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 6 146214396 146214396 + Missense_Mutation SNP T T C TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr6:146214396T>C c.4829A>G c.(4828-4830)cAt>cGt p.H1610R ACC 6 146248371 146248371 + Missense_Mutation SNP C C T TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr6:146248371C>T c.3155G>A c.(3154-3156)cGc>cAc p.R1052H BLCA 6 146207828 146207828 + Silent SNP C C T TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr6:146207828C>T c.5051G>A c.(5050-5052)tGa>tAa p.*1684* BLCA 6 146216072 146216072 + Silent SNP C C G TCGA-FD-A6TB-01A-12D-A339-08 TCGA-FD-A6TB-10A-21D-A339-08 g.chr6:146216072C>G c.4557G>C c.(4555-4557)ctG>ctC p.L1519L BLCA 6 146231621 146231621 + Missense_Mutation SNP G G A TCGA-XF-A9SP-01A-11D-A391-08 TCGA-XF-A9SP-10A-01D-A394-08 g.chr6:146231621G>A c.4478C>T c.(4477-4479)tCa>tTa p.S1493L BLCA 6 146242491 146242491 + Missense_Mutation SNP C C T TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr6:146242491C>T c.3820G>A c.(3820-3822)Gaa>Aaa p.E1274K BLCA 6 146243906 146243906 + Silent SNP C C T TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr6:146243906C>T c.3612G>A c.(3610-3612)caG>caA p.Q1204Q BLCA 6 146256146 146256146 + Missense_Mutation SNP C C T TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr6:146256146C>T c.2887G>A c.(2887-2889)Gac>Aac p.D963N BLCA 6 146256489 146256489 + Missense_Mutation SNP C C G TCGA-FD-A3B6-01A-21D-A20D-08 TCGA-FD-A3B6-10A-01D-A20D-08 g.chr6:146256489C>G c.2658G>C c.(2656-2658)aaG>aaC p.K886N BLCA 6 146264544 146264544 + Missense_Mutation SNP C C A TCGA-XF-A9SL-01A-11D-A391-08 TCGA-XF-A9SL-10A-01D-A394-08 g.chr6:146264544C>A c.1973G>T c.(1972-1974)cGc>cTc p.R658L BLCA 6 146264805 146264805 + Missense_Mutation SNP C C T TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr6:146264805C>T c.1712G>A c.(1711-1713)aGa>aAa p.R571K BLCA 6 146268656 146268656 + Silent SNP G G A TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr6:146268656G>A c.1185C>T c.(1183-1185)gtC>gtT p.V395V BLCA 6 146269463 146269463 + Nonsense_Mutation SNP G G A TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr6:146269463G>A c.1006C>T c.(1006-1008)Cga>Tga p.R336* BLCA 6 146271550 146271550 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr6:146271550G>C c.832C>G c.(832-834)Cac>Gac p.H278D BLCA 6 146275900 146275900 + Missense_Mutation SNP C C G TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr6:146275900C>G c.559G>C c.(559-561)Gaa>Caa p.E187Q BLCA 6 146275900 146275900 + Missense_Mutation SNP C C G TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr6:146275900C>G c.559G>C c.(559-561)Gaa>Caa p.E187Q BLCA 6 146275906 146275906 + Missense_Mutation SNP T T C TCGA-BL-A13I-01A-11D-A13W-08 TCGA-BL-A13I-11A-11D-A13W-08 g.chr6:146275906T>C c.553A>G c.(553-555)Atg>Gtg p.M185V BRCA 6 146240555 146240555 + Nonsense_Mutation SNP G G A TCGA-A2-A1FV-01A-11D-A13L-09 TCGA-A2-A1FV-10A-01D-A13O-09 g.chr6:146240555G>A c.4081C>T c.(4081-4083)Cga>Tga p.R1361* BRCA 6 146242419 146242419 + Missense_Mutation SNP C C G TCGA-B6-A0WZ-01A-11D-A10G-09 TCGA-B6-A0WZ-10A-01D-A10G-09 g.chr6:146242419C>G c.3892G>C c.(3892-3894)Gag>Cag p.E1298Q BRCA 6 146247363 146247363 + Missense_Mutation SNP G G A TCGA-E2-A1LS-01A-12D-A159-09 TCGA-E2-A1LS-11A-32W-A16L-09 g.chr6:146247363G>A c.3271C>T c.(3271-3273)Cgt>Tgt p.R1091C BRCA 6 146256180 146256180 + Silent SNP C C T TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr6:146256180C>T c.2853G>A c.(2851-2853)aaG>aaA p.K951K BRCA 6 146256486 146256486 + Silent SNP C C T TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr6:146256486C>T c.2661G>A c.(2659-2661)aaG>aaA p.K887K BRCA 6 146262775 146262776 + Frame_Shift_Ins INS - - C TCGA-B6-A0IN-01A-11W-A050-09 TCGA-B6-A0IN-10A-01W-A055-09 g.chr6:146262775_146262776insC c.2473_2474insG c.(2473-2475)gagfs p.E825fs BRCA 6 146264518 146264518 + Missense_Mutation SNP C C T TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr6:146264518C>T c.1999G>A c.(1999-2001)Gat>Aat p.D667N BRCA 6 146268666 146268666 + Missense_Mutation SNP C C T TCGA-AC-A3W6-01A-12D-A228-09 TCGA-AC-A3W6-10A-01D-A22A-09 g.chr6:146268666C>T c.1175G>A c.(1174-1176)cGa>cAa p.R392Q BRCA 6 146275931 146275931 + Silent SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr6:146275931C>T c.528G>A c.(526-528)ctG>ctA p.L176L BRCA 6 146276233 146276233 + Missense_Mutation SNP C C G TCGA-BH-A18H-01A-11D-A12B-09 TCGA-BH-A18H-10A-01D-A12B-09 g.chr6:146276233C>G c.226G>C c.(226-228)Gtg>Ctg p.V76L BRCA 6 146276419 146276419 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr6:146276419C>T c.40G>A c.(40-42)Gat>Aat p.D14N BRCA 6 146276436 146276436 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr6:146276436G>A c.23C>T c.(22-24)gCt>gTt p.A8V BRCA 6 146276440 146276440 + Missense_Mutation SNP G G C TCGA-D8-A142-01A-11D-A10Y-09 TCGA-D8-A142-10A-01D-A110-09 g.chr6:146276440G>C c.19C>G c.(19-21)Cgt>Ggt p.R7G CESC 6 146256116 146256116 + Missense_Mutation SNP G G A TCGA-C5-A1BI-01B-11D-A13W-08 TCGA-C5-A1BI-10A-01D-A13W-08 g.chr6:146256116G>A c.2917C>T c.(2917-2919)Cca>Tca p.P973S CESC 6 146264850 146264850 + Missense_Mutation SNP G G A TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr6:146264850G>A c.1667C>T c.(1666-1668)tCt>tTt p.S556F CESC 6 146275945 146275945 + Missense_Mutation SNP C C T TCGA-JW-A5VJ-01A-11D-A28B-09 TCGA-JW-A5VJ-10A-01D-A28E-09 g.chr6:146275945C>T c.514G>A c.(514-516)Gac>Aac p.D172N CHOL 6 146256253 146256253 + Missense_Mutation SNP G G T TCGA-W5-AA2T-01A-12D-A417-09 TCGA-W5-AA2T-10A-01D-A41A-09 g.chr6:146256253G>T c.2780C>A c.(2779-2781)tCt>tAt p.S927Y CHOL 6 146268687 146268687 + Missense_Mutation SNP G G T TCGA-3X-AAV9-01A-72D-A417-09 TCGA-3X-AAV9-10A-01D-A41A-09 g.chr6:146268687G>T c.1154C>A c.(1153-1155)gCt>gAt p.A385D COAD 6 146207910 146207910 + Missense_Mutation SNP A A T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr6:146207910A>T c.4969T>A c.(4969-4971)Tca>Aca p.S1657T COAD 6 146231664 146231664 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr6:146231664G>A c.4435C>T c.(4435-4437)Cgc>Tgc p.R1479C COAD 6 146234627 146234627 + Missense_Mutation SNP T T C TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr6:146234627T>C c.4313A>G c.(4312-4314)cAg>cGg p.Q1438R COAD 6 146240543 146240543 + Missense_Mutation SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr6:146240543G>A c.4093C>T c.(4093-4095)Cgt>Tgt p.R1365C COAD 6 146240543 146240543 + Missense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr6:146240543G>A c.4093C>T c.(4093-4095)Cgt>Tgt p.R1365C COAD 6 146240543 146240543 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr6:146240543G>A c.4093C>T c.(4093-4095)Cgt>Tgt p.R1365C COAD 6 146243832 146243832 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr6:146243832C>T c.3686G>A c.(3685-3687)tGt>tAt p.C1229Y COAD 6 146244873 146244873 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:146244873C>A c.3451G>T c.(3451-3453)Gaa>Taa p.E1151* COAD 6 146245970 146245970 + Nonsense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:146245970G>A c.3307C>T c.(3307-3309)Cga>Tga p.R1103* COAD 6 146248372 146248372 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:146248372G>A c.3154C>T c.(3154-3156)Cgc>Tgc p.R1052C COAD 6 146261868 146261869 + Frame_Shift_Del DEL CT CT - TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr6:146261868_146261869delCT c.2559_2560delAG c.(2557-2562)agaggafs p.G854fs COAD 6 146262867 146262867 + Silent SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr6:146262867G>A c.2382C>T c.(2380-2382)cgC>cgT p.R794R COAD 6 146262964 146262964 + Frame_Shift_Del DEL A A - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr6:146262964delA c.2285delT c.(2284-2286)ttgfs p.L762fs COAD 6 146264544 146264544 + Missense_Mutation SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr6:146264544C>T c.1973G>A c.(1972-1974)cGc>cAc p.R658H COAD 6 146264800 146264800 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:146264800G>A c.1717C>T c.(1717-1719)Cgc>Tgc p.R573C COAD 6 146264827 146264827 + Missense_Mutation SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr6:146264827A>G c.1690T>C c.(1690-1692)Tat>Cat p.Y564H COAD 6 146264843 146264843 + Silent SNP A A G TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr6:146264843A>G c.1674T>C c.(1672-1674)gaT>gaC p.D558D COAD 6 146264891 146264891 + Frame_Shift_Del DEL C C - TCGA-D5-5540-01A-01D-1650-10 TCGA-D5-5540-10A-01D-1650-10 g.chr6:146264891delC c.1626delG c.(1624-1626)gggfs p.G542fs COAD 6 146266724 146266724 + Frame_Shift_Del DEL T T - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr6:146266724delT c.1371delA c.(1369-1371)aaafs p.K457fs COAD 6 146275864 146275864 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:146275864T>G c.595A>C c.(595-597)Aaa>Caa p.K199Q COAD 6 146276107 146276107 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:146276107C>A c.352G>T c.(352-354)Gaa>Taa p.E118* COAD 6 146276213 146276213 + Silent SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr6:146276213T>C c.246A>G c.(244-246)ccA>ccG p.P82P COADREAD 6 146207910 146207910 + Missense_Mutation SNP A A T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr6:146207910A>T c.4969T>A c.(4969-4971)Tca>Aca p.S1657T COADREAD 6 146231664 146231664 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr6:146231664G>A c.4435C>T c.(4435-4437)Cgc>Tgc p.R1479C COADREAD 6 146234627 146234627 + Missense_Mutation SNP T T C TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr6:146234627T>C c.4313A>G c.(4312-4314)cAg>cGg p.Q1438R COADREAD 6 146240543 146240543 + Missense_Mutation SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr6:146240543G>A c.4093C>T c.(4093-4095)Cgt>Tgt p.R1365C COADREAD 6 146240543 146240543 + Missense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr6:146240543G>A c.4093C>T c.(4093-4095)Cgt>Tgt p.R1365C COADREAD 6 146240543 146240543 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr6:146240543G>A c.4093C>T c.(4093-4095)Cgt>Tgt p.R1365C COADREAD 6 146243422 146243422 + Splice_Site SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146243422G>A c.3782C>T c.(3781-3783)aCa>aTa p.T1261I COADREAD 6 146243832 146243832 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr6:146243832C>T c.3686G>A c.(3685-3687)tGt>tAt p.C1229Y COADREAD 6 146244873 146244873 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:146244873C>A c.3451G>T c.(3451-3453)Gaa>Taa p.E1151* COADREAD 6 146245970 146245970 + Nonsense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:146245970G>A c.3307C>T c.(3307-3309)Cga>Tga p.R1103* COADREAD 6 146248372 146248372 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:146248372G>A c.3154C>T c.(3154-3156)Cgc>Tgc p.R1052C COADREAD 6 146261868 146261869 + Frame_Shift_Del DEL CT CT - TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr6:146261868_146261869delCT c.2559_2560delAG c.(2557-2562)agaggafs p.G854fs COADREAD 6 146262867 146262867 + Silent SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr6:146262867G>A c.2382C>T c.(2380-2382)cgC>cgT p.R794R COADREAD 6 146262922 146262922 + Missense_Mutation SNP C C T TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr6:146262922C>T c.2327G>A c.(2326-2328)cGt>cAt p.R776H COADREAD 6 146262964 146262964 + Frame_Shift_Del DEL A A - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr6:146262964delA c.2285delT c.(2284-2286)ttgfs p.L762fs COADREAD 6 146264506 146264506 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146264506G>A c.2011C>T c.(2011-2013)Cgt>Tgt p.R671C COADREAD 6 146264544 146264544 + Missense_Mutation SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr6:146264544C>T c.1973G>A c.(1972-1974)cGc>cAc p.R658H COADREAD 6 146264622 146264622 + Missense_Mutation SNP C C G TCGA-DC-6158-01A-11D-1657-10 TCGA-DC-6158-10A-01D-1657-10 g.chr6:146264622C>G c.1895G>C c.(1894-1896)tGt>tCt p.C632S COADREAD 6 146264800 146264800 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:146264800G>A c.1717C>T c.(1717-1719)Cgc>Tgc p.R573C COADREAD 6 146264827 146264827 + Missense_Mutation SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr6:146264827A>G c.1690T>C c.(1690-1692)Tat>Cat p.Y564H COADREAD 6 146264843 146264843 + Silent SNP A A G TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr6:146264843A>G c.1674T>C c.(1672-1674)gaT>gaC p.D558D COADREAD 6 146264891 146264891 + Frame_Shift_Del DEL C C - TCGA-D5-5540-01A-01D-1650-10 TCGA-D5-5540-10A-01D-1650-10 g.chr6:146264891delC c.1626delG c.(1624-1626)gggfs p.G542fs COADREAD 6 146264908 146264908 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146264908C>A c.1609G>T c.(1609-1611)Gaa>Taa p.E537* COADREAD 6 146266724 146266724 + Frame_Shift_Del DEL T T - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr6:146266724delT c.1371delA c.(1369-1371)aaafs p.K457fs COADREAD 6 146267402 146267402 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146267402C>T c.1288G>A c.(1288-1290)Gaa>Aaa p.E430K COADREAD 6 146275864 146275864 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:146275864T>G c.595A>C c.(595-597)Aaa>Caa p.K199Q COADREAD 6 146276034 146276034 + Missense_Mutation SNP C C A TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr6:146276034C>A c.425G>T c.(424-426)aGt>aTt p.S142I COADREAD 6 146276107 146276107 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:146276107C>A c.352G>T c.(352-354)Gaa>Taa p.E118* COADREAD 6 146276213 146276213 + Silent SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr6:146276213T>C c.246A>G c.(244-246)ccA>ccG p.P82P COADREAD 6 146276446 146276446 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr6:146276446G>A c.13C>T c.(13-15)Cgg>Tgg p.R5W DLBC 6 146267376 146267376 + Silent SNP T T C TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr6:146267376T>C c.1314A>G c.(1312-1314)caA>caG p.Q438Q DLBC 6 146276280 146276280 + Missense_Mutation SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr6:146276280C>T c.179G>A c.(178-180)aGt>aAt p.S60N ESCA 6 146243864 146243864 + Silent SNP T T C TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr6:146243864T>C c.3654A>G c.(3652-3654)ccA>ccG p.P1218P ESCA 6 146264331 146264331 + Missense_Mutation SNP T T A TCGA-L5-A8NE-01A-11D-A37C-09 TCGA-L5-A8NE-11A-11D-A37F-09 g.chr6:146264331T>A c.2186A>T c.(2185-2187)cAg>cTg p.Q729L ESCA 6 146266723 146266723 + Nonsense_Mutation SNP C C A TCGA-LN-A7HX-01A-11D-A33E-09 TCGA-LN-A7HX-10A-01D-A33H-09 g.chr6:146266723C>A c.1372G>T c.(1372-1374)Gga>Tga p.G458* ESCA 6 146268631 146268631 + Missense_Mutation SNP C C T TCGA-IG-A5B8-01A-11D-A28B-09 TCGA-IG-A5B8-10A-01D-A28E-09 g.chr6:146268631C>T c.1210G>A c.(1210-1212)Gag>Aag p.E404K ESCA 6 146269407 146269407 + Splice_Site SNP C C T TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chr6:146269407C>T c.e5+1 ESCA 6 146275889 146275889 + Frame_Shift_Del DEL C C - TCGA-XP-A8T6-01A-11D-A36J-09 TCGA-XP-A8T6-10A-01D-A36M-09 g.chr6:146275889delC c.570delG c.(568-570)gggfs p.G190fs ESCA 6 146276380 146276380 + Missense_Mutation SNP C C T TCGA-X8-AAAR-01A-11D-A403-09 TCGA-X8-AAAR-10A-01D-A403-09 g.chr6:146276380C>T c.79G>A c.(79-81)Gag>Aag p.E27K GBM 6 146215353 146215353 + Missense_Mutation SNP A A G TCGA-12-3652-01A-01D-1495-08 TCGA-12-3652-10A-01D-1495-08 g.chr6:146215353A>G c.4628T>C c.(4627-4629)aTt>aCt p.I1543T GBM 6 146269445 146269445 + Missense_Mutation SNP C C T TCGA-02-0003-01A-01D-1490-08 TCGA-02-0003-10A-01D-1490-08 g.chr6:146269445C>T c.1024G>A c.(1024-1026)Gag>Aag p.E342K GBMLGG 6 146215310 146215310 + Silent SNP T T C TCGA-DU-6395-01A-12D-1705-08 TCGA-DU-6395-10A-01D-1705-08 g.chr6:146215310T>C c.4671A>G c.(4669-4671)caA>caG p.Q1557Q GBMLGG 6 146215353 146215353 + Missense_Mutation SNP A A G TCGA-12-3652-01A-01D-1495-08 TCGA-12-3652-10A-01D-1495-08 g.chr6:146215353A>G c.4628T>C c.(4627-4629)aTt>aCt p.I1543T GBMLGG 6 146266768 146266768 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:146266768G>A c.1327C>T c.(1327-1329)Cgt>Tgt p.R443C GBMLGG 6 146269445 146269445 + Missense_Mutation SNP C C T TCGA-02-0003-01A-01D-1490-08 TCGA-02-0003-10A-01D-1490-08 g.chr6:146269445C>T c.1024G>A c.(1024-1026)Gag>Aag p.E342K GBMLGG 6 146271526 146271526 + Nonsense_Mutation SNP G G A TCGA-HT-7616-01A-11D-2253-08 TCGA-HT-7616-10A-01D-2253-08 g.chr6:146271526G>A c.856C>T c.(856-858)Caa>Taa p.Q286* HNSC 6 146244822 146244822 + Missense_Mutation SNP T T A TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr6:146244822T>A c.3502A>T c.(3502-3504)Agc>Tgc p.S1168C HNSC 6 146245960 146245960 + Missense_Mutation SNP T T A TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr6:146245960T>A c.3317A>T c.(3316-3318)tAc>tTc p.Y1106F HNSC 6 146247394 146247394 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:146247394T>C c.3240A>G c.(3238-3240)atA>atG p.I1080M HNSC 6 146247400 146247400 + Silent SNP C C T TCGA-CQ-5334-01A-01D-1683-08 TCGA-CQ-5334-10A-01D-1683-08 g.chr6:146247400C>T c.3234G>A c.(3232-3234)ttG>ttA p.L1078L HNSC 6 146262872 146262872 + Missense_Mutation SNP G G A TCGA-MZ-A5BI-01A-31D-A34J-08 TCGA-MZ-A5BI-10C-01D-A34M-08 g.chr6:146262872G>A c.2377C>T c.(2377-2379)Cgt>Tgt p.R793C HNSC 6 146262922 146262922 + Missense_Mutation SNP C C A TCGA-CV-7242-01A-11D-2012-08 TCGA-CV-7242-10A-01D-2013-08 g.chr6:146262922C>A c.2327G>T c.(2326-2328)cGt>cTt p.R776L HNSC 6 146263002 146263002 + Missense_Mutation SNP T T G TCGA-CV-7242-01A-11D-2012-08 TCGA-CV-7242-10A-01D-2013-08 g.chr6:146263002T>G c.2247A>C c.(2245-2247)caA>caC p.Q749H HNSC 6 146264599 146264599 + Missense_Mutation SNP C C T TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr6:146264599C>T c.1918G>A c.(1918-1920)Gat>Aat p.D640N HNSC 6 146264650 146264650 + Missense_Mutation SNP A A C TCGA-QK-A6II-01A-11D-A31L-08 TCGA-QK-A6II-10A-01D-A31J-08 g.chr6:146264650A>C c.1867T>G c.(1867-1869)Ttc>Gtc p.F623V HNSC 6 146267421 146267421 + Missense_Mutation SNP C C G TCGA-4P-AA8J-01A-11D-A391-08 TCGA-4P-AA8J-10A-01D-A394-08 g.chr6:146267421C>G c.1269G>C c.(1267-1269)aaG>aaC p.K423N HNSC 6 146267451 146267451 + Silent SNP C C T TCGA-CN-5363-01A-01D-1434-08 TCGA-CN-5363-10A-01D-1434-08 g.chr6:146267451C>T c.1239G>A c.(1237-1239)ccG>ccA p.P413P HNSC 6 146268684 146268684 + Missense_Mutation SNP A A G TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr6:146268684A>G c.1157T>C c.(1156-1158)cTg>cCg p.L386P HNSC 6 146271470 146271470 + Missense_Mutation SNP C C G TCGA-CN-4734-01A-01D-1434-08 TCGA-CN-4734-10A-01D-1434-08 g.chr6:146271470C>G c.912G>C c.(910-912)ttG>ttC p.L304F HNSC 6 146271502 146271502 + Missense_Mutation SNP C C A TCGA-CN-6992-01A-11D-1912-08 TCGA-CN-6992-10A-01D-1912-08 g.chr6:146271502C>A c.880G>T c.(880-882)Gat>Tat p.D294Y HNSC 6 146271503 146271503 + Silent SNP C C T TCGA-CN-6992-01A-11D-1912-08 TCGA-CN-6992-10A-01D-1912-08 g.chr6:146271503C>T c.879G>A c.(877-879)gtG>gtA p.V293V HNSC 6 146273490 146273490 + Missense_Mutation SNP A A G TCGA-F7-A622-01A-11D-A28R-08 TCGA-F7-A622-10A-01D-A28U-08 g.chr6:146273490A>G c.758T>C c.(757-759)aTt>aCt p.I253T HNSC 6 146276246 146276246 + Silent SNP C C T TCGA-HD-8635-01A-11D-2394-08 TCGA-HD-8635-10A-01D-2394-08 g.chr6:146276246C>T c.213G>A c.(211-213)aaG>aaA p.K71K HNSC 6 146276439 146276439 + Missense_Mutation SNP C C T TCGA-CV-5979-01A-11D-1683-08 TCGA-CV-5979-11A-01D-1683-08 g.chr6:146276439C>T c.20G>A c.(19-21)cGt>cAt p.R7H KIPAN 6 146215295 146215296 + Frame_Shift_Ins INS - - T TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr6:146215295_146215296insT c.4685_4686insA c.(4684-4686)aagfs p.K1562fs KIPAN 6 146234630 146234630 + Missense_Mutation SNP C C G TCGA-A4-7585-01A-11D-2136-08 TCGA-A4-7585-11A-01D-2136-08 g.chr6:146234630C>G c.4310G>C c.(4309-4311)cGa>cCa p.R1437P KIPAN 6 146262786 146262786 + Silent SNP A A T TCGA-5P-A9KA-01A-11D-A42J-10 TCGA-5P-A9KA-10A-01D-A42M-10 g.chr6:146262786A>T c.2463T>A c.(2461-2463)gcT>gcA p.A821A KIPAN 6 146264642 146264642 + Frame_Shift_Del DEL T T - TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr6:146264642delT c.1875delA c.(1873-1875)caafs p.Q625fs KIPAN 6 146273498 146273498 + Missense_Mutation SNP A A T TCGA-CZ-5984-01A-11D-1669-08 TCGA-CZ-5984-11A-01D-1669-08 g.chr6:146273498A>T c.750T>A c.(748-750)aaT>aaA p.N250K KIRC 6 146273498 146273498 + Missense_Mutation SNP A A T TCGA-CZ-5984-01A-11D-1669-08 TCGA-CZ-5984-11A-01D-1669-08 g.chr6:146273498A>T c.750T>A c.(748-750)aaT>aaA p.N250K KIRP 6 146215295 146215296 + Frame_Shift_Ins INS - - T TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr6:146215295_146215296insT c.4685_4686insA c.(4684-4686)aagfs p.K1562fs KIRP 6 146234630 146234630 + Missense_Mutation SNP C C G TCGA-A4-7585-01A-11D-2136-08 TCGA-A4-7585-11A-01D-2136-08 g.chr6:146234630C>G c.4310G>C c.(4309-4311)cGa>cCa p.R1437P KIRP 6 146262786 146262786 + Silent SNP A A T TCGA-5P-A9KA-01A-11D-A42J-10 TCGA-5P-A9KA-10A-01D-A42M-10 g.chr6:146262786A>T c.2463T>A c.(2461-2463)gcT>gcA p.A821A KIRP 6 146264642 146264642 + Frame_Shift_Del DEL T T - TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr6:146264642delT c.1875delA c.(1873-1875)caafs p.Q625fs LGG 6 146215310 146215310 + Silent SNP T T C TCGA-DU-6395-01A-12D-1705-08 TCGA-DU-6395-10A-01D-1705-08 g.chr6:146215310T>C c.4671A>G c.(4669-4671)caA>caG p.Q1557Q LGG 6 146266768 146266768 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:146266768G>A c.1327C>T c.(1327-1329)Cgt>Tgt p.R443C LGG 6 146271526 146271526 + Nonsense_Mutation SNP G G A TCGA-HT-7616-01A-11D-2253-08 TCGA-HT-7616-10A-01D-2253-08 g.chr6:146271526G>A c.856C>T c.(856-858)Caa>Taa p.Q286* LIHC 6 146243830 146243830 + Missense_Mutation SNP G G T TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr6:146243830G>T c.3688C>A c.(3688-3690)Cac>Aac p.H1230N LIHC 6 146243946 146243946 + Missense_Mutation SNP A A G TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr6:146243946A>G c.3572T>C c.(3571-3573)tTc>tCc p.F1191S LIHC 6 146248366 146248366 + Missense_Mutation SNP A A G TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr6:146248366A>G c.3160T>C c.(3160-3162)Tcg>Ccg p.S1054P LIHC 6 146254194 146254194 + Splice_Site DEL T T - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr6:146254194delT c.3111delA c.(3109-3111)aaa>aa p.K1037fs LIHC 6 146256475 146256475 + Missense_Mutation SNP T T C TCGA-DD-AADE-01A-11D-A40R-10 TCGA-DD-AADE-10A-01D-A40U-10 g.chr6:146256475T>C c.2672A>G c.(2671-2673)cAt>cGt p.H891R LIHC 6 146264427 146264427 + Missense_Mutation SNP T T C TCGA-DD-AAEA-01A-11D-A40R-10 TCGA-DD-AAEA-10A-01D-A40U-10 g.chr6:146264427T>C c.2090A>G c.(2089-2091)aAg>aGg p.K697R LIHC 6 146275926 146275926 + Missense_Mutation SNP T T A TCGA-DD-A4NK-01A-11D-A28X-10 TCGA-DD-A4NK-10A-01D-A28X-10 g.chr6:146275926T>A c.533A>T c.(532-534)gAg>gTg p.E178V LIHC 6 146276072 146276072 + Missense_Mutation SNP T T G TCGA-DD-AAD2-01A-11D-A40R-10 TCGA-DD-AAD2-10A-01D-A40U-10 g.chr6:146276072T>G c.387A>C c.(385-387)ttA>ttC p.L129F LIHC 6 146276324 146276324 + Silent SNP T T A TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr6:146276324T>A c.135A>T c.(133-135)ccA>ccT p.P45P LUAD 6 146215302 146215302 + Missense_Mutation SNP C C T TCGA-86-6562-01A-11D-1753-08 TCGA-86-6562-10A-01D-1753-08 g.chr6:146215302C>T c.4679G>A c.(4678-4680)cGt>cAt p.R1560H LUAD 6 146234621 146234621 + Missense_Mutation SNP C C T TCGA-17-Z060-01A-01W-0747-08 TCGA-17-Z060-11A-01W-0747-08 g.chr6:146234621C>T c.4319G>A c.(4318-4320)gGa>gAa p.G1440E LUAD 6 146234666 146234666 + Missense_Mutation SNP C C T TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr6:146234666C>T c.4274G>A c.(4273-4275)gGa>gAa p.G1425E LUAD 6 146247376 146247376 + Silent SNP T T A TCGA-44-4112-01A-01D-1105-08 TCGA-44-4112-10A-01D-1458-08 g.chr6:146247376T>A c.3258A>T c.(3256-3258)atA>atT p.I1086I LUAD 6 146247397 146247397 + Missense_Mutation SNP C C G TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr6:146247397C>G c.3237G>C c.(3235-3237)ttG>ttC p.L1079F LUAD 6 146256096 146256096 + Missense_Mutation SNP C C A TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr6:146256096C>A c.2937G>T c.(2935-2937)caG>caT p.Q979H LUAD 6 146256253 146256253 + Missense_Mutation SNP G G A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr6:146256253G>A c.2780C>T c.(2779-2781)tCt>tTt p.S927F LUAD 6 146262871 146262871 + Missense_Mutation SNP C C G TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr6:146262871C>G c.2378G>C c.(2377-2379)cGt>cCt p.R793P LUAD 6 146262927 146262927 + Silent SNP T T C TCGA-91-6847-01A-11D-1945-08 TCGA-91-6847-11A-01D-1945-08 g.chr6:146262927T>C c.2322A>G c.(2320-2322)gtA>gtG p.V774V LUAD 6 146262953 146262953 + Missense_Mutation SNP C C G TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr6:146262953C>G c.2296G>C c.(2296-2298)Gat>Cat p.D766H LUAD 6 146264343 146264343 + Missense_Mutation SNP G G T TCGA-49-6742-01A-11D-1855-08 TCGA-49-6742-11A-01D-1855-08 g.chr6:146264343G>T c.2174C>A c.(2173-2175)tCc>tAc p.S725Y LUAD 6 146264414 146264414 + Missense_Mutation SNP A A T TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr6:146264414A>T c.2103T>A c.(2101-2103)ttT>ttA p.F701L LUAD 6 146264551 146264551 + Missense_Mutation SNP C C G TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr6:146264551C>G c.1966G>C c.(1966-1968)Gat>Cat p.D656H LUAD 6 146264813 146264813 + Missense_Mutation SNP C C A TCGA-17-Z042-01A-01W-0746-08 TCGA-17-Z042-11A-01W-0746-08 g.chr6:146264813C>A c.1704G>T c.(1702-1704)aaG>aaT p.K568N LUAD 6 146266576 146266576 + Missense_Mutation SNP T T A TCGA-67-6216-01A-11D-1753-08 TCGA-67-6216-10A-01D-1753-08 g.chr6:146266576T>A c.1519A>T c.(1519-1521)Act>Tct p.T507S LUAD 6 146266716 146266716 + Missense_Mutation SNP G G A TCGA-55-8096-01A-11D-2238-08 TCGA-55-8096-10A-01D-2238-08 g.chr6:146266716G>A c.1379C>T c.(1378-1380)tCc>tTc p.S460F LUAD 6 146266723 146266723 + Nonsense_Mutation SNP C C A TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr6:146266723C>A c.1372G>T c.(1372-1374)Gga>Tga p.G458* LUAD 6 146268732 146268732 + Missense_Mutation SNP A A C TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr6:146268732A>C c.1109T>G c.(1108-1110)aTt>aGt p.I370S LUAD 6 146269413 146269413 + Silent SNP T T C TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr6:146269413T>C c.1056A>G c.(1054-1056)acA>acG p.T352T LUAD 6 146271525 146271525 + Missense_Mutation SNP T T G TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr6:146271525T>G c.857A>C c.(856-858)cAa>cCa p.Q286P LUAD 6 146275836 146275836 + Missense_Mutation SNP T T A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr6:146275836T>A c.623A>T c.(622-624)cAc>cTc p.H208L LUAD 6 146275911 146275911 + Missense_Mutation SNP C C T TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr6:146275911C>T c.548G>A c.(547-549)gGt>gAt p.G183D LUAD 6 146275957 146275957 + Missense_Mutation SNP T T C TCGA-75-6207-01A-11D-1753-08 TCGA-75-6207-10A-01D-1753-08 g.chr6:146275957T>C c.502A>G c.(502-504)Atg>Gtg p.M168V LUAD 6 146276084 146276084 + Silent SNP A A T TCGA-55-7726-01A-11D-2167-08 TCGA-55-7726-10A-01D-2167-08 g.chr6:146276084A>T c.375T>A c.(373-375)ccT>ccA p.P125P LUAD 6 146276182 146276182 + Frame_Shift_Del DEL A A - TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr6:146276182delA c.277delT c.(277-279)tccfs p.S93fs LUAD 6 146276325 146276325 + Missense_Mutation SNP G G T TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr6:146276325G>T c.134C>A c.(133-135)cCa>cAa p.P45Q LUAD 6 146276454 146276454 + Missense_Mutation SNP C C A TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr6:146276454C>A c.5G>T c.(4-6)aGc>aTc p.S2I LUSC 6 146216035 146216035 + Missense_Mutation SNP G G C TCGA-66-2786-01A-01D-1522-08 TCGA-66-2786-11A-01D-1522-08 g.chr6:146216035G>C c.4594C>G c.(4594-4596)Ctc>Gtc p.L1532V LUSC 6 146243814 146243814 + Missense_Mutation SNP C C T TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr6:146243814C>T c.3704G>A c.(3703-3705)aGa>aAa p.R1235K LUSC 6 146244844 146244844 + Silent SNP C C T TCGA-60-2708-01A-01D-1522-08 TCGA-60-2708-11A-01D-1522-08 g.chr6:146244844C>T c.3480G>A c.(3478-3480)caG>caA p.Q1160Q LUSC 6 146248399 146248399 + Missense_Mutation SNP C C T TCGA-21-5786-01A-01D-1632-08 TCGA-21-5786-10A-01D-1632-08 g.chr6:146248399C>T c.3127G>A c.(3127-3129)Gca>Aca p.A1043T LUSC 6 146256083 146256083 + Missense_Mutation SNP G G T TCGA-66-2744-01A-01D-0983-08 TCGA-66-2744-11A-01D-0983-08 g.chr6:146256083G>T c.2950C>A c.(2950-2952)Cca>Aca p.P984T LUSC 6 146262959 146262959 + Nonsense_Mutation SNP C C A TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chr6:146262959C>A c.2290G>T c.(2290-2292)Gaa>Taa p.E764* LUSC 6 146264293 146264293 + Missense_Mutation SNP A A T TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr6:146264293A>T c.2224T>A c.(2224-2226)Tct>Act p.S742T LUSC 6 146264545 146264545 + Missense_Mutation SNP G G T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr6:146264545G>T c.1972C>A c.(1972-1974)Cgc>Agc p.R658S LUSC 6 146275940 146275940 + Missense_Mutation SNP C C A TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr6:146275940C>A c.519G>T c.(517-519)aaG>aaT p.K173N LUSC 6 146276093 146276093 + Missense_Mutation SNP C C A TCGA-66-2777-01A-01D-1267-08 TCGA-66-2777-11A-01D-1267-08 g.chr6:146276093C>A c.366G>T c.(364-366)caG>caT p.Q122H OV 6 146264368 146264368 + Missense_Mutation SNP C C T TCGA-13-1484-01A-01W-0545-08 TCGA-13-1484-10A-01W-0545-08 g.chr6:146264368C>T c.2149G>A c.(2149-2151)Gca>Aca p.A717T PAAD 6 146207836 146207836 + Silent SNP C C T TCGA-FZ-5919-01A-11D-1609-08 TCGA-FZ-5919-11A-02D-1609-08 g.chr6:146207836C>T c.5043G>A c.