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 1 160265920 160265920 + Silent SNP T T C TCGA-OR-A5K4-01A-11D-A29I-10 TCGA-OR-A5K4-10A-01D-A29L-10 g.chr1:160265920T>C c.2283A>G c.(2281-2283)acA>acG p.T761T BLCA 1 160261131 160261131 + Silent SNP G G T TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr1:160261131G>T c.3414C>A c.(3412-3414)gcC>gcA p.A1138A BLCA 1 160261157 160261157 + Missense_Mutation SNP C C G TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr1:160261157C>G c.3388G>C c.(3388-3390)Gaa>Caa p.E1130Q BLCA 1 160261692 160261692 + Missense_Mutation SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr1:160261692C>T c.3175G>A c.(3175-3177)Gag>Aag p.E1059K BLCA 1 160261931 160261931 + Silent SNP G G A TCGA-DK-A3X2-01A-11D-A22Z-08 TCGA-DK-A3X2-10A-01D-A22Z-08 g.chr1:160261931G>A c.3018C>T c.(3016-3018)ctC>ctT p.L1006L BLCA 1 160262955 160262955 + Splice_Site SNP C C T TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr1:160262955C>T c.e27+1 BLCA 1 160264384 160264384 + Splice_Site SNP C C G TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr1:160264384C>G c.e25-1 BLCA 1 160265889 160265889 + Missense_Mutation SNP C C G TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr1:160265889C>G c.2314G>C c.(2314-2316)Gag>Cag p.E772Q BLCA 1 160267134 160267134 + Splice_Site SNP C C G TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr1:160267134C>G c.2262G>C c.(2260-2262)caG>caC p.Q754H BLCA 1 160267169 160267169 + Missense_Mutation SNP A A G TCGA-KQ-A41P-01A-12D-A339-08 TCGA-KQ-A41P-10F-01D-A339-08 g.chr1:160267169A>G c.2227T>C c.(2227-2229)Tca>Cca p.S743P BLCA 1 160268719 160268719 + Silent SNP C C T TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr1:160268719C>T c.1893G>A c.(1891-1893)aaG>aaA p.K631K BLCA 1 160268894 160268894 + Missense_Mutation SNP C C G TCGA-UY-A78O-01A-12D-A339-08 TCGA-UY-A78O-10A-01D-A339-08 g.chr1:160268894C>G c.1828G>C c.(1828-1830)Gag>Cag p.E610Q BLCA 1 160268936 160268936 + Nonsense_Mutation SNP C C A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr1:160268936C>A c.1786G>T c.(1786-1788)Gag>Tag p.E596* BLCA 1 160275264 160275264 + Silent SNP G G A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr1:160275264G>A c.1626C>T c.(1624-1626)atC>atT p.I542I BLCA 1 160280027 160280027 + Silent SNP G G A TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr1:160280027G>A c.1098C>T c.(1096-1098)ttC>ttT p.F366F BLCA 1 160281792 160281792 + Missense_Mutation SNP C C G TCGA-GU-AATO-01A-11D-A391-08 TCGA-GU-AATO-10A-01D-A394-08 g.chr1:160281792C>G c.942G>C c.(940-942)atG>atC p.M314I BLCA 1 160282926 160282926 + Missense_Mutation SNP C C A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr1:160282926C>A c.874G>T c.(874-876)Gat>Tat p.D292Y BLCA 1 160282929 160282929 + Missense_Mutation SNP G G T TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr1:160282929G>T c.871C>A c.(871-873)Cat>Aat p.H291N BLCA 1 160283854 160283854 + Silent SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr1:160283854G>C c.768C>G c.(766-768)gtC>gtG p.V256V BRCA 1 160259952 160259952 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:160259952G>A c.3670C>T c.(3670-3672)Cgc>Tgc p.R1224C BRCA 1 160261648 160261648 + Silent SNP C C T TCGA-A2-A4S3-01A-21D-A25Q-09 TCGA-A2-A4S3-10A-01D-A25Q-09 g.chr1:160261648C>T c.3219G>A c.(3217-3219)ctG>ctA p.L1073L BRCA 1 160261650 160261650 + Missense_Mutation SNP G G C TCGA-E2-A15O-01A-11D-A10Y-09 TCGA-E2-A15O-10A-01D-A110-09 g.chr1:160261650G>C c.3217C>G c.(3217-3219)Ctg>Gtg p.L1073V BRCA 1 160261861 160261861 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:160261861G>A c.3088C>T c.(3088-3090)Cgt>Tgt p.R1030C BRCA 1 160264342 160264342 + Missense_Mutation SNP G G A TCGA-A7-A26I-01A-11D-A167-09 TCGA-A7-A26I-10A-01D-A167-09 g.chr1:160264342G>A c.2608C>T c.(2608-2610)Ctt>Ttt p.L870F BRCA 1 160267442 160267442 + Missense_Mutation SNP C C T TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr1:160267442C>T c.2071G>A c.(2071-2073)Gaa>Aaa p.E691K BRCA 1 160275320 160275320 + Missense_Mutation SNP T T C TCGA-AC-A3W5-01A-11D-A228-09 TCGA-AC-A3W5-10A-01D-A22A-09 g.chr1:160275320T>C c.1570A>G c.(1570-1572)Att>Gtt p.I524V BRCA 1 160275509 160275509 + Silent SNP G G A TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr1:160275509G>A c.1497C>T c.(1495-1497)gaC>gaT p.D499D BRCA 1 160276146 160276146 + Silent SNP C C T TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr1:160276146C>T c.1440G>A c.(1438-1440)aaG>aaA p.K480K BRCA 1 160279994 160279994 + Silent SNP G G A TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr1:160279994G>A c.1131C>T c.(1129-1131)gtC>gtT p.V377V BRCA 1 160280016 160280016 + Missense_Mutation SNP T T A TCGA-C8-A12L-01A-11D-A10Y-09 TCGA-C8-A12L-10A-01D-A110-09 g.chr1:160280016T>A c.1109A>T c.(1108-1110)tAc>tTc p.Y370F BRCA 1 160280018 160280018 + Silent SNP T T C TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr1:160280018T>C c.1107A>G c.(1105-1107)tcA>tcG p.S369S BRCA 1 160280027 160280027 + Silent SNP G G A TCGA-AC-A3YJ-01A-11D-A22X-09 TCGA-AC-A3YJ-10A-01D-A22X-09 g.chr1:160280027G>A c.1098C>T c.(1096-1098)ttC>ttT p.F366F BRCA 1 160280035 160280035 + Missense_Mutation SNP G G A TCGA-AC-A3YJ-01A-11D-A22X-09 TCGA-AC-A3YJ-10A-01D-A22X-09 g.chr1:160280035G>A c.1090C>T c.(1090-1092)Cca>Tca p.P364S CESC 1 160261692 160261692 + Missense_Mutation SNP C C T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr1:160261692C>T c.3175G>A c.(3175-3177)Gag>Aag p.E1059K CESC 1 160276954 160276954 + Splice_Site SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr1:160276954G>A c.1301C>T c.(1300-1302)tCg>tTg p.S434L CHOL 1 160263008 160263008 + Missense_Mutation SNP G G T TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr1:160263008G>T c.2771C>A c.(2770-2772)tCt>tAt p.S924Y CHOL 1 160269048 160269048 + Silent SNP G G A TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr1:160269048G>A c.1674C>T c.(1672-1674)caC>caT p.H558H COAD 1 160264296 160264298 + In_Frame_Del DEL TCT TCT - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr1:160264296_160264298delTCT c.2652_2654delAGA c.(2650-2655)gaagat>gat p.E884del COAD 1 160264308 160264308 + Missense_Mutation SNP T T C TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr1:160264308T>C c.2642A>G c.(2641-2643)gAt>gGt p.D881G COAD 1 160264314 160264314 + Missense_Mutation SNP C C A TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr1:160264314C>A c.2636G>T c.(2635-2637)gGc>gTc p.G879V COAD 1 160267156 160267156 + Missense_Mutation SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr1:160267156C>A c.2240G>T c.(2239-2241)cGg>cTg p.R747L COAD 1 160267380 160267380 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr1:160267380G>A c.2133C>T c.(2131-2133)ggC>ggT p.G711G COAD 1 160268918 160268918 + Missense_Mutation SNP C C A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr1:160268918C>A c.1804G>T c.(1804-1806)Gcc>Tcc p.A602S COAD 1 160268940 160268940 + Silent SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr1:160268940G>A c.1782C>T c.(1780-1782)ccC>ccT p.P594P COAD 1 160268940 160268940 + Silent SNP G G A TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr1:160268940G>A c.1782C>T c.(1780-1782)ccC>ccT p.P594P COAD 1 160268940 160268940 + Silent SNP G G T TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr1:160268940G>T c.1782C>A c.(1780-1782)ccC>ccA p.P594P COAD 1 160268941 160268941 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr1:160268941G>A c.1781C>T c.(1780-1782)cCc>cTc p.P594L COAD 1 160268942 160268942 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr1:160268942G>A c.1780C>T c.(1780-1782)Ccc>Tcc p.P594S COAD 1 160276982 160276982 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr1:160276982G>A c.1273C>T c.(1273-1275)Cgg>Tgg p.R425W COAD 1 160280047 160280047 + Splice_Site SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr1:160280047C>A c.1078G>T c.(1078-1080)Ggt>Tgt p.G360C COAD 1 160283843 160283843 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:160283843C>T c.779G>A c.(778-780)cGc>cAc p.R260H COAD 1 160309764 160309764 + Nonsense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr1:160309764G>A c.163C>T c.(163-165)Cga>Tga p.R55* COADREAD 1 160264296 160264298 + In_Frame_Del DEL TCT TCT - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr1:160264296_160264298delTCT c.2652_2654delAGA c.(2650-2655)gaagat>gat p.E884del COADREAD 1 160264308 160264308 + Missense_Mutation SNP T T C TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr1:160264308T>C c.2642A>G c.(2641-2643)gAt>gGt p.D881G COADREAD 1 160264314 160264314 + Missense_Mutation SNP C C A TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr1:160264314C>A c.2636G>T c.(2635-2637)gGc>gTc p.G879V COADREAD 1 160267156 160267156 + Missense_Mutation SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr1:160267156C>A c.2240G>T c.(2239-2241)cGg>cTg p.R747L COADREAD 1 160267380 160267380 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr1:160267380G>A c.2133C>T c.(2131-2133)ggC>ggT p.G711G COADREAD 1 160268918 160268918 + Missense_Mutation SNP C C A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr1:160268918C>A c.1804G>T c.(1804-1806)Gcc>Tcc p.A602S COADREAD 1 160268940 160268940 + Silent SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr1:160268940G>A c.1782C>T c.(1780-1782)ccC>ccT p.P594P COADREAD 1 160268940 160268940 + Silent SNP G G A TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr1:160268940G>A c.1782C>T c.(1780-1782)ccC>ccT p.P594P COADREAD 1 160268940 160268940 + Silent SNP G G T TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr1:160268940G>T c.1782C>A c.(1780-1782)ccC>ccA p.P594P COADREAD 1 160268941 160268941 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr1:160268941G>A c.1781C>T c.(1780-1782)cCc>cTc p.P594L COADREAD 1 160268942 160268942 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr1:160268942G>A c.1780C>T c.(1780-1782)Ccc>Tcc p.P594S COADREAD 1 160276982 160276982 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr1:160276982G>A c.1273C>T c.(1273-1275)Cgg>Tgg p.R425W COADREAD 1 160280047 160280047 + Splice_Site SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr1:160280047C>A c.1078G>T c.(1078-1080)Ggt>Tgt p.G360C COADREAD 1 160283843 160283843 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr1:160283843C>T c.779G>A c.(778-780)cGc>cAc p.R260H COADREAD 1 160293311 160293311 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:160293311G>A c.616C>T c.(616-618)Cgt>Tgt p.R206C COADREAD 1 160309764 160309764 + Nonsense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr1:160309764G>A c.163C>T c.(163-165)Cga>Tga p.R55* DLBC 1 160302298 160302298 + Missense_Mutation SNP T T C TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr1:160302298T>C c.436A>G c.(436-438)Aca>Gca p.T146A ESCA 1 160261861 160261861 + Missense_Mutation SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr1:160261861G>A c.3088C>T c.(3088-3090)Cgt>Tgt p.R1030C ESCA 1 160263226 160263226 + Missense_Mutation SNP C C T TCGA-L5-A891-01A-11D-A36J-09 TCGA-L5-A891-11A-21D-A36M-09 g.chr1:160263226C>T c.2704G>A c.(2704-2706)Gct>Act p.A902T ESCA 1 160264608 160264608 + Missense_Mutation SNP G G T TCGA-2H-A9GR-01A-12D-A37C-09 TCGA-2H-A9GR-11A-11D-A37F-09 g.chr1:160264608G>T c.2516C>A c.(2515-2517)aCt>aAt p.T839N ESCA 1 160268910 160268910 + Missense_Mutation SNP G G C TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr1:160268910G>C c.1812C>G c.(1810-1812)atC>atG p.I604M ESCA 1 160276271 160276271 + Missense_Mutation SNP T T A TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr1:160276271T>A c.1315A>T c.(1315-1317)Aat>Tat p.N439Y ESCA 1 160278920 160278920 + Frame_Shift_Del DEL G G - TCGA-JY-A6FE-01A-11D-A33E-09 TCGA-JY-A6FE-10A-01D-A33H-09 g.chr1:160278920delG c.1190delC c.(1189-1191)cctfs p.P397fs ESCA 1 160281732 160281732 + Missense_Mutation SNP G G T TCGA-2H-A9GL-01A-12D-A37C-09 TCGA-2H-A9GL-11A-11D-A37F-09 g.chr1:160281732G>T c.1002C>A c.(1000-1002)caC>caA p.H334Q ESCA 1 160283886 160283886 + Silent SNP G G T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr1:160283886G>T c.736C>A c.(736-738)Cgg>Agg p.R246R ESCA 1 160302324 160302324 + Missense_Mutation SNP T T C TCGA-IG-A50L-01A-11D-A27G-09 TCGA-IG-A50L-10A-01D-A27G-09 g.chr1:160302324T>C c.410A>G c.(409-411)tAt>tGt p.Y137C ESCA 1 160305050 160305050 + Silent SNP G G A TCGA-L5-A4OX-01A-21D-A28B-09 TCGA-L5-A4OX-11A-13D-A28E-09 g.chr1:160305050G>A c.291C>T c.(289-291)cgC>cgT p.R97R GBM 1 160268961 160268961 + Silent SNP G G A TCGA-06-0142-01A-01D-1490-08 TCGA-06-0142-10A-01D-1490-08 g.chr1:160268961G>A c.1761C>T c.(1759-1761)ccC>ccT p.P587P GBMLGG 1 160261620 160261620 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:160261620G>A c.3247C>T c.(3247-3249)Cgc>Tgc p.R1083C GBMLGG 1 160268752 160268752 + Silent SNP T T C TCGA-DU-5849-01A-11D-1705-08 TCGA-DU-5849-10A-01D-1705-08 g.chr1:160268752T>C c.1860A>G c.(1858-1860)ctA>ctG p.L620L GBMLGG 1 160268961 160268961 + Silent SNP G G A TCGA-06-0142-01A-01D-1490-08 TCGA-06-0142-10A-01D-1490-08 g.chr1:160268961G>A c.1761C>T c.(1759-1761)ccC>ccT p.P587P GBMLGG 1 160275249 160275249 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:160275249G>A c.1641C>T c.(1639-1641)aaC>aaT p.N547N GBMLGG 1 160283846 160283846 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:160283846G>T c.776C>A c.(775-777)cCt>cAt p.P259H HNSC 1 160260441 160260441 + Silent SNP G G A TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr1:160260441G>A c.3456C>T c.(3454-3456)ccC>ccT p.P1152P HNSC 1 160261152 160261152 + Silent SNP G G C TCGA-BA-A8YP-01A-11D-A391-08 TCGA-BA-A8YP-10A-01D-A394-08 g.chr1:160261152G>C c.3393C>G c.(3391-3393)ctC>ctG p.L1131L HNSC 1 160261696 160261696 + Silent SNP G G A TCGA-CN-4737-01A-01D-1434-08 TCGA-CN-4737-10A-01D-1434-08 g.chr1:160261696G>A c.3171C>T c.(3169-3171)tgC>tgT p.C1057C HNSC 1 160264643 160264662 + Splice_Site DEL CTTCCCTACAGAGGGAAGGA CTTCCCTACAGAGGGAAGGA - TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr1:160264643_160264662delCTTCCCTACAGAGGGAAGGA c.2477_2481delTCCTTCCCTCTGTAGGGAAG c.(2476-2481)gtcctt>g p.VL826fs HNSC 1 160267363 160267363 + Missense_Mutation SNP C C T TCGA-DQ-7588-01A-11D-2078-08 TCGA-DQ-7588-10B-01D-2078-08 g.chr1:160267363C>T c.2150G>A c.(2149-2151)cGc>cAc p.R717H HNSC 1 160275281 160275281 + Missense_Mutation SNP C C T TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr1:160275281C>T c.1609G>A c.(1609-1611)Gag>Aag p.E537K HNSC 1 160275290 160275290 + Missense_Mutation SNP C C T TCGA-QK-A6IJ-01A-11D-A31L-08 TCGA-QK-A6IJ-10A-01D-A31J-08 g.chr1:160275290C>T c.1600G>A c.(1600-1602)Gcc>Acc p.A534T HNSC 1 160276193 160276193 + Silent SNP G G A TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr1:160276193G>A c.1393C>T c.(1393-1395)Ctg>Ttg p.L465L HNSC 1 160276272 160276272 + Silent SNP C C T TCGA-CQ-6219-01A-11D-1912-08 TCGA-CQ-6219-10A-01D-1912-08 g.chr1:160276272C>T c.1314G>A c.(1312-1314)aaG>aaA p.K438K HNSC 1 160281696 160281696 + Silent SNP G G A TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr1:160281696G>A c.1038C>T c.(1036-1038)ttC>ttT p.F346F HNSC 1 160303419 160303419 + Nonsense_Mutation SNP C C T TCGA-CV-7406-01A-11D-2078-08 TCGA-CV-7406-10A-01D-2078-08 g.chr1:160303419C>T c.360G>A c.(358-360)tgG>tgA p.W120* HNSC 1 160309718 160309718 + Missense_Mutation SNP C C G TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr1:160309718C>G c.209G>C c.(208-210)gGa>gCa p.G70A HNSC 1 160309984 160309984 + Silent SNP A A G TCGA-UF-A71E-01A-31D-A34J-08 TCGA-UF-A71E-10B-01D-A34M-08 g.chr1:160309984A>G c.141T>C c.(139-141)ttT>ttC p.F47F HNSC 1 160312934 160312934 + Silent SNP G G A TCGA-CR-6491-01A-11D-1870-08 TCGA-CR-6491-10A-01D-1870-08 g.chr1:160312934G>A c.27C>T c.(25-27)agC>agT p.S9S KICH 1 160275563 160275563 + Splice_Site SNP C C G TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr1:160275563C>G c.1443G>C c.(1441-1443)cgG>cgC p.R481R KIPAN 1 160261203 160261203 + Missense_Mutation SNP C C A TCGA-BP-4330-01A-01D-1366-10 TCGA-BP-4330-11A-01D-1366-10 g.chr1:160261203C>A c.3342G>T c.(3340-3342)aaG>aaT p.K1114N KIPAN 1 160261217 160261217 + Missense_Mutation SNP T T C TCGA-B8-5158-01A-01D-1421-08 TCGA-B8-5158-10A-01D-1421-08 g.chr1:160261217T>C c.3328A>G c.(3328-3330)Aat>Gat p.N1110D KIPAN 1 160267213 160267220 + Frame_Shift_Del DEL TCCTTTCT TCCTTTCT - TCGA-B2-5635-01A-01D-1534-10 TCGA-B2-5635-10A-01D-1535-10 g.chr1:160267213_160267220delTCCTTTCT c.2176_2183delAGAAAGGA c.(2176-2184)agaaaggacfs p.RKD726fs KIPAN 1 160275563 160275563 + Splice_Site SNP C C G TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr1:160275563C>G c.1443G>C c.(1441-1443)cgG>cgC p.R481R KIPAN 1 160295426 160295427 + Frame_Shift_Ins INS - - T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr1:160295426_160295427insT c.512_513insA c.(511-513)aacfs p.N171fs KIPAN 1 160302290 160302290 + Missense_Mutation SNP G G C TCGA-BP-5178-01A-01D-1429-08 TCGA-BP-5178-11A-01D-1429-08 g.chr1:160302290G>C c.444C>G c.(442-444)gaC>gaG p.D148E KIPAN 1 160305059 160305059 + Silent SNP A A G TCGA-A4-8517-01A-11D-2396-08 TCGA-A4-8517-10A-01D-2396-08 g.chr1:160305059A>G c.282T>C c.(280-282)gaT>gaC p.D94D KIPAN 1 160310032 160310032 + Silent SNP C C A TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chr1:160310032C>A c.93G>T c.(91-93)ggG>ggT p.G31G KIRC 1 160261203 160261203 + Missense_Mutation SNP C C A TCGA-BP-4330-01A-01D-1366-10 TCGA-BP-4330-11A-01D-1366-10 g.chr1:160261203C>A c.3342G>T c.(3340-3342)aaG>aaT p.K1114N KIRC 1 160261217 160261217 + Missense_Mutation SNP T T C TCGA-B8-5158-01A-01D-1421-08 TCGA-B8-5158-10A-01D-1421-08 g.chr1:160261217T>C c.3328A>G c.(3328-3330)Aat>Gat p.N1110D KIRC 1 160267213 160267220 + Frame_Shift_Del DEL TCCTTTCT TCCTTTCT - TCGA-B2-5635-01A-01D-1534-10 TCGA-B2-5635-10A-01D-1535-10 g.chr1:160267213_160267220delTCCTTTCT c.2176_2183delAGAAAGGA c.(2176-2184)agaaaggacfs p.RKD726fs KIRC 1 160295426 160295427 + Frame_Shift_Ins INS - - T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr1:160295426_160295427insT c.512_513insA c.(511-513)aacfs p.N171fs KIRC 1 160302290 160302290 + Missense_Mutation SNP G G C TCGA-BP-5178-01A-01D-1429-08 TCGA-BP-5178-11A-01D-1429-08 g.chr1:160302290G>C c.444C>G c.(442-444)gaC>gaG p.D148E KIRC 1 160310032 160310032 + Silent SNP C C A TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chr1:160310032C>A c.93G>T c.(91-93)ggG>ggT p.G31G KIRP 1 160305059 160305059 + Silent SNP A A G TCGA-A4-8517-01A-11D-2396-08 TCGA-A4-8517-10A-01D-2396-08 g.chr1:160305059A>G c.282T>C c.(280-282)gaT>gaC p.D94D LGG 1 160261620 160261620 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:160261620G>A c.3247C>T c.(3247-3249)Cgc>Tgc p.R1083C LGG 1 160268752 160268752 + Silent SNP T T C TCGA-DU-5849-01A-11D-1705-08 TCGA-DU-5849-10A-01D-1705-08 g.chr1:160268752T>C c.1860A>G c.(1858-1860)ctA>ctG p.L620L LGG 1 160275249 160275249 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:160275249G>A c.1641C>T c.(1639-1641)aaC>aaT p.N547N LGG 1 160283846 160283846 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:160283846G>T c.776C>A c.(775-777)cCt>cAt p.P259H LIHC 1 160264344 160264344 + Missense_Mutation SNP G G A TCGA-UB-A7MA-01A-11D-A33Q-10 TCGA-UB-A7MA-10A-01D-A33Q-10 g.chr1:160264344G>A c.2606C>T c.(2605-2607)gCt>gTt p.A869V LIHC 1 160303437 160303437 + Silent SNP A A G TCGA-DD-AADF-01A-11D-A40R-10 TCGA-DD-AADF-10A-01D-A40U-10 g.chr1:160303437A>G c.342T>C c.(340-342)gaT>gaC p.D114D LIHC 1 160303442 160303442 + Missense_Mutation SNP C C A TCGA-DD-AADM-01A-11D-A40R-10 TCGA-DD-AADM-10A-01D-A40U-10 g.chr1:160303442C>A c.337G>T c.(337-339)Gat>Tat p.D113Y LIHC 1 160305090 160305090 + Missense_Mutation SNP C C A TCGA-DD-A1EL-01A-11D-A152-10 TCGA-DD-A1EL-10A-01D-A152-10 g.chr1:160305090C>A c.251G>T c.(250-252)cGc>cTc p.R84L LIHC 1 160309715 160309715 + Missense_Mutation SNP T T C TCGA-DD-AAD0-01A-11D-A40R-10 TCGA-DD-AAD0-10A-01D-A40U-10 g.chr1:160309715T>C c.212A>G c.(211-213)gAt>gGt p.D71G LUAD 1 160259998 160259998 + Missense_Mutation SNP C C G TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr1:160259998C>G c.3624G>C c.(3622-3624)gaG>gaC p.E1208D LUAD 1 160261252 160261254 + In_Frame_Del DEL GGC GGC - TCGA-78-8655-01A-11D-2393-08 TCGA-78-8655-10A-01D-2393-08 g.chr1:160261252_160261254delGGC c.3291_3293delGCC c.(3289-3294)cagcct>cat p.1097_1098QP>H LUAD 1 160261813 160261813 + Missense_Mutation SNP C C G TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr1:160261813C>G c.3136G>C c.(3136-3138)Gag>Cag p.E1046Q LUAD 1 160265889 160265889 + Missense_Mutation SNP C C G TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr1:160265889C>G c.2314G>C c.(2314-2316)Gag>Cag p.E772Q LUAD 1 160268683 160268689 + Frame_Shift_Del DEL CTTGACA CTTGACA - TCGA-17-Z047-01A-01W-0747-08 TCGA-17-Z047-11A-01W-0746-08 g.chr1:160268683_160268689delCTTGACA c.1923_1929delTGTCAAG c.(1921-1929)tttgtcaagfs p.FVK641fs LUAD 1 160268767 160268767 + Silent SNP C C T TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr1:160268767C>T c.1845G>A c.(1843-1845)gtG>gtA p.V615V LUAD 1 160269029 160269029 + Missense_Mutation SNP C C G TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr1:160269029C>G c.1693G>C c.(1693-1695)Gat>Cat p.D565H LUAD 1 160275308 160275308 + Missense_Mutation SNP T T C TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr1:160275308T>C c.1582A>G c.(1582-1584)Att>Gtt p.I528V LUAD 1 160275343 160275343 + Missense_Mutation SNP C C A TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chr1:160275343C>A c.1547G>T c.(1546-1548)cGc>cTc p.R516L LUAD 1 160276211 160276211 + Missense_Mutation SNP C C A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr1:160276211C>A c.1375G>T c.(1375-1377)Gct>Tct p.A459S LUAD 1 160281721 160281721 + Missense_Mutation SNP T T C TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr1:160281721T>C c.1013A>G c.(1012-1014)gAc>gGc p.D338G LUAD 1 160283840 160283840 + Missense_Mutation SNP T T A TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr1:160283840T>A c.782A>T c.(781-783)cAa>cTa p.Q261L LUAD 1 160293231 160293231 + Missense_Mutation SNP C C A TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr1:160293231C>A c.696G>T c.(694-696)tgG>tgT p.W232C LUAD 1 160293299 160293299 + Missense_Mutation SNP A A T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr1:160293299A>T c.628T>A c.(628-630)Tgg>Agg p.W210R LUAD 1 160293314 160293314 + Missense_Mutation SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr1:160293314C>A c.613G>T c.(613-615)Gat>Tat p.D205Y LUSC 1 160260349 160260349 + Missense_Mutation SNP T T C TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chr1:160260349T>C c.3548A>G c.(3547-3549)gAa>gGa p.E1183G LUSC 1 160261286 160261286 + Splice_Site SNP T T C TCGA-63-5128-01A-01D-1441-08 TCGA-63-5128-10A-01D-1441-08 g.chr1:160261286T>C c.3259A>G c.(3259-3261)Atg>Gtg p.M1087V LUSC 1 160262293 160262293 + Missense_Mutation SNP C C A TCGA-21-5784-01A-01D-1632-08 TCGA-21-5784-10A-01D-1632-08 g.chr1:160262293C>A c.2941G>T c.(2941-2943)Ggc>Tgc p.G981C LUSC 1 160262323 160262323 + Missense_Mutation SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr1:160262323G>C c.2911C>G c.(2911-2913)Cag>Gag p.Q971E LUSC 1 160264286 160264287 + Missense_Mutation DNP GA GA AG TCGA-51-4079-01A-01D-1458-08 TCGA-51-4079-11A-01D-1458-08 g.chr1:160264286_160264287GA>AG c.2663_2664TC>CT c.(2662-2664)cTC>cCT p.L888P LUSC 1 160281683 160281683 + Missense_Mutation SNP C C A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr1:160281683C>A c.1051G>T c.(1051-1053)Gat>Tat p.D351Y LUSC 1 160281763 160281763 + Missense_Mutation SNP G G T TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr1:160281763G>T c.971C>A c.