA-AU 4 85593666 85593666 single base substitution G C exon_variant MELA-AU 4 85593889 85593889 single base substitution G A 3_prime_UTR_variant MELA-AU 4 85593889 85593889 single base substitution G A exon_variant MELA-AU 4 85594125 85594125 single base substitution C T exon_variant MELA-AU 4 85594125 85594125 single base substitution C T missense_variant E3476K 10426G>A MELA-AU 4 85594125 85594125 single base substitution C T missense_variant E3493K 10477G>A MELA-AU 4 85594129 85594129 single base substitution T A exon_variant MELA-AU 4 85594129 85594129 single base substitution T A missense_variant Q3474H 10422A>T MELA-AU 4 85594129 85594129 single base substitution T A missense_variant Q3491H 10473A>T MELA-AU 4 85594156 85594156 single base substitution G A intron_variant MELA-AU 4 85594391 85594391 single base substitution A T intron_variant MELA-AU 4 85595129 85595129 single base substitution A T intron_variant MELA-AU 4 85596138 85596138 single base substitution G A intron_variant MELA-AU 4 85596219 85596219 single base substitution G A intron_variant MELA-AU 4 85596481 85596481 single base substitution G A intron_variant MELA-AU 4 85596833 85596833 single base substitution G A intron_variant MELA-AU 4 85596885 85596885 single base substitution G A intron_variant MELA-AU 4 85596977 85596977 single base substitution G A intron_variant MELA-AU 4 85597211 85597211 single base substitution C A intron_variant MELA-AU 4 85597782 85597782 single base substitution G A intron_variant MELA-AU 4 85598688 85598688 single base substitution G A intron_variant MELA-AU 4 85598721 85598721 single base substitution G A intron_variant MELA-AU 4 85598721 85598721 single base substitution G T intron_variant MELA-AU 4 85598875 85598875 single base substitution G A intron_variant MELA-AU 4 85599404 85599404 single base substitution G A exon_variant MELA-AU 4 85599404 85599404 single base substitution G A synonymous_variant F3375F 10125C>T MELA-AU 4 85599404 85599404 single base substitution G A synonymous_variant F3392F 10176C>T MELA-AU 4 85599664 85599664 single base substitution G A intron_variant MELA-AU 4 85600107 85600107 single base substitution G A exon_variant MELA-AU 4 85600107 85600107 single base substitution G A missense_variant P3354L 10061C>T MELA-AU 4 85600107 85600107 single base substitution G A missense_variant P3371L 10112C>T MELA-AU 4 85600875 85600875 single base substitution G C intron_variant MELA-AU 4 85600994 85600994 single base substitution T C intron_variant MELA-AU 4 85601731 85601731 single base substitution G A intron_variant MELA-AU 4 85601732 85601732 single base substitution G A intron_variant MELA-AU 4 85601811 85601811 single base substitution G A intron_variant MELA-AU 4 85602748 85602748 single base substitution A C intron_variant MELA-AU 4 85602806 85602806 single base substitution G A intron_variant MELA-AU 4 85603495 85603495 single base substitution G A intron_variant MELA-AU 4 85604329 85604329 single base substitution G A intron_variant MELA-AU 4 85604329 85604329 single base substitution G A upstream_gene_variant MELA-AU 4 85604726 85604726 single base substitution G A intron_variant MELA-AU 4 85604726 85604726 single base substitution G A upstream_gene_variant MELA-AU 4 85605620 85605620 single base substitution T C intron_variant MELA-AU 4 85605620 85605620 single base substitution T C upstream_gene_variant MELA-AU 4 85605625 85605625 single base substitution T A intron_variant MELA-AU 4 85605625 85605625 single base substitution T A upstream_gene_variant MELA-AU 4 85606929 85606929 single base substitution G A intron_variant MELA-AU 4 85606929 85606929 single base substitution G A upstream_gene_variant MELA-AU 4 85607141 85607141 single base substitution G A intron_variant MELA-AU 4 85607141 85607141 single base substitution G A upstream_gene_variant MELA-AU 4 85607255 85607255 single base substitution G A intron_variant MELA-AU 4 85607255 85607255 single base substitution G A upstream_gene_variant MELA-AU 4 85607275 85607276 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85607275 85607276 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 4 85607325 85607325 single base substitution G A intron_variant MELA-AU 4 85607325 85607325 single base substitution G A upstream_gene_variant MELA-AU 4 85607717 85607717 single base substitution G A intron_variant MELA-AU 4 85607717 85607717 single base substitution G A upstream_gene_variant MELA-AU 4 85608182 85608182 single base substitution C T downstream_gene_variant MELA-AU 4 85608182 85608182 single base substitution C T intron_variant MELA-AU 4 85608182 85608182 single base substitution C T upstream_gene_variant MELA-AU 4 85608191 85608191 single base substitution A T downstream_gene_variant MELA-AU 4 85608191 85608191 single base substitution A T intron_variant MELA-AU 4 85608191 85608191 single base substitution A T upstream_gene_variant MELA-AU 4 85608359 85608359 single base substitution C T downstream_gene_variant MELA-AU 4 85608359 85608359 single base substitution C T intron_variant MELA-AU 4 85608359 85608359 single base substitution C T upstream_gene_variant MELA-AU 4 85608857 85608857 single base substitution G A downstream_gene_variant MELA-AU 4 85608857 85608857 single base substitution G A intron_variant MELA-AU 4 85608857 85608857 single base substitution G A upstream_gene_variant MELA-AU 4 85609617 85609617 single base substitution G A downstream_gene_variant MELA-AU 4 85609617 85609617 single base substitution G A intron_variant MELA-AU 4 85611055 85611055 single base substitution C T downstream_gene_variant MELA-AU 4 85611055 85611055 single base substitution C T intron_variant MELA-AU 4 85611154 85611154 single base substitution T C downstream_gene_variant MELA-AU 4 85611154 85611154 single base substitution T C intron_variant MELA-AU 4 85611551 85611551 single base substitution C T downstream_gene_variant MELA-AU 4 85611551 85611551 single base substitution C T intron_variant MELA-AU 4 85611810 85611810 single base substitution G A downstream_gene_variant MELA-AU 4 85611810 85611810 single base substitution G A missense_variant T3054I 9161C>T MELA-AU 4 85611810 85611810 single base substitution G A missense_variant T3071I 9212C>T MELA-AU 4 85612671 85612671 single base substitution G A downstream_gene_variant MELA-AU 4 85612671 85612671 single base substitution G A intron_variant MELA-AU 4 85612935 85612935 single base substitution A G missense_variant L3001P 9002T>C MELA-AU 4 85612935 85612935 single base substitution A G missense_variant L3018P 9053T>C MELA-AU 4 85612935 85612935 single base substitution A G missense_variant L621P 1862T>C MELA-AU 4 85613331 85613331 single base substitution G C intron_variant MELA-AU 4 85613358 85613359 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85613613 85613618 deletion of <=200bp TACCAT - intron_variant MELA-AU 4 85614087 85614087 single base substitution G A synonymous_variant I2983I 8949C>T MELA-AU 4 85614087 85614087 single base substitution G A synonymous_variant I3000I 9000C>T MELA-AU 4 85614087 85614087 single base substitution G A synonymous_variant I603I 1809C>T MELA-AU 4 85614222 85614222 single base substitution G A intron_variant MELA-AU 4 85614326 85614326 single base substitution G A intron_variant MELA-AU 4 85614813 85614813 single base substitution G A intron_variant MELA-AU 4 85615142 85615142 single base substitution A G intron_variant MELA-AU 4 85615230 85615230 single base substitution G A intron_variant MELA-AU 4 85615243 85615243 single base substitution G A intron_variant MELA-AU 4 85615857 85615857 single base substitution G C intron_variant MELA-AU 4 85616167 85616167 single base substitution G A intron_variant MELA-AU 4 85616344 85616344 single base substitution G A intron_variant MELA-AU 4 85616355 85616355 single base substitution C T intron_variant MELA-AU 4 85617279 85617279 single base substitution G A synonymous_variant F2898F 8694C>T MELA-AU 4 85617279 85617279 single base substitution G A synonymous_variant F2915F 8745C>T MELA-AU 4 85617279 85617279 single base substitution G A synonymous_variant F518F 1554C>T MELA-AU 4 85617421 85617421 single base substitution G A intron_variant MELA-AU 4 85617893 85617893 single base substitution G A missense_variant H2877Y 8629C>T MELA-AU 4 85617893 85617893 single base substitution G A missense_variant H2894Y 8680C>T MELA-AU 4 85617893 85617893 single base substitution G A missense_variant H497Y 1489C>T MELA-AU 4 85618595 85618595 single base substitution G A intron_variant MELA-AU 4 85618668 85618668 single base substitution C T intron_variant MELA-AU 4 85619066 85619066 single base substitution T A intron_variant MELA-AU 4 85619146 85619146 single base substitution G A intron_variant MELA-AU 4 85619268 85619269 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85619302 85619302 single base substitution C T intron_variant MELA-AU 4 85619615 85619615 single base substitution G A intron_variant MELA-AU 4 85619774 85619774 single base substitution G A intron_variant MELA-AU 4 85619820 85619820 single base substitution G A intron_variant MELA-AU 4 85620061 85620061 single base substitution G A intron_variant MELA-AU 4 85620133 85620133 single base substitution G A intron_variant MELA-AU 4 85620268 85620268 single base substitution T A intron_variant MELA-AU 4 85620297 85620297 single base substitution G A intron_variant MELA-AU 4 85620451 85620451 single base substitution G A intron_variant MELA-AU 4 85621232 85621233 multiple base substitution (>=2bp and <=200bp) TT GG intron_variant MELA-AU 4 85622007 85622007 single base substitution G A intron_variant MELA-AU 4 85622083 85622083 single base substitution G A intron_variant MELA-AU 4 85622867 85622867 single base substitution G A intron_variant MELA-AU 4 85623493 85623493 single base substitution T A intron_variant MELA-AU 4 85623919 85623919 single base substitution A T intron_variant MELA-AU 4 85624012 85624012 single base substitution G A intron_variant MELA-AU 4 85625192 85625192 single base substitution T A intron_variant MELA-AU 4 85625444 85625444 single base substitution G A intron_variant MELA-AU 4 85625644 85625644 single base substitution G A intron_variant MELA-AU 4 85626097 85626097 single base substitution G A intron_variant MELA-AU 4 85626279 85626279 single base substitution G A intron_variant MELA-AU 4 85626521 85626521 single base substitution G A intron_variant MELA-AU 4 85626552 85626552 single base substitution G T missense_variant P2760H 8279C>A MELA-AU 4 85626552 85626552 single base substitution G T missense_variant P2777H 8330C>A MELA-AU 4 85626552 85626552 single base substitution G T missense_variant P380H 1139C>A MELA-AU 4 85626664 85626664 single base substitution C T missense_variant E2723K 8167G>A MELA-AU 4 85626664 85626664 single base substitution C T missense_variant E2740K 8218G>A MELA-AU 4 85626664 85626664 single base substitution C T missense_variant E343K 1027G>A MELA-AU 4 85626758 85626758 single base substitution A C intron_variant MELA-AU 4 85626760 85626760 single base substitution A G intron_variant MELA-AU 4 85626996 85626996 single base substitution G A intron_variant MELA-AU 4 85627109 85627109 single base substitution A G intron_variant MELA-AU 4 85627152 85627152 single base substitution G A intron_variant MELA-AU 4 85627221 85627221 single base substitution C T intron_variant MELA-AU 4 85627322 85627322 single base substitution G A intron_variant MELA-AU 4 85627774 85627774 single base substitution G A intron_variant MELA-AU 4 85627831 85627831 single base substitution G A intron_variant MELA-AU 4 85628182 85628182 single base substitution C T intron_variant MELA-AU 4 85628404 85628404 single base substitution G A intron_variant MELA-AU 4 85629088 85629089 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 85629973 85629973 single base substitution G A intron_variant MELA-AU 4 85630092 85630092 single base substitution G A synonymous_variant F2712F 8136C>T MELA-AU 4 85630092 85630092 single base substitution G A synonymous_variant F2729F 8187C>T MELA-AU 4 85630092 85630092 single base substitution G A synonymous_variant F332F 996C>T MELA-AU 4 85630903 85630903 single base substitution G A intron_variant MELA-AU 4 85631402 85631402 single base substitution G A intron_variant MELA-AU 4 85632289 85632289 single base substitution G A intron_variant MELA-AU 4 85632570 85632570 single base substitution G A intron_variant MELA-AU 4 85632930 85632931 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85633429 85633429 single base substitution C T intron_variant MELA-AU 4 85634112 85634112 single base substitution G A intron_variant MELA-AU 4 85634215 85634215 single base substitution G A intron_variant MELA-AU 4 85634387 85634387 single base substitution A G missense_variant L259S 776T>C MELA-AU 4 85634387 85634387 single base substitution A G missense_variant L2639S 7916T>C MELA-AU 4 85634387 85634387 single base substitution A G missense_variant L2656S 7967T>C MELA-AU 4 85634546 85634546 single base substitution G A intron_variant MELA-AU 4 85634561 85634561 single base substitution G A intron_variant MELA-AU 4 85635437 85635437 single base substitution C T intron_variant MELA-AU 4 85635484 85635484 single base substitution A G intron_variant MELA-AU 4 85635900 85635900 single base substitution G A intron_variant MELA-AU 4 85636030 85636030 single base substitution G A intron_variant MELA-AU 4 85636069 85636069 single base substitution C T intron_variant MELA-AU 4 85636232 85636232 single base substitution A C intron_variant MELA-AU 4 85636350 85636350 single base substitution G A intron_variant MELA-AU 4 85636370 85636370 single base substitution A G intron_variant MELA-AU 4 85636633 85636633 single base substitution G A intron_variant MELA-AU 4 85636645 85636645 single base substitution C G intron_variant MELA-AU 4 85636932 85636932 single base substitution A G intron_variant MELA-AU 4 85637427 85637427 insertion of <=200bp - A intron_variant MELA-AU 4 85637745 85637745 single base substitution C T intron_variant MELA-AU 4 85638485 85638485 single base substitution G A intron_variant MELA-AU 4 85638508 85638508 single base substitution G A intron_variant MELA-AU 4 85638587 85638587 single base substitution G A intron_variant MELA-AU 4 85638707 85638707 single base substitution G A intron_variant MELA-AU 4 85638939 85638939 single base substitution C T intron_variant MELA-AU 4 85639071 85639071 single base substitution G A intron_variant MELA-AU 4 85639130 85639130 single base substitution G A intron_variant MELA-AU 4 85639198 85639198 single base substitution G A intron_variant MELA-AU 4 85639216 85639216 single base substitution A T intron_variant MELA-AU 4 85641067 85641067 single base substitution G A intron_variant MELA-AU 4 85641441 85641441 single base substitution G A intron_variant MELA-AU 4 85641443 85641443 single base substitution G A intron_variant MELA-AU 4 85641656 85641656 single base substitution G A intron_variant MELA-AU 4 85641759 85641759 single base substitution C T intron_variant MELA-AU 4 85641983 85641983 single base substitution A T intron_variant MELA-AU 4 85642068 85642068 single base substitution G A intron_variant MELA-AU 4 85643042 85643042 single base substitution G A intron_variant MELA-AU 4 85643369 85643369 single base substitution C T intron_variant MELA-AU 4 85643732 85643732 single base substitution G A intron_variant MELA-AU 4 85644527 85644527 single base substitution A T intron_variant MELA-AU 4 85645132 85645132 single base substitution A T intron_variant MELA-AU 4 85646714 85646714 single base substitution G A intron_variant MELA-AU 4 85647189 85647189 single base substitution C T intron_variant MELA-AU 4 85647419 85647419 single base substitution T A intron_variant MELA-AU 4 85647799 85647799 single base substitution A T intron_variant MELA-AU 4 85649033 85649033 single base substitution T C intron_variant MELA-AU 4 85649046 85649046 single base substitution A G intron_variant MELA-AU 4 85649466 85649466 single base substitution G A intron_variant MELA-AU 4 85649594 85649594 single base substitution G A intron_variant MELA-AU 4 85649623 85649623 single base substitution C T intron_variant MELA-AU 4 85650712 85650712 single base substitution G A intron_variant MELA-AU 4 85651211 85651211 single base substitution G A intron_variant MELA-AU 4 85651427 85651427 single base substitution G A downstream_gene_variant MELA-AU 4 85651427 85651427 single base substitution G A intron_variant MELA-AU 4 85652170 85652170 single base substitution G T downstream_gene_variant MELA-AU 4 85652170 85652170 single base substitution G T intron_variant MELA-AU 4 85652220 85652220 single base substitution G A downstream_gene_variant MELA-AU 4 85652220 85652220 single base substitution G A intron_variant MELA-AU 4 85652799 85652799 single base substitution G A downstream_gene_variant MELA-AU 4 85652799 85652799 single base substitution G A intron_variant MELA-AU 4 85653131 85653131 single base substitution G A downstream_gene_variant MELA-AU 4 85653131 85653131 single base substitution G A intron_variant MELA-AU 4 85653636 85653636 single base substitution G A downstream_gene_variant MELA-AU 4 85653636 85653636 single base substitution G A intron_variant MELA-AU 4 85654047 85654047 single base substitution G A downstream_gene_variant MELA-AU 4 85654047 85654047 single base substitution G A intron_variant MELA-AU 4 85654086 85654086 single base substitution C T downstream_gene_variant MELA-AU 4 85654086 85654086 single base substitution C T intron_variant MELA-AU 4 85654674 85654674 single base substitution G A downstream_gene_variant MELA-AU 4 85654674 85654674 single base substitution G A missense_variant P2361L 7082C>T MELA-AU 4 85654674 85654674 single base substitution G A upstream_gene_variant MELA-AU 4 85655241 85655241 single base substitution G A downstream_gene_variant MELA-AU 4 85655241 85655241 single base substitution G A intron_variant MELA-AU 4 85655241 85655241 single base substitution G A upstream_gene_variant MELA-AU 4 85656574 85656574 single base substitution G A intron_variant MELA-AU 4 85656574 85656574 single base substitution G A upstream_gene_variant MELA-AU 4 85657211 85657211 single base substitution T C intron_variant MELA-AU 4 85657211 85657211 single base substitution T C upstream_gene_variant MELA-AU 4 85657268 85657268 single base substitution A C intron_variant MELA-AU 4 85657268 85657268 single base substitution A C upstream_gene_variant MELA-AU 4 85657680 85657680 single base substitution G A intron_variant MELA-AU 4 85657680 85657680 single base substitution G A upstream_gene_variant MELA-AU 4 85658039 85658039 single base substitution G T intron_variant MELA-AU 4 85658039 85658039 single base substitution G T upstream_gene_variant MELA-AU 4 85658041 85658041 single base substitution T A intron_variant MELA-AU 4 85658041 85658041 single base substitution T A upstream_gene_variant MELA-AU 4 85658168 85658168 single base substitution C T intron_variant MELA-AU 4 85658168 85658168 single base substitution C T upstream_gene_variant MELA-AU 4 85658343 85658343 single base substitution G A exon_variant MELA-AU 4 85658343 85658343 single base substitution G A missense_variant H2251Y 6751C>T MELA-AU 4 85658343 85658343 single base substitution G A upstream_gene_variant MELA-AU 4 85658428 85658428 single base substitution A G exon_variant MELA-AU 4 85658428 85658428 single base substitution A G synonymous_variant T2222T 6666T>C MELA-AU 4 85658428 85658428 single base substitution A G upstream_gene_variant MELA-AU 4 85658561 85658561 single base substitution G A intron_variant MELA-AU 4 85658561 85658561 single base substitution G A upstream_gene_variant MELA-AU 4 85658772 85658772 single base substitution G A intron_variant MELA-AU 4 85658772 85658772 single base substitution G A upstream_gene_variant MELA-AU 4 85658833 85658833 single base substitution A T intron_variant MELA-AU 4 85658833 85658833 single base substitution A T upstream_gene_variant MELA-AU 4 85658936 85658936 single base substitution G A intron_variant MELA-AU 4 85658936 85658936 single base substitution G A upstream_gene_variant MELA-AU 4 85659488 85659488 single base substitution A C intron_variant MELA-AU 4 85659488 85659488 single base substitution A C upstream_gene_variant MELA-AU 4 85659972 85659972 single base substitution G A intron_variant MELA-AU 4 85660354 85660354 single base substitution A G exon_variant MELA-AU 4 85660354 85660354 single base substitution A G intron_variant MELA-AU 4 85660748 85660748 single base substitution C T intron_variant MELA-AU 4 85660748 85660748 single base substitution C T upstream_gene_variant MELA-AU 4 85661333 85661333 single base substitution G A splice_region_variant MELA-AU 4 85661333 85661333 single base substitution G A upstream_gene_variant MELA-AU 4 85661562 85661562 deletion of <=200bp C - frameshift_variant R2081 MELA-AU 4 85661562 85661562 deletion of <=200bp C - upstream_gene_variant MELA-AU 4 85661879 85661879 single base substitution C T intron_variant MELA-AU 4 85661879 85661879 single base substitution C T upstream_gene_variant MELA-AU 4 85662516 85662516 single base substitution G A intron_variant MELA-AU 4 85662516 85662516 single base substitution G A upstream_gene_variant MELA-AU 4 85663669 85663669 single base substitution C T intron_variant MELA-AU 4 85663669 85663669 single base substitution C T upstream_gene_variant MELA-AU 4 85663703 85663703 single base substitution T C intron_variant MELA-AU 4 85663703 85663703 single base substitution T C upstream_gene_variant MELA-AU 4 85664391 85664391 single base substitution T A intron_variant MELA-AU 4 85664391 85664391 single base substitution T A upstream_gene_variant MELA-AU 4 85666143 85666143 single base substitution A G intron_variant MELA-AU 4 85666229 85666230 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 4 85666960 85666960 single base substitution C T intron_variant MELA-AU 4 85667016 85667016 single base substitution A C intron_variant MELA-AU 4 85667405 85667405 single base substitution G A downstream_gene_variant MELA-AU 4 85667405 85667405 single base substitution G A intron_variant MELA-AU 4 85667665 85667665 single base substitution G A downstream_gene_variant MELA-AU 4 85667665 85667665 single base substitution G A intron_variant MELA-AU 4 85668130 85668130 single base substitution G A downstream_gene_variant MELA-AU 4 85668130 85668130 single base substitution G A intron_variant MELA-AU 4 85668266 85668266 single base substitution G A downstream_gene_variant MELA-AU 4 85668266 85668266 single base substitution G A intron_variant MELA-AU 4 85668871 85668871 single base substitution G A downstream_gene_variant MELA-AU 4 85668871 85668871 single base substitution G A intron_variant MELA-AU 4 85669068 85669068 single base substitution G A downstream_gene_variant MELA-AU 4 85669068 85669068 single base substitution G A intron_variant MELA-AU 4 85669069 85669069 single base substitution G A downstream_gene_variant MELA-AU 4 85669069 85669069 single base substitution G A intron_variant MELA-AU 4 85669333 85669333 single base substitution G A downstream_gene_variant MELA-AU 4 85669333 85669333 single base substitution G A intron_variant MELA-AU 4 85669848 85669848 single base substitution G A downstream_gene_variant MELA-AU 4 85669848 85669848 single base substitution G A intron_variant MELA-AU 4 85670226 85670226 single base substitution G A downstream_gene_variant MELA-AU 4 85670226 85670226 single base substitution G A intron_variant MELA-AU 4 85670388 85670388 single base substitution T A downstream_gene_variant MELA-AU 4 85670388 85670388 single base substitution T A intron_variant MELA-AU 4 85670877 85670877 single base substitution G A downstream_gene_variant MELA-AU 4 85670877 85670877 single base substitution G A intron_variant MELA-AU 4 85671060 85671060 single base substitution A G downstream_gene_variant MELA-AU 4 85671060 85671060 single base substitution A G intron_variant MELA-AU 4 85671571 85671592 deletion of <=200bp GTTTTCAGGTTTCTATTTATAA - downstream_gene_variant MELA-AU 4 85671571 85671592 deletion of <=200bp GTTTTCAGGTTTCTATTTATAA - intron_variant MELA-AU 4 85671616 85671616 single base substitution G A downstream_gene_variant MELA-AU 4 85671616 85671616 single base substitution G A intron_variant MELA-AU 4 85671617 85671617 single base substitution G A downstream_gene_variant MELA-AU 4 85671617 85671617 single base substitution G A intron_variant MELA-AU 4 85672726 85672726 single base substitution G A exon_variant MELA-AU 4 85672726 85672726 single base substitution G A synonymous_variant F1961F 5883C>T MELA-AU 4 85673250 85673250 single base substitution T C intron_variant MELA-AU 4 85673671 85673671 single base substitution G A intron_variant MELA-AU 4 85673710 85673710 single base substitution G A intron_variant MELA-AU 4 85673903 85673903 single base substitution C A intron_variant MELA-AU 4 85673920 85673920 single base substitution G A intron_variant MELA-AU 4 85675039 85675039 single base substitution G A intron_variant MELA-AU 4 85675196 85675196 single base substitution G A intron_variant MELA-AU 4 85675243 85675243 single base substitution G A intron_variant MELA-AU 4 85675405 85675405 single base substitution G A intron_variant MELA-AU 4 85675468 85675468 single base substitution G A intron_variant MELA-AU 4 85676154 85676154 single base substitution G A intron_variant MELA-AU 4 85676411 85676411 single base substitution G A intron_variant MELA-AU 4 85676411 85676411 single base substitution G A splice_region_variant MELA-AU 4 85677346 85677346 single base substitution C T intron_variant MELA-AU 4 85677346 85677346 single base substitution C T upstream_gene_variant MELA-AU 4 85677402 85677402 single base substitution G A intron_variant MELA-AU 4 85677402 85677402 single base substitution G A upstream_gene_variant MELA-AU 4 85677740 85677744 deletion of <=200bp AAATA - intron_variant MELA-AU 4 85677740 85677744 deletion of <=200bp AAATA - upstream_gene_variant MELA-AU 4 85678995 85678995 single base substitution G A intron_variant MELA-AU 4 85678995 85678995 single base substitution G A upstream_gene_variant MELA-AU 4 85679319 85679319 single base substitution G A intron_variant MELA-AU 4 85679319 85679319 single base substitution G A upstream_gene_variant MELA-AU 4 85680025 85680025 single base substitution C T intron_variant MELA-AU 4 85680025 85680025 single base substitution C T upstream_gene_variant MELA-AU 4 85680150 85680150 single base substitution G A intron_variant MELA-AU 4 85680150 85680150 single base substitution G A upstream_gene_variant MELA-AU 4 85681776 85681776 single base substitution C T intron_variant MELA-AU 4 85682899 85682899 single base substitution G A intron_variant MELA-AU 4 85682913 85682913 single base substitution T C intron_variant MELA-AU 4 85684102 85684102 single base substitution A G intron_variant MELA-AU 4 85684935 85684935 single base substitution A T intron_variant MELA-AU 4 85684986 85684986 single base substitution A T intron_variant MELA-AU 4 85685161 85685161 single base substitution A T intron_variant MELA-AU 4 85685629 85685629 single base substitution A G intron_variant MELA-AU 4 85685811 85685811 single base substitution G A intron_variant MELA-AU 4 85686124 85686124 single base substitution G A intron_variant MELA-AU 4 85686228 85686228 single base substitution G A intron_variant MELA-AU 4 85686862 85686862 single base substitution T C intron_variant MELA-AU 4 85687298 85687298 single base substitution G A intron_variant MELA-AU 4 85687689 85687689 single base substitution T A intron_variant MELA-AU 4 85687799 85687799 single base substitution G A intron_variant MELA-AU 4 85687974 85687974 single base substitution A T intron_variant MELA-AU 4 85688192 85688192 single base substitution A G intron_variant MELA-AU 4 85688349 85688349 single base substitution T C intron_variant MELA-AU 4 85688918 85688918 single base substitution G A intron_variant MELA-AU 4 85689088 85689088 single base substitution G A intron_variant MELA-AU 4 85689426 85689426 single base substitution A G intron_variant MELA-AU 4 85689880 85689880 single base substitution T G intron_variant MELA-AU 4 85689901 85689901 single base substitution G A intron_variant MELA-AU 4 85690320 85690320 single base substitution G A intron_variant MELA-AU 4 85691021 85691021 single base substitution G A intron_variant MELA-AU 4 85691241 85691241 single base substitution G C intron_variant MELA-AU 4 85691487 85691487 single base substitution T C intron_variant MELA-AU 4 85692158 85692158 single base substitution A G intron_variant MELA-AU 4 85693135 85693135 single base substitution C T intron_variant MELA-AU 4 85693167 85693167 single base substitution G A intron_variant MELA-AU 4 85693493 85693493 single base substitution G A intron_variant MELA-AU 4 85693515 85693515 single base substitution G A intron_variant MELA-AU 4 85693754 85693754 single base substitution G A intron_variant MELA-AU 4 85694094 85694094 single base substitution G A intron_variant MELA-AU 4 85694110 85694110 single base substitution G A intron_variant MELA-AU 4 85694474 85694474 single base substitution G A intron_variant MELA-AU 4 85694714 85694714 single base substitution G A intron_variant MELA-AU 4 85694715 85694715 single base substitution G A intron_variant MELA-AU 4 85694736 85694736 single base substitution A G intron_variant MELA-AU 4 85695316 85695316 single base substitution G A intron_variant MELA-AU 4 85696257 85696257 single base substitution G A missense_variant S1518F 4553C>T