(5041-5043)gaG>gaA p.E1681E PAAD 6 146214385 146214385 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:146214385C>T c.4840G>A c.(4840-4842)Gcc>Acc p.A1614T PAAD 6 146214434 146214434 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:146214434A>G c.4791T>C c.(4789-4791)acT>acC p.T1597T PAAD 6 146264761 146264761 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:146264761T>G c.1756A>C c.(1756-1758)Aaa>Caa p.K586Q PAAD 6 146264834 146264836 + In_Frame_Del DEL ATC ATC - TCGA-2J-AABP-01A-11D-A40W-08 TCGA-2J-AABP-10A-01D-A40W-08 g.chr6:146264834_146264836delATC c.1681_1683delGAT c.(1681-1683)gatdel p.D561del PAAD 6 146264834 146264836 + In_Frame_Del DEL ATC ATC - TCGA-F2-A44G-01A-11D-A26I-08 TCGA-F2-A44G-10A-01D-A26I-08 g.chr6:146264834_146264836delATC c.1681_1683delGAT c.(1681-1683)gatdel p.D561del PAAD 6 146264834 146264836 + In_Frame_Del DEL ATC ATC - TCGA-HV-A7OP-01A-11D-A33T-08 TCGA-HV-A7OP-10A-01D-A33W-08 g.chr6:146264834_146264836delATC c.1681_1683delGAT c.(1681-1683)gatdel p.D561del PAAD 6 146264834 146264836 + In_Frame_Del DEL ATC ATC - TCGA-XD-AAUL-01A-21D-A397-08 TCGA-XD-AAUL-10A-01D-A39A-08 g.chr6:146264834_146264836delATC c.1681_1683delGAT c.(1681-1683)gatdel p.D561del PAAD 6 146275891 146275891 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:146275891C>A c.568G>T c.(568-570)Ggg>Tgg p.G190W PCPG 6 146262866 146262866 + Missense_Mutation SNP G G T TCGA-WB-A820-01A-11D-A35I-08 TCGA-WB-A820-10A-01D-A35G-08 g.chr6:146262866G>T c.2383C>A c.(2383-2385)Cta>Ata p.L795I PRAD 6 146242326 146242326 + Missense_Mutation SNP C C T TCGA-V1-A8WV-01A-11D-A377-08 TCGA-V1-A8WV-10A-01D-A37A-08 g.chr6:146242326C>T c.3985G>A c.(3985-3987)Gaa>Aaa p.E1329K PRAD 6 146243842 146243842 + Missense_Mutation SNP C C G TCGA-EJ-5511-01A-01D-1576-08 TCGA-EJ-5511-10A-01D-1577-08 g.chr6:146243842C>G c.3676G>C c.(3676-3678)Gca>Cca p.A1226P PRAD 6 146264543 146264543 + Silent SNP G G A TCGA-HC-A48F-01A-11D-A257-08 TCGA-HC-A48F-10A-01D-A25A-08 g.chr6:146264543G>A c.1974C>T c.(1972-1974)cgC>cgT p.R658R PRAD 6 146266673 146266673 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:146266673G>A c.1422C>T c.(1420-1422)taC>taT p.Y474Y READ 6 146243422 146243422 + Splice_Site SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146243422G>A c.3782C>T c.(3781-3783)aCa>aTa p.T1261I READ 6 146262922 146262922 + Missense_Mutation SNP C C T TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr6:146262922C>T c.2327G>A c.(2326-2328)cGt>cAt p.R776H READ 6 146264506 146264506 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146264506G>A c.2011C>T c.(2011-2013)Cgt>Tgt p.R671C READ 6 146264622 146264622 + Missense_Mutation SNP C C G TCGA-DC-6158-01A-11D-1657-10 TCGA-DC-6158-10A-01D-1657-10 g.chr6:146264622C>G c.1895G>C c.(1894-1896)tGt>tCt p.C632S READ 6 146264908 146264908 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146264908C>A c.1609G>T c.(1609-1611)Gaa>Taa p.E537* READ 6 146267402 146267402 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:146267402C>T c.1288G>A c.(1288-1290)Gaa>Aaa p.E430K READ 6 146276034 146276034 + Missense_Mutation SNP C C A TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr6:146276034C>A c.425G>T c.(424-426)aGt>aTt p.S142I READ 6 146276446 146276446 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr6:146276446G>A c.13C>T c.(13-15)Cgg>Tgg p.R5W SARC 6 146256227 146256227 + Missense_Mutation SNP G G C TCGA-QQ-A8VH-01A-11D-A37C-09 TCGA-QQ-A8VH-10A-01D-A37F-09 g.chr6:146256227G>C c.2806C>G c.(2806-2808)Cgt>Ggt p.R936G SARC 6 146264415 146264415 + Missense_Mutation SNP A A G TCGA-DX-AB35-01A-21D-A417-09 TCGA-DX-AB35-11A-11D-A41A-09 g.chr6:146264415A>G c.2102T>C c.(2101-2103)tTt>tCt p.F701S SARC 6 146268768 146268768 + Missense_Mutation SNP T T C TCGA-IW-A3M5-01A-22D-A21Q-09 TCGA-IW-A3M5-10A-01D-A21Q-09 g.chr6:146268768T>C c.1073A>G c.(1072-1074)gAg>gGg p.E358G SKCM 6 146214476 146214476 + Silent SNP G G A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr6:146214476G>A c.4749C>T c.(4747-4749)ccC>ccT p.P1583P SKCM 6 146231636 146231636 + Missense_Mutation SNP G G A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr6:146231636G>A c.4463C>T c.(4462-4464)tCg>tTg p.S1488L SKCM 6 146243875 146243875 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr6:146243875C>T c.3643G>A c.(3643-3645)Gag>Aag p.E1215K SKCM 6 146256182 146256182 + Missense_Mutation SNP T T C TCGA-EE-A2MF-06A-11D-A21A-08 TCGA-EE-A2MF-10B-01D-A21A-08 g.chr6:146256182T>C c.2851A>G c.(2851-2853)Aag>Gag p.K951E SKCM 6 146256482 146256482 + Missense_Mutation SNP G G A TCGA-EE-A2MF-06A-11D-A21A-08 TCGA-EE-A2MF-10B-01D-A21A-08 g.chr6:146256482G>A c.2665C>T c.(2665-2667)Cct>Tct p.P889S SKCM 6 146256503 146256503 + Missense_Mutation SNP G G C TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:146256503G>C c.2644C>G c.(2644-2646)Cgg>Ggg p.R882G SKCM 6 146262942 146262942 + Silent SNP G G A TCGA-D3-A3MV-06A-11D-A21A-08 TCGA-D3-A3MV-10A-01D-A21A-08 g.chr6:146262942G>A c.2307C>T c.(2305-2307)atC>atT p.I769I SKCM 6 146264611 146264611 + Silent SNP G G A TCGA-D3-A2JN-06A-11D-A196-08 TCGA-D3-A2JN-10A-01D-A198-08 g.chr6:146264611G>A c.1906C>T c.(1906-1908)Cta>Tta p.L636L SKCM 6 146264734 146264734 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr6:146264734G>A c.1783C>T c.(1783-1785)Ccc>Tcc p.P595S SKCM 6 146266711 146266711 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr6:146266711G>A c.1384C>T c.(1384-1386)Ctt>Ttt p.L462F SKCM 6 146271487 146271487 + Missense_Mutation SNP C C A TCGA-EE-A3J8-06A-11D-A20D-08 TCGA-EE-A3J8-10A-01D-A20D-08 g.chr6:146271487C>A c.895G>T c.(895-897)Gca>Tca p.A299S SKCM 6 146276122 146276122 + Missense_Mutation SNP T T C TCGA-EE-A2MQ-06A-11D-A197-08 TCGA-EE-A2MQ-10A-01D-A199-08 g.chr6:146276122T>C c.337A>G c.(337-339)Aaa>Gaa p.K113E SKCM 6 146276180 146276180 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr6:146276180G>A c.279C>T c.(277-279)tcC>tcT p.S93S

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 6 146239363 146239363 single base substitution T C 3_prime_UTR_variant BLCA-CN 6 146239363 146239363 single base substitution T C downstream_gene_variant BLCA-CN 6 146239363 146239363 single base substitution T C synonymous_variant E1386E 4158A>G BLCA-CN 6 146239363 146239363 single base substitution T C synonymous_variant E1390E 4170A>G BLCA-CN 6 146248331 146248331 single base substitution T A 3_prime_UTR_variant BLCA-CN 6 146248331 146248331 single base substitution T A exon_variant BLCA-CN 6 146248331 146248331 single base substitution T A synonymous_variant S1065S 3195A>T BLCA-CN 6 146248331 146248331 single base substitution T A synonymous_variant S1074S 3222A>T BLCA-CN 6 146264320 146264320 single base substitution C G 3_prime_UTR_variant BLCA-CN 6 146264320 146264320 single base substitution C G downstream_gene_variant BLCA-CN 6 146264320 146264320 single base substitution C G exon_variant BLCA-CN 6 146264320 146264320 single base substitution C G missense_variant E733Q 2197G>C BLCA-CN 6 146264539 146264539 single base substitution C G 3_prime_UTR_variant BLCA-CN 6 146264539 146264539 single base substitution C G downstream_gene_variant BLCA-CN 6 146264539 146264539 single base substitution C G exon_variant BLCA-CN 6 146264539 146264539 single base substitution C G missense_variant E660Q 1978G>C BLCA-CN 6 146273567 146273567 single base substitution C G exon_variant BLCA-CN 6 146273567 146273567 single base substitution C G missense_variant L227F 681G>C BLCA-US 6 146242491 146242491 single base substitution C T 3_prime_UTR_variant BLCA-US 6 146242491 146242491 single base substitution C T exon_variant BLCA-US 6 146242491 146242491 single base substitution C T missense_variant E1274K 3820G>A BLCA-US 6 146242491 146242491 single base substitution C T missense_variant E1278K 3832G>A BLCA-US 6 146256489 146256489 single base substitution C G 3_prime_UTR_variant BLCA-US 6 146256489 146256489 single base substitution C G exon_variant BLCA-US 6 146256489 146256489 single base substitution C G missense_variant K886N 2658G>C BLCA-US 6 146275900 146275900 single base substitution C G exon_variant BLCA-US 6 146275900 146275900 single base substitution C G missense_variant E187Q 559G>C BLCA-US 6 146275900 146275900 single base substitution C G upstream_gene_variant BLCA-US 6 146275906 146275906 single base substitution T C exon_variant BLCA-US 6 146275906 146275906 single base substitution T C missense_variant M185V 553A>G BLCA-US 6 146275906 146275906 single base substitution T C upstream_gene_variant BOCA-FR 6 146261479 146261479 single base substitution C T intron_variant BOCA-FR 6 146261479 146261479 single base substitution C T upstream_gene_variant BRCA-EU 6 146181335 146181335 single base substitution A T downstream_gene_variant BRCA-EU 6 146183951 146183951 insertion of <=200bp - T downstream_gene_variant BRCA-EU 6 146184210 146184210 single base substitution A G downstream_gene_variant BRCA-EU 6 146184990 146184990 single base substitution A G downstream_gene_variant BRCA-EU 6 146185888 146185888 single base substitution C T intron_variant BRCA-EU 6 146186053 146186053 single base substitution C G intron_variant BRCA-EU 6 146186221 146186221 single base substitution C G intron_variant BRCA-EU 6 146188588 146188588 single base substitution C G intron_variant BRCA-EU 6 146189125 146189125 single base substitution G T intron_variant BRCA-EU 6 146190575 146190575 single base substitution C T intron_variant BRCA-EU 6 146190787 146190794 deletion of <=200bp TTTATGGG - intron_variant BRCA-EU 6 146191381 146191381 single base substitution G C intron_variant BRCA-EU 6 146192654 146192654 single base substitution T A intron_variant BRCA-EU 6 146193474 146193474 single base substitution C T intron_variant BRCA-EU 6 146195477 146195477 single base substitution C A intron_variant BRCA-EU 6 146196198 146196198 single base substitution T A intron_variant BRCA-EU 6 146197512 146197512 deletion of <=200bp A - intron_variant BRCA-EU 6 146198445 146198445 single base substitution C G intron_variant BRCA-EU 6 146198905 146198905 single base substitution A T intron_variant BRCA-EU 6 146199337 146199337 single base substitution A G intron_variant BRCA-EU 6 146200663 146200663 single base substitution C T intron_variant BRCA-EU 6 146200911 146200911 single base substitution G A intron_variant BRCA-EU 6 146202103 146202103 single base substitution A C downstream_gene_variant BRCA-EU 6 146202103 146202103 single base substitution A C intron_variant BRCA-EU 6 146202693 146202693 single base substitution C T downstream_gene_variant BRCA-EU 6 146202693 146202693 single base substitution C T intron_variant BRCA-EU 6 146202948 146202948 insertion of <=200bp - G downstream_gene_variant BRCA-EU 6 146202948 146202948 insertion of <=200bp - G intron_variant BRCA-EU 6 146203005 146203009 deletion of <=200bp CGAGG - downstream_gene_variant BRCA-EU 6 146203005 146203009 deletion of <=200bp CGAGG - intron_variant BRCA-EU 6 146203243 146203243 single base substitution G A downstream_gene_variant BRCA-EU 6 146203243 146203243 single base substitution G A intron_variant BRCA-EU 6 146203969 146203969 single base substitution T C downstream_gene_variant BRCA-EU 6 146203969 146203969 single base substitution T C intron_variant BRCA-EU 6 146204119 146204119 single base substitution A G downstream_gene_variant BRCA-EU 6 146204119 146204119 single base substitution A G intron_variant BRCA-EU 6 146205099 146205099 single base substitution A T downstream_gene_variant BRCA-EU 6 146205099 146205099 single base substitution A T intron_variant BRCA-EU 6 146205783 146205783 single base substitution G A downstream_gene_variant BRCA-EU 6 146205783 146205783 single base substitution G A intron_variant BRCA-EU 6 146207231 146207231 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 146207231 146207231 single base substitution C T intron_variant BRCA-EU 6 146207559 146207559 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 146207559 146207559 single base substitution C T intron_variant BRCA-EU 6 146210434 146210434 single base substitution G A intron_variant BRCA-EU 6 146210467 146210467 single base substitution G A intron_variant BRCA-EU 6 146210971 146210971 single base substitution G A intron_variant BRCA-EU 6 146211096 146211096 single base substitution C T intron_variant BRCA-EU 6 146212042 146212042 single base substitution A G intron_variant BRCA-EU 6 146212195 146212195 single base substitution G C intron_variant BRCA-EU 6 146215548 146215548 single base substitution T C intron_variant BRCA-EU 6 146215548 146215548 single base substitution T C upstream_gene_variant BRCA-EU 6 146216362 146216362 single base substitution C T intron_variant BRCA-EU 6 146216362 146216362 single base substitution C T upstream_gene_variant BRCA-EU 6 146218815 146218815 single base substitution C G intron_variant BRCA-EU 6 146218815 146218815 single base substitution C G upstream_gene_variant BRCA-EU 6 146220122 146220122 insertion of <=200bp - T downstream_gene_variant BRCA-EU 6 146220122 146220122 insertion of <=200bp - T intron_variant BRCA-EU 6 146220803 146220803 single base substitution G A downstream_gene_variant BRCA-EU 6 146220803 146220803 single base substitution G A intron_variant BRCA-EU 6 146221889 146221889 single base substitution C T downstream_gene_variant BRCA-EU 6 146221889 146221889 single base substitution C T intron_variant BRCA-EU 6 146224332 146224332 single base substitution T C downstream_gene_variant BRCA-EU 6 146224332 146224332 single base substitution T C intron_variant BRCA-EU 6 146225477 146225477 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 146225477 146225477 single base substitution C T intron_variant BRCA-EU 6 146226501 146226501 single base substitution C G 3_prime_UTR_variant BRCA-EU 6 146226501 146226501 single base substitution C G intron_variant BRCA-EU 6 146226664 146226664 single base substitution A C 3_prime_UTR_variant BRCA-EU 6 146226664 146226664 single base substitution A C intron_variant BRCA-EU 6 146226733 146226733 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 146226733 146226733 single base substitution C T intron_variant BRCA-EU 6 146226957 146226957 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 146226957 146226957 single base substitution C T intron_variant BRCA-EU 6 146227450 146227450 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 146227450 146227450 single base substitution C T intron_variant BRCA-EU 6 146229587 146229587 single base substitution G A 3_prime_UTR_variant BRCA-EU 6 146229587 146229587 single base substitution G A intron_variant BRCA-EU 6 146230167 146230167 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 146230167 146230167 single base substitution C T intron_variant BRCA-EU 6 146230759 146230759 single base substitution C G 3_prime_UTR_variant BRCA-EU 6 146230759 146230759 single base substitution C G intron_variant BRCA-EU 6 146231312 146231312 single base substitution G C 3_prime_UTR_variant BRCA-EU 6 146231312 146231312 single base substitution G C intron_variant BRCA-EU 6 146232363 146232363 single base substitution C G intron_variant BRCA-EU 6 146232411 146232411 single base substitution T C intron_variant BRCA-EU 6 146233403 146233403 insertion of <=200bp - A downstream_gene_variant BRCA-EU 6 146233403 146233403 insertion of <=200bp - A intron_variant BRCA-EU 6 146233703 146233703 single base substitution C G downstream_gene_variant BRCA-EU 6 146233703 146233703 single base substitution C G intron_variant BRCA-EU 6 146237183 146237183 single base substitution C G downstream_gene_variant BRCA-EU 6 146237183 146237183 single base substitution C G intron_variant BRCA-EU 6 146237635 146237635 single base substitution G T downstream_gene_variant BRCA-EU 6 146237635 146237635 single base substitution G T intron_variant BRCA-EU 6 146238808 146238808 single base substitution T C 3_prime_UTR_variant BRCA-EU 6 146238808 146238808 single base substitution T C downstream_gene_variant BRCA-EU 6 146238808 146238808 single base substitution T C intron_variant BRCA-EU 6 146240326 146240326 single base substitution G C exon_variant BRCA-EU 6 146240326 146240326 single base substitution G C intron_variant BRCA-EU 6 146241487 146241487 single base substitution A G intron_variant BRCA-EU 6 146242007 146242032 deletion of <=200bp GTGGAAGATCAAGCTAATAATAGAAT - intron_variant BRCA-EU 6 146242203 146242203 single base substitution A C intron_variant BRCA-EU 6 146244023 146244023 single base substitution C G intron_variant BRCA-EU 6 146245126 146245126 single base substitution A G intron_variant BRCA-EU 6 146249400 146249400 single base substitution A T intron_variant BRCA-EU 6 146249400 146249400 single base substitution A T upstream_gene_variant BRCA-EU 6 146250304 146250304 deletion of <=200bp A - intron_variant BRCA-EU 6 146250304 146250304 deletion of <=200bp A - upstream_gene_variant BRCA-EU 6 146250740 146250740 single base substitution A G intron_variant BRCA-EU 6 146250740 146250740 single base substitution A G upstream_gene_variant BRCA-EU 6 146251998 146251998 single base substitution C T downstream_gene_variant BRCA-EU 6 146251998 146251998 single base substitution C T intron_variant BRCA-EU 6 146251998 146251998 single base substitution C T upstream_gene_variant BRCA-EU 6 146252453 146252453 deletion of <=200bp T - downstream_gene_variant BRCA-EU 6 146252453 146252453 deletion of <=200bp T - intron_variant BRCA-EU 6 146252453 146252453 deletion of <=200bp T - upstream_gene_variant BRCA-EU 6 146252724 146252724 single base substitution G A downstream_gene_variant BRCA-EU 6 146252724 146252724 single base substitution G A intron_variant BRCA-EU 6 146252724 146252724 single base substitution G A upstream_gene_variant BRCA-EU 6 146253204 146253204 single base substitution A G downstream_gene_variant BRCA-EU 6 146253204 146253204 single base substitution A G intron_variant BRCA-EU 6 146253204 146253204 single base substitution A G upstream_gene_variant BRCA-EU 6 146253604 146253604 single base substitution T C downstream_gene_variant BRCA-EU 6 146253604 146253604 single base substitution T C intron_variant BRCA-EU 6 146254065 146254065 single base substitution C G downstream_gene_variant BRCA-EU 6 146254065 146254065 single base substitution C G intron_variant BRCA-EU 6 146254776 146254776 single base substitution C A downstream_gene_variant BRCA-EU 6 146254776 146254776 single base substitution C A intron_variant BRCA-EU 6 146258883 146258883 single base substitution C T intron_variant BRCA-EU 6 146258883 146258883 single base substitution C T upstream_gene_variant BRCA-EU 6 146261303 146261303 single base substitution C G intron_variant BRCA-EU 6 146261303 146261303 single base substitution C G upstream_gene_variant BRCA-EU 6 146261880 146261880 single base substitution G C 3_prime_UTR_variant BRCA-EU 6 146261880 146261880 single base substitution G C downstream_gene_variant BRCA-EU 6 146261880 146261880 single base substitution G C exon_variant BRCA-EU 6 146261880 146261880 single base substitution G C missense_variant P850A 2548C>G BRCA-EU 6 146261880 146261880 single base substitution G C upstream_gene_variant BRCA-EU 6 146262325 146262325 single base substitution T C downstream_gene_variant BRCA-EU 6 146262325 146262325 single base substitution T C intron_variant BRCA-EU 6 146263093 146263093 single base substitution A G downstream_gene_variant BRCA-EU 6 146263093 146263093 single base substitution A G intron_variant BRCA-EU 6 146265684 146265684 single base substitution G A downstream_gene_variant BRCA-EU 6 146265684 146265684 single base substitution G A intron_variant BRCA-EU 6 146266032 146266032 insertion of <=200bp - A downstream_gene_variant BRCA-EU 6 146266032 146266032 insertion of <=200bp - A intron_variant BRCA-EU 6 146267678 146267678 single base substitution T G intron_variant BRCA-EU 6 146267930 146267930 single base substitution T A intron_variant BRCA-EU 6 146269928 146269928 single base substitution T C intron_variant BRCA-EU 6 146270213 146270213 single base substitution G A intron_variant BRCA-EU 6 146270222 146270222 deletion of <=200bp A - intron_variant BRCA-EU 6 146270226 146270226 single base substitution A G intron_variant BRCA-EU 6 146270450 146270450 single base substitution T C intron_variant BRCA-EU 6 146270956 146270956 deletion of <=200bp A - intron_variant BRCA-EU 6 146271348 146271348 single base substitution C G intron_variant BRCA-EU 6 146272367 146272367 single base substitution C T intron_variant BRCA-EU 6 146272785 146272785 single base substitution G A intron_variant BRCA-EU 6 146274045 146274045 single base substitution C A intron_variant BRCA-EU 6 146274881 146274881 single base substitution C T intron_variant BRCA-EU 6 146275923 146275923 single base substitution G A exon_variant BRCA-EU 6 146275923 146275923 single base substitution G A missense_variant S179L 536C>T BRCA-EU 6 146275923 146275923 single base substitution G A upstream_gene_variant BRCA-EU 6 146277468 146277468 single base substitution C G intron_variant BRCA-EU 6 146277468 146277468 single base substitution C G upstream_gene_variant BRCA-EU 6 146278428 146278428 deletion of <=200bp A - intron_variant BRCA-EU 6 146278428 146278428 deletion of <=200bp A - upstream_gene_variant BRCA-EU 6 146278724 146278724 single base substitution A T intron_variant BRCA-EU 6 146278724 146278724 single base substitution A T upstream_gene_variant BRCA-EU 6 146278726 146278726 single base substitution A T intron_variant BRCA-EU 6 146278726 146278726 single base substitution A T upstream_gene_variant BRCA-EU 6 146279896 146279896 single base substitution T C intron_variant BRCA-EU 6 146279896 146279896 single base substitution T C upstream_gene_variant BRCA-EU 6 146280016 146280016 single base substitution T C intron_variant BRCA-EU 6 146280016 146280016 single base substitution T C upstream_gene_variant BRCA-EU 6 146280445 146280445 single base substitution T G intron_variant BRCA-EU 6 146280445 146280445 single base substitution T G upstream_gene_variant BRCA-EU 6 146281026 146281026 single base substitution C T intron_variant BRCA-EU 6 146281026 146281026 single base substitution C T upstream_gene_variant BRCA-EU 6 146281056 146281056 single base substitution G C intron_variant BRCA-EU 6 146281056 146281056 single base substitution G C upstream_gene_variant BRCA-EU 6 146281209 146281209 single base substitution T C intron_variant BRCA-EU 6 146281209 146281209 single base substitution T C upstream_gene_variant BRCA-EU 6 146281663 146281664 deletion of <=200bp AG - intron_variant BRCA-EU 6 146282719 146282719 single base substitution G A intron_variant BRCA-EU 6 146283123 146283123 single base substitution C G intron_variant BRCA-EU 6 146283484 146283484 single base substitution C T intron_variant BRCA-EU 6 146283678 146283678 single base substitution G A intron_variant BRCA-EU 6 146283687 146283687 single base substitution G C intron_variant BRCA-EU 6 146283708 146283708 single base substitution A G intron_variant BRCA-EU 6 146284087 146284087 single base substitution T G intron_variant BRCA-EU 6 146284868 146284868 single base substitution C T intron_variant BRCA-EU 6 146284868 146284868 single base substitution C T splice_region_variant BRCA-EU 6 146285009 146285009 single base substitution G A 5_prime_UTR_variant BRCA-EU 6 146285009 146285009 single base substitution G A intron_variant BRCA-EU 6 146286755 146286755 single base substitution G T upstream_gene_variant BRCA-EU 6 146286784 146286784 single base substitution G T upstream_gene_variant BRCA-FR 6 146185760 146185760 single base substitution G T intron_variant BRCA-FR 6 146186053 146186053 single base substitution C G intron_variant BRCA-FR 6 146188588 146188588 single base substitution C G intron_variant BRCA-FR 6 146189125 146189125 single base substitution G T intron_variant BRCA-FR 6 146196198 146196198 single base substitution T A intron_variant BRCA-FR 6 146197017 146197017 single base substitution C T intron_variant BRCA-FR 6 146198445 146198445 single base substitution C G intron_variant BRCA-FR 6 146203969 146203969 single base substitution T C downstream_gene_variant BRCA-FR 6 146203969 146203969 single base substitution T C intron_variant BRCA-FR 6 146205099 146205099 single base substitution A T downstream_gene_variant BRCA-FR 6 146205099 146205099 single base substitution A T intron_variant BRCA-FR 6 146210467 146210467 single base substitution G A intron_variant BRCA-FR 6 146225477 146225477 single base substitution C T 3_prime_UTR_variant BRCA-FR 6 146225477 146225477 single base substitution C T intron_variant BRCA-FR 6 146232363 146232363 single base substitution C G intron_variant BRCA-FR 6 146238516 146238516 single base substitution C T 3_prime_UTR_variant BRCA-FR 6 146238516 146238516 single base substitution C T downstream_gene_variant BRCA-FR 6 146238516 146238516 single base substitution C T intron_variant BRCA-FR 6 146242203 146242203 single base substitution A C intron_variant BRCA-FR 6 146251968 146251968 single base substitution G A downstream_gene_variant BRCA-FR 6 146251968 146251968 single base substitution G A intron_variant BRCA-FR 6 146251968 146251968 single base substitution G A upstream_gene_variant BRCA-FR 6 146254776 146254776 single base substitution C A downstream_gene_variant BRCA-FR 6 146254776 146254776 single base substitution C A intron_variant BRCA-FR 6 146272367 146272367 single base substitution C T intron_variant BRCA-FR 6 146283123 146283123 single base substitution C G intron_variant BRCA-FR 6 146283484 146283484 single base substitution C T intron_variant BRCA-UK 6 146192355 146192355 single base substitution G A intron_variant BRCA-UK 6 146202056 146202056 single base substitution C G downstream_gene_variant BRCA-UK 6 146202056 146202056 single base substitution C G intron_variant BRCA-UK 6 146238763 146238763 single base substitution C G 3_prime_UTR_variant BRCA-UK 6 146238763 146238763 single base substitution C G downstream_gene_variant BRCA-UK 6 146238763 146238763 single base substitution C G intron_variant BRCA-UK 6 146260013 146260013 single base substitution C G intron_variant BRCA-UK 6 146260013 146260013 single base substitution C G upstream_gene_variant BRCA-UK 6 146264599 146264599 single base substitution C T 3_prime_UTR_variant BRCA-UK 6 146264599 146264599 single base substitution C T downstream_gene_variant BRCA-UK 6 146264599 146264599 single base substitution C T exon_variant BRCA-UK 6 146264599 146264599 single base substitution C T missense_variant D640N 1918G>A BRCA-US 6 146240555 146240555 single base substitution G A 3_prime_UTR_variant BRCA-US 6 146240555 146240555 single base substitution G A exon_variant BRCA-US 6 146240555 146240555 single base substitution G A stop_gained R1361* 4081C>T BRCA-US 6 146240555 146240555 single base substitution G A stop_gained R1365* 4093C>T BRCA-US 6 146242419 146242419 single base substitution C G 3_prime_UTR_variant BRCA-US 6 146242419 146242419 single base substitution C G exon_variant BRCA-US 6 146242419 146242419 single base substitution C G missense_variant E1298Q 3892G>C BRCA-US 6 146242419 146242419 single base substitution C G missense_variant E1302Q 3904G>C BRCA-US 6 146247363 146247363 single base substitution G A 3_prime_UTR_variant BRCA-US 6 146247363 146247363 single base substitution G A exon_variant BRCA-US 6 146247363 146247363 single base substitution G A missense_variant R1091C 3271C>T BRCA-US 6 146247363 146247363 single base substitution G A missense_variant R1100C 3298C>T BRCA-US 6 146256180 146256180 single base substitution C T 3_prime_UTR_variant BRCA-US 6 146256180 146256180 single base substitution C T exon_variant BRCA-US 6 146256180 146256180 single base substitution C T synonymous_variant K951K 2853G>A BRCA-US 6 146256486 146256486 single base substitution C T 3_prime_UTR_variant BRCA-US 6 146256486 146256486 single base substitution C T exon_variant BRCA-US 6 146256486 146256486 single base substitution C T synonymous_variant K887K 2661G>A BRCA-US 6 146262775 146262775 insertion of <=200bp - C 3_prime_UTR_variant BRCA-US 6 146262775 146262775 insertion of <=200bp - C downstream_gene_variant BRCA-US 6 146262775 146262775 insertion of <=200bp - C exon_variant BRCA-US 6 146262775 146262775 insertion of <=200bp - C frameshift_variant E825E? BRCA-US 6 146264518 146264518 single base substitution C T 3_prime_UTR_variant BRCA-US 6 146264518 146264518 single base substitution C T downstream_gene_variant BRCA-US 6 146264518 146264518 single base substitution C T exon_variant BRCA-US 6 146264518 146264518 single base substitution C T missense_variant D667N 1999G>A BRCA-US 6 146268666 146268666 single base substitution C T 3_prime_UTR_variant BRCA-US 6 146268666 146268666 single base substitution C T exon_variant BRCA-US 6 146268666 146268666 single base substitution C T missense_variant R392Q 1175G>A BRCA-US 6 146275931 146275931 single base substitution C T exon_variant BRCA-US 6 146275931 146275931 single base substitution C T synonymous_variant L176L 528G>A BRCA-US 6 146275931 146275931 single base substitution C T upstream_gene_variant BRCA-US 6 146276233 146276233 single base substitution C G exon_variant BRCA-US 6 146276233 146276233 single base substitution C G intron_variant BRCA-US 6 146276233 146276233 single base substitution C G missense_variant V76L 226G>C BRCA-US 6 