(970-972)cCa>cAa p.P324Q LUSC 1 160281809 160281809 + Splice_Site SNP C C A TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr1:160281809C>A c.e11-1 OV 1 160268941 160268941 + Missense_Mutation SNP G G A TCGA-20-0991-01A-03D-0428-08 TCGA-20-0991-10A-01D-0428-08 g.chr1:160268941G>A c.1781C>T c.(1780-1782)cCc>cTc p.P594L OV 1 160293228 160293228 + Silent SNP G G T TCGA-29-1761-01A-01W-0633-09 TCGA-29-1761-10A-01W-0633-09 g.chr1:160293228G>T c.699C>A c.(697-699)cgC>cgA p.R233R PAAD 1 160261125 160261125 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:160261125C>A c.3420G>T c.(3418-3420)caG>caT p.Q1140H PAAD 1 160261696 160261696 + Silent SNP G G A TCGA-FB-AAPZ-01A-11D-A40W-08 TCGA-FB-AAPZ-11A-11D-A40W-08 g.chr1:160261696G>A c.3171C>T c.(3169-3171)tgC>tgT p.C1057C PAAD 1 160261696 160261696 + Silent SNP G G A TCGA-HV-A7OL-01A-11D-A33T-08 TCGA-HV-A7OL-10A-01D-A33W-08 g.chr1:160261696G>A c.3171C>T c.(3169-3171)tgC>tgT p.C1057C PAAD 1 160261696 160261696 + Silent SNP G G A TCGA-LB-A8F3-01A-11D-A36O-08 TCGA-LB-A8F3-10A-01D-A367-08 g.chr1:160261696G>A c.3171C>T c.(3169-3171)tgC>tgT p.C1057C PAAD 1 160277034 160277034 + Splice_Site SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:160277034C>T c.1221G>A c.(1219-1221)gcG>gcA p.A407A PAAD 1 160295426 160295427 + Frame_Shift_Ins INS - - T TCGA-LB-A7SX-01A-11D-A33T-08 TCGA-LB-A7SX-10A-01D-A33W-08 g.chr1:160295426_160295427insT c.512_513insA c.(511-513)aacfs p.N171fs PAAD 1 160295426 160295427 + Frame_Shift_Ins INS - - T TCGA-LB-A8F3-01A-11D-A36O-08 TCGA-LB-A8F3-10A-01D-A367-08 g.chr1:160295426_160295427insT c.512_513insA c.(511-513)aacfs p.N171fs PAAD 1 160295426 160295427 + Frame_Shift_Ins INS - - T TCGA-YH-A8SY-01A-11D-A377-08 TCGA-YH-A8SY-10A-01D-A37A-08 g.chr1:160295426_160295427insT c.512_513insA c.(511-513)aacfs p.N171fs PAAD 1 160302256 160302256 + Missense_Mutation SNP G G A TCGA-IB-A6UF-01A-23D-A33T-08 TCGA-IB-A6UF-10A-01D-A33W-08 g.chr1:160302256G>A c.478C>T c.(478-480)Cgc>Tgc p.R160C PAAD 1 160312937 160312937 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:160312937C>A c.24G>T c.(22-24)aaG>aaT p.K8N PCPG 1 160261696 160261696 + Silent SNP G G A TCGA-S7-A7WV-01A-11D-A35I-08 TCGA-S7-A7WV-10A-01D-A35G-08 g.chr1:160261696G>A c.3171C>T c.(3169-3171)tgC>tgT p.C1057C PCPG 1 160276973 160276973 + Missense_Mutation SNP C C A TCGA-WB-A81J-01A-11D-A35I-08 TCGA-WB-A81J-10A-01D-A35G-08 g.chr1:160276973C>A c.1282G>T c.(1282-1284)Gtc>Ttc p.V428F PRAD 1 160276964 160276964 + Missense_Mutation SNP G G A TCGA-EJ-5522-01A-01D-1576-08 TCGA-EJ-5522-10A-01D-1577-08 g.chr1:160276964G>A c.1291C>T c.(1291-1293)Cgg>Tgg p.R431W PRAD 1 160309737 160309737 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:160309737G>A c.190C>T c.(190-192)Cca>Tca p.P64S READ 1 160293311 160293311 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:160293311G>A c.616C>T c.(616-618)Cgt>Tgt p.R206C SKCM 1 160260464 160260464 + Silent SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr1:160260464G>A c.3433C>T c.(3433-3435)Ctg>Ttg p.L1145L SKCM 1 160260465 160260465 + Silent SNP G G A TCGA-EE-A17Y-06A-11D-A196-08 TCGA-EE-A17Y-10B-01D-A198-08 g.chr1:160260465G>A c.3432C>T c.(3430-3432)atC>atT p.I1144I SKCM 1 160261862 160261862 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr1:160261862G>A c.3087C>T c.(3085-3087)ttC>ttT p.F1029F SKCM 1 160261901 160261901 + Silent SNP G G A TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr1:160261901G>A c.3048C>T c.(3046-3048)ctC>ctT p.L1016L SKCM 1 160261985 160261985 + Silent SNP C C T TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr1:160261985C>T c.2964G>A c.(2962-2964)aaG>aaA p.K988K SKCM 1 160262336 160262336 + Silent SNP G G A TCGA-DA-A3F3-06A-11D-A20D-08 TCGA-DA-A3F3-10A-01D-A20D-08 g.chr1:160262336G>A c.2898C>T c.(2896-2898)ggC>ggT p.G966G SKCM 1 160263246 160263246 + Missense_Mutation SNP G G A TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr1:160263246G>A c.2684C>T c.(2683-2685)tCc>tTc p.S895F SKCM 1 160263246 160263246 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr1:160263246G>A c.2684C>T c.(2683-2685)tCc>tTc p.S895F SKCM 1 160265560 160265560 + Silent SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr1:160265560G>A c.2442C>T c.(2440-2442)tcC>tcT p.S814S SKCM 1 160275485 160275485 + Silent SNP G G C TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr1:160275485G>C c.1521C>G c.(1519-1521)gcC>gcG p.A507A SKCM 1 160276187 160276187 + Nonsense_Mutation SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr1:160276187G>A c.1399C>T c.(1399-1401)Cga>Tga p.R467* SKCM 1 160278903 160278903 + Missense_Mutation SNP G G T TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr1:160278903G>T c.1207C>A c.(1207-1209)Cag>Aag p.Q403K SKCM 1 160280027 160280027 + Silent SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr1:160280027G>A c.1098C>T c.(1096-1098)ttC>ttT p.F366F SKCM 1 160281719 160281719 + Silent SNP G G T TCGA-D3-A1Q1-06A-21D-A196-08 TCGA-D3-A1Q1-10A-01D-A198-08 g.chr1:160281719G>T c.1015C>A c.(1015-1017)Cga>Aga p.R339R SKCM 1 160281796 160281796 + Missense_Mutation SNP C C T TCGA-ER-A3EV-06A-11D-A20D-08 TCGA-ER-A3EV-10A-01D-A20D-08 g.chr1:160281796C>T c.938G>A c.(937-939)gGt>gAt p.G313D SKCM 1 160282958 160282958 + Splice_Site SNP C C T TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr1:160282958C>T c.e10-1 SKCM 1 160293284 160293284 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr1:160293284G>A c.643C>T c.(643-645)Ccc>Tcc p.P215S SKCM 1 160295426 160295427 + Frame_Shift_Ins INS - - T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr1:160295426_160295427insT c.512_513insA c.(511-513)aacfs p.N171fs SKCM 1 160303462 160303462 + Missense_Mutation SNP G G A TCGA-D3-A5GS-06A-11D-A27K-08 TCGA-D3-A5GS-10A-01D-A27N-08 g.chr1:160303462G>A c.317C>T c.(316-318)cCc>cTc p.P106L SKCM 1 160305037 160305037 + Missense_Mutation SNP G G A TCGA-ER-A19J-06A-11D-A196-08 TCGA-ER-A19J-10A-01D-A198-08 g.chr1:160305037G>A c.304C>T c.(304-306)Cat>Tat p.H102Y

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 1 160263226 160263226 single base substitution C T downstream_gene_variant BLCA-CN 1 160263226 160263226 single base substitution C T missense_variant A902T 2704G>A BLCA-CN 1 160263226 160263226 single base substitution C T missense_variant A911T 2731G>A BLCA-CN 1 160313204 160313204 single base substitution T G upstream_gene_variant BLCA-CN 1 160314540 160314540 single base substitution G A upstream_gene_variant BLCA-US 1 160261692 160261692 single base substitution C T downstream_gene_variant BLCA-US 1 160261692 160261692 single base substitution C T missense_variant E1059K 3175G>A BLCA-US 1 160261692 160261692 single base substitution C T missense_variant E1068K 3202G>A BLCA-US 1 160262955 160262955 single base substitution C T downstream_gene_variant BLCA-US 1 160262955 160262955 single base substitution C T splice_donor_variant BLCA-US 1 160267134 160267134 single base substitution C G missense_variant Q754H 2262G>C BLCA-US 1 160267134 160267134 single base substitution C G missense_variant Q763H 2289G>C BLCA-US 1 160267134 160267134 single base substitution C G splice_region_variant BLCA-US 1 160282929 160282929 single base substitution G T missense_variant H291N 871C>A BLCA-US 1 160282929 160282929 single base substitution G T upstream_gene_variant BRCA-EU 1 160254773 160254773 single base substitution C G downstream_gene_variant BRCA-EU 1 160254971 160254971 single base substitution C A downstream_gene_variant BRCA-EU 1 160255142 160255142 single base substitution G A downstream_gene_variant BRCA-EU 1 160255562 160255562 single base substitution C T downstream_gene_variant BRCA-EU 1 160255692 160255692 single base substitution C G downstream_gene_variant BRCA-EU 1 160256709 160256709 single base substitution A T downstream_gene_variant BRCA-EU 1 160256987 160256987 single base substitution C T downstream_gene_variant BRCA-EU 1 160257315 160257315 single base substitution C T downstream_gene_variant BRCA-EU 1 160257638 160257638 single base substitution G C downstream_gene_variant BRCA-EU 1 160257776 160257776 single base substitution A C downstream_gene_variant BRCA-EU 1 160258770 160258770 deletion of <=200bp T - downstream_gene_variant BRCA-EU 1 160259265 160259265 single base substitution C A 3_prime_UTR_variant BRCA-EU 1 160259614 160259614 single base substitution C G 3_prime_UTR_variant BRCA-EU 1 160259614 160259614 single base substitution C G downstream_gene_variant BRCA-EU 1 160260990 160260990 single base substitution G T downstream_gene_variant BRCA-EU 1 160260990 160260990 single base substitution G T intron_variant BRCA-EU 1 160261228 160261228 single base substitution C T downstream_gene_variant BRCA-EU 1 160261228 160261228 single base substitution C T missense_variant R1106H 3317G>A BRCA-EU 1 160261228 160261228 single base substitution C T missense_variant R1115H 3344G>A BRCA-EU 1 160261572 160261572 single base substitution G C downstream_gene_variant BRCA-EU 1 160261572 160261572 single base substitution G C intron_variant BRCA-EU 1 160264669 160264669 single base substitution C T intron_variant BRCA-EU 1 160264743 160264743 single base substitution T A intron_variant BRCA-EU 1 160264902 160264902 single base substitution T C intron_variant BRCA-EU 1 160266069 160266069 single base substitution C T intron_variant BRCA-EU 1 160266992 160266992 single base substitution A T intron_variant BRCA-EU 1 160266994 160266994 single base substitution C T intron_variant BRCA-EU 1 160267870 160267870 single base substitution C G intron_variant BRCA-EU 1 160268321 160268321 single base substitution C G intron_variant BRCA-EU 1 160269097 160269097 single base substitution T G intron_variant BRCA-EU 1 160269097 160269097 single base substitution T G upstream_gene_variant BRCA-EU 1 160272418 160272418 single base substitution C T downstream_gene_variant BRCA-EU 1 160272418 160272418 single base substitution C T intron_variant BRCA-EU 1 160272418 160272418 single base substitution C T upstream_gene_variant BRCA-EU 1 160273175 160273175 single base substitution T A downstream_gene_variant BRCA-EU 1 160273175 160273175 single base substitution T A intron_variant BRCA-EU 1 160273175 160273175 single base substitution T A upstream_gene_variant BRCA-EU 1 160273427 160273427 single base substitution T A downstream_gene_variant BRCA-EU 1 160273427 160273427 single base substitution T A intron_variant BRCA-EU 1 160273427 160273427 single base substitution T A upstream_gene_variant BRCA-EU 1 160273532 160273532 single base substitution G C downstream_gene_variant BRCA-EU 1 160273532 160273532 single base substitution G C intron_variant BRCA-EU 1 160273532 160273532 single base substitution G C upstream_gene_variant BRCA-EU 1 160274732 160274732 single base substitution C G downstream_gene_variant BRCA-EU 1 160274732 160274732 single base substitution C G intron_variant BRCA-EU 1 160275012 160275012 insertion of <=200bp - T downstream_gene_variant BRCA-EU 1 160275012 160275012 insertion of <=200bp - T intron_variant BRCA-EU 1 160275153 160275153 single base substitution C T downstream_gene_variant BRCA-EU 1 160275153 160275153 single base substitution C T exon_variant BRCA-EU 1 160275153 160275153 single base substitution C T intron_variant BRCA-EU 1 160275378 160275378 single base substitution G T downstream_gene_variant BRCA-EU 1 160275378 160275378 single base substitution G T intron_variant BRCA-EU 1 160275378 160275378 single base substitution G T stop_gained C513* 1539C>A BRCA-EU 1 160276284 160276284 single base substitution C A downstream_gene_variant BRCA-EU 1 160276284 160276284 single base substitution C A splice_acceptor_variant BRCA-EU 1 160276284 160276284 single base substitution C A upstream_gene_variant BRCA-EU 1 160276434 160276434 single base substitution G A downstream_gene_variant BRCA-EU 1 160276434 160276434 single base substitution G A intron_variant BRCA-EU 1 160276434 160276434 single base substitution G A upstream_gene_variant BRCA-EU 1 160276435 160276435 single base substitution C A downstream_gene_variant BRCA-EU 1 160276435 160276435 single base substitution C A intron_variant BRCA-EU 1 160276435 160276435 single base substitution C A upstream_gene_variant BRCA-EU 1 160277970 160277970 single base substitution A G downstream_gene_variant BRCA-EU 1 160277970 160277970 single base substitution A G intron_variant BRCA-EU 1 160277970 160277970 single base substitution A G upstream_gene_variant BRCA-EU 1 160278003 160278003 single base substitution C G downstream_gene_variant BRCA-EU 1 160278003 160278003 single base substitution C G intron_variant BRCA-EU 1 160278003 160278003 single base substitution C G upstream_gene_variant BRCA-EU 1 160278506 160278506 single base substitution A T downstream_gene_variant BRCA-EU 1 160278506 160278506 single base substitution A T intron_variant BRCA-EU 1 160278506 160278506 single base substitution A T upstream_gene_variant BRCA-EU 1 160278758 160278758 single base substitution T A exon_variant BRCA-EU 1 160278758 160278758 single base substitution T A intron_variant BRCA-EU 1 160278758 160278758 single base substitution T A upstream_gene_variant BRCA-EU 1 160279981 160279981 single base substitution C A splice_donor_variant BRCA-EU 1 160279981 160279981 single base substitution C A upstream_gene_variant BRCA-EU 1 160281060 160281060 single base substitution C T intron_variant BRCA-EU 1 160281060 160281060 single base substitution C T upstream_gene_variant BRCA-EU 1 160281374 160281374 deletion of <=200bp A - intron_variant BRCA-EU 1 160281374 160281374 deletion of <=200bp A - upstream_gene_variant BRCA-EU 1 160281537 160281537 deletion of <=200bp A - intron_variant BRCA-EU 1 160281537 160281537 deletion of <=200bp A - upstream_gene_variant BRCA-EU 1 160282250 160282250 deletion of <=200bp T - intron_variant BRCA-EU 1 160282250 160282250 deletion of <=200bp T - upstream_gene_variant BRCA-EU 1 160283015 160283015 single base substitution T C intron_variant BRCA-EU 1 160283015 160283015 single base substitution T C upstream_gene_variant BRCA-EU 1 160283223 160283223 deletion of <=200bp G - intron_variant BRCA-EU 1 160283223 160283223 deletion of <=200bp G - upstream_gene_variant BRCA-EU 1 160283788 160283788 single base substitution C G missense_variant M278I 834G>C BRCA-EU 1 160283788 160283788 single base substitution C G upstream_gene_variant BRCA-EU 1 160285210 160285210 single base substitution C T intron_variant BRCA-EU 1 160285210 160285210 single base substitution C T upstream_gene_variant BRCA-EU 1 160285419 160285419 single base substitution G A intron_variant BRCA-EU 1 160285420 160285420 single base substitution C T intron_variant BRCA-EU 1 160285421 160285421 single base substitution T A intron_variant BRCA-EU 1 160285878 160285878 single base substitution G T intron_variant BRCA-EU 1 160286067 160286067 single base substitution G C intron_variant BRCA-EU 1 160287781 160287781 single base substitution G A intron_variant BRCA-EU 1 160287877 160287877 single base substitution C A intron_variant BRCA-EU 1 160288618 160288618 deletion of <=200bp T - intron_variant BRCA-EU 1 160289232 160289232 single base substitution G T intron_variant BRCA-EU 1 160289260 160289260 single base substitution C G intron_variant BRCA-EU 1 160289318 160289318 single base substitution C A intron_variant BRCA-EU 1 160289876 160289876 single base substitution C G intron_variant BRCA-EU 1 160290004 160290004 deletion of <=200bp A - intron_variant BRCA-EU 1 160290005 160290005 single base substitution A G intron_variant BRCA-EU 1 160290386 160290386 single base substitution G C intron_variant BRCA-EU 1 160293473 160293473 single base substitution G C intron_variant BRCA-EU 1 160293813 160293813 single base substitution G C intron_variant BRCA-EU 1 160294335 160294335 single base substitution G A intron_variant BRCA-EU 1 160295661 160295661 single base substitution T C intron_variant BRCA-EU 1 160296423 160296423 single base substitution T C intron_variant BRCA-EU 1 160297025 160297025 single base substitution C A intron_variant BRCA-EU 1 160297160 160297160 single base substitution C G intron_variant BRCA-EU 1 160298317 160298317 single base substitution C G downstream_gene_variant BRCA-EU 1 160298317 160298317 single base substitution C G intron_variant BRCA-EU 1 160298695 160298695 single base substitution G T downstream_gene_variant BRCA-EU 1 160298695 160298695 single base substitution G T intron_variant BRCA-EU 1 160299243 160299243 insertion of <=200bp - A downstream_gene_variant BRCA-EU 1 160299243 160299243 insertion of <=200bp - A intron_variant BRCA-EU 1 160299701 160299701 single base substitution G A downstream_gene_variant BRCA-EU 1 160299701 160299701 single base substitution G A intron_variant BRCA-EU 1 160299911 160299911 insertion of <=200bp - C downstream_gene_variant BRCA-EU 1 160299911 160299911 insertion of <=200bp - C intron_variant BRCA-EU 1 160300699 160300699 single base substitution C T downstream_gene_variant BRCA-EU 1 160300699 160300699 single base substitution C T intron_variant BRCA-EU 1 160301246 160301246 single base substitution C A downstream_gene_variant BRCA-EU 1 160301246 160301246 single base substitution C A intron_variant BRCA-EU 1 160301540 160301540 single base substitution C G downstream_gene_variant BRCA-EU 1 160301540 160301540 single base substitution C G intron_variant BRCA-EU 1 160301648 160301648 single base substitution T C downstream_gene_variant BRCA-EU 1 160301648 160301648 single base substitution T C intron_variant BRCA-EU 1 160301893 160301893 single base substitution C G downstream_gene_variant BRCA-EU 1 160301893 160301893 single base substitution C G intron_variant BRCA-EU 1 160302340 160302340 single base substitution T A downstream_gene_variant BRCA-EU 1 160302340 160302340 single base substitution T A missense_variant T132S 394A>T BRCA-EU 1 160303470 160303470 single base substitution C A splice_acceptor_variant BRCA-EU 1 160304867 160304867 single base substitution C T downstream_gene_variant BRCA-EU 1 160304867 160304867 single base substitution C T intron_variant BRCA-EU 1 160305981 160305981 deletion of <=200bp A - downstream_gene_variant BRCA-EU 1 160305981 160305981 deletion of <=200bp A - intron_variant BRCA-EU 1 160308690 160308690 single base substitution C G downstream_gene_variant BRCA-EU 1 160308690 160308690 single base substitution C G intron_variant BRCA-EU 1 160309393 160309393 single base substitution C T exon_variant BRCA-EU 1 160309393 160309393 single base substitution C T intron_variant BRCA-EU 1 160309932 160309932 single base substitution T G intron_variant BRCA-EU 1 160309959 160309959 single base substitution G C intron_variant BRCA-EU 1 160310663 160310663 single base substitution G A intron_variant BRCA-EU 1 160310663 160310663 single base substitution G A upstream_gene_variant BRCA-EU 1 160310931 160310931 single base substitution T A intron_variant BRCA-EU 1 160310931 160310931 single base substitution T A upstream_gene_variant BRCA-EU 1 160310989 160310989 single base substitution T C intron_variant BRCA-EU 1 160310989 160310989 single base substitution T C upstream_gene_variant BRCA-EU 1 160311217 160311217 single base substitution C T intron_variant BRCA-EU 1 160311217 160311217 single base substitution C T upstream_gene_variant BRCA-EU 1 160311606 160311606 deletion of <=200bp T - intron_variant BRCA-EU 1 160311606 160311606 deletion of <=200bp T - upstream_gene_variant BRCA-EU 1 160312212 160312212 single base substitution G T intron_variant BRCA-EU 1 160312212 160312212 single base substitution G T upstream_gene_variant BRCA-EU 1 160312305 160312305 deletion of <=200bp A - intron_variant BRCA-EU 1 160312305 160312305 deletion of <=200bp A - upstream_gene_variant BRCA-EU 1 160312508 160312508 single base substitution A G intron_variant BRCA-EU 1 160312508 160312508 single base substitution A G upstream_gene_variant BRCA-EU 1 160313567 160313567 single base substitution A G upstream_gene_variant BRCA-EU 1 160315549 160315549 insertion of <=200bp - C upstream_gene_variant BRCA-EU 1 160317267 160317267 single base substitution C T upstream_gene_variant BRCA-EU 1 160317344 160317344 insertion of <=200bp - T upstream_gene_variant BRCA-FR 1 160257638 160257638 single base substitution G C downstream_gene_variant BRCA-FR 1 160261228 160261228 single base substitution C T downstream_gene_variant BRCA-FR 1 160261228 160261228 single base substitution C T missense_variant R1106H 3317G>A BRCA-FR 1 160261228 160261228 single base substitution C T missense_variant R1115H 3344G>A BRCA-FR 1 160273532 160273532 single base substitution G C downstream_gene_variant BRCA-FR 1 160273532 160273532 single base substitution G C intron_variant BRCA-FR 1 160273532 160273532 single base substitution G C upstream_gene_variant BRCA-FR 1 160276268 160276268 single base substitution G C downstream_gene_variant BRCA-FR 1 160276268 160276268 single base substitution G C missense_variant L440V 1318C>G BRCA-FR 1 160276268 160276268 single base substitution G C upstream_gene_variant BRCA-FR 1 160277970 160277970 single base substitution A G downstream_gene_variant BRCA-FR 1 160277970 160277970 single base substitution A G intron_variant BRCA-FR 1 160277970 160277970 single base substitution A G upstream_gene_variant BRCA-FR 1 160284759 160284759 single base substitution G C intron_variant BRCA-FR 1 160284759 160284759 single base substitution G C upstream_gene_variant BRCA-FR 1 160285210 160285210 single base substitution C T intron_variant BRCA-FR 1 160285210 160285210 single base substitution C T upstream_gene_variant BRCA-FR 1 160285878 160285878 single base substitution G T intron_variant BRCA-FR 1 160297025 160297025 single base substitution C A intron_variant BRCA-FR 1 160297160 160297160 single base substitution C G intron_variant BRCA-UK 1 160264902 160264902 single base substitution T C intron_variant BRCA-UK 1 160267870 160267870 single base substitution C G intron_variant BRCA-UK 1 160273427 160273427 single base substitution T A downstream_gene_variant BRCA-UK 1 160273427 160273427 single base substitution T A intron_variant BRCA-UK 1 160273427 160273427 single base substitution T A upstream_gene_variant BRCA-UK 1 160278506 160278506 single base substitution A T downstream_gene_variant BRCA-UK 1 160278506 160278506 single base substitution A T intron_variant BRCA-UK 1 160278506 160278506 single base substitution A T upstream_gene_variant BRCA-UK 1 160287166 160287166 single base substitution A C intron_variant BRCA-UK 1 160289232 160289232 single base substitution G T intron_variant BRCA-UK 1 160298177 160298177 single base substitution G C intron_variant BRCA-UK 1 160298319 160298319 single base substitution C T downstream_gene_variant BRCA-UK 1 160298319 160298319 single base substitution C T intron_variant BRCA-UK 1 160299701 160299701 single base substitution G A downstream_gene_variant BRCA-UK 1 160299701 160299701 single base substitution G A intron_variant BRCA-UK 1 160301893 160301893 single base substitution C G downstream_gene_variant BRCA-UK 1 160301893 160301893 single base substitution C G intron_variant BRCA-UK 1 160304867 160304867 single base substitution C T downstream_gene_variant BRCA-UK 1 160304867 160304867 single base substitution C T intron_variant BRCA-US 1 160259952 160259952 single base substitution G A downstream_gene_variant BRCA-US 1 160259952 160259952 single base substitution G A missense_variant R1224C 3670C>T BRCA-US 1 160259952 160259952 single base substitution G A missense_variant R1233C 3697C>T BRCA-US 1 160261648 160261648 single base substitution C T downstream_gene_variant BRCA-US 1 160261648 160261648 single base substitution C T synonymous_variant L1073L 3219G>A BRCA-US 1 160261648 160261648 single base substitution C T synonymous_variant L1082L 3246G>A BRCA-US 1 160261650 160261650 single base substitution