MELA-AU 4 85697142 85697142 single base substitution G A intron_variant MELA-AU 4 85697697 85697697 single base substitution G A intron_variant MELA-AU 4 85698176 85698176 single base substitution G A intron_variant MELA-AU 4 85698320 85698320 single base substitution G A intron_variant MELA-AU 4 85698387 85698387 single base substitution G A intron_variant MELA-AU 4 85698492 85698492 single base substitution G A intron_variant MELA-AU 4 85699073 85699073 single base substitution G A intron_variant MELA-AU 4 85699528 85699528 single base substitution G A intron_variant MELA-AU 4 85699936 85699936 single base substitution C T intron_variant MELA-AU 4 85699946 85699946 single base substitution G A intron_variant MELA-AU 4 85700039 85700039 single base substitution A T intron_variant MELA-AU 4 85700225 85700225 single base substitution G C intron_variant MELA-AU 4 85700855 85700855 single base substitution G A intron_variant MELA-AU 4 85701072 85701072 single base substitution G T intron_variant MELA-AU 4 85701688 85701688 single base substitution G A intron_variant MELA-AU 4 85701904 85701904 single base substitution G A intron_variant MELA-AU 4 85702148 85702148 single base substitution G A intron_variant MELA-AU 4 85702208 85702208 single base substitution G A intron_variant MELA-AU 4 85702673 85702673 single base substitution G A intron_variant MELA-AU 4 85703377 85703377 single base substitution C T intron_variant MELA-AU 4 85703916 85703916 single base substitution T A intron_variant MELA-AU 4 85704072 85704072 single base substitution T G intron_variant MELA-AU 4 85704114 85704114 single base substitution A G splice_donor_variant MELA-AU 4 85704170 85704170 single base substitution C T missense_variant G1374R 4120G>A MELA-AU 4 85704422 85704422 single base substitution G A intron_variant MELA-AU 4 85704580 85704580 single base substitution G A intron_variant MELA-AU 4 85704713 85704713 single base substitution G A intron_variant MELA-AU 4 85704945 85704945 single base substitution C T intron_variant MELA-AU 4 85706632 85706633 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 85707411 85707411 single base substitution G A intron_variant MELA-AU 4 85707469 85707469 single base substitution G A intron_variant MELA-AU 4 85708548 85708548 single base substitution A G intron_variant MELA-AU 4 85708757 85708757 single base substitution G A missense_variant S1260L 3779C>T MELA-AU 4 85709019 85709019 single base substitution G A intron_variant MELA-AU 4 85709798 85709798 single base substitution G A intron_variant MELA-AU 4 85709857 85709857 single base substitution G A intron_variant MELA-AU 4 85709920 85709920 single base substitution C T intron_variant MELA-AU 4 85710180 85710180 single base substitution G A intron_variant MELA-AU 4 85710325 85710325 single base substitution T C intron_variant MELA-AU 4 85711202 85711202 single base substitution A T intron_variant MELA-AU 4 85711511 85711511 single base substitution A G intron_variant MELA-AU 4 85711790 85711790 single base substitution G A intron_variant MELA-AU 4 85711821 85711821 single base substitution G A intron_variant MELA-AU 4 85712031 85712031 single base substitution G A intron_variant MELA-AU 4 85712190 85712190 single base substitution G A intron_variant MELA-AU 4 85712563 85712563 single base substitution G A intron_variant MELA-AU 4 85713203 85713203 single base substitution C T intron_variant MELA-AU 4 85713536 85713536 single base substitution G A intron_variant MELA-AU 4 85714544 85714544 single base substitution G A intron_variant MELA-AU 4 85714923 85714923 single base substitution G A intron_variant MELA-AU 4 85714933 85714933 single base substitution A G intron_variant MELA-AU 4 85714934 85714934 single base substitution C T intron_variant MELA-AU 4 85715099 85715099 single base substitution A T intron_variant MELA-AU 4 85715948 85715948 single base substitution G A intron_variant MELA-AU 4 85716767 85716767 single base substitution C T intron_variant MELA-AU 4 85716823 85716823 single base substitution G A intron_variant MELA-AU 4 85717223 85717223 single base substitution T A intron_variant MELA-AU 4 85717464 85717464 single base substitution C T intron_variant MELA-AU 4 85717809 85717809 single base substitution G A missense_variant S1011F 3032C>T MELA-AU 4 85718231 85718231 single base substitution T C downstream_gene_variant MELA-AU 4 85718231 85718231 single base substitution T C intron_variant MELA-AU 4 85718692 85718692 single base substitution G A downstream_gene_variant MELA-AU 4 85718692 85718692 single base substitution G A intron_variant MELA-AU 4 85718711 85718711 insertion of <=200bp - TTAT downstream_gene_variant MELA-AU 4 85718711 85718711 insertion of <=200bp - TTAT intron_variant MELA-AU 4 85718711 85718711 insertion of <=200bp - TTATTTAT downstream_gene_variant MELA-AU 4 85718711 85718711 insertion of <=200bp - TTATTTAT intron_variant MELA-AU 4 85718732 85718732 single base substitution T C downstream_gene_variant MELA-AU 4 85718732 85718732 single base substitution T C intron_variant MELA-AU 4 85718897 85718897 single base substitution C G downstream_gene_variant MELA-AU 4 85718897 85718897 single base substitution C G intron_variant MELA-AU 4 85720493 85720493 single base substitution T A downstream_gene_variant MELA-AU 4 85720493 85720493 single base substitution T A intron_variant MELA-AU 4 85720689 85720689 single base substitution G A downstream_gene_variant MELA-AU 4 85720689 85720689 single base substitution G A intron_variant MELA-AU 4 85720728 85720728 single base substitution G A downstream_gene_variant MELA-AU 4 85720728 85720728 single base substitution G A intron_variant MELA-AU 4 85721815 85721815 single base substitution G A downstream_gene_variant MELA-AU 4 85721815 85721815 single base substitution G A intron_variant MELA-AU 4 85721892 85721892 single base substitution G A downstream_gene_variant MELA-AU 4 85721892 85721892 single base substitution G A intron_variant MELA-AU 4 85721894 85721894 single base substitution T A downstream_gene_variant MELA-AU 4 85721894 85721894 single base substitution T A intron_variant MELA-AU 4 85721985 85721985 single base substitution G A downstream_gene_variant MELA-AU 4 85721985 85721985 single base substitution G A intron_variant MELA-AU 4 85723263 85723263 single base substitution G A intron_variant MELA-AU 4 85723294 85723294 single base substitution T A intron_variant MELA-AU 4 85723447 85723447 single base substitution C T intron_variant MELA-AU 4 85723526 85723526 single base substitution C T intron_variant MELA-AU 4 85723690 85723690 single base substitution G A intron_variant MELA-AU 4 85724593 85724593 single base substitution G A exon_variant MELA-AU 4 85724593 85724593 single base substitution G A synonymous_variant P819P 2457C>T MELA-AU 4 85724706 85724706 single base substitution A G intron_variant MELA-AU 4 85724767 85724767 single base substitution G A intron_variant MELA-AU 4 85725012 85725012 single base substitution T C intron_variant MELA-AU 4 85725429 85725429 single base substitution G A downstream_gene_variant MELA-AU 4 85725429 85725429 single base substitution G A intron_variant MELA-AU 4 85725429 85725429 single base substitution G A upstream_gene_variant MELA-AU 4 85725765 85725765 single base substitution T C downstream_gene_variant MELA-AU 4 85725765 85725765 single base substitution T C intron_variant MELA-AU 4 85725765 85725765 single base substitution T C upstream_gene_variant MELA-AU 4 85726125 85726125 single base substitution G A downstream_gene_variant MELA-AU 4 85726125 85726125 single base substitution G A intron_variant MELA-AU 4 85726125 85726125 single base substitution G A upstream_gene_variant MELA-AU 4 85726517 85726517 single base substitution G A downstream_gene_variant MELA-AU 4 85726517 85726517 single base substitution G A intron_variant MELA-AU 4 85726517 85726517 single base substitution G A upstream_gene_variant MELA-AU 4 85726682 85726682 single base substitution G A downstream_gene_variant MELA-AU 4 85726682 85726682 single base substitution G A intron_variant MELA-AU 4 85726682 85726682 single base substitution G A upstream_gene_variant MELA-AU 4 85726833 85726833 single base substitution G A downstream_gene_variant MELA-AU 4 85726833 85726833 single base substitution G A intron_variant MELA-AU 4 85726833 85726833 single base substitution G A upstream_gene_variant MELA-AU 4 85727068 85727068 single base substitution G A downstream_gene_variant MELA-AU 4 85727068 85727068 single base substitution G A intron_variant MELA-AU 4 85727068 85727068 single base substitution G A upstream_gene_variant MELA-AU 4 85727613 85727613 single base substitution C T downstream_gene_variant MELA-AU 4 85727613 85727613 single base substitution C T intron_variant MELA-AU 4 85727613 85727613 single base substitution C T upstream_gene_variant MELA-AU 4 85727715 85727715 single base substitution G A downstream_gene_variant MELA-AU 4 85727715 85727715 single base substitution G A intron_variant MELA-AU 4 85727715 85727715 single base substitution G A upstream_gene_variant MELA-AU 4 85727893 85727893 single base substitution G A downstream_gene_variant MELA-AU 4 85727893 85727893 single base substitution G A intron_variant MELA-AU 4 85727893 85727893 single base substitution G A upstream_gene_variant MELA-AU 4 85728443 85728444 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 4 85728443 85728444 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 85728443 85728444 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 4 85729123 85729123 single base substitution G A downstream_gene_variant MELA-AU 4 85729123 85729123 single base substitution G A intron_variant MELA-AU 4 85729123 85729123 single base substitution G A upstream_gene_variant MELA-AU 4 85729529 85729529 single base substitution G A downstream_gene_variant MELA-AU 4 85729529 85729529 single base substitution G A intron_variant MELA-AU 4 85729529 85729529 single base substitution G A missense_variant S796F 2387C>T MELA-AU 4 85729529 85729529 single base substitution G A upstream_gene_variant MELA-AU 4 85729554 85729554 single base substitution G A downstream_gene_variant MELA-AU 4 85729554 85729554 single base substitution G A intron_variant MELA-AU 4 85729554 85729554 single base substitution G A missense_variant P788S 2362C>T MELA-AU 4 85729554 85729554 single base substitution G A upstream_gene_variant MELA-AU 4 85729987 85729987 single base substitution G A downstream_gene_variant MELA-AU 4 85729987 85729987 single base substitution G A intron_variant MELA-AU 4 85729987 85729987 single base substitution G A upstream_gene_variant MELA-AU 4 85730105 85730105 deletion of <=200bp G - exon_variant MELA-AU 4 85730105 85730105 deletion of <=200bp G - intron_variant MELA-AU 4 85730105 85730105 deletion of <=200bp G - upstream_gene_variant MELA-AU 4 85730632 85730632 single base substitution G A exon_variant MELA-AU 4 85730632 85730632 single base substitution G A intron_variant MELA-AU 4 85731467 85731467 single base substitution G A exon_variant MELA-AU 4 85731467 85731467 single base substitution G A missense_variant R640C 1918C>T MELA-AU 4 85731467 85731467 single base substitution G A upstream_gene_variant MELA-AU 4 85732348 85732348 single base substitution C T intron_variant MELA-AU 4 85732348 85732348 single base substitution C T upstream_gene_variant MELA-AU 4 85733043 85733043 single base substitution C T intron_variant MELA-AU 4 85733043 85733043 single base substitution C T upstream_gene_variant MELA-AU 4 85733218 85733218 single base substitution A T intron_variant MELA-AU 4 85733218 85733218 single base substitution A T upstream_gene_variant MELA-AU 4 85735617 85735617 single base substitution G A intron_variant MELA-AU 4 85735617 85735617 single base substitution G A upstream_gene_variant MELA-AU 4 85735963 85735968 deletion of <=200bp TATGAA - intron_variant MELA-AU 4 85735963 85735968 deletion of <=200bp TATGAA - upstream_gene_variant MELA-AU 4 85736686 85736686 single base substitution A G intron_variant MELA-AU 4 85736788 85736788 single base substitution G A intron_variant MELA-AU 4 85736819 85736819 single base substitution C T intron_variant MELA-AU 4 85736837 85736837 single base substitution G A intron_variant MELA-AU 4 85737580 85737580 single base substitution C T intron_variant MELA-AU 4 85737748 85737748 single base substitution A G intron_variant MELA-AU 4 85738523 85738523 single base substitution G A intron_variant MELA-AU 4 85738575 85738575 single base substitution C T exon_variant MELA-AU 4 85738575 85738575 single base substitution C T synonymous_variant T619T 1857G>A MELA-AU 4 85738749 85738749 single base substitution G A intron_variant MELA-AU 4 85739055 85739055 single base substitution A G intron_variant MELA-AU 4 85740079 85740079 single base substitution G A intron_variant MELA-AU 4 85741103 85741103 single base substitution G A intron_variant MELA-AU 4 85742679 85742679 single base substitution G T exon_variant MELA-AU 4 85742679 85742679 single base substitution G T synonymous_variant A383A 1149C>A MELA-AU 4 85742718 85742718 single base substitution G A intron_variant MELA-AU 4 85743302 85743303 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85743305 85743305 single base substitution G A intron_variant MELA-AU 4 85743428 85743428 single base substitution C T intron_variant MELA-AU 4 85744176 85744176 single base substitution G A intron_variant MELA-AU 4 85744410 85744410 single base substitution A G intron_variant MELA-AU 4 85745125 85745125 single base substitution A T intron_variant MELA-AU 4 85745597 85745597 single base substitution G A intron_variant MELA-AU 4 85745751 85745751 single base substitution G A intron_variant MELA-AU 4 85747618 85747618 single base substitution G A intron_variant MELA-AU 4 85748152 85748152 single base substitution A G intron_variant MELA-AU 4 85748625 85748625 single base substitution C T intron_variant MELA-AU 4 85748870 85748870 single base substitution C T intron_variant MELA-AU 4 85748899 85748899 single base substitution G A intron_variant MELA-AU 4 85749256 85749256 single base substitution G A intron_variant MELA-AU 4 85749544 85749544 single base substitution G A intron_variant MELA-AU 4 85749705 85749705 single base substitution A C intron_variant MELA-AU 4 85749985 85749985 single base substitution G A intron_variant MELA-AU 4 85751000 85751000 single base substitution A G intron_variant MELA-AU 4 85751436 85751436 deletion of <=200bp A - intron_variant MELA-AU 4 85751868 85751868 single base substitution T A intron_variant MELA-AU 4 85751965 85751965 single base substitution G A intron_variant MELA-AU 4 85751987 85751987 single base substitution G A intron_variant MELA-AU 4 85752140 85752140 single base substitution G A intron_variant MELA-AU 4 85752258 85752258 single base substitution G A intron_variant MELA-AU 4 85752439 85752439 single base substitution C T intron_variant MELA-AU 4 85752470 85752470 single base substitution A G intron_variant MELA-AU 4 85752916 85752916 single base substitution G A intron_variant MELA-AU 4 85753081 85753081 single base substitution G A intron_variant MELA-AU 4 85753167 85753167 single base substitution C T intron_variant MELA-AU 4 85753812 85753812 single base substitution G A intron_variant MELA-AU 4 85754654 85754654 single base substitution A G intron_variant MELA-AU 4 85754779 85754779 single base substitution T A intron_variant MELA-AU 4 85754846 85754846 single base substitution G A intron_variant MELA-AU 4 85755040 85755040 single base substitution G A intron_variant MELA-AU 4 85755466 85755466 single base substitution G A intron_variant MELA-AU 4 85755498 85755498 single base substitution A T intron_variant MELA-AU 4 85755699 85755699 single base substitution G A intron_variant MELA-AU 4 85755702 85755702 single base substitution G C intron_variant MELA-AU 4 85755779 85755779 single base substitution G A intron_variant MELA-AU 4 85755781 85755781 single base substitution G A intron_variant MELA-AU 4 85756506 85756506 single base substitution C T intron_variant MELA-AU 4 85756622 85756622 single base substitution G A intron_variant MELA-AU 4 85756651 85756651 single base substitution G A intron_variant MELA-AU 4 85757440 85757440 single base substitution T C downstream_gene_variant MELA-AU 4 85757440 85757440 single base substitution T C intron_variant MELA-AU 4 85757589 85757589 single base substitution G T downstream_gene_variant MELA-AU 4 85757589 85757589 single base substitution G T intron_variant MELA-AU 4 85757703 85757703 single base substitution G A downstream_gene_variant MELA-AU 4 85757703 85757703 single base substitution G A intron_variant MELA-AU 4 85758125 85758125 single base substitution G A downstream_gene_variant MELA-AU 4 85758125 85758125 single base substitution G A exon_variant MELA-AU 4 85758125 85758125 single base substitution G A missense_variant P178L 533C>T MELA-AU 4 85759075 85759075 single base substitution T C downstream_gene_variant MELA-AU 4 85759075 85759075 single base substitution T C intron_variant MELA-AU 4 85759612 85759612 single base substitution A G downstream_gene_variant MELA-AU 4 85759612 85759612 single base substitution A G intron_variant MELA-AU 4 85760577 85760577 single base substitution G A downstream_gene_variant MELA-AU 4 85760577 85760577 single base substitution G A intron_variant MELA-AU 4 85760778 85760778 single base substitution A G downstream_gene_variant MELA-AU 4 85760778 85760778 single base substitution A G intron_variant MELA-AU 4 85761761 85761761 single base substitution G A downstream_gene_variant MELA-AU 4 85761761 85761761 single base substitution G A intron_variant MELA-AU 4 85761817 85761817 single base substitution A G downstream_gene_variant MELA-AU 4 85761817 85761817 single base substitution A G intron_variant MELA-AU 4 85762240 85762240 single base substitution A T downstream_gene_variant MELA-AU 4 85762240 85762240 single base substitution A T intron_variant MELA-AU 4 85762354 85762354 single base substitution C T exon_variant MELA-AU 4 85762354 85762354 single base substitution C T missense_variant G123S 367G>A MELA-AU 4 85762354 85762354 single base substitution C T missense_variant G77S 229G>A MELA-AU 4 85762407 85762407 single base substitution C T exon_variant MELA-AU 4 85762407 85762407 single base substitution C T missense_variant S105N 314G>A MELA-AU 4 85762407 85762407 single base substitution C T missense_variant S59N 176G>A MELA-AU 4 85762747 85762747 single base substitution G C intron_variant MELA-AU 4 85762920 85762920 single base substitution G A intron_variant MELA-AU 4 85762984 85762984 single base substitution G A intron_variant MELA-AU 4 85763142 85763142 single base substitution A G intron_variant MELA-AU 4 85763256 85763256 single base substitution C T intron_variant MELA-AU 4 85763443 85763443 single base substitution A T intron_variant MELA-AU 4 85763921 85763921 single base substitution G A intron_variant MELA-AU 4 85763928 85763928 single base substitution C T intron_variant MELA-AU 4 85764148 85764148 single base substitution T A intron_variant MELA-AU 4 85764158 85764158 single base substitution A G intron_variant MELA-AU 4 85764708 85764708 single base substitution T G intron_variant MELA-AU 4 85764948 85764948 single base substitution G A intron_variant MELA-AU 4 85765075 85765075 single base substitution G A intron_variant MELA-AU 4 85765306 85765306 single base substitution G A intron_variant MELA-AU 4 85765697 85765697 single base substitution G A intron_variant MELA-AU 4 85766964 85766964 single base substitution G A downstream_gene_variant MELA-AU 4 85766964 85766964 single base substitution G A intron_variant MELA-AU 4 85767280 85767280 single base substitution G A downstream_gene_variant MELA-AU 4 85767280 85767280 single base substitution G A intron_variant MELA-AU 4 85767741 85767741 single base substitution G A downstream_gene_variant MELA-AU 4 85767741 85767741 single base substitution G A intron_variant MELA-AU 4 85768382 85768382 single base substitution G A downstream_gene_variant MELA-AU 4 85768382 85768382 single base substitution G A intron_variant MELA-AU 4 85770133 85770133 single base substitution G A downstream_gene_variant MELA-AU 4 85770133 85770133 single base substitution G A intron_variant MELA-AU 4 85770520 85770520 single base substitution G A downstream_gene_variant MELA-AU 4 85770520 85770520 single base substitution G A intron_variant MELA-AU 4 85771484 85771484 single base substitution T G intron_variant MELA-AU 4 85771484 85771484 single base substitution T G upstream_gene_variant MELA-AU 4 85771535 85771535 single base substitution G A intron_variant MELA-AU 4 85771535 85771535 single base substitution G A upstream_gene_variant MELA-AU 4 85771783 85771783 single base substitution G A intron_variant MELA-AU 4 85771783 85771783 single base substitution G A upstream_gene_variant MELA-AU 4 85773122 85773122 single base substitution A G intron_variant MELA-AU 4 85773122 85773122 single base substitution A G upstream_gene_variant MELA-AU 4 85773757 85773757 single base substitution T A intron_variant MELA-AU 4 85773757 85773757 single base substitution T A upstream_gene_variant MELA-AU 4 85773937 85773937 single base substitution G C intron_variant MELA-AU 4 85773937 85773937 single base substitution G C upstream_gene_variant MELA-AU 4 85774086 85774086 deletion of <=200bp T - intron_variant MELA-AU 4 85774086 85774086 deletion of <=200bp T - upstream_gene_variant MELA-AU 4 85774375 85774375 single base substitution G T intron_variant MELA-AU 4 85774375 85774375 single base substitution G T upstream_gene_variant MELA-AU 4 85775230 85775230 single base substitution G A intron_variant MELA-AU 4 85775230 85775230 single base substitution G A upstream_gene_variant MELA-AU 4 85775232 85775232 single base substitution G A intron_variant MELA-AU 4 85775232 85775232 single base substitution G A upstream_gene_variant MELA-AU 4 85775420 85775420 single base substitution T G intron_variant MELA-AU 4 85775420 85775420 single base substitution T G upstream_gene_variant MELA-AU 4 85775588 85775588 single base substitution G A intron_variant MELA-AU 4 85775588 85775588 single base substitution G A upstream_gene_variant MELA-AU 4 85776101 85776101 single base substitution G C intron_variant MELA-AU 4 85776101 85776101 single base substitution G C upstream_gene_variant MELA-AU 4 85776553 85776553 single base substitution T C intron_variant MELA-AU 4 85776677 85776677 single base substitution G A downstream_gene_variant MELA-AU 4 85776677 85776677 single base substitution G A intron_variant MELA-AU 4 85776719 85776719 single base substitution A T downstream_gene_variant MELA-AU 4 85776719 85776719 single base substitution A T intron_variant MELA-AU 4 85776779 85776779 single base substitution G A downstream_gene_variant MELA-AU 4 85776779 85776779 single base substitution G A intron_variant MELA-AU 4 85777999 85777999 single base substitution G A downstream_gene_variant MELA-AU 4 85777999 85777999 single base substitution G A intron_variant MELA-AU 4 85778589 85778589 single base substitution C T downstream_gene_variant MELA-AU 4 85778589 85778589 single base substitution C T intron_variant MELA-AU 4 85778788 85778788 single base substitution G A downstream_gene_variant MELA-AU 4 85778788 85778788 single base substitution G A intron_variant MELA-AU 4 85779221 85779221 single base substitution C T downstream_gene_variant MELA-AU 4 85779221 85779221 single base substitution C T intron_variant MELA-AU 4 85779470 85779470 single base substitution C T downstream_gene_variant MELA-AU 4 85779470 85779470 single base substitution C T intron_variant MELA-AU 4 85779614 85779614 single base substitution A T downstream_gene_variant MELA-AU 4 85779614 85779614 single base substitution A T intron_variant MELA-AU 4 85779617 85779617 single base substitution G A downstream_gene_variant MELA-AU 4 85779617 85779617 single base substitution G A intron_variant MELA-AU 4 85779990 85779990 single base substitution G A downstream_gene_variant MELA-AU 4 85779990 85779990 single base substitution G A intron_variant MELA-AU 4 85780034 85780034 single base substitution G A downstream_gene_variant MELA-AU 4 85780034 85780034 single base substitution G A intron_variant MELA-AU 4 85780894 85780894 single base substitution G A downstream_gene_variant MELA-AU 4 85780894 85780894 single base substitution G A intron_variant MELA-AU 4 85780998 85780998 single base substitution G A downstream_gene_variant MELA-AU 4 85780998 85780998 single base substitution G A intron_variant MELA-AU 4 85781388 85781388 single base substitution G A downstream_gene_variant MELA-AU 4 85781388 85781388 single base substitution G A intron_variant MELA-AU 4 85781437 85781437 single base substitution G A downstream_gene_variant MELA-AU 4 85781437 85781437 single base substitution G A intron_variant MELA-AU 4 85781713 85781713 single base substitution G A downstream_gene_variant MELA-AU 4 85781713 85781713 single base substitution G A exon_variant MELA-AU 4 85781713 85781713 single base substitution G A missense_variant P11L 32C>T MELA-AU 4 85782415 85782415 single base substitution G A intron_variant MELA-AU 4 85782415 85782415 single base substitution G A upstream_gene_variant MELA-AU 4 85782587 85782587 single base substitution G A intron_variant MELA-AU 4 85782587 85782587 single base substitution G A upstream_gene_variant MELA-AU 4 85783592 85783592 single base substitution G A intron_variant MELA-AU 4 85783592 85783592 single base substitution G A upstream_gene_variant MELA-AU 4 85783816 85783817 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85783816 85783817 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 4 85783851 85783851 single base substitution T G intron_variant MELA-AU 4 85783851 85783851 single base substitution T G upstream_gene_variant MELA-AU 4 85783916 85783916 single base substitution G A intron_variant MELA-AU 4 85783916 85783916 single base substitution G A upstream_gene_variant MELA-AU 4 85785037 85785037 single base substitution C T intron_variant MELA-AU 4 85785037 85785037 single base substitution C T upstream_gene_variant MELA-AU 4 85785188 85785188 deletion of <=200bp A - intron_variant MELA-AU 4 85785188 85785188 deletion of <=200bp A - upstream_gene_variant MELA-AU 4 85785269 85785269 single base substitution C T intron_variant MELA-AU 4 85785269 85785269 single base substitution C T upstream_gene_variant MELA-AU 4 85785610 85785610 single base substitution G A intron_variant MELA-AU 4 85785610 85785610 single base substitution G A upstream_gene_variant MELA-AU 4 85785843 85785843 single base substitution G A intron_variant MELA-AU 4 85785843 85785843 single base substitution G A upstream_gene_variant MELA-AU 4 85786835 85786835 single base substitution G A intron_variant MELA-AU 4 85787472 85787472 single base substitution C T intron_variant MELA-AU 4 85787657 85787657 single base substitution G A intron_variant MELA-AU 4 85788077 85788077 single base substitution G A intron_variant MELA-AU 4 85789249 85789249 single base substitution G A intron_variant MELA-AU 4 85789629 85789629 single base substitution G A intron_variant MELA-AU 4 85789775 85789775 single base substitution C T intron_variant MELA-AU 4 85791124 85791124 single base substitution G A intron_variant MELA-AU 4 85791372 85791372 single base substitution G A intron_variant MELA-AU 4 85791541 85791541 single base substitution G A intron_variant MELA-AU 4 85791890 85791890 single base substitution G A intron_variant MELA-AU 4 85792399 85792399 single base substitution G A intron_variant MELA-AU 4 85792476 85792476 single base substitution G A intron_variant MELA-AU 4 85792656 85792656 single base substitution C T intron_variant MELA-AU 4 85792814 85792815 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85793969 85793969 single base substitution G A intron_variant MELA-AU 4 85793998 85793998 single base substitution G A intron_variant MELA-AU 4 85794002 85794002 single base substitution T A intron_variant MELA-AU 4 85794171 85794171 single base substitution G A intron_variant MELA-AU 4 85794440 85794440 single base substitution C T intron_variant MELA-AU 4 85794649 85794649 single base substitution G A intron_variant MELA-AU 4 85795123 85795123 single base substitution G A intron_variant MELA-AU 4 85795285 85795285 single base substitution G A intron_variant MELA-AU 4 85795681 85795681 single base substitution G C intron_variant MELA-AU 4 85796353 85796353 single base substitution G A intron_variant MELA-AU 4 85796534 85796534 single base substitution T A intron_variant MELA-AU 4 85796870 85796870 single base substitution A G intron_variant MELA-AU 4 85796888 85796888 single base substitution T G intron_variant MELA-AU 4 85796994 85796995 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85797943 85797943 single base substitution A C intron_variant MELA-AU 4 85798296 85798296 single base substitution C T intron_variant MELA-AU 4 85798605 85798605 single base substitution G A intron_variant MELA-AU 4 85799528 85799528 single base substitution C A intron_variant MELA-AU 4 85799735 85799735 single base substitution G A intron_variant MELA-AU 4 85799818 85799818 single base substitution C T intron_variant MELA-AU 4 85800110 85800110 single base substitution G A intron_variant MELA-AU 4 85800914 85800914 single base substitution G A intron_variant MELA-AU 4 85802031 85802031 single base substitution C G intron_variant MELA-AU 4 85802290 85802290 single base substitution A G intron_variant MELA-AU 4 85802805 85802805 single