146276233 146276233 single base substitution C G upstream_gene_variant BRCA-US 6 146276419 146276419 single base substitution C T exon_variant BRCA-US 6 146276419 146276419 single base substitution C T missense_variant D14N 40G>A BRCA-US 6 146276419 146276419 single base substitution C T upstream_gene_variant BRCA-US 6 146276436 146276436 single base substitution G A exon_variant BRCA-US 6 146276436 146276436 single base substitution G A missense_variant A8V 23C>T BRCA-US 6 146276436 146276436 single base substitution G A upstream_gene_variant BRCA-US 6 146276440 146276440 single base substitution G C exon_variant BRCA-US 6 146276440 146276440 single base substitution G C missense_variant R7G 19C>G BRCA-US 6 146276440 146276440 single base substitution G C upstream_gene_variant BTCA-JP 6 146214367 146214367 single base substitution G A stop_gained R1620* 4858C>T BTCA-JP 6 146214367 146214367 single base substitution G A stop_gained R1624* 4870C>T BTCA-JP 6 146214367 146214367 single base substitution G A stop_gained R42* 124C>T BTCA-JP 6 146242689 146242689 single base substitution T A intron_variant BTCA-JP 6 146243485 146243485 single base substitution C T splice_acceptor_variant BTCA-JP 6 146256021 146256021 deletion of <=200bp A - downstream_gene_variant BTCA-JP 6 146256021 146256021 deletion of <=200bp A - intron_variant BTCA-JP 6 146267320 146267320 single base substitution G T intron_variant BTCA-JP 6 146269483 146269483 single base substitution C T 3_prime_UTR_variant BTCA-JP 6 146269483 146269483 single base substitution C T exon_variant BTCA-JP 6 146269483 146269483 single base substitution C T missense_variant S329N 986G>A BTCA-JP 6 146273082 146273082 single base substitution T A intron_variant BTCA-JP 6 146275907 146275907 single base substitution T C exon_variant BTCA-JP 6 146275907 146275907 single base substitution T C synonymous_variant E184E 552A>G BTCA-JP 6 146275907 146275907 single base substitution T C upstream_gene_variant BTCA-JP 6 146275990 146275990 single base substitution C T exon_variant BTCA-JP 6 146275990 146275990 single base substitution C T missense_variant G157S 469G>A BTCA-JP 6 146275990 146275990 single base substitution C T splice_acceptor_variant BTCA-JP 6 146275990 146275990 single base substitution C T upstream_gene_variant BTCA-JP 6 146276440 146276440 single base substitution G A exon_variant BTCA-JP 6 146276440 146276440 single base substitution G A missense_variant R7C 19C>T BTCA-JP 6 146276440 146276440 single base substitution G A upstream_gene_variant CESC-US 6 146256116 146256116 single base substitution G A 3_prime_UTR_variant CESC-US 6 146256116 146256116 single base substitution G A exon_variant CESC-US 6 146256116 146256116 single base substitution G A missense_variant P973S 2917C>T CESC-US 6 146264850 146264850 single base substitution G A 3_prime_UTR_variant CESC-US 6 146264850 146264850 single base substitution G A downstream_gene_variant CESC-US 6 146264850 146264850 single base substitution G A exon_variant CESC-US 6 146264850 146264850 single base substitution G A missense_variant S556F 1667C>T CESC-US 6 146275945 146275945 single base substitution C T exon_variant CESC-US 6 146275945 146275945 single base substitution C T missense_variant D172N 514G>A CESC-US 6 146275945 146275945 single base substitution C T upstream_gene_variant CLLE-ES 6 146186621 146186621 single base substitution T G intron_variant CLLE-ES 6 146190049 146190049 single base substitution A T intron_variant CLLE-ES 6 146195981 146195981 single base substitution G C intron_variant CLLE-ES 6 146219689 146219689 single base substitution T G downstream_gene_variant CLLE-ES 6 146219689 146219689 single base substitution T G intron_variant CLLE-ES 6 146264389 146264389 single base substitution T C 3_prime_UTR_variant CLLE-ES 6 146264389 146264389 single base substitution T C downstream_gene_variant CLLE-ES 6 146264389 146264389 single base substitution T C exon_variant CLLE-ES 6 146264389 146264389 single base substitution T C missense_variant M710V 2128A>G CLLE-ES 6 146269535 146269535 single base substitution C T intron_variant CLLE-ES 6 146274965 146274965 single base substitution A C intron_variant CLLE-ES 6 146275272 146275272 single base substitution G A intron_variant COAD-US 6 146214532 146214532 deletion of <=200bp A - splice_region_variant COAD-US 6 146214532 146214532 deletion of <=200bp A - upstream_gene_variant COAD-US 6 146240543 146240543 single base substitution G A 3_prime_UTR_variant COAD-US 6 146240543 146240543 single base substitution G A exon_variant COAD-US 6 146240543 146240543 single base substitution G A missense_variant R1365C 4093C>T COAD-US 6 146240543 146240543 single base substitution G A missense_variant R1369C 4105C>T COAD-US 6 146242529 146242529 single base substitution C G splice_acceptor_variant COAD-US 6 146248324 146248324 single base substitution C A splice_donor_variant COAD-US 6 146261868 146261869 deletion of <=200bp CT - 3_prime_UTR_variant COAD-US 6 146261868 146261869 deletion of <=200bp CT - downstream_gene_variant COAD-US 6 146261868 146261869 deletion of <=200bp CT - exon_variant COAD-US 6 146261868 146261869 deletion of <=200bp CT - frameshift_variant RG853 COAD-US 6 146261868 146261869 deletion of <=200bp CT - upstream_gene_variant COAD-US 6 146262867 146262867 single base substitution G A 3_prime_UTR_variant COAD-US 6 146262867 146262867 single base substitution G A downstream_gene_variant COAD-US 6 146262867 146262867 single base substitution G A exon_variant COAD-US 6 146262867 146262867 single base substitution G A synonymous_variant R794R 2382C>T COAD-US 6 146262964 146262964 deletion of <=200bp A - 3_prime_UTR_variant COAD-US 6 146262964 146262964 deletion of <=200bp A - downstream_gene_variant COAD-US 6 146262964 146262964 deletion of <=200bp A - exon_variant COAD-US 6 146262964 146262964 deletion of <=200bp A - frameshift_variant L762 COAD-US 6 146264800 146264800 single base substitution G A 3_prime_UTR_variant COAD-US 6 146264800 146264800 single base substitution G A downstream_gene_variant COAD-US 6 146264800 146264800 single base substitution G A exon_variant COAD-US 6 146264800 146264800 single base substitution G A missense_variant R573C 1717C>T COAD-US 6 146266724 146266724 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 6 146266724 146266724 deletion of <=200bp T - exon_variant COAD-US 6 146266724 146266724 deletion of <=200bp T - frameshift_variant K457 COAD-US 6 146275963 146275963 insertion of <=200bp - T exon_variant COAD-US 6 146275963 146275963 insertion of <=200bp - T frameshift_variant E166E? COAD-US 6 146275963 146275963 insertion of <=200bp - T upstream_gene_variant COAD-US 6 146276213 146276213 single base substitution T C exon_variant COAD-US 6 146276213 146276213 single base substitution T C intron_variant COAD-US 6 146276213 146276213 single base substitution T C synonymous_variant P82P 246A>G COAD-US 6 146276213 146276213 single base substitution T C upstream_gene_variant COCA-CN 6 146183579 146183579 single base substitution A C downstream_gene_variant COCA-CN 6 146183582 146183582 single base substitution C A downstream_gene_variant COCA-CN 6 146186079 146186079 single base substitution T A intron_variant COCA-CN 6 146207996 146207996 single base substitution G A intron_variant COCA-CN 6 146214370 146214370 single base substitution G A missense_variant H1619Y 4855C>T COCA-CN 6 146214370 146214370 single base substitution G A missense_variant H1623Y 4867C>T COCA-CN 6 146214370 146214370 single base substitution G A missense_variant H41Y 121C>T COCA-CN 6 146229365 146229365 single base substitution G C 3_prime_UTR_variant COCA-CN 6 146229365 146229365 single base substitution G C intron_variant COCA-CN 6 146244128 146244128 single base substitution A G intron_variant COCA-CN 6 146244810 146244810 single base substitution G A 3_prime_UTR_variant COCA-CN 6 146244810 146244810 single base substitution G A exon_variant COCA-CN 6 146244810 146244810 single base substitution G A stop_gained Q1172* 3514C>T COCA-CN 6 146244810 146244810 single base substitution G A stop_gained Q1181* 3541C>T COCA-CN 6 146245833 146245833 single base substitution C A intron_variant COCA-CN 6 146248863 146248863 single base substitution C T intron_variant COCA-CN 6 146248863 146248863 single base substitution C T upstream_gene_variant COCA-CN 6 146256486 146256486 single base substitution C A 3_prime_UTR_variant COCA-CN 6 146256486 146256486 single base substitution C A exon_variant COCA-CN 6 146256486 146256486 single base substitution C A missense_variant K887N 2661G>T COCA-CN 6 146262640 146262640 single base substitution T G downstream_gene_variant COCA-CN 6 146262640 146262640 single base substitution T G intron_variant COCA-CN 6 146264717 146264717 single base substitution G A 3_prime_UTR_variant COCA-CN 6 146264717 146264717 single base substitution G A downstream_gene_variant COCA-CN 6 146264717 146264717 single base substitution G A exon_variant COCA-CN 6 146264717 146264717 single base substitution G A synonymous_variant H600H 1800C>T COCA-CN 6 146264765 146264765 single base substitution T C 3_prime_UTR_variant COCA-CN 6 146264765 146264765 single base substitution T C downstream_gene_variant COCA-CN 6 146264765 146264765 single base substitution T C exon_variant COCA-CN 6 146264765 146264765 single base substitution T C synonymous_variant T584T 1752A>G COCA-CN 6 146266422 146266422 single base substitution G A downstream_gene_variant COCA-CN 6 146266422 146266422 single base substitution G A intron_variant COCA-CN 6 146268882 146268882 single base substitution C A intron_variant COCA-CN 6 146273685 146273685 single base substitution G T intron_variant COCA-CN 6 146276062 146276062 single base substitution A C exon_variant COCA-CN 6 146276062 146276062 single base substitution A C intron_variant COCA-CN 6 146276062 146276062 single base substitution A C missense_variant F133V 397T>G COCA-CN 6 146276062 146276062 single base substitution A C upstream_gene_variant EOPC-DE 6 146254179 146254179 single base substitution C G downstream_gene_variant EOPC-DE 6 146254179 146254179 single base substitution C G intron_variant EOPC-DE 6 146254179 146254179 single base substitution C G splice_region_variant ESAD-UK 6 146180681 146180681 single base substitution C T downstream_gene_variant ESAD-UK 6 146180737 146180737 single base substitution C A downstream_gene_variant ESAD-UK 6 146183579 146183579 single base substitution A G downstream_gene_variant ESAD-UK 6 146184512 146184512 single base substitution A T downstream_gene_variant ESAD-UK 6 146190345 146190345 single base substitution G T intron_variant ESAD-UK 6 146192625 146192625 single base substitution G C intron_variant ESAD-UK 6 146193483 146193483 deletion of <=200bp A - intron_variant ESAD-UK 6 146193666 146193666 deletion of <=200bp A - intron_variant ESAD-UK 6 146194103 146194103 single base substitution A C intron_variant ESAD-UK 6 146194140 146194140 single base substitution C T intron_variant ESAD-UK 6 146194180 146194180 single base substitution G C intron_variant ESAD-UK 6 146194483 146194484 deletion of <=200bp TA - intron_variant ESAD-UK 6 146194581 146194581 single base substitution A G intron_variant ESAD-UK 6 146195769 146195769 single base substitution T G intron_variant ESAD-UK 6 146197581 146197581 single base substitution T C intron_variant ESAD-UK 6 146199413 146199413 single base substitution G A intron_variant ESAD-UK 6 146199694 146199694 single base substitution C G intron_variant ESAD-UK 6 146200589 146200589 single base substitution C A intron_variant ESAD-UK 6 146204764 146204764 single base substitution T C downstream_gene_variant ESAD-UK 6 146204764 146204764 single base substitution T C intron_variant ESAD-UK 6 146207972 146207972 single base substitution C A intron_variant ESAD-UK 6 146208957 146208957 single base substitution T C intron_variant ESAD-UK 6 146209237 146209237 single base substitution C T splice_acceptor_variant ESAD-UK 6 146209498 146209498 single base substitution G A intron_variant ESAD-UK 6 146212220 146212220 single base substitution A G intron_variant ESAD-UK 6 146212499 146212499 single base substitution T G intron_variant ESAD-UK 6 146212533 146212533 single base substitution G A intron_variant ESAD-UK 6 146212911 146212911 single base substitution T C intron_variant ESAD-UK 6 146213807 146213807 single base substitution C A intron_variant ESAD-UK 6 146213968 146213968 single base substitution C T intron_variant ESAD-UK 6 146214654 146214654 single base substitution T G intron_variant ESAD-UK 6 146214654 146214654 single base substitution T G upstream_gene_variant ESAD-UK 6 146214686 146214686 single base substitution A T intron_variant ESAD-UK 6 146214686 146214686 single base substitution A T upstream_gene_variant ESAD-UK 6 146215210 146215210 single base substitution G T intron_variant ESAD-UK 6 146215210 146215210 single base substitution G T upstream_gene_variant ESAD-UK 6 146216691 146216691 single base substitution C G intron_variant ESAD-UK 6 146216691 146216691 single base substitution C G upstream_gene_variant ESAD-UK 6 146219469 146219469 single base substitution A G downstream_gene_variant ESAD-UK 6 146219469 146219469 single base substitution A G intron_variant ESAD-UK 6 146219469 146219469 single base substitution A G upstream_gene_variant ESAD-UK 6 146219673 146219673 single base substitution G A downstream_gene_variant ESAD-UK 6 146219673 146219673 single base substitution G A intron_variant ESAD-UK 6 146220296 146220296 single base substitution C T downstream_gene_variant ESAD-UK 6 146220296 146220296 single base substitution C T intron_variant ESAD-UK 6 146221167 146221167 single base substitution G A downstream_gene_variant ESAD-UK 6 146221167 146221167 single base substitution G A intron_variant ESAD-UK 6 146224402 146224402 single base substitution T A 3_prime_UTR_variant ESAD-UK 6 146224402 146224402 single base substitution T A intron_variant ESAD-UK 6 146224721 146224721 single base substitution C A 3_prime_UTR_variant ESAD-UK 6 146224721 146224721 single base substitution C A intron_variant ESAD-UK 6 146225830 146225830 single base substitution T C 3_prime_UTR_variant ESAD-UK 6 146225830 146225830 single base substitution T C intron_variant ESAD-UK 6 146226141 146226141 single base substitution G A 3_prime_UTR_variant ESAD-UK 6 146226141 146226141 single base substitution G A intron_variant ESAD-UK 6 146226159 146226159 single base substitution G A 3_prime_UTR_variant ESAD-UK 6 146226159 146226159 single base substitution G A intron_variant ESAD-UK 6 146230835 146230835 single base substitution C A 3_prime_UTR_variant ESAD-UK 6 146230835 146230835 single base substitution C A intron_variant ESAD-UK 6 146233669 146233669 single base substitution C T downstream_gene_variant ESAD-UK 6 146233669 146233669 single base substitution C T intron_variant ESAD-UK 6 146235484 146235484 single base substitution C T downstream_gene_variant ESAD-UK 6 146235484 146235484 single base substitution C T intron_variant ESAD-UK 6 146236302 146236302 single base substitution T C downstream_gene_variant ESAD-UK 6 146236302 146236302 single base substitution T C intron_variant ESAD-UK 6 146237845 146237845 single base substitution T G downstream_gene_variant ESAD-UK 6 146237845 146237845 single base substitution T G intron_variant ESAD-UK 6 146237950 146237950 single base substitution G A downstream_gene_variant ESAD-UK 6 146237950 146237950 single base substitution G A intron_variant ESAD-UK 6 146238979 146238979 single base substitution C T 3_prime_UTR_variant ESAD-UK 6 146238979 146238979 single base substitution C T downstream_gene_variant ESAD-UK 6 146238979 146238979 single base substitution C T intron_variant ESAD-UK 6 146241187 146241187 single base substitution T C intron_variant ESAD-UK 6 146242258 146242258 single base substitution A C intron_variant ESAD-UK 6 146242425 146242425 single base substitution C A 3_prime_UTR_variant ESAD-UK 6 146242425 146242425 single base substitution C A exon_variant ESAD-UK 6 146242425 146242425 single base substitution C A stop_gained E1296* 3886G>T ESAD-UK 6 146242425 146242425 single base substitution C A stop_gained E1300* 3898G>T ESAD-UK 6 146244027 146244027 single base substitution T G intron_variant ESAD-UK 6 146244679 146244679 deletion of <=200bp A - intron_variant ESAD-UK 6 146245970 146245970 single base substitution G A 3_prime_UTR_variant ESAD-UK 6 146245970 146245970 single base substitution G A exon_variant ESAD-UK 6 146245970 146245970 single base substitution G A stop_gained R1103* 3307C>T ESAD-UK 6 146245970 146245970 single base substitution G A stop_gained R1112* 3334C>T ESAD-UK 6 146248107 146248107 single base substitution C A intron_variant ESAD-UK 6 146250718 146250718 single base substitution A C intron_variant ESAD-UK 6 146250718 146250718 single base substitution A C upstream_gene_variant ESAD-UK 6 146250803 146250803 single base substitution C T intron_variant ESAD-UK 6 146250803 146250803 single base substitution C T upstream_gene_variant ESAD-UK 6 146251641 146251641 single base substitution G T downstream_gene_variant ESAD-UK 6 146251641 146251641 single base substitution G T intron_variant ESAD-UK 6 146251641 146251641 single base substitution G T upstream_gene_variant ESAD-UK 6 146253869 146253869 single base substitution T G downstream_gene_variant ESAD-UK 6 146253869 146253869 single base substitution T G intron_variant ESAD-UK 6 146254110 146254110 single base substitution A C downstream_gene_variant ESAD-UK 6 146254110 146254110 single base substitution A C intron_variant ESAD-UK 6 146254438 146254438 deletion of <=200bp T - downstream_gene_variant ESAD-UK 6 146254438 146254438 deletion of <=200bp T - intron_variant ESAD-UK 6 146254438 146254438 insertion of <=200bp - T downstream_gene_variant ESAD-UK 6 146254438 146254438 insertion of <=200bp - T intron_variant ESAD-UK 6 146255112 146255112 single base substitution G C downstream_gene_variant ESAD-UK 6 146255112 146255112 single base substitution G C intron_variant ESAD-UK 6 146255421 146255421 single base substitution G A downstream_gene_variant ESAD-UK 6 146255421 146255421 single base substitution G A intron_variant ESAD-UK 6 146258178 146258178 single base substitution G A intron_variant ESAD-UK 6 146258178 146258178 single base substitution G A upstream_gene_variant ESAD-UK 6 146258960 146258960 single base substitution C G intron_variant ESAD-UK 6 146258960 146258960 single base substitution C G upstream_gene_variant ESAD-UK 6 146261303 146261303 single base substitution C G intron_variant ESAD-UK 6 146261303 146261303 single base substitution C G upstream_gene_variant ESAD-UK 6 146262447 146262447 single base substitution T A downstream_gene_variant ESAD-UK 6 146262447 146262447 single base substitution T A intron_variant ESAD-UK 6 146265486 146265486 single base substitution C T downstream_gene_variant ESAD-UK 6 146265486 146265486 single base substitution C T intron_variant ESAD-UK 6 146266627 146266627 single base substitution A G 3_prime_UTR_variant ESAD-UK 6 146266627 146266627 single base substitution A G downstream_gene_variant ESAD-UK 6 146266627 146266627 single base substitution A G exon_variant ESAD-UK 6 146266627 146266627 single base substitution A G synonymous_variant L490L 1468T>C ESAD-UK 6 146267870 146267870 deletion of <=200bp A - intron_variant ESAD-UK 6 146269084 146269084 single base substitution C T intron_variant ESAD-UK 6 146270222 146270222 deletion of <=200bp A - intron_variant ESAD-UK 6 146270497 146270497 single base substitution C A intron_variant ESAD-UK 6 146270725 146270725 single base substitution G C intron_variant ESAD-UK 6 146272376 146272376 single base substitution G A intron_variant ESAD-UK 6 146273940 146273940 single base substitution A T intron_variant ESAD-UK 6 146276166 146276166 single base substitution T A exon_variant ESAD-UK 6 146276166 146276166 single base substitution T A intron_variant ESAD-UK 6 146276166 146276166 single base substitution T A missense_variant K98M 293A>T ESAD-UK 6 146276166 146276166 single base substitution T A upstream_gene_variant ESAD-UK 6 146276557 146276557 single base substitution G A intron_variant ESAD-UK 6 146276557 146276557 single base substitution G A upstream_gene_variant ESAD-UK 6 146277089 146277089 insertion of <=200bp - T intron_variant ESAD-UK 6 146277089 146277089 insertion of <=200bp - T upstream_gene_variant ESAD-UK 6 146277095 146277095 insertion of <=200bp - G intron_variant ESAD-UK 6 146277095 146277095 insertion of <=200bp - G upstream_gene_variant ESAD-UK 6 146277191 146277191 single base substitution A C intron_variant ESAD-UK 6 146277191 146277191 single base substitution A C upstream_gene_variant ESAD-UK 6 146277383 146277383 single base substitution T G intron_variant ESAD-UK 6 146277383 146277383 single base substitution T G upstream_gene_variant ESAD-UK 6 146277837 146277837 single base substitution T G intron_variant ESAD-UK 6 146277837 146277837 single base substitution T G upstream_gene_variant ESAD-UK 6 146277943 146277943 single base substitution A C intron_variant ESAD-UK 6 146277943 146277943 single base substitution A C upstream_gene_variant ESAD-UK 6 146279264 146279264 single base substitution A T intron_variant ESAD-UK 6 146279264 146279264 single base substitution A T upstream_gene_variant ESAD-UK 6 146281443 146281443 single base substitution C T intron_variant ESAD-UK 6 146282525 146282525 single base substitution C G intron_variant ESAD-UK 6 146284569 146284569 single base substitution A G intron_variant ESAD-UK 6 146285732 146285732 single base substitution G A upstream_gene_variant ESAD-UK 6 146288620 146288620 insertion of <=200bp - A upstream_gene_variant ESAD-UK 6 146288664 146288664 single base substitution T C upstream_gene_variant ESAD-UK 6 146288928 146288928 single base substitution T C upstream_gene_variant ESCA-CN 6 146207871 146207871 single base substitution C G intron_variant ESCA-CN 6 146207871 146207871 single base substitution C G missense_variant D1670H 5008G>C ESCA-CN 6 146207871 146207871 single base substitution C G missense_variant D1674H 5020G>C ESCA-CN 6 146244012 146244012 single base substitution G A intron_variant ESCA-CN 6 146254100 146254100 insertion of <=200bp - C downstream_gene_variant ESCA-CN 6 146254100 146254100 insertion of <=200bp - C intron_variant ESCA-CN 6 146256313 146256313 single base substitution C A intron_variant ESCA-CN 6 146273459 146273459 single base substitution A G intron_variant GBM-US 6 146215353 146215353 single base substitution A G missense_variant I1543T 4628T>C GBM-US 6 146215353 146215353 single base substitution A G missense_variant I1547T 4640T>C GBM-US 6 146215353 146215353 single base substitution A G upstream_gene_variant GBM-US 6 146269445 146269445 single base substitution C T 3_prime_UTR_variant GBM-US 6 146269445 146269445 single base substitution C T exon_variant GBM-US 6 146269445 146269445 single base substitution C T missense_variant E342K 1024G>A KIRC-US 6 146273498 146273498 single base substitution A T exon_variant KIRC-US 6 146273498 146273498 single base substitution A T missense_variant N250K 750T>A KIRP-US 6 146234630 146234630 single base substitution C G 3_prime_UTR_variant KIRP-US 6 146234630 146234630 single base substitution C G downstream_gene_variant KIRP-US 6 146234630 146234630 single base substitution C G missense_variant R1437P 4310G>C KIRP-US 6 146234630 146234630 single base substitution C G missense_variant R1441P 4322G>C KIRP-US 6 146264642 146264642 deletion of <=200bp T - 3_prime_UTR_variant KIRP-US 6 146264642 146264642 deletion of <=200bp T - downstream_gene_variant KIRP-US 6 146264642 146264642 deletion of <=200bp T - exon_variant KIRP-US 6 146264642 146264642 deletion of <=200bp T - frameshift_variant Q625 LAML-KR 6 146206875 146206875 single base substitution C T 3_prime_UTR_variant LAML-KR 6 146206875 146206875 single base substitution C T intron_variant LAML-KR 6 146207563 146207563 single base substitution A G 3_prime_UTR_variant LAML-KR 6 146207563 146207563 single base substitution A G intron_variant LAML-KR 6 146209058 146209058 single base substitution C A intron_variant LAML-KR 6 146221091 146221091 single base substitution C T downstream_gene_variant LAML-KR 6 146221091 146221091 single base substitution C T intron_variant LAML-KR 6 146255363 146255363 single base substitution G T downstream_gene_variant LAML-KR 6 146255363 146255363 single base substitution G T intron_variant LGG-US 6 146271526 146271526 single base substitution G A 3_prime_UTR_variant LGG-US 6 146271526 146271526 single base substitution G A exon_variant LGG-US 6 146271526 146271526 single base substitution G A stop_gained Q286* 856C>T LICA-CN 6 146262833 146262833 single base substitution T C 3_prime_UTR_variant LICA-CN 6 146262833 146262833 single base substitution T C downstream_gene_variant LICA-CN 6 146262833 146262833 single base substitution T C exon_variant LICA-CN 6 146262833 146262833 single base substitution T C missense_variant S806G 2416A>G LICA-CN 6 146266676 146266676 single base substitution T A 3_prime_UTR_variant LICA-CN 6 146266676 146266676 single base substitution T A downstream_gene_variant LICA-CN 6 146266676 146266676 single base substitution T A exon_variant LICA-CN 6 146266676 146266676 single base substitution T A missense_variant R473S 1419A>T LICA-FR 6 146208300 146208300 single base substitution C T intron_variant LICA-FR 6 146243488 146243488 insertion of <=200bp - A splice_region_variant LICA-FR 6 146252227 146252227 single base substitution C T downstream_gene_variant LICA-FR 6 146252227 146252227 single base substitution C T intron_variant LICA-FR 6 146252227 146252227 single base substitution C T upstream_gene_variant LICA-FR 6 146261913 146261913 single base substitution T A 3_prime_UTR_variant LICA-FR 6 146261913 146261913 single base substitution T A downstream_gene_variant LICA-FR 6 146261913 146261913 single base substitution T A exon_variant LICA-FR 6 146261913 146261913 single base substitution T A missense_variant S839C 2515A>T LICA-FR 6 146261913 146261913 single base substitution T A upstream_gene_variant LICA-FR 6 146262689 146262689 single base substitution T C downstream_gene_variant LICA-FR 6 146262689 146262689 single base substitution T C intron_variant LICA-FR 6 146262886 146262886 single base substitution T C 3_prime_UTR_variant LICA-FR 6 146262886 146262886 single base substitution T C downstream_gene_variant LICA-FR 6 146262886 146262886 single base substitution T C exon_variant LICA-FR 6 146262886 146262886 single base substitution T C missense_variant N788S 2363A>G LIHC-US 6 146243946 146243946 single base substitution A G 3_prime_UTR_variant LIHC-US 6 146243946 146243946 single base substitution A G exon_variant LIHC-US 6 146243946 146243946 single base substitution A G missense_variant F1191S 3572T>C LIHC-US 6 146243946 146243946 single base substitution A G missense_variant F1195S 3584T>C LIHC-US 6 146248354 146248354 single base substitution T C 3_prime_UTR_variant LIHC-US 6 146248354 146248354 single base substitution T C exon_variant LIHC-US 6 146248354 146248354 single base substitution T C missense_variant K1058E 3172A>G LIHC-US 6 146248354 146248354 single base substitution T C missense_variant K1067E 3199A>G LIHC-US 6 146264289 146264289 single base substitution A G 3_prime_UTR_variant LIHC-US 6 146264289 146264289 single base substitution A G downstream_gene_variant LIHC-US 6 146264289 146264289 single base substitution A G exon_variant LIHC-US 6 146264289 146264289 single base substitution A G missense_variant L743P 2228T>C LIHC-US 6 146264776 146264776 single base substitution C A 3_prime_UTR_variant LIHC-US 6 146264776 146264776 single base substitution C A downstream_gene_variant LIHC-US 6 146264776 146264776 single base substitution C A exon_variant LIHC-US 6 146264776 146264776 single base substitution C A missense_variant V581F 1741G>T LIHC-US 6 146275926 146275926 single base substitution T A exon_variant LIHC-US 6 146275926 146275926 single base substitution T A missense_variant E178V 533A>T LIHC-US 6 146275926 146275926 single base substitution T A upstream_gene_variant LIHC-US 6 146276324 146276324 single base substitution T A exon_variant LIHC-US 6 146276324 146276324 single base substitution T A splice_region_variant LIHC-US 6 146276324 146276324 single base substitution T A synonymous_variant P45P 135A>T LIHC-US 6 146276324 146276324 single base substitution T A upstream_gene_variant LINC-JP 6 146189065 146189065 single base substitution T C intron_variant LINC-JP 6 146192840 146192840 single base substitution T A intron_variant LINC-JP 6 146194849 146194849 single base substitution A G intron_variant LINC-JP 6 146208023 146208023 single base substitution T A intron_variant LINC-JP 6 146213340 146213340 single base substitution C G intron_variant LINC-JP 6 146215051 146215051 deletion of <=200bp A - intron_variant LINC-JP 6 146215051 146215051 deletion of <=200bp A - upstream_gene_variant LINC-JP 6 146226686 146226686 single base substitution A G 3_prime_UTR_variant LINC-JP 6 146226686 146226686 single base substitution A G intron_variant LINC-JP 6 146236623 146236623 single base substitution T C downstream_gene_variant LINC-JP 6 146236623 146236623 