G C downstream_gene_variant BRCA-US 1 160261650 160261650 single base substitution G C missense_variant L1073V 3217C>G BRCA-US 1 160261650 160261650 single base substitution G C missense_variant L1082V 3244C>G BRCA-US 1 160261861 160261861 single base substitution G A downstream_gene_variant BRCA-US 1 160261861 160261861 single base substitution G A missense_variant R1030C 3088C>T BRCA-US 1 160261861 160261861 single base substitution G A missense_variant R1039C 3115C>T BRCA-US 1 160264342 160264342 single base substitution G A downstream_gene_variant BRCA-US 1 160264342 160264342 single base substitution G A missense_variant L870F 2608C>T BRCA-US 1 160264342 160264342 single base substitution G A missense_variant L879F 2635C>T BRCA-US 1 160267442 160267442 single base substitution C T exon_variant BRCA-US 1 160267442 160267442 single base substitution C T missense_variant E691K 2071G>A BRCA-US 1 160267442 160267442 single base substitution C T missense_variant E700K 2098G>A BRCA-US 1 160275320 160275320 single base substitution T C downstream_gene_variant BRCA-US 1 160275320 160275320 single base substitution T C exon_variant BRCA-US 1 160275320 160275320 single base substitution T C missense_variant I524V 1570A>G BRCA-US 1 160275320 160275320 single base substitution T C missense_variant I533V 1597A>G BRCA-US 1 160275509 160275509 single base substitution G A downstream_gene_variant BRCA-US 1 160275509 160275509 single base substitution G A exon_variant BRCA-US 1 160275509 160275509 single base substitution G A synonymous_variant D499D 1497C>T BRCA-US 1 160276146 160276146 single base substitution C T downstream_gene_variant BRCA-US 1 160276146 160276146 single base substitution C T splice_region_variant BRCA-US 1 160276146 160276146 single base substitution C T upstream_gene_variant BRCA-US 1 160279994 160279994 single base substitution G A exon_variant BRCA-US 1 160279994 160279994 single base substitution G A synonymous_variant V377V 1131C>T BRCA-US 1 160279994 160279994 single base substitution G A upstream_gene_variant BRCA-US 1 160280016 160280016 single base substitution T A exon_variant BRCA-US 1 160280016 160280016 single base substitution T A missense_variant Y370F 1109A>T BRCA-US 1 160280016 160280016 single base substitution T A upstream_gene_variant BRCA-US 1 160280018 160280018 single base substitution T C exon_variant BRCA-US 1 160280018 160280018 single base substitution T C synonymous_variant S369S 1107A>G BRCA-US 1 160280018 160280018 single base substitution T C upstream_gene_variant BRCA-US 1 160280027 160280027 single base substitution G A exon_variant BRCA-US 1 160280027 160280027 single base substitution G A synonymous_variant F366F 1098C>T BRCA-US 1 160280027 160280027 single base substitution G A upstream_gene_variant BRCA-US 1 160280035 160280035 single base substitution G A exon_variant BRCA-US 1 160280035 160280035 single base substitution G A missense_variant P364S 1090C>T BRCA-US 1 160280035 160280035 single base substitution G A upstream_gene_variant BRCA-US 1 160314596 160314596 single base substitution C G upstream_gene_variant BTCA-JP 1 160260177 160260177 single base substitution C T downstream_gene_variant BTCA-JP 1 160260177 160260177 single base substitution C T intron_variant BTCA-JP 1 160263192 160263192 single base substitution C G downstream_gene_variant BTCA-JP 1 160263192 160263192 single base substitution C G missense_variant G913A 2738G>C BTCA-JP 1 160263192 160263192 single base substitution C G missense_variant G922A 2765G>C BTCA-JP 1 160263302 160263302 single base substitution T G downstream_gene_variant BTCA-JP 1 160263302 160263302 single base substitution T G intron_variant BTCA-JP 1 160264296 160264298 deletion of <=200bp TCT - disruptive_inframe_deletion ED884D BTCA-JP 1 160264296 160264298 deletion of <=200bp TCT - disruptive_inframe_deletion ED893D BTCA-JP 1 160264296 160264298 deletion of <=200bp TCT - downstream_gene_variant BTCA-JP 1 160267522 160267522 single base substitution G A exon_variant BTCA-JP 1 160267522 160267522 single base substitution G A missense_variant A664V 1991C>T BTCA-JP 1 160267522 160267522 single base substitution G A missense_variant A673V 2018C>T BTCA-JP 1 160283074 160283074 single base substitution A G intron_variant BTCA-JP 1 160283074 160283074 single base substitution A G upstream_gene_variant BTCA-JP 1 160302298 160302298 single base substitution T C downstream_gene_variant BTCA-JP 1 160302298 160302298 single base substitution T C missense_variant T146A 436A>G CESC-US 1 160261692 160261692 single base substitution C T downstream_gene_variant CESC-US 1 160261692 160261692 single base substitution C T missense_variant E1059K 3175G>A CESC-US 1 160261692 160261692 single base substitution C T missense_variant E1068K 3202G>A CESC-US 1 160276954 160276954 single base substitution G A downstream_gene_variant CESC-US 1 160276954 160276954 single base substitution G A missense_variant S434L 1301C>T CESC-US 1 160276954 160276954 single base substitution G A upstream_gene_variant CLLE-ES 1 160260442 160260442 single base substitution G A downstream_gene_variant CLLE-ES 1 160260442 160260442 single base substitution G A missense_variant P1152L 3455C>T CLLE-ES 1 160260442 160260442 single base substitution G A missense_variant P1161L 3482C>T CLLE-ES 1 160316040 160316040 single base substitution C T upstream_gene_variant COAD-US 1 160254899 160254899 single base substitution C T downstream_gene_variant COAD-US 1 160264296 160264298 deletion of <=200bp TCT - disruptive_inframe_deletion ED884D COAD-US 1 160264296 160264298 deletion of <=200bp TCT - disruptive_inframe_deletion ED893D COAD-US 1 160264296 160264298 deletion of <=200bp TCT - downstream_gene_variant COAD-US 1 160264314 160264314 single base substitution C A downstream_gene_variant COAD-US 1 160264314 160264314 single base substitution C A missense_variant G879V 2636G>T COAD-US 1 160264314 160264314 single base substitution C A missense_variant G888V 2663G>T COAD-US 1 160265586 160265586 single base substitution T G exon_variant COAD-US 1 160265586 160265586 single base substitution T G missense_variant T806P 2416A>C COAD-US 1 160265586 160265586 single base substitution T G missense_variant T815P 2443A>C COAD-US 1 160267380 160267380 single base substitution G A exon_variant COAD-US 1 160267380 160267380 single base substitution G A synonymous_variant G711G 2133C>T COAD-US 1 160267380 160267380 single base substitution G A synonymous_variant G720G 2160C>T COAD-US 1 160276982 160276982 single base substitution G A downstream_gene_variant COAD-US 1 160276982 160276982 single base substitution G A missense_variant R425W 1273C>T COAD-US 1 160276982 160276982 single base substitution G A upstream_gene_variant COAD-US 1 160277001 160277001 single base substitution G A downstream_gene_variant COAD-US 1 160277001 160277001 single base substitution G A synonymous_variant A418A 1254C>T COAD-US 1 160277001 160277001 single base substitution G A upstream_gene_variant COAD-US 1 160283843 160283843 single base substitution C T missense_variant R260H 779G>A COAD-US 1 160283843 160283843 single base substitution C T upstream_gene_variant COAD-US 1 160303416 160303416 single base substitution G A exon_variant COAD-US 1 160303416 160303416 single base substitution G A synonymous_variant N121N 363C>T COAD-US 1 160309764 160309764 single base substitution G A exon_variant COAD-US 1 160309764 160309764 single base substitution G A stop_gained R55* 163C>T COAD-US 1 160313199 160313199 deletion of <=200bp G - upstream_gene_variant COCA-CN 1 160260297 160260297 single base substitution G T downstream_gene_variant COCA-CN 1 160260297 160260297 single base substitution G T synonymous_variant I1200I 3600C>A COCA-CN 1 160260297 160260297 single base substitution G T synonymous_variant I1209I 3627C>A COCA-CN 1 160262281 160262281 single base substitution G A downstream_gene_variant COCA-CN 1 160262281 160262281 single base substitution G A missense_variant R985C 2953C>T COCA-CN 1 160262281 160262281 single base substitution G A missense_variant R994C 2980C>T COCA-CN 1 160263011 160263011 single base substitution T G downstream_gene_variant COCA-CN 1 160263011 160263011 single base substitution T G missense_variant N923T 2768A>C COCA-CN 1 160263011 160263011 single base substitution T G missense_variant N932T 2795A>C COCA-CN 1 160268629 160268629 single base substitution T G splice_region_variant COCA-CN 1 160275290 160275290 single base substitution C T downstream_gene_variant COCA-CN 1 160275290 160275290 single base substitution C T exon_variant COCA-CN 1 160275290 160275290 single base substitution C T missense_variant A534T 1600G>A COCA-CN 1 160275290 160275290 single base substitution C T missense_variant A543T 1627G>A COCA-CN 1 160276967 160276967 single base substitution C A downstream_gene_variant COCA-CN 1 160276967 160276967 single base substitution C A missense_variant D430Y 1288G>T COCA-CN 1 160276967 160276967 single base substitution C A upstream_gene_variant COCA-CN 1 160281598 160281598 single base substitution G A intron_variant COCA-CN 1 160281598 160281598 single base substitution G A upstream_gene_variant COCA-CN 1 160282854 160282854 single base substitution A G intron_variant COCA-CN 1 160282854 160282854 single base substitution A G upstream_gene_variant COCA-CN 1 160293230 160293230 single base substitution G A missense_variant R233C 697C>T COCA-CN 1 160293351 160293351 single base substitution C A intron_variant COCA-CN 1 160295183 160295183 single base substitution G A intron_variant COCA-CN 1 160303549 160303549 single base substitution G T intron_variant COCA-CN 1 160313740 160313740 single base substitution T C upstream_gene_variant ESAD-UK 1 160257262 160257262 single base substitution C A downstream_gene_variant ESAD-UK 1 160259265 160259265 single base substitution C G 3_prime_UTR_variant ESAD-UK 1 160260297 160260297 single base substitution G T downstream_gene_variant ESAD-UK 1 160260297 160260297 single base substitution G T synonymous_variant I1200I 3600C>A ESAD-UK 1 160260297 160260297 single base substitution G T synonymous_variant I1209I 3627C>A ESAD-UK 1 160260339 160260339 single base substitution T A downstream_gene_variant ESAD-UK 1 160260339 160260339 single base substitution T A synonymous_variant P1186P 3558A>T ESAD-UK 1 160260339 160260339 single base substitution T A synonymous_variant P1195P 3585A>T ESAD-UK 1 160264324 160264324 single base substitution C T downstream_gene_variant ESAD-UK 1 160264324 160264324 single base substitution C T missense_variant E876K 2626G>A ESAD-UK 1 160264324 160264324 single base substitution C T missense_variant E885K 2653G>A ESAD-UK 1 160264984 160264984 single base substitution G A intron_variant ESAD-UK 1 160267363 160267363 single base substitution C T exon_variant ESAD-UK 1 160267363 160267363 single base substitution C T missense_variant R717H 2150G>A ESAD-UK 1 160267363 160267363 single base substitution C T missense_variant R726H 2177G>A ESAD-UK 1 160267914 160267914 single base substitution T C intron_variant ESAD-UK 1 160270006 160270006 single base substitution T A intron_variant ESAD-UK 1 160270006 160270006 single base substitution T A upstream_gene_variant ESAD-UK 1 160270088 160270088 single base substitution C T downstream_gene_variant ESAD-UK 1 160270088 160270088 single base substitution C T intron_variant ESAD-UK 1 160270088 160270088 single base substitution C T upstream_gene_variant ESAD-UK 1 160270727 160270727 single base substitution G A downstream_gene_variant ESAD-UK 1 160270727 160270727 single base substitution G A intron_variant ESAD-UK 1 160270727 160270727 single base substitution G A upstream_gene_variant ESAD-UK 1 160275020 160275020 single base substitution T A downstream_gene_variant ESAD-UK 1 160275020 160275020 single base substitution T A intron_variant ESAD-UK 1 160277629 160277629 single base substitution G A downstream_gene_variant ESAD-UK 1 160277629 160277629 single base substitution G A intron_variant ESAD-UK 1 160277629 160277629 single base substitution G A upstream_gene_variant ESAD-UK 1 160279383 160279383 single base substitution G T intron_variant ESAD-UK 1 160279383 160279383 single base substitution G T upstream_gene_variant ESAD-UK 1 160281991 160281991 single base substitution C T intron_variant ESAD-UK 1 160281991 160281991 single base substitution C T upstream_gene_variant ESAD-UK 1 160283693 160283693 single base substitution G T intron_variant ESAD-UK 1 160283693 160283693 single base substitution G T upstream_gene_variant ESAD-UK 1 160284706 160284706 single base substitution C T intron_variant ESAD-UK 1 160284706 160284706 single base substitution C T upstream_gene_variant ESAD-UK 1 160285646 160285646 single base substitution C A intron_variant ESAD-UK 1 160287708 160287708 single base substitution C G intron_variant ESAD-UK 1 160289850 160289850 deletion of <=200bp A - intron_variant ESAD-UK 1 160293971 160293971 single base substitution G A intron_variant ESAD-UK 1 160295324 160295324 single base substitution G T intron_variant ESAD-UK 1 160296119 160296119 single base substitution T C intron_variant ESAD-UK 1 160296275 160296275 single base substitution C T intron_variant ESAD-UK 1 160297375 160297375 single base substitution C T intron_variant ESAD-UK 1 160297881 160297881 single base substitution G T intron_variant ESAD-UK 1 160297968 160297968 single base substitution A G intron_variant ESAD-UK 1 160299911 160299911 insertion of <=200bp - C downstream_gene_variant ESAD-UK 1 160299911 160299911 insertion of <=200bp - C intron_variant ESAD-UK 1 160300300 160300300 single base substitution C T downstream_gene_variant ESAD-UK 1 160300300 160300300 single base substitution C T intron_variant ESAD-UK 1 160303102 160303102 single base substitution G C downstream_gene_variant ESAD-UK 1 160303102 160303102 single base substitution G C intron_variant ESAD-UK 1 160304045 160304045 single base substitution T G intron_variant ESAD-UK 1 160304825 160304825 single base substitution T A downstream_gene_variant ESAD-UK 1 160304825 160304825 single base substitution T A intron_variant ESAD-UK 1 160305171 160305171 single base substitution G C downstream_gene_variant ESAD-UK 1 160305171 160305171 single base substitution G C intron_variant ESAD-UK 1 160306211 160306211 single base substitution G C downstream_gene_variant ESAD-UK 1 160306211 160306211 single base substitution G C intron_variant ESAD-UK 1 160309844 160309844 single base substitution G T intron_variant ESAD-UK 1 160311590 160311590 deletion of <=200bp T - intron_variant ESAD-UK 1 160311590 160311590 deletion of <=200bp T - upstream_gene_variant ESAD-UK 1 160314340 160314340 single base substitution G A upstream_gene_variant ESAD-UK 1 160315460 160315460 single base substitution C T upstream_gene_variant ESAD-UK 1 160316232 160316232 single base substitution A G upstream_gene_variant ESCA-CN 1 160263286 160263286 insertion of <=200bp - T downstream_gene_variant ESCA-CN 1 160263286 160263286 insertion of <=200bp - T intron_variant ESCA-CN 1 160265874 160265874 single base substitution T C exon_variant ESCA-CN 1 160265874 160265874 single base substitution T C missense_variant T777A 2329A>G ESCA-CN 1 160265874 160265874 single base substitution T C missense_variant T786A 2356A>G ESCA-CN 1 160267386 160267386 single base substitution G C exon_variant ESCA-CN 1 160267386 160267386 single base substitution G C missense_variant I709M 2127C>G ESCA-CN 1 160267386 160267386 single base substitution G C missense_variant I718M 2154C>G ESCA-CN 1 160275265 160275265 single base substitution A G downstream_gene_variant ESCA-CN 1 160275265 160275265 single base substitution A G exon_variant ESCA-CN 1 160275265 160275265 single base substitution A G missense_variant I542T 1625T>C ESCA-CN 1 160275265 160275265 single base substitution A G missense_variant I551T 1652T>C ESCA-CN 1 160287208 160287208 deletion of <=200bp A - intron_variant ESCA-CN 1 160293225 160293225 single base substitution C G missense_variant M234I 702G>C ESCA-CN 1 160305080 160305080 single base substitution G A downstream_gene_variant ESCA-CN 1 160305080 160305080 single base substitution G A exon_variant ESCA-CN 1 160305080 160305080 single base substitution G A synonymous_variant F87F 261C>T ESCA-CN 1 160309709 160309709 single base substitution T C exon_variant ESCA-CN 1 160309709 160309709 single base substitution T C missense_variant Y73C 218A>G GBM-US 1 160254853 160254853 single base substitution A G downstream_gene_variant GBM-US 1 160268961 160268961 single base substitution G A exon_variant GBM-US 1 160268961 160268961 single base substitution G A synonymous_variant P587P 1761C>T GBM-US 1 160268961 160268961 single base substitution G A synonymous_variant P596P 1788C>T KIRC-US 1 160261203 160261203 single base substitution C A downstream_gene_variant KIRC-US 1 160261203 160261203 single base substitution C A missense_variant K1114N 3342G>T KIRC-US 1 160261203 160261203 single base substitution C A missense_variant K1123N 3369G>T KIRC-US 1 160261217 160261217 single base substitution T C downstream_gene_variant KIRC-US 1 160261217 160261217 single base substitution T C missense_variant N1110D 3328A>G KIRC-US 1 160261217 160261217 single base substitution T C missense_variant N1119D 3355A>G KIRC-US 1 160267213 160267220 deletion of <=200bp TCCTTTCT - exon_variant KIRC-US 1 160267213 160267220 deletion of <=200bp TCCTTTCT - frameshift_variant RKD726 KIRC-US 1 160267213 160267220 deletion of <=200bp TCCTTTCT - frameshift_variant RKD735 KIRC-US 1 160302290 160302290 single base substitution G C downstream_gene_variant KIRC-US 1 160302290 160302290 single base substitution G C missense_variant D148E 444C>G KIRC-US 1 160310032 160310032 single base substitution C A exon_variant KIRC-US 1 160310032 160310032 single base substitution C A synonymous_variant G31G 93G>T KIRC-US 1 160310032 160310032 single base substitution C A upstream_gene_variant KIRC-US 1 160313253 160313253 single base substitution T A upstream_gene_variant KIRP-US 1 160305059 160305059 single base substitution A G downstream_gene_variant KIRP-US 1 160305059 160305059 single base substitution A G exon_variant KIRP-US 1 160305059 160305059 single base substitution A G synonymous_variant D94D 282T>C LGG-US 1 160268752 160268752 single base substitution T C exon_variant LGG-US 1 160268752 160268752 single base substitution T C synonymous_variant L620L 1860A>G LGG-US 1 160268752 160268752 single base substitution T C synonymous_variant L629L 1887A>G LICA-FR 1 160260355 160260355 deletion of <=200bp G - downstream_gene_variant LICA-FR 1 160260355 160260355 deletion of <=200bp G - frameshift_variant P1181 LICA-FR 1 160260355 160260355 deletion of <=200bp G - frameshift_variant P1190 LICA-FR 1 160261399 160261399 single base substitution T A downstream_gene_variant LICA-FR 1 160261399 160261399 single base substitution T A intron_variant LICA-FR 1 160265434 160265434 single base substitution A C intron_variant LICA-FR 1 160269024 160269024 single base substitution T C exon_variant LICA-FR 1 160269024 160269024 single base substitution T C synonymous_variant L566L 1698A>G LICA-FR 1 160269024 160269024 single base substitution T C synonymous_variant L575L 1725A>G LICA-FR 1 160281041 160281041 single base substitution C T intron_variant LICA-FR 1 160281041 160281041 single base substitution C T upstream_gene_variant LICA-FR 1 160294076 160294076 deletion of <=200bp T - intron_variant LICA-FR 1 160294248 160294251 deletion of <=200bp TTTT - intron_variant LICA-FR 1 160308469 160308469 single base substitution T C downstream_gene_variant LICA-FR 1 160308469 160308469 single base substitution T C intron_variant LICA-FR 1 160313745 160313745 deletion of <=200bp T - upstream_gene_variant LIHC-US 1 160264344 160264344 single base substitution G A downstream_gene_variant LIHC-US 1 160264344 160264344 single base substitution G A missense_variant A869V 2606C>T LIHC-US 1 160264344 160264344 single base substitution G A missense_variant A878V 2633C>T LIHC-US 1 160295377 160295377 single base substitution C T missense_variant D188N 562G>A LIHC-US 1 160305090 160305090 single base substitution C A downstream_gene_variant LIHC-US 1 160305090 160305090 single base substitution C A exon_variant LIHC-US 1 160305090 160305090 single base substitution C A missense_variant R84L 251G>T LIHC-US 1 160314603 160314606 deletion of <=200bp GATT - upstream_gene_variant LINC-JP 1 160257200 160257200 single base substitution A C downstream_gene_variant LINC-JP 1 160260066 160260066 single base substitution A C downstream_gene_variant LINC-JP 1 160260066 160260066 single base substitution A C intron_variant LINC-JP 1 160260161 160260161 single base substitution T A downstream_gene_variant LINC-JP 1 160260161 160260161 single base substitution T A intron_variant LINC-JP 1 160260540 160260540 single base substitution A C downstream_gene_variant LINC-JP 1 160260540 160260540 single base substitution A C intron_variant LINC-JP 1 160261523 160261523 single base substitution T G downstream_gene_variant LINC-JP 1 160261523 160261523 single base substitution T G intron_variant LINC-JP 1 160262258 160262258 single base substitution G C downstream_gene_variant LINC-JP 1 160262258 160262258 single base substitution G C intron_variant LINC-JP 1 160264781 160264781 single base substitution T C intron_variant LINC-JP 1 160265683 160265683 single base substitution T C intron_variant LINC-JP 1 160266724 160266724 single base substitution T A intron_variant LINC-JP 1 160266951 160266951 single base substitution T G intron_variant LINC-JP 1 160275867 160275867 single base substitution A G downstream_gene_variant LINC-JP 1 160275867 160275867 single base substitution A G intron_variant LINC-JP 1 160275867 160275867 single base substitution A G upstream_gene_variant LINC-JP 1 160279123 160279123 single base substitution A G intron_variant LINC-JP 1 160279123 160279123 single base substitution A G upstream_gene_variant LINC-JP 1 160280009 160280009 single base substitution T G exon_variant LINC-JP 1 160280009 160280009 single base substitution T G synonymous_variant P372P 1116A>C LINC-JP 1 160280009 160280009 single base substitution T G upstream_gene_variant LINC-JP 1 160280271 160280271 single base substitution T G exon_variant LINC-JP 1 160280271 160280271 single base substitution T G intron_variant LINC-JP 1 160280271 160280271 single base substitution T G upstream_gene_variant LINC-JP 1 160281617 160281617 single base substitution C T intron_variant LINC-JP 1 160281617 160281617 single base substitution C T upstream_gene_variant LINC-JP 1 160287836 160287836 single base substitution T C intron_variant LINC-JP 1 160296041 160296041 single base substitution G C intron_variant LINC-JP 1 160298932 160298932 single base substitution G A downstream_gene_variant LINC-JP 1 160298932 160298932 single base substitution G A intron_variant LINC-JP 1 160302370 160302370 single base substitution T C downstream_gene_variant LINC-JP 1 160302370 160302370 single base substitution T C intron_variant LINC-JP 1 160303580 160303580 single base substitution A T intron_variant LINC-JP 1 160303773 160303773 single base substitution G A intron_variant LINC-JP 1 160303775 160303775 single base substitution G T intron_variant LINC-JP 1 160304496 160304496 single base substitution A T downstream_gene_variant LINC-JP 1 160304496 160304496 single base substitution A T intron_variant LINC-JP 1 160309746 160309746 single base substitution T C exon_variant LINC-JP 1 160309746 160309746 single base substitution T C missense_variant K61E 181A>G LIRI-JP 1 160254550 160254550 insertion of <=200bp - T downstream_gene_variant LIRI-JP 1 160255433 160255433 single base substitution C A downstream_gene_variant LIRI-JP 1 160257177 160257177 single base substitution A C downstream_gene_variant LIRI-JP 1 160258641 160258641 insertion of <=200bp - A downstream_gene_variant LIRI-JP 1 160260220 160260220 insertion of <=200bp - TGTTTC downstream_gene_variant LIRI-JP 1 160260220 160260220 insertion of <=200bp - TGTTTC intron_variant LIRI-JP 1 160260916 160260916 single base substitution T G downstream_gene_variant LIRI-JP 1 160260916 160260916 single base substitution T G intron_variant LIRI-JP 1 160261809 160261809 single base substitution A C downstream_gene_variant LIRI-JP 1 160261809 160261809 single base substitution A C missense_variant I1047S 3140T>G LIRI-JP 1 160261809 160261809 single base substitution A C missense_variant I1056S 3167T>G LIRI-JP 1 160262627 160262627 single base substitution A G downstream_gene_variant LIRI-JP 1 160262627 160262627 single base substitution A G intron_variant LIRI-JP 1 160262906 160262906 single base substitution C A downstream_gene_variant LIRI-JP 1 160262906 160262906 single base substitution C A intron_variant LIRI-JP 1 160264534 160264534 single base substitution A G downstream_gene_variant LIRI-JP 1 160264534 160264534 single base substitution A G intron_variant LIRI-JP 1 160264804 160264804 single base substitution G A intron_variant LIRI-JP 1 160264828 160264828 single base substitution C A intron_variant LIRI-JP 1 160265550 160265550 single base substitution A T exon_variant LIRI-JP 1 160265550 160265550 single base substitution A T missense_variant F818I 2452T>A LIRI-JP 1 160265550 160265550 single base substitution A T missense_variant F827I 2479T>A LIRI-JP 1 160265601 160265601 single base substitution T C exon_variant LIRI-JP 1 160265601 160265601 single base substitution T C missense_variant I801V 2401A>G LIRI-JP 1 160265601 160265601 single base substitution T C missense_variant I810V 2428A>G LIRI-JP 1 160266491 160266491 single base substitution A G intron_variant LIRI-JP 1 160267618 160267618 single base substitution T C intron_variant LIRI-JP 1 160267922 160267922 single base substitution G A intron_variant LIRI-JP 1 160269451 160269451 single base substitution A C intron_variant LIRI-JP 1 160269451 160269451 single base substitution A C upstream_gene_variant LIRI-JP 1 160269789 160269789 single base substitution A G intron_variant LIRI-JP 1 160269789 160269789 single base substitution A G upstream_gene_variant LIRI-JP 1 160273770 160273770 single base substitution C T downstream_gene_variant LIRI-JP 1 160273770 160273770 single base substitution C T intron_variant LIRI-JP 1 160273770 160273770 single base substitution C T upstream_gene_variant LIRI-JP 1 160278066 160278066 single base substitution T C downstream_gene_variant LIRI-JP 1 160278066 160278066 single base substitution T C intron_variant LIRI-JP 1 160278066 160278066 single base substitution T C upstream_gene_variant LIRI-JP 1 160278637 160278649 deletion of <=200bp GCTGAAAGAGAGA - downstream_gene_variant LIRI-JP 1 160278637 160278649 deletion of <=200bp GCTGAAAGAGAGA - intron_variant LIRI-JP 1 160278637 160278649 deletion of <=200bp GCTGAAAGAGAGA - upstream_gene_variant LIRI-JP 1 160280159 160280159 single base substitution A C exon_variant LIRI-JP 1 160280159 160280159 single base substitution A C intron_variant LIRI-JP 1 160280159 160280159 single base substitution A C upstream_gene_variant LIRI-JP 1 160280761 160280761 single base substitution C G intron_variant LIRI-JP 1 160280761 160280761 single base substitution C G upstream_gene_variant LIRI-JP 1 160281730 160281730 single base substitution T C missense_variant Y335C 1004A>G LIRI-JP 1 160281730 160281730 single base substitution T C upstream_gene_variant LIRI-JP 1 160282445 160282445 single base substitution A C intron_variant LIRI-JP 1 160282445 160282445 single base substitution A C upstream_gene_variant LIRI-JP 1 160285221 160285221 single base substitution C A intron_variant LIRI-JP 1 160285221 160285221 single base substitution C A upstream_gene_variant LIRI-JP 1 160286847 160286847 single base substitution C A intron_variant LIRI-JP 1 160287280 160287280 single base substitution T C intron_variant LIRI-JP 1 160287628 160287628 single base substitution T G intron_variant LIRI-JP 1 160287983 160287983 single base substitution T C intron_variant LIRI-JP 1 160288458 160288458 single base substitution T C intron_variant LIRI-JP 1 160290764 160290764 single base substitution C T intron_variant LIRI-JP 1 160291672 160291672 single base substitution C T intron_variant LIRI-JP 1 160291745 160291745 single base substitution A G intron_variant LIRI-JP 1 160292386 160292387 deletion of <=200bp AT - intron_variant LIRI-JP 1 160293066 160293066 single base substitution A G intron_variant LIRI-JP 1 160293534 160293534 single base substitution T C intron_variant LIRI-JP 1 160294668 160294668 single base substitution C T intron_variant LIRI-JP 1 160300539 160300539 single base substitution C T downstream_gene_variant LIRI-JP 1 160300539 160300539 single base substitution C T intron_variant LIRI-JP 1 160300889 160300889 single base substitution T C downstream_gene_variant LIRI-JP 1 160300889 160300889 single base substitution T C intron_variant LIRI-JP 1 160303832 160303832 single base substitution T C intron_variant LIRI-JP 1 160306500 160306500 single base substitution T C downstream_gene_variant LIRI-JP 1 160306500 160306500 single base substitution T C intron_variant LIRI-JP 1 160306642 160306642 single base substitution T C downstream_gene_variant LIRI-JP 1 160306642 160306642 single base substitution T C intron_variant LIRI-JP 1 160307442 160307442 single base substitution G A downstream_gene_variant LIRI-JP 1 160307442 160307442 single base substitution G A intron_variant LIRI-JP 1 160308083 160308088 deletion of <=200bp GGATGT - downstream_gene_variant LIRI-JP 1 160308083 160308088 deletion of <=200bp GGATGT - intron_variant LIRI-JP 1 160308222 160308222 single base substitution A C downstream_gene_variant LIRI-JP 1 160308222 160308222 single base substitution A C intron_variant LIRI-JP 1 160308829 160308829 single base substitution G T downstream_gene_variant LIRI-JP 1 160308829 160308829 single base substitution G T intron_variant LIRI-JP 1 160310029 160310029 single base substitution G A exon_variant LIRI-JP 1 160310029 160310029 single base substitution G A synonymous_variant V32V 96C>T LIRI-JP 1 160310029 160310029 single base substitution G A upstream_gene_variant LIRI-JP 1 160312233 160312233 single base substitution G C intron_variant LIRI-JP 1 160312233 160312233 single base substitution G C upstream_gene_variant LIRI-JP 1 160312321 160312321 single base substitution T C intron_variant LIRI-JP 1 160312321 160312321 single base substitution T C upstream_gene_variant LIRI-JP 1 160313549 160313549 single base substitution T G upstream_gene_variant LIRI-JP 1 160315960 160315960 single base substitution A G upstream_gene_variant LUSC-KR 1 160257559 160257559 single base substitution C G downstream_gene_variant LUSC-KR 1 160260233 160260233 single base substitution T C downstream_gene_variant LUSC-KR 1 160260233 160260233 single base substitution T C intron_variant LUSC-KR 1 160263124 160263124 single base substitution C T downstream_gene_variant LUSC-KR 1 160263124 160263124 single base substitution C T intron_variant LUSC-KR 1 160265515 160265515 single base substitution T C intron_variant LUSC-KR 1 160271554 160271554 single base substitution T C downstream_gene_variant LUSC-KR 1 160271554 160271554 single base substitution T C intron_variant LUSC-KR 1 160271554 160271554 single base substitution T C upstream_gene_variant LUSC-KR 1 160275607 160275607 single base substitution C A downstream_gene_variant LUSC-KR 1 160275607 160275607 single base substitution C A exon_variant LUSC-KR 1 160275607 160275607 single base substitution C A intron_variant LUSC-KR 1 160277358 160277358 single base substitution C A downstream_gene_variant LUSC-KR 1 160277358 160277358 single base substitution C A intron_variant LUSC-KR 1 160277358 160277358 single base substitution C A upstream_gene_variant LUSC-KR 1 160283917 160283917 single base substitution T G splice_acceptor_variant LUSC-KR 1 160283917 160283917 single base substitution T G upstream_gene_variant LUSC-KR 1 160284844 160284844 single base substitution T A intron_variant LUSC-KR 1 160284844 160284844 single base substitution T A upstream_gene_variant LUSC-KR 1 160285981 160285981 single base substitution C G intron_variant LUSC-KR 1 160295507 160295507 single base substitution C G intron_variant LUSC-KR 1 160300240 160300240 single base substitution C G downstream_gene_variant LUSC-KR 1 160300240 160300240 single base substitution C G intron_variant LUSC-KR 1 160300776 160300776 single base substitution C T downstream_gene_variant LUSC-KR 1 160300776 160300776 single base substitution C T intron_variant LUSC-KR 1 160302138 160302138 single base substitution C G downstream_gene_variant LUSC-KR 1 160302138 160302138 single base substitution C G intron_variant LUSC-KR 1 160302444 160302444 single base substitution G A downstream_gene_variant LUSC-KR 1 160302444 160302444 single base substitution G A intron_variant LUSC-KR 1 160302543 160302543 single base substitution C G downstream_gene_variant LUSC-KR 1 160302543 160302543 single base substitution C G intron_variant LUSC-KR 1 160303416 160303416 single base substitution G A exon_variant LUSC-KR 1 160303416 160303416 single base substitution G A synonymous_variant N121N 363C>T LUSC-KR 1 160307656 160307656 single base substitution T C downstream_gene_variant LUSC-KR 1 160307656 160307656 single base substitution T C intron_variant LUSC-KR 1 160308574 160308574 single base substitution C A downstream_gene_variant LUSC-KR 1 160308574 160308574 single base substitution C A intron_variant LUSC-KR 1 160309664 160309664 single base substitution T G exon_variant LUSC-KR 1 160309664 160309664 single base substitution T G intron_variant LUSC-KR 1 160312371 160312371 single base substitution T C intron_variant LUSC-KR 1 160312371 160312371 single base substitution T C upstream_gene_variant LUSC-KR 1 160312437 160312437 single base substitution C A intron_variant LUSC-KR 1 160312437 160312437 single base substitution C A upstream_gene_variant LUSC-KR 1 160316390 160316390 single base substitution A T upstream_gene_variant LUSC-US 1 160260349 160260349 single base substitution T C downstream_gene_variant LUSC-US 1 160260349 160260349 single base substitution T C missense_variant E1183G 3548A>G LUSC-US 1 160260349 160260349 single base substitution T C missense_variant E1192G 3575A>G LUSC-US 1 160261286 160261286 single base substitution T C downstream_gene_variant LUSC-US 1 160261286 160261286 single base substitution T C missense_variant M1087V 3259A>G LUSC-US 1 160261286 160261286 single base substitution T C missense_variant M1096V 3286A>G LUSC-US 1 160262293 160262293 single base substitution C A downstream_gene_variant LUSC-US 1 160262293 160262293 single base substitution C A missense_variant G981C 2941G>T LUSC-US 1 160262293 160262293 single base substitution C A missense_variant G990C 2968G>T LUSC-US 1 160262323 160262323 single base substitution G C downstream_gene_variant LUSC-US 1 160262323 160262323 single base substitution G C missense_variant Q971E 2911C>G LUSC-US 1 160262323 160262323 single base substitution G C missense_variant Q980E 2938C>G LUSC-US 1 160264286 160264286 single base substitution G A downstream_gene_variant LUSC-US 1 160264286 160264286 single base substitution G A synonymous_variant L888L 2664C>T LUSC-US 1 160264286 160264286 single base substitution G A synonymous_variant L897L 2691C>T LUSC-US 1 160264287 160264287 single base substitution A G downstream_gene_variant LUSC-US 1 160264287 160264287 single base substitution A G missense_variant L888P 2663T>C LUSC-US 1 160264287 160264287 single base substitution A G missense_variant L897P 2690T>C LUSC-US 1 160281683 160281683 single base substitution C A missense_variant D351Y 1051G>T LUSC-US 1 160281683 160281683 single base substitution C A upstream_gene_variant LUSC-US 1 160281763 160281763 single base substitution G T missense_variant P324Q 971C>A LUSC-US 1 160281763 160281763 single base substitution G T upstream_gene_variant LUSC-US 1 160281809 160281809 single base substitution C A splice_acceptor_variant LUSC-US 1 160281809 160281809 single base substitution C A upstream_gene_variant LUSC-US 1 160314557 160314557 single base substitution T A upstream_gene_variant MALY-DE 1 160261836 160261836 single base substitution A C downstream_gene_variant MALY-DE 1 160261836 160261836 single base substitution A C missense_variant L1038R 3113T>G MALY-DE 1 160261836 160261836 single base substitution A C missense_variant L1047R 3140T>G MALY-DE 1 160264127 160264127 single base substitution T A downstream_gene_variant MALY-DE 1 160264127 160264127 single base substitution T A intron_variant MALY-DE 1 160264233 160264233 single base substitution A G downstream_gene_variant MALY-DE 1 160264233 160264233 single base substitution A G intron_variant MALY-DE 1 160281648 160281648 single base substitution T A intron_variant MALY-DE 1 160281648 160281648 single base substitution T A upstream_gene_variant MALY-DE 1 160284609 160284609 single base substitution T A intron_variant MALY-DE 1 160284609 160284609 single base substitution T A upstream_gene_variant MALY-DE 1 160290800 160290800 single base substitution G A intron_variant MALY-DE 1 160313388 160313388 single base substitution A G upstream_gene_variant MALY-DE 1 160317404 160317405 deletion of <=200bp GT - upstream_gene_variant MELA-AU 1 160254384 160254384 single base substitution G A downstream_gene_variant MELA-AU 1 160254926 160254926 single base substitution C T downstream_gene_variant MELA-AU 1 160254939 160254939 single base substitution G A downstream_gene_variant MELA-AU 1 160254946 160254946 single base substitution G A downstream_gene_variant MELA-AU 1 160254948 160254948 single base substitution C T downstream_gene_variant MELA-AU 1 160254969 160254969 single base substitution C T downstream_gene_variant MELA-AU 1 160254971 160254971 single base substitution C T downstream_gene_variant MELA-AU 1 160254980 160254980 single base substitution C T downstream_gene_variant MELA-AU 1 160254984 160254984 single base substitution C T downstream_gene_variant MELA-AU 1 160254995 160254995 single base substitution C T downstream_gene_variant MELA-AU 1 160255172 160255172 single base substitution A G downstream_gene_variant MELA-AU 1 160255652 160255652 single base substitution C T downstream_gene_variant MELA-AU 1 160256393 160256393 single base substitution A T downstream_gene_variant MELA-AU 1 160256695 160256695 single base substitution A G downstream_gene_variant MELA-AU 1 160257334 160257334 single base substitution T G downstream_gene_variant MELA-AU 1 160257563 160257563 single base substitution G A downstream_gene_variant MELA-AU 1 160258242 160258242 single base substitution G A downstream_gene_variant MELA-AU 1 160258891 160258891 single base substitution C T downstream_gene_variant MELA-AU 1 160259331 160259331 single base substitution G A 3_prime_UTR_variant MELA-AU 1 160259429 160259429 single base substitution G A 3_prime_UTR_variant MELA-AU 1 160260482 160260483 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 160260482 160260483 multiple base substitution (>=2bp and <=200bp) GG AA splice_region_variant MELA-AU 1 160260594 160260594 single base substitution G C downstream_gene_variant MELA-AU 1 160260594 160260594 single base substitution G C intron_variant MELA-AU 1 160260614 160260614 single base substitution G A downstream_gene_variant MELA-AU 1 160260614 160260614 single base substitution G A intron_variant MELA-AU 1 160261561 160261561 single base substitution G A downstream_gene_variant MELA-AU 1 160261561 160261561 single base substitution G A intron_variant MELA-AU 1 160261901 160261901 single base substitution G A downstream_gene_variant MELA-AU 1 160261901 160261901 single base substitution G A synonymous_variant L1016L 3048C>T MELA-AU 1 160261901 160261901 single base substitution G A synonymous_variant L1025L 3075C>T MELA-AU 1 160262102 160262102 single base substitution G A downstream_gene_variant MELA-AU 1 160262102 160262102 single base substitution G A intron_variant MELA-AU 1 160262229 160262229 single base substitution G A downstream_gene_variant MELA-AU 1 160262229 160262229 single base substitution G A intron_variant MELA-AU 1 160263903 160263903 single base substitution G A downstream_gene_variant MELA-AU 1 160263903 160263903 single base substitution G A intron_variant MELA-AU 1 160264073 160264073 single base substitution G A downstream_gene_variant MELA-AU 1 160264073 160264073 single base substitution G A intron_variant MELA-AU 1 160264105 160264105 single base substitution G A downstream_gene_variant MELA-AU 1 160264105 160264105 single base substitution G A intron_variant MELA-AU 1 160264125 160264125 single base substitution G A downstream_gene_variant MELA-AU 1 160264125 160264125 single base substitution G A intron_variant MELA-AU 1 160264391 160264391 single base substitution G A downstream_gene_variant MELA-AU 1 160264391 160264391 single base substitution G A splice_region_variant MELA-AU 1 160264860 160264860 single base substitution G A intron_variant MELA-AU 1 160265124 160265124 single base substitution G A intron_variant MELA-AU 1 160265214 160265214 single base substitution G A intron_variant MELA-AU 1 160266015 160266015 single base substitution G A intron_variant MELA-AU 1 160266253 160266253 single base substitution G A intron_variant MELA-AU 1 160267241 160267241 single base substitution A T intron_variant MELA-AU 1 160267310 160267310 single base substitution G A intron_variant MELA-AU 1 160267594 160267594 single base substitution G A intron_variant MELA-AU 1 160269133 160269133 single base substitution G A intron_variant MELA-AU 1 160269133 160269133 single base substitution G A upstream_gene_variant MELA-AU 1 160269228 160269228 single base substitution G A intron_variant MELA-AU 1 160269228 160269228 single base substitution G A upstream_gene_variant MELA-AU 1 160270135 160270135 insertion of <=200bp - AAAT downstream_gene_variant MELA-AU 1 160270135 160270135 insertion of <=200bp - AAAT intron_variant MELA-AU 1 160270135 160270135 insertion of <=200bp - AAAT upstream_gene_variant MELA-AU 1 160270180 160270180 single base substitution A G downstream_gene_variant MELA-AU 1 160270180 160270180 single base substitution A G intron_variant MELA-AU 1 160270180 160270180 single base substitution A G upstream_gene_variant MELA-AU 1 160270356 160270356 single base substitution G A downstream_gene_variant MELA-AU 1 160270356 160270356 single base substitution G A intron_variant MELA-AU 1 160270356 160270356 single base substitution G A upstream_gene_variant MELA-AU 1 160270474 160270474 single base substitution G A downstream_gene_variant MELA-AU 1 160270474 160270474 single base substitution G A intron_variant MELA-AU 1 160270474 160270474 single base substitution G A upstream_gene_variant MELA-AU 1 160270605 160270605 single base substitution G A downstream_gene_variant MELA-AU 1 160270605 160270605 single base substitution G A intron_variant MELA-AU 1 160270605 160270605 single base substitution G A upstream_gene_variant MELA-AU 1 160271562 160271562 single base substitution A C downstream_gene_variant MELA-AU 1 160271562 160271562 single base substitution A C intron_variant MELA-AU 1 160271562 160271562 single base substitution A C upstream_gene_variant MELA-AU 1 160271582 160271582 single base substitution T A downstream_gene_variant MELA-AU 1 160271582 160271582 single base substitution T A intron_variant MELA-AU 1 160271582 160271582 single base substitution T A upstream_gene_variant MELA-AU 1 160271591 160271591 single base substitution G A downstream_gene_variant MELA-AU 1 160271591 160271591 single base substitution G A intron_variant MELA-AU 1 160271591 160271591 single base substitution G A upstream_gene_variant MELA-AU 1 160272612 160272612 single base substitution G A downstream_gene_variant MELA-AU 1 160272612 160272612 single base substitution G A intron_variant MELA-AU 1 160272612 160272612 single base substitution G A upstream_gene_variant MELA-AU 1 160273089 160273089 single base substitution G A downstream_gene_variant MELA-AU 1 160273089 160273089 single base substitution G A intron_variant MELA-AU 1 160273089 160273089 single base substitution G A upstream_gene_variant MELA-AU 1 160273233 160273233 single base substitution G T downstream_gene_variant MELA-AU 1 160273233 160273233 single base substitution G T intron_variant MELA-AU 1 160273233 160273233 single base substitution G T upstream_gene_variant MELA-AU 1 160273585 160273585 single base substitution G A downstream_gene_variant MELA-AU 1 160273585 160273585 single base substitution G A intron_variant MELA-AU 1 160273585 160273585 single base substitution G A upstream_gene_variant MELA-AU 1 160273603 160273603 single base substitution G A downstream_gene_variant MELA-AU 1 160273603 160273603 single base substitution G A intron_variant MELA-AU 1 160273603 160273603 single base substitution G A upstream_gene_variant MELA-AU 1 160273790 160273790 single base substitution G A downstream_gene_variant MELA-AU 1 160273790 160273790 single base substitution G A intron_variant MELA-AU 1 160273790 160273790 single base substitution G A upstream_gene_variant MELA-AU 1 160273800 160273800 single base substitution G A downstream_gene_variant MELA-AU 1 160273800 160273800 single base substitution G A intron_variant MELA-AU 1 160273800 160273800 single base substitution G A upstream_gene_variant MELA-AU 1 160274110 160274110 single base substitution G A downstream_gene_variant MELA-AU 1 160274110 160274110 single base substitution G A intron_variant MELA-AU 1 160275800 160275800 single base substitution G A downstream_gene_variant MELA-AU 1 160275800 160275800 single base substitution G A intron_variant MELA-AU 1 160275800 160275800 single base substitution G A upstream_gene_variant MELA-AU 1 160276068 160276068 single base substitution G A downstream_gene_variant MELA-AU 1 160276068 160276068 single base substitution G A intron_variant MELA-AU 1 160276068 160276068 single base substitution G A upstream_gene_variant MELA-AU 1 160276729 160276729 single base substitution G A downstream_gene_variant MELA-AU 1 160276729 160276729 single base substitution G A intron_variant MELA-AU 1 160276729 160276729 single base substitution G A upstream_gene_variant MELA-AU 1 160276823 160276823 single base substitution G A downstream_gene_variant MELA-AU 1 160276823 160276823 single base substitution G A intron_variant MELA-AU 1 160276823 160276823 single base substitution G A upstream_gene_variant MELA-AU 1 160277811 160277811 single base substitution G A downstream_gene_variant MELA-AU 1 160277811 160277811 single base substitution G A intron_variant MELA-AU 1 160277811 160277811 single base substitution G A upstream_gene_variant MELA-AU 1 160277967 160277967 single base substitution G A downstream_gene_variant MELA-AU 1 160277967 160277967 single base substitution G A intron_variant MELA-AU 1 160277967 160277967 single base substitution G A upstream_gene_variant MELA-AU 1 160278507 160278507 single base substitution T C downstream_gene_variant MELA-AU 1 160278507 160278507 single base substitution T C intron_variant MELA-AU 1 160278507 160278507 single base substitution T C upstream_gene_variant MELA-AU 1 160278905 160278905 single base substitution