base substitution C T intron_variant MELA-AU 4 85803577 85803578 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 85803736 85803736 single base substitution A C intron_variant MELA-AU 4 85804195 85804195 single base substitution G A intron_variant MELA-AU 4 85804360 85804360 single base substitution T G intron_variant MELA-AU 4 85804611 85804611 single base substitution G A intron_variant MELA-AU 4 85805026 85805026 single base substitution G A intron_variant MELA-AU 4 85805512 85805512 single base substitution T C intron_variant MELA-AU 4 85805787 85805787 single base substitution G A intron_variant MELA-AU 4 85806322 85806322 single base substitution T C intron_variant MELA-AU 4 85807249 85807249 single base substitution G A intron_variant MELA-AU 4 85807301 85807301 single base substitution A C intron_variant MELA-AU 4 85807314 85807314 single base substitution T A intron_variant MELA-AU 4 85807514 85807514 single base substitution T C intron_variant MELA-AU 4 85807737 85807737 single base substitution T A intron_variant MELA-AU 4 85807814 85807814 single base substitution G A intron_variant MELA-AU 4 85807830 85807831 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 4 85808802 85808802 single base substitution G A intron_variant MELA-AU 4 85808931 85808931 single base substitution T A intron_variant MELA-AU 4 85809080 85809080 single base substitution T C intron_variant MELA-AU 4 85809188 85809188 single base substitution G A intron_variant MELA-AU 4 85809354 85809354 single base substitution G A intron_variant MELA-AU 4 85809368 85809368 single base substitution G A intron_variant MELA-AU 4 85809392 85809392 single base substitution G A intron_variant MELA-AU 4 85809397 85809397 single base substitution A T intron_variant MELA-AU 4 85810523 85810523 single base substitution C T intron_variant MELA-AU 4 85811425 85811425 single base substitution G T intron_variant MELA-AU 4 85812152 85812152 single base substitution G A intron_variant MELA-AU 4 85812886 85812886 single base substitution G A intron_variant MELA-AU 4 85812907 85812908 multiple base substitution (>=2bp and <=200bp) GG CA intron_variant MELA-AU 4 85813153 85813153 single base substitution G A intron_variant MELA-AU 4 85813867 85813867 single base substitution A C intron_variant MELA-AU 4 85815121 85815121 single base substitution G A intron_variant MELA-AU 4 85815215 85815215 single base substitution G A intron_variant MELA-AU 4 85815794 85815794 single base substitution G C intron_variant MELA-AU 4 85816153 85816153 single base substitution A C intron_variant MELA-AU 4 85816744 85816744 single base substitution G A intron_variant MELA-AU 4 85816935 85816935 single base substitution G A intron_variant MELA-AU 4 85817100 85817100 single base substitution G A intron_variant MELA-AU 4 85817129 85817129 single base substitution G A intron_variant MELA-AU 4 85817690 85817690 single base substitution G A intron_variant MELA-AU 4 85817745 85817745 single base substitution G A intron_variant MELA-AU 4 85818081 85818081 single base substitution G A 5_prime_UTR_variant MELA-AU 4 85818081 85818081 single base substitution G A exon_variant MELA-AU 4 85818081 85818081 single base substitution G A intron_variant MELA-AU 4 85818207 85818207 single base substitution G A intron_variant MELA-AU 4 85818207 85818207 single base substitution G A upstream_gene_variant MELA-AU 4 85819439 85819439 single base substitution T A intron_variant MELA-AU 4 85819439 85819439 single base substitution T A upstream_gene_variant MELA-AU 4 85819652 85819652 single base substitution G A intron_variant MELA-AU 4 85819652 85819652 single base substitution G A upstream_gene_variant MELA-AU 4 85819881 85819881 single base substitution A G intron_variant MELA-AU 4 85819881 85819881 single base substitution A G upstream_gene_variant MELA-AU 4 85819904 85819904 single base substitution G A intron_variant MELA-AU 4 85819904 85819904 single base substitution G A upstream_gene_variant MELA-AU 4 85819987 85819987 single base substitution T A intron_variant MELA-AU 4 85819987 85819987 single base substitution T A upstream_gene_variant MELA-AU 4 85820171 85820171 single base substitution G A intron_variant MELA-AU 4 85820171 85820171 single base substitution G A upstream_gene_variant MELA-AU 4 85820263 85820263 single base substitution A G intron_variant MELA-AU 4 85820263 85820263 single base substitution A G upstream_gene_variant MELA-AU 4 85821189 85821189 single base substitution A G intron_variant MELA-AU 4 85821189 85821189 single base substitution A G upstream_gene_variant MELA-AU 4 85821966 85821966 single base substitution A G intron_variant MELA-AU 4 85821966 85821966 single base substitution A G upstream_gene_variant MELA-AU 4 85821978 85821978 single base substitution T C intron_variant MELA-AU 4 85821978 85821978 single base substitution T C upstream_gene_variant MELA-AU 4 85822247 85822247 single base substitution G A intron_variant MELA-AU 4 85822247 85822247 single base substitution G A upstream_gene_variant MELA-AU 4 85822617 85822617 single base substitution G A intron_variant MELA-AU 4 85822617 85822617 single base substitution G A upstream_gene_variant MELA-AU 4 85822628 85822628 single base substitution G A intron_variant MELA-AU 4 85822628 85822628 single base substitution G A upstream_gene_variant MELA-AU 4 85822631 85822631 single base substitution G A intron_variant MELA-AU 4 85822631 85822631 single base substitution G A upstream_gene_variant MELA-AU 4 85823010 85823010 single base substitution G A intron_variant MELA-AU 4 85823010 85823010 single base substitution G A upstream_gene_variant MELA-AU 4 85823514 85823514 single base substitution G A intron_variant MELA-AU 4 85823734 85823738 deletion of <=200bp AAGAA - intron_variant MELA-AU 4 85824203 85824203 single base substitution G A intron_variant MELA-AU 4 85824386 85824386 single base substitution G A intron_variant MELA-AU 4 85824452 85824452 single base substitution T C intron_variant MELA-AU 4 85824487 85824487 single base substitution G A intron_variant MELA-AU 4 85824665 85824665 single base substitution G A intron_variant MELA-AU 4 85824683 85824683 single base substitution G A intron_variant MELA-AU 4 85825167 85825167 single base substitution G A intron_variant MELA-AU 4 85825442 85825442 single base substitution G A intron_variant MELA-AU 4 85825514 85825514 single base substitution G A intron_variant MELA-AU 4 85825544 85825544 single base substitution G A intron_variant MELA-AU 4 85826248 85826248 single base substitution G A intron_variant MELA-AU 4 85826321 85826321 single base substitution T A intron_variant MELA-AU 4 85826472 85826472 single base substitution G A intron_variant MELA-AU 4 85828268 85828268 single base substitution A T intron_variant MELA-AU 4 85828295 85828295 single base substitution G A intron_variant MELA-AU 4 85828804 85828804 single base substitution A T intron_variant MELA-AU 4 85829113 85829113 single base substitution G T intron_variant MELA-AU 4 85829262 85829262 single base substitution G A intron_variant MELA-AU 4 85829436 85829436 single base substitution G A intron_variant MELA-AU 4 85829545 85829545 single base substitution G A intron_variant MELA-AU 4 85830201 85830201 single base substitution G A intron_variant MELA-AU 4 85830230 85830230 single base substitution G A intron_variant MELA-AU 4 85830350 85830350 single base substitution G A intron_variant MELA-AU 4 85830418 85830418 single base substitution A T intron_variant MELA-AU 4 85831118 85831118 single base substitution G A intron_variant MELA-AU 4 85831647 85831647 single base substitution G A intron_variant MELA-AU 4 85831842 85831842 single base substitution G A intron_variant MELA-AU 4 85832109 85832109 single base substitution G A intron_variant MELA-AU 4 85832412 85832412 single base substitution G A intron_variant MELA-AU 4 85833389 85833389 single base substitution A T intron_variant MELA-AU 4 85834014 85834014 single base substitution G A intron_variant MELA-AU 4 85834041 85834041 single base substitution G A intron_variant MELA-AU 4 85834072 85834072 single base substitution G A intron_variant MELA-AU 4 85834224 85834224 single base substitution T G intron_variant MELA-AU 4 85835597 85835597 single base substitution C A intron_variant MELA-AU 4 85835833 85835833 single base substitution G A intron_variant MELA-AU 4 85835885 85835885 single base substitution T C intron_variant MELA-AU 4 85837294 85837294 single base substitution G A intron_variant MELA-AU 4 85837704 85837704 single base substitution G A intron_variant MELA-AU 4 85837890 85837890 single base substitution A T intron_variant MELA-AU 4 85838109 85838109 single base substitution G A intron_variant MELA-AU 4 85838159 85838159 single base substitution G A intron_variant MELA-AU 4 85838206 85838206 single base substitution G A intron_variant MELA-AU 4 85838278 85838278 single base substitution C T intron_variant MELA-AU 4 85838434 85838434 single base substitution G A intron_variant MELA-AU 4 85838442 85838442 single base substitution G A intron_variant MELA-AU 4 85839060 85839060 single base substitution C T intron_variant MELA-AU 4 85839544 85839544 single base substitution G C intron_variant MELA-AU 4 85839846 85839846 single base substitution G A intron_variant MELA-AU 4 85840359 85840359 single base substitution G A intron_variant MELA-AU 4 85840812 85840812 single base substitution G A intron_variant MELA-AU 4 85840864 85840864 single base substitution G A intron_variant MELA-AU 4 85841031 85841031 single base substitution A T intron_variant MELA-AU 4 85841102 85841102 single base substitution G A intron_variant MELA-AU 4 85841114 85841114 single base substitution A T intron_variant MELA-AU 4 85841514 85841514 single base substitution G A intron_variant MELA-AU 4 85841795 85841795 single base substitution A C intron_variant MELA-AU 4 85841972 85841972 single base substitution G A intron_variant MELA-AU 4 85842431 85842431 single base substitution G A intron_variant MELA-AU 4 85842459 85842459 single base substitution G A intron_variant MELA-AU 4 85842524 85842524 single base substitution G A intron_variant MELA-AU 4 85843245 85843245 single base substitution G A intron_variant MELA-AU 4 85843378 85843378 single base substitution G A intron_variant MELA-AU 4 85843488 85843488 single base substitution A T intron_variant MELA-AU 4 85843670 85843670 single base substitution G A intron_variant MELA-AU 4 85843792 85843792 single base substitution G A intron_variant MELA-AU 4 85844040 85844040 single base substitution G A intron_variant MELA-AU 4 85844119 85844119 single base substitution G A intron_variant MELA-AU 4 85845754 85845754 single base substitution G A intron_variant MELA-AU 4 85845870 85845870 single base substitution A C intron_variant MELA-AU 4 85846404 85846404 single base substitution C T intron_variant MELA-AU 4 85846743 85846743 single base substitution T C intron_variant MELA-AU 4 85846939 85846939 single base substitution A G intron_variant MELA-AU 4 85847691 85847691 single base substitution C G intron_variant MELA-AU 4 85848219 85848219 single base substitution G A intron_variant MELA-AU 4 85848787 85848787 single base substitution C T intron_variant MELA-AU 4 85849126 85849126 single base substitution G A intron_variant MELA-AU 4 85849294 85849294 single base substitution G A intron_variant MELA-AU 4 85849400 85849400 single base substitution C T intron_variant MELA-AU 4 85849628 85849628 single base substitution A C intron_variant MELA-AU 4 85849671 85849671 single base substitution G A intron_variant MELA-AU 4 85849928 85849928 single base substitution G A intron_variant MELA-AU 4 85850081 85850081 single base substitution G A intron_variant MELA-AU 4 85850172 85850172 single base substitution G A intron_variant MELA-AU 4 85850173 85850173 single base substitution G A intron_variant MELA-AU 4 85850198 85850198 single base substitution G A intron_variant MELA-AU 4 85850959 85850959 single base substitution G A intron_variant MELA-AU 4 85851522 85851522 single base substitution G A intron_variant MELA-AU 4 85851531 85851531 single base substitution G A intron_variant MELA-AU 4 85853917 85853917 single base substitution T A intron_variant MELA-AU 4 85854224 85854224 single base substitution G C intron_variant MELA-AU 4 85854283 85854283 single base substitution G A intron_variant MELA-AU 4 85854651 85854651 single base substitution G A intron_variant MELA-AU 4 85856567 85856567 single base substitution G A intron_variant MELA-AU 4 85857056 85857056 single base substitution G A intron_variant MELA-AU 4 85857697 85857697 single base substitution G A intron_variant MELA-AU 4 85858075 85858075 single base substitution G A intron_variant MELA-AU 4 85858494 85858494 single base substitution C T intron_variant MELA-AU 4 85859313 85859313 single base substitution T C intron_variant MELA-AU 4 85859986 85859986 single base substitution G A intron_variant MELA-AU 4 85860361 85860361 single base substitution C T intron_variant MELA-AU 4 85860581 85860581 single base substitution G A intron_variant MELA-AU 4 85860611 85860611 single base substitution C T intron_variant MELA-AU 4 85860782 85860782 single base substitution G A intron_variant MELA-AU 4 85860889 85860889 single base substitution T G intron_variant MELA-AU 4 85861156 85861156 single base substitution G A intron_variant MELA-AU 4 85861254 85861254 single base substitution C T intron_variant MELA-AU 4 85862416 85862416 single base substitution G A intron_variant MELA-AU 4 85862743 85862743 single base substitution G A intron_variant MELA-AU 4 85862869 85862869 single base substitution T A intron_variant MELA-AU 4 85862876 85862876 single base substitution G A intron_variant MELA-AU 4 85862898 85862898 single base substitution G A intron_variant MELA-AU 4 85863073 85863073 single base substitution G A intron_variant MELA-AU 4 85863405 85863405 single base substitution G A intron_variant MELA-AU 4 85863425 85863425 single base substitution G A intron_variant MELA-AU 4 85863884 85863884 single base substitution A C intron_variant MELA-AU 4 85863903 85863903 single base substitution G A intron_variant MELA-AU 4 85864606 85864606 single base substitution G A intron_variant MELA-AU 4 85865336 85865336 single base substitution T A intron_variant MELA-AU 4 85865449 85865449 single base substitution G A intron_variant MELA-AU 4 85865457 85865457 single base substitution C T intron_variant MELA-AU 4 85865506 85865506 single base substitution G A intron_variant MELA-AU 4 85865784 85865784 single base substitution C T intron_variant MELA-AU 4 85866398 85866398 single base substitution G A intron_variant MELA-AU 4 85867879 85867879 single base substitution C T intron_variant MELA-AU 4 85867939 85867939 single base substitution G A intron_variant MELA-AU 4 85868094 85868094 single base substitution G A intron_variant MELA-AU 4 85868697 85868697 single base substitution A T intron_variant MELA-AU 4 85868700 85868700 single base substitution T A intron_variant MELA-AU 4 85869513 85869513 single base substitution C T intron_variant MELA-AU 4 85869724 85869724 single base substitution C T intron_variant MELA-AU 4 85870044 85870044 single base substitution A G intron_variant MELA-AU 4 85870185 85870185 single base substitution A C intron_variant MELA-AU 4 85870919 85870919 single base substitution G A intron_variant MELA-AU 4 85871806 85871806 single base substitution G A intron_variant MELA-AU 4 85872256 85872256 single base substitution T A intron_variant MELA-AU 4 85872372 85872372 single base substitution G A intron_variant MELA-AU 4 85872580 85872580 single base substitution A G intron_variant MELA-AU 4 85873188 85873188 single base substitution A G intron_variant MELA-AU 4 85874094 85874094 single base substitution A C intron_variant MELA-AU 4 85874172 85874172 single base substitution G A intron_variant MELA-AU 4 85874459 85874459 single base substitution G A intron_variant MELA-AU 4 85874768 85874768 single base substitution T C intron_variant MELA-AU 4 85875583 85875583 single base substitution G A intron_variant MELA-AU 4 85877069 85877069 single base substitution G A intron_variant MELA-AU 4 85877411 85877411 single base substitution G A intron_variant MELA-AU 4 85878813 85878813 single base substitution G A intron_variant MELA-AU 4 85878904 85878904 single base substitution G A intron_variant MELA-AU 4 85879304 85879304 single base substitution G A intron_variant MELA-AU 4 85879664 85879664 single base substitution G A intron_variant MELA-AU 4 85881729 85881729 single base substitution G A intron_variant MELA-AU 4 85881792 85881792 single base substitution G A intron_variant MELA-AU 4 85881841 85881841 single base substitution G A intron_variant MELA-AU 4 85882165 85882165 single base substitution C A intron_variant MELA-AU 4 85883875 85883875 single base substitution G A intron_variant MELA-AU 4 85884504 85884504 single base substitution G A intron_variant MELA-AU 4 85884621 85884621 single base substitution G A intron_variant MELA-AU 4 85885397 85885397 single base substitution G A intron_variant MELA-AU 4 85888077 85888077 single base substitution C T upstream_gene_variant MELA-AU 4 85888479 85888479 single base substitution C T upstream_gene_variant MELA-AU 4 85890140 85890140 single base substitution C T upstream_gene_variant MELA-AU 4 85890628 85890628 single base substitution G C upstream_gene_variant MELA-AU 4 85890867 85890867 single base substitution C T upstream_gene_variant MELA-AU 4 85891783 85891783 single base substitution C T upstream_gene_variant MELA-AU 4 85891808 85891808 single base substitution G A upstream_gene_variant MELA-AU 4 85892179 85892179 single base substitution C T upstream_gene_variant MELA-AU 4 85892192 85892192 single base substitution C T upstream_gene_variant MELA-AU 4 85892358 85892358 single base substitution G A upstream_gene_variant ORCA-IN 4 85606073 85606073 single base substitution A T intron_variant ORCA-IN 4 85606073 85606073 single base substitution A T upstream_gene_variant ORCA-IN 4 85607084 85607084 single base substitution C G intron_variant ORCA-IN 4 85607084 85607084 single base substitution C G upstream_gene_variant ORCA-IN 4 85607452 85607452 single base substitution C G intron_variant ORCA-IN 4 85607452 85607452 single base substitution C G upstream_gene_variant ORCA-IN 4 85617317 85617317 single base substitution C A missense_variant V2886L 8656G>T ORCA-IN 4 85617317 85617317 single base substitution C A missense_variant V2903L 8707G>T ORCA-IN 4 85617317 85617317 single base substitution C A missense_variant V506L 1516G>T ORCA-IN 4 85619486 85619486 single base substitution G A intron_variant ORCA-IN 4 85621257 85621257 single base substitution C A intron_variant ORCA-IN 4 85646540 85646540 single base substitution T C intron_variant ORCA-IN 4 85713148 85713148 single base substitution C G intron_variant ORCA-IN 4 85722843 85722843 single base substitution C G downstream_gene_variant ORCA-IN 4 85722843 85722843 single base substitution C G missense_variant E928Q 2782G>C ORCA-IN 4 85781398 85781398 single base substitution C G downstream_gene_variant ORCA-IN 4 85781398 85781398 single base substitution C G intron_variant ORCA-IN 4 85787973 85787973 single base substitution G T intron_variant ORCA-IN 4 85808483 85808483 single base substitution G C intron_variant ORCA-IN 4 85885325 85885325 single base substitution G C intron_variant OV-AU 4 85608054 85608054 single base substitution T A downstream_gene_variant OV-AU 4 85608054 85608054 single base substitution T A intron_variant OV-AU 4 85608054 85608054 single base substitution T A upstream_gene_variant OV-AU 4 85612176 85612176 single base substitution C A downstream_gene_variant OV-AU 4 85612176 85612176 single base substitution C A intron_variant OV-AU 4 85616965 85616965 single base substitution A C intron_variant OV-AU 4 85633524 85633524 single base substitution A T intron_variant OV-AU 4 85652918 85652918 single base substitution T C downstream_gene_variant OV-AU 4 85652918 85652918 single base substitution T C intron_variant OV-AU 4 85656141 85656141 single base substitution C A downstream_gene_variant OV-AU 4 85656141 85656141 single base substitution C A intron_variant OV-AU 4 85656141 85656141 single base substitution C A upstream_gene_variant OV-AU 4 85657377 85657377 single base substitution T C exon_variant OV-AU 4 85657377 85657377 single base substitution T C synonymous_variant G2287G 6861A>G OV-AU 4 85657377 85657377 single base substitution T C upstream_gene_variant OV-AU 4 85662180 85662180 single base substitution C G intron_variant OV-AU 4 85662180 85662180 single base substitution C G upstream_gene_variant OV-AU 4 85663811 85663811 single base substitution C T intron_variant OV-AU 4 85663811 85663811 single base substitution C T upstream_gene_variant OV-AU 4 85664828 85664828 single base substitution C G intron_variant OV-AU 4 85664828 85664828 single base substitution C G upstream_gene_variant OV-AU 4 85691097 85691097 single base substitution C A intron_variant OV-AU 4 85697657 85697657 single base substitution A G intron_variant OV-AU 4 85698658 85698658 single base substitution T A intron_variant OV-AU 4 85716148 85716148 single base substitution C A intron_variant OV-AU 4 85718434 85718434 single base substitution T C downstream_gene_variant OV-AU 4 85718434 85718434 single base substitution T C intron_variant OV-AU 4 85730409 85730409 single base substitution T C exon_variant OV-AU 4 85730409 85730409 single base substitution T C intron_variant OV-AU 4 85736054 85736054 single base substitution C G intron_variant OV-AU 4 85736054 85736054 single base substitution C G upstream_gene_variant OV-AU 4 85739097 85739097 single base substitution G T intron_variant OV-AU 4 85740500 85740500 single base substitution G A intron_variant OV-AU 4 85743798 85743798 single base substitution G A intron_variant OV-AU 4 85744372 85744372 single base substitution A C intron_variant OV-AU 4 85746373 85746373 single base substitution T C intron_variant OV-AU 4 85748430 85748430 single base substitution G T intron_variant OV-AU 4 85750398 85750398 single base substitution A T intron_variant OV-AU 4 85761749 85761749 single base substitution T C downstream_gene_variant OV-AU 4 85761749 85761749 single base substitution T C intron_variant OV-AU 4 85766695 85766695 single base substitution T A downstream_gene_variant OV-AU 4 85766695 85766695 single base substitution T A intron_variant OV-AU 4 85771457 85771457 single base substitution A T intron_variant OV-AU 4 85771457 85771457 single base substitution A T upstream_gene_variant OV-AU 4 85774280 85774280 single base substitution G A intron_variant OV-AU 4 85774280 85774280 single base substitution G A upstream_gene_variant OV-AU 4 85776996 85776996 single base substitution G C downstream_gene_variant OV-AU 4 85776996 85776996 single base substitution G C intron_variant OV-AU 4 85781115 85781115 single base substitution T C downstream_gene_variant OV-AU 4 85781115 85781115 single base substitution T C intron_variant OV-AU 4 85785997 85785997 single base substitution C G intron_variant OV-AU 4 85785997 85785997 single base substitution C G upstream_gene_variant OV-AU 4 85795130 85795130 single base substitution C T intron_variant OV-AU 4 85795431 85795431 single base substitution T G intron_variant OV-AU 4 85796624 85796624 single base substitution A G intron_variant OV-AU 4 85798276 85798276 single base substitution G C intron_variant OV-AU 4 85805406 85805406 single base substitution T G intron_variant OV-AU 4 85809806 85809806 single base substitution T C intron_variant OV-AU 4 85816181 85816181 single base substitution A C intron_variant OV-AU 4 85817417 85817417 single base substitution A T intron_variant OV-AU 4 85833578 85833578 single base substitution T C intron_variant OV-AU 4 85836271 85836271 single base substitution A T intron_variant OV-AU 4 85841966 85841966 single base substitution C T intron_variant OV-AU 4 85858092 85858092 single base substitution T C intron_variant OV-AU 4 85869609 85869609 single base substitution C G intron_variant OV-AU 4 85869658 85869658 single base substitution G A intron_variant OV-AU 4 85881586 85881586 single base substitution A G intron_variant OV-AU 4 85882398 85882398 single base substitution T G intron_variant OV-AU 4 85890906 85890906 single base substitution T G upstream_gene_variant OV-US 4 85609123 85609123 single base substitution G A downstream_gene_variant OV-US 4 85609123 85609123 single base substitution G A intron_variant PACA-AU 4 85597046 85597046 deletion of <=200bp A - intron_variant PACA-AU 4 85601018 85601018 single base substitution C T intron_variant PACA-AU 4 85608056 85608056 single base substitution C G downstream_gene_variant PACA-AU 4 85608056 85608056 single base substitution C G intron_variant PACA-AU 4 85608056 85608056 single base substitution C G upstream_gene_variant PACA-AU 4 85609177 85609177 single base substitution T C downstream_gene_variant PACA-AU 4 85609177 85609177 single base substitution T C intron_variant PACA-AU 4 85609810 85609810 single base substitution T C downstream_gene_variant PACA-AU 4 85609810 85609810 single base substitution T C intron_variant PACA-AU 4 85610260 85610260 single base substitution G C downstream_gene_variant PACA-AU 4 85610260 85610260 single base substitution G C intron_variant PACA-AU 4 85613137 85613137 single base substitution C T intron_variant PACA-AU 4 85614270 85614270 single base substitution C A intron_variant PACA-AU 4 85614759 85614759 single base substitution A G intron_variant PACA-AU 4 85619447 85619447 single base substitution T A intron_variant PACA-AU 4 85619675 85619675 single base substitution C T intron_variant PACA-AU 4 85622173 85622173 single base substitution G C intron_variant PACA-AU 4 85624209 85624209 single base substitution C T intron_variant PACA-AU 4 85624921 85624921 single base substitution C T intron_variant PACA-AU 4 85626476 85626476 single base substitution G A intron_variant PACA-AU 4 85626903 85626903 single base substitution A G intron_variant PACA-AU 4 85627110 85627110 single base substitution C T intron_variant PACA-AU 4 85628732 85628732 single base substitution A C intron_variant PACA-AU 4 85632998 85632998 single base substitution C A intron_variant PACA-AU 4 85637451 85637451 single base substitution G A intron_variant PACA-AU 4 85642824 85642824 single base substitution G A intron_variant PACA-AU 4 85651444 85651444 single base substitution C T downstream_gene_variant PACA-AU 4 85651444 85651444 single base substitution C T intron_variant PACA-AU 4 85657085 85657085 single base substitution C T intron_variant PACA-AU 4 85657085 85657085 single base substitution C T upstream_gene_variant PACA-AU 4 85657287 85657287 single base substitution C G intron_variant PACA-AU 4 85657287 85657287 single base substitution C G upstream_gene_variant PACA-AU 4 85658675 85658675 single base substitution A C intron_variant PACA-AU 4 85658675 85658675 single base substitution A C upstream_gene_variant PACA-AU 4 85662516 85662516 single base substitution G A intron_variant PACA-AU 4 85662516 85662516 single base substitution G A upstream_gene_variant PACA-AU 4 85662760 85662760 single base substitution G A intron_variant PACA-AU 4 85662760 85662760 single base substitution G A upstream_gene_variant PACA-AU 4 85670997 85670997 single base substitution C T downstream_gene_variant PACA-AU 4 85670997 85670997 single base substitution C T intron_variant PACA-AU 4 85674854 85674854 single base substitution T A exon_variant PACA-AU 4 85674854 85674854 single base substitution T A missense_variant E1912V 5735A>T PACA-AU 4 85675101 85675101 single base substitution A G intron_variant PACA-AU 4 85676636 85676636 single base substitution C A intron_variant PACA-AU 4 85676636 85676636 single base substitution C A upstream_gene_variant PACA-AU 4 85677038 85677038 single base substitution C G intron_variant PACA-AU 4 85677038 85677038 single base substitution C G upstream_gene_variant PACA-AU 4 85682693 85682693 single base substitution G A intron_variant PACA-AU 4 85690581 85690581 single base substitution T A intron_variant PACA-AU 4 85693622 85693622 single base substitution G C intron_variant PACA-AU 4 85695316 85695316 single base substitution G T intron_variant PACA-AU 4 85696178 85696178 single base substitution C G intron_variant PACA-AU 4 85699262 85699262 single base substitution A C intron_variant PACA-AU 4 85714780 85714780 single base substitution C T intron_variant PACA-AU 4 85715767 85715767 single base substitution G C missense_variant S1131C 3392C>G PACA-AU 4 85716062 85716062 single base substitution C G missense_variant D1080H 3238G>C PACA-AU 4 85720479 85720479 insertion of <=200bp - AT downstream_gene_variant PACA-AU 4 85720479 85720479 insertion of <=200bp - AT intron_variant PACA-AU 4 85720494 85720494 single base substitution T A downstream_gene_variant PACA-AU 4 85720494 85720494 single base substitution T A intron_variant PACA-AU 4 85721146 85721146 single base substitution C G downstream_gene_variant PACA-AU 4 85721146 85721146 single base substitution C G intron_variant PACA-AU 4 85726511 85726511 deletion of <=200bp A - downstream_gene_variant PACA-AU 4 85726511 85726511 deletion of <=200bp A - intron_variant PACA-AU 4 85726511 85726511 deletion of <=200bp A - upstream_gene_variant PACA-AU 4 85726570 85726570 single base substitution C G downstream_gene_variant PACA-AU 4 85726570 85726570 single base substitution C G intron_variant PACA-AU 4 85726570 85726570 single base substitution C G