single base substitution T C intron_variant LINC-JP 6 146242689 146242689 single base substitution T A intron_variant LINC-JP 6 146246778 146246778 single base substitution T G intron_variant LINC-JP 6 146253636 146253636 single base substitution A C downstream_gene_variant LINC-JP 6 146253636 146253636 single base substitution A C intron_variant LINC-JP 6 146254404 146254405 deletion of <=200bp TA - downstream_gene_variant LINC-JP 6 146254404 146254405 deletion of <=200bp TA - intron_variant LINC-JP 6 146256050 146256050 single base substitution G A 3_prime_UTR_variant LINC-JP 6 146256050 146256050 single base substitution G A exon_variant LINC-JP 6 146256050 146256050 single base substitution G A stop_gained Q995* 2983C>T LINC-JP 6 146262578 146262578 single base substitution T C downstream_gene_variant LINC-JP 6 146262578 146262578 single base substitution T C intron_variant LINC-JP 6 146265638 146265638 insertion of <=200bp - C downstream_gene_variant LINC-JP 6 146265638 146265638 insertion of <=200bp - C intron_variant LINC-JP 6 146266701 146266701 single base substitution T C 3_prime_UTR_variant LINC-JP 6 146266701 146266701 single base substitution T C exon_variant LINC-JP 6 146266701 146266701 single base substitution T C missense_variant Y465C 1394A>G LINC-JP 6 146266859 146266859 single base substitution A G intron_variant LIRI-JP 6 146182354 146182354 single base substitution T C downstream_gene_variant LIRI-JP 6 146183646 146183646 single base substitution C G downstream_gene_variant LIRI-JP 6 146184389 146184389 single base substitution A G downstream_gene_variant LIRI-JP 6 146184427 146184427 single base substitution T C downstream_gene_variant LIRI-JP 6 146184486 146184486 single base substitution C A downstream_gene_variant LIRI-JP 6 146185133 146185133 single base substitution T C downstream_gene_variant LIRI-JP 6 146185532 146185532 single base substitution A C missense_variant L106W 317T>G LIRI-JP 6 146185609 146185609 single base substitution C T synonymous_variant A80A 240G>A LIRI-JP 6 146186297 146186297 single base substitution A G intron_variant LIRI-JP 6 146186304 146186304 single base substitution A C intron_variant LIRI-JP 6 146186379 146186379 single base substitution G A intron_variant LIRI-JP 6 146188878 146188878 single base substitution C T intron_variant LIRI-JP 6 146189878 146189878 single base substitution C T intron_variant LIRI-JP 6 146190025 146190025 single base substitution T C intron_variant LIRI-JP 6 146190662 146190662 single base substitution A G intron_variant LIRI-JP 6 146200073 146200073 single base substitution T G intron_variant LIRI-JP 6 146203914 146203914 single base substitution T C downstream_gene_variant LIRI-JP 6 146203914 146203914 single base substitution T C intron_variant LIRI-JP 6 146204588 146204588 single base substitution T C downstream_gene_variant LIRI-JP 6 146204588 146204588 single base substitution T C intron_variant LIRI-JP 6 146208311 146208311 single base substitution T C intron_variant LIRI-JP 6 146212188 146212188 single base substitution G T intron_variant LIRI-JP 6 146215190 146215190 single base substitution T C intron_variant LIRI-JP 6 146215190 146215190 single base substitution T C upstream_gene_variant LIRI-JP 6 146215456 146215456 single base substitution G C intron_variant LIRI-JP 6 146215456 146215456 single base substitution G C upstream_gene_variant LIRI-JP 6 146216628 146216628 single base substitution T G intron_variant LIRI-JP 6 146216628 146216628 single base substitution T G upstream_gene_variant LIRI-JP 6 146221205 146221205 single base substitution A T downstream_gene_variant LIRI-JP 6 146221205 146221205 single base substitution A T intron_variant LIRI-JP 6 146222078 146222078 single base substitution T C downstream_gene_variant LIRI-JP 6 146222078 146222078 single base substitution T C intron_variant LIRI-JP 6 146222096 146222096 single base substitution A T downstream_gene_variant LIRI-JP 6 146222096 146222096 single base substitution A T intron_variant LIRI-JP 6 146222135 146222135 single base substitution A C downstream_gene_variant LIRI-JP 6 146222135 146222135 single base substitution A C intron_variant LIRI-JP 6 146225632 146225632 single base substitution A C 3_prime_UTR_variant LIRI-JP 6 146225632 146225632 single base substitution A C intron_variant LIRI-JP 6 146226671 146226671 single base substitution T C 3_prime_UTR_variant LIRI-JP 6 146226671 146226671 single base substitution T C intron_variant LIRI-JP 6 146226762 146226762 single base substitution C A 3_prime_UTR_variant LIRI-JP 6 146226762 146226762 single base substitution C A intron_variant LIRI-JP 6 146227086 146227086 single base substitution G A 3_prime_UTR_variant LIRI-JP 6 146227086 146227086 single base substitution G A intron_variant LIRI-JP 6 146229063 146229063 single base substitution C T 3_prime_UTR_variant LIRI-JP 6 146229063 146229063 single base substitution C T intron_variant LIRI-JP 6 146233035 146233035 single base substitution T C intron_variant LIRI-JP 6 146233345 146233345 single base substitution T C downstream_gene_variant LIRI-JP 6 146233345 146233345 single base substitution T C intron_variant LIRI-JP 6 146235427 146235427 single base substitution A C downstream_gene_variant LIRI-JP 6 146235427 146235427 single base substitution A C intron_variant LIRI-JP 6 146235626 146235626 single base substitution A G downstream_gene_variant LIRI-JP 6 146235626 146235626 single base substitution A G intron_variant LIRI-JP 6 146244714 146244714 single base substitution G C intron_variant LIRI-JP 6 146246840 146246840 single base substitution T C intron_variant LIRI-JP 6 146249483 146249483 single base substitution T C intron_variant LIRI-JP 6 146249483 146249483 single base substitution T C upstream_gene_variant LIRI-JP 6 146250215 146250215 single base substitution T C intron_variant LIRI-JP 6 146250215 146250215 single base substitution T C upstream_gene_variant LIRI-JP 6 146251333 146251333 single base substitution A G downstream_gene_variant LIRI-JP 6 146251333 146251333 single base substitution A G intron_variant LIRI-JP 6 146251333 146251333 single base substitution A G upstream_gene_variant LIRI-JP 6 146251343 146251343 single base substitution A C downstream_gene_variant LIRI-JP 6 146251343 146251343 single base substitution A C intron_variant LIRI-JP 6 146251343 146251343 single base substitution A C upstream_gene_variant LIRI-JP 6 146252291 146252291 single base substitution G A downstream_gene_variant LIRI-JP 6 146252291 146252291 single base substitution G A intron_variant LIRI-JP 6 146252291 146252291 single base substitution G A upstream_gene_variant LIRI-JP 6 146252400 146252400 single base substitution C A downstream_gene_variant LIRI-JP 6 146252400 146252400 single base substitution C A intron_variant LIRI-JP 6 146252400 146252400 single base substitution C A upstream_gene_variant LIRI-JP 6 146252918 146252918 single base substitution T C downstream_gene_variant LIRI-JP 6 146252918 146252918 single base substitution T C intron_variant LIRI-JP 6 146252918 146252918 single base substitution T C upstream_gene_variant LIRI-JP 6 146253042 146253042 single base substitution C T downstream_gene_variant LIRI-JP 6 146253042 146253042 single base substitution C T intron_variant LIRI-JP 6 146253042 146253042 single base substitution C T upstream_gene_variant LIRI-JP 6 146254052 146254052 single base substitution T C downstream_gene_variant LIRI-JP 6 146254052 146254052 single base substitution T C intron_variant LIRI-JP 6 146254256 146254256 single base substitution C T 3_prime_UTR_variant LIRI-JP 6 146254256 146254256 single base substitution C T downstream_gene_variant LIRI-JP 6 146254256 146254256 single base substitution C T exon_variant LIRI-JP 6 146254256 146254256 single base substitution C T missense_variant E1017K 3049G>A LIRI-JP 6 146254256 146254256 single base substitution C T missense_variant E1026K 3076G>A LIRI-JP 6 146255865 146255865 single base substitution C A downstream_gene_variant LIRI-JP 6 146255865 146255865 single base substitution C A intron_variant LIRI-JP 6 146257172 146257172 single base substitution T A intron_variant LIRI-JP 6 146257172 146257172 single base substitution T A upstream_gene_variant LIRI-JP 6 146263157 146263157 single base substitution G C downstream_gene_variant LIRI-JP 6 146263157 146263157 single base substitution G C intron_variant LIRI-JP 6 146265311 146265311 single base substitution T C downstream_gene_variant LIRI-JP 6 146265311 146265311 single base substitution T C intron_variant LIRI-JP 6 146266580 146266580 single base substitution A G 3_prime_UTR_variant LIRI-JP 6 146266580 146266580 single base substitution A G downstream_gene_variant LIRI-JP 6 146266580 146266580 single base substitution A G exon_variant LIRI-JP 6 146266580 146266580 single base substitution A G synonymous_variant S505S 1515T>C LIRI-JP 6 146266601 146266601 single base substitution C T 3_prime_UTR_variant LIRI-JP 6 146266601 146266601 single base substitution C T downstream_gene_variant LIRI-JP 6 146266601 146266601 single base substitution C T exon_variant LIRI-JP 6 146266601 146266601 single base substitution C T synonymous_variant Q498Q 1494G>A LIRI-JP 6 146267115 146267115 single base substitution C G intron_variant LIRI-JP 6 146267116 146267116 single base substitution C A intron_variant LIRI-JP 6 146268896 146268896 single base substitution A G intron_variant LIRI-JP 6 146269406 146269406 single base substitution A C splice_donor_variant LIRI-JP 6 146269689 146269691 deletion of <=200bp CTC - intron_variant LIRI-JP 6 146270176 146270176 single base substitution G A intron_variant LIRI-JP 6 146271097 146271097 deletion of <=200bp G - intron_variant LIRI-JP 6 146271378 146271378 single base substitution T C intron_variant LIRI-JP 6 146272051 146272051 single base substitution A C intron_variant LIRI-JP 6 146272073 146272073 single base substitution A C intron_variant LIRI-JP 6 146273980 146273980 single base substitution T C intron_variant LIRI-JP 6 146275553 146275553 single base substitution A C intron_variant LIRI-JP 6 146277594 146277594 single base substitution C T intron_variant LIRI-JP 6 146277594 146277594 single base substitution C T upstream_gene_variant LIRI-JP 6 146277942 146277942 single base substitution A T intron_variant LIRI-JP 6 146277942 146277942 single base substitution A T upstream_gene_variant LIRI-JP 6 146278444 146278444 single base substitution A G intron_variant LIRI-JP 6 146278444 146278444 single base substitution A G upstream_gene_variant LIRI-JP 6 146281021 146281021 single base substitution A C intron_variant LIRI-JP 6 146281021 146281021 single base substitution A C upstream_gene_variant LIRI-JP 6 146282614 146282614 single base substitution T C intron_variant LIRI-JP 6 146288783 146288783 single base substitution G A upstream_gene_variant LUSC-KR 6 146181180 146181180 single base substitution A G downstream_gene_variant LUSC-KR 6 146183599 146183599 single base substitution A T downstream_gene_variant LUSC-KR 6 146189893 146189893 single base substitution A T intron_variant LUSC-KR 6 146191564 146191564 single base substitution A T intron_variant LUSC-KR 6 146191852 146191852 single base substitution T C intron_variant LUSC-KR 6 146192971 146192971 single base substitution G A intron_variant LUSC-KR 6 146209224 146209224 single base substitution T A synonymous_variant V1629V 4887A>T LUSC-KR 6 146209224 146209224 single base substitution T A synonymous_variant V1633V 4899A>T LUSC-KR 6 146209224 146209224 single base substitution T A synonymous_variant V51V 153A>T LUSC-KR 6 146214382 146214382 single base substitution T C missense_variant I1615V 4843A>G LUSC-KR 6 146214382 146214382 single base substitution T C missense_variant I1619V 4855A>G LUSC-KR 6 146214382 146214382 single base substitution T C missense_variant I37V 109A>G LUSC-KR 6 146215534 146215534 single base substitution A T intron_variant LUSC-KR 6 146215534 146215534 single base substitution A T upstream_gene_variant LUSC-KR 6 146216687 146216687 single base substitution G T intron_variant LUSC-KR 6 146216687 146216687 single base substitution G T upstream_gene_variant LUSC-KR 6 146228967 146228967 single base substitution C T 3_prime_UTR_variant LUSC-KR 6 146228967 146228967 single base substitution C T intron_variant LUSC-KR 6 146233575 146233575 single base substitution A G downstream_gene_variant LUSC-KR 6 146233575 146233575 single base substitution A G intron_variant LUSC-KR 6 146234653 146234653 single base substitution T C 3_prime_UTR_variant LUSC-KR 6 146234653 146234653 single base substitution T C downstream_gene_variant LUSC-KR 6 146234653 146234653 single base substitution T C synonymous_variant P1429P 4287A>G LUSC-KR 6 146234653 146234653 single base substitution T C synonymous_variant P1433P 4299A>G LUSC-KR 6 146235670 146235670 single base substitution G A downstream_gene_variant LUSC-KR 6 146235670 146235670 single base substitution G A intron_variant LUSC-KR 6 146236251 146236251 single base substitution A G downstream_gene_variant LUSC-KR 6 146236251 146236251 single base substitution A G intron_variant LUSC-KR 6 146238607 146238607 single base substitution C A 3_prime_UTR_variant LUSC-KR 6 146238607 146238607 single base substitution C A downstream_gene_variant LUSC-KR 6 146238607 146238607 single base substitution C A intron_variant LUSC-KR 6 146240671 146240671 single base substitution T C intron_variant LUSC-KR 6 146243581 146243581 single base substitution C T intron_variant LUSC-KR 6 146243991 146243991 single base substitution C T intron_variant LUSC-KR 6 146246126 146246126 single base substitution C T intron_variant LUSC-KR 6 146246588 146246588 single base substitution C G intron_variant LUSC-KR 6 146246787 146246787 single base substitution A C intron_variant LUSC-KR 6 146249598 146249598 single base substitution C A intron_variant LUSC-KR 6 146249598 146249598 single base substitution C A upstream_gene_variant LUSC-KR 6 146252546 146252546 single base substitution T C downstream_gene_variant LUSC-KR 6 146252546 146252546 single base substitution T C intron_variant LUSC-KR 6 146252546 146252546 single base substitution T C upstream_gene_variant LUSC-KR 6 146254065 146254065 single base substitution C T downstream_gene_variant LUSC-KR 6 146254065 146254065 single base substitution C T intron_variant LUSC-KR 6 146254783 146254783 single base substitution C A downstream_gene_variant LUSC-KR 6 146254783 146254783 single base substitution C A intron_variant LUSC-KR 6 146255104 146255104 single base substitution C T downstream_gene_variant LUSC-KR 6 146255104 146255104 single base substitution C T intron_variant LUSC-KR 6 146257563 146257563 single base substitution T A intron_variant LUSC-KR 6 146257563 146257563 single base substitution T A upstream_gene_variant LUSC-KR 6 146258956 146258956 single base substitution C T intron_variant LUSC-KR 6 146258956 146258956 single base substitution C T upstream_gene_variant LUSC-KR 6 146262218 146262218 single base substitution T A downstream_gene_variant LUSC-KR 6 146262218 146262218 single base substitution T A intron_variant LUSC-KR 6 146268623 146268623 single base substitution T A splice_region_variant LUSC-KR 6 146272607 146272607 single base substitution T C intron_variant LUSC-KR 6 146273769 146273769 single base substitution C T intron_variant LUSC-KR 6 146275236 146275236 single base substitution T C intron_variant LUSC-KR 6 146278296 146278296 single base substitution T C intron_variant LUSC-KR 6 146278296 146278296 single base substitution T C upstream_gene_variant LUSC-KR 6 146284786 146284786 single base substitution A G intron_variant LUSC-KR 6 146285204 146285204 single base substitution C A 5_prime_UTR_variant LUSC-KR 6 146285204 146285204 single base substitution C A intron_variant LUSC-KR 6 146285205 146285205 single base substitution C T 5_prime_UTR_variant LUSC-KR 6 146285205 146285205 single base substitution C T intron_variant LUSC-KR 6 146289417 146289417 single base substitution G A upstream_gene_variant LUSC-KR 6 146290435 146290435 single base substitution G A upstream_gene_variant LUSC-US 6 146216035 146216035 single base substitution G C missense_variant L1532V 4594C>G LUSC-US 6 146216035 146216035 single base substitution G C missense_variant L1536V 4606C>G LUSC-US 6 146216035 146216035 single base substitution G C upstream_gene_variant LUSC-US 6 146243814 146243814 single base substitution C T 3_prime_UTR_variant LUSC-US 6 146243814 146243814 single base substitution C T exon_variant LUSC-US 6 146243814 146243814 single base substitution C T missense_variant R1235K 3704G>A LUSC-US 6 146243814 146243814 single base substitution C T missense_variant R1239K 3716G>A LUSC-US 6 146244844 146244844 single base substitution C T 3_prime_UTR_variant LUSC-US 6 146244844 146244844 single base substitution C T exon_variant LUSC-US 6 146244844 146244844 single base substitution C T synonymous_variant Q1160Q 3480G>A LUSC-US 6 146244844 146244844 single base substitution C T synonymous_variant Q1169Q 3507G>A LUSC-US 6 146248399 146248399 single base substitution C T 3_prime_UTR_variant LUSC-US 6 146248399 146248399 single base substitution C T exon_variant LUSC-US 6 146248399 146248399 single base substitution C T missense_variant A1043T 3127G>A LUSC-US 6 146248399 146248399 single base substitution C T missense_variant A1052T 3154G>A LUSC-US 6 146256083 146256083 single base substitution G T 3_prime_UTR_variant LUSC-US 6 146256083 146256083 single base substitution G T exon_variant LUSC-US 6 146256083 146256083 single base substitution G T missense_variant P984T 2950C>A LUSC-US 6 146262959 146262959 single base substitution C A 3_prime_UTR_variant LUSC-US 6 146262959 146262959 single base substitution C A downstream_gene_variant LUSC-US 6 146262959 146262959 single base substitution C A exon_variant LUSC-US 6 146262959 146262959 single base substitution C A stop_gained E764* 2290G>T LUSC-US 6 146264293 146264293 single base substitution A T 3_prime_UTR_variant LUSC-US 6 146264293 146264293 single base substitution A T downstream_gene_variant LUSC-US 6 146264293 146264293 single base substitution A T exon_variant LUSC-US 6 146264293 146264293 single base substitution A T missense_variant S742T 2224T>A LUSC-US 6 146264545 146264545 single base substitution G T 3_prime_UTR_variant LUSC-US 6 146264545 146264545 single base substitution G T downstream_gene_variant LUSC-US 6 146264545 146264545 single base substitution G T exon_variant LUSC-US 6 146264545 146264545 single base substitution G T missense_variant R658S 1972C>A LUSC-US 6 146275940 146275940 single base substitution C A exon_variant LUSC-US 6 146275940 146275940 single base substitution C A missense_variant K173N 519G>T LUSC-US 6 146275940 146275940 single base substitution C A upstream_gene_variant LUSC-US 6 146276093 146276093 single base substitution C A exon_variant LUSC-US 6 146276093 146276093 single base substitution C A intron_variant LUSC-US 6 146276093 146276093 single base substitution C A missense_variant Q122H 366G>T LUSC-US 6 146276093 146276093 single base substitution C A upstream_gene_variant MALY-DE 6 146195180 146195180 single base substitution C A intron_variant MALY-DE 6 146197794 146197794 single base substitution C G intron_variant MALY-DE 6 146206163 146206163 single base substitution G T 3_prime_UTR_variant MALY-DE 6 146206163 146206163 single base substitution G T downstream_gene_variant MALY-DE 6 146206163 146206163 single base substitution G T intron_variant MALY-DE 6 146214397 146214397 single base substitution G T missense_variant H1610N 4828C>A MALY-DE 6 146214397 146214397 single base substitution G T missense_variant H1614N 4840C>A MALY-DE 6 146214397 146214397 single base substitution G T missense_variant H32N 94C>A MALY-DE 6 146215217 146215217 single base substitution A C intron_variant MALY-DE 6 146215217 146215217 single base substitution A C upstream_gene_variant MALY-DE 6 146217253 146217253 single base substitution C A intron_variant MALY-DE 6 146217253 146217253 single base substitution C A upstream_gene_variant MALY-DE 6 146225292 146225292 single base substitution A G 3_prime_UTR_variant MALY-DE 6 146225292 146225292 single base substitution A G intron_variant MALY-DE 6 146239355 146239355 single base substitution C T 3_prime_UTR_variant MALY-DE 6 146239355 146239355 single base substitution C T downstream_gene_variant MALY-DE 6 146239355 146239355 single base substitution C T missense_variant R1389Q 4166G>A MALY-DE 6 146239355 146239355 single base substitution C T missense_variant R1393Q 4178G>A MALY-DE 6 146239585 146239585 single base substitution C T exon_variant MALY-DE 6 146239585 146239585 single base substitution C T intron_variant MALY-DE 6 146243172 146243172 single base substitution T A intron_variant MALY-DE 6 146249670 146249671 deletion of <=200bp AT - intron_variant MALY-DE 6 146249670 146249671 deletion of <=200bp AT - upstream_gene_variant MALY-DE 6 146253691 146253691 single base substitution G T downstream_gene_variant MALY-DE 6 146253691 146253691 single base substitution G T intron_variant MALY-DE 6 146254832 146254832 single base substitution T G downstream_gene_variant MALY-DE 6 146254832 146254832 single base substitution T G intron_variant MALY-DE 6 146255804 146255804 insertion of <=200bp - A downstream_gene_variant MALY-DE 6 146255804 146255804 insertion of <=200bp - A intron_variant MALY-DE 6 146259190 146259190 single base substitution C T intron_variant MALY-DE 6 146259190 146259190 single base substitution C T upstream_gene_variant MALY-DE 6 146265791 146265791 single base substitution A T downstream_gene_variant MALY-DE 6 146265791 146265791 single base substitution A T intron_variant MALY-DE 6 146267451 146267451 single base substitution C T 3_prime_UTR_variant MALY-DE 6 146267451 146267451 single base substitution C T exon_variant MALY-DE 6 146267451 146267451 single base substitution C T synonymous_variant P413P 1239G>A MALY-DE 6 146267590 146267590 single base substitution T C intron_variant MALY-DE 6 146270657 146270657 single base substitution G C intron_variant MALY-DE 6 146277357 146277357 single base substitution C T intron_variant MALY-DE 6 146277357 146277357 single base substitution C T upstream_gene_variant MALY-DE 6 146277451 146277451 single base substitution G T intron_variant MALY-DE 6 146277451 146277451 single base substitution G T upstream_gene_variant MALY-DE 6 146285574 146285574 single base substitution T C upstream_gene_variant MALY-DE 6 146287246 146287246 single base substitution G C upstream_gene_variant MALY-DE 6 146287911 146287911 single base substitution A T upstream_gene_variant MALY-DE 6 146289859 146289859 single base substitution G C upstream_gene_variant MELA-AU 6 146181182 146181182 single base substitution G A downstream_gene_variant MELA-AU 6 146181708 146181708 single base substitution C T downstream_gene_variant MELA-AU 6 146181821 146181821 single base substitution G A downstream_gene_variant MELA-AU 6 146182820 146182820 single base substitution G A downstream_gene_variant MELA-AU 6 146182971 146182971 single base substitution G A downstream_gene_variant MELA-AU 6 146183579 146183579 single base substitution A C downstream_gene_variant MELA-AU 6 146183591 146183591 single base substitution C A downstream_gene_variant MELA-AU 6 146184272 146184272 single base substitution G A downstream_gene_variant MELA-AU 6 146184669 146184669 single base substitution G A downstream_gene_variant MELA-AU 6 146184885 146184885 single base substitution G A downstream_gene_variant MELA-AU 6 146185884 146185884 single base substitution G A intron_variant MELA-AU 6 146186397 146186397 single base substitution G A intron_variant MELA-AU 6 146187864 146187864 single base substitution G A intron_variant MELA-AU 6 146187965 146187965 single base substitution C A intron_variant MELA-AU 6 146188529 146188529 single base substitution G A intron_variant MELA-AU 6 146189431 146189431 single base substitution G A intron_variant MELA-AU 6 146189648 146189648 single base substitution A G intron_variant MELA-AU 6 146189878 146189878 single base substitution C T intron_variant MELA-AU 6 146189998 146189998 single base substitution G A intron_variant MELA-AU 6 146191657 146191657 single base substitution C T intron_variant MELA-AU 6 146192383 146192383 single base substitution G A intron_variant MELA-AU 6 146192450 146192450 single base substitution T A intron_variant MELA-AU 6 146192974 146192974 single base substitution C A intron_variant MELA-AU 6 146193410 146193410 single base substitution G A intron_variant MELA-AU 6 146193541 146193541 single base substitution G A intron_variant MELA-AU 6 146193801 146193801 single base substitution C T intron_variant MELA-AU 6 146194067 146194067 single base substitution G A intron_variant MELA-AU 6 146194831 146194831 single base substitution G A intron_variant MELA-AU 6 146196070 146196070 single base substitution G A intron_variant MELA-AU 6 146196517 146196517 single base substitution C A intron_variant MELA-AU 6 146198061 146198061 single base substitution G A intron_variant MELA-AU 6 146198973 146198973 single base substitution C G intron_variant MELA-AU 6 146199704 146199704 single base substitution G A intron_variant MELA-AU 6 146201439 146201439 single base substitution A G downstream_gene_variant MELA-AU 6 146201439 146201439 single base substitution A G intron_variant MELA-AU 6 146201703 146201703 single base substitution T A downstream_gene_variant MELA-AU 6 146201703 146201703 single base substitution T A intron_variant MELA-AU 6 146201948 146201948 single base substitution G A downstream_gene_variant MELA-AU 6 146201948 146201948 single base substitution G A intron_variant MELA-AU 6 146202589 146202589 single base substitution C T downstream_gene_variant MELA-AU 6 146202589 146202589 single base substitution C T intron_variant MELA-AU 6 146202715 146202715 single base substitution G A downstream_gene_variant MELA-AU 6 146202715 146202715 single base substitution G A intron_variant MELA-AU 6 146202908 146202908 single base substitution G A downstream_gene_variant MELA-AU 6 146202908 146202908 single base substitution G A intron_variant MELA-AU 6 146204251 146204251 single base substitution G A downstream_gene_variant MELA-AU 6 146204251 146204251 single base substitution G A intron_variant MELA-AU 6 146204274 146204274 single base substitution T C downstream_gene_variant MELA-AU 6 146204274 146204274 single base substitution T C intron_variant MELA-AU 6 146204341 146204341 single base substitution G A downstream_gene_variant MELA-AU 6 146204341 146204341 single base substitution G A intron_variant MELA-AU 6 146204442 146204442 single base substitution G A downstream_gene_variant MELA-AU 6 146204442 146204442 single base substitution G A intron_variant MELA-AU 6 146205093 146205093 deletion of <=200bp T - downstream_gene_variant MELA-AU 6 146205093 146205093 deletion of <=200bp T - intron_variant MELA-AU 6 146205103 146205103 single base substitution G A downstream_gene_variant MELA-AU 6 146205103 146205103 single base substitution G A intron_variant MELA-AU 6 146206100 146206100 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146206100 146206100 single base substitution G A downstream_gene_variant MELA-AU 6 146206100 146206100 single base substitution G A intron_variant MELA-AU 6 146206234 146206234 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146206234 146206234 single base substitution C T downstream_gene_variant MELA-AU 6 146206234 146206234 single base substitution C T intron_variant MELA-AU 6 146206269 146206269 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146206269 146206269 single base substitution C T downstream_gene_variant MELA-AU 6 146206269 146206269 single base substitution C T intron_variant MELA-AU 6 146206787 146206787 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146206787 146206787 single base substitution C T intron_variant MELA-AU 6 146207177 146207177 single base substitution C A 3_prime_UTR_variant MELA-AU 6 146207177 146207177 single base substitution C A intron_variant MELA-AU 6 146208891 146208891 single base substitution G A intron_variant MELA-AU 6 146209305 146209305 single base substitution T A intron_variant MELA-AU 6 146209760 146209760 single base substitution A G intron_variant MELA-AU 6 146210242 146210242 single base substitution G A intron_variant MELA-AU 6 146210360 146210360 single base substitution G A intron_variant MELA-AU 6 146211132 146211132 single base substitution A T intron_variant MELA-AU 6 146211720 146211720 single base substitution G C intron_variant MELA-AU 6 146214144 146214144 single base substitution G A intron_variant MELA-AU 6 146215321 146215321 single base substitution C A stop_gained E1554* 4660G>T MELA-AU 6 146215321 146215321 single base substitution C A stop_gained E1558* 4672G>T MELA-AU 6 146215321 146215321 single base substitution C A upstream_gene_variant MELA-AU 6 146215971 146215971 single base substitution G A intron_variant MELA-AU 6 146215971 146215971 single base substitution G A upstream_gene_variant MELA-AU 6 146216274 146216274 single base substitution G A intron_variant MELA-AU 6 146216274 146216274 single base substitution G A upstream_gene_variant MELA-AU 6 146217540 