G A exon_variant MELA-AU 1 160278905 160278905 single base substitution G A missense_variant S402F 1205C>T MELA-AU 1 160278905 160278905 single base substitution G A upstream_gene_variant MELA-AU 1 160278911 160278911 single base substitution G C exon_variant MELA-AU 1 160278911 160278911 single base substitution G C missense_variant A400G 1199C>G MELA-AU 1 160278911 160278911 single base substitution G C upstream_gene_variant MELA-AU 1 160279378 160279380 deletion of <=200bp AAG - intron_variant MELA-AU 1 160279378 160279380 deletion of <=200bp AAG - upstream_gene_variant MELA-AU 1 160279660 160279660 single base substitution G A intron_variant MELA-AU 1 160279660 160279660 single base substitution G A upstream_gene_variant MELA-AU 1 160281134 160281134 single base substitution A T intron_variant MELA-AU 1 160281134 160281134 single base substitution A T upstream_gene_variant MELA-AU 1 160282521 160282521 single base substitution G A intron_variant MELA-AU 1 160282521 160282521 single base substitution G A upstream_gene_variant MELA-AU 1 160283228 160283228 single base substitution G A intron_variant MELA-AU 1 160283228 160283228 single base substitution G A upstream_gene_variant MELA-AU 1 160283253 160283253 single base substitution G A intron_variant MELA-AU 1 160283253 160283253 single base substitution G A upstream_gene_variant MELA-AU 1 160283473 160283473 single base substitution G A intron_variant MELA-AU 1 160283473 160283473 single base substitution G A upstream_gene_variant MELA-AU 1 160283974 160283975 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 160283974 160283975 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 1 160284011 160284011 single base substitution A T intron_variant MELA-AU 1 160284011 160284011 single base substitution A T upstream_gene_variant MELA-AU 1 160284031 160284031 single base substitution C A intron_variant MELA-AU 1 160284031 160284031 single base substitution C A upstream_gene_variant MELA-AU 1 160284195 160284195 single base substitution G A intron_variant MELA-AU 1 160284195 160284195 single base substitution G A upstream_gene_variant MELA-AU 1 160284324 160284324 single base substitution G A intron_variant MELA-AU 1 160284324 160284324 single base substitution G A upstream_gene_variant MELA-AU 1 160284325 160284325 single base substitution G A intron_variant MELA-AU 1 160284325 160284325 single base substitution G A upstream_gene_variant MELA-AU 1 160284327 160284327 single base substitution G A intron_variant MELA-AU 1 160284327 160284327 single base substitution G A upstream_gene_variant MELA-AU 1 160285391 160285391 single base substitution G A intron_variant MELA-AU 1 160285558 160285558 single base substitution G A intron_variant MELA-AU 1 160285872 160285872 single base substitution G A intron_variant MELA-AU 1 160286667 160286667 single base substitution G A intron_variant MELA-AU 1 160287043 160287043 single base substitution G A intron_variant MELA-AU 1 160287085 160287086 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 1 160287105 160287105 single base substitution G A intron_variant MELA-AU 1 160287120 160287120 single base substitution A G intron_variant MELA-AU 1 160287378 160287379 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 160287425 160287425 single base substitution G A intron_variant MELA-AU 1 160287756 160287756 single base substitution G A intron_variant MELA-AU 1 160287889 160287889 single base substitution G T intron_variant MELA-AU 1 160287986 160287986 single base substitution C T intron_variant MELA-AU 1 160288892 160288892 single base substitution G A intron_variant MELA-AU 1 160289564 160289564 single base substitution C T intron_variant MELA-AU 1 160291764 160291764 single base substitution G A intron_variant MELA-AU 1 160292147 160292147 single base substitution A G intron_variant MELA-AU 1 160292558 160292558 single base substitution G A intron_variant MELA-AU 1 160292780 160292780 insertion of <=200bp - CA intron_variant MELA-AU 1 160292780 160292781 deletion of <=200bp CA - intron_variant MELA-AU 1 160292839 160292839 single base substitution A G intron_variant MELA-AU 1 160292994 160292994 single base substitution G A intron_variant MELA-AU 1 160293112 160293112 single base substitution A T intron_variant MELA-AU 1 160293964 160293964 single base substitution A G intron_variant MELA-AU 1 160295452 160295452 single base substitution G A intron_variant MELA-AU 1 160295545 160295545 single base substitution G A intron_variant MELA-AU 1 160295671 160295671 single base substitution G A intron_variant MELA-AU 1 160295937 160295937 single base substitution G A intron_variant MELA-AU 1 160296657 160296657 single base substitution G A intron_variant MELA-AU 1 160296896 160296896 single base substitution G A intron_variant MELA-AU 1 160297254 160297254 single base substitution G A intron_variant MELA-AU 1 160297256 160297256 single base substitution G A intron_variant MELA-AU 1 160297281 160297281 single base substitution G A intron_variant MELA-AU 1 160298034 160298034 single base substitution G A intron_variant MELA-AU 1 160300688 160300688 single base substitution G A downstream_gene_variant MELA-AU 1 160300688 160300688 single base substitution G A intron_variant MELA-AU 1 160301203 160301203 single base substitution G A downstream_gene_variant MELA-AU 1 160301203 160301203 single base substitution G A intron_variant MELA-AU 1 160302153 160302153 single base substitution C T downstream_gene_variant MELA-AU 1 160302153 160302153 single base substitution C T intron_variant MELA-AU 1 160302617 160302617 single base substitution T C downstream_gene_variant MELA-AU 1 160302617 160302617 single base substitution T C intron_variant MELA-AU 1 160302848 160302849 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 160302848 160302849 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 160303811 160303811 deletion of <=200bp T - intron_variant MELA-AU 1 160305165 160305165 single base substitution G A downstream_gene_variant MELA-AU 1 160305165 160305165 single base substitution G A intron_variant MELA-AU 1 160305297 160305297 single base substitution G A downstream_gene_variant MELA-AU 1 160305297 160305297 single base substitution G A intron_variant MELA-AU 1 160305381 160305381 single base substitution G A downstream_gene_variant MELA-AU 1 160305381 160305381 single base substitution G A intron_variant MELA-AU 1 160306165 160306165 single base substitution A G downstream_gene_variant MELA-AU 1 160306165 160306165 single base substitution A G intron_variant MELA-AU 1 160306409 160306409 single base substitution G A downstream_gene_variant MELA-AU 1 160306409 160306409 single base substitution G A intron_variant MELA-AU 1 160306790 160306790 single base substitution G A downstream_gene_variant MELA-AU 1 160306790 160306790 single base substitution G A intron_variant MELA-AU 1 160307174 160307174 single base substitution G A downstream_gene_variant MELA-AU 1 160307174 160307174 single base substitution G A intron_variant MELA-AU 1 160308322 160308322 single base substitution G A downstream_gene_variant MELA-AU 1 160308322 160308322 single base substitution G A intron_variant MELA-AU 1 160309305 160309305 deletion of <=200bp C - exon_variant MELA-AU 1 160309305 160309305 deletion of <=200bp C - intron_variant MELA-AU 1 160310482 160310482 single base substitution G A intron_variant MELA-AU 1 160310482 160310482 single base substitution G A upstream_gene_variant MELA-AU 1 160310798 160310798 single base substitution G A intron_variant MELA-AU 1 160310798 160310798 single base substitution G A upstream_gene_variant MELA-AU 1 160311355 160311355 single base substitution A C intron_variant MELA-AU 1 160311355 160311355 single base substitution A C upstream_gene_variant MELA-AU 1 160312234 160312234 single base substitution C T intron_variant MELA-AU 1 160312234 160312234 single base substitution C T upstream_gene_variant MELA-AU 1 160312527 160312527 single base substitution G A intron_variant MELA-AU 1 160312527 160312527 single base substitution G A upstream_gene_variant MELA-AU 1 160313679 160313679 single base substitution G A upstream_gene_variant MELA-AU 1 160314385 160314385 single base substitution C T upstream_gene_variant MELA-AU 1 160314441 160314441 single base substitution G A upstream_gene_variant MELA-AU 1 160314553 160314553 single base substitution C T upstream_gene_variant MELA-AU 1 160314720 160314720 single base substitution A T upstream_gene_variant MELA-AU 1 160315231 160315232 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 1 160315464 160315464 single base substitution C T upstream_gene_variant MELA-AU 1 160315645 160315645 single base substitution C T upstream_gene_variant MELA-AU 1 160316360 160316360 single base substitution C T upstream_gene_variant MELA-AU 1 160317190 160317190 single base substitution C T upstream_gene_variant MELA-AU 1 160317198 160317198 single base substitution C T upstream_gene_variant MELA-AU 1 160317217 160317217 single base substitution C T upstream_gene_variant MELA-AU 1 160317746 160317746 single base substitution C T upstream_gene_variant MELA-AU 1 160317986 160317986 single base substitution T A upstream_gene_variant MELA-AU 1 160318187 160318187 single base substitution C T upstream_gene_variant ORCA-IN 1 160261831 160261831 single base substitution C T downstream_gene_variant ORCA-IN 1 160261831 160261831 single base substitution C T missense_variant V1040I 3118G>A ORCA-IN 1 160261831 160261831 single base substitution C T missense_variant V1049I 3145G>A ORCA-IN 1 160263244 160263244 single base substitution G T downstream_gene_variant ORCA-IN 1 160263244 160263244 single base substitution G T missense_variant P896T 2686C>A ORCA-IN 1 160263244 160263244 single base substitution G T missense_variant P905T 2713C>A ORCA-IN 1 160266357 160266357 single base substitution G T intron_variant ORCA-IN 1 160267980 160267980 deletion of <=200bp G - intron_variant ORCA-IN 1 160274406 160274406 single base substitution G T downstream_gene_variant ORCA-IN 1 160274406 160274406 single base substitution G T intron_variant ORCA-IN 1 160295556 160295556 single base substitution G C intron_variant ORCA-IN 1 160303773 160303773 single base substitution G A intron_variant ORCA-IN 1 160306473 160306473 single base substitution G A downstream_gene_variant ORCA-IN 1 160306473 160306473 single base substitution G A intron_variant ORCA-IN 1 160315757 160315757 single base substitution T A upstream_gene_variant OV-AU 1 160254974 160254974 single base substitution C G downstream_gene_variant OV-AU 1 160259278 160259278 single base substitution A G 3_prime_UTR_variant OV-AU 1 160259352 160259352 single base substitution T C 3_prime_UTR_variant OV-AU 1 160264671 160264671 single base substitution G C intron_variant OV-AU 1 160264786 160264786 single base substitution T C intron_variant OV-AU 1 160268416 160268416 single base substitution G T intron_variant OV-AU 1 160271893 160271893 single base substitution T C downstream_gene_variant OV-AU 1 160271893 160271893 single base substitution T C intron_variant OV-AU 1 160271893 160271893 single base substitution T C upstream_gene_variant OV-AU 1 160274900 160274900 single base substitution G C downstream_gene_variant OV-AU 1 160274900 160274900 single base substitution G C intron_variant OV-AU 1 160302219 160302219 single base substitution C G downstream_gene_variant OV-AU 1 160302219 160302219 single base substitution C G intron_variant OV-AU 1 160310489 160310489 single base substitution A G intron_variant OV-AU 1 160310489 160310489 single base substitution A G upstream_gene_variant PACA-AU 1 160256574 160256574 single base substitution T C downstream_gene_variant PACA-AU 1 160261913 160261913 single base substitution C T downstream_gene_variant PACA-AU 1 160261913 160261913 single base substitution C T synonymous_variant L1012L 3036G>A PACA-AU 1 160261913 160261913 single base substitution C T synonymous_variant L1021L 3063G>A PACA-AU 1 160268057 160268057 single base substitution T A intron_variant PACA-AU 1 160268722 160268722 single base substitution C T exon_variant PACA-AU 1 160268722 160268722 single base substitution C T synonymous_variant Q630Q 1890G>A PACA-AU 1 160268722 160268722 single base substitution C T synonymous_variant Q639Q 1917G>A PACA-AU 1 160269135 160269135 single base substitution T A intron_variant PACA-AU 1 160269135 160269135 single base substitution T A upstream_gene_variant PACA-AU 1 160270135 160270135 insertion of <=200bp - AAATAAAT downstream_gene_variant PACA-AU 1 160270135 160270135 insertion of <=200bp - AAATAAAT intron_variant PACA-AU 1 160270135 160270135 insertion of <=200bp - AAATAAAT upstream_gene_variant PACA-AU 1 160270135 160270135 insertion of <=200bp - AAAT downstream_gene_variant PACA-AU 1 160270135 160270135 insertion of <=200bp - AAAT intron_variant PACA-AU 1 160270135 160270135 insertion of <=200bp - AAAT upstream_gene_variant PACA-AU 1 160271027 160271027 single base substitution G A downstream_gene_variant PACA-AU 1 160271027 160271027 single base substitution G A intron_variant PACA-AU 1 160271027 160271027 single base substitution G A upstream_gene_variant PACA-AU 1 160271849 160271856 deletion of <=200bp AATATAGT - downstream_gene_variant PACA-AU 1 160271849 160271856 deletion of <=200bp AATATAGT - intron_variant PACA-AU 1 160271849 160271856 deletion of <=200bp AATATAGT - upstream_gene_variant PACA-AU 1 160271863 160271863 single base substitution T C downstream_gene_variant PACA-AU 1 160271863 160271863 single base substitution T C intron_variant PACA-AU 1 160271863 160271863 single base substitution T C upstream_gene_variant PACA-AU 1 160282855 160282855 single base substitution A G intron_variant PACA-AU 1 160282855 160282855 single base substitution A G upstream_gene_variant PACA-AU 1 160283717 160283717 single base substitution T C intron_variant PACA-AU 1 160283717 160283717 single base substitution T C upstream_gene_variant PACA-AU 1 160286273 160286273 single base substitution G C intron_variant PACA-AU 1 160289535 160289535 single base substitution T A intron_variant PACA-AU 1 160292780 160292781 deletion of <=200bp CA - intron_variant PACA-AU 1 160294435 160294435 single base substitution T C intron_variant PACA-AU 1 160295065 160295065 single base substitution C T intron_variant PACA-AU 1 160301802 160301802 single base substitution C T downstream_gene_variant PACA-AU 1 160301802 160301802 single base substitution C T intron_variant PACA-AU 1 160308233 160308233 single base substitution G A downstream_gene_variant PACA-AU 1 160308233 160308233 single base substitution G A intron_variant PACA-AU 1 160312746 160312746 single base substitution G T intron_variant PACA-AU 1 160312746 160312746 single base substitution G T upstream_gene_variant PACA-AU 1 160313688 160313688 single base substitution T G upstream_gene_variant PACA-CA 1 160256483 160256483 single base substitution C G downstream_gene_variant PACA-CA 1 160258581 160258581 single base substitution T C downstream_gene_variant PACA-CA 1 160261431 160261431 single base substitution G C downstream_gene_variant PACA-CA 1 160261431 160261431 single base substitution G C intron_variant PACA-CA 1 160267120 160267120 single base substitution C T intron_variant PACA-CA 1 160267304 160267304 single base substitution C T intron_variant PACA-CA 1 160268512 160268512 deletion of <=200bp A - intron_variant PACA-CA 1 160270169 160270169 single base substitution A G downstream_gene_variant PACA-CA 1 160270169 160270169 single base substitution A G intron_variant PACA-CA 1 160270169 160270169 single base substitution A G upstream_gene_variant PACA-CA 1 160270684 160270684 single base substitution G A downstream_gene_variant PACA-CA 1 160270684 160270684 single base substitution G A intron_variant PACA-CA 1 160270684 160270684 single base substitution G A upstream_gene_variant PACA-CA 1 160271758 160271758 single base substitution C G downstream_gene_variant PACA-CA 1 160271758 160271758 single base substitution C G intron_variant PACA-CA 1 160271758 160271758 single base substitution C G upstream_gene_variant PACA-CA 1 160271895 160271895 single base substitution A G downstream_gene_variant PACA-CA 1 160271895 160271895 single base substitution A G intron_variant PACA-CA 1 160271895 160271895 single base substitution A G upstream_gene_variant PACA-CA 1 160271949 160271949 single base substitution A T downstream_gene_variant PACA-CA 1 160271949 160271949 single base substitution A T intron_variant PACA-CA 1 160271949 160271949 single base substitution A T upstream_gene_variant PACA-CA 1 160272455 160272456 deletion of <=200bp CT - downstream_gene_variant PACA-CA 1 160272455 160272456 deletion of <=200bp CT - intron_variant PACA-CA 1 160272455 160272456 deletion of <=200bp CT - upstream_gene_variant PACA-CA 1 160277197 160277197 single base substitution G A downstream_gene_variant PACA-CA 1 160277197 160277197 single base substitution G A intron_variant PACA-CA 1 160277197 160277197 single base substitution G A upstream_gene_variant PACA-CA 1 160278944 160278944 single base substitution C T exon_variant PACA-CA 1 160278944 160278944 single base substitution C T missense_variant S389N 1166G>A PACA-CA 1 160278944 160278944 single base substitution C T upstream_gene_variant PACA-CA 1 160281607 160281607 single base substitution A G intron_variant PACA-CA 1 160281607 160281607 single base substitution A G upstream_gene_variant PACA-CA 1 160282174 160282174 single base substitution C A intron_variant PACA-CA 1 160282174 160282174 single base substitution C A upstream_gene_variant PACA-CA 1 160283146 160283146 single base substitution G C intron_variant PACA-CA 1 160283146 160283146 single base substitution G C upstream_gene_variant PACA-CA 1 160284294 160284294 single base substitution G A intron_variant PACA-CA 1 160284294 160284294 single base substitution G A upstream_gene_variant PACA-CA 1 160291401 160291401 single base substitution A G intron_variant PACA-CA 1 160292345 160292345 single base substitution A G intron_variant PACA-CA 1 160292617 160292617 single base substitution T C intron_variant PACA-CA 1 160292667 160292667 single base substitution G T intron_variant PACA-CA 1 160293021 160293021 single base substitution T A intron_variant PACA-CA 1 160293331 160293331 single base substitution G C intron_variant PACA-CA 1 160295426 160295426 insertion of <=200bp - T frameshift_variant N171N? PACA-CA 1 160296000 160296000 single base substitution A C intron_variant PACA-CA 1 160299548 160299548 single base substitution C A downstream_gene_variant PACA-CA 1 160299548 160299548 single base substitution C A intron_variant PACA-CA 1 160305842 160305842 single base substitution A C downstream_gene_variant PACA-CA 1 160305842 160305842 single base substitution A C intron_variant PACA-CA 1 160307288 160307288 single base substitution C G downstream_gene_variant PACA-CA 1 160307288 160307288 single base substitution C G intron_variant PACA-CA 1 160307458 160307458 single base substitution G A downstream_gene_variant PACA-CA 1 160307458 160307458 single base substitution G A intron_variant PACA-CA 1 160307481 160307481 single base substitution C A downstream_gene_variant PACA-CA 1 160307481 160307481 single base substitution C A intron_variant PACA-CA 1 160313644 160313644 single base substitution A G upstream_gene_variant PACA-CA 1 160316542 160316542 single base substitution C T upstream_gene_variant PACA-CA 1 160317884 160317884 single base substitution A T upstream_gene_variant PAEN-AU 1 160270135 160270135 insertion of <=200bp - AAAT downstream_gene_variant PAEN-AU 1 160270135 160270135 insertion of <=200bp - AAAT intron_variant PAEN-AU 1 160270135 160270135 insertion of <=200bp - AAAT upstream_gene_variant PAEN-AU 1 160270135 160270138 deletion of <=200bp AAAT - downstream_gene_variant PAEN-AU 1 160270135 160270138 deletion of <=200bp AAAT - intron_variant PAEN-AU 1 160270135 160270138 deletion of <=200bp AAAT - upstream_gene_variant PAEN-AU 1 160316269 160316269 single base substitution T G upstream_gene_variant PAEN-IT 1 160258240 160258240 single base substitution G A downstream_gene_variant PBCA-DE 1 160258243 160258244 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 1 160270956 160270956 insertion of <=200bp - A downstream_gene_variant PBCA-DE 1 160270956 160270956 insertion of <=200bp - A intron_variant PBCA-DE 1 160270956 160270956 insertion of <=200bp - A upstream_gene_variant PBCA-DE 1 160273631 160273631 single base substitution T C downstream_gene_variant PBCA-DE 1 160273631 160273631 single base substitution T C intron_variant PBCA-DE 1 160273631 160273631 single base substitution T C upstream_gene_variant PBCA-DE 1 160276306 160276306 single base substitution G A downstream_gene_variant PBCA-DE 1 160276306 160276306 single base substitution G A intron_variant PBCA-DE 1 160276306 160276306 single base substitution G A upstream_gene_variant PBCA-DE 1 160286149 160286149 insertion of <=200bp - A intron_variant PBCA-DE 1 160292445 160292445 single base substitution G A intron_variant PBCA-DE 1 160292780 160292781 deletion of <=200bp CA - intron_variant PBCA-DE 1 160299918 160299918 single base substitution C A downstream_gene_variant PBCA-DE 1 160299918 160299918 single base substitution C A intron_variant PBCA-DE 1 160303310 160303310 single base substitution G C exon_variant PBCA-DE 1 160303310 160303310 single base substitution G C intron_variant PBCA-DE 1 160317404 160317405 deletion of <=200bp GT - upstream_gene_variant PRAD-CA 1 160267980 160267980 single base substitution G A intron_variant PRAD-CA 1 160273491 160273491 single base substitution T G downstream_gene_variant PRAD-CA 1 160273491 160273491 single base substitution T G intron_variant PRAD-CA 1 160273491 160273491 single base substitution T G upstream_gene_variant PRAD-CA 1 160276275 160276275 single base substitution G A downstream_gene_variant PRAD-CA 1 160276275 160276275 single base substitution G A synonymous_variant I437I 1311C>T PRAD-CA 1 160276275 160276275 single base substitution G A upstream_gene_variant PRAD-CA 1 160294580 160294580 single base substitution C G intron_variant PRAD-CA 1 160296658 160296658 single base substitution G C intron_variant PRAD-CA 1 160309729 160309729 single base substitution G A exon_variant PRAD-CA 1 160309729 160309729 single base substitution G A synonymous_variant F66F 198C>T PRAD-CA 1 160311140 160311140 single base substitution T C intron_variant PRAD-CA 1 160311140 160311140 single base substitution T C upstream_gene_variant PRAD-UK 1 160260302 160260302 single base substitution G C downstream_gene_variant PRAD-UK 1 160260302 160260302 single base substitution G C missense_variant Q1199E 3595C>G PRAD-UK 1 160260302 160260302 single base substitution G C missense_variant Q1208E 3622C>G PRAD-UK 1 160260309 160260309 single base substitution G A downstream_gene_variant PRAD-UK 1 160260309 160260309 single base substitution G A synonymous_variant F1196F 3588C>T PRAD-UK 1 160260309 160260309 single base substitution G A synonymous_variant F1205F 3615C>T PRAD-UK 1 160261046 160261046 single base substitution G A downstream_gene_variant PRAD-UK 1 160261046 160261046 single base substitution G A intron_variant PRAD-UK 1 160261214 160261214 single base substitution G C downstream_gene_variant PRAD-UK 1 160261214 160261214 single base substitution G C missense_variant L1111V 3331C>G PRAD-UK 1 160261214 160261214 single base substitution G C missense_variant L1120V 3358C>G PRAD-UK 1 160261320 160261320 single base substitution G T downstream_gene_variant PRAD-UK 1 160261320 160261320 single base substitution G T intron_variant PRAD-UK 1 