upstream_gene_variant PACA-AU 4 85726909 85726909 single base substitution C T downstream_gene_variant PACA-AU 4 85726909 85726909 single base substitution C T intron_variant PACA-AU 4 85726909 85726909 single base substitution C T upstream_gene_variant PACA-AU 4 85735281 85735281 single base substitution G A intron_variant PACA-AU 4 85735281 85735281 single base substitution G A upstream_gene_variant PACA-AU 4 85736389 85736389 single base substitution A C intron_variant PACA-AU 4 85740984 85740984 single base substitution G T intron_variant PACA-AU 4 85745451 85745451 single base substitution T C intron_variant PACA-AU 4 85746895 85746895 single base substitution T C intron_variant PACA-AU 4 85750985 85750985 single base substitution A G intron_variant PACA-AU 4 85750986 85750986 insertion of <=200bp - ATAG intron_variant PACA-AU 4 85751784 85751784 single base substitution A G intron_variant PACA-AU 4 85751970 85751970 single base substitution G C intron_variant PACA-AU 4 85753084 85753084 single base substitution G A intron_variant PACA-AU 4 85753632 85753632 single base substitution G T intron_variant PACA-AU 4 85756864 85756864 single base substitution G A intron_variant PACA-AU 4 85757421 85757421 single base substitution G T downstream_gene_variant PACA-AU 4 85757421 85757421 single base substitution G T intron_variant PACA-AU 4 85761738 85761738 single base substitution A G downstream_gene_variant PACA-AU 4 85761738 85761738 single base substitution A G intron_variant PACA-AU 4 85764175 85764175 insertion of <=200bp - T intron_variant PACA-AU 4 85764338 85764338 single base substitution T C intron_variant PACA-AU 4 85765207 85765207 single base substitution C A intron_variant PACA-AU 4 85785808 85785808 insertion of <=200bp - C intron_variant PACA-AU 4 85785808 85785808 insertion of <=200bp - C upstream_gene_variant PACA-AU 4 85792729 85792732 deletion of <=200bp GAAA - intron_variant PACA-AU 4 85795016 85795016 single base substitution G A intron_variant PACA-AU 4 85806081 85806081 single base substitution G A intron_variant PACA-AU 4 85808848 85808848 single base substitution C T intron_variant PACA-AU 4 85810296 85810296 single base substitution G A intron_variant PACA-AU 4 85812726 85812726 single base substitution G A intron_variant PACA-AU 4 85813592 85813592 single base substitution A T intron_variant PACA-AU 4 85816296 85816296 single base substitution A G intron_variant PACA-AU 4 85817082 85817082 single base substitution G A intron_variant PACA-AU 4 85817971 85817971 single base substitution C G intron_variant PACA-AU 4 85818178 85818178 deletion of <=200bp A - intron_variant PACA-AU 4 85818178 85818178 deletion of <=200bp A - upstream_gene_variant PACA-AU 4 85836787 85836787 single base substitution T A intron_variant PACA-AU 4 85844471 85844471 single base substitution C T intron_variant PACA-AU 4 85849046 85849046 single base substitution T C intron_variant PACA-AU 4 85849820 85849820 single base substitution T A intron_variant PACA-AU 4 85852436 85852436 single base substitution C T intron_variant PACA-AU 4 85859367 85859367 deletion of <=200bp A - intron_variant PACA-AU 4 85870752 85870752 single base substitution C A intron_variant PACA-AU 4 85873959 85873959 single base substitution A G intron_variant PACA-AU 4 85874708 85874708 single base substitution T A intron_variant PACA-AU 4 85879236 85879236 single base substitution G C intron_variant PACA-CA 4 85585726 85585726 single base substitution C T downstream_gene_variant PACA-CA 4 85588054 85588054 deletion of <=200bp A - downstream_gene_variant PACA-CA 4 85588610 85588610 single base substitution T G downstream_gene_variant PACA-CA 4 85592617 85592617 single base substitution A T 3_prime_UTR_variant PACA-CA 4 85592617 85592617 single base substitution A T downstream_gene_variant PACA-CA 4 85597066 85597066 single base substitution T A intron_variant PACA-CA 4 85598988 85598988 single base substitution C T intron_variant PACA-CA 4 85599495 85599495 single base substitution C A intron_variant PACA-CA 4 85600113 85600113 single base substitution G A exon_variant PACA-CA 4 85600113 85600113 single base substitution G A missense_variant P3352L 10055C>T PACA-CA 4 85600113 85600113 single base substitution G A missense_variant P3369L 10106C>T PACA-CA 4 85600996 85600996 single base substitution C T intron_variant PACA-CA 4 85601860 85601860 deletion of <=200bp T - intron_variant PACA-CA 4 85606188 85606188 single base substitution G A intron_variant PACA-CA 4 85606188 85606188 single base substitution G A upstream_gene_variant PACA-CA 4 85608277 85608287 deletion of <=200bp ATTTTCAACAC - downstream_gene_variant PACA-CA 4 85608277 85608287 deletion of <=200bp ATTTTCAACAC - intron_variant PACA-CA 4 85608277 85608287 deletion of <=200bp ATTTTCAACAC - upstream_gene_variant PACA-CA 4 85608307 85608307 deletion of <=200bp T - downstream_gene_variant PACA-CA 4 85608307 85608307 deletion of <=200bp T - intron_variant PACA-CA 4 85608307 85608307 deletion of <=200bp T - upstream_gene_variant PACA-CA 4 85612661 85612661 single base substitution T C downstream_gene_variant PACA-CA 4 85612661 85612661 single base substitution T C intron_variant PACA-CA 4 85613726 85613726 insertion of <=200bp - T intron_variant PACA-CA 4 85614685 85614685 single base substitution C T intron_variant PACA-CA 4 85614733 85614733 single base substitution G A intron_variant PACA-CA 4 85622515 85622515 single base substitution T G intron_variant PACA-CA 4 85625327 85625327 single base substitution A G intron_variant PACA-CA 4 85625881 85625881 single base substitution T C intron_variant PACA-CA 4 85627718 85627718 single base substitution C A intron_variant PACA-CA 4 85638138 85638138 single base substitution T C missense_variant R199G 595A>G PACA-CA 4 85638138 85638138 single base substitution T C missense_variant R2579G 7735A>G PACA-CA 4 85638138 85638138 single base substitution T C missense_variant R2596G 7786A>G PACA-CA 4 85642421 85642421 single base substitution C T intron_variant PACA-CA 4 85643636 85643636 single base substitution G A intron_variant PACA-CA 4 85644131 85644131 single base substitution C T intron_variant PACA-CA 4 85650383 85650383 single base substitution A T intron_variant PACA-CA 4 85654169 85654169 single base substitution A T downstream_gene_variant PACA-CA 4 85654169 85654169 single base substitution A T intron_variant PACA-CA 4 85655840 85655840 single base substitution C A downstream_gene_variant PACA-CA 4 85655840 85655840 single base substitution C A intron_variant PACA-CA 4 85655840 85655840 single base substitution C A upstream_gene_variant PACA-CA 4 85656061 85656061 single base substitution A T downstream_gene_variant PACA-CA 4 85656061 85656061 single base substitution A T intron_variant PACA-CA 4 85656061 85656061 single base substitution A T upstream_gene_variant PACA-CA 4 85657211 85657211 single base substitution T C intron_variant PACA-CA 4 85657211 85657211 single base substitution T C upstream_gene_variant PACA-CA 4 85660156 85660156 single base substitution C G intron_variant PACA-CA 4 85660156 85660156 single base substitution C G splice_region_variant PACA-CA 4 85666597 85666597 single base substitution C A intron_variant PACA-CA 4 85666600 85666600 deletion of <=200bp T - intron_variant PACA-CA 4 85666938 85666938 single base substitution G C intron_variant PACA-CA 4 85667161 85667161 single base substitution G C intron_variant PACA-CA 4 85669668 85669668 single base substitution G T downstream_gene_variant PACA-CA 4 85669668 85669668 single base substitution G T intron_variant PACA-CA 4 85671841 85671841 single base substitution T C downstream_gene_variant PACA-CA 4 85671841 85671841 single base substitution T C intron_variant PACA-CA 4 85676436 85676436 single base substitution G A exon_variant PACA-CA 4 85676436 85676436 single base substitution G A missense_variant R1848C 5542C>T PACA-CA 4 85680369 85680370 deletion of <=200bp AG - intron_variant PACA-CA 4 85680369 85680370 deletion of <=200bp AG - upstream_gene_variant PACA-CA 4 85687458 85687458 single base substitution A C missense_variant D1639E 4917T>G PACA-CA 4 85689427 85689427 single base substitution C T intron_variant PACA-CA 4 85690628 85690628 single base substitution C T intron_variant PACA-CA 4 85691688 85691688 single base substitution G A intron_variant PACA-CA 4 85699201 85699201 single base substitution A G intron_variant PACA-CA 4 85700011 85700011 single base substitution C A intron_variant PACA-CA 4 85700994 85700994 single base substitution T A intron_variant PACA-CA 4 85701935 85701935 single base substitution T A intron_variant PACA-CA 4 85701948 85701948 single base substitution A T intron_variant PACA-CA 4 85703535 85703535 single base substitution T A intron_variant PACA-CA 4 85703711 85703711 single base substitution C T intron_variant PACA-CA 4 85705685 85705685 single base substitution G C intron_variant PACA-CA 4 85706048 85706048 single base substitution C T intron_variant PACA-CA 4 85707186 85707186 single base substitution C T synonymous_variant V1336V 4008G>A PACA-CA 4 85708490 85708490 single base substitution A G intron_variant PACA-CA 4 85710032 85710032 single base substitution G A intron_variant PACA-CA 4 85711288 85711288 single base substitution A C intron_variant PACA-CA 4 85717089 85717089 single base substitution T C intron_variant PACA-CA 4 85720506 85720506 single base substitution G T downstream_gene_variant PACA-CA 4 85720506 85720506 single base substitution G T intron_variant PACA-CA 4 85721057 85721057 single base substitution T C downstream_gene_variant PACA-CA 4 85721057 85721057 single base substitution T C intron_variant PACA-CA 4 85728901 85728901 single base substitution G C downstream_gene_variant PACA-CA 4 85728901 85728901 single base substitution G C intron_variant PACA-CA 4 85728901 85728901 single base substitution G C upstream_gene_variant PACA-CA 4 85728920 85728920 insertion of <=200bp - C downstream_gene_variant PACA-CA 4 85728920 85728920 insertion of <=200bp - C intron_variant PACA-CA 4 85728920 85728920 insertion of <=200bp - C upstream_gene_variant PACA-CA 4 85730623 85730623 single base substitution G A exon_variant PACA-CA 4 85730623 85730623 single base substitution G A intron_variant PACA-CA 4 85732884 85732884 single base substitution A T intron_variant PACA-CA 4 85732884 85732884 single base substitution A T upstream_gene_variant PACA-CA 4 85733427 85733427 single base substitution C T intron_variant PACA-CA 4 85733427 85733427 single base substitution C T upstream_gene_variant PACA-CA 4 85733738 85733738 single base substitution A T intron_variant PACA-CA 4 85733738 85733738 single base substitution A T upstream_gene_variant PACA-CA 4 85735055 85735055 single base substitution A T intron_variant PACA-CA 4 85735055 85735055 single base substitution A T upstream_gene_variant PACA-CA 4 85742400 85742400 insertion of <=200bp - T exon_variant PACA-CA 4 85742400 85742400 insertion of <=200bp - T frameshift_variant Y476Y? PACA-CA 4 85743047 85743047 single base substitution C T intron_variant PACA-CA 4 85743306 85743306 single base substitution A G intron_variant PACA-CA 4 85750986 85750986 insertion of <=200bp - TAAATAAATAAG intron_variant PACA-CA 4 85752451 85752451 insertion of <=200bp - T intron_variant PACA-CA 4 85754814 85754814 insertion of <=200bp - AAAAG intron_variant PACA-CA 4 85755537 85755537 single base substitution C T intron_variant PACA-CA 4 85756512 85756512 single base substitution C T intron_variant PACA-CA 4 85757205 85757205 single base substitution A C intron_variant PACA-CA 4 85761914 85761914 single base substitution A T downstream_gene_variant PACA-CA 4 85761914 85761914 single base substitution A T intron_variant PACA-CA 4 85765174 85765174 single base substitution G T intron_variant PACA-CA 4 85765346 85765346 single base substitution G A intron_variant PACA-CA 4 85765669 85765669 single base substitution A T intron_variant PACA-CA 4 85765669 85765669 single base substitution A T splice_region_variant PACA-CA 4 85766424 85766424 deletion of <=200bp T - downstream_gene_variant PACA-CA 4 85766424 85766424 deletion of <=200bp T - intron_variant PACA-CA 4 85767134 85767134 deletion of <=200bp A - downstream_gene_variant PACA-CA 4 85767134 85767134 deletion of <=200bp A - intron_variant PACA-CA 4 85767521 85767521 insertion of <=200bp - A downstream_gene_variant PACA-CA 4 85767521 85767521 insertion of <=200bp - A intron_variant PACA-CA 4 85767953 85767953 single base substitution C T downstream_gene_variant PACA-CA 4 85767953 85767953 single base substitution C T intron_variant PACA-CA 4 85769506 85769506 single base substitution A T downstream_gene_variant PACA-CA 4 85769506 85769506 single base substitution A T intron_variant PACA-CA 4 85778900 85778900 single base substitution T C downstream_gene_variant PACA-CA 4 85778900 85778900 single base substitution T C intron_variant PACA-CA 4 85778960 85778960 single base substitution G A downstream_gene_variant PACA-CA 4 85778960 85778960 single base substitution G A intron_variant PACA-CA 4 85779065 85779065 single base substitution A C downstream_gene_variant PACA-CA 4 85779065 85779065 single base substitution A C intron_variant PACA-CA 4 85779115 85779115 single base substitution C A downstream_gene_variant PACA-CA 4 85779115 85779115 single base substitution C A intron_variant PACA-CA 4 85780981 85780981 single base substitution G T downstream_gene_variant PACA-CA 4 85780981 85780981 single base substitution G T intron_variant PACA-CA 4 85781164 85781164 single base substitution T C downstream_gene_variant PACA-CA 4 85781164 85781164 single base substitution T C intron_variant PACA-CA 4 85781727 85781727 single base substitution C T exon_variant PACA-CA 4 85781727 85781727 single base substitution C T synonymous_variant R6R 18G>A PACA-CA 4 85781727 85781727 single base substitution C T upstream_gene_variant PACA-CA 4 85783671 85783671 single base substitution G A intron_variant PACA-CA 4 85783671 85783671 single base substitution G A upstream_gene_variant PACA-CA 4 85785150 85785150 single base substitution C T intron_variant PACA-CA 4 85785150 85785150 single base substitution C T upstream_gene_variant PACA-CA 4 85788339 85788339 single base substitution A G intron_variant PACA-CA 4 85790932 85790932 single base substitution C T intron_variant PACA-CA 4 85794945 85794945 insertion of <=200bp - T intron_variant PACA-CA 4 85795078 85795078 single base substitution C A intron_variant PACA-CA 4 85805292 85805292 single base substitution C T intron_variant PACA-CA 4 85806957 85806957 single base substitution G A intron_variant PACA-CA 4 85807733 85807733 single base substitution T A intron_variant PACA-CA 4 85811120 85811120 single base substitution C T intron_variant PACA-CA 4 85812206 85812206 single base substitution A G intron_variant PACA-CA 4 85812445 85812445 single base substitution G C intron_variant PACA-CA 4 85819149 85819149 single base substitution G C intron_variant PACA-CA 4 85819149 85819149 single base substitution G C upstream_gene_variant PACA-CA 4 85821788 85821788 single base substitution A G intron_variant PACA-CA 4 85821788 85821788 single base substitution A G upstream_gene_variant PACA-CA 4 85822511 85822511 single base substitution G A intron_variant PACA-CA 4 85822511 85822511 single base substitution G A upstream_gene_variant PACA-CA 4 85823462 85823462 single base substitution A T intron_variant PACA-CA 4 85824035 85824048 deletion of <=200bp GTCTTTGACTTAGT - intron_variant PACA-CA 4 85824347 85824347 single base substitution G T intron_variant PACA-CA 4 85825377 85825377 insertion of <=200bp - CATT intron_variant PACA-CA 4 85828507 85828507 single base substitution A G intron_variant PACA-CA 4 85828630 85828630 single base substitution T A intron_variant PACA-CA 4 85829193 85829193 single base substitution G T intron_variant PACA-CA 4 85830201 85830201 single base substitution G A intron_variant PACA-CA 4 85830921 85830921 single base substitution C A intron_variant PACA-CA 4 85833211 85833211 single base substitution G T intron_variant PACA-CA 4 85838195 85838195 single base substitution A G intron_variant PACA-CA 4 85839559 85839559 single base substitution T C intron_variant PACA-CA 4 85847213 85847213 single base substitution A G intron_variant PACA-CA 4 85849185 85849185 single base substitution G A intron_variant PACA-CA 4 85852912 85852912 single base substitution C A intron_variant PACA-CA 4 85857458 85857458 single base substitution G A intron_variant PACA-CA 4 85858103 85858103 single base substitution C T intron_variant PACA-CA 4 85868071 85868071 single base substitution C T intron_variant PACA-CA 4 85871584 85871584 single base substitution T A intron_variant PACA-CA 4 85871846 85871846 single base substitution G T intron_variant PACA-CA 4 85876171 85876171 single base substitution A G intron_variant PACA-CA 4 85876756 85876756 single base substitution T C intron_variant PACA-CA 4 85882814 85882814 insertion of <=200bp - T intron_variant PACA-CA 4 85892125 85892125 single base substitution C T upstream_gene_variant PAEN-AU 4 85592701 85592701 single base substitution C A 3_prime_UTR_variant PAEN-AU 4 85592701 85592701 single base substitution C A downstream_gene_variant PAEN-AU 4 85659210 85659210 single base substitution T C intron_variant PAEN-AU 4 85659210 85659210 single base substitution T C upstream_gene_variant PAEN-AU 4 85718711 85718711 insertion of <=200bp - TTATTTAT downstream_gene_variant PAEN-AU 4 85718711 85718711 insertion of <=200bp - TTATTTAT intron_variant PAEN-AU 4 85735245 85735245 single base substitution G A intron_variant PAEN-AU 4 85735245 85735245 single base substitution G A upstream_gene_variant PAEN-AU 4 85759971 85759971 single base substitution C T downstream_gene_variant PAEN-AU 4 85759971 85759971 single base substitution C T intron_variant PAEN-AU 4 85771443 85771443 single base substitution A G intron_variant PAEN-AU 4 85771443 85771443 single base substitution A G upstream_gene_variant PAEN-AU 4 85815799 85815799 single base substitution G C intron_variant PAEN-AU 4 85873197 85873197 single base substitution A G intron_variant PAEN-IT 4 85668950 85668950 single base substitution C T downstream_gene_variant PAEN-IT 4 85668950 85668950 single base substitution C T intron_variant PAEN-IT 4 85715779 85715779 single base substitution C T missense_variant R1127H 3380G>A PAEN-IT 4 85731934 85731934 single base substitution C A intron_variant PAEN-IT 4 85731934 85731934 single base substitution C A upstream_gene_variant PAEN-IT 4 85732212 85732212 single base substitution A C intron_variant PAEN-IT 4 85732212 85732212 single base substitution A C upstream_gene_variant PAEN-IT 4 85767262 85767262 single base substitution G A downstream_gene_variant PAEN-IT 4 85767262 85767262 single base substitution G A intron_variant PAEN-IT 4 85775408 85775408 single base substitution G A intron_variant PAEN-IT 4 85775408 85775408 single base substitution G A upstream_gene_variant PAEN-IT 4 85783847 85783847 single base substitution A T intron_variant PAEN-IT 4 85783847 85783847 single base substitution A T upstream_gene_variant PAEN-IT 4 85799859 85799859 single base substitution C A intron_variant PAEN-IT 4 85826089 85826089 single base substitution C T intron_variant PAEN-IT 4 85829783 85829783 single base substitution C T intron_variant PBCA-DE 4 85601028 85601029 deletion of <=200bp TA - intron_variant PBCA-DE 4 85601635 85601635 single base substitution C T intron_variant PBCA-DE 4 85613550 85613550 deletion of <=200bp T - intron_variant PBCA-DE 4 85621894 85621894 single base substitution C G intron_variant PBCA-DE 4 85631966 85631966 single base substitution C T intron_variant PBCA-DE 4 85639555 85639555 single base substitution C A intron_variant PBCA-DE 4 85640850 85640850 insertion of <=200bp - AC intron_variant PBCA-DE 4 85650383 85650383 single base substitution A T intron_variant PBCA-DE 4 85651091 85651091 single base substitution C T intron_variant PBCA-DE 4 85661746 85661746 insertion of <=200bp - CATCAATAT intron_variant PBCA-DE 4 85661746 85661746 insertion of <=200bp - CATCAATAT upstream_gene_variant PBCA-DE 4 85663139 85663139 insertion of <=200bp - A intron_variant PBCA-DE 4 85663139 85663139 insertion of <=200bp - A upstream_gene_variant PBCA-DE 4 85685694 85685694 single base substitution C T intron_variant PBCA-DE 4 85691481 85691482 deletion of <=200bp GA - intron_variant PBCA-DE 4 85691912 85691912 single base substitution A G intron_variant PBCA-DE 4 85705016 85705017 deletion of <=200bp AC - intron_variant PBCA-DE 4 85708914 85708922 deletion of <=200bp AGGAAAATA - intron_variant PBCA-DE 4 85718419 85718419 deletion of <=200bp G - downstream_gene_variant PBCA-DE 4 85718419 85718419 deletion of <=200bp G - intron_variant PBCA-DE 4 85747600 85747600 single base substitution T C intron_variant PBCA-DE 4 85766267 85766267 insertion of <=200bp - A downstream_gene_variant PBCA-DE 4 85766267 85766267 insertion of <=200bp - A intron_variant PBCA-DE 4 85771477 85771477 insertion of <=200bp - T intron_variant PBCA-DE 4 85771477 85771477 insertion of <=200bp - T upstream_gene_variant PBCA-DE 4 85772012 85772012 single base substitution G T intron_variant PBCA-DE 4 85772012 85772012 single base substitution G T upstream_gene_variant PBCA-DE 4 85783867 85783867 single base substitution G A intron_variant PBCA-DE 4 85783867 85783867 single base substitution G A upstream_gene_variant PBCA-DE 4 85787480 85787480 deletion of <=200bp G - intron_variant PBCA-DE 4 85797077 85797077 single base substitution G A intron_variant PBCA-DE 4 85811428 85811428 insertion of <=200bp - T intron_variant PBCA-DE 4 85815479 85815479 single base substitution A G intron_variant PBCA-DE 4 85830183 85830184 deletion of <=200bp AC - intron_variant PBCA-DE 4 85833206 85833206 single base substitution C A intron_variant PBCA-DE 4 85835349 85835349 single base substitution C A intron_variant PBCA-DE 4 85847424 85847424 single base substitution T C intron_variant PBCA-DE 4 85848231 85848231 single base substitution C G intron_variant PBCA-DE 4 85853400 85853400 insertion of <=200bp - A intron_variant PBCA-DE 4 85867597 85867597 single base substitution G A intron_variant PBCA-DE 4 85873750 85873750 single base substitution C A intron_variant PBCA-DE 4 85874254 85874254 insertion of <=200bp - A intron_variant PBCA-DE 4 85879235 85879235 single base substitution C T intron_variant PRAD-CA 4 85601624 85601624 single base substitution T G intron_variant PRAD-CA 4 85606903 85606903 single base substitution A C intron_variant PRAD-CA 4 85606903 85606903 single base substitution A C upstream_gene_variant PRAD-CA 4 85641881 85641881 single base substitution T C intron_variant PRAD-CA 4 85672029 85672029 single base substitution A C downstream_gene_variant PRAD-CA 4 85672029 85672029 single base substitution A C intron_variant PRAD-CA 4 85706019 85706019 single base substitution A G intron_variant PRAD-CA 4 85734329 85734329 single base substitution A G intron_variant PRAD-CA 4 85734329 85734329 single base substitution A G upstream_gene_variant PRAD-CA 4 85753856 85753856 single base substitution A C intron_variant PRAD-CA 4 85813833 85813833 single base substitution C A intron_variant PRAD-CA 4 85836112 85836112 single base substitution A C intron_variant PRAD-CA 4 85838399 85838399 single base substitution A C intron_variant PRAD-CA 4 85847314 85847314 single base substitution C T intron_variant PRAD-CA 4 85871247 85871247 single base substitution T C intron_variant PRAD-UK 4 85597779 85597779 single base substitution A G intron_variant PRAD-UK 4 85654070 85654070 single base substitution T G downstream_gene_variant PRAD-UK 4 85654070 85654070 single base substitution T G intron_variant PRAD-UK 4 85659783 85659783 deletion of <=200bp A - intron_variant PRAD-UK 4 85680792 85680792 single base substitution T A intron_variant PRAD-UK 4 85680792 85680792 single base substitution T A upstream_gene_variant PRAD-UK 4 85684443 85684443 single base substitution A G intron_variant PRAD-UK 4 85689088 85689088 single base substitution G A intron_variant PRAD-UK 4 85692346 85692346 single base substitution G T intron_variant PRAD-UK 4 85699670 85699670 single base substitution G C missense_variant L1502V 4504C>G PRAD-UK 4 85702314 85702314 single base substitution A C intron_variant PRAD-UK 4 85704719 85704719 single base substitution G C intron_variant PRAD-UK 4 85705452 85705452 single base substitution G A intron_variant PRAD-UK 4 85713971 85713971 single base substitution G A intron_variant PRAD-UK 4 85718011 85718011 deletion of <=200bp T - downstream_gene_variant PRAD-UK 4 85718011 85718011 deletion of <=200bp T - intron_variant PRAD-UK 4 85722998 85722998 single base substitution A T exon_variant PRAD-UK 4 85722998 85722998 single base substitution A T missense_variant L876H 2627T>A PRAD-UK 4 85724625 85724625 insertion of <=200bp - A splice_region_variant PRAD-UK 4 85731823 85731823 single base substitution T C intron_variant PRAD-UK 4 85731823 85731823 single base substitution T C upstream_gene_variant PRAD-UK 4 85732195 85732195 single base substitution G C intron_variant PRAD-UK 4 85732195 85732195 single base substitution G C upstream_gene_variant PRAD-UK 4 85734297 85734297 single base substitution A G intron_variant PRAD-UK 4 85734297 85734297 single base substitution A G upstream_gene_variant PRAD-UK 4 85759104 85759104 single base substitution C G downstream_gene_variant PRAD-UK 4 85759104 85759104 single base substitution C G intron_variant PRAD-UK 4 85763845 85763845 single base substitution G T intron_variant PRAD-UK 4 85781793 85781793 single base substitution T A intron_variant PRAD-UK 4 85781793 85781793 single base substitution T A upstream_gene_variant PRAD-UK 4 85803577 85803577 single base substitution G A intron_variant PRAD-UK 4 85838806 85838807 deletion of <=200bp TT - intron_variant PRAD-UK 4 85860877 85860877 single base substitution A T intron_variant PRAD-UK 4 85877212 85877212 single base substitution T G intron_variant PRAD-UK 4 85879584 85879584 single base substitution A T intron_variant PRAD-UK 4 85882069 85882069 single base substitution A G intron_variant PRAD-UK 4 85891118 85891118 single base substitution T C upstream_gene_variant PRAD-US 4 85603587 85603587 single base substitution G A exon_variant PRAD-US 4 85603587 85603587 single base substitution G A missense_variant P3238S 9712C>T PRAD-US 4 85603587 85603587 single base substitution G A missense_variant P3255S 9763C>T PRAD-US 4 85699758 85699758 single base substitution G A synonymous_variant I1472I 4416C>T PRAD-US 4 85719250 85719250 single base substitution C T downstream_gene_variant PRAD-US 4 85719250 85719250 single base substitution C T missense_variant R945H 2834G>A PRAD-US 4 85758212 85758212 single base substitution A G downstream_gene_variant PRAD-US 4 85758212 85758212 single base substitution A G exon_variant PRAD-US 4 85758212 85758212 single base substitution A G missense_variant V149A 446T>C READ-US 4 85626556 85626556 single base substitution C T missense_variant D2759N 8275G>A READ-US 4 85626556 85626556 single base substitution C T missense_variant D2776N 8326G>A READ-US 4 85626556 85626556 single base substitution C T missense_variant D379N 1135G>A READ-US 4 85657363 85657363 single base substitution C T exon_variant READ-US 4 85657363 85657363 single base substitution C T missense_variant R2292Q 6875G>A READ-US 4 85657363 85657363 single base substitution C T upstream_gene_variant READ-US 4 85678299 85678299 single base substitution C T missense_variant R1735K 5204G>A READ-US 4 85678299 85678299 single base substitution C T upstream_gene_variant READ-US 4 85694026 85694026 single base substitution A G missense_variant V1604A 4811T>C RECA-EU 4 85586459 85586459 single base substitution T C downstream_gene_variant RECA-EU 4 85587966 85587966 single base substitution C A downstream_gene_variant RECA-EU 4 85594028 85594028 single base substitution T G exon_variant RECA-EU 4 85594028 85594028 single base substitution T G missense_variant N3508T 10523A>C RECA-EU 4 85594028 85594028 single base substitution T G missense_variant N3525T 10574A>C RECA-EU 4 85595503 85595503 single base substitution G A intron_variant RECA-EU 4 85597736 85597736 single base substitution A T intron_variant RECA-EU 4 85606728 85606728 single base substitution G T intron_variant RECA-EU 4 85606728 85606728 single base substitution G T upstream_gene_variant RECA-EU 4 85612933 85612933 single base substitution T A stop_gained K3002* 9004A>T RECA-EU 4 85612933 85612933 single base substitution T A stop_gained K3019* 9055A>T RECA-EU 4 85612933 85612933 single base substitution T A stop_gained K622* 1864A>T RECA-EU 4 85617206 85617206 single base substitution C T missense_variant V2923M 8767G>A RECA-EU 4 85617206 85617206 single base substitution C T missense_variant V2940M 8818G>A RECA-EU 4 85617206 85617206 single base substitution C T missense_variant V543M 1627G>A RECA-EU 4 85621780 85621780 single base substitution G T intron_variant RECA-EU 4 85625540 85625540 single base substitution G T stop_gained S2781* 8342C>A RECA-EU 4 85625540 85625540 single base substitution G T stop_gained S2798* 8393C>A RECA-EU 4 85625540 85625540 single base substitution G T stop_gained S401* 1202C>A RECA-EU 4 85630481 85630481 single base substitution A C missense_variant L2671V 8011T>G RECA-EU 4 85630481 85630481 single base substitution A C missense_variant L2688V 8062T>G RECA-EU 4 85630481 85630481 single base substitution A C missense_variant L291V 871T>G RECA-EU 4 85633327 85633327 single