146217540 single base substitution G A intron_variant MELA-AU 6 146217540 146217540 single base substitution G A upstream_gene_variant MELA-AU 6 146218277 146218277 single base substitution G A intron_variant MELA-AU 6 146218277 146218277 single base substitution G A upstream_gene_variant MELA-AU 6 146218856 146218856 single base substitution G A intron_variant MELA-AU 6 146218856 146218856 single base substitution G A upstream_gene_variant MELA-AU 6 146218902 146218902 single base substitution G A intron_variant MELA-AU 6 146218902 146218902 single base substitution G A upstream_gene_variant MELA-AU 6 146220075 146220075 single base substitution G A downstream_gene_variant MELA-AU 6 146220075 146220075 single base substitution G A intron_variant MELA-AU 6 146220326 146220326 single base substitution G A downstream_gene_variant MELA-AU 6 146220326 146220326 single base substitution G A intron_variant MELA-AU 6 146220704 146220704 single base substitution G A downstream_gene_variant MELA-AU 6 146220704 146220704 single base substitution G A intron_variant MELA-AU 6 146220722 146220722 single base substitution A G downstream_gene_variant MELA-AU 6 146220722 146220722 single base substitution A G intron_variant MELA-AU 6 146220977 146220977 single base substitution G A downstream_gene_variant MELA-AU 6 146220977 146220977 single base substitution G A intron_variant MELA-AU 6 146221502 146221502 single base substitution G A downstream_gene_variant MELA-AU 6 146221502 146221502 single base substitution G A intron_variant MELA-AU 6 146221719 146221719 single base substitution G A downstream_gene_variant MELA-AU 6 146221719 146221719 single base substitution G A intron_variant MELA-AU 6 146221868 146221868 single base substitution C T downstream_gene_variant MELA-AU 6 146221868 146221868 single base substitution C T intron_variant MELA-AU 6 146222201 146222201 single base substitution A T downstream_gene_variant MELA-AU 6 146222201 146222201 single base substitution A T intron_variant MELA-AU 6 146223144 146223144 single base substitution G A downstream_gene_variant MELA-AU 6 146223144 146223144 single base substitution G A intron_variant MELA-AU 6 146223543 146223543 single base substitution G A downstream_gene_variant MELA-AU 6 146223543 146223543 single base substitution G A intron_variant MELA-AU 6 146225882 146225882 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146225882 146225882 single base substitution G A intron_variant MELA-AU 6 146226295 146226295 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146226295 146226295 single base substitution G A intron_variant MELA-AU 6 146228475 146228475 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146228475 146228475 single base substitution C T intron_variant MELA-AU 6 146228485 146228485 single base substitution T C 3_prime_UTR_variant MELA-AU 6 146228485 146228485 single base substitution T C intron_variant MELA-AU 6 146228836 146228836 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146228836 146228836 single base substitution C T intron_variant MELA-AU 6 146229990 146229990 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146229990 146229990 single base substitution G A intron_variant MELA-AU 6 146230073 146230073 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146230073 146230073 single base substitution G A intron_variant MELA-AU 6 146231199 146231199 single base substitution T C 3_prime_UTR_variant MELA-AU 6 146231199 146231199 single base substitution T C intron_variant MELA-AU 6 146231201 146231201 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146231201 146231201 single base substitution C T intron_variant MELA-AU 6 146231684 146231684 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146231684 146231684 single base substitution G A missense_variant S1472F 4415C>T MELA-AU 6 146231684 146231684 single base substitution G A missense_variant S1476F 4427C>T MELA-AU 6 146232596 146232596 single base substitution G A intron_variant MELA-AU 6 146233333 146233333 single base substitution G A downstream_gene_variant MELA-AU 6 146233333 146233333 single base substitution G A intron_variant MELA-AU 6 146233782 146233782 single base substitution A T downstream_gene_variant MELA-AU 6 146233782 146233782 single base substitution A T intron_variant MELA-AU 6 146234523 146234523 single base substitution G A downstream_gene_variant MELA-AU 6 146234523 146234523 single base substitution G A intron_variant MELA-AU 6 146235069 146235069 single base substitution G A downstream_gene_variant MELA-AU 6 146235069 146235069 single base substitution G A intron_variant MELA-AU 6 146235718 146235718 single base substitution G A downstream_gene_variant MELA-AU 6 146235718 146235718 single base substitution G A intron_variant MELA-AU 6 146236023 146236023 single base substitution G A downstream_gene_variant MELA-AU 6 146236023 146236023 single base substitution G A intron_variant MELA-AU 6 146236531 146236531 single base substitution T C downstream_gene_variant MELA-AU 6 146236531 146236531 single base substitution T C intron_variant MELA-AU 6 146236617 146236617 single base substitution G A downstream_gene_variant MELA-AU 6 146236617 146236617 single base substitution G A intron_variant MELA-AU 6 146237395 146237395 single base substitution C T downstream_gene_variant MELA-AU 6 146237395 146237395 single base substitution C T intron_variant MELA-AU 6 146237633 146237633 single base substitution G A downstream_gene_variant MELA-AU 6 146237633 146237633 single base substitution G A intron_variant MELA-AU 6 146237900 146237900 single base substitution G A downstream_gene_variant MELA-AU 6 146237900 146237900 single base substitution G A intron_variant MELA-AU 6 146238013 146238013 single base substitution G A downstream_gene_variant MELA-AU 6 146238013 146238013 single base substitution G A intron_variant MELA-AU 6 146238502 146238502 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146238502 146238502 single base substitution G A downstream_gene_variant MELA-AU 6 146238502 146238502 single base substitution G A intron_variant MELA-AU 6 146238836 146238836 single base substitution T C 3_prime_UTR_variant MELA-AU 6 146238836 146238836 single base substitution T C downstream_gene_variant MELA-AU 6 146238836 146238836 single base substitution T C intron_variant MELA-AU 6 146239050 146239050 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146239050 146239050 single base substitution G A downstream_gene_variant MELA-AU 6 146239050 146239050 single base substitution G A intron_variant MELA-AU 6 146240598 146240598 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146240598 146240598 single base substitution C T exon_variant MELA-AU 6 146240598 146240598 single base substitution C T synonymous_variant R1346R 4038G>A MELA-AU 6 146240598 146240598 single base substitution C T synonymous_variant R1350R 4050G>A MELA-AU 6 146244149 146244150 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 146244257 146244257 single base substitution G A intron_variant MELA-AU 6 146244575 146244575 single base substitution G A intron_variant MELA-AU 6 146244721 146244721 single base substitution C A intron_variant MELA-AU 6 146245100 146245100 single base substitution G A intron_variant MELA-AU 6 146245647 146245647 single base substitution T C intron_variant MELA-AU 6 146245769 146245769 single base substitution G A intron_variant MELA-AU 6 146245835 146245835 single base substitution G A intron_variant MELA-AU 6 146246166 146246166 single base substitution A C intron_variant MELA-AU 6 146247786 146247786 single base substitution G A intron_variant MELA-AU 6 146247802 146247802 single base substitution T A intron_variant MELA-AU 6 146248364 146248364 single base substitution C T 3_prime_UTR_variant MELA-AU 6 146248364 146248364 single base substitution C T exon_variant MELA-AU 6 146248364 146248364 single base substitution C T synonymous_variant S1054S 3162G>A MELA-AU 6 146248364 146248364 single base substitution C T synonymous_variant S1063S 3189G>A MELA-AU 6 146248520 146248520 single base substitution T A intron_variant MELA-AU 6 146248520 146248520 single base substitution T A upstream_gene_variant MELA-AU 6 146248762 146248762 single base substitution G A intron_variant MELA-AU 6 146248762 146248762 single base substitution G A upstream_gene_variant MELA-AU 6 146248837 146248837 single base substitution A C intron_variant MELA-AU 6 146248837 146248837 single base substitution A C upstream_gene_variant MELA-AU 6 146249946 146249946 single base substitution A C intron_variant MELA-AU 6 146249946 146249946 single base substitution A C upstream_gene_variant MELA-AU 6 146249987 146249987 single base substitution G A intron_variant MELA-AU 6 146249987 146249987 single base substitution G A upstream_gene_variant MELA-AU 6 146250682 146250682 single base substitution G A intron_variant MELA-AU 6 146250682 146250682 single base substitution G A upstream_gene_variant MELA-AU 6 146250873 146250873 single base substitution G A intron_variant MELA-AU 6 146250873 146250873 single base substitution G A upstream_gene_variant MELA-AU 6 146251736 146251736 single base substitution G A downstream_gene_variant MELA-AU 6 146251736 146251736 single base substitution G A intron_variant MELA-AU 6 146251736 146251736 single base substitution G A upstream_gene_variant MELA-AU 6 146252491 146252491 single base substitution A C downstream_gene_variant MELA-AU 6 146252491 146252491 single base substitution A C intron_variant MELA-AU 6 146252491 146252491 single base substitution A C upstream_gene_variant MELA-AU 6 146253048 146253048 single base substitution G A downstream_gene_variant MELA-AU 6 146253048 146253048 single base substitution G A intron_variant MELA-AU 6 146253048 146253048 single base substitution G A upstream_gene_variant MELA-AU 6 146253129 146253129 single base substitution C T downstream_gene_variant MELA-AU 6 146253129 146253129 single base substitution C T intron_variant MELA-AU 6 146253129 146253129 single base substitution C T upstream_gene_variant MELA-AU 6 146256182 146256182 single base substitution T C 3_prime_UTR_variant MELA-AU 6 146256182 146256182 single base substitution T C exon_variant MELA-AU 6 146256182 146256182 single base substitution T C missense_variant K951E 2851A>G MELA-AU 6 146256482 146256482 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146256482 146256482 single base substitution G A exon_variant MELA-AU 6 146256482 146256482 single base substitution G A missense_variant P889S 2665C>T MELA-AU 6 146256896 146256896 single base substitution G A exon_variant MELA-AU 6 146256896 146256896 single base substitution G A intron_variant MELA-AU 6 146257070 146257070 single base substitution A T intron_variant MELA-AU 6 146257070 146257070 single base substitution A T upstream_gene_variant MELA-AU 6 146258152 146258152 single base substitution C T intron_variant MELA-AU 6 146258152 146258152 single base substitution C T upstream_gene_variant MELA-AU 6 146258873 146258873 single base substitution C A intron_variant MELA-AU 6 146258873 146258873 single base substitution C A upstream_gene_variant MELA-AU 6 146259805 146259805 single base substitution T A intron_variant MELA-AU 6 146259805 146259805 single base substitution T A upstream_gene_variant MELA-AU 6 146259881 146259881 single base substitution G A intron_variant MELA-AU 6 146259881 146259881 single base substitution G A upstream_gene_variant MELA-AU 6 146260358 146260358 single base substitution G A intron_variant MELA-AU 6 146260358 146260358 single base substitution G A upstream_gene_variant MELA-AU 6 146261140 146261140 single base substitution G A intron_variant MELA-AU 6 146261140 146261140 single base substitution G A upstream_gene_variant MELA-AU 6 146261432 146261432 single base substitution A C intron_variant MELA-AU 6 146261432 146261432 single base substitution A C upstream_gene_variant MELA-AU 6 146261767 146261767 single base substitution G A downstream_gene_variant MELA-AU 6 146261767 146261767 single base substitution G A intron_variant MELA-AU 6 146261767 146261767 single base substitution G A upstream_gene_variant MELA-AU 6 146262195 146262195 single base substitution G A downstream_gene_variant MELA-AU 6 146262195 146262195 single base substitution G A intron_variant MELA-AU 6 146263276 146263276 single base substitution G A downstream_gene_variant MELA-AU 6 146263276 146263276 single base substitution G A intron_variant MELA-AU 6 146263542 146263542 single base substitution A C downstream_gene_variant MELA-AU 6 146263542 146263542 single base substitution A C intron_variant MELA-AU 6 146263586 146263586 single base substitution A C downstream_gene_variant MELA-AU 6 146263586 146263586 single base substitution A C intron_variant MELA-AU 6 146263629 146263629 single base substitution A C downstream_gene_variant MELA-AU 6 146263629 146263629 single base substitution A C intron_variant MELA-AU 6 146264349 146264350 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 6 146264349 146264350 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 6 146264349 146264350 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 6 146264349 146264350 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P723L 2167CC>TT MELA-AU 6 146264734 146264734 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146264734 146264734 single base substitution G A downstream_gene_variant MELA-AU 6 146264734 146264734 single base substitution G A exon_variant MELA-AU 6 146264734 146264734 single base substitution G A missense_variant P595S 1783C>T MELA-AU 6 146265084 146265084 single base substitution G A downstream_gene_variant MELA-AU 6 146265084 146265084 single base substitution G A intron_variant MELA-AU 6 146266348 146266348 single base substitution G A downstream_gene_variant MELA-AU 6 146266348 146266348 single base substitution G A intron_variant MELA-AU 6 146266538 146266538 single base substitution T A 3_prime_UTR_variant MELA-AU 6 146266538 146266538 single base substitution T A downstream_gene_variant MELA-AU 6 146266538 146266538 single base substitution T A exon_variant MELA-AU 6 146266538 146266538 single base substitution T A synonymous_variant I519I 1557A>T MELA-AU 6 146266913 146266913 insertion of <=200bp - A intron_variant MELA-AU 6 146267268 146267268 single base substitution A C intron_variant MELA-AU 6 146267777 146267777 single base substitution G A intron_variant MELA-AU 6 146268287 146268287 single base substitution C T intron_variant MELA-AU 6 146268865 146268865 single base substitution G A intron_variant MELA-AU 6 146269420 146269420 single base substitution G A 3_prime_UTR_variant MELA-AU 6 146269420 146269420 single base substitution G A exon_variant MELA-AU 6 146269420 146269420 single base substitution G A missense_variant P350L 1049C>T MELA-AU 6 146269700 146269700 single base substitution C T intron_variant MELA-AU 6 146269854 146269854 single base substitution G A intron_variant MELA-AU 6 146270554 146270554 single base substitution G A intron_variant MELA-AU 6 146270758 146270758 single base substitution G A intron_variant MELA-AU 6 146271701 146271701 single base substitution G A intron_variant MELA-AU 6 146271944 146271944 single base substitution G A intron_variant MELA-AU 6 146272398 146272398 single base substitution C T intron_variant MELA-AU 6 146272445 146272445 single base substitution G A intron_variant MELA-AU 6 146272851 146272851 single base substitution G A intron_variant MELA-AU 6 146273845 146273845 single base substitution C T intron_variant MELA-AU 6 146273914 146273914 single base substitution C T intron_variant MELA-AU 6 146274167 146274167 single base substitution G A intron_variant MELA-AU 6 146274381 146274381 single base substitution C T intron_variant MELA-AU 6 146274780 146274780 single base substitution G A intron_variant MELA-AU 6 146276205 146276205 single base substitution T G exon_variant MELA-AU 6 146276205 146276205 single base substitution T G intron_variant MELA-AU 6 146276205 146276205 single base substitution T G missense_variant K85T 254A>C MELA-AU 6 146276205 146276205 single base substitution T G upstream_gene_variant MELA-AU 6 146276395 146276395 single base substitution G A exon_variant MELA-AU 6 146276395 146276395 single base substitution G A missense_variant H22Y 64C>T MELA-AU 6 146276395 146276395 single base substitution G A upstream_gene_variant MELA-AU 6 146276597 146276597 single base substitution G A intron_variant MELA-AU 6 146276597 146276597 single base substitution G A upstream_gene_variant MELA-AU 6 146277814 146277814 single base substitution C T intron_variant MELA-AU 6 146277814 146277814 single base substitution C T upstream_gene_variant MELA-AU 6 146277926 146277926 single base substitution G A intron_variant MELA-AU 6 146277926 146277926 single base substitution G A upstream_gene_variant MELA-AU 6 146279609 146279609 single base substitution G A intron_variant MELA-AU 6 146279609 146279609 single base substitution G A upstream_gene_variant MELA-AU 6 146279609 146279609 single base substitution G T intron_variant MELA-AU 6 146279609 146279609 single base substitution G T upstream_gene_variant MELA-AU 6 146281093 146281093 single base substitution G A intron_variant MELA-AU 6 146281093 146281093 single base substitution G A upstream_gene_variant MELA-AU 6 146281448 146281448 single base substitution G A intron_variant MELA-AU 6 146281684 146281684 single base substitution G A intron_variant MELA-AU 6 146281896 146281896 single base substitution G A intron_variant MELA-AU 6 146282403 146282403 single base substitution G A intron_variant MELA-AU 6 146284110 146284110 single base substitution C T intron_variant MELA-AU 6 146286101 146286102 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 6 146287062 146287062 single base substitution G A upstream_gene_variant MELA-AU 6 146287175 146287175 single base substitution C T upstream_gene_variant MELA-AU 6 146287838 146287839 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 6 146289107 146289107 single base substitution C T upstream_gene_variant MELA-AU 6 146289136 146289136 single base substitution C T upstream_gene_variant MELA-AU 6 146289704 146289704 single base substitution A G upstream_gene_variant MELA-AU 6 146289707 146289707 single base substitution C T upstream_gene_variant MELA-AU 6 146290065 146290065 single base substitution T C upstream_gene_variant MELA-AU 6 146290216 146290216 single base substitution C T upstream_gene_variant MELA-AU 6 146290254 146290254 single base substitution C T upstream_gene_variant ORCA-IN 6 146210981 146210981 single base substitution G C intron_variant ORCA-IN 6 146212930 146212931 deletion of <=200bp AA - intron_variant ORCA-IN 6 146243158 146243158 single base substitution C T intron_variant ORCA-IN 6 146268646 146268646 single base substitution C T 3_prime_UTR_variant ORCA-IN 6 146268646 146268646 single base substitution C T exon_variant ORCA-IN 6 146268646 146268646 single base substitution C T missense_variant A399T 1195G>A OV-AU 6 146181777 146181777 single base substitution A C downstream_gene_variant OV-AU 6 146182238 146182238 single base substitution C G downstream_gene_variant OV-AU 6 146183517 146183517 single base substitution G A downstream_gene_variant OV-AU 6 146185391 146185391 single base substitution T G 3_prime_UTR_variant OV-AU 6 146185412 146185412 single base substitution A T 3_prime_UTR_variant OV-AU 6 146186833 146186833 single base substitution G C intron_variant OV-AU 6 146187627 146187627 single base substitution C A intron_variant OV-AU 6 146195599 146195599 single base substitution C T intron_variant OV-AU 6 146198165 146198165 single base substitution T C intron_variant OV-AU 6 146205636 146205636 single base substitution T C downstream_gene_variant OV-AU 6 146205636 146205636 single base substitution T C intron_variant OV-AU 6 146216321 146216321 single base substitution A C intron_variant OV-AU 6 146216321 146216321 single base substitution A C upstream_gene_variant OV-AU 6 146226544 146226544 single base substitution C T 3_prime_UTR_variant OV-AU 6 146226544 146226544 single base substitution C T intron_variant OV-AU 6 146232487 146232487 single base substitution G C intron_variant OV-AU 6 146233117 146233117 single base substitution C G intron_variant OV-AU 6 146233574 146233574 single base substitution C A downstream_gene_variant OV-AU 6 146233574 146233574 single base substitution C A intron_variant OV-AU 6 146241342 146241342 single base substitution A G intron_variant OV-AU 6 146251865 146251865 single base substitution A T downstream_gene_variant OV-AU 6 146251865 146251865 single base substitution A T intron_variant OV-AU 6 146251865 146251865 single base substitution A T upstream_gene_variant OV-AU 6 146273699 146273699 single base substitution C G intron_variant OV-AU 6 146274503 146274503 single base substitution G T intron_variant OV-AU 6 146274504 146274504 single base substitution G T intron_variant OV-AU 6 146274969 146274969 single base substitution A C intron_variant OV-AU 6 146275179 146275179 single base substitution A G intron_variant OV-AU 6 146275627 146275627 single base substitution G A intron_variant OV-AU 6 146275702 146275702 single base substitution G T intron_variant OV-AU 6 146278428 146278428 single base substitution A C intron_variant OV-AU 6 146278428 146278428 single base substitution A C upstream_gene_variant OV-AU 6 146286278 146286278 single base substitution G T upstream_gene_variant OV-AU 6 146289531 146289531 single base substitution T A upstream_gene_variant PACA-AU 6 146186614 146186614 single base substitution T G intron_variant PACA-AU 6 146191466 146191466 single base substitution T C intron_variant PACA-AU 6 146192296 146192296 single base substitution C G intron_variant PACA-AU 6 146192935 146192935 single base substitution C T intron_variant PACA-AU 6 146193184 146193184 single base substitution A T intron_variant PACA-AU 6 146194331 146194331 insertion of <=200bp - T intron_variant PACA-AU 6 146198502 146198502 deletion of <=200bp T - intron_variant PACA-AU 6 146208210 146208210 single base substitution A G intron_variant PACA-AU 6 146223332 146223332 single base substitution G A downstream_gene_variant PACA-AU 6 146223332 146223332 single base substitution G A intron_variant PACA-AU 6 146231591 146231591 single base substitution G A 3_prime_UTR_variant PACA-AU 6 146231591 146231591 single base substitution G A missense_variant P1503L 4508C>T PACA-AU 6 146231591 146231591 single base substitution G A missense_variant P1507L 4520C>T PACA-AU 6 146235832 146235832 single base substitution A T downstream_gene_variant PACA-AU 6 146235832 146235832 single base substitution A T intron_variant PACA-AU 6 146248051 146248051 deletion of <=200bp G - intron_variant PACA-AU 6 146249378 146249378 single base substitution T C intron_variant PACA-AU 6 146249378 146249378 single base substitution T C upstream_gene_variant PACA-AU 6 146249670 146249670 insertion of <=200bp - AT intron_variant PACA-AU 6 146249670 146249670 insertion of <=200bp - AT upstream_gene_variant PACA-AU 6 146253455 146253455 deletion of <=200bp A - downstream_gene_variant PACA-AU 6 146253455 146253455 deletion of <=200bp A - intron_variant PACA-AU 6 146253455 146253455 deletion of <=200bp A - upstream_gene_variant PACA-AU 6 146260631 146260631 single base substitution G A intron_variant PACA-AU 6 146260631 146260631 single base substitution G A upstream_gene_variant PACA-AU 6 146261843 146261843 single base substitution G C downstream_gene_variant PACA-AU 6 146261843 146261843 single base substitution G C intron_variant PACA-AU 6 146261843 146261843 single base substitution G C upstream_gene_variant PACA-AU 6 146262936 146262936 single base substitution G A 3_prime_UTR_variant PACA-AU 6 146262936 146262936 single base substitution G A downstream_gene_variant PACA-AU 6 146262936 146262936 single base substitution G A exon_variant PACA-AU 6 146262936 146262936 single base substitution G A synonymous_variant T771T 2313C>T PACA-AU 6 146266724 146266724 deletion of <=200bp T - 3_prime_UTR_variant PACA-AU 6 146266724 146266724 deletion of <=200bp T - exon_variant PACA-AU 6 146266724 146266724 deletion of <=200bp T - frameshift_variant K457 PACA-AU 6 146268592 146268592 single base substitution G A intron_variant PACA-AU 6 146286178 146286178 single base substitution C T upstream_gene_variant PACA-AU 6 146286634 146286634 single base substitution A G upstream_gene_variant PACA-CA 6 146186976 146186976 deletion of <=200bp T - intron_variant PACA-CA 6 146187006 146187006 single base substitution C T intron_variant PACA-CA 6 146193995 146193995 single base substitution A T intron_variant PACA-CA 6 146194849 146194849 single base substitution A G intron_variant PACA-CA 6 146197670 146197670 single base substitution A G intron_variant PACA-CA 6 146198046 146198046 single base substitution C T intron_variant PACA-CA 6 146199053 146199053 single base substitution T C intron_variant PACA-CA 6 146204102 146204102 single base substitution C T downstream_gene_variant PACA-CA 6 146204102 146204102 single base substitution C T intron_variant PACA-CA 6 146206765 146206765 single base substitution C T 3_prime_UTR_variant PACA-CA 6 146206765 146206765 single base substitution C T intron_variant PACA-CA 6 146215570 146215570 single base substitution G T intron_variant PACA-CA 6 146215570 146215570 single base substitution G T upstream_gene_variant PACA-CA 6 146225760 146225760 single base substitution C T 3_prime_UTR_variant PACA-CA 6 146225760 146225760 single base substitution C T intron_variant PACA-CA 6 146234976 146234976 single base substitution T C downstream_gene_variant PACA-CA 6 146234976 146234976 single base substitution T C intron_variant PACA-CA 6 146237118 146237118 single base substitution A G downstream_gene_variant PACA-CA 6 146237118 146237118 single base substitution A G intron_variant PACA-CA 6 146240345 146240345 single base substitution C A exon_variant PACA-CA 6 146240345 146240345 single base substitution C A intron_variant PACA-CA 6 146244823 146244823 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 6 146244823 146244823 insertion of <=200bp - T exon_variant PACA-CA 6 146244823 146244823 insertion of <=200bp - T frameshift_variant T1167T? PACA-CA 6 146244823 146244823 insertion of <=200bp - T frameshift_variant T1176T? PACA-CA 6 146246959 146246959 single base substitution C T intron_variant PACA-CA 6 146251057 146251057 single base substitution T A downstream_gene_variant PACA-CA 6 146251057 146251057 single base substitution T A intron_variant PACA-CA 6 146251057 146251057 single base substitution T A upstream_gene_variant PACA-CA 6 146257373 146257373 single base substitution A G intron_variant PACA-CA 6 146257373 146257373 single base substitution A G upstream_gene_variant PACA-CA 6 146262855 146262855 single base substitution C T 3_prime_UTR_variant PACA-CA 6 146262855 146262855 single base substitution C T downstream_gene_variant PACA-CA 6 146262855 146262855 single base substitution C T exon_variant PACA-CA 6 146262855 146262855 single base substitution C T synonymous_variant Q798Q 2394G>A PACA-CA 6 146267595 146267595 single base substitution G C intron_variant PACA-CA 6 146267682 146267682 single base substitution C A intron_variant PACA-CA 6 146268740 146268740 single base substitution A G 3_prime_UTR_variant PACA-CA 6 146268740 146268740 single base substitution A G exon_variant PACA-CA 6 146268740 146268740 single base substitution A G synonymous_variant L367L 1101T>C PACA-CA 6 146274061 146274061 single base substitution C A intron_variant PACA-CA 6 146275126 146275126 single base substitution G A intron_variant PACA-CA 6 146277335 146277335 single base substitution C T intron_variant PACA-CA 6 146277335 146277335 single base substitution C T upstream_gene_variant PACA-CA 6 146278123 146278123 single base substitution T C intron_variant PACA-CA 6 146278123 146278123 single base substitution T C upstream_gene_variant PACA-CA 6 146282740 146282740 single base substitution A T intron_variant PACA-CA 6 146283953 146283953 single base substitution G A intron_variant PACA-CA 6 146286407 146286407 single base substitution G T upstream_gene_variant PACA-CA 6 146288027 146288027 single base substitution T C upstream_gene_variant PAEN-AU 6 146191466 146191466 single base substitution T C intron_variant PAEN-IT 6 146236633 146236633 single base substitution T C downstream_gene_variant PAEN-IT 6 146236633 146236633 single base substitution T C intron_variant PAEN-IT 6 146259074 146259074 single base substitution A C intron_variant PAEN-IT 6 146259074 146259074 single base substitution A C upstream_gene_variant PAEN-IT 6 146265564 146265564 single base substitution G A downstream_gene_variant PAEN-IT 6 146265564 146265564 single base substitution G A intron_variant PBCA-DE 6 146182515 146182515 single base substitution C T downstream_gene_variant PBCA-DE 6 146183430 146183430 insertion of <=200bp - A downstream_gene_variant PBCA-DE 6 146184310 146184310 single base substitution C T downstream_gene_variant PBCA-DE 6 146194331 146194331 insertion of <=200bp - T intron_variant PBCA-DE 6 146205794 146205794 single base substitution T C downstream_gene_variant PBCA-DE 6 146205794 146205794 single base substitution