160271817 160271817 single base substitution T G downstream_gene_variant PRAD-UK 1 160271817 160271817 single base substitution T G intron_variant PRAD-UK 1 160271817 160271817 single base substitution T G upstream_gene_variant PRAD-UK 1 160277970 160277970 single base substitution A G downstream_gene_variant PRAD-UK 1 160277970 160277970 single base substitution A G intron_variant PRAD-UK 1 160277970 160277970 single base substitution A G upstream_gene_variant PRAD-UK 1 160283833 160283833 single base substitution C T synonymous_variant L263L 789G>A PRAD-UK 1 160283833 160283833 single base substitution C T upstream_gene_variant PRAD-UK 1 160294474 160294474 single base substitution A C intron_variant PRAD-UK 1 160304447 160304447 single base substitution G A downstream_gene_variant PRAD-UK 1 160304447 160304447 single base substitution G A intron_variant PRAD-US 1 160276964 160276964 single base substitution G A downstream_gene_variant PRAD-US 1 160276964 160276964 single base substitution G A missense_variant R431W 1291C>T PRAD-US 1 160276964 160276964 single base substitution G A upstream_gene_variant PRAD-US 1 160314573 160314573 single base substitution C A upstream_gene_variant READ-US 1 160269037 160269037 single base substitution C T exon_variant READ-US 1 160269037 160269037 single base substitution C T missense_variant R562Q 1685G>A READ-US 1 160269037 160269037 single base substitution C T missense_variant R571Q 1712G>A RECA-EU 1 160265082 160265082 single base substitution A C intron_variant RECA-EU 1 160275270 160275270 single base substitution T C downstream_gene_variant RECA-EU 1 160275270 160275270 single base substitution T C exon_variant RECA-EU 1 160275270 160275270 single base substitution T C synonymous_variant V540V 1620A>G RECA-EU 1 160275270 160275270 single base substitution T C synonymous_variant V549V 1647A>G RECA-EU 1 160275279 160275279 single base substitution C T downstream_gene_variant RECA-EU 1 160275279 160275279 single base substitution C T exon_variant RECA-EU 1 160275279 160275279 single base substitution C T synonymous_variant E537E 1611G>A RECA-EU 1 160275279 160275279 single base substitution C T synonymous_variant E546E 1638G>A RECA-EU 1 160280919 160280919 single base substitution A C intron_variant RECA-EU 1 160280919 160280919 single base substitution A C upstream_gene_variant RECA-EU 1 160283043 160283043 single base substitution C A intron_variant RECA-EU 1 160283043 160283043 single base substitution C A upstream_gene_variant RECA-EU 1 160295943 160295943 single base substitution G A intron_variant RECA-EU 1 160299467 160299467 single base substitution G C downstream_gene_variant RECA-EU 1 160299467 160299467 single base substitution G C intron_variant RECA-EU 1 160306034 160306034 single base substitution G A downstream_gene_variant RECA-EU 1 160306034 160306034 single base substitution G A intron_variant RECA-EU 1 160307423 160307423 single base substitution C A downstream_gene_variant RECA-EU 1 160307423 160307423 single base substitution C A intron_variant RECA-EU 1 160307682 160307682 single base substitution G T downstream_gene_variant RECA-EU 1 160307682 160307682 single base substitution G T intron_variant RECA-EU 1 160310255 160310255 single base substitution G C intron_variant RECA-EU 1 160310255 160310255 single base substitution G C upstream_gene_variant RECA-EU 1 160311215 160311215 single base substitution T A intron_variant RECA-EU 1 160311215 160311215 single base substitution T A upstream_gene_variant SKCA-BR 1 160257898 160257898 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 1 160260525 160260525 single base substitution C T downstream_gene_variant SKCA-BR 1 160260525 160260525 single base substitution C T intron_variant SKCA-BR 1 160260526 160260526 single base substitution C T downstream_gene_variant SKCA-BR 1 160260526 160260526 single base substitution C T intron_variant SKCA-BR 1 160266087 160266087 single base substitution T G intron_variant SKCA-BR 1 160266819 160266819 single base substitution G A intron_variant SKCA-BR 1 160270134 160270134 insertion of <=200bp - AAAAT downstream_gene_variant SKCA-BR 1 160270134 160270134 insertion of <=200bp - AAAAT intron_variant SKCA-BR 1 160270134 160270134 insertion of <=200bp - AAAAT upstream_gene_variant SKCA-BR 1 160273992 160273992 single base substitution G A downstream_gene_variant SKCA-BR 1 160273992 160273992 single base substitution G A intron_variant SKCA-BR 1 160273992 160273992 single base substitution G A upstream_gene_variant SKCA-BR 1 160274110 160274110 single base substitution G A downstream_gene_variant SKCA-BR 1 160274110 160274110 single base substitution G A intron_variant SKCA-BR 1 160276355 160276355 single base substitution C T downstream_gene_variant SKCA-BR 1 160276355 160276355 single base substitution C T intron_variant SKCA-BR 1 160276355 160276355 single base substitution C T upstream_gene_variant SKCA-BR 1 160277100 160277100 single base substitution T G downstream_gene_variant SKCA-BR 1 160277100 160277100 single base substitution T G intron_variant SKCA-BR 1 160277100 160277100 single base substitution T G upstream_gene_variant SKCA-BR 1 160281341 160281341 single base substitution C T intron_variant SKCA-BR 1 160281341 160281341 single base substitution C T upstream_gene_variant SKCA-BR 1 160284524 160284524 single base substitution C T intron_variant SKCA-BR 1 160284524 160284524 single base substitution C T upstream_gene_variant SKCA-BR 1 160285129 160285129 single base substitution G A intron_variant SKCA-BR 1 160285129 160285129 single base substitution G A upstream_gene_variant SKCA-BR 1 160285131 160285131 single base substitution A G intron_variant SKCA-BR 1 160285131 160285131 single base substitution A G upstream_gene_variant SKCA-BR 1 160286618 160286618 single base substitution T A intron_variant SKCA-BR 1 160296697 160296697 single base substitution G A intron_variant SKCA-BR 1 160296754 160296754 single base substitution G T intron_variant SKCA-BR 1 160297924 160297924 single base substitution C T intron_variant SKCA-BR 1 160307060 160307060 single base substitution C A downstream_gene_variant SKCA-BR 1 160307060 160307060 single base substitution C A intron_variant SKCA-BR 1 160312183 160312183 single base substitution G A intron_variant SKCA-BR 1 160312183 160312183 single base substitution G A upstream_gene_variant SKCA-BR 1 160316486 160316486 single base substitution C T upstream_gene_variant SKCM-US 1 160254895 160254895 single base substitution C T downstream_gene_variant SKCM-US 1 160260340 160260340 single base substitution G A downstream_gene_variant SKCM-US 1 160260340 160260340 single base substitution G A missense_variant P1186L 3557C>T SKCM-US 1 160260340 160260340 single base substitution G A missense_variant P1195L 3584C>T SKCM-US 1 160260356 160260356 single base substitution G A downstream_gene_variant SKCM-US 1 160260356 160260356 single base substitution G A missense_variant P1181S 3541C>T SKCM-US 1 160260356 160260356 single base substitution G A missense_variant P1190S 3568C>T SKCM-US 1 160260464 160260464 single base substitution G A downstream_gene_variant SKCM-US 1 160260464 160260464 single base substitution G A synonymous_variant L1145L 3433C>T SKCM-US 1 160260464 160260464 single base substitution G A synonymous_variant L1154L 3460C>T SKCM-US 1 160260465 160260465 single base substitution G A downstream_gene_variant SKCM-US 1 160260465 160260465 single base substitution G A synonymous_variant I1144I 3432C>T SKCM-US 1 160260465 160260465 single base substitution G A synonymous_variant I1153I 3459C>T SKCM-US 1 160261862 160261862 single base substitution G A downstream_gene_variant SKCM-US 1 160261862 160261862 single base substitution G A synonymous_variant F1029F 3087C>T SKCM-US 1 160261862 160261862 single base substitution G A synonymous_variant F1038F 3114C>T SKCM-US 1 160261985 160261985 single base substitution C T downstream_gene_variant SKCM-US 1 160261985 160261985 single base substitution C T synonymous_variant K988K 2964G>A SKCM-US 1 160261985 160261985 single base substitution C T synonymous_variant K997K 2991G>A SKCM-US 1 160262336 160262336 single base substitution G A downstream_gene_variant SKCM-US 1 160262336 160262336 single base substitution G A synonymous_variant G966G 2898C>T SKCM-US 1 160262336 160262336 single base substitution G A synonymous_variant G975G 2925C>T SKCM-US 1 160262956 160262956 single base substitution C T downstream_gene_variant SKCM-US 1 160262956 160262956 single base substitution C T splice_region_variant SKCM-US 1 160263246 160263246 single base substitution G A downstream_gene_variant SKCM-US 1 160263246 160263246 single base substitution G A missense_variant S895F 2684C>T SKCM-US 1 160263246 160263246 single base substitution G A missense_variant S904F 2711C>T SKCM-US 1 160265560 160265560 single base substitution G A exon_variant SKCM-US 1 160265560 160265560 single base substitution G A synonymous_variant S814S 2442C>T SKCM-US 1 160265560 160265560 single base substitution G A synonymous_variant S823S 2469C>T SKCM-US 1 160275485 160275485 single base substitution G C downstream_gene_variant SKCM-US 1 160275485 160275485 single base substitution G C exon_variant SKCM-US 1 160275485 160275485 single base substitution G C synonymous_variant A507A 1521C>G SKCM-US 1 160276187 160276187 single base substitution G A downstream_gene_variant SKCM-US 1 160276187 160276187 single base substitution G A stop_gained R467* 1399C>T SKCM-US 1 160276187 160276187 single base substitution G A upstream_gene_variant SKCM-US 1 160278903 160278903 single base substitution G T exon_variant SKCM-US 1 160278903 160278903 single base substitution G T missense_variant Q403K 1207C>A SKCM-US 1 160278903 160278903 single base substitution G T upstream_gene_variant SKCM-US 1 160280027 160280027 single base substitution G A exon_variant SKCM-US 1 160280027 160280027 single base substitution G A synonymous_variant F366F 1098C>T SKCM-US 1 160280027 160280027 single base substitution G A upstream_gene_variant SKCM-US 1 160281719 160281719 single base substitution G T synonymous_variant R339R 1015C>A SKCM-US 1 160281719 160281719 single base substitution G T upstream_gene_variant SKCM-US 1 160281796 160281796 single base substitution C T missense_variant G313D 938G>A SKCM-US 1 160281796 160281796 single base substitution C T upstream_gene_variant SKCM-US 1 160282899 160282899 single base substitution G A missense_variant P301S 901C>T SKCM-US 1 160282899 160282899 single base substitution G A upstream_gene_variant SKCM-US 1 160282958 160282958 single base substitution C T splice_acceptor_variant SKCM-US 1 160282958 160282958 single base substitution C T upstream_gene_variant SKCM-US 1 160293284 160293284 single base substitution G A missense_variant P215S 643C>T SKCM-US 1 160295426 160295426 insertion of <=200bp - T frameshift_variant N171N? SKCM-US 1 160303462 160303462 single base substitution G A exon_variant SKCM-US 1 160303462 160303462 single base substitution G A missense_variant P106L 317C>T SKCM-US 1 160305037 160305037 single base substitution G A downstream_gene_variant SKCM-US 1 160305037 160305037 single base substitution G A exon_variant SKCM-US 1 160305037 160305037 single base substitution G A missense_variant H102Y 304C>T STAD-US 1 160261161 160261161 single base substitution T C downstream_gene_variant STAD-US 1 160261161 160261161 single base substitution T C synonymous_variant L1128L 3384A>G STAD-US 1 160261161 160261161 single base substitution T C synonymous_variant L1137L 3411A>G STAD-US 1 160261166 160261166 single base substitution G A downstream_gene_variant STAD-US 1 160261166 160261166 single base substitution G A missense_variant R1127C 3379C>T STAD-US 1 160261166 160261166 single base substitution G A missense_variant R1136C 3406C>T STAD-US 1 160261218 160261218 insertion of <=200bp - GA downstream_gene_variant STAD-US 1 160261218 160261218 insertion of <=200bp - GA frameshift_variant L1109L? STAD-US 1 160261218 160261218 insertion of <=200bp - GA frameshift_variant L1118L? STAD-US 1 160262393 160262393 single base substitution T C downstream_gene_variant STAD-US 1 160262393 160262393 single base substitution T C synonymous_variant V947V 2841A>G STAD-US 1 160262393 160262393 single base substitution T C synonymous_variant V956V 2868A>G STAD-US 1 160264607 160264607 single base substitution A G exon_variant STAD-US 1 160264607 160264607 single base substitution A G synonymous_variant T839T 2517T>C STAD-US 1 160264607 160264607 single base substitution A G synonymous_variant T848T 2544T>C STAD-US 1 160265548 160265548 deletion of <=200bp A - exon_variant STAD-US 1 160265548 160265548 deletion of <=200bp A - frameshift_variant F818 STAD-US 1 160265548 160265548 deletion of <=200bp A - frameshift_variant F827 STAD-US 1 160267456 160267456 single base substitution T C exon_variant STAD-US 1 160267456 160267456 single base substitution T C missense_variant N686S 2057A>G STAD-US 1 160267456 160267456 single base substitution T C missense_variant N695S 2084A>G STAD-US 1 160268702 160268702 single base substitution A G exon_variant STAD-US 1 160268702 160268702 single base substitution A G missense_variant V637A 1910T>C STAD-US 1 160268702 160268702 single base substitution A G missense_variant V646A 1937T>C STAD-US 1 160268779 160268779 single base substitution T C splice_region_variant STAD-US 1 160268902 160268902 single base substitution T G exon_variant STAD-US 1 160268902 160268902 single base substitution T G missense_variant K607T 1820A>C STAD-US 1 160268902 160268902 single base substitution T G missense_variant K616T 1847A>C STAD-US 1 160269047 160269047 single base substitution C T exon_variant STAD-US 1 160269047 160269047 single base substitution C T missense_variant G559R 1675G>A STAD-US 1 160269047 160269047 single base substitution C T missense_variant G568R 1702G>A STAD-US 1 160275305 160275305 single base substitution G A downstream_gene_variant STAD-US 1 160275305 160275305 single base substitution G A exon_variant STAD-US 1 160275305 160275305 single base substitution G A missense_variant R529C 1585C>T STAD-US 1 160275305 160275305 single base substitution G A missense_variant R538C 1612C>T STAD-US 1 160276963 160276963 single base substitution C T downstream_gene_variant STAD-US 1 160276963 160276963 single base substitution C T missense_variant R431Q 1292G>A STAD-US 1 160276963 160276963 single base substitution C T upstream_gene_variant STAD-US 1 160293315 160293315 single base substitution G A synonymous_variant H204H 612C>T STAD-US 1 160313199 160313199 deletion of <=200bp G - upstream_gene_variant UCEC-US 1 160254895 160254895 single base substitution C T downstream_gene_variant UCEC-US 1 160259952 160259952 single base substitution G A downstream_gene_variant UCEC-US 1 160259952 160259952 single base substitution G A missense_variant R1224C 3670C>T UCEC-US 1 160259952 160259952 single base substitution G A missense_variant R1233C 3697C>T UCEC-US 1 160260410 160260410 single base substitution G A downstream_gene_variant UCEC-US 1 160260410 160260410 single base substitution G A missense_variant H1163Y 3487C>T UCEC-US 1 160260410 160260410 single base substitution G A missense_variant H1172Y 3514C>T UCEC-US 1 160261165 160261165 single base substitution C T downstream_gene_variant UCEC-US 1 160261165 160261165 single base substitution C T missense_variant R1127H 3380G>A UCEC-US 1 160261165 160261165 single base substitution C T missense_variant R1136H 3407G>A UCEC-US 1 160261863 160261863 single base substitution A C downstream_gene_variant UCEC-US 1 160261863 160261863 single base substitution A C missense_variant F1029C 3086T>G UCEC-US 1 160261863 160261863 single base substitution A C missense_variant F1038C 3113T>G UCEC-US 1 160261966 160261966 single base substitution C A downstream_gene_variant UCEC-US 1 160261966 160261966 single base substitution C A missense_variant G1004C 3010G>T UCEC-US 1 160261966 160261966 single base substitution C A missense_variant G995C 2983G>T UCEC-US 1 160265890 160265890 single base substitution A G exon_variant UCEC-US 1 160265890 160265890 single base substitution A G synonymous_variant A771A 2313T>C UCEC-US 1 160265890 160265890 single base substitution A G synonymous_variant A780A 2340T>C UCEC-US 1 160267364 160267364 single base substitution G A exon_variant UCEC-US 1 160267364 160267364 single base substitution G A missense_variant R717C 2149C>T UCEC-US 1 160267364 160267364 single base substitution G A missense_variant R726C 2176C>T UCEC-US 1 160268672 160268672 single base substitution G T exon_variant UCEC-US 1 160268672 160268672 single base substitution G T missense_variant T647N 1940C>A UCEC-US 1 160268672 160268672 single base substitution G T missense_variant T656N 1967C>A UCEC-US 1 160269028 160269028 single base substitution T C exon_variant UCEC-US 1 160269028 160269028 single base substitution T C missense_variant D565G 1694A>G UCEC-US 1 160269028 160269028 single base substitution T C missense_variant D574G 1721A>G UCEC-US 1 160275322 160275322 single base substitution T G downstream_gene_variant UCEC-US 1 160275322 160275322 single base substitution T G exon_variant UCEC-US 1 160275322 160275322 single base substitution T G missense_variant N523T 1568A>C UCEC-US 1 160275322 160275322 single base substitution T G missense_variant N532T 1595A>C UCEC-US 1 160275358 160275358 single base substitution A T downstream_gene_variant UCEC-US 1 160275358 160275358 single base substitution A T exon_variant UCEC-US 1 160275358 160275358 single base substitution A T missense_variant I511N 1532T>A UCEC-US 1 160275358 160275358 single base substitution A T missense_variant I520N 1559T>A UCEC-US 1 160275367 160275367 single base substitution A C downstream_gene_variant UCEC-US 1 160275367 160275367 single base substitution A C intron_variant UCEC-US 1 160275367 160275367 single base substitution A C missense_variant L517R 1550T>G UCEC-US 1 160275367 160275367 single base substitution A C splice_region_variant UCEC-US 1 160278942 160278942 single base substitution T A exon_variant UCEC-US 1 160278942 160278942 single base substitution T A missense_variant T390S 1168A>T UCEC-US 1 160278942 160278942 single base substitution T A upstream_gene_variant UCEC-US 1 160280028 160280028 single base substitution A C exon_variant UCEC-US 1 160280028 160280028 single base substitution A C missense_variant F366C 1097T>G UCEC-US 1 160280028 160280028 single base substitution A C upstream_gene_variant UCEC-US 1 160281662 160281662 single base substitution G A missense_variant R358W 1072C>T UCEC-US 1 160281662 160281662 single base substitution G A upstream_gene_variant UCEC-US 1 160283780 160283780 single base substitution C T missense_variant R281Q 842G>A UCEC-US 1 160283780 160283780 single base substitution C T upstream_gene_variant UCEC-US 1 160283821 160283821 single base substitution A T missense_variant N267K 801T>A UCEC-US 1 160283821 160283821 single base substitution A T upstream_gene_variant UCEC-US 1 160283886 160283886 single base substitution G A missense_variant R246W 736C>T UCEC-US 1 160283886 160283886 single base substitution G A upstream_gene_variant UCEC-US 1 160295403 160295403 single base substitution G A missense_variant S179L 536C>T UCEC-US 1 160305094 160305094 single base substitution G A downstream_gene_variant UCEC-US 1 160305094 160305094 single base substitution G A exon_variant UCEC-US 1 160305094 160305094 single base substitution G A missense_variant R83W 247C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 587278 COSM1202065 c.1196A>G p.D399G Substitution - Missense 1:160309124-160309124 - SNU-175 COSM1335507 c.512delA p.N171fs*11 Deletion - Frameshift 1:160325637-160325637 - GC_364T-GC_364N COSM4772671 c.387-8delT p.? Unknown 1:160332565-160332565 - PD8969a COSM5799156 c.394A>T p.T132S Substitution - Missense 1:160332550-160332550 - TCGA-BC-A10U-01 COSM4942474 c.562G>A p.D188N Substitution - Missense 1:160325587-160325587 - CSCC-31-T COSM4448923 c.1443-1G>A p.? Unknown 1:160305774-160305774 - HCC2998 COSM1335501 c.1273C>T p.R425W Substitution - Missense 1:160307192-160307192 - B86-Tumor COSM3930454 c.2731G>A p.A911T Substitution - Missense 1:160293436-160293436 - TCGA-AC-A3YJ-01 COSM3476832 c.1098C>T p.F366F Substitution - coding silent 1:160310237-160310237 - CSCC-27-T COSM4530516 c.1704G>A p.G568G Substitution - coding silent 1:160299255-160299255 - TCGA-06-0142-01 COSM3399887 c.1788C>T p.P596P Substitution - coding silent 1:160299171-160299171 - TCGA-EE-A3AC-06 COSM3476823 c.2469C>T p.S823S Substitution - coding silent 1:160295770-160295770 - sysucc-834T COSM5485471 c.3600C>A p.I1200I Substitution - coding silent 1:160290507-160290507 - TCGA-AC-A5XS-01 COSM4391283 c.2098G>A p.E700K Substitution - Missense 1:160297652-160297652 - TCGA-GV-A3JZ-01 COSM1295336 c.2289G>C p.Q763H Substitution - Missense 1:160297344-160297344 - TCGA-AP-A056-01 COSM898277 c.247C>T p.R83W Substitution - Missense 1:160335304-160335304 - CSCC-40-T COSM1335483 c.2679_2681delAGA p.E893delE Deletion - In frame 1:160294506-160294508 - TCGA-AP-A051-01 COSM898275 c.736C>T p.R246W Substitution - Missense 1:160314096-160314096 - TCGA-BR-4184-01 COSM4024129 c.3406C>T p.R1136C Substitution - Missense 1:160291376-160291376 - TCGA-BP-4330-01 COSM3360428 c.3342G>T p.K1114N Substitution - Missense 1:160291413-160291413 - S00831 COSM5660390 c.453A>G p.V151V Substitution - coding silent 1:160332491-160332491 - ESCC-009T COSM3934188 c.261C>T p.F87F Substitution - coding silent 1:160335290-160335290 - TCGA-IH-A3EA-01 COSM3476819 c.2850G>A p.R950R Substitution - coding silent 1:160293166-160293166 - TCGA-BR-8591-01 COSM4024148 c.612C>T p.H204H Substitution - coding silent 1:160323525-160323525 - TCGA-B5-A0JY-01 COSM1583648 c.1721A>G p.D574G Substitution - Missense 1:160299238-160299238 - TCGA-60-2698-01 COSM676754 c.2911C>G p.Q971E Substitution - Missense 1:160292533-160292533 - HCC2998 COSM1335500 c.1273C>T p.R425W Substitution - Missense 1:160307192-160307192 - T578 COSM4674157 c.3600C>T p.I1200I Substitution - coding silent 1:160290507-160290507 - NPC2F COSM4995304 c.3644T>A p.V1215E Substitution - Missense 1:160290215-160290215 - TCGA-EB-A4IS-01 COSM3476809 c.3568C>T p.P1190S Substitution - Missense 1:160290566-160290566 - TARGET-30-PATDXG COSM1284263 c.754G>A p.V252I Substitution - Missense 1:160314078-160314078 - TCGA-CW-5580-01 COSM1134750 c.93G>T p.G31G Substitution - coding silent 1:160340242-160340242 - TCGA-AN-A046-01 COSM898257 c.3670C>T p.R1224C Substitution - Missense 1:160290162-160290162 - 0091_CRUK_PC_0091_T1_DNA COSM4420914 c.3331C>G p.L1111V Substitution - Missense 1:160291424-160291424 - 2492720 COSM5723497 c.2899C>T p.R967C Substitution - Missense 1:160292545-160292545 - SJRHB023 COSM3738115 c.2535C>G p.D845E Substitution - Missense 1:160294826-160294826 - 3N44-VS-3T44 COSM4982137 c.1293G>C p.R431R Substitution - coding silent 1:160307172-160307172 - TCGA-BP-5178-01 COSM463253 c.444C>G p.D148E Substitution - Missense 1:160332500-160332500 - CSCC-49-T COSM4570993 c.3586T>G p.F1196V Substitution - Missense 1:160290521-160290521 - CHC051T COSM3667385 c.1725A>G p.L575L Substitution - coding silent 1:160299234-160299234 - pfg008T COSM1639580 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - CSCC-27-T COSM4530517 c.1677G>A p.G559G Substitution - coding silent 1:160299255-160299255 - T578 COSM4674156 c.3627C>T p.I1209I Substitution - coding silent 1:160290507-160290507 - SC_9032 COSM5558212 c.1922A>G p.K641R Substitution - Missense 1:160298927-160298927 - 22T COSM110343 c.470A>C p.Q157P Substitution - Missense 1:160332474-160332474 - TCGA-33-4532-01 