base substitution A C intron_variant RECA-EU 4 85638281 85638281 single base substitution T A intron_variant RECA-EU 4 85651745 85651745 single base substitution T A downstream_gene_variant RECA-EU 4 85651745 85651745 single base substitution T A intron_variant RECA-EU 4 85657323 85657323 single base substitution C A missense_variant Q2305H 6915G>T RECA-EU 4 85657323 85657323 single base substitution C A splice_region_variant RECA-EU 4 85657323 85657323 single base substitution C A upstream_gene_variant RECA-EU 4 85658371 85658371 single base substitution T C exon_variant RECA-EU 4 85658371 85658371 single base substitution T C synonymous_variant E2241E 6723A>G RECA-EU 4 85658371 85658371 single base substitution T C upstream_gene_variant RECA-EU 4 85679410 85679410 single base substitution T G intron_variant RECA-EU 4 85679410 85679410 single base substitution T G upstream_gene_variant RECA-EU 4 85685325 85685325 single base substitution G A intron_variant RECA-EU 4 85704683 85704683 single base substitution C T intron_variant RECA-EU 4 85722197 85722197 single base substitution G A downstream_gene_variant RECA-EU 4 85722197 85722197 single base substitution G A intron_variant RECA-EU 4 85731441 85731441 single base substitution A C exon_variant RECA-EU 4 85731441 85731441 single base substitution A C synonymous_variant V648V 1944T>G RECA-EU 4 85731441 85731441 single base substitution A C upstream_gene_variant RECA-EU 4 85742864 85742864 single base substitution C G intron_variant RECA-EU 4 85745756 85745756 single base substitution A T intron_variant RECA-EU 4 85749887 85749887 single base substitution G T intron_variant RECA-EU 4 85751232 85751232 single base substitution G T intron_variant RECA-EU 4 85752349 85752349 single base substitution A G intron_variant RECA-EU 4 85754023 85754023 single base substitution C G intron_variant RECA-EU 4 85754846 85754846 single base substitution G A intron_variant RECA-EU 4 85762397 85762397 single base substitution T A exon_variant RECA-EU 4 85762397 85762397 single base substitution T A synonymous_variant I108I 324A>T RECA-EU 4 85762397 85762397 single base substitution T A synonymous_variant I62I 186A>T RECA-EU 4 85762501 85762501 single base substitution A T intron_variant RECA-EU 4 85765701 85765701 single base substitution T A intron_variant RECA-EU 4 85774143 85774143 single base substitution C G intron_variant RECA-EU 4 85774143 85774143 single base substitution C G upstream_gene_variant RECA-EU 4 85781716 85781716 single base substitution C A downstream_gene_variant RECA-EU 4 85781716 85781716 single base substitution C A exon_variant RECA-EU 4 85781716 85781716 single base substitution C A missense_variant R10L 29G>T RECA-EU 4 85793965 85793965 single base substitution C A intron_variant RECA-EU 4 85799721 85799721 single base substitution T G intron_variant RECA-EU 4 85801502 85801502 single base substitution G C intron_variant RECA-EU 4 85806347 85806347 single base substitution G T intron_variant RECA-EU 4 85808672 85808672 single base substitution C A intron_variant RECA-EU 4 85814583 85814583 single base substitution T G intron_variant RECA-EU 4 85816542 85816542 single base substitution A G intron_variant RECA-EU 4 85824922 85824922 single base substitution A G intron_variant RECA-EU 4 85829310 85829310 single base substitution A T intron_variant RECA-EU 4 85834672 85834672 single base substitution A T intron_variant RECA-EU 4 85842528 85842528 single base substitution G T intron_variant RECA-EU 4 85844230 85844230 single base substitution T C intron_variant RECA-EU 4 85849764 85849764 single base substitution T G intron_variant RECA-EU 4 85859284 85859284 single base substitution T C intron_variant RECA-EU 4 85872472 85872472 single base substitution T C intron_variant RECA-EU 4 85875129 85875129 single base substitution T C intron_variant RECA-EU 4 85879711 85879711 single base substitution G C intron_variant RECA-EU 4 85881644 85881644 single base substitution A T intron_variant RECA-EU 4 85886992 85886992 single base substitution G A intron_variant RECA-EU 4 85890101 85890101 single base substitution G A upstream_gene_variant SKCA-BR 4 85588790 85588790 single base substitution C G downstream_gene_variant SKCA-BR 4 85589633 85589633 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 4 85594560 85594560 single base substitution G A intron_variant SKCA-BR 4 85597400 85597400 single base substitution G A intron_variant SKCA-BR 4 85599012 85599012 single base substitution G A intron_variant SKCA-BR 4 85599141 85599141 single base substitution G A intron_variant SKCA-BR 4 85599147 85599147 single base substitution G A intron_variant SKCA-BR 4 85600300 85600300 single base substitution T G exon_variant SKCA-BR 4 85600300 85600300 single base substitution T G missense_variant T3290P 9868A>C SKCA-BR 4 85600300 85600300 single base substitution T G missense_variant T3307P 9919A>C SKCA-BR 4 85602296 85602296 single base substitution A C intron_variant SKCA-BR 4 85602889 85602889 single base substitution G A intron_variant SKCA-BR 4 85607719 85607719 single base substitution G A intron_variant SKCA-BR 4 85607719 85607719 single base substitution G A upstream_gene_variant SKCA-BR 4 85609286 85609286 single base substitution G A downstream_gene_variant SKCA-BR 4 85609286 85609286 single base substitution G A stop_gained R3149* 9445C>T SKCA-BR 4 85609286 85609286 single base substitution G A stop_gained R3166* 9496C>T SKCA-BR 4 85615048 85615049 deletion of <=200bp CA - intron_variant SKCA-BR 4 85615090 85615090 single base substitution C A intron_variant SKCA-BR 4 85615181 85615181 single base substitution G A intron_variant SKCA-BR 4 85617421 85617421 single base substitution G A intron_variant SKCA-BR 4 85617687 85617687 insertion of <=200bp - TTA intron_variant SKCA-BR 4 85618786 85618786 single base substitution G A intron_variant SKCA-BR 4 85626861 85626861 single base substitution T C intron_variant SKCA-BR 4 85629856 85629856 single base substitution G A intron_variant SKCA-BR 4 85631402 85631402 single base substitution G A intron_variant SKCA-BR 4 85634952 85634952 single base substitution G T intron_variant SKCA-BR 4 85635920 85635920 single base substitution G A intron_variant SKCA-BR 4 85636651 85636651 single base substitution G A intron_variant SKCA-BR 4 85637178 85637178 single base substitution G A intron_variant SKCA-BR 4 85638237 85638237 single base substitution G A intron_variant SKCA-BR 4 85638240 85638240 single base substitution T A intron_variant SKCA-BR 4 85641655 85641655 single base substitution G A intron_variant SKCA-BR 4 85645142 85645142 single base substitution A C intron_variant SKCA-BR 4 85654483 85654483 single base substitution G A downstream_gene_variant SKCA-BR 4 85654483 85654483 single base substitution G A intron_variant SKCA-BR 4 85661244 85661244 single base substitution G A intron_variant SKCA-BR 4 85661244 85661244 single base substitution G A upstream_gene_variant SKCA-BR 4 85662469 85662469 single base substitution G T intron_variant SKCA-BR 4 85662469 85662469 single base substitution G T upstream_gene_variant SKCA-BR 4 85665628 85665628 single base substitution T C intron_variant SKCA-BR 4 85671444 85671444 single base substitution T C downstream_gene_variant SKCA-BR 4 85671444 85671444 single base substitution T C intron_variant SKCA-BR 4 85674260 85674260 single base substitution G A intron_variant SKCA-BR 4 85676034 85676034 single base substitution G A intron_variant SKCA-BR 4 85677512 85677512 single base substitution T G intron_variant SKCA-BR 4 85677512 85677512 single base substitution T G upstream_gene_variant SKCA-BR 4 85678725 85678725 single base substitution G A intron_variant SKCA-BR 4 85678725 85678725 single base substitution G A upstream_gene_variant SKCA-BR 4 85681278 85681278 single base substitution G A intron_variant SKCA-BR 4 85681278 85681278 single base substitution G A upstream_gene_variant SKCA-BR 4 85683628 85683628 single base substitution A G intron_variant SKCA-BR 4 85684278 85684278 single base substitution G A intron_variant SKCA-BR 4 85684472 85684472 single base substitution G A intron_variant SKCA-BR 4 85685297 85685297 single base substitution A T intron_variant SKCA-BR 4 85686035 85686035 single base substitution G A intron_variant SKCA-BR 4 85689169 85689169 single base substitution G A intron_variant SKCA-BR 4 85690923 85690923 single base substitution G A intron_variant SKCA-BR 4 85695316 85695316 single base substitution G A intron_variant SKCA-BR 4 85702222 85702222 single base substitution G A intron_variant SKCA-BR 4 85706042 85706046 deletion of <=200bp TATAC - intron_variant SKCA-BR 4 85706044 85706046 deletion of <=200bp TAC - intron_variant SKCA-BR 4 85706072 85706074 deletion of <=200bp CAT - intron_variant SKCA-BR 4 85712083 85712083 single base substitution G A intron_variant SKCA-BR 4 85715331 85715331 single base substitution T G intron_variant SKCA-BR 4 85717676 85717676 single base substitution A G splice_region_variant SKCA-BR 4 85718710 85718710 insertion of <=200bp - CTTAT downstream_gene_variant SKCA-BR 4 85718710 85718710 insertion of <=200bp - CTTAT intron_variant SKCA-BR 4 85720492 85720492 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 4 85720492 85720492 insertion of <=200bp - TA intron_variant SKCA-BR 4 85720494 85720494 single base substitution T A downstream_gene_variant SKCA-BR 4 85720494 85720494 single base substitution T A intron_variant SKCA-BR 4 85720650 85720650 single base substitution T A downstream_gene_variant SKCA-BR 4 85720650 85720650 single base substitution T A intron_variant SKCA-BR 4 85722197 85722197 single base substitution G A downstream_gene_variant SKCA-BR 4 85722197 85722197 single base substitution G A intron_variant SKCA-BR 4 85727660 85727660 single base substitution G A downstream_gene_variant SKCA-BR 4 85727660 85727660 single base substitution G A intron_variant SKCA-BR 4 85727660 85727660 single base substitution G A upstream_gene_variant SKCA-BR 4 85733138 85733138 single base substitution G A intron_variant SKCA-BR 4 85733138 85733138 single base substitution G A upstream_gene_variant SKCA-BR 4 85735525 85735525 single base substitution G A intron_variant SKCA-BR 4 85735525 85735525 single base substitution G A upstream_gene_variant SKCA-BR 4 85738518 85738518 single base substitution G A intron_variant SKCA-BR 4 85738694 85738694 single base substitution C T exon_variant SKCA-BR 4 85738694 85738694 single base substitution C T missense_variant V580I 1738G>A SKCA-BR 4 85744699 85744699 single base substitution G A intron_variant SKCA-BR 4 85745239 85745239 single base substitution G A intron_variant SKCA-BR 4 85746383 85746383 single base substitution G A intron_variant SKCA-BR 4 85746408 85746408 single base substitution G A intron_variant SKCA-BR 4 85749984 85749984 single base substitution C T intron_variant SKCA-BR 4 85750380 85750380 single base substitution C A intron_variant SKCA-BR 4 85754846 85754846 single base substitution G A intron_variant SKCA-BR 4 85761935 85761935 single base substitution T C downstream_gene_variant SKCA-BR 4 85761935 85761935 single base substitution T C intron_variant SKCA-BR 4 85763872 85763872 single base substitution T G intron_variant SKCA-BR 4 85767325 85767325 single base substitution G A downstream_gene_variant SKCA-BR 4 85767325 85767325 single base substitution G A intron_variant SKCA-BR 4 85770371 85770371 single base substitution G A downstream_gene_variant SKCA-BR 4 85770371 85770371 single base substitution G A intron_variant SKCA-BR 4 85770722 85770722 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 4 85770722 85770722 insertion of <=200bp - TA intron_variant SKCA-BR 4 85771484 85771484 insertion of <=200bp - TG intron_variant SKCA-BR 4 85771484 85771484 insertion of <=200bp - TG upstream_gene_variant SKCA-BR 4 85778527 85778527 single base substitution G A downstream_gene_variant SKCA-BR 4 85778527 85778527 single base substitution G A intron_variant SKCA-BR 4 85781192 85781192 single base substitution G A downstream_gene_variant SKCA-BR 4 85781192 85781192 single base substitution G A intron_variant SKCA-BR 4 85783915 85783915 single base substitution T G intron_variant SKCA-BR 4 85783915 85783915 single base substitution T G upstream_gene_variant SKCA-BR 4 85785648 85785648 single base substitution A C intron_variant SKCA-BR 4 85785648 85785648 single base substitution A C upstream_gene_variant SKCA-BR 4 85789038 85789038 single base substitution T C intron_variant SKCA-BR 4 85799900 85799900 single base substitution G A intron_variant SKCA-BR 4 85802737 85802737 insertion of <=200bp - TA intron_variant SKCA-BR 4 85804270 85804270 single base substitution T G intron_variant SKCA-BR 4 85817642 85817642 single base substitution C A intron_variant SKCA-BR 4 85820230 85820230 single base substitution G A intron_variant SKCA-BR 4 85820230 85820230 single base substitution G A upstream_gene_variant SKCA-BR 4 85822971 85822971 single base substitution G A intron_variant SKCA-BR 4 85822971 85822971 single base substitution G A upstream_gene_variant SKCA-BR 4 85823051 85823051 single base substitution G A intron_variant SKCA-BR 4 85823051 85823051 single base substitution G A upstream_gene_variant SKCA-BR 4 85827504 85827504 single base substitution A T intron_variant SKCA-BR 4 85828204 85828212 deletion of <=200bp GAACCTGTA - intron_variant SKCA-BR 4 85831096 85831096 single base substitution T C intron_variant SKCA-BR 4 85831190 85831190 single base substitution G A intron_variant SKCA-BR 4 85839623 85839623 single base substitution G A intron_variant SKCA-BR 4 85840340 85840340 single base substitution G A intron_variant SKCA-BR 4 85840611 85840611 single base substitution C T intron_variant SKCA-BR 4 85841242 85841242 single base substitution G A intron_variant SKCA-BR 4 85848577 85848577 single base substitution G A intron_variant SKCA-BR 4 85855102 85855102 single base substitution G A intron_variant SKCA-BR 4 85868126 85868126 single base substitution A T intron_variant SKCA-BR 4 85868467 85868467 single base substitution C A intron_variant SKCA-BR 4 85869065 85869065 single base substitution A C intron_variant SKCA-BR 4 85871417 85871417 single base substitution G A intron_variant SKCA-BR 4 85871418 85871418 single base substitution G A intron_variant SKCA-BR 4 85871722 85871722 single base substitution A G intron_variant SKCA-BR 4 85890539 85890539 single base substitution G A upstream_gene_variant SKCM-US 4 85594031 85594031 single base substitution C T exon_variant SKCM-US 4 85594031 85594031 single base substitution C T missense_variant R3507Q 10520G>A SKCM-US 4 85594031 85594031 single base substitution C T missense_variant R3524Q 10571G>A SKCM-US 4 85594125 85594125 single base substitution C T exon_variant SKCM-US 4 85594125 85594125 single base substitution C T missense_variant E3476K 10426G>A SKCM-US 4 85594125 85594125 single base substitution C T missense_variant E3493K 10477G>A SKCM-US 4 85599427 85599427 single base substitution G A exon_variant SKCM-US 4 85599427 85599427 single base substitution G A stop_gained R3368* 10102C>T SKCM-US 4 85599427 85599427 single base substitution G A stop_gained R3385* 10153C>T SKCM-US 4 85600096 85600096 single base substitution G A exon_variant SKCM-US 4 85600096 85600096 single base substitution G A missense_variant R3358W 10072C>T SKCM-US 4 85600096 85600096 single base substitution G A missense_variant R3375W 10123C>T SKCM-US 4 85611675 85611675 single base substitution G A downstream_gene_variant SKCM-US 4 85611675 85611675 single base substitution G A missense_variant T3099I 9296C>T SKCM-US 4 85611675 85611675 single base substitution G A missense_variant T3116I 9347C>T SKCM-US 4 85611810 85611810 single base substitution G A downstream_gene_variant SKCM-US 4 85611810 85611810 single base substitution G A missense_variant T3054I 9161C>T SKCM-US 4 85611810 85611810 single base substitution G A missense_variant T3071I 9212C>T SKCM-US 4 85612913 85612913 single base substitution G A synonymous_variant I3008I 9024C>T SKCM-US 4 85612913 85612913 single base substitution G A synonymous_variant I3025I 9075C>T SKCM-US 4 85612913 85612913 single base substitution G A synonymous_variant I628I 1884C>T SKCM-US 4 85617207 85617207 single base substitution T C synonymous_variant Q2922Q 8766A>G SKCM-US 4 85617207 85617207 single base substitution T C synonymous_variant Q2939Q 8817A>G SKCM-US 4 85617207 85617207 single base substitution T C synonymous_variant Q542Q 1626A>G SKCM-US 4 85617227 85617227 single base substitution G A missense_variant H2916Y 8746C>T SKCM-US 4 85617227 85617227 single base substitution G A missense_variant H2933Y 8797C>T SKCM-US 4 85617227 85617227 single base substitution G A missense_variant H536Y 1606C>T SKCM-US 4 85617242 85617242 single base substitution C T missense_variant V2911I 8731G>A SKCM-US 4 85617242 85617242 single base substitution C T missense_variant V2928I 8782G>A SKCM-US 4 85617242 85617242 single base substitution C T missense_variant V531I 1591G>A SKCM-US 4 85623601 85623601 single base substitution G A missense_variant S2817L 8450C>T SKCM-US 4 85623601 85623601 single base substitution G A missense_variant S2834L 8501C>T SKCM-US 4 85623601 85623601 single base substitution G A missense_variant S437L 1310C>T SKCM-US 4 85639647 85639647 single base substitution T C missense_variant H164R 491A>G SKCM-US 4 85639647 85639647 single base substitution T C missense_variant H2544R 7631A>G SKCM-US 4 85639647 85639647 single base substitution T C missense_variant H2561R 7682A>G SKCM-US 4 85642710 85642710 single base substitution G A missense_variant P2469L 7406C>T SKCM-US 4 85642710 85642710 single base substitution G A missense_variant P2486L 7457C>T SKCM-US 4 85642710 85642710 single base substitution G A missense_variant P89L 266C>T SKCM-US 4 85642712 85642712 single base substitution A T synonymous_variant P2468P 7404T>A SKCM-US 4 85642712 85642712 single base substitution A T synonymous_variant P2485P 7455T>A SKCM-US 4 85642712 85642712 single base substitution A T synonymous_variant P88P 264T>A SKCM-US 4 85645656 85645656 single base substitution G A missense_variant A2438V 7313C>T SKCM-US 4 85645656 85645656 single base substitution G A missense_variant A2455V 7364C>T SKCM-US 4 85645656 85645656 single base substitution G A missense_variant A58V 173C>T SKCM-US 4 85654607 85654607 single base substitution C T downstream_gene_variant SKCM-US 4 85654607 85654607 single base substitution C T synonymous_variant K2383K 7149G>A SKCM-US 4 85654607 85654607 single base substitution C T synonymous_variant K3K 9G>A SKCM-US 4 85657478 85657478 single base substitution G A missense_variant H2254Y 6760C>T SKCM-US 4 85657478 85657478 single base substitution G A splice_region_variant SKCM-US 4 85657478 85657478 single base substitution G A upstream_gene_variant SKCM-US 4 85658343 85658343 single base substitution G A exon_variant SKCM-US 4 85658343 85658343 single base substitution G A missense_variant H2251Y 6751C>T SKCM-US 4 85658343 85658343 single base substitution G A upstream_gene_variant SKCM-US 4 85663060 85663060 single base substitution G A synonymous_variant L2030L 6088C>T SKCM-US 4 85663060 85663060 single base substitution G A upstream_gene_variant SKCM-US 4 85664947 85664947 single base substitution G A synonymous_variant S1993S 5979C>T SKCM-US 4 85664947 85664947 single base substitution G A upstream_gene_variant SKCM-US 4 85672726 85672726 single base substitution G A exon_variant SKCM-US 4 85672726 85672726 single base substitution G A synonymous_variant F1961F 5883C>T SKCM-US 4 85674877 85674877 single base substitution G A exon_variant SKCM-US 4 85674877 85674877 single base substitution G A synonymous_variant P1904P 5712C>T SKCM-US 4 85674967 85674967 single base substitution G A exon_variant SKCM-US 4 85674967 85674967 single base substitution G A synonymous_variant F1874F 5622C>T SKCM-US 4 85676491 85676491 single base substitution G A exon_variant SKCM-US 4 85676491 85676491 single base substitution G A synonymous_variant V1829V 5487C>T SKCM-US 4 85676507 85676507 single base substitution G A exon_variant SKCM-US 4 85676507 85676507 single base substitution G A missense_variant S1824F 5471C>T SKCM-US 4 85694049 85694049 single base substitution G A synonymous_variant T1596T 4788C>T SKCM-US 4 85695995 85695995 single base substitution G A missense_variant P1578S 4732C>T SKCM-US 4 85696067 85696067 single base substitution G A stop_gained R1554* 4660C>T SKCM-US 4 85696089 85696089 single base substitution G A synonymous_variant I1546I 4638C>T SKCM-US 4 85701308 85701308 single base substitution T A missense_variant S1440C 4318A>T SKCM-US 4 85707256 85707256 single base substitution G A missense_variant P1313L 3938C>T SKCM-US 4 85710914 85710914 single base substitution G A missense_variant L1212F 3634C>T SKCM-US 4 85711007 85711007 single base substitution G A missense_variant R1181C 3541C>T SKCM-US 4 85711043 85711043 single base substitution C T missense_variant E1169K 3505G>A SKCM-US 4 85715819 85715819 single base substitution G A missense_variant P1114S 3340C>T SKCM-US 4 85715876 85715876 single base substitution G A missense_variant P1095S 3283C>T SKCM-US 4 85724537 85724537 single base substitution G C exon_variant SKCM-US 4 85724537 85724537 single base substitution G C missense_variant S838C 2513C>G SKCM-US 4 85724567 85724567 single base substitution G A exon_variant SKCM-US 4 85724567 85724567 single base substitution G A missense_variant A828V 2483C>T SKCM-US 4 85729554 85729554 single base substitution G A downstream_gene_variant SKCM-US 4 85729554 85729554 single base substitution G A intron_variant SKCM-US 4 85729554 85729554 single base substitution G A missense_variant P788S 2362C>T SKCM-US 4 85729554 85729554 single base substitution G A upstream_gene_variant SKCM-US 4 85731300 85731300 single base substitution T G exon_variant SKCM-US 4 85731300 85731300 single base substitution T G synonymous_variant A695A 2085A>C SKCM-US 4 85731300 85731300 single base substitution T G upstream_gene_variant SKCM-US 4 85731436 85731436 single base substitution C A exon_variant SKCM-US 4 85731436 85731436 single base substitution C A missense_variant G650V 1949G>T SKCM-US 4 85731436 85731436 single base substitution C A upstream_gene_variant SKCM-US 4 85731442 85731442 single base substitution A G exon_variant SKCM-US 4 85731442 85731442 single base substitution A G missense_variant V648A 1943T>C SKCM-US 4 85731442 85731442 single base substitution A G upstream_gene_variant SKCM-US 4 85731467 85731467 single base substitution G A exon_variant SKCM-US 4 85731467 85731467 single base substitution G A missense_variant R640C 1918C>T SKCM-US 4 85731467 85731467 single base substitution G A upstream_gene_variant SKCM-US 4 85731479 85731479 single base substitution G A exon_variant SKCM-US 4 85731479 85731479 single base substitution G A stop_gained R636* 1906C>T SKCM-US 4 85731479 85731479 single base substitution G A upstream_gene_variant SKCM-US 4 85742315 85742315 single base substitution G A exon_variant SKCM-US 4 85742315 85742315 single base substitution G A missense_variant L505F 1513C>T SKCM-US 4 85742573 85742573 single base substitution A G exon_variant SKCM-US 4 85742573 85742573 single base substitution A G missense_variant F419L 1255T>C SKCM-US 4 85742679 85742679 single base substitution G A exon_variant SKCM-US 4 85742679 85742679 single base substitution G A synonymous_variant A383A 1149C>T SKCM-US 4 85748118 85748118 single base substitution C T exon_variant SKCM-US 4 85748118 85748118 single base substitution C T missense_variant E325K 973G>A SKCM-US 4 85752612 85752612 single base substitution G A exon_variant SKCM-US 4 85752612 85752612 single base substitution G A synonymous_variant T241T 723C>T SKCM-US 4 85781645 85781645 single base substitution C T downstream_gene_variant SKCM-US 4 85781645 85781645 single base substitution C T exon_variant SKCM-US 4 85781645 85781645 single base substitution C T missense_variant E34K 100G>A STAD-US 4 85598426 85598426 single base substitution T C exon_variant STAD-US 4 85598426 85598426 single base substitution T C synonymous_variant S3444S 10332A>G STAD-US 4 85598426 85598426 single base substitution T C synonymous_variant S3461S 10383A>G STAD-US 4 85600249 85600249 single base substitution T C exon_variant STAD-US 4 85600249 85600249 single base substitution T C missense_variant T3307A 9919A>G STAD-US 4 85600249 85600249 single base substitution T C missense_variant T3324A 9970A>G STAD-US 4 85605111 85605111 single base substitution T C synonymous_variant S3220S 9660A>G STAD-US 4 85605111 85605111 single base substitution T C synonymous_variant S3237S 9711A>G STAD-US 4 85605111 85605111 single base substitution T C upstream_gene_variant STAD-US 4 85609395 85609395 single base substitution G A downstream_gene_variant STAD-US 4 85609395 85609395 single base substitution G A synonymous_variant T3112T 9336C>T STAD-US 4 85609395 85609395 single base substitution G A synonymous_variant T3129T 9387C>T STAD-US 4 85611684 85611684 single base substitution T A downstream_gene_variant STAD-US 4 85611684 85611684 single base substitution T A missense_variant K3096M 9287A>T STAD-US 4 85611684 85611684 single base substitution T A missense_variant K3113M 9338A>T STAD-US 4 85612938 85612938 single base substitution T C missense_variant E3000G 8999A>G STAD-US 4 85612938 85612938 single base substitution T C missense_variant E3017G 9050A>G STAD-US 4 85612938 85612938 single base substitution T C missense_variant E620G 1859A>G STAD-US 4 85617218 85617218 deletion of <=200bp A - frameshift_variant Y2919 STAD-US 4 85617218 85617218 deletion of <=200bp A - frameshift_variant Y2936 STAD-US 4 85617218 85617218 deletion of <=200bp A - frameshift_variant Y539 STAD-US 4 85617299 85617299 single base substitution C T missense_variant E2892K 8674G>A STAD-US 4 85617299 85617299 single base substitution C T missense_variant E2909K 8725G>A STAD-US 4 85617299 85617299 single base substitution C T missense_variant E512K 1534G>A STAD-US 4 85617311 85617311 single base substitution C T missense_variant A2888T 8662G>A STAD-US 4 85617311 85617311 single base substitution C T missense_variant A2905T 8713G>A STAD-US 4 85617311 85617311 single base substitution C T missense_variant A508T 1522G>A STAD-US 4 85636503 85636503 single base substitution G A missense_variant R240W 718C>T STAD-US 4 85636503 85636503 single base substitution G A missense_variant R2620W 7858C>T STAD-US 4 85636503 85636503 single base substitution G A missense_variant R2637W 7909C>T STAD-US 4 85638104 85638104 single base substitution C A missense_variant S210I 629G>T STAD-US 4 85638104 85638104 single base substitution C A missense_variant S2590I 7769G>T STAD-US 4 85638104 85638104 single base substitution C A missense_variant S2607I 7820G>T STAD-US 4 85645698 85645698 single base substitution T C missense_variant Y2424C 7271A>G STAD-US 4 85645698 85645698 single base substitution T C missense_variant Y2441C 7322A>G STAD-US 4 85645698 85645698 single base substitution T C missense_variant Y44C 131A>G STAD-US 4 85654581 85654581 single base substitution T C downstream_gene_variant STAD-US 4 85654581 85654581 single base substitution T C missense_variant N12S 35A>G STAD-US 4 85654581 85654581 single base substitution T C missense_variant N2392S 7175A>G STAD-US 4 85654602 85654602 single base substitution A G downstream_gene_variant STAD-US 4 85654602 85654602 single base substitution A G missense_variant V2385A 7154T>C STAD-US 4 85654602 85654602 single base substitution A G missense_variant V5A 14T>C STAD-US 4 85657439 85657439 single base substitution G A exon_variant STAD-US 4 85657439 85657439 single base substitution G A missense_variant P2267S 6799C>T STAD-US 4 85657439 85657439 single base substitution G A upstream_gene_variant STAD-US 4 85658383 85658383 single base substitution C T exon_variant STAD-US 4 85658383 85658383 single base substitution C T synonymous_variant R2237R 6711G>A STAD-US 4 85658383 85658383 single base substitution C T upstream_gene_variant STAD-US 4 85658471 85658471 single base substitution A T exon_variant STAD-US 4 85658471 85658471 single base substitution A T missense_variant I2208K 6623T>A STAD-US 4 85658471 85658471 single base substitution A T upstream_gene_variant STAD-US 4 85660161 85660161 single base substitution A G splice_donor_variant STAD-US 4 85660241 85660241 single base substitution C T exon_variant STAD-US 4 85660241 85660241 single base substitution C T missense_variant A2166T 6496G>A STAD-US 4 85661406 85661406 single base substitution G A missense_variant P2133L 6398C>T STAD-US 4 85661406 85661406 single base substitution G A upstream_gene_variant STAD-US 4 85661555 85661555 single base substitution T A synonymous_variant S2083S 6249A>T STAD-US 4 85661555 85661555 single base substitution T A upstream_gene_variant STAD-US 4 85672710 85672710 single base substitution G A exon_variant STAD-US 4 85672710 85672710 single base substitution G A missense_variant R1967W 5899C>T STAD-US 4 85674913 85674913 single base substitution A G exon_variant STAD-US 4 85674913 85674913 single base substitution A G synonymous_variant P1892P 5676T>C STAD-US 4 85675010 85675012 deletion of <=200bp TCT - disruptive_inframe_deletion EE1859E STAD-US 4 85675010 85675012 deletion of <=200bp TCT - exon_variant STAD-US 4 85676453 85676453 deletion of <=200bp A - exon_variant STAD-US 4 85676453 85676453 deletion of <=200bp A - frameshift_variant L1842 STAD-US 4 85676453 85676453 insertion of <=200bp - A exon_variant STAD-US 4 85676453 85676453 insertion of <=200bp - A frameshift_variant L1842F? STAD-US 4 85678171 85678171 single base substitution C T missense_variant A1778T 5332G>A STAD-US 4 85678171 85678171 single base substitution C T upstream_gene_variant STAD-US 4 85687073 85687073 single base substitution A G missense_variant V1693A 5078T>C STAD-US 4 85694043 85694043 single base substitution C T synonymous_variant A1598A 4794G>A STAD-US 4 85696261 85696261 single base substitution G T missense_variant L1517I 4549C>A STAD-US 4 85701357 85701357 single base substitution A G synonymous_variant D1423D 4269T>C STAD-US 4 85701365 85701365 single base substitution C T missense_variant A1421T 4261G>A STAD-US 4 85707176 85707176 single base substitution G A missense_variant R1340W 4018C>T STAD-US 4 85707196 85707196 single base substitution G A missense_variant S1333F 3998C>T STAD-US 4 85707266 85707266 single base substitution C A missense_variant V1310L 3928G>T STAD-US 4 85708634 85708634 single base substitution C T splice_donor_variant STAD-US 4 85708803 85708803 single base substitution C T missense_variant V1245I 3733G>A STAD-US 4 85708812 85708812 single base substitution C T missense_variant V1242M 3724G>A STAD-US 4 85708820 85708820 single base substitution G T missense_variant P1239Q 3716C>A STAD-US 4 85715780 85715780 single base substitution G A missense_variant R1127C 3379C>T STAD-US 4 85715865 85715865 single base substitution G A synonymous_variant S1098S 3294C>T STAD-US 4 85716121 85716121 deletion of <=200bp A - frameshift_variant L1060 STAD-US 4 85719168 85719168 single base substitution A G downstream_gene_variant STAD-US 4 85719168 85719168 single base substitution A G synonymous_variant S972S 2916T>C STAD-US 4 85719240 85719240 single base substitution A G downstream_gene_variant STAD-US 4 85719240 85719240 single base substitution A G synonymous_variant S948S 2844T>C STAD-US 4 85722917 85722917 single base substitution C T downstream_gene_variant STAD-US 4 85722917 85722917 single base substitution C T missense_variant R903Q 2708G>A STAD-US 4 85731038 85731038 single base substitution A G exon_variant STAD-US 4 85731038 85731038 single base substitution A G splice_donor_variant STAD-US 4 85731148 85731148 single base substitution C A exon_variant STAD-US 4 85731148 85731148 single base substitution C A missense_variant R746I 2237G>T STAD-US 4 85731320 85731320 single base substitution A G exon_variant STAD-US 4 85731320 85731320 single base substitution A G missense_variant F689L 2065T>C STAD-US 4 85731320 85731320 single base substitution A G upstream_gene_variant STAD-US 4 85731422 85731422 single base substitution T C exon_variant STAD-US 4 85731422 85731422 single base substitution T C missense_variant T655A 1963A>G STAD-US 4 85731422 85731422 single base substitution T C upstream_gene_variant STAD-US 4 85738729 85738729 single base substitution C T exon_variant STAD-US 4 85738729 85738729 single base substitution C T missense_variant R568Q 1703G>A STAD-US 4 85741342 85741342 deletion of <=200bp A - splice_region_variant STAD-US 4 85750185 85750185 single base substitution A G exon_variant STAD-US 4 85750185 85750185 single base substitution A G missense_variant Y310H 928T>C STAD-US 4 85750257 85750257 single base substitution G C exon_variant STAD-US 4 85750257 85750257 single base substitution G C missense_variant L286V 856C>G STAD-US 4 85758175 85758175 insertion of <=200bp - A downstream_gene_variant STAD-US 4 85758175 85758175 insertion of <=200bp - A exon_variant STAD-US 4 85758175 85758175 insertion of <=200bp - A frameshift_variant F161F? STAD-US 4 85762336 85762336 single base substitution T C downstream_gene_variant STAD-US 4 85762336 85762336 single base substitution T C exon_variant STAD-US 4 85762336 85762336 single base substitution T C missense_variant T129A 385A>G STAD-US 4 85771148 85771148 single base substitution T C exon_variant STAD-US 4 85771148 85771148 single base substitution T C missense_variant T71A 211A>G STAD-US 4 85771148 85771148 single base substitution T C missense_variant T7A 19A>G STAD-US 4 85781643 85781643 single base substitution C G downstream_gene_variant STAD-US 4 85781643 85781643 single base substitution C G exon_variant STAD-US 4 85781643 85781643 single base substitution C G missense_variant E34D 102G>C THCA-US 4 85639709 85639709 single base substitution G A synonymous_variant Y143Y 429C>T THCA-US 4 85639709 85639709 single base substitution G A synonymous_variant Y2523Y 7569C>T THCA-US 4 85639709 85639709 single base substitution G A synonymous_variant Y2540Y 7620C>T THCA-US 4 85696234 85696234 insertion of <=200bp - T frameshift_variant L1526H? UCEC-US 4 85594131 85594131 single base substitution G A exon_variant UCEC-US 4 85594131 85594131 single base substitution G A stop_gained Q3474* 10420C>T UCEC-US 4 85594131 85594131 single base substitution G A stop_gained Q3491* 10471C>T UCEC-US 4 85600238 85600238 single base substitution G A exon_variant UCEC-US 4 85600238 85600238 single base substitution G A synonymous_variant G3310G 9930C>T UCEC-US 4 85600238 85600238 single base substitution G A synonymous_variant G3327G 9981C>T UCEC-US 4 85600284 85600284 single base substitution C T exon_variant UCEC-US 4 85600284 85600284 single base substitution C T missense_variant R3295Q 9884G>A UCEC-US 4 85600284 85600284 single base substitution C T missense_variant R3312Q 9935G>A UCEC-US 4 85600322 85600322 single base substitution G A exon_variant UCEC-US 4 85600322 85600322 single base substitution G A synonymous_variant D3282D 9846C>T UCEC-US 4 85600322 85600322 single base substitution G A synonymous_variant D3299D 9897C>T UCEC-US 4 85605097 85605097 single base substitution C T missense_variant R3225Q 9674G>A UCEC-US 4 85605097 85605097 single base substitution C T missense_variant R3242Q 9725G>A UCEC-US 4 85605097 85605097 single base substitution C T upstream_gene_variant UCEC-US 4 85605186 85605186 single base substitution G A synonymous_variant S3195S 9585C>T UCEC-US 4 85605186 85605186 single base substitution G A synonymous_variant S3212S 9636C>T UCEC-US 4 85605186 85605186 single base substitution G A upstream_gene_variant UCEC-US 4 85609264 85609264 single base substitution G T downstream_gene_variant UCEC-US 4 85609264 85609264 single base substitution G T missense_variant S3156Y 9467C>A UCEC-US 4 85609264 85609264 single base substitution G T missense_variant S3173Y 9518C>A UCEC-US 4 85609357 85609357 single base substitution A C downstream_gene_variant UCEC-US 4 85609357 85609357 single base substitution A C missense_variant I3125S 9374T>G UCEC-US 4 85609357 85609357 single base substitution A C missense_variant I3142S 9425T>G UCEC-US 4 85614055 85614055 single base substitution G T missense_variant S2994Y 8981C>A UCEC-US 4 85614055 85614055 single base substitution G T missense_variant S3011Y 9032C>A UCEC-US 4 85614055 85614055 single base substitution G T missense_variant S614Y 1841C>A UCEC-US 4 85617182 85617182 single base substitution G T missense_variant P2931T 8791C>A UCEC-US 4 85617182 85617182 single base substitution G T missense_variant P2948T 8842C>A UCEC-US 4 85617182 85617182 single base substitution G T missense_variant P551T 1651C>A UCEC-US 4 85617254 85617254 single base substitution C T missense_variant A2907T 8719G>A UCEC-US 4 85617254 85617254 single base substitution C T missense_variant A2924T 8770G>A UCEC-US 4 85617254 85617254 single base substitution C T missense_variant A527T 1579G>A UCEC-US 4 85617256 85617256 single base substitution G A missense_variant A2906V 8717C>T UCEC-US 4 85617256 85617256 single base substitution G A missense_variant A2923V 8768C>T UCEC-US 4 85617256 85617256 single base substitution G A missense_variant A526V 1577C>T UCEC-US 4 85623569 85623569 single base substitution C A stop_gained E2828* 8482G>T UCEC-US 4 85623569 85623569 single base substitution C A stop_gained E2845* 8533G>T UCEC-US 4 85623569 85623569 single base substitution C A stop_gained E448* 1342G>T UCEC-US 4 85625503 85625503 single base substitution G C missense_variant F2793L 8379C>G UCEC-US 4 85625503 85625503 single base substitution G C missense_variant F2810L 8430C>G UCEC-US 4 85625503 85625503 single base substitution G C missense_variant F413L 1239C>G UCEC-US 4 85634327 85634327 single base substitution G A missense_variant T2659M 7976C>T UCEC-US 4 85634327 85634327 single base substitution G A missense_variant T2676M 8027C>T UCEC-US 4 85634327 85634327 single base substitution G A missense_variant T279M 836C>T UCEC-US 4 85645642 85645642 single base substitution A C missense_variant S2443A 7327T>G UCEC-US 4 85645642 85645642 single base substitution A C missense_variant S2460A 7378T>G UCEC-US 4 85645642 85645642 single base substitution A C missense_variant S63A 187T>G UCEC-US 4 85645693 85645693 single base substitution G A stop_gained R2426* 7276C>T UCEC-US 4 85645693 85645693 single base substitution G A stop_gained R2443* 7327C>T UCEC-US 4 85645693 85645693 single base substitution G A stop_gained R46* 136C>T UCEC-US 4 85654536 85654536 single base substitution G A downstream_gene_variant UCEC-US 4 85654536 85654536 single base substitution G A missense_variant A2407V 7220C>T UCEC-US 4 85654536 85654536 single base substitution G A missense_variant A27V 80C>T UCEC-US 4 85654599 85654599 single base substitution C T downstream_gene_variant UCEC-US 4 85654599 85654599 single base substitution C T missense_variant R2386Q 7157G>A UCEC-US 4 85654599 85654599 single base substitution C T missense_variant R6Q 17G>A UCEC-US 4 85654715 85654715 single base substitution G A downstream_gene_variant UCEC-US 4 85654715 85654715 single base substitution G A synonymous_variant I2347I 7041C>T UCEC-US 4 85654715 85654715 single base substitution G A upstream_gene_variant UCEC-US 4 85654761 85654761 single base substitution C T downstream_gene_variant UCEC-US 4 85654761 85654761 single base substitution C T missense_variant R2332H 6995G>A UCEC-US 4 85654761 85654761 single base substitution C T upstream_gene_variant UCEC-US 4 85657353 85657353 single base substitution A G exon_variant UCEC-US 4 85657353 85657353 single base substitution A G synonymous_variant S2295S 6885T>C UCEC-US 4 85657353 85657353 single base substitution A G upstream_gene_variant UCEC-US 4 85658480 85658480 single base substitution G A exon_variant UCEC-US 4 85658480 85658480 single base substitution G A missense_variant T2205I 6614C>T UCEC-US 4 85658480 85658480 single base substitution G A upstream_gene_variant UCEC-US 4 85658516 85658516 single base substitution C T exon_variant UCEC-US 4 85658516 85658516 single base substitution C T missense_variant R2193H 6578G>A UCEC-US 4 85658516 85658516 single base substitution C T upstream_gene_variant UCEC-US 4 85660238 85660238 single base substitution G A exon_variant UCEC-US 4 85660238 85660238 single base substitution G A missense_variant R2167C 6499C>T UCEC-US 4 85661544 85661544 single base substitution G A missense_variant S2087L 6260C>T UCEC-US 4 85661544 85661544 single base substitution G A upstream_gene_variant UCEC-US 4 85663004 85663004 single base substitution G T missense_variant F2048L 6144C>A UCEC-US 4 85663004 85663004 single base substitution G T upstream_gene_variant UCEC-US 4 85664916 85664916 single base substitution C A stop_gained E2004* 6010G>T UCEC-US 4 85664916 85664916 single base substitution C A upstream_gene_variant UCEC-US 4 85674932 85674932 single base substitution G A exon_variant UCEC-US 4 85674932 85674932 single base substitution G A missense_variant A1886V 5657C>T UCEC-US 4 85676502 85676502 single base substitution C T exon_variant UCEC-US 4 85676502 85676502 single base substitution C T missense_variant G1826R 5476G>A UCEC-US 4 85678244 85678244 single base substitution A T missense_variant F1753L 5259T>A UCEC-US 4 85678244 85678244 single base substitution A T upstream_gene_variant UCEC-US 4 85687154 85687154 single base substitution A G missense_variant L1666P 4997T>C UCEC-US 4 85694034 85694034 single base substitution C T synonymous_variant E1601E 4803G>A UCEC-US 4 85696066 85696066 single base substitution C T missense_variant R1554Q 4661G>A UCEC-US 4 85699690 85699690 single base substitution G T stop_gained S1495* 4484C>A UCEC-US 4 85699713 85699713 single base substitution A G synonymous_variant H1487H 4461T>C UCEC-US 4 85699781 85699781 single base substitution G A missense_variant R1465C 4393C>T UCEC-US 4 85701277 85701277 single base substitution C A missense_variant R1450I 4349G>T UCEC-US 4 85707234 85707234 single base substitution C A missense_variant E1320D 3960G>T UCEC-US 4 85707251 85707251 single base substitution A C missense_variant S1315A 3943T>G UCEC-US 4 85711000 85711000 single base substitution C T missense_variant R1183Q 3548G>A UCEC-US 4 85715751 85715751 single base substitution G A synonymous_variant Y1136Y 3408C>T UCEC-US 4 85717840 85717840 single base substitution G A missense_variant H1001Y 3001C>T UCEC-US 4 85719193 85719193 single base substitution C A downstream_gene_variant UCEC-US 4 85719193 85719193 single base substitution C A missense_variant R964M 2891G>T UCEC-US 4 85724513 85724513 single base substitution A G exon_variant UCEC-US 4 85724513 85724513 single base substitution A G missense_variant I846T 2537T>C UCEC-US 4 85731098 85731098 single base substitution G A exon_variant UCEC-US 4 85731098 85731098 single base substitution G A missense_variant R763W 2287C>T UCEC-US 4 85731102 85731102 single base substitution C T exon_variant UCEC-US 4 85731102 85731102 single base substitution C T synonymous_variant T761T 2283G>A UCEC-US 4 85731226 85731226 single base substitution C T exon_variant UCEC-US 4 85731226 85731226 single base substitution C T missense_variant R720Q 2159G>A UCEC-US 4 85731274 85731274 single base substitution T C exon_variant UCEC-US 4 85731274 85731274 single base substitution T C missense_variant H704R 2111A>G UCEC-US 4 85731274 85731274 single base substitution T C upstream_gene_variant UCEC-US 4 85731296 85731296 single base substitution G A exon_variant UCEC-US 4 85731296 85731296 single base substitution G A missense_variant R697C 2089C>T UCEC-US 4 85731296 85731296 single base substitution G A upstream_gene_variant UCEC-US 4 85731460 85731460 single base substitution C A exon_variant UCEC-US 4 85731460 85731460 single base substitution C A missense_variant R642I 1925G>T UCEC-US 4 85731460 85731460 single base substitution C A upstream_gene_variant UCEC-US 4 85742581 85742581 single base substitution G A exon_variant UCEC-US 4 85742581 85742581 single base substitution G A missense_variant A416V 1247C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand YUDIALE COSM1694631 c.10033G>C p.G3345R Substitution - Missense 4:84679033-84679033 - sysucc-880T COSM5463366 c.9254C>T p.A3085V Substitution - Missense 4:84690615-84690615 - TCGA-AX-A0J1-01 COSM1058336 c.9981C>T p.G3327G Substitution - coding silent 4:84679085-84679085 - EGC15 COSM5060516 c.10511G>A p.R3504H Substitution - Missense 4:84672938-84672938 - HCC067T COSM5824037 c.7488A>T p.G2496G Substitution - coding silent 4:84721526-84721526 - OST10T COSM1732603 c.4493T>A p.F1498Y Substitution - Missense 4:84778528-84778528 - HCC118T COSM5813705 c.5833T>A p.C1945S Substitution - Missense 4:84751623-84751623 - SC_9047 COSM5565676 c.10297C>T p.R3433* Substitution - Nonsense 4:84677359-84677359 - TCGA-G2-A2EL-01 COSM1310334 c.5971G>C p.E1991Q Substitution - Missense 4:84751485-84751485 - TCGA-B5-A11Y-01 COSM1058386 c.2111A>G p.H704R Substitution - Missense 4:84810121-84810121 - DLD1 COSM2956241 c.9792A>G p.E3264E Substitution - coding silent 4:84682405-84682405 - TCGA-B6-A40C-01 COSM4391305 c.7297G>A p.V2433I Substitution - Missense 4:84724570-84724570 - sysucc-1163T COSM5459125 c.1058C>T p.A353V Substitution - Missense 4:84826880-84826880 - BD202T COSM5501334 c.688C>A p.P230T Substitution - Missense 4:84831494-84831494 - ATL018 COSM5709375 c.692G>A p.W231* Substitution - Nonsense 4:84831490-84831490 - SC_9038 COSM5559315 c.10014C>A p.L3338L Substitution - coding silent 4:84679052-84679052 - PT48 COSM5931568 c.7082C>T p.P2361L Substitution - Missense 4:84733521-84733521 - CSCC-7-T COSM128479 c.2682C>T p.V894V Substitution - coding silent 4:84801790-84801790 - 587342 COSM1232519 c.6091C>T p.P2031S Substitution - Missense 4:84741904-84741904 - TCGA-CA-6717-01 COSM1431467 c.7670T>G p.F2557C Substitution - Missense 4:84718506-84718506 - TCGA-D3-A2JF-06 COSM3606702 c.2362C>T p.P788S Substitution - Missense 4:84808401-84808401 - TCGA-CG-4442-01 COSM4126445 c.3716C>A p.P1239Q Substitution - Missense 4:84787667-84787667 - I2L-P7-Tumor-Organoid COSM1431476 c.5525delT p.L1842fs*10 Deletion - Frameshift 4:84755300-84755300 - Pat_22_B COSM5866879 c.5245G>T p.D1749Y Substitution - Missense 4:84757105-84757105 - SWE-1A COSM1179334 c.2630C>A p.A877D Substitution - Missense 4:84801842-84801842 - TCGA-D3-A3C7-06 COSM3606707 c.1906C>T p.R636* Substitution - Nonsense 4:84810326-84810326 - ATL014 COSM5575150 c.846G>C p.M282I Substitution - Missense 4:84829114-84829114 - YUGOE COSM1694634 c.4477C>T p.P1493S Substitution - Missense 4:84778544-84778544 - TCGA-DK-A1AC-01 COSM1310335 c.5807G>C p.G1936A Substitution - Missense 4:84751649-84751649 - TCGA-29-1701-01 COSM1328363 c.1501A>G p.R501G Substitution - Missense 4:84821174-84821174 - TCGA-BP-4340-01 COSM3365726 c.971A>G p.K324R Substitution - Missense 4:84826967-84826967 - TCGA-DK-A3WY-01 COSM3776042 c.8721A>G p.L2907L Substitution - coding silent 4:84696150-84696150 - HCC53T COSM1619171 c.3524T>A p.I1175N Substitution - Missense 4:84789871-84789871 - HCC163 COSM3661239 c.5144A>C p.E1715A Substitution - Missense 4:84765854-84765854 - TCGA-BP-4965-01 COSM1495894 c.2477A>G p.N826S Substitution - Missense 4:84803420-84803420 - TCGA-BR-6452-01 COSM4126440 c.3998C>T p.S1333F Substitution - Missense 4:84786043-84786043 - TCGA-FV-A23B-01 COSM4913970 c.6108A>G p.G2036G Substitution - coding silent 4:84741887-84741887 - Gp2D COSM2956416 c.1380T>C p.C460C Substitution - coding silent 4:84821295-84821295 - TCGA-66-2759-01 COSM734417 c.812C>G p.S271* Substitution - Nonsense 4:84829148-84829148 - TCGA-EI-6917-01 COSM3428722 c.6875G>A p.R2292Q Substitution - Missense 4:84736210-84736210 - I2L-P24Tb-Tumor-Biopsy COSM5356065 c.7098C>T p.L2366L Substitution - coding silent 4:84733505-84733505 - HCC172 COSM3661242 c.3132T>C p.A1044A Substitution - coding silent 4:84796556-84796556 - T3118 COSM1431476 c.5525delT p.L1842fs*10 Deletion - Frameshift 4:84755300-84755300 - TCGA-IR-A3LK-01 COSM4816840 c.8967C>G p.I2989M Substitution - Missense 4:84692967-84692967 - TCGA-AX-A0J1-01 COSM1058353 c.7220C>T p.A2407V Substitution - Missense 4:84733383-84733383 - TCGA-D7-6820-01 COSM4126432 c.5676T>C p.P1892P Substitution - coding silent 4:84753760-84753760 - BD183T COSM5508038 c.7962-3C>T p.? Unknown 4:84713242-84713242 - PD13302a COSM5783421 c.2632G>A p.V878M Substitution - Missense 4:84801840-84801840 - TCGA-CA-6717-01 COSM1431480 c.3564C>T p.I1188I Substitution - coding silent 4:84789831-84789831 - ATL081 COSM5709371 c.10326G>T p.Q3442H Substitution - Missense 4:84677330-84677330 - EV007-R3 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 - TCGA-B5-A0JY-01 COSM1058370 c.4803G>A p.E1601E Substitution - coding silent 4:84772881-84772881 - TCGA-BS-A0UF-01 COSM1058347 c.8533G>T p.E2845* Substitution - Nonsense 4:84702416-84702416 - HCC53 COSM1619171 c.3524T>A p.I1175N Substitution - Missense 4:84789871-84789871 - T613 COSM4740818 c.5134G>T p.G1712* Substitution - Nonsense 4:84765864-84765864 - BN31T COSM1619168 c.7863A>G p.R2621R Substitution - coding silent 4:84716908-84716908 - B104-0-Tumor COSM4005812 c.643C>T p.L215F Substitution - Missense 4:84831539-84831539 - EV007-R1 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 - C0084T COSM4165042 c.10574A>C p.N3525T Substitution - Missense 4:84672875-84672875 - I2L-P7-Tumor-Organoid COSM5356249 c.8139C>T p.N2713N Substitution - coding silent 4:84708987-84708987 - CRC-03T COSM5451781 c.8828A>G p.Y2943C Substitution - Missense 4:84696043-84696043 - TCGA-BH-A1F8-01 COSM1486132 c.5243G>A p.R1748Q Substitution - Missense 4:84757107-84757107 - LUAD-RT-S01840 COSM384808 c.8193G>C p.W2731C Substitution - Missense 4:84708933-84708933 - TCGA-B5-A0K9-01 COSM1058368 c.5259T>A p.F1753L Substitution - Missense 4:84757091-84757091 - CDGLIV0707A0251_T COSM5040419 c.957-2A>T p.? Unknown 4:84826983-84826983 - 477 COSM4438816 c.5397C>G p.I1799M Substitution - Missense 4:84756953-84756953 - TCGA-EW-A1IZ-01 COSM1486130 c.7051C>T p.L2351L Substitution - coding silent 4:84733552-84733552 - TCGA-CG-5721-01 COSM1431474 c.5899C>T p.R1967W Substitution - Missense 4:84751557-84751557 - TCGA-D7-8576-01 COSM4126418 c.8725G>A p.E2909K Substitution - Missense 4:84696146-84696146 - DLBCL-PatientG COSM220376 c.3084G>A p.M1028I Substitution - Missense 4:84796604-84796604 - TCGA-B5-A0JY-01 COSM278115 c.3548G>A p.R1183Q Substitution - Missense 4:84789847-84789847 - GHE0605 COSM5714045 c.3386C>A p.A1129E Substitution - Missense 4:84794620-84794620 - TCGA-A6-6653-01 COSM1431470 c.6824G>A p.R2275H Substitution - Missense 4:84736261-84736261 - TCGA-BP-4326-01 COSM3365725 c.2583T>A p.S861S Substitution - coding silent 4:84803314-84803314 - TCGA-BQ-7059-01 COSM3993826 c.121C>T p.H41Y Substitution - Missense 4:84860471-84860471 - TCGA-61-2009-01 COSM73275 c.1232A>C p.Y411S Substitution - Missense 4:84821443-84821443 - I2L-P7-Tumor-Organoid COSM5356181 c.2938A>C p.S980R Substitution - Missense 4:84796750-84796750 - TCGA-CS-5397-01 COSM3975080 c.9194A>T p.E3065V Substitution - Missense 4:84691641-84691641 - TCGA-AR-A24H-01 COSM1486131 c.6126G>A p.V2042V Substitution - coding silent 4:84741869-84741869 - TCGA-CG-5721-01 COSM4126428 c.6574+2T>C p.? Unknown 4:84739008-84739008 - C0097T COSM4165043 c.8393C>A p.S2798* Substitution - Nonsense 4:84704387-84704387 - TCGA-BC-A10X-01 COSM4927746 c.5095T>C p.S1699P Substitution - Missense 4:84765903-84765903 - CSCC-27-T COSM3606708 c.1513C>T p.L505F Substitution - Missense 4:84821162-84821162 - TCGA-HU-A4H4-01 COSM4126441 c.3928G>T p.V1310L Substitution - Missense 4:84786113-84786113 - TCGA-EK-A3GK-01 COSM4853525 c.5990C>G p.S1997C Substitution - Missense 4:84743783-84743783 - YUFIT COSM3606679 c.9075C>T p.I3025I Substitution - coding silent 4:84691760-84691760 - TCGA-EE-A29M-06 COSM3606685 c.7364C>T p.A2455V Substitution - Missense 4:84724503-84724503 - L13 COSM5369135 c.1105_1106CC>AT p.P369I Substitution - Missense 4:84826832-84826833 - TCGA-B5-A0K8-01 COSM1058379 c.3343C>G p.P1115A Substitution - Missense 4:84794663-84794663 - T578 COSM4740810 c.10210C>T p.R3404* Substitution - Nonsense 4:84678217-84678217 - D9 COSM5007798 c.991G>A p.A331T Substitution - Missense 4:84826947-84826947 - SWE-1A COSM1179334 c.2630C>A p.A877D Substitution - Missense 4:84801842-84801842 - TCGA-EE-A29D-06 COSM3606690 c.5712C>T p.P1904P Substitution - coding silent 4:84753724-84753724 - NPC10D COSM4996469 c.7622G>A p.R2541H Substitution - Missense 4:84718554-84718554 - QC2-39-T2 COSM5655485 c.10308C>G p.S3436R Substitution - Missense 4:84677348-84677348 - T3091 COSM4740815 c.6009_6010insA p.E2004fs*9 Insertion - Frameshift 4:84743763-84743764 - S02400 COSM5699899 c.1810G>T p.D604Y Substitution - Missense 4:84817469-84817469 - TCGA-DA-A1I4-06 COSM3606695 c.4732C>T p.P1578S Substitution - Missense 4:84774842-84774842 - T3118 COSM4740822 c.1954G>A p.V652M Substitution - Missense 4:84810278-84810278 - TCGA-AA-A010-01 COSM286495 c.3541C>T p.R1181C Substitution - Missense 4:84789854-84789854 - TCGA-AP-A059-01 COSM1058345 c.8770G>A p.A2924T Substitution - Missense 4:84696101-84696101 - LUAD-B02515 COSM336225 c.8961A>T p.A2987A Substitution - coding silent 4:84692973-84692973 - TCGA-66-2768-01 COSM734429 c.10571G>A p.R3524Q Substitution - Missense 4:84672878-84672878 - 3N53-VS-3T53 COSM4983599 c.10114A>G p.I3372V Substitution - Missense 4:84678952-84678952 - TCGA-B0-5692-01 COSM481628 c.5719A>G p.I1907V Substitution - Missense 4:84753717-84753717 - TCGA-27-1832-01 COSM3409589 c.6823C>T p.R2275C Substitution - Missense 4:84736262-84736262 - pfg317T COSM4758380 c.6032A>G p.D2011G Substitution - Missense 4:84743741-84743741 - J52_T COSM3946606 c.6734T>G p.L2245R Substitution - Missense 4:84737207-84737207 - 3006_T COSM3946607 c.4831G>T p.E1611* Substitution - Nonsense 4:84772853-84772853 - SJMB027 COSM255937 c.6691G>A p.V2231M Substitution - Missense 4:84737250-84737250 - TCGA-EE-A3AC-06 COSM3606704 c.1949G>T p.G650V Substitution - Missense 4:84810283-84810283 - LUAD-RT-S01774 COSM381539 c.3057G>T p.L1019L Substitution - coding silent 4:84796631-84796631 - TCGA-HJ-7597-01 COSM4126443 c.3733G>A p.V1245I Substitution - Missense 4:84787650-84787650 - BD121T COSM5515018 c.2158C>T p.R720* Substitution - Nonsense 4:84810074-84810074 - TCGA-B5-A0JY-01 COSM1058367 c.5476G>A p.G1826R Substitution - Missense 4:84755349-84755349 - PDA_042 COSM5000254 c.1801A>G p.N601D Substitution - Missense 4:84817478-84817478 - SJMB131 COSM255278 c.9544-10C>G p.? Unknown 4:84684135-84684135 - TCGA-DA-A1I8-06 COSM3606680 c.8817A>G p.Q2939Q Substitution - coding silent 4:84696054-84696054 - T3152 COSM4740811 c.9314_9315insTG p.W3105fs*34 Insertion - Frameshift 4:84690554-84690555 - HCC129T COSM2956330 c.5883C>T p.F1961F Substitution - coding silent 4:84751573-84751573 - TCGA-EE-A3AF-06 COSM3606687 c.6751C>T p.H2251Y Substitution - Missense 4:84737190-84737190 - TCGA-H4-A2HQ-01 COSM1310333 c.8028G>T p.T2676T Substitution - coding silent 4:84713173-84713173 - TCGA-B5-A0JY-01 COSM1058351 c.7378T>G p.S2460A Substitution - Missense 4:84724489-84724489 - T1743 COSM4740813 c.8125T>G p.L2709V Substitution - Missense 4:84709001-84709001 - pfg016T COSM1431491 c.32C>T p.P11L Substitution - Missense 4:84860560-84860560 - Pat_34_A COSM4488202 c.3290C>T p.P1097L Substitution - Missense 4:84794716-84794716 - CSCC-60-T COSM4462796 c.1260C>T p.I420I Substitution - coding silent 4:84821415-84821415 - TCGA-BG-A0VT-01 COSM1058350 c.7692G>A p.V2564V Substitution - coding silent 4:84718484-84718484 - ESCC-246T COSM1058371 c.4661G>A p.R1554Q Substitution - Missense 4:84774913-84774913 - CHC326T COSM4806023 c.6461G>A p.G2154E Substitution - Missense 4:84740190-84740190 - 585270 COSM324281 c.2800G>C p.A934P Substitution - Missense 4:84801672-84801672 - Au2 COSM5600848 c.5270C>T p.P1757L Substitution - Missense 4:84757080-84757080 - TCGA-EE-A2M5-06 COSM3606694 c.4788C>T p.T1596T Substitution - coding silent 4:84772896-84772896 - Br27P COSM40758 c.1126C>T p.H376Y Substitution - Missense 4:84821549-84821549 - WA11 COSM242236 c.1A>G p.M1V Substitution - Missense 4:84860591-84860591 - 7T COSM3714954 c.2782G>C p.E928Q Substitution - Missense 4:84801690-84801690 - LOVO COSM4645520 c.6501C>T p.R2167R Substitution - coding silent 4:84739083-84739083 - LUAD-S01478 COSM399974 c.9727T>G p.F3243V Substitution - Missense 4:84682470-84682470 - H2009 COSM1193892 c.3625A>G p.T1209A Substitution - Missense 4:84789770-84789770 - EV007-R7 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 - C092 COSM5543698 c.8662C>T p.R2888* Substitution - Nonsense 4:84696758-84696758 - TCGA-FS-A1ZQ-06 COSM3606692 c.5487C>T p.V1829V Substitution - coding silent 4:84755338-84755338 - T2999 COSM4740816 c.5502C>T p.N1834N Substitution - coding silent 4:84755323-84755323 - T3535 COSM1431476 c.5525delT p.L1842fs*10 Deletion - Frameshift 4:84755300-84755300 - 011T COSM1727697 c.6482G>T p.G2161V Substitution - Missense 4:84739102-84739102 - Pat_59_B COSM5866876 c.9052C>T p.L3018F Substitution - Missense 4:84691783-84691783 - SNU-175 COSM2956362 c.3918C>T p.S1306S Substitution - coding silent 4:84786123-84786123 - TCGA-F5-6864-01 COSM3428723 c.4811T>C p.V1604A Substitution - Missense 4:84772873-84772873 - 6115122 COSM5574015 c.9569_9570insA p.Y3191fs*21 Insertion - Frameshift 4:84684099-84684100 - ATLL_A-01 COSM5575150 c.846G>C p.M282I Substitution - Missense 4:84829114-84829114 - TCGA-BR-A4QM-01 COSM4126431 c.6249A>T p.S2083S Substitution - coding silent 4:84740402-84740402 - ESO-173 COSM1270367 c.419C>A p.T140N Substitution - Missense 4:84837086-84837086 - TCGA-C5-A2LX-01 COSM4827523 c.9608T>C p.V3203A Substitution - Missense 4:84684061-84684061 - LC_C1 COSM1186610 c.2868C>A p.D956E Substitution - Missense 4:84798063-84798063 - C391 COSM4441792 c.6923C>T p.S2308L Substitution - Missense 4:84735113-84735113 - TCGA-B5-A0JY-01 COSM1058365 c.6010G>T p.E2004* Substitution - Nonsense 4:84743763-84743763 - WA38 COSM242235 c.10466G>A p.R3489H Substitution - Missense 4:84672983-84672983 - OSCC-GB_00070111 COSM3714954 c.2782G>C p.E928Q Substitution - Missense 4:84801690-84801690 - 092T COSM1731392 c.1006G>T p.V336F Substitution - Missense 4:84826932-84826932 - TCGA-BR-6566-01 COSM4126420 c.7909C>T p.R2637W Substitution - Missense 4:84715350-84715350 - ESCC_141 COSM5643587 c.3919G>T p.E1307* Substitution - Nonsense 4:84786122-84786122 - NPC15F COSM4996471 c.1480T>C p.Y494H Substitution - Missense 4:84821195-84821195 - TCGA-22-4591-01 COSM734422 c.2973T>G p.D991E Substitution - Missense 4:84796715-84796715 - GC_315T-GC_315N COSM734416 c.415-4C>T p.? Unknown 4:84837094-84837094 - UM-SCC-47 COSM4600164 c.2782G>A p.E928K Substitution - Missense 4:84801690-84801690 - TCGA-BR-6452-01 COSM4126417 c.9050A>G p.E3017G Substitution - Missense 4:84691785-84691785 - PCSI_0469_Pa_P_526 COSM4808826 c.4917T>G p.D1639E Substitution - Missense 4:84766305-84766305 - TCGA-EJ-5524-01 COSM1131011 c.2834G>A p.R945H Substitution - Missense 4:84798097-84798097 - TCGA-BR-6452-01 COSM4126459 c.211A>G p.T71A Substitution - Missense 4:84849995-84849995 - CSCC-27-T COSM4485241 c.290C>T p.S97L Substitution - Missense 4:84849916-84849916 - HT115 COSM2956415 c.1390A>G p.I464V Substitution - Missense 4:84821285-84821285 - HCC134T COSM3661240 c.4107A>G p.I1369M Substitution - Missense 4:84783030-84783030 - sysucc-274T COSM5476541 c.2346T>A p.S782R Substitution - Missense 4:84808417-84808417 - TCGA-D7-A4YX-01 COSM4126429 c.6496G>A p.A2166T Substitution - Missense 4:84739088-84739088 - SNUH_G73_S1 COSM4415548 c.4174+8G>T p.? Unknown 4:84782955-84782955 - 2492730 COSM5729845 c.6895A>C p.K2299Q Substitution - Missense 4:84736190-84736190 - 2492729 COSM5727236 c.7481C>T p.P2494L Substitution - Missense 4:84721533-84721533 - S02328 COSM5692129 c.4911T>C p.L1637L Substitution - coding silent 4:84766311-84766311 - TCGA-BR-4370-01 COSM4126421 c.7820G>T p.S2607I Substitution - Missense 4:84716951-84716951 - HN_62854 COSM128479 c.2682C>T p.V894V Substitution - coding silent 4:84801790-84801790 - TCGA-AA-A00N-01 COSM278114 c.9980G>T p.G3327V Substitution - Missense 4:84679086-84679086 - HCC163T COSM3661239 c.5144A>C p.E1715A Substitution - Missense 4:84765854-84765854 - TCGA-EB-A3Y7-01 COSM3606711 c.973G>A p.E325K Substitution - Missense 4:84826965-84826965 - BD114T COSM5502872 c.6574G>C p.G2192R Substitution - Missense 4:84739010-84739010 - sysucc-1512T COSM5450786 c.8763C>T p.G2921G Substitution - coding silent 4:84696108-84696108 - 5_RESISTANT COSM1724972 c.1592-3delT p.? Unknown 4:84820189-84820189 - TCGA-CS-5393-01 COSM3975079 c.9952G>A p.A3318T Substitution - Missense 4:84679114-84679114 - TCGA-AC-A23H-01 COSM3826353 c.3589G>T p.V1197F Substitution - Missense 4:84789806-84789806 - 49M COSM2956330 c.5883C>T p.F1961F Substitution - coding silent 4:84751573-84751573 - TCGA-CG-5728-01 COSM2956249 c.9387C>T p.T3129T Substitution - coding silent 4:84688242-84688242 - YURED COSM1694635 c.3289C>T p.P1097S Substitution - Missense 4:84794717-84794717 - HCT8 COSM4635166 c.923A>G p.Q308R Substitution - Missense 4:84829037-84829037 - ESCC_170 COSM5649499 c.5660C>A p.S1887Y Substitution - Missense 4:84753776-84753776 - PCSI_0112_Pa_P COSM3381028 c.18G>A p.R6R Substitution - coding silent 4:84860574-84860574 - TCGA-AP-A0LE-01 COSM1058373 c.4461T>C p.H1487H Substitution - coding silent 4:84778560-84778560 - DLD1 COSM4625356 c.2935A>G p.S979G Substitution - Missense 4:84797996-84797996 - KM12 COSM2956396 c.2227C>T p.P743S Substitution - Missense 4:84810005-84810005 - TCGA-G2-A2ES-01 COSM1310336 c.5147A>T p.Q1716L Substitution - Missense 4:84765851-84765851 - CSCC-49-T COSM4519097 c.9677_9678GG>AA p.W3226* Substitution - Nonsense 4:84683991-84683992 - 0047_CRUK_PC_0047_T1_DNA COSM5421829 c.2430-6_2430-5insT p.? Unknown 4:84803472-84803473 - TCGA-CC-5262-01 COSM4919228 c.3954A>G p.P1318P Substitution - coding silent 4:84786087-84786087 - RK219_C01 COSM3768040 c.8364C>T p.T2788T Substitution - coding silent 4:84704416-84704416 - SJDOSTEOS009 COSM5760110 c.10523A>G p.N3508S Substitution - Missense 4:84672926-84672926 - TCGA-BS-A0U8-01 COSM1058361 c.6577C>T p.R2193C Substitution - Missense 4:84737364-84737364 - LUAD-CHTN-MAD06-00668 COSM359939 c.2815G>A p.V939M Substitution - Missense 4:84801657-84801657 - J63_T COSM3946604 c.9961G>T p.A3321S Substitution - Missense 4:84679105-84679105 - TCGA-AX-A0J1-01 COSM1058374 c.4393C>T p.R1465C Substitution - Missense 4:84778628-84778628 - TCGA-AP-A051-01 COSM1058380 c.3001C>T p.H1001Y Substitution - Missense 4:84796687-84796687 - TCGA-EB-A44O-01 COSM734429 c.10571G>A p.R3524Q Substitution - Missense 4:84672878-84672878 - TCGA-AA-3966-01 COSM273466 c.3179delT p.L1060fs*41 Deletion - Frameshift 4:84794968-84794968 - TCGA-HT-7485-01 COSM3975081 c.9082A>G p.T3028A Substitution - Missense 4:84691753-84691753 - TCGA-DD-A119-01 COSM4919978 c.1969T>C p.L657L Substitution - coding silent 4:84810263-84810263 - TCGA-EB-A4IS-01 COSM2956330 c.5883C>T p.F1961F Substitution - coding silent 4:84751573-84751573 - TCGA-A6-6781-01 COSM1431477 c.5475C>T p.S1825S Substitution - coding silent 4:84755350-84755350 - T3202 COSM4740824 c.984C>G p.S328S Substitution - coding silent 4:84826954-84826954 - Pat_41_B COSM5866875 c.9061C>T p.P3021S Substitution - Missense 4:84691774-84691774 - TCGA-AS-3777-01 COSM1495895 c.7579C>T p.L2527L Substitution - coding silent 4:84721435-84721435 - PCSI_0591_Pa_P_526 COSM5760579 c.10106C>T p.P3369L Substitution - Missense 4:84678960-84678960 - Pat_41_B COSM5866881 c.3400C>T p.Q1134* Substitution - Nonsense 4:84794606-84794606 - LUAD-S01467 COSM404618 c.3683A>G p.H1228R Substitution - Missense 4:84787700-84787700 - EV007-R6 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 - sysucc-311T COSM5466227 c.6874C>T p.R2292* Substitution - Nonsense 4:84736211-84736211 - TCGA-FJ-A3ZE-01 COSM3776041 c.10415G>C p.R3472T Substitution - Missense 4:84677241-84677241 - TCGA-BR-A452-01 COSM4126430 c.6398C>T p.P2133L Substitution - Missense 4:84740253-84740253 - TCGA-AC-A3W5-01 COSM3826351 c.4593-1G>C p.? Unknown 4:84774982-84774982 - TCGA-BR-8487-01 COSM4126449 c.2844T>C p.S948S Substitution - coding silent 4:84798087-84798087 - T1240 COSM4740817 c.5404C>T p.R1802W Substitution - Missense 4:84756946-84756946 - TCGA-AD-5900-01 COSM1431481 c.3443G>A p.R1148Q Substitution - Missense 4:84794563-84794563 - BD202T COSM5501333 c.689C>T p.P230L Substitution - Missense 4:84831493-84831493 - LAU165 COSM233756 c.5477G>A p.G1826E Substitution - Missense 4:84755348-84755348 - TCGA-BR-6452-01 COSM4126425 c.6799C>T p.P2267S Substitution - Missense 4:84736286-84736286 - TCGA-D5-6535-01 COSM1431485 c.1872G>C p.K624N Substitution - Missense 4:84817407-84817407 - CAL33 COSM2956418 c.1264G>C p.E422Q Substitution - Missense 4:84821411-84821411 - pfg016T COSM1642536 c.331T>C p.F111L Substitution - Missense 4:84841237-84841237 - LUAD-F00368 COSM341410 c.9706C>T p.H3236Y Substitution - Missense 4:84683963-84683963 - CSCC-7-T COSM4505970 c.7077C>T p.G2359G Substitution - coding silent 4:84733526-84733526 - TCGA-EE-A29E-06 COSM3606708 c.1513C>T p.L505F Substitution - Missense 4:84821162-84821162 - RK180_C01 COSM1633821 c.6289A>G p.R2097G Substitution - Missense 4:84740362-84740362 - HCC172T COSM3661242 c.3132T>C p.A1044A Substitution - coding silent 4:84796556-84796556 - Pat_41_B COSM5866877 c.8179C>T p.P2727S Substitution - Missense 4:84708947-84708947 - SNU-175 COSM2956430 c.509T>C p.V170A Substitution - Missense 4:84836996-84836996 - TCGA-AP-A051-01 COSM1058352 c.7327C>T p.R2443* Substitution - Nonsense 4:84724540-84724540 - PT37 COSM2956391 c.2398C>T p.P800S Substitution - Missense 4:84808365-84808365 - PCSI_0090_Pa_X COSM3381001 c.7786A>G p.R2596G Substitution - Missense 4:84716985-84716985 - 19 COSM5746312 c.6487G>T p.E2163* Substitution - Nonsense 4:84739097-84739097 - TCGA-33-4566-01 COSM734420 c.2632G>T p.V878L Substitution - Missense 4:84801840-84801840 - SJMB025 COSM255913 c.4037T>A p.L1346* Substitution - Nonsense 4:84786004-84786004 - BCM375T COSM4799242 c.3441C>A p.D1147E Substitution - Missense 4:84794565-84794565 - TCGA-AP-A051-01 COSM1058383 c.2287C>T p.R763W Substitution - Missense 4:84809945-84809945 - MO_1336 COSM5568842 c.2336C>G p.S779C Substitution - Missense 4:84809896-84809896 - ESO-0167 COSM1270365 c.9226T>A p.L3076M Substitution - Missense 4:84690643-84690643 - TCGA-A4-A5Y0-01 COSM3993825 c.2786G>T p.R929L Substitution - Missense 4:84801686-84801686 - LOVO COSM2956256 c.9102G>A p.A3034A Substitution - coding silent 4:84691733-84691733 - HCA7 COSM4630970 c.7988C>T p.T2663M Substitution - Missense 4:84713213-84713213 - TCGA-B5-A11E-01 COSM1058381 c.2891G>T p.R964M Substitution - Missense 4:84798040-84798040 - C0075T COSM4165046 c.1944T>G p.V648V Substitution - coding silent 4:84810288-84810288 - TCGA-21-5782-01 COSM734418 c.870C>T p.L290L Substitution - coding silent 4:84829090-84829090 - TCGA-EE-A29D-06 COSM3606713 c.100G>A p.E34K Substitution - Missense 4:84860492-84860492 - TCGA-AA-A010-01 COSM286493 c.8550C>A p.F2850L Substitution - Missense 4:84702399-84702399 - TCGA-19-5955 COSM1131011 c.2834G>A p.R945H Substitution - Missense 4:84798097-84798097 - pfg222T COSM4758388 c.2855G>C p.C952S Substitution - Missense 4:84798076-84798076 - BZ32 COSM242235 c.10466G>A p.R3489H Substitution - Missense 4:84672983-84672983 - TCGA-34-5231-01 COSM734428 c.10413A>C p.E3471D Substitution - Missense 4:84677243-84677243 - TCGA-BR-8680-01 COSM4126436 c.4549C>A p.L1517I Substitution - Missense 4:84775108-84775108 - 938T COSM4599519 c.3380G>A p.R1127H Substitution - Missense 4:84794626-84794626 - HCC080T COSM5810621 c.7830A>C p.A2610A Substitution - coding silent 4:84716941-84716941 - 19 COSM5746311 c.7336T>C p.S2446P Substitution - Missense 4:84724531-84724531 - TCGA-C5-A1BL-01 COSM4837023 c.1925G>C p.R642T Substitution - Missense 4:84810307-84810307 - TCGA-CJ-4918-01 COSM481625 c.7103A>T p.K2368M Substitution - Missense 4:84733500-84733500 - C0017T COSM4422491 c.9055A>T p.K3019* Substitution - Nonsense 4:84691780-84691780 - 2530678 COSM5885719 c.2557C>G p.L853V Substitution - Missense 4:84803340-84803340 - 49M COSM5593955 c.10038C>T p.F3346F Substitution - coding silent 4:84679028-84679028 - TCGA-AP-A0LM-01 COSM1058357 c.6885T>C p.S2295S Substitution - coding silent 4:84736200-84736200 - LIM2099 COSM4641222 c.1138A>G p.N380D Substitution - Missense 4:84821537-84821537 - GHE0955 COSM4444978 c.10486C>T p.R3496C Substitution - Missense 4:84672963-84672963 - TCGA-D1-A16X-01 COSM1058354 c.7157G>A p.R2386Q Substitution - Missense 4:84733446-84733446 - TCGA-EE-A2GB-06 COSM3606674 c.10477G>A p.E3493K Substitution - Missense 4:84672972-84672972 - BD114T COSM5502873 c.1930G>A p.V644I Substitution - Missense 4:84810302-84810302 - DU-145 COSM1671121 c.10439G>C p.G3480A Substitution - Missense 4:84677217-84677217 - TCGA-AA-A010-01 COSM286497 c.251T>A p.V84D Substitution - Missense 4:84849955-84849955 - UM-SCC-2 COSM4599519 c.3380G>A p.R1127H Substitution - Missense 4:84794626-84794626 - PCSI_0112_Pa_P COSM3381002 c.6574+7G>C p.? Unknown 4:84739003-84739003 - TCGA-EE-A2A2-06 COSM3606696 c.4638C>T p.I1546I Substitution - coding silent 4:84774936-84774936 - TCGA-BR-6566-01 COSM4126415 c.9711A>G p.S3237S Substitution - coding silent 4:84683958-84683958 - 587332 COSM1232517 c.7402G>C p.E2468Q Substitution - Missense 4:84724465-84724465 - TCGA-GN-A269-01 COSM3606712 c.723C>T p.T241T Substitution - coding silent 4:84831459-84831459 - CSCC-16-T COSM4513962 c.9576C>T p.I3192I Substitution - coding silent 4:84684093-84684093 - TCGA-BR-4361-01 COSM4126448 c.2916T>C p.S972S Substitution - coding silent 4:84798015-84798015 - YUKLAB COSM1694633 c.7348G>A p.A2450T Substitution - Missense 4:84724519-84724519 - TCGA-BR-4370-01 COSM4126455 c.1703G>A p.R568Q Substitution - Missense 4:84817576-84817576 - CHC892T COSM4795194 c.6118G>A p.V2040I Substitution - Missense 4:84741877-84741877 - TCGA-A5-A0VP-01 COSM1058339 c.9725G>A p.R3242Q Substitution - Missense 4:84683944-84683944 - SW948 COSM2956253 c.9243G>A p.Q3081Q Substitution - coding silent 4:84690626-84690626 - TCGA-A5-A0GW-01 COSM1058335 c.10443G>A p.Q3481Q Substitution - coding silent 4:84677213-84677213 - TCGA-EE-A29E-06 COSM3606699 c.3340C>T p.P1114S Substitution - Missense 4:84794666-84794666 - ESCC_60 COSM5632771 c.3178T>G p.L1060V Substitution - Missense 4:84794969-84794969 - TCGA-BH-A0BA-01 COSM448265 c.3825A>C p.L1275F Substitution - Missense 4:84787558-84787558 - MO_1249 COSM5572181 c.10310G>A p.W3437* Substitution - Nonsense 4:84677346-84677346 - TCGA-F4-6806-01 COSM1431488 c.913C>T p.R305W Substitution - Missense 4:84829047-84829047 - TCGA-B0-5080-01 COSM481624 c.7540T>A p.S2514T Substitution - Missense 4:84721474-84721474 - BK0100 COSM4189116 c.7032G>T p.W2344C Substitution - Missense 4:84733571-84733571 - 8P2 COSM3734632 c.3202G>A p.A1068T Substitution - Missense 4:84794945-84794945 - PT55 COSM5941932 c.8139C>G p.N2713K Substitution - Missense 4:84708987-84708987 - pfg010T COSM1642535 c.803T>A p.M268K Substitution - Missense 4:84829157-84829157 - ASHPC_0023_Pa_P COSM4806681 c.4008G>A p.V1336V Substitution - coding silent 4:84786033-84786033 - TCGA-D9-A4Z3-01 COSM3606676 c.10123C>T p.R3375W Substitution - Missense 4:84678943-84678943 - TCGA-66-2785-01 COSM734426 c.9251G>T p.C3084F Substitution - Missense 4:84690618-84690618 - 587228 COSM1232515 c.197C>T p.P66L Substitution - Missense 4:84850009-84850009 - TCGA-AM-5820-01 COSM3760791 c.9094A>G p.I3032V Substitution - Missense 4:84691741-84691741 - TCGA-AZ-4315-01 COSM1431465 c.8941C>T p.R2981* Substitution - Nonsense 4:84692993-84692993 - T3724 COSM4740821 c.3585T>G p.H1195Q Substitution - Missense 4:84789810-84789810 - TCGA-CG-4437-01 COSM4126457 c.856C>G p.L286V Substitution - Missense 4:84829104-84829104 - C658 COSM4443491 c.6497C>A p.A2166D Substitution - Missense 4:84739087-84739087 - Pat_11_B COSM1270363 c.9313_9314delTG p.W3105fs*23 Deletion - Frameshift 4:84690555-84690556 - TCGA-GV-A3JZ-01 COSM1310338 c.1669C>T p.L557F Substitution - Missense 4:84820109-84820109 - TCGA-E2-A14V-01 COSM448259 c.7498G>A p.E2500K Substitution - Missense 4:84721516-84721516 - TCGA-CC-A7IK-01 COSM4924706 c.8523A>C p.A2841A Substitution - coding silent 4:84702426-84702426 - TCGA-BH-A0BZ-01 COSM448262 c.5873C>T p.A1958V Substitution - Missense 4:84751583-84751583 - RKO COSM4648817 c.6674T>C p.V2225A Substitution - Missense 4:84737267-84737267 - TCGA-AP-A0LT-01 COSM1058334 c.10471C>T p.Q3491* Substitution - Nonsense 4:84672978-84672978 - LS174T COSM2956402 c.1951T>C p.F651L Substitution - Missense 4:84810281-84810281 - STC246 COSM2956272 c.8486G>A p.R2829H Substitution - Missense 4:84702463-84702463 - 8066446 COSM3784428 c.3392C>G p.S1131C Substitution - Missense 4:84794614-84794614 - SNUH_G76_S1 COSM2956228 c.10392G>A p.S3464S Substitution - coding silent 4:84677264-84677264 - PT33 COSM5908462 c.8197C>T p.L2733F Substitution - Missense 4:84708929-84708929 - T2944 COSM4740827 c.238T>G p.F80V Substitution - Missense 4:84849968-84849968 - 467 COSM4437351 c.8801T>G p.L2934R Substitution - Missense 4:84696070-84696070 - CSCC-27-T COSM4505525 c.6955C>T p.R2319C Substitution - Missense 4:84735081-84735081 - LC_C21 COSM1186608 c.6773G>T p.C2258F Substitution - Missense 4:84736312-84736312 - HT115 COSM4638315 c.9844G>A p.D3282N Substitution - Missense 4:84679222-84679222 - TCGA-AP-A059-01 COSM1058375 c.4349G>T p.R1450I Substitution - Missense 4:84780124-84780124 - TCGA-EE-A2GO-06 COSM3606689 c.5979C>T p.S1993S Substitution - coding silent 4:84743794-84743794 - HCC134 COSM3661240 c.4107A>G p.I1369M Substitution - Missense 4:84783030-84783030 - ATL001 COSM5709374 c.1283C>T p.S428L Substitution - Missense 4:84821392-84821392 - TCGA-KK-A6E4-01 COSM4876478 c.4416C>T p.I1472I Substitution - coding silent 4:84778605-84778605 - CRC-06T COSM5457143 c.7363G>A p.A2455T Substitution - Missense 4:84724504-84724504 - TCGA-CM-5348-01 COSM1431464 c.9329C>T p.S3110F Substitution - Missense 4:84690540-84690540 - ME009T COSM222924 c.4579C>T p.L1527F Substitution - Missense 4:84775078-84775078 - BN31 COSM1619168 c.7863A>G p.R2621R Substitution - coding silent 4:84716908-84716908 - TCGA-CU-A0YN-01 COSM420491 c.179G>A p.R60K Substitution - Missense 4:84860413-84860413 - S02323 COSM4387361 c.8539A>G p.I2847V Substitution - Missense 4:84702410-84702410 - TCGA-AA-A010-01 COSM286492 c.9121C>A p.L3041I Substitution - Missense 4:84691714-84691714 - PT53 COSM1694635 c.3289C>T p.P1097S Substitution - Missense 4:84794717-84794717 - TCGA-BR-4184-01 COSM4126438 c.4261G>A p.A1421T Substitution - Missense 4:84780212-84780212 - LC_C18 COSM1186609 c.4289C>G p.A1430G Substitution - Missense 4:84780184-84780184 - 1_RESISTANT COSM1720973 c.10112C>T p.P3371L Substitution - Missense 4:84678954-84678954 - TCGA-GN-A266-06 COSM3606691 c.5622C>T p.F1874F Substitution - coding silent 4:84753814-84753814 - DLD1 COSM4625355 c.2965G>T p.G989C Substitution - Missense 4:84796723-84796723 - TCGA-BR-8059-01 COSM4126460 c.102G>C p.E34D Substitution - Missense 4:84860490-84860490 - TCGA-25-1634-01 COSM78770 c.2994A>T p.E998D Substitution - Missense 4:84796694-84796694 - TCGA-D1-A16E-01 COSM1058359 c.6614C>T p.T2205I Substitution - Missense 4:84737327-84737327 - TCGA-BS-A0TE-01 COSM1058389 c.1247C>T p.A416V Substitution - Missense 4:84821428-84821428 - DLD1 COSM4625354 c.5994A>G p.T1998T Substitution - coding silent 4:84743779-84743779 - TCGA-BT-A20J-01 COSM420492 c.6202C>G p.L2068V Substitution - Missense 4:84741793-84741793 - TCGA-AX-A0J0-01 COSM1058372 c.4484C>A p.S1495* Substitution - Nonsense 4:84778537-84778537 - TCGA-FY-A3W9-01 COSM3373590 c.7620C>T p.Y2540Y Substitution - coding silent 4:84718556-84718556 - TCGA-BR-8487-01 COSM4126451 c.2345+2T>C p.? Unknown 4:84809885-84809885 - TCGA-AP-A051-01 COSM1058369 c.4997T>C p.L1666P Substitution - Missense 4:84766001-84766001 - TCGA-AR-A0TX-01 COSM448263 c.5670G>A p.M1890I Substitution - Missense 4:84753766-84753766 - SJMB027 COSM255937 c.6691G>A p.V2231M Substitution - Missense 4:84737250-84737250 - TCGA-AP-A0LM-01 COSM1058349 c.8027C>T p.T2676M Substitution - Missense 4:84713174-84713174 - 5_PRE-TREATMENT COSM1270363 c.9313_9314delTG p.W3105fs*23 Deletion - Frameshift 4:84690555-84690556 - Pat_70_B COSM1270363 c.9313_9314delTG p.W3105fs*23 Deletion - Frameshift 4:84690555-84690556 - TCGA-AP-A059-01 COSM1058342 c.9425T>G p.I3142S Substitution - Missense 4:84688204-84688204 - TCGA-AX-A05Z-01 COSM1058388 c.1925G>T p.R642I Substitution - Missense 4:84810307-84810307 - CHOL37 COSM1744736 c.4093C>T p.P1365S Substitution - Missense 4:84783044-84783044 - TCGA-FW-A3R5-06 COSM3918278 c.4660C>T p.R1554* Substitution - Nonsense 4:84774914-84774914 - 2492703 COSM5600848 c.5270C>T p.P1757L Substitution - Missense 4:84757080-84757080 - TCGA-FP-A4BE-01 COSM4126458 c.385A>G p.T129A Substitution - Missense 4:84841183-84841183 - PAPNNX COSM1431465 c.8941C>T p.R2981* Substitution - Nonsense 4:84692993-84692993 - TCGA-EE-A2MJ-06 COSM3606683 c.8501C>T p.S2834L Substitution - Missense 4:84702448-84702448 - HCC69 COSM1619169 c.5103C>G p.L1701L Substitution - coding silent 4:84765895-84765895 - TCGA-CH-5739-01 COSM3674235 c.5980C>A p.P1994T Substitution - Missense 4:84743793-84743793 - Ad2 COSM4440885 c.2150A>T p.D717V Substitution - Missense 4:84810082-84810082 - TCGA-BT-A42C-01 COSM4390200 c.5932C>G p.P1978A Substitution - Missense 4:84751524-84751524 - DLBCL-PatientB COSM220206 c.8277A>C p.Q2759H Substitution - Missense 4:84705452-84705452 - TCGA-HE-A5NK-01 COSM4908481 c.3205C>A p.P1069T Substitution - Missense 4:84794942-84794942 - TCGA-BR-8372-01 COSM4126456 c.928T>C p.Y310H Substitution - Missense 4:84829032-84829032 - TCGA-BR-8680-01 COSM4126452 c.2237G>T p.R746I Substitution - Missense 4:84809995-84809995 - TCGA-EJ-5518-01 COSM1131012 c.9763C>T p.P3255S Substitution - Missense 4:84682434-84682434 - PR-02-254 COSM248315 c.6241A>C p.R2081R Substitution - coding silent 4:84740410-84740410 - H1993 COSM1196820 c.7114G>A p.E2372K Substitution - Missense 4:84733489-84733489 - BZ18 COSM5758472 c.576G>C p.Q192H Substitution - Missense 4:84836929-84836929 - S01366 COSM316504 c.7221+1G>T p.? Unknown 4:84733381-84733381 - TCGA-BH-A0BW-01 COSM448267 c.1014G>C p.L338L Substitution - coding silent 4:84826924-84826924 - EWS834 COSM4585260 c.10056A>G p.S3352S Substitution - coding silent 4:84679010-84679010 - TCGA-BT-A42C-01 COSM4390497 c.5962C>G p.L1988V Substitution - Missense 4:84751494-84751494 - S00022 COSM316503 c.39G>T p.Q13H Substitution - Missense 4:84860553-84860553 - TCGA-AP-A051-01 COSM1058384 c.2283G>A p.T761T Substitution - coding silent 4:84809949-84809949 - TCGA-AX-A05Z-01 COSM1058378 c.3408C>T p.Y1136Y Substitution - coding silent 4:84794598-84794598 - TCGA-39-5031-01 COSM734424 c.5988G>A p.R1996R Substitution - coding silent 4:84743785-84743785 - TCGA-AP-A051-01 COSM1058344 c.8842C>A p.P2948T Substitution - Missense 4:84696029-84696029 - TCGA-AP-A0LM-01 COSM1058377 c.3943T>G p.S1315A Substitution - Missense 4:84786098-84786098 - TCGA-DA-A1I4-06 COSM3606700 c.2513C>G p.S838C Substitution - Missense 4:84803384-84803384 - TCGA-EE-A2MD-06 COSM3606706 c.1918C>T p.R640C Substitution - Missense 4:84810314-84810314 - TCGA-G4-6320-01 COSM3696762 c.9300G>A p.T3100T Substitution - coding silent 4:84690569-84690569 - S01366 COSM316504 c.7221+1G>T p.? Unknown 4:84733381-84733381 - TCGA-19-5955-01 COSM1131011 c.2834G>A p.R945H Substitution - Missense 4:84798097-84798097 - NPC15F COSM4996470 c.4706T>A p.V1569D Substitution - Missense 4:84774868-84774868 - CSCC-30-T COSM4508705 c.7852C>T p.H2618Y Substitution - Missense 4:84716919-84716919 - TCGA-37-4133-01 COSM734427 c.10356G>C p.V3452V Substitution - coding silent 4:84677300-84677300 - TCGA-EE-A2MG-06 COSM3606703 c.2085A>C p.A695A Substitution - coding silent 4:84810147-84810147 - C0076T COSM4165044 c.8062T>G p.L2688V Substitution - Missense 4:84709328-84709328 - YURAY COSM5401753 c.10101C>T p.P3367P Substitution - coding silent 4:84678965-84678965 - pfg068T COSM1058389 c.1247C>T p.A416V Substitution - Missense 4:84821428-84821428 - ESO-0129 COSM1270364 c.10090C>A p.L3364I Substitution - Missense 4:84678976-84678976 - TCGA-CG-5723-01 COSM4126419 c.8713G>A p.A2905T Substitution - Missense 4:84696158-84696158 - TCGA-BP-4973-01 COSM1495896 c.8241G>C p.K2747N Substitution - Missense 4:84705488-84705488 - LC_C8 COSM1186607 c.9952G>T p.A3318S Substitution - Missense 4:84679114-84679114 - TCGA-EB-A24D-01 COSM3606677 c.9347C>T p.T3116I Substitution - Missense 4:84690522-84690522 - SK-MEL-5 COSM1671123 c.238T>C p.F80L Substitution - Missense 4:84849968-84849968 - CSCC-35-T COSM4551844 c.541G>A p.E181K Substitution - Missense 4:84836964-84836964 - TCGA-ER-A19E-06 COSM3606686 c.6760C>T p.H2254Y Substitution - Missense 4:84736325-84736325 - S02249 COSM5680171 c.10345G>A p.D3449N Substitution - Missense 4:84677311-84677311 - TCGA-AP-A051-01 COSM1058366 c.5657C>T p.A1886V Substitution - Missense 4:84753779-84753779 - TCGA-AA-3715-01 COSM270549 c.7605G>T p.K2535N Substitution - Missense 4:84721409-84721409 - TCGA-28-5213-01 COSM3409588 c.8041G>A p.G2681R Substitution - Missense 4:84713160-84713160 - TCGA-AU-6004-01 COSM1431474 c.5899C>T p.R1967W Substitution - Missense 4:84751557-84751557 - C0082T COSM4165045 c.6723A>G p.E2241E Substitution - coding silent 4:84737218-84737218 - T3021 COSM4740825 c.461T>C p.V154A Substitution - Missense 4:84837044-84837044 - LP6007533-DNA_A01 COSM5032965 c.3189G>T p.L1063F Substitution - Missense 4:84794958-84794958 - PT15_1 COSM5897513 c.1210C>T p.L404F Substitution - Missense 4:84821465-84821465 - TCGA-D3-A5GO-06 COSM3606675 c.10153C>T p.R3385* Substitution - Nonsense 4:84678274-84678274 - DU-145 COSM1671122 c.7631G>T p.R2544L Substitution - Missense 4:84718545-84718545 - TCGA-B2-5633-01 COSM481632 c.436A>G p.T146A Substitution - Missense 4:84837069-84837069 - TCGA-AP-A059-01 COSM1058382 c.2537T>C p.I846T Substitution - Missense 4:84803360-84803360 - CHC892T COSM4797880 c.1502G>A p.R501K Substitution - Missense 4:84821173-84821173 - PT48 COSM1694635 c.3289C>T p.P1097S Substitution - Missense 4:84794717-84794717 - Pat_41_B COSM5866883 c.2429G>A p.R810K Substitution - Missense 4:84808334-84808334 - 587376 COSM1232522 c.2387C>A p.S796Y Substitution - Missense 4:84808376-84808376 - TCGA-CG-5728-01 COSM4126450 c.2708G>A p.R903Q Substitution - Missense 4:84801764-84801764 - TCGA-D1-A16J-01 COSM1058348 c.8430C>G p.F2810L Substitution - Missense 4:84704350-84704350 - SA236 COSM212824 c.7523A>C p.Q2508P Substitution - Missense 4:84721491-84721491 - C0009T COSM4165048 c.29G>T p.R10L Substitution - Missense 4:84860563-84860563 - 7285 COSM5615427 c.8293G>A p.A2765T Substitution - Missense 4:84705436-84705436 - TCGA-BH-A0HP-01 COSM448258 c.7778G>C p.R2593T Substitution - Missense 4:84716993-84716993 - TCGA-DD-A4NN-01 COSM4935266 c.2545C>T p.P849S Substitution - Missense 4:84803352-84803352 - TCGA-EE-A2MS-06 COSM3606682 c.8782G>A p.V2928I Substitution - Missense 4:84696089-84696089 - 587332 COSM1232518 c.4105A>G p.I1369V Substitution - Missense 4:84783032-84783032 - CHC097T COSM4790784 c.4118C>T p.A1373V Substitution - Missense 4:84783019-84783019 - T56 COSM1177670 c.6821C>T p.S2274F Substitution - Missense 4:84736264-84736264 - LUAD-RT-S01852 COSM384957 c.8108T>A p.I2703N Substitution - Missense 4:84709018-84709018 - TCGA-BS-A0UF-01 COSM1058343 c.9032C>A p.S3011Y Substitution - Missense 4:84692902-84692902 - 56516 COSM1582919 c.10474T>C p.S3492P Substitution - Missense 4:84672975-84672975 - CHC1731T COSM4792080 c.7985T>C p.L2662P Substitution - Missense 4:84713216-84713216 - HCC17T COSM1619166 c.8270G>T p.G2757V Substitution - Missense 4:84705459-84705459 - PD8618a COSM5795200 c.8243C>T p.T2748M Substitution - Missense 4:84705486-84705486 - TCGA-BH-A0DZ-01 COSM448269 c.305-1G>T p.? Unknown 4:84841264-84841264 - TCGA-FW-A3R5-06 COSM3918279 c.3634C>T p.L1212F Substitution - Missense 4:84789761-84789761 - Gp5D COSM2956416 c.1380T>C p.C460C Substitution - coding silent 4:84821295-84821295 - CSCC-38-T COSM4500053 c.556C>T p.L186F Substitution - Missense 4:84836949-84836949 - YUKAT COSM5401756 c.4121G>A p.G1374E Substitution - Missense 4:84783016-84783016 - CCK81 COSM2956429 c.554T>C p.L185P Substitution - Missense 4:84836951-84836951 - KM12 COSM2956265 c.8764C>T p.P2922S Substitution - Missense 4:84696107-84696107 - 8P3 COSM3734632 c.3202G>A p.A1068T Substitution - Missense 4:84794945-84794945 - T3236 COSM4740819 c.4385A>G p.K1462R Substitution - Missense 4:84778636-84778636 - S01366 COSM316505 c.9017_9018AC>CT p.D3006>? Complex 4:84692916-84692917 - CLL115 COSM1291979 c.795T>G p.V265V Substitution - coding silent 4:84829165-84829165 - B47 COSM1753863 c.5534G>A p.G1845E Substitution - Missense 4:84755291-84755291 - 447 COSM4435147 c.14A>T p.K5M Substitution - Missense 4:84860578-84860578 - C467 COSM4442183 c.643C>A p.L215I Substitution - Missense 4:84831539-84831539 - TCGA-HU-A4GN-01 COSM4126442 c.3901+1G>A p.? Unknown 4:84787481-84787481 - TCGA-BR-4362-01 COSM4126414 c.9970A>G p.T3324A Substitution - Missense 4:84679096-84679096 - CML038T COSM5802695 c.7295C>G p.A2432G Substitution - Missense 4:84724572-84724572 - TCGA-AY-6197-01 COSM1431484 c.2346T>C p.S782S Substitution - coding silent 4:84808417-84808417 - TCGA-36-2547-01 COSM1328364 c.4657C>G p.L1553V Substitution - Missense 4:84774917-84774917 - TCGA-BS-A0UF-01 COSM1058341 c.9518C>A p.S3173Y Substitution - Missense 4:84688111-84688111 - 345973 COSM3726442 c.64G>A p.A22T Substitution - Missense 4:84860528-84860528 - CHC326T COSM4806023 c.6461G>A p.G2154E Substitution - Missense 4:84740190-84740190 - TCGA-D1-A167-01 COSM1058362 c.6499C>T p.R2167C Substitution - Missense 4:84739085-84739085 - CSCC-55-T COSM4498549 c.5225C>T p.T1742M Substitution - Missense 4:84757125-84757125 - TCGA-28-5214-01 COSM3409587 c.9318G>C p.E3106D Substitution - Missense 4:84690551-84690551 - EV007-R5 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 - TCGA-D3-A3ML-06 COSM3918277 c.7149G>A p.K2383K Substitution - coding silent 4:84733454-84733454 - LAU618 COSM235568 c.529C>T p.L177L Substitution - coding silent 4:84836976-84836976 - TCGA-39-5022-01 COSM734423 c.5124C>T p.L1708L Substitution - coding silent 4:84765874-84765874 - TCGA-BR-4256-01 COSM4126422 c.7322A>G p.Y2441C Substitution - Missense 4:84724545-84724545 - TCGA-AC-A3W6-01 COSM3826352 c.4314C>G p.V1438V Substitution - coding silent 4:84780159-84780159 - TCGA-EE-A29L-06 COSM3606678 c.9212C>T p.T3071I Substitution - Missense 4:84690657-84690657 - TCGA-66-2782-01 COSM448258 c.7778G>C p.R2593T Substitution - Missense 4:84716993-84716993 - Pat_41_B COSM5866874 c.10363G>A p.E3455K Substitution - Missense 4:84677293-84677293 - PT08_2 COSM5893022 c.9512C>T p.P3171L Substitution - Missense 4:84688117-84688117 - PT17_1 COSM5898852 c.4063-3C>T p.? Unknown 4:84783077-84783077 - C0037T COSM4422544 c.8818G>A p.V2940M Substitution - Missense 4:84696053-84696053 - TCGA-FJ-A3Z7-01 COSM1431487 c.1128C>T p.H376H Substitution - coding silent 4:84821547-84821547 - TCGA-HU-A4GQ-01 COSM4126433 c.5332G>A p.A1778T Substitution - Missense 4:84757018-84757018 - CHC892T COSM4795194 c.6118G>A p.V2040I Substitution - Missense 4:84741877-84741877 - I2L-P24Tb-Tumor-Organoid COSM5356065 c.7098C>T p.L2366L Substitution - coding silent 4:84733505-84733505 - 8049749 COSM3393028 c.5735A>T p.E1912V Substitution - Missense 4:84753701-84753701 - LUAD-RT-S01487 COSM377941 c.1014G>T p.L338L Substitution - coding silent 4:84826924-84826924 - YUTUCO COSM3606695 c.4732C>T p.P1578S Substitution - Missense 4:84774842-84774842 - PD4937a COSM165552 c.561G>C p.Q187H Substitution - Missense 4:84836944-84836944 - CSCC-62-T COSM4557795 c.7417G>A p.E2473K Substitution - Missense 4:84724450-84724450 - LUAD-E00918 COSM365279 c.5459G>T p.G1820V Substitution - Missense 4:84755366-84755366 - HCC89 COSM1619170 c.4849+6T>C p.? Unknown 4:84772829-84772829 - CLL143 COSM1291978 c.7337C>T p.S2446F Substitution - Missense 4:84724530-84724530 - D28 COSM5546120 c.9606C>T p.I3202I Substitution - coding silent 4:84684063-84684063 - TCGA-FD-A3N5-01 COSM1310337 c.1985A>G p.E662G Substitution - Missense 4:84810247-84810247 - SH-3000 COSM2956362 c.3918C>T p.S1306S Substitution - coding silent 4:84786123-84786123 - TCGA-HU-A4H4-01 COSM4126423 c.7175A>G p.N2392S Substitution - Missense 4:84733428-84733428 - HCC89 COSM1619167 c.8059A>G p.T2687A Substitution - Missense 4:84709331-84709331 - HCC69T COSM1619169 c.5103C>G p.L1701L Substitution - coding silent 4:84765895-84765895 - TCGA-BR-6452-01 COSM4126424 c.7154T>C p.V2385A Substitution - Missense 4:84733449-84733449 - TCGA-EE-A3JA-06 COSM3606710 c.1149C>T p.A383A Substitution - coding silent 4:84821526-84821526 - TCGA-A3-3362-01 COSM481626 c.6782G>T p.R2261L Substitution - Missense 4:84736303-84736303 - AOCS-094-6-X COSM4138532 c.6861A>G p.G2287G Substitution - coding silent 4:84736224-84736224 - C135 COSM4618440 