T C intron_variant PBCA-DE 6 146229471 146229471 single base substitution G T 3_prime_UTR_variant PBCA-DE 6 146229471 146229471 single base substitution G T intron_variant PBCA-DE 6 146244173 146244173 insertion of <=200bp - A intron_variant PBCA-DE 6 146244374 146244374 single base substitution G T intron_variant PBCA-DE 6 146248912 146248912 single base substitution C T intron_variant PBCA-DE 6 146248912 146248912 single base substitution C T upstream_gene_variant PBCA-DE 6 146252368 146252368 single base substitution G T downstream_gene_variant PBCA-DE 6 146252368 146252368 single base substitution G T intron_variant PBCA-DE 6 146252368 146252368 single base substitution G T upstream_gene_variant PBCA-DE 6 146260028 146260028 single base substitution T G intron_variant PBCA-DE 6 146260028 146260028 single base substitution T G upstream_gene_variant PBCA-DE 6 146265847 146265847 single base substitution C G downstream_gene_variant PBCA-DE 6 146265847 146265847 single base substitution C G intron_variant PBCA-DE 6 146270969 146270969 single base substitution G T intron_variant PRAD-CA 6 146201463 146201463 single base substitution A C downstream_gene_variant PRAD-CA 6 146201463 146201463 single base substitution A C intron_variant PRAD-CA 6 146206619 146206619 single base substitution G A 3_prime_UTR_variant PRAD-CA 6 146206619 146206619 single base substitution G A downstream_gene_variant PRAD-CA 6 146206619 146206619 single base substitution G A intron_variant PRAD-UK 6 146193475 146193475 deletion of <=200bp A - intron_variant PRAD-UK 6 146195842 146195842 single base substitution G C intron_variant PRAD-UK 6 146196515 146196515 single base substitution A G intron_variant PRAD-UK 6 146213945 146213945 single base substitution C A intron_variant PRAD-UK 6 146256014 146256014 single base substitution T C downstream_gene_variant PRAD-UK 6 146256014 146256014 single base substitution T C intron_variant PRAD-UK 6 146273478 146273478 single base substitution A C splice_region_variant PRAD-UK 6 146277871 146277871 single base substitution T C intron_variant PRAD-UK 6 146277871 146277871 single base substitution T C upstream_gene_variant PRAD-UK 6 146280009 146280009 single base substitution G T intron_variant PRAD-UK 6 146280009 146280009 single base substitution G T upstream_gene_variant PRAD-UK 6 146283227 146283227 single base substitution G A intron_variant PRAD-US 6 146243842 146243842 single base substitution C G 3_prime_UTR_variant PRAD-US 6 146243842 146243842 single base substitution C G exon_variant PRAD-US 6 146243842 146243842 single base substitution C G missense_variant A1226P 3676G>C PRAD-US 6 146243842 146243842 single base substitution C G missense_variant A1230P 3688G>C PRAD-US 6 146264543 146264543 single base substitution G A 3_prime_UTR_variant PRAD-US 6 146264543 146264543 single base substitution G A downstream_gene_variant PRAD-US 6 146264543 146264543 single base substitution G A exon_variant PRAD-US 6 146264543 146264543 single base substitution G A synonymous_variant R658R 1974C>T READ-US 6 146209198 146209198 single base substitution A G missense_variant I1638T 4913T>C READ-US 6 146209198 146209198 single base substitution A G missense_variant I1642T 4925T>C READ-US 6 146209198 146209198 single base substitution A G missense_variant I60T 179T>C READ-US 6 146256428 146256428 single base substitution C A 3_prime_UTR_variant READ-US 6 146256428 146256428 single base substitution C A exon_variant READ-US 6 146256428 146256428 single base substitution C A missense_variant D907Y 2719G>T READ-US 6 146264622 146264622 single base substitution C G 3_prime_UTR_variant READ-US 6 146264622 146264622 single base substitution C G downstream_gene_variant READ-US 6 146264622 146264622 single base substitution C G exon_variant READ-US 6 146264622 146264622 single base substitution C G missense_variant C632S 1895G>C READ-US 6 146276034 146276034 single base substitution C A exon_variant READ-US 6 146276034 146276034 single base substitution C A intron_variant READ-US 6 146276034 146276034 single base substitution C A missense_variant S142I 425G>T READ-US 6 146276034 146276034 single base substitution C A upstream_gene_variant READ-US 6 146276446 146276446 single base substitution G A exon_variant READ-US 6 146276446 146276446 single base substitution G A missense_variant R5W 13C>T READ-US 6 146276446 146276446 single base substitution G A upstream_gene_variant RECA-EU 6 146189371 146189371 single base substitution T G intron_variant RECA-EU 6 146207183 146207183 single base substitution C A 3_prime_UTR_variant RECA-EU 6 146207183 146207183 single base substitution C A intron_variant RECA-EU 6 146208331 146208331 single base substitution T C intron_variant RECA-EU 6 146209703 146209703 single base substitution T A intron_variant RECA-EU 6 146217953 146217953 single base substitution T G intron_variant RECA-EU 6 146217953 146217953 single base substitution T G upstream_gene_variant RECA-EU 6 146226648 146226648 single base substitution C T 3_prime_UTR_variant RECA-EU 6 146226648 146226648 single base substitution C T intron_variant RECA-EU 6 146226963 146226963 single base substitution G A 3_prime_UTR_variant RECA-EU 6 146226963 146226963 single base substitution G A intron_variant RECA-EU 6 146229862 146229862 single base substitution T G 3_prime_UTR_variant RECA-EU 6 146229862 146229862 single base substitution T G intron_variant RECA-EU 6 146240413 146240413 single base substitution T C exon_variant RECA-EU 6 146240413 146240413 single base substitution T C intron_variant RECA-EU 6 146240665 146240665 single base substitution T C intron_variant RECA-EU 6 146247303 146247303 single base substitution A C intron_variant RECA-EU 6 146249496 146249496 single base substitution C G intron_variant RECA-EU 6 146249496 146249496 single base substitution C G upstream_gene_variant RECA-EU 6 146259451 146259451 single base substitution G A intron_variant RECA-EU 6 146259451 146259451 single base substitution G A upstream_gene_variant RECA-EU 6 146265831 146265831 single base substitution C A downstream_gene_variant RECA-EU 6 146265831 146265831 single base substitution C A intron_variant RECA-EU 6 146265833 146265833 single base substitution T A downstream_gene_variant RECA-EU 6 146265833 146265833 single base substitution T A intron_variant RECA-EU 6 146270740 146270740 single base substitution A T intron_variant RECA-EU 6 146273865 146273865 single base substitution T C intron_variant RECA-EU 6 146274312 146274312 single base substitution A G intron_variant RECA-EU 6 146284210 146284210 single base substitution A G intron_variant RECA-EU 6 146286887 146286887 single base substitution A T upstream_gene_variant SKCA-BR 6 146186079 146186079 insertion of <=200bp - TCA intron_variant SKCA-BR 6 146186079 146186079 single base substitution T A intron_variant SKCA-BR 6 146188654 146188654 single base substitution G A intron_variant SKCA-BR 6 146188767 146188767 insertion of <=200bp - TATAGAGAG intron_variant SKCA-BR 6 146188902 146188902 single base substitution T G intron_variant SKCA-BR 6 146191403 146191403 single base substitution T A intron_variant SKCA-BR 6 146191662 146191662 single base substitution T A intron_variant SKCA-BR 6 146193482 146193482 insertion of <=200bp - CA intron_variant SKCA-BR 6 146194831 146194831 single base substitution G A intron_variant SKCA-BR 6 146205005 146205005 single base substitution G A downstream_gene_variant SKCA-BR 6 146205005 146205005 single base substitution G A intron_variant SKCA-BR 6 146206996 146206996 single base substitution A C 3_prime_UTR_variant SKCA-BR 6 146206996 146206996 single base substitution A C intron_variant SKCA-BR 6 146208669 146208669 single base substitution G T intron_variant SKCA-BR 6 146208806 146208806 single base substitution A G intron_variant SKCA-BR 6 146210846 146210846 single base substitution A G intron_variant SKCA-BR 6 146214048 146214048 single base substitution T C intron_variant SKCA-BR 6 146215556 146215556 insertion of <=200bp - GT intron_variant SKCA-BR 6 146215556 146215556 insertion of <=200bp - GT upstream_gene_variant SKCA-BR 6 146219689 146219689 single base substitution T G downstream_gene_variant SKCA-BR 6 146219689 146219689 single base substitution T G intron_variant SKCA-BR 6 146221324 146221324 single base substitution G A downstream_gene_variant SKCA-BR 6 146221324 146221324 single base substitution G A intron_variant SKCA-BR 6 146223775 146223775 single base substitution G A downstream_gene_variant SKCA-BR 6 146223775 146223775 single base substitution G A intron_variant SKCA-BR 6 146229803 146229803 single base substitution G A 3_prime_UTR_variant SKCA-BR 6 146229803 146229803 single base substitution G A intron_variant SKCA-BR 6 146235698 146235698 single base substitution A G downstream_gene_variant SKCA-BR 6 146235698 146235698 single base substitution A G intron_variant SKCA-BR 6 146237163 146237163 single base substitution C T downstream_gene_variant SKCA-BR 6 146237163 146237163 single base substitution C T intron_variant SKCA-BR 6 146240125 146240125 single base substitution G A exon_variant SKCA-BR 6 146240125 146240125 single base substitution G A intron_variant SKCA-BR 6 146242583 146242583 single base substitution A G intron_variant SKCA-BR 6 146244081 146244081 insertion of <=200bp - GT intron_variant SKCA-BR 6 146252232 146252232 single base substitution T C downstream_gene_variant SKCA-BR 6 146252232 146252232 single base substitution T C intron_variant SKCA-BR 6 146252232 146252232 single base substitution T C upstream_gene_variant SKCA-BR 6 146255609 146255609 insertion of <=200bp - TAAATA downstream_gene_variant SKCA-BR 6 146255609 146255609 insertion of <=200bp - TAAATA intron_variant SKCA-BR 6 146258114 146258116 deletion of <=200bp CTT - intron_variant SKCA-BR 6 146258114 146258116 deletion of <=200bp CTT - upstream_gene_variant SKCA-BR 6 146258119 146258119 single base substitution T C intron_variant SKCA-BR 6 146258119 146258119 single base substitution T C upstream_gene_variant SKCA-BR 6 146259593 146259593 single base substitution A G intron_variant SKCA-BR 6 146259593 146259593 single base substitution A G upstream_gene_variant SKCA-BR 6 146261681 146261681 single base substitution A T intron_variant SKCA-BR 6 146261681 146261681 single base substitution A T upstream_gene_variant SKCA-BR 6 146271985 146271985 single base substitution A T intron_variant SKCA-BR 6 146283743 146283743 single base substitution A T intron_variant SKCM-US 6 146214476 146214476 single base substitution G A synonymous_variant P1583P 4749C>T SKCM-US 6 146214476 146214476 single base substitution G A synonymous_variant P1587P 4761C>T SKCM-US 6 146214476 146214476 single base substitution G A synonymous_variant P5P 15C>T SKCM-US 6 146231636 146231636 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146231636 146231636 single base substitution G A missense_variant S1488L 4463C>T SKCM-US 6 146231636 146231636 single base substitution G A missense_variant S1492L 4475C>T SKCM-US 6 146243875 146243875 single base substitution C T 3_prime_UTR_variant SKCM-US 6 146243875 146243875 single base substitution C T exon_variant SKCM-US 6 146243875 146243875 single base substitution C T missense_variant E1215K 3643G>A SKCM-US 6 146243875 146243875 single base substitution C T missense_variant E1219K 3655G>A SKCM-US 6 146256071 146256071 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146256071 146256071 single base substitution G A exon_variant SKCM-US 6 146256071 146256071 single base substitution G A missense_variant R988C 2962C>T SKCM-US 6 146256182 146256182 single base substitution T C 3_prime_UTR_variant SKCM-US 6 146256182 146256182 single base substitution T C exon_variant SKCM-US 6 146256182 146256182 single base substitution T C missense_variant K951E 2851A>G SKCM-US 6 146256482 146256482 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146256482 146256482 single base substitution G A exon_variant SKCM-US 6 146256482 146256482 single base substitution G A missense_variant P889S 2665C>T SKCM-US 6 146256503 146256503 single base substitution G C 3_prime_UTR_variant SKCM-US 6 146256503 146256503 single base substitution G C exon_variant SKCM-US 6 146256503 146256503 single base substitution G C missense_variant R882G 2644C>G SKCM-US 6 146262942 146262942 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146262942 146262942 single base substitution G A downstream_gene_variant SKCM-US 6 146262942 146262942 single base substitution G A exon_variant SKCM-US 6 146262942 146262942 single base substitution G A synonymous_variant I769I 2307C>T SKCM-US 6 146264611 146264611 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146264611 146264611 single base substitution G A downstream_gene_variant SKCM-US 6 146264611 146264611 single base substitution G A exon_variant SKCM-US 6 146264611 146264611 single base substitution G A synonymous_variant L636L 1906C>T SKCM-US 6 146264734 146264734 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146264734 146264734 single base substitution G A downstream_gene_variant SKCM-US 6 146264734 146264734 single base substitution G A exon_variant SKCM-US 6 146264734 146264734 single base substitution G A missense_variant P595S 1783C>T SKCM-US 6 146266598 146266598 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146266598 146266598 single base substitution G A downstream_gene_variant SKCM-US 6 146266598 146266598 single base substitution G A exon_variant SKCM-US 6 146266598 146266598 single base substitution G A synonymous_variant I499I 1497C>T SKCM-US 6 146266711 146266711 single base substitution G A 3_prime_UTR_variant SKCM-US 6 146266711 146266711 single base substitution G A exon_variant SKCM-US 6 146266711 146266711 single base substitution G A missense_variant L462F 1384C>T SKCM-US 6 146271487 146271487 single base substitution C A 3_prime_UTR_variant SKCM-US 6 146271487 146271487 single base substitution C A exon_variant SKCM-US 6 146271487 146271487 single base substitution C A missense_variant A299S 895G>T SKCM-US 6 146276122 146276122 single base substitution T C exon_variant SKCM-US 6 146276122 146276122 single base substitution T C intron_variant SKCM-US 6 146276122 146276122 single base substitution T C missense_variant K113E 337A>G SKCM-US 6 146276122 146276122 single base substitution T C upstream_gene_variant SKCM-US 6 146276180 146276180 single base substitution G A exon_variant SKCM-US 6 146276180 146276180 single base substitution G A intron_variant SKCM-US 6 146276180 146276180 single base substitution G A synonymous_variant S93S 279C>T SKCM-US 6 146276180 146276180 single base substitution G A upstream_gene_variant STAD-US 6 146214432 146214432 single base substitution T C missense_variant H1598R 4793A>G STAD-US 6 146214432 146214432 single base substitution T C missense_variant H1602R 4805A>G STAD-US 6 146214432 146214432 single base substitution T C missense_variant H20R 59A>G STAD-US 6 146240548 146240548 single base substitution C G 3_prime_UTR_variant STAD-US 6 146240548 146240548 single base substitution C G exon_variant STAD-US 6 146240548 146240548 single base substitution C G missense_variant R1363T 4088G>C STAD-US 6 146240548 146240548 single base substitution C G missense_variant R1367T 4100G>C STAD-US 6 146240594 146240594 single base substitution G A 3_prime_UTR_variant STAD-US 6 146240594 146240594 single base substitution G A exon_variant STAD-US 6 146240594 146240594 single base substitution G A missense_variant R1348C 4042C>T STAD-US 6 146240594 146240594 single base substitution G A missense_variant R1352C 4054C>T STAD-US 6 146243472 146243472 single base substitution A G 3_prime_UTR_variant STAD-US 6 146243472 146243472 single base substitution A G exon_variant STAD-US 6 146243472 146243472 single base substitution A G synonymous_variant C1244C 3732T>C STAD-US 6 146243472 146243472 single base substitution A G synonymous_variant C1248C 3744T>C STAD-US 6 146244889 146244889 single base substitution C G 3_prime_UTR_variant STAD-US 6 146244889 146244889 single base substitution C G exon_variant STAD-US 6 146244889 146244889 single base substitution C G synonymous_variant V1145V 3435G>C STAD-US 6 146244889 146244889 single base substitution C G synonymous_variant V1154V 3462G>C STAD-US 6 146247355 146247355 single base substitution G A 3_prime_UTR_variant STAD-US 6 146247355 146247355 single base substitution G A exon_variant STAD-US 6 146247355 146247355 single base substitution G A synonymous_variant G1093G 3279C>T STAD-US 6 146247355 146247355 single base substitution G A synonymous_variant G1102G 3306C>T STAD-US 6 146247425 146247425 single base substitution T C 3_prime_UTR_variant STAD-US 6 146247425 146247425 single base substitution T C exon_variant STAD-US 6 146247425 146247425 single base substitution T C missense_variant H1070R 3209A>G STAD-US 6 146247425 146247425 single base substitution T C missense_variant H1079R 3236A>G STAD-US 6 146254276 146254276 single base substitution T G 3_prime_UTR_variant STAD-US 6 146254276 146254276 single base substitution T G downstream_gene_variant STAD-US 6 146254276 146254276 single base substitution T G exon_variant STAD-US 6 146254276 146254276 single base substitution T G missense_variant K1010T 3029A>C STAD-US 6 146254276 146254276 single base substitution T G missense_variant K1019T 3056A>C STAD-US 6 146256106 146256106 single base substitution C A 3_prime_UTR_variant STAD-US 6 146256106 146256106 single base substitution C A exon_variant STAD-US 6 146256106 146256106 single base substitution C A missense_variant R976M 2927G>T STAD-US 6 146256278 146256278 single base substitution C T 3_prime_UTR_variant STAD-US 6 146256278 146256278 single base substitution C T exon_variant STAD-US 6 146256278 146256278 single base substitution C T missense_variant E919K 2755G>A STAD-US 6 146256569 146256569 insertion of <=200bp - A 3_prime_UTR_variant STAD-US 6 146256569 146256569 insertion of <=200bp - A exon_variant STAD-US 6 146256569 146256569 insertion of <=200bp - A frameshift_variant G860V? STAD-US 6 146256570 146256570 insertion of <=200bp - A 3_prime_UTR_variant STAD-US 6 146256570 146256570 insertion of <=200bp - A exon_variant STAD-US 6 146256570 146256570 insertion of <=200bp - A frameshift_variant F859F? STAD-US 6 146262872 146262872 single base substitution G A 3_prime_UTR_variant STAD-US 6 146262872 146262872 single base substitution G A downstream_gene_variant STAD-US 6 146262872 146262872 single base substitution G A exon_variant STAD-US 6 146262872 146262872 single base substitution G A missense_variant R793C 2377C>T STAD-US 6 146262928 146262928 single base substitution A G 3_prime_UTR_variant STAD-US 6 146262928 146262928 single base substitution A G downstream_gene_variant STAD-US 6 146262928 146262928 single base substitution A G exon_variant STAD-US 6 146262928 146262928 single base substitution A G missense_variant V774A 2321T>C STAD-US 6 146264379 146264379 single base substitution A G 3_prime_UTR_variant STAD-US 6 146264379 146264379 single base substitution A G downstream_gene_variant STAD-US 6 146264379 146264379 single base substitution A G exon_variant STAD-US 6 146264379 146264379 single base substitution A G missense_variant V713A 2138T>C STAD-US 6 146264759 146264759 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 6 146264759 146264759 deletion of <=200bp T - downstream_gene_variant STAD-US 6 146264759 146264759 deletion of <=200bp T - exon_variant STAD-US 6 146264759 146264759 deletion of <=200bp T - frameshift_variant K586 STAD-US 6 146264834 146264834 insertion of <=200bp - ATC 3_prime_UTR_variant STAD-US 6 146264834 146264834 insertion of <=200bp - ATC downstream_gene_variant STAD-US 6 146264834 146264834 insertion of <=200bp - ATC exon_variant STAD-US 6 146264834 146264834 insertion of <=200bp - ATC inframe_insertion D561DD STAD-US 6 146266640 146266640 single base substitution C T 3_prime_UTR_variant STAD-US 6 146266640 146266640 single base substitution C T downstream_gene_variant STAD-US 6 146266640 146266640 single base substitution C T exon_variant STAD-US 6 146266640 146266640 single base substitution C T synonymous_variant R485R 1455G>A STAD-US 6 146266673 146266673 single base substitution G A 3_prime_UTR_variant STAD-US 6 146266673 146266673 single base substitution G A downstream_gene_variant STAD-US 6 146266673 146266673 single base substitution G A exon_variant STAD-US 6 146266673 146266673 single base substitution G A synonymous_variant Y474Y 1422C>T STAD-US 6 146266724 146266724 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 6 146266724 146266724 deletion of <=200bp T - exon_variant STAD-US 6 146266724 146266724 deletion of <=200bp T - frameshift_variant K457 STAD-US 6 146267451 146267451 single base substitution C T 3_prime_UTR_variant STAD-US 6 146267451 146267451 single base substitution C T exon_variant STAD-US 6 146267451 146267451 single base substitution C T synonymous_variant P413P 1239G>A UCEC-US 6 146207903 146207903 single base substitution T C intron_variant UCEC-US 6 146207903 146207903 single base substitution T C missense_variant K1659R 4976A>G UCEC-US 6 146207903 146207903 single base substitution T C missense_variant K1663R 4988A>G UCEC-US 6 146214414 146214414 single base substitution G A missense_variant P1604L 4811C>T UCEC-US 6 146214414 146214414 single base substitution G A missense_variant P1608L 4823C>T UCEC-US 6 146214414 146214414 single base substitution G A missense_variant P26L 77C>T UCEC-US 6 146215302 146215302 single base substitution C G missense_variant R1560P 4679G>C UCEC-US 6 146215302 146215302 single base substitution C G missense_variant R1564P 4691G>C UCEC-US 6 146215302 146215302 single base substitution C G upstream_gene_variant UCEC-US 6 146234648 146234648 single base substitution G T 3_prime_UTR_variant UCEC-US 6 146234648 146234648 single base substitution G T downstream_gene_variant UCEC-US 6 146234648 146234648 single base substitution G T missense_variant P1431H 4292C>A UCEC-US 6 146234648 146234648 single base substitution G T missense_variant P1435H 4304C>A UCEC-US 6 146240488 146240488 single base substitution T C 3_prime_UTR_variant UCEC-US 6 146240488 146240488 single base substitution T C exon_variant UCEC-US 6 146240488 146240488 single base substitution T C missense_variant H1383R 4148A>G UCEC-US 6 146240488 146240488 single base substitution T C missense_variant H1387R 4160A>G UCEC-US 6 146242464 146242464 single base substitution G A 3_prime_UTR_variant UCEC-US 6 146242464 146242464 single base substitution G A exon_variant UCEC-US 6 146242464 146242464 single base substitution G A stop_gained R1283* 3847C>T UCEC-US 6 146242464 146242464 single base substitution G A stop_gained R1287* 3859C>T UCEC-US 6 146243935 146243935 single base substitution T G 3_prime_UTR_variant UCEC-US 6 146243935 146243935 single base substitution T G exon_variant UCEC-US 6 146243935 146243935 single base substitution T G missense_variant T1195P 3583A>C UCEC-US 6 146243935 146243935 single base substitution T G missense_variant T1199P 3595A>C UCEC-US 6 146244781 146244781 single base substitution C A missense_variant E1181D 3543G>T UCEC-US 6 146244781 146244781 single base substitution C A missense_variant E1190D 3570G>T UCEC-US 6 146244781 146244781 single base substitution C A splice_region_variant UCEC-US 6 146244837 146244837 single base substitution G A 3_prime_UTR_variant UCEC-US 6 146244837 146244837 single base substitution G A exon_variant UCEC-US 6 146244837 146244837 single base substitution G A stop_gained R1163* 3487C>T UCEC-US 6 146244837 146244837 single base substitution G A stop_gained R1172* 3514C>T UCEC-US 6 146256575 146256575 single base substitution G T exon_variant UCEC-US 6 146256575 146256575 single base substitution G T missense_variant L858I 2572C>A UCEC-US 6 146256575 146256575 single base substitution G T splice_region_variant UCEC-US 6 146262773 146262773 single base substitution A G 3_prime_UTR_variant UCEC-US 6 146262773 146262773 single base substitution A G downstream_gene_variant UCEC-US 6 146262773 146262773 single base substitution A G exon_variant UCEC-US 6 146262773 146262773 single base substitution A G missense_variant C826R 2476T>C UCEC-US 6 146262922 146262922 single base substitution C T 3_prime_UTR_variant UCEC-US 6 146262922 146262922 single base substitution C T downstream_gene_variant UCEC-US 6 146262922 146262922 single base substitution C T exon_variant UCEC-US 6 146262922 146262922 single base substitution C T missense_variant R776H 2327G>A UCEC-US 6 146262963 146262963 single base substitution C T 3_prime_UTR_variant UCEC-US 6 146262963 146262963 single base substitution C T downstream_gene_variant UCEC-US 6 146262963 146262963 single base substitution C T exon_variant UCEC-US 6 146262963 146262963 single base substitution C T synonymous_variant L762L 2286G>A UCEC-US 6 146264362 146264362 single base substitution G A 3_prime_UTR_variant UCEC-US 6 146264362 146264362 single base substitution G A downstream_gene_variant UCEC-US 6 146264362 146264362 single base substitution G A exon_variant UCEC-US 6 146264362 146264362 single base substitution G A synonymous_variant L719L 2155C>T UCEC-US 6 146264653 146264653 single base substitution C A 3_prime_UTR_variant UCEC-US 6 146264653 146264653 single base substitution C A downstream_gene_variant UCEC-US 6 146264653 146264653 single base substitution C A exon_variant UCEC-US 6 146264653 146264653 single base substitution C A stop_gained E622* 1864G>T UCEC-US 6 146264800 146264800 single base substitution G A 3_prime_UTR_variant UCEC-US 6 146264800 146264800 single base substitution G A downstream_gene_variant UCEC-US 6 146264800 146264800 single base substitution G A exon_variant UCEC-US 6 146264800 146264800 single base substitution G A missense_variant R573C 1717C>T UCEC-US 6 146266555 146266555 single base substitution A C 3_prime_UTR_variant UCEC-US 6 146266555 146266555 single base substitution A C downstream_gene_variant UCEC-US 6 146266555 146266555 single base substitution A C exon_variant UCEC-US 6 146266555 146266555 single base substitution A C missense_variant Y514D 1540T>G UCEC-US 6 146266636 146266636 single base substitution G A 3_prime_UTR_variant UCEC-US 6 146266636 146266636 single base substitution G A downstream_gene_variant UCEC-US 6 146266636 146266636 single base substitution G A exon_variant UCEC-US 6 146266636 146266636 single base substitution G A synonymous_variant L487L 1459C>T UCEC-US 6 146267368 146267368 single base substitution C T splice_donor_variant UCEC-US 6 146267452 146267452 single base substitution G T 3_prime_UTR_variant UCEC-US 6 146267452 146267452 single base substitution G T exon_variant UCEC-US 6 146267452 146267452 single base substitution G T missense_variant P413Q 1238C>A UCEC-US 6 146267458 146267458 single base substitution A C 3_prime_UTR_variant UCEC-US 6 146267458 146267458 single base substitution A C exon_variant UCEC-US 6 146267458 146267458 single base substitution A C missense_variant F411C 1232T>G UCEC-US 6 146273496 146273496 single base substitution G T exon_variant UCEC-US 6 146273496 146273496 single base substitution G T missense_variant S251Y 752C>A UCEC-US 6 146276186 146276186 single base substitution A C exon_variant UCEC-US 6 146276186 146276186 single base substitution A C intron_variant UCEC-US 6 146276186 146276186 single base substitution A C missense_variant I91M 273T>G UCEC-US 6 146276186 146276186 single base substitution A C upstream_gene_variant UCEC-US 6 146276252 146276252 single base substitution A C exon_variant UCEC-US 6 146276252 146276252 single base substitution A C intron_variant UCEC-US 6 146276252 146276252 single base substitution A C missense_variant D69E 207T>G UCEC-US 6 146276252 146276252 single base substitution A C upstream_gene_variant UCEC-US 6 146276266 146276266 single base substitution C T exon_variant UCEC-US 6 146276266 146276266 single base substitution C T intron_variant UCEC-US 6 146276266 146276266 single base substitution C T missense_variant V65M 193G>A UCEC-US 6 146276266 146276266 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-61-2113-01 COSM115726 c.2741T>G p.I914R Substitution - Missense 6:145935156-145935156 - J74_T COSM3948116 c.4843A>G p.I1615V Substitution - Missense 6:145893246-145893246 - TCGA-AC-A23H-01 COSM3829238 c.40G>A p.D14N Substitution - Missense 6:145955283-145955283 - MB104X COSM87919 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - ESCC_47 COSM5630798 c.3045A>G p.T1015T Substitution - coding silent 6:145933151-145933151 - ESO-107 COSM1265550 c.3997G>A p.E1333K Substitution - Missense 6:145921190-145921190 - TCGA-66-2744-01 COSM4862413 c.2950C>A p.P984T Substitution - Missense 6:145934947-145934947 - TCGA-BS-A0UV-01 COSM4864611 c.1864G>T p.E622* Substitution - Nonsense 6:145943517-145943517 - BCM337T COSM4799044 c.2363A>G p.N788S Substitution - Missense 6:145941750-145941750 - LP6005500-DNA_G01 COSM5036526 c.3307C>T p.R1103* Substitution - Nonsense 6:145924834-145924834 - TCGA-JW-A5VJ-01 COSM4818428 c.514G>A p.D172N Substitution - Missense 6:145954809-145954809 - TCGA-EE-A2MQ-06 COSM3621310 c.337A>G p.K113E Substitution - Missense 6:145954986-145954986 - TCGA-AC-A23H-01 COSM3829236 c.528G>A p.L176L Substitution - coding silent 6:145954795-145954795 - TCGA-AC-A3W6-01 COSM3829233 c.1175G>A p.R392Q Substitution - Missense 6:145947530-145947530 - TCGA-AP-A051-01 COSM4872428 c.2476T>C p.C826R Substitution - Missense 6:145941637-145941637 - BCM723T COSM5348497 c.3720-5_3720-4insT p.? Unknown 6:145922352-145922353 - TCGA-BR-A4J4-01 COSM3858837 c.4088G>C p.R1363T Substitution - Missense 6:145919412-145919412 - CRC-02T COSM5455451 c.4855C>T p.H1619Y Substitution - Missense 6:145893234-145893234 - LS411 COSM3017659 c.1371delA p.G458fs*26 Deletion - Frameshift 6:145945588-145945588 - TCGA-BR-A4J4-01 COSM3858838 c.4100G>C p.R1367T Substitution - Missense 6:145919412-145919412 - 587376 COSM1225670 c.3983C>A p.S1328* Substitution - Nonsense 6:145921204-145921204 - TCGA-AP-A051-01 COSM1074176 c.4823C>T p.P1608L Substitution - Missense 6:145893278-145893278 - Pat_40_A COSM5869478 c.199C>T p.H67Y Substitution - Missense 6:145955124-145955124 - TCGA-B2-5633-01 COSM483495 c.2046G>T p.L682L Substitution - coding silent 6:145943335-145943335 - 61 COSM5737797 c.2701T>C p.W901R Substitution - Missense 6:145935310-145935310 - PCSI_0019_Pa_P_526 COSM3381443 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - 61 COSM5737796 c.2701T>C p.W901R Substitution - Missense 6:145935310-145935310 - CHEWS024 COSM3017624 c.2085T>G p.N695K Substitution - Missense 6:145943296-145943296 - PCSI_0083_Pa_X COSM3381445 c.1101T>C p.L367L Substitution - coding silent 6:145947604-145947604 - 66 COSM5083640 c.1758delA p.G587fs*23 Deletion - Frameshift 6:145943623-145943623 - LUAD-CHTN-Z4716A COSM362500 c.4052A>T p.N1351I Substitution - Missense 6:145919460-145919460 - TCGA-CM-6171-01 COSM3017694 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - TCGA-BS-A0UF-01 COSM4586287 c.3487C>T p.R1163* Substitution - Nonsense 6:145923701-145923701 - 13542 COSM740719 c.3507G>A p.Q1169Q Substitution - coding silent 6:145923708-145923708 - HT55 COSM1074205 c.1717C>T p.R573C Substitution - Missense 6:145943664-145943664 - S01504 COSM4387359 c.1283A>G p.N428S Substitution - Missense 6:145946271-145946271 - S02248 COSM5679773 c.1984A>T p.I662L Substitution - Missense 6:145943397-145943397 - 0036_CRUK_PC_0036_T1_DNA COSM5423466 c.763+7T>G p.? Unknown 6:145952342-145952342 - 721LT COSM328199 c.476A>C p.D159A Substitution - Missense 6:145954847-145954847 - LIM2551 COSM1440972 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - TCGA-AP-A051-01 COSM4874101 c.4811C>T p.P1604L Substitution - Missense 6:145893278-145893278 - ESO-0009 COSM1265548 c.2057C>A p.A686E Substitution - Missense 6:145943324-145943324 - B47 COSM1754570 c.4158A>G p.E1386E Substitution - coding silent 6:145918227-145918227 - YUKAT COSM5404528 c.1365A>G p.G455G Substitution - coding silent 6:145945594-145945594 - 2293776 COSM4607935 c.3556C>A p.L1186I Substitution - Missense 6:145923659-145923659 - TCGA-ER-A193-06 COSM3621294 c.3655G>A p.E1219K Substitution - Missense 6:145922739-145922739 - TCGA-B6-A0WZ-01 COSM4815121 c.3892G>C p.E1298Q Substitution - Missense 6:145921283-145921283 - 2318494 COSM4777263 c.3671A>C p.E1224A Substitution - Missense 6:145922711-145922711 - HCC058T COSM5805502 c.1419A>T p.R473S Substitution - Missense 6:145945540-145945540 - TCGA-EP-A26S-01 COSM4913527 c.1741G>T p.V581F Substitution - Missense 6:145943640-145943640 - TCGA-BG-A0MQ-01 COSM4874458 c.2286G>A p.L762L Substitution - coding silent 6:145941827-145941827 - T36 COSM4725914 c.908T>C p.V303A Substitution - Missense 6:145950338-145950338 - TCGA-BR-6452-01 COSM3858857 c.2138T>C p.V713A Substitution - Missense 6:145943243-145943243 - T3064 COSM1642886 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - sysucc-1317T COSM5450192 c.1800C>T p.H600H Substitution - coding silent 6:145943581-145943581 - B80-5 COSM1754575 c.2197G>C p.E733Q Substitution - Missense 6:145943184-145943184 - TCGA-BR-8360-01 COSM3858853 c.2755G>A p.E919K Substitution - Missense 6:145935142-145935142 - TCGA-AP-A059-01 COSM4866108 c.1321+1G>A p.? Unknown 6:145946232-145946232 - TCGA-BR-6706-01 COSM3858848 c.3029A>C p.K1010T Substitution - Missense 6:145933140-145933140 - PCSI0019 COSM216735 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - TCGA-A5-A0GA-01 COSM1595893 c.4976A>G p.K1659R Substitution - Missense 6:145886767-145886767 - T3024 COSM4725910 c.1984A>G p.I662V Substitution - Missense 6:145943397-145943397 - T636 COSM3017599 c.2644C>T p.R882W Substitution - Missense 6:145935367-145935367 - TCGA-BR-7707-01 COSM3017615 c.2321T>C p.V774A Substitution - Missense 6:145941792-145941792 - CSCC-56-T COSM4516155 c.1632_1633GG>TA p.K544_D545>NN Complex - compound substitution 6:145943748-145943749 - T2568 COSM4725918 c.500C>T p.P167L Substitution - Missense 6:145954823-145954823 - TCGA-66-2786-01 COSM740721 c.4606C>G p.L1536V Substitution - Missense 6:145894899-145894899 - HT55 COSM3017642 c.1717C>T p.R573C Substitution - Missense 6:145943664-145943664 - TCGA-CA-6718-01 COSM4787022 c.246A>G p.P82P Substitution - coding silent 6:145955077-145955077 - T1154 COSM4725904 c.4221T>C p.L1407L Substitution - coding silent 6:145918164-145918164 - TCGA-AC-A23H-01 COSM3829237 c.40G>A p.D14N Substitution - Missense 6:145955283-145955283 - TCGA-D1-A101-01 COSM1074180 c.4608C>T p.L1536L Substitution - coding silent 6:145894897-145894897 - RK001_C01 COSM1634545 c.3076G>A p.E1026K Substitution - Missense 6:145933120-145933120 - WA16 COSM241604 c.2021G>A p.R674H Substitution - Missense 6:145943360-145943360 - ESCC_6 COSM5623388 c.873C>T p.I291I Substitution - coding silent 6:145950373-145950373 - TCGA-AN-A046-01 COSM3829239 c.23C>T p.A8V Substitution - Missense 6:145955300-145955300 - DLD1 COSM1642887 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - RK065_C01 COSM1634547 c.1494G>A p.Q498Q Substitution - coding silent 6:145945465-145945465 - XHDG38 COSM4769770 c.764-9G>C p.? Unknown 6:145950491-145950491 - TCGA-37-4141-01 COSM4859206 c.2290G>T p.E764* Substitution - Nonsense 6:145941823-145941823 - HT115 COSM3017530 c.4871G>A p.R1624Q Substitution - Missense 6:145893230-145893230 - TCGA-E2-A1LS-01 COSM1487295 c.3298C>T p.R1100C Substitution - Missense 6:145926227-145926227 - Pat_41_B COSM1440972 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - TCGA-A2-A1FV-01 COSM4814155 c.4081C>T p.R1361* Substitution - Nonsense 6:145919419-145919419 - SNUH_G61_S1 COSM4003714 c.2632C>T p.R878* Substitution - Nonsense 6:145935379-145935379 - TCGA-CA-6718-01 COSM1440973 c.246A>G p.P82P Substitution - coding silent 6:145955077-145955077 - pfg127T COSM3017612 c.2398C>T p.R800C Substitution - Missense 6:145941715-145941715 - TCGA-HC-A48F-01 COSM3783941 c.1974C>T p.R658R Substitution - coding silent 6:145943407-145943407 - SNUH_G61_S1 COSM4003715 c.2632C>T p.R878* Substitution - Nonsense 6:145935379-145935379 - CRC-02T COSM5455452 c.4867C>T p.H1623Y Substitution - Missense 6:145893234-145893234 - S00472 COSM315157 c.1373G>T p.G458V Substitution - Missense 6:145945586-145945586 - TCGA-B5-A0JY-01 COSM1074219 c.752C>A p.S251Y Substitution - Missense 6:145952360-145952360 - TCGA-ES-A2HT-01 COSM4938823 c.2228T>C p.L743P Substitution - Missense 6:145943153-145943153 - YUKAT COSM5404521 c.3344C>T p.A1115V Substitution - Missense 6:145924797-145924797 - TCGA-G4-6294-01 COSM3697554 c.3783-1G>C p.? Unknown 6:145921393-145921393 - pfg127T COSM3017611 c.2398C>T p.R800C Substitution - Missense 6:145941715-145941715 - Gp5D COSM3017526 c.4903A>G p.R1635G Substitution - Missense 6:145888084-145888084 - HCC2998 COSM205721 c.3181C>T p.R1061C Substitution - Missense 6:145927236-145927236 - TCGA-CZ-5984-01 COSM483496 c.750T>A p.N250K Substitution - Missense 6:145952362-145952362 - TCGA-AP-A059-01 COSM1074215 c.1232T>G p.F411C Substitution - Missense 6:145946322-145946322 - PCSI_0019_Pa_P COSM216735 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - Capan-1 COSM328199 c.476A>C p.D159A Substitution - Missense 6:145954847-145954847 - TCGA-AX-A0J0-01 COSM1074207 c.1540T>G p.Y514D Substitution - Missense 6:145945419-145945419 - ESO-963 COSM1265551 c.2414C>T p.P805L Substitution - Missense 6:145941699-145941699 - B59-0 COSM1754578 c.681G>C p.L227F Substitution - Missense 6:145952431-145952431 - CSCC-27-T COSM4570253 c.249T>C p.I83I Substitution - coding silent 6:145955074-145955074 - HCC2998 COSM3017708 c.267T>C p.V89V Substitution - coding silent 6:145955056-145955056 - TCGA-EI-6507-01 COSM4946056 c.13C>T p.R5W Substitution - Missense 6:145955310-145955310 - 134427 COSM323317 c.817A>T p.I273F Substitution - Missense 6:145950429-145950429 - SC_9031 COSM5548716 c.4552G>A p.A1518T Substitution - Missense 6:145894953-145894953 - TCGA-BS-A0UF-01 COSM1074192 c.3514C>T p.R1172* Substitution - Nonsense 6:145923701-145923701 - TCGA-HU-A4G8-01 COSM3858850 c.2927G>T p.R976M Substitution - Missense 6:145934970-145934970 - S00472 COSM5657942 c.1373G>T p.G458V Substitution - Missense 6:145945586-145945586 - CSCC-49-T COSM4525948 c.1364G>A p.G455E Substitution - Missense 6:145945595-145945595 - CSCC-18-T COSM4572839 c.882T>G p.D294E Substitution - Missense 6:145950364-145950364 - TCGA-37-4141-01 COSM740716 c.2290G>T p.E764* Substitution - Nonsense 6:145941823-145941823 - HCT15 COSM3017643 c.1709G>T p.R570M Substitution - Missense 6:145943672-145943672 - 10-162 COSM305479 c.2775C>G p.H925Q Substitution - Missense 6:145935122-145935122 - TCGA-AA-3715-01 COSM270142 c.3698G>A p.C1233Y Substitution - Missense 6:145922696-145922696 - PR-00-1165 COSM247315 c.2386C>T p.R796W Substitution - Missense 6:145941727-145941727 - CSCC-49-T COSM3621298 c.2307C>T p.I769I Substitution - coding silent 6:145941806-145941806 - BK0006 COSM4185582 c.1363G>T p.G455* Substitution - Nonsense 6:145945596-145945596 - B60-Tumor COSM1754576 c.1978G>C p.E660Q Substitution - Missense 6:145943403-145943403 - TCGA-EE-A3JI-06 COSM3621289 c.4749C>T p.P1583P Substitution - coding silent 6:145893340-145893340 - T3255 COSM4725903 c.4476G>A p.S1492S Substitution - coding silent 6:145910499-145910499 - T2269 COSM4725921 c.403G>A p.E135K Substitution - Missense 6:145954920-145954920 - TCGA-FD-A3SS-01 COSM3777167 c.3832G>A p.E1278K Substitution - Missense 6:145921355-145921355 - TCGA-DM-A28F-01 COSM5170628 c.2559_2560delAG p.G854fs*14 Deletion - Frameshift 6:145940732-145940733 - Pat_41_B COSM5869475 c.203G>A p.R68K Substitution - Missense 6:145955120-145955120 - HCT8 COSM4635334 c.1815C>T p.S605S Substitution - coding silent 6:145943566-145943566 - T12 COSM5345049 c.2199G>C p.E733D Substitution - Missense 6:145943182-145943182 - TCGA-BR-4280-01 COSM247316 c.4054C>T p.R1352C Substitution - Missense 6:145919458-145919458 - 587222 COSM1225667 c.3252G>T p.L1084F Substitution - Missense 6:145926273-145926273 - T12 COSM5345050 c.2199G>C p.E733D Substitution - Missense 6:145943182-145943182 - TCGA-BH-A2L8-01 COSM3829229 c.2661G>A p.K887K Substitution - coding silent 6:145935350-145935350 - HCC2998 COSM1672814 c.3154C>T p.R1052C Substitution - Missense 6:145927236-145927236 - HCT15 COSM3017645 c.1691A>G p.Y564C Substitution - Missense 6:145943690-145943690 - 016-0040-02TD COSM145928 c.2128A>G p.M710V Substitution - Missense 6:145943253-145943253 - 07-P075 COSM4586284 c.4560C>T p.V1520V Substitution - coding silent 6:145894945-145894945 - 1N52-VS-1T52 COSM4976825 c.1856G>T p.C619F Substitution - Missense 6:145943525-145943525 - T1154 COSM4725905 c.4233T>C p.L1411L Substitution - coding silent 6:145918164-145918164 - TCGA-FW-A3R5-06 COSM3920817 c.2644C>G p.R882G Substitution - Missense 6:145935367-145935367 - TCGA-G4-6294-01 COSM3697555 c.3795-1G>C p.? Unknown 6:145921393-145921393 - ESCC_82 COSM5636159 c.2296G>T p.D766Y Substitution - Missense 6:145941817-145941817 - TCGA-AP-A0LM-01 COSM1074190 c.3570G>T p.E1190D Substitution - Missense 6:145923645-145923645 - TCGA-C8-A26Y-01 COSM3829231 c.1999G>A p.D667N Substitution - Missense 6:145943382-145943382 - TCGA-B5-A11U-01 COSM1074209 c.1459C>T p.L487L Substitution - coding silent 6:145945500-145945500 - KM12 COSM4612819 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - TCGA-DD-A4NK-01 COSM4935147 c.533A>T p.E178V Substitution - Missense 6:145954790-145954790 - HCT116 COSM1642887 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - 8015858 COSM1159235 c.2313C>T p.T771T Substitution - coding silent 6:145941800-145941800 - PT46 COSM5928859 c.1724A>T p.K575I Substitution - Missense 6:145943657-145943657 - S00472 COSM315157 c.1373G>T p.G458V Substitution - Missense 6:145945586-145945586 - TCGA-B6-A0IN-01 COSM5835118 c.2473_2474insG p.E825fs*18 Insertion - Frameshift 6:145941639-145941640 - YUPTER COSM5404526 c.1433G>A p.R478Q Substitution - Missense 6:145945526-145945526 - IGROV-1 COSM1672813 c.4093C>T p.R1365C Substitution - Missense 6:145919407-145919407 - Pat_06_A COSM5869471 c.1898C>T p.A633V Substitution - Missense 6:145943483-145943483 - 8016470 COSM3393840 c.4520C>T p.P1507L Substitution - Missense 6:145910455-145910455 - BN31 COSM1621008 c.1394A>G p.Y465C Substitution - Missense 6:145945565-145945565 - TCGA-EE-A20C-06 COSM3621302 c.1783C>T p.P595S Substitution - Missense 6:145943598-145943598 - TCGA-12-3652-01 COSM3410645 c.4640T>C p.I1547T Substitution - Missense 6:145894217-145894217 - TCGA-AP-A0LM-01 COSM4872929 c.4679G>C p.R1560P Substitution - Missense 6:145894166-145894166 - CSCC-46-T COSM4569885 c.2124T>C p.V708V Substitution - coding silent 6:145943257-145943257 - TCGA-02-0003-01 COSM2148892 c.1024G>A p.E342K Substitution - Missense 6:145948309-145948309 - TCGA-ER-A193-06 COSM3621293 c.3643G>A p.E1215K Substitution - Missense 6:145922739-145922739 - TCGA-D8-A142-01 COSM4814008 c.19C>G p.R7G Substitution - Missense 6:145955304-145955304 - 35 COSM4172405 c.2219C>T p.S740L Substitution - Missense 6:145943162-145943162 - TCGA-BH-A18H-01 COSM4813360 c.226G>C p.V76L Substitution - Missense 6:145955097-145955097 - J52_T COSM3948115 c.4899A>T p.V1633V Substitution - coding silent 6:145888088-145888088 - T98G COSM3017619 c.2180G>T p.C727F Substitution - Missense 6:145943201-145943201 - B47 COSM1754571 c.4170A>G p.E1390E Substitution - coding silent 6:145918227-145918227 - 8015858 COSM4945836 c.2313C>T p.T771T Substitution - coding silent 6:145941800-145941800 - BK0006 COSM4185583 c.1363G>T p.G455* Substitution - Nonsense 6:145945596-145945596 - ESCC_47 COSM5630797 c.3018A>G p.T1006T Substitution - coding silent 6:145933151-145933151 - TCGA-EP-A26S-01 COSM4913526 c.1741G>T p.V581F Substitution - Missense 6:145943640-145943640 - HCC007T COSM3017609 c.2416A>G p.S806G Substitution - Missense 6:145941697-145941697 - TCGA-BR-8680-01 COSM3017657 c.1422C>T p.Y474Y Substitution - coding silent 6:145945537-145945537 - BD124T COSM5492147 c.19C>T p.R7C Substitution - Missense 6:145955304-145955304 - TCGA-B5-A11E-01 COSM4870612 c.4292C>A p.P1431H Substitution - Missense 6:145913512-145913512 - TCGA-DM-A28F-01 COSM1440966 c.2559_2560delAG p.G854fs*14 Deletion - Frameshift 6:145940732-145940733 - CSCC-27-T COSM4503855 c.64C>T p.H22Y Substitution - Missense 6:145955259-145955259 - XHDG38 COSM4769769 c.764-9G>C p.? Unknown 6:145950491-145950491 - T2979 COSM4725917 c.646C>G p.L216V Substitution - Missense 6:145952466-145952466 - TCGA-22-5473-01 COSM4862753 c.3704G>A p.R1235K Substitution - Missense 6:145922678-145922678 - T636 COSM3017600 c.2644C>T p.R882W Substitution - Missense 6:145935367-145935367 - T3024 COSM4725908 c.2390A>G p.N797S Substitution - Missense 6:145941723-145941723 - BD124T COSM5492146 c.19C>T p.R7C Substitution - Missense 6:145955304-145955304 - PCSI_0083_Pa_P_526 COSM3381444 c.1101T>C p.L367L Substitution - coding silent 6:145947604-145947604 - HCC2998 COSM1672814 c.3154C>T p.R1052C Substitution - Missense 6:145927236-145927236 - B59-0-Tumor COSM1754579 c.681G>C p.L227F Substitution - Missense 6:145952431-145952431 - LUAD-B01811 COSM334684 c.1796G>T p.G599V Substitution - Missense 6:145943585-145943585 - PT44 COSM5926573 c.2278C>T p.H760Y Substitution - Missense 6:145941835-145941835 - PD4120a COSM164321 c.1918G>A p.D640N Substitution - Missense 6:145943463-145943463 - HCC2998 COSM1672815 c.1288G>A p.E430K Substitution - Missense 6:145946266-145946266 - TCGA-66-2777-01 COSM4861869 c.366G>T p.Q122H Substitution - Missense 6:145954957-145954957 - LIM2551 COSM4612819 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - YUKAT COSM5404522 c.3371C>T p.A1124V Substitution - Missense 6:145924797-145924797 - TCGA-66-2787-01 COSM740715 c.2224T>A p.S742T Substitution - Missense 6:145943157-145943157 - LUAD-S01302 COSM396172 c.4560C>G p.V1520V Substitution - coding silent 6:145894945-145894945 - BD49T COSM5497863 c.469G>A p.G157S Substitution - Missense 6:145954854-145954854 - S02342 COSM5692973 c.2455G>C p.D819H Substitution - Missense 6:145941658-145941658 - TCGA-EI-6917-01 COSM3430084 c.4925T>C p.I1642T Substitution - Missense 6:145888062-145888062 - CSCC-27-T COSM4003715 c.2632C>T p.R878* Substitution - Nonsense 6:145935379-145935379 - sysucc-880T COSM5463498 c.2661G>T p.K887N Substitution - Missense 6:145935350-145935350 - CHEWS020 COSM4586285 c.4269A>G p.T1423T Substitution - coding silent 6:145913535-145913535 - TCGA-EE-A20C-06 COSM3621301 c.1783C>T p.P595S Substitution - Missense 6:145943598-145943598 - CSCC-37-T COSM4538219 c.2519G>A p.G840E Substitution - Missense 6:145940773-145940773 - B23-Tumor COSM1754573 c.3222A>T p.S1074S Substitution - coding silent 6:145927195-145927195 - BCM723T COSM5348498 c.3732-5_3732-4insT p.? Unknown 6:145922352-145922353 - CSCC-44-T COSM3381443 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - Pat_40_B COSM5869477 c.199C>T p.H67Y Substitution - Missense 6:145955124-145955124 - TCGA-BR-6706-01 COSM3858849 c.3056A>C p.K1019T Substitution - Missense 6:145933140-145933140 - BD53T COSM5509251 c.986G>A p.S329N Substitution - Missense 6:145948347-145948347 - 016 COSM145928 c.2128A>G p.M710V Substitution - Missense 6:145943253-145943253 - NB06C COSM1236367 c.3907C>T p.R1303* Substitution - Nonsense 6:145921280-145921280 - YUPTER COSM5404525 c.1433G>A p.R478Q Substitution - Missense 6:145945526-145945526 - SNU-C2B COSM3017556 c.4106G>A p.R1369H Substitution - Missense 6:145919406-145919406 - TCGA-D5-6928-01 COSM1672813 c.4093C>T p.R1365C Substitution - Missense 6:145919407-145919407 - PCSI_0019_Pa_P COSM3381443 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - SC_9031 COSM5548715 c.4540G>A p.A1514T Substitution - Missense 6:145894953-145894953 - T2269 COSM4725905 c.4233T>C p.L1411L Substitution - coding silent 6:145918164-145918164 - TCGA-B5-A0JY-01 COSM4869262 c.1238C>A p.P413Q Substitution - Missense 6:145946316-145946316 - HCC2998 COSM1672815 c.1288G>A p.E430K Substitution - Missense 6:145946266-145946266 - TCGA-D7-8573-01 COSM3858835 c.4793A>G p.H1598R Substitution - Missense 6:145893296-145893296 - T3255 COSM4725902 c.4464G>A p.S1488S Substitution - coding silent 6:145910499-145910499 - CHEWS024 COSM3017623 c.2085T>G p.N695K Substitution - Missense 6:145943296-145943296 - TCGA-CM-6674-01 COSM3017694 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - PT37 COSM4172406 c.2219C>T p.S740L Substitution - Missense 6:145943162-145943162 - TCGA-66-2786-01 COSM4860393 c.4594C>G p.L1532V Substitution - Missense 6:145894899-145894899 - sysucc-1397T COSM5474877 c.3541C>T p.Q1181* Substitution - Nonsense 6:145923674-145923674 - TCGA-B5-A11X-01 COSM1074223 c.207T>G p.D69E Substitution - Missense 6:145955116-145955116 - J52_T COSM3948114 c.4887A>T p.V1629V Substitution - coding silent 6:145888088-145888088 - TCGA-12-3652-01 COSM3410644 c.4628T>C p.I1543T Substitution - Missense 6:145894217-145894217 - TCGA-D5-6928-01 COSM205718 c.4105C>T p.R1369C Substitution - Missense 6:145919407-145919407 - TCGA-AP-A0LM-01 COSM4873603 c.2155C>T p.L719L Substitution - coding silent 6:145943226-145943226 - TCGA-CC-A3MB-01 COSM4933696 c.3584T>C p.F1195S Substitution - Missense 6:145922810-145922810 - TCGA-13-0905-01 COSM133463 c.2829_2830GG>AT p.D944Y Substitution - Missense 6:145935067-145935068 - TCGA-DK-A3WW-01 COSM3777168 c.559G>C p.E187Q Substitution - Missense 6:145954764-145954764 - CSCC-44-T COSM4452993 c.2396A>T p.K799M Substitution - Missense 6:145941717-145941717 - TCGA-EE-A3JD-06 COSM4395686 c.279C>T p.S93S Substitution - coding silent 6:145955044-145955044 - YUOMEGA COSM5404523 c.1686T>C p.P562P Substitution - coding silent 6:145943695-145943695 - CSCC-18-T COSM4572840 c.882T>G p.D294E Substitution - Missense 6:145950364-145950364 - BD124T COSM5492144 c.4858C>T p.R1620* Substitution - Nonsense 6:145893231-145893231 - ESO-0023 COSM1265549 c.3598C>A p.Q1200K Substitution - Missense 6:145922796-145922796 - TCGA-AP-A0LM-01 COSM1074178 c.4691G>C p.R1564P Substitution - Missense 6:145894166-145894166 - TCGA-AP-A0LM-01 COSM4872946 c.3543G>T p.E1181D Substitution - Missense 6:145923645-145923645 - sysucc-880T COSM5463497 c.2661G>T p.K887N Substitution - Missense 6:145935350-145935350 - CHC442T COSM5419689 c.2515A>T p.S839C Substitution - Missense 6:145940777-145940777 - TCGA-A4-7585-01 COSM3994638 c.4310G>C p.R1437P Substitution - Missense 6:145913494-145913494 - CHEWS025 COSM1074192 c.3514C>T p.R1172* Substitution - Nonsense 6:145923701-145923701 - B60 COSM1754576 c.1978G>C p.E660Q Substitution - Missense 6:145943403-145943403 - TCGA-B5-A0JN-01 COSM4874334 c.2572C>A p.L858I Substitution - Missense 6:145935439-145935439 - TCGA-D8-A27G-01 COSM3829227 c.2853G>A p.K951K Substitution - coding silent 6:145935044-145935044 - TCGA-B5-A11U-01 COSM4871176 c.1459C>T p.L487L Substitution - coding silent 6:145945500-145945500 - B80-5 COSM1754574 c.2197G>C p.E733Q Substitution - Missense 6:145943184-145943184 - TCGA-HC-A48F-01 COSM3783942 c.1974C>T p.R658R Substitution - coding silent 6:145943407-145943407 - CSCC-49-T COSM3621297 c.2307C>T p.I769I Substitution - coding silent 6:145941806-145941806 - BCM337T COSM4799044 c.2363A>G p.N788S Substitution - Missense 6:145941750-145941750 - T3262 COSM1440972 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - 123E COSM5966961 c.3922A>G p.I1308V Substitution - Missense 6:145921265-145921265 - tumor_4191799 COSM3357961 c.1239G>A p.P413P Substitution - coding silent 6:145946315-145946315 - DLD1 COSM4625679 c.1268A>G p.K423R Substitution - Missense 6:145946286-145946286 - GC_315T-GC_315N COSM4773794 c.611C>A p.P204Q Substitution - Missense 6:145954712-145954712 - sysucc-1317T COSM5450191 c.1800C>T p.H600H Substitution - coding silent 6:145943581-145943581 - CSCC-44-T COSM4452994 c.2396A>T p.K799M Substitution - Missense 6:145941717-145941717 - 13542 COSM4863102 c.3480G>A p.Q1160Q Substitution - coding silent 6:145923708-145923708 - TCGA-13-1484-01 COSM72635 c.2149G>A p.A717T Substitution - Missense 6:145943232-145943232 - PD3295a COSM51937 c.3677T>A p.V1226D Substitution - Missense 6:145922717-145922717 - TCGA-E2-A1LS-01 COSM4813283 c.3271C>T p.R1091C Substitution - Missense 6:145926227-145926227 - TCGA-AP-A051-01 COSM1074196 c.2476T>C p.C826R Substitution - Missense 6:145941637-145941637 - CSCC-27-T COSM4503856 c.64C>T p.H22Y Substitution - Missense 6:145955259-145955259 - 07-P075 COSM4586283 c.4548C>T p.V1516V Substitution - coding silent 6:145894945-145894945 - 35 COSM4172406 c.2219C>T p.S740L Substitution - Missense 6:145943162-145943162 - HCC058T COSM5805501 c.1419A>T p.R473S Substitution - Missense 6:145945540-145945540 - S01563 COSM315158 c.2415delG p.S806fs*4 Deletion - Frameshift 6:145941698-145941698 - IGROV-1 COSM205718 c.4105C>T p.R1369C Substitution - Missense 6:145919407-145919407 - TCGA-EB-A3XD-01 COSM3621304 c.1497C>T p.I499I Substitution - coding silent 6:145945462-145945462 - HCT8 COSM4635333 c.1815C>T p.S605S Substitution - coding silent 6:145943566-145943566 - TCGA-BH-A18H-01 COSM450632 c.226G>C p.V76L Substitution - Missense 6:145955097-145955097 - TCGA-DC-6158-01 COSM4946151 c.1895G>C p.C632S Substitution - Missense 6:145943486-145943486 - TCGA-CM-4743-01 COSM3017659 c.1371delA p.G458fs*26 Deletion - Frameshift 6:145945588-145945588 - P07-837 COSM247316 c.4054C>T p.R1352C Substitution - Missense 6:145919458-145919458 - 587342 COSM1225669 c.2192T>C p.V731A Substitution - Missense 6:145943189-145943189 - TCGA-HT-7616-01 COSM3928139 c.856C>T p.Q286* Substitution - Nonsense 6:145950390-145950390 - 447 COSM3723538 c.20G>A p.R7H Substitution - Missense 6:145955303-145955303 - TCGA-EE-A2MF-06 COSM4893044 c.2851A>G p.K951E Substitution - Missense 6:145935046-145935046 - ATL072 COSM5709885 c.2527C>T p.R843* Substitution - Nonsense 6:145940765-145940765 - TCGA-AP-A059-01 COSM1074225 c.193G>A p.V65M Substitution - Missense 6:145955130-145955130 - TCGA-BR-4362-01 COSM3858844 c.3279C>T p.G1093G Substitution - coding silent 6:145926219-145926219 - tumor_4131095 COSM5948759 c.4840C>A p.H1614N Substitution - Missense 6:145893261-145893261 - TCGA-CZ-5984-01 COSM4857720 c.750T>A p.N250K Substitution - Missense 6:145952362-145952362 - TCGA-BH-A2L8-01 COSM3829230 c.2661G>A p.K887K Substitution - coding silent 6:145935350-145935350 - TCGA-AX-A0J0-01 COSM4867079 c.1540T>G p.Y514D Substitution - Missense 6:145945419-145945419 - TCGA-60-2708-01 COSM4863102 c.3480G>A p.Q1160Q Substitution - coding silent 6:145923708-145923708 - T3024 COSM4725909 c.2390A>G p.N797S Substitution - Missense 6:145941723-145941723 - T3064 COSM1642887 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - TCGA-ER-A193-06 COSM3621305 c.1384C>T p.L462F Substitution - Missense 6:145945575-145945575 - YUPTER COSM5404530 c.669A>G p.K223K Substitution - coding silent 6:145952443-145952443 - YUOMEGA COSM5404524 c.1686T>C p.P562P Substitution - coding silent 6:145943695-145943695 - TCGA-AP-A0LM-01 COSM1074221 c.273T>G p.I91M Substitution - Missense 6:145955050-145955050 - 1517_PT COSM4612819 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - TCGA-EE-A20F-06 COSM3621291 c.4463C>T p.S1488L Substitution - Missense 6:145910500-145910500 - CHEWS020 COSM4586286 c.4281A>G p.T1427T Substitution - coding silent 6:145913535-145913535 - TCGA-CH-5746-01 COSM1132023 c.4088C>A p.T1363K Substitution - Missense 6:145919424-145919424 - YUPAER COSM5404532 c.559G>A p.E187K Substitution - Missense 6:145954764-145954764 - TCGA-C8-A26Y-01 COSM3829232 c.1999G>A p.D667N Substitution - Missense 6:145943382-145943382 - OSCC-GB_01100111 COSM4888524 c.1195G>A p.A399T Substitution - Missense 6:145947510-145947510 - Pat_40_B COSM5869478 c.199C>T p.H67Y Substitution - Missense 6:145955124-145955124 - PT46 COSM5928860 c.1724A>T p.K575I Substitution - Missense 6:145943657-145943657 - HCT15 COSM3017646 c.1691A>G p.Y564C Substitution - Missense 6:145943690-145943690 - HCC2998 COSM3017707 c.267T>C p.V89V Substitution - coding silent 6:145955056-145955056 - BN31T COSM1621008 c.1394A>G p.Y465C Substitution - Missense 6:145945565-145945565 - CHC442T COSM5419688 c.2515A>T p.S839C Substitution - Missense 6:145940777-145940777 - TCGA-AP-A059-01 COSM1074211 c.1321+1G>A p.? Unknown 6:145946232-145946232 - CSCC-49-T COSM4525947 c.1364G>A p.G455E Substitution - Missense 6:145945595-145945595 - LIM2405 COSM4643052 c.2408C>T p.A803V Substitution - Missense 6:145941705-145941705 - ESCC_82 COSM5636158 c.2296G>T p.D766Y Substitution - Missense 6:145941817-145941817 - TCGA-B5-A0JY-01 COSM4869283 c.752C>A p.S251Y Substitution - Missense 6:145952360-145952360 - TCGA-CC-A3MB-01 COSM4933695 c.3572T>C p.F1191S Substitution - Missense 6:145922810-145922810 - T26 COSM5618252 c.3707G>A p.R1236Q Substitution - Missense 6:145922687-145922687 - T578 COSM4725899 c.4962G>A p.T1654T Substitution - coding silent 6:145886781-145886781 - TCGA-FD-A3SS-01 COSM3777166 c.3820G>A p.E1274K Substitution - Missense 6:145921355-145921355 - I2L-P7-Tumor-Organoid COSM5357673 c.1209C>T p.P403P Substitution - coding silent 6:145947496-145947496 - T2940 COSM1642886 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - Gp5D COSM3017525 c.4891A>G p.R1631G Substitution - Missense 6:145888084-145888084 - TCGA-66-2787-01 COSM4859726 c.2224T>A p.S742T Substitution - Missense 6:145943157-145943157 - CCK81 COSM3017659 c.1371delA p.G458fs*26 Deletion - Frameshift 6:145945588-145945588 - 381 COSM1672815 c.1288G>A p.E430K Substitution - Missense 6:145946266-145946266 - SNU-175 COSM3017626 c.1987T>C p.C663R Substitution - Missense 6:145943394-145943394 - TCGA-AZ-6598-01 COSM5140759 c.2285delT p.L762fs*6 Deletion - Frameshift 6:145941828-145941828 - I2L-P7-Tumor-Organoid COSM5357672 c.1209C>T p.P403P Substitution - coding silent 6:145947496-145947496 - TCGA-D8-A142-01 COSM450633 c.19C>G p.R7G Substitution - Missense 6:145955304-145955304 - TCGA-B5-A0JY-01 COSM1074213 c.1238C>A p.P413Q Substitution - Missense 6:145946316-145946316 - TCGA-EE-A2MQ-06 COSM3621309 c.337A>G p.K113E Substitution - Missense 6:145954986-145954986 - CHEWS034 COSM4586288 c.1173T>G p.T391T Substitution - coding silent 6:145947532-145947532 - ESCC_6 COSM5623387 c.873C>T p.I291I Substitution - coding silent 6:145950373-145950373 - TCGA-66-2744-01 COSM740717 c.2950C>A p.P984T Substitution - Missense 6:145934947-145934947 - TCGA-HT-7616-01 COSM3928138 c.856C>T p.Q286* Substitution - Nonsense 6:145950390-145950390 - TCGA-CA-6717-01 COSM3697557 c.3228+1G>T p.? Unknown 6:145927188-145927188 - TCGA-AP-A0LM-01 COSM4873023 c.273T>G p.I91M Substitution - Missense 6:145955050-145955050 - TCGA-CM-6171-01 COSM87919 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - TCGA-FW-A3R5-06 COSM3920818 c.2644C>G p.R882G Substitution - Missense 6:145935367-145935367 - TCGA-BR-4292-01 COSM3858855 c.2377C>T p.R793C Substitution - Missense 6:145941736-145941736 - TCGA-BR-4292-01 