COSM1146007 c.971C>A p.P324Q Substitution - Missense 1:160311973-160311973 - TCGA-B5-A0JY-01 COSM898262 c.2149C>T p.R717C Substitution - Missense 1:160297574-160297574 - CSCC-38-T COSM4483579 c.2685C>T p.S895S Substitution - coding silent 1:160293455-160293455 - ESCC-009T COSM3934189 c.261C>T p.F87F Substitution - coding silent 1:160335290-160335290 - TCGA-AC-A3W5-01 COSM3802483 c.1597A>G p.I533V Substitution - Missense 1:160305530-160305530 - T3658 COSM4674160 c.3252A>G p.K1084K Substitution - coding silent 1:160291852-160291852 - TCGA-C8-A12L-01 COSM424322 c.1109A>T p.Y370F Substitution - Missense 1:160310226-160310226 - CSCC-18-T COSM4472485 c.1787C>T p.P596L Substitution - Missense 1:160299172-160299172 - OSCC-GB_00910111 COSM4888131 c.3145G>A p.V1049I Substitution - Missense 1:160292041-160292041 - CRC-06T COSM5456144 c.2004+6A>C p.? Unknown 1:160298839-160298839 - TCGA-D3-A5GS-06 COSM3476842 c.317C>T p.P106L Substitution - Missense 1:160333672-160333672 - EGC3 COSM5052717 c.303_304insT p.H102fs*3 Insertion - Frameshift 1:160335247-160335248 - HCC131T COSM1601109 c.1116A>C p.P372P Substitution - coding silent 1:160310219-160310219 - TCGA-D3-A51T-06 COSM3476827 c.1399C>T p.R467* Substitution - Nonsense 1:160306397-160306397 - SNU-C2B COSM2085522 c.2809G>A p.E937K Substitution - Missense 1:160293180-160293180 - 0091_CRUK_PC_0091_T1_DNA COSM4420899 c.3588C>T p.F1196F Substitution - coding silent 1:160290519-160290519 - TARGET-30-PATDXG COSM1151881 c.761G>A p.C254Y Substitution - Missense 1:160314071-160314071 - TCGA-BR-8591-01 COSM4024147 c.612C>T p.H204H Substitution - coding silent 1:160323525-160323525 - BD177T COSM5517268 c.436A>G p.T146A Substitution - Missense 1:160332508-160332508 - TCGA-BT-A20J-01 COSM414387 c.871C>A p.H291N Substitution - Missense 1:160313139-160313139 - HCC2998 COSM1639580 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - EGC3 COSM4024147 c.612C>T p.H204H Substitution - coding silent 1:160323525-160323525 - ESCC_93 COSM4674159 c.3520C>T p.R1174W Substitution - Missense 1:160290587-160290587 - T3498 COSM2085515 c.2981G>A p.R994H Substitution - Missense 1:160292490-160292490 - ESCC_13 COSM5625013 c.1969C>G p.R657G Substitution - Missense 1:160298880-160298880 - 2492723 COSM5723497 c.2899C>T p.R967C Substitution - Missense 1:160292545-160292545 - TCGA-A5-A0GB-01 COSM1151878 c.3407G>A p.R1136H Substitution - Missense 1:160291375-160291375 - TCGA-BR-6452-01 COSM4024127 c.3411A>G p.L1137L Substitution - coding silent 1:160291371-160291371 - ccRCC-44 COSM1661248 c.2672T>C p.V891A Substitution - Missense 1:160294515-160294515 - TCGA-60-2698-01 COSM676750 c.1051G>T p.D351Y Substitution - Missense 1:160311893-160311893 - TCGA-DK-A1AC-01 COSM1295332 c.3202G>A p.E1068K Substitution - Missense 1:160291902-160291902 - TCGA-EJ-5522-01 COSM1127304 c.1291C>T p.R431W Substitution - Missense 1:160307174-160307174 - HDC82 COSM4636566 c.2584T>C p.L862L Substitution - coding silent 1:160294777-160294777 - TCGA-BS-A0UJ-01 COSM1583651 c.2340T>C p.A780A Substitution - coding silent 1:160296100-160296100 - TCGA-63-5128-01 COSM676757 c.3259A>G p.M1087V Substitution - Missense 1:160291496-160291496 - TCGA-CG-5721-01 COSM4024136 c.2057A>G p.N686S Substitution - Missense 1:160297666-160297666 - TCGA-AM-5820-01 COSM146664 c.363C>T p.N121N Substitution - coding silent 1:160333626-160333626 - TCGA-IR-A3LK-01 COSM2085597 c.1301C>T p.S434L Substitution - Missense 1:160307164-160307164 - TCGA-EJ-7123-01 COSM3671467 c.1576G>T p.E526* Substitution - Nonsense 1:160305524-160305524 - CHC051T COSM3667386 c.1698A>G p.L566L Substitution - coding silent 1:160299234-160299234 - ESCC-129T COSM3934191 c.218A>G p.Y73C Substitution - Missense 1:160339919-160339919 - TCGA-A5-A0GB-01 COSM898259 c.3380G>A p.R1127H Substitution - Missense 1:160291375-160291375 - LUAD-S01357 COSM386156 c.3557C>T p.P1186L Substitution - Missense 1:160290550-160290550 - TCGA-AN-A0AK-01 COSM3802488 c.1440G>A p.K480K Substitution - coding silent 1:160306356-160306356 - GC8_T COSM146664 c.363C>T p.N121N Substitution - coding silent 1:160333626-160333626 - LUAD-NYU846 COSM376463 c.2477G>A p.G826E Substitution - Missense 1:160294857-160294857 - TCGA-B8-5158-01 COSM1134747 c.3355A>G p.N1119D Substitution - Missense 1:160291427-160291427 - PCSI_0269_Pa_P_526 COSM4961940 c.1166G>A p.S389N Substitution - Missense 1:160309154-160309154 - TCGA-AM-5820-01 COSM3750511 c.2416A>C p.T806P Substitution - Missense 1:160295796-160295796 - TCGA-D3-A1Q1-06 COSM3476834 c.1015C>A p.R339R Substitution - coding silent 1:160311929-160311929 - TCGA-AX-A05Z-01 COSM1583652 c.3113T>G p.F1038C Substitution - Missense 1:160292073-160292073 - TCGA-B5-A11J-01 COSM1583645 c.1168A>T p.T390S Substitution - Missense 1:160309152-160309152 - CSCC-47-T COSM4494326 c.430C>T p.H144Y Substitution - Missense 1:160332514-160332514 - PD4847a COSM5778088 c.834G>C p.M278I Substitution - Missense 1:160313998-160313998 - S0078 COSM5881549 c.2879A>T p.Q960L Substitution - Missense 1:160292592-160292592 - PD7199a COSM5781842 c.1143+1G>T p.? Unknown 1:160310191-160310191 - TCGA-BH-A2L8-01 COSM3802490 c.1131C>T p.V377V Substitution - coding silent 1:160310204-160310204 - 855_CLM COSM4777945 c.490A>G p.I164V Substitution - Missense 1:160332454-160332454 - 2492721 COSM5723496 c.2926C>T p.R976C Substitution - Missense 1:160292545-160292545 - CSCC-44-T COSM3476841 c.317C>T p.P106L Substitution - Missense 1:160333672-160333672 - B86-Tumor COSM3930455 c.2704G>A p.A902T Substitution - Missense 1:160293436-160293436 - TCGA-D1-A103-01 COSM898257 c.3670C>T p.R1224C Substitution - Missense 1:160290162-160290162 - TCGA-BR-6452-01 COSM4024139 c.1860A>G p.V620V Substitution - coding silent 1:160298989-160298989 - TCGA-CG-5721-01 COSM4024145 c.1292G>A p.R431Q Substitution - Missense 1:160307173-160307173 - SC_9096 COSM5552316 c.1606G>T p.D536Y Substitution - Missense 1:160305494-160305494 - KYSE-510 COSM2085614 c.877C>T p.R293C Substitution - Missense 1:160313133-160313133 - T16 COSM146664 c.363C>T p.N121N Substitution - coding silent 1:160333626-160333626 - TCGA-29-1761-01 COSM1319824 c.699C>A p.R233R Substitution - coding silent 1:160323438-160323438 - TCGA-AN-A046-01 COSM3802482 c.3088C>T p.R1030C Substitution - Missense 1:160292071-160292071 - TCGA-D3-A2JD-06 COSM3476826 c.1521C>G p.A507A Substitution - coding silent 1:160305695-160305695 - CHC051T COSM3667386 c.1698A>G p.L566L Substitution - coding silent 1:160299234-160299234 - TCGA-B5-A11J-01 COSM898269 c.1168A>T p.T390S Substitution - Missense 1:160309152-160309152 - TCGA-D1-A103-01 COSM898271 c.1072C>T p.R358W Substitution - Missense 1:160311872-160311872 - ESCC-038T COSM3934185 c.1625T>C p.I542T Substitution - Missense 1:160305475-160305475 - CRC-06T COSM5456145 c.1977+6A>C p.? Unknown 1:160298839-160298839 - TCGA-DA-A3F3-06 COSM3476818 c.2898C>T p.G966G Substitution - coding silent 1:160292546-160292546 - TCGA-B5-A0JV-01 COSM530110 c.2983G>T p.G995C Substitution - Missense 1:160292176-160292176 - ESO-152 COSM1248963 c.2428A>G p.I810V Substitution - Missense 1:160295811-160295811 - 0091_CRUK_PC_0091_T1_DNA COSM4420153 c.3595C>G p.Q1199E Substitution - Missense 1:160290512-160290512 - TCGA-A6-6781-01 COSM3750512 c.1254C>T p.A418A Substitution - coding silent 1:160307211-160307211 - TCGA-DU-5849-01 COSM3965946 c.1887A>G p.L629L Substitution - coding silent 1:160298962-160298962 - PD9004a COSM5792789 c.1539C>A p.C513* Substitution - Nonsense 1:160305588-160305588 - PT37 COSM5917105 c.2132G>A p.G711D Substitution - Missense 1:160297591-160297591 - CSCC-44-T COSM3476842 c.317C>T p.P106L Substitution - Missense 1:160333672-160333672 - PD7248a COSM5792059 c.1303-1G>T p.? Unknown 1:160306494-160306494 - TCGA-IH-A3EA-01 COSM386156 c.3557C>T p.P1186L Substitution - Missense 1:160290550-160290550 - TCGA-BS-A0UF-01 COSM898270 c.1097T>G p.F366C Substitution - Missense 1:160310238-160310238 - 0091_CRUK_PC_0091_T1_DNA COSM4420913 c.3358C>G p.L1120V Substitution - Missense 1:160291424-160291424 - HCC2998 COSM1639579 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - TCGA-AA-3510-01 COSM1335501 c.1273C>T p.R425W Substitution - Missense 1:160307192-160307192 - HCC131 COSM1601110 c.1116A>C p.P372P Substitution - coding silent 1:160310219-160310219 - TCGA-AM-5820-01 COSM3750514 c.363C>T p.N121N Substitution - coding silent 1:160333626-160333626 - TCGA-EQ-A4SO-01 COSM4024131 c.2868A>G p.V956V Substitution - coding silent 1:160292603-160292603 - TCGA-D3-A51T-06 COSM3476828 c.1399C>T p.R467* Substitution - Nonsense 1:160306397-160306397 - T3535 COSM4674163 c.2673G>T p.E891D Substitution - Missense 1:160294487-160294487 - HDC82 COSM4636567 c.2557T>C p.L853L Substitution - coding silent 1:160294777-160294777 - 23 COSM5748416 c.1176_1196del21 p.L393_D399delLYTIPKD Deletion - In frame 1:160309124-160309144 - ESCC_BICR_038T COSM5434503 c.2356A>G p.T786A Substitution - Missense 1:160296084-160296084 - C089 COSM5542780 c.2831C>T p.S944F Substitution - Missense 1:160293185-160293185 - TCGA-D3-A5GS-06 COSM3476841 c.317C>T p.P106L Substitution - Missense 1:160333672-160333672 - CPCG0040-F1 COSM4880122 c.198C>T p.F66F Substitution - coding silent 1:160339939-160339939 - GC_364T-GC_364N COSM4772672 c.387-8delT p.? Unknown 1:160332565-160332565 - ML2 COSM1165461 c.961C>T p.R321W Substitution - Missense 1:160311983-160311983 - pfg008T COSM1639579 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - ESCC_134 COSM5642654 c.844A>C p.T282P Substitution - Missense 1:160313166-160313166 - WA53 COSM236713 c.3344T>G p.L1115R Substitution - Missense 1:160291411-160291411 - TCGA-AC-A5XS-01 COSM4391284 c.2071G>A p.E691K Substitution - Missense 1:160297652-160297652 - TCGA-AP-A056-01 COSM1583637 c.247C>T p.R83W Substitution - Missense 1:160335304-160335304 - TCGA-DK-A1AC-01 COSM1295333 c.3175G>A p.E1059K Substitution - Missense 1:160291902-160291902 - 8015271 COSM1159252 c.1890G>A p.Q630Q Substitution - coding silent 1:160298932-160298932 - S0078 COSM5881550 c.2852A>T p.Q951L Substitution - Missense 1:160292592-160292592 - ESCC_93 COSM4674158 c.3547C>T p.R1183W Substitution - Missense 1:160290587-160290587 - TCGA-DA-A1HY-06 COSM3476831 c.1098C>T p.F366F Substitution - coding silent 1:160310237-160310237 - TCGA-B5-A0JY-01 COSM898264 c.1694A>G p.D565G Substitution - Missense 1:160299238-160299238 - TCGA-AX-A0J1-01 COSM1583649 c.1967C>A p.T656N Substitution - Missense 1:160298882-160298882 - ESO-H01 COSM1248965 c.3355A>T p.N1119Y Substitution - Missense 1:160291427-160291427 - TCGA-ER-A19J-06 COSM3476844 c.304C>T p.H102Y Substitution - Missense 1:160335247-160335247 - C0002T COSM2085579 c.1638G>A p.E546E Substitution - coding silent 1:160305489-160305489 - PAPNNX COSM5004922 c.164G>A p.R55Q Substitution - Missense 1:160339973-160339973 - TCGA-EI-6917-01 COSM3418212 c.1685G>A p.R562Q Substitution - Missense 1:160299247-160299247 - TCGA-BR-4184-01 COSM4024130 c.3379C>T p.R1127C Substitution - Missense 1:160291376-160291376 - TCGA-A5-A0GP-01 COSM898267 c.1529-6T>G p.? Unknown 1:160305577-160305577 - RK140_C01 COSM3700517 c.2479T>A p.F827I Substitution - Missense 1:160295760-160295760 - T3262 COSM1335506 c.512delA p.N171fs*11 Deletion - Frameshift 1:160325637-160325637 - RK176_C01 COSM1248963 c.2428A>G p.I810V Substitution - Missense 1:160295811-160295811 - C089 COSM5542781 c.2804C>T p.S935F Substitution - Missense 1:160293185-160293185 - TCGA-CG-5721-01 COSM4024137 c.1937T>C p.V646A Substitution - Missense 1:160298912-160298912 - LUAD-F00368 COSM367616 c.2729C>T p.P910L Substitution - Missense 1:160293411-160293411 - TCGA-A3-3367-01 COSM414388 c.2900G>A p.R967H Substitution - Missense 1:160292544-160292544 - sysucc-1317T COSM5448217 c.1627G>A p.A543T Substitution - Missense 1:160305500-160305500 - LUAD-S01315 COSM344869 c.2385C>G p.L795L Substitution - coding silent 1:160295827-160295827 - TCGA-E2-A15O-01 COSM1472867 c.3244C>G p.L1082V Substitution - Missense 1:160291860-160291860 - TCGA-A6-6781-01 COSM3750513 c.1254C>T p.A418A Substitution - coding silent 1:160307211-160307211 - ICGC_0053 COSM1159252 c.1890G>A p.Q630Q Substitution - coding silent 1:160298932-160298932 - BD124T COSM5491222 c.1991C>T p.A664V Substitution - Missense 1:160297732-160297732 - TCGA-ER-A19J-06 COSM3476843 c.304C>T p.H102Y Substitution - Missense 1:160335247-160335247 - TCGA-D1-A103-01 COSM1583654 c.3697C>T p.R1233C Substitution - Missense 1:160290162-160290162 - PD8969a COSM5799157 c.394A>T p.T132S Substitution - Missense 1:160332550-160332550 - TCGA-A7-A26I-01 COSM1472869 c.2608C>T p.L870F Substitution - Missense 1:160294552-160294552 - TCGA-BS-A0UF-01 COSM1583644 c.1097T>G p.F366C Substitution - Missense 1:160310238-160310238 - TCGA-A5-A0GP-01 COSM1583646 c.1550T>G p.L517R Substitution - Missense 1:160305577-160305577 - HCC159 COSM3705162 c.181A>G p.K61E Substitution - Missense 1:160339956-160339956 - SC_9020 COSM5570621 c.3643G>A p.V1215M Substitution - Missense 1:160290216-160290216 - TCGA-D3-A5GN-06 COSM3476829 c.1207C>A p.Q403K Substitution - Missense 1:160309113-160309113 - TCGA-E2-A15O-01 COSM424321 c.3217C>G p.L1073V Substitution - Missense 1:160291860-160291860 - KYSE-510 COSM2085615 c.877C>T p.R293C Substitution - Missense 1:160313133-160313133 - TCGA-AP-A051-01 COSM1583641 c.736C>T p.R246W Substitution - Missense 1:160314096-160314096 - ESCC-009T COSM3934187 c.702G>C p.M234I Substitution - Missense 1:160323435-160323435 - Pat_28_B COSM5844173 c.2399C>G p.P800R Substitution - Missense 1:160295813-160295813 - TCGA-BT-A3PH-01 COSM1295335 c.2823+1G>A p.? Unknown 1:160293165-160293165 - SC_9090 COSM5572983 c.3616-1G>A p.? Unknown 1:160290217-160290217 - T2269 COSM4674168 c.1291C>T p.R431W Substitution - Missense 1:160307174-160307174 - Pat_01_B COSM4494325 c.430C>T p.H144Y Substitution - Missense 1:160332514-160332514 - TCGA-39-5030-01 COSM676758 c.3548A>G p.E1183G Substitution - Missense 1:160290559-160290559 - PD24314a COSM5795444 c.310-1G>T p.? Unknown 1:160333680-160333680 - TCGA-AX-A0J1-01 COSM898263 c.1940C>A p.T647N Substitution - Missense 1:160298882-160298882 - 459 COSM4436346 c.962G>A p.R321Q Substitution - Missense 1:160311982-160311982 - TCGA-IH-A3EA-01 COSM3476808 c.3584C>T p.P1195L Substitution - Missense 1:160290550-160290550 - TCGA-EI-6917-01 COSM3418211 c.1712G>A p.R571Q Substitution - Missense 1:160299247-160299247 - CSCC-38-T COSM4483578 c.2712C>T p.S904S Substitution - coding silent 1:160293455-160293455 - 3N44-VS-3T44 COSM4982136 c.1293G>C p.R431R Substitution - coding silent 1:160307172-160307172 - TCGA-06-0142-01 COSM3399888 c.1761C>T p.P587P Substitution - coding silent 1:160299171-160299171 - LUAD-E00897 COSM364215 c.3406G>A p.E1136K Substitution - Missense 1:160291349-160291349 - TCGA-AZ-4315-01 COSM1335504 c.779G>A p.R260H Substitution - Missense 1:160314053-160314053 - HCC2998 COSM1639580 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - S02249 COSM5679943 c.562G>C p.D188H Substitution - Missense 1:160325587-160325587 - TCGA-BR-8363-01 COSM4024144 c.1675G>A p.G559R Substitution - Missense 1:160299257-160299257 - TCGA-AA-3511-01 COSM1335487 c.2663G>T p.G888V Substitution - Missense 1:160294524-160294524 - PT35 COSM5911275 c.3671G>T p.R1224L Substitution - Missense 1:160290161-160290161 - 1425-01-01TD COSM5418734 c.3482C>T p.P1161L Substitution - Missense 1:160290652-160290652 - PCSI_0269_Pa_P_526 COSM4961939 c.1166G>A p.S389N Substitution - Missense 1:160309154-160309154 - TCGA-CW-6087-01 COSM463252 c.2859C>T p.G953G Substitution - coding silent 1:160292585-160292585 - TCGA-51-4079-01 COSM676753 c.2664C>T p.L888L Substitution - coding silent 1:160294496-160294496 - TCGA-51-4079-01 COSM676751 c.2663T>C p.L888P Substitution - Missense 1:160294497-160294497 - TCGA-EE-A2MR-06 COSM3476839 c.643C>T p.P215S Substitution - Missense 1:160323494-160323494 - ESCC-002T COSM3934183 c.2127C>G p.I709M Substitution - Missense 1:160297596-160297596 - ESCC_BICR_038T COSM5434504 c.2329A>G p.T777A Substitution - Missense 1:160296084-160296084 - sysucc-1370T COSM5469674 c.697C>T p.R233C Substitution - Missense 1:160323440-160323440 - TCGA-BT-A3PH-01 COSM1295334 c.2850+1G>A p.? Unknown 1:160293165-160293165 - RK290_C01 COSM4780107 c.3140T>G p.I1047S Substitution - Missense 1:160292019-160292019 - CSCC-49-T COSM4570992 c.3613T>G p.F1205V Substitution - Missense 1:160290521-160290521 - TCGA-39-5030-01 COSM1145998 c.3575A>G p.E1192G Substitution - Missense 1:160290559-160290559 - TCGA-EE-A3AC-06 COSM3476824 c.2442C>T p.S814S Substitution - coding silent 1:160295770-160295770 - OSCC-GB_00910111 COSM4888132 c.3118G>A p.V1040I Substitution - Missense 1:160292041-160292041 - TCGA-IH-A3EA-01 COSM3476820 c.2823G>A p.R941R Substitution - coding silent 1:160293166-160293166 - QGP1 COSM2085564 c.1882T>C p.Y628H Substitution - Missense 1:160298940-160298940 - TCGA-BR-6452-01 COSM4024134 c.2517T>C p.T839T Substitution - coding silent 1:160294817-160294817 - EGC3 COSM4024148 c.612C>T p.H204H Substitution - coding silent 1:160323525-160323525 - TCGA-D1-A17H-01 COSM898266 c.1532T>A p.I511N Substitution - Missense 1:160305568-160305568 - TCGA-A6-6781-01 COSM1335492 c.2133C>T p.G711G Substitution - coding silent 1:160297590-160297590 - CCRF-CEM COSM1668138 c.3173G>A p.R1058H Substitution - Missense 1:160291904-160291904 - TCGA-BH-A2L8-01 COSM3802489 c.1131C>T p.V377V Substitution - coding silent 1:160310204-160310204 - ccRCC-44 COSM1661249 c.2645T>C p.V882A Substitution - Missense 1:160294515-160294515 - pfg008T COSM1639580 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - ICGC_0053 COSM1159251 c.1917G>A p.Q639Q Substitution - coding silent 1:160298932-160298932 - TCGA-A8-A09Z-01 COSM3802491 c.1107A>G p.S369S Substitution - coding silent 1:160310228-160310228 - TCGA-AC-A3YJ-01 COSM3802493 c.1090C>T p.P364S Substitution - Missense 1:160310245-160310245 - TCGA-A6-6781-01 COSM1335491 c.2160C>T p.G720G Substitution - coding silent 1:160297590-160297590 - HCC159T COSM3705163 c.181A>G p.K61E Substitution - Missense 1:160339956-160339956 - 61 COSM5735704 c.928C>A p.H310N Substitution - Missense 1:160312016-160312016 - TCGA-63-5128-01 COSM1145999 c.3286A>G p.M1096V Substitution - Missense 1:160291496-160291496 - TCGA-51-4079-01 COSM1146005 c.2690T>C p.L897P Substitution - Missense 1:160294497-160294497 - TCGA-DA-A3F3-06 COSM3476817 c.2925C>T p.G975G Substitution - coding silent 1:160292546-160292546 - TCGA-51-4079-01 COSM1146003 c.2691C>T p.L897L Substitution - coding silent 1:160294496-160294496 - CSCC-40-T COSM1335484 c.2652_2654delAGA p.E884delE Deletion - In frame 1:160294506-160294508 - TCGA-B8-5158-01 COSM463251 c.3328A>G p.N1110D Substitution - Missense 1:160291427-160291427 - Pat_06_B COSM5844175 c.2383C>T p.L795F Substitution - Missense 1:160295829-160295829 - QGP1 COSM2085563 c.1909T>C p.Y637H Substitution - Missense 1:160298940-160298940 - Pat_01_B COSM4494326 c.430C>T p.H144Y Substitution - Missense 1:160332514-160332514 - T2225 COSM4674159 c.3520C>T p.R1174W Substitution - Missense 1:160290587-160290587 - T256 COSM4674165 c.2416A>G p.T806A Substitution - Missense 1:160295796-160295796 - TCGA-37-5819-01 COSM676748 c.926-1G>T p.? Unknown 1:160312019-160312019 - TCGA-21-5784-01 COSM676755 c.2941G>T p.G981C Substitution - Missense 1:160292503-160292503 - HCC2998 COSM1335500 c.1273C>T p.R425W Substitution - Missense 1:160307192-160307192 - HCC159T COSM3705162 c.181A>G p.K61E Substitution - Missense 1:160339956-160339956 - TCGA-EJ-7123-01 COSM3671466 c.1603G>T p.E535* Substitution - Nonsense 1:160305524-160305524 - 27 COSM5748768 c.1162_1194del33 p.N388_K398del11 Deletion - In frame 1:160309126-160309158 - SNUH_G10_S1 COSM3677424 c.297G>A p.T99T Substitution - coding silent 1:160335254-160335254 - HCC2998 COSM1335501 c.1273C>T p.R425W Substitution - Missense 1:160307192-160307192 - TCGA-A8-A09Z-01 COSM3802492 c.1107A>G p.S369S Substitution - coding silent 1:160310228-160310228 - YUKLAB COSM1335504 c.779G>A p.R260H Substitution - Missense 1:160314053-160314053 - TCGA-EB-A41A-01 COSM3476836 c.901C>T p.P301S Substitution - Missense 1:160313109-160313109 - TCGA-AM-5820-01 COSM3750510 c.2443A>C p.T815P Substitution - Missense 1:160295796-160295796 - TCGA-GV-A3JZ-01 COSM1295337 c.2262G>C p.Q754H Substitution - Missense 1:160297344-160297344 - TCGA-BP-4330-01 COSM3360427 c.3369G>T p.K1123N Substitution - Missense 1:160291413-160291413 - TCGA-37-5819-01 COSM1146008 c.926-1G>T p.? Unknown 1:160312019-160312019 - TCGA-EQ-A4SO-01 COSM4024132 c.2841A>G p.V947V Substitution - coding silent 1:160292603-160292603 - CPCG0040-F1 COSM4880121 c.198C>T p.F66F Substitution - coding silent 1:160339939-160339939 - TCGA-20-0991-01 COSM70275 c.1781C>T p.P594L Substitution - Missense 1:160299151-160299151 - TCGA-AP-A056-01 COSM1583640 c.536C>T p.S179L Substitution - Missense 1:160325613-160325613 - 28 COSM4777945 c.490A>G p.I164V Substitution - Missense 1:160332454-160332454 - TCGA-D3-A1Q1-06 COSM3476833 c.1015C>A p.R339R Substitution - coding silent 1:160311929-160311929 - TCGA-B5-A11E-01 COSM898258 c.3487C>T p.H1163Y Substitution - Missense 1:160290620-160290620 - TCGA-AA-3510-01 COSM1335500 c.1273C>T p.R425W Substitution - Missense 1:160307192-160307192 - TCGA-D1-A103-01 COSM1583643 c.1072C>T p.R358W Substitution - Missense 1:160311872-160311872 - 855_CLM COSM4777944 c.490A>G p.I164V Substitution - Missense 1:160332454-160332454 - CHC1744T COSM5348017 c.3542delC p.P1181fs*2 Deletion - Frameshift 1:160290565-160290565 - LP6007398-DNA_A01 COSM5951670 c.2626G>A p.E876K Substitution - Missense 1:160294534-160294534 - S00501 COSM310283 c.3276C>T p.T1092T Substitution - coding silent 1:160291479-160291479 - TCGA-EE-A2MT-06 COSM3476816 c.2964G>A p.K988K Substitution - coding silent 1:160292195-160292195 - RK140_C01 COSM3700518 c.2452T>A p.F818I Substitution - Missense 1:160295760-160295760 - SC_9032 COSM5558213 c.1895A>G p.K632R Substitution - Missense 1:160298927-160298927 - PTC-14C COSM4142894 c.2369C>A p.P790H Substitution - Missense 1:160295843-160295843 - TCGA-CG-5721-01 COSM4024138 c.1910T>C p.V637A Substitution - Missense 1:160298912-160298912 - TCGA-DK-A2I1-01 COSM1295338 c.2048_2049GG>TT p.W683F Substitution - Missense 1:160297701-160297702 - BD114T COSM5502354 c.2765G>C p.G922A Substitution - Missense 1:160293402-160293402 - TCGA-60-2698-01 COSM1146002 c.2938C>G p.Q980E Substitution - Missense 1:160292533-160292533 - T256 COSM4674164 c.2443A>G p.T815A Substitution - Missense 1:160295796-160295796 - GCT28 COSM5749642 c.3251A>T p.K1084I Substitution - Missense 1:160291853-160291853 - T3535 COSM4674162 c.2700G>T p.E900D Substitution - Missense 1:160294487-160294487 - SJMB008 COSM255448 c.155G>A p.G52D Substitution - Missense 1:160339982-160339982 - 61 COSM5735705 c.928C>A p.H310N Substitution - Missense 1:160312016-160312016 - 71 COSM5744426 c.1174_1191del18 p.D392_P397delDLYTIP Deletion - In frame 1:160309129-160309146 - T3658 COSM4674161 c.3225A>G p.K1075K Substitution - coding silent 1:160291852-160291852 - TCGA-BG-A0LX-01 COSM898273 c.801T>A p.N267K Substitution - Missense 1:160314031-160314031 - LUAD-RT-S01774 COSM381266 c.1756C>T p.R586C Substitution - Missense 1:160299176-160299176 - 71 COSM5744423 c.2029C>G p.L677V Substitution - Missense 1:160297721-160297721 - CSCC-47-T COSM4494325 c.430C>T p.H144Y Substitution - Missense 1:160332514-160332514 - SJMB008 COSM4775209 c.155G>A p.G52D Substitution - Missense 1:160339982-160339982 - TCGA-D3-A51R-06 COSM3476822 c.2684C>T p.S895F Substitution - Missense 1:160293456-160293456 - LP6007398-DNA_A01 COSM5951669 c.2653G>A p.E885K Substitution - Missense 1:160294534-160294534 - TCGA-BR-6452-01 COSM4024133 c.2544T>C p.T848T Substitution - coding silent 1:160294817-160294817 - SNU-C2B COSM2085521 c.2836G>A p.E946K Substitution - Missense 1:160293180-160293180 - TCGA-EE-A2MT-06 COSM3476815 c.2991G>A p.K997K Substitution - coding silent 1:160292195-160292195 - Pat_41_B COSM5844170 c.3253G>A p.E1085K Substitution - Missense 1:160291851-160291851 - TCGA-AO-A128-01 COSM3802486 c.1497C>T p.D499D Substitution - coding silent 1:160305719-160305719 - 0091_CRUK_PC_0091_T1_DNA COSM4420152 c.3622C>G p.Q1208E Substitution - Missense 1:160290512-160290512 - CSCC-29-T COSM4503403 c.639C>T p.F213F Substitution - coding silent 1:160323498-160323498 - 27 COSM5748767 c.1162_1194del33 p.N388_K398del11 Deletion - In frame 1:160309126-160309158 - CHC051T COSM3667385 c.1725A>G p.L575L Substitution - coding silent 1:160299234-160299234 - 8015271 COSM1159251 c.1917G>A p.Q639Q Substitution - coding silent 1:160298932-160298932 - Gp2D COSM1335507 c.512delA p.N171fs*11 Deletion - Frameshift 1:160325637-160325637 - TCGA-EE-A29B-06 COSM3476837 c.843-1G>A p.? Unknown 1:160313168-160313168 - TCGA-BR-8363-01 COSM4024143 c.1702G>A p.G568R Substitution - Missense 1:160299257-160299257 - PT35 COSM5911274 c.3698G>T p.R1233L Substitution - Missense 1:160290161-160290161 - 2492723 COSM5723496 c.2926C>T p.R976C Substitution - Missense 1:160292545-160292545 - ESO-152 COSM1248964 c.2401A>G p.I801V Substitution - Missense 1:160295811-160295811 - TCGA-EE-A17Y-06 COSM3476813 c.3459C>T p.I1153I Substitution - coding silent 1:160290675-160290675 - TCGA-A2-A4S3-01 COSM3802479 c.3246G>A p.L1082L Substitution - coding silent 1:160291858-160291858 - Gp2D COSM1335506 c.512delA p.N171fs*11 Deletion - Frameshift 1:160325637-160325637 - TCGA-BR-A4QL-01 COSM2085582 c.1585C>T p.R529C Substitution - Missense 1:160305515-160305515 - 8064559 COSM1159252 c.1890G>A p.Q630Q Substitution - coding silent 1:160298932-160298932 - TCGA-A4-8517-01 COSM3984383 c.282T>C p.D94D Substitution - coding silent 1:160335269-160335269 - YUDUTY COSM1688955 c.3374A>G p.K1125R Substitution - Missense 1:160291408-160291408 - TCGA-BC-A10U-01 COSM4942475 c.562G>A p.D188N Substitution - Missense 1:160325587-160325587 - 28 COSM4777944 c.490A>G p.I164V Substitution - Missense 1:160332454-160332454 - TCGA-D3-A51R-06 COSM3476821 c.2711C>T p.S904F Substitution - Missense 1:160293456-160293456 - TCGA-A7-A26I-01 COSM1472868 c.2635C>T p.L879F Substitution - Missense 1:160294552-160294552 - TCGA-B5-A0JV-01 COSM1138706 c.3010G>T p.G1004C Substitution - Missense 1:160292176-160292176 - tumor_4158726 COSM3356457 c.1076+10A>T p.? Unknown 1:160311858-160311858 - PA195 COSM1162637 c.1268G>A p.R423Q Substitution - Missense 1:160307197-160307197 - TCGA-EE-A2MR-06 COSM3476840 c.643C>T p.P215S Substitution - Missense 1:160323494-160323494 - 587278 COSM1202064 c.1196A>G p.D399G Substitution - Missense 1:160309124-160309124 - ESCC-038T COSM3934184 c.1652T>C p.I551T Substitution - Missense 1:160305475-160305475 - PD4847a COSM5778089 c.834G>C p.M278I Substitution - Missense 1:160313998-160313998 - TCGA-CW-5580-01 COSM463254 c.93G>T p.G31G Substitution - coding silent 1:160340242-160340242 - ESO-H01 COSM1248966 c.3328A>T p.N1110Y Substitution - Missense 1:160291427-160291427 - TCGA-BT-A20J-01 COSM1133275 c.871C>A p.H291N Substitution - Missense 1:160313139-160313139 - PA195 COSM1162638 c.1268G>A p.R423Q Substitution - Missense 1:160307197-160307197 - HCC2998 COSM1639579 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - TCGA-AC-A3YJ-01 COSM3476831 c.1098C>T p.F366F Substitution - coding silent 1:160310237-160310237 - TCGA-A4-8517-01 COSM3984384 c.282T>C p.D94D Substitution - coding silent 1:160335269-160335269 - SJRHB023 COSM3738116 c.2508C>G p.D836E Substitution - Missense 1:160294826-160294826 - HCT8 COSM4633367 c.3048C>T p.L1016L Substitution - coding silent 1:160292111-160292111 - TCGA-BR-6452-01 COSM4024140 c.1833A>G p.V611V Substitution - coding silent 1:160298989-160298989 - RK166_C01 COSM1626574 c.96C>T p.V32V Substitution - coding silent 1:160340239-160340239 - CSCC-49-T COSM4465205 c.1371C>T p.F457F Substitution - coding silent 1:160306425-160306425 - ESO-859 COSM1238577 c.1747A>G p.R583G Substitution - Missense 1:160299185-160299185 - 2492722 COSM5723496 c.2926C>T p.R976C Substitution - Missense 1:160292545-160292545 - TCGA-BR-A4QL-01 COSM2085581 c.1612C>T p.R538C Substitution - Missense 1:160305515-160305515 - TCGA-DD-A1EL-01 COSM4925854 c.251G>T p.R84L Substitution - Missense 1:160335300-160335300 - HCC2998 COSM2085571 c.1674C>A p.I558I Substitution - coding silent 1:160305453-160305453 - TCGA-ER-A3EV-06 COSM3863265 c.938G>A p.G313D Substitution - Missense 1:160312006-160312006 - sysucc-1370T COSM5469673 c.697C>T p.R233C Substitution - Missense 1:160323440-160323440 - TCGA-AX-A05Z-01 COSM898260 c.3086T>G p.F1029C Substitution - Missense 1:160292073-160292073 - TCGA-33-4532-01 COSM676749 c.971C>A p.P324Q Substitution - Missense 1:160311973-160311973 - TCGA-BG-A0LX-01 COSM1151880 c.801T>A p.N267K Substitution - Missense 1:160314031-160314031 - CSCC-31-T COSM4448922 c.1443-1G>A p.? Unknown 1:160305774-160305774 - TCGA-C8-A12L-01 COSM1472870 c.1109A>T p.Y370F Substitution - Missense 1:160310226-160310226 - TCGA-EE-A3JD-06 COSM4397002 c.3114C>T p.F1038F Substitution - coding silent 1:160292072-160292072 - TCGA-DD-A1EL-01 COSM4925853 c.251G>T p.R84L Substitution - Missense 1:160335300-160335300 - ATL059 COSM5704978 c.968G>A p.R323Q Substitution - Missense 1:160311976-160311976 - BD177T COSM5517269 c.436A>G p.T146A Substitution - Missense 1:160332508-160332508 - 8057783 COSM1159251 c.1917G>A p.Q639Q Substitution - coding silent 1:160298932-160298932 - TCGA-AC-A3YJ-01 COSM3802494 c.1090C>T p.P364S Substitution - Missense 1:160310245-160310245 - TCGA-EE-A3JD-06 COSM4397003 c.3087C>T p.F1029F Substitution - coding silent 1:160292072-160292072 - 71 COSM5744425 c.1174_1191del18 p.D392_P397delDLYTIP Deletion - In frame 1:160309129-160309146 - TCGA-60-2698-01 COSM1146006 c.1051G>T p.D351Y Substitution - Missense 1:160311893-160311893 - TCGA-29-1761-01 COSM1319825 c.699C>A p.R233R Substitution - coding silent 1:160323438-160323438 - TCGA-AU-6004-01 COSM1335483 c.2679_2681delAGA p.E893delE Deletion - In frame 1:160294506-160294508 - TCGA-AO-A128-01 COSM3802485 c.1497C>T p.D499D Substitution - coding silent 1:160305719-160305719 - ESCC-129T COSM3934190 c.218A>G p.Y73C Substitution - Missense 1:160339919-160339919 - 2492720 COSM5723496 c.2926C>T p.R976C Substitution - Missense 1:160292545-160292545 - RK162_C01 COSM2085608 c.1004A>G p.Y335C Substitution - Missense 1:160311940-160311940 - TCGA-EE-A2A2-06 COSM3476812 c.3433C>T p.L1145L Substitution - coding silent 1:160290674-160290674 - TCGA-B5-A11E-01 COSM1583653 c.3514C>T p.H1172Y Substitution - Missense 1:160290620-160290620 - HT115 COSM2085629 c.599T>C p.V200A Substitution - Missense 1:160325550-160325550 - BD114T COSM5502355 c.2738G>C p.G913A Substitution - Missense 1:160293402-160293402 - RK176_C01 COSM1248964 c.2401A>G p.I801V Substitution - Missense 1:160295811-160295811 - sysucc-834T COSM5485470 c.3627C>A p.I1209I Substitution - coding silent 1:160290507-160290507 - 2334191 COSM319638 c.1331T>C p.I444T Substitution - Missense 1:160306465-160306465 - TCGA-GN-A266-06 COSM3476821 c.2711C>T p.S904F Substitution - Missense 1:160293456-160293456 - TCGA-21-5784-01 COSM1146001 c.2968G>T p.G990C Substitution - Missense 1:160292503-160292503 - BD124T COSM1335483 c.2679_2681delAGA p.E893delE Deletion - In frame 1:160294506-160294508 - TCGA-EB-A41A-01 COSM3476835 c.901C>T p.P301S Substitution - Missense 1:160313109-160313109 - TCGA-AU-6004-01 COSM1335484 c.2652_2654delAGA p.E884delE Deletion - In frame 1:160294506-160294508 - PAPNNX COSM5004921 c.164G>A p.R55Q Substitution - Missense 1:160339973-160339973 - S00501 COSM310283 c.3276C>T p.T1092T Substitution - coding silent 1:160291479-160291479 - T2225 COSM4674158 c.3547C>T p.R1183W Substitution - Missense 1:160290587-160290587 - TCGA-EB-A4IS-01 COSM3476810 c.3541C>T p.P1181S Substitution - Missense 1:160290566-160290566 - ESO-859 COSM1238576 c.1774A>G p.R592G Substitution - Missense 1:160299185-160299185 - PD7199a COSM5781841 c.1143+1G>T p.? Unknown 1:160310191-160310191 - ESCC-002T COSM3934182 c.2154C>G p.I718M Substitution - Missense 1:160297596-160297596 - RK162_C01 COSM2085609 c.1004A>G p.Y335C Substitution - Missense 1:160311940-160311940 - SC_9096 COSM5552315 c.1633G>T p.D545Y Substitution - Missense 1:160305494-160305494 - TCGA-IR-A3LK-01 COSM2085596 c.1301C>T p.S434L Substitution - Missense 1:160307164-160307164 - HCC2998 COSM2085572 c.1647C>A p.I549I Substitution - coding silent 1:160305453-160305453 - TCGA-AN-A046-01 COSM3802481 c.3115C>T p.R1039C Substitution - Missense 1:160292071-160292071 - RK290_C01 COSM4780106 c.3167T>G p.I1056S Substitution - Missense 1:160292019-160292019 - 23 COSM5748415 c.1176_1196del21 p.L393_D399delLYTIPKD Deletion - In frame 1:160309124-160309144 - PTC-14C COSM4142893 c.2396C>A p.P799H Substitution - Missense 1:160295843-160295843 - OSCC-GB_00620111 COSM4881275 c.2686C>A p.P896T Substitution - Missense 1:160293454-160293454 - S00831 COSM5660391 c.453A>G p.V151V Substitution - coding silent 1:160332491-160332491 - Pat_28_B COSM5844172 c.2426C>G p.P809R Substitution - Missense 1:160295813-160295813 - 8064559 COSM1159251 c.1917G>A p.Q639Q Substitution - coding silent 1:160298932-160298932 - 2492722 COSM5723497 c.2899C>T p.R967C Substitution - Missense 1:160292545-160292545 - LP6007544-DNA_A01 COSM5034548 c.2150G>A p.R717H Substitution - Missense 1:160297573-160297573 - tumor_4158726 COSM3356458 c.1076+10A>T p.? Unknown 1:160311858-160311858 - YUDUTY COSM1688956 c.3347A>G p.K1116R Substitution - Missense 1:160291408-160291408 - BD124T COSM5491221 c.2018C>T p.A673V Substitution - Missense 1:160297732-160297732 - TCGA-CA-6718-01 COSM1335509 c.163C>T p.R55* Substitution - Nonsense 1:160339974-160339974 - T3011 COSM2085558 c.2087G>A p.R696H Substitution - Missense 1:160297636-160297636 - 71 COSM5744424 c.2002C>G p.L668V Substitution - Missense 1:160297721-160297721 - TARGET-30-PATDXG COSM898274 c.761G>A p.C254Y Substitution - Missense 1:160314071-160314071 - TCGA-AP-A056-01 COSM898276 c.536C>T p.S179L Substitution - Missense 1:160325613-160325613 - ATL059 COSM5704977 c.968G>A p.R323Q Substitution - Missense 1:160311976-160311976 - TCGA-Q1-A73O-01 COSM1295332 c.3202G>A p.E1068K Substitution - Missense 1:160291902-160291902 - ESCC_13 COSM5625014 c.1942C>G p.R648G Substitution - Missense 1:160298880-160298880 - ESCC-009T COSM3934186 c.702G>C p.M234I Substitution - Missense 1:160323435-160323435 - RK166_C01 COSM1626573 c.96C>T p.V32V Substitution - coding silent 1:160340239-160340239 - NPC2F COSM4995305 c.3617T>A p.V1206E Substitution - Missense 1:160290215-160290215 - SC_9020 COSM5570622 c.3616G>A p.V1206M Substitution - Missense 1:160290216-160290216 - TCGA-B5-A0JY-01 COSM1583650 c.2176C>T p.R726C Substitution - Missense 1:160297574-160297574 - TCGA-ER-A3EV-06 COSM3863266 c.938G>A p.G313D Substitution - Missense 1:160312006-160312006 - TCGA-UB-A7MA-01 COSM4909971 c.2633C>T p.A878V Substitution - Missense 1:160294554-160294554 - SNU-175 COSM1335506 c.512delA p.N171fs*11 Deletion - Frameshift 1:160325637-160325637 - 8057783 COSM1159252 c.1890G>A p.Q630Q Substitution - coding silent 1:160298932-160298932 - 1425-01-01TD COSM5418735 c.3455C>T p.P1152L Substitution - Missense 1:160290652-160290652 - Pat_41_B COSM5844171 c.3226G>A p.E1076K Substitution - Missense 1:160291851-160291851 - TCGA-D3-A2JD-06 COSM3476825 c.1521C>G p.A507A Substitution - coding silent 1:160305695-160305695 - EGC3 COSM5052716 c.303_304insT p.H102fs*3 Insertion - Frameshift 1:160335247-160335248 - TCGA-BS-A0UJ-01 COSM898261 c.2313T>C p.A771A Substitution - coding silent 1:160296100-160296100 - 2492721 COSM5723497 c.2899C>T p.R967C Substitution - Missense 1:160292545-160292545 - TCGA-GN-A266-06 COSM3476822 c.2684C>T p.S895F Substitution - Missense 1:160293456-160293456 - 8067944 COSM4389902 c.3063G>A p.L1021L Substitution - coding silent 1:160292123-160292123 - TCGA-BR-6452-01 COSM4024128 c.3384A>G p.L1128L Substitution - coding silent 1:160291371-160291371 - TCGA-AZ-4315-01 COSM1335505 c.779G>A p.R260H Substitution - Missense 1:160314053-160314053 - GCT28 COSM5749643 c.3224A>T p.K1075I Substitution - Missense 1:160291853-160291853 - OSCC-GB_00620111 COSM4881274 c.2713C>A p.P905T Substitution - Missense 1:160293454-160293454 - TCGA-DA-A1HY-06 COSM3476832 c.1098C>T p.F366F Substitution - coding silent 1:160310237-160310237 - TCGA-CG-5721-01 COSM4024146 c.1292G>A p.R431Q Substitution - Missense 1:160307173-160307173 - HCC131T COSM1601110 c.1116A>C p.P372P Substitution - coding silent 1:160310219-160310219 - T2269 COSM4674167 c.1328A>C p.E443A Substitution - Missense 1:160306468-160306468 - PD24314a COSM5795445 c.310-1G>T p.? Unknown 1:160333680-160333680 - TCGA-AC-A3W5-01 COSM3802484 c.1570A>G p.I524V Substitution - Missense 1:160305530-160305530 - CCRF-CEM COSM1668137 c.3200G>A p.R1067H Substitution - Missense 1:160291904-160291904 - TCGA-A5-A0VP-01 COSM898272 c.842G>A p.R281Q Substitution - Missense 1:160313990-160313990 - TCGA-D3-A5GN-06 COSM3476830 c.1207C>A p.Q403K Substitution - Missense 1:160309113-160309113 - TCGA-EE-A29B-06 COSM3476838 c.843-1G>A p.? Unknown 1:160313168-160313168 - TCGA-AA-3511-01 COSM1335488 c.2636G>T p.G879V Substitution - Missense 1:160294524-160294524 - TCGA-BR-8680-01 COSM4024141 c.1847A>C p.K616T Substitution - Missense 1:160299112-160299112 - CSCC-49-T COSM4465204 c.1371C>T p.F457F Substitution - coding silent 1:160306425-160306425 - T3262 COSM1335507 c.512delA p.N171fs*11 Deletion - Frameshift 1:160325637-160325637 - T3011 COSM2085557 c.2114G>A p.R705H Substitution - Missense 1:160297636-160297636 - TCGA-EE-A17Y-06 COSM3476814 c.3432C>T p.I1144I Substitution - coding silent 1:160290675-160290675 - SJMB008 COSM255448 c.155G>A p.G52D Substitution - Missense 1:160339982-160339982 - sysucc-1317T COSM5448218 c.1600G>A p.A534T Substitution - Missense 1:160305500-160305500 - TCGA-DK-A2I1-01 COSM1295339 c.2021_2022GG>TT p.W674F Substitution - Missense 1:160297701-160297702 - pfg008T COSM1639579 c.841C>T p.R281W Substitution - Missense 1:160313991-160313991 - CSCC-29-T COSM4503404 c.639C>T p.F213F Substitution - coding silent 1:160323498-160323498 - CHC1744T COSM5348016 c.3569delC p.P1190fs*2 Deletion - Frameshift 1:160290565-160290565 - 0091_CRUK_PC_0091_T1_DNA COSM4420898 c.3615C>T p.F1205F Substitution - coding silent 1:160290519-160290519 - TCGA-CA-6718-01 COSM1335508 c.163C>T p.R55* Substitution - Nonsense 1:160339974-160339974 - SC_9090 COSM5572982 c.3643-1G>A p.? Unknown 1:160290217-160290217 - TCGA-A2-A4S3-01 COSM3802480 c.3219G>A p.L1073L Substitution - coding silent 1:160291858-160291858 - TCGA-AN-A0AK-01 COSM3802487 c.1440G>A p.K480K Substitution - coding silent 1:160306356-160306356 - TCGA-BR-8680-01 COSM4024142 c.1820A>C p.K607T Substitution - Missense 1:160299112-160299112 - TCGA-BP-5178-01 COSM1134749 c.444C>G p.D148E Substitution - Missense 1:160332500-160332500 - BD124T COSM1335484 c.2652_2654delAGA p.E884delE Deletion - In frame 1:160294506-160294508 - 459 COSM4436345 c.962G>A p.R321Q Substitution - Missense 1:160311982-160311982 - C0002T COSM2085576 c.1620A>G p.V540V Substitution - coding silent 1:160305480-160305480 - TCGA-B5-A11E-01 COSM1583647 c.1595A>C p.N532T Substitution - Missense 1:160305532-160305532 - Pat_06_B COSM5844174 c.2410C>T p.L804F Substitution - Missense 1:160295829-160295829 - LUAD-RT-S01769 COSM380772 c.167G>A p.G56D Substitution - Missense 1:160339970-160339970 - LUAD-E00918 COSM364917 c.3543A>G p.P1181P Substitution - coding silent 1:160290564-160290564 - PR-09-5630 COSM243813 c.3059G>A p.G1020D Substitution - Missense 1:160292100-160292100 - T3498 COSM2085516 c.2954G>A p.R985H Substitution - Missense 1:160292490-160292490 - TCGA-UB-A7MA-01 COSM4909972 c.2606C>T p.A869V Substitution - Missense 1:160294554-160294554 - LP6007544-DNA_A01 COSM5034547 c.2177G>A p.R726H Substitution - Missense 1:160297573-160297573 - TCGA-A5-A0VP-01 COSM1583642 c.842G>A p.R281Q Substitution - Missense 1:160313990-160313990 - T2269 COSM1127304 c.1291C>T p.R431W Substitution - Missense 1:160307174-160307174 - TCGA-CG-5721-01 COSM4024135 c.2084A>G p.N695S Substitution - Missense 1:160297666-160297666 - TCGA-AN-A046-01 COSM1583654 c.3697C>T p.R1233C Substitution - Missense 1:160290162-160290162 - TCGA-DU-5849-01 COSM3965947 c.1860A>G p.L620L Substitution - coding silent 1:160298962-160298962 - SNUH_G10_S1 COSM3677425 c.297G>A p.T99T Substitution - coding silent 1:160335254-160335254 - HT115 COSM2085628 c.599T>C p.V200A Substitution - Missense 1:160325550-160325550 - YUKLAB COSM1335505 c.779G>A p.R260H Substitution - Missense 1:160314053-160314053 - TCGA-EE-A2A2-06 COSM3476811 c.3460C>T p.L1154L Substitution - coding silent 1:160290674-160290674 - TCGA-A5-A0GD-01 COSM898274 c.761G>A p.C254Y Substitution - Missense 1:160314071-160314071 - HCT8 COSM4633366 c.3075C>T p.L1025L Substitution - coding silent 1:160292111-160292111 - C0002T COSM2085580 c.1611G>A p.E537E Substitution - coding silent 1:160305489-160305489 - ESCC_134 COSM5642653 c.844A>C p.T282P Substitution - Missense 1:160313166-160313166 - TCGA-Q1-A73O-01 COSM1295333 c.3175G>A p.E1059K Substitution - Missense 1:160291902-160291902 - T2269 COSM4674166 c.1328A>C p.E443A Substitution - Missense 1:160306468-160306468 - HCC131 COSM1601109 c.1116A>C p.P372P Substitution - coding silent 1:160310219-160310219 - TCGA-B5-A11E-01 COSM898265 c.1568A>C p.N523T Substitution - Missense 1:160305532-160305532 - S00501 COSM5658067 c.3303C>T p.T1101T Substitution - coding silent 1:160291479-160291479 - ML2 COSM1165460 c.961C>T p.R321W Substitution - Missense 1:160311983-160311983 - PT37 COSM5917104 c.2159G>A p.G720D Substitution - Missense 1:160297591-160297591 - 8067944 COSM4389903 c.3036G>A p.L1012L Substitution - coding silent 1:160292123-160292123 - C0002T COSM2085575 c.1647A>G p.V549V Substitution - coding silent 1:160305480-160305480 - CSCC-18-T COSM4472486 c.1760C>T p.P587L Substitution - Missense 1:160299172-160299172 - T16 COSM3750514 c.363C>T p.N121N Substitution - coding silent 1:160333626-160333626 - TCGA-EJ-5522-01 COSM4674168 c.1291C>T p.R431W Substitution - Missense 1:160307174-160307174 - PD7248a COSM5792058 c.1303-1G>T p.? Unknown 1:160306494-160306494 - S02249 COSM5679942 c.562G>C p.D188H Substitution - Missense 1:160325587-160325587 - TCGA-D1-A17H-01 COSM1151879 c.1559T>A p.I520N Substitution - Missense 1:160305568-160305568 - HCC159 COSM3705163 c.181A>G p.K61E Substitution - Missense 1:160339956-160339956 - TARGET-30-PATDXG COSM1284262 c.754G>A p.V252I Substitution - Missense 1:160314078-160314078 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.162105;Hs.162121 1q23.2 601924 2391295|CGAP|BC038447|G/T|coding|Lys81Asn|331|Candidate; 2391305|CGAP|BC038447|C/T|coding|Asn121Asn|451|Validated Hs.684921;Hs.684922;Hs.684923;Hs.684924;Hs.684925;Hs.684926;Hs.684927;Hs.684928;Hs.684931;Hs.684932;Hs.684933;Hs.684934;Hs.684935;Hs.684936;Hs.684937;Hs.684938;Hs.684939;Hs.684940;Hs.684941;Hs.684942;Hs.684943;Hs.684944;Hs.684945;Hs.684947;Hs.684948;Hs.684949;Hs.684950;Hs.684951;Hs.684953;Hs.684954;Hs.684955;Hs.684956;Hs.684957;Hs.684958;Hs.684959;Hs.684960;Hs.684961;Hs.684962;Hs.684963;Hs.684964;Hs.684965;Hs.684966;Hs.684967;Hs.684968;Hs.684969;Hs.684970;Hs.684971;Hs.684972;Hs.684973;Hs.684974;Hs.684975;Hs.684976;Hs.684977;Hs.684978;Hs.684979;Hs.684981;Hs.684982;Hs.684983;Hs.684984;Hs.684985;Hs.684986;Hs.684987;Hs.684988;Hs.684989;Hs.684990;Hs.684991;Hs.684992;Hs.684993;Hs.684994;Hs.684995;Hs.684996;Hs.684998;Hs.684999;Hs.685001;Hs.685002;Hs.685003;Hs.685004;Hs.685005;Hs.685006;Hs.685007;Hs.685008;Hs.685009;Hs.685010;Hs.685011;Hs.685012;Hs.685013;Hs.685016;Hs.685017;Hs.685020;Hs.685021;Hs.685022;Hs.685023;Hs.685025 1q23.2 601924 2391295|CGAP|BC038447|G/T|coding|Lys81Asn|331|Candidate; 2391305|CGAP|BC038447|C/T|coding|Asn121Asn|451|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.L517R c.1550T>G 1 160275367 UCEC A G Missense p.I444T c.1331T>C 1 160276255 SCLC A G Missense p.L897P c.2690T>C 1 160264287 LUSC A T Missense p.I520N c.1559T>A 1 160275358 UCEC A T Missense p.N267K c.801T>A 1 160283821 UCEC C A Missense p.G1004C c.3010G>T 1 160261966 UCEC C A Missense p.G568W c.1702G>T 1 160269047 LUAD C A Missense p.G990C c.2968G>T 1 160262293 LUSC C A Missense p.K1123N c.3369G>T 1 160261203 RCCC C A Missense p.R525L c.1574G>T 1 160275343 LUAD C A Missense p.R581L c.1742G>T 1 160269007 LUAD C A SpliceAcceptorSNV . c.926-1G>T 1 160281809 LUSC C A Synonymous p.G31G c.93G>T 1 160310032 RCCC CC AA Missense p.W683F c.2048_2049delinsTT 1 160267491 BLCA C G Missense p.G70A c.209G>C 1 160309718 HNSC C G Missense p.Q763H c.2289G>C 1 160267134 BLCA C - IntronicDeletion . c.842+1delG 1 160283779 HNSC CTC - 5-UTRDeletion . c.1-12_1-10delGAG 1 160312970 ESCA C T Missense p.E546K c.1636G>A 1 160275281 HNSC C T Missense p.G313D c.938G>A 1 160281796 CM C T Missense p.R1136H c.3407G>A 1 160261165 UCEC C T Missense p.R281Q c.842G>A 1 160283780 UCEC C T Missense p.R726H c.2177G>A 1 160267363 HNSC C T Missense p.R976H c.2927G>A 1 160262334 HNSC C T Missense p.V252I c.754G>A 1 160283868 NB C T Nonsense p.W120* c.360G>A 1 160303419 HNSC C T SpliceAcceptorSNV . c.843-1G>A 1 160282958 CM C T SpliceDonorSNV . c.2850+1G>A 1 160262955 BLCA C T Synonymous p.K438K c.1314G>A 1 160276272 HNSC C T Synonymous p.K997K c.2991G>A 1 160261985 CM C T Synonymous p.Q639Q c.1917G>A 1 160268722 PAAD C T Synonymous p.R39R c.117G>A 1 160310008 CM C T Synonymous p.R950R c.2850G>A 1 160262956 CM C T Synonymous p.V624V c.1872G>A 1 160268767 LUAD CTTCCCTACAGAGGGAAGGA - SpliceAcceptorDeletion . c.2504-15_2508delTCCTTCCCTCTGTAGGGAAG 1 160264643 HNSC CTTGACA - Frameshift p.F650Lfs*71 c.1950_1956delTGTCAAG 1 160268683 LUAD G A 3-UTRSNV . c.3699+84C>T 1 160259866 CM G A Missense p.H102Y c.304C>T 1 160305037 CM G A Missense p.L879F c.2635C>T 1 160264342 BRCA G A Missense p.P1195L c.3584C>T 1 160260340 CM G A Missense p.P603L c.1808C>T 1 160268941 OV G A Missense p.R1183W c.3547C>T 1 160260377 CM G A Missense p.R281W c.841C>T 1 160283781 STAD G A Missense p.R431W c.1291C>T 1 160276964 PRAD G A Missense p.S1202F c.3605C>T 1 160260319 CM G A Missense p.S944F c.2831C>T 1 160262975 CM G A Synonymous p.F1038F c.3114C>T 1 160261862 CM G A Synonymous p.F346F c.1038C>T 1 160281696 HNSC G A Synonymous p.F366F c.1098C>T 1 160280027 CM G A Synonymous p.G853G c.2559C>T 1 160264592 CM G A Synonymous p.G975G c.2925C>T 1 160262336 CM G A Synonymous p.I1153I c.3459C>T 1 160260465 CM G A Synonymous p.L1154L c.3460C>T 1 160260464 CM G A Synonymous p.L748L c.2242C>T 1 160267181 CM G A Synonymous p.L897L c.2691C>T 1 160264286 LUSC G A Synonymous p.L951L c.2853C>T 1 160262408 CM G A Synonymous p.P596P c.1788C>T 1 160268961 GBM G A Synonymous p.S823S c.2469C>T 1 160265560 CM G A Synonymous p.S9S c.27C>T 1 160312934 HNSC G A Synonymous p.T1101T c.3303C>T 1 160261269 SCLC G C Missense p.D148E c.444C>G 1 160302290 RCCC G C Missense p.L1082V c.3244C>G 1 160261650 BRCA G C Synonymous p.A507A c.1521C>G 1 160275485 CM G T Missense p.H291N c.871C>A 1 160282929 BLCA G T Missense p.P324Q c.971C>A 1 160281763 LUSC G T Missense p.P514H c.1541C>A 1 160275376 CM G T Missense p.P789Q c.2366C>A 1 160265864 LUAD G T Synonymous p.R339R c.1015C>A 1 160281719 CM T A Missense p.N1119Y c.3355A>T 1 160261217 ESCA T A Missense p.T390S c.1168A>T 1 160278942 UCEC T A Missense p.Y370F c.1109A>T 1 160280016 BRCA TCCTTTCT - Frameshift p.R735Hfs*13 c.2203_2210delAGAAAGGA 1 160267213 RCCC T C Missense p.E1192G c.3575A>G 1 160260349 LUSC T C Missense p.I537V c.1609A>G 1 160275308 LUAD T C Missense p.I810V c.2428A>G 1 160265601 ESCA T C Missense p.M1096V c.3286A>G 1 160261286 LUSC T C Missense p.N1119D c.3355A>G 1 160261217 RCCC T C Synonymous p.L629L c.1887A>G 1 160268752 LGG - T Frameshift p.N171Kfs*18 c.512dupA 1 160295427 CM TGTG - IntronicDeletion . c.310-290_310-287delCACA 1 160303756 CM