c.9076G>A p.V3026I Substitution - Missense 4:84691759-84691759 - S01366 COSM316505 c.9017_9018AC>CT p.D3006>? Complex 4:84692916-84692917 - TCGA-B5-A0K9-01 COSM1058358 c.6726A>G p.E2242E Substitution - coding silent 4:84737215-84737215 - TCGA-RP-A694-06 COSM4893711 c.7455T>A p.P2485P Substitution - coding silent 4:84721559-84721559 - 2492702 COSM5600848 c.5270C>T p.P1757L Substitution - Missense 4:84757080-84757080 - TCGA-AD-6964-01 COSM1431476 c.5525delT p.L1842fs*10 Deletion - Frameshift 4:84755300-84755300 - CSCC-11-T COSM4447469 c.8901+3A>T p.? Unknown 4:84695967-84695967 - sysucc-274T COSM5476540 c.2407A>G p.T803A Substitution - Missense 4:84808356-84808356 - TCGA-39-5036-01 COSM734415 c.304+2T>C p.? Unknown 4:84849900-84849900 - TCGA-E2-A573-01 COSM3826350 c.9747G>T p.L3249F Substitution - Missense 4:84682450-84682450 - KM12 COSM2956235 c.10122G>A p.V3374V Substitution - coding silent 4:84678944-84678944 - LUAD-S00484 COSM343055 c.9687G>A p.Q3229Q Substitution - coding silent 4:84683982-84683982 - TCGA-AC-A23H-01 COSM448258 c.7778G>C p.R2593T Substitution - Missense 4:84716993-84716993 - SNU-175 COSM2956339 c.5525_5526insT p.L1842fs*52 Insertion - Frameshift 4:84755299-84755300 - SC_9072 COSM1058384 c.2283G>A p.T761T Substitution - coding silent 4:84809949-84809949 - sysucc-1247T COSM5764650 c.550G>A p.G184R Substitution - Missense 4:84836955-84836955 - TCGA-A2-A0YH-01 COSM448257 c.8811G>A p.E2937E Substitution - coding silent 4:84696060-84696060 - S00022 COSM316503 c.39G>T p.Q13H Substitution - Missense 4:84860553-84860553 - SNUH_G26_S1 COSM3606676 c.10123C>T p.R3375W Substitution - Missense 4:84678943-84678943 - TCGA-AX-A063-01 COSM1058340 c.9636C>T p.S3212S Substitution - coding silent 4:84684033-84684033 - YURUS COSM1694632 c.9148T>A p.F3050I Substitution - Missense 4:84691687-84691687 - C0031T COSM4422451 c.6915G>T p.Q2305H Substitution - Missense 4:84736170-84736170 - TCGA-AP-A059-01 COSM1058363 c.6260C>T p.S2087L Substitution - Missense 4:84740391-84740391 - 2492701 COSM5600848 c.5270C>T p.P1757L Substitution - Missense 4:84757080-84757080 - TCGA-AD-6964-01 COSM1431475 c.5751T>C p.L1917L Substitution - coding silent 4:84751705-84751705 - HCC17 COSM1619166 c.8270G>T p.G2757V Substitution - Missense 4:84705459-84705459 - T3724 COSM1431476 c.5525delT p.L1842fs*10 Deletion - Frameshift 4:84755300-84755300 - TCGA-FU-A3HZ-01 COSM4839991 c.8573T>C p.F2858S Substitution - Missense 4:84702376-84702376 - S02354 COSM5695637 c.4365G>A p.Q1455Q Substitution - coding silent 4:84780108-84780108 - CSCC-30-T COSM4488202 c.3290C>T p.P1097L Substitution - Missense 4:84794716-84794716 - TCGA-CM-6166-01 COSM1058361 c.6577C>T p.R2193C Substitution - Missense 4:84737364-84737364 - YURAY COSM2956408 c.1702C>T p.R568* Substitution - Nonsense 4:84817577-84817577 - EV007-R4 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 - TCGA-AX-A060-01 COSM1058371 c.4661G>A p.R1554Q Substitution - Missense 4:84774913-84774913 - T3152 COSM4740823 c.1040T>C p.V347A Substitution - Missense 4:84826898-84826898 - DLBCL-PatientL COSM220442 c.5084T>A p.L1695Q Substitution - Missense 4:84765914-84765914 - TCGA-EJ-A46D-01 COSM3783831 c.446T>C p.V149A Substitution - Missense 4:84837059-84837059 - HDC101 COSM4636111 c.8709G>A p.V2903V Substitution - coding silent 4:84696162-84696162 - CRC-19T COSM5481905 c.8663G>A p.R2888Q Substitution - Missense 4:84696757-84696757 - TCGA-AH-6544-01 COSM1567222 c.5204G>A p.R1735K Substitution - Missense 4:84757146-84757146 - CSCC-27-T COSM4512022 c.8892C>T p.I2964I Substitution - coding silent 4:84695979-84695979 - TCGA-FW-A3R5-06 COSM3918281 c.3283C>T p.P1095S Substitution - Missense 4:84794723-84794723 - TCGA-EE-A3J5-06 COSM3606701 c.2483C>T p.A828V Substitution - Missense 4:84803414-84803414 - LIM2405 COSM4613633 c.8913_8914insA p.P2972fs*27 Insertion - Frameshift 4:84693020-84693021 - TCGA-CK-4947-01 COSM1431491 c.32C>T p.P11L Substitution - Missense 4:84860560-84860560 - TCGA-FS-A1ZZ-06 COSM3606688 c.6088C>T p.L2030L Substitution - coding silent 4:84741907-84741907 - CSCC-49-T COSM4472203 c.1767C>T p.A589A Substitution - coding silent 4:84817512-84817512 - TCGA-AD-5900-01 COSM1431486 c.1814A>T p.D605V Substitution - Missense 4:84817465-84817465 - CCK81 COSM2956367 c.3745A>G p.I1249V Substitution - Missense 4:84787638-84787638 - CRC-36T COSM5460896 c.6291G>T p.R2097S Substitution - Missense 4:84740360-84740360 - TCGA-BT-A3PK-01 COSM3776045 c.5358T>A p.S1786R Substitution - Missense 4:84756992-84756992 - TCGA-BR-6452-01 COSM4126453 c.2065T>C p.F689L Substitution - Missense 4:84810167-84810167 - TCGA-RP-A694-06 COSM4893971 c.7457C>T p.P2486L Substitution - Missense 4:84721557-84721557 - ESCC_BICR_042T COSM5443822 c.1398C>G p.V466V Substitution - coding silent 4:84821277-84821277 - TCGA-B5-A0JZ-01 COSM1058346 c.8768C>T p.A2923V Substitution - Missense 4:84696103-84696103 - T3535 COSM4740812 c.8233A>G p.N2745D Substitution - Missense 4:84705496-84705496 - HDC82 COSM4636751 c.4587G>A p.E1529E Substitution - coding silent 4:84775070-84775070 - HCC172T COSM3661241 c.3712A>T p.N1238Y Substitution - Missense 4:84787671-84787671 - QC2-30-T2 COSM1058337 c.9935G>A p.R3312Q Substitution - Missense 4:84679131-84679131 - 16461 COSM5615428 c.3803C>G p.T1268R Substitution - Missense 4:84787580-84787580 - 587376 COSM1232521 c.3547C>T p.R1183* Substitution - Nonsense 4:84789848-84789848 - 587376 COSM1232520 c.9145A>G p.T3049A Substitution - Missense 4:84691690-84691690 - pfg181T COSM4758389 c.2792C>A p.A931D Substitution - Missense 4:84801680-84801680 - TCGA-EE-A29G-06 COSM3606705 c.1943T>C p.V648A Substitution - Missense 4:84810289-84810289 - TCGA-E2-A10B-01 COSM448261 c.6891_6894delTAAT p.K2299fs*22 Deletion - Frameshift 4:84736191-84736194 - TCGA-D1-A16O-01 COSM1058337 c.9935G>A p.R3312Q Substitution - Missense 4:84679131-84679131 - ESO-081 COSM1243733 c.6302A>G p.Y2101C Substitution - Missense 4:84740349-84740349 - J52_T COSM3946605 c.7221+3G>A p.? Unknown 4:84733379-84733379 - ATL089 COSM5709372 c.9692T>C p.V3231A Substitution - Missense 4:84683977-84683977 - BD72T COSM1431476 c.5525delT p.L1842fs*10 Deletion - Frameshift 4:84755300-84755300 - TCGA-EK-A2PL-01 COSM4838400 c.4004C>T p.T1335I Substitution - Missense 4:84786037-84786037 - Pat_41_B COSM5866880 c.5000G>A p.G1667D Substitution - Missense 4:84765998-84765998 - CSCC-7-T COSM4492863 c.404C>T p.S135F Substitution - Missense 4:84841164-84841164 - 1_PRE-TREATMENT COSM1720973 c.10112C>T p.P3371L Substitution - Missense 4:84678954-84678954 - RH30SJ_ COSM2956310 c.6550A>G p.S2184G Substitution - Missense 4:84739034-84739034 - TCGA-EB-A431-01 COSM3606709 c.1255T>C p.F419L Substitution - Missense 4:84821420-84821420 - TCGA-AN-A0XW-01 COSM448268 c.561G>A p.Q187Q Substitution - coding silent 4:84836944-84836944 - TCGA-13-0916-01 COSM120018 c.8491G>T p.A2831S Substitution - Missense 4:84702458-84702458 - C91 COSM4444978 c.10486C>T p.R3496C Substitution - Missense 4:84672963-84672963 - 011T COSM1727698 c.1328A>T p.K443I Substitution - Missense 4:84821347-84821347 - TCGA-AX-A0J1-01 COSM1058387 c.2089C>T p.R697C Substitution - Missense 4:84810143-84810143 - TCGA-FU-A3HZ-01 COSM734429 c.10571G>A p.R3524Q Substitution - Missense 4:84672878-84672878 - TCGA-EE-A2MR-06 COSM3606681 c.8797C>T p.H2933Y Substitution - Missense 4:84696074-84696074 - TCGA-BR-A4J2-01 COSM4126447 c.3294C>T p.S1098S Substitution - coding silent 4:84794712-84794712 - TCGA-22-5492-01 COSM734425 c.7837G>T p.D2613Y Substitution - Missense 4:84716934-84716934 - TCGA-CZ-4866-01 COSM481629 c.2645T>C p.L882S Substitution - Missense 4:84801827-84801827 - DN1401F COSM5961181 c.9232G>C p.E3078Q Substitution - Missense 4:84690637-84690637 - HCC89T COSM1619170 c.4849+6T>C p.? Unknown 4:84772829-84772829 - TCGA-AP-A056-01 COSM1058355 c.7041C>T p.I2347I Substitution - coding silent 4:84733562-84733562 - S02248 COSM5679737 c.4348A>G p.R1450G Substitution - Missense 4:84780125-84780125 - SNU-C2B COSM2956433 c.350G>A p.S117N Substitution - Missense 4:84841218-84841218 - ESO-120 COSM1270366 c.8612G>C p.G2871A Substitution - Missense 4:84696808-84696808 - TCGA-FW-A3R5-06 COSM3918280 c.3505G>A p.E1169K Substitution - Missense 4:84789890-84789890 - SC_9038 COSM5553181 c.8106A>G p.E2702E Substitution - coding silent 4:84709020-84709020 - RK288_C01 COSM4625356 c.2935A>G p.S979G Substitution - Missense 4:84797996-84797996 - Pat_46_B COSM5866882 c.2762C>T p.P921L Substitution - Missense 4:84801710-84801710 - Pat_46_A COSM5866882 c.2762C>T p.P921L Substitution - Missense 4:84801710-84801710 - TCGA-AA-3492-01 COSM1431489 c.567T>C p.V189V Substitution - coding silent 4:84836938-84836938 - ESO-0590 COSM1270363 c.9313_9314delTG p.W3105fs*23 Deletion - Frameshift 4:84690555-84690556 - S02246 COSM5679112 c.10188G>T p.L3396L Substitution - coding silent 4:84678239-84678239 - TCGA-A8-A09G-01 COSM448264 c.5037_5038insA p.H1680fs*18 Insertion - Frameshift 4:84765960-84765961 - TCGA-BR-4361-01 COSM4126416 c.9338A>T p.K3113M Substitution - Missense 4:84690531-84690531 - CHC892T COSM4797880 c.1502G>A p.R501K Substitution - Missense 4:84821173-84821173 - TCGA-EE-A3JI-06 COSM3606679 c.9075C>T p.I3025I Substitution - coding silent 4:84691760-84691760 - ESCC_152 COSM5645482 c.9724C>T p.R3242W Substitution - Missense 4:84683945-84683945 - NCI-H835 COSM2956374 c.3467A>G p.E1156G Substitution - Missense 4:84794539-84794539 - D28 COSM5546119 c.9392C>T p.T3131I Substitution - Missense 4:84688237-84688237 - HX14T COSM1619172 c.1018A>G p.T340A Substitution - Missense 4:84826920-84826920 - TCGA-AA-A010-01 COSM286494 c.7965T>A p.F2655L Substitution - Missense 4:84713236-84713236 - DLD1 COSM4625357 c.1104A>G p.V368V Substitution - coding silent 4:84826834-84826834 - S0045 COSM2956251 c.9349G>A p.V3117I Substitution - Missense 4:84690520-84690520 - SJMB118 COSM255319 c.929A>G p.Y310C Substitution - Missense 4:84829031-84829031 - pfg122T COSM4758390 c.572T>C p.V191A Substitution - Missense 4:84836933-84836933 - PT55 COSM5941931 c.2009A>G p.K670R Substitution - Missense 4:84810223-84810223 - H1672 COSM316502 c.2436A>T p.A812A Substitution - coding silent 4:84803461-84803461 - 9-RS COSM1731898 c.1858G>C p.E620Q Substitution - Missense 4:84817421-84817421 - TCGA-BR-6452-01 COSM4126434 c.5078T>C p.V1693A Substitution - Missense 4:84765920-84765920 - Ad4 COSM4441040 c.5843G>A p.G1948D Substitution - Missense 4:84751613-84751613 - ESCC_44 COSM5630145 c.5663T>C p.M1888T Substitution - Missense 4:84753773-84753773 - LUAD-B00416 COSM331421 c.6176G>A p.G2059D Substitution - Missense 4:84741819-84741819 - HCC89T COSM1619167 c.8059A>G p.T2687A Substitution - Missense 4:84709331-84709331 - MO_1263 COSM5564941 c.6152G>A p.R2051H Substitution - Missense 4:84741843-84741843 - EV007-R2 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 - TCGA-D1-A17Q-01 COSM1058388 c.1925G>T p.R642I Substitution - Missense 4:84810307-84810307 - PT48 COSM2956391 c.2398C>T p.P800S Substitution - Missense 4:84808365-84808365 - TCGA-C5-A1BQ-01 COSM4841669 c.2261C>G p.S754* Substitution - Nonsense 4:84809971-84809971 - TCGA-DY-A1DD-01 COSM1567223 c.8326G>A p.D2776N Substitution - Missense 4:84705403-84705403 - TCGA-AR-A24R-01 COSM5212275 c.2046delT p.F682fs*11 Deletion - Frameshift 4:84810186-84810186 - 0062_CRUK_PC_0062_T1_DNA COSM5421214 c.4504C>G p.L1502V Substitution - Missense 4:84778517-84778517 - TCGA-DK-A3IU-01 COSM3776044 c.7842C>G p.I2614M Substitution - Missense 4:84716929-84716929 - TCGA-BR-8591-01 COSM4126413 c.10383A>G p.S3461S Substitution - coding silent 4:84677273-84677273 - Pat_28_B COSM5866878 c.5389C>T p.P1797S Substitution - Missense 4:84756961-84756961 - TCGA-29-1707-01 COSM1328365 c.10415G>T p.R3472I Substitution - Missense 4:84677241-84677241 - TCGA-HU-A4H3-01 COSM4126444 c.3724G>A p.V1242M Substitution - Missense 4:84787659-84787659 - TCGA-AO-A0JL-01 COSM448260 c.7227G>A p.E2409E Substitution - coding silent 4:84726906-84726906 - TCGA-CJ-4912-01 COSM481627 c.6024C>T p.Y2008Y Substitution - coding silent 4:84743749-84743749 - TCGA-B5-A0K1-01 COSM1058338 c.9897C>T p.D3299D Substitution - coding silent 4:84679169-84679169 - T3262 COSM2956384 c.2763G>A p.P921P Substitution - coding silent 4:84801709-84801709 - SW403 COSM4343452 c.2957A>T p.E986V Substitution - Missense 4:84796731-84796731 - SJMB025 COSM255913 c.4037T>A p.L1346* Substitution - Nonsense 4:84786004-84786004 - LUAD-NYU315 COSM373661 c.8589T>C p.F2863F Substitution - coding silent 4:84702360-84702360 - YUMOBER COSM5401754 c.9438C>G p.S3146S Substitution - coding silent 4:84688191-84688191 - TCGA-GM-A2DK-01 COSM3826354 c.1290T>C p.F430F Substitution - coding silent 4:84821385-84821385 - PT08_1 COSM5893022 c.9512C>T p.P3171L Substitution - Missense 4:84688117-84688117 - LUAD-E00934 COSM393685 c.7222-2A>C p.? Unknown 4:84726913-84726913 - YUTUCO COSM3606700 c.2513C>G p.S838C Substitution - Missense 4:84803384-84803384 - TCGA-FW-A3I3-06 COSM3606684 c.7682A>G p.H2561R Substitution - Missense 4:84718494-84718494 - 9-RS COSM1731899 c.1850C>A p.P617Q Substitution - Missense 4:84817429-84817429 - CSCC-15-T COSM4126425 c.6799C>T p.P2267S Substitution - Missense 4:84736286-84736286 - GHE0536 COSM5713546 c.1592-3_1592-2insT p.? Unknown 4:84820188-84820189 - sysucc-1370T COSM5471923 c.9951C>T p.R3317R Substitution - coding silent 4:84679115-84679115 - HN_63058 COSM130190 c.4015A>G p.I1339V Substitution - Missense 4:84786026-84786026 - TCGA-D3-A5GU-06 COSM3606698 c.3938C>T p.P1313L Substitution - Missense 4:84786103-84786103 - LS180 COSM2956402 c.1951T>C p.F651L Substitution - Missense 4:84810281-84810281 - TCGA-GV-A40G-01 COSM3776043 c.7962-1G>A p.? Unknown 4:84713240-84713240 - HCC097T COSM5816479 c.9320T>A p.M3107K Substitution - Missense 4:84690549-84690549 - OSCC-GB_01090111 COSM4886415 c.8707G>T p.V2903L Substitution - Missense 4:84696164-84696164 - PT48 COSM2956390 c.2399C>T p.P800L Substitution - Missense 4:84808364-84808364 - MO_1249 COSM5555310 c.10149G>C p.G3383G Substitution - coding silent 4:84678278-84678278 - TCGA-D7-8573-01 COSM4126437 c.4269T>C p.D1423D Substitution - coding silent 4:84780204-84780204 - LAU108 COSM233757 c.7901G>A p.G2634E Substitution - Missense 4:84715358-84715358 - TCGA-BR-8368-01 COSM4126439 c.4018C>T p.R1340W Substitution - Missense 4:84786023-84786023 - TCGA-EJ-7125-01 COSM3674233 c.9595G>T p.G3199W Substitution - Missense 4:84684074-84684074 - HCC152T COSM5807176 c.1809C>T p.D603D Substitution - coding silent 4:84817470-84817470 - TCGA-D1-A17Q-01 COSM1058376 c.3960G>T p.E1320D Substitution - Missense 4:84786081-84786081 - SW620 COSM4616051 c.7032_7034delGTG p.W2344delW Deletion - In frame 4:84733569-84733571 - TCGA-EE-A3AA-06 COSM286495 c.3541C>T p.R1181C Substitution - Missense 4:84789854-84789854 - T263 COSM4740814 c.6803C>G p.T2268S Substitution - Missense 4:84736282-84736282 - TCGA-BR-4184-01 COSM4126446 c.3379C>T p.R1127C Substitution - Missense 4:84794627-84794627 - C0028T COSM4165047 c.324A>T p.I108I Substitution - coding silent 4:84841244-84841244 - YUHAMA COSM5401757 c.3554G>T p.G1185V Substitution - Missense 4:84789841-84789841 - HCC172 COSM3661241 c.3712A>T p.N1238Y Substitution - Missense 4:84787671-84787671 - TCGA-AA-3663-01 COSM1431473 c.6314G>A p.R2105Q Substitution - Missense 4:84740337-84740337 - LOVO COSM2956427 c.731G>A p.R244H Substitution - Missense 4:84831451-84831451 - Pat_27_B COSM1270363 c.9313_9314delTG p.W3105fs*23 Deletion - Frameshift 4:84690555-84690556 - TCGA-AA-A00N-01 COSM278115 c.3548G>A p.R1183Q Substitution - Missense 4:84789847-84789847 - LUAD_E00945 COSM389926 c.6691G>T p.V2231L Substitution - Missense 4:84737250-84737250 - TCGA-EE-A29G-06 COSM3606693 c.5471C>T p.S1824F Substitution - Missense 4:84755354-84755354 - ESOSCC155T COSM1173070 c.6784G>A p.G2262R Substitution - Missense 4:84736301-84736301 - HCT15 COSM2956241 c.9792A>G p.E3264E Substitution - coding silent 4:84682405-84682405 - TCGA-CG-5721-01 COSM4126435 c.4794G>A p.A1598A Substitution - coding silent 4:84772890-84772890 - sysucc-2026T COSM5461045 c.3901+8A>C p.? Unknown 4:84787474-84787474 - YUKAT COSM5401758 c.533C>T p.P178L Substitution - Missense 4:84836972-84836972 - TCGA-AA-A010-01 COSM286496 c.840C>T p.V280V Substitution - coding silent 4:84829120-84829120 - TCGA-CG-5721-01 COSM4126454 c.1963A>G p.T655A Substitution - Missense 4:84810269-84810269 - TCGA-AX-A0J1-01 COSM1058360 c.6578G>A p.R2193H Substitution - Missense 4:84737363-84737363 - TCGA-AX-A05Z-01 COSM1058364 c.6144C>A p.F2048L Substitution - Missense 4:84741851-84741851 - sysucc-657T COSM5459943 c.318G>T p.R106R Substitution - coding silent 4:84841250-84841250 - TCGA-B8-4622-01 COSM481631 c.1136G>C p.R379T Substitution - Missense 4:84821539-84821539 - TCGA-BR-4361-01 COSM4126426 c.6711G>A p.R2237R Substitution - coding silent 4:84737230-84737230 - LOVO COSM2956230 c.10298G>A p.R3433Q Substitution - Missense 4:84677358-84677358 - KPOPBR-49-T COSM5963438 c.2554A>C p.M852L Substitution - Missense 4:84803343-84803343 - SH-1537 COSM5018562 c.7628C>T p.A2543V Substitution - Missense 4:84718548-84718548 - T1154 COSM4740820 c.4176A>T p.G1392G Substitution - coding silent 4:84780297-84780297 - BCM375T COSM4799242 c.3441C>A p.D1147E Substitution - Missense 4:84794565-84794565 - CHC097T COSM4790784 c.4118C>T p.A1373V Substitution - Missense 4:84783019-84783019 - 8016470 COSM3393029 c.3238G>C p.D1080H Substitution - Missense 4:84794909-84794909 - 448 COSM4435279 c.6916G>T p.E2306* Substitution - Nonsense 4:84735120-84735120 - YUOMEGA COSM5401755 c.9369A>G p.L3123L Substitution - coding silent 4:84688260-84688260 - CHC1731T COSM4792080 c.7985T>C p.L2662P Substitution - Missense 4:84713216-84713216 - TCGA-CK-5916-01 COSM1431490 c.63C>T p.N21N Substitution - coding silent 4:84860529-84860529 - TCGA-D3-A51T-06 COSM3606697 c.4318A>T p.S1440C Substitution - Missense 4:84780155-84780155 - T20 COSM4740826 c.307G>T p.A103S Substitution - Missense 4:84841261-84841261 - ccRCC-9 COSM1664981 c.3897G>A p.M1299I Substitution - Missense 4:84787486-84787486 - TCGA-CM-5864-01 COSM1431469 c.7472G>T p.R2491L Substitution - Missense 4:84721542-84721542 - TCGA-BR-6452-01 COSM4126427 c.6623T>A p.I2208K Substitution - Missense 4:84737318-84737318 - TCGA-G4-6302-01 COSM3696763 c.2094T>C p.Y698Y Substitution - coding silent 4:84810138-84810138 - 2492700 COSM5600848 c.5270C>T p.P1757L Substitution - Missense 4:84757080-84757080 - TCGA-F4-6570-01 COSM1431472 c.6465-1G>A p.? Unknown 4:84739120-84739120 - SNUH_G10_S1 COSM4003176 c.336A>G p.L112L Substitution - coding silent 4:84841232-84841232 - RK035_C01 COSM1633822 c.3504A>G p.E1168E Substitution - coding silent 4:84789891-84789891 - TCGA-A5-A0GP-01 COSM1058385 c.2159G>A p.R720Q Substitution - Missense 4:84810073-84810073 - MO_1249 COSM5573119 c.10148-1G>A p.? Unknown 4:84678280-84678280 - TCGA-P4-A5ED-01 COSM3993824 c.5568A>G p.Q1856Q Substitution - coding silent 4:84753868-84753868 - TCGA-FU-A3HZ-01 COSM175297 c.4605G>T p.K1535N Substitution - Missense 4:84774969-84774969 - LUAD-F00170 COSM366835 c.6375A>C p.V2125V Substitution - coding silent 4:84740276-84740276 - 587346 COSM1232516 c.3007C>T p.R1003W Substitution - Missense 4:84796681-84796681 - LOVO COSM2956304 c.7006G>A p.A2336T Substitution - Missense 4:84733597-84733597 - TCGA-G9-6351-01 COSM3674234 c.7910G>T p.R2637L Substitution - Missense 4:84715349-84715349 - ATL074 COSM5709373 c.9081T>G p.C3027W Substitution - Missense 4:84691754-84691754 - ESCC_42 COSM5629741 c.6646G>C p.E2216Q Substitution - Missense 4:84737295-84737295 - TCGA-A5-A0VP-01 COSM1058356 c.6995G>A p.R2332H Substitution - Missense 4:84733608-84733608 - EV007-R9 COSM4410943 c.9576C>G p.I3192M Substitution - Missense 4:84684093-84684093 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.480116 4q21.23

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.6993+513T>G 4 85655683 CLL A C Missense p.C3218G c.9652T>G 4 85605170 LUAD A C Missense p.D991E c.2973T>G 4 85717868 LUSC A C Missense p.H997Q c.2991T>G 4 85717850 CM A C Nonsense p.Y1162* c.3486T>G 4 85715673 CM A C Synonymous p.V265V c.795T>G 4 85750318 CLL A - Frameshift p.L1060Cfs*41 c.3179delT 4 85716121 STAD A - Frameshift p.Y2852Ifs*14 c.8554delT 4 85623548 LUAD A G IntronicSNV . c.1-96116T>C 4 85877860 CLL A G Missense p.F111L c.331T>C 4 85762390 STAD A G Missense p.L882S c.2645T>C 4 85722980 RCCC A G Missense p.S97P c.289T>C 4 85771070 LUAD A G Missense p.V149A c.446T>C 4 85758212 PRAD A G Missense p.V648A c.1943T>C 4 85731442 CM A G SpliceDonorSNV . c.304+2T>C 4 85771053 LUSC A G Synonymous p.H1487H c.4461T>C 4 85699713 UCEC A - IntronicDeletion . c.7222-34delT 4 85648098 STAD A T Missense p.F1753L c.5259T>A 4 85678244 UCEC A T Missense p.I2141N c.6422T>A 4 85661382 HNSC A T Missense p.L3076M c.9226T>A 4 85611796 ESCA A T Missense p.M268K c.803T>A 4 85750310 STAD A T Missense p.S1786R c.5358T>A 4 85678145 BLCA A T Missense p.S2514T c.7540T>A 4 85642627 RCCC A T Synonymous p.S861S c.2583T>A 4 85724467 RCCC ATTA - Frameshift p.K2299Tfs*22 c.6891_6894delTAAT 4 85657344 BRCA CAAT - Frameshift p.I1151Ffs*48 c.3451_3454delATTG 4 85715705 LGG CA - Frameshift p.W3105Gfs*23 c.9313_9314delTG 4 85611708 BLCA C A Missense p.A1412S c.4234G>T 4 85701392 HNSC C A Missense p.A1430S c.4288G>T 4 85701338 LUAD C A Missense p.A2831S c.8491G>T 4 85623611 OV C A Missense p.D1423Y c.4267G>T 4 85701359 HNSC C A Missense p.D2613Y c.7837G>T 4 85638087 LUSC C A Missense p.G2553W c.7657G>T 4 85639672 LUAD C A Missense p.G650V c.1949G>T 4 85731436 CM C A Missense p.M144I c.432G>T 4 85758226 CM C A Missense p.Q13H c.39G>T 4 85781706 SCLC C A Missense p.R2167L c.6500G>T 4 85660237 LUAD C A Missense p.S2607I c.7820G>T 4 85638104 STAD C A Missense p.V1331L c.3991G>T 4 85707203 LUAD C A Nonsense p.E205* c.613G>T 4 85752722 LUAD C A Nonsense p.E2255* c.6763G>T 4 85657475 HNSC C A Nonsense p.G309* c.925G>T 4 85750188 LUAD C A SpliceAcceptorSNV . c.2430-1G>T 4 85724621 LUAD C A SpliceAcceptorSNV . c.6074-1G>T 4 85663075 STAD C A SpliceDonorSNV . c.1887+1G>T 4 85738544 LUAD C A SpliceDonorSNV . c.7221+1G>T 4 85654534 SCLC C A SpliceDonorSNV . c.8596+1G>T 4 85623505 LUAD C A Synonymous p.G1739G c.5217G>T 4 85678286 LUAD C A Synonymous p.T2676T c.8028G>T 4 85634326 BLCA C A Synonymous p.V1331V c.3993G>T 4 85707201 LUAD CC AG MultiAAMissense p.L1063_A1064delinsFS c.3189_3190delinsCT 4 85716110 LUAD CC TT Missense p.E2163K c.6486_6487delinsAA 4 85660250 CM CC TT Missense p.G1233N c.3697_3698delinsAA 4 85708838 CM C G Missense p.A934P c.2800G>C 4 85722825 SCLC C G Missense p.E1273Q c.3817G>C 4 85708719 COREAD C G Missense p.E1991Q c.5971G>C 4 85672638 BLCA C G Missense p.E3106D c.9318G>C 4 85611704 GBM C G Missense p.G2871A c.8612G>C 4 85617961 ESCA C G Missense p.Q187H c.561G>C 4 85758097 BRCA C G Missense p.R2381T c.7142G>C 4 85654614 HNSC C G Missense p.R2593T c.7778G>C 4 85638146 BRCA C G Missense p.R2593T c.7778G>C 4 85638146 LUSC C G Missense p.R379T c.1136G>C 4 85742692 RCCC C G Missense p.V1401L c.4201G>C 4 85701425 LUAD C G Missense p.W1105S c.3314G>C 4 85715845 CM C G Synonymous p.L338L c.1014G>C 4 85748077 BRCA C G Synonymous p.V3452V c.10356G>C 4 85598453 LUSC C G Synonymous p.V676V c.2028G>C 4 85731357 RCCC C T Missense p.A2765T c.8293G>A 4 85626589 NSCLC C T Missense p.A3318T c.9952G>A 4 85600267 LGG C T Missense p.C36Y c.107G>A 4 85781638 LUAD C T Missense p.E2500K c.7498G>A 4 85642669 BRCA C T Missense p.E3493K c.10477G>A 4 85594125 CM C T Missense p.G2681R c.8041G>A 4 85634313 GBM C T Missense p.H376Y c.1126C>T 4 85742702 GBM C T Missense p.R1554Q c.4661G>A 4 85696066 UCEC C T Missense p.R1748Q c.5243G>A 4 85678260 BRCA C T Missense p.R2332H c.6995G>A 4 85654761 UCEC C T Missense p.R3242Q c.9725G>A 4 85605097 UCEC C T Missense p.R3312Q c.9935G>A 4 85600284 UCEC C T Missense p.R3524Q c.10571G>A 4 85594031 LUSC C T Missense p.R40Q c.119G>A 4 85781626 COREAD C T Missense p.R568Q c.1703G>A 4 85738729 STAD C T Missense p.R60K c.179G>A 4 85781566 BLCA C T Missense p.R720Q c.2159G>A 4 85731226 UCEC C T Missense p.R903Q c.2708G>A 4 85722917 STAD C T Missense p.R945H c.2834G>A 4 85719250 GBM C T Missense p.R945H c.2834G>A 4 85719250 PRAD C T Missense p.V2928I c.8782G>A 4 85617242 CM C T Nonsense p.W2310* c.6930G>A 4 85656259 LUAD C T Synonymous p.E2409E c.7227G>A 4 85648059 BRCA C T Synonymous p.E2937E c.8811G>A 4 85617213 BRCA C T Synonymous p.K2383K c.7149G>A 4 85654607 CM C T Synonymous p.K2999K c.8997G>A 4 85614090 CM C T Synonymous p.K3486K c.10458G>A 4 85594144 CM C T Synonymous p.Q187Q c.561G>A 4 85758097 BRCA C T Synonymous p.R1996R c.5988G>A 4 85664938 LUSC C T Synonymous p.V1663V c.4989G>A 4 85687162 LUAD C T Synonymous p.V195V c.585G>A 4 85752750 HNSC C T Synonymous p.V2042V c.6126G>A 4 85663022 BRCA GAA - InFrameDeletion p.L685delL c.2054_2056delTTC 4 85731329 LGG G A IntronicSNV . c.1-101538C>T 4 85883282 CLL G A Missense p.A1958V c.5873C>T 4 85672736 BRCA G A Missense p.A2455V c.7364C>T 4 85645656 CM G A Missense p.A2923V c.8768C>T 4 85617256 UCEC G A Missense p.A416V c.1247C>T 4 85742581 UCEC G A Missense p.A828V c.2483C>T 4 85724567 CM G A Missense p.H2251Y c.6751C>T 4 85658343 CM G A Missense p.H2254Y c.6760C>T 4 85657478 CM G A Missense p.L1527F c.4579C>T 4 85696231 CM G A Missense p.L557F c.1669C>T 4 85741262 BLCA G A Missense p.P11L c.32C>T 4 85781713 STAD G A Missense p.P1578S c.4732C>T 4 85695995 CM G A Missense p.P1754S c.5260C>T 4 85678243 CM G A Missense p.P1904S c.5710C>T 4 85674879 CM G A Missense p.P1994S c.5980C>T 4 85664946 CM G A Missense p.P2948L c.8843C>T 4 85617181 LUAD G A Missense p.P3255S c.9763C>T 4 85603587 PRAD G A Missense p.P788S c.2362C>T 4 85729554 CM G A Missense p.R1181C c.3541C>T 4 85711007 CM G A Missense p.R1381W c.4141C>T 4 85704149 COREAD G A Missense p.R2051C c.6151C>T 4 85662997 LUAD G A Missense p.R2275C c.6823C>T 4 85657415 GBM G A Missense p.R244C c.730C>T 4 85752605 COREAD G A Missense p.R2528C c.7582C>T 4 85642585 STAD G A Missense p.R640C c.1918C>T 4 85731467 CM G A Missense p.S1592F c.4775C>T 4 85694062 COREAD G A Missense p.S1824F c.5471C>T 4 85676507 CM G A Missense p.S2446F c.7337C>T 4 85645683 CLL G A Missense p.S2834L c.8501C>T 4 85623601 CM G A Missense p.T2205I c.6614C>T 4 85658480 UCEC G A Missense p.T3071I c.9212C>T 4 85611810 CM G A Missense p.T3116I c.9347C>T 4 85611675 CM G A Missense p.T82I c.245C>T 4 85771114 LUAD G A Nonsense p.Q3491* c.10471C>T 4 85594131 UCEC G A Nonsense p.Q933* c.2797C>T 4 85722828 BRCA G A Nonsense p.R636* c.1906C>T 4 85731479 CM G A Synonymous p.A383A c.1149C>T 4 85742679 CM G A Synonymous p.D3299D c.9897C>T 4 85600322 UCEC G A Synonymous p.F80F c.240C>T 4 85771119 LUAD G A Synonymous p.I1472I c.4416C>T 4 85699758 PRAD G A Synonymous p.I1546I c.4638C>T 4 85696089 CM G A Synonymous p.I3025I c.9075C>T 4 85612913 CM G A Synonymous p.L1334L c.4000C>T 4 85707194 COREAD G A Synonymous p.L1708L c.5124C>T 4 85687027 LUSC G A Synonymous p.L2030L c.6088C>T 4 85663060 CM G A Synonymous p.L2752L c.8254C>T 4 85626628 LUAD G A Synonymous p.L290L c.870C>T 4 85750243 LUSC G A Synonymous p.S1993S c.5979C>T 4 85664947 CM G A Synonymous p.S3212S c.9636C>T 4 85605186 UCEC G A Synonymous p.S3378S c.10134C>T 4 85600085 HNSC G A Synonymous p.T1596T c.4788C>T 4 85694049 CM G A Synonymous p.T241T c.723C>T 4 85752612 CM G A Synonymous p.T3129T c.9387C>T 4 85609395 STAD G A Synonymous p.V1829V c.5487C>T 4 85676491 CM G A Synonymous p.V894V c.2682C>T 4 85722943 HNSC G A Synonymous p.Y2008Y c.6024C>T 4 85664902 RCCC G A Synonymous p.Y2540Y c.7620C>T 4 85639709 THCA G C Missense p.A1958G c.5873C>G 4 85672736 HNSC G C Missense p.F2810L c.8430C>G 4 85625503 UCEC G C Missense p.I2614M c.7842C>G 4 85638082 BLCA G C Missense p.L2068V c.6202C>G 4 85662946 BLCA G C Missense p.L286V c.856C>G 4 85750257 STAD G C Missense p.L316V c.946C>G 4 85750167 LUAD G C Missense p.P798R c.2393C>G 4 85729523 CM G C Missense p.S656C c.1967C>G 4 85731418 LUAD G C Missense p.S838C c.2513C>G 4 85724537 CM G C Missense p.T1268R c.3803C>G 4 85708733 NSCLC G C Nonsense p.S271* c.812C>G 4 85750301 LUSC GT AG Missense p.D3006A c.9017_9018delinsCT 4 85614069 SCLC G T Missense p.A2477D c.7430C>A 4 85645590 COREAD G T Missense p.L3364I c.10090C>A 4 85600129 ESCA G T Missense p.P1994T c.5980C>A 4 85664946 STAD G T Missense p.T140N c.419C>A 4 85758239 ESCA T A Missense p.E3065V c.9194A>T 4 85612794 LGG T A Missense p.E998D c.2994A>T 4 85717847 OV T A Missense p.K2368M c.7103A>T 4 85654653 RCCC T A Missense p.K3381N c.10143A>T 4 85600076 BRCA T A Missense p.Q1716L c.5147A>T 4 85687004 BLCA T A Missense p.S2142C c.6424A>T 4 85661380 COREAD T A Synonymous p.P352P c.1056A>T 4 85748035 HNSC T A Synonymous p.V775V c.2325A>T 4 85731060 HNSC T C 3-UTRSNV . c.10578+322A>G 4 85593702 HC T C Missense p.E662G c.1985A>G 4 85731400 BLCA T C Missense p.H2561R c.7682A>G 4 85639647 CM T C Missense p.H3193R c.9578A>G 4 85605244 LUAD T C Missense p.H704R c.2111A>G 4 85731274 UCEC T C Missense p.I1339V c.4015A>G 4 85707179 HNSC T C Missense p.I1907V c.5719A>G 4 85674870 RCCC T C Missense p.K324R c.971A>G 4 85748120 RCCC T C Missense p.K329R c.986A>G 4 85748105 LUAD T C Missense p.T146A c.436A>G 4 85758222 RCCC T C Missense p.Y2441C c.7322A>G 4 85645698 STAD T C Synonymous p.E1168E c.3504A>G 4 85711044 HC T C Synonymous p.K1349K c.4047A>G 4 85707147 HNSC T C Synonymous p.Q2506Q c.7518A>G 4 85642649 LUAD T C Synonymous p.Q2939Q c.8817A>G 4 85617207 CM T - Frameshift p.K581Sfs*10 c.1742delA 4 85738690 RCCC - T Frameshift p.L1526Tfs*7 c.4575dupA 4 85696235 THCA - T Frameshift p.Q3121Tfs*8 c.9360dupA 4 85611662 RCCC T G Missense p.E3471D c.10413A>C 4 85598396 LUSC T G Missense p.L1275F c.3825A>C 4 85708711 BRCA T G Missense p.Q2508P c.7523A>C 4 85642644 BRCA T G Missense p.Y411S c.1232A>C 4 85742596 OV T G Synonymous p.A695A c.2085A>C 4 85731300 CM - T IntronicInsertion . c.8597-2222dupA 4 85620198 CM