COSM3858854 c.2377C>T p.R793C Substitution - Missense 6:145941736-145941736 - TCGA-C5-A1BI-01 COSM4841600 c.2917C>T p.P973S Substitution - Missense 6:145934980-145934980 - YUKAT COSM5404527 c.1365A>G p.G455G Substitution - coding silent 6:145945594-145945594 - TCGA-18-3409-01 COSM4861151 c.1972C>A p.R658S Substitution - Missense 6:145943409-145943409 - T3080 COSM1642886 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - TCGA-AN-A046-01 COSM3829240 c.23C>T p.A8V Substitution - Missense 6:145955300-145955300 - tumor_4102009 COSM3357958 c.4166G>A p.R1389Q Substitution - Missense 6:145918219-145918219 - S01563 COSM5670080 c.2415delG p.S806fs*4 Deletion - Frameshift 6:145941698-145941698 - TCGA-AC-A23H-01 COSM3829235 c.528G>A p.L176L Substitution - coding silent 6:145954795-145954795 - S02290 COSM5686772 c.348A>T p.L116L Substitution - coding silent 6:145954975-145954975 - HCT15 COSM3017644 c.1709G>T p.R570M Substitution - Missense 6:145943672-145943672 - Pat_41_B COSM5869473 c.590G>A p.R197K Substitution - Missense 6:145954733-145954733 - PCSI_0019_Pa_P_526 COSM216735 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - pfg212T COSM4762378 c.2020C>T p.R674C Substitution - Missense 6:145943361-145943361 - Pat_40_A COSM5869477 c.199C>T p.H67Y Substitution - Missense 6:145955124-145955124 - TCGA-CG-5721-01 COSM3357960 c.1239G>A p.P413P Substitution - coding silent 6:145946315-145946315 - SNUH_G76_S1 COSM4418131 c.2569+6G>T p.? Unknown 6:145940717-145940717 - S02342 COSM5692974 c.2455G>C p.D819H Substitution - Missense 6:145941658-145941658 - pfg016T COSM1642887 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - PT37 COSM4172405 c.2219C>T p.S740L Substitution - Missense 6:145943162-145943162 - TCGA-JW-A5VJ-01 COSM4818429 c.514G>A p.D172N Substitution - Missense 6:145954809-145954809 - 1N57-VS-1T57 COSM4977450 c.1038C>G p.L346L Substitution - coding silent 6:145948295-145948295 - BD53T COSM5509250 c.986G>A p.S329N Substitution - Missense 6:145948347-145948347 - 0036_CRUK_PC_0036_T1_DNA COSM5423467 c.763+7T>G p.? Unknown 6:145952342-145952342 - LOVO COSM3017538 c.4609G>A p.V1537I Substitution - Missense 6:145894896-145894896 - T98G COSM3017620 c.2180G>T p.C727F Substitution - Missense 6:145943201-145943201 - HX21T COSM3662183 c.2983C>T p.Q995* Substitution - Nonsense 6:145934914-145934914 - TCGA-D3-A3MV-06 COSM3621297 c.2307C>T p.I769I Substitution - coding silent 6:145941806-145941806 - 1N57-VS-1T57 COSM4977449 c.1038C>G p.L346L Substitution - coding silent 6:145948295-145948295 - CSCC-37-T COSM4538220 c.2519G>A p.G840E Substitution - Missense 6:145940773-145940773 - CCK81 COSM1440971 c.1371delA p.G458fs*26 Deletion - Frameshift 6:145945588-145945588 - TCGA-EJ-5511-01 COSM4876304 c.3676G>C p.A1226P Substitution - Missense 6:145922706-145922706 - TCGA-C5-A1BQ-01 COSM4842485 c.1667C>T p.S556F Substitution - Missense 6:145943714-145943714 - MPCC_0039_Pa_C COSM216735 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - T3262 COSM4612819 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - ESCC_BICR_040T COSM5430155 c.5008G>C p.D1670H Substitution - Missense 6:145886735-145886735 - HDC54 COSM87919 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - SNU-175 COSM3017625 c.1987T>C p.C663R Substitution - Missense 6:145943394-145943394 - TCGA-BS-A0UM-01 COSM4864284 c.4148A>G p.H1383R Substitution - Missense 6:145919352-145919352 - HCC007T COSM3017610 c.2416A>G p.S806G Substitution - Missense 6:145941697-145941697 - TCGA-ER-A193-06 COSM3621306 c.1384C>T p.L462F Substitution - Missense 6:145945575-145945575 - PR-3051 COSM247317 c.1333A>G p.M445V Substitution - Missense 6:145945626-145945626 - RK004_C01 COSM1634549 c.1061+2T>G p.? Unknown 6:145948270-145948270 - HCC2998 COSM205721 c.3181C>T p.R1061C Substitution - Missense 6:145927236-145927236 - Pat_41_B COSM5869474 c.590G>A p.R197K Substitution - Missense 6:145954733-145954733 - TCGA-EB-A41A-01 COSM3621296 c.2962C>T p.R988C Substitution - Missense 6:145934935-145934935 - TCGA-HU-8604-01 COSM3858842 c.3435G>C p.V1145V Substitution - coding silent 6:145923753-145923753 - PT44 COSM5926572 c.2278C>T p.H760Y Substitution - Missense 6:145941835-145941835 - T2269 COSM4725920 c.403G>A p.E135K Substitution - Missense 6:145954920-145954920 - T2269 COSM4725904 c.4221T>C p.L1407L Substitution - coding silent 6:145918164-145918164 - CHEWS025 COSM4586287 c.3487C>T p.R1163* Substitution - Nonsense 6:145923701-145923701 - TCGA-BC-A217-01 COSM4936873 c.3172A>G p.K1058E Substitution - Missense 6:145927218-145927218 - TCGA-EB-A3XD-01 COSM3621303 c.1497C>T p.I499I Substitution - coding silent 6:145945462-145945462 - TCGA-AA-A010-01 COSM284974 c.3478G>T p.E1160* Substitution - Nonsense 6:145923737-145923737 - CSCC-46-T COSM4569884 c.2124T>C p.V708V Substitution - coding silent 6:145943257-145943257 - TCGA-D3-A2JN-06 COSM3621300 c.1906C>T p.L636L Substitution - coding silent 6:145943475-145943475 - B47-Tumor COSM1754570 c.4158A>G p.E1386E Substitution - coding silent 6:145918227-145918227 - TCGA-DD-A4NK-01 COSM4935148 c.533A>T p.E178V Substitution - Missense 6:145954790-145954790 - PT23_1 COSM5902809 c.2906C>T p.S969F Substitution - Missense 6:145934991-145934991 - TCGA-BR-8680-01 COSM3017658 c.1422C>T p.Y474Y Substitution - coding silent 6:145945537-145945537 - 082T COSM1730922 c.2456A>G p.D819G Substitution - Missense 6:145941657-145941657 - BD114T COSM5503175 c.3720-1G>A p.? Unknown 6:145922349-145922349 - HDC54 COSM3017694 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - TCGA-BR-4280-01 COSM3858839 c.4042C>T p.R1348C Substitution - Missense 6:145919458-145919458 - HCC2998 COSM263650 c.1288G>A p.E430K Substitution - Missense 6:145946266-145946266 - TCGA-02-0003-01 COSM2148891 c.1024G>A p.E342K Substitution - Missense 6:145948309-145948309 - 66 COSM5083639 c.1758delA p.G587fs*23 Deletion - Frameshift 6:145943623-145943623 - Pat_41_B COSM4612819 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - T2979 COSM4725916 c.646C>G p.L216V Substitution - Missense 6:145952466-145952466 - T36 COSM4725915 c.908T>C p.V303A Substitution - Missense 6:145950338-145950338 - TCGA-B5-A11E-01 COSM1074182 c.4304C>A p.P1435H Substitution - Missense 6:145913512-145913512 - DLD1 COSM1642886 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - TCGA-CM-5861-01 COSM1440967 c.2382C>T p.R794R Substitution - coding silent 6:145941731-145941731 - TCGA-AP-A059-01 COSM4866354 c.1232T>G p.F411C Substitution - Missense 6:145946322-145946322 - TCGA-AX-A05S-01 COSM4872200 c.2327G>A p.R776H Substitution - Missense 6:145941786-145941786 - Pat_41_B COSM5869476 c.203G>A p.R68K Substitution - Missense 6:145955120-145955120 - BN31T COSM323318 c.1394A>G p.Y465C Substitution - Missense 6:145945565-145945565 - T26 COSM5618251 c.3695G>A p.R1232Q Substitution - Missense 6:145922687-145922687 - TCGA-DC-6158-01 COSM1568040 c.1895G>C p.C632S Substitution - Missense 6:145943486-145943486 - TCGA-EI-6917-01 COSM3430083 c.4913T>C p.I1638T Substitution - Missense 6:145888062-145888062 - TCGA-AP-A059-01 COSM4866116 c.193G>A p.V65M Substitution - Missense 6:145955130-145955130 - TCGA-D1-A16X-01 COSM4865748 c.3847C>T p.R1283* Substitution - Nonsense 6:145921328-145921328 - TCGA-66-2777-01 COSM740712 c.366G>T p.Q122H Substitution - Missense 6:145954957-145954957 - TCGA-D3-A2JN-06 COSM3621299 c.1906C>T p.L636L Substitution - coding silent 6:145943475-145943475 - TCGA-B6-A0WZ-01 COSM450631 c.3904G>C p.E1302Q Substitution - Missense 6:145921283-145921283 - 587284 COSM1225668 c.4853C>T p.A1618V Substitution - Missense 6:145893248-145893248 - CSCC-56-T COSM4516154 c.1632_1633GG>TA p.K544_D545>NN Complex - compound substitution 6:145943748-145943749 - TCGA-HU-A4G8-01 COSM3858851 c.2927G>T p.R976M Substitution - Missense 6:145934970-145934970 - 447 COSM3723539 c.20G>A p.R7H Substitution - Missense 6:145955303-145955303 - TCGA-EE-A2MF-06 COSM4893043 c.2851A>G p.K951E Substitution - Missense 6:145935046-145935046 - TCGA-B6-A0IN-01 COSM5835117 c.2473_2474insG p.E825fs*18 Insertion - Frameshift 6:145941639-145941640 - tumor_4131095 COSM5948758 c.4828C>A p.H1610N Substitution - Missense 6:145893261-145893261 - TCGA-EE-A2MF-06 COSM4893053 c.2665C>T p.P889S Substitution - Missense 6:145935346-145935346 - TCGA-D7-8573-01 COSM3858836 c.4805A>G p.H1602R Substitution - Missense 6:145893296-145893296 - 082T COSM1730923 c.2456A>G p.D819G Substitution - Missense 6:145941657-145941657 - TCGA-AX-A05S-01 COSM170013 c.2327G>A p.R776H Substitution - Missense 6:145941786-145941786 - PCSI_0083_Pa_P_526 COSM3381445 c.1101T>C p.L367L Substitution - coding silent 6:145947604-145947604 - TCGA-BL-A13I-01 COSM4812073 c.553A>G p.M185V Substitution - Missense 6:145954770-145954770 - TCGA-BG-A0MQ-01 COSM1074199 c.2286G>A p.L762L Substitution - coding silent 6:145941827-145941827 - T2568 COSM4725919 c.500C>T p.P167L Substitution - Missense 6:145954823-145954823 - TCGA-CG-5733-01 COSM3858858 c.1455G>A p.R485R Substitution - coding silent 6:145945504-145945504 - S02290 COSM5686771 c.348A>T p.L116L Substitution - coding silent 6:145954975-145954975 - TCGA-02-0003 COSM2148892 c.1024G>A p.E342K Substitution - Missense 6:145948309-145948309 - TCGA-HU-8604-01 COSM3858843 c.3462G>C p.V1154V Substitution - coding silent 6:145923753-145923753 - T3080 COSM1642887 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - 587376 COSM1225671 c.1536G>T p.K512N Substitution - Missense 6:145945423-145945423 - TCGA-EE-A2MF-06 COSM4893054 c.2665C>T p.P889S Substitution - Missense 6:145935346-145935346 - BD49T COSM5497862 c.469G>A p.G157S Substitution - Missense 6:145954854-145954854 - TCGA-C5-A1BQ-01 COSM4842484 c.1667C>T p.S556F Substitution - Missense 6:145943714-145943714 - T3145 COSM4725913 c.1563T>A p.D521E Substitution - Missense 6:145945396-145945396 - TCGA-AG-A002-01 COSM263649 c.1609G>T p.E537* Substitution - Nonsense 6:145943772-145943772 - TCGA-A4-7585-01 COSM3994639 c.4322G>C p.R1441P Substitution - Missense 6:145913494-145913494 - TCGA-CM-5861-01 COSM4787175 c.2382C>T p.R794R Substitution - coding silent 6:145941731-145941731 - I2L-P7-Tumor-Organoid COSM5357083 c.3720-4delT p.? Unknown 6:145922352-145922352 - TCGA-EF-5830-01 COSM4946012 c.425G>T p.S142I Substitution - Missense 6:145954898-145954898 - pfg016T COSM1642886 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - LOVO COSM3017537 c.4597G>A p.V1533I Substitution - Missense 6:145894896-145894896 - S01563 COSM315158 c.2415delG p.S806fs*4 Deletion - Frameshift 6:145941698-145941698 - TCGA-AA-3966-01 COSM273240 c.1690T>C p.Y564H Substitution - Missense 6:145943691-145943691 - B59-0-Tumor COSM1754578 c.681G>C p.L227F Substitution - Missense 6:145952431-145952431 - TCGA-02-0003 COSM2148891 c.1024G>A p.E342K Substitution - Missense 6:145948309-145948309 - DLD1 COSM4625678 c.1268A>G p.K423R Substitution - Missense 6:145946286-145946286 - TCGA-EE-A3JI-06 COSM3621290 c.4761C>T p.P1587P Substitution - coding silent 6:145893340-145893340 - 2334188 COSM323318 c.1394A>G p.Y465C Substitution - Missense 6:145945565-145945565 - TCGA-D8-A27G-01 COSM3829228 c.2853G>A p.K951K Substitution - coding silent 6:145935044-145935044 - Pat_06_A COSM5869472 c.1898C>T p.A633V Substitution - Missense 6:145943483-145943483 - pfg212T COSM4762377 c.2020C>T p.R674C Substitution - Missense 6:145943361-145943361 - TCGA-21-5786-01 COSM740718 c.3154G>A p.A1052T Substitution - Missense 6:145927263-145927263 - TCGA-BR-6452-01 COSM3858856 c.2138T>C p.V713A Substitution - Missense 6:145943243-145943243 - TCGA-BS-A0UM-01 COSM1074184 c.4160A>G p.H1387R Substitution - Missense 6:145919352-145919352 - CSCC-27-T COSM4003714 c.2632C>T p.R878* Substitution - Nonsense 6:145935379-145935379 - RK004_C01 COSM1634548 c.1061+2T>G p.? Unknown 6:145948270-145948270 - TCGA-CG-5721-01 COSM3357961 c.1239G>A p.P413P Substitution - coding silent 6:145946315-145946315 - TCGA-A2-A1FV-01 COSM1487294 c.4093C>T p.R1365* Substitution - Nonsense 6:145919419-145919419 - TCGA-BR-4201-01 COSM3858846 c.3209A>G p.H1070R Substitution - Missense 6:145926289-145926289 - TCGA-BR-4256-01 COSM3858841 c.3744T>C p.C1248C Substitution - coding silent 6:145922336-145922336 - BD114T COSM5503176 c.3732-1G>A p.? Unknown 6:145922349-145922349 - TCGA-EI-6507-01 COSM1568038 c.13C>T p.R5W Substitution - Missense 6:145955310-145955310 - 721LT COSM4386430 c.476A>C p.D159A Substitution - Missense 6:145954847-145954847 - B60-Tumor COSM1754577 c.1978G>C p.E660Q Substitution - Missense 6:145943403-145943403 - ESCC_3 COSM5622663 c.4789A>G p.I1597V Substitution - Missense 6:145893312-145893312 - OSCC-GB_01100111 COSM4888523 c.1195G>A p.A399T Substitution - Missense 6:145947510-145947510 - CHEWS034 COSM4586289 c.1173T>G p.T391T Substitution - coding silent 6:145947532-145947532 - B59-0 COSM1754579 c.681G>C p.L227F Substitution - Missense 6:145952431-145952431 - TCGA-EE-A20F-06 COSM3621292 c.4475C>T p.S1492L Substitution - Missense 6:145910500-145910500 - KM12 COSM1440972 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 - TCGA-60-2708-01 COSM740719 c.3507G>A p.Q1169Q Substitution - coding silent 6:145923708-145923708 - LIM2405 COSM4643051 c.2408C>T p.A803V Substitution - Missense 6:145941705-145941705 - TCGA-18-3409-01 COSM740714 c.1972C>A p.R658S Substitution - Missense 6:145943409-145943409 - TCGA-C5-A1BI-01 COSM4841599 c.2917C>T p.P973S Substitution - Missense 6:145934980-145934980 - 123E COSM5966960 c.3910A>G p.I1304V Substitution - Missense 6:145921265-145921265 - SNU-C2B COSM3017555 c.4094G>A p.R1365H Substitution - Missense 6:145919406-145919406 - TCGA-EE-A3J8-06 COSM3621308 c.895G>T p.A299S Substitution - Missense 6:145950351-145950351 - J74_T COSM3948117 c.4855A>G p.I1619V Substitution - Missense 6:145893246-145893246 - TCGA-CM-4743-01 COSM1440971 c.1371delA p.G458fs*26 Deletion - Frameshift 6:145945588-145945588 - TCGA-F5-6814-01 COSM3430085 c.2719G>T p.D907Y Substitution - Missense 6:145935292-145935292 - 2318494 COSM4777264 c.3683A>C p.E1228A Substitution - Missense 6:145922711-145922711 - TCGA-F5-6814-01 COSM3430086 c.2719G>T p.D907Y Substitution - Missense 6:145935292-145935292 - HCT116 COSM1642886 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - BCM337T COSM4799043 c.2363A>G p.N788S Substitution - Missense 6:145941750-145941750 - SNUH_G76_S1 COSM4418130 c.2569+6G>T p.? Unknown 6:145940717-145940717 - TCGA-A6-6781-01 COSM3686332 c.4708-3delT p.? Unknown 6:145893396-145893396 - TCGA-AG-A002-01 COSM263647 c.3794C>T p.T1265I Substitution - Missense 6:145922286-145922286 - TCGA-BR-4256-01 COSM3858840 c.3732T>C p.C1244C Substitution - coding silent 6:145922336-145922336 - TCGA-A6-6781-01 COSM3017694 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - TCGA-BR-4201-01 COSM3858847 c.3236A>G p.H1079R Substitution - Missense 6:145926289-145926289 - CSCC-16-T COSM4496449 c.4759C>T p.P1587S Substitution - Missense 6:145893342-145893342 - 2293776 COSM4607934 c.3529C>A p.L1177I Substitution - Missense 6:145923659-145923659 - T3088 COSM4725901 c.4816G>T p.V1606L Substitution - Missense 6:145893285-145893285 - PA285 COSM1163422 c.743T>C p.L248S Substitution - Missense 6:145952369-145952369 - T3145 COSM4725912 c.1563T>A p.D521E Substitution - Missense 6:145945396-145945396 - TCGA-B5-A11E-01 COSM4869929 c.3583A>C p.T1195P Substitution - Missense 6:145922799-145922799 - TCGA-EE-A3JD-06 COSM4395687 c.279C>T p.S93S Substitution - coding silent 6:145955044-145955044 - BN31 COSM323318 c.1394A>G p.Y465C Substitution - Missense 6:145945565-145945565 - TCGA-BL-A13I-01 COSM421047 c.553A>G p.M185V Substitution - Missense 6:145954770-145954770 - TCGA-EF-5830-01 COSM1568039 c.425G>T p.S142I Substitution - Missense 6:145954898-145954898 - ESO-963 COSM1265547 c.1644_1664del21 p.E549_T555delEYLPSDT Deletion - In frame 6:145943717-145943737 - TCGA-21-5786-01 COSM4862641 c.3127G>A p.A1043T Substitution - Missense 6:145927263-145927263 - TCGA-FD-A3B6-01 COSM1311636 c.2658G>C p.K886N Substitution - Missense 6:145935353-145935353 - TCGA-BR-4362-01 COSM3858845 c.3306C>T p.G1102G Substitution - coding silent 6:145926219-145926219 - TCGA-CA-6717-01 COSM3017642 c.1717C>T p.R573C Substitution - Missense 6:145943664-145943664 - 381 COSM263650 c.1288G>A p.E430K Substitution - Missense 6:145946266-145946266 - BD124T COSM5492145 c.4870C>T p.R1624* Substitution - Nonsense 6:145893231-145893231 - I2L-P7-Tumor-Organoid COSM5357084 c.3732-4delT p.? Unknown 6:145922352-145922352 - B47-Tumor COSM1754571 c.4170A>G p.E1390E Substitution - coding silent 6:145918227-145918227 - HT115 COSM3017529 c.4859G>A p.R1620Q Substitution - Missense 6:145893230-145893230 - LUAD-B02594 COSM336860 c.2348A>T p.D783V Substitution - Missense 6:145941765-145941765 - T3024 COSM4725911 c.1984A>G p.I662V Substitution - Missense 6:145943397-145943397 - CSCC-44-T COSM216735 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - TCGA-D3-A3MV-06 COSM3621298 c.2307C>T p.I769I Substitution - coding silent 6:145941806-145941806 - MPCC_0039_Pa_C COSM3381443 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - B80-5-Tumor COSM1754575 c.2197G>C p.E733Q Substitution - Missense 6:145943184-145943184 - RK065_C01 COSM1634546 c.1494G>A p.Q498Q Substitution - coding silent 6:145945465-145945465 - TCGA-B5-A0JN-01 COSM1074194 c.2572C>A p.L858I Substitution - Missense 6:145935439-145935439 - TCGA-A6-6781-01 COSM3686331 c.4696-3delT p.? Unknown 6:145893396-145893396 - ATL072 COSM5709884 c.2527C>T p.R843* Substitution - Nonsense 6:145940765-145940765 - TCGA-D1-A16X-01 COSM1074186 c.3859C>T p.R1287* Substitution - Nonsense 6:145921328-145921328 - YUROL COSM5404519 c.4448C>T p.S1483F Substitution - Missense 6:145910515-145910515 - ESCC_3 COSM5622662 c.4777A>G p.I1593V Substitution - Missense 6:145893312-145893312 - LS411 COSM1440971 c.1371delA p.G458fs*26 Deletion - Frameshift 6:145945588-145945588 - PCSI_0083_Pa_X COSM3381444 c.1101T>C p.L367L Substitution - coding silent 6:145947604-145947604 - CSCC-16-T COSM4496448 c.4747C>T p.P1583S Substitution - Missense 6:145893342-145893342 - TCGA-AZ-6598-01 COSM1440968 c.2285delT p.L762fs*6 Deletion - Frameshift 6:145941828-145941828 - TCGA-CA-6717-01 COSM3697556 c.3201+1G>T p.? Unknown 6:145927188-145927188 - 016-0040-02TD COSM4782228 c.2128A>G p.M710V Substitution - Missense 6:145943253-145943253 - TCGA-FD-A3B6-01 COSM4810802 c.2658G>C p.K886N Substitution - Missense 6:145935353-145935353 - TCGA-B5-A11X-01 COSM4872300 c.207T>G p.D69E Substitution - Missense 6:145955116-145955116 - 1N52-VS-1T52 COSM4976824 c.1856G>T p.C619F Substitution - Missense 6:145943525-145943525 - TCGA-A3-3363-01 COSM1496182 c.4485T>C p.F1495F Substitution - coding silent 6:145910490-145910490 - TCGA-ES-A2HT-01 COSM4938822 c.2228T>C p.L743P Substitution - Missense 6:145943153-145943153 - LUAD-S01404 COSM404518 c.1239G>T p.P413P Substitution - coding silent 6:145946315-145946315 - TCGA-33-4583-01 COSM740713 c.519G>T p.K173N Substitution - Missense 6:145954804-145954804 - HCC2998 COSM263650 c.1288G>A p.E430K Substitution - Missense 6:145946266-145946266 - TCGA-EE-A3J8-06 COSM3621307 c.895G>T p.A299S Substitution - Missense 6:145950351-145950351 - T3499 COSM4725906 c.2534G>A p.C845Y Substitution - Missense 6:145940758-145940758 - TCGA-33-4583-01 COSM4858583 c.519G>T p.K173N Substitution - Missense 6:145954804-145954804 - sysucc-1397T COSM5474876 c.3514C>T p.Q1172* Substitution - Nonsense 6:145923674-145923674 - ME009T COSM223128 c.4341G>T p.W1447C Substitution - Missense 6:145910634-145910634 - YUPAER COSM5404531 c.559G>A p.E187K Substitution - Missense 6:145954764-145954764 - TCGA-BS-A0UV-01 COSM1074203 c.1864G>T p.E622* Substitution - Nonsense 6:145943517-145943517 - TCGA-CG-5733-01 COSM3858859 c.1455G>A p.R485R Substitution - coding silent 6:145945504-145945504 - 90226 COSM330493 c.4266+9delT p.? Unknown 6:145918122-145918122 - TCGA-AG-A002-01 COSM263650 c.1288G>A p.E430K Substitution - Missense 6:145946266-145946266 - 8016470 COSM3393839 c.4508C>T p.P1503L Substitution - Missense 6:145910455-145910455 - LP6005500-DNA_G01 COSM205720 c.3334C>T p.R1112* Substitution - Nonsense 6:145924834-145924834 - B60 COSM1754577 c.1978G>C p.E660Q Substitution - Missense 6:145943403-145943403 - TCGA-CM-6674-01 COSM87919 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - YUROL COSM5404520 c.4460C>T p.S1487F Substitution - Missense 6:145910515-145910515 - RK001_C01 COSM1634544 c.3049G>A p.E1017K Substitution - Missense 6:145933120-145933120 - B23-Tumor COSM1754572 c.3195A>T p.S1065S Substitution - coding silent 6:145927195-145927195 - TCGA-EJ-5511-01 COSM1132021 c.3688G>C p.A1230P Substitution - Missense 6:145922706-145922706 - TCGA-BC-A217-01 COSM4936874 c.3199A>G p.K1067E Substitution - Missense 6:145927218-145927218 - TCGA-AC-A3W6-01 COSM3829234 c.1175G>A p.R392Q Substitution - Missense 6:145947530-145947530 - ICGC_0052 COSM1159235 c.2313C>T p.T771T Substitution - coding silent 6:145941800-145941800 - T3088 COSM4725900 c.4804G>T p.V1602L Substitution - Missense 6:145893285-145893285 - PCSI_0019_Pa_X COSM216735 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - TCGA-BS-A0UV-01 COSM3017642 c.1717C>T p.R573C Substitution - Missense 6:145943664-145943664 - PCSI_0019_Pa_X COSM3381443 c.2394G>A p.Q798Q Substitution - coding silent 6:145941719-145941719 - TCGA-BR-7707-01 COSM3017616 c.2321T>C p.V774A Substitution - Missense 6:145941792-145941792 - tumor_4191799 COSM3357960 c.1239G>A p.P413P Substitution - coding silent 6:145946315-145946315 - TCGA-EB-A41A-01 COSM3621295 c.2962C>T p.R988C Substitution - Missense 6:145934935-145934935 - TCGA-UB-A7MB-01 COSM4932877 c.135A>T p.P45P Substitution - coding silent 6:145955188-145955188 - CSCC-27-T COSM4570254 c.249T>C p.I83I Substitution - coding silent 6:145955074-145955074 - HX21T COSM3662184 c.2983C>T p.Q995* Substitution - Nonsense 6:145934914-145934914 - TCGA-22-5473-01 COSM740720 c.3716G>A p.R1239K Substitution - Missense 6:145922678-145922678 - TCGA-UB-A7MB-01 COSM4932876 c.135A>T p.P45P Substitution - coding silent 6:145955188-145955188 - TCGA-DK-A3WW-01 COSM3777169 c.559G>C p.E187Q Substitution - Missense 6:145954764-145954764 - TCGA-AP-A0LT-01 COSM1074217 c.783A>C p.E261D Substitution - Missense 6:145950463-145950463 - T3499 COSM4725907 c.2534G>A p.C845Y Substitution - Missense 6:145940758-145940758 - WA22 COSM241603 c.2264G>T p.G755V Substitution - Missense 6:145941849-145941849 - S01504 COSM4387358 c.1283A>G p.N428S Substitution - Missense 6:145946271-145946271 - S02248 COSM5679774 c.1984A>T p.I662L Substitution - Missense 6:145943397-145943397 - B80-5-Tumor COSM1754574 c.2197G>C p.E733Q Substitution - Missense 6:145943184-145943184 - BCM337T COSM4799043 c.2363A>G p.N788S Substitution - Missense 6:145941750-145941750 - TCGA-BR-8360-01 COSM3858852 c.2755G>A p.E919K Substitution - Missense 6:145935142-145935142 - TCGA-AA-A010-01 COSM284975 c.352G>T p.E118* Substitution - Nonsense 6:145954971-145954971 - TCGA-CA-6717-01 COSM1074205 c.1717C>T p.R573C Substitution - Missense 6:145943664-145943664 - TCGA-BS-A0UV-01 COSM1074205 c.1717C>T p.R573C Substitution - Missense 6:145943664-145943664 - TCGA-AA-A00N-01 COSM277265 c.595A>C p.K199Q Substitution - Missense 6:145954728-145954728 - B23 COSM1754573 c.3222A>T p.S1074S Substitution - coding silent 6:145927195-145927195 - TCGA-B5-A11E-01 COSM1074188 c.3595A>C p.T1199P Substitution - Missense 6:145922799-145922799 - PT23_1 COSM5902808 c.2906C>T p.S969F Substitution - Missense 6:145934991-145934991 - GC_315T-GC_315N COSM4773795 c.611C>A p.P204Q Substitution - Missense 6:145954712-145954712 - TCGA-A6-6781-01 COSM87919 c.495_496insA p.E166fs*7 Insertion - Frameshift 6:145954827-145954828 - TCGA-AG-A002-01 COSM263648 c.2011C>T p.R671C Substitution - Missense 6:145943370-145943370 - T2940 COSM1642887 c.277delT p.S93fs*5 Deletion - Frameshift 6:145955046-145955046 - tumor_4102009 COSM3357959 c.4178G>A p.R1393Q Substitution - Missense 6:145918219-145918219 - YUPTER COSM5404529 c.669A>G p.K223K Substitution - coding silent 6:145952443-145952443 - TCGA-AP-A0LM-01 COSM1074201 c.2155C>T p.L719L Substitution - coding silent 6:145943226-145943226 - B23 COSM1754572 c.3195A>T p.S1065S Substitution - coding silent 6:145927195-145927195 - 1517_PT COSM1440972 c.495delA p.E166fs*3 Deletion - Frameshift 6:145954828-145954828 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.723269;Hs.723273;Hs.723295;Hs.723297 6q24.3 608048

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.4515+5952T>G 6 146225632 HC A C Missense p.D69E c.207T>G 6 146276252 UCEC A C Missense p.I914R c.2741T>G 6 146256292 OV A - Frameshift p.S93Pfs*5 c.277delT 6 146276182 LUAD A - Frameshift p.S93Pfs*5 c.277delT 6 146276182 STAD A G Missense p.I1543T c.4628T>C 6 146215353 GBM A G SpliceDonorSNV . c.1061+2T>C 6 146269406 STAD A G Synonymous p.C1244C c.3732T>C 6 146243472 STAD A T Missense p.N250K c.750T>A 6 146273498 RCCC A T Missense p.S742T c.2224T>A 6 146264293 LUSC C A IntronicSNV . c.4515+4822G>T 6 146226762 HC C A Missense p.A299S c.895G>T 6 146271487 CM C A Missense p.G458V c.1373G>T 6 146266722 SCLC C A Missense p.K173N c.519G>T 6 146275940 LUSC C A Missense p.K568N c.1704G>T 6 146264813 LUAD C A Missense p.Q122H c.366G>T 6 146276093 LUSC C A Missense p.Q979H c.2937G>T 6 146256096 LUAD C A Missense p.R776L c.2327G>T 6 146262922 HNSC C A Nonsense p.E764* c.2290G>T 6 146262959 LUSC CC AT Missense p.D294Y c.879_880delinsAT 6 146271502 HNSC CC AT Missense p.D944Y c.2829_2830delinsAT 6 146256203 OV C - Frameshift p.S806Afs*4 c.2415delG 6 146262834 SCLC C G Missense p.A1226P c.3676G>C 6 146243842 PRAD C G Missense p.D766H c.2296G>C 6 146262953 LUAD C G Missense p.E1298Q c.3892G>C 6 146242419 BRCA C G Missense p.K886N c.2658G>C 6 146256489 BLCA C G Missense p.L304F c.912G>C 6 146271470 HNSC C G Missense p.R793P c.2378G>C 6 146262871 LUAD C G Missense p.V76L c.226G>C 6 146276233 BRCA C T Missense p.A1043T c.3127G>A 6 146248399 LUSC C T Missense p.A1210T c.3628G>A 6 146243890 STAD C T Missense p.A717T c.2149G>A 6 146264368 OV C T Missense p.D640N c.1918G>A 6 146264599 BRCA C T Missense p.D640N c.1918G>A 6 146264599 HNSC C T Missense p.E1017K c.3049G>A 6 146254256 HC C T Missense p.E1215K c.3643G>A 6 146243875 CM C T Missense p.E1329K c.3985G>A 6 146242326 ESCA C T Missense p.E342K c.1024G>A 6 146269445 GBM C T Missense p.E919K c.2755G>A 6 146256278 STAD C T Missense p.G1440E c.4319G>A 6 146234621 LUAD C T Missense p.G183D c.548G>A 6 146275911 LUAD C T Missense p.R1235K c.3704G>A 6 146243814 LUSC C T Missense p.R1560H c.4679G>A 6 146215302 LUAD C T Missense p.R776H c.2327G>A 6 146262922 COREAD C T Missense p.R776H c.2327G>A 6 146262922 UCEC C T Missense p.R7H c.20G>A 6 146276439 HNSC C T Missense p.V946M c.2836G>A 6 146256197 STAD C T Synonymous p.L1078L c.3234G>A 6 146247400 HNSC C T Synonymous p.L762L c.2286G>A 6 146262963 UCEC C T Synonymous p.Q1160Q c.3480G>A 6 146244844 LUSC C T Synonymous p.Q1160Q c.3480G>A 6 146244844 NSCLC C T Synonymous p.Q1404Q c.4212G>A 6 146239309 CM C T Synonymous p.Q798Q c.2394G>A 6 146262855 PAAD G A 3-UTRSNV . c.5049+247C>T 6 146207583 CM G A IntronicSNV . c.3720-63C>T 6 146243547 NSCLC G A Missense p.L462F c.1384C>T 6 146266711 CM G A Missense p.P45L c.134C>T 6 146276325 CM G A Missense p.P582L c.1745C>T 6 146264772 CM G A Missense p.P595S c.1783C>T 6 146264734 CM G A Missense p.P805L c.2414C>T 6 146262835 ESCA G A Missense p.P889S c.2665C>T 6 146256482 CM G A Missense p.R1091C c.3271C>T 6 146247363 BRCA G A Missense p.R1348C c.4042C>T 6 146240594 STAD G A Missense p.R793C c.2377C>T 6 146262872 STAD G A Missense p.S1488L c.4463C>T 6 146231636 CM G A Missense p.S927F c.2780C>T 6 146256253 LUAD G A Missense p.T648I c.1943C>T 6 146264574 LUAD G A Nonsense p.Q286* c.856C>T 6 146271526 LGG G A Nonsense p.R1299* c.3895C>T 6 146242416 NB G A Nonsense p.R1361* c.4081C>T 6 146240555 BRCA G A Nonsense p.R336* c.1006C>T 6 146269463 STAD G A Synonymous p.I769I c.2307C>T 6 146262942 CM G A Synonymous p.L487L c.1459C>T 6 146266636 UCEC G A Synonymous p.L636L c.1906C>T 6 146264611 CM G A Synonymous p.P1583P c.4749C>T 6 146214476 CM G A Synonymous p.S93S c.279C>T 6 146276180 CM G A Synonymous p.T771T c.2313C>T 6 146262936 PAAD G C Missense p.L1532V c.4594C>G 6 146216035 LUSC G C Missense p.R7G c.19C>G 6 146276440 BRCA G T 3-UTRSNV . c.5049+299C>A 6 146207531 CM GTGTCTGATGGCAAGTATTCA - InFrameDeletion p.E549_T555delEYLPSDT c.1644_1664delTGAATACTTGCCATCAGACAC 6 146264853 ESCA G T IntronicSNV . c.4515+2113C>A 6 146229471 MB G T Missense p.L858I c.2572C>A 6 146256575 UCEC G T Missense p.P984T c.2950C>A 6 146256083 LUSC G T Missense p.Q1022K c.3064C>A 6 146254241 CM G T Missense p.Q1196K c.3586C>A 6 146243932 ESCA G T Missense p.S725Y c.2174C>A 6 146264343 LUAD T A Missense p.I273F c.817A>T 6 146271565 SCLC T A Missense p.S1168C c.3502A>T 6 146244822 HNSC T A Missense p.T507S c.1519A>T 6 146266576 LUAD T A Missense p.Y1106F c.3317A>T 6 146245960 HNSC T A Synonymous p.I1086I c.3258A>T 6 146247376 LUAD T C Missense p.H1070R c.3209A>G 6 146247425 STAD T C Missense p.H1383R c.4148A>G 6 146240488 UCEC T C Missense p.K113E c.337A>G 6 146276122 CM T C Missense p.K1659R c.4976A>G 6 146207903 UCEC T C Missense p.K951E c.2851A>G 6 146256182 CM T C Missense p.M168V c.502A>G 6 146275957 LUAD T C Missense p.M185V c.553A>G 6 146275906 BLCA T C Missense p.Y465C c.1394A>G 6 146266701 SCLC T C Synonymous p.Q1557Q c.4671A>G 6 146215310 LGG T G Missense p.K1010T c.3029A>C 6 146254276 STAD T G Missense p.Q749H c.2247A>C 6 146263002 HNSC T - IntronicDeletion . c.3403-35delA 6 146244956 STAD